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Kawasaki Disease in the Time of COVID-19 and MIS-C - The International Kawasaki Disease Registry.
Harahsheh, Ashraf S; Shah, Samay; Dallaire, Frederic; Manlhiot, Cedric; Khoury, Michael; Lee, Simon; Fabi, Marianna; Mauriello, Daniel; Selamet Tierney, Elif Seda; Sabati, Arash A; Dionne, Audrey; Dahdah, Nagib; Choueiter, Nadine; Thacker, Deepika; Giglia, Therese M; Truong, Dongngan T; Jain, Supriya; Portman, Michael; Orr, William B; Harris, Tyler H; Szmuszkovicz, Jacqueline R; Farid, Pedrom; McCrindle, Brian W.
  • Harahsheh AS; Division of Cardiology, Department of Pediatrics, Children's National Hospital; George Washington University School of Medicine & Health Sciences; 111 Michigan Ave, NW Washington, DC 20010, USA. Electronic address: aharahsh@childrensnational.org.
  • Shah S; Medical student at George Washington University School of Medicine & Health Sciences, Washington, DC.
  • Dallaire F; Department of pediatrics, Université de Sherbrooke, and Centre de Recherche du Centre Hospitalier Universitaire de Sherbrooke, Sherbrooke, QC, Canada.
  • Manlhiot C; Blalock-Taussig-Thomas Congenital Heart Center at Johns Hopkins University, Baltimore, MD, USA.
  • Khoury M; Division of Pediatric Cardiology, Department of Pediatrics, University of Alberta, Edmonton, AB, Canada.
  • Lee S; The Heart Center at Nationwide Children's Hospital, Columbus, OH, USA.
  • Fabi M; Pediatric Emergency Unit, IRCCS Azienda Ospedaliero Universitaria di Bologna, Bologna, Italy.
  • Mauriello D; Johns Hopkins All Children's Hospital, Saint Petersburg, FL, USA.
  • Selamet Tierney ES; Department of Pediatrics, Division of Cardiology, Lucile Packard Children's Hospital, Stanford University Medical Center, Palo Alto, CA, USA.
  • Sabati AA; Phoenix Children's Hospital, Phoenix, AZ, USA.
  • Dionne A; Boston Children's Hospital, Harvard Medical School, Boston, MA, USA.
  • Dahdah N; Division of Pediatric Cardiology, CHU Ste-Justine, University of Montreal, Montreal, QC, Canada.
  • Choueiter N; Children's Hospital at Montefiore, Albert Einstein College of Medicine, Bronx, NY, USA.
  • Thacker D; Nemours Children's Hospital, Wilmington, DE, USA.
  • Giglia TM; Children's Hospital of Philadelphia, Philadelphia, PA, USA.
  • Truong DT; University of Utah and Primary Children's Hospital, Salt Lake City, UT, USA.
  • Jain S; New York Medical College/Maria Fareri Children's Hospital at Westchester Medical Center, Valhalla, NY, USA.
  • Portman M; Seattle Children's Hospital, Seattle, WA, USA.
  • Orr WB; Division of Pediatric Cardiology, Department of Pediatrics, Washington University School of Medicine, St Louis, MO, USA.
  • Harris TH; UPMC Children's Hospital of Pittsburgh, Pittsburgh, PA, USA.
  • Szmuszkovicz JR; Children's Hospital of Los Angeles, Los Angeles, CA, USA.
  • Farid P; Labatt Family Heart Centre, The Hospital for Sick Children, Department of Pediatrics, University of Toronto, Toronto, ON, Canada.
  • McCrindle BW; Labatt Family Heart Centre, The Hospital for Sick Children, Department of Pediatrics, University of Toronto, Toronto, ON, Canada.
Can J Cardiol ; 2023 Jun 06.
Article in English | MEDLINE | ID: covidwho-20236553
ABSTRACT

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 by evidence of prior SARS-CoV-2 infection.

METHODS:

The International KD Registry (IKDR) enrolled KD and MIS-C patients from sites from North, Central and South America, Europe, Asia and Middle East. Evidence of prior infection was defined as Positive (+ve household contact or positive PCR/serology), Possible (suggestive clinical features of MIS-C 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 89 (4%), Negative 404 (17%) and Unknown for 311 (13%) patients. Clinical outcomes varied significantly between 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, while patients in the Negative and Unknown groups had more severe coronary artery abnormalities. results

CONCLUSION:

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 prior acute SARS CoV2 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.
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Full text: Available Collection: International databases Database: MEDLINE Type of study: Experimental Studies / Observational study / Prognostic study / Randomized controlled trials Language: English Journal subject: Cardiology Year: 2023 Document Type: Article

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Full text: Available Collection: International databases Database: MEDLINE Type of study: Experimental Studies / Observational study / Prognostic study / Randomized controlled trials Language: English Journal subject: Cardiology Year: 2023 Document Type: Article