Committee report: Questionnaire survey on the treatment of COVID-19 in patients receiving dialysis therapy.

Coronavirus disease 2019 Dialysis Renal replacement therapy Steroids

Journal

Renal replacement therapy
ISSN: 2059-1381
Titre abrégé: Ren Replace Ther
Pays: England
ID NLM: 101698599

Informations de publication

Date de publication:
2022
Historique:
received: 05 03 2022
accepted: 01 04 2022
entrez: 2 5 2022
pubmed: 3 5 2022
medline: 3 5 2022
Statut: ppublish

Résumé

Patients with coronavirus disease 2019 (COVID-19) who receive dialysis therapy develop more severe disease and have a poorer prognosis than patients who do not. Although various data on the treatment of patients not receiving dialysis therapy have been reported, clinical practice for patients on dialysis is challenging as data is limited. The Infection Control Committee of the Japanese Society for Dialysis Therapy decided to clarify the status of treatment in COVID-19 patients on dialysis. A questionnaire survey of 105 centers that had treated at least five COVID-19 patients on dialysis was conducted in August 2021. Sixty-six centers (62.9%) responded to the questionnaire. Antivirals were administered in 27.7% of facilities treating mild disease (most patients received favipiravir) and 66.7% of facilities treating moderate disease (most patients with moderate or more severe conditions received remdesivir). Whether and how remdesivir is administered varies between centers. Steroids were initiated most frequently in moderate II disease (50.8%), while 43.1% of the facilities initiated steroids in mild or moderate I disease. The type of steroid, dose, and the duration of administration were generally consistent, with most facilities administering dexamethasone 6 mg orally or 6.6 mg intravenously for 10 days. Steroid pulse therapy was administered in 48.5% of the facilities, and tocilizumab was administered in 25.8% of the facilities, mainly to patients on ventilators or equivalent medications, or to the cases of exacerbations. Furthermore, some facilities used a polymethylmethacrylate membrane during dialysis, nafamostat as an anticoagulant, and continuous hemodiafiltration in severe cases. There was limited experience of polymyxin B-immobilized fiber column-direct hemoperfusion and extracorporeal membrane oxygenation. The discharge criteria for patients receiving dialysis therapy were longer than those set by the Ministry of Health, Labor and Welfare in 22.7% of the facilities. Our survey revealed a variety of treatment practices in each facility. Further evidence and innovations are required to improve the prognosis of patients with COVID-19 receiving dialysis therapy.

Sections du résumé

Background UNASSIGNED
Patients with coronavirus disease 2019 (COVID-19) who receive dialysis therapy develop more severe disease and have a poorer prognosis than patients who do not. Although various data on the treatment of patients not receiving dialysis therapy have been reported, clinical practice for patients on dialysis is challenging as data is limited. The Infection Control Committee of the Japanese Society for Dialysis Therapy decided to clarify the status of treatment in COVID-19 patients on dialysis.
Methods UNASSIGNED
A questionnaire survey of 105 centers that had treated at least five COVID-19 patients on dialysis was conducted in August 2021.
Results UNASSIGNED
Sixty-six centers (62.9%) responded to the questionnaire. Antivirals were administered in 27.7% of facilities treating mild disease (most patients received favipiravir) and 66.7% of facilities treating moderate disease (most patients with moderate or more severe conditions received remdesivir). Whether and how remdesivir is administered varies between centers. Steroids were initiated most frequently in moderate II disease (50.8%), while 43.1% of the facilities initiated steroids in mild or moderate I disease. The type of steroid, dose, and the duration of administration were generally consistent, with most facilities administering dexamethasone 6 mg orally or 6.6 mg intravenously for 10 days. Steroid pulse therapy was administered in 48.5% of the facilities, and tocilizumab was administered in 25.8% of the facilities, mainly to patients on ventilators or equivalent medications, or to the cases of exacerbations. Furthermore, some facilities used a polymethylmethacrylate membrane during dialysis, nafamostat as an anticoagulant, and continuous hemodiafiltration in severe cases. There was limited experience of polymyxin B-immobilized fiber column-direct hemoperfusion and extracorporeal membrane oxygenation. The discharge criteria for patients receiving dialysis therapy were longer than those set by the Ministry of Health, Labor and Welfare in 22.7% of the facilities.
Conclusions UNASSIGNED
Our survey revealed a variety of treatment practices in each facility. Further evidence and innovations are required to improve the prognosis of patients with COVID-19 receiving dialysis therapy.

