Literature DB >> 1679661

Hemodynamic interactions of a new beta blocker, celiprolol, with nifedipine in angina pectoris.

B Silke1, S P Verma, S Guy.   

Abstract

The hemodynamic consequences of blockade at both beta-adrenoceptors and slow calcium channels is of therapeutic importance for patients with angina pectoris. The hemodynamic interaction of a new cardioselective beta blocker, celiprolol, and nifedipine was examined in an acute hemodynamic study using three prospectively matched groups with angiographically confirmed coronary artery disease (n = 10/group). Patients were randomly allocated to intravenous celiprolol (8 mg), sublingual nifedipine (20 mg), or their combination. Rest and exercise (supine bicycle) hemodynamics were determined before and following each therapy. At rest, celiprolol did not alter pumping function; nifedipine reduced diastolic blood pressure and systemic vascular resistance index (SVRI), with a small increase in heart rate. Combination therapy reduced systemic arterial pressure and SVRI; heart rate and cardiac stroke volume index increased. During exercise celiprolol tended to reduce heart rate and cardiac index; nifedipine reduced exercise SVR and cardiac stroke work indices. Combination therapy reduced all components of blood pressure; cardiac stroke work and SVR indices fell. These hemodynamic data suggest that beta blockade with celiprolol may result in a slight depression of cardiac pumping during exercise; however, such effects are offset by the vasodilating actions of nifedipine (reflex sympathetic action offsetting cardiodepression). Thus the acute hemodynamic effects of this combination were seemingly safe in these patients; the longer term effects during maintained therapy should be further assessed.

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Year:  1991        PMID: 1679661     DOI: 10.1007/bf03029741

Source DB:  PubMed          Journal:  Cardiovasc Drugs Ther        ISSN: 0920-3206            Impact factor:   3.727


  37 in total

1.  Cardiac output measurement by thermal dilution: reproducibility and comparison with the dye-dilution technique.

Authors:  M B Sorensen; N E Bille-Brahe; H C Engell
Journal:  Ann Surg       Date:  1976-01       Impact factor: 12.969

2.  Celiprolol--pharmacological profile of an unconventional beta-blocker.

Authors:  P S Wolf; R D Smith; A Khandwala; R G Van Inwegen; R J Gordon; W S Mann; D V Romano; T P Pruss
Journal:  Br J Clin Pract Suppl       Date:  1985-06

3.  Haemodynamic dose-response effects of i.v. nicardipine in coronary artery disease.

Authors:  B Silke; S P Verma; G I Nelson; M Hussain; S H Taylor
Journal:  Br J Clin Pharmacol       Date:  1984-11       Impact factor: 4.335

Review 4.  Pharmacological basis for the therapeutic applications of slow-channel blocking drugs.

Authors:  B N Singh
Journal:  Angiology       Date:  1982-08       Impact factor: 3.619

5.  Haemodynamic dose-response effects of i.v. metoprolol in coronary heart disease.

Authors:  W G Hendry; B Silke; S H Taylor
Journal:  Eur J Clin Pharmacol       Date:  1981       Impact factor: 2.953

6.  Acute influence of different beta-blocking agents upon left heart hemodynamics at rest and during exercise in patients with coronary artery disease.

Authors:  A Reale; A Nigri; P A Gioffrè; M Motolese
Journal:  Eur J Cardiol       Date:  1979-02

7.  Left ventricular angiography on exercise. A new method of assessing left ventricular function in ischaemic heart disease.

Authors:  B Sharma; J F Goodwin; M J Raphael; R E Steiner; R G Rainbow; S H Taylor
Journal:  Br Heart J       Date:  1976-01

8.  Hemodynamic effects of verapamil and practolol in man.

Authors:  R Seabra-Gomes; A Rickards; R Sutton
Journal:  Eur J Cardiol       Date:  1976-03

9.  Effect of oral propranolol on rest and exercise left ventricular ejection fraction, volumes, and segmental wall motion in patients with angina pectoris. Assessment with equilibrium gated blood pool imaging.

Authors:  G J Dehmer; M Falkoff; S E Lewis; L D Hillis; R W Parkey; J T Willerson
Journal:  Br Heart J       Date:  1981-06

10.  Hemodynamic effects of nifedipine during upright exercise in stable angina pectoris and either normal or severely impaired left ventricular function.

Authors:  G I Nelson; B Silke; R C Ahuja; S P Verma; M Hussain; S H Taylor
Journal:  Am J Cardiol       Date:  1984-02-01       Impact factor: 2.778

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  1 in total

1.  Interactions of a new beta-blocker, celiprolol, with the calcium antagonists, diltiazem and nifedipine, on atrioventricular conduction.

Authors:  S Motomura; K Hashimoto
Journal:  Cardiovasc Drugs Ther       Date:  1995-06       Impact factor: 3.727

  1 in total

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