Key result
The first-dose blood pressure response to ACE inhibitors in CHF was poorly predicted by baseline variables, with baseline mean arterial pressure being the strongest single predictor (r2=5.8%, P=0.02).
Why the study?
Can baseline clinical and laboratory variables predict the blood pressure response to the first dose of ACE inhibitor in patients with mild to moderate congestive heart failure?
Observational (n=132)
Can baseline clinical and laboratory variables predict the blood pressure response to the first dose of ACE inhibitor in patients with mild to moderate congestive heart failure?
The first-dose blood pressure response to ACE inhibitors in mild to moderate heart failure is primarily related to plasma drug concentration and cannot be accurately predicted by baseline clinical or laboratory variables.
Answers are grounded in this paper and cite their sources.
Baseline variables should not guide first-dose ACEI monitoring in CHF; leaves open better predictors including pharmacokinetics.
AIMS: To investigate the relationship in patients with heart failure between BP response to the first dose of ACE inhibitor and (1) plasma drug concentration and (2) baseline clinical and laboratory variables. METHODS: We studied individual placebo-corrected BP responses to initiation of treatment with one of a number ACE inhibitor preparations in 132 patients with mild to moderate CHF. Various pharmacokinetic/pharmacodynamic models were compared. We assessed the strength of association between baseline physiological and laboratory variables and the BP response as assessed directly from the AUC(0,10 h) and indirectly from the slope of the PK/PD relationship. Predictive models for response variables were developing using regression analysis. RESULTS: BP response was primarily related to plasma drug concentration. The association between the fall in BP and baseline variables was weak. The strongest single predictor of BP response was baseline mean arterial pressure (r2 = 5.8%, P = 0.02). The best combinations of predictor variables contained mean arterial pressure, plasma renin activity, creatinine concentration and age (r2 = 14.4%, P = 0.37). When the choice of ACE inhibitor was added, the predictive power of the model increased (r = 23.6%, P < 0.01) but left the majority of the variability in response unexplained. CONCLUSIONS: The first-dose blood pressure response to ACE inhibition cannot be accurately predicted from baseline pathophysiological variables in patients with mild to moderate CHF. The choice of ACE inhibitor accounts for a small proportion of the variability in response but wide inter-individual variability exists in the response to each treatment.
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Murray et al. (1998) conducted an observational in mild to moderate congestive heart failure (n=132). ACE inhibitor vs. placebo was evaluated on Blood pressure response. The first-dose blood pressure response to ACE inhibitors in CHF was poorly predicted by baseline variables, with baseline mean arterial pressure being the strongest single predictor (r2=5.8%, P=0.02).
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