Journal
JOURNAL OF PEDIATRIC SURGERY
Volume 58, Issue 10, Pages 2054-2058Publisher
W B SAUNDERS CO-ELSEVIER INC
DOI: 10.1016/j.jpedsurg.2023.05.005
Keywords
Liver transplantation; Pediatric; Tacrolimus; Once-daily; Adherence
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This study examined the effects of conversion from twice-daily tacrolimus to once-daily tacrolimus in 179 pediatric liver transplant recipients. The results showed that most recipients had uneventful follow-up after the conversion, and there was a significant decrease in the variation of tacrolimus trough levels.
Background: Nonadherence to immunosuppression is the most common cause of late acute rejection in pediatric liver transplant (LT) recipients. A prolonged-release once-daily tacrolimus formulation was developed to improve adherence and long-term allograft survival. Methods: We screened 179 pediatric LT recipients who converted from twice-daily tacrolimus (TD-TAC) to once-daily tacrolimus (OD-TAC) between February 2011 and September 2019. Results: One hundred seventy-nine recipients converted to OD-TAC and were followed for 18 months. 152 OD-TAC-converted recipients (84.9%) experienced uneventful follow-up, while 21 recipients showed LFT elevation. Four recipients had biopsy-proven acute rejection within six months of conversion, all of which were successfully treated with steroid pulse. 166 recipients (92.7%) remain on OD-TAC and 13 (7.3%) were switched back to TD-TAC. The mean tacrolimus trough level significantly decreased three months following conversion (3.14 +/- 1.9 ng/mL) compared with pre-conversion levels (3.69 +/- 1.98 ng/ mL). Mean tacrolimus trough levels remained unchanged from 3 months to 12 months following conversion. Percent coefficient of variation of tacrolimus trough levels decreased significantly from 32.5 +/- 16.4 ng/mL to 27.5 +/- 15.6 ng/mL after conversion to OD-TAC, reflecting a decrease in variation of tacrolimus trough levels following conversion. Conclusions: Conversion to OD-TAC in pediatric LT recipients with stable graft function is safe and effective. Level of evidence: Level IV.
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