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Práctica de la hemorragia obstétrica, Resúmenes de Obstetricia

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e168 VOL. 130, NO. 4, OCTOBER 2017 OBSTETRICS & GYNECOLOGY
Postpartum Hemorrhage
Maternal hemorrhage, defined as a cumulative blood loss of greater than or equal to 1,000 mL or blood loss accom-
panied by signs or symptoms of hypovolemia within 24 hours after the birth process, remains the leading cause of
maternal mortality worldwide (1). Additional important secondary sequelae from hemorrhage exist and include adult
respiratory distress syndrome, shock, disseminated intravascular coagulation, acute renal failure, loss of fertility, and
pituitary necrosis (Sheehan syndrome).
Hemorrhage that leads to blood transfusion is the leading cause of severe maternal morbidity in the United States
closely followed by disseminated intravascular coagulation (2). In the United States, the rate of postpartum hemor-
rhage increased 26% between 1994 and 2006 primarily because of increased rates of atony (3). In contrast, maternal
mortality from postpartum obstetric hemorrhage has decreased since the late 1980s and accounted for slightly more
than 10% of maternal mortalities (approximately 1.7 deaths per 100,000 live births) in 2009 (2, 4). This observed
decrease in mortality is associated with increasing rates of transfusion and peripartum hysterectomy (2–4).
The purpose of this Practice Bulletin is to discuss the risk factors for postpartum hemorrhage as well as its evalu-
ation, prevention, and management. In addition, this document will encourage obstetrician–gynecologists and other
obstetric care providers to play key roles in implementing standardized bundles of care (eg, policies, guidelines, and
algorithms) for the management of postpartum hemorrhage.
Number 183, OctOber 2017 (Replaces Practice Bulletin Number 76, October 2006)
ACOG PRACTICE BULLETIN
Clinical Management Guidelines for Obstetrician–Gynecologists
Background
The American College of Obstetricians and Gynecolo-
gists’ (ACOG) reVITALize program defines postpartum
hemorrhage as cumulative blood loss greater than or
equal to 1,000 mL or blood loss accompanied by signs
or symptoms of hypovolemia within 24 hours after the
birth process (includes intrapartum loss) regardless of
route of delivery (5). This is in contrast to the more
traditional definitions of postpartum hemorrhage as an
estimated blood loss in excess of 500 mL after a vaginal
birth or a loss of greater than 1,000 mL after a cesarean
birth (6). This new classification is likely to reduce the
number of individuals labeled with postpartum hemor-
rhage. However, despite this new characterization, a
blood loss greater than 500 mL in a vaginal delivery
should be considered abnormal and should serve as an
indication for the health care provider to investigate the
increased blood deficit. Although visually estimated
blood loss is considered inaccurate, use of an educa-
tional process, with limited instruction on estimating
blood loss, has been shown to improve the accuracy of
such estimates (7). Historically, a decrease in hematocrit
of 10% had been proposed as an alternative marker to
define postpartum hemorrhage; however, determinations
of hemoglobin or hematocrit concentrations are often
delayed, may not reflect current hematologic status, and
are not clinically useful in the setting of acute postpartum
hemorrhage (8).
In postpartum women, it is important to recognize
that the signs or symptoms of considerable blood loss
(eg, tachycardia and hypotension) often do not present or
do not present until blood loss is substantial (9). There-
fore, in a patient with tachycardia and hypotension, the
obstetrician–gynecologist or other obstetric care provider
should be concerned that considerable blood loss, usually
Committee on Practice Bulletins—Obstetrics. This Practice Bulletin was developed by the American College of Obstetricians and Gynecologists’
Committee on Practice Bulletins–Obstetrics in collaboration with Laurence E. Shields, MD; Dena Goffman, MD; and Aaron B. Caughey, MD, PhD.
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e168 VOL. 130, NO. 4, OCTOBER 2017 OBSTETRICS & GYNECOLOGY

Postpartum Hemorrhage

Maternal hemorrhage , defined as a cumulative blood loss of greater than or equal to 1,000 mL or blood loss accom-

panied by signs or symptoms of hypovolemia within 24 hours after the birth process, remains the leading cause of

maternal mortality worldwide (1). Additional important secondary sequelae from hemorrhage exist and include adult

respiratory distress syndrome, shock, disseminated intravascular coagulation, acute renal failure, loss of fertility, and

pituitary necrosis (Sheehan syndrome).

Hemorrhage that leads to blood transfusion is the leading cause of severe maternal morbidity in the United States

closely followed by disseminated intravascular coagulation (2). In the United States, the rate of postpartum hemor-

rhage increased 26% between 1994 and 2006 primarily because of increased rates of atony (3). In contrast, maternal

mortality from postpartum obstetric hemorrhage has decreased since the late 1980s and accounted for slightly more

than 10% of maternal mortalities (approximately 1.7 deaths per 100,000 live births) in 2009 (2, 4). This observed

decrease in mortality is associated with increasing rates of transfusion and peripartum hysterectomy (2–4).

The purpose of this Practice Bulletin is to discuss the risk factors for postpartum hemorrhage as well as its evalu-

ation, prevention, and management. In addition, this document will encourage obstetrician–gynecologists and other

obstetric care providers to play key roles in implementing standardized bundles of care (eg, policies, guidelines, and

algorithms) for the management of postpartum hemorrhage.

Number 183, O ctOber 2017 (Replaces Practice Bulletin Number 76, October 2006)

ACOG P RACTICE BULLET IN

Clinical Management Guidelines for Obstetrician–Gynecologists

Background

The American College of Obstetricians and Gynecolo-

gists’ (ACOG) reVITALize program defines postpartum

hemorrhage as cumulative blood loss greater than or

equal to 1,000 mL or blood loss accompanied by signs

or symptoms of hypovolemia within 24 hours after the

birth process (includes intrapartum loss) regardless of

route of delivery (5). This is in contrast to the more

traditional definitions of postpartum hemorrhage as an

estimated blood loss in excess of 500 mL after a vaginal

birth or a loss of greater than 1,000 mL after a cesarean

birth (6). This new classification is likely to reduce the

number of individuals labeled with postpartum hemor-

rhage. However, despite this new characterization, a

blood loss greater than 500 mL in a vaginal delivery

should be considered abnormal and should serve as an

indication for the health care provider to investigate the

increased blood deficit. Although visually estimated

blood loss is considered inaccurate, use of an educa-

tional process, with limited instruction on estimating

blood loss, has been shown to improve the accuracy of

such estimates (7). Historically, a decrease in hematocrit

of 10% had been proposed as an alternative marker to

define postpartum hemorrhage; however, determinations

of hemoglobin or hematocrit concentrations are often

delayed, may not reflect current hematologic status, and

are not clinically useful in the setting of acute postpartum

hemorrhage (8).

