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Гипертрофическая кардиомиопатия
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Габрусенко С.А., Селезнёв Д.М., Наумов В.Г. Генетические аспекты гипертрофической кардиомиопатии (обзор литературы) // Практикующий врач. 2000. Т. 18. № 2. С. 2–5.
Шляхто Е.В. и др. Первичные кардиомиопатии, современное представление // Терапевтический архив. 2005. Т. 77. № 12. С. 77–83.
Gersh B.J. et al. 2011 ACCF/AHA guideline for the diagnosis and treatment of hypertrophic cardiomyopathy: Executive summary: A report of the American College of cardiology foundation/American heart association task force on practice guidelines // Circulation. 2011. Vol. 124, № 24. P. 2761–2796.
Elliott P. et al. 2014 ESC guidelines on diagnosis and management of hypertrophic cardiomyopathy: The task force for the diagnosis and management of hypertrophic cardiomyopathy of the European Society of Cardiology (ESC) // Eur. Heart J. 2014. Vol. 35, № 39. P. 2733–2779.
Alfares A.A. et al. Results of clinical genetic testing of 2,912 probands with hypertrophic cardiomyopathy: Expanded panels offer limited additional sensitivity // Genet. Med. 2015. Vol. 17, № 11. P. 880–888.
Coats C.J., Elliott P.M. Genetic biomarkers in hypertrophic cardiomyopathy // Biomark. Med. 2013. Vol. 7, № 4. P. 505–516.
Elliott P., McKenna W.J. Hypertrophic cardiomyopathy // Lancet. 2004. Vol. 363, № 9424. P. 1881–1891.
Kelly M.A. et al. Adaptation and validation of the ACMG/AMP variant classification framework for MYH7-associated inherited cardiomyopathies: Recommendations by ClinGen’s Inherited Cardiomyopathy Expert Panel // Genet. Med. 2018. Vol. 20, № 3. P. 351–359.
Kokado H. et al. Clinical features of hypertrophic cardiomyopathy caused by a Lys183 deletion mutation in the cardiac troponin I gene // Circulation. 2000. Vol. 102, № 6. P. 663–669.
Kostareva A. et al. Deletion in TNNI3 gene is associated with restrictive cardiomyopathy // Int. J. Cardiol. 2009. Vol. 131, № 3. P. 410–412.
Maron B.J. Hypertrophic Cardiomyopathy: A Systematic Review // JAMA. 2002. Vol. 287, № 10. P. 1308–1320.
Maron B.J. et al. Moving Beyond the Sarcomere to Explain Heterogeneity in Hypertrophic Cardiomyopathy: JACC Review Topic of the Week // J. Am. Coll. Cardiol. 2019. Vol. 73, № 15. P. 1978–1986.
Mogensen J. et al. Frequency and Clinical Expression of Cardiac Troponin I Mutations in 748 Consecutive Families With Hypertrophic Cardiomyopathy // J. Am. Coll. Cardiol. 2004. Vol. 44. P. 2315–2325.
Селезнёв Д.М. и др. Роль мутаций в гене тяжелой цепи сердечного бета-миозина в российской популяции больных с гипертрофической кардиомиопатией // Кардиология. 2005. Т. 45. № 4. С. 15–20.
Туральчук М.В., Новик Г.А., Гудкова А.Я. Особенности течения кардиомиопатий с рестриктивным фенотипом, обусловленных мутациями генов сердечного тропонина I и десмина, и алгоритмы их диагностики // Педиатрическая фармакология. 2011. Т. 8. № 4. С. 112–116.
Burton D. et al. Two mutations in troponin I that cause hypertrophic cardiomyopathy have contrasting effects on cardiac muscle contractility // Biochem. J. 2002. Vol. 362, № 2. P. 443–451.
Zhou N. et al. Whole-exome sequencing identifies rare compound heterozygous mutations in the MYBPC3 gene associated with severe familial hypertrophic cardiomyopathy // Eur. J. Med. Genet. 2018. Vol. 61, № 8. P. 434–441.
Charron P. et al. Accuracy of European diagnostic criteria for familial hypertrophic cardiomyopathy in a genotyped population // Int. J. Cardiol. 2003. Vol. 90, № 1. P. 33–38.
Lopes L.R. et al. Use of high-throughput targeted exome-sequencing to screen for copy number variation in hypertrophic cardiomyopathy // Eur. J. Med. Genet. 2015. Vol. 58, № 11. P. 611–616.
Brignole M. et al. 2013 ESC Guidelines on cardiac pacing and cardiac resynchronization therapy: The Task Force on cardiac pacing and resynchronization therapy of the European Society of Cardiology (ESC). Developed in collaboration with the European Heart Rhythm Association // Europace. 2013. Vol. 15, № 8. P. 1070–1118.
Hiemstra Y.L. et al. Development of and Progression of Overt Heart Failure in Nonobstructive Hypertrophic Cardiomyopathy // Am. J. Cardiol. 2018. Vol. 122, № 4. P. 656–662.
Ho C.Y. et al. The burden of early phenotypes and the influence of wall thickness in hypertrophic cardiomyopathy mutation carriers: Findings from the HCMNet study // JAMA Cardiol. 2017. Vol. 2, № 4. P. 419–428.
Hodatsu A. et al. Compound heterozygosity deteriorates phenotypes of hypertrophic cardiomyopathy with founder MYBPC3 mutation: Evidence from patients and zebrafish models // Am. J. Physiol. - Hear. Circ. Physiol. 2014. Vol. 307, № 11. P. H1594–H1604.
Horimoto M. et al. Development of obstructive hypertrophic cardiomyopathy from nonobstructive hypertrophic cardiomyopathy // Am. J. Cardiol. 1998. Vol. 82, № 3. P. 403–405.
Ansari-Lari M.A., Ali S.Z. Fine-Needle Aspiration of Abdominal Fat Pad for Amyloid Detection: A Clinically Useful Test? // Diagn. Cytopathol. 2004. Vol. 30, № 3. P. 178–181.
Canepa M. et al. Comparison of clinical presentation, left ventricular morphology, hemodynamics, and exercise tolerance in obese versus nonobese patients with hypertrophic cardiomyopathy // Am. J. Cardiol. 2013. Vol. 112, № 8. P. 1182–1189.
Charron P. et al. Genetic counselling and testing in cardiomyopathies: A position statement of the European Society of Cardiology Working Group on Myocardial and Pericardial Diseases // Eur. Heart J. 2010. Vol. 31, № 22. P. 2715–2728.
Finocchiaro G. et al. Impact of demographic features, lifestyle, and comorbidities on the clinical expression of hypertrophic cardiomyopathy // J. Am. Heart Assoc. 2017. Vol. 6, № 12. P. e007161.
Bos J.M., Ommen S.R., Ackerman M.J. Genetics of hypertrophic cardiomyopathy: one, two, or more diseases? // Curr. Opin. Cardiol. 2007. Vol. 22, № 3. P. 193–199.
Richards S. et al. Standards and guidelines for the interpretation of sequence variants: A joint consensus recommendation of the American College of Medical Genetics and Genomics and the Association for Molecular Pathology // Genet. Med. 2015. Vol. 17, № 5. P. 405–424.
Marian A.J., Braunwald E. Hypertrophic cardiomyopathy: Genetics, pathogenesis, clinical manifestations, diagnosis, and therapy // Circ. Res. 2017. Vol. 121, № 7. P. 749–770.
Бокерия Л.А. и др. Экспрессия генов матриксной металлопротеиназы-1 (ММР-1), тканевого ингибитора матриксных металлопротеиназ-1 (TIMP-1), коллагена I и III типов в миокарде больных идиопатической гипертрофической кардиомиопатией // Бюллетень НЦССХ им. А.Н. Бакулева РАМН. 2005. Т. 6. № 4. С. 35–42.
Гудкова А.Я. и др. Гипертрофическая кардиомиопатия. Клинико-морфологические сопоставления // Архив патологии. 2012. Т. 74. № 4. С. 8–11.
Гудкова А.Я. Характеристика течения обструктивной гипертрофической кардиомиопатии у взрослых (обзор литературы и результаты собственных исследований) // Артериальная гипертензия. 2008. Т. 14. № 2, Приложение 2. С. 39–49.
Гудкова А.Я., Шляхто Е.В. Клеточные механизмы гипертрофии миокарда при гипертрофической кардиомиопатии и эссенциальной артериальной гипертензии // Артериальная гипертензия. 2008. Т. 14. № 4. С. 364–380.
Shlyakhto E. V. et al. Cellular aspects of pathogenesis of hypertrophic cardiomyopathy: Role of cardiomyocyte polyploidy and activation of nuclear antigen of the proliferating cell in myocardium // Cell tissue biol. 2007. Vol. 1, № 6. P. 582–588.
Frustaci A., Russo M.A., Chimenti C. Diagnostic contribution of left ventricular endomyocardial biopsy in patients with clinical phenotype of hypertrophic cardiomyopathy // Hum. Pathol. 2013. Vol. 44, № 1. P. 133–141.
Leone O. et al. 2011 Consensus statement on endomyocardial biopsy from the Association for European Cardiovascular Pathology and the Society for Cardiovascular Pathology // Cardiovasc. Pathol. 2012. Vol. 21, № 4. P. 245–274.
Philipson D.J. et al. Emerging pharmacologic and structural therapies for hypertrophic cardiomyopathy // Heart Fail. Rev. 2017. Vol. 22, № 6. P. 879–888.
Roberts R., Sigwart U. Current concepts of the pathogenesis and treatment of hypertrophic cardiomyopathy // Circulation. 2005. Vol. 112, № 2. P. 293–296.
Varnava A.M. et al. Hypertrophic cardiomyopathy: The interrelation of disarray, fibrosis and small vessel disease // Heart. 2000. Vol. 84, № 5. P. 476–482.
Зайцев В.В. и др. Клиническое значение различных методов оценки миокардиального фиброза при гипертрофической кардиомиопатии // Кардиология. 2020. Т. 60. № 3. С. 44–50.
Arbustini E. et al. The MOGE(S) classification for a phenotype-genotype nomenclature of cardiomyopathy: Endorsed by the world heart federation // J. Am. Coll. Cardiol. 2013. Vol. 62, № 22. P. 2046–2072.
Barcia G. et al. Pitfalls in molecular diagnosis of Friedreich ataxia // Eur. J. Med. Genet. 2018. Vol. 61, № 8. P. 455–458.
Bokhari S. et al. 99mTc-pyrophosphate scintigraphy for differentiating light-chain cardiac amyloidosis from the transthyretin-related familial and senile cardiac amyloidoses // Circ. Cardiovasc. Imaging. 2013. Vol. 6, № 2. P. 195–201.
Charron P. et al. Danon’s disease as a cause of hypertrophic cardiomyopathy: A systematic survey // Heart. 2004. Vol. 90, № 8. P. 842–846.
Cook A., Giunti P. Friedreich’s ataxia: Clinical features, pathogenesis and management // Br. Med. Bull. 2017. Vol. 124, № 1. P. 19–30.
D’souza A. et al. Localized insulin-derived amyloidosis: A potential pitfall in the diagnosis of systemic amyloidosis by fat aspirate // Am. J. Hematol. 2012. Vol. 87, № 11. P. E131-132.
Dubrey S.W., Hawkins P.N., Falk R.H. Amyloid diseases of the heart: Assessment, diagnosis, and referral // Heart. 2011. Vol. 97, № 1. P. 75–84.
Frustaci A. et al. Evolution of cardiac pathology in classic Fabry disease: Progressive cardiomyocyte enlargement leads to increased cell death and fibrosis, and correlates with severity of ventricular hypertrophy // Int. J. Cardiol. 2017. Vol. 248. P. 257–262.
Monserrat L. et al. Prevalence of Fabry Disease in a Cohort of 508 Unrelated Patients With Hypertrophic Cardiomyopathy // J. Am. Coll. Cardiol. 2007. Vol. 50, № 25. P. 2399–2403.
Planté-Bordeneuve V., Said G. Familial amyloid polyneuropathy // Lancet Neurol. 2011. Vol. 10, № 12. P. 1086–1097.
Quarta C.C. et al. Defining the diagnosis in echocardiographically suspected senile systemic amyloidosis // JACC Cardiovasc. Imaging. 2012. Vol. 5, № 7. P. 755–758.
European Reference Networks in the Field of Rare Diseases: State of the Art and Future Directions. Third Report [Electronic resource]. 2008. URL:
http://www.eucerd.eu/? post_type=document&p=1204
.
Sado D.M. et al. Identification and assessment of anderson-fabry disease by cardiovascular magnetic resonance noncontrast myocardial T1 mapping // Circ. Cardiovasc. Imaging. 2013. Vol. 6, № 3. P. 392–398.
