Справка
x
Поиск
Закладки
Озвучить книгу
Изменить режим чтения
Изменить размер шрифта
Оглавление
Для озвучивания и цитирования книги перейдите в режим постраничного просмотра.
Легочная артериальная гипертензия, ассоциированная с врожденными пороками сердца у взрослых
Литература
Поставить закладку
Galiè N, Humbert M, Vachiery JL, Gibbs S, Lang I, Torbicki A. et al. 2015 ESC/ERS Guidelines for the diagnosis and treatment of pulmonary hypertension: The Joint Task Force for the Diagnosis and Treatment of Pulmonary Hypertension of the European Society of Cardiology (ESC) and the European Respiratory Society (ERS): Endorsed by: Association for European Paediatric and Congenital Cardiology (AEPC), International Society for Heart and Lung Transplantation (ISHLT). Eur Heart J. 2016; 37(1).
Galiè N, Simonneau G. (eds). Updates in Pulmonary Hypertension Proceedings of the 5
th
World Symposium on Pulmonary Hypertension. J Am Coll Cardiol. 2013; 62 (25), Suppl D.
Чазова И.Е., Мартынюк Т.В. (ред.). Легочная гипертензия. М., 2015.
Choussat A., Fontan F., Besse P. Selection criteria for Fontan's procedure. - In: Anderson R.H, Shineborne E.A. (eds). Pediatric cardiology. Edinburgh: Churchhill Livingstone; 1977: 559-570.
Hosein RB, Clarke AJ, McGuirk SP, Griselli M, Stumper O, De Giovanni JV et. al. Factors influencing early and late outcome following the Fontan procedure in the current era. The 'Two Commandments'? Eur J Cardiothorac Surg. 2007; 31(3): 344-52.
Cerro MJ, Abman S, Diaz G, Freudenthal AH, Freudenthal F, Harikrishnan S et al. A consensus approach to the classification of pediatric pulmonary hypertensive vascular disease: Report from the PVRI Pediatric Taskforce, Panama 2011. Pulm Circ. 2011; (2): 286–298.
Dimopoulos K, Wort SJ, Gatzoulis MA. Pulmonary hypertension related to congenital heart disease: a call for action. Eur Heart J. 2014; 35(11): 691-700.
Nadas AS, Fyler DF. Pediatric cardiology. Philadelphia: WB Saunders; 1972: 684.
Heath D, Edwards JE. The pathology of hypertensive pulmonary vascular disease. Circulation. 1958; 18: 533-547.
Baumgartner H, Bonhoeffer P, De Groot NM, de Haan F, Deanfield JE, Galie N et al. ESC Guidelines for the management of grown-up congenital heart disease (new version 2010). Eur Heart J. 2010; 31(23):2915-57.
D'Alto M, Mahadevan VS. Pulmonary arterial hypertension associated with congenital heart disease. Eur Respir Rev. 2012; 21(126):328-37.
Gorbachevsky SV, Shmalts AA and Zaets SB. What Can Cause Pulmonary Vascular Disease in Functionally Single Ventricle? Anatomy & Physiology. 2016; 6(1):1000е137. Available at: http: //dx.doi.org/ 10.4172/2161-0940.1000e137.
Therrien J, Rambihar S, Newman B, Siminovitch K, Langleben D, Webb G et al. Eisenmenger syndrome and atrial septal defect: nature or nurture? Can J Cardiol. 2006; 22:1133–1136.
Manes A, Palazzini M, Leci E, Bacchi Reggiani ML, Branzi A, Galiè N. Current era survival of patients with pulmonary arterial hypertension associated with congenital heart disease: a comparison between clinical subgroups. Eur Heart J. 2014; 35(11): 716-24.
D'Alto M, Romeo E, Argiento P, Correra A, Santoro G, Gaio G et al. Hemodynamics of patients developing pulmonary arterial hypertension after shunt closure. Int J Cardiol. 2013; 168(4): 3797-801.
D’Alto M, Romeo E, Argiento P, Santoro G, Sarubbi B, Gaio G et al. Pulmonary vasoreactivity predicts long-term outcome in patients with Eisenmenger syndrome receiving bosentan therapy. Heart Br Card Soc. 2010; 96:1475–1479.
Post MC, Janssens S, Van deWerf F, BudtsW. Responsiveness to inhaled nitric oxide is a predictor for mid-term survival in adult patients with congenital heart defects and pulmonary arterial hypertension. Eur Heart J. 2004; 25:1651-1656.
Бураковский В.И., Бухарин В.А., Плотникова Л.Р. Легочная гипертензия при врожденных пороках сердца. М.: Медицина; 1975.
Горбачевский С.В., Шмальц А.А.
Гипертензионная сосудистая болезнь легких, ассоциированная с врожденными пороками сердца. В кн.: Детская кардиохирургия. Руководство для врачей. М., 2016: 833-850.
