Evidence map›Paper›PMID 25807932›Full record

Trial reportClinical pharmacology and therapeutics2015

Pharmacokinetics, Pharmacodynamics, and Safety of Lisinopril in Pediatric Kidney Transplant Patients: Implications for Starting Dose Selection.

H Trachtman, A Frymoyer, A Lewandowski, L A Greenbaum, D I Feig, D S Gipson, B A Warady, J W Goebel, G J Schwartz, K Lewis and 3 more

Open access · bronzeAbstract readClinical Trial
In one paragraph

Trial report in Clinical pharmacology and therapeutics, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
2.6field-weighted citation impact, top 12% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

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

8 citing papers in PubMed, 22 citations in OpenAlex.

  1. Article
  2. Characterization of ACE Inhibitors and ATLife (Basel, Switzerland) · 2021
    Article
  3. Article
  4. Article
  5. Article
  6. Article
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  8. Review
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

13 authors at 10 institutions in 1 country.

H TrachtmanDepartment of Pediatrics, New York University, New York, New York, USA.
A FrymoyerDepartment of Pediatrics, Stanford University, Palo Alto, California, USA.
A LewandowskiEmmes Corp., Rockville, Maryland, USA.
L A GreenbaumDepartment of Pediatric Nephrology, Emory University, Atlanta, Georgia, USA.
D I FeigDivision of Pediatric Nephrology, University of Alabama, Birmingham, Alabama, USA.
D S GipsonDepartment of Pediatrics, University of Michigan, Ann Arbor, Michigan, USA.
B A WaradyDepartment of Pediatrics, Children's Mercy Hospital, Kansas City, Missouri, USA.
J W GoebelDivision of Nephrology and Hypertension, Cincinnati Children's Hospital, Cincinnati, Ohio, USA.
G J SchwartzDivision of Pediatric Nephrology, University of Rochester, Rochester, New York, USA.
K LewisOpAns, LLC, Durham, North Carolina, USA.
R AnandEmmes Corp., Rockville, Maryland, USA.
U D PatelDuke Clinical Research Institute, Duke University Medical Center, Durham, North Carolina, USA.
Best Pharmaceuticals for Children Act-Pediatric Trials Network Administrative Core Committee
Emmes (United States) · USChildren's Mercy Hospital · USCincinnati Children's Hospital Medical Center · USClinical Research Institute · USEmory University · USNew York University · USStanford University · USUniversity of Alabama · USUniversity of Michigan–Ann Arbor · USUniversity of Rochester · US

Funding

Mentorship of early-career pediatricians in quantitiative methods and therapeuticK24HD058735 · NICHD · DUKE UNIVERSITY · PI BENJAMIN, DANIEL K. · 2009 to 2018
$1.5M
Pharmacology of Aminophylline for Acute Kidney Injury in Neonates and ChildrenK23HD079557 · NICHD · STANFORD UNIVERSITY · PI FRYMOYER, ADAM · 2014 to 2018
$732k
NICHD NIH HHS HHSN267200700051CNICHD NIH HHS HHSN275201000001GNICHD NIH HHS HHSN275201000001ZNICHD NIH HHS HHSN275201000003CNICHD NIH HHS HHSN275201000003INICHD NIH HHS K23 HD079557NICHD NIH HHS K24 HD058735NIDDK NIH HHS HHSN267200700051C
6 · The paper itself

Abstract

Hypertension in pediatric kidney transplant recipients contributes to long-term graft loss, yet treatment options--including angiotensin-converting enzyme inhibitors--are poorly characterized in this vulnerable population. We conducted a multicenter, open-label pharmacokinetic (PK) study of daily oral lisinopril in 22 children (ages 7-17 years) with stable kidney transplant function. Standard noncompartmental PK analyses were performed at steady state. Effects on blood pressure were examined in lisinopril-naïve patients (n = 13). Oral clearance declined in proportion to underlying kidney function; however, in patients with low estimated glomerular filtration rate (30-59 ml/min per 1.73m(2)), exposure (standardized to 0.1 mg/kg/day dose) was within the range reported previously in children without a kidney transplant. In lisinopril-naïve patients, 85% and 77% had a ≥ 6 mmHg reduction in systolic and diastolic blood pressure, respectively. Lisinopril was well tolerated. Our study provides initial insight on lisinopril use in children with a kidney transplant, including starting dose considerations.

Indexed as

Kidney TransplantationAdolescentAngiotensin-Converting Enzyme InhibitorsChildFemaleHumansHypertensionLisinoprilMaleAngiotensin-Converting Enzyme InhibitorsLisinopril

Identifiers

PMID25807932
PMCPMC4536255
OpenAlexW2086977817

What Socratic holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

None linked

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 Socratic graph.