PMID- 15958835 OWN - NLM STAT- MEDLINE DCOM- 20051219 LR - 20220330 IS - 0269-9370 (Print) IS - 0269-9370 (Linking) VI - 19 IP - 10 DP - 2005 Jul 1 TI - Incidence and risk factors of immune reconstitution inflammatory syndrome complicating HIV-associated cryptococcosis in France. PG - 1043-9 AB - BACKGROUND: Immune reconstitution inflammatory syndrome (IRIS) in association with cryptococcosis has been anecdotically reported following administration of highly active antiretroviral therapy (HAART). OBJECTIVE: To analyse the incidence and risk factors for IRIS-associated cryptococcosis among HIV-infected patients. DESIGN: Retrospective multicentre study between 1996 and 2000 through the French Cryptococcosis Database. METHODS: Subsequent occurrence of IRIS examined in 120 HIV-infected adult patients treated with HAART and experiencing a first episode of culture-confirmed cryptococcosis. RESULTS: Ten patients developed IRIS during the study period, giving an incidence of 10/239, or 4.2/100 person-years [95% confidence interval (CI), 2.2-7.8]. IRIS consisted of acute symptoms consistent with inflammation occurring within a median of 8 months (range, 2-37) after the diagnosis of cryptococcosis in the context of negative cultures and immunological and/or virological response to HAART. Radiology and histopathology detected features compatible with inflammation. Symptom severity required transfer into intensive care units for three patients and use of anti-inflammatory drugs for four. Three patients with evolutive IRIS died. Compared with patients without IRIS for whom complete clinical and microbiological information were available at baseline, previously unknown HIV infection [odds ratio (OR), 4.8; 95% CI, 1.0-21.7], CD4 cell count < 7 x 10 cells/l (OR, 4.0; 95% CI, 0.9-17.2), fungaemia (OR, 6.1; 95% CI, 1.1-35.2) and HAART initiation within 2 months of cryptococcosis diagnosis (OR, 5.50; 95% CI, 1.0-29.6) were independently associated with the risk of subsequent IRIS. CONCLUSIONS: IRIS-related cryptococcosis was observed more frequently in severely immunocompromised patients with disseminated infection and HAART initiation soon after the diagnosis. FAU - Lortholary, Olivier AU - Lortholary O AD - National Reference Centre for Mycoses and Antifungals, Molecular Mycology Unit bEmerging Diseases Epidemiology Unit, Institut Pasteur, Paris, France. olortho@pasteur.fr FAU - Fontanet, Arnaud AU - Fontanet A FAU - Memain, Nathalie AU - Memain N FAU - Martin, Antoine AU - Martin A FAU - Sitbon, Karine AU - Sitbon K FAU - Dromer, Francoise AU - Dromer F CN - French Cryptococcosis Study Group LA - eng PT - Journal Article PT - Multicenter Study PL - England TA - AIDS JT - AIDS (London, England) JID - 8710219 RN - 0 (Anti-Inflammatory Agents) SB - IM CIN - AIDS. 2005 Nov 18;19(17):2050-2. PMID: 16260920 MH - AIDS-Related Opportunistic Infections/*chemically induced MH - Adult MH - Anti-Inflammatory Agents/therapeutic use MH - Antiretroviral Therapy, Highly Active/*adverse effects MH - Critical Care MH - Cryptococcosis/*chemically induced/immunology MH - Female MH - HIV Infections/*drug therapy/immunology MH - Humans MH - Immune Tolerance/*drug effects MH - Incidence MH - Inflammation/*chemically induced MH - Male MH - Middle Aged MH - Retrospective Studies MH - Risk Factors MH - Syndrome EDAT- 2005/06/17 09:00 MHDA- 2005/12/20 09:00 CRDT- 2005/06/17 09:00 PHST- 2005/06/17 09:00 [pubmed] PHST- 2005/12/20 09:00 [medline] PHST- 2005/06/17 09:00 [entrez] AID - 00002030-200507010-00009 [pii] AID - 10.1097/01.aids.0000174450.70874.30 [doi] PST - ppublish SO - AIDS. 2005 Jul 1;19(10):1043-9. doi: 10.1097/01.aids.0000174450.70874.30.