Department of Pediatrics and Adolescent Medicine, Ulm University Medical Center, Eythstrasse 24, 89075, Ulm, Germany.
Department of Pediatrics, Medizinische Fakultät Carl Gustav Carus, Technische Universität Dresden, Dresden, Germany.
Rheumatol Int. 2021 May;41(5):911-920. doi: 10.1007/s00296-021-04824-4. Epub 2021 Mar 8.
Data on therapy of COVID-19 in immunocompetent and immunosuppressed children are scarce. We aimed to explore management strategies of pediatric rheumatologists. All subscribers to international Pediatric Rheumatology Bulletin Board were invited to take part in an online survey on therapeutic approaches to COVID-19 in healthy children and children with autoimmune/inflammatory diseases (AID). Off-label therapies would be considered by 90.3% of the 93 participating respondents. In stable patients with COVID-19 on oxygen supply (stage I), use of remdesivir (48.3%), azithromycin (26.6%), oral corticosteroids (25.4%) and/or hydroxychloroquine (21.9%) would be recommended. In case of early signs of "cytokine storm" (stage II) or in critically ill patients (stage III) (a) anakinra (79.5% stage II; 83.6% stage III) or tocilizumab (58.0% and 87.0%, respectively); (b) corticosteroids (oral 67.2% stage II, intravenously 81.7% stage III); (c) intravenous immunoglobulins (both stages 56.5%); or (d) remdesivir (both stages 46.7%) were considered. In AID, > 94.2% of the respondents would not support a preventive adaptation of the immunomodulating therapy. In case of mild COVID-19, more than 50% of the respondents would continue pre-existing treatment with immunoglobulins (100%), hydroxychloroquine (94.2%), anakinra (79.2%) or canakinumab (72.5%), or tocilizumab (69.8%). Long-term corticosteroids would be reduced by 26.9% (< = 2 mg/kg/d) and 50.0% (> 2 mg/kg/day), respectively, with only 5.8% of respondents voting to discontinue the therapy. Conversely, more than 75% of respondents would refrain from administering cyclophosphamide and anti-CD20-antibodies. As evidence on management of pediatric COVID-19 is incomplete, continuous and critical expert opinion and knowledge exchange is helpful.
免疫功能正常和免疫抑制儿童的 COVID-19 治疗数据很少。我们旨在探索儿科风湿病学家的管理策略。邀请国际儿科风湿病学公告板的所有订阅者参加一项关于健康儿童和自身免疫性/炎症性疾病(AID)儿童 COVID-19 治疗方法的在线调查。93 名参与调查的受访者中有 90.3%会考虑使用未经批准的治疗方法。对于接受氧气供应的 COVID-19 稳定患者(I 期),建议使用瑞德西韦(48.3%)、阿奇霉素(26.6%)、口服皮质类固醇(25.4%)和/或羟氯喹(21.9%)。如果出现“细胞因子风暴”早期迹象(II 期)或危重症患者(III 期)(a)使用阿那白滞素(79.5%II 期;83.6%III 期)或托珠单抗(58.0%和 87.0%,分别);(b)皮质类固醇(口服 67.2%II 期,静脉内 81.7%III 期);(c)静脉内免疫球蛋白(两个阶段均为 56.5%);或(d)瑞德西韦(两个阶段均为 46.7%)。在 AID 中,超过 94.2%的受访者不支持预防性调整免疫调节治疗。在 COVID-19 轻症的情况下,超过 50%的受访者会继续进行免疫球蛋白(100%)、羟氯喹(94.2%)、阿那白滞素(79.2%)或卡那单抗(72.5%)或托珠单抗(69.8%)的现有治疗。长期皮质类固醇将分别减少 26.9%(< = 2mg/kg/d)和 50.0%(> 2mg/kg/d),只有 5.8%的受访者投票决定停止治疗。相反,超过 75%的受访者会避免使用环磷酰胺和抗 CD20 抗体。由于儿科 COVID-19 管理的证据不完整,因此持续和关键的专家意见和知识交流是有帮助的。