Department of Medicine, Division of Clinical Pharmacology, University of Cape Town, Cape Town, South Africa.
BMC Infect Dis. 2009 Dec 15;9:205. doi: 10.1186/1471-2334-9-205.
High rates of mortality and morbidity have been described in sub-Saharan African patients within the first few months of starting highly active antiretroviral therapy (HAART). There is limited data on the causes of early morbidity on HAART and the associated resource utilization.
A cross-sectional study was conducted of medical admissions at a secondary-level hospital in Cape Town, South Africa. Patients on HAART were identified from a register and HIV-infected patients not on HAART were matched by gender, month of admission, and age group to correspond with the first admission of each case. Primary reasons for admission were determined by chart review. Direct health care costs were determined from the provider's perspective.
There were 53 in the HAART group with 70 admissions and 53 in the no-HAART group with 60 admissions. The median duration of HAART was 1 month (interquartile range 1-3 months). Median baseline CD4 count in the HAART group was 57 x 106 cells/L (IQR 15-115). The primary reasons for admission in the HAART group were more likely to be due to adverse drug reactions and less likely to be due to AIDS events than the no-HAART group (34% versus 7%; p < 0.001 and 39% versus 63%; p = 0.005 respectively). Immune reconstitution inflammatory syndrome was the primary reason for admission in 10% of the HAART group. Lengths of hospital stay per admission and inpatient survival were not significantly different between the two groups. Five of the 15 deaths in the HAART group were due to IRIS or adverse drug reactions. Median costs per admission of diagnostic and therapeutic services (laboratory investigations, radiology, intravenous fluids and blood, and non-ART medications) were higher in the HAART group compared with the no-HAART group (US$190 versus US$111; p = 0.001), but the more expensive non-curative costs (overhead, capital, and clinical staff) were not significantly different (US$1199 versus US$1128; p = 0.525).
Causes of early morbidity are different and more complex in HIV-infected patients on HAART. This results in greater resource utilization of diagnostic and therapeutic services.
在撒哈拉以南非洲地区,开始高效抗逆转录病毒治疗(HAART)后的最初几个月,死亡率和发病率均较高。有关 HAART 早期发病原因以及相关资源利用的资料有限。
对南非开普敦一家二级医院的住院患者进行了一项横断面研究。从登记处中确定正在接受 HAART 的患者,并通过性别、入院月份和年龄组与每位病例的首次入院进行匹配,以确定未接受 HAART 的 HIV 感染者。通过病历回顾确定主要入院原因。从提供者的角度确定直接医疗费用。
HAART 组有 53 例,共 70 例入院,未接受 HAART 组有 53 例,共 60 例入院。HAART 的中位疗程为 1 个月(四分位距 1-3 个月)。HAART 组的中位基线 CD4 计数为 57×106 个细胞/L(IQR 15-115)。HAART 组的主要入院原因更可能是药物不良反应,而不太可能是艾滋病事件,与未接受 HAART 组相比(34%对 7%;p<0.001 和 39%对 63%;p=0.005)。免疫重建炎症综合征是 HAART 组 10%的主要入院原因。两组之间每次住院的住院时间和住院生存率无显著差异。HAART 组的 15 例死亡中有 5 例归因于 IRIS 或药物不良反应。每次住院的诊断和治疗服务(实验室检查、放射学、静脉补液和血液、非抗逆转录病毒药物)费用中位数在 HAART 组中高于未接受 HAART 组(190 美元对 111 美元;p=0.001),但更昂贵的非治愈性费用(间接费用、资本和临床人员)并无显著差异(1199 美元对 1128 美元;p=0.525)。
HAART 治疗的 HIV 感染者的早期发病原因不同且更为复杂,这导致对诊断和治疗服务的资源利用增加。