Adherence, per‐protocol effects, and the estimands framework

Author:

Keene Oliver1ORCID

Affiliation:

1. KeeneONStatistics Berkshire UK

Abstract

AbstractIn the statistical literature, treatment effects in clinical trials are frequently described as either ITT or per‐protocol effects. The estimand given for the per‐protocol effect is the effect in adherers, where adherers are typically defined as adhering to the intervention as specified in the trial protocol. This dichotomy of treatment effects is unhelpful when there are in reality multiple treatment effects that can be of clinical interest and relevance. The terms “per‐protocol” and “adherence” are confusing to non‐statisticians. Protocols always allow for discontinuation of randomized treatment so participants discontinuing have actually followed the protocol. When rescue or additional medication is available, the effect in adherers could mean the effect regardless of use of these medications or the effect in a counterfactual world where the participant did not take the medication. Adherence can mean continuing to be prescribed a treatment or some arbitrary level of compliance with a medication that has been prescribed. The ICH E9 (R1) estimands framework provides an improved alternative for the description of treatment effects in clinical trials. Identification of important intercurrent events and the strategy used to handle these events is key to determining the treatment effect. When designing a trial, estimands should be properly defined according to this framework. It is time the statistical literature abandoned describing treatment effects as the effect in adherers or the per‐protocol effect.

Publisher

Wiley

Subject

Pharmacology (medical),Pharmacology,Statistics and Probability

Reference14 articles.

1. RoB 2: a revised tool for assessing risk of bias in randomised trials;Sterne JA;BMJ,2019

2. Interval-cohort designs and bias in the estimation of per-protocol effects: a simulation study

3. Estimands, Estimators, and Estimates

4. International Council for Harmonisation of Technical Requirements for Pharmaceuticals for Human Use. ICH E9 (R1) addendum on estimands and sensitivity analysis in clinical trials to the guideline on statistical principles for clinical trials Final version Adopted Nov 2019. Accessed November 7 2022https://database.ich.org/sites/default/files/E9-R1_Step4_Guideline_2019_1203.pdf

同舟云学术

1.学者识别学者识别

2.学术分析学术分析

3.人才评估人才评估

"同舟云学术"是以全球学者为主线,采集、加工和组织学术论文而形成的新型学术文献查询和分析系统,可以对全球学者进行文献检索和人才价值评估。用户可以通过关注某些学科领域的顶尖人物而持续追踪该领域的学科进展和研究前沿。经过近期的数据扩容,当前同舟云学术共收录了国内外主流学术期刊6万余种,收集的期刊论文及会议论文总量共计约1.5亿篇,并以每天添加12000余篇中外论文的速度递增。我们也可以为用户提供个性化、定制化的学者数据。欢迎来电咨询!咨询电话:010-8811{复制后删除}0370

www.globalauthorid.com

TOP

Copyright © 2019-2024 北京同舟云网络信息技术有限公司
京公网安备11010802033243号  京ICP备18003416号-3