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3岁以下感染艾滋病毒的非洲儿童一线抗逆转录病毒疗法的成本效益

Cost-effectiveness of first-line antiretroviral therapy for HIV-infected African children less than 3 years of age.

作者信息

Ciaranello Andrea L, Doherty Kathleen, Penazzato Martina, Lindsey Jane C, Harrison Linda, Kelly Kathleen, Walensky Rochelle P, Essajee Shaffiq, Losina Elena, Muhe Lulu, Wools-Kaloustian Kara, Ayaya Samuel, Weinstein Milton C, Palumbo Paul, Freedberg Kenneth A

机构信息

aDivision of Infectious Diseases bDivision of General Medicine cMedical Practice Evaluation Center, Department of Medicine, Massachusetts General Hospital, Boston, Massachusetts, USA dThe Medical Research Council Clinical Trials Unit, London, UK eWorld Health Organization, Geneva, Switzerland fCenter for Biostatistics in AIDS Research gDepartment of Health Policy and Management, Harvard School of Public Health hDivision of Infectious Diseases, Department of Medicine iDepartment of Orthopedic Surgery, Brigham and Women's Hospital, Boston jCenter for AIDS Research, Harvard University, Cambridge, Massachusetts kClinton Health Access Initiative, New York lDepartments of Biostatistics and Epidemiology, Boston University School of Public Health, Boston, Massachusetts mDivision of Infectious Diseases, Department of Medicine, Indiana University School of Medicine, Indianapolis, Indiana, USA nDepartment of Child Health and Pediatrics, Moi University, Eldoret, Kenya oDepartment of Medicine and Department of Pediatrics16, Dartmouth-Hitchcock Medical Center, Lebanon, New Hampshire, USA.

出版信息

AIDS. 2015 Jun 19;29(10):1247-59. doi: 10.1097/QAD.0000000000000672.

Abstract

BACKGROUND

The International Maternal, Pediatric, and Adolescent Clinical Trials P1060 trial demonstrated superior outcomes for HIV-infected children less than 3 years old initiating antiretroviral therapy (ART) with lopinavir/ritonavir compared to nevirapine, but lopinavir/ritonavir is four-fold costlier.

DESIGN/METHODS: We used the Cost-Effectiveness of Preventing AIDS Complications (CEPAC)-Pediatric model, with published and P1060 data, to project outcomes under three strategies: no ART; first-line nevirapine (with second-line lopinavir/ritonavir); and first-line lopinavir/ritonavir (second-line nevirapine). The base-case examined South African children initiating ART at age 12 months; sensitivity analyses varied all key model parameters. Outcomes included life expectancy, lifetime costs, and incremental cost-effectiveness ratios [ICERs; dollars/year of life saved ($/YLS)]. We considered interventions with ICERs less than 1× per-capita gross domestic product (South Africa: $7500)/YLS as 'very cost-effective,' interventions with ICERs below 3× gross domestic product/YLS as 'cost-effective,' and interventions leading to longer life expectancy and lower lifetime costs as 'cost-saving'.

RESULTS

Projected life expectancy was 2.8 years with no ART. Both ART regimens markedly improved life expectancy and were very cost-effective, compared to no ART. First-line lopinavir/ritonavir led to longer life expectancy (28.8 years) and lower lifetime costs ($41 350/person, from lower second-line costs) than first-line nevirapine (27.6 years, $44 030). First-line lopinavir/ritonavir remained cost-saving or very cost-effective compared to first-line nevirapine unless: liquid lopinavir/ritonavir led to two-fold higher virologic failure rates or 15-fold greater costs than in the base-case, or second-line ART following first-line lopinavir/ritonavir was very ineffective.

CONCLUSIONS

On the basis of P1060 data, first-line lopinavir/ritonavir leads to longer life expectancy and is cost-saving or very cost-effective compared to first-line nevirapine. This supports WHO guidelines, but increasing access to pediatric ART is critical regardless of the regimen used.

摘要

背景

国际孕产妇、儿科和青少年临床试验P1060试验表明,与奈韦拉平相比,3岁以下开始使用洛匹那韦/利托那韦进行抗逆转录病毒治疗(ART)的HIV感染儿童的治疗效果更佳,但洛匹那韦/利托那韦的成本是奈韦拉平的四倍。

设计/方法:我们使用预防艾滋病并发症成本效益(CEPAC)-儿科模型以及已发表的数据和P1060试验数据,预测三种策略下的结果:不进行抗逆转录病毒治疗;一线使用奈韦拉平(二线使用洛匹那韦/利托那韦);一线使用洛匹那韦/利托那韦(二线使用奈韦拉平)。基础病例研究的是12个月大开始接受抗逆转录病毒治疗的南非儿童;敏感性分析对所有关键模型参数进行了变动。结果包括预期寿命、终身成本和增量成本效益比[ICERs;挽救生命年数的美元数($/YLS)]。我们将ICERs低于人均国内生产总值1倍(南非:7500美元)/YLS的干预措施视为“非常具有成本效益”,ICERs低于国内生产总值3倍/YLS的干预措施视为“具有成本效益”,导致更长预期寿命和更低终身成本的干预措施视为“节省成本”。

结果

不进行抗逆转录病毒治疗时预测的预期寿命为2.8年。与不进行抗逆转录病毒治疗相比,两种抗逆转录病毒治疗方案均显著提高了预期寿命且非常具有成本效益。一线使用洛匹那韦/利托那韦导致的预期寿命(28.8年)比一线使用奈韦拉平(27.6年)更长,终身成本更低(每人41350美元,因为二线成本更低)。与一线使用奈韦拉平相比,一线使用洛匹那韦/利托那韦仍然具有节省成本或非常具有成本效益的优势,除非:液体洛匹那韦/利托那韦导致的病毒学失败率比基础病例高两倍或成本比基础病例高15倍,或者一线使用洛匹那韦/利托那韦后的二线抗逆转录病毒治疗效果非常差。

结论

基于P1060试验数据,一线使用洛匹那韦/利托那韦可带来更长的预期寿命,与一线使用奈韦拉平相比具有节省成本或非常具有成本效益的优势。这支持了世界卫生组织的指南,但无论使用何种治疗方案,增加儿科抗逆转录病毒治疗的可及性都至关重要。

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