Literature DB >> 685992

Selection of vasodilator, inotropic or combined therapy for the management of heart failure.

J N Cohn, J A Franciosa.   

Abstract

Vasodilator and inotropic drugs work through independent mechanisms in augmenting left ventricular pump function in patients with heart failure. The selection between these two classes of pharmacologic agents for an individual patient may be based on the control blood pressure as well as the underlying disease. Although vasodilator drugs are easiest and safest to employ in patients with normal or high arterial presure levels, even in relatively hypotensive subjects (systolic arterial pressure less than 105 mm Hg), a salutary hemodynamic effect can be achieved without an undue decrease in pressure. Inotropic drugs may be safest to administer to patients without coronary artery disease, but the oxygen-consuming effect of these drugs need not necessarily have an adverse effect on patients with ischemic heart disease. Combined vasodilator and inotropic drug therapy is the most potent pharmacologic means of restoring pump function in patients with severe heart failure. The long-term use of vasodilator and inotropic drugs in the treatment of heart failure is dependent on the availability of agents that will produce a sustained hemodynamic effect. Hydralazine, nitrates and prazosin have been employed alone or in combination and provide a promising approach to vasodilator treatment of heart failure. Better and more selective oral inotropic agents are needed to allow this therapeutic modality to be employed optimally.

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Year:  1978        PMID: 685992     DOI: 10.1016/0002-9343(78)90708-8

Source DB:  PubMed          Journal:  Am J Med        ISSN: 0002-9343            Impact factor:   4.965


  10 in total

Review 1.  The rationale for combined use of diuretics, digitalis, and vasodilators in congestive heart failure.

Authors:  T W Smith; M A Pfeffer
Journal:  Cardiovasc Drugs Ther       Date:  1989-03       Impact factor: 3.727

Review 2.  Vasodilator therapy in the perioperative period.

Authors:  P N Fyman; J E Cottrell; L Kushins; P A Casthely
Journal:  Can Anaesth Soc J       Date:  1986-09

3.  Haemodynamic effects, plasma concentrations and tolerance of orally administered prenalterol in man.

Authors:  A Weiss; B Pfister; P Imhof; P H Degen; D Burckhardt; U C Dubach
Journal:  Eur J Clin Pharmacol       Date:  1980-11       Impact factor: 2.953

4.  Mathematical model of cardiovascular mechanics for diagnostic analysis and treatment of heart failure: Part 2. Analysis of vasodilator therapy and planning of optimal drug therapy.

Authors:  H Tsuruta; T Sato; N Ikeda
Journal:  Med Biol Eng Comput       Date:  1994-01       Impact factor: 2.602

5.  A comparative study of the cardiovascular and biochemical actions of the imidazo [4,5b] pyridine sulmazole and an imidazo [4,5c] pyridine analogue, BW A746C.

Authors:  G Allan; D Cambridge; M J Follenfant; D Stone; M V Whiting
Journal:  Br J Pharmacol       Date:  1988-02       Impact factor: 8.739

6.  Short- and long-term effects of hydralazine and combined hydralazine-prenalterol therapy in severe chronic congestive heart failure.

Authors:  H Drexler; H Löllgen; H Just
Journal:  Klin Wochenschr       Date:  1981-06-15

7.  Contributions of hemodynamic monitoring to the treatment of chronic congestive heart failure.

Authors:  P W Armstrong
Journal:  Can Med Assoc J       Date:  1979-10-06       Impact factor: 8.262

8.  The cardiovascular pharmacology of ICI 170777 ((6RS)-6-methyl-5-(pyrid-4-yl)-3H,6H-1,3,4- thiadiazin-2-one) a novel compound with positive inotropic and vasodilator effects.

Authors:  M G Collis; J R Keddie; W Rouse
Journal:  Br J Pharmacol       Date:  1989-06       Impact factor: 8.739

9.  Haemodynamic response to dopexamine hydrochloride in postinfarction heart failure: lack of tolerance after continuous infusion.

Authors:  G Svenson; L E Strandberg; B Lindvall; L Erhardt
Journal:  Br Heart J       Date:  1988-12

Review 10.  cGMP Signaling and Modulation in Heart Failure.

Authors:  Robert M Blanton
Journal:  J Cardiovasc Pharmacol       Date:  2020-05       Impact factor: 3.271

  10 in total

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