In postpartum women, it is important to recognize

that the signs or symptoms of considerable blood loss

(eg, tachycardia and hypotension) often do not present or

do not present until blood loss is substantial (9). There-

fore, in a patient with tachycardia and hypotension, the

obstetrician–gynecologist or other obstetric care provider

should be concerned that considerable blood loss, usually

Committee on Practice Bulletins—Obstetrics. This Practice Bulletin was developed by the American College of Obstetricians and Gynecologists’

Committee on Practice Bulletins–Obstetrics in collaboration with Laurence E. Shields, MD; Dena Goffman, MD; and Aaron B. Caughey, MD, PhD.

VOL. 130, NO. 4, OCTOBER 2017 Practice Bulletin Postpartum Hemorrhage e

uterine massage, bimanual compression, and uterotonic

drugs (15). Maternal trauma is indicated by lacerations,

expanding hematomas, or uterine rupture. Retention of

placental tissue can be readily diagnosed with manual

examination or bedside ultrasonography of the uterine

cavity and is addressed with manual removal or uter-

ine curettage. Thrombin is a reminder to evaluate the

patient’s coagulation status and if abnormal to correct

with replacement of clotting factors, fibrinogen, or other

factor replacement sources (see sections on Transfusion

Therapy and Massive Transfusion). It is important to

identify the most likely diagnosis or diagnoses to ini-

tiate appropriate interventions. These diagnoses are

outlined individually in the Clinical Considerations and

Recommendations section.

Risk Factors

Because obstetric hemorrhage is unpredictable, relatively

common, and leads to severe morbidity and mortality, all

obstetric unit members, including the physicians, mid-

wives, and nurses who provide obstetric care, should be

prepared to manage women who experience it. A number

of well-established risk factors such as prolonged labor

or chorioamnionitis are associated with postpartum hem-

orrhage (Table 1). However, many women without these

risk factors can experience a postpartum hemorrhage

(16). State and national organizations have suggested

that a maternal risk assessment should be conducted

antenatally and at the time of admission and continuously

modified as other risk factors develop during labor or the

postpartum period (17).

Risk assessment tools are readily available (18, 19)

and have been shown to identify 60–85% of patients

who will experience a significant obstetric hemorrhage

(17, 20, 21). An example of this type of assessment

tool is outlined in Table 2. However, a validation study

of this tool among a retrospective cohort of more than

10,000 women showed that although the tool correctly

identified more than 80% of patients with severe post-

partum hemorrhage, more than 40% of women who did

not experience hemorrhage were placed into the high-

risk group giving the tool a specificity of just below

60% (20). Additionally, approximately 1% of women

in the low-risk group experienced a severe postpartum

hemorrhage, which indicates that the clinical value for

identifying patients through risk assessment is low.

These findings reinforce the need for diligent surveil-

lance in all patients, including those initially thought to

be at low risk.

Prevention

Many organizations have recommended active manage-

ment of the third stage of labor as a method to reduce

representing 25% of the woman’s total blood volume

(or approximately 1,500 mL or more), has occurred (10).

Thus, earlier recognition of postpartum hemorrhage (eg,

before deterioration in vital signs) should be the goal in

order to improve outcomes.

Differential Diagnosis

The initial management of any patient with obstetric

hemorrhage requires that the obstetrician–gynecologist

or other obstetric care provider first identify the source

of bleeding (uterine, cervical, vaginal, periurethral, peri-

clitoral, perineal, perianal, or rectal). This can be quickly

done with a careful physical examination. After the

anatomic site is identified, it is important to identify the

cause because treatment may vary. The most common

etiologies (see Box 1) are broken into primary or sec-

ondary causes. Primary postpartum hemorrhage occurs

within the first 24 hours of birth, whereas secondary

postpartum hemorrhage is defined as excessive bleeding

that occurs more than 24 hours after delivery and up to

12 weeks postpartum (11, 12).

When evaluating a patient who is bleeding, it may be

helpful to consider “the 4 Ts” mnemonic device—tone,

trauma, tissue, and thrombin (13). Abnormal uterine

tone (uterine atony) is estimated to cause 70–80% of

postpartum hemorrhage and usually should be suspected

first as the etiology of postpartum hemorrhage (14).

Recommended interventions for uterine atony include

Box 1. Etiology of Postpartum Hemorrhage ^

Primary:

  • Uterine atony
  • Lacerations
  • Retained placenta
  • Abnormally adherent placenta (accreta)
  • Defects of coagulation (eg, disseminated intravascular

coagulation)*

  • Uterine inversion

Secondary:

  • Subinvolution of the placental site
  • Retained products of conception
  • Infection
  • Inherited coagulation defects (eg, factor deficiency

such as von Willebrand)

*These include inherited coagulation defects as well as acute coagulopathies that may develop from events such as amniotic fluid embolism, placental abruption, or severe preeclampsia.

VOL. 130, NO. 4, OCTOBER 2017 Practice Bulletin Postpartum Hemorrhage e

aimed at treating cases early and consistently to reduce

severe maternal morbidity and mortality as well as to

identify the need for more aggressive interventions (such

as hysterectomy or other surgeries) and intensive care

unit admissions. Although it does appear that hemor-

rhage is treated earlier with such approaches, evidence

regarding maternal outcomes, such as severe maternal

morbidity or intensive care unit admission, is inconsis-

tent (12).

Facilities With Limited Resources

Many hospitals that provide maternal services are

located in rural or small communities. In the United

States, obstetric services are provided in 50% of criti-

cal access hospitals and 92% of rural hospitals (37).

