Obstetrical bleeding: Difference between revisions
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{{Short description|Bleeding in pregnancy that occurs before, during, or after childbirth}} |
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{{Infobox medical condition (new) |
{{Infobox medical condition (new) |
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| name = Obstetrical bleeding |
| name = Obstetrical bleeding |
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| synonyms = Maternal bleeding, obstetrical hemorrhage, maternal hemorrhage |
| synonyms = Maternal bleeding, obstetrical hemorrhage, obstetric haemorrhage,<ref name="ICD-11 JA4">{{cite web | title=ICD-11 for Mortality and Morbidity Statistics | url=https://icd.who.int/browse11/l-m/en#/http%3A%2F%2Fid.who.int%2Ficd%2Fentity%2F903303141 |website= World Health Organization | access-date=2023-12-05}}</ref> maternal hemorrhage |
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<!-- Epidemiology --> |
<!-- Epidemiology --> |
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About 8.7 million cases of severe maternal bleeding occurred in 2015<ref name=GBD2016Inc>{{cite journal | title = Global, regional, and national incidence, prevalence, and years lived with disability for 310 diseases and injuries, 1990-2015: a systematic analysis for the Global Burden of Disease Study 2015 | journal = Lancet | volume = 388 | issue = 10053 | pages = 1545–1602 | date = October 2016 | pmid = 27733282 | pmc = 5055577 | doi = 10.1016/S0140-6736(16)31678-6 | last1 = Vos | first1 = Theo | last2 = Allen | first2 = Christine | last3 = Arora | first3 = Megha | last4 = Barber | first4 = Ryan M. | last5 = Bhutta | first5 = Zulfiqar A. | last6 = Brown | first6 = Alexandria | last7 = Carter | first7 = Austin | last8 = Casey | first8 = Daniel C. | last9 = Charlson | first9 = Fiona J. | last10 = Chen | first10 = Alan Z. | last11 = Coggeshall | first11 = Megan | last12 = Cornaby | first12 = Leslie | last13 = Dandona | first13 = Lalit | last14 = Dicker | first14 = Daniel J. | last15 = Dilegge | first15 = Tina | last16 = Erskine | first16 = Holly E. | last17 = Ferrari | first17 = Alize J. | last18 = Fitzmaurice | first18 = Christina | last19 = Fleming | first19 = Tom | last20 = Forouzanfar | first20 = Mohammad H. | last21 = Fullman | first21 = Nancy | last22 = Gething | first22 = Peter W. | last23 = Goldberg | first23 = Ellen M. | last24 = Graetz | first24 = Nicholas | last25 = Haagsma | first25 = Juanita A. | last26 = Hay | first26 = Simon I. | last27 = Johnson | first27 = Catherine O. | last28 = Kassebaum | first28 = Nicholas J. | last29 = Kawashima | first29 = Toana | last30 = Kemmer | first30 = Laura | |
About 8.7 million cases of severe maternal bleeding occurred in 2015<ref name=GBD2016Inc>{{cite journal | title = Global, regional, and national incidence, prevalence, and years lived with disability for 310 diseases and injuries, 1990-2015: a systematic analysis for the Global Burden of Disease Study 2015 | journal = Lancet | volume = 388 | issue = 10053 | pages = 1545–1602 | date = October 2016 | pmid = 27733282 | pmc = 5055577 | doi = 10.1016/S0140-6736(16)31678-6 | last1 = Vos | first1 = Theo | last2 = Allen | first2 = Christine | last3 = Arora | first3 = Megha | last4 = Barber | first4 = Ryan M. | last5 = Bhutta | first5 = Zulfiqar A. | last6 = Brown | first6 = Alexandria | last7 = Carter | first7 = Austin | last8 = Casey | first8 = Daniel C. | last9 = Charlson | first9 = Fiona J. | last10 = Chen | first10 = Alan Z. | last11 = Coggeshall | first11 = Megan | last12 = Cornaby | first12 = Leslie | last13 = Dandona | first13 = Lalit | last14 = Dicker | first14 = Daniel J. | last15 = Dilegge | first15 = Tina | last16 = Erskine | first16 = Holly E. | last17 = Ferrari | first17 = Alize J. | last18 = Fitzmaurice | first18 = Christina | last19 = Fleming | first19 = Tom | last20 = Forouzanfar | first20 = Mohammad H. | last21 = Fullman | first21 = Nancy | last22 = Gething | first22 = Peter W. | last23 = Goldberg | first23 = Ellen M. | last24 = Graetz | first24 = Nicholas | last25 = Haagsma | first25 = Juanita A. | last26 = Hay | first26 = Simon I. | last27 = Johnson | first27 = Catherine O. | last28 = Kassebaum | first28 = Nicholas J. | last29 = Kawashima | first29 = Toana | last30 = Kemmer | first30 = Laura | display-authors = 29 }}</ref> resulting in 83,000 deaths.