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Therapie kardiovaskulärer Erkrankungen

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Praktische Arzneitherapie
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Zusammenfassung

Diese Medikamentengruppe wird eingesetzt, um erhöhte Blutdruckwerte (>140/90 mg/Hg) zu senken bzw. zu normalisieren. Es handelt sich bei der medikamentösen antihypertensiven Behandlung in der Regel um eine symptomatische, aber nicht um eine kausale Therapie. Die Kooperation der Patienten (Compliance) ist Voraussetzung, um auf lange Sicht die Hypertonie zu kontrollieren und deren kardiovaskuläre und renale Komplikationen zu verhindern. Beginn, Absetzen oder die Dosisanpassung einer antihypertensiven Therapie sollten niemals ohne ärztliche Überwachung erfolgen, wobei Arzt und Patient auf rechtzeitige Wiederverschreibung der Medikation achten müssen (Vermeidung eines „Rebound-Phänomens“). Arzneimittelwechselwirkungen von Antihypertensiva mit gleichzeitig verabreichten Pharmaka sind zahlreich und können zur Wirkabschwächung (z. B. nichtsteroidale Antirheumatika) oder zur Wirkverstärkung der blutdrucksenkenden Medikamente führen (z. B. bei gleichzeitiger Gabe weiterer antihypertensiver Substanzen, von Nitraten oder Neuroleptika). An Nebenwirkungen verursachen Antihypertensiva häufig Müdigkeit, Schwindel und Benommenheit, sodass die Fahrtüchtigkeit und Tätigkeiten, die erhöhte geistige Aufmerksamkeit erfordern, beeinträchtigt werden können. Gleichzeitiger Alkoholgenuss bzw. die Einnahme sedierender Medikamente kann die o. g. unerwünschten Effekte verstärken, insbesondere können diese nach dem Aufrichten aus sitzender oder liegender Position auftreten. Die ganz überwiegende Anzahl der Hypertoniker hat eine leichte bis mittelschwere Form der Hypertonie. Diese kann in der Mehrzahl mit diätetischer Salzrestriktion, z. B. Vermeidung stark salzhaltiger Nahrungsmittel wie Pökelfleisch (Kassler), von gesalzenen Nüssen, Büchsennahrung, und Minimierung der Salzzugabe beim Kochen sowie einem Diuretikum in niedriger bis mittlerer Dosierung (z. B. Chlortalidon 25–50 mg/Tag) gut behandelt werden. Da zahlreiche andere Antihypertensiva eine Natriumretention bewirken, können Diuretika in niedriger Dosis auch zusätzlich gegeben werden. Die Kombination aus einem Diuretikum und Beta-Rezeptorenblocker, falls das Diuretikum allein nicht ausreichend wirksam ist, hat sich bewährt. Spezielle Patientengruppen:

  • Hypertoniker mit Diabetes mellitus: Diese Patienten sind vorzugsweise mit ACE-Hemmern zu therapieren, weil dadurch das Fortschreiten der diabetischen Nephropathie verzögert wird. Sie sollten keine Dihydropyridin-Kalziumkanalblocker erhalten.

  • Auch Altershypertoniker profitieren von einer antihypertensiven Therapie. Bei Patienten mit isolierter systolischer Hypertonie können z. B. durch Therapie mit Chlortalidon und Atenolol das Auftreten von Herzinfarkt, Schlaganfall und Herzinsuffizienz deutlich gesenkt werden.

  • Schwangere sollten mit Methyldopa oder kardioselektiven Beta-Rezeptorenblockern — wie z. B. Metoprolol oder Atenolol — behandelt werden. ACE-Hemmer oder AT1- Blocker führen eventuell zu einem Oligohydrammion und einer Nierenfunktionsverschlechterung beim Neugeborenen. Somit ist ihr Einsatz nicht angezeigt. Es existieren vielfältige Empfehlungen zur antihypertensiven Therapie. In den deutschsprachigen Ländern findet in dieser Hinsicht das Schema der Deutschen Liga zur Bekämpfung des hohen Blutdrucks besondere Beachtung (Abb. 14.1; [1]).

