Evidence map›Paper›PMID 29439674›Full record

ArticleBMC nephrology2018

Establishing a clinical phenotype for cachexia in end stage kidney disease - study protocol.

Joanne Reid, Helen R Noble, Gary Adamson, Andrew Davenport, Ken Farrington, Denis Fouque, Kamyar Kalantar-Zadeh, John Mallett, C McKeaveney, S Porter and 5 more

Open access · goldAbstract read
In one paragraph

Article in BMC nephrology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing 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

7 citing papers in PubMed, 17 citations in OpenAlex.

  1. Review
  2. Article
  3. The lived experience of renal cachexia: An interpretive phenomenological analysis.International journal of nursing studies advances · 2024
    Article
  4. Article
  5. Article
  6. Article
  7. Cardiovascular risk factors in children on dialysis: an update.Pediatric nephrology (Berlin, Germany) · 2020
    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

15 authors at 10 institutions in 3 countries.

Joanne ReidSchool of Nursing and Midwifery, Queen's University Belfast Medical Biology Centre, 97 Lisburn Rd, Belfast, BT9 7BL, UK. j.reid@qub.ac.uk.ORCID 0000-0001-5820-862X
Helen R NobleSchool of Nursing and Midwifery, Queen's University Belfast Medical Biology Centre, 97 Lisburn Rd, Belfast, BT9 7BL, UK.
Gary AdamsonSchool of Psychology, Ulster University Magee Campus, Londonderry, BT48 7JL, UK.
Andrew DavenportUCL Centre for Nephrology, Royal Free Hospital, University College London, Pond Street, London, NW3 2QG, UK.
Ken FarringtonEast and North Hertfordshire University NHS Trust, Lister Hospital, Coreys Mill Lane, Stevenage, SG1 4AB, UK.
Denis FouqueDepartment of Nephrology, Université de Lyon, UCBL, Carmen, Centre Hospitalier Lyon Sud, F-69495, Pierre-Bénite, France.
Kamyar Kalantar-ZadehDivision of Nephrology and Hypertension, Pediatrics and Public Health, University of California, Los Angeles, USA.
John MallettSchool of Psychology, Ulster University Magee Campus, Londonderry, BT48 7JL, UK.
C McKeaveneySchool of Nursing and Midwifery, Queen's University Belfast Medical Biology Centre, 97 Lisburn Rd, Belfast, BT9 7BL, UK.
S PorterDepartment of Social Sciences and Social Work, Bournemouth University, Poole, UK.
David S SeresColumbia University Medical Centre, NY Presbyterian Hospital, New York, USA.
Joanne ShieldsRegional Nephrology Unit, Belfast City Hospital, Belfast HSC Trust, Belfast, UK.
Adrian SleeUCL, Faculty of Medical Sciences, Gower St, Bloomsbury, London, WC1E 6BT, UK.
Miles D WithamSchool of Medicine, Ninewells Hospital, Dundee, DD1 9SY, UK.
Alexander P MaxwellSchool of Medicine, Dentistry and Biomedical Sciences, Queens University Belfast and Regional Nephrology Unit, Belfast City Hospital, Belfast HSC Trust, Belfast, UK.
Queen's University Belfast · GBUniversity of Ulster · GBBournemouth University · GBLister Hospital · GBNinewells Hospital · GBPresbyterian Hospital · USThe Royal Free Hospital · GBUniversité Claude Bernard Lyon 1 · FRUniversity College London · GBUniversity of California, Los Angeles · US

Funding

Medical Research Council MC_PC_15025
6 · The paper itself

Abstract

backgroundSurveys using traditional measures of nutritional status indicate that muscle wasting is common among persons with end-stage kidney disease (ESKD). Up to 75% of adults undergoing maintenance dialysis show some evidence of muscle wasting. ESKD is associated with an increase in inflammatory cytokines and can result in cachexia, with the loss of muscle and fat stores. At present, only limited data are available on the classification of wasting experienced by persons with ESKD. Individuals with ESKD often exhibit symptoms of anorexia, loss of lean muscle mass and altered energy expenditure. These symptoms are consistent with the syndrome of cachexia observed in other chronic diseases, such as cancer, heart failure, and acquired immune deficiency syndrome. While definitions of cachexia have been developed for some diseases, such as cardiac failure and cancer, no specific cachexia definition has been established for chronic kidney disease. The importance of developing a definition of cachexia in a population with ESKD is underscored by the negative impact that symptoms of cachexia have on quality of life and the association of cachexia with a substantially increased risk of premature mortality. The aim of this study is to determine the clinical phenotype of cachexia specific to individuals with ESKD.

methodsA longitudinal study which will recruit adult patients with ESKD receiving haemodialysis attending a Regional Nephrology Unit within the United Kingdom. Patients will be followed 2 monthly over 12 months and measurements of weight; lean muscle mass (bioelectrical impedance, mid upper arm muscle circumference and tricep skin fold thickness); muscle strength (hand held dynamometer), fatigue, anorexia and quality of life collected. We will determine if they experience (and to what degree) the known characteristics associated with cachexia. DISCUSSION: Cachexia is a debilitating condition associated with an extremely poor outcome. Definitions of cachexia in chronic illnesses are required to reflect specific nuances associated with each disease. These discrete cachexia definitions help with the precision of research and the subsequent clinical interventions to improve outcomes for patients suffering from cachexia. The absence of a definition for cachexia in an ESKD population makes it particularly difficult to study the incidence of cachexia or potential treatments, as there are no standardised inclusion criteria for patients with ESKD who have cachexia. Outcomes from this study will provide much needed data to inform development and testing of potential treatment modalities, aimed at enhancing current clinical practice, policy and education.

Indexed as

Patient SelectionPhenotypeCachexiaHumansKidney Failure, ChronicLongitudinal StudiesRenal DialysisUnited KingdomCachexiaDefinitionEnd-stage kidney diseaseLongitudinalPhenotype

Identifiers

PMID29439674
PMCPMC5812213
OpenAlexW2787535938

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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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.