Tsai S.B. et al. Myocardial infarction with “clean coronaries” caused by amyloid light-chain AL amyloidosis: A case report and literature review // Amyloid. 2011. Vol. 18, № 3. P. 160–164.
Vogelsberg H. et al. Cardiovascular Magnetic Resonance in Clinically Suspected Cardiac Amyloidosis. Noninvasive Imaging Compared to Endomyocardial Biopsy // J. Am. Coll. Cardiol. 2008. Vol. 51, № 10. P. 1022–1030.
Wilkinson J.D. et al. Outcomes in children with Noonan syndrome and hypertrophic cardiomyopathy: A study from the Pediatric Cardiomyopathy Registry // Am. Heart J. 2012. Vol. 164, № 3. P. 442–448.
Yang Z., Vatta M. Danon disease as a cause of autophagic vacuolar myopathy // Congenit. Heart Dis. 2007. Vol. 2, № 6. P. 404–409.
Yang Z. et al. Danon Disease as an Underrecognized Cause of Hypertrophic Cardiomyopathy in Children // Circulation. 2005. Vol. 112, № 11. P. 1612–1617.
Ibrahim M. et al. Modern Management of Systolic Anterior Motion of the Mitral Valve // Eur J Cardiothorac Surg. 2012. Vol. 41. P. 60–70.
Deng L. et al. Numerical simulation study on systolic anterior motion of the mitral valve in hypertrophic obstructive cardiomyopathy // Int. J. Cardiol. 2018. Vol. 266. P. 167–173.
Manabe S. et al. Management of systolic anterior motion of the mitral valve: a mechanism-based approach // Gen. Thorac. Cardiovasc. Surg. 2018. Vol. 66, № 7. P. 379–389.
Ro R. et al. Vector flow mapping in obstructive hypertrophic cardiomyopathy to assess the relationship of early systolic left ventricular flow and the mitral valve // J. Am. Coll. Cardiol. 2014. Vol. 64, № 19. P. 1984–1995.
Hymel B.J., Townsley M.M. Echocardiographic assessment of systolic anterior motion of the mitral valve // Anesth. Analg. 2014. Vol. 118, № 6. P. 1197–1201.
Sherrid M. V. et al. Systolic anterior motion begins at low left ventricular outflow tract velocity in obstructive hypertrophic cardiomyopathy // J. Am. Coll. Cardiol. 2000. Vol. 36, № 4. P. 1344–1354.
Silbiger J.J. Abnormalities of the Mitral Apparatus in Hypertrophic Cardiomyopathy: Echocardiographic, Pathophysiologic, and Surgical Insights // J. Am. Soc. Echocardiogr. 2016. Vol. 29, № 7. P. 622–639.
Shah J.S. et al. Prevalence of exercise-induced left ventricular outflow tract obstruction in symptomatic patients with non-obstructive hypertrophic cardiomyopathy // Heart. 2008. Vol. 94, № 10. P. 1288–1294.
Geske J.B. et al. Variability of left ventricular outflow tract gradient during cardiac catheterization in patients with hypertrophic cardiomyopathy // JACC Cardiovasc. Interv. 2011. Vol. 4, № 6. P. 704–709.
Efthimiadis G.K. et al. Clinical characteristics and natural history of hypertrophic cardiomyopathy with midventricular obstruction // Circ. J. 2013. Vol. 77, № 9. P. 2366–2374.
Minami Y. et al. Clinical implications of midventricular obstruction in patients with hypertrophic cardiomyopathy // J. Am. Coll. Cardiol. 2011. Vol. 57, № 23. P. 2346–2355.
Yan L.R. et al. Clinical characteristics and prognosis of 60 patients with midventricular obstructive hypertrophic cardiomyopathy // J. Cardiovasc. Med. 2015. Vol. 16, № 11. P. 751–760.
Hang D. et al. Combined transaortic and transapical approach to septal myectomy in patients with complex hypertrophic cardiomyopathy // J. Thorac. Cardiovasc. Surg. 2018. Vol. 155, № 5. P. 2096–2102.
Pacheco Claudio C. et al. Why names matter for women: MINOCA/INOCA (myocardial infarction/ischemia and no obstructive coronary artery disease) // Clin. Cardiol. 2018. Vol. 41, № 2. P. 185–193.
Аверкина Н.В. и др. Оценка перфузии миокарда у больных с гипертрофической кардиомиопатией в сопоставлении с клиническими и эхокардиографическими данными // Терапевтический архив. 2003. Т. 75. № 4. С. 20–25.
Аверков О.В. и др. Дифференцированный подход в диагностике, формулировке диагноза, ведении больных и статистическом учете инфаркта миокарда 2 типа (согласованная позиция) // Российский кардиологический журнал. 2019. Т. 24. № 6. С. 7–21.
Каплунова В.Ю. и др. Гипертрофическая кардиомиопатия и ишемическая болезнь сердца. Варианты сочетанной патологии // Кардиология. 2017. Т. 57. № 12. С. 16–24.
Костин С.И. Морфологические и морфометрические особенности гипертрофической кардиомиопатии // Архив патологии. 1989. Т. 51. № 1. С. 47–52.
Мухарлямов Н. Кардиомиопатии. Москва, 1990. 283 с. с.
Aletras A.H. et al. Heterogeneity of intramural function in hypertrophic cardiomyopathy mechanistic insights from MRI late gadolinium enhancement and high-resolution displacement encoding with stimulated echoes strain maps // Circ. Cardiovasc. Imaging. 2011. Vol. 4, № 4. P. 425–434.
Camici P.G., Olivotto I., Rimoldi O.E. The coronary circulation and blood flow in left ventricular hypertrophy // J. Mol. Cell. Cardiol. 2012. Vol. 52, № 4. P. 857–864.
Einarsen E. et al. Comparison of Frequency of Ischemic Cardiovascular Events in Patients With Aortic Stenosis With Versus Without Asymmetric Septal Hypertrophy (from the SEAS Trial) // Am. J. Cardiol. 2017. Vol. 119, № 7. P. 1082–1087.
Foà A. et al. Histopathological comparison of intramural coronary artery remodeling and myocardial fibrosis in obstructive versus end-stage hypertrophic cardiomyopathy // Int. J. Cardiol. 2019. Vol. 291. P. 77–82.
Kwon D.H. et al. Cardiac Magnetic Resonance Detection of Myocardial Scarring in Hypertrophic Cardiomyopathy. Correlation With Histopathology and Prevalence of Ventricular Tachycardia // J. Am. Coll. Cardiol. 2009. Vol. 54, № 3. P. 242–249.
Maron M.S. et al. The Case for Myocardial Ischemia in Hypertrophic Cardiomyopathy // J. Am. Coll. Cardiol. 2009. Vol. 54, № 9. P. 866–875.
Mundhenke M., Schwartzkopff B., Strauer B.E. Structural analysis of arteriolar and myocardial remodelling in the subendocardial region of patients with hypertensive heart disease and hypertrophic cardiomyopathy // Virchows Arch. 1997. Vol. 431, № 4. P. 265–273.
Nakamura T. et al. Increased plasma brain natriuretic peptide level as a guide for silent myocardial ischemia in patients with non-obstructive hypertrophic cardiomyopathy // J. Am. Coll. Cardiol. 2002. Vol. 39, № 10. P. 1657–1663.
Raphael C.E. et al. Mechanisms of Myocardial Ischemia in Hypertrophic Cardiomyopathy: Insights From Wave Intensity Analysis and Magnetic Resonance // J. Am. Coll. Cardiol. 2016. Vol. 68, № 15. P. 1651–1660.
Sciagrà R. et al. Myocardial blood flow and left ventricular functional reserve in hypertrophic cardiomyopathy: a 13NH3 gated PET study // Eur. J. Nucl. Med. Mol. Imaging. 2017. Vol. 44, № 5. P. 866–875.
Shin Y.J. et al. Clinical significance of evaluating coronary atherosclerosis in adult patients with hypertrophic cardiomyopathy who have chest pain // Eur. Radiol. 2019. Vol. 29, № 9. P. 4593– 4602.
Liu W., Sun D., Yang J. Diastolic Dysfunction of Hypertrophic Cardiomyopathy Genotype-Positive Subjects Without Hypertrophy Is Detected by Tissue Doppler Imaging: A Systematic Review and Meta-analysis: A // J. Ultrasound Med. 2017. Vol. 36, № 10. P. 2093–2103.
Covella M. et al. Mechanism of Progressive Heart Failure and Significance of Pulmonary Hypertension in Obstructive Hypertrophic Cardiomyopathy // Circ. Hear. Fail. 2017. Vol. 10, № 4. P. e003689.
Germans T. et al. How do hypertrophic cardiomyopathy mutations affect myocardial function in carriers with normal wall thickness? Assessment with cardiovascular magnetic resonance // J. Cardiovasc. Magn. Reson. 2010. Vol. 12, № 1. P. 13.
Huang X. et al. Assessment of left ventricular systolic and diastolic abnormalities in patients with hypertrophic cardiomyopathy using real-time three-dimensional echocardiography and two-dimensional speckle tracking imaging // Cardiovasc. Ultrasound. 2018. Vol. 16, № 1. P. 23.
Matsumura Y. et al. Left ventricular diastolic function assessed using Doppler tissue imaging in patients with hypertrophic cardiomyopathy: Relation to symptoms and exercise capacity // Heart. 2002. Vol. 87, № 3. P. 247–251.
Бокерия Л.А., Борисов К.В., Синев А.Ф. Улучшение диастолической функции левого и правого желудочков сердца после хирургической коррекции гипертрофической обструктивной кардиомиопатии при помощи оригинального способа // Грудная и сердечно-сосудистая хирургия. 1999. Т. 4. С. 4–10.
Harris K.M. et al. Prevalence, clinical profile, and significance of left ventricular remodeling in the end-stage phase of hypertrophic cardiomyopathy // Circulation. 2006. Vol. 114, № 3. P. 216– 225.
Biagini E. et al. Prognostic Implications of the Doppler Restrictive Filling Pattern in Hypertrophic Cardiomyopathy // Am. J. Cardiol. 2009. Vol. 104, № 12. P. 1727–1731.
Bravo P.E. et al. Late gadolinium enhancement confined to the right ventricular insertion points in hypertrophic cardiomyopathy: An intermediate stage phenotype? // Eur. Heart J. Cardiovasc. Imaging. 2016. Vol. 17, № 3. P. 293–300.
Fernández A. et al. Comparison of prevalence, clinical course, and pathological findings of left ventricular systolic impairment versus normal systolic function in patients with hypertrophic cardiomyopathy // Am. J. Cardiol. 2011. Vol. 108, № 4. P. 548–555.
Melacini P. et al. Clinicopathological profiles of progressive heart failure in hypertrophic cardiomyopathy // Eur. Heart J. 2010. Vol. 31, № 17. P. 2111–2123.
Maron M.S. et al. Right Ventricular Involvement in Hypertrophic Cardiomyopathy // Am. J. Cardiol. 2007. Vol. 100, № 8. P. 1293–1298.
Falcone D.M., Moore D., Lambert E.C. Idiopathic hypertrophic cardiomyopathy involving the right ventricle. // Am. J. Cardiol. 1967. Vol. 19, № 5. P. 735–740.
Shimizu M. et al. Echocardiographic assessment of right ventricular obstruction in hypertrophic cardiomyopathy // Circ. J. 2003. Vol. 67, № 10. P. 855–860.
Бокерия Л.А., Борисов К.В. Обструктивная гипертрофическая кардиомиопатия: методы хирургической коррекции // Грудная и сердечно-сосудистая хирургия. 1997. Т. 1. С. 61–65.
Бокерия Л.А. и др. Результаты медикаментозного и хирургического лечения гипертрофической кардиомиопатии с обструкцией выводных отделов левого и правого желудочков сердца // Грудная и сердечно-сосудистая хирургия. 2004. № 2. С. 4–9.
Бокерия Л.А. и др. Хирургическая коррекция ранее неоперабельных форм гипертрофической обструктивной кардиомиопатии // Грудная и сердечно-сосудистая хирургия. 1999. Т. 6. С. 130–136.
Pagourelias E.D. et al. Prognostic Value of Right Ventricular Diastolic Function Indices in Hypertrophic Cardiomyopathy // Eur. J. Echocardiogr. 2011. Vol. 12, № 11. P. 809–817.
Shah J.P. et al. Prevalence and Prognostic Significance of Right Ventricular Dysfunction in Patients With Hypertrophic Cardiomyopathy // Am. J. Cardiol. 2018. Vol. 122, № 11. P. 1932–1938.
Кактурский Л. Внезапная смерть (клиническая морфология). Москва, 2000. 126 с. с.