Because these centers typically do not have the same

resources as most urban centers, developing a compre-

hensive plan for dealing with obstetric emergencies such

as postpartum hemorrhage is important. In particular,

these small centers should consider establishing guide-

lines regarding appropriate case selection to triage or

transfer patients to higher-level centers. Additionally,

assessing available resources and developing a com-

prehensive plan for evaluating and managing obstetric

hemorrhage are important for reducing morbidity. For

more information see Obstetric Care Consensus No. 2,

Levels of Maternal Care (38).

Clinical Considerations and

Recommendations

What should be considered in the initial evaluation and management of a patient with excessive bleeding in the immediate postpartum period?

When postpartum bleeding exceeds expected volumes

(500 mL in a vaginal delivery or 1,000 mL in a cesarean

delivery), a careful and thorough evaluation should be

undertaken. A rapid physical examination of the uterus,

cervix, vagina, vulva, and perineum can often identify

the etiology (sometimes multiple sources) of the postpar-

tum hemorrhage. Obstetrician–gynecologists and other

obstetric care providers should be familiar with algo-

rithms for the diagnosis and management of postpartum

hemorrhage (18, 39) and, ideally, these should be posted

on labor and delivery units (see For More Information).

The most common etiologies include uterine atony, gen-

ital tract lacerations, retained placental tissue and, less

commonly, placental abruption, coagulopathy (acquired

or inherited), amniotic fluid embolism, placenta accreta,

or uterine inversion.

or with placental delivery—has not been adequately

studied or found to be associated with a difference in

the risk of hemorrhage (28). Specifically, delaying

oxytocin until after delayed umbilical cord clamping

has not been found to increase the risk of hemorrhage

(29). The World Health Organization, ACOG, American

Academy of Family Physicians, and Association of

Women’s Health, Obstetric and Neonatal Nurses recom-

mend administering uterotonics (usually oxytocin) after

all births for the prevention of postpartum hemorrhage

(13, 22, 24). Therefore, all obstetric care facilities should

have guidelines for the routine administration of utero-

tonics in the immediate postpartum period.

Although the number of well-conducted studies is

limited, one small study found that the use of uterine

massage was associated with reduced postpartum blood

loss and reduced need for additional uterotonic agents

(30); however, a Cochrane review found no statistical

differences and found the evidence inconclusive (31).

Furthermore, neither early umbilical cord clamping nor

umbilical cord traction have been shown to have a sig-

nificant effect on the incidence or volume of postpartum

hemorrhage (32). Additionally, in a Cochrane review,

two trials examining nipple stimulation or breastfeeding

did not demonstrate a difference in postpartum hemor-

rhage (33, 34).

Techniques for Management

Management may vary greatly among patients and

depends on the etiology and available treatment options.

In general, management of postpartum hemorrhage

should use a multidisciplinary and multifaceted approach

that involves maintaining hemodynamic stability while

simultaneously identifying and treating the cause of

blood loss. Treatment options for postpartum hemor-

rhage because of uterine atony include administration of

uterotonics or pharmacologic agents, tamponade of the

uterus (eg, intrauterine balloons), surgical techniques to

control the bleeding (eg, the B-Lynch procedure), embo-

lization of pelvic arteries or, ultimately, hysterectomy.

Generally, less invasive methods should be tried initially

if possible; however, if unsuccessful, more invasive

measures may be required. More specific guidance for

these management approaches is delineated later in the

document.

Systematic approaches to postpartum hemorrhage

based on algorithms have been created, and these

approaches have been used more widely at individual

hospitals and in health systems (19, 35, 36). These

approaches employ a multidisciplinary (eg, obstet-

rics, nursing, anesthesia, transfusion medicine), multi-

faceted, stepwise approach to the detection and manage-

ment of postpartum hemorrhage. The approaches are

e172 Practice Bulletin Postpartum Hemorrhage OBSTETRICS & GYNECOLOGY

precipitous uncontrolled delivery or an operative vaginal

delivery. Labial, rectal, pelvic pressure or pain, or vital

sign deterioration may be the only symptoms of genital

tract hematomas and may not be recognized until hours

after delivery. Once identified, most genital tract hema-

tomas can be managed conservatively. However, rapid

progressive enlargement of the hematoma, particularly

in the setting of abnormal vital signs, indicates a need

for incision and drainage. One reason that opening a

hematoma is reserved for only the most severe cases

is that often a single bleeding source is not identified

when a hematoma is incised. Exploration with sutur-

ing or packing may be needed to achieve hemostasis.

Arterial embolization is another option for management

of a hematoma and should be considered as a possibility

before opening the hematoma.

Deterioration of maternal vital signs without obvi-

ous bleeding should alert the obstetric team that there

may be intraperitoneal or retroperitoneal bleeding. In

this setting, resuscitative measures, diagnostic imaging,

and surgical intervention or an interventional radiology

procedure should not be delayed.

Retained Placenta

Detailed visual inspection of the placenta for complete-

ness should be conducted after all deliveries. Even when

the placenta appears intact, there may be additional

remaining products of conception (eg, succenturiate

lobe) within the uterine cavity. Manual removal of the

placenta, prior uterine surgery, or other risk factors

for morbidly adherent placenta should raise suspi-

cion for retained placental tissue or placenta accreta.

Ultrasonography or intrauterine manual examination

is usually used to diagnose retained placental tissue.

Retained placental tissue is unlikely when ultrasonog-

raphy reveals a normal endometrial stripe. However,

although ultrasonographic images of retained placental

tissue can be inconsistent, detection of an echogenic

mass within the uterus is highly suspicious. When a

retained placenta is identified, the first step is to attempt

manual removal of the tissue. If a woman has adequate

regional analgesia, assessment of the uterine cavity may

be performed. If manual extraction fails, either a “banjo”

curette or large oval forceps (Sopher or Bierer) can be

used for removal. Because of the concern for uterine

perforation in the postpartum uterus and to ensure

removal of all tissue, ultrasound guidance may be used.

If the placental tissue is adherent to the uterine wall,

there should be increased suspicion for placenta accreta,

particularly in the presence of risk factors for placenta

accreta. Management of placenta accreta is discussed

later in the document.

