Imperial College London
Alternate

ProfessorDianaBilton

Faculty of Medicine, National Heart & Lung Institute

Honorary Clinical Senior Lecturer
 
 
 
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Contact

 

+44 (0)7801 067 057diana.bilton

 
 
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Location

 

Fulham RoadRoyal Brompton Campus

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Summary

 

Publications

Citation

BibTex format

@article{Mohindru:2020:10.1007/s41669-019-0144-1,
author = {Mohindru, B and Turner, D and Sach, T and Bilton, D and Carr, S and Archangelidi, O and Bhadhuri, A and Whitty, JA},
doi = {10.1007/s41669-019-0144-1},
journal = {PharmacoEconomics - Open},
pages = {13--25},
title = {Health state utility data in cystic fibrosis: a systematic review},
url = {http://dx.doi.org/10.1007/s41669-019-0144-1},
volume = {4},
year = {2020}
}
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RIS format (EndNote, RefMan)

TY  - JOUR
AB  - INTRODUCTION: Cystic fibrosis (CF) is a life-limiting, hereditable condition, with the highest prevalence in Europe. CF treatments have led to improvements in clinical symptoms, disease management and decelerated disease progression. However, little is known about the health state utility (HSU) associated with CF disease states, adverse events, and changes in disease severity. Although HSU data have contributed to existing health economic modelling studies, a lack of such data have been highlighted. This systematic review aims to provide a summary of HSU-related research in CF and highlight related research gaps. METHODS: Online searches were performed in six databases and studies in any of the following categories were included: (1) estimation of HSUs in CF; (2) mapping studies between patient-reported outcome measures (PROMs) and HSUs; (3) economic evaluations on the management of CF that report primary HSU data; and (4) any CF clinical trial that reported HSU as an outcome. RESULTS: A total of 17 studies were reviewed, of which 12 provided HSU values for specific CF populations. The remaining five articles provided HSU data that were broken down by CF relevant health states, including lung transplantations, pulmonary exacerbation (PEx) events and forced expiratory volume in 1 s (FEV1). CONCLUSION: Current HSU data in CF are limited and there is considerable scope for further research, both in providing HSU values for CF and in investigating methods for HSU elicitation/evaluation in CF populations.
AU  - Mohindru,B
AU  - Turner,D
AU  - Sach,T
AU  - Bilton,D
AU  - Carr,S
AU  - Archangelidi,O
AU  - Bhadhuri,A
AU  - Whitty,JA
DO  - 10.1007/s41669-019-0144-1
EP  - 25
PY  - 2020///
SN  - 2509-4254
SP  - 13
TI  - Health state utility data in cystic fibrosis: a systematic review
T2  - PharmacoEconomics - Open
UR  - http://dx.doi.org/10.1007/s41669-019-0144-1
UR  - https://www.ncbi.nlm.nih.gov/pubmed/31054048
UR  - http://hdl.handle.net/10044/1/79064
VL  - 4
ER  -
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