Miltefosine implementation for treatment of cutaneous leishmaniasis: access indicators in the state of Minas Gerais, 2021-2024.

Sarah Nascimento Silva, Mell Ferreira Saliba, Laís Raquel Ribeiro, Gláucia Cota
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Abstract

Objective: To describe and evaluate the initial indicators of the pilot implementation of miltefosine in Minas Gerais for the treatment of cutaneous leishmaniasis.

Methods: This is a descriptive, cross-sectional study based on regulatory documents and secondary administrative data generated during the dispensing of miltefosine in Minas Gerais between May 2021 and April 2024. Indicators related to access and operability of the strategy implemented were calculated for the steps involved in approving the request for use and dispensing of the drug.

Results: The authorization rate was 97.5% for 281 valid requests. The outpatient clinic of the René Rachou Institute, a reference center for leishmaniasis in Minas Gerais, was responsible for the largest number of requests during the period. The health macro-regions Centre and North concentrated the largest number of requests (48.9% and 33.6%), which coincided with the regions with the highest number of reported cases. Median time for analyzing requests and for the person to access the medicine was 1.0 (0-76) and 10.0 (0-340) days, with significant variation between the health macro-regions. One hundred and nineteen people were treated in a municipality other than their place of residence. Of these, 49 needed to travel to another health macro-region. The miltefosine diffusion rate was 11.3% for the three-year period monitored, with significant variation between the macro-regions.

Conclusion: The indicators confirmed that miltefosine has been implemented, but revealed low diffusion and regional disparities. Barriers need to be identified and strategies developed to expand equitable access to new technologies.

米替福辛用于治疗皮肤利什曼病:2021-2024年米纳斯吉拉斯州可及性指标
目的:描述和评价米地福辛在米纳斯吉拉斯州试点实施治疗皮肤利什曼病的初步指标。方法:这是一项描述性横断面研究,基于2021年5月至2024年4月在米纳斯吉拉斯州分配米替福辛期间产生的监管文件和二级行政数据。计算了与所实施战略的可及性和可操作性有关的指标,以确定批准使用和配发药物请求所涉及的步骤。结果:281例有效申请的授权率为97.5%。在本报告所述期间,米纳斯吉拉斯的利什曼病参考中心ren Rachou研究所的门诊部处理了最多的请求。卫生宏观区域中心和北部集中了最多的请求(48.9%和33.6%),这与报告病例数量最多的区域相吻合。分析请求和个人获得药物的中位数时间分别为1.0(0-76)天和10.0(0-340)天,卫生宏观区域之间差异很大。119人在其居住地以外的城市接受治疗。其中49人需要前往另一个卫生宏观区域。在监测的三年期间,米氟辛扩散率为11.3%,宏观区域之间差异显著。结论:各项指标均证实米替福辛已得到实施,但存在低扩散和地区差异。需要确定障碍并制定战略以扩大公平获得新技术的机会。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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