优化人类狂犬病疫苗供应链:一项建模研究。

Vaccine Pub Date : 2025-04-30 Epub Date: 2025-04-23 DOI:10.1016/j.vaccine.2025.127108
Martha M Luka, Elaine A Ferguson, Eleanor Rees, Husna Hoffu, Joel Changalucha, Kennedy Lushasi, Lwitiko Sikana, Mumbua Mutunga, S M Thumbi, Katie Hampson
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引用次数: 0

摘要

背景:在低收入和中等收入国家,狂犬病每年造成数千人死亡。尽管有用于暴露后预防的有效疫苗,但其费用高昂,加上供应链失灵,导致供应短缺和可预防的死亡。全球疫苗免疫联盟的投资旨在改善接触后疫苗的可及性。我们评估了坦桑尼亚和肯尼亚的PEP需求,并研究了改善全球免疫联盟合格国家供应链的库存管理策略。方法:我们拟合坦桑尼亚(6646例患者,20个地区)和肯尼亚(199112例患者,47个县)5年咬伤患者数据的负二项分布,以参数化世卫组织推荐的肌内注射(IM)和皮内注射(ID)方案下暴露后疫苗需求的模拟。在观察到的需求范围内,我们比较了模拟疫苗使用、缺货和库存管理策略的影响。结果:患者咬伤发生率差异显著;需求激增远远超过月平均水平(6%的月份超过患者每月平均咬伤次数的3倍),在低发病率环境中最为极端。免疫接种可使小瓶使用量减少55%,并减少缺货风险。在ID下,疫苗瓶的节省在高通量环境下最大,而风险缓解在低通量环境下最大。将PEP分散到更多的设施可以改善获取途径,但减少了共用小瓶的机会,从而增加了小瓶的使用。根据患者吞吐量确定弹性供应链策略,允许适应不断变化的需求。结论:免疫接种减少了小瓶的使用和库存,即使在低通量环境中也是如此。定制库存管理——通过调整警报阈值和补充库存量——可以简化将狂犬病疫苗纳入基本免疫供应链的过程,提高疫苗的可得性并防止不必要的死亡。然而,还必须考虑后勤方面的权衡。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Optimising human rabies vaccine supply chains: A modelling study.

Background: Rabies causes thousands of deaths annually in low- and middle-income countries. Despite effective vaccines for post-exposure prophylaxis (PEP), their expense, coupled with supply chain failures, leads to stockouts and preventable deaths. Investment by Gavi, the Vaccine Alliance, aims to improve access to post-exposure vaccines. We evaluate PEP demand in Tanzania and Kenya and examine stock management strategies for improving supply chains in Gavi-eligible countries.

Methods: We fitted negative binomial distributions to five years of bite patient data from Tanzania (6646 patients, 20 districts) and Kenya (199,112 patients, 47 counties) to parameterise simulations of post-exposure vaccine demand under WHO-recommended intramuscular (IM) and intradermal (ID) regimens. We compared simulated vaccine use, stockouts, and the impact of stock management strategies across the observed range in demand.

Results: Bite patient incidence varied dramatically; demand surges far exceeded monthly averages (in 6 % of months exceeding 3× average monthly bite patient presentations) and were most extreme in low-incidence settings. ID vaccination reduces vial use by >55 % and reduces stockout risk. Under ID vaccination vial savings are greatest in high-throughput settings, whilst risk mitigation is maximised in low-throughput settings. Decentralizing PEP to more facilities improves access, though reduces vial-sharing opportunities and so increases vial use. Resilient supply chain strategies were identified according to patient throughput, allowing for adaptation to changing demand.

Conclusions: ID vaccination reduces vial use and stockouts, even in low-throughput settings. Tailoring stock management-through adjusted alert thresholds and restocking volumes-can simplify the integration of rabies vaccines into essential immunisation supply chains, improving their availability and preventing unnecessary deaths. However, logistical trade-offs must also be considered.

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