PMID- 22095568 OWN - NLM STAT- MEDLINE DCOM- 20120509 LR - 20220311 IS - 1537-6591 (Electronic) IS - 1058-4838 (Print) IS - 1058-4838 (Linking) VI - 54 IP - 3 DP - 2012 Feb 1 TI - Paradoxical immune reconstitution inflammatory syndrome in HIV-infected patients treated with combination antiretroviral therapy after AIDS-defining opportunistic infection. PG - 424-33 LID - 10.1093/cid/cir802 [doi] AB - BACKGROUND: The incidence of immune reconstitution inflammatory syndrome (IRIS) when antiretroviral therapy (ART) is initiated after an AIDS-defining opportunistic infection (OI) is uncertain and understudied for the most common OIs. METHODS: We examined patients in the University of Washington Human Immunodeficiency Virus Cohort initiating potent ART subsequent to an AIDS-defining OI. IRIS was determined through retrospective medical record review and adjudication using a standardized data collection process and clinical case definition. We compared demographic and clinical characteristics, and immunologic changes in patients with and without IRIS. RESULTS: Among 196 patients with 260 OIs, 21 (11%; 95% confidence interval, 7%-16%) developed paradoxical IRIS in the first year on ART. The 3 most common OIs among study patients were Pneumocystis pneumonia (PCP, 28%), Candida esophagitis (23%), and Kaposi sarcoma (KS, 16%). Cumulative 1-year incidence of IRIS was 29% (12/41) for KS, 16% (4/25) for tuberculosis, 14% (1/7) for Cryptococcus, 10% (1/10) for Mycobacterium avium complex, and 4% (3/72) for PCP. Morbidity and mortality were highest in those with visceral KS-IRIS compared with other types of IRIS (100% [6/6] vs 7% [1/15], P < .01). Patients with mucocutaneous KS and tuberculosis-IRIS experienced greater median increase in CD4(+) cell count during the first 6 months of ART compared with those without IRIS (+158 vs +53 cells/muL, P = .04, mucocutaneous KS; +261 vs +113, P = .04, tuberculosis). CONCLUSIONS: Cumulative incidence and features of IRIS varied depending on the OI. IRIS occurred in >10% of patients with KS, tuberculosis, or Cryptococcus. Visceral KS-IRIS led to considerable morbidity and mortality. FAU - Achenbach, Chad J AU - Achenbach CJ AD - Department of Medicine, Feinberg School of Medicine, Division of Infectious Diseases and Center for Global Health, Northwestern University, Chicago, Illinois 60611, USA. c-achenbach@northwestern.edu FAU - Harrington, Robert D AU - Harrington RD FAU - Dhanireddy, Shireesha AU - Dhanireddy S FAU - Crane, Heidi M AU - Crane HM FAU - Casper, Corey AU - Casper C FAU - Kitahata, Mari M AU - Kitahata MM LA - eng GR - P30 AI027757/AI/NIAID NIH HHS/United States GR - T32 AI007140/AI/NIAID NIH HHS/United States GR - T32 AI07140-31/AI/NIAID NIH HHS/United States PT - Journal Article PT - Research Support, N.I.H., Extramural DEP - 20111117 PL - United States TA - Clin Infect Dis JT - Clinical infectious diseases : an official publication of the Infectious Diseases Society of America JID - 9203213 RN - 0 (Anti-HIV Agents) SB - IM CIN - Clin Infect Dis. 2012 Jul;55(1):157-8; author reply 158-9. PMID: 22491336 MH - *AIDS-Related Opportunistic Infections MH - Acquired Immunodeficiency Syndrome/*drug therapy MH - Adult MH - Anti-HIV Agents/administration & dosage/*adverse effects/*therapeutic use MH - CD4 Lymphocyte Count MH - CD8-Positive T-Lymphocytes MH - Cohort Studies MH - Drug Therapy, Combination MH - Female MH - Humans MH - Immune Reconstitution Inflammatory Syndrome/*chemically induced MH - Male MH - Middle Aged MH - Odds Ratio MH - Retrospective Studies PMC - PMC3258272 EDAT- 2011/11/19 06:00 MHDA- 2012/05/10 06:00 PMCR- 2013/02/01 CRDT- 2011/11/19 06:00 PHST- 2011/11/19 06:00 [entrez] PHST- 2011/11/19 06:00 [pubmed] PHST- 2012/05/10 06:00 [medline] PHST- 2013/02/01 00:00 [pmc-release] AID - cir802 [pii] AID - 10.1093/cid/cir802 [doi] PST - ppublish SO - Clin Infect Dis. 2012 Feb 1;54(3):424-33. doi: 10.1093/cid/cir802. Epub 2011 Nov 17.