Informace o publikaci

COVID-19-Associated Paediatric Inflammatory Multisystem Syndrome (PIMS-TS) in Intensive Care: A Retrospective Cohort Trial (PIMS-TS INT)

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MUSILOVÁ Tereza JONAS Jakub GOMBALA Tomas DAVID Jan FENCL Filip KLABUSAYOVÁ Eva KLUČKA Jozef KRATOCHVÍL Milan HAVRÁNKOVÁ Pavla VRTKOVA Adela SLABÁ Kateřina TUČKOVÁ Jana HOMOLA Lukáš ŠTOURAČ Petr VYMAZAL Tomáš

Rok publikování 2023
Druh Článek v odborném periodiku
Časopis / Zdroj Children
Fakulta / Pracoviště MU

Lékařská fakulta

Citace
www https://www.mdpi.com/2227-9067/10/2/348
Doi http://dx.doi.org/10.3390/children10020348
Klíčová slova PIMS-TS; COVID-19; SARS-CoV-2; paediatric patient; post-COVID syndrome
Popis Paediatric inflammatory multisystem syndrome temporally associated with COVID-19 (PIMS-TS) is a new disease in children and adolescents that occurs after often asymptomatic or mild COVID-19. It can be manifested by different clinical symptomatology and varying severity of disease based on multisystemic inflammation. The aim of this retrospective cohort trial was to describe the initial clinical presentation, diagnostics, therapy and clinical outcome of paediatric patients with a diagnosis of PIMS-TS admitted to one of the 3 PICUs. All paediatric patients who were admitted to the hospital with a diagnosis of paediatric inflammatory multisystem syndrome temporally associated with SARS-CoV-2 (PIMS-TS) during the study period were enrolled in the study. A total of 180 patients were analysed. The most common symptoms upon admission were fever (81.6%, n = 147), rash (70.6%, n = 127), conjunctivitis (68.9%, n = 124) and abdominal pain (51.1%, n = 92). Acute respiratory failure occurred in 21.1% of patients (n = 38). Vasopressor support was used in 20.6% (n = 37) of cases. Overall, 96.7% of patients (n = 174) initially tested positive for SARS-CoV-2 IgG antibodies. Almost all patients received antibiotics during in-hospital stays. No patient died during the hospital stay or after 28 days of follow-up. Initial clinical presentation and organ system involvement of PIMS-TS including laboratory manifestations and treatment were identified in this trial. Early identification of PIMS-TS manifestation is essential for early treatment and proper management of patients.
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