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:
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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.
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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.
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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
Deutsche Liga zur Bekämpfung des hohen Blutdruckes e.V. (2003) Empfehlungen zur Hochdruckbehandlung in der Praxis und zur Bekämpfung hypertensiver Notfälle. 11. Auflage. Heidelberg
Flockhart, D (2002) Cytochrome P450 Drug Interactions. [online aufgerufen am 25.11.2002] URL: http://medicine.iupui.edu/flockhart/
Routledge PA, Shand DG (1979) Clinical pharmacokinetics of propranolol. Clin Pharmacokinet 4: 73–90
Dollery C (1991) Propranolol. A Pharmacopoeia. Churchill Livingstone, Edinburgh, p 272–278
Toon S, Davidson EM, Garstang FM et al. (1988) The racemic metoprolol-H2antagonist interaction. Clin Pharmacol Ther 43: 283–289
Sandstrom B (1978) Antihypertensive treatment with the adrenergic p-receptor blocker metoprolol during pregnancy. Gynecol Obst 9: 195–204
Kirch W, Köhler H, Mutschier E et al. (1981) Pharmacokinetics of atenolol in relation to renal function. Eur J clin Pharmacol 19: 65–71
Rubin PC, Butters L, Clark DM (1983) Placebo-controlled trial of atenolol in treatment of pregnancy-associated hypertension. Lancet 1: 431–434
CIBIS-II Investigators and Committees (1999) The Cardiac Insufficiency Bisoprolol Study II (CIBIS-II): a randomised trial. Lancet 353: 9–13
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
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
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
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
Blair AD, Burgess ED, Maxwell BM et al. (1981) Sotalol kinetics in renal insufficiency. Clin Pharmacol Ther 29: 457–463
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
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
von Mollendorff E, Reiff K, Neugebauer G (1987) Pharmacokinetics and bioavailability of carvedilol, a vasodilating beta-blocker. Eur J clin Pharmacol 33: 511–513
Hamann SR, Blouin RA, McAllister RG (1984) Clinical pharmacokinetics of verapamil. Clin Pharmacokinet 9: 26–41
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
Belz GG, Doering W, Hankes R et al (1983) Interaction between digoxin and calcium antagonists and antiarrhythmic drugs. Clin Pharmacol Ther 33: 410–417
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
Smith MS, Verghese CP, Shand DG (1983) Pharmacokinetic and pharmacodynamic effects of diltiazem. Am J Cardiol 51: 1369–1374
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
Kirch W, Hutt HJ, Dylewicz P et al. (1986) Dose depedence of the nifedipine/digoxin interaction? Clin Pharmacol Ther 39: 35–39
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
Blychert E, Edgar B, Elmfeldt D, Shapiro D (1995) Plasma concentrations vs. effect for felodipine. J Cardiovasc Pharmacol 15 (suppl 4): S57
Hayduk K (1995) Initiale Dosistitration von Amlodipin bei leichter bis mittlerer Hypertonie. Munch Med Wschr 23: 381–386
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
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
Abernethy D (1989) The pharmacokinetic profile of amlodipine. Am Heart J 118: 1100–1103
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
Captopril Multicentre Research Group (1987) A placebo controlled trial of captopril in refractory chronic congestive heart failure. J Am Coll Cardiol 2: 755–763
Belz GG, de Mey CA (1992) A case for sublinggual captopril. Blood Pressure 1: 120–122
Duchin KL, Singhvi SM, Willard DA (1982) Captopril kinetics. Clin Pharmacol Ther 31: 452–458
Swedberg K (1991) Lack of beneficial effects on mortality by early intervention with enalapril in acute myocardial infarction. Circulation 84: II - 366
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
Davies RO, Irvin JD, Kramsch DK (1984) Enalapril worldwide experiences. Am J Med 77 (suppl 2A): 23–35
Goa KL, Wagstaff AJ (1996) Losartan Potassium. Drugs 51: 820–845
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
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
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
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
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
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
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
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
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