Uterine Atony

Because uterine atony causes 70–80% of cases of post-

partum hemorrhage, it remains the single most common

cause, and its incidence appears to be increasing (14,

21, 40). At the time of delivery, risk factors include, but

are not limited to, prolonged labor, induction of labor,

prolonged use of oxytocin, chorioamnionitis, multiple

gestation, polyhydramnios, and uterine leiomyomas (see

Table 1 and Table 2).

In the setting of postpartum hemorrhage, identifica-

tion of a soft, poorly contracted (boggy) uterus suggests

atony as a causative factor. When atony is suspected,

the bladder should be emptied and a bimanual pelvic

examination conducted, any intrauterine clots should

be removed, and uterine massage should be performed.

In addition to oxytocin, a second uterotonic agent is

required in 3–25% of cases of postpartum hemorrhage

(15). Supplemental uterotonics that are most com-

monly administered include methylergonovine, 15-

methyl prostaglandin F 2 a, or misoprostol. As discussed

in a 2015 systematic review, there is a lack of evidence

that suggests which specific additional uterotonics are

the most effective (12). Treatment of refractory atony

may require the use of secondary methods such as uter-

ine tamponade with an intrauterine tamponade balloon

or compression sutures (41, 42).

Occasionally, the fundus is firm and contracted

down, but the lower uterine segment is dilated and

atonic. In this setting, the usual approach is to manually

remove any clots and to use bimanual compression to

reduce the blood loss while waiting for the uterotonic

agents to work. Treatment with the intrauterine tampon-

ade balloon can be considered if there is persistent lower

uterine segment atony.

Obstetric Trauma

Genital tract lacerations are the most common complica-

tions of obstetric trauma. Although such lacerations are

predominantly venous bleeding, they can be the primary

source of a postpartum hemorrhage. Rapid identification

and repair of cervical lacerations, lacerations compli-

cated by arterial bleeding, and high vaginal lacerations

should be performed. Similarly, distal vaginal, vulvar,

periclitoral, and perineal lacerations should be repaired

if contributing significantly to blood loss. If a uterine

artery laceration is suspected, interventional radiology

or surgical exploration and ligation should be consid-

ered. Repair may require assistance from anesthesia and

transfer to a well-equipped operating room.

Genital tract hematomas (labial, vaginal, broad

ligament, or retroperitoneal) also can lead to significant

blood loss and should be suspected in the setting of a

e174 Practice Bulletin Postpartum Hemorrhage OBSTETRICS & GYNECOLOGY

ending with extension of the gauze through the cervi-

cal os. To avoid leaving gauze in the uterus at time of

removal, it can be carefully counted and tied together.

Similarly, multiple large Foley catheters (which were

common before the development of commercial intra-

uterine tamponade devices) can still be used, but the

challenge is placing multiple devices and keeping

Tamponade Techniques

When uterotonics and bimanual uterine massage fail to

sustain uterine contractions and satisfactorily control

hemorrhage, the use of compression (including manual

compression), intrauterine tamponade or packing can be

effective in decreasing hemorrhage secondary to uterine

atony (Table 4). Although the evidence that compares

these approaches is poor or absent, it is important for

institutions to adopt an approach and train personnel

in this approach. For example, the California Maternal

Quality Care Collaborative recommends the use of an

intrauterine balloon for tamponade after uterotonics

have failed.

Evidence for the benefits of use of intrauterine bal-

loon tamponade is limited; however, in one study, 86%

of women who had balloon tamponade did not require

further procedures or surgeries (12, 51). Similarly, a

summary of studies showed that 75% of patients did

not need further treatment after intrauterine balloon

tamponade (12). In some refractory cases, intrauterine

tamponade and uterine compression sutures (described

later) may be used together (52).

If a balloon tamponade system is not available, the

uterus may be packed with gauze. This requires careful

layering of the material back and forth from one uterine

cornu to the other repeatedly using a sponge stick, and

Table 3. Acute Medical Management of Postpartum Hemorrhage ^

Drug Dose and Route Frequency Contraindications Adverse Effects*

Oxytocin IV: 10–40 units per 500–1,000 mL Continuous Rare, hypersensitivity to Usually none. as continuous infusion medication Nausea, vomiting, or hyponatremia with IM: 10 units prolonged dosing. Hypotension can result from IV push, which is not recommended.

Methylergonovine IM: 0.2 mg Every 2–4 h Hypertension, preeclampsia, Nausea, vomiting, severe cardiovascular disease, hypertension particularly hypersensitivity to drug when given IV, which is not recommended

15-methyl PGF 2 a IM: 0.25 mg Every 15–90 min, Asthma. Relative Nausea, vomiting, Intramyometrial: 0.25 mg eight doses contraindication for diarrhea, fever (transient), maximum hypertension, active hepatic, headache, chills, pulmonary, or cardiac disease shivering hypertension, bronchospasm

Misoprostol 600–1,000 micrograms oral, One time Rare, hypersensitivity to Nausea, vomiting, diarrhea sublingual, or rectal medication or to prostaglandins shivering, fever (transient), headache

Abbreviations: IV, intravenously; IM, intramuscularly; PG, prostaglandin. *All agents can cause nausea and vomiting. Modified from Lyndon A, Lagrew D, Shields L, Main E, Cape V, editors. Improving health care response to obstetric hemorrhage version 2.0. A California quality improve- ment toolkit. Stamford (CA): California Maternal Quality Care Collaborative; Sacramento (CA): California Department of Public Health; 2015.

Table 4. Tamponade Techniques for Postpartum Hemorrhage

^

Technique Comment

Commercially available intrauterine balloon tamponade devices

  • Bakri Balloon
  • ebb uterine tamponade system

Foley catheter Insert one or more 60 mL bulbs and fill with 60 mL of saline. Uterine packing 4-inch gauze, can be soaked with 5,000 units of thrombin in 5 mL of saline then insert from one cornua to the other with ring forceps.

Inserted transcervically or through cesarean incision; has an exit port for blood drainage Inflated with 300–500 mL of saline Double Balloon: maximum rec- ommended fill volumes are 750 mL for the uterine balloon and 300 mL for the vaginal balloon.

