Short- and Long-term Risks of Highly Active Antiretroviral Treatment with Incident Opportunistic Infections among People Living with HIV/AIDS

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作者
Yung-Feng Yen
Marcelo Chen
I.-An Jen
Pei-Hung Chuang
Chun-Yuan Lee
Su-I. Lin
Yi-Ming Arthur Chen
机构
[1] Taipei City Hospital,Section of Infectious Diseases
[2] Kaohsiung Medical University,Center for Infectious Disease and Cancer Research
[3] National Yang-Ming University,Department and Institute of Public Health
[4] National Taipei University of Nursing and Health Sciences,Department of Health Care Management
[5] Mackay Memorial Hospital,Department of Urology
[6] Mackay Junior College of Medicine,Department of Cosmetic Applications and Management
[7] Nursing and Management,Division of Infectious Diseases, Department of Internal Medicine
[8] Taipei Association of Health and Welfare Data Science,Clinical Pharmacogenomics and Pharmacoproteomics Program, School of Pharmacy
[9] Kaohsiung Medical University Hospital,undefined
[10] Kaohsiung Medical University,undefined
[11] National Mosquito-Borne Diseases Control Research Center,undefined
[12] National Health Research Institutes,undefined
[13] Taipei Medical University,undefined
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Highly active antiretroviral therapy (HAART) causes a rapid increase of CD4 + T cells counts during the first 3–6 months of treatment and may enhance the development of opportunistic infections (OIs). However, the short- and long-term effects of HAART exposure on the development of incident OIs has not been extensively studied. This nationwide longitudinal study followed up a total of 26,258 people living with HIV/AIDS (PLWHA) to ascertain the short- and long-term effects of HAART on incident OIs. During 150,196 person-years of follow-up, 6,413 (24.4%) PLWHA had new onset of OIs. After adjusting for demographics, comorbidities, and AIDS status, PLWHA who received HAART were more likely to develop OIs than those who did not receive HAART. Considering the short- and long-term effects of HAART on the development of OIs, HAART was found to be a risk factor for developing OIs during the first 90 days of treatment, but a protective factor against OIs after 180 days of HAART use. The risk for the development of active OIs significantly decreased as the duration of HAART increased (P < 0.001). Our study suggests that HAART is a risk factor for developing OIs in the short term, but is a protective factor in the long term.
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