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Immunoglobulin for Kawasaki disease: a 3-year retrospective audit

AIM: To evaluate whether intravenous immunoglobulin (IVIG) use in children with suspected Kawasaki disease (KD) was given according to local trust and the newly revised American Heart Association (AHA) guidelines. METHODS: In our tertiary hospital, any child with suspected KD given IVIG, over the pa...

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Autores principales: Pascall, Beth, Thakker, Arjuna, Foo, Ying, Thakker, Pradip
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BMJ Publishing Group 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6733330/
https://www.ncbi.nlm.nih.gov/pubmed/31548996
http://dx.doi.org/10.1136/bmjpo-2019-000451
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author Pascall, Beth
Thakker, Arjuna
Foo, Ying
Thakker, Pradip
author_facet Pascall, Beth
Thakker, Arjuna
Foo, Ying
Thakker, Pradip
author_sort Pascall, Beth
collection PubMed
description AIM: To evaluate whether intravenous immunoglobulin (IVIG) use in children with suspected Kawasaki disease (KD) was given according to local trust and the newly revised American Heart Association (AHA) guidelines. METHODS: In our tertiary hospital, any child with suspected KD given IVIG, over the past 3 years, was identified. Their electronic notes were then reviewed. RESULTS: Ten patients were identified. Nine patients had a fever lasting 5 days or more. Four patients had either 5/5 or 4/5 of the diagnostic criteria for KD and were diagnosed with complete KD. The remaining six patients were suspected to have incomplete KD. 7/10 patients received IVIG within 10 days of onset of illness. Patients suspected to have incomplete KD experienced a mean delay in administration of IVIG of 5.3 days compared with those with complete KD. In four patients, an alternative diagnosis was established. Three patients had coronary artery abnormalities on first echocardiogram. From these patients, only one had a follow-up echocardiogram recorded in their notes. No patient had more than one follow-up echocardiogram (at both 2 and 6 weeks). CONCLUSION: Identifying patients with incomplete KD is more difficult than identifying those with complete KD and any delay in giving IVIG could be due to this reason. This audit suggests that increasing awareness of incomplete KD and a clear guideline will aid prompter diagnosis and administration of IVIG. This audit also suggests that all patients with KD should receive more than one follow-up echocardiogram.
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spelling pubmed-67333302019-09-23 Immunoglobulin for Kawasaki disease: a 3-year retrospective audit Pascall, Beth Thakker, Arjuna Foo, Ying Thakker, Pradip BMJ Paediatr Open General Paediatrics AIM: To evaluate whether intravenous immunoglobulin (IVIG) use in children with suspected Kawasaki disease (KD) was given according to local trust and the newly revised American Heart Association (AHA) guidelines. METHODS: In our tertiary hospital, any child with suspected KD given IVIG, over the past 3 years, was identified. Their electronic notes were then reviewed. RESULTS: Ten patients were identified. Nine patients had a fever lasting 5 days or more. Four patients had either 5/5 or 4/5 of the diagnostic criteria for KD and were diagnosed with complete KD. The remaining six patients were suspected to have incomplete KD. 7/10 patients received IVIG within 10 days of onset of illness. Patients suspected to have incomplete KD experienced a mean delay in administration of IVIG of 5.3 days compared with those with complete KD. In four patients, an alternative diagnosis was established. Three patients had coronary artery abnormalities on first echocardiogram. From these patients, only one had a follow-up echocardiogram recorded in their notes. No patient had more than one follow-up echocardiogram (at both 2 and 6 weeks). CONCLUSION: Identifying patients with incomplete KD is more difficult than identifying those with complete KD and any delay in giving IVIG could be due to this reason. This audit suggests that increasing awareness of incomplete KD and a clear guideline will aid prompter diagnosis and administration of IVIG. This audit also suggests that all patients with KD should receive more than one follow-up echocardiogram. BMJ Publishing Group 2019-09-06 /pmc/articles/PMC6733330/ /pubmed/31548996 http://dx.doi.org/10.1136/bmjpo-2019-000451 Text en © Author(s) (or their employer(s)) 2019. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ. This is an open access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited, appropriate credit is given, any changes made indicated, and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/4.0/.
spellingShingle General Paediatrics
Pascall, Beth
Thakker, Arjuna
Foo, Ying
Thakker, Pradip
Immunoglobulin for Kawasaki disease: a 3-year retrospective audit
title Immunoglobulin for Kawasaki disease: a 3-year retrospective audit
title_full Immunoglobulin for Kawasaki disease: a 3-year retrospective audit
title_fullStr Immunoglobulin for Kawasaki disease: a 3-year retrospective audit
title_full_unstemmed Immunoglobulin for Kawasaki disease: a 3-year retrospective audit
title_short Immunoglobulin for Kawasaki disease: a 3-year retrospective audit
title_sort immunoglobulin for kawasaki disease: a 3-year retrospective audit
topic General Paediatrics
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6733330/
https://www.ncbi.nlm.nih.gov/pubmed/31548996
http://dx.doi.org/10.1136/bmjpo-2019-000451
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