Ревишвили А.Ш. и др. Клинические рекомендации по проведению электрофизиологических исследований, катетерной абляции и применению имплантируемых антиаритмических устройств. Москва, 2017. 701 с. с.
Adabag A.S. et al. Spectrum and prognostic significance of arrhythmias on ambulatory Holter electrocardiogram in hypertrophic cardiomyopathy // J. Am. Coll. Cardiol. 2005. Vol. 45, № 5. P. 697–704.
Zipes D.P. et al. ACC/AHA/ESC 2006 guidelines for management of patients with ventricular arrhythmias and the prevention of sudden cardiac death // Europace. 2006. Vol. 8, № 9. P. 746–837.
Czosek R.J. et al. Arrhythmic Burden and Ambulatory Monitoring of Pediatric Patients with Cardiomyopathy. // Pacing Clin. Electrophysiol. 2016. Vol. 39, № 5. P. 443–451.
Desai M.Y., Mentias A. Risk stratification in hypertrophic cardiomyopathy // Aging (Albany. NY). 2019. Vol. 11, № 6. P. 1617–1618.
Elliott P.M. et al. Sudden death in hypertrophic cardiomyopathy: Identification of high risk patients // J. Am. Coll. Cardiol. 2000. Vol. 36, № 7. P. 2212–2218.
Goyal V., Jassal D.S., Dhalla N.S. Pathophysiology and prevention of sudden cardiac death // Can. J. Physiol. Pharmacol. 2015. Vol. 94, № 3. P. 237–244.
Marrakchi S. et al. Risk stratification in hypertrophic cardiomyopathy // Herz. 2020. Vol. 45, № 1. P. 50–64.
Weissler-Snir A. et al. Prevention of Sudden Death in Hypertrophic Cardiomyopathy: Bridging the Gaps in Knowledge // Eur Hear. J. 2017. Vol. 38, № 22. P. 1728–1737.
Weissler-Snir A. et al. Usefulness of 14-Day Holter for Detection of Nonsustained Ventricular Tachycardia in Patients With Hypertrophic Cardiomyopathy // Am. J. Cardiol. 2016. Vol. 118, № 8. P. 1258–1263.
Goff Z.D., Calkins H. Sudden death related cardiomyopathies - Hypertrophic cardiomyopathy // Prog. Cardiovasc. Dis. 2019. Vol. 62, № 3. P. 212–216.
Bois J.P. et al. Relation between temperature extremes and symptom exacerbation in patients with hypertrophic cardiomyopathy // Am. J. Cardiol. 2016. Vol. 117, № 6. P. 961–965.
Haghjoo M. et al. Predictors of syncope in patients with hypertrophic cardiomyopathy // PACE - Pacing Clin. Electrophysiol. 2009. Vol. 32, № 5. P. 642–647.
Seggewiß H. et al. Syncope in hypertrophic (obstructive) cardiomyopathy // Herzschrittmachertherapie und Elektrophysiologie. 2018. Vol. 29, № 2. P. 178–182.
Williams L., Frenneaux M. Syncope in Hypertrophic Cardiomyopathy: Mechanisms and Consequences for Treatment // Europace. 2007. Vol. 9, № 9. P. 817–822.
Farhad H. et al. Left Atrial structure and function in hypertrophic cardiomyopathy sarcomere mutation carriers with and without left ventricular hypertrophy // J. Cardiovasc. Magn. Reson. 2017. Vol. 19, № 1. P. 107.
Burstein B., Nattel S. Atrial Fibrosis: Mechanisms and Clinical Relevance in Atrial Fibrillation // J. Am. Coll. Cardiol. 2008. Vol. 51, № 8. P. 802–809.
Philipson D.J., Rader F., Siegel R.J. Risk factors for atrial fibrillation in hypertrophic cardiomyopathy // Eur. J. Prev. Cardiol. 2019. P. doi: 10.1177/2047487319828474. Epub ahead of print.
Garg L. et al. Atrial fibrillation in hypertrophic cardiomyopathy: prevalence, clinical impact, and management // Heart Fail. Rev. 2019. Vol. 24, № 2. P. 189–197.
Killu A.M. et al. Cardiac Resynchronization Therapy in Patients With End-Stage Hypertrophic Cardiomyopathy // Europace. 2018. Vol. 20, № 1. P. 82–88.
Kirchhof P. et al. 2016 ESC Guidelines for the Management of Atrial Fibrillation Developed in Collaboration With EACTS // Eur. Heart J. 2016. Vol. 37. P. 2893–2962.
Maron B.J. et al. Clinical Spectrum and Management of Heart Failure in Hypertrophic Cardiomyopathy // JACC Hear. Fail. Elsevier Inc., 2018. Vol. 6, № 5. P. 353–363.
Seferović P.M. et al. Heart failure in cardiomyopathies: a position paper from the Heart Failure Association of the European Society of Cardiology // Eur. J. Heart Fail. 2019. Vol. 21, № 5. P. 553–576.
Maron B.J. et al. Epidemiology of Hypertrophic Cardiomyopathy–Related Death // Circulation. 2000. Vol. 102, № 8. P. 858–864.
Semsarian C. et al. New perspectives on the prevalence of hypertrophic cardiomyopathy // J. Am. Coll. Cardiol. 2015. Vol. 65, № 12. P. 1249–1254.
Amano Y. et al. MRI classification of asymmetric septal hypertrophic cardiomyopathy and its relation to the presence of risk factors // Int. J. Cardiovasc. Imaging. 2012. Vol. 28, № 8. P. 2019– 2025.
Geske J.B., Ommen S.R., Gersh B.J. Hypertrophic Cardiomyopathy: Clinical Update // JACC Hear. Fail. 2018. Vol. 6, № 5. P. 364–375.
Дземешкевич С.Л. и др. Анатомические и морфологические признаки диффузно-генерализованной формы гипертрофической кардиомиопатии // Российский кардиологический журнал. 2015. Т. 5. № 121. С. 58–63.
Gudkova A. et al. Diagnostic challenge in desmin cardiomyopathy with transformation of clinical phenotypes // Pediatr. Cardiol. 2013. Vol. 34, № 2. P. 467–470.
Rowin E.J. et al. Interaction of Adverse Disease Related Pathways in Hypertrophic Cardiomyopathy // Am. J. Cardiol. 2017. Vol. 120, № 12. P. 2256–2264.
Габрусенко С.А. и др. Клинико-гемодинамический статус и сердечные натрийуретические пептиды в плазме больных гипертрофической кардиомиопатией // Кардиологический вестник (Бюллетень РКНПК). 2006. Т. 1. № 2. С. 25–31.
Стрельцова А.А., Гудкова А.Я., Костарева А.А. Фибрилляция предсердий при гипертрофической кардиомиопатии: современные аспекты эпидемиологии, факторов риска, патогенеза и фармакотерапии // Cons. Medicum. 2018. Т. 20. № 5. С. 34–39.
Стрельцова А.А. и др. Полиморфный вариант rs1739843 гена белка теплового шока 7 (HSPB7) и его связь с вариантами клинического течения и исходами у пациентов с гипертрофической кардиомиопатией (результаты 10-летнего наблюдения) // Российский кардиологический журнал. 2019. № 10. С. 7–15.
Binder J. et al. Echocardiography-guided genetic testing in hypertrophic cardiomyopathy: Septal morphological features predict the presence of myofilament mutations // Mayo Clin. Proc. 2006. Vol. 81, № 4. P. 459–467.
Elliott P., Spirito P. Prevention of hypertrophic cardiomyopathy-related deaths: Theory and practice // Heart. 2008. Vol. 94, № 10. P. 1269–1275.
Elliott P.M. et al. Historical trends in reported survival rates in patients with hypertrophic cardiomyopathy // Heart. 2006. Vol. 92, № 6. P. 785–791.
Kawai C. et al. Hypertrophic obstructive and non-obstructive cardiomyopathy in Japan. Diagnosis of the disease with special reference to endomyocardial catheter biopsy // Eur Hear. J. 1983. Vol. 4, № 1. P. 121–125.
Kitaoka H. et al. Hypertrophic Cardiomyopathy With Progression From Apical Hypertrophy to Asymmetrical Septal Hypertrophy: A Case Report // J. Cardiol. 2005. Vol. 45, № 4. P. 155–159.
Klues H.G., Schiffers A., Maron B.J. Phenotypic spectrum and patterns of left ventricular hypertrophy in hypertrophic cardiomyopathy: Morphologic observations and significance as assessed by two-dimensional echocardiography in 600 patients // J. Am. Coll. Cardiol. 1995. Vol. 26, № 7. P. 1699–1708.
Maron B.J. et al. Clinical profile of stroke in 900 patients with hypertrophic cardiomyopathy // J. Am. Coll. Cardiol. 2002. Vol. 39, № 2. P. 301–307.
Thaman R. et al. Progressive left ventricular remodeling in patients with hypertrophic cardiomyopathy and severe left ventricular hypertrophy // J. Am. Coll. Cardiol. 2004. Vol. 44, № 2. P. 398–405.
Lancellotti P. et al. The Clinical Use of Stress Echocardiography in Non-Ischaemic Heart Disease: Recommendations from the European Association of Cardiovascular Imaging and the American Society of Echocardiography. // J. Am. Soc. Echocardiogr. 2017. Vol. 30, № 2. P. 101–138.
Parato V.M. et al. Echocardiographic diagnosis of the different phenotypes of hypertrophic cardiomyopathy // Cardiovasc. Ultrasound. 2016. Vol. 14, № 1. P. 30.
Lambiase P.D. et al. Worldwide Experience With a Totally Subcutaneous Implantable Defibrillator: Early Results From the EFFORTLESS S-ICD Registry // Eur Hear. J. 2014. Vol. 35, № 25. P. 1657–1665.
Ponikowski P. et al. 2016 ESC Guidelines for the diagnosis and treatment of acute and chronic heart failure: The Task Force for the diagnosis and treatment of acute and chronic heart failure of the European Society of Cardiology (ESC). Developed with the special contribution // Eur. J. Heart Fail. 2016. Vol. 18, № 8. P. 891–975.
Maron B.J. et al. American College of Cardiology/European Society of Cardiology Clinical Expert Consensus Document on Hypertrophic Cardiomyopathy: A report of the American College of Cardiology Foundation Task Force on Clinical Expert Consensus Documents and the European S // Eur. Heart J. 2003. Vol. 24, № 21. P. 1965–1991.
Barrett M.J., Ayub B., Martinez M.W. Cardiac auscultation in sports medicine: Strategies to improve clinical care // Curr. Sports Med. Rep. 2012. Vol. 11, № 2. P. 78–84.
Cantwell J.D. Preparticipation physical evaluation: Getting to the heart of the matter // Med. Sci. Sports Exerc. 1998. Vol. 30, № 10. P. 341–344.
Efthimiadis G.K. et al. Prevalence and Clinical Outcomes of Incidentally Diagnosed Hypertrophic Cardiomyopathy // Am. J. Cardiol. 2010. Vol. 105, № 10. P. 1445–1450.
Harmon K.G., Zigman M., Drezner J.A. The effectiveness of screening history, physical exam, and ECG to detect potentially lethal cardiac disorders in athletes: A systematic review/meta-analysis // J. Electrocardiol. 2015. Vol. 48, № 3. P. 329–338.
Raviele A. et al. Management of Patients With Palpitations: A Position Paper From the European Heart Rhythm Association // Europace. 2011. Vol. 13, № 7. P. 920–934.
Attenhofer Jost C.H. et al. Echocardiography in the evaluation of systolic murmurs of unknown cause // Am. J. Med. 2000. Vol. 108, № 8. P. 614–620.
Rapezzi C. et al. Diagnostic work-up in cardiomyopathies: bridging the gap between clinical phenotypes and final diagnosis. A position statement from the ESC Working Group on Myocardial and Pericardial Diseases // Eur Hear. J. 2013. Vol. 34. P. 1448–1458.
Rapezzi C. et al. Disease profile and differential diagnosis of hereditary transthyretin-related amyloidosis with exclusively cardiac phenotype: an Italian perspective // Eur Hear. J. 2013. Vol. 34, № 7. P. 520–528.
Sarkozy A., Digilio M.C., Dallapiccola B. Leopard syndrome // Orphanet J. Rare Dis. 2008. Vol. 3, № 1. P. 13.
Scaglia F. et al. Clinical Spectrum, Morbidity, and Mortality in 113 Pediatric Patients with Mitochondrial Disease // Pediatrics. 2004. Vol. 114, № 4. P. 925–931.
Pagourelias E.D. et al. Efficacy of various “classic” echocardiographic and laboratory indices in distinguishing the “gray zone” between athlete’s heart and hypertrophic cardiomyopathy: A pilot study // Echocardiography. 2013. Vol. 30, № 2. P. 131–139.