VOL. 130, NO. 4, OCTOBER 2017 Practice Bulletin Postpartum Hemorrhage e

to postpartum hemorrhage, the median success of vascu-

lar ligation is 92% (12).

However, because these less invasive vascular tech-

niques appear to be effective, it appears that internal iliac

(hypogastric) artery ligation is performed less frequently

than in the past. The procedure has been found to be con-

siderably less successful than originally thought (57) and

because practitioners have become less familiar with this

technique (which requires a retroperitoneal approach) it

is rarely used today.

Uterine Compression Sutures

Although there are no good-quality studies that pro-

vide evidence for the success of uterine compression

sutures, the B-Lynch technique probably is the most

common uterine compression technique for atony (42);

however, other techniques, such as Cho and Hayman,

have been described (42, 58–61). The effectiveness of

uterine compression sutures as a secondary treatment

for uterine atony unresponsive to medical management

appears to be approximately 60–75%, with none of the

techniques shown to be superior to another (12, 62, 63).

B-lynch sutures are placed from the cervix to fundus

and provide physical compression of the uterus. A large

suture (eg, a number 1 chromic suture) should be used

to prevent breaking and the suture should be rapidly

absorbed to prevent risk of bowel herniation through

a persistent loop of suture after uterine involution.

Physicians should be familiar with the technique and it

could be helpful to have diagrams available on labor and

delivery for quick reference such as those available in

the Alliance for Innovation on Maternal Health Obstetric

Hemorrhage Bundle (64) (see For More Information).

Direct comparisons between compression sutures and

uterine balloons have been described in small case series

and suggest they have similar effectiveness (65). Uterine

necrosis after placement of compression sutures has

been reported; however, the exact incidence is not clear

because of the small number of patients in case reports

and series.

Hysterectomy

When more conservative therapies have failed, hys-

terectomy is considered the definitive treatment and is

not only associated with permanent sterility but also

potential surgical complications. For example, six small

studies have shown that bladder injuries range from 6%

to 12% and ureteral injuries range from 0.4% to 41%

(12). There are inadequate studies that compared hyster-

ectomy to other management approaches. Additionally,

there is inadequate evidence examining different surgi-

cal approaches to hysterectomy (eg, total hysterectomy

versus supracervical hysterectomy). Therefore, in the

careful count of them. In cases where compression, or

intrauterine tamponade, or both, fail to adequately con-

trol hemorrhage, they may be used to temporize while

planning to move to uterine artery embolization (UAE)

or hysterectomy.

Uterine Artery Embolization

Candidates for UAE typically are hemodynamically

stable, appear to have persistent slow bleeding and have

failed less invasive therapy (uterotonic agents, uterine

massage, uterine compression, and manual removal of

any clots) (12). When successful, UAE also has the

benefit of a woman retaining her uterus and, potentially,

future fertility. Fluoroscopic identification of bleeding

vessels allows embolization with absorbable gelatin

sponges, coils, or microparticles. Studies (n=15) have

shown that UAE for postpartum hemorrhage has a

median success rate of 89%, ranging from 58% to 98%

(12). Moreover, one of the largest series (114 UAE pro-

cedures) reported a success rate greater than 80%, with

15% requiring subsequent hysterectomy (53). The risk

of significant harm (uterine necrosis, deep vein throm-

bosis, or peripheral neuropathy) appears to be low (less

than 5%) based on reports from small case series (12).

After UAE, infertility has been reported in up to 43% of

women (12). Other studies have reported that in women

who have had a UAE, subsequent pregnancy complica-

tions such as preterm birth (5–15%) and fetal growth

restriction (7%) appear to be similar to the general

obstetric population (12, 54).

Surgical Management

Vascular Ligation

When less invasive approaches such as uterotonic agents

(with or without tamponade measures) or UAE fail to

control bleeding in the setting of postpartum hemor-

rhage, exploratory laparotomy is indicated. In the setting

of a vaginal delivery, it is common to use a midline verti-

cal abdominal incision to optimize exposure and reduce

risk of surgical bleeding. In the setting of cesarean birth,

the existing surgical incision may be used. Several tech-

niques are available to control bleeding with limited evi-

dence for each (12). The general aim of vascular ligation

in the setting of atony is to diminish the pulse pressure of

blood flowing to the uterus. A common first approach is

bilateral uterine artery ligation (O’Leary sutures), which

commonly accomplishes this goal of reducing blood

flow to the uterus, and is quickly and easily performed

(55, 56). Similarly, to further diminish blood flow to

the uterus, sutures also can be placed across the vessels

within the utero–ovarian ligaments. Reports from case

series indicate that, when used as a second-line approach

VOL. 130, NO. 4, OCTOBER 2017 Practice Bulletin Postpartum Hemorrhage e

tributes to secondary hemorrhage. Ultrasound evalua-

tion can help identify intrauterine tissue. Endometritis

should be strongly suspected in the presence of uterine

tenderness and a low grade fever. Secondary postpartum

hemorrhage also may be the first indication of bleeding

disorders such as von Willebrand disease.

Treatment should be focused on the etiology of

the hemorrhage and may include uterotonic agents and

antibiotics, but if these fail to resolve the problem or if

retained products of conception are suspected, uterine

curettage may be necessary. If treating endometritis,

broad antibiotic coverage with clindamycin and genta-

micin is a common choice, although other combinations

also are used (86). Often the volume of tissue removed

by curettage is relatively small, yet bleeding usually

subsides promptly. Concurrent ultrasound assessment

at the time of curettage can help prevent uterine per-

foration. Patients should be counseled about the pos-

sibility of hysterectomy before initiating any operative

procedure.

What is best practice for blood product replacement during and after a postpartum hemorrhage?

The Timing of Transfusion Therapy ^

Initiation of transfusion therapy generally is based

on estimated blood deficit and ongoing blood loss.

However, in the setting of postpartum hemorrhage,

acute changes in hemoglobin or hematocrit will not

accurately reflect blood loss. As noted previously,

maternal vital signs typically do not change drasti-

cally until significant blood loss has occurred (10).

