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南非耐利福平结核病治疗期间管理药物不良反应的直接成本。

Direct costs of managing adverse drug reactions during rifampicin-resistant tuberculosis treatment in South Africa.

机构信息

Health Economics Unit, School of Family and Public Health, Faculty of Health Sciences, University of Cape Town, Cape Town.

Clinical HIV Research Unit, Department of Internal Medicine, Faculty of Health Sciences, University of the Witwatersrand, Johannesburg, South Africa.

出版信息

Int J Tuberc Lung Dis. 2018 Apr 1;22(4):393-398. doi: 10.5588/ijtld.17.0661.

Abstract

OBJECTIVE

To estimate the provider costs of managing adverse drug reactions (ADRs) to standard long-course treatment for multidrug- and rifampicin-resistant tuberculosis (MDR/RR-TB) according to South African guidelines.

METHODS

We parameterised a published Markov health state model for MDR/RR-TB with guidelines-based, bottom-up public-sector provider costing of ADR management. Frequency of ADR occurrence was extracted from the literature. Costs were estimated over 10 years, discounted 3% annually and tested using probabilistic sensitivity analysis.

RESULTS

On average, guidelines-based costing of moderate ADRs weighted by the frequency of occurrence was US$135.76 (standard deviation [SD] US$17.18) and the cost of serious ADRs was US$521.29 (SD US$55.99). We estimated that the incremental costs of ADR management were US$380.17 annually per patient initiating MDR/RR-TB treatment. The incremental costs of ADR management for the public health sector in South Africa was US$4.76 million, 8.3% of the estimated cohort costs of MDR/RR-TB treatment ($57.55 million) for the 2015 cohort of 12 527 patients.

CONCLUSIONS

Management of multiple ADRs and serious ADRs, which are common during the first 6 months of standard, long-course MDR/RR-TB treatment, substantially increases provider treatment costs. These results need to be taken into account when comparing regimen costs, and highlight the urgent need to identify drug regimens with improved safety profiles.

摘要

目的

根据南非指南,估算标准长程治疗方案治疗耐多药和利福平耐药结核病(MDR/RR-TB)时管理药物不良反应(ADR)的医疗服务提供方成本。

方法

我们利用基于指南的药物不良反应管理的自下而上公共部门提供者成本参数化了一份发表的 MDR/RR-TB 马尔可夫健康状态模型。从文献中提取药物不良反应发生的频率。10 年内估计成本,每年贴现 3%,并使用概率敏感性分析进行检验。

结果

根据发生频率加权的中度 ADR 指南成本为 135.76 美元(标准差 17.18 美元),严重 ADR 的成本为 521.29 美元(标准差 55.99 美元)。我们估计,每位开始 MDR/RR-TB 治疗的患者每年因药物不良反应管理而增加的成本为 380.17 美元。南非公共卫生部门因药物不良反应管理而增加的成本为每年 476 万美元,占 2015 年 12527 名患者队列中 MDR/RR-TB 治疗估计队列成本(5755 万美元)的 8.3%。

结论

在标准长程 MDR/RR-TB 治疗的前 6 个月中,管理多种药物不良反应和严重药物不良反应会显著增加医疗服务提供方的治疗成本。在比较治疗方案的成本时,需要考虑这些结果,并强调迫切需要确定具有改善安全性特征的药物方案。

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