Cargando…
Torsades de Pointes During Myringotomy in a Child with Congenital Long QT Syndrome: A Case Report
Patient: Male, 7-year-old Final Diagnosis: Torsades de pointes Symptoms: Ventricular tachycardia Medication: Propranolol • Magnesium Clinical Procedure: Bilateral myringotomy tubes Specialty: Anesthesiology • Cardiology • Pediatrics and Neonatology OBJECTIVE: Congenital defects/diseases BACKGROUND:...
Autores principales: | , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
International Scientific Literature, Inc.
2020
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7571281/ https://www.ncbi.nlm.nih.gov/pubmed/33056945 http://dx.doi.org/10.12659/AJCR.925602 |
_version_ | 1783597140410368000 |
---|---|
author | Coleman, Melissa Imundo, Jason R. Cortez, Daniel Cohen, Mark H. Dhar, Padmani Dalal, Priti G. |
author_facet | Coleman, Melissa Imundo, Jason R. Cortez, Daniel Cohen, Mark H. Dhar, Padmani Dalal, Priti G. |
author_sort | Coleman, Melissa |
collection | PubMed |
description | Patient: Male, 7-year-old Final Diagnosis: Torsades de pointes Symptoms: Ventricular tachycardia Medication: Propranolol • Magnesium Clinical Procedure: Bilateral myringotomy tubes Specialty: Anesthesiology • Cardiology • Pediatrics and Neonatology OBJECTIVE: Congenital defects/diseases BACKGROUND: Long QT syndrome (LQTS) is an arrhythmogenic heart condition that can be congenital or acquired. Prolonged ventricular repolarizations in individuals with the disorder can cause fatal arrhythmias. Abnormal functioning of cardiac ion channels leads to arrhythmias such as torsades de pointes (TdP) and may be triggered by stress or medications. Many medications used in the perioperative period are triggers for the arrythmia. CASE REPORT: A 7-year-old patient with known congenital LQTS type 2 presented for bilateral myringotomy and tube placement. The patient was otherwise healthy and taking propranolol daily. Preoperative midazolam was administered for anxiolysis, and induction of anesthesia was uneventful. He sustained an episode of TdP immediately following general anesthetic induction after failure of an in situ automatic implantable cardioverter-defibrillator (AICD). External defibrillation succeeded, and the patient was stabilized in the Postanesthesia Recovery Unit before transfer to the Pediatric Intensive Care Unit. Interrogation of the AICD revealed several undelivered defibrillation attempts. A chest X-ray showed an area suggestive of an epicardial electrode fracture. The following day, the AICD was replaced with no arrythmias noted. The patient had an uneventful recovery. CONCLUSIONS: In patients with a known history of LQTS, preparation and prevention are cornerstones of anesthesia care. Minimizing the use of triggering medications and emotional stress in the perioperative period, combined with ready equipment and medications to respond to arrythmias, are essential. In children, there is a greater chance of lead fracture and resulting device failure. Preoperative history of device function or interrogation of the AICD and possibly a chest X-ray are essential to ensure the integrity of the leads. |
format | Online Article Text |
id | pubmed-7571281 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | International Scientific Literature, Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-75712812020-11-04 Torsades de Pointes During Myringotomy in a Child with Congenital Long QT Syndrome: A Case Report Coleman, Melissa Imundo, Jason R. Cortez, Daniel Cohen, Mark H. Dhar, Padmani Dalal, Priti G. Am J Case Rep Articles Patient: Male, 7-year-old Final Diagnosis: Torsades de pointes Symptoms: Ventricular tachycardia Medication: Propranolol • Magnesium Clinical Procedure: Bilateral myringotomy tubes Specialty: Anesthesiology • Cardiology • Pediatrics and Neonatology OBJECTIVE: Congenital defects/diseases BACKGROUND: Long QT syndrome (LQTS) is an arrhythmogenic heart condition that can be congenital or acquired. Prolonged ventricular repolarizations in individuals with the disorder can cause fatal arrhythmias. Abnormal functioning of cardiac ion channels leads to arrhythmias such as torsades de pointes (TdP) and may be triggered by stress or medications. Many medications used in the perioperative period are triggers for the arrythmia. CASE REPORT: A 7-year-old patient with known congenital LQTS type 2 presented for bilateral myringotomy and tube placement. The patient was otherwise healthy and taking propranolol daily. Preoperative midazolam was administered for anxiolysis, and induction of anesthesia was uneventful. He sustained an episode of TdP immediately following general anesthetic induction after failure of an in situ automatic implantable cardioverter-defibrillator (AICD). External defibrillation succeeded, and the patient was stabilized in the Postanesthesia Recovery Unit before transfer to the Pediatric Intensive Care Unit. Interrogation of the AICD revealed several undelivered defibrillation attempts. A chest X-ray showed an area suggestive of an epicardial electrode fracture. The following day, the AICD was replaced with no arrythmias noted. The patient had an uneventful recovery. CONCLUSIONS: In patients with a known history of LQTS, preparation and prevention are cornerstones of anesthesia care. Minimizing the use of triggering medications and emotional stress in the perioperative period, combined with ready equipment and medications to respond to arrythmias, are essential. In children, there is a greater chance of lead fracture and resulting device failure. Preoperative history of device function or interrogation of the AICD and possibly a chest X-ray are essential to ensure the integrity of the leads. International Scientific Literature, Inc. 2020-10-15 /pmc/articles/PMC7571281/ /pubmed/33056945 http://dx.doi.org/10.12659/AJCR.925602 Text en © Am J Case Rep, 2020 This work is licensed under Creative Common Attribution-NonCommercial-NoDerivatives 4.0 International (CC BY-NC-ND 4.0 (https://creativecommons.org/licenses/by-nc-nd/4.0/) ) |
spellingShingle | Articles Coleman, Melissa Imundo, Jason R. Cortez, Daniel Cohen, Mark H. Dhar, Padmani Dalal, Priti G. Torsades de Pointes During Myringotomy in a Child with Congenital Long QT Syndrome: A Case Report |
title | Torsades de Pointes During Myringotomy in a Child with Congenital Long QT Syndrome: A Case Report |
title_full | Torsades de Pointes During Myringotomy in a Child with Congenital Long QT Syndrome: A Case Report |
title_fullStr | Torsades de Pointes During Myringotomy in a Child with Congenital Long QT Syndrome: A Case Report |
title_full_unstemmed | Torsades de Pointes During Myringotomy in a Child with Congenital Long QT Syndrome: A Case Report |
title_short | Torsades de Pointes During Myringotomy in a Child with Congenital Long QT Syndrome: A Case Report |
title_sort | torsades de pointes during myringotomy in a child with congenital long qt syndrome: a case report |
topic | Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7571281/ https://www.ncbi.nlm.nih.gov/pubmed/33056945 http://dx.doi.org/10.12659/AJCR.925602 |
work_keys_str_mv | AT colemanmelissa torsadesdepointesduringmyringotomyinachildwithcongenitallongqtsyndromeacasereport AT imundojasonr torsadesdepointesduringmyringotomyinachildwithcongenitallongqtsyndromeacasereport AT cortezdaniel torsadesdepointesduringmyringotomyinachildwithcongenitallongqtsyndromeacasereport AT cohenmarkh torsadesdepointesduringmyringotomyinachildwithcongenitallongqtsyndromeacasereport AT dharpadmani torsadesdepointesduringmyringotomyinachildwithcongenitallongqtsyndromeacasereport AT dalalpritig torsadesdepointesduringmyringotomyinachildwithcongenitallongqtsyndromeacasereport |