How has the COVID-19 pandemic affected our rheumatology patients using biological/targeted DMARDs?

Semih Gulle1, Yesim Erez1, Ali Karakas1

  • 1Department of Rheumatology, Dokuz Eylul University School of Medicine, Izmir, Turkey.

Insights

During the COVID-19 pandemic, about one-fifth of inflammatory rheumatic disease patients delayed biologic or targeted synthetic disease-modifying antirheumatic drug (b/tsDMARD) treatment. However, with good patient communication, treatment was successfully restarted, showing high 12-month drug retention rates.

Area of Science:

  • Rheumatology
  • Infectious Diseases
  • Pharmacology

Background:

  • The COVID-19 pandemic significantly impacted healthcare delivery and patient management.
  • Patients with inflammatory rheumatic musculoskeletal diseases (iRMD) on b/tsDMARDs faced unique challenges and concerns regarding treatment continuity.
  • Understanding the pandemic's effects on iRMD treatment is crucial for maintaining patient health and drug efficacy.

Purpose of the Study:

  • To investigate the impact of the COVID-19 pandemic on the treatment course of iRMD patients using b/tsDMARDs.
  • To analyze treatment delays and identify factors influencing drug retention during the pandemic.
  • To assess the risk of SARS-CoV-2 infection in iRMD patients based on their treatment and comorbidities.

Main Methods:

  • A two-stage study design was employed to assess treatment delays and long-term retention.
  • Data on 521 iRMD patients were analyzed, including diagnoses (e.g., SpA, RA) and medication use (b/tsDMARDs, hydroxychloroquine, glucocorticoids).
  • Statistical analysis, including hazard ratios (HR), was used to identify factors affecting drug retention and SARS-CoV-2 infection risk.

Main Results:

  • Approximately 20% of iRMD patients on b/tsDMARDs delayed treatment in the initial 3 months of the pandemic due to COVID-19 fears.
  • Factors reducing 12-month drug retention included concurrent hydroxychloroquine use, IV bDMARD administration, and initial treatment discontinuation.
  • Glucocorticoid use and pre-existing interstitial lung disease/COPD significantly increased SARS-CoV-2 infection risk.

Conclusions:

  • Despite initial treatment delays driven by pandemic-related fears, effective patient communication facilitated treatment resumption.
  • High 12-month drug retention rates were observed, indicating the resilience of b/tsDMARD therapy in iRMD patients.
  • Identifying risk factors for SARS-CoV-2 infection is vital for protecting vulnerable iRMD patients during pandemics.
Abstract

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