Coutu M. et al. Cardiac transplantation for hypertrophic cardiomyopathy: a valid therapeutic option. // J. Heart Lung Transplant. 2004. Vol. 23, № 4. P. 413–417.
Zhang C., Huang X., Li J. Light chain amyloidosis: Where are the light chains from and how they play their pathogenic role? // Blood Rev. 2017. Vol. 31, № 4. P. 261–270.
Ingles J. et al. Nonfamilial Hypertrophic Cardiomyopathy: Prevalence, Natural History, and Clinical Implications // Circ. Cardiovasc. Genet. 2017. Vol. 10, № 2. P. e001620.
Maron B.J., Pelliccia A., Spirito P. Cardiac disease in young trained athletes: Insights into methods for distinguishing athlete’s heart from structural heart disease, with particular emphasis on hypertrophic cardiomyopathy // Circulation. 1995. Vol. 91, № 5. P. 1596–1601.
Young L. et al. Hypertrophic cardiomyopathy: A complex disease // Cleve. Clin. J. Med. 2018. Vol. 85, № 5. P. 399–411.
Efthimiadis G.K. et al. Hypertrophic cardiomyopathy in 2013: Current speculations and future perspectives // World J Cardiol. 2014. Vol. 6, № 2. P. 26–37.
Hershberger R.E. et al. Genetic Evaluation of Cardiomyopathy–A Heart Failure Society of America Practice Guideline // J. Card. Fail. 2018. Vol. 24, № 5. P. 281–302.
Efthimiadis G.K. et al. An Overview of Pharmacotherapy in Hypertrophic Cardiomyopathy: Current Speculations and Clinical Perspectives. // Rev. Cardiovasc. Med. 2016. Vol. 17, № 3–4. P. 115–123.
Fananapazir L. et al. Electrophysiologic abnormalities in patients with hypertrophic cardiomyopathy. A consecutive analysis in 155 patients // Circulation. 1989. Vol. 80, № 5. P. 1259– 1268.
Kelly B.S., Mattu A., Brady W.J. Hypertrophic cardiomyopathy: electrocardiographic manifestations and other important considerations for the emergency physician // Am. J. Emerg. Med. 2007. Vol. 25, № 1. P. 72–79.
McLeod C.J. et al. Outcome of Patients With Hypertrophic Cardiomyopathy and a Normal Electrocardiogram // J. Am. Coll. Cardiol. 2009. Vol. 54, № 3. P. 229–233.
Wilke I. et al. High Incidence of De Novo and Subclinical Atrial Fibrillation in Patients With Hypertrophic Cardiomyopathy and Cardiac Rhythm Management Device // J. Cardiovasc. Electrophysiol. 2016. Vol. 27, № 7. P. 779–784.
Хирманов В.Н. и др. Электрокардиографические методы в диагностике, выборе метода и тактики лечения гипертрофической кардиомиопатии // Prog. Biomed. Res. 1997. Т. 2. № 1. С. 7–22.
O’Mahony C. et al. A novel clinical risk prediction model for sudden cardiac death in hypertrophic cardiomyopathy (HCM Risk-SCD) // Eur Hear. J. 2014. Vol. 35, № 30. P. 2010–2020.
Wasfy M.M., Weiner R.B. Differentiating the athlete’s heart from hypertrophic cardiomyopathy // Current Opinion in Cardiology. 2015. Vol. 30, № 5. P. 500–505.
Weigner M.J. et al. Risk for clinical thromboembolism associated with conversion to sinus rhythm in patients with atrial fibrillation lasting less than 48 hours // Ann. Intern. Med. 1997. Vol. 126, № 8. P. 615–620.
Guttmann O.P. et al. Atrial fibrillation and thromboembolism in patients with hypertrophic cardiomyopathy: Systematic review // Heart. 2014. Vol. 100, № 6. P. 465–472.
Brignole M. et al. Indications for the use of diagnostic implantable and external ECG loop recorders. // Europace. 2009. Vol. 11, № 5. P. 671–687.
Frangini P.A. et al. How revealing are insertable loop recorders in pediatrics? // Pacing Clin. Electrophysiol. 2008. Vol. 31, № 3. P. 338–343.
Solano A. et al. Incidence, diagnostic yield and safety of the implantable loop-recorder to detect the mechanism of syncope in patients with and without structural heart disease // Eur. Heart J. 2004. Vol. 25, № 13. P. 1116–1119.
Moon J.C.C. et al. The histologic basis of late gadolinium enhancement cardiovascular magnetic resonance in hypertrophic cardiomyopathy // J. Am. Coll. Cardiol. 2004. Vol. 43, № 12. P. 2260–2264.
O’Hanlon R. et al. Prognostic significance of myocardial fibrosis in hypertrophic cardiomyopathy // J. Am. Coll. Cardiol. 2010. Vol. 56, № 11. P. 867–874.
Pernat A., Pohar B., Horvat M. Heart conduction disturbances and cardiovascular collapse after disopyramide and low-dose metoprolol in a patient with hypertrophic obstructive cardiomyopathy // J. Electrocardiol. 1997. Vol. 30, № 4. P. 341–344.
Cerqueira M.D. et al. Standardized Myocardial Segmentation and Nomenclature for Tomographic Imaging of the Heart A Statement for Healthcare Professionals From the Cardiac Imaging Committee // Circulation. 2002. Vol. 105, № 4. P. 539–542.
Flachskampf F. et al. Recommendations for Transoesophageal Echocardiography: Update 2010 // Eur. J. Echocardiogr. 2010. Vol. 11, № 7. P. 557–576.
Lang R.M. et al. Recommendations for cardiac chamber quantification by echocardiography in adults: An update from the American society of echocardiography and the European association of cardiovascular imaging // Eur. Heart J. Cardiovasc. Imaging. 2015. Vol. 16, № 3. P. 233–271.
Mitchell C. et al. Guidelines for Performing a Comprehensive Transthoracic Echocardiographic Examination in Adults: Recommendations from the American Society of Echocardiography // J. Am. Soc. Echocardiogr. 2018. Vol. 32, № 1. P. 1–64.
Nagueh S.F. et al. Recommendations for the Evaluation of Left Ventricular Diastolic Function by Echocardiography // Eur. J. Echocardiogr. 2009. Vol. 10, № 2. P. 165–193.
Senior R. et al. Contrast echocardiography: evidence-based recommendations by European Association of Echocardiography // Eur J Echocardiogr. 2009. Vol. 10, № 2. P. 194–212.
Maron B.J. et al. Clinical course of hypertrophic cardiomyopathy with survival to advanced age // J. Am. Coll. Cardiol. 2003. Vol. 42, № 5. P. 882–888.
Maron B.J. et al. Nonobstructive Hypertrophic Cardiomyopathy Out of the Shadows: Known from the Beginning but Largely Ignored … Until Now // Am. J. Med. 2017. Vol. 130, № 2. P. 119–123.
Maron M.S. et al. Hypertrophic cardiomyopathy is predominantly a disease of left ventricular outflow tract obstruction // Circulation. 2006. Vol. 114, № 21. P. 2232–2239.
Spirito P. et al. Risk of sudden death and outcome in patients with hypertrophic cardiomyopathy with benign presentation and without risk factors // Am. J. Cardiol. 2014. Vol. 113, № 9. P. 1550–1555.
Spirito P. et al. Magnitude of left ventricular hypertrophy and risk of sudden death in hypertrophic cardiomyopathy // N. Engl. J. Med. 2000. Vol. 342, № 24. P. 1778–1785.
Belenkie I., MacDonald R.P.R., Smith E.R. Localized septal hypertrophy: Part of the spectrum of hypertrophic cardiomyopathy or an incidental echocardiographic finding? // Am. Heart J. 1988. Vol. 115, № 2. P. 385–390.
Gardin J. et al. Localized basal ventricular septal hypertrophy - prevalence, functional and clinical correlates in a population referred for echocardiography // Am J Noninvas Card. 1998. Vol. 6, № 1. P. 5–8.
Losi M.A. et al. Echocardiography in patients with hypertrophic cardiomyopathy: Usefulness of old and new techniques in the diagnosis and pathophysiological assessment // Cardiovasc. Ultrasound. 2010. Vol. 8, № 1. P. 7.
Alvares R.F., Goodwin J.F. Non-invasive assessment of diastolic function in hypertrophic cardiomyopathy on and off beta adrenergic blocking drugs // Br. Heart J. 1982. Vol. 48, № 3. P. 204– 212.
Dimitrow P.P. et al. Left ventricular outflow tract gradient provoked by upright position or exercise in treated patients with hypertrophic cardiomyopathy without obstruction at rest. // Echocardiography. 2009. Vol. 26, № 5. P. 513–520.
Elliott P. et al. Left ventricular outflow tract obstruction and sudden death in hypertrophic cardiomyopathy // Eur. Heart J. 2006. Vol. 27, № 24. P. 3073–3074.
Nistri S. et al. Timing and significance of exercise-induced left ventricular outflow tract pressure gradients in hypertrophic cardiomyopathy // Am. J. Cardiol. 2010. Vol. 106, № 9. P. 1301– 1306.
Olivotto I. et al. Clinical utility and safety of exercise testing in patients with hypertrophic cardiomyopathy // G. Ital. Cardiol. 1999. Vol. 29. P. 11–19.
Sadoul N. et al. Prospective prognostic assessment of blood pressure response during exercise in patients with hypertrophic cardiomyopathy // Circulation. 1997. Vol. 96, № 9. P. 2987– 2991.
Tower-Rader A. et al. A Comprehensive Review of Stress Testing in Hypertrophic Cardiomyopathy: Assessment of Functional Capacity, Identification of Prognostic Indicators, and Detection of Coronary Artery Disease // J. Am. Soc. Echocardiogr. 2017. Vol. 30, № 9. P. 829–844.
Yalçin F. et al. The effect of dobutamine stress on left ventricular outflow tract gradients in hypertensive patients with basal septal hypertrophy // Angiology. 2004. Vol. 55, № 3. P. 295–301.
Mestres C.A. et al. Hypertrophic Obstructive Cardiomyopathy: What, When, Why, for Whom? // Eur J Cardiothorac Surg. 2018. Vol. 53, № 4. P. 700–707.
Mickelsen S. et al. Doppler evaluation of the descending aorta in patients with hypertrophic cardiomyopathy: Potential for assessing the functional significance of outflow tract gradients and for optimizing pacemaker function // J. Interv. Card. Electrophysiol. 2004. Vol. 11, № 1. P. 47–53.
Tezuka A. et al. Bisoprolol successfully improved the intraventricular pressure gradient in a patient with midventricular obstructive hypertrophic cardiomyopathy with an apex aneurysm due to apical myocardial damage // Intern. Med. 2019. Vol. 58, № 4. P. 535–539.
Cardim N. et al. Role of multimodality cardiac imaging in the management of patients with hypertrophic cardiomyopathy: An expert consensus of the European Association of Cardiovascular Imaging Endorsed by the Saudi Heart Association // Eur. Heart J. Cardiovasc. Imaging. 2015. Vol. 16, № 3. P. 280.
Kim M.S. et al. Left Ventricular Outflow Tract Obstruction in the Presence of Asymmetric Septal Hypertrophy and Accessory Mitral Valve Tissue Treated With Alcohol Septal Ablation // Eur. J. Echocardiogr. 2008. Vol. 9, № 5. P. 720–724.
Monakier D. et al. Usefulness of myocardial contrast echocardiographic quantification of risk area for predicting postprocedural complications in patients undergoing septal ethanol ablation for obstructive hypertrophic cardiomyopathy // Am. J. Cardiol. 2004. Vol. 94, № 12. P. 1515–1522.
Wallace E.L. et al. Septal perforator anatomy and variability of perfusion bed by myocardial contrast echocardiography: A study of hypertrophic cardiomyopathy patients undergoing alcohol septal ablation // J. Interv. Cardiol. 2013. Vol. 26, № 6. P. 604–612.
Grigg L.E. et al. Transesophageal Doppler echocardiography in obstructive hypertrophic cardiomyopathy: Clarification of pathophysiology and importance in intraoperative decision making // J. Am. Coll. Cardiol. 1992. Vol. 20, № 1. P. 42–52.
Marwick T.H. et al. Benefits of intraoperative echocardiography in the surgical management of hypertrophic cardiomyopathy // J. Am. Coll. Cardiol. 1992. Vol. 20, № 5. P. 1066–1072.
Oki T. et al. Transesophageal echocardiographic evaluation of mitral regurgitation in hypertrophic cardiomyopathy: Contributions of eccentric left ventricular hypertrophy and related abnormalities of the mitral complex // J. Am. Soc. Echocardiogr. 1995. Vol. 8, № 4. P. 503–510.
