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{{Short description|Methods to achieve pregnancy by artificial or partially artificial means}}
{{Infobox medical intervention
{{Infobox medical intervention
| Name = Assisted reproductive technology
| Name = Assisted reproductive technology
| Image = Blausen 0060 AssistedReproductiveTechnology.png
| Image = Blausen 0060 AssistedReproductiveTechnology.png
| Caption = Illustration depicting intracytoplasmic sperm injection (ICSI), an example of assisted reproductive technology.
| Caption = Illustration depicting intracytoplasmic sperm injection (ICSI), an example of assisted reproductive technology
| ICD10 =
| ICD10 =
| ICD9 =
| ICD9 =
| MeshID = D027724
| MeshID = D027724
| OPS301 =
| OPS301 =
| OtherCodes =
| Synonyms =ART
}}
}}
'''Assisted reproductive technology''' ('''ART''') are medical procedures used primarily to address [[infertility]]. It includes procedures such as [[in vitro fertilization]]. It may include [[intracytoplasmic sperm injection]] (ICSI), [[cryopreservation]] of gametes or embryos, and/or may involve the use of [[fertility medication]]. When used to address infertility, it may also be referred to as '''fertility treatment.''' ART mainly belongs to the field of [[reproductive endocrinology and infertility]]. Some forms of ART are also used with regard to fertile couples for genetic reasons ([[preimplantation genetic diagnosis]]). ART may also be used in [[surrogacy]] arrangements, although not all surrogacy arrangements involve ART.
'''Assisted reproductive technology''' ('''ART''') includes medical procedures used primarily to address [[infertility]]. This subject involves procedures such as [[in vitro fertilization]] (IVF), [[intracytoplasmic sperm injection]] (ICSI), [[cryopreservation]] of gametes or embryos, and/or the use of [[fertility medication]]. When used to address infertility, ART may also be referred to as '''fertility treatment.''' ART mainly belongs to the field of [[reproductive endocrinology and infertility]]. Some forms of ART may be used with regard to fertile couples for genetic purpose (see [[preimplantation genetic diagnosis]]). ART may also be used in [[surrogacy]] arrangements, although not all surrogacy arrangements involve ART.
The existence of sterility will not always require ART to be the first option to consider, as there are occasions when its cause is a mild disorder that can be solved with more conventional treatments or with behaviors based on promoting health and reproductive habits.


== Procedures ==
== Procedures ==
=== General ===
=== General ===
With ART, the process of [[sexual intercourse]] is bypassed and fertilization of the [[oocyte]]s occurs in the laboratory environment (i.e., [[in vitro fertilization]]).
With ART, the process of [[sexual intercourse]] is bypassed and fertilization of the [[oocyte]]s occurs in the laboratory environment (i.e., [[in vitro fertilization]]).{{citation needed|date=February 2022}}


In the US, the [[Centers for Disease Control and Prevention]] (CDC)—which is required as a result of the 1992 ''Fertility Clinic Success Rate and Certification Act'' to publish the annual ART success rates at U.S. fertility clinics—defines ART to include "all fertility treatments in which both eggs and sperm are handled. In general, ART procedures involve surgically removing eggs from a woman's ovaries, combining them with sperm in the laboratory, and returning them to the woman's body or donating them to another woman." According to CDC, "they do not include treatments in which only sperm are handled (i.e., intrauterine—or artificial—insemination) or procedures in which a woman takes medicine only to stimulate egg production without the intention of having eggs retrieved."<ref>{{cite web|title=What is Assisted Reproductive Technology? {{!}} Reproductive Health {{!}} CDC|url=https://www.cdc.gov/art/whatis.html|publisher=CDC|date=November 14, 2014|url-status=live|archiveurl=https://web.archive.org/web/20171101183209/https://www.cdc.gov/art/whatis.html|archivedate=November 1, 2017}}</ref>
In the US, the [[Centers for Disease Control and Prevention]] (CDC) defines ART to include "all fertility treatments in which both eggs and sperm are handled. In general, ART procedures involve surgically removing eggs from a woman's ovaries, combining them with sperm in the laboratory, and returning them to the woman's body or donating them to another woman." According to CDC, "they do not include treatments in which only sperm are handled (i.e., intrauterine—or artificial—insemination) or procedures in which a woman takes medicine only to stimulate egg production without the intention of having eggs retrieved."<ref>{{cite web|title=What is Assisted Reproductive Technology? {{!}} Reproductive Health {{!}} CDC|url=https://www.cdc.gov/art/whatis.html|publisher=CDC|date=November 14, 2014|url-status=live|archive-url=https://web.archive.org/web/20171101183209/https://www.cdc.gov/art/whatis.html|archive-date=November 1, 2017}}</ref>


In Europe, ART also excludes artificial insemination and includes only procedures where oocytes are handled.<ref>{{cite journal|last1=European IVF-Monitoring Consortium (EIM) for the European Society of Human Reproduction and Embryology|last2=Calhaz-Jorge|first2=C.|display-authors=et al|last10=Wyns|title=Assisted reproductive technology in Europe, 2012: results generated from European registers by ESHRE.|journal=Human Reproduction (Oxford, England)|date=August 2016|volume=31|issue=8|pages=1638–52|pmid=27496943|doi=10.1093/humrep/dew151}}</ref><ref>{{cite journal|last1=Sorenson|first1=Corinna|title=ART in the European Union|journal=Euro Observer Euro Observer|date=Autumn 2006|volume=8|issue=4|url=http://www.euro.who.int/__data/assets/pdf_file/0019/80371/EuroObserver8_4.pdf?ua=1|url-status=live|archiveurl=https://web.archive.org/web/20161129022850/http://www.euro.who.int/__data/assets/pdf_file/0019/80371/EuroObserver8_4.pdf?ua=1|archivedate=2016-11-29}}</ref>
In Europe, ART also excludes artificial insemination and includes only procedures where oocytes are handled.<ref>{{cite journal|last1=European IVF-Monitoring Consortium (EIM) for the European Society of Human Reproduction and Embryology|last2=Calhaz-Jorge|first2=C.|display-authors=et al|last10=Wyns|title=Assisted reproductive technology in Europe, 2012: results generated from European registers by ESHRE.|journal=Human Reproduction (Oxford, England)|date=August 2016|volume=31|issue=8|pages=1638–52|pmid=27496943|doi=10.1093/humrep/dew151|doi-access=free}}</ref><ref>{{cite journal|last1=Sorenson|first1=Corinna|title=ART in the European Union|journal=Euro Observer Euro Observer|date=Autumn 2006|volume=8|issue=4|url=http://www.euro.who.int/__data/assets/pdf_file/0019/80371/EuroObserver8_4.pdf?ua=1|url-status=live|archive-url=https://web.archive.org/web/20161129022850/http://www.euro.who.int/__data/assets/pdf_file/0019/80371/EuroObserver8_4.pdf?ua=1|archive-date=2016-11-29}}</ref>


The WHO, or World Health Organization, also defines ART this way.<ref>{{cite journal|last1=Zegers-Hochschild|first1=F|display-authors=et al|last2=for the International Committee for Monitoring Assisted Reproductive Technology and the World Health Organization|title=International Committee for Monitoring Assisted Reproductive Technology (ICMART) and the World Health Organization (WHO) revised glossary of ART terminology, 2009.|journal=Fertility and Sterility|date=November 2009|volume=92|issue=5|pages=1520–4|pmid=19828144|url=http://www.who.int/reproductivehealth/publications/infertility/art_terminology2.pdf?ua=1|doi=10.1016/j.fertnstert.2009.09.009|url-status=live|archiveurl=https://web.archive.org/web/20161129024154/http://www.who.int/reproductivehealth/publications/infertility/art_terminology2.pdf?ua=1|archivedate=2016-11-29}}</ref>
The [[World Health Organization]] (WHO), also defines ART this way.<ref>{{cite journal|last1=Zegers-Hochschild|first1=F|display-authors=et al|last2=for the International Committee for Monitoring Assisted Reproductive Technology and the World Health Organization|title=International Committee for Monitoring Assisted Reproductive Technology (ICMART) and the World Health Organization (WHO) revised glossary of ART terminology, 2009.|journal=Fertility and Sterility|date=November 2009|volume=92|issue=5|pages=1520–4|pmid=19828144|url=https://www.who.int/reproductivehealth/publications/infertility/art_terminology2.pdf?ua=1|doi=10.1016/j.fertnstert.2009.09.009|url-status=live|archive-url=https://web.archive.org/web/20161129024154/http://www.who.int/reproductivehealth/publications/infertility/art_terminology2.pdf?ua=1|archive-date=2016-11-29}}</ref>


=== Ovulation induction ===
=== Ovulation induction ===
{{Main|Ovulation induction}}
{{Main|Ovulation induction}}
[[Ovulation induction]] is usually used in the sense of stimulation of the development of [[ovarian follicles]]<ref name=advancedfertility>[http://www.advancedfertility.com/inducovu.htm Ovulation Problems and Infertility: Treatment of ovulation problems with Clomid and other fertility drugs.] Advanced Fertility Center of Chicago. Gurnee & Crystal Lake, Illinois. Retrieved on Mars 7, 2010</ref><ref name=flinders>[http://www.flindersivf.com.au/resources/ovulation.induction/ Flinders reproductive medicine > Ovulation Induction] {{Webarchive|url=https://web.archive.org/web/20091003075946/http://www.flindersivf.com.au/resources/ovulation.induction/ |date=2009-10-03 }} Retrieved on Mars 7, 2010</ref><ref>[http://www.fertilitylifelines.com/fertilitytreatments/ovulationinduction.jsp fertilityLifeLines > Ovulation Induction] {{Webarchive|url=https://web.archive.org/web/20130310222621/http://www.fertilitylifelines.com/fertilitytreatments/ovulationinduction.jsp |date=2013-03-10 }} Retrieved on Mars 7, 2010</ref> by [[fertility medication]] to reverse [[anovulation]] or [[oligoovulation]].
[[Ovulation induction]] is usually used in the sense of stimulation of the development of [[ovarian follicles]]<ref name=advancedfertility>[http://www.advancedfertility.com/inducovu.htm Ovulation Problems and Infertility: Treatment of ovulation problems with Clomid and other fertility drugs.] Advanced Fertility Center of Chicago. Gurnee & Crystal Lake, Illinois. Retrieved on Mars 7, 2010</ref><ref name=flinders>[http://www.flindersivf.com.au/resources/ovulation.induction/ Flinders reproductive medicine > Ovulation Induction] {{Webarchive|url=https://web.archive.org/web/20091003075946/http://www.flindersivf.com.au/resources/ovulation.induction/ |date=2009-10-03 }} Retrieved on Mars 7, 2010</ref><ref>[http://www.fertilitylifelines.com/fertilitytreatments/ovulationinduction.jsp fertilityLifeLines > Ovulation Induction] {{Webarchive|url=https://web.archive.org/web/20130310222621/http://www.fertilitylifelines.com/fertilitytreatments/ovulationinduction.jsp |date=2013-03-10 }} Retrieved on Mars 7, 2010</ref> by [[fertility medication]] to reverse [[anovulation]] or [[oligoovulation]]. These medications are given by injection for 8 to 14 days. A health care provider closely monitors the development of the eggs using transvaginal ultrasound and blood tests to assess follicle growth and estrogen production by the ovaries. When follicles have reached an adequate size and the eggs are mature enough, an injection of the hormone hCG initiates the ovulation process. Egg retrieval should occur 36 hours before ovulation.


=== In vitro fertilization ===
=== In vitro fertilization ===
{{See|In vitro fertilization}}
{{Further|In vitro fertilization}}
[[File:2902 IVF-02.jpg|thumb|315x315px|Steps of IVF Treatment]]
In [[vitro fertilization]] is the technique of letting [[fertilization]] of the male and female [[gametes]] (sperm and egg) occur outside the female body.
[[In vitro fertilization]] is the technique of letting [[Human fertilization|fertilization]] of the male and female [[gametes]] (sperm and egg) occur outside the female body.


Techniques usually used in in vitro fertilization include:
Techniques usually used in in vitro fertilization include:
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Less commonly used techniques in in vitro fertilization are:
Less commonly used techniques in in vitro fertilization are:
* [[Assisted zona hatching]] (AZH) is performed shortly before the embryo is transferred to the uterus. A small opening is made in the outer layer surrounding the egg in order to help the embryo hatch out and aid in the implantation process of the growing embryo.
* [[Assisted zona hatching]] (AZH) is performed shortly before the embryo is transferred to the uterus. A small opening is made in the outer layer surrounding the egg in order to help the embryo hatch out and aid in the implantation process of the growing embryo.
* [[File:In vitro fertilization.jpg|right|250px|thumb|Intracytoplasmic sperm injection (ICSI)]][[Intracytoplasmic sperm injection]] (ICSI) is beneficial in the case of male factor infertility where sperm counts are very low or failed fertilization occurred with previous IVF attempt(s). The ICSI procedure involves a single sperm carefully injected into the center of an egg using a microneedle. With ICSI, only one sperm per egg is needed. Without ICSI, you need between 50,000 and 100,000. This method is also sometimes employed when donor sperm is used.
* [[File:In vitro fertilization.jpg|right|250px|thumb|Intracytoplasmic sperm injection (ICSI)]] [[Intracytoplasmic sperm injection]] (ICSI) is beneficial in the case of male factor infertility where sperm counts are very low or failed fertilization occurred with previous IVF attempt(s). The ICSI procedure involves a single sperm carefully injected into the center of an egg using a microneedle. With ICSI, only one sperm per egg is needed. Without ICSI, you need between 50,000 and 100,000. This method is also sometimes employed when donor sperm is used.
* [[Autologous endometrial coculture]] is a possible treatment for patients who have failed previous IVF attempts or who have poor embryo quality. The patient's fertilized eggs are placed on top of a layer of cells from the patient's own uterine lining, creating a more natural environment for embryo development.
* [[Autologous endometrial coculture]] is a possible treatment for patients who have failed previous IVF attempts or who have poor embryo quality. The patient's fertilized eggs are placed on top of a layer of cells from the patient's own uterine lining, creating a more natural environment for embryo development.
* In [[zygote intrafallopian transfer]] (ZIFT), egg cells are removed from the woman's ovaries and fertilized in the laboratory; the resulting zygote is then placed into the fallopian tube.
* In [[zygote intrafallopian transfer]] (ZIFT), egg cells are removed from the woman's ovaries and fertilized in the laboratory; the resulting zygote is then placed into the fallopian tube.
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* [[Sperm donation]] may provide the source for the sperm used in IVF procedures where the male partner produces no sperm or has an inheritable disease, or where the woman being treated has no male partner.
* [[Sperm donation]] may provide the source for the sperm used in IVF procedures where the male partner produces no sperm or has an inheritable disease, or where the woman being treated has no male partner.
* [[Preimplantation genetic diagnosis]] (PGD) involves the use of genetic screening mechanisms such as fluorescent in-situ hybridization (FISH) or comparative genomic hybridization (CGH) to help identify genetically abnormal embryos and improve healthy outcomes.
* [[Preimplantation genetic diagnosis]] (PGD) involves the use of genetic screening mechanisms such as fluorescent in-situ hybridization (FISH) or comparative genomic hybridization (CGH) to help identify genetically abnormal embryos and improve healthy outcomes.
* [[Embryo splitting (disambiguation)|Embryo splitting]] can be used for twinning to increase the number of available embryos.<ref>{{cite journal |vauthors=Illmensee K, Levanduski M, Vidali A, Husami N, Goudas VT |title=Human embryo twinning with applications in reproductive medicine |journal=Fertil. Steril. |volume= 93|issue= 2|pages= 423–7|date=February 2009 |pmid=19217091 |doi=10.1016/j.fertnstert.2008.12.098 |url=}}</ref>
* [[Embryo splitting (disambiguation)|Embryo splitting]] can be used for twinning to increase the number of available embryos.<ref>{{cite journal |vauthors=Illmensee K, Levanduski M, Vidali A, Husami N, Goudas VT |title=Human embryo twinning with applications in reproductive medicine |journal=Fertil. Steril. |volume= 93|issue= 2|pages= 423–7|date=February 2009 |pmid=19217091 |doi=10.1016/j.fertnstert.2008.12.098 |doi-access=free }}</ref>


