Kawasaki disease: an unexpected etiology of shock and multiple organ dysfunction syndrome

Pauline Gatterre1, Mehdi Oualha, Laurent Dupic

  • 1Service de Réanimation Pédiatrique, Hôpital Necker Enfants-Malades, Assistance Publique-Hôpitaux de Paris, Faculté de Médecine, Université Paris-Descartes, 149, Rue de Sèvres, 75743, Paris Cedex 15, France.

Intensive Care Medicine
|January 26, 2012
PubMed

Insights

Severe Kawasaki disease (KD) with shock can cause multiple organ dysfunction syndrome (MODS). Prompt diagnosis and treatment of these severe KD cases led to complete recovery in all pediatric patients studied.

Area of Science:

  • Pediatric critical care medicine
  • Infectious diseases
  • Rheumatology

Background:

  • Severe forms of Kawasaki disease (KD) are increasingly associated with shock and coronary artery abnormalities (CAA).
  • Limited data exists on non-cardiovascular organ involvement and outcomes in severe KD presenting with shock.

Purpose of the Study:

  • To analyze organ involvement beyond cardiovascular aspects in severe KD patients admitted to the PICU.
  • To assess the outcomes of severe KD with shock compared to common forms.

Main Methods:

  • Retrospective study of 11 patients diagnosed with KD and admitted to a pediatric intensive care unit (PICU) between 2001 and 2009.
  • Analysis of clinical data, including organ involvement, diagnostic delays, treatment duration, and patient outcomes.

Main Results:

  • Seven patients (63%) developed CAA, with complete regression observed.
  • Non-specific encephalopathy and acute kidney injury were common findings.
  • Eight patients experienced Multiple Organ Dysfunction Syndrome (MODS), yet all 11 children survived without sequelae despite predicted high mortality.

Conclusions:

  • Moderate shock is a primary reason for PICU admission in KD patients.
  • Severe KD with shock can present with significant MODS, highlighting the need for early recognition.
  • Timely diagnosis and treatment are crucial for favorable outcomes in these severe KD cases.
Abstract

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