Горбачевский С.В., Шмальц А.А., Белкина М.В. Гренадеров М.А., Барышникова И.Ю., Пурсанов М.Г. и др. Алгоритм диагностики гипертензионной сосудистой болезни легких, ассоциированной с врожденными пороками сердца. Бюллетень НЦССХ им. А.Н. Бакулева РАМН Сердечно-сосудистые заболевания. 2015; 16(S3): 12.
Горбачевский С.В., Шмальц А.А., Белкина М.В., Гренадеров М.А., Рахмонов К.Х. Алгоритм определения показаний к хирургическому лечению врожденных пороков сердца с гипертензионной сосудистой болезнью легких. Бюллетень НЦССХ им. А.Н. Бакулева РАМН Сердечно-сосудистые заболевания. 2015; 16(S3): 12.
Lopes AA, Leary PW. Measurement, interpretation and use of hemodynamic parameters. Cardiol Young. 2009; 19(Suppl 1):8–12.
Douwes JM, van Loon RL, Hoendermis ES, Vonk-Noordegraaf A, Roofthooft MT, Talsma MD et al. Acute pulmonary vasodilator response in paediatric and adult pulmonary arterial hypertension: occurrence and prognostic value when comparing three response criteria. Eur Heart J. 2011; 32(24): 3137-46.
Nakanishi T. Pulmonary arterial hypertension associated with congenital heart disease. Personal perspectives. Int Heart J. 2015; 56. Suppl: S1-3. doi: 10.1536/ihj.15-064.
Moller JH, Patton C, Varco RL, Lillehei CW. Late results (30 to 35 years) after operative closure of isolated ventricular septal defect from 1954 to 1960. Am J Cardiol 1991; 68:1491–1497.
Galie` N, Manes A, Palazzini M, Negro L, Marinelli A, Gambetti S et al. Management of pulmonary arterial hypertension associated with congenital systemic-to-pulmonary shunts and Eisenmenger’s syndrome. Drugs. 2008;68:1049–1066.
Kaemmerer H, Niwa K, Oechslin E, Ewert P, Webb GD, Hess J. Pulmonary Arterial Hypertension in Congenital Heart Disease: Eisenmenger's Syndrome – A Global Perspective. Bremen: UNI-MED, 2013
Broberg CS, Ujita M, Prasad S, Li W, Rubens M, Bax BE et al. Pulmonary arterial thrombosis in Eisenmenger syndrome is associated with biventricular dysfunction and decreased pulmonary flow velocity. J Am Coll Cardiol. 2007;50:634–642.
Sandoval J, Aguirre JS, Pulido T, Martinez-Guerra ML, Santos E, Alvarado P et al. Nocturnal oxygen therapy in patients with the Eisenmenger syndrome. Am J Respir Crit Care Med. 2001; 164:1682-1687.
Diller GP, Lammers AE, Haworth SG, Dimopoulos K, Derrick G, Bonhoeffer P et al. A modelling study of atrial septostomy for pulmonary arterial hypertension, and its effect on the state of tissue oxygenation and systemic blood flow. Cardiol Young. 2010; 20:25–32.
Broberg CS, Bax BE, Okonko DO, Rampling MW, Bayne S, Harries C et al. Blood viscosity and its relationship to iron deficiency, symptoms, and exercise capacity in adults with cyanotic congenital heart disease. J Am Coll Cardiol. 2006; 48:356–365.
Rhodes CJ, Howard LS, Busbridge M, Ashby D, Kondili E, Gibbs JS et al. Iron deficiency and raised hepcidin in idiopathic pulmonary arterial hypertension clinical prevalence, outcomes, and mechanistic insights. J Am Coll Cardiol. 2011;58:300–309.
Galie` N, Beghetti M, Gatzoulis MA Granton J, Berger RM, Lauer A et al. Bosentan therapy in patients with Eisenmenger syndrome: a multicenter, double-blind, randomized, placebo-controlled study. Circulation. 2006;114: 48–54.
Gatzoulis MA, Beghetti M, Galie` N, Granton J, Berger RM, Lauer A et al. Longer-term bosentan therapy improves functional capacity in Eisenmenger syndrome: results of the BREATHE-5 open-label extension study. Int J Cardiol. 2007; 127:27–32.
ZuckermanWA, Leaderer D, Rowan CA, Mituniewicz JD, Rosenzweig EB. Ambrisentan for pulmonary arterial hypertension due to congenital heart disease. J Am Coll Cardiol. 2011;107:1381–1385.
Mukhopadhyay S, Sharma M, Ramakrishnan S, Yusuf J, Gupta MD, Bhamri N et al. Phosphodiesterase-5 inhibitor in Eisenmenger syndrome: a preliminary observational study. Circulation. 2006;114:1807–1810.
Rosenzweig EB, Kerstein D, Barst RJ. Long-term prostacyclin for pulmonary hypertension with associated congenital heart defects. Circulation. 1999; 99: 1858–1865
Tay EL, Papaphylactou M, Diller GP, Alonso-Gonzalez R, Inuzuka R, Giannakoulas G et al. Quality of life and functional capacity can be improved in patients with Eisenmenger syndrome with oral sildenafil therapy. Int J Cardiol 2011; 149: 372–376.