=== Pre-implantation genetic diagnosis ===
=== Pre-implantation genetic diagnosis ===
A [[pre-implantation genetic diagnosis]] procedure may be conducted on [[embryo]]s prior to [[Implantation (human embryo)|implantation]] (as a form of [[embryo profiling]]), and sometimes even of [[oocyte]]s prior to [[Fertilisation|fertilization]]. PGD is considered in a similar fashion to [[prenatal diagnosis]]. When used to screen for a specific [[genetic disease]], its main advantage is that it avoids selective [[abortion|pregnancy termination]] as the method makes it highly likely that the baby will be free of the disease under consideration.<ref>{{Cite news|url=https://www.technologyreview.com/s/612258/are-we-designing-inequality-into-our-genes/|title=Designer babies aren't futuristic. They're already here.|last=Hercher|first=Laura|date=2018-10-22|work=MIT Technology Review|access-date=2018-10-26|language=en}}</ref> PGD thus is an adjunct to ART procedures, and requires in vitro fertilization to obtain [[oocytes]] or [[embryo]]s for evaluation. Embryos are generally obtained through blastomere or blastocyst biopsy. The latter technique has proved to be less deleterious for the embryo, therefore it is advisable to perform the biopsy around day 5 or 6 of development.<ref name=Sullivan-Pyke2018>{{cite journal |last1=Sullivan-Pyke |first1=C |last2=Dokras |first2=A |title=Preimplantation Genetic Screening and Preimplantation Genetic Diagnosis. |journal=Obstetrics and Gynecology Clinics of North America |date=March 2018 |volume=45 |issue=1 |pages=113–125 |doi=10.1016/j.ogc.2017.10.009 |pmid=29428279}}</ref> [[Sex selection]] is the attempt to control the sex of offspring to achieve a desired sex. It can be accomplished in several ways, both pre- and post-implantation of an embryo, as well as at birth. Pre-implantation techniques include PGD, but also [[sperm sorting]].
A [[pre-implantation genetic diagnosis]] procedure may be conducted on [[embryo]]s prior to [[Implantation (human embryo)|implantation]] (as a form of [[embryo profiling]]), and sometimes even of [[oocyte]]s prior to [[Human fertilization|fertilization]]. PGD is considered in a similar fashion to [[prenatal diagnosis]]. PGD is an adjunct to ART procedures, and requires in vitro fertilization to obtain [[oocytes]] or [[embryo]]s for evaluation. Embryos are generally obtained through blastomere or blastocyst biopsy. The latter technique has proved to be less deleterious for the embryo, therefore it is advisable to perform the biopsy around day 5 or 6 of development.<ref name=Sullivan-Pyke2018>{{cite journal |last1=Sullivan-Pyke |first1=C |last2=Dokras |first2=A |title=Preimplantation Genetic Screening and Preimplantation Genetic Diagnosis. |journal=Obstetrics and Gynecology Clinics of North America |date=March 2018 |volume=45 |issue=1 |pages=113–125 |doi=10.1016/j.ogc.2017.10.009 |pmid=29428279}}</ref> [[Sex selection]] is the attempt to control the sex of offspring to achieve a desired sex in case of X chromosome linked diseases. It can be accomplished in several ways, both pre- and post-implantation of an embryo, as well as at birth. Pre-implantation techniques include PGD, but also [[sperm sorting]].{{citation needed|date=February 2022}}


=== Others ===
=== Others ===
Other assisted reproduction techniques include:
Other assisted reproduction techniques include:
* [[Mitochondrial replacement therapy]] (MRT, sometimes called mitochondrial donation) is the replacement of [[mitochondria]] in one or more cells to prevent or ameliorate disease. MRT originated as a special form of IVF in which some or all of the future baby's [[mitochondrial DNA]] comes from a third party. This technique is used in cases when mothers carry genes for [[mitochondrial diseases]]. The therapy is approved for use in the United Kingdom.<ref name=NAS2016ethics>{{cite book|last1=Committee on the Ethical and Social Policy Considerations of Novel Techniques for Prevention of Maternal Transmission of Mitochondrial DNA Diseases|last2=Board on Health Sciences Policy|last3=Institute of Medicine|editor1-last=Claiborne|editor1-first=Anne|editor2-last=English|editor2-first=Rebecca|editor3-last=Kahn|editor3-first=Jeffrey|title=Mitochondrial Replacement Techniques: Ethical, Social, and Policy Considerations|date=2016|publisher=National Academies Press|isbn=978-0-309-38870-2|url=https://www.nap.edu/read/21871/chapter/1}} [http://nationalacademies.org/hmd/reports/2016/Mitochondrial-Replacement-Techniques Index page] with links to summaries including [http://www.nationalacademies.org/hmd/~/media/Files/Report%20Files/2016/Mitochondrial%20Replacement%20Techniques/mito%20ethics%20infographic_FINAL.pdf one page summary flyer].</ref><ref name=2015CreeRev>{{cite journal|last1=Cree|first1=L|last2=Loi|first2=P|title=Mitochondrial replacement: from basic research to assisted reproductive technology portfolio tool-technicalities and possible risks.|journal=Molecular Human Reproduction|date=January 2015|volume=21|issue=1|pages=3–10|pmid=25425606|doi=10.1093/molehr/gau082}} {{open access}}</ref>
* [[Mitochondrial replacement therapy]] (MRT, sometimes called mitochondrial donation) is the replacement of [[mitochondria]] in one or more cells to prevent or ameliorate disease. MRT originated as a special form of IVF in which some or all of the future baby's [[mitochondrial DNA]] comes from a third party. This technique is used in cases when mothers carry genes for [[mitochondrial diseases]]. The therapy is approved for use in the United Kingdom.<ref>{{Cite journal |last=Scully |first=Jackie Leach |date=January 2017 |title=A Mitochondrial Story: Mitochondrial Replacement, Identity and Narrative |url=https://pubmed.ncbi.nlm.nih.gov/27973722/ |journal=Bioethics |volume=31 |issue=1 |pages=37–45 |doi=10.1111/bioe.12310 |issn=1467-8519 |pmid=27973722|hdl=1959.4/unsworks_66960 |hdl-access=free }}</ref><ref name=NAS2016ethics>{{cite book|editor1-last=Claiborne|editor1-first=Anne|editor2-last=English|editor2-first=Rebecca|editor3-last=Kahn|editor3-first=Jeffrey|title=Mitochondrial Replacement Techniques: Ethical, Social, and Policy Considerations|date=2016|publisher=National Academies Press|doi=10.17226/21871 |pmid=27054230 |isbn=978-0-309-38870-2|url=https://www.nap.edu/read/21871/chapter/1|last1=Claiborne |first1=A. |last2=English |first2=R. |last3=Kahn |first3=J. }} [http://nationalacademies.org/hmd/reports/2016/Mitochondrial-Replacement-Techniques Index page] {{Webarchive|url=https://web.archive.org/web/20181126135516/http://www.nationalacademies.org/hmd/reports/2016/Mitochondrial-Replacement-Techniques |date=2018-11-26 }} with links to summaries including [http://www.nationalacademies.org/hmd/~/media/Files/Report%20Files/2016/Mitochondrial%20Replacement%20Techniques/mito%20ethics%20infographic_FINAL.pdf one page summary flyer] {{Webarchive|url=https://web.archive.org/web/20171030233717/http://www.nationalacademies.org/hmd/~/media/Files/Report%20Files/2016/Mitochondrial%20Replacement%20Techniques/mito%20ethics%20infographic_FINAL.pdf |date=2017-10-30 }}.</ref><ref name=2015CreeRev>{{cite journal|last1=Cree|first1=L|last2=Loi|first2=P|title=Mitochondrial replacement: from basic research to assisted reproductive technology portfolio tool-technicalities and possible risks.|journal=Molecular Human Reproduction|date=January 2015|volume=21|issue=1|pages=3–10|pmid=25425606|doi=10.1093/molehr/gau082|doi-access=free}} {{open access}}</ref>
* In [[gamete intrafallopian transfer]] (GIFT) a mixture of sperm and eggs is placed directly into a woman's fallopian tubes using laparoscopy following a transvaginal ovum retrieval.
* In [[gamete intrafallopian transfer]] (GIFT), a mixture of sperm and eggs is placed directly into a woman's fallopian tubes using laparoscopy following a transvaginal ovum retrieval.
* [[Reproductive surgery]], treating e.g. [[fallopian tube obstruction]] and [[vas deferens obstruction]], or reversing a [[vasectomy]] by a [[reverse vasectomy]]. In [[surgical sperm retrieval]] (SSR) the reproductive urologist obtains sperm from the vas deferens, epididymis or directly from the testis in a short outpatient procedure.
* [[Reproductive surgery]], treating e.g. [[fallopian tube obstruction]] and [[vas deferens obstruction]], or reversing a [[vasectomy]] by a [[reverse vasectomy]]. In [[surgical sperm retrieval]] (SSR), the reproductive urologist obtains sperm from the vas deferens, epididymis or directly from the testis in a short outpatient procedure.
* By [[cryopreservation]], eggs, sperm and reproductive tissue can be preserved for later IVF.
* By [[cryopreservation]], eggs, sperm and reproductive tissue can be preserved for later IVF.


== Risks ==
== Risks ==
The majority of IVF-conceived infants do not have [[congenital disorder|birth defects]].<ref name="Van Voorhis 2007">{{cite journal |author=Van Voorhis BJ |year=2007 |title=Clinical practice. In vitro fertilization |journal=[[New England Journal of Medicine|N Engl J Med]] |volume=356 |issue=4 |pages=379–86 |pmid=17251534 |doi=10.1056/NEJMcp065743}}</ref>
The majority of IVF-conceived infants do not have [[congenital disorder|birth defects]].<ref name="Van Voorhis 2007">{{cite journal |author=Van Voorhis BJ |year=2007 |title=Clinical practice. In vitro fertilization |journal=[[New England Journal of Medicine|N Engl J Med]] |volume=356 |issue=4 |pages=379–86 |pmid=17251534 |doi=10.1056/NEJMcp065743}}</ref>
However, some studies have suggested that assisted reproductive technology is associated with an increased risk of birth defects.<ref name="Kurinczuk 2004">{{cite journal |vauthors=Kurinczuk JJ, Hansen M, Bower C |year=2004 |title=The risk of birth defects in children born after assisted reproductive technologies |journal=Current Opinion in Obstetrics and Gynecology |volume=16 |issue=3 |pages=201–9 |pmid=15129049 |doi=10.1097/00001703-200406000-00002}}</ref><ref name="Hansen 2005">{{cite journal |vauthors=Hansen M, Bower C, Milne E, de Klerk N, Kurinczuk JJ |year=2005 |title=Assisted reproductive technologies and the risk of birth defects—a systematic review |journal=Hum Reprod |volume=20 |issue=2 |pages=328–38 |pmid=15567881 |doi=10.1093/humrep/deh593}}</ref>
However, some studies have suggested that assisted reproductive technology is associated with an increased risk of birth defects.<ref name="Kurinczuk 2004">{{cite journal |vauthors=Kurinczuk JJ, Hansen M, Bower C |year=2004 |title=The risk of birth defects in children born after assisted reproductive technologies |journal=Current Opinion in Obstetrics and Gynecology |volume=16 |issue=3 |pages=201–9 |pmid=15129049 |doi=10.1097/00001703-200406000-00002|s2cid=23159787 }}</ref><ref name="Hansen 2005">{{cite journal |vauthors=Hansen M, Bower C, Milne E, de Klerk N, Kurinczuk JJ |year=2005 |title=Assisted reproductive technologies and the risk of birth defects—a systematic review |journal=Hum Reprod |volume=20 |issue=2 |pages=328–38 |pmid=15567881 |doi=10.1093/humrep/deh593|doi-access=free }}</ref>
Artificial reproductive technology is becoming more available. Early studies suggest that there could be an increased risk for medical complications with both the mother and baby. Some of these include low birth weight, placental insufficiency, chromosomal disorders, preterm deliveries, gestational diabetes, and pre-eclampsia(Aiken and Brockelsby).<ref>{{Cite journal|doi=10.1017/S096553951600005X|title=Fetal and Maternal Consequences of Pregnancies Conceived Using Art|journal=Fetal and Maternal Medicine Review|volume=25|issue=3–4|pages=281–294|year=2016|last1=Aiken|first1=Catherine E. M.|last2=Brockelsby|first2=Jeremy C.}}</ref>
Artificial reproductive technology is becoming more available. Early studies suggest that there could be an increased risk for medical complications with both the mother and baby. Some of these include low birth weight, placental insufficiency, chromosomal disorders, preterm deliveries, gestational diabetes, and [[pre-eclampsia]] (Aiken and Brockelsby).<ref>{{Cite journal|doi=10.1017/S096553951600005X|title=Fetal and Maternal Consequences of Pregnancies Conceived Using Art|journal=Fetal and Maternal Medicine Review|volume=25|issue=3–4|pages=281–294|year=2016|last1=Aiken|first1=Catherine E. M.|last2=Brockelsby|first2=Jeremy C.}}</ref>


In the largest U.S. study, which used data from a statewide registry of birth defects,<ref name="Olson 2005">{{cite journal |vauthors=Olson CK, Keppler-Noreuil KM, Romitti PA, Budelier WT, Ryan G, Sparks AE, Van Voorhis BJ |year=2005 |title=In vitro fertilization is associated with an increase in major birth defects |journal=Fertil Steril |volume=84 |issue=5 |pages=1308–15 |pmid=16275219 |doi=10.1016/j.fertnstert.2005.03.086}}</ref>
In the largest U.S. study, which used data from a statewide registry of birth defects,<ref name="Olson 2005">{{cite journal |vauthors=Olson CK, Keppler-Noreuil KM, Romitti PA, Budelier WT, Ryan G, Sparks AE, Van Voorhis BJ |year=2005 |title=In vitro fertilization is associated with an increase in major birth defects |journal=Fertil Steril |volume=84 |issue=5 |pages=1308–15 |pmid=16275219 |doi=10.1016/j.fertnstert.2005.03.086}}</ref>
Line 62: Line 65:
The main risks are:
The main risks are:
* [[Genetic disorder]]s
* [[Genetic disorder]]s
* [[Low birth weight]].<ref>{{Cite web|url=https://medlineplus.gov/ency/article/007279.htm|title=In vitro fertilization (IVF): MedlinePlus Medical Encyclopedia|website=medlineplus.gov|language=en|access-date=2018-11-07}}</ref> In IVF and ICSI, a risk factor is the decreased expression of proteins in [[energy metabolism]]; [[Ferritin light chain]] and [[ATP5A1]].<ref name=zhang>{{cite journal |vauthors=Zhang Y, Zhang YL, Feng C |title=Comparative proteomic analysis of human placenta derived from assisted reproductive technology |journal=Proteomics |volume= 8|issue= 20|pages= 4344–56|date=September 2008 |pmid=18792929 |doi=10.1002/pmic.200800294 |url=|display-authors=etal}}</ref>
* [[Low birth weight]].<ref>{{Cite web|url=https://medlineplus.gov/ency/article/007279.htm|title=In vitro fertilization (IVF): MedlinePlus Medical Encyclopedia|website=medlineplus.gov|language=en|access-date=2018-11-07}}</ref> In IVF and ICSI, a risk factor is the decreased expression of proteins in [[energy metabolism]]; [[Ferritin light chain]] and [[ATP5A1]].<ref name=zhang>{{cite journal |vauthors=Zhang Y, Zhang YL, Feng C |title=Comparative proteomic analysis of human placenta derived from assisted reproductive technology |journal=Proteomics |volume= 8|issue= 20|pages= 4344–56|date=September 2008 |pmid=18792929 |doi=10.1002/pmic.200800294 |s2cid=206362532 |display-authors=etal}}</ref>
* [[Preterm birth]]. Low birth weight and preterm birth are strongly associated with many health problems, such as [[visual impairment]] and [[cerebral palsy]], and children born after IVF are roughly twice as likely to have cerebral palsy.<ref>{{cite journal |journal=Arch Pediatr Adolesc Med |year=2009 |volume=163 |issue=1 |pages=72–83 |title=Cerebral palsy, autism spectrum disorders, and developmental delay in children born after assisted conception: a systematic review and meta-analysis |vauthors=Hvidtjørn D, Schieve L, Schendel D, Jacobsson B, Sværke C, Thorsen P |pmid=19124707 |doi=10.1001/archpediatrics.2008.507 }}</ref>
* [[Preterm birth]]. Low birth weight and preterm birth are strongly associated with many health problems, such as [[visual impairment]] and [[cerebral palsy]]. Children born after IVF are roughly twice as likely to have cerebral palsy.<ref>{{cite journal |journal=Arch Pediatr Adolesc Med |year=2009 |volume=163 |issue=1 |pages=72–83 |title=Cerebral palsy, autism spectrum disorders, and developmental delay in children born after assisted conception: a systematic review and meta-analysis |vauthors=Hvidtjørn D, Schieve L, Schendel D, Jacobsson B, Sværke C, Thorsen P |pmid=19124707 |doi=10.1001/archpediatrics.2008.507 |doi-access=free }}</ref>