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Literatur

  1. Deutsche Liga zur Bekämpfung des hohen Blutdruckes e.V. (2003) Empfehlungen zur Hochdruckbehandlung in der Praxis und zur Bekämpfung hypertensiver Notfälle. 11. Auflage. Heidelberg

    Google Scholar 

  2. Flockhart, D (2002) Cytochrome P450 Drug Interactions. [online aufgerufen am 25.11.2002] URL: http://medicine.iupui.edu/flockhart/

  3. Routledge PA, Shand DG (1979) Clinical pharmacokinetics of propranolol. Clin Pharmacokinet 4: 73–90

    PubMed  CAS  Google Scholar 

  4. Dollery C (1991) Propranolol. A Pharmacopoeia. Churchill Livingstone, Edinburgh, p 272–278

    Google Scholar 

  5. Toon S, Davidson EM, Garstang FM et al. (1988) The racemic metoprolol-H2antagonist interaction. Clin Pharmacol Ther 43: 283–289

    PubMed  CAS  Google Scholar 

  6. Sandstrom B (1978) Antihypertensive treatment with the adrenergic p-receptor blocker metoprolol during pregnancy. Gynecol Obst 9: 195–204

    CAS  Google Scholar 

  7. Kirch W, Köhler H, Mutschier E et al. (1981) Pharmacokinetics of atenolol in relation to renal function. Eur J clin Pharmacol 19: 65–71

    PubMed  CAS  Google Scholar 

  8. Rubin PC, Butters L, Clark DM (1983) Placebo-controlled trial of atenolol in treatment of pregnancy-associated hypertension. Lancet 1: 431–434

    PubMed  CAS  Google Scholar 

  9. CIBIS-II Investigators and Committees (1999) The Cardiac Insufficiency Bisoprolol Study II (CIBIS-II): a randomised trial. Lancet 353: 9–13

    Google Scholar 

  10. Kirch W, Rose I, Demers HG et al. (1987) Pharmacokinetics of bisoprolol during repeated oral administration to healthy volunteers and patients with kidney or liver disease. Clin Pharmacokinet 13: 110–113

    PubMed  CAS  Google Scholar 

  11. Leopold G, Ungethüm W, Pabst J et al. (1986) Pharmacodynamic profile of bisoprolol a new β1-selective adrenoceptor antagonist. Brit J clin Pharmacol 22: 293–300

    CAS  Google Scholar 

  12. Anderson JL (1990) Effectiveness of sotalol for therapy of complex ventricular arrhythmias and comparisons with placebo and class 1 antiarrhythmic drugs. Am J Cardiol 65: 37A - 42A

    PubMed  CAS  Google Scholar 

  13. Woosley RL, Barbey JT, Wang T et al. (1990) Concentration/response relations for the multiple antiarrhythmic actions of sotalol. Am J Cardiol 65: 22A - 27A

    PubMed  CAS  Google Scholar 

  14. Blair AD, Burgess ED, Maxwell BM et al. (1981) Sotalol kinetics in renal insufficiency. Clin Pharmacol Ther 29: 457–463

    PubMed  CAS  Google Scholar 

  15. Lund-Johansen P, Omvik P (1992) Chronic hemodynamic effects of carvedilol in essential hypertension at rest and during exercise. Eur Heart J 13 (2): 281–286

    PubMed  CAS  Google Scholar 

  16. Packer M, Bristow MR, Cohn JN et al. (1996) The effect of carvedilol on morbidity and mortality in patients with chronic heart failure. N Engl J Med 334: 1349–1355

    PubMed  CAS  Google Scholar 

  17. von Mollendorff E, Reiff K, Neugebauer G (1987) Pharmacokinetics and bioavailability of carvedilol, a vasodilating beta-blocker. Eur J clin Pharmacol 33: 511–513

    Google Scholar 

  18. Hamann SR, Blouin RA, McAllister RG (1984) Clinical pharmacokinetics of verapamil. Clin Pharmacokinet 9: 26–41

    PubMed  CAS  Google Scholar 

  19. Hoon TJ, Baumann JL, Rodvold KA (1986) The pharmacodynamic and pharmacokinetic differences of the D-and L-isomers of verapamil: implications in the treatment of paroxysmal supraventricular tachycardia. Am Heart J 112: 396–403

    PubMed  CAS  Google Scholar 

  20. Belz GG, Doering W, Hankes R et al (1983) Interaction between digoxin and calcium antagonists and antiarrhythmic drugs. Clin Pharmacol Ther 33: 410–417