<ref name=GBD2016De>{{cite journal | title = Global, regional, and national life expectancy, all-cause mortality, and cause-specific mortality for 249 causes of death, 1980-2015: a systematic analysis for the Global Burden of Disease Study 2015 | journal = Lancet | volume = 388 | issue = 10053 | pages = 1459–1544 | date = October 2016 | pmid = 27733281 | pmc = 5388903 | doi = 10.1016/S0140-6736(16)31012-1 | last1 = Wang | first1 = Haidong | last2 = Naghavi | first2 = Mohsen | last3 = Allen | first3 = Christine | last4 = Barber | first4 = Ryan M. | last5 = Bhutta | first5 = Zulfiqar A. | last6 = Carter | first6 = Austin | last7 = Casey | first7 = Daniel C. | last8 = Charlson | first8 = Fiona J. | last9 = Chen | first9 = Alan Zian | last10 = Coates | first10 = Matthew M. | last11 = Coggeshall | first11 = Megan | last12 = Dandona | first12 = Lalit | last13 = Dicker | first13 = Daniel J. | last14 = Erskine | first14 = Holly E. | last15 = Ferrari | first15 = Alize J. | last16 = Fitzmaurice | first16 = Christina | last17 = Foreman | first17 = Kyle | last18 = Forouzanfar | first18 = Mohammad H. | last19 = Fraser | first19 = Maya S. | last20 = Fullman | first20 = Nancy | last21 = Gething | first21 = Peter W. | last22 = Goldberg | first22 = Ellen M. | last23 = Graetz | first23 = Nicholas | last24 = Haagsma | first24 = Juanita A. | last25 = Hay | first25 = Simon I. | last26 = Huynh | first26 = Chantal | last27 = Johnson | first27 = Catherine O. | last28 = Kassebaum | first28 = Nicholas J. | last29 = Kinfu | first29 = Yohannes | last30 = Kulikoff | first30 = Xie Rachel | display-authors = 29 }}</ref> Between 2003 and 2009, bleeding accounted for 27% of maternal deaths globally.<ref name="SayChou2014">{{cite journal|last1=Say|first1=Lale|last2=Chou|first2=Doris|last3=Gemmill|first3=Alison|last4=Tunçalp|first4=Özge|last5=Moller|first5=Ann-Beth|last6=Daniels|first6=Jane|last7=Gülmezoglu|first7=A Metin|last8=Temmerman|first8=Marleen|last9=Alkema|first9=Leontine|title=Global causes of maternal death: a WHO systematic analysis|journal=The Lancet Global Health|volume=2|issue=6|year=2014|pages=e323–e333|issn=2214-109X|doi=10.1016/S2214-109X(14)70227-X|pmid=25103301|doi-access=free|hdl=1854/LU-5796925|hdl-access=free}}</ref> |
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==Later pregnancy== |
==Later pregnancy== |
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{{main|Antepartum bleeding}} |
{{main|Antepartum bleeding}} |
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[[Antepartum bleeding]] (APH), also prepartum hemorrhage, is bleeding during pregnancy from the 24th week<ref name=":0">[http://patient.info/doctor/antepartum-haemorrhage patient.info » PatientPlus » Antepartum Haemorrhage] Last Updated: 5 May 2009</ref> (sometimes defined as from the 20th week<ref>[http://www.thewomens.org.au/AntepartumHaemorrhage The Royal Women’s Hospital > antepartum haemorrhage] {{webarchive|url=https://web.archive.org/web/20100108223247/http://www.thewomens.org.au/AntepartumHaemorrhage |date=2010-01-08 }} Retrieved on Jan 13, 2009</ref><ref name=":0" />) [[gestational age]] up to the birth of the baby.