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Biomedical subjects

L G Dryburgh

Publications and source records attributed to L G Dryburgh.

5 recordsLinked to original sources

Forearm vasoconstriction during dynamic leg exercise in patients with chronic heart failure.

Previous studies assessing vascular responses in nonexercising beds during exercise in patients with chronic heart failure (CHF) have yielded varying results. We proposed that the clinical and hemodynamic severity of heart failure may explain some of the variation. We reasoned that diastolic ventricular interaction (DVI), by limiting the ability of such patients to increase left ventricular (LV) volume and stroke volume during exercise, would attenuate baroreflex activation, resulting in increased sympathetic activation and hence exaggerated vasoconstriction. We hypothesized therefore that vasoconstriction in nonexercising beds would be exaggerated in patients with symptomatic and hemodynamically severe heart failure, particularly if associated with DVI. We measured forearm vascular resistance (FVR) during semierect cycle exercise in 22 CHF patients and 23 control subjects. DVI was assessed by measuring changes in ventricular volumes (radionuclide ventriculography) during volume unloading (-30 mm Hg lower-body negative pressure) in the heart failure patients and was inferred when LV end-diastolic volume paradoxically increased. Patients with symptoms of heart failure developed larger increases in FVR during exercise than did asymptomatic patients. There were significant correlations between the change in FVR during peak exercise and the resting mean pulmonary arterial pressure and pulmonary vascular resistance. CHF patients with DVI developed exaggerated increases in FVR (median [25th to 75th percentile]) compared with the remaining patients during low-workload exercise (138 [66 to 171] vs 6.4 [-4.3 to 28] units, P = 0.002) and during peak exercise (160 [90 to 384] vs 61 [-7.4 to 75] units, P < 0.02). Vasoconstriction in nonexercising beds is exaggerated in CHF patients with clinically and hemodynamically severe heart failure, particularly if associated with DVI. This may explain some of the reported variation in the degree of sympathetic activation that occurs during exercise in CHF patients.

Analysis of Variance↗

Indices of left ventricular systolic function derived by computer analysis of digitised M-mode echocardiograms.

In order to determine the value of computer-assisted analysis of echocardiograms we digitised 980 M-mode studies in normal subjects and patients with pressure and volume overload and heart muscle disease to derive left ventricular dimensions (D), peak systolic rate of change of dimension, normalized for instantaneous dimension (dD/dt/D), mean velocity of circumferential fiber shortening (mean Vcf) and percentage fractional shortening (%FS). The systolic phase indices which, in these patients averaged greater than normal in those with aortic stenosis and hypertrophic cardiomyopathy and lower than normal in those with aortic regurgitation, mitral stenosis and dilated cardiomyopathy, were closely related to each other in all categories of patients. Measurement of % FS appears to describe left ventricular function as well as the more complex indices (mean Vcf, peak dD/dt/D).

Adolescent↗

Beat-to-beat variation in echocardiographic measurements of left ventricular dimensions and function.

M-mode echocardiography was used to explore the extent of spontaneous variation in left ventricular dimensions and indices of systolic and diastolic function. Extended records made in 26 subjects at rest were digitized and analyzed by computer. We found considerable beat-to-beat variation, in that measurements of five or more consecutive cycles were necessary to provide representative values for minor axis dimensions, while the degree of scatter for derived indices of function was greater. This has to be recognized when serial echocardiography is used to study the progress of disease or the effects of treatment.

Adolescent↗

Effect of disopyramide on left ventricular performance: the relationship of free and total concentrations of the drug and of its mono-N-dealkylated metabolite to noninvasive indices of function.

We used M-mode echocardiography and recordings of systolic time intervals to follow changes in left ventricular systolic function of 10 normal subjects during administration of 200 mg oral disopyramide every 8 h. Left ventricular function was significantly depressed (peak rate of change of dimension - 17%, p less than 0.001; mean velocity of circumferential fiber shortening - 15%, p less than 0.01; percent fractional shortening - 16%, p less than 0.05) for as long as 7 h after a dose. These changes could be correlated with those in plasma concentrations of free and total disopyramide, and of its mono-N-dealkylated metabolite (change in peak rate of change of dimension versus levels of disopyramide plus metabolite, r = -0.41, p less than 0.03; changes in ratio preejection time/ejection time versus levels of disopyramide and metabolite, r = 0.62, p less than 0.002).

Adult↗