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Chapter 14 - Surgery for Cardiomyopathy and Pericardial Disease

from Section 2 - Anaesthesia for Specific Procedures

Published online by Cambridge University Press:  12 May 2020

Joseph Arrowsmith
Affiliation:
Royal Papworth Hospital, Cambridge
Andrew Roscoe
Affiliation:
Singapore General Hospital
Jonathan Mackay
Affiliation:
Royal Papworth Hospital, Cambridge
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Summary

Cardiomyopathy is a disease spectrum that alters the shape, function and conduction of cardiac muscle. Affecting 1 in 500 people it is often incurable; however, symptom control can improve life quality and expectancy.

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Publisher: Cambridge University Press
Print publication year: 2020

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References

Corrado, D, Link, MS, Calkins, H. Arrhythmogenic right ventricular cardiomyopathy. N Engl J Med 2017; 376: 6172.CrossRefGoogle ScholarPubMed
Irpachi, K, Kumar, KA, Kapoor, PM. Echocardiography for hypertrophic obstructive cardiomyopathy. Ann Card Anaesth 2017; 20: 279.Google ScholarPubMed
Marcus, FI, Fontaine, GH, Guiraudon, G, et al. Right ventricular dysplasia: a report of 24 adult cases. Circulation 1982; 65: 384–98.CrossRefGoogle ScholarPubMed
Pick, JM, Batra, AS. Implantable cardioverter–defibrillator implantation for primary and secondary prevention: indications and outcomes. Cardiol Young 2017; 27: S126S131.CrossRefGoogle ScholarPubMed
Varian, K, Tang, WHW. Therapeutic strategies targeting inherited cardiomyopathies. Curr Heart Fail Rep 2017; 14: 321–30.CrossRefGoogle ScholarPubMed
Weintraub, RG, Semsarian, C, Macdonald, P. Dilated cardiomyopathy. Lancet 2017; 390: 400–14.CrossRefGoogle ScholarPubMed
Zhang, L, Piña, IL. Stress-induced cardiomyopathy. Heart Fail Clin 2019; 15: 4153.CrossRefGoogle ScholarPubMed

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