Post Partum Hemorrhage – Mini Review

Mini Review

Charalampos Voros, Kalliopi Pappa

1st department of Obstetrics and Gynecology, Alexandra Hospital, National and Kapodistrian University of Athens, Greece

Correspondence: Charalampos Voros, 2-4 Lourou str, Athens, Greece. Email:



Postpartum hemorrhage (PPH) is an obstetric emergency. It is one of the top causes of maternal mortality in both high and low income countries, although the absolute risk of death from PPH is much lower in high-income countries. Several risk factors predispose to the development of PPH including prolonged labor, precipitous labor, uterine distension. In 2017, the American College of Obstetricians and Gynecologists revised the definition of PPH to help guide its management. In the present mini-review we focus on specific medical and minimally invasive interventions, and surgical interventions at laparotomy.

Key words: postpartum; hemorrhage, blood loss, bleeding


Postpartum hemorrhage (PPH) is an obstetric emergency. It is one of the top causes of maternal mortality in both high and low income countries, although the absolute risk of death from PPH is much lower in high-income countries. Timely diagnosis, appropriate resources, and  management are critical for preventing death.

Postpartum bleeding is often defined as the loss of more than 500 ml or 1,000 ml of blood within the first 24 hours following childbirth.1,2

In 2017, the American College of Obstetricians and Gynecologists revised their definition of PPH from the classic one (≥500 mL after vaginal birth or ≥1000 mL after cesarean delivery) to (1) cumulative blood loss ≥1000 mL or (2) bleeding associated with signs/symptoms of hypovolemia within 24 hours of the birth process regardless of delivery route in order to reduce the number of women inappropriately labeled with this diagnosis.3

This topic will present an overview of major issues relating to PPH. Clinical use of specific medical and minimally invasive interventions, and surgical interventions at laparotomy.4

Although vasodilatation due to neuraxial anesthesia and vasovagal reactions may result in lightheadedness/syncope, tachycardia, and hypotension, these entities are less likely postpartum than PPH, and they are readily reversible and generally not dangerous. Lightheadedness, tachycardia, or hypotension is unlikely to be due to neuraxial anesthesia if the woman was hemodynamically stable prior to delivery, the level of the block did not become significantly higher immediately following delivery, and symptoms did not abruptly follow systemic administration of a drug known to cause hypotension. 5


The most common cause of PPH is uterine atony, which complicates 1 in 40 births in the United States and is responsible for at least 75 percent of cases of PPH .Risk factors for uterine atony include prolonged labor, precipitous labor, uterine distension (multi-fetal gestation, polyhydramnios, fetal macrosomia), fibroid uterus, chorioamnionitis, indicated magnesium sulfate infusions, and prolonged use of oxytocin. Ineffective uterine contraction, either focally or diffusely, is additionally associated with a diverse range of etiologies including retained placental tissue, placental disorders (such as morbidly adherent placenta, placenta previa, and abruption placentae), coagulopathy (increased fibrin degradation products) and uterine inversion. Body mass index (BMI) above 40 (class III obesity) is also a recognized risk factor for postpartum uterine atony .The diagnosis of atony is generally made when the uterus does not become firm after routine management of the third stage of labor.  Atony may or may not be associated with retained tissue. .6  Placental disorders (eg, morbidly adherent placenta, placenta previa, abruptio placentae), retained products of conception, and uterine inversion result in PPH because they inhibit effective uterine contraction. With diffuse atony, blood loss can be much greater than observed because a flaccid and dilated uterus may contain a significant amount of blood. With focal localized atony, the fundal region may be well contracted while the lower uterine segment is dilated (ballooning) and atonic, which is difficult to appreciate on abdominal examination, but may be detected on vaginal examination.

Trauma-related bleeding can be due to lacerations or surgical incisions. Cervical and vaginal lacerations may develop as a result of the natural processes of delivery or may be related to provider interventions. They may not be noted until excessive postpartum vaginal bleeding prompts lower genital tract examination, including examination for vaginal and vulvar hematomas.Corpus lacerations may be complete transmyometrial ruptures or incomplete lacerations of the inner myometrium.7

At cesarean delivery, hemorrhage from the uterine incision is generally caused by lateral extension of the incision, which can result from spontaneous tearing of an edematous lower segment during an otherwise uneventful cesarean delivery after prolonged labor, from an incision made too low or not sufficiently curved on the lower segment, or from delivery of the fetus through an incision that is too small.

