CAMBIOS CARDIOVASCULARES EN LA CIRROSIS. EL IMPACTO DE LAS COMPLICACIONES Y LOS TRATAMIENTOS

(especial para SIIC © Derechos reservados)
El reconocimiento de cambios leves en la estructura cardíaca que pueden ser detectados incluso en las etapas iniciales de la cirrosis preascítica ha contribuido a una mejor comprensión de los trastornos cardiovasculares que se observan a medida que progresa la enfermedad.
pozzi9.jpg Autor:
Massimo Pozzi
Columnista Experto de SIIC

Institución:
Università degli Studi Milano-Bicocca


Artículos publicados por Massimo Pozzi
Coautores
Daniela Prata Pizzala* Laura Ratti* Maria Milanese* Alberto Doretti* Guido Grassi* Giuseppe Mancia* 
Università degli Studi Milano-Bicocca, Monza, Italia*
Recepción del artículo
4 de Abril, 2008
Aprobación
8 de Mayo, 2008
Primera edición
19 de Marzo, 2009
Segunda edición, ampliada y corregida
7 de Junio, 2021

Resumen
En tiempos recientes, la miocardiopatía cirrótica ha pasado a ser considerada una nueva entidad clínica. El reconocimiento de cambios leves en la estructura cardíaca que pueden ser detectados incluso en las etapas iniciales de la cirrosis preascítica ha contribuido a una mejor comprensión de los trastornos cardiovasculares que se observan a medida que progresa la enfermedad. Se han categorizado cambios cardíacos estructurales y se diagnóstica, con frecuencia, la disfunción diastólica. La cirrosis descompensada se caracteriza por una disminución de la presión sanguínea y de la resistencia vascular periférica, y un aumento del gasto cardíaco y de la frecuencia cardíaca, los cuales se producen en un escenario de circulación hiperdinámica favorecida por la expansión del volumen total sanguíneo, la sobrecarga circulatoria y la hiperactividad de los sistemas endógenos vasoactivos. La vasodilatación periférica evita la insuficiencia cardíaca. Recientemente se ha reconocido la existencia de una menor respuesta cardíaca en situaciones de estrés como son los cambios en las condiciones de la carga cardíaca en presencia de un mayor deterioro de la función hepática, tales como la ascitis refractaria, el síndrome hepatorrenal, la peritonitis bacteriana espontánea y la hemorragia de várices esofágicas. Ante la disponibilidad de intervenciones terapéuticas (paracentesis, comunicación portosistémica intrahepática transyugular, comunicación venosa peritoneal, trasplante hepático) utilizadas actualmente para manejar las complicaciones potencialmente mortalesen las formas más avanzadas de cirrosis, el conocimiento del impacto que tienen en la función cardiovascular es de suma importancia. Se encuentran en progreso las intervenciones terapéuticas dirigidas a prevenir y manejar el deterioro cardiovascular.

Palabras clave
miocardiopatía cirrótica, ascitis, circulación hiperdinámica


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Abstract
Cirrhotic cardiomyopathy has recently gained the dignity of a new clinical entity. The knowledge of subtle cardiostructural changes that can be detected even in the early stages of preascitic cirrhosis have contributed to a better understanding of the cardiovascular derangement observed as disease severity progresses. Diastolic dysfunction is frequently detected in this setting and heart structural changes are being characterized. Decompensated cirrhosis is characterized by decreased arterial blood pressure and peripheral vascular resistances, increased cardiac output and heart rate in the setting of hyperdynamic circulation favoured by total blood volume expansion, circulatory overload and overactivity of the endogenous vasoactive systems. Peripheral vasodilation prevents over heart failure. Reduced heart responses to stressful conditions such as changes in cardiac loading conditions in presence of further deterioration of liver function, such as refractory ascites, hepatorenal syndrome, spontaneous bacterial peritonitis and bleeding esophageal varices, have been recently identified. Facing the availability of therapeutic interventions (paracentesis, transjugular intrahepatic porto-systemic shunt -TIPS, peritoneovenous shunt, liver transplantation) currently employed to manage the life-threatening complications of the most advanced phases of cirrhosis, the knowledge of their impact on cardiovascular function is of paramount relevance. Therapeutic interventions targeted to prevent and manage cardiovascular deterioration are in progress.