Other risk factors are:
* [[Membrane damage]]{{Citation needed|reason=The reference Zhang'08 does not contain any direct data on membrane damage.|date=January 2014}}, which may be reflected by increased expression of the [[membrane fusion protein]]s [[NAPA (gene)|NAPA]] and [[Annexin A3]].<ref name=zhang />
[[Sperm donation]] is an exception, with a birth defect rate of almost a fifth compared to the general population. It may be explained by that sperm banks accept only people with high sperm count.
[[Sperm donation]] is an exception, with a birth defect rate of almost a fifth compared to the general population. It may be explained by that sperm banks accept only people with high sperm count.


[[Germ cell]]s of the mouse normally have a frequency of spontaneous point [[mutation]]s that is 5 to 10-fold lower than that in [[somatic cell]]s from the same individual.<ref name="McCarrey2009">McCarrey JR. Maintenance of genetic integrity during natural and assisted reproduction. Reprod Biomed Online. 2009;18 Suppl 2:51-5. doi: 10.1016/s1472-6483(10)60449-x. PMID 19406032</ref> This low frequency in the [[germline]] leads to [[embryo]]s that have a low frequency of point mutations in the next generation. No significant differences were observed in the frequency or spectrum of mutations between naturally conceived fetuses and assisted-conception fetuses.<ref name = McCarrey2009/> This suggests that with respect to the maintenance of genetic integrity assisted conception is safe.<ref name = McCarrey2009/>
Current data indicate little or no increased risk for [[postpartum depression]] among women who use ART.<ref>{{cite journal|doi=10.1093/humupd/dmq025|title=Risk for postpartum depression associated with assisted reproductive technologies and multiple births: A systematic review|year=2010|last1=Ross|first1=L. E.|last2=McQueen|first2=K.|last3=Vigod|first3=S.|last4=Dennis|first4=C.-L.|journal=Human Reproduction Update|volume=17|pages=96–106|pmid=20605900|issue=1}}</ref>


Usage of assisted reproductive technology including [[Ovulation induction|ovarian stimulation]] and [[in vitro fertilization]] have been associated with an increased overall risk of [[childhood cancer]] in the offspring, which may be caused by the same original disease or condition that caused the infertility or subfertility in the mother or father.<ref>{{cite journal|pmid=23562045|doi=10.1016/j.fertnstert.2013.03.017|title=Fertility treatment and childhood cancer risk: A systematic meta-analysis|year=2013|last1=Hargreave|first1=Marie|last2=Jensen|first2=Allan|last3=Toender|first3=Anita|last4=Andersen|first4=Klaus Kaae|last5=Kjaer|first5=Susanne Krüger|journal=Fertility and Sterility|volume=100|pages=150–61|issue=1}}</ref>
Current data indicate little or no increased risk for [[postpartum depression]] among women who use ART.<ref>{{cite journal|doi=10.1093/humupd/dmq025|title=Risk for postpartum depression associated with assisted reproductive technologies and multiple births: A systematic review|year=2010|last1=Ross|first1=L. E.|last2=McQueen|first2=K.|last3=Vigod|first3=S.|last4=Dennis|first4=C.-L.|journal=Human Reproduction Update|volume=17|pages=96–106|pmid=20605900|issue=1|doi-access=free}}</ref>

Study results indicate that ART can affect both women and men's sexual health negatively.<ref>{{Cite journal |last1=Piva |first1=Isabella |last2=Lo Monte |first2=Giuseppe |last3=Graziano |first3=Angela |last4=Marci |first4=Roberto |date=August 2014 |title=A literature review on the relationship between infertility and sexual dysfunction: Does fun end with baby making? |url=http://www.tandfonline.com/doi/full/10.3109/13625187.2014.919379 |journal=The European Journal of Contraception & Reproductive Health Care |language=en |volume=19 |issue=4 |pages=231–237 |doi=10.3109/13625187.2014.919379 |pmid=24901746 |issn=1362-5187}}</ref>

Usage of assisted reproductive technology including [[Ovulation induction|ovarian stimulation]] and [[in vitro fertilization]] have been associated with an increased overall risk of [[childhood cancer]] in the offspring, which may be caused by the same original disease or condition that caused the infertility or subfertility in the mother or father.<ref>{{cite journal|pmid=23562045|doi=10.1016/j.fertnstert.2013.03.017|title=Fertility treatment and childhood cancer risk: A systematic meta-analysis|year=2013|last1=Hargreave|first1=Marie|last2=Jensen|first2=Allan|last3=Toender|first3=Anita|last4=Andersen|first4=Klaus Kaae|last5=Kjaer|first5=Susanne Krüger|journal=Fertility and Sterility|volume=100|pages=150–61|issue=1|doi-access=free}}</ref>


That said, In a landmark paper by Jacques Balayla et al. it was determined that infants born after ART have similar neurodevelopment than infants born after natural conception.<ref>Balayla, Jacques, Odile Sheehy, William D. Fraser, Jean R. Séguin, Jacquetta Trasler, Patricia Monnier, Andrea A. MacLeod, Marie-Noëlle Simard, Gina Muckle, and Anick Bérard. "Neurodevelopmental Outcomes After Assisted Reproductive Technologies." Obstetrics & Gynecology (2017).</ref>
That said, In a landmark paper by Jacques Balayla et al. it was determined that infants born after ART have similar neurodevelopment than infants born after natural conception.<ref>Balayla, Jacques, Odile Sheehy, William D. Fraser, Jean R. Séguin, Jacquetta Trasler, Patricia Monnier, Andrea A. MacLeod, Marie-Noëlle Simard, Gina Muckle, and Anick Bérard. "Neurodevelopmental Outcomes After Assisted Reproductive Technologies." Obstetrics & Gynecology (2017).</ref>


ART may also pose risks to the mother. A large US database study compared pregnancy outcomes among 106,000 assisted conception pregnancies with 34 million natural conception pregnancies. It found that assisted conception pregnancies were associated with an increased risk of [[cardiovascular disease]]s, including [[acute kidney injury]] and [[arrhythmia]]. Assisted conception pregnancies were also associated with a higher risk of [[Caesarean section|caesarean delivery]] and [[Preterm birth|premature birth]].<ref>{{Cite journal |date=2022-09-20 |title=Assisted conception is linked to cardiovascular disease and birth complications |url=https://evidence.nihr.ac.uk/alert/assisted-conception-linked-to-cardiovascular-disease-birth-complications/ |journal=NIHR Evidence |language=en |doi=10.3310/nihrevidence_53388|s2cid=252416365 }}</ref><ref>{{Cite journal |last1=Wu |first1=Pensée |last2=Sharma |first2=Garima V. |last3=Mehta |first3=Laxmi S. |last4=Chew-Graham |first4=Carolyn A. |last5=Lundberg |first5=Gina P. |last6=Nerenberg |first6=Kara A. |last7=Graham |first7=Michelle M. |last8=Chappell |first8=Lucy C. |last9=Kadam |first9=Umesh T. |last10=Jordan |first10=Kelvin P. |last11=Mamas |first11=Mamas A. |date=2022-02-22 |title=In-Hospital Complications in Pregnancies Conceived by Assisted Reproductive Technology |journal=Journal of the American Heart Association |language=en |volume=11 |issue=5 |pages=e022658 |doi=10.1161/JAHA.121.022658 |issn=2047-9980 |pmc=9075081 |pmid=35191320}}</ref>
== Usage ==
Assisted reproductive technology procedures performed in the U.S. has over than doubled over the last 10 years, with 140,000 procedures in 2006,<ref name=chicagoART>[http://www.chicagotribune.com/features/arts/chi-0621-fertility-dramas-side1jun21,0,7805988.story chicagotribune.com Infertility by the numbers] {{webarchive|url=https://web.archive.org/web/20090705084623/http://www.chicagotribune.com/features/arts/chi-0621-fertility-dramas-side1jun21,0,7805988.story |date=2009-07-05 }} Colleen Mastony. June 21, 2009</ref> resulting in 55,000 births.<ref name=chicagoART />


In theory, ART can solve almost all reproductive problems, except for severe pathology or the absence of a uterus (or womb), using specific gamete or embryo donation techniques. However, this does not mean that all women can be treated with assisted reproductive techniques, or that all women who are treated will achieve pregnancy.
In [[Australia]], 3.1% of births are a result of ART.<ref>[http://www.theaustralian.news.com.au/story/0,25197,26117922-12377,00.html 'More IVF babies but less multiple births'] {{webarchive|url=https://web.archive.org/web/20090924235447/http://www.theaustralian.news.com.au/story/0,25197,26117922-12377,00.html |date=2009-09-24 }} THE AUSTRALIAN. September 24, 2009</ref>


== Usage ==
In case of discontinuation of fertility treatment, the most common reasons have been estimated to be: postponement of treatment (39%), physical and psychological burden (19%, psychological burden 14%, physical burden 6.32%), relational and personal problems (17%, personal reasons 9%, relational problems 9%), treatment rejection (13%) and organizational (12%) and clinic (8%) problems.<ref>{{cite journal|doi=10.1093/humupd/dms031|title=Why do patients discontinue fertility treatment? A systematic review of reasons and predictors of discontinuation in fertility treatment|year=2012|last1=Gameiro|first1=S.|last2=Boivin|first2=J.|last3=Peronace|first3=L.|last4=Verhaak|first4=C. M.|journal=Human Reproduction Update|volume=18|issue=6|pages=652–69|pmid=22869759|pmc=3461967}}</ref>
As a result of the 1992 Fertility Clinic Success Rate and Certification Act, the CDC is required to publish the annual ART success rates at U.S. fertility clinics.<ref>{{Cite web|url=https://www.cdc.gov/art/nass/policy.html|title=Policy Document {{!}} Assisted Reproductive Technology (ART) {{!}} Reproductive Health {{!}} CDC|date=2019-01-31|website=www.cdc.gov|language=en-us|access-date=2019-11-14}}</ref> Assisted reproductive technology procedures performed in the U.S. has over than doubled over the last 10 years, with 140,000 procedures in 2006,<ref name=chicagoART>[http://www.chicagotribune.com/features/arts/chi-0621-fertility-dramas-side1jun21,0,7805988.story chicagotribune.com Infertility by the numbers] {{webarchive|url=https://web.archive.org/web/20090705084623/http://www.chicagotribune.com/features/arts/chi-0621-fertility-dramas-side1jun21,0,7805988.story |date=2009-07-05 }} Colleen Mastony. June 21, 2009</ref> resulting in 55,000 births.<ref name=chicagoART />


In [[Australia]], 3.1% of births in the late 2000's are a result of ART.<ref>[http://www.theaustralian.news.com.au/story/0,25197,26117922-12377,00.html 'More IVF babies but less multiple births'] {{webarchive|url=https://web.archive.org/web/20090924235447/http://www.theaustralian.news.com.au/story/0,25197,26117922-12377,00.html |date=2009-09-24 }} THE AUSTRALIAN. September 24, 2009</ref>
== Society and culture ==
=== Ethics ===
Some couples find it difficult to stop treatment despite very bad prognosis, resulting in futile therapies. This may give ART providers a difficult decision of whether to continue or refuse treatment.<ref>{{cite journal | author1 = Ethics Committee of the American Society for Reproductive Medicine | title = Fertility treatment when the prognosis is very poor or futile | journal = Fertility and Sterility | volume = 92 | issue = 4 | pages = 1194–7 | year = 2009 | pmid = 19726040 | doi = 10.1016/j.fertnstert.2009.07.979 }}</ref>


The most common reasons for discontinuation of fertility treatment have been estimated to be: postponement of treatment (39%), physical and psychological burden (19%), psychological burden (14%), physical burden (6.32%), relational and personal problems (17%), personal reasons (9%), relational problems (9%), treatment rejection (13%) and organizational (12%) and clinic (8%) problems.<ref>{{cite journal|doi=10.1093/humupd/dms031|title=Why do patients discontinue fertility treatment? A systematic review of reasons and predictors of discontinuation in fertility treatment|year=2012|last1=Gameiro|first1=S.|last2=Boivin|first2=J.|last3=Peronace|first3=L.|last4=Verhaak|first4=C. M.|journal=Human Reproduction Update|volume=18|issue=6|pages=652–69|pmid=22869759|pmc=3461967}}</ref>
''For treatment-specific ethical considerations, see entries in individual subarticles, e.g. [[In vitro fertilisation#Ethics|In vitro fertilisation]], [[Surrogacy#Ethical issues|Surrogacy]] and [[Sperm donation#Ethical considerations|Sperm donation]]


==By country==
Some assisted reproductive technologies can in fact be harmful to both the mother and child. Posing a psychological and a physical health risk, which may impact the ongoing use of these treatments. The adverse effects may cause for alarm, and they should be tightly regulated to ensure candidates are not only mentally, but physically prepared.<ref>{{cite journal | author1 = Noah, Lars | title = Assisted Reproductive Technologies and the Pitfalls of Unregulated Biomedical Innovation | journal = Florida Law Review | volume = 55 | issue = 2 | pages = 604–609 | year = 2003 }}</ref>


=== Costs ===
=== United States ===
Many Americans do not have [[health insurance|insurance]] coverage for fertility investigations and treatments. Many states are starting to mandate coverage, and the rate of use is 278% higher in states with complete coverage.<ref>{{cite journal |vauthors=Jain T, Harlow BL, Hornstein MD |title=Insurance coverage and outcomes of ''in vitro'' fertilization |journal=N. Engl. J. Med. |volume=347 |issue=9 |pages=661–6 |date=August 2002 |pmid=12200554 |doi=10.1056/NEJMsa013491|doi-access=free }}</ref>
==== United States ====
Many Americans do not have [[health insurance|insurance]] coverage for fertility investigations and treatments. Many states are starting to mandate coverage, and the rate of use is 278% higher in states with complete coverage.<ref>{{cite journal |vauthors=Jain T, Harlow BL, Hornstein MD |title=Insurance coverage and outcomes of ''in vitro'' fertilization |journal=N. Engl. J. Med. |volume=347 |issue=9 |pages=661–6 |date=August 2002 |pmid=12200554 |doi=10.1056/NEJMsa013491}}</ref>


