Journal of Clinical Medicine Research, ISSN 1918-3003 print, 1918-3011 online, Open Access |
Article copyright, the authors; Journal compilation copyright, J Clin Med Res and Elmer Press Inc |
Journal website https://www.jocmr.org |
Review
Volume 15, Number 1, January 2023, pages 1-9
Sudden Cardiac Death in Young Individuals: A Current Review of Evaluation, Screening and Prevention
Table
AHA 14 points | Modified four points |
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AAP: American Academy of Pediatrics; AHA: American Heart Association; CPVT: catecholaminergic polymorphic ventricular tachycardia; DCM: dilated cardiomyopathy; HCM: hypertrophic cardiomyopathy; LQTS: long QT syndrome; SIDS: sudden infant death syndrome. | |
Personal history | 1. Have you ever fainted, passed out, or had an unexplained seizure suddenly and without warning, especially during exercise or in response to sudden loud noises, such as doorbells, alarm clocks, and ringing telephones? |
1. History of chest pain/discomfort/tightness on exertion? | |
2. History of unexplained syncope? | |
3. History of excessive and unexplained dyspnea or palpitations associated with exertion | |
2. Have you ever experienced breathlessness or chest pain while exercise? | |
4. Prior history of heart murmur on examination | |
3. Has anyone in your immediate family or more distant relatives (aunts, uncles, cousins) passed away suddenly or unexpectedly before the age of 50 due to cardiac issues? This includes unexpected drownings, unexplained auto crashes in which the relative was the driver, or SIDS? | |
5. History of increased blood pressure | |
6. Any prior restriction on sports activity | |
7. Were you ever ordered heart disease investigations by a physician? | |
Family history | |
8. Early death of > 1 relative before the age of 50 years due to heart disease | 4. Is there anyone in your family under the age of 50 who has a pacemaker or implantable defibrillator, or to anyone with hypertrophic obstructive cardiomyopathy, Marfan syndrome, LQTS, arrhythmogenic cardiomyopathy, short QT syndrome, Brugada syndrome, or CPVT? |
9. Close relative of < 50 years with heart disease | |
10. Family history HCM or DCM, LQTS or other channelopathies, Marfan syndrome, symptomatic arrhythmias or any other known genetic cardiac condition | |
Physical examination | |
11. Audible heart murmur | |
12. Check for femoral pulses | |
13. Marfan syndrome findings (Kyphoscoliosis, high arch palate, pectus excavatum, arachnodactyly, arm span > height, hyperlaxity, myopia, mitral valve prolapse, aortic insufficiency, systemic arterial hypertension) | |
14. Brachial artery pressure |