Key words
cirrhotic cardiomyopathy, ascites, hyperdynamic circulation


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Clasificación en siicsalud
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Especialidades
Principal: Cardiología
Relacionadas: Cuidados Intensivos, Gastroenterología, Medicina Interna, Trasplantes



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Massimo Pozzi, Clinica Medica A.O. San Gerardo (Monza), 20052, Via Pergolesi 33, Monza, Italia
Bibliografía del artículo

1. Kowalski HJ, Abelmann WH. The cardiac output at rest in Laennec's cirrhosis. J Clin Invest 32(10):1025-1033, 1953.
2. Schrier RW, Arroyo V, Bernardi M, Epstein M, Henriksen JH, Rodes J. Peripheral arterial vasodilation hypothesis: a proposal for the initiation of renal sodium and water retention in cirrhosis. Hepatology 8(5):1151-1157, 1988.
3. Henriksen JH, Moller S, Ring-Larsen H, Christensen NJ. The sympathetic nervous system in liver disease. J Hepatol 29(2):328-341, 1998.
4. Moller S, Henriksen JH. Cirrhotic cardiomyopathy: a pathophysiological review of circulatory dysfunction in liver disease. Heart 87(1):9-15, 2002.
5. Bernardi M, Li BS, Arienti V, et al. Systemic and regional hemodynamics in pre-ascitic cirrhosis: effects of posture. J Hepatol 39(4):502-508, 2003.
6. Moller S, Bendtsen F, Henriksen JH. Vasoactive substances in the circulatory dysfunction of cirrhosis. Scand J Clin Lab Invest 61(6):421-429, 2001.
7. Vallance P, Moncada S. Hyperdynamic circulation in cirrhosis: a role for nitric oxide? Lancet 337(8744):776-778, 1991.
8. Martin PY, Gines P, Schrier RW. Nitric oxide as a mediator of hemodynamic abnormalities and sodium and water retention in cirrhosis. N Engl J Med 339(8):533-541, 1998.
9. Ma Z, Lee SS. Cirrhotic cardiomyopathy: getting to the heart of the matter. Hepatology 24(2):451-459, 1996.
10. Liu H, Song D, Lee SS. Cirrhotic cardiomyopathy. Gastroenterol Clin Biol 26(10):842-847, 2002.
11. Moller S, Henriksen JH. Cardiovascular dysfunction in cirrhosis. Pathophysiological evidence of a cirrhotic cardiomyopathy. Scand J Gastroenterol 36(8):785-794, 2001.
12. Finucci G, Desideri A, Sacerdoti D, et al. Left ventricular diastolic function in liver cirrhosis. Scand J Gastroenterol 31(3):279-284, 1996.
13. Pozzi M, Carugo S, Boari G, et al. Evidence of functional and structural cardiac abnormalities in cirrhotic patients with and without ascites. Hepatology 26(5):1131-1137, 1997.
14. Pozzi M, Redaelli E, Ratti L, et al. Time-course of diastolic dysfunction in different stages of chronic HCV related liver diseases. Minerva Gastroenterol Dietol 51(2):179-186, 2005.
15. Wong F, Liu P, Lilly L, Bomzon A, Blendis L. Role of cardiac structural and functional abnormalities in the pathogenesis of hyperdynamic circulation and renal sodium retention in cirrhosis. Clin Sci (Lond) 97(3):259-267, 1999.
16. Valeriano V, Funaro S, Lionetti R, et al. Modification of cardiac function in cirrhotic patients with and without ascites. Am J Gastroenterol 95(11):3200-3205, 2000.
17. De BK, Majumdar D, Das D, et al. Cardiac dysfunction in portal hypertension among patients with cirrhosis and non-cirrhotic portal fibrosis. J Hepatol 39(3):315-319, 2003.
18. Blendis L, Wong F. Is there a cirrhotic cardiomyopathy? Am J Gastroenterol 95(11):3026-3028, 2000.
19. Kelbaek H, Rabol A, Brynjolf I, et al. Haemodynamic response to exercise in patients with alcoholic liver cirrhosis. Clin Physiol 7(1):35-41, 1987.