Jaillon P (1980) Clinical pharmacokinetics of prazosin: Clin Pharmacokinet 5: 365–376
Dominiak P (1993) Ein postsynaptischer al-Adrenozeptorenblocker in der Hochdrucktherapie. Internist 34: 682–687
The Treatment of Mild Hypertension Research Group (1991) The Treatment of Mild Hypertension Study. Arch Intern Med 151: 1413–23
Kirch W, Axthelm T (1982) Endralazine, a new peripheral vasodilator–a randomized crossover trial against dihydralazine. J Cardiovasc Pharmacol 4: 562–566
Shepherd AMM, Ludden TM, McNay JL (1980) Hydralazine kinetics after single and repeated oral doses. Clin Pharmacol Ther 28: 804–11
Bammel A, Stern R, Sterry W (1993) Therapy der antrogenetischen Alopezie. Dtsch Med Wschr 118: 787–789
Lowenthal DT, Affrime MB (1980) Pharmacology and pharmacokinetics of minoxidil. J Cardiovasc Pharmacol 2 (suppl 2): S93 - S106
Vesey CJ, Cole PV (1985) Blood cyanide and thiocyanate concentrations produced by long-term therapy with sodium nitroprusside. Br J Anaest 57: 148–155
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
Kirch W, Ohnhaus EE (1986) Double blind comparison of ketanserin with atenolol: Antihypertensive activity and platelet function. J Hypertension 4 (suppl 1), 67–70
Cameron HC, Waller PC, Ramsay LE (1987) The effect of ketanserin on the QT interval. Br clin Pharmacol 23: 630 P
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
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
Washton AM, Resnick RB (1981) Clonidine in opiate withdrawal: review and appraisal of clinical findings. Pharmacotherapy 1: 140–146
Shaw JE (1984) Pharmacokinetics of nitroglycerin and clonidine delivered by the transdermal route. Am Heart J 108: 217–223
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
Kirch W, Hutt HJ, Plänitz V (1988) The influence of renal function on clinical pharmacokinetics of moxonidine. J Clin Pharmacol 15: 245–253
Jerie P (1980) Clinical experience with guanfacine in long-term treatment of hypertension. Part I: efficacy and dosage. Br clin Pharmacol 10: 37S - 47S
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
Kwan KC, Foltz EL, Breault GO (1976) Pharmacokinetics of methyldopa in man. J Pharmacol Exp Ther 198: 264–277
Johnson P, Kitchin AH, Lowther CP (1966) Treatment of hypertension with methyldopa. Br Med J 5480: 133–137
Fozaned JR, Mir AR (1987) Are 5 HT-receptors involved in the antihypertensive effect of urapidil? Brit J Pharmacol 90: 24–30
Kirsten R, Nelson K, Steinigans VW (1988) Clinical pharmacokinetics of urapidil. Clin Pharmacokinet 14: 129–140
Stitzel RE (1977) The biological fate of reserpine. Pharmacol Rev 28: 179–205
Hypertension Stroke Cooperative Study Group (1974) Effects of antihypertensive treatment on stroke recurrence. JAMA 229: 09–418
Lant A (1983) Diuretics: Clinical pharmacology and therapeutics use (2 Parts): Drugs 29: 57–87, 162–188
Kokko JP (1984) Site and mechanism of action of diuretics. Am J Med 77: 11–17
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
Cutler RE, Blair AD (1979) Clinical pharmacokinetics of furosemide. Clin Pharmacokinet 4: 279–296
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
McNabb WR, Noormohamed FH, Brooks BA (1984) Renal actions of piretanide and three other „loop“ diuretics. Clin Pharmacol Ther 35: 328–337
Clissold SP, Brogden RN (1985) Piretanide: A preliminary review of its pharmacodynamic and pharmacokinetic properties, and therapeutic efficacy. Drugs 29: 489–530
Khatri I, Goltdiener U, Notargiacomo A et al. (1980) Effect of therapy on left ventricular function in hypertension. Clin Sci 59: 435–439
Beerman B, Groschinsky-Grind M (1980) Clinical pharmacokinetics of diuretics. Clin Pharmacokinet 5: 221–245
Wilkinson PR, Hesp R, Issler H (1975) Total body and serum potassium during prolonged thiazide therapy for essential hypertension. Lancet 1: 759–762
Mulley BA, Parr GD, Rye RM (1980) Pharmacokinetics of chlorthalidone. Eur J Pharmacol 17: 203–207
Anon (1972) Potassium-sparing diuretics: Spironolactone v triamterene and amiloride. Drug Ther Bull 10: 30–32
Burnakis TG, Mioduch HJ (1984) Triamterene. Arch Int Med 144: 2371–2372
Smith AJ, Smith RN (1973) Kinetics and bioavialability of two formulations of amiloride in man. Brit J Pharmacol 48: 646–649
Macfie HL, Colvin CL, Anderson PO (1981) Amiloride; Drug Intell Clin Pharm 15: 94–98
Ramsay LE, Hettiarachchi J, Fraser R (1980) Amiloride, spironolactone, and potassium chloride in thiazide-treated hypertensive patients. Clin Pharmacol Ther 27: 533–543
Eggert RC (1970) Spironolactone diuretics in patients with cirrhosis and ascites. Brit Med J 4: 401–403
