Evidence map›Paper›PMID 32219405›Full record

ArticleJAMA network open2020

Comparison of US Federal and Foundation Funding of Research for Sickle Cell Disease and Cystic Fibrosis and Factors Associated With Research Productivity.

Faheem Farooq, Peter J Mogayzel, Sophie Lanzkron, Carlton Haywood, John J Strouse

Registry-linked trialOpen access · goldAbstract readComparative Study
In one paragraph

Article in JAMA network open, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT07540767 (Development of a Provider-Focused Intervention to Improve Health Outcomes in Pediatric Sickle Cell Disease), which is not on this map. Cited by 73 papers.

0numbers the graph read from it
0cells of the map it votes in
73citing papers in PubMed
12.9field-weighted citation impact, top 1% 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.

NCT07540767 nanot yet recruitingnot on this mapstarted 2027, after this paper: background citation

Development of a Provider-Focused Intervention to Improve Health Outcomes in Pediatric Sickle Cell Disease

TypeinterventionalSponsorConnecticut Children's Medical CenterRan2027 to 2030Enrolled30ConditionsSickle Cell Disease, Sickle Cell Anemia in Children, Sickle Cell Disease (SCD), Sickle CellArmsIndividuation and Perspective-Taking (IPT), pediatric SCD pain management education session
3 · Its place in the literature

Who cites it

73 citing papers in PubMed, 176 citations in OpenAlex.

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13 more citing papers are in PubMed but not listed here.

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

5 authors at 3 institutions in 1 country.

Faheem FarooqDeparment of Pediatrics and Medicine, Stony Brook University Hospital, Stony Brook, New York.
Peter J MogayzelDivision of Pediatric Pulmonology, Department of Pediatrics, Johns Hopkins University School of Medicine, Baltimore, Maryland.
Sophie LanzkronDivision of Hematology, Department of Medicine, Johns Hopkins University School of Medicine, Baltimore, Maryland.
Carlton HaywoodDivision of Hematology, Department of Medicine, Johns Hopkins University School of Medicine, Baltimore, Maryland.
John J StrouseDivision of Hematology, Department of Medicine, Duke University School of Medicine, Durham, North Carolina.
Johns Hopkins University · USDuke University · USStony Brook University Hospital · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Importance: Sickle cell disease (SCD) and cystic fibrosis (CF) are severe autosomal recessive disorders associated with intermittent disease exacerbations that require hospitalizations, progressive chronic organ injury, and substantial premature mortality. Research funding is a limited resource and may contribute to health care disparities, especially for rare diseases that disproportionally affect economically disadvantaged groups. Objective: To compare disease-specific funding between SCD and CF and the association between funding and research productivity. Design, Setting, and Participants: This cross-sectional study examined federal and foundation funding, publications indexed in PubMed, clinical trials registered in ClinicalTrials.gov, and new drug approvals from January 1, 2008, to December 31, 2018, in an estimated US population of approximately 90 000 individuals with SCD and approximately 30 000 individuals with CF. Main Outcomes and Measures: Federal and foundation funding, publications indexed in PubMed, clinical trial registrations, and new drug approvals. Results: From 2008 through 2018, federal funding was greater per person with CF compared with SCD (mean [SD], $2807 [$175] vs $812 [$147]; P < .001). Foundation expenditures were greater for CF than for SCD (mean [SD], $7690 [$3974] vs $102 [$13.7]; P < .001). Significantly more research articles (mean [SD], 1594 [225] vs 926 [157]; P < .001) and US Food and Drug Administration drug approvals (4 vs 1) were found for CF compared with SCD, but the total number of clinical trials was similar (mean [SD], 27.3 [6.9] vs 23.8 [6.3]; P = .22). Conclusions and Relevance: The findings show that disparities in funding between SCD and CF may be associated with decreased research productivity and novel drug development for SCD. Increased federal and foundation funding is needed for SCD and other diseases that disproportionately affect economically disadvantaged groups to address health care disparities.

Indexed as

Biomedical ResearchResearch Support as TopicAnemia, Sickle CellCross-Sectional StudiesCystic FibrosisDrug DevelopmentFoundationsHumansUnited States

Identifiers

PMID32219405
PMCPMC12549141
OpenAlexW3014078140

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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.