    PubMed  CAS  Google Scholar 

  21. Petru MA, Crawford MH, Kennedy GT (1985) Long term efficacy of high-dose diltiazem for chronic stable angina-pectoris: 16-month serial studies with placebo controls. Am Heart J 109: 99–103

    PubMed  CAS  Google Scholar 

  22. Smith MS, Verghese CP, Shand DG (1983) Pharmacokinetic and pharmacodynamic effects of diltiazem. Am J Cardiol 51: 1369–1374

    PubMed  CAS  Google Scholar 

  23. Sorkin EM, Clissold SP, Brogden RN (1985) Nifedipine. A review of its pharmacodynamic and pharmacokinetic properties and therapeutic efficacy in ischemic heart disease, hypertension and related cardiovascular disorders. Drugs 30: 182–274

    PubMed  CAS  Google Scholar 

  24. Kirch W, Hutt HJ, Dylewicz P et al. (1986) Dose depedence of the nifedipine/digoxin interaction? Clin Pharmacol Ther 39: 35–39

    PubMed  CAS  Google Scholar 

  25. Petry JMR, DeCoster PM, Renkin J (1983) Hemodynamic effects of felodipine at rest and during exercise in exertional angina pectoris. Am J Cardiol 52: 453–457

    Google Scholar 

  26. Blychert E, Edgar B, Elmfeldt D, Shapiro D (1995) Plasma concentrations vs. effect for felodipine. J Cardiovasc Pharmacol 15 (suppl 4): S57

    Google Scholar 

  27. Hayduk K (1995) Initiale Dosistitration von Amlodipin bei leichter bis mittlerer Hypertonie. Munch Med Wschr 23: 381–386

    Google Scholar 

  28. Deanfield JE, Detry JM, Lichtlen PR, et al for the CAPE Study Group (1994) Amlodipine reduces transient myocardial ischemia in patients with coronary artery disease: a double-blind circadian anti-ischemia program in Europe ( CAPE Trial ). J Am Coll Cardiol 24: 1460–1467

    PubMed  CAS  Google Scholar 

  29. Packer M, O’Conner CM, Ghali JK et al. for the Prospective Randomized Amlodipine Survival Evaluation Group (1996) Effect of amlodipine on morbidity and mortality in severe chronic heart failure. N Engl J Med 335: 1107–1114

    PubMed  CAS  Google Scholar 

  30. Abernethy D (1989) The pharmacokinetic profile of amlodipine. Am Heart J 118: 1100–1103

    PubMed  CAS  Google Scholar 

  31. Veterans Administration Cooperative Study Group on Antihypertensive Agents (1984) Low-dose captopril for the treatment of mild to moderate hypertension. I Results of a 14-week trial. Arch Intern Med 144: 1947–1953

    Google Scholar 

  32. Captopril Multicentre Research Group (1987) A placebo controlled trial of captopril in refractory chronic congestive heart failure. J Am Coll Cardiol 2: 755–763

    Google Scholar 

  33. Belz GG, de Mey CA (1992) A case for sublinggual captopril. Blood Pressure 1: 120–122

    PubMed  CAS  Google Scholar 

  34. Duchin KL, Singhvi SM, Willard DA (1982) Captopril kinetics. Clin Pharmacol Ther 31: 452–458

    PubMed  CAS  Google Scholar 

  35. Swedberg K (1991) Lack of beneficial effects on mortality by early intervention with enalapril in acute myocardial infarction. Circulation 84: II - 366

    Google Scholar 

  36. Schwartz JB, Taylor A, Abernethy D (1985) Pharmacokinetics and pharmacodynamics of enalapril in patients with congestive heart failure and patients with hypertension. J Cardiovasc Pharmacol 7: 767–776

    PubMed  CAS  Google Scholar 

  37. Davies RO, Irvin JD, Kramsch DK (1984) Enalapril worldwide experiences. Am J Med 77 (suppl 2A): 23–35

    PubMed  CAS  Google Scholar 

  38. Goa KL, Wagstaff AJ (1996) Losartan Potassium. Drugs 51: 820–845

    PubMed  CAS  Google Scholar 

  39. Goldberg AI, Dunlay MC, Sweet CS (1995) Sicherheit and Verträglichkeit des Angiotensin II-Rezeptor-Antagonisten Losartan-Kalium im Vergleich zu Hydrochlorothiazid, Atenolol, Felodipin in Retardform and AngiotensinConverting-Enzym-Hemmern bei der Behandlung der arteriellen Hypertonie. Am J Cardiol 75: 793–795

