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Hypertrophic cardiomyopathy in childhood and adolescence - strategies to prevent sudden death.

Author: Ostman-SmithIngegerd

Journal ArticleAn article published in an academic or professional journal that reports original research or scholarly analysis.
ReviewAn article that critically examines existing research on a particular topic and summarizes the current state of knowledge in the field.

Overview

Hypertrophic cardiomyopathy is a common cause of sudden death in childhood, particularly in the 8- to 16-year age range. Beta-blocker therapy with lipophilic beta-blockers significantly reduces sudden death risk. Other treatments, like disopyramide and internal cardioverter defibrillator implantation, are also used.
Paper Details　
Original Abstract of the Article :
Clinically overt hypertrophic cardiomyopathy is the most common cause of sudden unexpected death in childhood and has significantly higher sudden death mortality in the 8- to 16-year age range than in the 17- to 30-year age range. A combination of electrocardiographic risk factors (a limb-lead ECG v...See full text at original site
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引用元：
https://doi.org/10.1111/j.1472-8206.2010.00869.x

データ提供：米国国立医学図書館（NLM）

Hypertrophic Cardiomyopathy: A Silent Killer in Children

Hypertrophic cardiomyopathy (HCM), a heart muscle disease, can be particularly dangerous in children and adolescents, increasing the risk of sudden cardiac death. This research focuses on strategies to prevent sudden death in children with HCM. The authors discuss the importance of identifying high-risk patients based on electrocardiographic risk factors and septal wall thickness. They also emphasize the role of beta-blockers, particularly lipophilic beta-blockers, in reducing the risk of sudden death. The study also discusses the potential benefits and risks of other treatments, such as disopyramide, calcium-channel blockers, amiodarone, and internal cardioverter defibrillators.

Preventing Sudden Death: A Multifaceted Approach

The study emphasizes the importance of early detection and risk stratification in managing HCM in children. Identifying high-risk patients through ECG and septal wall thickness measurements allows for targeted interventions to reduce the risk of sudden cardiac death. The study highlights the crucial role of beta-blockers, particularly lipophilic beta-blockers, in reducing the risk of sudden death in these patients.

HCM in Children: A Complex Challenge

This research highlights the challenges of managing HCM in children and adolescents. The study emphasizes the importance of careful patient selection, appropriate treatment strategies, and ongoing monitoring to minimize the risk of sudden cardiac death. Understanding the diverse risk factors and treatment options for HCM in children is crucial for ensuring the health and safety of these vulnerable individuals.

Dr. Camel's Conclusion

This research provides essential information for healthcare professionals managing HCM in children and adolescents. The study highlights the critical need for early detection, risk stratification, and appropriate treatment strategies to prevent sudden cardiac death. The study's findings emphasize the importance of ongoing research and collaborative efforts to improve the management of HCM in children and adolescents, ultimately contributing to healthier and safer futures for these individuals.

Date :
  1. Date Completed 2011-01-05
  2. Date Revised 2020-12-16
Further Info :

Pubmed ID

20727015

DOI: Digital Object Identifier

10.1111/j.1472-8206.2010.00869.x

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English

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