TY - JOUR
T1 - COVID-19 in children treated with immunosuppressive medication for kidney diseases
AU - Marlais, Matko
AU - Wlodkowski, Tanja
AU - Al-Akash, Samhar
AU - Ananin, Petr
AU - Bandi, Varun Kumar
AU - Baudouin, Veronique
AU - Boyer, Olivia
AU - Vásquez, Luciola
AU - Govindan, Sukanya
AU - Hooman, Nakysa
AU - Ijaz, Iftikhar
AU - Loza, Reyner
AU - Melgosa, Marta
AU - Pande, Nivedita
AU - Pape, Lars
AU - Saha, Anshuman
AU - Samsonov, Dmitry
AU - Schreuder, Michiel F.
AU - Sharma, Jyoti
AU - Siddiqui, Sahar
AU - Sinha, Rajiv
AU - Stewart, Heather
AU - Tasic, Velibor
AU - Tönshoff, Burkhard
AU - Twombley, Katherine
AU - Upadhyay, Kiran
AU - Vivarelli, Marina
AU - Weaver, Donald J.
AU - Woroniecki, Robert
AU - Schaefer, Franz
AU - Tullus, Kjell
N1 - Publisher Copyright:
© Author(s) (or their employer(s)) 2021. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ.
PY - 2021/7/19
Y1 - 2021/7/19
N2 - BACKGROUND: Children are recognised as at lower risk of severe COVID-19 compared with adults, but the impact of immunosuppression is yet to be determined. This study aims to describe the clinical course of COVID-19 in children with kidney disease taking immunosuppressive medication and to assess disease severity. METHODS: Cross-sectional study hosted by the European Rare Kidney Disease Reference Network and supported by the European, Asian and International paediatric nephrology societies. Anonymised data were submitted online for any child (age <20 years) with COVID-19 taking immunosuppressive medication for a kidney condition. Study recruited for 16 weeks from 15 March 2020 to 05 July 2020. The primary outcome was severity of COVID-19. RESULTS: 113 children were reported in this study from 30 different countries. Median age: 13 years (49% male). Main underlying reasons for immunosuppressive therapy: kidney transplant (47%), nephrotic syndrome (27%), systemic lupus erythematosus (10%). Immunosuppressive medications used include: glucocorticoids (76%), mycophenolate mofetil (MMF) (54%), tacrolimus/ciclosporine A (58%), rituximab/ofatumumab (11%). 78% required no respiratory support during COVID-19 illness, 5% required bi-level positive airway pressure or ventilation. Four children died; all deaths reported were from low-income countries with associated comorbidities. There was no significant difference in severity of COVID-19 based on gender, dialysis status, underlying kidney condition, and type or number of immunosuppressive medications. CONCLUSIONS: This global study shows most children with a kidney disease taking immunosuppressive medication have mild disease with SARS-CoV-2 infection. We therefore suggest that children on immunosuppressive therapy should not be more strictly isolated than children who are not on immunosuppressive therapy.
AB - BACKGROUND: Children are recognised as at lower risk of severe COVID-19 compared with adults, but the impact of immunosuppression is yet to be determined. This study aims to describe the clinical course of COVID-19 in children with kidney disease taking immunosuppressive medication and to assess disease severity. METHODS: Cross-sectional study hosted by the European Rare Kidney Disease Reference Network and supported by the European, Asian and International paediatric nephrology societies. Anonymised data were submitted online for any child (age <20 years) with COVID-19 taking immunosuppressive medication for a kidney condition. Study recruited for 16 weeks from 15 March 2020 to 05 July 2020. The primary outcome was severity of COVID-19. RESULTS: 113 children were reported in this study from 30 different countries. Median age: 13 years (49% male). Main underlying reasons for immunosuppressive therapy: kidney transplant (47%), nephrotic syndrome (27%), systemic lupus erythematosus (10%). Immunosuppressive medications used include: glucocorticoids (76%), mycophenolate mofetil (MMF) (54%), tacrolimus/ciclosporine A (58%), rituximab/ofatumumab (11%). 78% required no respiratory support during COVID-19 illness, 5% required bi-level positive airway pressure or ventilation. Four children died; all deaths reported were from low-income countries with associated comorbidities. There was no significant difference in severity of COVID-19 based on gender, dialysis status, underlying kidney condition, and type or number of immunosuppressive medications. CONCLUSIONS: This global study shows most children with a kidney disease taking immunosuppressive medication have mild disease with SARS-CoV-2 infection. We therefore suggest that children on immunosuppressive therapy should not be more strictly isolated than children who are not on immunosuppressive therapy.
KW - nephrology
KW - virology
UR - https://www.scopus.com/pages/publications/85199813366
U2 - 10.1136/archdischild-2020-320616
DO - 10.1136/archdischild-2020-320616
M3 - Article
C2 - 33355203
AN - SCOPUS:85199813366
SN - 0003-9888
VL - 106
SP - 798
EP - 801
JO - Archives of Disease in Childhood
JF - Archives of Disease in Childhood
IS - 8
ER -