    Google Scholar 

  40. Pitt B, Segal R, Martinez FA et al. (1997) Randomisierte Studie von Losartan gegenüber Captopril bei Patienten über 65 mit Herzinsuffizienz (Studie „Evaluation of Losartan in the Elderly“, ELITE ). Lancet 349: 747–752

    PubMed  CAS  Google Scholar 

  41. Andersson OK, Neldam S (1998) The antihypertensive effect and tolerability of candesartan cilexetil, a new generation angiotensin II antagonist, in comparison with losartan. Blood Press 7: 53–59

    PubMed  CAS  Google Scholar 

  42. Heuer HJ, Schöndorfer G, Högemann AM (1997) 24-hour blood pressure profile of different doses of candesartan cilexetil in patients with mild to moderate hypertension. J Hum Hyptertens. 11 (Suppl. 2 ): 55–56

    Google Scholar 

  43. de Zeeuw D, Remuzzi G, Kirch W (1997) Pharmcokinetics of candesartan cilexetil in volunteers with renal or hepatic impairment. J Hum Hypertens 11 (Suppl. 2): 37–42

    Google Scholar 

  44. Pool JL, Guthrie RM, Littlejohn III TW et al. (1998) Dose-Related antihypertensive Effects of Irbesartan in Patients with Mild-to-Moderate Hypertension. Am J Hypertens 11: 462–470

    PubMed  CAS  Google Scholar 

  45. Stumpe KO, Haworth D, Hoglund C et al. (1998) Comparison of the Agntiotensin II Receptor Antagonist Irbesartan with Atenolol for Treatment of Hypertension. Blood Press 7: 31–37

    PubMed  CAS  Google Scholar 

  46. Sica DA, Marino MR, Hammett JL et al. (1997) The pharmacokinetics of irbesartan in renal failure and maintenance hemodialysis. Clin Pharmacol Ther 62: 610–618

    PubMed  CAS  Google Scholar 

  47. Brodgen RN, Heel RL, Speight TM et al. (1977) Prazosin: A review of its pharmacological properties and therapeutic efficacy in hypertension. Drugs 14: 163–197

    Google Scholar 

  48. Jaillon P (1980) Clinical pharmacokinetics of prazosin: Clin Pharmacokinet 5: 365–376

    PubMed  CAS  Google Scholar 

  49. Dominiak P (1993) Ein postsynaptischer al-Adrenozeptorenblocker in der Hochdrucktherapie. Internist 34: 682–687

    PubMed  CAS  Google Scholar 

  50. The Treatment of Mild Hypertension Research Group (1991) The Treatment of Mild Hypertension Study. Arch Intern Med 151: 1413–23

    Google Scholar 

  51. Kirch W, Axthelm T (1982) Endralazine, a new peripheral vasodilator–a randomized crossover trial against dihydralazine. J Cardiovasc Pharmacol 4: 562–566

    PubMed  CAS  Google Scholar 

  52. Shepherd AMM, Ludden TM, McNay JL (1980) Hydralazine kinetics after single and repeated oral doses. Clin Pharmacol Ther 28: 804–11

    PubMed  CAS  Google Scholar 

  53. Bammel A, Stern R, Sterry W (1993) Therapy der antrogenetischen Alopezie. Dtsch Med Wschr 118: 787–789

    PubMed  CAS  Google Scholar 

  54. Lowenthal DT, Affrime MB (1980) Pharmacology and pharmacokinetics of minoxidil. J Cardiovasc Pharmacol 2 (suppl 2): S93 - S106

    PubMed  Google Scholar 

  55. Vesey CJ, Cole PV (1985) Blood cyanide and thiocyanate concentrations produced by long-term therapy with sodium nitroprusside. Br J Anaest 57: 148–155

    CAS  Google Scholar 

  56. Schulz V, Bonn R, Kindler J (1979) Kinetics and elimination of thiocyanate in 7 healthy subjects and in 8 subjects with renal failure. Klin Wochenschr 57: 243–247