Nissenson AR, Weston RE, Kleeman CR (1979) Mannitol: West J Med 131: 277–284
Parker JO (1987) Nitrate therapy in stable angina pectoris. N Engl J Med 316: 1635–1642
Abrams J (1985) Pharmacology of nitroglycerin and long-acting nitrates. Am J Cardiol 56: 12A - 18A
Reynen K (1993) Nitrate. Dtsch Med Wschr 118: 1532–1539
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
Parker JO, Vankoughnett KA, Farrell B (1986) Nitroglycerin lingual spray: Clinical efficacy and dose-response relation. Am J Cardiol 57: 1–5
Tremblay G (1985) High dose isosorbide dinitrate in management of angina pectoris. Am Heart J 110: 280–284
Abrams J (1980) Nitrate tolerance and dependence. Am Heart J 99: 113–123
Sporl-Radun S, Betzien G, Kaufmann B (1980) Effects and pharmacokinetis of isosorbide dinitrate in normal man. Eur J Clin Pharmacol 18: 237–244
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
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
Kukovetz WR, Holzmann S (1985) Mechanisms of vasodilation by molsidomine. Am Heart J 109: 637–640
Ostrowski J, Resag K (1985) Pharmacokinetics of molsidomine in humans. Am Heart J 109: 641–643
Bresnahan JF, Vlietstra RE (1979) Digitalis glycosides. Mayo Clin Proc 54: 675–684
Lisalo E (1977) Clinical pharmacokinetics of digoxin. Clin Pharmacokinet 2: 1–16
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
Perrier D, Mayersohn M, Marcus FI (1977) Clinical pharmacokinetics of digitoxin. Clin Pharmacokinet 2: 292–311
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
Kuhlmann J (1985) Effects of verapamil, diltiazem and nifedipine on plasma levels and renal excretion of digitoxin. Clin Pharmacol Ther 38: 667–673
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
Surawicz B (1993) Pharmacologic treatment of cardiac arrhythmias: 25 years progress. J Am Coll Cardiol 1: 365–381
Vaughan Williams EM (1984) A Classification of antiarrhythmic actions reassessed after a decade of new drugs. J Clin Pharmacol 24: 129–147
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
Ochs HR, Greenblatt DJ, Woo E (1980) Clinical pharmacokinetics of quinidine. Clin Pharmacokinet 5: 150–168
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
Koch-Weser J (1979) Disopyramide. N Engl J Med 300: 957–962
Kleinsorge H (1959) Klinische Untersuchungen über die Wirkungsweise des Rauwolfia-Alkaloids Ajmalin bei Herzrhythmusstörungen, insbesondere der Extrasystolie. Med Klin 10: 409–414
Giardina E-GV, Heissenbuttel RH, Bigger JT (1973) Intermittent intravenous procainamide to treat ventricular arrhythmias. Ann Intern Med 78: 183–193
Greenspan AM et al. (1980) Large dose procainamide therapy for ventricular tachyarrhythmia. Am J Cardiol 46: 453–463
Connolly SJ, Kates RE (1982) Clinical pharmacokinetics of N-acetylprocainamide. Clin Pharmacokinet 7: 206–220
Benowitz NL, Meister W (1978) Clinical pharmacokinetics of lidocaine. Clin Pharmacokinet 3: 177–201
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
Ribner HS, Isaacs ES, Frishman WH (1979) Lidocaine prophylaxis against ventricular fibrillation in acute myocardical infarction. Prog Cardiovasc Dis 21: 287–313
Schrader BJ, Bauman JL (1986) Mexiletine: A new type I antiarrhythmic agent. Drug Intell Clin Pharmacol 20: 255–260
Woosley RL, Wang T, Stone W et al. (1984) Pharmacology, electrophysiology,and pharmacokinetics of mexiletine. Am Heart J 107: 1058–1065
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
Roden DM, Woosley RL (1986) Tocainide. N Engl J Med 315: 41–45
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
Munsat TL (1967) Therapy of myotonia. A double-blind evaluation of diphenylhydantoin, procainamide and placebo. Neurology 17: 359–367
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
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
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
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
Holmes B, Heel RC (1985) Flecainide. A preliminary review of its pharmacokinetic properties and therapeutic efficacy. Drugs 29: 1–33
Nappi JM, Anderson JL (1985) Flecainide: A new prototype antiarrhythmic agent. Pharmacotherapy 5: 209–221
Sing BN (1983) Amiodarone: Historical development and pharmacologic profile. Am Heart J 106: 788–797
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
Holt DW, Tucker GT, Jackson PR et al. (1983) Amiodarone pharmacokinetics. Am Heart J 106: 840–847
Camm AJ, Garratt CJ (1991) Adenosine and supraventricular tachycardia. N Engl J Med 325: 1621–1629
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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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