The use of once‐daily LCP‐Tacrolimus with adolescent and young adult solid organ transplant recipients

Author:

Householder Sarah12ORCID,Ramakrishnan Adarsh3,Chen Justin K.45ORCID,Gorsch Lindsey1ORCID,Tsapepas Demetra4,Lobritto Steven6,Rundle Anna6,Vittorio Jennifer M.67ORCID

Affiliation:

1. Vagelos College of Physicians and Surgeons New York New York USA

2. Department of Pediatrics, Department of Internal Medicine Yale‐New Haven Hospital New Haven Connecticut USA

3. New York‐Presbyterian Hospital New York New York USA

4. Department of Pharmacy New York‐Presbyterian Hospital New York New York USA

5. Department of Pharmacy Children's Healthcare of Atlanta Atlanta Georgia USA

6. Division of Pediatric Gastroenterology and Hepatology, Department of Pediatrics Columbia University Irving Medical Center New York New York USA

7. Division of Pediatric Gastroenterology and Hepatology, Department of Pediatrics Hassenfeld Children's Hospital at NYU Langone New York New York USA

Abstract

AbstractBackgroundAdolescent and young adult (AYA) solid organ transplant (SOT) recipients experience increased rates of rejection and graft loss surrounding the time of health care transition, in part due to poor medication adherence. This study aims to examine the impact of a once‐daily formulation of tacrolimus, LCP‐tacrolimus (LCPT), on medication adherence for AYA SOT patients.MethodsA retrospective descriptive analysis was performed for all patients who underwent SOT and were prescribed LCPT after the age of 12 at our single‐center pediatric hospital. Medication adherence was assessed via provider documentation and the medication level variability index (MLVI).ResultsTwenty‐nine patients were prescribed LCPT as part of their immunosuppression regimen. Twenty patients were converted to LCPT from immediate‐acting (IR) tacrolimus; six patients were initiated immediately following transplant, and three patients were unable to receive LCPT due to insurance denial. There was a numeric improvement in medication adherence for converted patients when measured by provider assessment (45.0% vs. 68.4%, p = .140) and MLVI (40.0% vs. 71.4%, p = .276), though these did not reach statistical significance. There were no differences in episodes of rejection or adverse effects. LCPT prescription was not associated with decreased medication burden, and two patients transitioned back to IR tacrolimus due to increased cost.ConclusionsLCPT use did not significantly improve patient adherence; however, it resulted in numerically higher perceived and measured adherence rates. LCPT appears to be safe and effective in the management of SOT recipients; however, it may not affect pill burden and may result in a higher financial burden. Use may be considered for a select group of AYA SOT recipients.

Publisher

Wiley

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