20. Wong F, Girgrah N, Graba J, Allidina Y, Liu P, Blendis L. The cardiac response to exercise in cirrhosis. Gut 49(2):268-275, 2001.
21. Grose RD, Nolan J, Dillon JF, et al. Exercise-induced left ventricular dysfunction in alcoholic and non-alcoholic cirrhosis. J Hepatol 22(3):326-332, 1995.
22. Limas CJ, Guiha NH, Lekagul O, Cohn JN. Impaired left ventricular function in alcoholic cirrhosis with ascites. Ineffectiveness of ouabain. Circulation 49(4):754-760, 1974.
23. Mikulic E, Munoz C, Puntoni LE, Lebrec D. Hemodynamic effects of dobutamine in patients with alcoholic cirrhosis. Clin Pharmacol Ther 34(1):56-59, 1983.
24. Lunzer MR, Newman SP, Bernard AG, Manghani KK, Sherlock SP, Ginsburg J. Impaired cardiovascular responsiveness in liver disease. Lancet 2(7931):382-385, 1975.
25. Blendis L, Wong F. The hyperdynamic circulation in cirrhosis: an overview. Pharmacol Ther 89(3):221-231, 2001.
26. Wong F, Liu P, Allidina Y, Blendis L. Pattern of sodium handling and its consequences in patients with preascitic cirrhosis. Gastroenterology 108(6):1820-1827, 1995.
27. Guazzi M, Polese A, Magrini F, Fiorentini C, Olivari MT. Negative influences of ascites on the cardiac function of cirrhotic patients. Am J Med 59(2):165-170, 1975.
28. Pozzi M, Osculati G, Boari G, et al. Time course of circulatory and humoral effects of rapid total paracentesis in cirrhotic patients with tense, refractory ascites. Gastroenterology 106(3):709-719, 1994.
29. Panos MZ, Moore K, Vlavianos P, et al. Single, total paracentesis for tense ascites: sequential hemodynamic changes and right atrial size. Hepatology 11(4):662-667, 1990.
30. Luca A, Feu F, Garcia-Pagan JC, et al. Favorable effects of total paracentesis on splanchnic hemodynamics in cirrhotic patients with tense ascites. Hepatology 20(1 Pt 1):30-33, 1994.
31. Jimenez W, Arroyo V. Origins of cardiac dysfunction in cirrhosis. Gut 52(10):1392-1394, 2003.
32. Salerno F, Merli M, Riggio O, et al. Randomized controlled study of TIPS versus paracentesis plus albumin in cirrhosis with severe ascites. Hepatology 40(3):629-635, 2004.
33. Lotterer E, Wengert A, Fleig WE. Transjugular intrahepatic portosystemic shunt: short-term and long-term effects on hepatic and systemic hemodynamics in patients with cirrhosis. Hepatology 29(3):632-639, 1999.
34. Huonker M, Schumacher YO, Ochs A, Sorichter S, Keul J, Rossle M. Cardiac function and haemodynamics in alcoholic cirrhosis and effects of the transjugular intrahepatic portosystemic stent shunt. Gut 44(5):743-748, 1999.
35. Ruiz del Arbol L, Monescillo A, Jimenez W, Garcia-Plaza A, Arroyo V, Rodes J. Paracentesis-induced circulatory dysfunction: mechanism and effect on hepatic hemodynamics in cirrhosis. Gastroenterology 113(2):579-586, 1997.
36. Gines P, Guevara M, De Las HD, Arroyo V. Review article: albumin for circulatory support in patients with cirrhosis. Aliment Pharmacol Ther 16(Suppl.):524-31, 2002.
37. Salerno F, Cazzaniga M, Pagnozzi G, et al. Humoral and cardiac effects of TIPS in cirrhotic patients with different "effective" blood volume. Hepatology 38(6):1370-1377, 2003.
38. Martinet JP, Fenyves D, Legault L, et al. Treatment of refractory ascites using transjugular intrahepatic portosystemic shunt (TIPS): a caution. Dig Dis Sci 42(1):161-166, 1997.
39. Moore KP, Wong F, Gines P, et al. The management of ascites in cirrhosis: report on the consensus conference of the International Ascites Club. Hepatology 38(1):258-266, 2003.
