Updated: Oct 21, 2009
Defining postpartum hemorrhage (PPH) is problematic and has been historically difficult. Waiting for a patient to meet the postpartum hemorrhage criteria, particularly in resource-poor settings or with sudden hemorrhage, may delay appropriate intervention. Postpartum hemorrhage is traditionally defined as blood loss greater than 500 mL during a vaginal delivery or greater than 1,000 mL with a cesarean delivery. However, significant blood loss can be well tolerated by most young healthy females, and an uncomplicated delivery often results in blood loss of more than 500 mL without any compromise of the mother's condition.
The addition of "a 10% drop in hemoglobin" to the definition provides an objective laboratory measure. However, this is not helpful in acute situations since it can take hours for losses to create laboratory changes in red blood cell measurements. Signs and symptoms of hypovolemia (lightheadedness, tachycardia, syncope, fatigue and oliguria) are also of limited utility as they can be late findings in a young and otherwise healthy female. As a result, any bleeding that has the potential to result in hemodynamic instability, if left untreated, should be considered postpartum hemorrhage and managed accordingly.
Postpartum hemorrhage can be divided into 2 types: early postpartum hemorrhage, which occurs within 24 hours of delivery, and late postpartum hemorrhage, which occurs 24 hours to 6 weeks after delivery. Most cases of postpartum hemorrhage, greater than 99%, are early postpartum hemorrhage. Notably, most women are still under the care of their delivering provider during this time. With many women delivering outside of hospitals and early postpartum hospital discharge being a growing trend, postpartum hemorrhage that presents to the emergency department may be either early or late.
Within this combined population, emergency medicine providers are likely to receive patients that fall into 1 of 3 categories:
At term, the uterus and placenta receive 500-800 mL of blood per minute through their low resistance network of vessels. This high flow predisposes a gravid uterus to significant bleeding if not well physiologically or medically controlled. By the third trimester, maternal blood volume increases by 50%, which increases the body's tolerance of blood loss during delivery.
Following delivery of the fetus, the gravid uterus is able to contract down significantly given the reduction in volume. This allows the placenta to separate from the uterine interface, exposing maternal blood vessels that interface with the placental surface. After separation and delivery of the placenta, the uterus initiates a process of contraction and retraction, shortening its fiber and kinking the supplying blood vessels, like physiologic sutures or "living ligatures."
If the uterus fails to contract, or the placenta fails to separate or deliver, then significant hemorrhage may ensue. Uterine atony, or diminished myometrial contractility, accounts for 80% of postpartum hemorrhage. The other major causes include abnormal placental attachment or retained placental tissue, laceration of tissues or blood vessels in the pelvis and genital tract, and maternal coagulopathies. An additional, though uncommon, cause is inversion of the uterus during placental delivery.
The traditional pneumonic "4Ts: tone, tissue, trauma, and thrombosis" can be used to remember the potential causes. Here, a 5th is added; “T” for uterine inversion that will be called “traction.”
The incidence of postpartum hemorrhage is about 1 in 5 pregnancies, but this figure varies widely due to differential definitions for postpartum hemorrhage.
Mortality
Although accountable for only 8% of maternal deaths in developed countries, postpartum hemorrhage is the second leading single cause of maternal mortality, ranking behind preeclampsia/eclampsia.1 Globally, postpartum hemorrhage is the leading cause of maternal mortality. The condition is responsible for 25% of delivery-associated deaths,2 and this figure is as high as 60% in some countries. International initiatives to improve outcomes have invested in training birth attendants (traditional or otherwise) and nurse midwives on the active management of the third stage of labor (the period immediately after delivering of the infant). Most efforts focus on uterine atony, which is the primary cause of postpartum hemorrhage. This has included education on manual techniques to increase uterine contraction-retraction and making pharmacologic uterotonic agents (oxytocin and misoprostol) more available.3,4,5
Morbidity
Postpartum hemorrhage is a potentially life-threatening complication of both vaginal and cesarean delivery. Associated morbidity is related to the direct consequences of blood loss as well as the potential complications of hemostatic and resuscitative interventions.