There are some health insurance companies that cover diagnosis of infertility but frequently once diagnosed will not cover any treatment costs.
There are some health insurance companies that cover diagnosis of infertility, but frequently once diagnosed will not cover any treatment costs.{{citation needed|date=February 2022}}


2005 approximate treatment/diagnosis costs (United States, costs in US$):
Approximate treatment/diagnosis costs in the United States, with inflation, as of {{Inflation/year|index=US}} (US$):
* Initial workup: [[hysteroscopy]], [[hysterosalpingogram]], [[blood test]]s ~$2,000
* Initial workup: [[hysteroscopy]], [[hysterosalpingogram]], [[blood test]]s ~${{Inflation|index=US|value=2000|start_year=2005|r=-2|fmt=c}}{{Citation needed|date=September 2024}}
* Sonohysterogram (SHG) ~ ${{Inflation|index=US|value=600|start_year=2005|r=-1|fmt=c}}–${{Inflation|index=US|value=1000|start_year=2005|r=-2|fmt=c}}{{Citation needed|date=September 2024}}
* Sonohysterogram (SHG) ~ $600–$1,000
* Clomiphene citrate cycle ~ ${{Inflation|index=US|value=200|start_year=2005|r=-1|fmt=c}}–${{Inflation|index=US|value=500|start_year=2005|r=-1|fmt=c}}{{Citation needed|date=September 2024}}
* Clomiphene citrate cycle ~ $200–$500
* IVF cycle ~ ${{Inflation|index=US|value=10000|start_year=2005|r=-2|fmt=c}}–${{Inflation|index=US|value=30000|start_year=2005|r=-2|fmt=c}}{{Citation needed|date=September 2024}}
* IVF cycle ~ $10,000–$30,000
* Use of a [[surrogate mother]] to carry the child – dependent on arrangements
* Use of a [[surrogate mother]] to carry the child – dependent on arrangements

Another way to look at costs is to determine the expected cost of establishing a pregnancy. Thus if a clomiphene treatment has a chance to establish a pregnancy in 8% of cycles and costs $500, the expected cost is $6,000 to establish a pregnancy, compared to an IVF cycle (cycle fecundity 40%) with a corresponding expected cost of $30,000 ($12,000/.4).
Another way to look at costs is to determine the expected cost of establishing a pregnancy. Thus, if a clomiphene treatment has a chance to establish a pregnancy in 8% of cycles and costs ${{Inflation|index=US|value=500|start_year=2005|r=-1|fmt=c}}, the expected cost is ${{Inflation|index=US|value=6000|start_year=2005|r=-2|fmt=c}} to establish a pregnancy, compared to an IVF cycle (cycle fecundity 40%) with a corresponding expected cost of ${{Inflation|index=US|value=30000|start_year=2005|r=-2|fmt=c}} (${{Inflation|index=US|value=12000|start_year=2005|r=-2|fmt=c}} × 40%).{{Citation needed|date=September 2024}}


For the community as a whole, the cost of IVF on average pays back by 700% by tax from future employment by the conceived human being.<ref>{{cite journal |vauthors=Connolly MP, Pollard MS, Hoorens S, Kaplan BR, Oskowitz SP, Silber SJ |title=Long-term economic benefits attributed to IVF-conceived children: a lifetime tax calculation |journal=Am J Manag Care |volume=14 |issue=9 |pages=598–604 |date=September 2008 |pmid=18778175 |url=http://www.ajmc.com/pubMed.php?pii=10709}}</ref>
For the community as a whole, the cost of IVF on average pays back by 700% by tax from future employment by the conceived human being.<ref>{{cite journal |vauthors=Connolly MP, Pollard MS, Hoorens S, Kaplan BR, Oskowitz SP, Silber SJ |title=Long-term economic benefits attributed to IVF-conceived children: a lifetime tax calculation |journal=Am J Manag Care |volume=14 |issue=9 |pages=598–604 |date=September 2008 |pmid=18778175 |url=http://www.ajmc.com/pubMed.php?pii=10709}}</ref>


==== United Kingdom ====
===European Union===
[[File:Europe and assisted reproductive technology.svg|thumb|Number of assisted reproductive technology cycles in Europe between 1997 and 2014<ref name=edjnet>{{cite news |last1=Jézéquélou |first1=Orlane |title=How does assisted reproductive technology work in Europe? |url=https://www.europeandatajournalism.eu/News/Data-news/How-does-assisted-reproductive-technology-work-in-Europe |access-date=29 November 2019 |work=Alternatives Economiques/EDJNet |date=23 October 2019}}</ref><ref>{{cite journal |last1=De Geyter |first1=Ch. |last2=Calhaz-Jorge |first2=C. |last3=Kupka |first3=M.S. |last4=Wyns |first4=C. |last5=Mocanu |first5=E. |last6=Motrenko |first6=T. |last7=Scaravelli |first7=G. |last8=Smeenk |first8=J. |last9=Vidakovic1 |first9=S. |last10=Goossens |first10=V. |title=ART in Europe, 2014: results generated from European registries by ESHRE: The European IVF-monitoring Consortium (EIM) for the European Society of Human Reproduction and Embryology (ESHRE) |journal=Human Reproduction |date=September 2018 |volume=33 |issue=9 |pages=1586–1601 |doi=10.1093/humrep/dey242 |pmid=30032255 |doi-access=free |hdl=10451/49519 |hdl-access=free }}</ref>]]
In the United Kingdom, all patients have the right to preliminary testing, provided free of charge by the [[National Health Service]]. However, treatment is not widely available on the NHS and there can be long waiting lists. Many patients therefore pay for immediate treatment within the NHS or seek help from private clinics.
In [[Europe]], 157,500 children were born using assisted reproductive technology in 2015, according to the [[European Society of Human Reproduction and Embryology]] (ESHRE).<ref name=edjnet /> But there are major differences in legislation across the Old Continent.
A [[Directive (European Union)|European directive]] fixes standards concerning the use of human tissue and cells,<ref>{{cite web |title=Directive 2004/23/EC of the European Parliament and of the Council of 31 March 2004 on setting standards of quality and safety for the donation, procurement, testing, processing, preservation, storage and distribution of human tissues and cells |url=https://eur-lex.europa.eu/legal-content/en/TXT/HTML/?uri=CELEX:32004L0023 |access-date=3 December 2019}}</ref> but all ethical and legal questions on ART remain the prerogative of [[Member state of the European Union|EU member states]].


[[File:Assisted reproductive technology across Europe.svg|left|thumb|Conditions of assisted reproductive technology in different European countries:<ref name=edjnet /><ref>{{Cite web|url=https://www.rainbow-europe.org/#0/8682/0|title=Rainbow Map|access-date=2019-11-12|language=en|publisher=ILGA-Europe}}</ref>
In 2013, the [[National Institute for Health and Care Excellence]] published new guidelines about who should have access to IVF treatment on the NHS in England and Wales.<ref>{{cite web|title=IVF|url=http://www.nhs.uk/conditions/IVF/Pages/Introduction.aspx|publisher=NHS Choices|accessdate=19 April 2014|url-status=live|archiveurl=https://web.archive.org/web/20140420030919/http://www.nhs.uk/conditions/IVF/Pages/Introduction.aspx|archivedate=20 April 2014}}</ref>
{{legend|#a6ce39|ART authorized for lesbian couples}}
{{legend|#b2df8a|ART authorized for single women}}
{{legend|#33a02c|ART authorized for single women and lesbian couples}}
{{legend|#6F2C91|ART prohibited for single women and lesbian couples}}]]
Across Europe, the legal criteria per availability vary somewhat.<ref>{{Cite web|url=https://www.ieb-eib.org/docs/pdf/2019-04/doc-1554801302-21.pdf|title=Encadrement juridique international dans les différents domaines de la bioéthique|access-date=2019-11-04|language=fr|publisher=Agence de la biomédecine}}</ref> In 11 countries all women may benefit; in 8 others only heterosexual couples are concerned; in 7 only single women; and in 2 ([[Austria]] and [[Germany]]) only lesbian couples.
[[Spain]] was the first European country to open ART to all women, in 1977, the year the first sperm bank was opened there. In [[France]], the right to ART is accorded to all women since 2019. In the last 15 years, legislation has evolved quickly. For example, [[Portugal]] made ART available in 2006 with conditions very similar to those in France, before amending the law in 2016 to allow lesbian couples and single women to benefit. [[Italy]] clarified its uncertain legal situation in 2004 by adopting Europe's strictest laws: ART is only available to heterosexual couples, married or otherwise, and sperm donation is prohibited.


Today, 21 countries provide partial public funding for ART treatment. The seven others, which do not, are [[Ireland]], [[Cyprus]], [[Estonia]], [[Latvia]], [[Luxembourg]], [[Malta]], and [[Romania]].
The guidelines also say women aged between 40 and 42 should be offered one cycle of IVF on the NHS if all of the following additional criteria are also met: They have never had IVF treatment before, have no evidence of low ovarian reserve (this is when eggs in the ovary are low in number or low in quality) and have been informed of the additional implications of IVF and pregnancy at this age. However, if tests show IVF is the only treatment likely to help them get pregnant, women should be referred for IVF straight away.
Such subsidies are subject to conditions, however. In [[Belgium]], a fixed payment of €1,073 is made for each full cycle of the IVF process. The woman must be aged under 43 and may not carry out more than six cycles of ART. There is also a limit on the number of transferable embryos, which varies according to age and the number of cycles completed.
In France, ART is subsidized in full by national health insurance for women up to age 43, with limits of 4 attempts at IVF and 6 at artificial insemination.
[[Germany]] tightened its conditions for public funding in 2004, which caused a sharp drop in the number of ART cycles carried out, from more than 102,000 in 2003 to fewer than 57,000 the following year. Since then the figure has remained stable.


17 countries limit access to ART according to the age of the woman. 10 countries have established an upper age limit, varying from 40 ([[Finland]], [[Netherlands]]) to 50 (including Spain, [[Greece]] and Estonia).
This policy is often modified by local Clinical Commissioning Groups, in a fairly blatant breach of the [[NHS Constitution for England]] which provides that patients have the right to drugs and treatments that have been recommended by NICE for use in the NHS. For example, the Cheshire, Merseyside and West Lancashire [[Clinical Commissioning Group]] insists on additional conditions:<ref>{{cite web|title=Services & how we can help|url=http://www.thehewittfertilitycentre.org.uk/funding-options/|publisher=Liverpool Women's NHS Foundation Trust|accessdate=19 April 2014|url-status=dead|archiveurl=https://web.archive.org/web/20140624054259/http://thehewittfertilitycentre.org.uk/funding-options/|archivedate=2014-06-24}}</ref>
Since 1994, France is one of a number of countries (including Germany, Spain, and the UK) which use the somewhat vague notion of "natural age of procreation". In 2017, the steering council of France's Agency of Biomedicine established an age limit of 43 for women using ART.
* The person undergoing treatment must have commenced treatment before her 40th birthday.
10 countries have no age limit for ART. These include Austria, [[Hungary]], Italy and [[Poland]].
* The person undergoing treatment must have a BMI of between 19 and 29.
* Neither partner must have any living children, from either the current or previous relationships. This includes adopted as well as biological children.
* Sub-fertility must not be the direct result of a sterilisation procedure in either partner (this does not include conditions where sterilisation occurs as a result of another medical problem). Couples who have undertaken a reversal of their sterilisation procedure are not eligible for treatment.


Most European countries allow donations of gametes by third parties. But the situations vary depending on whether sperm or eggs are concerned. Sperm donations are authorized in 20 EU member states; in 11 of them anonymity is allowed. Egg donations are possible in 17 states, including 8 under anonymous conditions.
==== Canada ====
On 12 April, the [[Council of Europe]] adopted a recommendation which encourages an end to anonymity.<ref>{{Cite web|url=http://assembly.coe.int/nw/xml/XRef/Xref-DocDetails-EN.asp?FileID=27680&lang=EN|title=Recommendation 2156 (2019) - Anonymous donation of sperm and oocytes: balancing the rights of parents, donors and children|access-date=2019-11-12}}</ref> In the UK, anonymous sperm donations ended in 2005 and children have access to the identity of the donor when they reach adulthood.
{{See also|Assisted Human Reproduction Act}}
In France, the principle of anonymous donations of sperm or embryos is maintained in the law of bioethics of 2011, but a new bill under discussion may change the situation.<ref>{{Cite web|url=https://www.alternatives-economiques.fr/pma-panique-filiation/00090402|title=PMA: panique dans la filiation|author=Céline Mouzon|access-date=2019-11-12|language=fr|date=2019-09-23}}</ref>
Some treatments are covered by OHIP (public health insurance) in Ontario and others are not. Those with bilaterally blocked fallopian tubes and under 40 have treatment is covered but are still required to pay lab fees (around $3,000–4,000). Coverage varies in other provinces. Most other patients are required to pay for treatments themselves.<ref>{{Cite web|url=http://www.ivfcanada.com/services/fees/general_fee_schedule.cfm|archiveurl=https://web.archive.org/web/20090808064341/http://www.ivfcanada.com/services/fees/general_fee_schedule.cfm|url-status=dead|title=IVF Canada|archivedate=August 8, 2009}}</ref>


==== Israel ====
=== United Kingdom ===
In the United Kingdom, all patients have the right to preliminary testing, provided free of charge by the [[National Health Service]] (NHS). However, treatment is not widely available on the NHS and there can be long waiting lists. Many patients therefore pay for immediate treatment within the NHS or seek help from private clinics.
Israel's national health insurance, which is mandatory for all Israeli citizens, covers nearly all fertility treatments. IVF costs are fully subsidized up to the birth of two children for all Israeli women, including single women and lesbian couples. Embryo transfers for purposes of gestational surrogacy are also covered.<ref>Teman, Elly. 2010. [http://www.ucpress.edu/books/pages/11401.php Birthing a Mother: the Surrogate Body and the Pregnant Self.] {{webarchive|url=https://web.archive.org/web/20091121040210/http://www.ucpress.edu/books/pages/11401.php |date=2009-11-21 }} Berkeley: University of California Press</ref>


In 2013, the [[National Institute for Health and Care Excellence]] (NICE) published new guidelines about who should have access to IVF treatment on the NHS in England and Wales.<ref>{{cite web|title=IVF|url=http://www.nhs.uk/conditions/IVF/Pages/Introduction.aspx|publisher=NHS Choices|access-date=19 April 2014|url-status=live|archive-url=https://web.archive.org/web/20140420030919/http://www.nhs.uk/conditions/IVF/Pages/Introduction.aspx|archive-date=20 April 2014}}</ref>
==== Germany ====
On 27 January 2009, the Federal Constitutional Court ruled that it is unconstitutional, that the health insurance companies have to bear only 50% of the cost for IVF.<ref>[http://www.samenspender-info.de/zuschuesse-kuenstliche-befruchtung.html Zuschüsse der Krankenversicherung für eine künstliche Befruchtung] {{webarchive|url=https://web.archive.org/web/20130208072207/http://www.samenspender-info.de/zuschuesse-kuenstliche-befruchtung.html |date=2013-02-08 }} Retrieved 2. January 2013.</ref> On 2 March 2012, the Federal Council has approved a draft law of some federal states, which provides that the federal government provides a subsidy of 25% to the cost. Thus, the share of costs borne for the pair would drop to just 25%.<ref>[http://www.insemination-erfolg.de/finanzierung-befruchtung.html Finanzierung künstlicher Befruchtung] {{webarchive|url=https://web.archive.org/web/20130219152136/http://www.insemination-erfolg.de/finanzierung-befruchtung.html |date=2013-02-19 }} Retrieved 2. January 2013.</ref>


