Evidence map›Paper›PMID 26345374›Full record

ReviewCardiology in the young2016

CHD associated with syndromic diagnoses: peri-operative risk factors and early outcomes.

Benjamin J Landis, David S Cooper, Robert B Hinton

Open access · greenAbstract readReview
In one paragraph

Review in Cardiology in the young, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed, 1 pooled it
2.4field-weighted citation impact, top 11% 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

25 citing papers in PubMed, 1 synthesis or guideline pooled it, 41 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Genes · 2023
    Article
  12. Article
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  14. Article
  15. Review
  16. Review
  17. Article
  18. Genetic Basis of Human Congenital Heart Disease.Cold Spring Harbor perspectives in biology · 2020
    Article
  19. Congenital heart defects in CHARGE: The molecular role of CHD7 and effects on cardiac phenotype and clinical outcomes.American journal of medical genetics. Part C, Seminars in medical genetics · 2020
    Review
  20. Article
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 1 institution in 1 country.

Benjamin J LandisHeart Institute,Cincinnati Children's Hospital Medical Center,Cincinnati,Ohio,United States of America.
David S CooperHeart Institute,Cincinnati Children's Hospital Medical Center,Cincinnati,Ohio,United States of America.
Robert B HintonHeart Institute,Cincinnati Children's Hospital Medical Center,Cincinnati,Ohio,United States of America.
Cincinnati Children's Hospital Medical Center · US

Funding

Indiana Pediatric Scientist Award(IPSA)K12HD068371 · NICHD · INDIANA UNIVERSITY INDIANAPOLIS · PI CLAPP, DAVID W · 2013 to 2017
$1.9M
NICHD NIH HHS K12 HD068371
6 · The paper itself

Abstract

CHD is frequently associated with a genetic syndrome. These syndromes often present specific cardiovascular and non-cardiovascular co-morbidities that confer significant peri-operative risks affecting multiple organ systems. Although surgical outcomes have improved over time, these co-morbidities continue to contribute substantially to poor peri-operative mortality and morbidity outcomes. Peri-operative morbidity may have long-standing ramifications on neurodevelopment and overall health. Recognising the cardiovascular and non-cardiovascular risks associated with specific syndromic diagnoses will facilitate expectant management, early detection of clinical problems, and improved outcomes--for example, the development of syndrome-based protocols for peri-operative evaluation and prophylactic actions may improve outcomes for the more frequently encountered syndromes such as 22q11 deletion syndrome.

Indexed as

22q11 Deletion SyndromeAlagille SyndromeHeart Defects, CongenitalHeart DiseasesHeterotaxy SyndromeHumansInfantMarfan SyndromeNoonan SyndromeRisk FactorsSyndromeTime FactorsTreatment OutcomeTurner SyndromeWilliams SyndromeCHDgeneticsyndrome

Identifiers

PMID26345374
PMCPMC5125077
OpenAlexW1914247950

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.