Evidence map›Paper›PMID 31001828›Full record

ArticleArtificial organs2019

Process of selecting and educating HCV-uninfected kidney waiting-list candidates for HCV-infected kidney transplantation.

Meghan E Sise, David Wojciechowski, Donald F Chute, Jenna Gustafson, Raymond T Chung, Winfred W Williams, Nahel Elias

Open access · greenAbstract read
In one paragraph

Article in Artificial organs, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.6field-weighted citation impact, top 34% 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

3 citing papers in PubMed, 5 citations in OpenAlex.

  1. Trial
  2. Article
  3. Article
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

7 authors at 1 institution in 1 country.

Meghan E SiseDepartment of Medicine, Division of Nephrology, Massachusetts General Hospital, Boston, Massachusetts.ORCID https://orcid.org/0000-0002-4327-9713
David WojciechowskiDepartment of Medicine, Division of Nephrology, Massachusetts General Hospital, Boston, Massachusetts.
Donald F ChuteDepartment of Medicine, Gastrointestinal Unit, Massachusetts General Hospital, Boston, Massachusetts.
Jenna GustafsonDepartment of Medicine, Gastrointestinal Unit, Massachusetts General Hospital, Boston, Massachusetts.
Raymond T ChungDepartment of Medicine, Gastrointestinal Unit, Massachusetts General Hospital, Boston, Massachusetts.
Winfred W WilliamsDepartment of Medicine, Division of Nephrology, Massachusetts General Hospital, Boston, Massachusetts.
Nahel EliasDepartment of Surgery, Division of Transplant Surgery, Massachusetts General Hospital, Boston, Massachusetts.
Massachusetts General Hospital · US

Funding

Patient-Oriented Research on Hepatitis in Special PopulationsK24DK078772 · NIDDK · MASSACHUSETTS GENERAL HOSPITAL · PI CHUNG, RAYMOND T · 2007 to 2016
$1.6M
Effect of Hepatitis C Virus Eradication on Chronic Kidney Disease ProgressionK23DK117014 · NIDDK · MASSACHUSETTS GENERAL HOSPITAL · PI SISE, MEGHAN E. · 2018 to 2022
$865k
NIDDK NIH HHS K23 DK117014NIDDK NIH HHS K24 DK078772NIDDK NIH HHS MES - NIH K23 DK117014. RTC - NIH K24DK078772NIDDK NIH HHS NIH K23 DK117014NIDDK NIH HHS NIH K24DK078772
6 · The paper itself

Abstract

Long waiting times for kidney transplant (KT) and the high risk of mortality on dialysis have prompted investigation into strategies to utilize hepatitis C virus (HCV)-infected organs to decrease discard rates of potentially viable kidneys. Due the opioid epidemic, the number of HCV-infected donors has increased significantly. With the development of direct-acting antiviral therapies for HCV infection, now more than 95% of patients who received treatment are cured. Experimental trials have used direct-acting antiviral therapy to treat HCV infection in HCV-uninfected transplant recipients of kidneys from HCV-viremic donors. To date, HCV has been eradicated in all cases. Though these strategies will potentially increase the donor pool of available kidneys, shorten waitlist times, and ultimately decrease mortality in patients waiting for KT, identifying the ideal candidates and educating them about a protocol to utilize direct-acting antiviral therapy to cure HCV after it is transmitted is essential. We present our approach to patient selection and education for a clinical trial in transplantation of HCV viremic kidneys into uninfected recipients.

Indexed as

Kidney TransplantationPatient Education as TopicAdultAgedAntiviral AgentsDonor SelectionHepacivirusHepatitis CHumansInformed ConsentKidney DiseasesMiddle AgedTissue DonorsYoung AdultAntiviral Agentsallocationhepatitis C viruskidney transplantpatient education

Identifiers

PMID31001828
PMCPMC6733639
OpenAlexW2937952672

What OpenQuestion 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 OpenQuestion graph.