    PubMed  CAS  Google Scholar 

  57. Kirch W, Ohnhaus EE (1986) Double blind comparison of ketanserin with atenolol: Antihypertensive activity and platelet function. J Hypertension 4 (suppl 1), 67–70

    Google Scholar 

  58. Cameron HC, Waller PC, Ramsay LE (1987) The effect of ketanserin on the QT interval. Br clin Pharmacol 23: 630 P

    Google Scholar 

  59. Trenk D, Mosier A, Kirch W et al. (1983) Pharmacokinetics and pharmacodynamics of the 5-HT2 receptor antagonist ketanserin in man. J Cardiovasc Pharmacol 5: 1034–1039

    PubMed  CAS  Google Scholar 

  60. Distler A, Kirch W, Luth B (1980) Antihypertensive effect of guanfacine: A double blind crossover comparison with clonidine. Brit J clin Pharmacol 10: 49S - 53S

    Google Scholar 

  61. Washton AM, Resnick RB (1981) Clonidine in opiate withdrawal: review and appraisal of clinical findings. Pharmacotherapy 1: 140–146

    PubMed  CAS  Google Scholar 

  62. Shaw JE (1984) Pharmacokinetics of nitroglycerin and clonidine delivered by the transdermal route. Am Heart J 108: 217–223

    PubMed  CAS  Google Scholar 

  63. Kirch W, Hutt HJ, Plänitz V (1990) Pharmacodynamic action and pharmacokinetics of moxonidine after single oral administration in hypertensive patients. J Clin Pharmacol 30: 1088–1095

    PubMed  CAS  Google Scholar 

  64. Kirch W, Hutt HJ, Plänitz V (1988) The influence of renal function on clinical pharmacokinetics of moxonidine. J Clin Pharmacol 15: 245–253

    CAS  Google Scholar 

  65. Jerie P (1980) Clinical experience with guanfacine in long-term treatment of hypertension. Part I: efficacy and dosage. Br clin Pharmacol 10: 37S - 47S

    Google Scholar 

  66. Kirch W, Kohler H, Braun W (1980) Elimination of guanfacine in patients with normal and impaired renal function. Brit J clin Pharmacol 10: 33S - 35S

    Google Scholar 

  67. Kwan KC, Foltz EL, Breault GO (1976) Pharmacokinetics of methyldopa in man. J Pharmacol Exp Ther 198: 264–277

    PubMed  CAS  Google Scholar 

  68. Johnson P, Kitchin AH, Lowther CP (1966) Treatment of hypertension with methyldopa. Br Med J 5480: 133–137

    Google Scholar 

  69. Fozaned JR, Mir AR (1987) Are 5 HT-receptors involved in the antihypertensive effect of urapidil? Brit J Pharmacol 90: 24–30

    Google Scholar 

  70. Kirsten R, Nelson K, Steinigans VW (1988) Clinical pharmacokinetics of urapidil. Clin Pharmacokinet 14: 129–140

    PubMed  CAS  Google Scholar 

  71. Stitzel RE (1977) The biological fate of reserpine. Pharmacol Rev 28: 179–205

    Google Scholar 

  72. Hypertension Stroke Cooperative Study Group (1974) Effects of antihypertensive treatment on stroke recurrence. JAMA 229: 09–418

    Google Scholar 

  73. Lant A (1983) Diuretics: Clinical pharmacology and therapeutics use (2 Parts): Drugs 29: 57–87, 162–188

    Google Scholar 

  74. Kokko JP (1984) Site and mechanism of action of diuretics. Am J Med 77: 11–17

    PubMed  CAS  Google Scholar 

  75. Anderson J, Goodfrey BE, Hill DM et al. (1971) A comparison of the effects of hydrochlorothiazide and of furosemide in the treatment of hypertensive patients. Q J Med 40: 541–560

    PubMed  CAS  Google Scholar 

  76. Cutler RE, Blair AD (1979) Clinical pharmacokinetics of furosemide. Clin Pharmacokinet 4: 279–296

    PubMed  CAS  Google Scholar 

  77. Dikshit K, Vyden JK, Forrester JS (1973) Renal and extrarenal hemodynamic effects of furosemide in congestive heart failure after acute myocardial infarction. N Engl J Med 288: 1087–1090

    PubMed  CAS  Google Scholar 

  78. McNabb WR, Noormohamed FH, Brooks BA (1984) Renal actions of piretanide and three other „loop“ diuretics. Clin Pharmacol Ther 35: 328–337

