Literature DB >> 1532321

Effect of captopril on functional, physiological and biochemical outcome criteria in aged heart failure patients.

C J O'Neill1, A Charlett, R J Dobbs, A A Deshmukh, S G Bowes, C Weller, P W Nicholson, J S Milledge, S M Dobbs.   

Abstract

1. Captopril was evaluated as an adjuvant to diuretic and digoxin therapy in heart failure in old age, using walking ability, minute ventilation and oxygen consumption and plasma atrial natriuretic factor (ANF) concentration as measures of outcome. 2. Twenty patients, mean (s.d.) age 81 (6) years, entered a double-blind, randomised, crossover study of three treatments, a twice daily regimen of captopril (AA), at a dosage established by titration against serum angiotensin converting enzyme (ACE) activity, the same dosage in the morning with placebo at night (AP), and twice daily placebo (PP). Each treatment lasted 3 weeks. A 2 week run-in period on triple therapy, with AA captopril, was used to assess stability and compliance. Seventeen completed all treatments: three completed two. 3. Any benefit of captopril was modest and there was deterioration in gait on the titrated dosage 3 months afterwards (P = 0.04). Efficacy in the old may be greatest when the titrated dose (25 or 50 mg) is given once daily: the multiple daily doses recommended may be unnecessarily demanding. 4. Walking performance was measured by gait analysis (GA) at free walking speed and by a simple walking test (SWT), in which patients stopped at the first relevant symptom. There was a consistent tendency for four measures of performance (GA: speed, stride length and double support time; SWT distance) to be best on the AP treatment, next best on AA, and worst on PP but for the fifth, SWT speed, AP and AA were similar. The trend appeared most marked for SWT distance, mean (s.e. mean) values for AP, AA and PP being 123 (15), 94 (16) and 75 (16) m, respectively. However, the treatment effect did not reach statistical significance at the 0.05 level. 5. There was no significant difference between treatments in minute ventilation, minute oxygen consumption, or their ratio, either at rest or on exercise. 6. Resting ANF concentrations were nearly four times higher (P = 0.0001) in the patients than those, mean (s.e. mean) 66 (5) pmol l-1, in eleven healthy volunteers of mean age 80 (6) years, and the increase on exercise, seen in the controls (P less than 0.01), was absent. In the patients the resting plasma ANF concentration was significantly affected by treatment (P = 0.03), being less on both AP, 245 (9), and AA, 214 (9) than on PP, 264 (10) pmol l-1 (P = 0.02 and 0.03, respectively). 7. Baseline serum ACE activity was induced on active treatment. The change in ACE activity at 3 h post an active dose was significantly greater on AP than AA (P = 0.005). The increased sensitivity to inhibition during once daily administration was reflected in mean arterial pressure. The pre-dose standing pressure was less on AP than on PP (P less than 0.05), and the change in postural fall (pre-dose minus 2 h post), was greater (P = 0.004), but AA and PP were similar in these respects.(ABSTRACT TRUNCATED AT 400 WORDS)

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Year:  1992        PMID: 1532321      PMCID: PMC1381303          DOI: 10.1111/j.1365-2125.1992.tb04020.x

Source DB:  PubMed          Journal:  Br J Clin Pharmacol        ISSN: 0306-5251            Impact factor:   4.335


  39 in total

1.  Carotid artery stenosis exposed by an adverse effect of captopril.

Authors:  H Jensen; H Ring-Larsen; P Garsdal; P Fruergaard
Journal:  Br Med J (Clin Res Ed)       Date:  1986-10-25

2.  A continuous monitoring spectrophotometric method for the measurement of angiotensin-converting enzyme in human serum.

Authors:  G A Maguire; C P Price
Journal:  Ann Clin Biochem       Date:  1985-03       Impact factor: 2.057

3.  Atrial natriuretic peptide in relation to physical exercise.

Authors:  J Bollerslev; J Svanegård; O Blaabjerg; T Pindborg
Journal:  Scand J Clin Lab Invest       Date:  1987-11       Impact factor: 1.713

4.  Measurement of plasma angiotensin II.

Authors:  J J Morton; D J Webb
Journal:  Clin Sci (Lond)       Date:  1985-04       Impact factor: 6.124

5.  Enalapril and hypertension.

Authors:  L M Cohen; G Anderson; R F White; G Griffing; J Melby
Journal:  Am J Psychiatry       Date:  1984-08       Impact factor: 18.112

6.  Compliance with anti-tuberculous therapy: a field trial of a pill-box with a concealed electronic recording device.

Authors:  R Cheung; J Dickins; P W Nicholson; A S Thomas; H H Smith; H E Larson; A A Deshmukh; R J Dobbs; S M Dobbs
Journal:  Eur J Clin Pharmacol       Date:  1988       Impact factor: 2.953

7.  Controlled trial of captopril in chronic heart failure: a rest and exercise hemodynamic study.

Authors:  B L Kramer; B M Massie; N Topic
Journal:  Circulation       Date:  1983-04       Impact factor: 29.690

8.  Effect of a new angiotensin converting enzyme inhibitor MK 421 and its lysine analogue on the components of the renin system in healthy subjects.

Authors:  D B Brunner; G Desponds; J Biollaz; I Keller; F Ferber; H Gavras; H R Brunner; J L Schelling
Journal:  Br J Clin Pharmacol       Date:  1981-05       Impact factor: 4.335

9.  Functional capacity of patients with chronic left ventricular failure. Relationship of bicycle exercise performance to clinical and hemodynamic characterization.

Authors:  J A Franciosa; S Ziesche; M Wilen
Journal:  Am J Med       Date:  1979-09       Impact factor: 4.965

10.  The effects of antihypertensive therapy on the quality of life.

Authors:  S H Croog; S Levine; M A Testa; B Brown; C J Bulpitt; C D Jenkins; G L Klerman; G H Williams
Journal:  N Engl J Med       Date:  1986-06-26       Impact factor: 91.245

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  2 in total

Review 1.  Optimising heart failure pharmacotherapy: the ideal combination.

Authors:  J G Cleland; D P Dutka
Journal:  Br Heart J       Date:  1994-08

2.  Objective evidence for tolerance, against a background of improvement, during maintenance therapy with controlled release levodopa/carbidopa.

Authors:  S G Bowes; R J Dobbs; M Henley; A Charlett; C J O'Neill; P W Nicholson; A G Purkiss; C Weller; S M Dobbs
Journal:  Eur J Clin Pharmacol       Date:  1992       Impact factor: 2.953

  2 in total

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