Adherence, per‐protocol effects, and the estimands framework
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Published:2023-07-21
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ISSN:1539-1604
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Container-title:Pharmaceutical Statistics
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language:en
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Short-container-title:Pharmaceutical Statistics
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.
Subject
Pharmacology (medical),Pharmacology,Statistics and Probability
Reference14 articles.
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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
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1 articles.
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