1999
DOI: 10.1001/jama.282.23.2220
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AIDS-Related Opportunistic Illnesses Occurring After Initiation of Potent Antiretroviral Therapy

Abstract: Our data indicate that the risk of developing an OI for a person receiving potent antiretroviral therapy is highest during the initial months of therapy. Baseline CD4 cell count and immunologic and virologic response to treatment were strong predictors of disease progression in patients receiving potent therapy. Individuals with CD4 cell counts of 50 x 10(6)/L or below may need close clinical surveillance after initiation of potent therapy.

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Cited by 438 publications
(297 citation statements)
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“…Advanced naïve patients should receive an intensive follow-up program, especially during the initial treatment phase (B-II) because the risk of opportunistic infections during the first 12 months is reduced, but not eliminated by cART [24][25][26][27].…”
Section: Opportunistic Diseases and Concomitant Conditionsmentioning
confidence: 99%
“…Advanced naïve patients should receive an intensive follow-up program, especially during the initial treatment phase (B-II) because the risk of opportunistic infections during the first 12 months is reduced, but not eliminated by cART [24][25][26][27].…”
Section: Opportunistic Diseases and Concomitant Conditionsmentioning
confidence: 99%
“…Based on recent sentinel surveillance data, the national adult prevalence rate is estimated at 6.6% (1). The introduction of highly active antiretroviral therapy (HAART) in 1997 has markedly improved the length of survival and the morbidity of HIV-infected patients through the improvement of the immunodeficiency caused by HIV infection (2)(3)(4)(5)(6)(7)(8)(9)(10). In recent years, the management of human immunodeficiency virus positive individuals has been based on HAART comprising a combination of nucleoside analogue reverse transcriptase inhibitors and at least one protease inhibitor and/or one non-nucleoside analogue reverse transcriptase inhibitor (11).…”
mentioning
confidence: 99%
“…Also, HIV-infected patients initiating both therapies are more prone to develop transient chest radiographic worsening than HIV-uninfected and HIV-infected patients not on AR therapy 4 . Enhancing host immunity following initiation of AR therapy or its intensification with a protease inhibitor has also been implicated in the emergence of cytomegalovirus retinitis 6 , Mycobacterium avium complex lymphadenitis 14 , development of zoster rash 9 , rapid worsening of Kaposi's sarcoma lesions 7 and development of multiple cerebral lesions compatible with progressive multifocal leukoencephalopathy in AIDS patients 7 .…”
Section: Discussionmentioning
confidence: 99%