Evidence map›Paper›PMID 28349207›Full record

ArticlePediatric cardiology2017

Trends in National Institutes of Health-Funded Congenital Heart Disease Research from 2005 to 2015.

Kristin M Burns, Victoria L Pemberton, Charlene A Schramm, Gail D Pearson, Jonathan R Kaltman

Abstract read
In one paragraph

Article in Pediatric cardiology, 2017. 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
–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

3 citing papers in PubMed.

  1. Review
  2. Article
  3. Congenital Heart Disease: The State-of-the-Art on Its Pharmacological Therapeutics.Journal of cardiovascular development and disease · 2022
    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

5 authors.

Kristin M BurnsNational Heart, Lung, and Blood Institute, National Institutes of Health, Bethesda, MD, USA. kristin.burns@nih.gov.ORCID http://orcid.org/0000-0001-8665-1303
Victoria L PembertonNational Heart, Lung, and Blood Institute, National Institutes of Health, Bethesda, MD, USA.
Charlene A SchrammNational Heart, Lung, and Blood Institute, National Institutes of Health, Bethesda, MD, USA.
Gail D PearsonNational Heart, Lung, and Blood Institute, National Institutes of Health, Bethesda, MD, USA.
Jonathan R KaltmanNational Heart, Lung, and Blood Institute, National Institutes of Health, Bethesda, MD, USA.

Funding

Intramural NIH HHS Z99 HL999999
6 · The paper itself

Abstract

In an era of ongoing need for research to enable evidence-based care for the expanding population with congenital heart disease (CHD), economic fluctuations have impacted research funding. We characterize trends in NIH-funded CHD research from 2005 to 2015. We searched the NIH RePORTER database from 2005 to 2015 using the terms "congenital heart" and "cardiac morphogenesis". Projects were characterized by year, institute, mechanism, costs, type and topic, and funding trends were analyzed. From 2005 to 2015, NIH funded 633 CHD research projects with total costs of $991 million. The National Heart, Lung, and Blood Institute funded 83% of CHD projects (528, $857 million). The R01 mechanism was used for 45% of projects (288, $421 million). Projects were 70% basic/early translational research, 27% clinical research, and 3% both. Cardiac developmental biology was the most common topic (52%), followed by technology/therapy development (15%), and diagnosis/management (12%). The total number of CHD projects ranged from 153 to 221 per year (30-58 new projects/year), and costs per year ranged from $58 to $116 million. The number of projects and total costs increased until 2012, but decreased again thereafter. CHD research did not experience as much erosion as overall NIH purchasing power; in constant dollars, CHD research funding levels in 2015 were $12 million higher than those in 2005. The NIH supported a diverse portfolio of CHD projects from 2005 to 2015. Support of CHD research projects trended upward until 2012, but declined thereafter due to fiscal austerity measures.

Indexed as

Heart Defects, CongenitalNational Institutes of Health (U.S.)Biomedical ResearchClinical Trials as TopicFinancing, GovernmentHumansUnited StatesCongenital heart defectFundingPediatricsResearchTrials

Identifiers

PMID28349207
PMCPMC5745797

What OpenQuestion holds

Textmetadata
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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.