The guidelines say women aged between 40 and 42 should be offered one cycle of IVF on the NHS if they have never had IVF treatment before, have no evidence of low ovarian reserve (this is when eggs in the ovary are low in number, or low in quality), and have been informed of the additional implications of IVF and pregnancy at this age. However, if tests show IVF is the only treatment likely to help them get pregnant, women should be referred for IVF straight away.
=== Fictional representation ===
Films and other fiction depicting emotional struggles of assisted reproductive technology have had an upswing in the latter part of the 2000s decade, although the techniques have been available for decades.<ref name=chicagotribune>[http://www.chicagotribune.com/entertainment/art/chi-0621-fertility-dramasjun21,0,2997759.story chicagotribune.com --> Heartache of infertility shared on stage, screen] {{webarchive|url=https://archive.is/20120703180716/http://articles.chicagotribune.com/2009-06-21/news/0906190243_1_fertility-treatments-ovulation-artificial-insemination |date=2012-07-03 }} By Colleen Mastony, Tribune reporter. June 21, 2009</ref> Yet, the number of people that can relate to it by personal experience in one way or another is ever growing, and the variety of trials and struggles are huge.<ref name=chicagotribune />


This policy is often modified by local [[Clinical commissioning group|Clinical Commissioning Groups]], in a fairly blatant breach of the [[NHS Constitution for England]] which provides that patients have the right to drugs and treatments that have been recommended by NICE for use in the NHS. For example, the Cheshire, Merseyside and West Lancashire Clinical Commissioning Group insists on additional conditions:<ref>{{cite web|title=Services & how we can help|url=http://www.thehewittfertilitycentre.org.uk/funding-options/|publisher=Liverpool Women's NHS Foundation Trust|access-date=19 April 2014|url-status=dead|archive-url=https://web.archive.org/web/20140624054259/http://thehewittfertilitycentre.org.uk/funding-options/|archive-date=2014-06-24}}</ref>
''For specific examples, refer to the fiction sections in individual subarticles, e.g. [[Surrogacy#Fictional representation|surrogacy]], [[Sperm donor#Fictional representation|sperm donation]] and [[fertility clinic]].''
* The person undergoing treatment must have commenced treatment before her 40th birthday;
* The person undergoing treatment must have a BMI of between 19 and 29;
* Neither partner must have any living children, from either the current or previous relationships. This includes adopted as well as biological children; and,
* Sub-fertility must not be the direct result of a sterilisation procedure in either partner (this does not include conditions where sterilisation occurs as a result of another medical problem). Couples who have undertaken a reversal of their sterilisation procedure are not eligible for treatment.


=== Canada ===
In addition, [[reproduction and pregnancy in speculative fiction]] has been present for many decades.
{{See also|Assisted Human Reproduction Act}}
Some treatments are covered by [[OHIP]] (public health insurance) in Ontario and others are not. Women with bilaterally blocked fallopian tubes and are under the age of 40 have treatment covered but are still required to pay test fees (around CA$3,000–4,000). Coverage varies in other provinces. Most other patients are required to pay for treatments themselves.<ref>{{Cite web|url=http://www.ivfcanada.com/services/fees/general_fee_schedule.cfm|archive-url=https://web.archive.org/web/20090808064341/http://www.ivfcanada.com/services/fees/general_fee_schedule.cfm|url-status=dead|title=IVF Canada|archive-date=August 8, 2009}}</ref>


=== Israel ===
== Research and speculative uses ==
Israel's national health insurance, which is mandatory for all Israeli citizens, covers nearly all fertility treatments. IVF costs are fully subsidized up to the birth of two children for all Israeli women, including single women and lesbian couples. Embryo transfers for purposes of gestational surrogacy are also covered.<ref>Teman, Elly. 2010. [http://www.ucpress.edu/books/pages/11401.php Birthing a Mother: the Surrogate Body and the Pregnant Self.] {{webarchive|url=https://web.archive.org/web/20091121040210/http://www.ucpress.edu/books/pages/11401.php |date=2009-11-21 }} Berkeley: University of California Press</ref>
The idea of using future ART techniques, including direct human germline engineering technologies, to select and genetically modify embryos for the purpose of [[human enhancement]] has been referred to as '''designer babies''', '''reprogenetics''', and '''liberal eugenics''' and has been discussed since the introduction of [[biotechnology]] in the late 1970s.<ref name="Gordon1999">{{cite journal |vauthors=Gordon JW |title=Genetic enhancement in humans |journal=Science |volume=283 |issue=5410 |pages=2023–4 |year=1999 |pmid=10206908 |doi=10.1126/science.283.5410.2023 |bibcode=1999Sci...283.2023G }}</ref><ref>[http://www.nature.com/scitable/topicpage/embryo-screening-and-the-ethics-of-human-60561 Pray, L. (2008) Embryo screening and the ethics of human genetic engineering. Nature Education 1(1):207 (Retrieved January 24, 2015).]</ref><ref>{{Cite journal| author = Erik Parens and Lori P. Knowles | title = Reprogenetics and Public Policy Reflections and Recommendations | publisher = [[Hastings Center]] | date = 2003 | url = http://www.thehastingscenter.org/uploadedFiles/Publications/Special_Reports/reprogenetics_and_public_policy.pdf| accessdate = January 24, 2015 }}</ref><ref name=RBO>{{Cite journal|last=Ishii|first=Tetsuya|date=August 2014|title=Potential impact of human mitochondrial replacement on global policy regarding germline gene modification|journal=Reproductive Biomedicine Online|volume=29|issue=2|pages=150–155|doi=10.1016/j.rbmo.2014.04.001|issn=1472-6491|pmid=24832374|hdl=2115/56864}}</ref><ref name=DaD>{{Cite book|url=https://books.google.com/?id=E3qsPJb44Q8C&pg=PR7&dq=human+germline+engineering#v=onepage&q=human%20germline%20engineering&f=false|title=Design and Destiny: Jewish and Christian Perspectives on Human Germline Modification|last=Cole-Turner|first=Ronald|date=2008|publisher=MIT Press|isbn=978-0-262-53301-0}}</ref><ref name=RedesigningHumans>{{Cite book|url=https://books.google.com/?id=XLjJ4AkYWUgC&pg=PR7&dq=human+germline+engineering#v=onepage&q=human%20germline%20engineering&f=false|title=Redesigning Humans: Choosing Our Genes, Changing Our Future|last=Stock|first=Gregory|date=2003|publisher=Houghton Mifflin Harcourt|isbn=978-0-618-34083-5}}</ref>


=== Germany ===
The term "liberal eugenics" was coined by bioethicist [[Nicholas Agar]].<ref name="Agar 2004">{{cite book|author = Agar, Nicholas|title = Liberal Eugenics: In Defence of Human Enhancement|year = 2004|isbn = 978-1-4051-2390-7|author-link = Nicholas Agar}}</ref><ref>{{Cite journal |last= |first= |date=2008 |title=Regulating Eugenics |url= http://harvardlawreview.org/2008/04/regulating-eugenics/ |journal=Harvard Law Review |access-date=May 2, 2015}}</ref> Liberal eugenics is aimed at "improving" the genotypes of future generations through screening and genetic modification to eliminate "undesirable" traits. The term "reprogenetics" was coined by [[Lee M. Silver]], a professor of [[molecular biology]] at [[Princeton University]], in his 1997 book ''Remaking Eden''.<ref name="Silver 1998">{{cite book| author=Silver, Lee M.| title=Remaking Eden: Cloning and Beyond in a Brave New World| publisher=Harper Perennial| year=1998| isbn=978-0-380-79243-6| author-link=Lee M. Silver| url=https://archive.org/details/remakingeden00leem}}</ref><ref name="Kistler 2001">{{Cite journal| author = Kistler, Walter P.| title = Genetics in the New Millennium: The Promise of Reprogenics| date = 2001 | url = http://www.wfs.org/kistler.htm| accessdate=2007-11-13 |archiveurl = https://web.archive.org/web/20071009162045/http://www.wfs.org/kistler.htm <!-- Bot retrieved archive --> |archivedate = 2007-10-09}}</ref>
On 27 January 2009, the [[Federal Constitutional Court]] ruled that it is unconstitutional, that the health insurance companies have to bear only 50% of the cost for IVF.<ref>[http://www.samenspender-info.de/zuschuesse-kuenstliche-befruchtung.html Zuschüsse der Krankenversicherung für eine künstliche Befruchtung] {{webarchive|url=https://web.archive.org/web/20130208072207/http://www.samenspender-info.de/zuschuesse-kuenstliche-befruchtung.html |date=2013-02-08 }} Retrieved 2. January 2013.</ref> On 2 March 2012, the [[Federal Council (Germany)|Federal Council]] has approved a draft law of some federal states, which provides that the federal government provides a subsidy of 25% to the cost. Thus, the share of costs borne for the pair would drop to just 25%.<ref>[http://www.insemination-erfolg.de/finanzierung-befruchtung.html Finanzierung künstlicher Befruchtung] {{webarchive|url=https://web.archive.org/web/20130219152136/http://www.insemination-erfolg.de/finanzierung-befruchtung.html |date=2013-02-19 }} Retrieved 2. January 2013.</ref> Since July 2017, assisted reproductive technology is also allowed for married lesbian couples, as German parliament allowed [[Same-sex marriage in Germany|same-sex marriages in Germany]].


=== France ===
The philosophical movement associated with these speculative uses is [[transhumanism]].<ref name="Wagner 2002">{{cite journal |author=Wagner, Cynthia G. |title=Germinal Choice Technology: Our Evolutionary Future. An Interview with Gregory Stock |year=2002 |url=http://www.wfs.org/intstock.htm |accessdate=2006-02-21 |url-status=dead |archiveurl=https://web.archive.org/web/20060207090538/http://www.wfs.org/intstock.htm |archivedate=2006-02-07 }}</ref><ref name="Black 2003">{{cite book |author-link=Edwin Black |last=Black |first=Edwin |title=War Against the Weak: Eugenics and America's Campaign to Create a Master Race |publisher=Four Walls Eight Windows |year=2003 |isbn=978-1-56858-258-0 |url=https://archive.org/details/isbn_9781568582580 }}</ref> When [[eugenics]] is discussed in this context it usually in context of allowing parents to select desirable traits in an unborn child and not in the use of genetics to destroy embryos or to prevent the formation of undesirable embryos.
In July 2020, the [[French Parliament]] allowed assisted reproductive technology also for lesbian couples and single women.<ref>[https://www.queer.de/detail.php?article_id=36724 Queer.de: Frankreich: Künstliche Befruchtung auch für lesbische Paare (german)], July 21, 2020</ref><ref>[https://www.noz.de/deutschland-welt/politik/artikel/2097957/frankreich-legalisiert-kuenstliche-befruchtung-fuer-alle-frauen NOZ.de: Beifall im Parlament: Frankreich legalisiert künstliche Befruchtung für alle Frauen (german)], July 31, 2020</ref>


=== Cuba ===
This procedure does not have to encompass liberal eugenics in terms of human enhancement though. It could be an option for both women and men unable to conceive a child naturally, as well as same-sex couples.<ref>{{Cite journal|last=Falloon|first=Katie|date=2014-01-01|title=ART and the Art of Medicine|journal=AMA Journal of Ethics|volume=16|issue=1|pages=3–4|doi=10.1001/virtualmentor.2014.16.1.fred1-1401|issn=2376-6980}}</ref>
Cuban sources mention that assisted reproduction is completely legal and free in the country.<ref>http://www.ahora.cu/fr/sante/5715-reproduction-assistee-et-droit-du-travail-a-cuba (in French), on ''Ahora''</ref><ref>http://www.granma.cu/cuba/2020-01-15/reproduccion-asistida-en-cuba-nuevas-razones-para-la-felicidad (in Spanish), on ''Granma.cu''</ref>


=== India ===
Safety is a major concern when it comes to the gene editing and mitochondrial transfer, as problems may not arise in the first children for many years, and their offspring may be affected, and problems may only appear in those subsequent generations.<ref name=":3">{{Cite journal|last=Anderson|first=W. French|date=1985-08-01|title=Human Gene Therapy: Scientific and Ethical Considerations|journal=Journal of Medicine and Philosophy|language=en|volume=10|issue=3|pages=275–292|doi=10.1093/jmp/10.3.275|issn=0360-5310|pmid=3900264}}</ref><ref name=":2" /><ref>{{cite journal|date=January 2016|title=Designer babies|journal=Obstetrics, Gynecology and Reproductive Medicine|volume=26|issue=2|pages=59–60|doi=10.1016/j.ogrm.2015.11.011|last1=Pang|first1=Ronald T.K|hdl=10722/234869}}</ref> New diseases may be introduced accidentally.<ref name="Green 2007">{{cite book | last = Green | first = Ronald M. | title = Babies By Design: The Ethics of Genetic Choice | publisher = Yale University Press | year = 2007 | location = New Haven | pages = 96–97 | id = 129954761 | isbn = 978-0-300-12546-7 | url = https://archive.org/details/babiesbydesignet00gree }}</ref><ref name="Agar2006">{{cite journal|last=Agar|first=Nicholas|year=2006|title=Designer Babies: Ethical Considerations|url=http://www.actionbioscience.org/biotechnology/agar.html|journal=ActionBioscience.org}}</ref>
The Government of India has notified the Surrogacy (Regulation) Act 2021 and the Assisted Reproductive Technology (Regulation) Act 2021<ref>{{Cite web|title=Govt notifies laws to regulate surrogacy, assisted reproductive technology|url=https://www.businesstoday.in/latest/policy/story/govt-notifies-laws-to-regulate-surrogacy-assisted-reproductive-technology-320438-2022-01-26|access-date=2022-02-03|website=Business Today|date=26 January 2022 |language=en}}</ref> to regulate the practice of ART. Prior to that, the National Guidelines for Accreditation, Supervision and Regulation of ART Clinics in India published by the Ministry for Health and Family Welfare, Government of India in the year 2005 was governing the field.<ref>{{Cite web|title=IVF Clinics|url=https://pib.gov.in/newsite/PrintRelease.aspx?relid=118621|access-date=2022-02-03|website=pib.gov.in}}</ref> Indian law recognises the right of a single woman, who is a major, to have children through ART.<ref>{{Cite web|last=A|first=Aruna|date=2021-09-14|title=Need to understand the rights of a single mother by choice.|url=https://www.legalbay.co.in/post/need-to-understand-the-rights-of-a-single-mother-by-choice|access-date=2022-02-03|website=Legal Bay|language=en}}</ref>


== Society and culture ==
Neither the first generation nor their offspring will have given consent to have been treated.<ref name=":2" /> On a larger scale, germline modification has the potential to impact the gene pool of the entire human race in a negative or positive way.<ref name=":5">{{Cite journal|last=Smith|first=Kevin R.|last2=Chan|first2=Sarah|last3=Harris|first3=John|title=Human Germline Genetic Modification: Scientific and Bioethical Perspectives|journal=Archives of Medical Research|volume=43|issue=7|pages=491–513|doi=10.1016/j.arcmed.2012.09.003|pmid=23072719|year=2012}}</ref>
=== Ethics ===
{{For|treatment-specific ethical considerations|In vitro fertilisation#Ethics|Surrogacy#Ethical issues|Sperm donation#Ethical and legal issues}}
Some couples may find it difficult to stop treatment despite very bad prognosis, resulting in futile therapies. This has the potential to give ART providers a difficult decision of whether to continue or refuse treatment.<ref>{{cite journal | author1 = Ethics Committee of the American Society for Reproductive Medicine | title = Fertility treatment when the prognosis is very poor or futile | journal = Fertility and Sterility | volume = 92 | issue = 4 | pages = 1194–7 | year = 2009 | pmid = 19726040 | doi = 10.1016/j.fertnstert.2009.07.979 | doi-access = free }}</ref>