Coagulopathy is a cause of PPH in women with an inherited or acquired bleeding diathesis, and a result of PPH when there is a severe reduction of clotting factors due to persistent heavy bleeding and hemodilution of the remaining clotting factors. Acute coagulopathies can be caused by amniotic fluid embolism, placental abruption, preeclampsia with severe features, or HELLP syndrome.

Risk classification

The California quality improvement.8  toolkit classifies patients as low, medium, or high risk for PPH:

Low Risk : Singleton pregnancy, fewer than four previous deliveries, chorioamnionitis, obesity( BMI > 35), estimated fetal weight >4,000 gr

Medium Risk: Prior uterine surgery,more than four previous deliveries,multiple gestation,large fibroids and chorioamnionitis

High Risk: Suspected placenta accreta or percretam hematocrit < 30%, platelets < 100,000 and active bleeding on admission


When hemorrhage is suspected as the cause of hemodynamic instability, initial (and expedited) management with blood and blood products is advised (as opposed to large volume crystalloid infusion). Hypovolemic hemorrhagic shock is treated with aggressive volume resuscitation with packed red cells and other appropriate blood products. Transfusion should keep up with blood loss, with early activation of a protocol for large volume transfusion in those patients with heavy bleeding. Development of a standardized institutional approach to massive transfusion improves outcome . There are no data from clinical trials of PPH to help guide management of transfusion specifically in PPH

Uterine massage is a simple first line treatment as it helps the uterus to contract to reduce bleeding. Although the evidence around the effectiveness of uterine massage is inconclusive, it is common practice after the delivery of the placenta.

Intravenous oxytocin is the drug of choice for postpartum hemorrhage.9 Ergotamine may also be used.10

Oxytocin helps the uterus to contract quickly and the contractions to last for longer.11 It is the first line treatment for PPH when its cause is the uterus not contracting well. A combination of syntocinon and ergometrine is commonly used as part of active management of the third stage of labor.12 This is called syntometrine. It does reduce the risk of PPH by improving the tone of the uterus when compared with no treatment however it has to be used with caution due to its effect raising blood pressure and causing worse after pains.

Carbetocin compared with oxytocin produced a reduction in women who needed uterine massage and further uterotonic drugs for women having caesarean sections.13 There was no difference in rates of PPH in women having caesarean sections or women having vaginal deliveries when given carbetocin.14 Carbetocin appears to cause less adverse effects. More research is needed to find the cost effectiveness of using carbetocin.15

Tranexamic acid, a clot stabilizing medication, may also be used to reduce bleeding and blood transfusions in low-risk women,16 however evidence as of 2015 was not strong.

Classification of hemorrhage
  1. Stage 0: normal – treated with fundal massage and oxytocin.
  2. Stage 1: more than normal bleeding – establish large-bore intravenous access, assemble personnel, increase oxytocin, consider use of methergine, perform fundal massage, prepare 2 units of packed red blood cells.
  3. Stage 2: bleeding continues – check coagulation status, assemble response team, move to operating room, place intrauterine balloon, administer additional uterotonics (misoprostol, carboprost tromethamine), consider: uterine artery embolization, dilatation and curettage, and laparotomy with uterine compression stitches or hysterectomy.
  4. Stage 3: bleeding continues – activate massive transfusion protocol, mobilize additional personnel, recheck laboratory tests, perform laparotomy, consider hysterectomy. .17

Surgery may be used  in case of cervical lacerations or tear or uterine rupture or medical management fails. Methods used may include uterine artery ligation, ovarian artery ligation, internal iliac artery ligation, selective arterial embolization, B-lynch suture, and hysterectomy.18, 19 20  Bleeding caused by traumatic causes should be management by surgical repair.


Active management of the third stage is a method of shortening the stage between when the baby is born and when the placenta is delivered.21 This stage is when the mother is at risk of having a PPH. Active management involves giving a drug which helps the uterus contract before delivering the placenta by a gentle but sustained pull on the umbilical cord whilst exerting upward pressure on the lower abdomen to support the uterus (controlled cord traction).22

Another method of active management which is not recommended now is fundal pressure during the delivery of the placenta. A review into this method found no research and advises controlled cord traction because fundal pressure can cause the mother unnecessary pain.23 Allowing the cord to drain appears to shorten the third stage and reduce blood loss but evidence around this subject is not strong enough to draw solid conclusions.24