Identifiants

pubmed: 35494536
doi: 10.1186/s41100-022-00405-8
pii: 405
pmc: PMC9035500
doi:

Types de publication

Journal Article

Langues

eng

Pagination

18

Informations de copyright

© The Author(s) 2022.

Déclaration de conflit d'intérêts

Competing interestsThe authors declare that they have no competing interests.

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Auteurs

Ayumi Yoshifuji (A)

Infection Control Committee, The Japanese Society for Dialysis Therapy, Tokyo, Japan.

Munekazu Ryuzaki (M)

Infection Control Committee, The Japanese Society for Dialysis Therapy, Tokyo, Japan.
Department of Nephrology, Tokyo Saiseikai Central Hospital, 1-4-17 Mita, Minato-ku, Tokyo, 108-0073 Japan.

Yuki Uehara (Y)

Infection Control Committee, The Japanese Society for Dialysis Therapy, Tokyo, Japan.

Norio Ohmagari (N)

Infection Control Committee, The Japanese Society for Dialysis Therapy, Tokyo, Japan.

Toru Kawai (T)

Infection Control Committee, The Japanese Society for Dialysis Therapy, Tokyo, Japan.

Yoshihiko Kanno (Y)

Infection Control Committee, The Japanese Society for Dialysis Therapy, Tokyo, Japan.

Kan Kikuchi (K)

Infection Control Committee, The Japanese Society for Dialysis Therapy, Tokyo, Japan.

Hiroshi Kon (H)

Infection Control Committee, The Japanese Society for Dialysis Therapy, Tokyo, Japan.

Ken Sakai (K)

Infection Control Committee, The Japanese Society for Dialysis Therapy, Tokyo, Japan.

Toshio Shinoda (T)

Infection Control Committee, The Japanese Society for Dialysis Therapy, Tokyo, Japan.

Yaoko Takano (Y)

Infection Control Committee, The Japanese Society for Dialysis Therapy, Tokyo, Japan.

Junko Tanaka (J)

Infection Control Committee, The Japanese Society for Dialysis Therapy, Tokyo, Japan.

Kazuhiko Hora (K)

Infection Control Committee, The Japanese Society for Dialysis Therapy, Tokyo, Japan.

Yasushi Nakazawa (Y)

Infection Control Committee, The Japanese Society for Dialysis Therapy, Tokyo, Japan.

Naoki Hasegawa (N)

Infection Control Committee, The Japanese Society for Dialysis Therapy, Tokyo, Japan.

Norio Hanafusa (N)

Infection Control Committee, The Japanese Society for Dialysis Therapy, Tokyo, Japan.

Fumihiko Hinoshita (F)

Infection Control Committee, The Japanese Society for Dialysis Therapy, Tokyo, Japan.

Keita Morikane (K)

Infection Control Committee, The Japanese Society for Dialysis Therapy, Tokyo, Japan.

Shu Wakino (S)

Infection Control Committee, The Japanese Society for Dialysis Therapy, Tokyo, Japan.

Hidetomo Nakamoto (H)

Infection Control Committee, The Japanese Society for Dialysis Therapy, Tokyo, Japan.

Yoshiaki Takemoto (Y)

Infection Control Committee, The Japanese Society for Dialysis Therapy, Tokyo, Japan.

Classifications MeSH