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Outcomes Associated with Giant Coronary Artery Aneurysms after Kawasaki Disease: A Single-Center United States Experience.
Elias, Matthew D; Brothers, Julie A; Hogarty, Alexa N; Martino, Jordy; O'Byrne, Michael L; Patel, Chandni; Stephens, Paul; Tingo, Jennifer; Vetter, Victoria L; Ravishankar, Chitra; Giglia, Therese M.
Afiliação
  • Elias MD; Division of Cardiology, Children's Hospital of Philadelphia, Philadelphia, PA. Electronic address: eliasm1@chop.edu.
  • Brothers JA; Division of Cardiology, Children's Hospital of Philadelphia, Philadelphia, PA.
  • Hogarty AN; Division of Cardiology, Children's Hospital of Philadelphia, Philadelphia, PA.
  • Martino J; Division of Cardiology, Children's Hospital of Philadelphia, Philadelphia, PA.
  • O'Byrne ML; Division of Cardiology, Children's Hospital of Philadelphia, Philadelphia, PA.
  • Patel C; Division of Cardiology, Children's Hospital of Philadelphia, Philadelphia, PA.
  • Stephens P; Division of Cardiology, Children's Hospital of Philadelphia, Philadelphia, PA.
  • Tingo J; Division of Cardiology, Children's Hospital of Philadelphia, Philadelphia, PA.
  • Vetter VL; Division of Cardiology, Children's Hospital of Philadelphia, Philadelphia, PA.
  • Ravishankar C; Division of Cardiology, Children's Hospital of Philadelphia, Philadelphia, PA.
  • Giglia TM; Division of Cardiology, Children's Hospital of Philadelphia, Philadelphia, PA.
J Pediatr ; 274: 114145, 2024 Jun 13.
Article em En | MEDLINE | ID: mdl-38878963
ABSTRACT

OBJECTIVES:

To determine the long-term outcomes among a cohort of patients with Kawasaki disease (KD) and a history of giant coronary artery aneurysms (CAAs) at a single US center. STUDY

DESIGN:

Medical records for all patients with KD and giant CAAs at a pediatric academic institution were reviewed. Primary outcomes included major adverse cardiovascular events (MACE) and normalization of CA luminal diameter, using Kaplan-Meier analyses.

RESULTS:

There were 60 patients with KD and giant CAAs identified between 1989 and 2023. The majority of patients were male (71.7%) with a median age at diagnosis of 0.9 years (range, 0.2-13.3 years). Patients were followed for a median of 11 years, up to 34.5 years. MACE occurred in 13 patients (21.7%) at a median of 1.4 years (range, 0.04-22.6 years) after KD diagnosis. The 10-, 20-, and 30-year MACE-free rates were 75%, 75%, and 60%. Patients with maximal CA z scores of ≥20 or bilateral CAA were more likely to have MACE. During follow-up, 26.7% of CAA regressed to a normal luminal diameter at a median of 3.6 years (range, 0.6-12.0 years). The 10-, 20- and 30-year likelihood of CA regression to normal luminal diameter was 36%, 46%, and 46%.

CONCLUSIONS:

Over 30 years, MACE occurred in nearly 22% of patients, more often in those with bilateral CAA or CA z scores of ≥20. Despite regression to a normal luminal diameter in >25% of CAAs, patients with a history of KD-associated giant CAA require ongoing surveillance for cardiac complications, even years after the initial disease.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: J Pediatr Ano de publicação: 2024 Tipo de documento: Article País de publicação: Estados Unidos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: J Pediatr Ano de publicação: 2024 Tipo de documento: Article País de publicação: Estados Unidos