Article Text
Abstract
Objectives To investigate how the first wave of COVID-19 pandemic influenced decisions of rheumatologists and health professionals in rheumatology regarding the management of patients with inflammatory rheumatic and musculoskeletal diseases (RMDs).
Methods An English-language questionnaire was developed by a EULAR working group and distributed via national rheumatology societies of EULAR countries, EMEUNET and individual working group members. Responses were collected using an online survey tool. Descriptive statistics were calculated.
Results We analysed 1286 responses from 35/45 EULAR countries. Due to containment measures, 82% of respondents indicated cancellation/postponement of face-to-face visits of new patients (84% of them offering remote consultation) and 91% of follow-up visits (96% with remote consultation). The majority of respondents (58%) perceived that the interval between symptom onset and first rheumatological consultations was longer during containment restrictions than before. Treatment decisions were frequently postponed (34%), and the majority (74%) of respondents stated that it was less likely to start a biological disease modifying anti-rheumatic drug (DMARD)/targeted synthetic DMARD during the pandemic, mainly because of patients’ fear, limited availability of screening procedures and decreased availability of rheumatological services. Use of (hydroxy)chloroquine (HCQ) and tocilizumab (TCZ) for the COVID-19 indication was reported by 47% and 42% of respondents, respectively, leading to a shortage of these drugs for RMDs indications according to 49% and 14% of respondents, respectively.
Conclusion Measures related to containment of COVID-19 pandemic led to a perceived delay between symptom onset and a first rheumatological visit, postponement of treatment decisions, and shortage of HCQ and TCZ, thereby negatively impacting early treatment and treat-to-target strategies.
- epidemiology
- arthritis
- rheumatoid
- autoimmune diseases
- health services research
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Footnotes
Handling editor Désirée van der Heijde
Twitter @pedrommcmachado, @FranciscaSivera
Contributors All authors designed the study and contributed to data collection. CD analysed the data and drafted the first version of the manuscript. All coauthors critically interpreted the results, discussed the findings together, critically reviewed the manuscript and approved its final version.
Funding This study was funded by the European League against Rheumatism (EULAR), project number EPI025.
Competing interests CD received consulting/speaker’s fees from Abbvie, Eli Lilly, Janssen, Novartis, Pfizer, Roche and Sanofi, all unrelated to this manuscript. AA has nothing to disclose. JWJB received honoraria from Lilly, Roche, Abbvie, Galapagos, SUN all unrelated to this manuscript. AB received research granst form Abbvie and Celgene, and consultation/speakers fees from Eli Lilly, Novartis, UCB and Galapagos all to here department and all unrelated to this manuscript. BC received honoraria from AbbVie; BMS; Gilead; Janssen; Lilly; Merck; Novartis; Pfizer; Roche-Chugai; Sanofi; and research grants from Novartis, Pfizer and Roche; all unrelated to this manuscript. AF has nothing to disclose. PMM received consulting/speaker’s fees from Abbvie, BMS, Celgene, Eli Lilly, Janssen, MSD, Novartis, Pfizer, Roche and UCB, all unrelated to this manuscript. IP received honoraria from Novartis, Sanofi, Abbvie, Sandoz and Roche, all unrelated to this manuscript. FS has nothing to disclose. TAS has nothing to disclose. FB received consulting/speaker’s fees from Abbvie, Lilly, Horizontherapeutics, Pfizer and Roche/Chugai, all unrelated to this manuscript.
Patient consent for publication Not required.
Provenance and peer review Not commissioned; externally peer reviewed.
Data availability statement Data are available upon reasonable request. The data will be shared if there is a reasonable request for it.
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