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Brief Summary

GUIDELINE TITLE

HIV screening in pregnancy.

BIBLIOGRAPHIC SOURCE(S)

GUIDELINE STATUS

This is the current release of the guideline.

BRIEF SUMMARY CONTENT

 
RECOMMENDATIONS
 EVIDENCE SUPPORTING THE RECOMMENDATIONS
 IDENTIFYING INFORMATION AND AVAILABILITY
 DISCLAIMER

 Go to the Complete Summary

RECOMMENDATIONS

MAJOR RECOMMENDATIONS

Definitions of the levels of evidence (I, II-1, II-2, II-3, and III) and grades of recommendations (A-E) are provided at the end of the "Major Recommendations" field.

Counselling

  1. All pregnant women should have human immunodeficiency virus (HIV) screening with appropriate counselling. This testing must be voluntary. Screening should be considered a standard of care, although women must be informed of the policy, its risks and benefits, and the right of refusal. Women must not be tested without their knowledge. (II-2 B)
  2. Pre-test counselling and the patient's decision about testing should be documented in the patient's chart. (III-B)
  3. Women who decline screening should still have concerns discussed and should continue to receive optimum antenatal care. (III-C)

When to Provide Screening

  1. Women should be offered HIV screening at their first prenatal visit. (I-A)
  2. Women who test negative for HIV and continue to engage in high-risk behaviour should be retested in each trimester of pregnancy. (II-3 B)
  3. Women with no prenatal care and unknown HIV status should be offered testing when admitted to hospital for labour and delivery. Women at high risk for HIV and with unknown status should be offered HIV prophylaxis in labour, and HIV prophylaxis should be given to the infant post partum. (III-B)

Appropriate Follow-Up

  1. Women who test positive for HIV should be followed by practitioners who are knowledgeable in the care of HIV-positive women. (III-C)

Definitions:

Quality of Evidence Assessment*

I: Evidence obtained from at least one properly randomized controlled trial

II-1: Evidence from well-designed controlled trials without randomization

II-2: Evidence from well-designed cohort (prospective or retrospective) or case-control studies, preferably from more than one centre or research group

II-3: Evidence obtained from comparisons between times or places with or without the intervention. Dramatic results in uncontrolled experiments (such as the results of treatment with penicillin in the 1940s) could also be included in this category

III: Opinions of respected authorities, based on clinical experience, descriptive studies, or reports of expert committees

Classification of Recommendations*

  1. There is good evidence to support the recommendation that the condition be specifically considered in a periodic health examination.
  2. There is fair evidence to support the recommendation that the condition be specifically considered in a periodic health examination.
  3. There is poor evidence regarding the inclusion or exclusion of the condition in a periodic health examination.
  4. There is fair evidence to support the recommendation that the condition not be considered in a periodic health examination.
  5. There is good evidence to support the recommendation that the condition be excluded from consideration in a periodic health examination.

*The quality of evidence reported in these guidelines has been adapted from the Evaluation of Evidence criteria described in the Canadian Task Force on the Periodic Health Exam.

**Recommendations included in these guidelines have been adapted from the Classification of Recommendations criteria described in the Canadian Task Force on the Periodic Health Exam.

CLINICAL ALGORITHM(S)

None provided

EVIDENCE SUPPORTING THE RECOMMENDATIONS

TYPE OF EVIDENCE SUPPORTING THE RECOMMENDATIONS

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

IDENTIFYING INFORMATION AND AVAILABILITY

BIBLIOGRAPHIC SOURCE(S)

ADAPTATION

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

DATE RELEASED

2006 Dec

GUIDELINE DEVELOPER(S)

Society of Obstetricians and Gynaecologists of Canada - Medical Specialty Society

SOURCE(S) OF FUNDING

Society of Obstetricians and Gynaecologists of Canada

GUIDELINE COMMITTEE

Infectious Disease Committee

COMPOSITION OF GROUP THAT AUTHORED THE GUIDELINE

Principal Authors: Lisa Keenan-Lindsay, RN, MN, Toronto ON; Mark H. Yudin, MD, MSc, FRCSC, Toronto ON

Committee Members: Marc Boucher, MD, FRCSC, Montreal QC; Howard Ronald Cohen, MD, FRCSC, Toronto ON; Andrée Gruslin, MD, FRCSC, Ottawa ON; Catherine Jane MacKinnon, MD, FRCSC, Brantford ON; Deborah M. Money, MD, FRCSC, Vancouver BC; Caroline Paquet, RM, MSc, Trois-Rivières QC; Marc Steben, MD, Montreal QC; Julie van Schalkwyk, MD, FRCSC, Vancouver BC; Thomas Wong, MD, MPH, FRCPC, Ottawa ON; Mark H. Yudin, MD, MSc, FRCSC, Toronto ON

FINANCIAL DISCLOSURES/CONFLICTS OF INTEREST

Not stated

GUIDELINE STATUS

This is the current release of the guideline.

GUIDELINE AVAILABILITY

Electronic copies: Available in Portable Document Format (PDF) from the Society of Obstetricians and Gynaecologists of Canada Web site.

Print copies: Available from the Society of Obstetricians and Gynaecologists of Canada, La société des obstétriciens et gynécologues du Canada (SOGC) 780 promenade Echo Drive Ottawa, ON K1S 5R7 (Canada); Phone: 1-800-561-2416

AVAILABILITY OF COMPANION DOCUMENTS

None available

PATIENT RESOURCES

None available

NGC STATUS

This NGC summary was completed by ECRI Institute on February 10, 2009. The information was verified by the guideline developer on March 4, 2009.

COPYRIGHT STATEMENT

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

DISCLAIMER

NGC DISCLAIMER

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