Comparison of the sensitivity of patient-reported outcomes for detecting the benefit of biologics in severe asthma

Author:

Hyland Michael E12ORCID,Lanario Joseph W2ORCID,Menzies-Gow Andrew3,Mansur Adel H4,Dodd James W5ORCID,Fowler Stephen J6,Hayes Gemma7,Jones Rupert C1,Masoli Matthew8

Affiliation:

1. Plymouth Marjon University, Plymouth, UK

2. Faculty of Health, University of Plymouth, Plymouth, UK

3. Royal Brompton Hospital, London, UK

4. University Hospitals Birmingham and University of Birmingham, Heartlands Hospital, Birmingham, UK

5. Academic Respiratory Unit, Southmead Hospital, North Bristol Hospital Trust, Bristol, UK

6. School of Biological Sciences, Faculty of Biology, Medicine and Health, University of Manchester, Manchester Academic Health Science Centre and NIHR Manchester Biomedical Research Centre, Manchester University Hospitals NHS Foundation Trust, Manchester, UK

7. University Hospitals Plymouth NHS Trust, Plymouth, UK

8. Royal Devon and Exeter Hospital, University of Exeter, Exeter, UK

Abstract

Background The sensitivity of patient-reported outcomes (PROs) to detect the effects of treatment change depends on the match between the change in items of the PRO and the change that takes place in a sample of people. The aim of this study is to compare the sensitivity of different PROs in detecting changes following the initiation of biologic treatment in asthma. Methods: Patients starting a biologic treatment as part of clinical care completed the Asthma Control Questionnaire (ACQ-6), the Severe Asthma Questionnaire (SAQ and SAQ-global scores) and the EQ5D (EQ-5D-5L and EQ5D-VAS) at baseline. They completed the ACQ-6, SAQ, SAQ-global and a retrospective global rating of change (GRoC) scale at weeks 4, 8 and 16 and completed the EQ-5D-5L and EQ5D-VAS at week 16. The SAQ-global and EQ5D-VAS differ but both are single item 100-point questions. Sensitivity was measured by Cohen’s D effect size at each of the three time points. Results: 110 patients were recruited. Depending on the time of assessment, effect size varied between 0.45 and 0.64 for the SAQ, between 0.50 and 0.77 for the SAQ-global; between 0.45 and 0.69 for ACQ-6; between 0.91 and 1.22 for GRoC; 0.32 for EQ-5D-5L and 0.49 for EQ5D-VAS. Conclusion: The sensitivity to change of a questionnaire varies with the time of measurement. The three asthma-specific prospective measures (SAQ, SAQ-global and ACQ-6) have similar sensitivity to change. The single-item EQ5D-VAS was less sensitive than the asthma specific measures and less sensitive than the single-item SAQ-global. The EQ-5D-5L was least sensitive.

Funder

GlaxoSmithKline

Publisher

SAGE Publications

Subject

Pulmonary and Respiratory Medicine

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