4.7 Article

Estimating the population health burden of musculoskeletal conditions using primary care electronic health records

Journal

RHEUMATOLOGY
Volume 60, Issue 10, Pages 4832-4843

Publisher

OXFORD UNIV PRESS
DOI: 10.1093/rheumatology/keab109

Keywords

electronic health records; primary care; musculoskeletal; health services research; surveillance; pain; quality of life; back pain; shoulder pain

Categories

Funding

  1. Versus Arthritis [21403]
  2. National Institute for Health Research (NIHR) Oxford Biomedical Research Centre (BRC)
  3. NIHR Senior Research Fellowship [SRF2018-11-ST2-004]
  4. NIHR Biomedical Research Centre at University Hospitals Bristol and Weston NHS Foundation Trust
  5. University of Bristol
  6. MRC [MC_U147585823, MC_UU_12011/5, MC_PC_15015] Funding Source: UKRI

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By collecting patient-reported measures of pain experience, function, and health status, and utilizing routine electronic health records, it is feasible to estimate population levels of musculoskeletal patients effectively.
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.

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