Yu E.H.C. et al. Mitral regurgitation in hypertrophic obstructive cardiomyopathy: Relationship to obstruction and relief with myectomy // J. Am. Coll. Cardiol. 2000. Vol. 36, № 7. P. 2219–2225.
McIntosh C.L. et al. Initial Results of Combined Anterior Mitral Leaflet Plication and Ventricular Septal Myotomy-Myectomy for Relief of Left Ventricular Outflow Tract Obstruction in Patients With Hypertrophic Cardiomyopathy // Circulation. 1992. Vol. 86, № 5. P. 60–67.
Green J.J. et al. Prognostic value of late gadolinium enhancement in clinical outcomes for hypertrophic cardiomyopathy // JACC Cardiovasc. Imaging. 2012. Vol. 5, № 4. P. 370–377.
Moon J.C.C. et al. Detection of apical hypertrophic cardiomyopathy by cardiovascular magnetic resonance in patients with non-diagnostic echocardiography // Heart. 2004. Vol. 90, № 6. P. 645–649.
Olivotto I. et al. Assessment and Significance of Left Ventricular Mass by Cardiovascular Magnetic Resonance in Hypertrophic Cardiomyopathy // J. Am. Coll. Cardiol. 2008. Vol. 52, № 7. P. 559–566.
Prinz C. et al. Myocardial Fibrosis Severity on Cardiac Magnetic Resonance Imaging Predicts Sustained Arrhythmic Events in Hypertrophic Cardiomyopathy // Can. J. Cardiol. 2013. Vol. 29, № 3. P. 358–363.
Rickers C. et al. Utility of cardiac magnetic resonance imaging in the diagnosis of hypertrophic cardiomyopathy // Circulation. 2005. Vol. 112, № 6. P. 855–861.
Rudolph A. et al. Noninvasive Detection of Fibrosis Applying Contrast-Enhanced Cardiac Magnetic Resonance in Different Forms of Left Ventricular Hypertrophy. Relation to Remodeling // J. Am. Coll. Cardiol. 2009. Vol. 53, № 3. P. 284–291.
Webb J. et al. The Emerging Role of Cardiac Magnetic Resonance Imaging in the Evaluation of Patients with HFpEF // Curr. Heart Fail. Rep. 2018. Vol. 15, № 1. P. 1–9.
Albano B.B.P. et al. Treating a Structural Heart Disease Using a Non-structural Approach: Role of Cardiac Pacing in Hypertrophic Cardiomyopathy // Cardiol. Res. 2017. Vol. 8, № 1. P. 20–25.
Puntmann V.O. et al. Left ventricular chamber dimensions and wall thickness by cardiovascular magnetic resonance: comparison with transthoracic echocardiography // Eur Hear. J Cardiovasc Imaging. 2013. Vol. 14. P. 240–246.
Falk R.H. Diagnosis and management of the cardiac amyloidoses // Circulation. 2005. Vol. 112, № 13. P. 2047–2060.
Gillmore J.D. et al. Nonbiopsy diagnosis of cardiac transthyretin amyloidosis // Circulation. 2016. Vol. 133, № 24. P. 2404–2412.
Syed I.S. et al. Role of Cardiac Magnetic Resonance Imaging in the Detection of Cardiac Amyloidosis // JACC Cardiovasc. Imaging. 2010. Vol. 3, № 2. P. 155–164.
Todiere G. et al. Progression of myocardial fibrosis assessed with cardiac magnetic resonance in hypertrophic cardiomyopathy // J. Am. Coll. Cardiol. 2012. Vol. 60, № 10. P. 922–929.
O’Hanlon R., Assomull R.G., Prasad S.K. Use of cardiovascular magnetic resonance for diagnosis and management in hypertrophic cardiomyopathy // Curr. Cardiol. Rep. 2007. Vol. 9, № 1. P. 51–56.
Patel P. et al. Left ventricular outflow tract obstruction in hypertrophic cardiomyopathy patients without severe septal hypertrophy: Implications of mitral valve and papillary muscle abnormalities assessed using cardiac magnetic resonance and echocardiography // Circ. Cardiovasc. Imaging. 2015. Vol. 8, № 7. P. e003132.
Gruner C. et al. Significance of left ventricular apical-basal muscle bundle identified by cardiovascular magnetic resonance imaging in patients with hypertrophic cardiomyopathy // Eur. Heart J. 2014. Vol. 35, № 39. P. 2706–2713.
Brouwer W.P. et al. Multiple myocardial crypts on modified long-axis view are a specific finding in pre-hypertrophic HCM mutation carriers // Eur Hear. J Cardiovasc Imaging. 2012. Vol. 13, № 4. P. 292–297.
Schroeder S. et al. Cardiac Computed Tomography: Indications, Applications, Limitations, and Training Requirements: Report of a Writing Group Deployed by the Working Group Nuclear Cardiology and Cardiac CT of the European Society of Cardiology and the European Council of Nuc // Eur Hear. J. 2008. Vol. 29, № 4. P. 531–556.
Esposito A. et al. Multidetector computed tomography for coronary stents imaging: High-voltage (140-KVP) prospective ecg-triggered versus standard-voltage (120-kvp) retrospective ecg-gated helical scanning // J. Comput. Assist. Tomogr. 2013. Vol. 37, № 3. P. 395–401.
Shiozaki A.A. et al. Myocardial fibrosis detected by cardiac CT predicts ventricular fibrillation/ventricular tachycardia events in patients with hypertrophic cardiomyopathy // J. Cardiovasc. Comput. Tomogr. 2013. Vol. 7, № 3. P. 173–181.
Rapezzi C. et al. Usefulness and limitations of 99mTc-3, 3-diphosphono-1, 2-propanodicarboxylic acid scintigraphy in the aetiological diagnosis of amyloidotic cardiomyopathy // Eur. J. Nucl. Med. Mol. Imaging. 2011. Vol. 38, № 3. P. 470–478.
Rapezzi C. et al. Role of 99mTc-DPD scintigraphy in diagnosis and prognosis of hereditary transthyretin-related cardiac amyloidosis // JACC Cardiovasc. Imaging. 2011. Vol. 4, № 6. P. 659– 670.
Katayama M. et al. Left ventricular septal hypertrophy in elderly patients with aortic stenosis // J. Ultrasound Med. 2017. Vol. 37, № 1. P. 217–224.
Mitsutake R. et al. Usefulness of multi-detector row computed tomography for the management of percutaneous transluminal septal myocardial ablation in patient with hypertrophic obstructive cardiomyopathy // Int. J. Cardiol. 2008. Vol. 129, № 2. P. 61–63.
Scalone G., Niccoli G., Crea F. Editor’s Choice-Pathophysiology, diagnosis and management of MINOCA: an update // Eur. Hear. journal. Acute Cardiovasc. care. 2019. Vol. 8, № 1. P. 54–62.
Okayama S. et al. Role of cardiac computed tomography in planning and evaluating percutaneous transluminal septal myocardial ablation for hypertrophic obstructive cardiomyopathy // J. Cardiovasc. Comput. Tomogr. 2010. Vol. 4, № 1. P. 62–65.
Villa A.D.M. et al. Microvascular ischemia in hypertrophic cardiomyopathy: New insights from high-resolution combined quantification of perfusion and late gadolinium enhancement // J. Cardiovasc. Magn. Reson. 2016. Vol. 18, № 4. P. doi:10.1186/s12968-016-0223-8. Epub ahead of print.
Chen J.M. et al. Reevaluating the significance of pulmonary hypertension before cardiac transplantation: Determination of optimal thresholds and quantification of the effect of reversibility on perioperative mortality // J. Thorac. Cardiovasc. Surg. 1997. Vol. 114, № 4. P. 627– 634.
Kato T.S. et al. Cardiac transplantation in patients with hypertrophic cardiomyopathy // Am. J. Cardiol. 2012. Vol. 110, № 4. P. 568–574.
Lindelöw B. et al. High and low pulmonary vascular resistance in heart transplant candidates. A 5-year follow-up after heart transplantation shows continuous reduction in resistance and no difference in complication rate // Eur. Heart J. 1999. Vol. 20, № 2. P. 148–156.
Maron M.S. et al. Survival after cardiac transplantation in patients with hypertrophic cardiomyopathy // Circ. Hear. Fail. 2010. Vol. 3, № 5. P. 574–579.
Mehra M.R. et al. Listing Criteria for Heart Transplantation: International Society for Heart and Lung Transplantation Guidelines for the Care of Cardiac Transplant Candidates-2006 // J. Hear. Lung Transplant. 2006. Vol. 25, № 9. P. 1024–1042.
Torres M.F., Perez-Villa F. Heart transplantation in patients with hypertrophic cardiomyopathy // Glob. Cardiol. Sci. Pract. 2018. Vol. 2018, № 3. P. 32.
Blomström-Lundqvist C. et al. ACC/AHA/ESC Guidelines for the Management of Patients with Supraventricular Arrhythmias - Executive Summary: A Report of the American College of Cardiology/American Heart Association Task Force on Practice Guidelines and the European Society of Cardiology // J. Am. Coll. Cardiol. 2003. Vol. 42, № 8. P. 1493–1531.
Бокерия Л.А., Берсенёва М.И., Маленков Д.А. Аритмогенные осложнения гипертрофической кардиомиопатии // Анналы аритмологии. 2010. Т. 7. № 3. С. 62–69.
Muresan L. et al. Recommendations for the use of electrophysiological study: Update 2018 // Hell. J. Cardiol. 2019. Vol. 60, № 2. P. 82–100.
Wang W. et al. Prognostic Implications of Nonsustained Ventricular Tachycardia in High-Risk Patients With Hypertrophic Cardiomyopathy // Circ. Arrhythm. Electrophysiol. 2017. Vol. 10, № 3. P. e004604.
Inada K. et al. Substrate characterization and catheter ablation for monomorphic ventricular tachycardia in patients with apical hypertrophic cardiomyopathy // J. Cardiovasc. Electrophysiol. 2011. Vol. 22, № 1. P. 41–48.
Lim K.K., Maron B.J., Knight B.P. Successful catheter ablation of hemodynamically unstable monomorphic ventricular tachycardia in a patient with hypertrophic cardiomyopathy and apical aneurysm // J. Cardiovasc. Electrophysiol. 2009. Vol. 20, № 4. P. 445–447.
Refaat M.M., Hotait M., Tseng Z.H. Utility of the exercise electrocardiogram testing in sudden cardiac death risk stratification // Ann. Noninvasive Electrocardiol. 2014. Vol. 19, № 4. P. 311–318.
Yi G. et al. Can the Assessment of Dynamic QT Dispersion on Exercise Electrocardiogram Predict Sudden Cardiac Death in Hypertrophic Cardiomyopathy? // Pacing Clin. Electrophysiol. 2000. Vol. 23, № 11Pt2. P. 1953–1956.
Nistri S. et al. β blockers for prevention of exercise-induced left ventricular outflow tract obstruction in patients with hypertrophic cardiomyopathy // Am. J. Cardiol. 2012. Vol. 110, № 5. P. 715–719.
Rowin E.J. et al. Role of Exercise Testing in Hypertrophic Cardiomyopathy // JACC Cardiovasc. Imaging. 2017. Vol. 10, № 11. P. 1374–1386.
Mancini D.M. et al. Value of peak exercise oxygen consumption for optimal timing of cardiac transplantation in ambulatory patients with heart failure // Circulation. 1991. Vol. 83, № 3. P. 778– 786.
Sharma S. et al. Utility of cardiopulmonary exercise in the assessment of clinical determinants of functional capacity in hypertrophic cardiomyopathy // Am. J. Cardiol. 2000. Vol. 86, № 2. P. 162–168.
Колоскова Н.Н., Шаталов К.В., Бокерия Л.А. Определение пикового потребления кислорода: клиническое использование и перспективы // Креативная кардиология. 2014. Т. 2. С. 20–28.
Coats C.J. et al. Cardiopulmonary Exercise Testing and Prognosis in Hypertrophic Cardiomyopathy // Circ. Hear. Fail. 2015. Vol. 8, № 6. P. 1022–1031.
Arena R. et al. Ventilatory efficiency and resting hemodynamics in hypertrophic cardiomyopathy // Med. Sci. Sports Exerc. 2008. Vol. 40, № 5. P. 799–805.
Olivotto I. et al. Prognostic value of systemic blood pressure response during exercise in a community-based patient population with hypertrophic cardiomyopathy // J. Am. Coll. Cardiol. 1999. Vol. 33, № 7. P. 2044–2051.
Diodati J.G. et al. Predictors of exercise benefit after operative relief of left ventricular outflow obstruction by the myotomy-myectomy procedure in hypertrophic cardiomyopathy // Am. J. Cardiol. 1992. Vol. 69, № 19. P. 1617–1622.