Some assisted reproductive technologies have the potential to be harmful to both the mother and child, posing a psychological and/or physical health risk, which may impact the ongoing use of these treatments.
Another concern, especially for people who believe that life begins at conception, is the fate of flawed or unchosen embryos created during the work of reaching an embryo with the desired qualities.<ref name=":2">{{Cite journal|last=Lappé|first=Marc|date=1991-12-01|title=Ethical Issues in Manipulating the Human Germ Line|journal=Journal of Medicine and Philosophy|language=en|volume=16|issue=6|pages=621–639|doi=10.1093/jmp/16.6.621|issn=0360-5310|pmid=1787391}}</ref> The embryo cannot give consent and some of the treatments have long-lasting and harmful implications.<ref name=":2" />


In Israel, there is research supporting using ART, including recycled lab materials from the IVF process, to help women work through some of these mixed emotions.<ref>Article link: Dr. Katan, Seven news, 14.1.2022, Hebrew [https://www.inn.co.il/news/537690 See section] on Artistic conception הפריה אומנותית.</ref><ref>
In many countries, editing embryos and germline modification is illegal.<ref name=Ishii2015>{{cite journal |last1=Ishii |first1=T |title=Germline genome-editing research and its socioethical implications. |journal=Trends in Molecular Medicine |date=August 2015 |volume=21 |issue=8 |pages=473–81 |doi=10.1016/j.molmed.2015.05.006 |pmid=26078206}}</ref> As of 2015, 15 of 22 Western European nations had outlawed human germline engineering.<ref>{{Cite journal|last=Lanphier|first=Edward|last2=Urnov|first2=Fyodor|last3=Haecker|first3=Sarah Ehlen|last4=Werner|first4=Michael|last5=Smolenski|first5=Joanna|date=2015-03-26|title=Don't edit the human germ line|journal=Nature|volume=519|issue=7544|pages=410–411|doi=10.1038/519410a|pmid=25810189|bibcode=2015Natur.519..410L}}</ref> Human germline modification has for many years has been heavily off limits. As of 2016 there was no legislation in the United States that explicitly prohibited germline engineering, however, the ''Consolidated Appropriation Act of 2016'' banned the use of [[Food and Drug Administration|U.S. Food and Drug Administration (FDA)]] funds to engage in research regarding human germline modifications.<ref>{{Cite journal|last=Cohen|first=I. Glenn|last2=Adashi|first2=Eli Y.|date=2016-08-05|title=The FDA is prohibited from going germline|journal=Science|volume=353|issue=6299|pages=545–546|doi=10.1126/science.aag2960|issn=0036-8075|pmid=27493171|bibcode=2016Sci...353..545C}}</ref>
Gilat Kupietzky-Sacks, IVF Embryologist and initiator of the project and Miriam Kupietzky, Art Therapist run a women's workshop using recycled lab material. [https://ivfcreativeart.wixsite.com/website about workshop]</ref><ref>Workshop on the Use of Life Cycle Concepts [https://www.epa.gov/sites/production/files/2016-09/documents/g7_us_workshop_summary_proceedings_final.pdf about workshop in the USA and other countries]</ref><ref>Angela Savage. "Works of ART: on creativity, infertility and Assisted Reproductive Technology." In ''Art'', 25.7.2016. Article on art produced in response to IVF treatment [https://www.wheelercentre.com/notes/work-of-art-on-creativity-and-assisted-reproductive-technology]</ref>


=== Fictional representation ===
Germline modification is considered a more ethically and morally acceptable treatment when one or both of the parents is a carrier for a harmful trait and is treated to improve the genotype and safety of the future generations.<ref name=":2" /> When the treatment is used for this purpose, it can fill the gaps that other technologies may not be able to accomplish.<ref name=":5" /> The American [[National Academy of Sciences]] and [[National Academy of Medicine]] gave qualified support to human genome editing in 2017 once answers have been found to safety and efficiency problems "but only for serious conditions under stringent oversight."<ref>{{Cite news|url=https://www.nytimes.com/2017/02/14/health/human-gene-editing-panel.html|title=Human Gene Editing Receives Science Panel's Support|last=Harmon|first=Amy|date=2017-02-14|newspaper=The New York Times|access-date=2017-02-17|issn=0362-4331}}</ref> Germline modification would be more practical if sampling methods were less destructive and used the polar bodies rather than embryos.<ref name=":2" /> In 2018, the [[Nuffield Council on Bioethics]] issued a report which concluded that under certain circumstances, editing of the DNA of human embryos could be acceptable.<ref>{{Cite journal|last=Hawkes|first=Nigel|date=2018-07-17|title=Human genome editing is not unethical, says Nuffield Council|url=https://www.bmj.com/content/362/bmj.k3140|journal=BMJ|language=en|volume=362|pages=k3140|doi=10.1136/bmj.k3140|issn=0959-8138|pmid=30018086}}</ref> The Nuffield Council is a British independent organisation that evaluates ethical questions in medicine and biology.
Films and other fiction depicting emotional struggles of assisted reproductive technology have had an upswing in the latter part of the 2000s decade, although the techniques have been available for decades.<ref name=chicagotribune>{{Cite web
|url=http://www.chicagotribune.com/entertainment/art/chi-0621-fertility-dramasjun21,0,2997759.story
|website=[[Chicago Tribune|chicagotribune.com]]
|title=Heartache of infertility shared on stage, screen
|access-date=2009-06-23
|archive-date=2012-07-03
|archive-url=https://archive.today/20120703180716/http://articles.chicagotribune.com/2009-06-21/news/0906190243_1_fertility-treatments-ovulation-artificial-insemination
|url-status=dead
}} By Colleen Mastony, Tribune reporter. June 21, 2009</ref> As ART becomes more utilized, the number of people that can relate to it by personal experience in one way or another is growing.<ref name=chicagotribune />


''For specific examples, refer to the fiction sections in individual subarticles, e.g. [[Surrogacy#Judaism|surrogacy]], [[Sperm donor#Fictional representation|sperm donation]] and [[fertility clinic]].''
Lee Silver has projected a [[dystopia]] in which a race of [[Übermensch|superior humans]] look down on those without genetic enhancements, though others have counseled against accepting this vision of the future.<ref name="Silver 1998" /> It has also been suggested that if designer babies were created through genetic engineering, that this could have deleterious effects on the human gene pool.<ref name="Baird2007">{{cite journal|last=Baird |first=Stephen L. |date=April 2007 |title=Designer Babies: Eugenics Repackaged or Consumer Options? |url=http://www.iteea.org/Publications/TTT/apr07.pdf |journal=Technology Teacher |volume=66 |issue=7 |pages=12–16 |archive-date=March 28, 2014 |url-status=dead |archiveurl=https://web.archive.org/web/20140328101105/http://www.iteea.org/Publications/TTT/apr07.pdf }}</ref> Some futurists claim that it would put the human species on a path to [[participant evolution]].<ref name="Silver 1998" /><ref name="Hughes 2004">{{cite book|author = Hughes, James| title = Citizen Cyborg: Why Democratic Societies Must Respond to the Redesigned Human of the Future| publisher = Westview Press| year = 2004| isbn = 978-0-8133-4198-9|authorlink = James Hughes (sociologist)| title-link = Citizen Cyborg}}</ref> It has also been argued that designer babies may have an important role as counter-acting an argued [[dysgenic]] trend.<ref name="ReferenceB">{{cite journal |last1=Lynn |first1=Richard |last2=Harvey |first2=John |title=The decline of the world's IQ |journal=Intelligence |volume=36 |issue=2 |year=2008 |pages=112–20 |doi=10.1016/j.intell.2007.03.004 }}</ref>


In addition, [[reproduction and pregnancy in speculative fiction]] has been present for many decades.
In November 2018, [[He Jiankui|Jiankui He]] announced that he had [[Genome editing|edited the genomes]] of two human embryos, to attempt to disable the gene for [[CCR5]], which codes for a receptor that [[HIV]] uses to enter cells. He said that twin girls, Lulu and Nana, had been born a few weeks earlier. He said that the girls still carried functional copies of CCR5 along with disabled CCR5 ([[mosaicism]]) and were still vulnerable to HIV. The work was widely condemned as unethical, dangerous, and premature.<ref>{{cite news |last1=Begley |first1=Sharon |title=Amid uproar, Chinese scientist defends creating gene-edited babies – STAT |url=https://www.statnews.com/2018/11/28/chinese-scientist-defends-creating-gene-edited-babies/ |work=STAT |date=28 November 2018}}</ref> [[Carl Zimmer]] compared the reaction to He's human gene editing experiment to the initial reactions and subsequent debate over [[mitochondrial replacement therapy]] (MRT) and the eventual regulatory approval of MRT in the United Kingdom.<ref name="NYT-20181201">{{cite news |last=Zimmer |first=Carl |authorlink=Carl Zimmer |title=Genetically Modified People Are Walking Among Us |url=https://www.nytimes.com/2018/12/01/sunday-review/crispr-china-babies-gene-editing.html |date=1 December 2018 |work=[[The New York Times]] |accessdate=2 December 2018 }}</ref>

==Historical facts==
25 July 1978, [[Louise Brown]] was born; this was the first successful birth of a child after [[IVF]] treatment. The procedure took place at Dr Kershaw's Cottage Hospital (now Dr Kershaw's Hospice) in Royton, Oldham, England. [[Patrick Steptoe]] (gynaecologist) and [[Robert Edwards (physiologist)]] worked together to develop the IVF technique.<ref>{{Cite news|url=http://news.bbc.co.uk/onthisday/hi/dates/stories/july/25/newsid_2499000/2499411.stm|title=1978: First 'test tube baby' born|date=July 25, 1978|via=news.bbc.co.uk}}</ref> Steptoe described a new method of egg extraction and Edwards were carrying out a way to fertilise eggs in the lab. Robert G. Edwards was awarded the [[Nobel Prize in Physiology or Medicine]] in 2010, but not Steptoe because the Nobel Prize is not awarded posthumously.<ref>{{Cite web | url=https://www.nobelprize.org/prizes/medicine/2010/summary/ |title = The Nobel Prize in Physiology or Medicine 2010}}</ref>

The first successful birth by ICSI ([[Intracytoplasmic sperm injection]]) took place on 14 January 1992. The technique was developed by [[Gianpiero D. Palermo]] at the [[Vrije Universiteit Brussel]], in the Center for Reproductive Medicine in Brussels. Actually, the discovery was made by a mistake when a spermatozoid was put into the cytoplasm.<ref>{{cite journal| pmid=1351601 | volume=340 | issue=8810 | title=Pregnancies after intracytoplasmic injection of single spermatozoon into an oocyte | year=1992 | last1=Palermo |first1=G |last2=Joris |first2=H |last3=Devroey |first3=P |last4=Van Steirteghem |first4=AC | journal=Lancet | pages=17–8 | doi=10.1016/0140-6736(92)92425-f| s2cid=2916063 }}</ref>


== See also ==
== See also ==
{{Commons category}}
* [[Artificial uterus]]
* [[Artificial uterus]]
* [[Diethylstilbestrol]]
* [[Artificial insemination]]
* [[Fertility fraud]]
* [[Human cloning]]
* [[Human cloning]]
* [[Religious response to ART]]
* [[Ova bank]]
* [[Sperm bank]]
* [[Sperm bank]]
* [[Sperm donation]]
* [[Sperm donation]]
* [[Spontaneous conception]], the unassisted conception of a subsequent child after prior use of assisted reproductive technology
* [[Spontaneous conception]], the unassisted conception of a subsequent child after prior use of assisted reproductive technology
* [[Egg donation]]
* [[Ralph L. Brinster]]
* [[Religious response to ART]]
* ''[[Repository for Germinal Choice]]''


== References ==
== References ==
{{Free-content attribution
|title= How does assisted reproductive technology work in Europe?
|author = Orlane Jézéquélou/Alternatives Economiques
|publisher = EDJNet
|documentURL= https://www.europeandatajournalism.eu/News/Data-news/How-does-assisted-reproductive-technology-work-in-Europe
|license=CC BY 4.0
}}
{{Reflist|30em}}
{{Reflist|30em}}

== Further reading ==
*Hauskeller, Michael. [http://ndpr.nd.edu/review.cfm?id=4541 Philosophical Review of Nicholas Agar's ''Liberal Eugenics: In Defence of Human Enhancement'']. Retrieved on 2008-08-03.
*Hari, Johann. [https://web.archive.org/web/20091109182742/http://www.independent.co.uk/opinion/commentators/johann-hari/johann-hari-why-i-support-liberal-eugenics-406804.html ''Why I support liberal eugenics'']. Retrieved on 2008-08-03
*Kanamori, Osamu. [https://web.archive.org/web/20120204083732/http://www.med.osaka-u.ac.jp/pub/eth/kanamori.doc ''Relief and Shadow of New Liberal Eugenics'']. Retrieved on 2008-08-03
*[[David Pearce (philosopher)|David, Pearce]] [http://hedweb.com/reproductive-revolution/liberal-eugenics.html "Liberal Eugenics?"]. Retrieved on 2010-6-27


== External links ==
== External links ==
* [https://www.cdc.gov/art/ Centers for Disease Control and Prevention (CDC), Assisted Reproductive Technology]
* [https://www.cdc.gov/art/ Centers for Disease Control and Prevention (CDC), Assisted Reproductive Technology]


{{Women's health|state=collapsed}}
{{Assisted reproductive technology}}
{{Assisted reproductive technology}}
{{Pregnancy}}
{{Pregnancy}}
{{Reproductive health}}
{{Reproductive health}}
{{Authority control}}


[[Category:Assisted reproductive technology| ]]
[[Category:Assisted reproductive technology| ]]
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[[Category:Biotechnology]]
[[Category:Biotechnology]]
[[Category:Bioethics]]
[[Category:Bioethics]]
[[Category:Eugenics]]
[[Category:Futurology]]
[[Category:Fertility medicine]]
[[Category:Fertility medicine]]
[[Category:Genetic engineering]]
[[Category:Genetic engineering]]

Latest revision as of 04:50, 5 January 2025

Assisted reproductive technology
Illustration depicting intracytoplasmic sperm injection (ICSI), an example of assisted reproductive technology
Other namesART
MeSHD027724

Assisted reproductive technology (ART) includes medical procedures used primarily to address infertility. This subject involves procedures such as in vitro fertilization (IVF), intracytoplasmic sperm injection (ICSI), cryopreservation of gametes or embryos, and/or the use of fertility medication. When used to address infertility, ART may also be referred to as fertility treatment. ART mainly belongs to the field of reproductive endocrinology and infertility. Some forms of ART may be used with regard to fertile couples for genetic purpose (see preimplantation genetic diagnosis). ART may also be used in surrogacy arrangements, although not all surrogacy arrangements involve ART. The existence of sterility will not always require ART to be the first option to consider, as there are occasions when its cause is a mild disorder that can be solved with more conventional treatments or with behaviors based on promoting health and reproductive habits.

Procedures

[edit]

General

[edit]

With ART, the process of sexual intercourse is bypassed and fertilization of the oocytes occurs in the laboratory environment (i.e., in vitro fertilization).[citation needed]

In the US, the Centers for Disease Control and Prevention (CDC) defines ART to include "all fertility treatments in which both eggs and sperm are handled. In general, ART procedures involve surgically removing eggs from a woman's ovaries, combining them with sperm in the laboratory, and returning them to the woman's body or donating them to another woman." According to CDC, "they do not include treatments in which only sperm are handled (i.e., intrauterine—or artificial—insemination) or procedures in which a woman takes medicine only to stimulate egg production without the intention of having eggs retrieved."[1]

In Europe, ART also excludes artificial insemination and includes only procedures where oocytes are handled.[2][3]

The World Health Organization (WHO), also defines ART this way.[4]

Ovulation induction

[edit]

Ovulation induction is usually used in the sense of stimulation of the development of ovarian follicles[5][6][7] by fertility medication to reverse anovulation or oligoovulation. These medications are given by injection for 8 to 14 days. A health care provider closely monitors the development of the eggs using transvaginal ultrasound and blood tests to assess follicle growth and estrogen production by the ovaries. When follicles have reached an adequate size and the eggs are mature enough, an injection of the hormone hCG initiates the ovulation process. Egg retrieval should occur 36 hours before ovulation.

