Evidence map›Paper›PMID 31004326›Full record

ArticleAdvances in therapy2019

The Association of Tacrolimus Formulation Switching with Trough Concentration Variability: A Retrospective Cohort Study of Tacrolimus Use Post-Kidney Transplantation Based on National Drug Code (NDC) Numbers.

Jason J Schwartz, Edward Lee, Ashley P Butler, David P Facklam, Billy Franks, James R Spalding, Maria E Vassilakis, Gary D Thal, William D Irish

Abstract read
In one paragraph

Article in Advances in therapy, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

What it found

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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

9 authors.

Jason J SchwartzMedical Affairs, Astellas Pharma Global Development, Inc., Northbrook, IL, USA. jason.schwartz@astellas.com.
Edward LeeFormerly Medical Affairs, Astellas Pharma Global Development, Inc., Northbrook, IL, USA.
Ashley P ButlerRegulatory and Scientific Affairs, CTI Clinical Trial and Consulting Services, Covington, KY, USA.
David P FacklamRegulatory and Scientific Affairs, CTI Clinical Trial and Consulting Services, Covington, KY, USA.
Billy FranksMedical Affairs, Astellas Pharma Global Development Inc., Leiden, The Netherlands.
James R SpaldingMedical Affairs, Astellas Pharma Global Development, Inc., Northbrook, IL, USA.
Maria E VassilakisMedical Affairs, Astellas Pharma Global Development, Inc., Northbrook, IL, USA.
Gary D ThalMedical Affairs, Astellas Pharma Global Development, Inc., Northbrook, IL, USA.
William D IrishFormerly Real World Evidence, CTI Clinical Trial and Consulting Services, Raleigh, NC, USA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionIt was hypothesized that patients experiencing at least one tacrolimus formulation switch may require more frequent therapeutic drug monitoring, subsequent dose adjustments, and a potential for untoward clinical outcomes than patients who remain on a single formulation.

methodsEligible patients were adult kidney transplant recipients with stable renal function at month 3 post-transplant and no evidence of acute rejection, receiving an oral, tacrolimus-based regimen. Patients were categorized into two groups (fixed or variable formulation) using the US National Drug Code (NDC) on the basis of tacrolimus formulation usage over the 12-month period.

resultsA total of 305 patients were enrolled from four US transplant centers; 44 (14.4%) received multiple formulations and 261 (85.6%) received a single formulation. Mean number of tacrolimus dose adjustments and mean cumulative milligram dose change were not statistically different between the two groups. Mean trough-to-dose ratio, frequency of trough level measurements, and mean number of excursions above 120% or below 80% of the patient's mean trough concentration were significantly higher in the variable compared to the fixed formulation group.

conclusionA variable tacrolimus formulation regimen was associated with a higher frequency of trough level measurements and a greater number of excursions in trough levels compared with continuing on a fixed formulation regimen of tacrolimus in this retrospective chart review study.

fundingAstellas Pharma Global Development, Inc. Plain language summary available for this article.

Indexed as

AdultAgedCohort StudiesDose-Response Relationship, DrugDrug CompoundingDrug MonitoringFemaleGraft RejectionHumansImmunosuppressive AgentsKidney TransplantationMaleMiddle AgedRetrospective StudiesTacrolimusUnited StatesImmunosuppressive AgentsTacrolimusAssessmentBioequivalenceElectronic medical recordKidney transplantationNephrologyPatient outcomesRetrospective studyTacrolimusTherapeutic drug monitoring

Identifiers

PMID31004326
PMCPMC6824386

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.