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1.
Clin Transplant ; 32(12): e13415, 2018 12.
Article in English | MEDLINE | ID: mdl-30276862

ABSTRACT

BACKGROUND: To investigate the impact of delayed calcineurin inhibitor (CNI) initiation in liver transplant recipients (LTR) with peri-operative renal insufficiency receiving basiliximab induction, we compared renal outcomes of LTR stratified by the degree of achieved post-operative renal recovery (RR) prior to CNI initiation. METHODS: All adult LTR transplanted between 01/2007 and 12/2015 who received basiliximab were included. Patients who received multi-organ transplantations, were repeat transplant recipients, or expired prior to post-operative day (POD) 90 were excluded. The primary outcome of our retrospective analysis was renal function at POD 90. RESULTS: A total of 210 patients were included in our final analysis. Most patients were Caucasian males undergoing liver transplantation for liver disease secondary to hepatitis C virus. Baseline characteristics were similar among the evaluable population. Estimated GFR was significantly higher among patients with the greatest degree of post-operative renal recovery at POD 90; however, this difference did not persist at POD 180. There was no significant difference in incidence or severity of biopsy-proven acute rejection (BPAR) at any measured time point. CONCLUSIONS: Delayed CNI initiation following liver transplantation in patients with post-operative renal insufficiency who receive basiliximab induction does not adversely affect the incidence of BPAR or long-term renal outcomes.


Subject(s)
Basiliximab/therapeutic use , Calcineurin Inhibitors/administration & dosage , Graft Rejection/mortality , Graft Survival/drug effects , Liver Transplantation/mortality , Postoperative Complications/mortality , Renal Insufficiency/mortality , Female , Follow-Up Studies , Graft Rejection/drug therapy , Graft Rejection/etiology , Humans , Immunosuppressive Agents/therapeutic use , Liver Transplantation/adverse effects , Male , Middle Aged , Postoperative Complications/drug therapy , Postoperative Complications/etiology , Prognosis , Renal Insufficiency/drug therapy , Renal Insufficiency/etiology , Risk Factors , Time-to-Treatment
2.
Pharmacotherapy ; 34(11): 1209-19, 2014 Nov.
Article in English | MEDLINE | ID: mdl-25251980

ABSTRACT

Widespread anecdotal use of sublingual tacrolimus administration has arisen, although little literature exists to guide practice. Given the paucity of data, we conducted a survey to evaluate the practice of sublingual tacrolimus administration at transplant centers across the United States and evaluated the literature that is currently available. A 10-question online survey assessing the current state of sublingual tacrolimus use was distributed to pharmacists at transplant centers that each performed more than 100 solid organ transplantations in 2013. In addition, a literature review was performed by searching the PubMed database to identify available evidence for the sublingual administration of tacrolimus. The online survey was completed by 59 (65.6%) of the 90 targeted transplant centers, representing 51.3% of all solid organ transplantations performed in 2013. Sublingual administration of tacrolimus was used in all solid organ transplant populations, with ~67% of lung transplant centers using this route for tacrolimus. The most common dose conversion was 2 mg oral to 1 mg sublingual, with 92% of centers opening oral capsules and administering the contents sublingually. Home use of sublingual administration and use in the pediatric population was uncommon. Seven peer-reviewed reports and one abstract were identified in the literature review. Seven of the eight publications reported favorably on sublingual administration, although no consistent dose conversion or method of administration was elucidated. The majority of the transplant centers surveyed found sublingual tacrolimus a viable alternative when oral administration is unavailable. A large robust prospective evaluation of sublingual administration of tacrolimus is imperative to provide the most effective care to solid organ transplant recipients and to ensure optimal safety for both patients and providers who administer the drug.


Subject(s)
Calcineurin Inhibitors/administration & dosage , Graft Rejection/prevention & control , Immunosuppressive Agents/administration & dosage , Organ Transplantation/adverse effects , Tacrolimus/administration & dosage , Administration, Sublingual , Calcineurin Inhibitors/adverse effects , Calcineurin Inhibitors/pharmacokinetics , Calcineurin Inhibitors/therapeutic use , Graft Rejection/immunology , Graft Rejection/metabolism , Health Care Surveys , Humans , Immunosuppressive Agents/adverse effects , Immunosuppressive Agents/pharmacokinetics , Immunosuppressive Agents/therapeutic use , Internet , Practice Patterns, Physicians' , Tacrolimus/adverse effects , Tacrolimus/pharmacokinetics , Tacrolimus/therapeutic use , United States
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