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Tirofiban in Suspected Left Ventricular Assist Device Pump Thrombosis
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Antithrombotic optimization with a glycoprotein IIb/IIIa inhibitor has been used for the treatment of suspected pump thrombosis, but available literature with tirofiban is lacking. This study aims to describe the use of tirofiban for suspected pump thrombosis. This was a single-center cohort study of left ventricular assist device patients who received tirofiban for the treatment of suspected pump thrombosis from January 1, 2016 to July 31, 2017. Tirofiban was initiated at 0.1 μg/kg/min in patients with normal renal function and subsequent dose adjustments for altered renal function or history of bleeding were employed. Success was defined as resolution of lactate dehydrogenase back to patients’ known baseline. Fourteen patients were included for 16 total instances of tirofiban use during the time period. Tirofiban was continued for a median of 5 days (range: 0.3–35 days). Successful treatment was achieved in 12 of the 16 tirofiban uses (75%). Seven bleeding events occurred while on therapy, two major and five minor. This study showed a majority of patients achieved success with tirofiban for suspected pump thrombosis. For patients who are not current candidates for pump exchange or transplant, tirofiban may be considered a therapeutic medical management option.
Ovid Technologies (Wolters Kluwer Health)
Title: Tirofiban in Suspected Left Ventricular Assist Device Pump Thrombosis
Description:
Antithrombotic optimization with a glycoprotein IIb/IIIa inhibitor has been used for the treatment of suspected pump thrombosis, but available literature with tirofiban is lacking.
This study aims to describe the use of tirofiban for suspected pump thrombosis.
This was a single-center cohort study of left ventricular assist device patients who received tirofiban for the treatment of suspected pump thrombosis from January 1, 2016 to July 31, 2017.
Tirofiban was initiated at 0.
1 μg/kg/min in patients with normal renal function and subsequent dose adjustments for altered renal function or history of bleeding were employed.
Success was defined as resolution of lactate dehydrogenase back to patients’ known baseline.
Fourteen patients were included for 16 total instances of tirofiban use during the time period.
Tirofiban was continued for a median of 5 days (range: 0.
3–35 days).
Successful treatment was achieved in 12 of the 16 tirofiban uses (75%).
Seven bleeding events occurred while on therapy, two major and five minor.
This study showed a majority of patients achieved success with tirofiban for suspected pump thrombosis.
For patients who are not current candidates for pump exchange or transplant, tirofiban may be considered a therapeutic medical management option.
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