Inadequate early resuscitation and hypoperfusion

may lead to lactic acidosis, systemic inflammatory

response syndrome with accompanying multiorgan

dysfunction, and coagulopathy (87). In women with

ongoing bleeding that equates to the blood loss of

1,500 mL or more or in women with abnormal vital signs

(tachycardia and hypotension), immediate preparation

for transfusion should be made (18, 19, 39). Because

such a large blood loss includes depletion of coagula-

tion factors, it is common for such patients to develop

a consumptive coagulopathy, commonly labeled as

disseminated intravascular coagulation, and the patients

will require platelets and coagulation factors in addition

to packed red blood cells.

Transfusion and Massive Obstetric Hemorrhage ^

Massive transfusion usually is defined as a transfusion

of 10 or more units of packed red blood cells within

at cesarean delivery (74, 75). Uterine inversion in a prior

pregnancy leads to an increased risk in a subsequent preg-

nancy (1 per 26 subsequent deliveries) although it is still

relatively uncommon (74). Upon bimanual examination,

the finding of a firm mass at or below the cervix, coupled

with the absence of identification of the uterine corpus

on abdominal examination, suggests inversion. If the

inversion occurs before placental separation, detachment

or removal of the placenta is generally not undertaken

before replacement of the uterus because, presumably,

this could lead to additional hemorrhage (76).

Manual replacement of the uterine corpus involves

placing the palm of the hand or a closed fist against the

fundus (now inverted and lowermost at or through the

cervix), as if holding a tennis ball, with the fingertips

exerting upward pressure circumferentially (77). To

restore normal anatomy, relaxation of the uterus may be

necessary. Terbutaline, magnesium sulfate, halogenated

general anesthetics, and nitroglycerin have all been used

for uterine relaxation without clear evidence supporting

any one approach as superior to the others (78). Manual

replacement with or without uterine relaxants usually

is successful with the large majority being successfully

replaced in one small series (76). In the unusual circum-

stance in which it is not, laparotomy is required. Two

procedures have been reported to return the uterine cor-

pus to the abdominal cavity. The Huntington procedure

involves progressive upward traction on the inverted

corpus using Babcock or Allis forceps (79). The Haultain

procedure involves incising the cervix posteriorly, which

allows for digital repositioning of the inverted corpus,

with subsequent repair of the incision (80).

Supportive measures and treatment of the associated

hemorrhage should be employed while the inversion is

corrected. In the setting of recurrent uterine inversion,

the use of intrauterine tamponade balloons has been

reported to prevent recurrent uterine inversion as well

as the accompanying hemorrhage in a number of case

reports (81–84). The use of uterine compression sutures

for prevention of acute recurrence also has been success-

ful in a limited number of case reports (59, 85).

What is the management approach for secondary or delayed postpartum hemorrhage?

Secondary postpartum hemorrhage , defined as excessive

bleeding that occurs more than 24 hours after delivery

and up to 12 weeks postpartum, occurs in approximately

1% of pregnancies (11). In the event of secondary

hemorrhage, a number of specific etiologies should be

considered. Uterine atony (perhaps secondary to retained

products of conception) with or without infection con-

e178 Practice Bulletin Postpartum Hemorrhage OBSTETRICS & GYNECOLOGY

It is also important to establish approaches to

address situations in which patients decline various treat-

ment approaches. For example, refusal of blood products

is common in patients who are Jehovah’s Witnesses.

This subset of patients has between a 44-fold to 130-

fold higher risk of maternal mortality from obstetric

hemorrhage because of refusal of blood products (94,

95). Because this population may accept some blood

products, a predelivery directive that can be used in the

event of a severe postpartum hemorrhage can be dis-

cussed with the patient during the prenatal period (18,

96). Greater detail on this issue is outlined in Committee

Opinion No. 664, Refusal of Medically Recommended

Treatment During Pregnancy.

Although transfusion is often lifesaving in obstet-

rics, usage of blood products, particularly in the setting

of massive transfusion, is not without risk. Massive

transfusion is associated with hyperkalemia from packed

red blood cells and citrate (used as a preservative in

stored blood products) toxicity that will typically worsen

hypocalcemia. The combination of acidosis, hypocalce-

mia, and hypothermia all contribute to worsening coagu-

lopathy and increased morbidity (87, 97). Overzealous

resuscitation with crystalloid also can be associated with

dilution-related coagulopathy and can contribute to pul-

monary edema (98). Other complications include transfu-

sion febrile nonhemolytic reactions (0.8 per 1,000 units

transfused), acute hemolytic transfusion reaction (0.

per 1,000 units transfused), and acute transfusion reac-

tions related lung injury (TRALI, 0.1 per 1,000 units

transfused) (99). Transfusion-associated infections (eg,

hepatitis, human immunodeficiency virus, West Nile

virus, Chagas disease, malaria, and Lyme disease) are

relatively rare (less than 1/100,000–1,000,000) (100).

Other Related Therapies

Cell Salvage

Intraoperative cell salvage—also known as autologous

blood transfusion—has been shown to be effective

and safe in obstetric patients. Limitations are primarily

related to availability of appropriate staff and equipment.

In certain settings where significant blood loss is antici-

pated, such as placenta previa and placenta accreta, hav-

ing this tool available may reduce the need for or volume

of allogeneic blood transfusion. Early concerns related

to amniotic fluid contamination have been dispelled

with higher quality filtering techniques (101). There is

some concern for anti-D isoimmunization, and appropri-

ate testing and treatment with anti-D immunoglobulin is

necessary (102, 103). However, because the large major-

ity of postpartum hemorrhage events are unpredictable,

cell salvage is rarely available or used.

24 hours, transfusion of 4 units of packed red blood

cells within 1 hour when ongoing need for more blood is

anticipated, or replacement of a complete blood volume

(87). Despite the low quality of evidence regarding the

benefit of massive transfusion for early postpartum hem-

orrhage (12), massive transfusion protocols should be

part of a comprehensive management plan for treatment

of postpartum hemorrhage in settings with adequate

blood banking.

