Kawasaki Disease Associated Acute Abdomen: Most Require No Surgery

J Inflamm Res. 2023 Nov 10:16:5157-5162. doi: 10.2147/JIR.S434982. eCollection 2023.

Abstract

Objective: To summarize the clinical features and treatment experiences of patients with Kawasaki disease (KD)-associated acute abdomen (KD-AA).

Methods: We conducted a retrospective case-control study of patients with KD-AA treated at our hospital between January 2006 and November 2022.

Results: Of the 917 children with KD, 43 (4.7%) presented with AA. Of these, 33 with complete information were included in the KD-AA group. Patients with KD-AA were significantly older, with higher neutrophil rate, C-reactive protein, procalcitonin, and alanine transaminase levels and lower hemoglobin, albumin, and serum sodium levels. Additionally, more patients with KD-AA presented with aseptic meningitis and KD shock syndrome than those with KD alone (all p<0.05). The two groups did not differ in the incidence of intravenous immunoglobulin (IVIG) resistance, incomplete KD, or coronary artery abnormalities. All patients received aspirin and IVIG therapy, with nine receiving a second dose of IVIG and 11 receiving corticosteroids. Only two patients with KD-AA underwent surgery, and the prognosis of all patients with KD-AA was good.

Conclusion: KD-AA should be suspected in febrile children with abdominal symptoms. Prompt diagnosis of KD-AA is important for early effective treatment to avoid unnecessary surgical harm. KD, complicated by acute abdomen, has a good prognosis.

Keywords: Kawasaki disease; acute abdomen; clinical manifestation; treatment.

Grants and funding

This study was supported by a research project from Mianyang Central Hospital (No.2023KY025).