40. Gines P, Cardenas A, Arroyo V, Rodes J. Management of cirrhosis and ascites. N Engl J Med 350(16):1646-1654, 2004.
41. Ruiz del Arbol L, Monescillo A, Arocena C, et al. Circulatory function and hepatorenal syndrome in cirrhosis. Hepatology 42(2):439-447, 2005.
42. Luca A, Garcia-Pagan JC, Bosch J, et al. Beneficial effects of intravenous albumin infusion on the hemodynamic and humoral changes after total paracentesis. Hepatology 22(3):753-758, 1995.
43. Pozzi M, Grassi G, Pecci V, et al. Early effects of total paracentesis and albumin infusion on muscle sympathetic nerve activity in cirrhotic patients with tense ascites. J Hepatol 30(1):95-100, 1999.
44. Merli M, Valeriano V, Funaro S, et al. Modifications of cardiac function in cirrhotic patients treated with transjugular intrahepatic portosystemic shunt (TIPS). Am J Gastroenterol 97(1):142-148, 2002.
45. Jalan R, Finlayson ND, Hayes PC. TIPSS trials: design determines outcome. Hepatology 26(5):1361-1365, 1997.
46. Sanyal AJ, Genning C, Reddy KR, et al. The North American Study for the Treatment of Refractory Ascites. Gastroenterology 124(3):634-641, 2003.
47. Azoulay D, Castaing D, Majno P, et al. Salvage transjugular intrahepatic portosystemic shunt for uncontrolled variceal bleeding in patients with decompensated cirrhosis. J Hepatol 35(5):590-597, 2001.
48. Cazzaniga M, Salerno F, Pagnozzi G, et al. Diastolic dysfunction is associated with poor survival in patients with cirrhosis with transjugular intrahepatic portosystemic shunt. Gut 56(6):869-875, 2007.
49. Llach J, Gines P, Arroyo V, et al. Prognostic value of arterial pressure, endogenous vasoactive systems, and renal function in cirrhotic patients admitted to the hospital for the treatment of ascites. Gastroenterology 94(2):482-487, 1988.
50. Tristani FE, Cohn JN. Systemic and renal hemodynamics in oliguric hepatic failure: effect of volume expansion. J Clin Invest 46(12):1894-1906, 1967.
51. Lebrec D. Review article: future indications for terlipressin therapy. Aliment Pharmacol Ther 20(Suppl.):365-67, 2004.
52. Navasa M, Rimola A, Rodes J. Bacterial infections in liver disease. Semin Liver Dis 17(4):323-333, 1997.
53. Ruiz del Arbol L, Urman J, Fernandez J, et al. Systemic, renal, and hepatic hemodynamic derangement in cirrhotic patients with spontaneous bacterial peritonitis. Hepatology 38(5):1210-1218, 2003.
54. Sharma AC. Sepsis-induced myocardial dysfunction. Shock 28(3):265-269, 2007.
55. Myers RP, Lee SS. Cirrhotic cardiomyopathy and liver transplantation. Liver Transpl 6(4 Suppl 1):S44-S52, 2000.
56. Donovan CL, Marcovitz PA, Punch JD, et al. Two-dimensional and dobutamine stress echocardiography in the preoperative assessment of patients with end-stage liver disease prior to orthotopic liver transplantation. Transplantation 1996; 61(8):1180-1188, 1996.
57. Nasraway SA, Klein RD, Spanier TB, et al. Hemodynamic correlates of outcome in patients undergoing orthotopic liver transplantation. Evidence for early postoperative myocardial depression. Chest 107(1):218-224, 1995.
58. Spanier TB, Klein RD, Nasraway SA, et al. Multiple organ failure after liver transplantation. Crit Care Med 23(3):466-473, 1995.
59. Torregrosa M, Aguade S, Dos L, et al. Cardiac alterations in cirrhosis: reversibility after liver transplantation. J Hepatol 42(1):68-74, 2005.
