TY - JOUR
T1 - Estimating the population health burden of musculoskeletal conditions using primary care electronic health records
AU - Yu, Dahai
AU - Peat, George
AU - Jordan, Kelvin P.
AU - Bailey, James
AU - Prieto-Alhambra, Daniel
AU - Robinson, Danielle E.
AU - Strauss, Victoria Y.
AU - Walker-Bone, Karen
AU - Silman, Alan
AU - Mamas, Mamas
AU - Blackburn, Steven
AU - Dent, Stephen
AU - Dunn, Kate
AU - Judge, Andrew
AU - Protheroe, Joanne
AU - Wilkie, Ross
N1 - Funding Information:
PRELIM was funded by Versus Arthritis (21403). G.P., K.J., R.W. and D.Y. hold Honorary Academic Consultant Contracts from Public Health England. K.J. is supported by matched funding awarded to the NIHR Applied Research Collaboration (West Midlands). This research was supported by the National Institute for Health Research (NIHR) Oxford Biomedical Research Centre (BRC). D.P.A. is funded through a NIHR Senior Research Fellowship (Grant Number SRF- 2018-11-ST2-004). A.J. was supported by the NIHR Biomedical Research Centre at University Hospitals Bristol and Weston NHS Foundation Trust and the University of Bristol.
Publisher Copyright:
© 2021 The Author(s) 2021.
PY - 2021/10
Y1 - 2021/10
N2 - Objectives: Better indicators from affordable, sustainable data sources are needed to monitor population burden of musculoskeletal conditions. We propose five indicators of musculoskeletal health and assessed if routinely available primary care electronic health records (EHR) can estimate population levels in musculoskeletal consulters. Methods: We collected validated patient-reported measures of pain experience, function and health status through a local survey of adults (≥35 years) presenting to English general practices over 12 months for low back pain, shoulder pain, osteoarthritis and other regional musculoskeletal disorders. Using EHR data we derived and validated models for estimating population levels of five self-reported indicators: prevalence of high impact chronic pain, overall musculoskeletal health (based on Musculoskeletal Health Questionnaire), quality of life (based on EuroQoL health utility measure), and prevalence of moderate-to-severe low back pain and moderate-to-severe shoulder pain. We applied models to a national EHR database (Clinical Practice Research Datalink) to obtain national estimates of each indicator for three successive years. Results: The optimal models included recorded demographics, deprivation, consultation frequency, analgesic and antidepressant prescriptions, and multimorbidity. Applying models to national EHR, we estimated that 31.9% of adults (≥35 years) presenting with non-inflammatory musculoskeletal disorders in England in 2016/17 experienced high impact chronic pain. Estimated population health levels were worse in women, older aged and those in the most deprived neighbourhoods, and changed little over 3 years. Conclusion: National and subnational estimates for a range of subjective indicators of non-inflammatory musculoskeletal health conditions can be obtained using information from routine electronic health records.
AB - Objectives: Better indicators from affordable, sustainable data sources are needed to monitor population burden of musculoskeletal conditions. We propose five indicators of musculoskeletal health and assessed if routinely available primary care electronic health records (EHR) can estimate population levels in musculoskeletal consulters. Methods: We collected validated patient-reported measures of pain experience, function and health status through a local survey of adults (≥35 years) presenting to English general practices over 12 months for low back pain, shoulder pain, osteoarthritis and other regional musculoskeletal disorders. Using EHR data we derived and validated models for estimating population levels of five self-reported indicators: prevalence of high impact chronic pain, overall musculoskeletal health (based on Musculoskeletal Health Questionnaire), quality of life (based on EuroQoL health utility measure), and prevalence of moderate-to-severe low back pain and moderate-to-severe shoulder pain. We applied models to a national EHR database (Clinical Practice Research Datalink) to obtain national estimates of each indicator for three successive years. Results: The optimal models included recorded demographics, deprivation, consultation frequency, analgesic and antidepressant prescriptions, and multimorbidity. Applying models to national EHR, we estimated that 31.9% of adults (≥35 years) presenting with non-inflammatory musculoskeletal disorders in England in 2016/17 experienced high impact chronic pain. Estimated population health levels were worse in women, older aged and those in the most deprived neighbourhoods, and changed little over 3 years. Conclusion: National and subnational estimates for a range of subjective indicators of non-inflammatory musculoskeletal health conditions can be obtained using information from routine electronic health records.
KW - back pain
KW - Electronic health records
KW - Health services research
KW - Musculoskeletal
KW - pain
KW - Primary care
KW - quality of life
KW - shoulder pain
KW - surveillance
UR - https://www.scopus.com/pages/publications/85117176866
U2 - 10.1093/rheumatology/keab109
DO - 10.1093/rheumatology/keab109
M3 - Article
C2 - 33560340
AN - SCOPUS:85117176866
SN - 1462-0324
VL - 60
SP - 4832
EP - 4843
JO - Rheumatology
JF - Rheumatology
IS - 10
ER -