<ref name=St2010Ant/> The primary consideration is the presence of a [[placenta previa]] which is a low lying placenta at or very near to the internal cervical os. This condition occurs in roughly 4 out of 1000 <ref name="pmid27902772">{{cite journal | vauthors = Soyama H, Miyamoto M, Ishibashi H, Takano M, Sasa H, Furuya K | title = Relation between Birth Weight and Intraoperative Hemorrhage during Cesarean Section in Pregnancy with Placenta Previa | journal = PLOS ONE | volume = 11 | issue = 11 | pages = e0167332 | date = 2016 | pmid = 27902772 | pmc = 5130260 | doi = 10.1371/journal.pone.0167332 }}</ref> pregnancies and usually needs to be resolved by delivering the baby via [[cesarean section]]. Also a placental [[abruption]] (in which there is premature separation of the placenta) can lead to obstetrical hemorrhage, sometimes concealed. This pathology is of important consideration after maternal trauma such as a motor vehicle accident or fall. |
[[Antepartum bleeding]] (APH), also prepartum hemorrhage, is bleeding during pregnancy from the 24th week<ref name=":0">[http://patient.info/doctor/antepartum-haemorrhage patient.info » PatientPlus » Antepartum Haemorrhage] Last Updated: 5 May 2009</ref> (sometimes defined as from the 20th week<ref>[http://www.thewomens.org.au/AntepartumHaemorrhage The Royal Women’s Hospital > antepartum haemorrhage] {{webarchive|url=https://web.archive.org/web/20100108223247/http://www.thewomens.org.au/AntepartumHaemorrhage |date=2010-01-08 }} Retrieved on Jan 13, 2009</ref><ref name=":0" />) [[Gestational age (obstetrics)|gestational age]] up to the birth of the baby.<ref name=St2010Ant/> The primary consideration is the presence of a [[placenta previa]] which is a low lying placenta at or very near to the internal cervical os. This condition occurs in roughly 4 out of 1000 <ref name="pmid27902772">{{cite journal | vauthors = Soyama H, Miyamoto M, Ishibashi H, Takano M, Sasa H, Furuya K | title = Relation between Birth Weight and Intraoperative Hemorrhage during Cesarean Section in Pregnancy with Placenta Previa | journal = PLOS ONE | volume = 11 | issue = 11 | pages = e0167332 | date = 2016 | pmid = 27902772 | pmc = 5130260 | doi = 10.1371/journal.pone.0167332 | bibcode = 2016PLoSO..1167332S | doi-access = free }}</ref> pregnancies and usually needs to be resolved by delivering the baby via [[cesarean section]]. Also a placental [[abruption]] (in which there is premature separation of the placenta) can lead to obstetrical hemorrhage, sometimes concealed. This pathology is of important consideration after maternal trauma such as a motor vehicle accident or fall. |
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Other considerations to include when assessing antepartum bleeding are: sterile vaginal exams that are performed in order to assess dilation of the patient when the 40th week is approaching. As well as cervical insufficiency defined as a midtrimester (14th-26th week) dilation of the cervix which may need medical intervention to assist in keeping the pregnancy sustainable.<ref>{{Cite web|url=https://www.uptodate.com/contents/cervical-insufficiency|title=Cervical insufficiency|last=Berghella, MD|first=Vincenzo|date=July 2017|website=UpToDate |
Other considerations to include when assessing antepartum bleeding are: sterile vaginal exams that are performed in order to assess dilation of the patient when the 40th week is approaching. As well as cervical insufficiency defined as a midtrimester (14th-26th week) dilation of the cervix which may need medical intervention to assist in keeping the pregnancy sustainable.<ref>{{Cite web|url=https://www.uptodate.com/contents/cervical-insufficiency|title=Cervical insufficiency|last=Berghella, MD|first=Vincenzo|date=July 2017|website=UpToDate}}</ref> |
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===During labor=== |
===During labor=== |
