已发表论文

川崎病相关急性腹部:大多数不需要手术

 

Authors She X , Chen J, Zhou YN, Guo J, Zhao FH, Yi C

Received 11 August 2023

Accepted for publication 7 November 2023

Published 10 November 2023 Volume 2023:16 Pages 5157—5162

DOI https://doi.org/10.2147/JIR.S434982

Checked for plagiarism Yes

Review by Single anonymous peer review

Peer reviewer comments 2

Editor who approved publication: Professor Ning Quan

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, Creactive 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 < 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