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No increased rate of SARS-CoV-2 infection for patients with inflammatory rheumatic diseases compared with the general population in the city of Hamburg (Germany)
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  1. Peer Aries1,
  2. Christof Iking-Konert2
  1. 1Rheumatologie und klinische Immunolgie, Rheumatologie im Struenseehaus, Hamburg, Germany
  2. 2Nephrology and Rheumatology, Department of Medicine III, University of Hamburg Faculty of Medicine, Hamburg, Germany
  1. Correspondence to Dr Christof Iking-Konert, Nephrology and Rheumatology, Department of Medicine III, University of Hamburg Faculty of Medicine, Hamburg 20146, Germany; c.iking-konert{at}uke.de

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We highly appreciated the work on the paper by Gianfrancesco et al.1 While this large international registry provides information, for example, about the course of the disease in regard to the intensity of immunosuppression or complications, they do not allow any conclusions about the actual incidence rate of infections in patients with rheumatic diseases compared with the overall population. In addition to the data by Gianfrancesco et al we here like to share our data and experience of the Hamburg COVID-19 registry.

Until 9 June 2020, a total of 5120 proven severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infections were reported in Hamburg.2 This corresponds to 0.28% of the total population of the city of Hamburg (1.814 million inhabitants), with a reported mortality rate of 4.4% (in total 226 patients).

With the beginning of the COVID-19 pandemic we initiated a SARS-CoV-2 registry, where all reported COVID cases were documented anonymously by all rheumatologists of the city of Hamburg. In total, 11 771 patients were prescribed any disease-modifying antirheumatic drug (DMARD) during this period. Of these, a total of 30 (0.25%) patients had a clinically tested SARS-CoV-2 infection (clinical symptoms and SARS-CoV-2 PCR and/or IgG positive). Three out of 30 patients with rheumatic diseases (10%) were treated with severe disease in intensive care unit, in contrast to 4.4% of patients with COVID of the general population. So far, no deaths were reported in our cohort (mortality rate 0%) (see table 1).

Table 1

Number of SARS-Cov-2 infections, ICU admissions and death in the general population compared to DMARD treated patients as well as calculated incidences

In analogy to the COVID-19 Global Rheumatology Alliance registry, our cohort found no evidence that individual rheumatological diseases lead to a higher risk for or a severe course of infection. Additionally, so far, no accumulation of infection among one of the therapy groups (conventional synthetic DMARD, biological DMARD or targeted synthetic DMARD) was apparent.1

To the best of our knowledge, this is the largest population-based study to date in this particular risk group. We consider the risk of unreported cases for the group of the general population comparable with that for the patients with rheumatic diseases.

In summary, patients with rheumatic diseases and under DMARD therapy do not seem to have a higher risk of a SARS-CoV-2 infection.

Additionally, in this cohort patients with rheumatic diseases did not have a higher rate of a severe course of SARS-CoV-2 infection.

Acknowledgments

We would like to thank all rheumatologists of the Rheumazentrum Hamburg who participated in the register.

References

Footnotes

  • Collaborators K Ahmadi, A von Alt Stutterheim, E Barth, H Bisinger, P Bremer, S El-Nawab-Becker, A Gödde, H Heintz, M Janneck, S Kahl, M Kern, B Panzer, C Platzek, L Roth, M Schaposchnikow, A Schiewek-Güsmer, U Schnoor, S Tatzis, H Tremel, B. Varoga, J. Veigel, W. Winter, J Wollenhaupt.

  • Contributors Both authors contributed equally in collecting and analysing the data as well as in writing the manuscript.

  • Funding The authors have not declared a specific grant for this research from any funding agency in the public, commercial or not-for-profit sectors.

  • Competing interests None declared.

  • Patient and public involvement Patients and/or the public were not involved in the design, or conduct, or reporting, or dissemination plans of this research.

  • Patient consent for publication Not required.

  • Provenance and peer review Not commissioned; internally peer reviewed.

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