Late-onset opportunistic infections while receiving anti-retroviral therapy in Latin America: burden and risk factors. (September 2022)
- Record Type:
- Journal Article
- Title:
- Late-onset opportunistic infections while receiving anti-retroviral therapy in Latin America: burden and risk factors. (September 2022)
- Main Title:
- Late-onset opportunistic infections while receiving anti-retroviral therapy in Latin America: burden and risk factors
- Authors:
- Núñez, Isaac
Crabtree-Ramirez, Brenda
Shepherd, Bryan E.
Sterling, Timothy R.
Cahn, Pedro
Veloso, Valdiléa G.
Cortes, Claudia P
Padgett, Denis
Gotuzzo, Eduardo
Sierra-Madero, Juan
McGowan, Catherine C.
Person, Anna K.
Caro-Vega, Yanink - Abstract:
- Highlights: Late opportunistic infections in HIV have not been properly characterized. Around 8% of more than 10, 000 patients had late-onset opportunistic infections. Most common infections were tuberculosis, esophageal candidiasis, and Pneumocystis jirovecii ( P. jirovecii ). Higher CD4 cell count and undetectable viral load were associated with lower risk. Treatment switch and prior history of AIDS were associated with higher risk. Abstract: Objectives: The aim of this study was to describe the incidence, clinical characteristics, and risk factors of late-onset opportunistic infections (LOI) in people who live with HIV (PWLHA) within the Caribbean, Central and South America network for HIV epidemiology. Methods: We performed a retrospective cohort study including treatment-naive PWLHA enrolled at seven sites (Argentina, Brazil, Chile, Peru, Mexico, and two sites in Honduras). Follow-up began at 6 months after treatment started. Outcomes were LOI, loss to follow-up, and death. We used a Cox proportional hazards model and a competing risks model to evaluate risk factors. Results: A total of 10, 583 patients were included. Median follow up was at 5.4 years. LOI occurred in 895 (8.4%) patients. Median time to opportunistic infection was 2.1 years. The most common infections were tuberculosis (39%), esophageal candidiasis (10%), and Pneumocystis jirovecii ( P. jirovecii ) pneumonia (10%). Death occurred in 576 (5.4%) patients, and 3021 (28.5%) patients were lost to follow-up.Highlights: Late opportunistic infections in HIV have not been properly characterized. Around 8% of more than 10, 000 patients had late-onset opportunistic infections. Most common infections were tuberculosis, esophageal candidiasis, and Pneumocystis jirovecii ( P. jirovecii ). Higher CD4 cell count and undetectable viral load were associated with lower risk. Treatment switch and prior history of AIDS were associated with higher risk. Abstract: Objectives: The aim of this study was to describe the incidence, clinical characteristics, and risk factors of late-onset opportunistic infections (LOI) in people who live with HIV (PWLHA) within the Caribbean, Central and South America network for HIV epidemiology. Methods: We performed a retrospective cohort study including treatment-naive PWLHA enrolled at seven sites (Argentina, Brazil, Chile, Peru, Mexico, and two sites in Honduras). Follow-up began at 6 months after treatment started. Outcomes were LOI, loss to follow-up, and death. We used a Cox proportional hazards model and a competing risks model to evaluate risk factors. Results: A total of 10, 583 patients were included. Median follow up was at 5.4 years. LOI occurred in 895 (8.4%) patients. Median time to opportunistic infection was 2.1 years. The most common infections were tuberculosis (39%), esophageal candidiasis (10%), and Pneumocystis jirovecii ( P. jirovecii ) pneumonia (10%). Death occurred in 576 (5.4%) patients, and 3021 (28.5%) patients were lost to follow-up. A protease inhibitor–based regimen (hazard ratio 1.25), AIDS-defining events during the first 6 months of antiretroviral-treatment (hazard ratio 2.12), starting antiretroviral-treatment in earlier years (hazard ratio 1.52 for 2005 vs 2010), and treatment switch (hazard ratio 1.31) were associated with a higher risk of LOI. Conclusion: LOI occurred in nearly one in 10 patients. People with risk factors could benefit from closer follow-up. … (more)
- Is Part Of:
- International journal of infectious diseases. Volume 122(2022)
- Journal:
- International journal of infectious diseases
- Issue:
- Volume 122(2022)
- Issue Display:
- Volume 122, Issue 2022 (2022)
- Year:
- 2022
- Volume:
- 122
- Issue:
- 2022
- Issue Sort Value:
- 2022-0122-2022-0000
- Page Start:
- 469
- Page End:
- 475
- Publication Date:
- 2022-09
- Subjects:
- Opportunistic infections -- HIV -- AIDS -- Latin America -- Tuberculosis -- Cohort studies
Communicable diseases -- Periodicals
Communicable Diseases -- Periodicals
Communicable diseases
Periodicals
Electronic journals
616.9 - Journal URLs:
- http://bibpurl.oclc.org/web/73769 ↗
http://www.journals.elsevier.com/international-journal-of-infectious-diseases/ ↗
http://www.sciencedirect.com/science/journal/12019712 ↗
http://www.clinicalkey.com/dura/browse/journalIssue/12019712 ↗
http://www.clinicalkey.com.au/dura/browse/journalIssue/12019712 ↗
http://www.elsevier.com/journals ↗ - DOI:
- 10.1016/j.ijid.2022.06.041 ↗
- Languages:
- English
- ISSNs:
- 1201-9712
- Deposit Type:
- Legaldeposit
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- Available online (eLD content is only available in our Reading Rooms) ↗
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- British Library DSC - 4542.304750
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