Bennett M.K. et al. Evaluation of the role of endomyocardial biopsy in 851 patients with unexplained heart failure from 2000-2009 // Circ. Hear. Fail. 2013. Vol. 6, № 4. P. 676–684.
Schönland S.O. et al. Immunohistochemistry in the classification of systemic forms of amyloidosis: A systematic investigation of 117 patients // Blood. 2012. Vol. 119, № 2. P. 488–493.
Quarta C.C. et al. Diagnostic Sensitivity of Abdominal Fat Aspiration in Cardiac Amyloidosis // Eur Hear. J. 2017. Vol. 38, № 24. P. 1905–1908.
Крылова Н.С. и др. Гипертрофическая кардиомиопатия и артериальная гипертензия: возможно ли сочетание? // Сердце журнал для практикующих врачей. 2015. Т. 14. № 3(83). С. 164–169.
Полякова А.А. и др. Гипертрофическая кардиомиопатия в старшей возрастной группе: влияние факторов кардиометаболического риска и полиморфизма гена MADD // Артериальная гипертензия. 2018. Т. 24. № 1. С. 29–40.
Abel E.D., Litwin S.E., Sweeney G. Cardiac remodeling in obesity // Physiological Reviews. 2008. Vol. 88, № 2. P. 389–419.
Ommen S.R., Lopez-Jimenez F. Obesity and hypertrophic cardiomyopathy: Chickens, eggs, and causality: Clinical skills remain the key to caring for patients // J. Am. Coll. Cardiol. 2013. Vol. 62, № 5. P. 458–459.
Olivotto I. et al. Obesity and its association to phenotype and clinical course in hypertrophic cardiomyopathy // J. Am. Coll. Cardiol. 2013. Vol. 62, № 5. P. 449–457.
Van Straten A.H.M. et al. Increased septum wall thickness in patients undergoing aortic valve replacement predicts worse late survival // Ann. Thorac. Surg. 2012. Vol. 94, № 1. P. 66–71.
Di Tommaso L. et al. Asymmetric septal hypertrophy in patients with severe aortic stenosis: The usefulness of associated septal myectomy // J. Thorac. Cardiovasc. Surg. 2013. Vol. 145, № 1. P. 171–175.
Dweck M.R. et al. Left ventricular remodeling and hypertrophy in patients with aortic stenosis: Insights from cardiovascular magnetic resonance // J. Cardiovasc. Magn. Reson. 2012. Vol. 14, № 1. P. 50.
Maron B.J., Edwards J.E., Epstein S.E. Disproportionate ventricular septal thickening in patients with systemic hypertension // Chest. 1978. Vol. 73, № 4. P. 466–470.
Rodrigues J.C.L. et al. Prevalence and Predictors of Asymmetric Hypertensive Heart Disease: Insights From Cardiac and Aortic Function With Cardiovascular Magnetic Resonance // Eur Hear. J Cardiovasc Imaging. 2016. Vol. 17, № 12. P. 1405–1413.
Tuseth N. et al. Asymmetric septal hypertrophy - A marker of hypertension in aortic stenosis (a SEAS substudy) // Blood Press. 2010. Vol. 19, № 3. P. 140–144.
Shapiro L.M. et al. An echocardiographic study of localized subaortic hypertrophy // Eur. Heart J. 1986. Vol. 7, № 2. P. 127–132.
Raissuni Z. et al. Hypertrophic cardiomyopathy mimicking STEMI: The role of cardiac magnetic resonance imaging in the detection of microvascular coronary dysfunction // Diagn. Interv. Imaging. 2014. Vol. 95, № 11. P. 1111–1112.
Timmer S.A.J., Knaapen P. Coronary Microvascular Function, Myocardial Metabolism, and Energetics in Hypertrophic Cardiomyopathy: Insights From Positron Emission Tomography // Eur Hear. J Cardiovasc Imaging. 2013. Vol. 14, № 2. P. 95–101.
Zhang Y.D. et al. Hypertrophic cardiomyopathy: Cardiac structural and microvascular abnormalities as evaluated with multi-parametric MRI // Eur. J. Radiol. 2015. Vol. 84, № 8. P. 1480– 1486.
Gutiérrez-Barrios A. et al. Invasive assessment of coronary microvascular dysfunction in hypertrophic cardiomyopathy: The index of microvascular resistance // Cardiovasc. Revascularization Med. 2015. Vol. 16, № 7. P. 426–428.
Ismail T.F. et al. Coronary microvascular ischemia in hypertrophic cardiomyopathy - A pixel-wise quantitative cardiovascular magnetic resonance perfusion study // J. Cardiovasc. Magn. Reson. 2014. Vol. 16, № 1. P. 49.
Olivotto I. et al. Microvascular function is selectively impaired in patients with hypertrophic cardiomyopathy and sarcomere myofilament gene mutations // J. Am. Coll. Cardiol. 2011. Vol. 58, № 8. P. 839–848.
Zipes D.P. et al. ACC/AHA/ESC 2006 guidelines for management of patients with ventricular arrhythmias and the prevention of sudden cardiac death // Circulation. 2006. Vol. 114, № 10. P. e385-484.
Basavarajaiah S. et al. Prevalence of Hypertrophic Cardiomyopathy in Highly Trained Athletes. Relevance to Pre-Participation Screening // J. Am. Coll. Cardiol. 2008. Vol. 51, № 10. P. 1033–1039.
Malhotra A., Sharma S. Hypertrophic cardiomyopathy in athletes // Eur. Cardiol. Rev. 2017. Vol. 12, № 2. P. 80–82.
Pelliccia A. et al. Recommendations for participation in competitive sport and leisure-time physical activity in individuals with cardiomyopathies, myocarditis and pericarditis // Eur. J. Prev. Cardiol. 2006. Vol. 13, № 6. P. 876–885.
Liebregts M. et al. Validation of the HCM Risk-SCD model in patients with hypertrophic cardiomyopathy following alcohol septal ablation // Europace. 2018. Vol. 20, № FI2. P. 198–203.
Spoladore R. et al. Pharmacological Treatment Options for Hypertrophic Cardiomyopathy: High Time for Evidence // Eur Hear. J. 2012. Vol. 33, № 14. P. 1724–1733.
Toshima H. et al. Comparable Effects of Oral Diltiazem and Verapamil in the Treatment of Hypertrophic Cardiomyopathy Double-blind Crossover Study // Jpn. Heart J. 1986. Vol. 27, № 5. P. 701–715.
Galve E. et al. Late benefits of dual-chamber pacing in obstructive hypertrophic cardiomyopathy: A 10-year follow-up study // Heart. 2010. Vol. 96, № 5. P. 352–356.
Gentry J.L. et al. Ranolazine for Treatment of Angina or Dyspnea in Hypertrophic Cardiomyopathy Patients (RHYME) // J. Am. Coll. Cardiol. 2016. Vol. 68, № 16. P. 1815–1817.
Kappenberger L. et al. Pacing in hypertrophic obstructive cardiomyopathy. A randomized crossover study // Eur. Heart J. 1997. Vol. 18, № 8. P. 1249–1256.
Maron B.J. et al. Assessment of Permanent Dual-Chamber Pacing as a Treatment for Drug-Refractory Symptomatic Patients With Obstructive Hypertrophic Cardiomyopathy // Circulation. 1999. Vol. 99, № 22. P. 2927–2933.
Maron M.S. et al. Effect of Spironolactone on Myocardial Fibrosis and Other Clinical Variables in Patients with Hypertrophic Cardiomyopathy // Am. J. Med. 2018. Vol. 131, № 7. P. 837– 841.
Nishimura R.A. et al. Dual-chamber pacing for hypertrophic cardiomyopathy: A randomized, double-blind, crossover trial // J. Am. Coll. Cardiol. 1997. Vol. 29, № 2. P. 435–441.
Olivotto I. et al. Efficacy of Ranolazine in Patients With Symptomatic Hypertrophic Cardiomyopathy: The RESTYLE-HCM Randomized, Double-Blind, Placebo-Controlled Study // Circ. Heart Fail. 2018. Vol. 11, № 1. P. e004124.
Slade A.K. et al. DDD pacing in hypertrophic cardiomyopathy: A multicentre clinical experience // Heart. 1996. Vol. 75, № 1. P. 44–49.
Jung H. et al. Effectiveness and Safety of Non-Vitamin K Antagonist Oral Anticoagulants in Patients With Atrial Fibrillation With Hypertrophic Cardiomyopathy: A Nationwide Cohort Study // Chest. 2019. Vol. 155, № 2. P. 354–363.
Zhou Y. et al. Non-vitamin K antagonist oral anticoagulants in patients with hypertrophic cardiomyopathy and atrial fibrillation: a systematic review and meta-analysis // J. Thromb. Thrombolysis. 2019. P. doi: 10.1007/s11239-019-02008-3. Epub ahead of print.
Rujirachun P. et al. Efficacy and safety of direct oral anticoagulants (DOACs) versus vitamin K antagonist (VKA) among patients with atrial fibrillation and hypertrophic cardiomyopathy: a systematic review and meta-analysis // Acta Cardiol. 2019. P. doi: 10.1080/00015385.2019.1668113. Epub ahead of print.
Patten M., Pecha S., Aydin A. Atrial fibrillation in hypertrophic cardiomyopathy: Diagnosis and considerations for management // J. Atr. Fibrillation. 2018. Vol. 10, № 5. P. 1556.
Dearani J.A. et al. Surgery Insight: Septal myectomy for obstructive hypertrophic cardiomyopathy - The Mayo Clinic experience // Nat. Clin. Pract. Cardiovasc. Med. 2007. Vol. 4, № 9. P. 503–512.
Leonardi R.A. et al. Meta-analyses of septal reduction therapies for obstructive hypertrophic cardiomyopathy comparative rates of overall mortality and sudden cardiac death after treatment // Circ. Cardiovasc. Interv. 2010. Vol. 3, № 2. P. 97–104.
Zeng Z. et al. Comparison of percutaneous transluminal septal myocardial ablation versus septal myectomy for the treatment of patients with hypertrophic obstructive cardiomyopathy-A meta analysis // Int. J. Cardiol. 2006. Vol. 112, № 1. P. 80–84.
Afanasyev A. V. et al. Single-Centre Experience of Surgical Myectomy for Hypertrophic Obstructive Cardiomyopathy // Hear. Lung Circ. 2019. Vol. 29, № 6. P. 949–955.
Veselka J. et al. Short- and long-term outcomes of alcohol septal ablation for hypertrophic obstructive cardiomyopathy in patients with mild left ventricular hypertrophy: a propensity score matching analysis // Eur Hear. J. 2019. Vol. 40, № 21. P. 1681–1687.
Майстренко А.Д. и др. Современное состояние проблемы хирургического лечения гипертрофической обструктивной кардиомиопатии // Вестник хирургии имени И.И. Грекова. 2013. Т. 172. № 2. С. 82–87.
Хитрова М.Э. и др. Метаанализ результатов хирургического лечения гипертрофической обструктивной кардиомиопатии // Креативная кардиология. 2017. Т. 11. № 4. С. 337–347.
Богданов Д.В., Шапошник И.И. Варианты клинического течения, исходы и прогноз гипертрофической необструктивной кардиомиопатии – результаты длительного наблюдения // Российский кардиологический журнал. 2019. Т. 24. № 11. С. 48–54.
Vriesendorp P.A. et al. Validation of the 2014 European Society of Cardiology Guidelines Risk Prediction Model for the Primary Prevention of Sudden Cardiac Death in Hypertrophic Cardiomyopathy // Circ. Arrhythmia Electrophysiol. 2015. Vol. 8, № 4. P. 829–835.
Falk V. et al. 2017 ESC/EACTS Guidelines for the management of valvular heart disease // Eur. J. Cardiothorac. Surg. 2017. Vol. 52, № 4. P. 616–664.
Lourenсo A.P. et al. An integrative translational approach to study heart failure with preserved ejection fraction: a position paper from the Working Group on Myocardial Function of the European Society of Cardiology // Eur. J. Heart Fail. 2018. Vol. 20, № 2. P. 216–227.
Мареев В.Ю. и др. Клинические рекомендации ОССН-РКО РНМОТ Сердечная недостаточность: хроническая (ХСН) и острая декомпенсированная (ОДСН). Диагностика, профилактика, лечение // Кардиология. 2018. Т. 58. № 6S. С. 8–158.
Российское кардиологическое общество. Клинические рекомендации “Артериальная гипертензия у взрослых” [Electronic resource]. 2020. URL:
https://scardio.ru/content/Guidelines/Clinic_rek_AG_2020.pdf
(accessed: 10.07.2020).
Гудкова А.Я., Стрельцова А.А., Костарева А.А. Гипертрофическая кардиомиопатия: современные возможности фармакологических подходов к лечению // Терапевтический архив. 2019. Т. 91. № 9. С. 129–136.
