Provision of HIV treatment in HIV preventive vaccine trials: a developing country perspective

被引:36
作者
Slack, C
Stobie, M
Milford, C
Lindegger, G
Wassenaar, D
Strode, A
IJsselmuiden, C
机构
[1] Univ KwaZulu Natal, Sch Psychol, HAVEG, ZA-3209 Scottsville, Pietermaritzbur, South Africa
[2] Univ KwaZulu Natal, Sch Human & Social Studies, Unilever Eth Ctr, ZA-3209 Scottsville, Pietermaritzbur, South Africa
[3] Univ KwaZulu Natal, Sch Law, ZA-3209 Scottsville, Pietermaritzbur, South Africa
[4] Univ Pretoria, Fac Med, Sch Hlth Syst & Publ Hlth, ZA-0001 Pretoria, South Africa
[5] Council Hlth Res Dev, COHRED, CH-1201 Geneva, Switzerland
关键词
HIV vaccines; consent; justice; research ethics; standard of care; South Africa;
D O I
10.1016/j.socscimed.2004.06.049
中图分类号
R1 [预防医学、卫生学];
学科分类号
1004 ; 120402 ;
摘要
HIV treatment for participants who become infected during HIV vaccine trials has been the focus of ethical controversy. The obligations of sponsors to ensure that participants have access to antiretrovirals have been a particular focus of this debate. This paper presents three arguments that have been made in this regard, and some of their limitations, in anticipation of HIV vaccine trials in South Africa. The first argument is that HIV risk behaviour increases in such trials, and HIV infection can be viewed as a research-related injury, justifying sponsor provision of treatment on grounds of compensation for harm. We conclude that risk-behaviour studies to date do not show general increases in risk behaviour that could constitute the basis for a general obligation. Participation may well adversely impact on risk behaviour for some individuals, and conceivably this could be demonstrated. This argument may, therefore, have merit at the individual level; however, it seems a weak platform from which to argue that sponsors should treat all HIV infections acquired during trials. The second argument is that treatment should be provided based on distributive justice. We conclude that traditional concepts of "distributive justice" in research appear limited in justifying obligations of sponsors to ensure access to antiretrovirals. Further, using research initiatives to reduce global health care inequities is controversial, and even proponents may disagree about the fairest use of finite resources. The third argument is that sponsors should ensure antiretroviral access on grounds of beneficence; namely, the maxim that if one can do something beneficial without sacrificing anything of comparable significance, it ought to be done. Thus, sponsors should provide more interventions than those minimally required to conduct the research. However, beneficence may demand levels of altruism that exceeds what is reasonable. While the latter arguments may provide stronger justifications than the first, it is difficult to use these arguments to establish that sponsor provision of antiretrovirals to infected individuals is obligatory. (C) 2004 Elsevier Ltd. All rights reserved.
引用
收藏
页码:1197 / 1208
页数:12
相关论文
共 50 条
  • [21] Ethics, human rights and HIV vaccine trials in low-income settings
    London, Leslie
    Kagee, Ashraf
    Moodley, Keymanthri
    Swartz, Leslie
    JOURNAL OF MEDICAL ETHICS, 2012, 38 (05) : 286 - 293
  • [22] Caveats and pitfalls associated with researching community engagement in the context of HIV vaccine trials
    Kagee, Ashraf
    De Wet, Anneliese
    Kafaar, Zuhayr
    Lesch, Anthea
    Swartz, Leslie
    Newman, Peter A.
    JOURNAL OF HEALTH PSYCHOLOGY, 2020, 25 (01) : 82 - 91
  • [23] Gender aspects on HIV prevention efforts and participation in HIV vaccine trials among Police officers in Dar es Salaam, Tanzania
    Tarimo, Edith A. M.
    Kakoko, Deodatus C. V.
    Kohi, Thecla W.
    Bakari, Muhammad
    Sandstrom, Eric
    Siyame, David
    Mhalu, Fred
    Kulane, Asli
    BMC PUBLIC HEALTH, 2018, 18
  • [24] “If It’s Not Working, Why Would They Be Testing It?”: mental models of HIV vaccine trials and preventive misconception among men who have sex with men in India
    Venkatesan Chakrapani
    Peter A Newman
    Neeti Singhal
    Ruban Nelson
    Murali Shunmugam
    BMC Public Health, 13
  • [25] I'm Positive, But I'm Negative: Competing Voices in Informed Consent and Implications for HIV Vaccine Trials
    Rautenbach, Clinton
    Lindegger, Graham
    Slack, Catherine
    Wallace, Melissa
    Newman, Peter
    JOURNAL OF EMPIRICAL RESEARCH ON HUMAN RESEARCH ETHICS, 2015, 10 (02) : 151 - 156
  • [26] "If It's Not Working, Why Would They Be Testing It?": mental models of HIV vaccine trials and preventive misconception among men who have sex with men in India
    Chakrapani, Venkatesan
    Newman, Peter A.
    Singhal, Neeti
    Nelson, Ruban
    Shunmugam, Murali
    BMC PUBLIC HEALTH, 2013, 13
  • [27] Randomized, controlled evaluation of a prototype informed consent process for HIV vaccine efficacy trials
    Coletti, AS
    Heagerty, P
    Sheon, AR
    Gross, M
    Koblin, BA
    Metzger, DS
    Seage, GR
    JAIDS-JOURNAL OF ACQUIRED IMMUNE DEFICIENCY SYNDROMES, 2003, 32 (02) : 161 - 169
  • [28] HIV VACCINE TRIALS - SOME DESIGN ISSUES INCLUDING SAMPLE-SIZE CALCULATION
    DIXON, DO
    RIDA, WN
    FAST, PE
    HOTH, DF
    JOURNAL OF ACQUIRED IMMUNE DEFICIENCY SYNDROMES AND HUMAN RETROVIROLOGY, 1993, 6 (05): : 485 - 496
  • [29] Ethical considerations in international HIV vaccine trials: summary of a consultative process conducted by the Joint United Nations Programme on HIV/AIDS (UNAIDS)
    Guenter, D
    Esparza, J
    Macklin, R
    JOURNAL OF MEDICAL ETHICS, 2000, 26 (01) : 37 - 43
  • [30] Primary and secondary tuberculosis preventive treatment in HIV clinics: simulating alternative strategies
    Basu, S.
    Maru, D.
    Poolman, E.
    Galvani, A.
    INTERNATIONAL JOURNAL OF TUBERCULOSIS AND LUNG DISEASE, 2009, 13 (05) : 652 - 658