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Besides placenta previa and placental abruption, [[uterine rupture]] can occur, which is a very serious condition leading to internal or external bleeding. Bleeding from the [[fetus]] is rare, but may occur with two conditions called vasa previa and velamentous umbilical cord insertion where the fetal blood vessels lie near the placental insertion site unprotected by Wharton's jelly of the cord.<ref>{{Cite web|url=http://stage0www.uptodate.com/contents/velamentous-umbilical-cord-insertion-and-vasa-previa?source=search_result&search=Vasa+previa&selectedTitle=1~17|title=Velamentous umbilical cord insertion and vasa previa|vauthors = ((Charles J Lockwood, MD, MHCM)), ((Karen Russo-Stieglitz, MD))|date=July 2017|website=UpToDate |
Besides [[Placenta praevia|placenta previa]] and [[placental abruption]], [[uterine rupture]] can occur, which is a very serious condition leading to internal or external bleeding. Bleeding from the [[fetus]] is rare, but may occur with two conditions called [[Vasa praevia|vasa previa]] and [[Velamentous cord insertion|velamentous umbilical cord insertion]] where the fetal blood vessels lie near the placental insertion site unprotected by Wharton's jelly of the cord.<ref>{{Cite web|url=http://stage0www.uptodate.com/contents/velamentous-umbilical-cord-insertion-and-vasa-previa?source=search_result&search=Vasa+previa&selectedTitle=1~17|title=Velamentous umbilical cord insertion and vasa previa|vauthors = ((Charles J Lockwood, MD, MHCM)), ((Karen Russo-Stieglitz, MD))|date=July 2017|website=UpToDate}}</ref> Occasionally this condition can be diagnosed by ultrasound. There are also tests to differentiate maternal blood from fetal blood which can help in determining the source of the bleed. |
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==After delivery== |
==After delivery== |
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{{main|Postpartum bleeding}} |
{{main|Postpartum bleeding}} |
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Abnormal bleeding after delivery, or postpartum hemorrhage, is the loss of greater than 500 ml of blood following vaginal delivery, or 1000 ml of blood following cesarean section. Other definitions of excessive postpartum bleeding are hemodynamic instability, drop of hemoglobin of more than 10%,<ref name="pmid27050823">{{cite journal | vauthors = Atukunda EC, Mugyenyi GR, Obua C, Atuhumuza EB, Musinguzi N, Tornes YF, Agaba AG, Siedner MJ | title = Measuring Post-Partum Haemorrhage in Low-Resource Settings: The Diagnostic Validity of Weighed Blood Loss versus Quantitative Changes in Hemoglobin | journal = PLOS ONE | volume = 11 | issue = 4 | pages = e0152408 | date = 2016 | pmid = 27050823 | pmc = 4822885 | doi = 10.1371/journal.pone.0152408 }}</ref> or requiring blood transfusion. In the literature, primary postpartum hemorrhage is defined as uncontrolled bleeding that occurs in the first 24 hours after delivery while secondary hemorrhage occurs between 24 hours and six weeks.<ref name=":1">Global burden of maternal haemorrhage in the year 2000 Carmen Dolea1, Carla AbouZahr2, Claudia Stein1 Evidence and Information for Policy (EIP), World Health Organization, Geneva, July 2003</ref> |
Abnormal bleeding after delivery, or postpartum hemorrhage, is the loss of greater than 500 ml of blood following vaginal delivery, or 1000 ml of blood following cesarean section. Other definitions of excessive postpartum bleeding are hemodynamic instability, drop of hemoglobin of more than 10%,<ref name="pmid27050823">{{cite journal | vauthors = Atukunda EC, Mugyenyi GR, Obua C, Atuhumuza EB, Musinguzi N, Tornes YF, Agaba AG, Siedner MJ | title = Measuring Post-Partum Haemorrhage in Low-Resource Settings: The Diagnostic Validity of Weighed Blood Loss versus Quantitative Changes in Hemoglobin | journal = PLOS ONE | volume = 11 | issue = 4 | pages = e0152408 | date = 2016 | pmid = 27050823 | pmc = 4822885 | doi = 10.1371/journal.pone.0152408 | bibcode = 2016PLoSO..1152408A | doi-access = free }}</ref> or requiring blood transfusion. In the literature, primary postpartum hemorrhage is defined as uncontrolled bleeding that occurs in the first 24 hours after delivery while secondary hemorrhage occurs between 24 hours and six weeks.<ref name=":1">Global burden of maternal haemorrhage in the year 2000 Carmen Dolea1, Carla AbouZahr2, Claudia Stein1 Evidence and Information for Policy (EIP), World Health Organization, Geneva, July 2003</ref> |