Zhang ZN, Jiang X, Zhang R, Li XL, Wu BX, Zhao QH et al. Oral sildenafil treatment for Eisenmenger syndrome: a prospective, open-label, multicentre study. Heart 2011; 97: 1876–1881.
Chau EM, Fan KY, Chow WH. Effects of chronic sildenafil in patients with Eisenmenger syndrome versus idiopathic pulmonary arterial hypertension. Int J Cardiol 2007; 120: 301–305.
Rosenkranz S, Ghofrani HA, Beghetti M, Ivy D, Frey R, Fritsch A et al. Riociguat for pulmonary arterial hypertension associated with congenital heart disease. Heart. 2015; 101(22):1792-9.
Pulido T, Adzerikho I, Channick RN, Delcroix M, Galiè N, Ghofrani HA et al. Macitentan and morbidity and mortality in pulmonary arterial hypertension. N Engl J Med. 2013; 369(9): 809-18.
Galiè N, Ghofrani HA, Torbicki A, Barst RJ, Rubin LJ, Badesch D et al. Sildenafil citrate therapy for pulmonary arterial hypertension. N Engl J Med. 2005; 353(20): 2148-57.
Galie` N, Rubin L, Hoeper M, Jansa P, Al-Hiti H, Meyer G et al. Treatment of patients with mildly symptomatic pulmonary arterial hypertension with bosentan (EARLY study): a double-blind, randomised controlled trial. Lancet. 2008; 371:2093–2100.
Hebert A, Mikkelsen UR, Thilen U, Idorn L, Jensen AS, Nagy E et al. Bosentan improves exercise capacity in adolescents and adults after Fontan operation: the TEMPO (Treatment With Endothelin Receptor Antagonist in Fontan Patients, a Randomized, Placebo-Controlled, Double-Blind Study Measuring Peak Oxygen Consumption) study. Circulation. 2014; 130(23):2021-30.
Goldberg DJ, French B, McBride MG, Marino BS, Mirarchi N, Hanna BD et al. Impact of oral sildenafil on exercise performance in children and young adults after the fontan operation: a randomized, double-blind, placebo-controlled, crossover trial. Circulation. 2011; 123(11):1185-93.
Shang XK, Lu R, Zhang X, Zhang CD, Xiao SN, Liu M J et al. Efficacy of Bosentan inpatients after Fontan procedures: a double-blind, randomized controlled trial. J Huazhong Univ Sci Technolog Med Sci. 2016; 36(4): 534-40.
Mori H, Park IS, Yamagishi H, Nakamura M, Ishikawa S, Takigiku K et al. Sildenafil reduces pulmonary vascular resistance in single ventricular physiology. Int J Cardiol. 2016; 221:122-7.
Hirono K, Yoshimura N, Taguchi M, Watanabe K, Nakamura T, Ichida F et al. Bosentan induces clinical and hemodynamic improvement in candidates for right-sided heart bypass surgery. J. Thorac. Cardiovasc. Surg. 2010; 140:346–351.
Inuzuka R, Tatebe S, Wakiguchi S, Nakajima H, Ohtsu H, Dimopoulos K et al. B-type natriuretic peptide at the early stage of univentricular circulation reflects inadequate adaptation to volume overload. Int J Cardiol. 2012; 159(2): 88–93.
Iversen K, Jensen AS, Jensen TV, Vejlstrup NG, Søndergaard L. et al. Combination therapy with bosentan and sildenafil in Eisenmenger syndrome: a randomized, placebocontrolled, double-blinded trial. Eur Heart J. 2010; 31:1124–1131.
D’Alto M, Romeo E, Argiento P, Sarubbi B, Santoro G, Grimaldi N et al. Bosentan-sildenafil association in patients with congenital heart disease-related pulmonary arterial hypertension and Eisenmenger physiology. Int J Cardiol. 2012;155:378–82.
Montani D, Savale L, Natali D, Jaïs X, Herve P, Garcia G et al. Long-term response to calcium-channel blockers in nonidiopathic pulmonary arterial hypertension. Eur Heart J. 2010; 31:1898–1907.
Для продолжения работы требуется
Регистрация
Предыдущая страница
Следующая страница
Оглавление
Рабочая группа по подготовке текста рекомендаций
АССОЦИАЦИЯ СЕРДЕЧНО-СОСУДИСТЫХ ХИРУРГОВ РОССИИ РОССИЙСКОЕ МЕДИЦИНСКОЕ ОБЩЕСТВО ПО АРТЕРИАЛЬНОЙ ГИПЕРТОНИИ
Определение, классификация и патофизиология.
Клиническое течение.
Диагностика
Хирургическое лечение
Медикаментозное лечение
Литература
Данный блок поддерживает скрол*