Evidence map›Paper›PMID 25923243›Full record

ArticlePloS one2015

Short and long-term effects of telaprevir on kidney function in patients with hepatitis C virus infection: a retrospective cohort study.

Meghan E Sise, Elke S Backman, Julia B Wenger, Brian R Wood, Paul E Sax, Raymond T Chung, Ravi Thadhani, Arthur Y Kim

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.6field-weighted citation impact, top 31% 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

2 citing papers in PubMed, 7 citations in OpenAlex.

  1. Review
  2. Treatment of chronic hepatitis C in patients with chronic kidney disease with Sofosbuvir-basead regimes.The Brazilian journal of infectious diseases : an official publication of the Brazilian Society of Infectious Diseases
    Observational
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

8 authors at 4 institutions in 1 country.

Meghan E SiseDivision of Nephrology, Department of Medicine, Massachusetts General Hospital, Harvard University, Boston, MA, United States of America.
Elke S BackmanDepartment of Pharmacy, Massachusetts General Hospital, Harvard University, Boston, MA, United States of America.
Julia B WengerDivision of Nephrology, Department of Medicine, Massachusetts General Hospital, Harvard University, Boston, MA, United States of America.
Brian R WoodDivision of Allergy and Infectious Diseases, University of Washington, Seattle, WA, United States of America.
Paul E SaxDivision of Infectious Diseases, Brigham and Women's Hospital, and Harvard Medical School, Boston, MA, United States of America.
Raymond T ChungGastrointestinal Unit, Department of Medicine, Massachusetts General Hospital, Harvard University, Boston, MA, United States of America.
Ravi ThadhaniDivision of Nephrology, Department of Medicine, Massachusetts General Hospital, Harvard University, Boston, MA, United States of America.
Arthur Y KimDivision of Infectious Diseases, Department of Medicine, Massachusetts General Hospital, Harvard University, Boston, MA, United States of America.
Massachusetts General Hospital · USHarvard University · USBrigham and Women's Hospital · USUniversity of Washington · US

Funding

Patient-Oriented Research on Hepatitis in Special PopulationsK24DK078772 · NIDDK · MASSACHUSETTS GENERAL HOSPITAL · PI CHUNG, RAYMOND T · 2007 to 2016
$1.6M
Patient Oriented Studies of Vitamin D in Chronic Kidney DiseaseK24DK094872 · NIDDK · MASSACHUSETTS GENERAL HOSPITAL · PI THADHANI, RAVI · 2012 to 2016
$546k
NIDDK NIH HHS K24 DK078772NIDDK NIH HHS K24 DK094872
6 · The paper itself

Abstract

backgroundRecent reports suggest that telaprevir, a protease inhibitor used to treat hepatitis C infection, is associated with decline in kidney function during therapy, particularly in patients with baseline renal impairment.

methodsPatients treated with telaprevir in a single healthcare network were retrospectively reviewed. Kidney function was determined at baseline, during therapy, and twelve weeks and twelve months after telaprevir discontinuation. Significant creatinine rise during therapy was defined as an increase in serum creatinine ≥ 0.3mg/dL from baseline during treatment with telaprevir.

resultsBetween July 2011 to January 2013,seventy-eight patients began treatment. The majority completed the prescribed twelve weeks of telaprevir therapy; 32% discontinued due to side effects. The average rise in serum creatinine during therapy was 0.22mg/dL (standard deviation 0.22mg/dL). Thirty-one percent experienced a significant creatinine rise during therapy. Decline in estimated glomerular filtration rate (eGFR) was lower in those with baseline eGFR < 90 mL/min/1.73m2 compared to the group with baseline eGFR ≥ 90 mL/min/1.73m2 (12 vs. 18 mL/min/1.73m2, P = 0.047). Serum creatinine fully normalized by twelve weeks after cessation of telaprevir in 83% of patients, however experiencing a significant creatinine rise during telaprevir use was associated with a 6.6mL/min/1.73m2 decrease in estimated glomerular filtration rate at twelve months in an adjusted model.

conclusionsDecline in kidney function during therapy with telaprevir is common and is not associated with baseline eGFR < 90mL/min/1.73m2 as previously reported.

Indexed as

AdultCohort StudiesCreatinineFemaleFollow-Up StudiesGlomerular Filtration RateHepatitis CHumansKidney DiseasesLogistic ModelsMaleMiddle AgedOdds RatioOligopeptidesProtease InhibitorsRetrospective StudiesCreatinineOligopeptidesProtease Inhibitorstelaprevir

Identifiers

PMID25923243
PMCPMC4414554
OpenAlexW2023978112

What OpenQuestion holds

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LicenceCC BY
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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 OpenQuestion graph.