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Have we got the optimal treatment for refractory Kawasaki disease in very young infants? A case report and literature review

A small group of patients with Kawasaki disease (KD) demonstrates resistance to standard therapy, putting them at high risk for an unfavorable prognosis, especially regarding coronary artery aneurysms. Although adding corticosteroids to first-line i.v. immunoglobulins (IVIGs) is considered beneficia...

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Autores principales: Lersch, Robert, Mandilaras, Guido, Schrader, Meike, Anselmino, Felicitas, Haas, Nikolaus A., Jakob, André
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10419265/
https://www.ncbi.nlm.nih.gov/pubmed/37576144
http://dx.doi.org/10.3389/fped.2023.1210940
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author Lersch, Robert
Mandilaras, Guido
Schrader, Meike
Anselmino, Felicitas
Haas, Nikolaus A.
Jakob, André
author_facet Lersch, Robert
Mandilaras, Guido
Schrader, Meike
Anselmino, Felicitas
Haas, Nikolaus A.
Jakob, André
author_sort Lersch, Robert
collection PubMed
description A small group of patients with Kawasaki disease (KD) demonstrates resistance to standard therapy, putting them at high risk for an unfavorable prognosis, especially regarding coronary artery aneurysms. Although adding corticosteroids to first-line i.v. immunoglobulins (IVIGs) is considered beneficial, and despite timely treatment initiation, very young infants, in particular, can present an unfavorable clinical course. We report on a 3-month-old boy with a clinically severe KD phenotype involving the early development of giant coronary artery aneurysms. Because of his poor response to the first course of IVIG and prednisolone, we administered infliximab. His clinical condition improved after that, and his temperature dropped. Inflammatory markers however did not recover completely, and he remained subfebrile. In addition, as the coronary artery dimensions deteriorated, a second IVIG course was administered and prednisolone continued at the initial dosage. Although fever and routine inflammatory parameters normalized, close follow-up investigations revealed both still increasing coronary artery dimensions and renewed rise in inflammatory parameters, necessitating two more infliximab administrations in addition to continuous prednisolone. Because of the coronary artery dimensions (left anterior descending artery, 4.9 mm, Z-score 11.1; right coronary artery 5.8 mm, Z-score 15.5), dual platelet inhibitory therapy with ASA and later clopidogrel combined with low-molecular heparin was indicated. Four weeks after his initial KD diagnosis, we detected no renewed increase in inflammatory markers; at that time, we observed a slight reduction in coronary dimensions. In summary, despite timely guideline-fulfilling therapy, the prolonged clinical course of this very young infant with KD entailing the development of giant coronary artery aneurysms makes us question whether this age group may benefit from early, even more intense therapy.
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spelling pubmed-104192652023-08-12 Have we got the optimal treatment for refractory Kawasaki disease in very young infants? A case report and literature review Lersch, Robert Mandilaras, Guido Schrader, Meike Anselmino, Felicitas Haas, Nikolaus A. Jakob, André Front Pediatr Pediatrics A small group of patients with Kawasaki disease (KD) demonstrates resistance to standard therapy, putting them at high risk for an unfavorable prognosis, especially regarding coronary artery aneurysms. Although adding corticosteroids to first-line i.v. immunoglobulins (IVIGs) is considered beneficial, and despite timely treatment initiation, very young infants, in particular, can present an unfavorable clinical course. We report on a 3-month-old boy with a clinically severe KD phenotype involving the early development of giant coronary artery aneurysms. Because of his poor response to the first course of IVIG and prednisolone, we administered infliximab. His clinical condition improved after that, and his temperature dropped. Inflammatory markers however did not recover completely, and he remained subfebrile. In addition, as the coronary artery dimensions deteriorated, a second IVIG course was administered and prednisolone continued at the initial dosage. Although fever and routine inflammatory parameters normalized, close follow-up investigations revealed both still increasing coronary artery dimensions and renewed rise in inflammatory parameters, necessitating two more infliximab administrations in addition to continuous prednisolone. Because of the coronary artery dimensions (left anterior descending artery, 4.9 mm, Z-score 11.1; right coronary artery 5.8 mm, Z-score 15.5), dual platelet inhibitory therapy with ASA and later clopidogrel combined with low-molecular heparin was indicated. Four weeks after his initial KD diagnosis, we detected no renewed increase in inflammatory markers; at that time, we observed a slight reduction in coronary dimensions. In summary, despite timely guideline-fulfilling therapy, the prolonged clinical course of this very young infant with KD entailing the development of giant coronary artery aneurysms makes us question whether this age group may benefit from early, even more intense therapy. Frontiers Media S.A. 2023-07-28 /pmc/articles/PMC10419265/ /pubmed/37576144 http://dx.doi.org/10.3389/fped.2023.1210940 Text en © 2023 Lersch, Mandilaras, Schrader, Anselmino, Haas and Jakob. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY) (https://creativecommons.org/licenses/by/4.0/) . The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Pediatrics
Lersch, Robert
Mandilaras, Guido
Schrader, Meike
Anselmino, Felicitas
Haas, Nikolaus A.
Jakob, André
Have we got the optimal treatment for refractory Kawasaki disease in very young infants? A case report and literature review
title Have we got the optimal treatment for refractory Kawasaki disease in very young infants? A case report and literature review
title_full Have we got the optimal treatment for refractory Kawasaki disease in very young infants? A case report and literature review
title_fullStr Have we got the optimal treatment for refractory Kawasaki disease in very young infants? A case report and literature review
title_full_unstemmed Have we got the optimal treatment for refractory Kawasaki disease in very young infants? A case report and literature review
title_short Have we got the optimal treatment for refractory Kawasaki disease in very young infants? A case report and literature review
title_sort have we got the optimal treatment for refractory kawasaki disease in very young infants? a case report and literature review
topic Pediatrics
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10419265/
https://www.ncbi.nlm.nih.gov/pubmed/37576144
http://dx.doi.org/10.3389/fped.2023.1210940
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