    PubMed  CAS  Google Scholar 

  79. Clissold SP, Brogden RN (1985) Piretanide: A preliminary review of its pharmacodynamic and pharmacokinetic properties, and therapeutic efficacy. Drugs 29: 489–530

    PubMed  CAS  Google Scholar 

  80. Khatri I, Goltdiener U, Notargiacomo A et al. (1980) Effect of therapy on left ventricular function in hypertension. Clin Sci 59: 435–439

    Google Scholar 

  81. Beerman B, Groschinsky-Grind M (1980) Clinical pharmacokinetics of diuretics. Clin Pharmacokinet 5: 221–245

    Google Scholar 

  82. Wilkinson PR, Hesp R, Issler H (1975) Total body and serum potassium during prolonged thiazide therapy for essential hypertension. Lancet 1: 759–762

    PubMed  CAS  Google Scholar 

  83. Mulley BA, Parr GD, Rye RM (1980) Pharmacokinetics of chlorthalidone. Eur J Pharmacol 17: 203–207

    CAS  Google Scholar 

  84. Anon (1972) Potassium-sparing diuretics: Spironolactone v triamterene and amiloride. Drug Ther Bull 10: 30–32

    Google Scholar 

  85. Burnakis TG, Mioduch HJ (1984) Triamterene. Arch Int Med 144: 2371–2372

    CAS  Google Scholar 

  86. Smith AJ, Smith RN (1973) Kinetics and bioavialability of two formulations of amiloride in man. Brit J Pharmacol 48: 646–649

    CAS  Google Scholar 

  87. Macfie HL, Colvin CL, Anderson PO (1981) Amiloride; Drug Intell Clin Pharm 15: 94–98

    CAS  Google Scholar 

  88. Ramsay LE, Hettiarachchi J, Fraser R (1980) Amiloride, spironolactone, and potassium chloride in thiazide-treated hypertensive patients. Clin Pharmacol Ther 27: 533–543

    PubMed  CAS  Google Scholar 

  89. Eggert RC (1970) Spironolactone diuretics in patients with cirrhosis and ascites. Brit Med J 4: 401–403

    PubMed  CAS  Google Scholar 

  90. Nissenson AR, Weston RE, Kleeman CR (1979) Mannitol: West J Med 131: 277–284

    PubMed  CAS  Google Scholar 

  91. Parker JO (1987) Nitrate therapy in stable angina pectoris. N Engl J Med 316: 1635–1642

    PubMed  CAS  Google Scholar 

  92. Abrams J (1985) Pharmacology of nitroglycerin and long-acting nitrates. Am J Cardiol 56: 12A - 18A

    PubMed  CAS  Google Scholar 

  93. Reynen K (1993) Nitrate. Dtsch Med Wschr 118: 1532–1539

    CAS  Google Scholar 

  94. Majid PA, De Feyter PJF, van der Wall et al. (1980) Molsidomine in the treatment of patients with angina pectoris. Acute haemodynamic effects and clinical efficacy. N Engl J Med 302: 1–6

    PubMed  CAS  Google Scholar 

  95. Parker JO, Vankoughnett KA, Farrell B (1986) Nitroglycerin lingual spray: Clinical efficacy and dose-response relation. Am J Cardiol 57: 1–5

    PubMed  CAS  Google Scholar 

  96. Tremblay G (1985) High dose isosorbide dinitrate in management of angina pectoris. Am Heart J 110: 280–284

    PubMed  CAS  Google Scholar 

  97. Abrams J (1980) Nitrate tolerance and dependence. Am Heart J 99: 113–123

    PubMed  CAS  Google Scholar 

  98. Sporl-Radun S, Betzien G, Kaufmann B (1980) Effects and pharmacokinetis of isosorbide dinitrate in normal man. Eur J Clin Pharmacol 18: 237–244

    PubMed  CAS  Google Scholar 

  99. Thadani U, Prasad R, Hamilton S (1987) Usefulness of twice-daily isosorbide 5mononitrate in prevention development of tolerance in angina pectoris. Am J Cardiol 447–482

    Google Scholar 

  100. Akpan W, Endele R, Neugebauer G et al. (1984) Pharmacokinetics of IS-S-MN after oral intravenous administration in patients with hepatic failure. In: Cohn JN, Rittinghausen R (eds) Mononitrates. Springer, Berlin pp 86–91