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== Risk factors == |
== Risk factors == |
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In rare cases, inherited bleeding disorders, like [[hemophilia]], [[von Willebrand disease]] (vWD), or [[Factor IX deficiency|factor IX]] or [[Haemophilia C|XI]] deficiency, may cause severe postpartum hemorrhage, with an increased risk of death particularly in the postpartum period.<ref name=":1" /> The risk of postpartum hemorrhage in patients with vWD and carriers of hemophilia has been found to be 18.5% and 22% respectively. This pathology occurs due to the normal physiological drop in maternal clotting factors after delivery which greatly increases the risk of secondary postpartum hemorrhage.<ref name="pmid11251653">{{cite journal | vauthors = Kadir RA, Aledort LM | title = Obstetrical and gynaecological bleeding: a common presenting symptom | journal = Clinical and Laboratory Haematology | volume = 22 |
In rare cases, inherited bleeding disorders, like [[hemophilia]], [[von Willebrand disease]] (vWD), or [[Factor IX deficiency|factor IX]] or [[Haemophilia C|XI]] deficiency, may cause severe postpartum hemorrhage, with an increased risk of death particularly in the postpartum period.<ref name=":1" /> The risk of postpartum hemorrhage in patients with vWD and carriers of hemophilia has been found to be 18.5% and 22% respectively. This pathology occurs due to the normal physiological drop in maternal clotting factors after delivery which greatly increases the risk of secondary postpartum hemorrhage.<ref name="pmid11251653">{{cite journal | vauthors = Kadir RA, Aledort LM | title = Obstetrical and gynaecological bleeding: a common presenting symptom | journal = Clinical and Laboratory Haematology | volume = 22 | pages = 12–6; discussion 30–2 | date = October 2000 | issue = Suppl 1 | pmid = 11251653 | doi = 10.1046/j.1365-2257.2000.00007.x}}</ref> |
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Another bleeding risk factor is thrombocytopenia, or decreased platelet levels, which is the most common hematological change associated with pregnancy induced hypertension. If platelet counts drop less than 100,000 per microliter the patient will be at a severe risk for inability to clot during and after delivery.<ref>{{Cite book|title=Pregnancy and birth sourcebook|last=Aldred|first=Heather E.|publisher=health reference series|year=1997|isbn=9780780802162 |
Another bleeding risk factor is thrombocytopenia, or decreased platelet levels, which is the most common hematological change associated with pregnancy induced hypertension. If platelet counts drop less than 100,000 per microliter the patient will be at a severe risk for inability to clot during and after delivery.<ref>{{Cite book|title=Pregnancy and birth sourcebook|last=Aldred|first=Heather E.|publisher=health reference series|year=1997|isbn=9780780802162}}</ref> |
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== Medical tests == |
== Medical tests == |
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If a small amount of bleeding is seen in early pregnancy a physician may request: |
If a small amount of bleeding is seen in early pregnancy a physician may request: |
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* A quantitative human chorionic gonadotropin (hCG) blood test to confirm the pregnancy or assist in diagnosing a potential miscarriage <ref name="HeineSwamy">{{Cite web|url=https://www.merckmanuals.com/professional/gynecology-and-obstetrics/symptoms-during-pregnancy/vaginal-bleeding-during-early-pregnancy|title=Vaginal bleeding during early pregnancy|vauthors = Heine PR, Swamy GK|date=August 2009|website=Merck Manual |
