Kawasaki Disease in the Time of COVID-19 and MIS-C: The International Kawasaki Disease Registry

被引:9
作者
Harahsheh, Ashraf S. [1 ,2 ,26 ,27 ,28 ]
Shah, Samay [3 ]
Dallaire, Frederic [4 ,5 ]
Manlhiot, Cedric [6 ]
Khoury, Michael [7 ]
Lee, Simon [8 ]
Fabi, Marianna [9 ]
Mauriello, Daniel [10 ]
Tierney, Elif Seda Selamet [11 ]
Sabati, Arash A. [12 ]
Dionne, Audrey [13 ]
Dahdah, Nagib [14 ]
Choueiter, Nadine [15 ]
Thacker, Deepika [16 ]
Giglia, Therese M. [17 ]
Truong, Dongngan T. [18 ,19 ]
Jain, Supriya [20 ]
Portman, Michael [21 ]
Orr, William B. [22 ]
Harris, Tyler H. [23 ]
Szmuszkovicz, Jacqueline R. [24 ]
Farid, Pedrom [25 ]
McCrindle, Brian W. [25 ]
机构
[1] Childrens Natl Hosp, Dept Pediat, Div Cardiol, Washington, DC USA
[2] George Washington Univ, Sch Med & Hlth Sci, Washington, DC USA
[3] George Washington Univ, Sch Med & Hlth Sci, Washington, DC USA
[4] Univ Sherbrooke, Dept Paediat, Sherbrooke, PQ, Canada
[5] Univ Sherbrooke, Ctr Rech Ctr Hosp, Sherbrooke, PQ, Canada
[6] Johns Hopkins Univ, Blalock Taussig Thomas Congenital Heart Ctr, Baltimore, MD USA
[7] Univ Alberta, Dept Paediat, Div Paediat Cardiol, Edmonton, AB, Canada
[8] Nationwide Childrens Hosp, Heart Ctr, Columbus, OH USA
[9] IRCCS Azienda Osped Univ Bologna, Paediat Emergency Unit, Bologna, Italy
[10] Johns Hopkins All Childrens Hosp, St Petersburg, FL USA
[11] Stanford Univ, Lucile Packard Childrens Hosp, Dept Pediat, Div Cardiol,Med Ctr, Palo Alto, CA USA
[12] Phoenix Childrens Hosp, Phoenix, AZ USA
[13] Harvard Med Sch, Boston Childrens Hosp, Boston, MA USA
[14] Univ Montreal, CHU Ste Justine, Div Paediat Cardiol, Montreal, PQ, Canada
[15] Albert Einstein Coll Med, Childrens Hosp Montefiore, Bronx, NY USA
[16] Nemours Childrens Hosp, Wilmington, DE USA
[17] Childrens Hosp Philadelphia, Philadelphia, PA USA
[18] Univ Utah, Salt Lake City, UT USA
[19] Primary Childrens Med Ctr, Salt Lake City, UT USA
[20] Maria Fareri Childrens Hosp, New York Med Coll, Westchester Med Ctr, Valhalla, NY USA
[21] Seattle Childrens Hosp, Seattle, WA USA
[22] Washington Univ, Sch Med, Dept Pediat, Div Pediat Cardiol, St Louis, MO USA
[23] UPMC Childrens Hosp Pittsburgh, Pittsburgh, PA USA
[24] Childrens Hosp Los Angeles, Los Angeles, CA USA
[25] Univ Toronto, Hosp Sick Children, Labatt Family Heart Ctr, Dept Pediat, Toronto, ON, Canada
[26] George Washington Univ, Sch Med & Hlth Sci, Dept Pediat, Washington, DC 20010 USA
[27] Childrens Natl Hosp, Div Cardiol, Washington, DC 20010 USA
[28] 111 Michigan Ave NW, Washington, DC 20010 USA
关键词
MULTISYSTEM INFLAMMATORY SYNDROME; RISK-FACTORS; CHILDREN; MANAGEMENT;
D O I
10.1016/j.cjca.2023.06.001
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background: Patients with multisystem inflammatory syndrome in children (MIS -C) and Kawasaki disease (KD) have overlapping clinical features. We compared demographics, clinical presentation, management, and outcomes of patients according to evidence of previous SARS-CoV-2 infection. Methods: The International Kawasaki Disease Registry (IKDR) enrolled KD and MIS -C patients from sites in North, Central, and South America, Europe, Asia, and the Middle East. Evidence of previous infection was defined as: Positive (household contact or positive polymerase chain reaction [PCR]/serology), Possible (suggestive clinical features of MISC and/or KD with negative PCR or serology but not both), Negative (negative PCR and serology and no known exposure), and Unknown (incomplete testing and no known exposure). Results: Of 2345 enrolled patients SARS-CoV-2 status was Positive for 1541 (66%) patients, Possible for 89 (4%), Negative for 404 (17%) and Unknown for 311 (13%). Clinical outcomes varied significantly among the groups, with more patients in the Positive/Possible groups presenting with shock, having admission to intensive care, receiving inotropic support, and having longer hospital stays. Regarding cardiac abnormalities, patients in the Positive/Possible groups had a higher prevalence of left ventricular dysfunction, and patients in the Negative and Unknown groups had more severe coronary artery abnormalities. Conclusions: There appears to be a spectrum of clinical features from MIS -C to KD with a great deal of heterogeneity, and one primary differentiating factor is evidence for previous acute SARS-CoV-2 infection/exposure. SARS-CoV-2 Positive/Possible patients had more severe presentations and required more intensive management, with a greater likelihood of ventricular dysfunction but less severe coronary artery adverse outcomes, in keeping with MIS -C.
引用
收藏
页码:58 / 72
页数:15
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