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Minimal clinically important difference in means in vulnerable populations: challenges and solutions

Peacock, JL; Lo, J; Rees, JR; Sauzet, O (2021) Minimal clinically important difference in means in vulnerable populations: challenges and solutions. BMJ Open, 11 (11). e052338-e052338. ISSN 2044-6055 https://doi.org/10.1136/bmjopen-2021-052338
SGUL Authors: Peacock, Janet Lesley

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Abstract

Introduction and motivation Many health studies measure a continuous outcome and compare means between groups. Since means for biological data are often difficult to interpret clinically, it is common to dichotomise using a cut-point and present the ‘percentage abnormal’ alongside or in place of means. Examples include birthweight where ‘abnormal’ is defined as <2500 g (low birthweight), systolic blood pressure with abnormal defined as >140 mm Hg (high blood pressure) and lung function with varying definitions of the ‘limit of normal’. In vulnerable populations with low means, for example, birthweight in a population of preterm babies, a given difference in means between two groups will represent a larger difference in the percentage with low birthweight than in a general population of babies where most will be full term. Thus, in general, the difference in percentage of patients with abnormal values for a given difference in means varies according to the reference population’s mean value. This phenomenon leads to challenges in interpreting differences in means in vulnerable populations and in defining an outcome-specific minimal clinically important difference (MCID) in means since the proportion abnormal, which is useful in interpreting means, is not constant—it varies with the population mean. This has relevance for study power calculations and data analyses in vulnerable populations where a small observed difference in means may be difficult to interpret clinically and may be disregarded, even if associated with a relatively large difference in percentage abnormal which is clinically relevant. Methods To address these issues, we suggest both difference in means and difference in percentage (proportion) abnormal are considered when choosing the MCID, and that both means and percentages abnormal are reported when analysing the data. Conclusions We describe a distributional approach to analyse proportions classified as abnormal that avoids the usual loss of precision and power associated with dichotomisation.

Item Type: Article
Additional Information: © Author(s) (or their employer(s)) 2021. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ. http://creativecommons.org/licenses/by-nc/4.0/ This is an open access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited, appropriate credit is given, any changes made indicated, and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/4.0/.
Keywords: epidemiology, public health, statistics & research methods, Birth Weight, Humans, Infant, Low Birth Weight, Infant, Newborn, Minimal Clinically Important Difference
SGUL Research Institute / Research Centre: Academic Structure > Population Health Research Institute (INPH)
Journal or Publication Title: BMJ Open
ISSN: 2044-6055
Language: en
Media of Output: Electronic
Related URLs:
Publisher License: Creative Commons: Attribution-Noncommercial 4.0
Dates:
Date Event
2021-11-09 Published
2021-10-13 Accepted
URI: https://openaccess.sgul.ac.uk/id/eprint/118534
Publisher's version: https://doi.org/10.1136/bmjopen-2021-052338

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