* A quantitative human chorionic gonadotropin (hCG) blood test to confirm the pregnancy or assist in diagnosing a potential miscarriage <ref name="HeineSwamy">{{Cite web|url=https://www.merckmanuals.com/professional/gynecology-and-obstetrics/symptoms-during-pregnancy/vaginal-bleeding-during-early-pregnancy|title=Vaginal bleeding during early pregnancy|vauthors = Heine PR, Swamy GK|date=August 2009|website=Merck Manual}}</ref> |
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* Transvaginal pelvic ultrasonography to confirm that the pregnancy is not outside of the uterus<ref name="HeineSwamy"/> |
* Transvaginal pelvic ultrasonography to confirm that the pregnancy is not outside of the uterus<ref name="HeineSwamy"/> |
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* Blood type and Rh test to rule out [[hemolytic disease of the newborn]]<ref name="HeineSwamy"/> |
* Blood type and Rh test to rule out [[hemolytic disease of the newborn]]<ref name="HeineSwamy"/> |
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==Unrelated bleeding== |
==Unrelated bleeding== |
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Pregnant patients may have bleeding from the reproductive tract due to trauma, including sexual trauma, neoplasm, most commonly [[cervical cancer]], and [[hematologic disorder]]s. Molar pregnancy (also called [[Molar pregnancy|hydatiform mole]]) is a type of pregnancy where the sperm and the egg have joined within the uterus, but the result is a cyst resembling a grape-like cluster rather than an embryo. Bleeding can be an early sign of this tumor developing.<ref>{{Cite book|title=Pregnancy and birth sourcebook|last=Aldred|first=Heather E.|publisher=Omnigraphics|year=1997|isbn=9780780802162 |
Pregnant patients may have bleeding from the reproductive tract due to trauma, including sexual trauma, neoplasm, most commonly [[cervical cancer]], and [[hematologic disorder]]s. Molar pregnancy (also called [[Molar pregnancy|hydatiform mole]]) is a type of pregnancy where the sperm and the egg have joined within the uterus, but the result is a cyst resembling a grape-like cluster rather than an embryo. Bleeding can be an early sign of this tumor developing.<ref>{{Cite book|title=Pregnancy and birth sourcebook|last=Aldred|first=Heather E.|publisher=Omnigraphics|year=1997|isbn=9780780802162}}</ref> |
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==See also== |
==See also== |
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{{offline|med}} |
{{offline|med}} |
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{{Women's health|state=collapsed}} |
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{{Pathology of pregnancy, childbirth and the puerperium}} |
{{Pathology of pregnancy, childbirth and the puerperium}} |
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{{Pregnancy}} |
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{{DEFAULTSORT:Obstetrical Hemorrhage}} |
{{DEFAULTSORT:Obstetrical Hemorrhage}} |
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[[Category:Health issues in pregnancy]] |
[[Category:Health issues in pregnancy]] |
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[[Category:Women's health]] |
[[Category:Women's health]] |
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[[Category:Obstetric haemorrhage]] |
Latest revision as of 23:36, 21 July 2024
Obstetrical bleeding | |
---|---|
Other names | Maternal bleeding, obstetrical hemorrhage, obstetric haemorrhage,[1] maternal hemorrhage |
Specialty | Obstetrics |
Frequency | 8.7 million (2015)[2] |
Deaths | 83,000 (2015)[3] |
Obstetrical bleeding is bleeding in pregnancy that occurs before, during, or after childbirth.[4] Bleeding before childbirth is that which occurs after 24 weeks of pregnancy.[4] Bleeding may be vaginal or less commonly into the abdominal cavity. Bleeding which occurs before 24 weeks is known as early pregnancy bleeding.
