Background
Heart failure (HF) guidelines recommend routine monitoring of serum potassium and renal function in patients treated with a mineralocorticoid receptor antagonist (MRA). How these recommendations are implemented in high risk patients or according to setting of drug initiation is poorly characterized.
Methods and Results
We conducted a retrospective cohort study of Medicare beneficiaries linked to laboratory data in 10 states with prevalent HF as of July 1, 2011 and incident MRA use between May 1 and September 30, 2011. Outcomes included laboratory testing prior to MRA initiation and in the early (day 1–10) and extended (day 11–90) post-initiation periods, based on setting of drug initiation and presence of renal insufficiency. Additional outcomes included abnormal laboratory results and adverse events proximate to MRA initiation. Of 10,443 Medicare beneficiaries with HF started on an MRA, 19.7% were initiated during a hospitalization. Appropriate follow-up lab testing across all time periods occurred in 25.2% of patients with inpatient initiation compared with 2.8% of patients begun as an outpatient. Patients with chronic kidney disease (CKD) had higher rates of both hyperkalemia and acute kidney failure in the early (1.3% and 2.7%, respectively) and extended (5.6% and 9.8%, respectively) post-initiation periods compared with those without CKD.
Conclusions
Patients initiated on MRA therapy as an outpatient had extremely poor rates of guideline indicated follow-up laboratory monitoring after drug initiation. In particular, patients with CKD are at high risk for adverse events after MRA initiation. Quality improvement initiatives focused on systems to improve appropriate laboratory monitoring are needed.