Evidence map›Paper›PMID 35744084›Full record

ArticleMedicina (Kaunas, Lithuania)2022

Decreasing Significance of Early Allograft Dysfunction with Rising Use of Nonconventional Donors.

Stephanie Ohara, Elizabeth Macdonough, Lena Egbert, Abigail Brooks, Blanca Lizaola-Mayo, Amit K Mathur, Bashar Aqel, Kunam S Reddy, Caroline C Jadlowiec

Open access · goldAbstract read
In one paragraph

Article in Medicina (Kaunas, Lithuania), 2022. 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
1.5field-weighted citation impact, top 18% 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. Article
  2. 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

9 authors at 4 institutions in 2 countries.

Stephanie OharaDivision of Surgery, Valleywise Health Medical Center, Creighton University, Phoenix, AZ 85008, USA.
Elizabeth MacdonoughDivision of Gastroenterology and Hepatology, Mayo Clinic, Phoenix, AZ 85054, USA.
Lena EgbertMayo Clinic Alix School of Medicine, Scottsdale, AZ 85259, USA.
Abigail BrooksSchool of Medicine, Tel Aviv University, Tel Aviv-Yafo 6997801, Israel.
Blanca Lizaola-MayoDivision of Gastroenterology and Hepatology, Mayo Clinic, Phoenix, AZ 85054, USA.
Amit K MathurDivision of Transplant Surgery, Department of Surgery, Mayo Clinic, Phoenix, AZ 85054, USA.ORCID 0000-0002-9215-2014
Bashar AqelDivision of Gastroenterology and Hepatology, Mayo Clinic, Phoenix, AZ 85054, USA.
Kunam S ReddyDivision of Transplant Surgery, Department of Surgery, Mayo Clinic, Phoenix, AZ 85054, USA.
Caroline C JadlowiecDivision of Transplant Surgery, Department of Surgery, Mayo Clinic, Phoenix, AZ 85054, USA.ORCID 0000-0001-7860-9519
WinnMed · USCHI Health Creighton University Medical Center - Bergan Mercy · USMayo Clinic in Arizona · USTel Aviv University · IL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background and Objectives: Early allograft dysfunction (EAD) is considered a surrogate marker for adverse post-liver transplant (LT) outcomes. With the increasing use of nonconventional donors, EAD has become a more frequent occurrence. Given this background, we aimed to assess the prevalence and impact of EAD in an updated cohort inclusive of both conventional and nonconventional liver allografts. Materials and Methods: Perioperative and one-year outcomes were assessed for a total of 611 LT recipients with and without EAD from Mayo Clinic Arizona. EAD was defined as the presence of one or more of the following: bilirubin > 10 mg/dL on day 7, INR > 1.6 on day 7, or ALT and/or AST > 2000 IU/L within the first 7 days of LT. Results: Within this cohort, 31.8% of grafts (n = 194) came from donation after circulatory death (DCD) donors, 17.7% (n = 108) were nationally shared, 16.4% (n = 100) were allocated as post-cross clamp, and 8.7% contained moderate steatosis. EAD was observed in 52.2% (n = 321) of grafts in the study cohort (79% in DCD grafts and 40% in DBD grafts). EAD grafts had higher donor risk index (DRI) scores (1.9 vs. 1.6, p < 0.0001), were more likely to come from DCD donors (48% vs. 13.8%, p < 0.0001), were regionally allocated (p = 0.003), and had higher cold ischemia times (median 6.0 vs. 5.5 h, p = 0.001). Primary nonfunction events were rare in both groups (1.3% vs. 0.3%, p = 0.22). Post-LT acute kidney injury occurred at a similar frequency in recipients with and without EAD (43.6% vs. 30.3%, p = 0.41), and there were no differences in ICU (median 2 vs. 1 day, p = 0.60) or hospital (6 vs. 5 days, p = 0.24) length of stay. For DCD grafts, the rate of ischemic cholangiopathy was similar in the two groups (14.9% EAD vs. 17.5% no EAD, p = 0.69). One-year patient survival for grafts with and without EAD was 96.0% and 94.1% (HR 1.2, 95% CI 0.7−1.8; p = 0.54); one-year graft survival was 92.5% and 92.1% (HR 1.0, 95% CI 0.7−1.5; p = 0.88). Conclusions: In this cohort, EAD occurred in 52% of grafts. The occurrence of EAD, however, did not portend inferior outcomes. Compared to those without EAD, recipients with EAD had similar post-operative outcomes, as well as one-year patient and graft survival. EAD should be managed supportively and should not be viewed as a deterrent to utilization of non-ideal grafts.

Indexed as

End Stage Liver DiseaseLiver TransplantationAllograftsGraft SurvivalHumansRetrospective StudiesTissue Donorsdeceased donordonation after circulatory deathdonor poolgraft typemarginal donororgan shortage

Identifiers

PMID35744084
PMCPMC9227373
OpenAlexW4283031676

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.