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Revising expectations from rapid HIV tests in the emergency department.
Walensky, Rochelle P; Arbelaez, Christian; Reichmann, William M; Walls, Ron M; Katz, Jeffrey N; Block, Brian L; Dooley, Matthew; Hetland, Adam; Kimmel, Simeon; Solomon, Jessica D; Losina, Elena.
Afiliação
  • Walensky RP; Brigham and Women's Hospital, Harvard Medical School, Boston, Massachusetts 02115, USA. rwalensky@partners.org
Ann Intern Med ; 149(3): 153-60, 2008 Aug 05.
Article em En | MEDLINE | ID: mdl-18678842
ABSTRACT

BACKGROUND:

Expanded HIV screening efforts in the United States have increased the use of rapid HIV tests in emergency departments. The reported sensitivity and specificity of rapid HIV tests exceed 99%.

OBJECTIVE:

To assess whether a reactive rapid oral HIV test result correctly identifies adults with HIV infection in the emergency department.

DESIGN:

Diagnostic test performance assessment within the framework of a randomized, clinical trial.

SETTING:

Brigham and Women's Hospital emergency department (Boston, Massachusetts) from 7 February to 1 October 2007. PATIENTS 849 adults with valid rapid oral HIV test results. INTERVENTION Rapid HIV testing with the OraQuick ADVANCE Rapid HIV-1/2 Antibody Test (OraSure Technologies, Bethlehem, Pennsylvania). Patients with reactive rapid test results were offered enzyme-linked immunoassay, Western blot, and plasma HIV-1 RNA testing for confirmation. MEASUREMENTS Specificity and positive likelihood ratio.

RESULTS:

39 patients had reactive results (4.6% [95% CI, 3.2% to 6.0%]). On confirmation, 5 patients were HIV-infected (prevalence, 0.6% [CI, 0.1% to 1.1%]) and 26 were non-HIV-infected (8 patients declined confirmation). The estimated rapid test specificity was 96.9% (CI, 95.7% to 98.1%). Sensitivity analyses of the true HIV status of unconfirmed cases and test sensitivity resulted in a positive likelihood ratio of 8 to 32. Western blot alone as a confirmation test provided conclusive HIV status in only 50.0% (CI, 30.8% to 69.2%) of patients at first follow-up. The addition of HIV-1 RNA testing to the confirmation protocol improved this rate to 96.2% (CI, 88.8% to 100.0%).

LIMITATION:

Test sensitivity cannot be assessed because nonreactive OraQuick test results were not confirmed.

CONCLUSION:

Although patients with a reactive oral OraQuick HIV screening test in the emergency department had an 8- to 32-fold increased odds of HIV infection compared with the pretest odds, the specificity of the test was lower than anticipated.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Kit de Reagentes para Diagnóstico / Infecções por HIV / Serviço Hospitalar de Emergência Tipo de estudo: Clinical_trials / Diagnostic_studies / Guideline / Prognostic_studies / Risk_factors_studies Limite: Adult / Female / Humans / Male / Middle aged País/Região como assunto: America do norte Idioma: En Revista: Ann Intern Med Ano de publicação: 2008 Tipo de documento: Article País de afiliação: Estados Unidos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Kit de Reagentes para Diagnóstico / Infecções por HIV / Serviço Hospitalar de Emergência Tipo de estudo: Clinical_trials / Diagnostic_studies / Guideline / Prognostic_studies / Risk_factors_studies Limite: Adult / Female / Humans / Male / Middle aged País/Região como assunto: America do norte Idioma: En Revista: Ann Intern Med Ano de publicação: 2008 Tipo de documento: Article País de afiliação: Estados Unidos