Risk Factors of Coronary Artery Abnormalities and Resistance to Intravenous Immunoglobulin Plus Corticosteroid Therapy in Severe Kawasaki Disease

Author:

Miyata Koichi1ORCID,Miura Masaru1ORCID,Kaneko Tetsuji23ORCID,Morikawa Yoshihiko2ORCID,Sakakibara Hiroshi4ORCID,Matsushima Takahiro4,Misawa Masahiro5ORCID,Takahashi Tsutomu6,Nakazawa Maki7,Tsuchihashi Takatoshi8ORCID,Yamashita Yukio9,Obonai Toshimasa10,Chiga Michiko11ORCID,Hori Naoaki12ORCID,Komiyama Osamu13ORCID,Yamagishi Hiroyuki1

Affiliation:

1. Department of Cardiology (K.M., M. Miura), Tokyo Metropolitan Children’s Medical Center, Japan.

2. Clinical Research Support Center (T.K., Y.M.), Tokyo Metropolitan Children’s Medical Center, Japan.

3. Teikyo Academic Research Center, Teikyo University, Tokyo, Japan (T.K.).

4. Department of General Pediatrics (H.S., T.M.), Tokyo Metropolitan Children’s Medical Center, Japan.

5. Department of Pediatrics, Tokyo Metropolitan Bokutoh Hospital, Japan (M. Misawa).

6. Department of Pediatrics, Saiseikai Utsunomiya Hospital, Tochigi, Japan (T. Takahashi).

7. Department of Pediatrics, National Hospital Organization Saitama National Hospital, Saitama, Japan (M.N.).

8. Department of Pediatrics, Kawasaki Municipal Hospital, Kanagawa, Japan (T. Tsuchihashi).

9. Department of Pediatrics, Yokohama Municipal Citizen’s Hospital, Kanagawa, Japan (Y.Y.).

10. Department of Pediatrics, Tama-Hokubu Medical Center, Tokyo, Japan (T.O.).

11. Department of Pediatrics, Tokyo Metropolitan Ohtsuka Hospital, Japan (M.C.).

12. Department of Pediatrics, Ota Memorial Hospital, Gunma, Japan (N.H.).

13. Department of Pediatrics, National Hospital Organization Tokyo Medical Center, Japan (O.K.).

Abstract

Background: Coronary artery abnormalities (CAAs) still occur in patients with Kawasaki disease receiving intensified treatment with corticosteroids. We aimed to determine the risk factors of CAA development and resistance to intensified treatment in Post RAISE (Prospective Observational Study on Stratified Treatment With Immunoglobulin Plus Steroid Efficacy for Kawasaki Disease)—the largest prospective cohort of Kawasaki disease patients to date. Methods: In Post RAISE, 2648 consecutive patients with Kawasaki disease were enrolled. The present study analyzed 724 patients predicted to be intravenous immunoglobulin (IVIG) nonresponders (Kobayashi score ≥5) who received intensified treatment consisting of IVIG plus prednisolone. The association between the baseline characteristics and CAA at 1 month after disease onset was examined. The association between the baseline characteristics and treatment resistance was also investigated. Results: Maximum Z score at baseline ≥2.5 (odds ratio, 3.4 [95% CI, 1.5–7.8]), age at fever onset <1 year (odds ratio, 3.4 [95% CI, 1.6–7.4]), and nonresponsiveness to IVIG plus prednisolone treatment (odds ratio, 6.8 [95% CI, 3.3–14.0]) were independent predictors of CAA development. Nonresponsiveness to IVIG plus prednisolone was significantly associated with 8 baseline variables. Baseline total bilirubin (odds ratio, 1.4 [95% CI, 1.2–1.7]) was the only significant independent predictor other than the variables included in the Kobayashi score, enabling treatment resistance to be identified at diagnosis. The area under the ROC curve was 0.74 (95% CI, 0.69–0.79). At a cutoff point of 1.0, the sensitivity and specificity for predicting treatment resistance were 71% and 65%, respectively. Conclusions: In Post RAISE, younger age at fever onset, a larger maximum Z score at baseline, and nonresponsiveness to IVIG plus prednisolone were risk factors significantly associated with CAA development. Nonresponders were able to be identified at diagnosis based on the total bilirubin value. To prevent CAA, more intensified or adjunctive therapies using other agents, such as pulsed methylprednisolone, ciclosporin, infliximab, and Anakinra, should be considered for patients with these risk factors. Registration: URL: https://www.umin.ac.jp/ctr/ ; Unique identifier: UMIN000007133.

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Cardiology and Cardiovascular Medicine

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