Spondyloarthritis & psoriatic arthritis

High burden of polypharmacy and comorbidity in persons with psoriatic arthritis: an analysis of claims data, stratified by age and sex

RMD OpenPublished Cross-sectional study

Authors' conclusion

Polypharmacy is common in PsA and is composed of PsA-specific medication as well as frequent medications for comorbidities, equally affecting women and men.

Study context

Population
Persons with psoriatic arthritis (PsA) on DMARD therapy in 2021, German BARMER health insurance database
Exposure
PsA on DMARD therapy vs sex- and age-matched controls without inflammatory arthritis
  • PsAn = 11,984
Outcome
Polypharmacy (≥5 concomitant drugs)
Methodological detailsclaims data analysis, sex-matched and age-matched controls, linear regression model
  • Claims data analysis
  • Sex-matched and age-matched controls
  • Linear regression model

Main finding

As reported in the abstract

Observational data: associations, not effects.

Further findings

OutcomePsADifference (units) (95% CI)
Number of medicationsWomenmean 4.9 (SD 2.8)2.4 (2.34–2.43)
Number of medicationsMen2.3 (2.21–2.35)
  • Polypharmacy in PsA by sex: Women 52%
  • Polypharmacy in PsA by sex: Men 45%

Polypharmacy in PsA by sex

Polypharmacy strongly increased with age and comorbidity

Anatomical Therapeutic Chemical (ATC) drug classes, PsA vs controls

Musculoskeletal drugs, PsA vs controls
81% vs 30%
Immunomodulatory drugs, PsA vs controls
56% vs 2.6%
Cardiovascular drugs, PsA vs controls
62% vs 48%
Alimentary tract/metabolic drugs, PsA vs controls
57% vs 31%
Nervous system drugs, PsA vs controls
50% vs 31%
  • All ATC drug classes significantly more frequent in PsA

Age-adjusted increase in number of medications per unit increase of Rheumatic Disease Comorbidity Index (RDCI)

Men
0.98 (95% CI 0.95 to 1.01)
Women
0.93 (95% CI 0.90 to 0.96)

Original publication

High burden of polypharmacy and comorbidity in persons with psoriatic arthritis: an analysis of claims data, stratified by age and sex. RMD Open. Published 9 March 2023. doi:10.1136/rmdopen-2022-002960

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