Risk scores for Kawasaki disease, a management tool developed by the KAWA-RACE cohort.

INTRODUCTION/OBJECTIVES: Asian scores developed to predict unresponsiveness to intravenous immunoglobulin (IVIG) or development of coronary artery aneurysms (CAA) in patients with Kawasaki disease (KD) are not appropriate in Western populations. The purpose of this study is to develop 2 scores, to predict unresponsiveness to IVIG and development of CAA, appropriate for Spanish population. METHOD: Data of 625 Spanish children with KD collected retrospectively (2011-2016) were used to identify variables to develop the 2 scores of interest: unresponsiveness to IVIG and development of CAA. A statistical model selected best variables to create the scores, and scores were validated with data from 98 patients collected prospectively. RESULTS: From 625 patients of the retrospective cohort, final analysis was performed in 439 subjects: 37 developed CAA, and 212 were unresponsive to IVIG. For the score to predict CAA, a cutoff ≥ 8 was considered for high risk, considering a score system with a different weight for each of the eight variables. External validation showed a sensitivity of 22% and a specificity of 75%. The score to predict unresponsiveness to IVIG established a cutoff ≥ 8 for high risk, considering a score system with a different weight for each of the nine variables. External validation showed a sensitivity of 78% and a specificity of 50%. CONCLUSIONS: Two risk scores for KD were developed from Spanish population, to predict development of CAA and unresponsiveness to IVIG; validation in other cohorts could help to implement these tools in the management of KD in other Western populations.

Kawasaki disease in children younger than 6 months of age: characteristics of a Spanish cohort.

A retrospective study that compared children younger than 6 months versus older children of a Spanish cohort of patients diagnosed with Kawasaki disease between 2011 and 2016 (Kawa-Race study). From the 598 patients recruited, 42 patients were younger than 6 months (7%) and presented more frequently with an incomplete diagnosis of Kawasaki disease (52.4 vs 27.9%, p = 0.001). Cardiac abnormalities detected by echocardiography were more common in younger patients (52.4 vs 30%, p = 0.002). These younger patients presented with a higher proportion of coronary aneurysms as well (19 vs 8.6%, p < 0.001). Shock at diagnosis (9.5 vs 1.9%, p = 0.016) and admission to intensive care units (17.7 vs 4.1%, p = 0.003) were more frequent in patients younger than 6 months. There were no statistically significant differences in relation to infections, non-response to IVIG, or mid- or long-term outcomes.Conclusion: Data of the Spanish cohort are consistent with other American and Asian studies, although Spanish children younger than 6 months had a lower rate of non-response to IVIG and better clinical outcomes. A high index of suspicion should be considered for this population due to a higher risk of coronary abnormalities, presentation of shock, and admission to the intensive care unit. What is Known: •Children below 6 months of age with Kawasaki disease (KD) have different features compared to older. •Younger patients usually have an incomplete form of KD and coronary artery abnormalities. What is New: •Younger than 6 months with KD presented with shock and required admission to PICU more frequently compared to older. •Infections play a similar role in KD despite the age of the patients.

Prevalence and Clinical Characteristics of SARS-CoV-2 Confirmed and Negative Kawasaki Disease Patients During the Pandemic in Spain.

Introduction: COVID-19 has a less severe course in children. In April 2020, some children presented with signs of multisystem inflammation with clinical signs overlapping with Kawasaki disease (KD), most of them requiring admission to the pediatric intensive care unit (PICU). This study aimed to describe the prevalence and clinical characteristics of KD SARS-CoV-2 confirmed and negative patients during the pandemic in Spain. Material and Methods: Medical data of KD patients from January 1, 2018 until May 30, 2020 was collected from the KAWA-RACE study group. We compared the KD cases diagnosed during the COVID-19 period (March 1-May 30, 2020) that were either SARS-CoV-2 confirmed (CoV+) or negative (CoV-) to those from the same period during 2018 and 2019 (PreCoV). Results: One hundred and twenty-four cases were collected. There was a significant increase in cases and PICU admissions in 2020 (P-trend = 0.001 and 0.0004, respectively). CoV+ patients were significantly older (7.5 vs. 2.5 yr) and mainly non-Caucasian (64 vs. 29%), had incomplete KD presentation (73 vs. 32%), lower leucocyte (9.5 vs. 15.5 × 109) and platelet count (174 vs. 423 × 109/L), higher inflammatory markers (C-Reactive Protein 18.5vs. 10.9 mg/dl) and terminal segment of the natriuretic atrial peptide (4,766 vs. 505 pg/ml), less aneurysm development (3.8 vs. 11.1%), and more myocardial dysfunction (30.8 vs. 1.6%) than PreCoV patients. Respiratory symptoms were not increased during the COVID-19 period. Conclusion: The KD CoV+ patients mostly meet pediatric inflammatory multisystem syndrome temporally associated with COVID-19/multisystem inflammatory syndrome in children criteria. Whether this is a novel entity or the same disease on different ends of the spectrum is yet to be clarified.

Factores influyentes en la evolución de la mortalidad de las cardiopatías congénitas. Estudio sobre 1.216 niños en la Comunidad Autónoma de Murcia (1978-1990) / Influential Factors in Mortality Rate from Congenital Heart Disease. Study on 1,216 Children in the Autonomous Community of Murcia, Spain (1978-1990)

Introducción. En los últimos años se han producido importantes progresos en el tratamiento de las cardiopatías congénitas. Estos cambios han afectado tanto al diagnóstico como al manejo preoperatorio, tratamiento quirúrgico y a los cuidados postoperatorios, todo lo cual ha contribuido a mejorar la evolución de los niños con cardiopatía congénita. Objetivos. Pretendemos valorar la evolución de las cardiopatías congénitas en un hospital de nivel terciario, comparando dos períodos distintos en cuanto al manejo diagnóstico y terapéutico. También pretendemos conocer la influencia que han tenido en la mortalidad factores como la presencia de anomalías extracardíacas asociadas y la realización o no de cirugía cardíaca. Pacientes y métodos. Analizamos, de manera retrospectiva, la evolución tanto global como por cardiopatías individualizadas, así como los factores relacionados con ésta, de 1.216 niños con cardiopatía congénita, de un día a 7 años de edad, nacidos a lo largo de 13 años y estudiados en la sección de cardiología pediátrica de un hospital de referencia para toda la Comunidad Autónoma de Murcia. El tiempo de estudio se dividió a su vez en dos períodos: 1978-1983 y 1984-1990, con diferencias en cuanto al diagnóstico y al tratamiento. Resultados. a) Se ha producido un descenso de la mortalidad en el período 1984-1990, con respecto al período 1978-1983, pasando del 28 al 21,7 por ciento (p < 0,05); b) individualmente, el descenso de la mortalidad ha sido estadísticamente significativo en dos entidades: la comunicación interventricular y el conducto arterioso persistente, y c) mayor mortalidad en pacientes no intervenidos y en presencia de anomalías extracardíacas asociadas.Conclusión. Los progresos en el manejo de las cardiopatías congénitas han conducido a un resultado más favorable en los últimos años (AU)