Risk of non-AIDS-related mortality may exceed risk of AIDS-related mortality among individuals enrolling into care with CD4+ counts greater than 200 cells/mm3

被引:92
作者
Lau, Bryan
Gange, Stephen J.
Moore, Richard D.
机构
[1] Johns Hopkins Univ, Sch Med, Dept Med, Baltimore, MD 21287 USA
[2] Johns Hopkins Bloomberg Sch Publ Hlth, Dept Epidemiol, Baltimore, MD USA
关键词
cohort; competing risks; epidemiologic methods; HIV; mortality;
D O I
10.1097/01.qai.0000247229.68246.c5
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Objective: To quantify cause-specific mortality risk attributable to non-AIDS-related and AIDS-related causes before and after the advent of highly active antiretroviral therapy (HAART). Methods: Competing-risk methods were used to determine the cumulative AIDS-related and non-AID S-related risk of mortality between 1990 and the end of 2003 in the Johns Hopkins HIV Clinical Cohort, a prospective cohort study. Results: Beginning in 1997 with the introduction of HAART, all-cause mortality declined and has remained stable at approximately 39 deaths per 1000 person-years. AIDS-related mortality continued to decline in this period (P = 0.008), whereas non-AIDS-related mortality increased (P < 0.001). Using competing-risk methods, the risk of dying attributable to AIDS-related causes remains significantly higher than the risk of dying attributable to non-AIDS-related causes for patients with a CD4(+) count : 200 cells/mm(3) in the HAART era. For those with a CD4(+) count > 200 cells/mm(3), however, non-AIDS-related mortality was greater than AIDS-related mortality, particularly among injection drug users. Other transmission categories had similar AIDS-related and non-AIDS-related cumulative mortalities. Conclusions: HAART has reduced mortality rates among HIV-infected individuals. but further efforts to reduce mortality in this population require increased attention to conditions that have not traditionally been considered to be HIV related.
引用
收藏
页码:179 / 187
页数:9
相关论文
共 28 条
[11]   ON THE USE OF CAUSE-SPECIFIC FAILURE AND CONDITIONAL FAILURE PROBABILITIES - EXAMPLES FROM CLINICAL ONCOLOGY DATA [J].
GAYNOR, JJ ;
FEUER, EJ ;
TAN, CC ;
WU, DH ;
LITTLE, CR ;
STRAUS, DJ ;
CLARKSON, BD ;
BRENNAN, MF .
JOURNAL OF THE AMERICAN STATISTICAL ASSOCIATION, 1993, 88 (422) :400-409
[12]   All cause mortality in the Swiss HIV cohort study from 1990 to 2001 in comparison with the Swiss population [J].
Keiser, O ;
Taffé, P ;
Zwahlen, M ;
Battegay, M ;
Bernasconi, E ;
Weber, R ;
Rickenbach, M .
AIDS, 2004, 18 (13) :1835-1843
[13]  
Lewden C, 2005, INT J EPIDEMIOL, V34, P121, DOI 10.1093/ije/dyh307
[14]   APPLYING COX REGRESSION TO COMPETING RISKS [J].
LUNN, M ;
MCNEIL, N .
BIOMETRICS, 1995, 51 (02) :524-532
[15]   Effects of antiretroviral therapy and opportunistic illness primary chemoprophylaxis on survival after AIDS diagnosis [J].
McNaghten, AD ;
Hanson, DL ;
Jones, JL ;
Dworkin, MS ;
Ward, JW .
AIDS, 1999, 13 (13) :1687-1695
[16]  
Mocroft A, 1999, J ACQ IMMUN DEF SYND, V22, P369
[17]   Causes of death in HIV infection: the key determinant to define the clinical response to anti-HIV therapy [J].
Mocroft, A ;
Gatell, J ;
Reiss, P ;
Ledergerber, B ;
Kirk, O ;
Vella, S ;
Blaxhult, A ;
Phillips, AN ;
Lundgren, J .
AIDS, 2004, 18 (17) :2333-2337
[18]   Decline in the AIDS and death rates in the EuroSIDA study: an observational study [J].
Mocroft, A ;
Ledergerber, B ;
Katlama, C ;
Kirk, O ;
Reiss, P ;
Monforte, AD ;
Knsyz, B ;
Dietrich, M ;
Phillips, AN ;
Lundgren, JD .
LANCET, 2003, 362 (9377) :22-29
[19]   Changes in the cause of death among HIV positive subjects across Europe: results from the EuroSIDA study [J].
Mocroft, A ;
Brettle, R ;
Kirk, O ;
Blaxhult, A ;
Parkin, JM ;
Antunes, F ;
Francioli, P ;
Monforte, AD ;
Fox, Z ;
Lundgren, JD .
AIDS, 2002, 16 (12) :1663-1671
[20]   Understanding the clinical and economic outcomes of HIV therapy: The Johns Hopkins HIV clinical practice cohort [J].
Moore, RD .
JOURNAL OF ACQUIRED IMMUNE DEFICIENCY SYNDROMES AND HUMAN RETROVIROLOGY, 1998, 17 :S38-S41