Evidence map›Paper›PMID 37502850›Full record

ArticlemedRxiv : the preprint server for health sciences2023

Development and Validation of a Computable Phenotype for Turner Syndrome Utilizing Electronic Health Records from a National Pediatric Network.

Sarah D Huang, Vaneeta Bamba, Samantha Bothwell, Patricia Y Fechner, Anna Furniss, Chijioke Ikomi, Leena Nahata, Natalie J Nokoff, Laura Pyle, Helina Seyoum and 1 more

Abstract readPreprint
In one paragraph

Article in medRxiv : the preprint server for health sciences, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

11 authors.

Sarah D HuangDepartment of Pediatrics, University of Colorado, Anschutz Medical Campus, Aurora, CO 80045.
Vaneeta BambaDivision Endocrinology and Diabetes, The Children's Hospital of Philadelphia, Philadelphia, PA 19104.
Samantha BothwellDepartment of Pediatrics, University of Colorado, Anschutz Medical Campus, Aurora, CO 80045.
Patricia Y FechnerDepartment of Pediatrics, University of Washington, Division of Endocrinology at Seattle Children's, Seattle, WA 98105.
Anna FurnissACCORDS, University of Colorado, Anschutz Medical Campus, Aurora, CO 80045.
Chijioke IkomiDivision of Endocrinology, Nemours Children's Health, Wilmington, DE 19803.
Leena NahataDivision of Endocrinology, Nationwide Children's Hospital, Columbus, OH 43205.
Natalie J NokoffDepartment of Pediatrics, University of Colorado, Anschutz Medical Campus, Aurora, CO 80045.
Laura PyleDepartment of Pediatrics, University of Colorado, Anschutz Medical Campus, Aurora, CO 80045.
Helina SeyoumDepartment of Pediatrics, University of Colorado, Anschutz Medical Campus, Aurora, CO 80045.
Shanlee M DavisDepartment of Pediatrics, University of Colorado, Anschutz Medical Campus, Aurora, CO 80045.

Funding

Pubertal Blockade and Estradiol Effects on Cardiometabolic Health for Transitioning Youth (PUBERTY)K23HL151868 · NHLBI · UNIVERSITY OF COLORADO DENVER · PI NOKOFF, NATALIE J · 2020 to 2024
$941k
TESTO: Testosterone Effects on Short-Term Outcomes in Infants with XXYK23HD092588 · NICHD · UNIVERSITY OF COLORADO DENVER · PI DAVIS, SHANLEE · 2017 to 2021
$826k
Population Health in Pediatric Sex Chromosome AneuploidiesR03HD102773 · NICHD · UNIVERSITY OF COLORADO DENVER · PI DAVIS, SHANLEE · 2020 to 2021
$156k
NHLBI NIH HHS K23 HL151868NICHD NIH HHS K23 HD092588NICHD NIH HHS R03 HD102773
6 · The paper itself

Abstract

Turner syndrome (TS) is a genetic condition occurring in ~1 in 2,000 females characterized by the complete or partial absence of the second sex chromosome. TS research faces similar challenges to many other pediatric rare disease conditions, with homogenous, single-center, underpowered studies. Secondary data analyses utilizing Electronic Health Record (EHR) have the potential to address these limitations, however, an algorithm to accurately identify TS cases in EHR data is needed. We developed a computable phenotype to identify patients with TS using PEDSnet, a pediatric research network. This computable phenotype was validated through chart review; true positives and negatives and false positives and negatives were used to assess accuracy at both primary and external validation sites. The optimal algorithm consisted of the following criteria: female sex, ≥1 outpatient encounter, and ≥3 encounters with a diagnosis code that maps to TS, yielding average sensitivity 0.97, specificity 0.88, and C-statistic 0.93 across all sites. The accuracy of any estradiol prescriptions yielded an average C-statistic of 0.91 across sites and 0.80 for transdermal and oral formulations separately. PEDSnet and computable phenotyping are powerful tools in providing large, diverse samples to pragmatically study rare pediatric conditions like TS.

Indexed as

computable phenotypeelectronic health recordpediatric rare diseasesex chromosome aneuploidyTurner syndrome

Identifiers

PMID37502850
PMCPMC10371114

What OpenQuestion holds

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LicenceCC BY-NC-ND
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.