Evidence map›Paper›PMID 29223439›Full record

ArticleAmerican heart journal2017

A unique linkage of administrative and clinical registry databases to expand analytic possibilities in pediatric heart transplantation research.

Justin Godown, Cary Thurm, Debra A Dodd, Jonathan H Soslow, Brian Feingold, Andrew H Smith, Bret A Mettler, Bryn Thompson, Matt Hall

Open access · greenAbstract readMulticenter Study
In one paragraph

Article in American heart journal, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
5.2field-weighted citation impact, top 4% 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

17 citing papers in PubMed, 33 citations in OpenAlex.

  1. Linkage of the CF Foundation Patient Registry with the Scientific Registry of Transplant Recipients database.Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society · 2025
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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

9 authors at 4 institutions in 1 country.

Justin GodownPediatric Cardiology, Monroe Carell Jr. Children's Hospital, Nashville, TN. Electronic address: justin.godown@vanderbilt.edu.
Cary ThurmChildren's Hospital Association, Lenexa, KS.
Debra A DoddPediatric Cardiology, Monroe Carell Jr. Children's Hospital, Nashville, TN.
Jonathan H SoslowPediatric Cardiology, Monroe Carell Jr. Children's Hospital, Nashville, TN.
Brian FeingoldPediatrics and Clinical and Translational Science, University of Pittsburgh School of Medicine, Pittsburgh, PA.
Andrew H SmithPediatric Critical Care, Monroe Carell Jr. Children's Hospital, Nashville, TN.
Bret A MettlerPediatric Cardiothoracic Surgery, Monroe Carell Jr. Children's Hospital, Nashville, TN.
Bryn ThompsonScientific Registry of Transplant Recipients, Minneapolis Medical Research Foundation, Minneapolis, MN.
Matt HallChildren's Hospital Association, Lenexa, KS.
Monroe Carell Jr. Children's Hospital · USChildren's Hospital Association · USOrthopaedic Research Foundation · USUniversity of Pittsburgh · US

Funding

Quantitative Assessment of Cardiac Disease in Duchenne Muscular DystrophyK23HL123938 · NHLBI · VANDERBILT UNIVERSITY MEDICAL CENTER · PI SOSLOW, JONATHAN HARVEY · 2014 to 2018
$829k
NHLBI NIH HHS K23 HL123938
6 · The paper itself

Abstract

backgroundLarge clinical, research, and administrative databases are increasingly utilized to facilitate pediatric heart transplant (HTx) research. Linking databases has proven to be a robust strategy across multiple disciplines to expand the possible analyses that can be performed while leveraging the strengths of each dataset. We describe a unique linkage of the Scientific Registry of Transplant Recipients (SRTR) database and the Pediatric Health Information System (PHIS) administrative database to provide a platform to assess resource utilization in pediatric HTx.

methodsAll pediatric patients (1999-2016) who underwent HTx at a hospital enrolled in the PHIS database were identified. A linkage was performed between the SRTR and PHIS databases in a stepwise approach using indirect identifiers. To determine the feasibility of using these linked data to assess resource utilization, total and post-HTx hospital costs were assessed.

resultsA total of 3188 unique transplants were identified as being present in both databases and amenable to linkage. Linkage of SRTR and PHIS data was successful in 3057 (95.9%) patients, of whom 2896 (90.8%) had complete cost data. Median total and post-HTx hospital costs were $518,906 (IQR $324,199-$889,738), and $334,490 (IQR $235,506-$498,803) respectively with significant differences based on patient demographics and clinical characteristics at HTx.

conclusionsLinkage of the SRTR and PHIS databases is feasible and provides an invaluable tool to assess resource utilization. Our analysis provides contemporary cost data for pediatric HTx from the largest US sample reported to date. It also provides a platform for expanded analyses in the pediatric HTx population.

Indexed as

Biomedical ResearchCardiologyRegistriesAdolescentChildChild, PreschoolDatabases, FactualFemaleHealth Information SystemsHeart Defects, CongenitalHeart TransplantationHospitals, PediatricHumansInfantMaleRetrospective Studies

Identifiers

PMID29223439
PMCPMC5726444
OpenAlexW2750194734

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.