Cefiderocol for treating severe aerobic Gram-negative bacterial infections: technology evaluation to inform a novel subscription-style payment model.

IF 3.5 2区 医学 Q1 HEALTH CARE SCIENCES & SERVICES Health technology assessment Pub Date : 2024-06-01 DOI:10.3310/YGWR4511
Beth Woods, Laetitia Schmitt, Dina Jankovic, Benjamin Kearns, Alison Scope, Shijie Ren, Tushar Srivastava, Chu Chang Ku, Jean Hamilton, Claire Rothery, Laura Bojke, Mark Sculpher, Sue Harnan
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Abstract

Background: To limit the use of antimicrobials without disincentivising the development of novel antimicrobials, there is interest in establishing innovative models that fund antimicrobials based on an evaluation of their value as opposed to the volumes used. The aim of this project was to evaluate the population-level health benefit of cefiderocol in the NHS in England, for the treatment of severe aerobic Gram-negative bacterial infections when used within its licensed indications. The results were used to inform the National Institute for Health and Care Excellence guidance in support of commercial discussions regarding contract value between the manufacturer and NHS England.

Methods: The health benefit of cefiderocol was first derived for a series of high-value clinical scenarios. These represented uses that were expected to have a significant impact on patients' mortality risks and health-related quality of life. The clinical effectiveness of cefiderocol relative to its comparators was estimated by synthesising evidence on susceptibility of the pathogens of interest to the antimicrobials in a network meta-analysis. Patient-level costs and health outcomes of cefiderocol under various usage scenarios compared with alternative management strategies were quantified using decision modelling. Results were reported as incremental net health effects expressed in quality-adjusted life-years, which were scaled to 20-year population values using infection number forecasts based on data from Public Health England. The outcomes estimated for the high-value clinical scenarios were extrapolated to other expected uses for cefiderocol.

Results: Among Enterobacterales isolates with the metallo-beta-lactamase resistance mechanism, the base-case network meta-analysis found that cefiderocol was associated with a lower susceptibility relative to colistin (odds ratio 0.32, 95% credible intervals 0.04 to 2.47), but the result was not statistically significant. The other treatments were also associated with lower susceptibility than colistin, but the results were not statistically significant. In the metallo-beta-lactamase Pseudomonas aeruginosa base-case network meta-analysis, cefiderocol was associated with a lower susceptibility relative to colistin (odds ratio 0.44, 95% credible intervals 0.03 to 3.94), but the result was not statistically significant. The other treatments were associated with no susceptibility. In the base case, patient-level benefit of cefiderocol was between 0.02 and 0.15 quality-adjusted life-years, depending on the site of infection, the pathogen and the usage scenario. There was a high degree of uncertainty surrounding the benefits of cefiderocol across all subgroups. There was substantial uncertainty in the number of infections that are suitable for treatment with cefiderocol, so population-level results are presented for a range of scenarios for the current infection numbers, the expected increases in infections over time and rates of emergence of resistance. The population-level benefits varied substantially across the base-case scenarios, from 896 to 3559 quality-adjusted life-years over 20 years.

Conclusion: This work has provided quantitative estimates of the value of cefiderocol within its areas of expected usage within the NHS.

Limitations: Given existing evidence, the estimates of the value of cefiderocol are highly uncertain.

Future work: Future evaluations of antimicrobials would benefit from improvements to NHS data linkages; research to support appropriate synthesis of susceptibility studies; and application of routine data and decision modelling to assess enablement value.

Study registration: No registration of this study was undertaken.

Funding: This award was funded by the National Institute for Health and Care Research (NIHR) Health Technology Assessment Policy Research Programme (NIHR award ref: NIHR135591), conducted through the Policy Research Unit in Economic Methods of Evaluation in Health and Social Care Interventions, PR-PRU-1217-20401, and is published in full in Health Technology Assessment; Vol. 28, No. 28. See the NIHR Funding and Awards website for further award information.

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治疗严重需氧革兰阴性菌感染的头孢羟氨苄:技术评估为新型订购式付费模式提供依据。
背景:为了限制抗菌药物的使用,同时又不抑制新型抗菌药物的开发,人们有兴趣建立创新模式,根据抗菌药物的价值评估而不是使用量来资助抗菌药物。该项目的目的是评估头孢羟氨苄在英格兰国家医疗服务体系中用于治疗严重需氧革兰阴性菌感染时,在其许可适应症范围内的人群健康效益。研究结果将为国家健康与护理卓越研究所提供指导,以支持生产商与英格兰国家医疗服务体系就合同价值进行商业讨论:方法:首先针对一系列高价值临床方案得出头孢羟氨苄的健康效益。这些方案代表了预计会对患者的死亡风险和健康相关生活质量产生重大影响的用途。在一项网络荟萃分析中,通过综合相关病原体对抗菌药物敏感性的证据,估算出头孢羟氨苄相对于同类药物的临床疗效。利用决策模型对头孢羟氨苄在不同使用情况下与其他管理策略相比的患者层面成本和健康结果进行了量化。结果以质量调整生命年表示的增量净健康效应进行报告,并根据英格兰公共卫生部门提供的数据进行感染人数预测,将其放大至 20 年人口值。高价值临床方案的估计结果被外推至头孢羟氨苄的其他预期用途:在具有金属-beta-内酰胺酶耐药机制的肠杆菌分离物中,基础案例网络荟萃分析发现,头孢羟氨苄与可乐定相比具有更低的敏感性(几率比 0.32,95% 可信区间 0.04 至 2.47),但该结果在统计学上并不显著。其他治疗方法的易感性也低于可乐定,但结果无统计学意义。在金属-β-内酰胺酶铜绿假单胞菌基础病例网络荟萃分析中,头孢克洛与较低的易感性相关(几率比 0.44,95% 可信区间 0.03 至 3.94),但结果无统计学意义。其他治疗方法与药敏性无关。在基础病例中,根据感染部位、病原体和使用方案的不同,头孢羟氨苄在患者层面的获益为 0.02 至 0.15 质量调整生命年。在所有亚组中,头孢羟氨苄的获益具有高度不确定性。适合使用头孢羟氨苄治疗的感染病例数存在很大的不确定性,因此,我们针对目前的感染病例数、随着时间推移感染病例数的预期增长情况以及耐药性的出现率等一系列情况,给出了人群水平的结果。在不同的基本假设情况下,人口层面的收益差异很大,20 年间质量调整生命年从 896 年到 3559 年不等:这项研究对头孢羟氨苄在国家医疗服务体系预期使用范围内的价值进行了量化估算:局限性:鉴于现有证据,头孢克洛的价值估算具有很大的不确定性:今后的工作:改进 NHS 数据链接、开展研究以支持对药敏性研究进行适当的综合、应用常规数据和决策建模来评估启用价值,将有利于今后对抗菌药物进行评估:本研究未进行注册:该奖项由国家健康与护理研究所(NIHR)健康技术评估政策研究计划(NIHR奖项编号:NIHR135591)资助,通过健康与社会护理干预措施经济评估方法政策研究组(PR-PRU-1217-20401)进行,全文发表于《健康技术评估》(Health Technology Assessment)第28卷第28期。更多奖项信息,请参阅 NIHR Funding and Awards 网站。
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来源期刊
Health technology assessment
Health technology assessment 医学-卫生保健
CiteScore
6.90
自引率
0.00%
发文量
94
审稿时长
>12 weeks
期刊介绍: Health Technology Assessment (HTA) publishes research information on the effectiveness, costs and broader impact of health technologies for those who use, manage and provide care in the NHS.
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