Recommendations for optimal blood product

replacement therapy and timing of transfusion in obstet-

ric patients have been primarily limited to consensus

opinion (18), protocols adapted from trauma literature

(88, 89), and a few clinical reports (19, 39, 90–92). All

recommend the use of multicomponent therapy with

fixed ratios of packed red blood cells, fresh or thawed

plasma, platelets, and cryoprecipitate. When a massive

transfusion protocol is needed, fixed ratios of packed

red blood cells, fresh frozen plasma, and platelets should

be used. The recommended initial transfusion ratio for

packed red blood cells:fresh frozen plasma:platelets

has been in the range of 1:1:1 and is designed to mimic

replacement of whole blood. In a recent survey, more

than 80% of institutions reported using the 1:1 red blood

cell:plasma ratio (93). These recommendations are dif-

ferent from protocols that have previously suggested

ratios such as 4:4:1 or 6:4:1 and are related to how a

unit of platelets is defined (18). What is more important

than the actual ratio is that there is a specific protocol

for multicomponent therapy in place at each institution.

In women with suspected disseminated intravascular

coagulation (ie, consumptive coagulopathy, or low

fibrinogen, or both) administration of cryoprecipitate

also should be considered. Findings of critically low

fibrinogen should be particularly anticipated in the set-

ting of placental abruption or amniotic fluid embolism,

and early use of cryoprecipitate is commonly included as

part of the resuscitation.

Although smaller hospitals may not have all blood

products, every obstetric unit should have a compre-

hensive maternal hemorrhage emergency management

plan that includes protocols for accessing packed red

blood cells. In emergency situations, type specific or

type O Rh-negative blood also should be readily avail-

able. Physicians should be familiar with their hospitals’

protocol and recommendations for use of combination

blood component therapy. No specific hemorrhage pro-

tocol has been proved to be more effective than another;

therefore, each hospital will need to address its specific

resources and make modifications specific to its unique

setting. For examples of algorithms, see For More

Information.

e180 Practice Bulletin Postpartum Hemorrhage OBSTETRICS & GYNECOLOGY

for escalation of care, and a functioning massive trans-

fusion protocol.

Every obstetric unit should have an organized, sys-

tematic obstetric hemorrhage response that coordinates

care among all critical personnel. Hospitals should

consider adopting a system to implement key elements

in four categories: 1) readiness to respond to a maternal

hemorrhage, 2) recognition and prevention measures in

place for all patients, 3) a multidisciplinary response

to excessive maternal bleeding, and 4) a systems-based

quality improvement process to improve responsiveness

through reporting and system learning. The Council on

Patient Safety in Women’s Healthcare has endorsed a

system and further details can be found on the For More

Information web page. Education, drills, and review of

team protocol compliance are needed to ensure everyone

remains proficient with the treatment algorithm and tools

at each facility.

Multidisciplinary simulation-based team training,

including postpartum hemorrhage scenarios, have been

associated with improved safety culture and outcomes in

obstetrics (113–115). Hemorrhage drills have been used

for multiple purposes, including the following: identify

management pitfalls (116), improve confidence and com-

petence in skills (117), pilot and modify checklists (118),

identify and correct systems issues (119, 120), famil-

iarize staff with management algorithms, and ensure

timely management of hemorrhage (19). Although one

standardized approach for drills, simulation, and team

training has not been established, there are several rec-

ommended tools and techniques that can be incorporated

into unit-based improvement strategies (121, 122).

Summary of

Recommendations and

Conclusions

The following recommendations and conclusions are based on good and consistent scientific evidence (Level A):

All obstetric care facilities should have guidelines

for the routine administration of uterotonics in the

immediate postpartum period.

Uterotonic agents should be the first-line treatment

for postpartum hemorrhage caused by uterine atony.

The specific agent selected, outside of recognized

contraindications, is at the health care provider’s dis-

cretion because none has been shown to have greater

efficacy than others for the treatment of uterine

atony.

The following recommendations and conclusions are based on limited or inconsistent scientific evidence (Level B):

When uterotonics fail to adequately control post-

partum hemorrhage, prompt escalation to other

interventions (such as tamponade or surgical tech-

niques) and escalation of intensity of care and sup-

port personnel are indicated.

Given the mortality reduction findings, tranexamic

acid should be considered in the setting of obstetric

hemorrhage when initial medical therapy fails.

Obstetrician–gynecologists and other obstetric care

providers should work with their institutions to

ensure the existence of a designated multidisciplinary

response team, a staged postpartum hemorrhage pro-

tocol that includes guidelines for escalation of care,

and a functioning massive transfusion protocol.

The following recommendations and conclusions are based primarily on consensus and expert opinion (Level C):

Management of postpartum hemorrhage should use

a multidisciplinary and multifaceted approach that

involves maintaining hemodynamic stability while

simultaneously identifying and treating the cause of

blood loss.

Generally, in the treatment of postpartum hemor-

rhage, less invasive methods should be used initially

if possible, but if unsuccessful, preservation of life

may require more aggressive interventions including

hysterectomy.

When a massive transfusion protocol is needed,

fixed ratios of packed red blood cells, fresh frozen

plasma, and platelets should be used.

Hospitals should consider adopting a system to

implement key elements in four categories: 1) readi-

ness to respond to a maternal hemorrhage, 2) recog-

nition and prevention measures in place for all

patients, 3) a multidisciplinary response to excessive

maternal bleeding, and 4) a systems-based quality

improvement process to improve responsiveness

through reporting and system learning.

