4.7 Article

Cryptococcal Antigenemia in Human Immunodeficiency Virus Antiretroviral Therapy-Experienced Ugandans With Virologic Failure

期刊

CLINICAL INFECTIOUS DISEASES
卷 71, 期 7, 页码 1726-1731

出版社

OXFORD UNIV PRESS INC
DOI: 10.1093/cid/ciz1069

关键词

cryptococcal antigenemia; virologic failure; ART experienced; HIV

资金

  1. National Institutes of Health Fogarty International Center [D43TW009345, K01TW010268]
  2. National Institute of Allergy and Infectious Diseases [K23AI138851, U01AI125003]
  3. Developing Excellence in Leadership, Training and Science (DELTAS) Africa Initiative [DEL-15-011]
  4. NEPAD
  5. Wellcome Trust [107742/Z/15/Z]
  6. UK government

向作者/读者索取更多资源

Background. Detectable serum or plasma cryptococcal antigen (CrAg) precedes symptomatic cryptococcal meningitis. The World Health Organization recommends CrAg screening for human immunodeficiency virus-positive persons with CD4 count <100 cells/mu L initiating antiretroviral therapy (ART). However, an increasing proportion of patients with cryptococcosis are now ART experienced. Whether CrAg screening is cost-effective in those with virologic failure is unknown. Methods. We retrospectively performed nationwide plasma CrAg testing among ART-experienced Ugandan adults with virologic failure (>= 1000 copies/mL) using leftover plasma after viral load testing during September 2017-January 2018. For those who were CrAg positive, we obtained ART history, meningitis occurrence, and 6-month survival via medical records review. Results. Among 1186 subjects with virologic failure, 35 (3.0%) were CrAg positive with median ART duration of 41 months (interquartile range, 10-84 months). Among 25 subjects with 6-month outcomes, 16 (64%) survived, 7 (28%) died, and 2 (8%) were lost. One survivor had suffered cryptococcal meningitis 2 years prior. Two others developed cryptococcal meningitis and survived. Five survivors were known to have received fluconazole. Thus, meningitis-free survival at 6 months was 61% (14/23). Overall, 91% (32/35) of CrAg-positive persons had viral load >= 5000 copies/mL compared with 64% (735/1151) of CrAg-negative persons (odds ratio, 6.0 [95% confidence interval, 1.8-19.8]; P = .001). CrAg prevalence was 4.2% (32/768) among those with viral loads >= 5000 copies/mL and 0.7% (3/419) among those with viral loads <5000 copies/mL. Conclusions. In addition to the CD4 threshold of <100 cells/mu L, reflexive CrAg screening should be considered in persons failing ART in Uganda with viral loads >= 5000 copies/mL.

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