Consequences of uncontrolled hemorrhage
Consequences of fluid resuscitation
Risks from exposure to blood products
Risks associated with surgical intervention
Need for permanent sterilization to control bleeding
If the bleeding cannot be controlled conservatively (removal of products of conception, suturing disrupted tissues, application of pressure) then surgical intervention may be necessary. In severe cases, the following may occur:
The clinical history should be taken as a primary survey (ABCs) of the patient. This should include collecting an initial set of vital signs to guide the patient’s management, as the patient is positioned to begin the physical examination. Keep in mind, that if the bleeding is very brisk, the patient’s mental status may wane. As a result, this first set of questions should include queries about signs and symptoms that are most crucial in managing potential circulatory collapse, identifying the cause of postpartum hemorrhage (PPH), and selecting appropriate therapies.10
As mentioned earlier, patients with postpartum hemorrhage (PPH) should be managed like all emergency department resuscitation situations, with the history and physical examination occurring simultaneously while following acute life support algorithms.
The physical examination should focus on determining the cause of the bleeding. The patient may not have the typical hemodynamic changes of shock early in the course of the hemorrhage due to physiologic maternal hypervolemia.
Important organ systems to assess include the pulmonary system (evidence of pulmonary edema), the cardiovascular (heart murmur, tachycardia, strength of peripheral pulses), and neurological systems (mental status changes from hypovolemia).The skin should also be checked for petechiae or oozing from skin puncture sites, which could indicate a coagulopathy, or a mottled appearance, which can be indicative of severe hypovolemia.
Looking for occult postpartum hemorrhagein the form of a pelvic, vaginal, uterine, or abdominal wall hematoma, or intra-abdominal or perihepatic bleedingis always an important consideration when unstable hemodynamic findings are present without evidence of excessive vaginal blood loss.
Having a gynecologic examination bed is helpful but not necessary. The patient's pelvis can always be elevated on an inverted bedpan (thick-side toward the patient's feet) cushioned with towels and a sheet for comfort. Ensure that good lighting and suction are available before beginning.The 4Ts of postpartum hemorrhage (PPH) +1: tone, trauma, tissue, thrombosis, and traction. More than one of these can cause postpartum hemorrhage in any given patient.
Endometritis
Endometritis: Consider uterine infection, or endometritis, particularly with late postpartum hemorrhage. Signs and symptoms that should peak the clinical suspicion for this diagnosis include fever, chills, foul discharge, tender abdomen/uterus, and elevated WBC count with a differential favoring bacterial infection (neutrophilia with or without bands). Start early broad-spectrum antibiotic coverage and consider sepsis.
Wound breakdown: Internal wound breakdown from repaired genital tract lacerations or previously closed cesarean delivery incisions should be considered as a potential cause of vaginal bleeding, internal bleeding, or hematoma.
Genital tract manipulation: Genital tract lacerations may be induced by intercourse, finger penetration, or foreign object insertion (including tampons) into the genital tract.
Nongenital sources of bleeding: Birth trauma may lead to retroperitoneal hematomas, which may be initially difficulty to identify. Women who have undergone cesarean delivery may have an abdominal wall or subfacial hematoma. Rarely, HELLP syndrome can produce life-threatening bleeding into and rupture of the liver capsule, and this should be suspected in the setting of severe epigastric or right upper quadrant pain. Ruptured splenic artery aneurysms have been reported in pregnancy as well.
Studies to be considered with vaginal bleeding and decreasing red blood cell counts in the postpartum patient include ultrasonography (U/S), computed tomography (CT), or magnetic resonance imaging (MRI).
Ultrasonography is a fast and helpful modality for imaging pelvic structures and should be the first-line study for pelvic pathology.
Ultrasonography
In a hemodynamically unstable patient, a bedside ultrasonography can be performed by an experienced emergency medicine provider as an extension of the physical examination. In general, a dedicated pelvic ultrasonography (transabdominal and/or transvaginal) is helpful in identifying large retained placental fragments, hematomas, or other intrauterine abnormalities. Retained placenta and hematoma can look ultrasonographically identical. Using a Doppler ultrasound to look for vascularity can help to differential between the two, with clots being avascular and retained placenta often receiving persistent blood flow from the uterus.
The abdominal views of the focused assessment with sonography in trauma (FAST) examination are helpful in identifying fluid within the peritoneum that may be the result of hemorrhage. This study is designed to identify intra-abdominal and pericardial fluid that requires early operative intervention in trauma patients. However, the abdominal views are useful in any patient with suspected intra-abdominal free fluid. These include views of the right upper quadrant (RUQ)/Morison's pouch area (the most dependent area of a supine patient's peritoneal cavity), the left upper quadrant (LUQ) spleno-renal recess, and views of the pelvis (sagittal and coronal views of the uterus and pouch of Douglas). This study can detect 250-500 mL of fluid in the peritoneum, but it is a poor study for identifying retroperitoneal or paravaginal hemorrhage (extra-peritoneal bleeding).