For More Information ^

The American College of Obstetricians and Gynecologists

has identified additional resources on topics related to

this document that may be helpful for ob-gyns, other

health care providers, and patients. You may view

VOL. 130, NO. 4, OCTOBER 2017 Practice Bulletin Postpartum Hemorrhage e

postpartum hemorrhage. Comparative Effectiveness Review No. 151. AHRQ Publication No. 15-EHC013- EF. Rockville (MD): Agency for Healthcare Research and Quality; 2015. (Systematic Review)^

  1. Anderson JM, Etches D. Prevention and manage- ment of postpartum hemorrhage. Am Fam Physician 2007;75:875–82. (Level III)^
  2. Bateman BT, Berman MF, Riley LE, Leffert LR. The epidemiology of postpartum hemorrhage in a large, nationwide sample of deliveries. Anesth Analg 2010;110:1368–73. (Level II-3)^
  3. Bateman BT, Tsen LC, Liu J, Butwick AJ, Huybrechts KF. Patterns of second-line uterotonic use in a large sample of hospitalizations for childbirth in the United States: 2007-2011. Anesth Analg 2014;119:1344–9. (Level II-3)^
  4. Wetta LA, Szychowski JM, Seals S, Mancuso MS, Biggio JR, Tita AT. Risk factors for uterine atony/post- partum hemorrhage requiring treatment after vaginal delivery. Am J Obstet Gynecol 2013;209:51.e1,51–6. (Level II-2)^
  5. Main EK, Goffman D, Scavone BM, Low LK, Bingham D, Fontaine PL, et al. National Partnership for Maternal Safety: consensus bundle on obstetric hemor- rhage. National Partnership for Maternal Safety, Council on Patient Safety in Women’s Health Care [published erratum appears in Obstet Gynecol 2015;126:1111]. Obstet Gynecol 2015;126:155–62. (Level III)^
  6. Lyndon A, Lagrew D, Shields L, Main E, Cape V, editors. Improving health care response to obstetric hemorrhage version 2.0. A California quality improve- ment toolkit. Stamford (CA): California Maternal Quality Care Collaborative; Sacramento (CA): California Department of Public Health; 2015. (Level III)^
  7. Shields LE, Smalarz K, Reffigee L, Mugg S, Burdumy TJ, Propst M. Comprehensive maternal hem- orrhage protocols improve patient safety and reduce utilization of blood products. Am J Obstet Gynecol 2011;205:368.e1–8. (Level II-3)^
  8. Dilla AJ, Waters JH, Yazer MH. Clinical validation of risk stratification criteria for peripartum hemorrhage. Obstet Gynecol 2013;122:120–6. (Level II-3)^
  9. Kramer MS, Berg C, Abenhaim H, Dahhou M, Rouleau J, Mehrabadi A, et al. Incidence, risk factors, and temporal trends in severe postpartum hemorrhage. Am J Obstet Gynecol 2013;209:449.e1–7. (Level II-3) ^
  10. Guidelines for oxytocin administration after birth. AWHONN Practice Brief Number 2. J Obstet Gynecol Neonatal Nurs 2015;44:161–3. (Level III)^
  11. Evensen A, Anderson JM, Fontaine P. Postpartum hemorrhage: prevention and treatment. Am Fam Phys- ician 2017;95:442–9. (Level III)^
  12. World Health Organization. WHO recommendations for the prevention and treatment of postpartum haemor- rhage. Geneva: WHO; 2012. (Level III)^
  13. Begley CM, Gyte GML, Devane D, McGuire W, Weeks A. Active versus expectant management for women in the third stage of labour. Cochrane Database of

these resources at www.acog.org/More–Info/Postpartum

Hemorrhage.

These resources are for information only and are not

meant to be comprehensive. Referral to these resources

does not imply the American College of Obstetricians

and Gynecologists’ endorsement of the organization, the

organization’s website, or the content of the resource.

These resources may change without notice.

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e186 Practice Bulletin Postpartum Hemorrhage OBSTETRICS & GYNECOLOGY

The MEDLINE database, the Cochrane Library, and ACOG’s own internal resources and documents were used to con duct a lit er a ture search to lo cate rel e vant ar ti cles pub lished between January 2000 and June 2017. The search was restricted to articles published in the English language. Priority was given to articles reporting results of original research, although review articles and commentaries also were consulted. Abstracts of research presented at sympo- sia and scientific conferences were not considered adequate for inclusion in this document. Guidelines published by organizations or institutions such as the National Institutes of Health and the American College of Obstetricians and Gynecologists were reviewed, and additional studies were located by reviewing bibliographies of identified articles. When reliable research was not available, expert opinions from obstetrician–gynecologists were used. Studies were reviewed and evaluated for quali ty according to the method outlined by the U.S. Pre ven tive Services Task Force: I Evidence obtained from at least one properly designed randomized controlled trial. II-1 Evidence obtained from well-designed controlled trials without randomization. II-2 Evidence obtained from well-designed cohort or case–control analytic studies, preferably from more than one center or research group. II-3 Evidence obtained from multiple time series with or without the intervention. Dramatic results in uncon- trolled experiments also could be regarded as this type of evidence. III Opinions of respected authorities, based on clinical experience, descriptive studies, or reports of expert committees. Based on the highest level of evidence found in the data, recommendations are provided and graded according to the following categories: Level A—Recommendations are based on good and con- sis tent sci en tif ic evidence. Level B—Recommendations are based on limited or incon- sistent scientific evidence. Level C—Recommendations are based primarily on con- sen sus and expert opinion.

Copyright October 2017 by the American College of Obstetri- cians and Gynecologists. All rights reserved. No part of this publication may be reproduced, stored in a retrieval system, posted on the Internet, or transmitted, in any form or by any means, electronic, mechanical, photocopying, recording, or otherwise, without prior written permission from the publisher. Requests for authorization to make photocopies should be directed to Copyright Clearance Center, 222 Rosewood Drive, Danvers, MA 01923, (978) 750-8400. ISSN 1099- The American College of Obstetricians and Gynecologists 409 12th Street, SW, PO Box 96920, Washington, DC 20090- Postpartum hemorrhage. Practice Bulletin No. 183. American College of Obstetricians and Gynecologists. Obstet Gynecol 2017;130: e168–86.

This information is designed as an educational resource to aid clinicians in providing obstetric and gynecologic care, and use of this information is

voluntary. This information should not be considered as inclusive of all proper treatments or methods of care or as a statement of the standard of care.

It is not intended to substitute for the independent professional judgment of the treating clinician. Variations in practice may be warranted when, in

the reasonable judgment of the treating clinician, such course of action is indicated by the condition of the patient, limitations of available resources, or

advances in knowledge or technology. The American College of Obstetricians and Gynecologists reviews its publications regularly; however, its publica-

tions may not reflect the most recent evidence. Any updates to this document can be found on www.acog.org or by calling the ACOG Resource Center.

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