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James Mason a Medicines Evaluation Group, Centre for Health Economics
University of York, York YO10 5DD, b Division of Primary Care, Public and
Occupational Health, School of Medicine, University of Birmingham,
Birmingham B15 2TT
Correspondence to: J Mason jmm7{at}york.ac.uk
Objective:
To estimate the costs and consequences of diagnosing symptomatic heart failure with left ventricular systolic dysfunction and initiating angiotensin converting enzyme inhibitors in
primary care.
Design:
Analysis of individual patient data from
studies of left ventricular dysfunction (SOLVD) to identify
complications during test dose and titration phases.
Setting:
Two randomised controlled trials in secondary care.
Participants:
7487 patients taking a test dose of
enalapril at enrolment to the treatment and prevention trials; 2569 patients with clinical signs of heart failure and established left
ventricular dysfunction entered the treatment trial.
Main outcome measures:
Discontinuation during the test
dose period. Discontinuation or reduction of dose during the first year
of treatment for heart failure. Costs of diagnosis and titration of treatment.
Results:
During the test dose phase, 585 patients
(7.8%) reported side effects; 136 (1.8%) of these discontinued
because of severe side effects. During the titration phase, compared
with placebo, enalapril was associated with an increased risk of dose reduction due to hypotension (odds ratio 2.09, 95% confidence interval
1.15 to 3.82). However, overall, there was no difference in the rates
of side effects leading to dose reduction or withdrawal between the
enalapril and placebo groups. The costs of diagnosing heart failure
with left ventricular systolic dysfunction and initiating and titrating
an angiotensin converting enzyme inhibitor in primary care are £300 to
£400.
Conclusions:
Treatment with angiotensin converting
enzyme inhibitors can be safely started for patients with heart failure and left ventricular systolic dysfunction in primary care.
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