Treatment of Multisystem Inflammatory Syndrome in Children

被引:251
作者
McArdle, Andrew J. [1 ]
Vito, Ortensia [1 ]
Patel, Harsita [1 ]
Seaby, Eleanor G. [1 ,5 ,6 ]
Shah, Priyen [1 ]
Wilson, Clare [1 ]
Broderick, Claire [1 ]
Nijman, Ruud [1 ,3 ]
Tremoulet, Adriana H. [7 ,8 ]
Munblit, Daniel [2 ,9 ]
Ulloa-Gutierrez, Rolando [10 ]
Carter, Michael J. [4 ]
De, Tisham [1 ]
Hoggart, Clive [11 ]
Whittaker, Elizabeth [1 ,3 ]
Herberg, Jethro A. [3 ]
Kaforou, Myrsini [1 ]
Cunnington, Aubrey J. [1 ,3 ]
Levin, Michael [1 ,3 ]
机构
[1] Imperial Coll London, Dept Infect Dis, Sect Pediat Infect Dis, London, England
[2] Imperial Coll London, Natl Heart & Lung Inst, Fac Med, Inflammat Repair & Dev Sect, London, England
[3] Imperial Coll Healthcare NHS Trust, Dept Pediat, London, England
[4] Kings Coll London, St Thomas Hosp, Sch Life Course Sci, Dept Women & Childrens Hlth, London, England
[5] Univ Southampton, Genom Informat Grp, Southampton, Hants, England
[6] Broad Inst MIT & Harvard, Translat Genom Grp, Cambridge, MA 02142 USA
[7] Univ Calif San Diego, Dept Pediat, San Diego, CA 92103 USA
[8] Rady Childrens Hosp, San Diego, CA USA
[9] Sechenov Univ, Dept Pediat & Pediat Infect Dis, Moscow, Russia
[10] Hosp Nacl Ninos Dr Carlos Saenz Herrera, Ctr Ciencias Med, Serv Infectol, Caja Costarricense Seguro Social, San Jose, Costa Rica
[11] Icahn Sch Med Mt Sinai, Dept Genet & Genom Sci, New York, NY 10029 USA
基金
英国惠康基金; 英国医学研究理事会; 美国国家卫生研究院; 欧盟地平线“2020”;
关键词
ACUTE RESPIRATORY SYNDROME; KAWASAKI-LIKE DISEASE; TOXIC-SHOCK-SYNDROME; MANAGEMENT; OUTCOMES;
D O I
10.1056/NEJMoa2102968
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
BACKGROUND Evidence is urgently needed to support treatment decisions for children with multisystem inflammatory syndrome (MIS-C) associated with severe acute respiratory syndrome coronavirus 2. METHODS We performed an international observational cohort study of clinical and outcome data regarding suspected MIS-C that had been uploaded by physicians onto a Web-based database. We used inverse-probability weighting and generalized linear models to evaluate intravenous immune globulin (IVIG) as a reference, as compared with IVIG plus glucocorticoids and glucocorticoids alone. There were two primary outcomes: the first was a composite of inotropic support or mechanical ventilation by day 2 or later or death; the second was a reduction in disease severity on an ordinal scale by day 2. Secondary outcomes included treatment escalation and the time until a reduction in organ failure and inflammation. RESULTS Data were available regarding the course of treatment for 614 children from 32 countries from June 2020 through February 2021; 490 met the World Health Organization criteria for MIS-C. Of the 614 children with suspected MIS-C, 246 received primary treatment with IVIG alone, 208 with IVIG plus glucocorticoids, and 99 with glucocorticoids alone; 22 children received other treatment combinations, including biologic agents, and 39 received no immunomodulatory therapy. Receipt of inotropic or ventilatory support or death occurred in 56 patients who received IVIG plus glucocorticoids (adjusted odds ratio for the comparison with IVIG alone, 0.77; 95% confidence interval [CI], 0.33 to 1.82) and in 17 patients who received glucocorticoids alone (adjusted odds ratio, 0.54; 95% CI, 0.22 to 1.33). The adjusted odds ratios for a reduction in disease severity were similar in the two groups, as compared with IVIG alone (0.90 for IVIG plus glucocorticoids and 0.93 for glucocorticoids alone). The time until a reduction in disease severity was similar in the three groups. CONCLUSIONS We found no evidence that recovery from MIS-C differed after primary treatment with IVIG alone, IVIG plus glucocorticoids, or glucocorticoids alone, although significant differences may emerge as more data accrue.
引用
收藏
页码:11 / 22
页数:12
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