Center for Global Health and Development, Boston University, MA, USA.
J Int AIDS Soc. 2010 Mar 6;13:8. doi: 10.1186/1758-2652-13-8.
While the number of HIV-positive patients on antiretroviral therapy (ART) in resource-limited settings has increased dramatically, some patients eligible for treatment do not initiate ART even when it is available to them. Understanding why patients opt out of care, or are unable to opt in, is important to achieving the goal of universal access.
We conducted a cross-sectional survey among 400 patients on ART (those who were able to access care) and 400 patients accessing home-based care (HBC), but who had not initiated ART (either they were not able to, or chose not to, access care) in two rural and two urban sites in Zambia to identify barriers to and facilitators of ART uptake.
HBC patients were 50% more likely to report that it would be very difficult to get to the ART clinic than those on ART (RR: 1.48; 95% CI: 1.21-1.82). Stigma was common in all areas, with 54% of HBC patients, but only 15% of ART patients, being afraid to go to the clinic (RR: 3.61; 95% CI: 3.12-4.18). Cost barriers differed by location: urban HBC patients were three times more likely to report needing to pay to travel to the clinic than those on ART (RR: 2.84; 95% CI: 2.02-3.98) and 10 times more likely to believe they would need to pay a fee at the clinic (RR: 9.50; 95% CI: 2.24-40.3). In rural areas, HBC subjects were more likely to report needing to pay non-transport costs to attend the clinic than those on ART (RR: 4.52; 95% CI: 1.91-10.7). HBC patients were twice as likely as ART patients to report not having enough food to take ART being a concern (27% vs. 13%, RR: 2.03; 95% CI: 1.71-2.41), regardless of location and gender.
Patients in home-based care for HIV/AIDS who never initiated ART perceived greater financial and logistical barriers to seeking HIV care and had more negative perceptions about the benefits of the treatment. Future efforts to expand access to antiretroviral care should consider ways to reduce these barriers in order to encourage more of those medically eligible for antiretrovirals to initiate care.
在资源有限的环境中,接受抗逆转录病毒疗法(ART)的艾滋病毒阳性患者数量显著增加,但仍有一些符合治疗条件的患者即使能够获得治疗也不开始接受治疗。了解患者为何选择不接受治疗或无法选择接受治疗,对于实现普及治疗目标至关重要。
我们在赞比亚两个农村和两个城市地区的 400 名接受抗逆转录病毒治疗的患者(能够获得治疗的患者)和 400 名接受家庭护理(HBC)但尚未开始接受治疗的患者(由于各种原因无法或选择不接受治疗)中进行了横断面调查,以确定接受抗逆转录病毒治疗的障碍和促进因素。
HBC 患者报告前往 ART 诊所非常困难的可能性比接受 ART 治疗的患者高 50%(RR:1.48;95%CI:1.21-1.82)。所有地区都普遍存在耻辱感,54%的 HBC 患者害怕去诊所,而只有 15%的接受 ART 治疗的患者害怕去诊所(RR:3.61;95%CI:3.12-4.18)。费用障碍因地点而异:城市 HBC 患者前往诊所的交通费用是接受 ART 治疗的患者的三倍(RR:2.84;95%CI:2.02-3.98),十倍以上的人认为他们需要在诊所支付费用(RR:9.50;95%CI:2.24-40.3)。在农村地区,HBC 患者比接受 ART 治疗的患者更有可能报告需要支付非交通费用才能去诊所(RR:4.52;95%CI:1.91-10.7)。HBC 患者比接受 ART 治疗的患者报告称,他们没有足够的食物来服用抗逆转录病毒药物的顾虑要大两倍(27%比 13%,RR:2.03;95%CI:1.71-2.41),无论地点和性别如何。
从未开始接受抗逆转录病毒治疗的艾滋病毒感染者的家庭护理患者认为寻求艾滋病毒护理存在更大的财务和后勤障碍,并且对治疗的益处有更负面的看法。未来扩大抗逆转录病毒治疗的努力应考虑减少这些障碍的方法,以鼓励更多符合抗逆转录病毒治疗条件的人开始接受治疗。