In vitro fertilization

[edit]
Steps of IVF Treatment

In vitro fertilization is the technique of letting fertilization of the male and female gametes (sperm and egg) occur outside the female body.

Techniques usually used in in vitro fertilization include:

  • Transvaginal ovum retrieval (OVR) is the process whereby a small needle is inserted through the back of the vagina and guided via ultrasound into the ovarian follicles to collect the fluid that contains the eggs.
  • Embryo transfer is the step in the process whereby one or several embryos are placed into the uterus of the female with the intent to establish a pregnancy.

Less commonly used techniques in in vitro fertilization are:

  • Assisted zona hatching (AZH) is performed shortly before the embryo is transferred to the uterus. A small opening is made in the outer layer surrounding the egg in order to help the embryo hatch out and aid in the implantation process of the growing embryo.
  • Intracytoplasmic sperm injection (ICSI)
    Intracytoplasmic sperm injection (ICSI) is beneficial in the case of male factor infertility where sperm counts are very low or failed fertilization occurred with previous IVF attempt(s). The ICSI procedure involves a single sperm carefully injected into the center of an egg using a microneedle. With ICSI, only one sperm per egg is needed. Without ICSI, you need between 50,000 and 100,000. This method is also sometimes employed when donor sperm is used.
  • Autologous endometrial coculture is a possible treatment for patients who have failed previous IVF attempts or who have poor embryo quality. The patient's fertilized eggs are placed on top of a layer of cells from the patient's own uterine lining, creating a more natural environment for embryo development.
  • In zygote intrafallopian transfer (ZIFT), egg cells are removed from the woman's ovaries and fertilized in the laboratory; the resulting zygote is then placed into the fallopian tube.
  • Cytoplasmic transfer is the technique in which the contents of a fertile egg from a donor are injected into the infertile egg of the patient along with the sperm.
  • Egg donors are resources for women with no eggs due to surgery, chemotherapy, or genetic causes; or with poor egg quality, previously unsuccessful IVF cycles or advanced maternal age. In the egg donor process, eggs are retrieved from a donor's ovaries, fertilized in the laboratory with the sperm from the recipient's partner, and the resulting healthy embryos are returned to the recipient's uterus.
  • Sperm donation may provide the source for the sperm used in IVF procedures where the male partner produces no sperm or has an inheritable disease, or where the woman being treated has no male partner.
  • Preimplantation genetic diagnosis (PGD) involves the use of genetic screening mechanisms such as fluorescent in-situ hybridization (FISH) or comparative genomic hybridization (CGH) to help identify genetically abnormal embryos and improve healthy outcomes.
  • Embryo splitting can be used for twinning to increase the number of available embryos.[8]

Pre-implantation genetic diagnosis

[edit]

A pre-implantation genetic diagnosis procedure may be conducted on embryos prior to implantation (as a form of embryo profiling), and sometimes even of oocytes prior to fertilization. PGD is considered in a similar fashion to prenatal diagnosis. PGD is an adjunct to ART procedures, and requires in vitro fertilization to obtain oocytes or embryos for evaluation. Embryos are generally obtained through blastomere or blastocyst biopsy. The latter technique has proved to be less deleterious for the embryo, therefore it is advisable to perform the biopsy around day 5 or 6 of development.[9] Sex selection is the attempt to control the sex of offspring to achieve a desired sex in case of X chromosome linked diseases. It can be accomplished in several ways, both pre- and post-implantation of an embryo, as well as at birth. Pre-implantation techniques include PGD, but also sperm sorting.[citation needed]

Others

[edit]

Other assisted reproduction techniques include:

Risks

[edit]

The majority of IVF-conceived infants do not have birth defects.[13] However, some studies have suggested that assisted reproductive technology is associated with an increased risk of birth defects.[14][15] Artificial reproductive technology is becoming more available. Early studies suggest that there could be an increased risk for medical complications with both the mother and baby. Some of these include low birth weight, placental insufficiency, chromosomal disorders, preterm deliveries, gestational diabetes, and pre-eclampsia (Aiken and Brockelsby).[16]

In the largest U.S. study, which used data from a statewide registry of birth defects,[17] 6.2% of IVF-conceived children had major defects, as compared with 4.4% of naturally conceived children matched for maternal age and other factors (odds ratio, 1.3; 95% confidence interval, 1.00 to 1.67).[13] ART carries with it a risk for heterotopic pregnancy (simultaneous intrauterine and extrauterine pregnancy).[18] The main risks are:

Sperm donation is an exception, with a birth defect rate of almost a fifth compared to the general population. It may be explained by that sperm banks accept only people with high sperm count.

Germ cells of the mouse normally have a frequency of spontaneous point mutations that is 5 to 10-fold lower than that in somatic cells from the same individual.[22] This low frequency in the germline leads to embryos that have a low frequency of point mutations in the next generation. No significant differences were observed in the frequency or spectrum of mutations between naturally conceived fetuses and assisted-conception fetuses.[22] This suggests that with respect to the maintenance of genetic integrity assisted conception is safe.[22]

Current data indicate little or no increased risk for postpartum depression among women who use ART.[23]

Study results indicate that ART can affect both women and men's sexual health negatively.[24]

Usage of assisted reproductive technology including ovarian stimulation and in vitro fertilization have been associated with an increased overall risk of childhood cancer in the offspring, which may be caused by the same original disease or condition that caused the infertility or subfertility in the mother or father.[25]

That said, In a landmark paper by Jacques Balayla et al. it was determined that infants born after ART have similar neurodevelopment than infants born after natural conception.[26]

ART may also pose risks to the mother. A large US database study compared pregnancy outcomes among 106,000 assisted conception pregnancies with 34 million natural conception pregnancies. It found that assisted conception pregnancies were associated with an increased risk of cardiovascular diseases, including acute kidney injury and arrhythmia. Assisted conception pregnancies were also associated with a higher risk of caesarean delivery and premature birth.[27][28]

In theory, ART can solve almost all reproductive problems, except for severe pathology or the absence of a uterus (or womb), using specific gamete or embryo donation techniques. However, this does not mean that all women can be treated with assisted reproductive techniques, or that all women who are treated will achieve pregnancy.

Usage

[edit]

As a result of the 1992 Fertility Clinic Success Rate and Certification Act, the CDC is required to publish the annual ART success rates at U.S. fertility clinics.[29] Assisted reproductive technology procedures performed in the U.S. has over than doubled over the last 10 years, with 140,000 procedures in 2006,[30] resulting in 55,000 births.[30]

In Australia, 3.1% of births in the late 2000's are a result of ART.[31]

The most common reasons for discontinuation of fertility treatment have been estimated to be: postponement of treatment (39%), physical and psychological burden (19%), psychological burden (14%), physical burden (6.32%), relational and personal problems (17%), personal reasons (9%), relational problems (9%), treatment rejection (13%) and organizational (12%) and clinic (8%) problems.[32]

By country

[edit]

United States

[edit]

Many Americans do not have insurance coverage for fertility investigations and treatments. Many states are starting to mandate coverage, and the rate of use is 278% higher in states with complete coverage.[33]

There are some health insurance companies that cover diagnosis of infertility, but frequently once diagnosed will not cover any treatment costs.[citation needed]

Approximate treatment/diagnosis costs in the United States, with inflation, as of 2023 (US$):

Another way to look at costs is to determine the expected cost of establishing a pregnancy. Thus, if a clomiphene treatment has a chance to establish a pregnancy in 8% of cycles and costs $780, the expected cost is $9,400 to establish a pregnancy, compared to an IVF cycle (cycle fecundity 40%) with a corresponding expected cost of $46,800 ($18,700 × 40%).[citation needed]

For the community as a whole, the cost of IVF on average pays back by 700% by tax from future employment by the conceived human being.[34]

European Union

[edit]
Number of assisted reproductive technology cycles in Europe between 1997 and 2014[35][36]

In Europe, 157,500 children were born using assisted reproductive technology in 2015, according to the European Society of Human Reproduction and Embryology (ESHRE).[35] But there are major differences in legislation across the Old Continent. A European directive fixes standards concerning the use of human tissue and cells,[37] but all ethical and legal questions on ART remain the prerogative of EU member states.

Conditions of assisted reproductive technology in different European countries:[35][38]
  ART authorized for lesbian couples
  ART authorized for single women
  ART authorized for single women and lesbian couples
  ART prohibited for single women and lesbian couples

Across Europe, the legal criteria per availability vary somewhat.[39] In 11 countries all women may benefit; in 8 others only heterosexual couples are concerned; in 7 only single women; and in 2 (Austria and Germany) only lesbian couples. Spain was the first European country to open ART to all women, in 1977, the year the first sperm bank was opened there. In France, the right to ART is accorded to all women since 2019. In the last 15 years, legislation has evolved quickly. For example, Portugal made ART available in 2006 with conditions very similar to those in France, before amending the law in 2016 to allow lesbian couples and single women to benefit. Italy clarified its uncertain legal situation in 2004 by adopting Europe's strictest laws: ART is only available to heterosexual couples, married or otherwise, and sperm donation is prohibited.

Today, 21 countries provide partial public funding for ART treatment. The seven others, which do not, are Ireland, Cyprus, Estonia, Latvia, Luxembourg, Malta, and Romania. Such subsidies are subject to conditions, however. In Belgium, a fixed payment of €1,073 is made for each full cycle of the IVF process. The woman must be aged under 43 and may not carry out more than six cycles of ART. There is also a limit on the number of transferable embryos, which varies according to age and the number of cycles completed. In France, ART is subsidized in full by national health insurance for women up to age 43, with limits of 4 attempts at IVF and 6 at artificial insemination. Germany tightened its conditions for public funding in 2004, which caused a sharp drop in the number of ART cycles carried out, from more than 102,000 in 2003 to fewer than 57,000 the following year. Since then the figure has remained stable.

17 countries limit access to ART according to the age of the woman. 10 countries have established an upper age limit, varying from 40 (Finland, Netherlands) to 50 (including Spain, Greece and Estonia). Since 1994, France is one of a number of countries (including Germany, Spain, and the UK) which use the somewhat vague notion of "natural age of procreation". In 2017, the steering council of France's Agency of Biomedicine established an age limit of 43 for women using ART. 10 countries have no age limit for ART. These include Austria, Hungary, Italy and Poland.

Most European countries allow donations of gametes by third parties. But the situations vary depending on whether sperm or eggs are concerned. Sperm donations are authorized in 20 EU member states; in 11 of them anonymity is allowed. Egg donations are possible in 17 states, including 8 under anonymous conditions. On 12 April, the Council of Europe adopted a recommendation which encourages an end to anonymity.[40] In the UK, anonymous sperm donations ended in 2005 and children have access to the identity of the donor when they reach adulthood. In France, the principle of anonymous donations of sperm or embryos is maintained in the law of bioethics of 2011, but a new bill under discussion may change the situation.[41]

United Kingdom

[edit]

In the United Kingdom, all patients have the right to preliminary testing, provided free of charge by the National Health Service (NHS). However, treatment is not widely available on the NHS and there can be long waiting lists. Many patients therefore pay for immediate treatment within the NHS or seek help from private clinics.

In 2013, the National Institute for Health and Care Excellence (NICE) published new guidelines about who should have access to IVF treatment on the NHS in England and Wales.[42]

The guidelines say women aged between 40 and 42 should be offered one cycle of IVF on the NHS if they have never had IVF treatment before, have no evidence of low ovarian reserve (this is when eggs in the ovary are low in number, or low in quality), and have been informed of the additional implications of IVF and pregnancy at this age. However, if tests show IVF is the only treatment likely to help them get pregnant, women should be referred for IVF straight away.

This policy is often modified by local Clinical Commissioning Groups, in a fairly blatant breach of the NHS Constitution for England which provides that patients have the right to drugs and treatments that have been recommended by NICE for use in the NHS. For example, the Cheshire, Merseyside and West Lancashire Clinical Commissioning Group insists on additional conditions:[43]

  • The person undergoing treatment must have commenced treatment before her 40th birthday;
  • The person undergoing treatment must have a BMI of between 19 and 29;
  • Neither partner must have any living children, from either the current or previous relationships. This includes adopted as well as biological children; and,
  • Sub-fertility must not be the direct result of a sterilisation procedure in either partner (this does not include conditions where sterilisation occurs as a result of another medical problem). Couples who have undertaken a reversal of their sterilisation procedure are not eligible for treatment.

Canada

[edit]

Some treatments are covered by OHIP (public health insurance) in Ontario and others are not. Women with bilaterally blocked fallopian tubes and are under the age of 40 have treatment covered but are still required to pay test fees (around CA$3,000–4,000). Coverage varies in other provinces. Most other patients are required to pay for treatments themselves.[44]

Israel

[edit]

Israel's national health insurance, which is mandatory for all Israeli citizens, covers nearly all fertility treatments. IVF costs are fully subsidized up to the birth of two children for all Israeli women, including single women and lesbian couples. Embryo transfers for purposes of gestational surrogacy are also covered.[45]

Germany

[edit]

On 27 January 2009, the Federal Constitutional Court ruled that it is unconstitutional, that the health insurance companies have to bear only 50% of the cost for IVF.[46] On 2 March 2012, the Federal Council has approved a draft law of some federal states, which provides that the federal government provides a subsidy of 25% to the cost. Thus, the share of costs borne for the pair would drop to just 25%.[47] Since July 2017, assisted reproductive technology is also allowed for married lesbian couples, as German parliament allowed same-sex marriages in Germany.

France

[edit]

In July 2020, the French Parliament allowed assisted reproductive technology also for lesbian couples and single women.[48][49]

Cuba

[edit]

Cuban sources mention that assisted reproduction is completely legal and free in the country.[50][51]

India

[edit]

The Government of India has notified the Surrogacy (Regulation) Act 2021 and the Assisted Reproductive Technology (Regulation) Act 2021[52] to regulate the practice of ART. Prior to that, the National Guidelines for Accreditation, Supervision and Regulation of ART Clinics in India published by the Ministry for Health and Family Welfare, Government of India in the year 2005 was governing the field.[53] Indian law recognises the right of a single woman, who is a major, to have children through ART.[54]

Society and culture

[edit]

Ethics

[edit]

Some couples may find it difficult to stop treatment despite very bad prognosis, resulting in futile therapies. This has the potential to give ART providers a difficult decision of whether to continue or refuse treatment.[55]

Some assisted reproductive technologies have the potential to be harmful to both the mother and child, posing a psychological and/or physical health risk, which may impact the ongoing use of these treatments.

In Israel, there is research supporting using ART, including recycled lab materials from the IVF process, to help women work through some of these mixed emotions.[56][57][58][59]

Fictional representation

[edit]

Films and other fiction depicting emotional struggles of assisted reproductive technology have had an upswing in the latter part of the 2000s decade, although the techniques have been available for decades.[60] As ART becomes more utilized, the number of people that can relate to it by personal experience in one way or another is growing.[60]

For specific examples, refer to the fiction sections in individual subarticles, e.g. surrogacy, sperm donation and fertility clinic.

In addition, reproduction and pregnancy in speculative fiction has been present for many decades.

