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Comorbidities and use of analgesics in people with knee pain: a study in the Nottingham Knee Pain and Health in the Community (KPIC) cohort.
Swain, Subhashisa; Fernandes, Gwen Sascha; Sarmanova, Aliya; Valdes, Ana M; Walsh, David A; Coupland, Carol; Doherty, Michael; Zhang, Weiya.
Afiliación
  • Swain S; Academic Rheumatology, School of Medicine, University of Nottingham, Nottingham City Hospital.
  • Fernandes GS; Population Health Sciences, Bristol Medical School, University of Bristol, Bristol.
  • Sarmanova A; Population Health Sciences, Bristol Medical School, University of Bristol, Bristol.
  • Valdes AM; Academic Rheumatology, School of Medicine, University of Nottingham, Nottingham City Hospital.
  • Walsh DA; Academic Rheumatology, School of Medicine, University of Nottingham, Nottingham City Hospital.
  • Coupland C; Centre for Academic Primary Care, School of Medicine, University of Nottingham, Nottingham, UK.
  • Doherty M; Academic Rheumatology, School of Medicine, University of Nottingham, Nottingham City Hospital.
  • Zhang W; Academic Rheumatology, School of Medicine, University of Nottingham, Nottingham City Hospital.
Rheumatol Adv Pract ; 6(2): rkac049, 2022.
Article en En | MEDLINE | ID: mdl-35784017
ABSTRACT

Objectives:

The aims were to examine the prevalence of comorbidities and role of oral analgesic use in people with knee pain (KP) compared with those without.

Methods:

The Knee Pain and related health In the Community (KPIC) cohort comprises community-derived adults aged ≥40 years, irrespective of knee pain. Thirty-six comorbidities across 10 systems were compared between people with KP and controls without KP or knee OA. Multivariable logistic regression analysis was used to determine the adjusted odds ratio (aOR) and 95% CI for multimorbidity (at least two chronic conditions) and each specific comorbidity. Both prescribed and over-the-counter analgesics were included in the model, and their interactions with KP for comorbidity outcomes were examined.

Results:

Two thousand eight hundred and thirty-two cases with KP and 2518 controls were selected from 9506 baseline participants. The mean age of KP cases was 62.2 years, and 57% were women. Overall, 29% of the total study population had multimorbidity (KP cases 34.4%; controls 23.8%). After adjustment for age, sex, BMI and analgesic use, KP was significantly associated with multimorbidity (aOR 1.35; 95% CI 1.17, 1.56) and with cardiovascular (aOR 1.25; 95% CI 1.08, 1.44), gastrointestinal (aOR 1.34; 95% CI 1.04, 1.92), chronic widespread pain (aOR 1.54; 95% CI 1.29, 1.86) and neurological (aOR 1.32; 95% CI 1.01, 1.76) comorbidities. For multimorbidity, the use of paracetamol and opioids interacted positively with KP, whereas the use of NSAIDs interacted negatively for seven comorbidities.

Conclusion:

People with KP are more likely to have other chronic conditions. The long-term benefits and harms of this change remain to be investigated. Trial registration ClinicalTrials.gov, http//clinicaltrials.gov, NCT02098070.
Palabras clave

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Tipo de estudio: Etiology_studies / Risk_factors_studies Idioma: En Revista: Rheumatol Adv Pract Año: 2022 Tipo del documento: Article

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Tipo de estudio: Etiology_studies / Risk_factors_studies Idioma: En Revista: Rheumatol Adv Pract Año: 2022 Tipo del documento: Article