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比较评估法国社区和医院药房中emicizumab(Hemlibra®)在血友病 A 患者中的可及性。

Comparative evaluation of access to emicizumab (Hemlibra®) for people with haemophilia A in community and hospital pharmacies in France.

机构信息

Haemophilia Treatment Centre and French Reference Centre on Haemophilia, Louis Pradel Hospital, Hospices Civils de Lyon, Bron, France.

Pharmaceutical Unit, Louis Pradel Hospital, Hospices Civils de Lyon, Bron, France.

出版信息

Eur J Public Health. 2024 Oct 1;34(5):866-871. doi: 10.1093/eurpub/ckae131.

Abstract

Since June 2021 in France, patients with haemophilia A with anti-factor VIII inhibitors and patients with severe haemophilia A without anti-factor VIII inhibitors have the choice between the community and the hospital pharmacy for dispensing emicizumab (Hemlibra®). This study aims to investigate patient-centred access to treatment by evaluating and comparing the dimensions of the Penchansky and Thomas model, between community and hospital pharmacies. The evaluation of access to treatment was based on the dimensions of the Penchansky and Thomas model: accessibility, availability, acceptability, accommodation and affordability. These were assessed using appropriate and specific indicators in the study context and calculated for patients choosing community pharmacy or hospital pharmacy for emicizumab dispensing. Geographical data collected as part of the national 'PASO DOBLE DEMI' study were used for this analysis. The findings reveal that dispensing emicizumab in community pharmacies improves accessibility by significantly reducing travel time. The availability of healthcare services is also improved due to the territorial coverage of community pharmacies. The extended opening hours and low waiting time also contribute to better access to emicizumab in community pharmacies. The dimension of acceptability must be improved, and further investigations are needed to address the affordability dimension. Several months after emicizumab became available in French community pharmacies, access to treatment has significantly improved, reducing the burden of this rare chronic disease for patients and their careers. These results suggest that this innovative model could be extended to other medicines and even other therapeutic areas.

摘要

自 2021 年 6 月起,在法国,患有抗凝血因子 VIII 抑制剂的血友病 A 患者和患有无抗凝血因子 VIII 抑制剂的重度血友病 A 患者,在社区药房和医院药房之间,可选择调配艾美赛珠单抗(Hemlibra®)。本研究旨在通过评估和比较潘昌斯基和托马斯模型的维度,调查以患者为中心的治疗途径,该模型包括可及性、可获得性、可接受性、适应性和可负担性。在研究背景下,使用适当和特定的指标来评估治疗的可及性,并计算选择社区药房或医院药房调配艾美赛珠单抗的患者的维度得分。该分析使用了国家“PASO DOBLE DEMI”研究中收集的地理数据。研究结果表明,在社区药房调配艾美赛珠单抗可显著减少出行时间,从而提高可及性。由于社区药房的地域覆盖范围更广,医疗服务的可获得性也得到了改善。此外,社区药房营业时间延长且等待时间较短,也有助于改善艾美赛珠单抗的可及性。可接受性维度需要进一步改善,还需要进一步调查以解决可负担性维度的问题。在艾美赛珠单抗在法国社区药房供应几个月后,治疗的可及性显著提高,减轻了患者及其护理人员的负担。这些结果表明,这种创新模式可以扩展到其他药物甚至其他治疗领域。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/69b5/11430965/47e9e1cc8c7b/ckae131f1.jpg

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