Ammirati E. et al. Pharmacological treatment of hypertrophic cardiomyopathy: current practice and novel perspectives // Eur. J. Heart Fail. 2016. Vol. 18, № 9. P. 1106–1118.
Spicer R.L. et al. Hemodynamic effects of verapamil in children and adolescents with hypertrophic cardiomyopathy // Circulation. 1983. Vol. 67, № 2. P. 413–420.
Flamm M.D., Harrison D.C., Hancock E.W. Muscular subaortic stenosis. Prevention of outflow obstruction with propranolol. // Circulation. 1968. Vol. 38, № 5. P. 846–858.
Sherrid M.V. Drug Therapy for Hypertrophic Cardiomypathy: Physiology and Practice // Curr. Cardiol. Rev. 2016. Vol. 12, № 1. P. 52–65.
Sherrid M.V., Gunsburg D., Sharma A. Medical treatment of hypertrophic cardiomyopathy // Curr. Cardiol. Rep. 2000. Vol. 2, № 2. P. 148–153.
Sherrid M. V. et al. Multicenter study of the efficacy and safety of disopyramide in obstructive hypertrophic cardiomyopathy // J. Am. Coll. Cardiol. 2005. Vol. 45, № 8. P. 1251–1258.
Sherrid M. V. et al. Treatment of obstructive hypertrophic cardiomyopathy symptoms and gradient resistant to first-line therapy with β-blockade or verapamil // Circ. Hear. Fail. 2013. Vol. 6, № 4. P. 694–702.
Adelman A.G. et al. Long-term propranolol therapy in muscular subaortic stenosis. // Br. Heart J. 1970. Vol. 32, № 6. P. 804–811.
Bonow R.O. et al. Verapamil-induced improvement in left ventricular diastolic filling and increased exercise tolerance in patients with hypertrophic cardiomyopathy: Short- and long-term effects // Circulation. 1985. Vol. 72, № 4. P. 853–864.
Bonow R.O., Rosing D.R., Epstein S.E. The acute and chronic effects of verapamil on left ventricular function in patients with hypertrophic cardiomyopathy // Eur. Heart J. 1983. Vol. 4, № suppl F. P. 57–65.
Gistri R. et al. Effect of verapamil on absolute myocardial blood flow in hypertrophic cardiomyopathy // Am. J. Cardiol. 1994. Vol. 74, № 4. P. 363–368.
Rosing D.R. et al. Verapamil therapy: A new approach to the pharmacologic treatment of hypertrophic cardiomyopathy: III. Effects of long-term administration // Am. J. Cardiol. 1981. Vol. 48, № 3. P. 545–553.
Rosing D.R. et al. Verapamil therapy: a new approach to the pharmacologic treatment of hypertrophic cardiomyopathy. I. Hemodynamic effects // Circulation. 1979. Vol. 60, № 6. P. 1201– 1207.
Maron B.J. Hypertrophic cardiomyopathy: A systematic review // JAMA 2002. Vol. 287, № 3. P. 1308-1320.
Said S.M. et al. Transapical approach for apical myectomy and relief of midventricular obstruction in hypertrophic cardiomyopathy // J. Card. Surg. 2012. Vol. 27, № 4. P. 443–448.
Shah A. et al. Severe symptoms in mid and apical hypertrophic cardiomyopathy // Echocardiography. 2009. Vol. 26, № 8. P. 922–933.
Maron M.S. et al. Contemporary Natural History and Management of Nonobstructive Hypertrophic Cardiomyopathy // J. Am. Coll. Cardiol. 2016. Vol. 67, № 12. P. 1399–1409.
McMurray J.J.V. et al. ESC Guidelines for the diagnosis and treatment of acute and chronic heart failure 2012: The Task Force for the Diagnosis and Treatment of Acute and Chronic Heart Failure 2012 of the European Society of Cardiology. Developed in collaboration with the Heart // Eur. Heart J. 2012. Vol. 33, № 14. P. 1787–1847.
Сафрыгина Ю.В. и др. Сердечные натрийуретические пептиды в плазме больных гипертрофической кардиомиопатией // Кардиология. 2007. Т. 47. № 5. С. 50–57.
Braunwald E. et al. Idiopathic hypertrophic subaortic stenosis: a description of the disease based upon an analysis of 64 patients // Circulation. 1964. Vol. 30, № 4. P. 3–119.
Okeie K. et al. Left ventricular systolic dysfunction during exercise and dobutamine stress in patients with hypertrophic cardiomyopathy // J. Am. Coll. Cardiol. 2000. Vol. 36, № 3. P. 856–863.
Epstein S.E., Rosing D.R. Verapamil: Its potential for causing serious complications in patients with hypertrophic cardiomyopathy // Circulation. 1981. Vol. 64, № 3. P. 437–441.
Shimada Y.J. et al. Effects of Losartan on Left Ventricular Hypertrophy and Fibrosis in Patients With Nonobstructive Hypertrophic Cardiomyopathy // JACC Hear. Fail. 2013. Vol. 1, № 6. P. 480–487.
Udelson J.E. et al. Verapamil prevents silent myocardial perfusion abnormalities during exercise in asymptomatic patients with hypertrophic cardiomyopathy // Circulation. 1989. Vol. 79, № 5. P. 1052–1060.
Wilmshurst P.T. et al. Effects of verapamil on haemodynamic function and myocardial metabolism in patients with hypertrophic cardiomyopathy // Heart. 1986. Vol. 56, № 6. P. 544–553.
Argulian E. et al. Antihypertensive therapy in hypertrophic cardiomyopathy // Am. J. Cardiol. 2013. Vol. 111, № 7. P. 1040–1045.
Olivotto I. et al. Patterns of disease progression in hypertrophic cardiomyopathy an individualized approach to clinical staging // Circ. Hear. Fail. 2012. Vol. 5, № 4. P. 535–546.
Robinson K. et al. Atrial fibrillation in hypertrophie cardiomyopathy: A longitudinal study // J. Am. Coll. Cardiol. 1990. Vol. 15, № 6. P. 1279–1285.
Olivotto I. et al. Impact of atrial fibrillation on the clinical course of hypertrophic cardiomyopathy // Circulation. 2001. Vol. 104, № 21. P. 2517–2524.
Maron B.J. et al. Prevalence of hypertrophic cardiomyopathy in a general population of young adults: Echocardiographic analysis of 4111 subjects in the CARDIA study // Circulation. 1995. Vol. 92, № 4. P. 785–789.
Camm A.J. et al. 2012 focused update of the ESC Guidelines for the management of atrial: Fibrillation An update of the 2010 ESC Guidelines for the management of atrial fibrillation: Developed with the special contribution of the European Heart Rhythm Association // Europace. 2012. Vol. 14, № 10. P. 1385–1413.
Camm C.F., Camm A.J. Atrial fibrillation and anticoagulation in hypertrophic cardiomyopathy // Arrhythmia Electrophysiol. Rev. 2017. Vol. 6, № 2. P. 63–68.
Di Cori A. et al. Role of cardiac electronic implantable device in the stratification and management of embolic risk of silent atrial fibrillation: are all atrial fibrillations created equal? // Expert Rev. Cardiovasc. Ther. 2018. Vol. 16, № 3. P. 175–181.
van Velzen H.G. et al. Incidence of Device-Detected Atrial Fibrillation and Long-Term Outcomes in Patients With Hypertrophic Cardiomyopathy // Am. J. Cardiol. 2017. Vol. 119, № 1. P. 100–105.
Brambatti M. et al. Temporal relationship between subclinical atrial fibrillation and embolic events // Circulation. 2014. Vol. 129, № 21. P. 2094–2099.
Camm A.J. et al. Guidelines for the management of atrial fibrillation: the Task Force for the Management of Atrial Fibrillation of the European Society of Cardiology (ESC) // Eur. Heart J. 2010. Vol. 31, № 19. P. 2369–2429.
Miller C.A.S. et al. Safety, Side Effects and Relative Efficacy of Medications for Rhythm Control of Atrial Fibrillation in Hypertrophic Cardiomyopathy // Am. J. Cardiol. 2019. Vol. 123, № 11. P. 1859–1862.
Schaufelberger M. Cardiomyopathy and pregnancy // Heart. 2019. Vol. 105, № 20. P. 1543– 1551.
Azarbal F. et al. Exercise capacity and paroxysmal atrial fibrillation in patients with hypertrophic cardiomyopathy // Heart. 2014. Vol. 100, № 8. P. 624–630.
Pisters R. et al. A novel user-friendly score (HAS-BLED) to assess 1-year risk of major bleeding in patients with atrial fibrillation: The euro heart survey // Chest. 2010. Vol. 138, № 5. P. 1093–1100.
Lee H.J. et al. Novel Oral Anticoagulants for Primary Stroke Prevention in Hypertrophic Cardiomyopathy Patients with Atrial Fibrillation // Stroke. 2019. Vol. 50, № 9. P. 2582–2586.
Dominguez F. et al. Direct oral anticoagulants in patients with hypertrophic cardiomyopathy and atrial fibrillation // Int. J. Cardiol. 2017. Vol. 248. P. 232–238.
Li B. et al. Could direct oral anticoagulants be an alternative to vitamin K antagonists in patients with hypertrophic cardiomyopathy and atrial fibrillation? // Int. J. Cardiol. 2018. Vol. 256. P. 39.
Lozier M.R. et al. Thromboembolic outcomes of different anticoagulation strategies for patients with atrial fibrillation in the setting of hypertrophic cardiomyopathy: A systematic review // J. Atr. Fibrillation. 2020. Vol. 12, № 4. P. 2207.
Ruff C.T. et al. Comparison of the efficacy and safety of new oral anticoagulants with warfarin in patients with atrial fibrillation: A meta-analysis of randomised trials // Lancet. 2014. Vol. 383, № 9921. P. 955–962.
Zhou Y. et al. Non-vitamin K antagonist oral anticoagulants in patients with hypertrophic cardiomyopathy and atrial fibrillation: a systematic review and meta-analysis // J. Thromb. Thrombolysis. 2019. P. doi: 10.1007/s11239-019-02008-3. Epub ahead of print.
Connolly S.J. et al. Dabigatran versus warfarin in patients with atrial fibrillation // N. Engl. J. Med. 2009. Vol. 361, № 12. P. 1139–1151.
Gómez-Outes A. et al. Dabigatran, Rivaroxaban, or Apixaban versus Warfarin in Patients with Nonvalvular Atrial Fibrillation: A Systematic Review and Meta-Analysis of Subgroups // Thrombosis. 2013. Vol. 2013. Article ID 640723.
Бокерия Л.А. и др. Клинические рекомендации «Фибрилляция предсердий». Москва, 2017. 65 с. с.
Connolly S.J. et al. Effect of clopidogrel added to aspirin in patients with atrial fibrillation // N. Engl. J. Med. 2009. Vol. 360, № 20. P. 2066–2078.
Бокерия Л.А. и др. Хирургическое лечение фибрилляции предсердий: современное состояние проблемы // Анналы аритмологии. 2009. Т. 6. № 2. С. 5–11.
Nishimura R.A., Schaff H. V. Septal myectomy for patients with hypertrophic cardiomyopathy: A new paradigm // J. Thorac. Cardiovasc. Surg. 2016. Vol. 151, № 2. P. 303–304.
Swistel D.G., Balaram S.K. Surgical Myectomy for Hypertrophic Cardiomyopathy in the 21st Century, the Evolution of the “RPR” Repair: Resection, Plication, and Release // Prog. Cardiovasc. Dis. 2012. Vol. 54, № 6. P. 498–502.
Swistel D.G., Sherrid M. V. The surgical management of obstructive hypertrophic cardiomyopathy: The RPR procedure-resection, plication, release // Ann. Cardiothorac. Surg. 2017. Vol. 6, № 4. P. 423–425.
Veselka J. et al. Long-term clinical outcome after alcohol septal ablation for obstructive hypertrophic cardiomyopathy: Results from the Euro-ASA registry // Eur. Heart J. 2016. Vol. 37, № 19. P. 1517–1523.
Afanasyev A.V. et al. Myectomy Versus Alcohol Septal Ablation in Patients With Hypertrophic Obstructive Cardiomyopathy // Interact. Cardiovasc. Thorac. Surg. 2020. Article number ivaa075. Epub ahead of print.
Bogachev-Prokophiev A. et al. Mitral Valve Repair or Replacement in Hypertrophic Obstructive Cardiomyopathy: A Prospective Randomized Study // Interact. Cardiovasc. Thorac. Surg. 2017. Vol. 25, № 3. P. 356–362.