Historical facts

[edit]

25 July 1978, Louise Brown was born; this was the first successful birth of a child after IVF treatment. The procedure took place at Dr Kershaw's Cottage Hospital (now Dr Kershaw's Hospice) in Royton, Oldham, England. Patrick Steptoe (gynaecologist) and Robert Edwards (physiologist) worked together to develop the IVF technique.[61] Steptoe described a new method of egg extraction and Edwards were carrying out a way to fertilise eggs in the lab. Robert G. Edwards was awarded the Nobel Prize in Physiology or Medicine in 2010, but not Steptoe because the Nobel Prize is not awarded posthumously.[62]

The first successful birth by ICSI (Intracytoplasmic sperm injection) took place on 14 January 1992. The technique was developed by Gianpiero D. Palermo at the Vrije Universiteit Brussel, in the Center for Reproductive Medicine in Brussels. Actually, the discovery was made by a mistake when a spermatozoid was put into the cytoplasm.[63]

See also

[edit]

References

[edit]

 This article incorporates text from a free content work. Licensed under CC BY 4.0. Text taken from How does assisted reproductive technology work in Europe?​, Orlane Jézéquélou/Alternatives Economiques, EDJNet.

  1. ^ "What is Assisted Reproductive Technology? | Reproductive Health | CDC". CDC. November 14, 2014. Archived from the original on November 1, 2017.
  2. ^ European IVF-Monitoring Consortium (EIM) for the European Society of Human Reproduction and Embryology; Calhaz-Jorge, C.; et al. (August 2016). "Assisted reproductive technology in Europe, 2012: results generated from European registers by ESHRE". Human Reproduction (Oxford, England). 31 (8): 1638–52. doi:10.1093/humrep/dew151. PMID 27496943.
  3. ^ Sorenson, Corinna (Autumn 2006). "ART in the European Union" (PDF). Euro Observer Euro Observer. 8 (4). Archived (PDF) from the original on 2016-11-29.
  4. ^ Zegers-Hochschild, F; for the International Committee for Monitoring Assisted Reproductive Technology and the World Health Organization; et al. (November 2009). "International Committee for Monitoring Assisted Reproductive Technology (ICMART) and the World Health Organization (WHO) revised glossary of ART terminology, 2009" (PDF). Fertility and Sterility. 92 (5): 1520–4. doi:10.1016/j.fertnstert.2009.09.009. PMID 19828144. Archived (PDF) from the original on 2016-11-29.
  5. ^ Ovulation Problems and Infertility: Treatment of ovulation problems with Clomid and other fertility drugs. Advanced Fertility Center of Chicago. Gurnee & Crystal Lake, Illinois. Retrieved on Mars 7, 2010
  6. ^ Flinders reproductive medicine > Ovulation Induction Archived 2009-10-03 at the Wayback Machine Retrieved on Mars 7, 2010
  7. ^ fertilityLifeLines > Ovulation Induction Archived 2013-03-10 at the Wayback Machine Retrieved on Mars 7, 2010
  8. ^ Illmensee K, Levanduski M, Vidali A, Husami N, Goudas VT (February 2009). "Human embryo twinning with applications in reproductive medicine". Fertil. Steril. 93 (2): 423–7. doi:10.1016/j.fertnstert.2008.12.098. PMID 19217091.
  9. ^ Sullivan-Pyke, C; Dokras, A (March 2018). "Preimplantation Genetic Screening and Preimplantation Genetic Diagnosis". Obstetrics and Gynecology Clinics of North America. 45 (1): 113–125. doi:10.1016/j.ogc.2017.10.009. PMID 29428279.
  10. ^ Scully, Jackie Leach (January 2017). "A Mitochondrial Story: Mitochondrial Replacement, Identity and Narrative". Bioethics. 31 (1): 37–45. doi:10.1111/bioe.12310. hdl:1959.4/unsworks_66960. ISSN 1467-8519. PMID 27973722.
  11. ^ Claiborne, A.; English, R.; Kahn, J. (2016). Claiborne, Anne; English, Rebecca; Kahn, Jeffrey (eds.). Mitochondrial Replacement Techniques: Ethical, Social, and Policy Considerations. National Academies Press. doi:10.17226/21871. ISBN 978-0-309-38870-2. PMID 27054230. Index page Archived 2018-11-26 at the Wayback Machine with links to summaries including one page summary flyer Archived 2017-10-30 at the Wayback Machine.
  12. ^ Cree, L; Loi, P (January 2015). "Mitochondrial replacement: from basic research to assisted reproductive technology portfolio tool-technicalities and possible risks". Molecular Human Reproduction. 21 (1): 3–10. doi:10.1093/molehr/gau082. PMID 25425606. Open access icon
  13. ^ a b Van Voorhis BJ (2007). "Clinical practice. In vitro fertilization". N Engl J Med. 356 (4): 379–86. doi:10.1056/NEJMcp065743. PMID 17251534.
  14. ^ Kurinczuk JJ, Hansen M, Bower C (2004). "The risk of birth defects in children born after assisted reproductive technologies". Current Opinion in Obstetrics and Gynecology. 16 (3): 201–9. doi:10.1097/00001703-200406000-00002. PMID 15129049. S2CID 23159787.
  15. ^ Hansen M, Bower C, Milne E, de Klerk N, Kurinczuk JJ (2005). "Assisted reproductive technologies and the risk of birth defects—a systematic review". Hum Reprod. 20 (2): 328–38. doi:10.1093/humrep/deh593. PMID 15567881.
  16. ^ Aiken, Catherine E. M.; Brockelsby, Jeremy C. (2016). "Fetal and Maternal Consequences of Pregnancies Conceived Using Art". Fetal and Maternal Medicine Review. 25 (3–4): 281–294. doi:10.1017/S096553951600005X.
  17. ^ Olson CK, Keppler-Noreuil KM, Romitti PA, Budelier WT, Ryan G, Sparks AE, Van Voorhis BJ (2005). "In vitro fertilization is associated with an increase in major birth defects". Fertil Steril. 84 (5): 1308–15. doi:10.1016/j.fertnstert.2005.03.086. PMID 16275219.
  18. ^ MD, Daniel M. Avery, MD, Marion D. Reed, MD, William L. Lenahan. "What you should know about heterotopic pregnancy : OBG Management". www.obgmanagement.com. Retrieved 2016-07-28.{{cite web}}: CS1 maint: multiple names: authors list (link)
  19. ^ "In vitro fertilization (IVF): MedlinePlus Medical Encyclopedia". medlineplus.gov. Retrieved 2018-11-07.
  20. ^ Zhang Y, Zhang YL, Feng C, et al. (September 2008). "Comparative proteomic analysis of human placenta derived from assisted reproductive technology". Proteomics. 8 (20): 4344–56. doi:10.1002/pmic.200800294. PMID 18792929. S2CID 206362532.
  21. ^ Hvidtjørn D, Schieve L, Schendel D, Jacobsson B, Sværke C, Thorsen P (2009). "Cerebral palsy, autism spectrum disorders, and developmental delay in children born after assisted conception: a systematic review and meta-analysis". Arch Pediatr Adolesc Med. 163 (1): 72–83. doi:10.1001/archpediatrics.2008.507. PMID 19124707.
  22. ^ a b c McCarrey JR. Maintenance of genetic integrity during natural and assisted reproduction. Reprod Biomed Online. 2009;18 Suppl 2:51-5. doi: 10.1016/s1472-6483(10)60449-x. PMID 19406032
  23. ^ Ross, L. E.; McQueen, K.; Vigod, S.; Dennis, C.-L. (2010). "Risk for postpartum depression associated with assisted reproductive technologies and multiple births: A systematic review". Human Reproduction Update. 17 (1): 96–106. doi:10.1093/humupd/dmq025. PMID 20605900.
  24. ^ Piva, Isabella; Lo Monte, Giuseppe; Graziano, Angela; Marci, Roberto (August 2014). "A literature review on the relationship between infertility and sexual dysfunction: Does fun end with baby making?". The European Journal of Contraception & Reproductive Health Care. 19 (4): 231–237. doi:10.3109/13625187.2014.919379. ISSN 1362-5187. PMID 24901746.
  25. ^ Hargreave, Marie; Jensen, Allan; Toender, Anita; Andersen, Klaus Kaae; Kjaer, Susanne Krüger (2013). "Fertility treatment and childhood cancer risk: A systematic meta-analysis". Fertility and Sterility. 100 (1): 150–61. doi:10.1016/j.fertnstert.2013.03.017. PMID 23562045.
  26. ^ Balayla, Jacques, Odile Sheehy, William D. Fraser, Jean R. Séguin, Jacquetta Trasler, Patricia Monnier, Andrea A. MacLeod, Marie-Noëlle Simard, Gina Muckle, and Anick Bérard. "Neurodevelopmental Outcomes After Assisted Reproductive Technologies." Obstetrics & Gynecology (2017).
  27. ^ "Assisted conception is linked to cardiovascular disease and birth complications". NIHR Evidence. 2022-09-20. doi:10.3310/nihrevidence_53388. S2CID 252416365.
  28. ^ Wu, Pensée; Sharma, Garima V.; Mehta, Laxmi S.; Chew-Graham, Carolyn A.; Lundberg, Gina P.; Nerenberg, Kara A.; Graham, Michelle M.; Chappell, Lucy C.; Kadam, Umesh T.; Jordan, Kelvin P.; Mamas, Mamas A. (2022-02-22). "In-Hospital Complications in Pregnancies Conceived by Assisted Reproductive Technology". Journal of the American Heart Association. 11 (5): e022658. doi:10.1161/JAHA.121.022658. ISSN 2047-9980. PMC 9075081. PMID 35191320.
  29. ^ "Policy Document | Assisted Reproductive Technology (ART) | Reproductive Health | CDC". www.cdc.gov. 2019-01-31. Retrieved 2019-11-14.
  30. ^ a b chicagotribune.com Infertility by the numbers Archived 2009-07-05 at the Wayback Machine Colleen Mastony. June 21, 2009
  31. ^ 'More IVF babies but less multiple births' Archived 2009-09-24 at the Wayback Machine THE AUSTRALIAN. September 24, 2009
  32. ^ Gameiro, S.; Boivin, J.; Peronace, L.; Verhaak, C. M. (2012). "Why do patients discontinue fertility treatment? A systematic review of reasons and predictors of discontinuation in fertility treatment". Human Reproduction Update. 18 (6): 652–69. doi:10.1093/humupd/dms031. PMC 3461967. PMID 22869759.
  33. ^ Jain T, Harlow BL, Hornstein MD (August 2002). "Insurance coverage and outcomes of in vitro fertilization". N. Engl. J. Med. 347 (9): 661–6. doi:10.1056/NEJMsa013491. PMID 12200554.
  34. ^ Connolly MP, Pollard MS, Hoorens S, Kaplan BR, Oskowitz SP, Silber SJ (September 2008). "Long-term economic benefits attributed to IVF-conceived children: a lifetime tax calculation". Am J Manag Care. 14 (9): 598–604. PMID 18778175.
  35. ^ a b c Jézéquélou, Orlane (23 October 2019). "How does assisted reproductive technology work in Europe?". Alternatives Economiques/EDJNet. Retrieved 29 November 2019.
  36. ^ De Geyter, Ch.; Calhaz-Jorge, C.; Kupka, M.S.; Wyns, C.; Mocanu, E.; Motrenko, T.; Scaravelli, G.; Smeenk, J.; Vidakovic1, S.; Goossens, V. (September 2018). "ART in Europe, 2014: results generated from European registries by ESHRE: The European IVF-monitoring Consortium (EIM) for the European Society of Human Reproduction and Embryology (ESHRE)". Human Reproduction. 33 (9): 1586–1601. doi:10.1093/humrep/dey242. hdl:10451/49519. PMID 30032255.{{cite journal}}: CS1 maint: numeric names: authors list (link)
  37. ^ "Directive 2004/23/EC of the European Parliament and of the Council of 31 March 2004 on setting standards of quality and safety for the donation, procurement, testing, processing, preservation, storage and distribution of human tissues and cells". Retrieved 3 December 2019.
  38. ^ "Rainbow Map". ILGA-Europe. Retrieved 2019-11-12.
  39. ^ "Encadrement juridique international dans les différents domaines de la bioéthique" (PDF) (in French). Agence de la biomédecine. Retrieved 2019-11-04.
  40. ^ "Recommendation 2156 (2019) - Anonymous donation of sperm and oocytes: balancing the rights of parents, donors and children". Retrieved 2019-11-12.
  41. ^ Céline Mouzon (2019-09-23). "PMA: panique dans la filiation" (in French). Retrieved 2019-11-12.
  42. ^ "IVF". NHS Choices. Archived from the original on 20 April 2014. Retrieved 19 April 2014.
  43. ^ "Services & how we can help". Liverpool Women's NHS Foundation Trust. Archived from the original on 2014-06-24. Retrieved 19 April 2014.
  44. ^ "IVF Canada". Archived from the original on August 8, 2009.
  45. ^ Teman, Elly. 2010. Birthing a Mother: the Surrogate Body and the Pregnant Self. Archived 2009-11-21 at the Wayback Machine Berkeley: University of California Press
  46. ^ Zuschüsse der Krankenversicherung für eine künstliche Befruchtung Archived 2013-02-08 at the Wayback Machine Retrieved 2. January 2013.
  47. ^ Finanzierung künstlicher Befruchtung Archived 2013-02-19 at the Wayback Machine Retrieved 2. January 2013.
  48. ^ Queer.de: Frankreich: Künstliche Befruchtung auch für lesbische Paare (german), July 21, 2020
  49. ^ NOZ.de: Beifall im Parlament: Frankreich legalisiert künstliche Befruchtung für alle Frauen (german), July 31, 2020
  50. ^ http://www.ahora.cu/fr/sante/5715-reproduction-assistee-et-droit-du-travail-a-cuba (in French), on Ahora
  51. ^ http://www.granma.cu/cuba/2020-01-15/reproduccion-asistida-en-cuba-nuevas-razones-para-la-felicidad (in Spanish), on Granma.cu
  52. ^ "Govt notifies laws to regulate surrogacy, assisted reproductive technology". Business Today. 26 January 2022. Retrieved 2022-02-03.
  53. ^ "IVF Clinics". pib.gov.in. Retrieved 2022-02-03.
  54. ^ A, Aruna (2021-09-14). "Need to understand the rights of a single mother by choice". Legal Bay. Retrieved 2022-02-03.
  55. ^ Ethics Committee of the American Society for Reproductive Medicine (2009). "Fertility treatment when the prognosis is very poor or futile". Fertility and Sterility. 92 (4): 1194–7. doi:10.1016/j.fertnstert.2009.07.979. PMID 19726040.
  56. ^ Article link: Dr. Katan, Seven news, 14.1.2022, Hebrew See section on Artistic conception הפריה אומנותית.
  57. ^ Gilat Kupietzky-Sacks, IVF Embryologist and initiator of the project and Miriam Kupietzky, Art Therapist run a women's workshop using recycled lab material. about workshop
  58. ^ Workshop on the Use of Life Cycle Concepts about workshop in the USA and other countries
  59. ^ Angela Savage. "Works of ART: on creativity, infertility and Assisted Reproductive Technology." In Art, 25.7.2016. Article on art produced in response to IVF treatment [1]
  60. ^ a b "Heartache of infertility shared on stage, screen". chicagotribune.com. Archived from the original on 2012-07-03. Retrieved 2009-06-23. By Colleen Mastony, Tribune reporter. June 21, 2009
  61. ^ "1978: First 'test tube baby' born". July 25, 1978 – via news.bbc.co.uk.
  62. ^ "The Nobel Prize in Physiology or Medicine 2010".
  63. ^ Palermo, G; Joris, H; Devroey, P; Van Steirteghem, AC (1992). "Pregnancies after intracytoplasmic injection of single spermatozoon into an oocyte". Lancet. 340 (8810): 17–8. doi:10.1016/0140-6736(92)92425-f. PMID 1351601. S2CID 2916063.
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