Supply of nirmatrelvir/ritonavir and molnupiravir for patients with COVID-19 in the first eight months since listing on the Australian Pharmaceutical Benefits Scheme: A retrospective observational study

IF 2.9 4区 医学 Q2 INFECTIOUS DISEASES
Derrick Lopez , Douglas Pritchard , Frank M. Sanfilippo , Erin Kelty , Amy Page , Christopher Etherton-Beer , Osvaldo P. Almeida , David B. Preen
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Abstract

Objectives

To compare the supply of molnupiravir and nirmatrelvir/ritonavir in relation to patient characteristics and other co-prescribed medicines and to estimate the number of patients without contraindications to nirmatrelvir/ritonavir who were treated with molnupiravir.

Study design, setting

Retrospective observational study of patients identified in the Pharmaceutical Benefits Scheme (PBS) 10 % sample dataset who were supplied with either molnupiravir or nirmatrelvir/ritonavir between May and December 2022. We supplemented the PBS dataset with aggregated counts from published literature to determine prevalence of clinical contraindications to nirmatrelvir/ritonavir.

Main outcome measures

We used multivariable Poisson regression to estimate risk ratios (RR) of receiving nirmatrelvir/ritonavir over molnupiravir.

Results

We identified 54,550 patients who received either nirmatrelvir/ritonavir (26.8 %) or molnupiravir (73.2 %). Their average age was 71.6 (SD = 13.4) years and 57.1 % were female. Patients were less likely to receive nirmatrelvir/ritonavir with increasing age (RR = 0.50; 95 % CI: 0.48–0.53; for ages 85 + compared to < 65 years) or who had received medicines contraindicated for use with nirmatrelvir/ritonavir (RR = 0.66; 95 % CI: 0.64–0.68). During the study period, we estimated that between 28.4 % and 45.4 % of patients aged ≥ 65 years had received molnupiravir in the absence of pharmacological and clinical contraindications to nirmatrelvir/ritonavir.

Conclusion

Many prescriptions were written for molnupiravir where there were no contraindications to nirmatrelvir/ritonavir. The benefits that followed from prompt government action in approving and obtaining nirmatrelvir/ritonavir were therefore likely to be less than they could potentially have been. Governments should consider investing in quality improvement systems to ensure the best outcomes in terms of efficacy and safety.

在澳大利亚药品福利计划上市后的前八个月中,为 COVID-19 患者供应的 nirmatrelvir/ritonavir 和 molnupiravir:回顾性观察研究。
目的比较莫仑匹韦和尼马瑞韦/利托那韦的供应量与患者特征和其他联合处方药物的关系,并估计无尼马瑞韦/利托那韦禁忌症但接受了莫仑匹韦治疗的患者人数:对药品福利计划(PBS)10%抽样数据集中确定的在2022年5月至12月期间接受过莫仑吡韦或尼马瑞韦/利托那韦治疗的患者进行回顾性观察研究。我们对 PBS 数据集进行了补充,并汇总了已发表文献中的计数,以确定尼马瑞韦/利托那韦临床禁忌症的流行率:我们使用多变量泊松回归来估计接受尼尔马特韦/利托那韦治疗的风险比(RR):我们发现有 54,550 名患者接受了 nirmatrelvir/ritonavir(26.8%)或 molnupiravir(73.2%)治疗。他们的平均年龄为 71.6 (SD = 13.4) 岁,57.1% 为女性。随着年龄的增长,患者接受 nirmatrelvir/ritonavir 治疗的可能性降低(RR = 0.50;95 % CI:0.48-0.53;85 岁以上与结论相比):许多处方都是在没有禁忌症的情况下开具的莫仑拉韦处方。因此,政府迅速采取行动批准和获得 nirmatrelvir/ritonavir 所带来的益处可能低于其可能带来的益处。各国政府应考虑对质量改进系统进行投资,以确保在疗效和安全性方面取得最佳成果。
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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来源期刊
Infectious diseases now
Infectious diseases now Medicine-Infectious Diseases
CiteScore
7.10
自引率
2.90%
发文量
116
审稿时长
40 days
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