Evidence map›Paper›PMID 21809369›Full record

ArticleAmerican journal of hematology2011

Recurrent, severe wheezing is associated with morbidity and mortality in adults with sickle cell disease.

Robyn T Cohen, Anusha Madadi, Morey A Blinder, Michael R DeBaun, Robert C Strunk, Joshua J Field

Open access · bronzeAbstract readMulticenter Study
In one paragraph

Article in American journal of hematology, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 35 papers.

0numbers the graph read from it
0cells of the map it votes in
35citing papers in PubMed
2.0field-weighted citation impact, top 14% 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

35 citing papers in PubMed, 63 citations in OpenAlex.

  1. Trial
  2. Trial
  3. Trial
  4. Trial
  5. Article
  6. Article
  7. Article
  8. Article
  9. Review
  10. Review
  11. The Cardiopulmonary Complications of Sickle Cell Disease.Hematology/oncology clinics of North America · 2022
    Review
  12. Observational
  13. Article
  14. Review
  15. Article
  16. Article
  17. Acute Chest Syndrome in Children with Sickle Cell Disease.Pediatric allergy, immunology, and pulmonology · 2017
    Review
  18. Article
  19. Article
  20. 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

6 authors at 5 institutions in 1 country.

Robyn T CohenDepartment of Pediatrics, Drexel University College of Medicine, Philadelphia, Pennsylvania, USA.
Anusha Madadi
Morey A Blinder
Michael R DeBaun
Robert C Strunk
Joshua J Field
Washington University in St. Louis · USDrexel University · USSt. Luke's Hospital · USVanderbilt University · USVersiti Blood Center of Wisconsin · US

Funding

Asthma and Nocturnal Hypoxemia in Sickle Cell Anemia IIR01HL079937 · NHLBI · WASHINGTON UNIVERSITY · PI DEBAUN, MICHAEL R., STRUNK, ROBERT · 2005 to 2013
$10.4M
CLINICAL HEMATOLOGY RESEARCH CAREER DEVELOPMENT PROGRAM AT WASHINGTON UNIVERSITYK12HL087107 · NHLBI · WASHINGTON UNIVERSITY · PI SADLER, J EVAN · 2006 to 2016
$3.8M
MEMBRANE-MEDIATED MECHANISMS OF TISSUE FACTOR FUNCTIONF32HL008710 · NHLBI · OKLAHOMA MEDICAL RESEARCH FOUNDATION · PI NEUENSCHWANDER, PIERRE FERNAND · 1992 to 1994
–
NHLBI NIH HHS HL079937NHLBI NIH HHS K12 HL08710NHLBI NIH HHS K12 HL087107NHLBI NIH HHS R01 HL079937
6 · The paper itself

Abstract

Prior studies of asthma in children with sickle cell disease (SCD) were based on reports of a doctor-diagnosis of asthma with limited description of asthma features. Doctor-diagnoses of asthma may represent asthma or wheezing unrelated to asthma. Objectives of this study were to determine if asthma characteristics are present in adults with a doctor-diagnosis of asthma and/or wheezing, and to examine the relationship between doctor-diagnosis of asthma, wheezing and SCD morbidity. This was an observational cohort study of 114 adults with SCD who completed respiratory symptom questionnaires and had serum IgE measurements. A subset of 79 participants completed pulmonary function testing. Survival analysis was based on a mean prospective follow-up of 28 months and data were censored at the time of death or loss to follow-up. Adults reporting a doctor-diagnosis of asthma (N = 34) were more likely to have features of asthma including wheeze, eczema, family history of asthma, and an elevated IgE level (all P < 0.05). However, there was no difference in pain or ACS rate, lung function, or risk of death between adults with and without a doctor-diagnosis of asthma. In contrast, adults who reported recurrent, severe episodes of wheezing (N = 34), regardless of asthma, had twice the rates of pain and ACS, decreased lung function and increased risk of death compared with adults without recurrent, severe wheezing. Asthma features were not associated with recurrent, severe wheezing. Our data suggest that wheezing in SCD may occur independently of asthma and is a marker of disease severity.

Indexed as

Acute Chest SyndromeAdolescentAdultAgedAnemia, Sickle CellAsthmaBiomarkersCohort StudiesFemaleHumansImmunoglobulin EMaleMiddle AgedMorbidityPain MeasurementProspective StudiesBiomarkersImmunoglobulin E

Identifiers

PMID21809369
PMCPMC4103016
OpenAlexW2083067465

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.