Ultrasonography cannot reliably differentiate between blood, urine, or ascites; however, in the setting of suspected hemorrhage, any fluid in the abdomen should prompt further investigation.
More stable patients can have their abdominal and/or pelvic ultrasonography confirmed with an official study performed by a radiologist.
Computed tomography
In the event that ultrasonography is not diagnostic, CT is a helpful follow-up study. This may also be the first-line study when a pelvic hematoma or abscess is suspected, which may be missed with a sonogram. The traditional teaching is that pelvic CT is a less than ideal study for pelvic structures, due to artifact from the surrounding pelvic bones that reduces the image quality. However, this is generally not the case with modern multidetector CT studies. When enhanced with intravenous (I+) and intra-intestinal (O/R+...either oral or rectal contrast), CT can detail pelvic hematomas, cesarean delivery wound dehiscence, and retained placental tissue.
Magnetic resonance imaging
MRI is a time consuming study that is rarely performed from the ED in these patients. It can be helpful in delineating tissue planes to determine if a fluid collection (hematoma or abscess) is intrauterine or extrauterine when this is not clear from ultrasonography or CT. It can also help to distinguish a placenta accreta from simple retained products of conception.
Limited literature is available on abdominopelvic imaging in postpartum hemorrhage since the presentation of significant bleeding prompts rapid resuscitation and immediate intervention based on the clinical picture rather than documented imaging. Nonetheless, all 3 imaging modalities can assist in the evaluation of a bleeding source, but ultrasonography is usually sufficient for emergent situations.
For any obstetric emergency medical services (EMS) field call, emergency medical technicians (EMTs) should be vigilant and prepared for postpartum hemorrhage (PPH) as a potential complication. After delivery, there are two patients to assess: the mother and the baby. Their intervention needs should be prioritized according to the airway, breathing, and circulation (ABCs) of acute life support.
The patient with suspected or obvious postpartum hemorrhage should be managed like any other hemorrhaging patient. Resuscitation measure should be started with the history and physical examination according to acute life support algorithms. Have someone call a consultant obstetrician/gynecologist (OB/GYN) immediately as care for the patient is initiated in order to make the patient's transition from resuscitative care to definitive care with the OB/GYN team smooth and early.
Also see the American College of Obstetricians and Gynecologist for guidelines on the treatment of postpartum hemorrhage.13
For all cases, do the following:
For cases of extreme hemorrhage or when it is not possible to identify the source of the bleeding after the secondary survey, consider an urgent transfer of the patient to an operating room with the OB/GYN or general surgery consulting team.
Medications used to control postpartum hemorrhage (PPH) are in the category of uterotonic drugs. These drugs stimulate contraction of the uterine muscle, helping to control PPH.
These agents are useful in the treatment and prophylaxis of PPH. The information below applies only following delivery of the fetus (the dosing, indications, and contraindications will vary prior to delivery).
Produces rhythmic uterine contractions, can stimulate the gravid uterus, and has vasopressive and antidiuretic effects. Can be used to control postpartum bleeding or hemorrhage. Some suggest its prophylactic use in the third stage of labor; one study of 1000 deliveries revealed a 32% reduction in the rate of PPH.14
Add 20 units of oxytocin to 1 L of crystalloid
Administer fluid at rate high enough to control uterine atony
If 20 units are added to 1 L, infuse at rate of 200-600 mL/h
Add 20 units of oxytocin to 1 L of crystalloid
Administer fluid at rate high enough to control uterine atony
It may also be given as 10-20 units in a single IM injection
If 20 units are added to 1 L, infuse at rate of 200-600 mL/h
<12 years: Not established
>12 years: Administer as in adults
Pressor effect of sympathomimetics may increase when used concomitantly with oxytocic drugs, causing postpartum hypertension
Documented hypersensitivity
C - Fetal risk revealed in studies in animals but not established or not studied in humans; may use if benefits outweigh risk to fetus
Rapid bolus may cause hypotension, myocardial arrhythmias, or cardiac arrest; higher doses may cause diuresis, making it difficult to monitor urine output as a measure of resuscitation; has an intrinsic antidiuretic effect that, when administered with continuous infusion in a patient receiving fluids by mouth, can cause water intoxication
Acts directly on uterine smooth muscle, causing a sustained tetanic uterotonic effect that reduces uterine bleeding and shortens the third stage of labor. Administer IM or intramyometrially during puerperium, during delivery of placenta, or after delivering anterior shoulder.
