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Published on: November 8, 2015
Diltiazem use in tacrolimus-treated renal transplant recipients
J Kothari1, M Nash, J Zaltzman
1St Michael's Hospital, University of Toronto, Ontario, Canada.
Insights
Diltiazem is safe and effective for managing post-kidney transplant hypertension in patients on tacrolimus. This calcium channel blocker can be a first-line treatment option without impacting tacrolimus levels or costs.
Area of Science:
- Nephrology
- Pharmacology
- Transplant Medicine
Background:
- Calcium channel blockers are used for post-transplant hypertension but may interact with calcineurin inhibitors.
- Limited data exist on diltiazem use with tacrolimus (immunosuppressant) in renal transplant recipients.
Purpose of the Study:
- To evaluate the safety and efficacy of diltiazem in renal transplant patients receiving tacrolimus-based immunosuppression.
- To assess the impact of diltiazem on renal function, blood pressure control, and tacrolimus exposure.
Main Methods:
- Retrospective analysis of renal transplant recipients from March 1997 to March 2002.
- Patients received tacrolimus, mycophenolate mofetil, and prednisone.
- Comparison of outcomes between patients who received diltiazem in the first postoperative week and a control group.
Main Results:
- No significant differences in renal function, graft survival, or patient survival at 2 years between groups.
- Similar blood pressure control, though the diltiazem group required more antihypertensive medications.
- No increased tacrolimus-related side effects or altered tacrolimus exposure/monitoring costs.
Conclusions:
- Diltiazem is safe and effective as a first-line antihypertensive in renal transplant recipients on tacrolimus.
- Diltiazem use is cost-neutral concerning tacrolimus monitoring and overall costs.
Background:
Calcium channel blockers are widely used in the treatment of post-transplant hypertension but have the potential for drug interaction with calcineurin inhibitors. Renal allograft outcomes when diltiazem is used with cyclosporine have been reported, but similar data with tacrolimus are not available.
Methods:
We performed a retrospective analysis of all our renal transplant recipients from March 1997 to March 2002 who were given tacrolimus, mycophenolate mofetil and prednisone. Patients were divided into two groups based on whether diltiazem was started in the first postoperative week. Outcome measures included renal function up to 2 years post-transplant, blood pressure (BP) control, tacrolimus exposure, and costs related to tacrolimus monitoring.
Results:
Sixty-four patients constituted the diltiazem group and 32 the control group. Their baseline characteristics were similar. The mean average daily dose of diltiazem used was 213.95 mg/day. There was no difference in renal function, graft survival, or patient survival over 2 years. BP control was similar although the diltiazem group required more medication. Diltiazem was discontinued in four patients due to side-effects. There was no difference in tacrolimus-related side-effects between the two groups. There was also no difference in tacrolimus exposure, cost related to tacrolimus monitoring, or combined costs when the expense of diltiazem was added.
Conclusion:
Diltiazem use is acceptably safe and efficacious in renal transplant recipients treated with tacrolimus-based immunosuppressive therapy. It can be considered as a first-line antihypertensive in these patients and is cost neutral for tacrolimus use.
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