Evidence map›Paper›PMID 37216689›Full record

ArticleBlood2023

New ASH initiatives to improve patient care in the long-overlooked sickle cell disease.

Venée N Tubman, Narla Mohandas, Charles S Abrams

Open access · bronzeAbstract read
In one paragraph

Article in Blood, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.9field-weighted citation impact, top 23% 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

3 citing papers in PubMed, 3 citations in OpenAlex.

  1. Article
  2. Review
  3. Hydroxyurea in the sickle cell disease modern era.Expert review of clinical pharmacology · 2024
    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

3 authors at 3 institutions in 1 country.

Venée N TubmanDepartment of Pediatrics, Baylor College of Medicine, Houston, TX.
Narla MohandasResearch Laboratory of Red Cell Physiology, New York Blood Center, New York, NY.ORCID 0000-0003-2271-5296
Charles S AbramsDepartment of Medicine, University of Pennsylvania, Philadelphia, PA.
Baylor College of Medicine · USNew York Blood Center · USUniversity of Pennsylvania · US

Funding

Characterization of B Lymphocyte Deficiency in Pediatric Sickle Cell DiseaseK23HL148548 · NHLBI · BAYLOR COLLEGE OF MEDICINE · PI TUBMAN, VENEE N · 2020 to 2024
$816k
NHLBI NIH HHS K23 HL148548
6 · The paper itself

Abstract

Because of the unique biology of sickle cell disease (SCD) as well as the societal disadvantages and racial inequities suffered by these patients, individuals with SCD have not benefited from the same remarkable advances in care and therapeutics as those with other hematologic disorders. Life expectancy of individuals with SCD is shortened by ∼20 years even with optimal clinical care, and infant mortality continues to be a major concern in low-income countries. As hematologists, we must do more. The American Society of Hematology (ASH) and the ASH Research Collaborative have instituted a multipronged initiative to improve the lives of individuals living with this disease. Here, we describe 2 components of this ASH initiative, the Consortium on Newborn Screening in Africa (CONSA) to improve the early diagnosis of infants in low-resource countries and the SCD Clinical Trial Network to accelerate the development of more effective therapeutics and care for those with this disorder. The combination of SCD-focused initiatives, ASH Research Collaborative, CONSA, and Sickle Cell Clinical Trials Network has enormous potential to dramatically alter the course of SCD worldwide. We believe that the timing is ripe to embark on these critical and worthwhile initiatives and improve the lives of individuals with this disease.

Indexed as

Anemia, Sickle CellHematologic DiseasesHumansInfantInfant, NewbornLife ExpectancyNeonatal ScreeningPatient Care

Identifiers

PMID37216689
PMCPMC13122306
OpenAlexW4377224216

What OpenQuestion holds

Textmetadata
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.