0.2 mg IM/IV repeat q2-4h if required
<12 years: Not established
>12 years: Administer as in adults
Concurrent administration of methylergonovine with vasoconstrictors or other ergot alkaloids may produce additive effect
Documented hypersensitivity; glaucoma; Tourette syndrome; anxiety; hypertension
C - Fetal risk revealed in studies in animals but not established or not studied in humans; may use if benefits outweigh risk to fetus
Caution in sepsis, obliterative vascular disease, or hepatic or renal insufficiency
Prostaglandin similar to F2-alpha, but it has a longer duration and produces myometrial contractions that induce hemostasis at the placentation site, which reduces postpartum bleeding.
250 mcg IM or intramyometrial q15-90min; not to exceed 2 mg
<12 years: Not established
>12 years: Administer as in adults
Despite reports that it increases the toxicity of uterotonic agents, they are often used in combination
Documented hypersensitivity; pelvic inflammatory disease; asthma
C - Fetal risk revealed in studies in animals but not established or not studied in humans; may use if benefits outweigh risk to fetus
Caution in cardiovascular disease, asthma, hypotension or hypertension, adrenal disease, diabetes, renal or hepatic disease, compromised uterus, and jaundice; do not inject IV (may induce hypertension and bronchospasm)
Synthetic prostaglandin E 1 analog.
600-1000 mcg PR for 1 dose
<12 years: Not established
>12 years: Administer as in adults
Despite reports of it increasing the toxicity of uterotonics, they are routinely used together
Allergy to prostaglandins
X - Contraindicated; benefit does not outweigh risk
Significant cardiac disease; may produce fever
Used to prevent and treat PPH due to uterine atony by producing firm contraction of the uterus within minutes. Although it is intended primarily for IM administration, a faster response can be achieved with IV use. Compared with IM route, IV route has a higher incidence of adverse effects; IV use should be reserved for emergencies (eg, excessive uterine bleeding). Severe uterine bleeding may require repeated doses, but it seldom requires more than one injection q2-4h.
0.2 mg IM/IV; repeat q2-4h prn
<12 years: Not established
>12 years: Administer as in adults
None reported
Documented hypersensitivity
X - Contraindicated; benefit does not outweigh risk
Discontinue if ergotism develops; caution in heart disease, hypertension, mitral-valve stenosis, venoatrial shunts, sepsis, obliterative vascular disease, hepatic or renal impairment
Man-made activated protein that promotes thrombosis.
40-90 mcg/kg IV
<12 years: Not established
>12 years: Administer as in adults
None reported
Documented hypersensitivity to product, mouse, hamster, or cow proteins
C - Fetal risk revealed in studies in animals but not established or not studied in humans; may use if benefits outweigh risk to fetus
Monitor for signs of thrombosis or activation of coagulation system; thrombotic events may increase in patients with advanced atherosclerotic disease, crush injury, sepsis, and disseminated intravascular coagulation; may also cause hypertension
If a patient is brought to a hospital without obstetric services, the EM providers should initiate resuscitation and transfer the patient as quickly as possible to a hospital with obstetric services for definitive care. Discuss an en route resuscitation plan with the EMS transport team, and make the receiving hospital aware of what the patient's status was upon departure from the ED so that the appropriate resources are mobilized before her arrival. Be sure to adhere to patient transfer laws set by the transferring facility, city, EMS transport organization, and state.
The active management of the third stage of labor has been shown to decrease the incidence and severity of postpartum hemorrhage (PPH). This includes the administration of oxytocin or misoprostol, uterine massage, gentle traction on the umbilical cord, and prompt placental delivery. Women with a known uterine scar or suspected placental abnormalities should be delivered and managed in a hospital setting, and instrumentation should be avoided, when possible, during vaginal delivery.
For further information, see the World Health Organizations recommendations on the prevention of postpartum hemorrhage.15
Consequences include the sequelae of hemorrhage; aggressive fluid resuscitation; blood-product exposure; and procedures done to control uterine, cervical, vaginal, or peritoneal hemorrhage. See Mortality/Morbidity for more detail.
