Rapid HIV-1 testing during labor - A multicenter study

被引:142
作者
Bulterys, M
Jamieson, DJ
O'Sullivan, MJ
Cohen, MH
Maupin, R
Nesheim, S
Webber, MP
Van Dyke, R
Wiener, J
Branson, BM
机构
[1] Ctr Dis Control & Prevent, Div HIV AIDS Prevent Surveillance & Epidemiol, Natl Ctr HIV STD & TB Prevent, Atlanta, GA 30333 USA
[2] Univ Miami, Sch Med, Dept Obstet & Gynecol, Miami, FL 33101 USA
[3] Cook Cty Hosp, Dept Med, Chicago, IL 60612 USA
[4] Louisiana State Univ, Sch Med, Dept Obstet & Gynecol, New Orleans, LA USA
[5] Emory Univ, Sch Med, Dept Pediat, Atlanta, GA USA
[6] Montefiore Med Ctr, Albert Einstein Coll Med, Dept Epidemiol & Populat Hlth, Bronx, NY 10467 USA
[7] Tulane Univ, Sch Med, Dept Pediat, New Orleans, LA 70112 USA
来源
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION | 2004年 / 292卷 / 02期
关键词
D O I
10.1001/jama.292.2.219
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Context Timely testing of women in labor with undocumented human immunodeficiency virus (HIV) status could enable immediate provision of antiretroviral prophylaxis. Objectives To determine the feasibility and acceptance of rapid HIV testing among women in labor and to assess rapid HIV assay performance. Design, Setting, and Patients The Mother-Infant Rapid Intervention At Delivery (MIRIAD) study implemented 24-hour counseling and voluntary rapid HIV testing for women in labor at 16 US hospitals from November 16, 2001, through November 15, 2003. A rapid HIV-1 antibody test for whole blood was used. Main Outcome Measures Acceptance of HIV testing; sensitivity, specificity, and predictive value of the rapid test; time from blood collection to patient notification of results. Results There were 91707 visits to the labor and delivery units in the study, 7381 of which were by eligible women without documentation of HIV testing. Of these, 5744 (78%) women were approached for rapid HIV testing and 4849 (84%) consented. HIV-1 test results were positive for 34 women (prevalence=7/1000). Sensitivity and specificity of the rapid test were 100% and 99.9%, respectively; positive predictive value was 90% compared with 76% for enzyme immunoassay (EIA). Factors independently associated with higher test acceptance included younger age, being black or Hispanic, gestational age less than 32 weeks, and having had no prenatal care. Lower acceptance was associated with being admitted between 4 Pm and midnight, particularly on Friday nights, but this may be explained in part by fewer available personnel. Median time from blood collection to patient notification of result was 66 minutes (interquartile range, 45-120 minutes), compared with 28 hours for EIA (P<.001). Conclusions Rapid HIV testing is feasible and delivers accurate and timely test results for women in labor. It provides HIV-positive women prompt access to intrapartum and neonatal antiretroviral prophylaxis, proven to reduce perinatal HIV transmission, and may be particularly applicable to higher-risk populations.
引用
收藏
页码:219 / 223
页数:5
相关论文
共 22 条
  • [1] [Anonymous], 2011, Categorical data analysis
  • [2] [Anonymous], The U.S. Public Health Service Syphilis Study at Tuskegee
  • [3] Branson B.M., 2000, AIDS REV, V2, P76
  • [4] Prevention of HIV infection in children
    Bulterys, M
    Fowler, MG
    [J]. PEDIATRIC CLINICS OF NORTH AMERICA, 2000, 47 (01) : 241 - +
  • [5] *CDCP, QUAL ASS GUID TEST O
  • [6] *CDCP, 2001, MMWR RECOMM REP, V50, P63
  • [7] *CDCP, 2003, MMWR-MORBID MORTAL W, V52, P866
  • [8] *CDCP, 2003, MMWR-MORBID MORTAL W, V52, P329
  • [9] Centers for Disease Control and prevention, 2004, RAP HIV ANT TEST LAB
  • [10] Using point-of-care testing to make rapid HIV-1 tests in labor really rapid
    Cohen, MH
    Olszewski, Y
    Branson, B
    Robey, M
    Love, F
    Jamieson, DJ
    Bulterys, M
    [J]. AIDS, 2003, 17 (14) : 2121 - 2124