Safety of Benazepril in 400 Azotemic and 110 Non-Azotemic Client-Owned Cats (2001–2012)

Author:

Lavallee Jennifer O.1,Norsworthy Gary D.1,Huston Carla L.1,Chew Dennis J.1

Affiliation:

1. From Cat Specialist, Castle Rock, Colorado (J.O.L.); Alamo Feline Health Center, San Antonio, Texas (G.D.N.); Department of Pathobiology and Population Medicine, Mississippi State College of Veterinary Medicine, Starkville, Mississippi (C.L.H.); and Department of Veterinary Clinical Sciences, The Ohio State University, Columbus, Ohio (D.J.C.).

Abstract

ABSTRACT This retrospective study examined cats after initiation of benazepril therapy to determine the frequency of systemic hypotension or elevations in serum creatinine and/or potassium. Medical records review identified azotemic and non-azotemic cats prescribed benazepril. Blood pressure was recorded at the first available time after initiation of therapy. No cats experienced documented systolic systemic hypotension (<90 mmHg). Serum creatinine, and potassium when available, were recorded at baseline and in time windows after initiation of treatment: 1–30 days and 31–60 days. Blood chemistry results were screened for hyperkalemia (≥6.0 mEq/L). During the first 2 mo after starting benazepril therapy, there was a low incidence (3.7%) and clinically insignificant magnitude of hyperkalemia. Serum creatinine increases of greater than 30% from baseline were noted. This change was found in 11.0% of cats during the first 30 days of therapy and in 13.7% of cats from days 31–60 after initiation of therapy. The long-term survival of the cats that had >30% increases in creatinine from baseline was not statistically different from the survival of those that did not experience these increases, which suggests this finding may not be a reason to discontinue therapy. Benazepril appeared safe in a heterogeneous population of cats.

Publisher

American Animal Hospital Association

Subject

Small Animals

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