Pre-existing musculoskeletal pain and its association with mortality in newly diagnosed co-morbid conditions: an electronic health record cohort study

Author:

Marshall Michelle1ORCID,Mason Kayleigh J1ORCID,Edwards John J1ORCID,Mamas Mamas A2,Bailey James1,Heron Neil13,Achana Felix A4,Frisher Martin5,Huntley Alyson L6,Mallen Christian D1ORCID,Png May Ee4,Tatton Stephen1,White Simon5ORCID,Jordan Kelvin P1ORCID

Affiliation:

1. Centre for Musculoskeletal Health Research, School of Medicine, Keele University , Keele, UK

2. Keele Cardiovascular Research Group, Centre for Prognosis Research, Keele University , Keele, UK

3. Centre for Public Health, Queen’s University Belfast , Belfast, UK

4. Nuffield Department of Primary Care Health Sciences, Oxford University , Oxford, UK

5. School of Pharmacy and Bioengineering, Keele University , Keele, UK

6. Centre for Academic Primary Care, Bristol Medical School, Bristol University , Bristol, UK

Abstract

Abstract Objective Musculoskeletal pain is a common risk factor for co-morbid conditions and might increase the risk of poor outcomes. The objective was to determine whether patients with pre-existing musculoskeletal pain have an increased risk for mortality following a new diagnosis of a co-morbid condition. Methods Patients aged ≥45 years with a new diagnosis of acute coronary syndrome (ACS), stroke, cancer, dementia or pneumonia recorded in a UK electronic primary care database linked to hospital and mortality records were examined. The association of mortality with musculoskeletal pain (inflammatory conditions, OA and regional pain) was determined. Results The sample size varied from 128 649 (stroke) to 406 289 (cancer) by cohort, with 22–31% having pre-existing musculoskeletal conditions. In the ACS cohort, there was a higher rate of mortality for all musculoskeletal types. There were also higher unadjusted mortality rates in patients with inflammatory arthritis compared with those without musculoskeletal pain in the stroke, cancer and dementia cohorts and for patients with OA in the stroke and cancer cohorts. After adjustment for the number of prescribed medications and age, the increased risk of mortality remained only for patients with inflammatory arthritis in the ACS cohort (adjusted hazard ratio = 1.07; 95% CI 1.03, 1.10). Conclusion Older adults with inflammatory arthritis and OA have increased risk of mortality when they develop a new condition, which seems to be related to the prescription of multiple medicines. Pre-existing musculoskeletal pain is an indicator of a complex patient who is at risk of poorer outcomes at the onset of new illnesses.

Funder

Nuffield Foundation

Publisher

Oxford University Press (OUP)

Subject

Rheumatology

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