1. Callaghan WM, Kuklina EV, Berg CJ. Trends in postpartum hemorrhage: United States, 1994-2006. Am J Obstet Gynecol 2010; 202:353.e1.
2. Marshall AL, Durani U, Bartley A, et al. The impact of postpartum hemorrhage on hospital length of stay and inpatient mortality: a National Inpatient Sample-based analysis. Am J Obstet Gynecol 2017; 217:344.e1.
3. Lockwood CJ, Schatz F. A biological model for the regulation of peri-implantational hemostasis and menstruation. J Soc Gynecol Investig 1996; 3:159.
4. Lockwood CJ, Nemerson Y, Krikun G, et al. Steroid-modulated stromal cell tissue factor expression: a model for the regulation of endometrial hemostasis and menstruation. J Clin Endocrinol Metab 1993; 77:1014.
5. Lockwood CJ. Regulation of plasminogen activator inhibitor 1 expression by interaction of epidermal growth factor with progestin during decidualization of human endometrial stromal cells. Am J Obstet Gynecol 2001; 184:798.
6. Lockwood CJ, Krikun G, Schatz F. The decidua regulates hemostasis in human endometrium. Semin Reprod Endocrinol 1999; 17:45.
7. Bateman BT, Berman MF, Riley LE, Leffert LR. The epidemiology of postpartum hemorrhage in a large, nationwide sample of deliveries. Anesth Analg 2010; 110:1368.
8. Conrad LB, Groome LJ, Black DR. Management of Persistent Postpartum Hemorrhage Caused by Inner Myometrial Lacerations. Obstet Gynecol 2015; 126:266.
9. Sheiner E, Sarid L, Levy A, et al. Obstetric risk factors and outcome of pregnancies complicated with early postpartum hemorrhage: a population-based study. J Matern Fetal Neonatal Med 2005; 18:149.
10. Mhyre JM, Shilkrut A, Kuklina EV, et al. Massive blood transfusion during hospitalization for delivery in New York State, 1998-2007. Obstet Gynecol 2013; 122:1288.
11. Rouse DJ, Leindecker S, Landon M, et al. The MFMU Cesarean Registry: uterine atony after primary cesarean delivery. Am J Obstet Gynecol 2005; 193:1056.
12. Cheng YW, Delaney SS, Hopkins LM, Caughey AB. The association between the length of first stage of labor, mode of delivery, and perinatal outcomes in women undergoing induction of labor. Am J Obstet Gynecol 2009; 201:477.e1.
13. Blomberg M. Maternal obesity and risk of postpartum hemorrhage. Obstet Gynecol 2011; 118:561.
14. Wetta LA, Szychowski JM, Seals S, et al. Risk factors for uterine atony/postpartum hemorrhage requiring treatment after vaginal delivery. Am J Obstet Gynecol 2013; 209:51.e1.
15. Kramer MS, Berg C, Abenhaim H, et al. Incidence, risk factors, and temporal trends in severe postpartum hemorrhage. Am J Obstet Gynecol 2013; 209:449.e1.
16. Sharp GC, Saunders PT, Greene SA, et al. Intergenerational transmission of postpartum hemorrhage risk: analysis of 2 Scottish birth cohorts. Am J Obstet Gynecol 2014; 211:51.e1.
17. Bruning AH, Heller HM, Kieviet N, et al. Antidepressants during pregnancy and postpartum hemorrhage: a systematic review. Eur J Obstet Gynecol Reprod Biol 2015; 189:38.
18. Oberg AS, Hernandéz-Diaź S, Frisell T, et al. Genetic contribution to postpartum haemorrhage in Swedish population: cohort study of 466,686 births. BMJ 2014; 349:g4984.
19. Giannella L, Mfuta K, Pedroni D, et al. Delays in the delivery room of a primary maternity unit: a retrospective analysis of obstetric outcomes. J Matern Fetal Neonatal Med 2013; 26:593.
20. Lim G, Melnyk V, Facco FL, et al. Cost-effectiveness Analysis of Intraoperative Cell Salvage for Obstetric Hemorrhage. Anesthesiology 2018; 128:328.
21. Salati JA, Leathersich SJ, Williams MJ, et al. Prophylactic oxytocin for the third stage of labour to prevent postpartum haemorrhage. Cochrane Database Syst Rev 2019; 4:CD001808.
22. Lakshmi SD, Abraham R. Role of Prophylactic Tranexamic Acid in Reducing Blood Loss during Elective Caesarean Section: A Randomized Controlled Study. J Clin Diagn Res 2016; 10:QC17.
23. Dilla AJ, Waters JH, Yazer MH. Clinical validation of risk stratification criteria for peripartum hemorrhage. Obstet Gynecol 2013; 122:120.
24. Novello A, King JC. Health advisory: Prevention of maternal deaths through improved management of hemorrhage. (Accessed on July 2019).