This study examined the hypothesis that patients who develop angiotensin-converting
enzyme inhibitor intolerance attributable to circulatory-renal limitations (CRLimit)
have more severe underlying disease and worse outcome.
Although the renin-angiotensin system contributes to the progression of heart failure
(HF), it also supports the failing circulation. Patients with the most severe disease
may not tolerate inhibition of this system.
Consecutive inpatient admissions to the cardiomyopathy service of the Brigham and
Women's Hospital between 2000 and 2002 were reviewed retrospectively for initial profiles,
discharge medications, and documented reasons for discontinuation of angiotensin-converting
enzyme inhibitors. Outcomes of death and transplantation were determined.
Of the 259 patients, 86 were not on an angiotensin-converting enzyme inhibitor at
discharge. Circulatory-renal limitations of symptomatic hypotension, progressive renal
dysfunction, or hyperkalemia were documented in 60 patients (23%); other adverse effects,
including cough, in 24 patients; and absent reasons in 2 patients. Compared with patients
on angiotensin-converting enzyme inhibitors, patients with CRLimit were older (60
vs. 55 years; p = 0.006), with longer history of HF (5 vs. 2 years; p = 0.009), lower
systolic blood pressure (104 vs. 110 mm Hg; p = 0.05), lower sodium (135 vs. 138 mEql/l;
p = 0.002), and higher initial creatinine (2.5 vs. 1.2 mg/dl; p = 0.0001). Mortality
was 57% in patients with CRLimit and 22% in the patients on angiotensin-converting
enzyme inhibitors during a median 8.5-month follow-up (p = 0.0001).
Development of CRLimit to angiotensin-converting enzyme inhibitor intolerance identifies
patients with severe disease who are likely to die during the next year. New treatment
strategies should be targeted to this population.