60. Poynard T, McHutchison J, Manns M, et al. Impact of pegylated interferon alfa-2b and ribavirin on liver fibrosis in patients with chronic hepatitis C. Gastroenterology 122(5):1303-1313, 2002.
61. Rincon D, Ripoll C, Lo IO, et al. Antiviral therapy decreases hepatic venous pressure gradient in patients with chronic hepatitis C and advanced fibrosis. Am J Gastroenterol 101(10):2269-2274, 2006.
62. Jensen GS, Trotter JF. Treatment of chronic HCV in advanced liver disease: unmet challenges, reason for optimism. J Hepatol 47(4):441-443, 2007.
63. Di Marco V, Almasio PL, Ferraro D, et al. Peg-interferon alone or combined with ribavirin in HCV cirrhosis with portal hypertension: a randomized controlled trial. J Hepatol 47(4):484-491, 2007.
64. Kweon YO, Goodman ZD, Dienstag JL, et al. Decreasing fibrogenesis: an immunohistochemical study of paired liver biopsies following lamivudine therapy for chronic hepatitis B. J Hepatol 35(6):749-755, 2001.
65. Wanless IR. Use of corticosteroid therapy in autoimmune hepatitis resulting in the resolution of cirrhosis. J Clin Gastroenterol 32(5):371-372, 2001.
66. Pozzi M, Grassi G, Ratti L, et al. Cardiac, neuroadrenergic, and portal hemodynamic effects of prolonged aldosterone blockade in postviral child A cirrhosis. Am J Gastroenterol 100(5):1110-1116, 2005.
67. Inserte J, Perello A, Agullo L, et al. Left ventricular hypertrophy in rats with biliary cirrhosis. Hepatology 38(3):589-598, 2003.
68. Kim S, Iwao H. Molecular and cellular mechanisms of angiotensin II-mediated cardiovascular and renal diseases. Pharmacol Rev 52(1):11-34, 2000.
69. Jimenez W, Martinez-Pardo A, Arroyo V, et al. Temporal relationship between hyperaldosteronism, sodium retention and ascites formation in rats with experimental cirrhosis. Hepatology 5(2):245-250, 1985.
70. Bernardi M, Di Marco C, Trevisani F, et al. Renal sodium retention during upright posture in preascitic cirrhosis. Gastroenterology 105(1):188-193, 1993.
71. Pozzi M, Grassi G, Redaelli E, et al. Patterns of regional sympathetic nerve traffic in preascitic and ascitic cirrhosis. Hepatology 34(6):1113-1118, 2001.
72. Morali GA, Floras JS, Legault L, Tobe S, Skorecki KL, Blendis LM. Muscle sympathetic nerve activity and renal responsiveness to atrial natriuretic factor during the development of hepatic ascites. Am J Med 91(4):383-392, 1991.
73. Stanton HC, Brenner G, Mayfield ED, Jr. Studies on isoproterenol-induced cardiomegaly in rats. Am Heart J 77(1):72-80, 1969.
74. Cohen J. Role of endocrine factors in the pathogenesis of cardiac hypertrophy. Circ Res 35(2):suppl-57, 1974.
75. Pozzi M, Prata Pizzala D, Ratti L, et al. Heart function and myocardial tissue characterization in patients with HCV related cirrhosis: diastolic dysfunction and cardiac hypertrophy. The Open Gastroenterology Journal 1(1):1-8, 2007.
76. Pozzi M, Ratti L, Guidi C, Milanese M, Mancia G. Potential therapeutic targets in cirrhotic cardiomyopathy. Cardiovasc Hematol Disord Drug Targets 7(1):21-26, 2007.
77. Gaskari SA, Honar H, Lee SS. Therapy insight: Cirrhotic cardiomyopathy. Nat Clin Pract Gastroenterol Hepatol 3(6):329-337, 2006.
78. Schepke M, Werner E, Biecker E, et al. Hemodynamic effects of the angiotensin II receptor antagonist irbesartan in patients with cirrhosis and portal hypertension. Gastroenterology 121(2):389-395, 2001.

 
 
 
 
 
 
 
 
 
 
 
 
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