Evidence map›Paper›PMID 32289544›Full record

ArticleClinical gastroenterology and hepatology : the official clinical practice journal of the American Gastroenterological Association2021

Physical and Mental Quality of Life in Patients With End-Stage Liver Disease and Their Informal Caregivers.

Lissi Hansen, Michael F Chang, Christopher S Lee, Shirin Hiatt, Evan J Firsick, Nathan F Dieckmann, Karen S Lyons

Open access · greenAbstract read
In one paragraph

Article in Clinical gastroenterology and hepatology : the official clinical practice journal of the American Gastroenterological Association, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers, 5 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed, 5 pooled it
2.9field-weighted citation impact, top 8% 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

19 citing papers in PubMed, 5 syntheses or guidelines pooled it, 43 citations in OpenAlex.

  1. Pooled it
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  9. Longitudinal changes in physical and psychological outcomes in spousal vs. non-spousal caregivers for patients with end-stage liver disease.Quality of life research : an international journal of quality of life aspects of treatment, care and rehabilitation · 2025
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  17. Hospice care for end stage liver disease in the United States.Expert review of gastroenterology & hepatology · 2021
    Review
  18. Opioids in Hemodialysis Patients.Seminars in nephrology · 2021
    Review
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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 3 institutions in 1 country.

Lissi HansenSchool of Nursing, Oregon Health & Science University, Portland, Oregon. Electronic address: hansenli@ohsu.edu.
Michael F ChangGastroenterology and Hepatology, VA Portland Health Care System, Portland, Oregon.
Christopher S LeeWilliam F. Connell School of Nursing, Boston College, Boston, Massachusetts.
Shirin HiattSchool of Nursing, Oregon Health & Science University, Portland, Oregon.
Evan J FirsickSchool of Nursing, Oregon Health & Science University, Portland, Oregon.
Nathan F DieckmannSchool of Nursing, Oregon Health & Science University, Portland, Oregon.
Karen S LyonsWilliam F. Connell School of Nursing, Boston College, Boston, Massachusetts.
Oregon Health & Science University · USBoston College · USVA Portland Health Care System · US

Funding

Symptom burden in End-Stage Liver Disease patient-caregiver dyadsR01NR016017 · NINR · OREGON HEALTH & SCIENCE UNIVERSITY · PI HANSEN, LISSI · 2016 to 2020
$1.9M
NINR NIH HHS R01 NR016017
6 · The paper itself

Abstract

BACKGROUND &

aimsManagement of end-stage liver disease (ESLD) has implications for not only patients' quality of life (QOL), but also their caregivers'. We aimed to identify characteristics of patients with ESLD and their caregivers that are associated with QOL.

methodsWe obtained cross-sectional baseline data from patients and their caregivers (132 dyads; 62% were married or partners), recruited from outpatient hepatology clinics within 2 healthcare centers. Patients were included if their model for end-stage liver disease score was 15 or more; caregivers were identified by the patient as the primary informal caregiver. QOL was measured by the SF-36 and relationship quality using the mutuality scale. We measured uncertainty using the uncertainty in illness scales for patients and caregivers. Multilevel modeling was used to analyze the data.

resultsRefractory ascites was associated with worse physical QOL for patients (unstandardized beta [B], -9.19; standard error [SE], 2.28) and caregivers (B, -5.41; SE, 2.33); history of hepatic encephalopathy was associated with worse patient physical QOL (B, -3.86; SE, 1.65). High levels of uncertainty were associated with worse physical and mental QOL for both members of the dyads; relationship quality was significantly associated with patient mental QOL (B, 2.73; SE, 1.19).

conclusionsClinicians and researchers should consider the effects of ESLD on caregivers as well as their patients to optimize the QOL for both.

Indexed as

End Stage Liver DiseaseQuality of LifeCaregiversCross-Sectional StudiesHumansSeverity of Illness IndexSurveys and QuestionnairesChildrenCirrhosisFamily MembersPsychologic Factor

Identifiers

PMID32289544
PMCPMC7554075
OpenAlexW3015513239

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.