Evidence map›Paper›PMID 29342203›Full record

Observational studyPloS one2018

Biological pathways underlying the association of red cell distribution width and adverse clinical outcome: Results of a prospective cohort study.

Giedre Zurauskaite, Marc Meier, Alaadin Voegeli, Daniel Koch, Sebastian Haubitz, Alexander Kutz, Luca Bernasconi, Andreas Huber, Mario Bargetzi, Beat Mueller and 1 more

Open access · goldAbstract readObservational Study
In one paragraph

Observational study in PloS one, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed, 1 pooled it
2.3field-weighted citation impact, top 9% 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

24 citing papers in PubMed, 1 synthesis or guideline pooled it, 41 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Observational
  11. Red cell distribution width is a predictor of all-cause mortality in hospitalized dogs.Journal of veterinary emergency and critical care (San Antonio, Tex. : 2001) · 2022
    Article
  12. Article
  13. RDW Value may Increase the Diagnostic Accuracy of MPS.Sisli Etfal Hastanesi tip bulteni · 2021
    Article
  14. Article
  15. Article
  16. Clonal Hematopoiesis and Premalignant Diseases.Cold Spring Harbor perspectives in medicine · 2020
    Review
  17. Article
  18. Article
  19. Article
  20. 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

11 authors at 1 institution in 1 country.

Giedre ZurauskaiteMedical University Department, Kantonsspital Aarau, Aarau, Switzerland.
Marc MeierMedical University Department, Kantonsspital Aarau, Aarau, Switzerland.
Alaadin VoegeliMedical University Department, Kantonsspital Aarau, Aarau, Switzerland.
Daniel KochMedical University Department, Kantonsspital Aarau, Aarau, Switzerland.ORCID 0000-0002-4660-5924
Sebastian HaubitzMedical University Department, Kantonsspital Aarau, Aarau, Switzerland.
Alexander KutzMedical University Department, Kantonsspital Aarau, Aarau, Switzerland.
Luca BernasconiInstitute of Laboratory Medicine, Kantonsspital Aarau, Aarau, Switzerland.
Andreas HuberInstitute of Laboratory Medicine, Kantonsspital Aarau, Aarau, Switzerland.
Mario BargetziDivision of Hematology, Oncology and Transfusion Medicine, Kantonsspital Aarau, Aarau, Switzerland.
Beat MuellerMedical University Department, Kantonsspital Aarau, Aarau, Switzerland.
Philipp SchuetzMedical University Department, Kantonsspital Aarau, Aarau, Switzerland.
Kantonsspital Aarau · CH

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundRed cell distribution width (RDW) predicts disease outcome in several patient populations, but its prognostic value in addition to other disease parameters in unselected medical inpatients remains unclear. Our aim was to investigate the association of admission RDW levels and mortality adjusted for several disease pathways in unselected medical patients from a previous multicenter study.

methodsWe included consecutive adult, medical patients at the time point of hospital admission through the emergency department into this observational, cohort study. The primary endpoint was mortality at 30-day. To study association of admission RDW and outcomes, we calculated regression analysis with step-wise inclusion of clinical and laboratory parameters from different biological pathways.

resultsThe 30-day mortality of the 4273 included patients was 5.6% and increased from 1.4% to 14.3% from the lowest to the highest RDW quartile. There was a strong association of RDW and mortality in unadjusted analysis (OR 1.32; 95%CI 1.27-1.39, p<0.001). RDW was strongly correlated with different pathways including inflammation (coefficient of determination (R2) 0.30; p<0.001), nutrition (R2 0.20; p<0.001) and blood diseases (R2 0.30; p<0.001 The association was eliminated after including different biological pathways into the models with the fully adjusted regression model showing an OR of 1.02 (95%CI 0.93-1.12; p = 0.664) for the association of RDW and mortality. Similar effects were found for other outcomes including intensive care unit admission and hospital readmission.

conclusionOur data suggests that RDW is a strong surrogate marker of mortality in unselected medical inpatients with most of the prognostic information being explained by other disease factors. The strong correlation of RDW and different biological pathways such as chronic inflammation, malnutrition and blood disease suggest that RDW may be viewed as an unspecific and general "chronic disease prognostic marker".

Indexed as

Erythrocyte IndicesAdultAgedAnemiaCohort StudiesEmergency Service, HospitalFemaleHospital MortalityHumansInpatientsMaleMiddle AgedPatient AdmissionPrognosisProspective Studies

Identifiers

PMID29342203
PMCPMC5771602
OpenAlexW2794347925

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.