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10.1016/j.cjca.2021.05.014

http://scihub22266oqcxt.onion/10.1016/j.cjca.2021.05.014
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34090979!8180353!34090979
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suck abstract from ncbi


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pmid34090979      Can+J+Cardiol 2021 ; 37 (10): 1619-1628
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  • Kawasaki Disease Shock Syndrome vs Classical Kawasaki Disease: A Meta-analysis and Comparison With SARS-CoV-2 Multisystem Inflammatory Syndrome #MMPMID34090979
  • Lamrani L; Manlhiot C; Elias MD; Choueiter NF; Dionne A; Harahsheh AS; Portman MA; McCrindle BW; Dahdah N
  • Can J Cardiol 2021[Oct]; 37 (10): 1619-1628 PMID34090979show ga
  • BACKGROUND: The emergence of increasing reports worldwide of a severe inflammatory process and shock in pediatric patients resembling Kawasaki disease (KD)-and, more specifically, Kawasaki disease shock syndrome (KDSS)-prompted us to explore KDSS in a preamble of a systematic comparison between the 2 conditions. METHODS: We completed a systematic review of KDSS and performed a meta-analysis comparison between reported KDSS cases and KD controls. RESULTS: A total of 10 case-control series were included in the meta-analysis. Patients with KDSS were older (38.4 +/- 30.6 vs 21.9 +/- 19.5 months; P < 0.001) compared with standard KD with equal sex distribution and completeness of clinical diagnostic criteria. KDSS present higher C-reactive protein (59.4 +/- 29.2 mg/dL vs 20.8 +/- 14.8 mg/dL; P < 0.001), lower albumin (2.7 +/- 0.5 g/dL vs 3.3 +/- 0.5 g/dL; P < 0.01), and lower platelets (255 +/- 149 109/L vs 394 +/- 132 109/L; P < 0.001) but only borderline higher white blood cells (P = 0.06). Differences in alanine transaminase, aspartate aminotransferase, and erythrocyte sedimentation rate were nonsignificant. The odds of intravenous immunoglobulin resistance (44.4% vs 9.6%; (P < 0.001) and the hospital length of stay (10.9 +/- 5.8 vs 5.0 +/- 3.0 days; P < 0.001) were higher in KDSS, as were the odds of coronary-artery abnormalities (33.9% vs 8.6%; P < 0.001). CONCLUSIONS: This first meta-analysis on KDSS vs KD represents a basis for future works on KDSS and opens the opportunity for future multicentre studies in the search of causal relationships between presenting elements and the eventual complications of KDSS. The similarities between SARS-CoV-2 multisystem inflammatory syndrome in children and KDSS open new horizons to the understanding of the etiology and pathophysiology related to KDSS.
  • |*Mucocutaneous Lymph Node Syndrome/blood/diagnosis[MESH]
  • |*Systemic Inflammatory Response Syndrome/blood/diagnosis/etiology/therapy[MESH]
  • |COVID-19/blood/*complications/diagnosis[MESH]
  • |Child, Preschool[MESH]
  • |Diagnosis, Differential[MESH]
  • |Humans[MESH]
  • |Outcome Assessment, Health Care[MESH]


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