Risk factors for early mortality on antiretroviral therapy in advanced HIV-infected adults

被引:2
|
作者
Bisson, Gregory P. [1 ]
Ramchandani, Ritesh [2 ]
Miyahara, Sachiko [2 ]
Mngqibisa, Rosie [3 ]
Matoga, Mitch [4 ]
Ngongondo, McNeil [4 ]
Samaneka, Wadzanai [5 ]
Koech, Lucy [6 ]
Naidoo, Kogieleum [7 ]
Rassool, Mohammed [8 ]
Kirui, Fredrick [6 ]
Banda, Peter [9 ,10 ]
Mave, Vidya [11 ]
Kadam, Dileep [11 ]
Leger, Paul [12 ]
Henestroza, German [13 ]
Manabe, Yukari C. [14 ]
Bao, Jing [15 ]
Kumwenda, Johnstone [9 ]
Gupta, Amita [14 ]
Hosseinipour, Mina C. [4 ,16 ]
机构
[1] Univ Penn, Perelman Sch Med, 832 Blockley Hall,423 Guardian Dr, Philadelphia, PA 19104 USA
[2] Harvard TH Chan Sch Publ Hlth, Boston, MA USA
[3] Enhancing Care Fdn, Durban Int CRS, Durban, South Africa
[4] UNC Project, Lilongwe, Malawi
[5] Univ Zimbabwe, Harare, Zimbabwe
[6] Kenya Med Res Inst KEMRI, Kericho, Kenya
[7] Univ Witwatersrand, South African MRC, CAPRISA HIV, TB Pathogenesis & Treatment Res Unit, Johannesburg, South Africa
[8] Univ Witwatersrand, Clin HIV Res Unit, Dept Med, Johannesburg, South Africa
[9] Johns Hopkins Project, Blantyre, Malawi
[10] Univ Malawi, Coll Med, Blantyre, Malawi
[11] BJ Med Coll, Johns Hopkins Clin Trials Unit, Pune, Maharashtra, India
[12] GHESKIO, Port Au Prince, Haiti
[13] Ctr Infect Dis Res, Lusaka, Zambia
[14] Johns Hopkins Univ, Sch Med, Baltimore, MD USA
[15] NIAID, HJF DAIDS, Div Henry M Jackson Fdn, Bethesda, MD 20892 USA
[16] Univ N Carolina, Sch Med, Chapel Hill, NC USA
基金
美国国家卫生研究院;
关键词
antiretroviral therapy; early mortality; HIV-1; Infection; isoniazid prophylaxis; opportunistic infections; tuberculosis; HIV-1-INFECTED PATIENTS; CD4; COUNT; RECONSTITUTION; FAILURE; RALTEGRAVIR; ACTIVATION; INITIATION; IMPACT; HAART; DEATH;
D O I
10.1097/QAD.0000000000001606
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Background: Many HIV-infected individuals present with advanced HIV disease. These patients are at high risk of death after antiretroviral therapy (ART) initiation, but risk factors for death in these patients are unclear. Methods: We used data from a multisite randomized trial comparing empiric vs. preventive tuberculosis therapy in HIV-infected adults initiating ART with CD4(+) T-cell counts less than 50 cells/mu l to evaluate risk factors for death within 48 weeks after ART initiation. Cox proportional hazards models were fit to evaluate characteristics present at baseline and at 4 weeks after ART initiation, including the week 4 CD4(+) T-cell response and new opportunistic infections. Results: Of 850 enrolled, the median pre-ART CD4(+) T-cell count was 18 cells/mu l and 67 (7.9%) died. Baseline risk factors for death included lymphadenopathy, lower CD4(+) T-cell count, lower serum albumin, high white blood cell count, elevated neutrophil percentage, and lower hemoglobin. Among 746 participants with data at week 4, the median changes in CD4(+) T-cell count and viral load for those who died (n = 43) vs. survived were 26 vs. 56 cells/ml and - 2.7 vs. - 2.7 log10 copies/mu l, respectively. Each 20 cell/mu l lower change in week 4 CD4(+) T-cell count was associated with a 20% increased risk of post week-4 mortality (adjusted hazard ratio 1.20, 1.01-1.42, P = .038). Conclusion: Evidence of active infection and suboptimal immunologic response during the first month of ART are associated with death in the first year after ART initiation in those with advanced HIV disease taking tuberculosis preventive therapy. Strategies to reduce early mortality in this population warrant further investigation. Copyright (C) 2017 Wolters Kluwer Health, Inc. All rights reserved.
引用
收藏
页码:2217 / 2225
页数:9
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