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  • Guideline Summary
  • NGC:005702
  • 2006 Oct (reaffirmed 2013)

Postpartum hemorrhage.

American College of Obstetricians and Gynecologists (ACOG). Postpartum hemorrhage. Washington (DC): American College of Obstetricians and Gynecologists (ACOG); 2006 Oct. 10 p. (ACOG practice bulletin; no. 76).  [40 references]

This is the current release of the guideline.

The American College of Obstetricians and Gynecologists (ACOG) reaffirmed the currency of the guideline in 2013.

Age Group

UMLS Concepts (what is this?)

SNOMEDCT_US
Antibacterial agent (346325008), Antibacterial agent (419241000), Antibiotic (255631004), Blood coagulation disorder (362970003), Blood coagulation disorder (64779008), Blood test (252275004), Blood test (396550006), Catheterization (45211000), Curettage - action (129319001), Curettage - action (68688001), Drainage procedure (122462000), Drainage procedure (129289008), Embolization procedure (122463005), Embolization procedure (129335008), Erythropoietin (111167001), Erythropoietin (83042003), Exploratory laparotomy (74770008), Hysterectomy (236886002), Iron (30729008), Iron (373755001), Iron (3829006), Laparotomy (86481000), Menorrhagia (386692008), Mineral (87918000), Operation on female genital organs (12658000), Oxytocic agent (410937004), Oxytocic agent (424999005), Postpartum hemorrhage (47821001), Transfusion of blood component (54790000), Ultrasonography (16310003), Ultrasonography (278292003), Ultrasonography (359659005), Uterine inversion (27215002), Vitamin (12968008), Vitamin (87708000)

Major Recommendations

The grades of evidence (I-III) and levels of recommendations (A-C) are defined at the end of the "Major Recommendations" field.

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

  • Uterotonic agents should be the first-line treatment for postpartum hemorrhage due to uterine atony.
  • Management may vary greatly among patients, depending on etiology and available treatment options, and often a multidisciplinary approach is required.
  • When uterotonics fail following vaginal delivery, exploratory laparotomy is the next step.
  • In the presence of conditions known to be associated with placenta accreta, the obstetric care provider must have a high clinical suspicion and take appropriate precautions.

Definitions:

Grades of Evidence

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 uncontrolled 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.

Levels of Recommendations

Level A — Recommendations are based on good and consistent scientific evidence.

Level B — Recommendations are based on limited or inconsistent scientific evidence.

Level C — Recommendations are based primarily on consensus and expert opinion.

Clinical Algorithm(s)

None provided

Disease/Condition(s)

Postpartum hemorrhage

Guideline Category

Evaluation

Management

Treatment

Clinical Specialty

Emergency Medicine

Family Practice

Obstetrics and Gynecology

Intended Users

Physicians

Guideline Objective(s)

  • To aid practitioners in making decisions about appropriate obstetric and gynecologic care
  • To review the etiology, evaluation, and management of postpartum hemorrhage

Target Population

  • Women during the first 24 hours after delivery (at risk for primary postpartum hemorrhage), especially those with:
    • Uterine atony
    • Retained placenta—especially placenta accreta
    • Defects in coagulation
    • Uterine inversion
  • Women between 24 hours and 6–12 weeks after delivery (at risk for secondary postpartum hemorrhage),especially those with:
    • Subinvolution of placental site
    • Retained products of conception
    • Infection
    • Inherited coagulation defects
  • Women with other risk factors for postpartum hemorrhage

Interventions and Practices Considered

Evaluation/Management

  1. Multi-disciplinary approach with high clinical suspicion
  2. Laboratory evaluation of lost blood
  3. Testing for bleeding disorders among patients with menorrhagia
  4. Medical management, including use of uterotonic agents
  5. Exploratory laparotomy
  6. Ultrasonography
  7. Drainage of hematomas
  8. Uterine compression or massage
  9. Tamponade: packing of the uterine cavity, Foley catheter insertion, Sengstaken-Blakemore tube insertion, SOS Bakri tamponade balloon use
  10. Surgical management, including uterine curettage and hysterectomy
  11. Arterial ligation or embolization
  12. Blood component therapy (donor or autologous): packed red cells, platelets, fresh frozen plasma, cryoprecipitate
  13. Manual replacement of the uterine corpus
  14. Antibiotics

Poststabilization Management

  1. Prenatal vitamin and mineral capsules
  2. Additional iron tablets
  3. Erythropoietin

Major Outcomes Considered

  • Time to cessation of bleeding
  • Incidence of serious sequelae (adult respiratory distress syndrome, coagulopathy, shock, loss of fertility, and pituitary necrosis)
  • Loss of fertility
  • Mortality

Methods Used to Collect/Select the Evidence

Hand-searches of Published Literature (Primary Sources)

Hand-searches of Published Literature (Secondary Sources)

Searches of Electronic Databases

Description of Methods Used to Collect/Select the Evidence

2006 Original Document

The MEDLINE database, the Cochrane Library, and the American College of Obstetricians and Gynecologists' own internal resources and documents were used to conduct a literature search to locate relevant articles published between January 1901 and June 2006. 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 symposia 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 American College of Obstetricians and Gynecologists were reviewed, and additional studies were located by reviewing bibliographies of identified articles.

2013 Reaffirmation

The NCBI database was searched from 2006 to 2013. Committee members conducted a literature search with the assistance from the ACOG Resource Center staff who routinely perform the Practice Bulletin literature searches.

