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运筹学作为改善世卫组织欧洲区域耐多药结核病治疗结果的一种机制。

Operational research as a mechanism to improve treatment outcomes for drug-resistant TB in the WHO European Region.

作者信息

Migliori G B, Korotych O, Achar J, Ciobanu A, Dravniece G, Germanovych M, Gurbanova E, Hovhannesyan A, Khachatryan N, Kuksa L, Lomtadze N, Rich M L, Skrahina A, Yedilbayev A

机构信息

Servizio di Epidemiologia Clinica delle Malattie Respiratorie, Istituti Clinici Scientifici Maugeri, Istituto di Ricovero e Cura a Carattere Scientifico, Tradate, Italy.

Joint Infectious Diseases Unit, World Health Organization Regional Office for Europe, Copenhagen, Denmark.

出版信息

IJTLD Open. 2024 Mar 1;1(3):103-110. doi: 10.5588/ijtldopen.24.0035. eCollection 2024 Mar.

Abstract

In 2022, the WHO European Region accounted for 15.1% of all incident rifampicin-resistant/multidrug-resistant TB (RR/MDR-TB) cases. Most occurred in 18 high-priority countries of eastern Europe and central Asia, many of which joined an initiative led by the WHO Regional Office for Europe. The aim was to introduce three, fully oral, 9-month modified shorter treatment regimens (mSTR) to treat RR/MDR-TB under operational research conditions. The three regimens were: 1) bedaquiline + linezolid + levofloxacin + clofazimine + cycloserine (BdqLzdLfxCfzCs); 2) BdqLzdLfxCfz + delamanid (Dlm) for children over 6 years of age and adults; and 3) DlmLzdLfxCfz for children under 6 years of age. The project aimed to enhance treatment success, facilitate mSTR implementation, promote quality of care and build research capacity, while also contributing to global knowledge on all-oral mSTR use. Between April 2020 and June 2022, >2,800 patients underwent mSTR treatment in the WHO European Region. This unique experience promoted further collaboration with national tuberculosis programmes, health authorities, experts and donors within and outside Europe, with a focus on implementing operational research and improving the quality of care in high TB burden countries of the region. In the hope of encouraging others to adopt this model, we have described the principles of the initiative, its strengths and weaknesses and next steps.

摘要

2022年,世卫组织欧洲区域的利福平耐药/耐多药结核病(RR/MDR-TB)新发病例占全球的15.1%。大多数病例发生在东欧和中亚的18个重点国家,其中许多国家参与了由世卫组织欧洲区域办事处牵头的一项倡议。其目的是在开展运营研究的条件下引入三种为期9个月的全口服改良短程治疗方案(mSTR),用于治疗RR/MDR-TB。这三种方案分别是:1)贝达喹啉+利奈唑胺+左氧氟沙星+氯法齐明+环丝氨酸(BdqLzdLfxCfzCs);2)6岁以上儿童及成人使用BdqLzdLfxCfz+德拉马尼(Dlm);3)6岁以下儿童使用DlmLzdLfxCfz。该项目旨在提高治疗成功率,促进mSTR的实施,提升医疗服务质量并增强研究能力,同时也为全球全口服mSTR的使用知识做出贡献。2020年4月至2022年6月期间,世卫组织欧洲区域有超过2800名患者接受了mSTR治疗。这一独特经验促进了与欧洲内外的国家结核病规划、卫生当局、专家和捐助方的进一步合作,重点是在该区域结核病高负担国家开展运营研究并提高医疗服务质量。为鼓励其他方采用这一模式,我们阐述了该倡议的原则、优缺点及后续步骤。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b172/11221584/30807d56860d/ijtldopen0035f1.jpg

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