Evidence map›Paper›PMID 36191963›Full record

ArticleBritish journal of haematology2022

Patients with sickle cell disease who develop end-stage kidney disease continue to experience poor survival - A 19-year United States Renal Data System study.

Jeffrey C Winer, Marianne E Yee, Kenneth I Ataga, Jeffrey D Lebensburger, Rima S Zahr

Erratum issuedAbstract readLetter
In one paragraph

Article in British journal of haematology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
–field-weighted citation impact
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

16 citing papers in PubMed.

  1. Article
  2. Review
  3. Review
  4. Observational
  5. Article
  6. Article
  7. Review
  8. Article
  9. Observational
  10. Article
  11. Article
  12. Article
  13. Article
  14. Sickle Cell Disease and CKD: An Update.American journal of nephrology · 2024
    Review
  15. Article
  16. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

5 authors.

Jeffrey C WinerDivision of Academic Hospital Medicine, Department of Pediatrics, University of Tennessee Health Science Center, Memphis, Tennessee, USA.
Marianne E YeeDepartment of Pediatrics, Aflac Cancer and Blood Disorders Center, Children's Healthcare of Atlanta, Emory University School of Medicine, Atlanta, Georgia, USA.ORCID 0000-0001-6082-8385
Kenneth I AtagaCenter for Sickle Cell Disease, University of Tennessee Health Science Center Memphis, Tennessee, USA.ORCID 0000-0002-4501-9982
Jeffrey D LebensburgerDivision of Pediatric Hematology and Oncology, University of Alabama at Birmingham, Birmingham, Alabama, USA.ORCID 0000-0001-5011-1022
Rima S ZahrDivision of Pediatric Nephrology and Hypertension, University of Tennessee Health Science Center Memphis, Tennessee, USA.ORCID 0000-0002-3631-7195

Funding

Genetic modifiers of Sickle Cell Kidney DiseaseK23HL157554 · NHLBI · UNIVERSITY OF TENNESSEE HEALTH SCI CTR · PI Rima Zahr · 2022 to 2026
$849k
NHLBI NIH HHS K23 HL157554
6 · The paper itself

Abstract

PubMed holds no abstract for this paper.

Indexed as

Anemia, Sickle CellKidney Failure, ChronicKidney TransplantationHumansUnited States

Identifiers

PMID36191963
PMCPMC10739628

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.