    Google Scholar 

  101. Kukovetz WR, Holzmann S (1985) Mechanisms of vasodilation by molsidomine. Am Heart J 109: 637–640

    PubMed  CAS  Google Scholar 

  102. Ostrowski J, Resag K (1985) Pharmacokinetics of molsidomine in humans. Am Heart J 109: 641–643

    PubMed  CAS  Google Scholar 

  103. Bresnahan JF, Vlietstra RE (1979) Digitalis glycosides. Mayo Clin Proc 54: 675–684

    PubMed  CAS  Google Scholar 

  104. Lisalo E (1977) Clinical pharmacokinetics of digoxin. Clin Pharmacokinet 2: 1–16

    Google Scholar 

  105. Kirch W, Laskowski M, Ohnhaus EE et al. (1989) Effects of felodipine on plasma digoxin levels and haemodymanics in patients with heart failure. J Intern Med (ehem Acta Medica Scand) 225: 237–241

    CAS  Google Scholar 

  106. Perrier D, Mayersohn M, Marcus FI (1977) Clinical pharmacokinetics of digitoxin. Clin Pharmacokinet 2: 292–311

    PubMed  CAS  Google Scholar 

  107. Kirch W, Ohnhaus EE, Pabst J et al. (1989) Digitoxin in patients with hepatorenal insufficiency after repeated oral administration. Eur Heart J 10: 40–44

    PubMed  CAS  Google Scholar 

  108. Kuhlmann J (1985) Effects of verapamil, diltiazem and nifedipine on plasma levels and renal excretion of digitoxin. Clin Pharmacol Ther 38: 667–673

    PubMed  CAS  Google Scholar 

  109. The Cardiac Arrhythmia Suppression Trial (CAST) (1989) Investigators: Preliminary report: Effect of encainidine and flecainide on mortality in a randomized trial of arrhythmia suppression after myocardial function. N Engl J Med 321: 406–412

    Google Scholar 

  110. Surawicz B (1993) Pharmacologic treatment of cardiac arrhythmias: 25 years progress. J Am Coll Cardiol 1: 365–381

    Google Scholar 

  111. Vaughan Williams EM (1984) A Classification of antiarrhythmic actions reassessed after a decade of new drugs. J Clin Pharmacol 24: 129–147

    Google Scholar 

  112. Carliner NH, Fisher ML, Crouthamel WG et al. (1980) Relation of ventricular premature beat suppression to serum quinidine concentration determined by a new and specific assay. Am Heart J 100: 483–489

    PubMed  CAS  Google Scholar 

  113. Ochs HR, Greenblatt DJ, Woo E (1980) Clinical pharmacokinetics of quinidine. Clin Pharmacokinet 5: 150–168

    PubMed  CAS  Google Scholar 

  114. Heel RC, Brogden RN, Speight TM et al. (1978) Disopyramide: A review of its pharmacological properties and therapeutic use in treating cardiac arrhythmias Drugs 15: 331–368

    CAS  Google Scholar 

  115. Koch-Weser J (1979) Disopyramide. N Engl J Med 300: 957–962

    CAS  Google Scholar 

  116. Kleinsorge H (1959) Klinische Untersuchungen über die Wirkungsweise des Rauwolfia-Alkaloids Ajmalin bei Herzrhythmusstörungen, insbesondere der Extrasystolie. Med Klin 10: 409–414

    Google Scholar 

  117. Giardina E-GV, Heissenbuttel RH, Bigger JT (1973) Intermittent intravenous procainamide to treat ventricular arrhythmias. Ann Intern Med 78: 183–193

    PubMed  CAS  Google Scholar 

  118. Greenspan AM et al. (1980) Large dose procainamide therapy for ventricular tachyarrhythmia. Am J Cardiol 46: 453–463

    PubMed  CAS  Google Scholar 

  119. Connolly SJ, Kates RE (1982) Clinical pharmacokinetics of N-acetylprocainamide. Clin Pharmacokinet 7: 206–220

    PubMed  CAS  Google Scholar 

  120. Benowitz NL, Meister W (1978) Clinical pharmacokinetics of lidocaine. Clin Pharmacokinet 3: 177–201

    PubMed  CAS  Google Scholar 

  121. Lie KJ, Weliens HJ, van Capelle FJ et al. (1974) Lidocaine in the prevention of primary ventricular fibrillation. N Engl J Med 291: 1324–1326