Causes of bleeding before and during childbirth include cervicitis, placenta previa, placental abruption and uterine rupture.[4][5] Causes of bleeding after childbirth include poor contraction of the uterus, retained products of conception, and bleeding disorders.[4]
About 8.7 million cases of severe maternal bleeding occurred in 2015[2] resulting in 83,000 deaths.[3] Between 2003 and 2009, bleeding accounted for 27% of maternal deaths globally.[6]
Later pregnancy
[edit]Antepartum bleeding (APH), also prepartum hemorrhage, is bleeding during pregnancy from the 24th week[7] (sometimes defined as from the 20th week[8][7]) gestational age up to the birth of the baby.[5] The primary consideration is the presence of a placenta previa which is a low lying placenta at or very near to the internal cervical os. This condition occurs in roughly 4 out of 1000 [9] pregnancies and usually needs to be resolved by delivering the baby via cesarean section. Also a placental abruption (in which there is premature separation of the placenta) can lead to obstetrical hemorrhage, sometimes concealed. This pathology is of important consideration after maternal trauma such as a motor vehicle accident or fall.
Other considerations to include when assessing antepartum bleeding are: sterile vaginal exams that are performed in order to assess dilation of the patient when the 40th week is approaching. As well as cervical insufficiency defined as a midtrimester (14th-26th week) dilation of the cervix which may need medical intervention to assist in keeping the pregnancy sustainable.[10]
During labor
[edit]Besides placenta previa and placental abruption, uterine rupture can occur, which is a very serious condition leading to internal or external bleeding. Bleeding from the fetus is rare, but may occur with two conditions called vasa previa and velamentous umbilical cord insertion where the fetal blood vessels lie near the placental insertion site unprotected by Wharton's jelly of the cord.[11] Occasionally this condition can be diagnosed by ultrasound. There are also tests to differentiate maternal blood from fetal blood which can help in determining the source of the bleed.
After delivery
[edit]Abnormal bleeding after delivery, or postpartum hemorrhage, is the loss of greater than 500 ml of blood following vaginal delivery, or 1000 ml of blood following cesarean section. Other definitions of excessive postpartum bleeding are hemodynamic instability, drop of hemoglobin of more than 10%,[12] or requiring blood transfusion. In the literature, primary postpartum hemorrhage is defined as uncontrolled bleeding that occurs in the first 24 hours after delivery while secondary hemorrhage occurs between 24 hours and six weeks.[13]
Risk factors
[edit]In rare cases, inherited bleeding disorders, like hemophilia, von Willebrand disease (vWD), or factor IX or XI deficiency, may cause severe postpartum hemorrhage, with an increased risk of death particularly in the postpartum period.[13] The risk of postpartum hemorrhage in patients with vWD and carriers of hemophilia has been found to be 18.5% and 22% respectively. This pathology occurs due to the normal physiological drop in maternal clotting factors after delivery which greatly increases the risk of secondary postpartum hemorrhage.[14] Another bleeding risk factor is thrombocytopenia, or decreased platelet levels, which is the most common hematological change associated with pregnancy induced hypertension. If platelet counts drop less than 100,000 per microliter the patient will be at a severe risk for inability to clot during and after delivery.[15]
Medical tests
[edit]If a small amount of bleeding is seen in early pregnancy a physician may request:
- A quantitative human chorionic gonadotropin (hCG) blood test to confirm the pregnancy or assist in diagnosing a potential miscarriage [16]
- Transvaginal pelvic ultrasonography to confirm that the pregnancy is not outside of the uterus[16]
- Blood type and Rh test to rule out hemolytic disease of the newborn[16]
For bleeding seen in later pregnancy tests may include:
- Complete blood count (CBC) and blood type and screen [16]
- Ultrasound to determine placental location [16]
- Kleihauer-Betke (KB) test especially if there was maternal trauma [16]
Unrelated bleeding
[edit]Pregnant patients may have bleeding from the reproductive tract due to trauma, including sexual trauma, neoplasm, most commonly cervical cancer, and hematologic disorders. Molar pregnancy (also called hydatiform mole) is a type of pregnancy where the sperm and the egg have joined within the uterus, but the result is a cyst resembling a grape-like cluster rather than an embryo. Bleeding can be an early sign of this tumor developing.[17]
See also
[edit]References
[edit]- ^ "ICD-11 for Mortality and Morbidity Statistics". World Health Organization. Retrieved 2023-12-05.