Bogachev-Prokophiev A. et al. Septal Myectomy With Vs Without Subvalvular Apparatus Intervention in Patients With Hypertrophic Obstructive Cardiomyopathy: A Prospective Randomized Study // Semin. Thorac. Cardiovasc. Surg. 2019. Vol. 31, № 3. P. 424–431.
Afanasyev A. et al. Myectomy With Mitral Valve Repair Versus Replacement in Adult Patients With Hypertrophic Obstructive Cardiomyopathy: A Systematic Review and Meta-Analysis // Interact. Cardiovasc. Thorac. Surg. 2019. Vol. 28, № 3. P. 465–472.
Гурщенков А.В. и др. Пятилетний опыт использования мобилизации сердца при септальной миоэктомии // Кардиология и сердечно-сосудистая хирургия. 2018. Т. 11. № 4. С. 54–58.
Agarwal S. et al. Updated Meta-Analysis of Septal Alcohol Ablation Versus Myectomy for Hypertrophic Cardiomyopathy // J. Am. Coll. Cardiol. 2010. Vol. 55, № 8. P. 823–834.
Alam M., Dokainish H., Lakkis N.M. Hypertrophic obstructive cardiomyopathy-alcohol septal ablation vs. myectomy: a meta-analysis // Eur. Heart J. 2009. Vol. 30, № 9. P. 1080–1087.
Swistel D.G., Balaram S.K. Resection, Plication, Release--the RPR Procedure for Obstructive Hypertrophic Cardiomyopathy // Anadolu Kardiyol Derg. 2006. Vol. 6, № Suppl 2. P. 31–36.
Каштанов М.Г. и др. Этаноловая септальная аблация в лечении обструктивной гипертрофической кардиомиопатии: отбор пациентов и рациональность ее применения // Патология кровообращения и кардиохирургия. 2017. Т. 21. № 1. С. 104–116.
Batzner A. et al. Hypertrophic obstructive cardiomyopathy–the role of myectomy and percutaneous septal ablation in drug-refractory disease // Dtsch. Aerzteblatt Online. 2019. Vol. 116, № 4. P. 47–53.
Сухов В.К. и др. Спиртовая септальная абляция при обструктивной гипертрофической кардиомиопатии // Международный журнал интервенционной кардиоангиологии. 2013. № 35. С. 75.
Schaff H. V. et al. Expanding the indications for septal myectomy in patients with hypertrophic cardiomyopathy: Results of operation in patients with latent obstruction // J. Thorac. Cardiovasc. Surg. 2012. Vol. 143, № 2. P. 303–309.
McCully R.B. et al. Extent of clinical improvement after surgical treatment of hypertrophic obstructive cardiomyopathy // Circulation. 1996. Vol. 94, № 3. P. 467–471.
Orme N.M. et al. Comparison of surgical septal myectomy to medical therapy alone in patients with hypertrophic cardiomyopathy and syncope // Am. J. Cardiol. 2013. Vol. 111, № 3. P. 388–392.
Halpern D.G. et al. Echocardiography before and after resect-plicate-release surgical myectomy for obstructive hypertrophic cardiomyopathy // J. Am. Soc. Echocardiogr. 2015. Vol. 28, № 11. P. 1318–1328.
Kaple R.K. et al. Mitral Valve Abnormalities in Hypertrophic Cardiomyopathy: Echocardiographic Features and Surgical Outcomes // Ann. Thorac. Surg. 2008. Vol. 85, № 5. P. 1527–1535.
Kofflard M.J. et al. Initial results of combined anterior mitral leaflet extension and myectomy in patients with obstructive hypertrophic cardiomyopathy // J. Am. Coll. Cardiol. 1996. Vol. 28, № 1. P. 197–202.
Schoendube F.A. et al. Long-term clinical and echocardiographic follow-up after surgical correction of hypertrophic obstructive cardiomyopathy with extended myectomy and reconstruction of the subvalvular mitral apparatus // Circulation. 1995. Vol. 92, № 9. P. ii122-127.
Steggerda R.C. et al. Periprocedural complications and long-term outcome after alcohol septal ablation versus surgical myectomy in hypertrophic obstructive cardiomyopathy a single-center experience // JACC Cardiovasc. Interv. 2014. Vol. 7, № 11. P. 1227–1234.
Богачев-Прокофьев А.В. и др. Эффективность расширенной миоэктомии у пациентов с желудочковой обструкцией при гипертрофической кардиомиопатии // Кардиология. 2017. Т. 57. № 5. С. 38–43.
Borisov K. V. Right ventricle myectomy // Ann. Cardiothorac. Surg. 2017. Vol. 6, № 4. P. 402– 409.
Wehman B. et al. Transmitral Septal Myectomy for Hypertrophic Obstructive Cardiomyopathy // Ann. Thorac. Surg. 2018. Vol. 105, № 4. P. 1102–1108.
Бокерия Л.А., Борисов К.В., Синев А.Ф. Улучшение диастолической функции левого и правого желудочков сердца после хирургической коррекции гипертрофической обструктивной кардиомиопатии при помощи оригинального способа // Грудная и сердечно-сосудистая хирургия. 1999. Т. 4. С. 4–10.
Бокерия Л.А. Гипертрофическая обструктивная кардиомиопатия // Анналы хирургии. 2013. Т. 5. С. 5–14.
Takahashi J. et al. Septal Myectomy, Papillary Muscle Resection, and Mitral Valve Replacement for Hypertrophic Obstructive Cardiomyopathy: A Case Report // Ann Thorac Cardiovasc Surg. 2008. Vol. 14, № 4. P. 258–262.
Cooley D.A., Wukasch D.C., Leachman R.D. Mitral valve replacement for idiopathic hypertrophic subaortic stenosis. Results in 27 patients. // J. Cardiovasc. Surg. 1976. Vol. 17, № 5. P. 380–387.
Stassano P. et al. Mitral Valve Replacement and Limited Myectomy for Hypertrophic Obstructive Cardiomyopathy: A 25-Year Follow-Up // Texas Hear. Inst. J. 2004. Vol. 31, № 2. P. 137– 142.
Reis R.L. et al. Anterion-superior displacement of papillary muscles producing obstruction and mitral regurgitation in idiopathic hypertrophic subaortic stenosis. Operative relief by posterior-superior realignment of papillary muscles following ventricular septal myectomy // Circulation. 1974. Vol. 50, № 2. P. ii181-188.
Shimahara Y. et al. Combined mechanical mitral valve replacement and transmitral myectomy for hypertrophic obstructive cardiomyopathy treatment: An experience of over 20 years // J. Cardiol. 2019. Vol. 73, № 4. P. 318–325.
Topilski I. et al. Long-Term Effects of Dual-Chamber Pacing With Periodic Echocardiographic Evaluation of Optimal Atrioventricular Delay in Patients With Hypertrophic Cardiomyopathy >50 Years of Age // Am. J. Cardiol. 2006. Vol. 97, № 12. P. 1769–1775.
Хирманов В.Н. и др. Отдаленные результаты лечения гипертрофической кардиомиопатии с помощью постоянной двукамерной электрокардиостимуляции // Кардиология. 2002. Т. 8. С. 46–47.
Трешкур Т.В. и др. Внутрисердечная гемодинамика у больных гипертрофической кардиомиопатией при лечении постоянной двукамерной электрокардиостимуляцией // Вестник аритмологии. 1995. Т. 4. С. 248.
Daubert C. et al. Pacing for hypertrophic obstructive cardiomyopathy: an update and future directions. // Europace. 2018. Vol. 20, № 6. P. 908–920.
Quintana E., Cox J.L. Surgical management of atrial fibrillation at the time of septal myectomy // Ann. Cardiothorac. Surg. 2017. Vol. 6, № 4. P. 386–393.
Бокерия Л.А. и др. Хирургическая коррекция обструктивной гипертрофической кардиомиопатии с SAM-синдромом и фибрилляцией предсердий // Анналы аритмологии. 2016. Т. 13. № 4. С. 216–221.
Бокерия Л.А. и др. Сочетанная операция миоэктомии межжелудочковой перегородки из правого желудочка и эпикардиальная криомодификация операции «лабиринт» // Анналы аритмологии. 2013. Т. 10. № 2. С. 64–68.
Bogachev-Prokophiev A. V. et al. Concomitant ablation for atrial fibrillation during septal myectomy in patients with hypertrophic obstructive cardiomyopathy // J. Thorac. Cardiovasc. Surg. 2018. Vol. 155, № 4. P. 1536-1542.
Monserrat L. et al. Non-sustained ventricular tachycardia in hypertrophic cardiomyopathy: An independent marker of sudden death risk in young patients // J. Am. Coll. Cardiol. 2003. Vol. 42, № 5. P. 873–879.
Moya A. et al. Guidelines for the diagnosis and management of syncope (version 2009) // Eur. Heart J. 2009. Vol. 30, № 21. P. 2631–2671.
Sherrid M. V., Massera D. Risk Stratification and Hypertrophic Cardiomyopathy Subtypes // J. Am. Coll. Cardiol. 2019. Vol. 74, № 19. P. 2346–2349.
Mentias A. et al. Late Gadolinium Enhancement in Patients With Hypertrophic Cardiomyopathy and Preserved Systolic Function // J. Am. Coll. Cardiol. 2018. Vol. 72, № 8. P. 857– 870.
Бельских Л.В. и др. Трансплантация сердца и механическая поддержка кровообращения. Национальные клинические рекомендации. 2016. 115 с. с.
Topilsky Y. et al. Left ventricular assist device therapy in patients with restrictive and hypertrophic cardiomyopathy // Circ. Hear. Fail. 2011. Vol. 4, № 3. P. 266–275.
Biagini E. et al. Heart Transplantation in Hypertrophic Cardiomyopathy // Am. J. Cardiol. 2008. Vol. 101, № 3. P. 387–392.
Стрюк Р.И. и др. Диагностика и лечение сердечно-сосудистых заболеваний при беременности 2018. Национальные рекомендации // Российский кардиологический журнал. 2018. Т. 3. № 155. С. 91–134.
Goland S. et al. Pregnancy in women with hypertrophic cardiomyopathy: data from the European Society of Cardiology initiated Registry of Pregnancy and Cardiac disease (ROPAC) // Eur Hear. J. 2017. Vol. 38, № 35. P. 2683–2690.
Regitz-Zagrosek V. et al. 2018 ESC Guidelines for the management of cardiovascular diseases during pregnancy // Eur. Heart J. 2018. Vol. 39, № 34. P. 3165–3241.
Bowyer L. The Confidential Enquiry into Maternal and Child Health (CEMACH). Saving Mothers’ Lives: reviewing maternal deaths to make motherhood safer 2003–2005. The Seventh Report of the Confidential Enquiries into Maternal Deaths in the UK // Obstet. Med. 2008. Vol. 1, № 1. P. 54–54.
Billebeau G. et al. Pregnancy in women with a cardiomyopathy: Outcomes and predictors from a retrospective cohort // Arch. Cardiovasc. Dis. 2018. Vol. 111, № 3. P. 199–209.
Krul S.P. et al. Systematic Review of Pregnancy in Women With Inherited Cardiomyopathies // Eur J Hear. Fail. 2011. Vol. 13. P. 584–594.
Tromp C.H.N. et al. Electrical cardioversion during pregnancy: Safe or not? // Netherlands Hear. J. 2011. Vol. 19, № 3. P. 134–136.
Maron M.S. et al. Prevalence, clinical significance, and natural history of left ventricular apical aneurysms in hypertrophic cardiomyopathy // Circulation. 2008. Vol. 118, № 15. P. 1541– 1549.
Burton H., Alberg C., Stewart A. Heart to Heart: Inherited Cardiovascular Conditions Services - A Needs Assessment and Service Review. 2009. 163 p.
Canepa M. et al. Distinguishing ventricular septal bulge versus hypertrophic cardiomyopathy in the elderly // Heart. 2016. Vol. 102, № 14. P. 1087–1094.
Olesen J.B. et al. Validation of risk stratification schemes for predicting stroke and thromboembolism in patients with atrial fibrillation: Nationwide cohort study // BMJ. 2011. Vol. 342, № 7792. P. 320.
Lip G.Y.H. et al. Comparative validation of a novel risk score for predicting bleeding risk in anticoagulated patients with atrial fibrillation: The HAS-BLED (hypertension, abnormal renal/liver function, stroke, bleeding history or predisposition, labile INR, elderly, drug // J. Am. Coll. Cardiol. 2011. Vol. 57, № 2. P. 173–180.
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Table of contents
Список сокращений
Термины и определения
Гипертрофическая кардиомиопатия
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Список литературы
Приложение А1. Состав рабочей группы
Приложение А2. Методология разработки клинических рекомендаций
Приложение А3. Связанные документы
Приложение Б. Алгоритмы ведения пациента
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Приложение В. Информация для пациентов
Приложение Г.
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