    PubMed  CAS  Google Scholar 

  122. Ribner HS, Isaacs ES, Frishman WH (1979) Lidocaine prophylaxis against ventricular fibrillation in acute myocardical infarction. Prog Cardiovasc Dis 21: 287–313

    PubMed  CAS  Google Scholar 

  123. Schrader BJ, Bauman JL (1986) Mexiletine: A new type I antiarrhythmic agent. Drug Intell Clin Pharmacol 20: 255–260

    CAS  Google Scholar 

  124. Woosley RL, Wang T, Stone W et al. (1984) Pharmacology, electrophysiology,and pharmacokinetics of mexiletine. Am Heart J 107: 1058–1065

    PubMed  CAS  Google Scholar 

  125. Breithardt G, Selpel L, Abendroth RR (1980) Comparative cross-over study of the effects of disopyramide and mexiletine on stimulus-induced ventricular tachycardia. Circulation 62 (suppl III): 153

    Google Scholar 

  126. Roden DM, Woosley RL (1986) Tocainide. N Engl J Med 315: 41–45

    CAS  Google Scholar 

  127. Elvin AT, Lalka D, Stoeckel K et al. (1980) Tocainide kinetics and metabolism. Effects of pheno-barbitone and substrates for glucuronyl transferase. Clin Pharmacol Ther 28: 652–658

    PubMed  CAS  Google Scholar 

  128. Munsat TL (1967) Therapy of myotonia. A double-blind evaluation of diphenylhydantoin, procainamide and placebo. Neurology 17: 359–367

    PubMed  CAS  Google Scholar 

  129. Bigger JT Jr, Schmidt DH, Kutt H (1968) Relationship between the plasma levels of diphenyl-hydantoin sodium and its cardiac antiarrhythmic effect. Circulation 38: 363–374

    PubMed  Google Scholar 

  130. Keller K, Meyer-Erstorf G, Beck OA et al. (1978) Correlation and pharmacological effect on atrio-ventricular conduction time of the antiarrhythmic drug propafenone. Eur J clin Pharmacol 13: 17–20

    PubMed  CAS  Google Scholar 

  131. Siddoway LA, Thompson KA, McAllister DB et al. (1987) Polymorphism of propafenone metabolism and disposition in man: clinical and pharmacokinetic consequences. Circulation 75: 785–791

    PubMed  CAS  Google Scholar 

  132. Salerno DM, Granrud G, Sharkey P et al. (1984) A controlled trial of propafenone for treatment of frequent and repetitive ventricular premature complexes. Am J Cardiol 53: 77–83

    PubMed  CAS  Google Scholar 

  133. Holmes B, Heel RC (1985) Flecainide. A preliminary review of its pharmacokinetic properties and therapeutic efficacy. Drugs 29: 1–33

    PubMed  CAS  Google Scholar 

  134. Nappi JM, Anderson JL (1985) Flecainide: A new prototype antiarrhythmic agent. Pharmacotherapy 5: 209–221

    PubMed  CAS  Google Scholar 

  135. Sing BN (1983) Amiodarone: Historical development and pharmacologic profile. Am Heart J 106: 788–797

    Google Scholar 

  136. Rotmensch HH, Belhassen B, Swanson BN et al. (1984) Steady-state serum amiodarone concentrations: relationship with antiarrhythmic efficacy and toxicity. Ann Intern Med 101: 462–469

    PubMed  CAS  Google Scholar 

  137. Holt DW, Tucker GT, Jackson PR et al. (1983) Amiodarone pharmacokinetics. Am Heart J 106: 840–847

    PubMed  CAS  Google Scholar 

  138. Camm AJ, Garratt CJ (1991) Adenosine and supraventricular tachycardia. N Engl J Med 325: 1621–1629

    PubMed  CAS  Google Scholar 

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Kirch, W. (2003). Therapie kardiovaskulärer Erkrankungen. In: Frölich, J.C., Kirch, W. (eds) Praktische Arzneitherapie. Springer, Berlin, Heidelberg. https://doi.org/10.1007/978-3-662-09397-9_14

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  • DOI: https://doi.org/10.1007/978-3-662-09397-9_14

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