- ^ a b Vos, Theo; Allen, Christine; Arora, Megha; Barber, Ryan M.; Bhutta, Zulfiqar A.; Brown, Alexandria; Carter, Austin; Casey, Daniel C.; Charlson, Fiona J.; Chen, Alan Z.; Coggeshall, Megan; Cornaby, Leslie; Dandona, Lalit; Dicker, Daniel J.; Dilegge, Tina; Erskine, Holly E.; Ferrari, Alize J.; Fitzmaurice, Christina; Fleming, Tom; Forouzanfar, Mohammad H.; Fullman, Nancy; Gething, Peter W.; Goldberg, Ellen M.; Graetz, Nicholas; Haagsma, Juanita A.; Hay, Simon I.; Johnson, Catherine O.; Kassebaum, Nicholas J.; Kawashima, Toana; et al. (October 2016). "Global, regional, and national incidence, prevalence, and years lived with disability for 310 diseases and injuries, 1990-2015: a systematic analysis for the Global Burden of Disease Study 2015". Lancet. 388 (10053): 1545–1602. doi:10.1016/S0140-6736(16)31678-6. PMC 5055577. PMID 27733282.
- ^ a b Wang, Haidong; Naghavi, Mohsen; Allen, Christine; Barber, Ryan M.; Bhutta, Zulfiqar A.; Carter, Austin; Casey, Daniel C.; Charlson, Fiona J.; Chen, Alan Zian; Coates, Matthew M.; Coggeshall, Megan; Dandona, Lalit; Dicker, Daniel J.; Erskine, Holly E.; Ferrari, Alize J.; Fitzmaurice, Christina; Foreman, Kyle; Forouzanfar, Mohammad H.; Fraser, Maya S.; Fullman, Nancy; Gething, Peter W.; Goldberg, Ellen M.; Graetz, Nicholas; Haagsma, Juanita A.; Hay, Simon I.; Huynh, Chantal; Johnson, Catherine O.; Kassebaum, Nicholas J.; Kinfu, Yohannes; et al. (October 2016). "Global, regional, and national life expectancy, all-cause mortality, and cause-specific mortality for 249 causes of death, 1980-2015: a systematic analysis for the Global Burden of Disease Study 2015". Lancet. 388 (10053): 1459–1544. doi:10.1016/S0140-6736(16)31012-1. PMC 5388903. PMID 27733281.
- ^ a b c d Walfish, M.; Neuman, A.; Wlody, D. (December 2009). "Maternal haemorrhage". British Journal of Anaesthesia. 103: i47 – i56. doi:10.1093/bja/aep303. PMID 20007990.
- ^ a b Stables, Dorothy; Rankin, Jean (2010). Physiology in Childbearing: With Anatomy and Related Biosciences. Elsevier Health Sciences. p. 429. ISBN 978-0702044113.
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