Nonsteroidal Antiinflammatory Drugs and Susceptibility to COVID‐19

Objective To identify whether active use of nonsteroidal antiinflammatory drugs (NSAIDs) increases susceptibility to developing suspected or confirmed coronavirus disease 2019 (COVID‐19) compared to the use of other common analgesics. Methods We performed a propensity score–matched cohort study with...

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Published inArthritis & rheumatology (Hoboken, N.J.) Vol. 73; no. 5; pp. 731 - 739
Main Authors Chandan, Joht Singh, Zemedikun, Dawit Tefra, Thayakaran, Rasiah, Byne, Nathan, Dhalla, Samir, Acosta‐Mena, Dionisio, Gokhale, Krishna M., Thomas, Tom, Sainsbury, Christopher, Subramanian, Anuradhaa, Cooper, Jennifer, Anand, Astha, Okoth, Kelvin O., Wang, Jingya, Adderley, Nicola J., Taverner, Thomas, Denniston, Alastair K., Lord, Janet, Thomas, G. Neil, Buckley, Christopher D., Raza, Karim, Bhala, Neeraj, Nirantharakumar, Krishnarajah, Haroon, Shamil
Format Journal Article
LanguageEnglish
Published United States Wiley Subscription Services, Inc 01.05.2021
John Wiley and Sons Inc
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Summary:Objective To identify whether active use of nonsteroidal antiinflammatory drugs (NSAIDs) increases susceptibility to developing suspected or confirmed coronavirus disease 2019 (COVID‐19) compared to the use of other common analgesics. Methods We performed a propensity score–matched cohort study with active comparators, using a large UK primary care data set. The cohort consisted of adult patients age ≥18 years with osteoarthritis (OA) who were followed up from January 30 to July 31, 2020. Patients prescribed an NSAID (excluding topical preparations) were compared to those prescribed either co‐codamol (paracetamol and codeine) or co‐dydramol (paracetamol and dihydrocodeine). A total of 13,202 patients prescribed NSAIDs were identified, compared to 12,457 patients prescribed the comparator drugs. The primary outcome measure was the documentation of suspected or confirmed COVID‐19, and the secondary outcome measure was all‐cause mortality. Results During follow‐up, the incidence rates of suspected/confirmed COVID‐19 were 15.4 and 19.9 per 1,000 person‐years in the NSAID‐exposed group and comparator group, respectively. Adjusted hazard ratios for suspected or confirmed COVID‐19 among the unmatched and propensity score–matched OA cohorts, using data from clinical consultations in primary care settings, were 0.82 (95% confidence interval [95% CI] 0.62–1.10) and 0.79 (95% CI 0.57–1.11), respectively, and adjusted hazard ratios for the risk of all‐cause mortality were 0.97 (95% CI 0.75–1.27) and 0.85 (95% CI 0.61–1.20), respectively. There was no effect modification by age or sex. Conclusion No increase in the risk of suspected or confirmed COVID‐19 or mortality was observed among patients with OA in a primary care setting who were prescribed NSAIDs as compared to those who received comparator drugs. These results are reassuring and suggest that in the absence of acute illness, NSAIDs can be safely prescribed during the ongoing pandemic.
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The views expressed are those of the authors and not necessarily those of the MRC, Arthritis Research UK, or Health Data Research UK.
Drs. Chandan, Zemedikun, and Thayakaran contributed equally to this work. Drs. Raza, Bhala, Nirantharakumar, and Haroon contributed equally to this work.
Supported in part by the MRC‐ARUK Centre for Musculoskeletal Ageing Research. Drs. Lord, Buckley, and Raza’s work was supported in part by the NIHR Birmingham Biomedical Research Centre. Dr. Nirantharakumar’s work was supported by Health Data Research UK.
No potential conflicts of interest relevant to this article were reported.
ISSN:2326-5191
2326-5205
DOI:10.1002/art.41593