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A clinically utilized intravenous continuous rate infusion of diltiazem does not significantly decrease systolic function in healthy dogs

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Abstract OBJECTIVE To determine if left ventricular systolic function on echocardiography, systemic blood pressure, and electrocardiography change with a clinically accepted intravenous (IV) diltiazem constant rate infusion (CRI) compared to a control. ANIMALS 10 healthy client-owned adult dogs. PROCEDURES Prospective, masked, crossover study from May 27, 2021, to August 22, 2021. Dogs were randomized to receive diltiazem (loading dose of 240 μg/kg, IV followed by a CRI of 6 μg/kg/min for 300 minutes) or the same volume of 5% dextrose in water (D5W) administered IV followed by the opposite intervention after a 7-day washout. Blood pressure was monitored during each CRI, and echocardiographic and electrocardiographic studies were performed immediately before the CRI and during the last hour of the CRI. RESULTS Postdiltiazem systolic time interval (STI) (median, 0.30; range, 0.16 to 0.34) was significantly lower than post-D5W STI (median, 0.32; range, 0.22 to 0.40; P = .046). All other echocardiographic parameters did not differ significantly between each of the groups after receiving diltiazem or D5W. Systemic blood pressure did not change significantly with either diltiazem (P = .450) or D5W (P = .940), and none of the dogs became hypotensive at any point in the study. Expectedly, negative dromotropy was observed with diltiazem. CLINICAL RELEVANCE A significant decrease in left ventricular systolic function was not appreciated in healthy dogs receiving diltiazem at a clinically accepted intravenous infusion rate at this dosing regimen. Further studies are needed in dogs with cardiac disease.
Title: A clinically utilized intravenous continuous rate infusion of diltiazem does not significantly decrease systolic function in healthy dogs
Description:
Abstract OBJECTIVE To determine if left ventricular systolic function on echocardiography, systemic blood pressure, and electrocardiography change with a clinically accepted intravenous (IV) diltiazem constant rate infusion (CRI) compared to a control.
ANIMALS 10 healthy client-owned adult dogs.
PROCEDURES Prospective, masked, crossover study from May 27, 2021, to August 22, 2021.
Dogs were randomized to receive diltiazem (loading dose of 240 μg/kg, IV followed by a CRI of 6 μg/kg/min for 300 minutes) or the same volume of 5% dextrose in water (D5W) administered IV followed by the opposite intervention after a 7-day washout.
Blood pressure was monitored during each CRI, and echocardiographic and electrocardiographic studies were performed immediately before the CRI and during the last hour of the CRI.
RESULTS Postdiltiazem systolic time interval (STI) (median, 0.
30; range, 0.
16 to 0.
34) was significantly lower than post-D5W STI (median, 0.
32; range, 0.
22 to 0.
40; P = .
046).
All other echocardiographic parameters did not differ significantly between each of the groups after receiving diltiazem or D5W.
Systemic blood pressure did not change significantly with either diltiazem (P = .
450) or D5W (P = .
940), and none of the dogs became hypotensive at any point in the study.
Expectedly, negative dromotropy was observed with diltiazem.
CLINICAL RELEVANCE A significant decrease in left ventricular systolic function was not appreciated in healthy dogs receiving diltiazem at a clinically accepted intravenous infusion rate at this dosing regimen.
Further studies are needed in dogs with cardiac disease.

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