Number of Source Documents

Not stated

Methods Used to Assess the Quality and Strength of the Evidence

Weighting According to a Rating Scheme (Scheme Given)

Rating Scheme for the Strength of the Evidence

Studies were reviewed and evaluated for quality according to the method outlined by the U.S. Preventive 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 uncontrolled 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.

Methods Used to Analyze the Evidence

Systematic Review

Description of the Methods Used to Analyze the Evidence

Not stated

Methods Used to Formulate the Recommendations

Expert Consensus

Description of Methods Used to Formulate the Recommendations

2006 Original Document

Analysis of available evidence was given priority in formulating recommendations. When reliable research was not available, expert opinions from obstetrician–gynecologists were used. See also the "Rating Scheme for the Strength of Recommendations" field regarding Grade C recommendations.

2013 Reaffirmation

The Committee on Practice Bulletins - Obstetrics met in October 2013 and reaffirmed this document. A committee member reviewed the document and new literature on the topic. The document was then reviewed by the committee and the committee agreed that it is current and accurate.

Rating Scheme for the Strength of the Recommendations

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 consistent scientific evidence.

Level B — Recommendations are based on limited or inconsistent scientific evidence.

Level C — Recommendations are based primarily on consensus and expert opinion.

Cost Analysis

A formal cost analysis was not performed and published cost analyses were not reviewed.

Method of Guideline Validation

Internal Peer Review

Description of Method of Guideline Validation

Practice Bulletins are validated by two internal clinical review panels composed of practicing obstetrician-gynecologists generalists and sub-specialists. The final guidelines are also reviewed and approved by the American College of Obstetricians and Gynecologists (ACOG) Executive Board.

Type of Evidence Supporting the Recommendations

The type of supporting evidence is identified and graded for each recommendation (see "Major Recommendations").

Potential Benefits

Appropriate evaluation and management of women with postpartum hemorrhage

Potential Harms

  • Undiluted rapid oxytocin IV infusion causes hypotension.
  • Care must be taken in performing curettage to avoid perforation of the uterus.

Contraindications

  • Relative contraindication for 15-methylprostaglandin F2a in patients with hepatic, renal, and cardiac disease. Diarrhea, fever, tachycardia can occur.
  • Avoid methylergonovine if patient is hypertensive.
  • Avoid 15-methylprostaglandin F2a in asthmatic patients.
  • Avoid dinoprostone if patient is hypotensive. Fever is common.

Qualifying Statements

These guidelines should not be construed as dictating an exclusive course of treatment or procedure. Variations in practice may be warranted based on the needs of the individual patient, resources, and limitations unique to the institution or type of practice.

Description of Implementation Strategy

An implementation strategy was not provided.

Implementation Tools

Audit Criteria/Indicators

For information about availability, see the Availability of Companion Documents and Patient Resources fields below.

IOM Care Need

Getting Better

IOM Domain

Effectiveness

Timeliness

Bibliographic Source(s)

American College of Obstetricians and Gynecologists (ACOG). Postpartum hemorrhage. Washington (DC): American College of Obstetricians and Gynecologists (ACOG); 2006 Oct. 10 p. (ACOG practice bulletin; no. 76).  [40 references]

Adaptation

Not applicable: The guideline was not adapted from another source.

Date Released

2006 Oct (reaffirmed 2013)

Guideline Developer(s)

American College of Obstetricians and Gynecologists - Medical Specialty Society

Source(s) of Funding

American College of Obstetricians and Gynecologists (ACOG)

Guideline Committee

American College of Obstetricians and Gynecologists (ACOG) Committee on Practice Bulletins-Obstetrics

Composition of Group That Authored the Guideline

Not stated

Financial Disclosures/Conflicts of Interest

Not stated

Guideline Status

This is the current release of the guideline.

The American College of Obstetricians and Gynecologists (ACOG) reaffirmed the currency of the guideline in 2013.

Guideline Availability

Electronic copies: None available

Print copies: Available for purchase from the American College of Obstetricians and Gynecologists (ACOG) Distribution Center, PO Box 933104, Atlanta, GA 31193-3104; telephone, 800-762-2264, ext. 192; e-mail: sales@acog.org. The ACOG Bookstore is available online at the ACOG Web site External Web Site Policy.

Availability of Companion Documents

Proposed performance measures are included in the original guideline document.

Patient Resources

None available

NGC Status

This NGC summary was completed by ECRI Institute on August 2, 2007. The information was verified by the guideline developer on September 10, 2007. This summary was updated by ECRI Institute on March 21, 2008 following the FDA advisory on Erythropoiesis Stimulating Agents. This summary was updated by ECRI Institute on August 15, 2008 following the U.S. Food and Drug Administration advisory on Erythropoiesis Stimulating Agents (ESAs). This summary was updated by ECRI Institute on April 1, 2010 following the U.S. Food and Drug Administration advisory on Erythropoiesis-Stimulating Agents (ESAs). The currency of the guideline was reaffirmed by the developer in 2008 and this summary was updated by ECRI Institute on November 30, 2011. The currency of the guideline was reaffirmed by the developer in 2013 and this summary was updated by ECRI Institute on March 7, 2014.

Copyright Statement

This NGC summary is based on the original guideline, which is subject to the guideline developer's copyright restrictions.

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