Preferences of inflammatory arthritis patients for biological disease-modifying antirheumatic drugs in the first 100 days of the COVID-19 pandemic

dc.contributor.authorKalyoncu, Umut
dc.contributor.authorPehlivan, Yavuz
dc.contributor.authorAkar, Servet
dc.contributor.authorKasifoglu, Timucin
dc.contributor.authorKimyon, Gezmis
dc.contributor.authorKaradag, Omer
dc.contributor.authorKiraz, Sedat
dc.date.accessioned2026-08-12T17:19:48Z
dc.date.issued2021
dc.departmentFırat Üniversitesi
dc.description.abstractBackground/aim: To evaluate treatment adherence and predictors of drug discontinuation among patients with inflammatory arthritis receiving bDMARDs within the first 100 days after the announcement of the COVID-19 pandemic. Materials and methods: A total of 1871 patients recorded in TReasure registry for whom advanced therapy was prescribed for rheumatoid arthritis (RA) or spondyloarthritis (SpA) within the 3 months (6-9 months for rituximab) before the declaration of COVID-19 pandemic were evaluated, and 1394 (74.5%) responded to the phone survey. Patients' data regarding demographic, clinical characteristics and disease activity before the pandemic were recorded. The patients were inquired about the diagnosis of COVID-19, the rate of continuation on bDMARDs, the reasons for treatment discontinuation, if any, and the current general disease activity (visual analog scale, [VAS]). Results: A total of 1394 patients (493 RA [47.3% on anti-TNF] patients and 901 SpA [90.0% on anti-TNF] patients) were included in the study. Overall, 2.8% of the patients had symptoms suggesting COVID-19, and 2 (0.15%) patients had PCR-confirmed COVID-19. Overall, 18.1% of all patients (13.8% of the RA and 20.5% of the SpA; p = 0.003) discontinued their bDMARDs. In the SpA group, the patients who discontinued bDMARDs were younger (40 [21-73] vs. 44 years [20-79]; p = 0.005) and had higher general disease activity; however, no difference was relevant for RA patients. Conclusion: Although the COVID-19 was quite uncommon in the first 100 days of the pandemic, nearly one-fifth of the patients discontinued bDMARDs within this period. The long-term effects of the pandemic should be monitored.
dc.description.sponsorshipHacettepe Rheumatology Society
dc.description.sponsorshipUK received honorary from Abbvie, Amgen, Johnson and Johnson, MSD, Novartis, Pfizer, Roche, UCB. YP received honorary from Abbvie, Roche, Novartis, MSD, Pfizer. SA received honorary from Abbvie, Amgen, MSD, Novartis, Pfizer, Roche, UCB. TK received honorary from Abbvie, Amgen, MSD, Novartis, Pfizer, Roche, UCB. GK received honorary from Abbvie, Amgen, Novartis, Pfizer, UCB. OK received honorary from Amgen, Johnson and Johnson, MSD, Novartis, Pfizer, Roche, UCB. ED received honorary from Abbvie, Amgen, Johnson and Johnson, MSD, Novartis, Pfizer, Roche, UCB. IE received honorary from Abbvie, Amgen, Johnson and Johnson, MSD, Novartis, Pfizer, Roche, UCB. LK received honorary from Abbvie, Amgen, MSD, Novartis, Pfizer, Roche, UCB. DE received honorary from Abbvie, Amgen, MSD, Novartis, Pfizer, UCB. CB received honorary from Abbvie, Amgen, MSD, Novartis, Pfizer, Roche, UCB. HE received honorary from Novartis, Roche. RM received honorary from Abbvie, Amgen, MSD, Novartis, Pfizer, Roche, UCB. NK received honorary from Novartis, UCB. MC received honorary from Abbvie, Amgen, MSD, Novartis, Pfizer, Roche, UCB. SSK received honorary from Abbvie, MSD, Novartis, Pfizer, Roche, UCB. OK received honorary from Amgen, Johnson and Johnson, MSD, Novartis, Pfizer, Roche, UCB. SK received honorary from Abbvie, Amgen, Johnson and Johnson, MSD, Novartis, Pfizer, Roche, UCB. Other authors declare no conflict of interest. This study was funded by Hacettepe Rheumatology Society.
dc.identifier.doi10.3906/sag-2012-5
dc.identifier.endpage1623
dc.identifier.issn1300-0144
dc.identifier.issn1303-6165
dc.identifier.issue4
dc.identifier.orcid0000-0002-2260-4660
dc.identifier.orcid0000-0002-3443-3117
dc.identifier.orcid0000-0002-3734-1242
dc.identifier.orcid0000-0003-3775-639X
dc.identifier.orcid0000-0003-4530-2304
dc.identifier.orcid0000-0002-6990-4206
dc.identifier.orcid0000-0001-6172-7762
dc.identifier.pmid33611869
dc.identifier.scopus2-s2.0-85114289836
dc.identifier.scopusqualityQ2
dc.identifier.startpage1615
dc.identifier.trdizinid479713
dc.identifier.urihttps://doi.org/10.3906/sag-2012-5
dc.identifier.urihttps://search.trdizin.gov.tr/tr/yayin/detay/479713
dc.identifier.urihttps://hdl.handle.net/11508/53327
dc.identifier.volume51
dc.identifier.wosWOS:000691544700002
dc.identifier.wosqualityQ3
dc.indekslendigikaynakWeb of Science
dc.indekslendigikaynakScopus
dc.indekslendigikaynakTR-Dizin
dc.indekslendigikaynakPubMed
dc.language.isoen
dc.publisherTubitak Scientific & Technological Research Council Turkey
dc.relation.ispartofTurkish Journal of Medical Sciences
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı
dc.rightsinfo:eu-repo/semantics/openAccess
dc.snmzKA_WoS_20260511
dc.subjectCOVID-19
dc.subjectbiologic DMARDs
dc.subjectrheumatoid arthritis
dc.subjectspondyloarthritis
dc.titlePreferences of inflammatory arthritis patients for biological disease-modifying antirheumatic drugs in the first 100 days of the COVID-19 pandemic
dc.typeArticle

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