The prognosis depends on the cause of the PPH, its duration, the amount of blood loss, comorbid conditions, and the effectiveness of treatment. Prompt diagnosis and treatment are essential to achieving the best outcome for any given patient. Most reproductive-age women will do well if managed promptly in a setting with operative and blood-product resources available.
Postpartum hemorrhage can be a frightening experience for patients. It is important to provide reassurance and communicate through each step of emergency care. Make patients aware of what to anticipate through their clinical course including expected procedures; transport; and the indication, risks, and benefits of interventions.
To avoid common medicolegal pitfalls consider the following:
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postpartum hemorrhage, postpartum bleeding, PPH, bleeding after delivery, vaginal delivery, cesarean delivery, birth, giving birth, blood loss after birth, blood loss after delivery, maternal death, 4 T's, 4 Ts, tone, tissue, thrombosis, uterine atony, uterine prolapse, oxytocin, hemorrhage, coagulopathy, living ligatures, physiologic sutures, DIC, uterine inversion, maternal mortality, uterotonic, oxytocin, Pitocin, misoprostol, Cytotec, ergotamine, methylergotamine, carboprost, Hemabate, recombinant factor VIIa, retained products of conception, retained placenta, obstetrics, pelvic ultrasound, bedside ultrasound, third stage of labor, 3rd stage of labor
Maame Yaa A B Yiadom, MPH, MD, Staff Physician, Department of Emergency Medicine, Brigham and Women's Hospital and Massachusetts General Hospital
Maame Yaa A B Yiadom, MPH, MD is a member of the following medical societies: Alpha Omega Alpha, American Academy of Emergency Medicine, American College of Emergency Physicians, American Medical Association, American Public Health Association, National Medical Association, and Society for Academic Emergency Medicine
Disclosure: Nothing to disclose.
Daniela Carusi, MSc, MD, Instructor, Obstetrics and Gynecology and Reproductive Biology, Harvard Medical School; Consulting Physician, Department of Obstetrics and Gynecology, Medical Director, Department of General Ambulatory Gynecology, Brigham and Women's Hospital
Daniela Carusi, MSc, MD is a member of the following medical societies: American College of Obstetricians and Gynecologists, Association of Reproductive Health Professionals, and Massachusetts Medical Society
Disclosure: Nothing to disclose.
Assaad J Sayah, MD, Chief, Department of Emergency Medicine, Cambridge Health Alliance
Assaad J Sayah, MD is a member of the following medical societies: National Association of EMS Physicians
Disclosure: Nothing to disclose.
Francisco Talavera, PharmD, PhD, Senior Pharmacy Editor, eMedicine
Disclosure: eMedicine Salary Employment
Mark Zwanger, MD, MBA, Assistant Professor, Department of Emergency Medicine, Thomas Jefferson University
Mark Zwanger, MD, MBA is a member of the following medical societies: American Academy of Emergency Medicine, American College of Emergency Physicians, and American Medical Association
Disclosure: Medicines Company Consulting fee Consulting; Pfizer Salary Employment
John D Halamka, MD, MS, Associate Professor of Medicine, Harvard Medical School, Beth Israel Deaconess Medical Center; Chief Information Officer, CareGroup Healthcare System and Harvard Medical School; Attending Physician, Division of Emergency Medicine, Beth Israel Deaconess Medical Center
John D Halamka, MD, MS is a member of the following medical societies: American College of Emergency Physicians, American Medical Informatics Association, Phi Beta Kappa, and Society for Academic Emergency Medicine
Disclosure: Nothing to disclose.
Pamela L Dyne, MD, Professor of Clinical Medicine/Emergency Medicine, David Geffen School of Medicine at UCLA; Attending Physician, Department of Emergency Medicine, Olive View-UCLA Medical Center
Pamela L Dyne, MD is a member of the following medical societies: American Academy of Emergency Medicine, American College of Emergency Physicians, and Society for Academic Emergency Medicine
Disclosure: Nothing to disclose.
Special thanks to Dr. Donnie Bell for his assistance with the "Imaging" section for this topic.
The authors and editors of eMedicine gratefully acknowledge the contributions of previous author, Michael P Wainscott, MD, to the development and writing of this article.
Postpartum Hemorrhage (PPH). Shahid M. Ahmad, Atif Farid, Demitra del Silva, Harish Kodi.
New Technologies to Save Mothers Lives from PPH. PATH/USAID.
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