Evidence map›Paper›PMID 33072941›Full record

ArticleInternational journal of neonatal screening2018

Congenital Hypothyroidism 3-Year Follow-Up Project: Region 4 Midwest Genetics Collaborative Results.

Kupper A Wintergerst, Erica Eugster, Karen Andruszewski, Mary Kleyn, Nancy Vanderburg, Joe Sockalosky, Ram Menon, Sharon Linard, Suzanne Kingery, Susan R Rose and 3 more

Abstract read
In one paragraph

Article in International journal of neonatal screening, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. 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

13 authors.

Kupper A WintergerstDepartment of Pediatrics, Endocrinology, University of Louisville, Louisville, KY 40202, USA.
Erica EugsterDepartment of Pediatrics, Endocrinology, Indiana University, Indianapolis, IN 46202, USA.
Karen AndruszewskiMichigan Department of Community Health, Lansing, MI 48933, USA.
Mary KleynMichigan Department of Community Health, Lansing, MI 48933, USA.
Nancy VanderburgMinnesota Department of Health, St. Paul, MN 55155, USA.
Joe SockaloskyChildren's Hospitals and Clinics of Minnesota, St. Paul, MN 55102, USA.
Ram MenonDepartment of Pediatrics, Endocrinology, University of Michigan, Ann Arbor, MI 48109, USA.
Sharon LinardOhio Department of Health Laboratory, Reynoldsburg, OH 43068, USA.ORCID https://orcid.org/0000-0001-7004-7769
Suzanne KingeryDepartment of Pediatrics, Endocrinology, University of Louisville, Louisville, KY 40202, USA.
Susan R RoseDepartment of Pediatrics, Endocrinology, College of Medicine, University of Cincinnati, Cincinnati, OH 45229, USA.ORCID https://orcid.org/0000-0003-1328-1289
Julie MooreRegion 4 Midwest Genetics Collaborative, Michigan Public Health Institute, Okemos, MI 48864, USA.
Gina GembelRegion 4 Midwest Genetics Collaborative, Michigan Public Health Institute, Okemos, MI 48864, USA.
Lisa GormanRegion 4 Midwest Genetics Collaborative, Michigan Public Health Institute, Okemos, MI 48864, USA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

To identify the 3-year follow-up management and education patterns of primary care clinicians and pediatric endocrinologists for children diagnosed with congenital hypothyroidism (CH) through newborn screening programs, the Region 4 Midwest Genetics Collaborative, made up of seven regional states (Illinois, Indiana, Kentucky, Michigan, Minnesota, Ohio, Wisconsin), performed a survey study of parents and physicians caring for children identified with CH. The clinicians and parents of 409 children with CH regionally identified in 2007 were invited to participate in a voluntary survey. Responses relating to treatment, monitoring practices, educational resources, genetic counseling, and services provided/received were collected from 214 clinicians and 77 parents. In total, 99% had undergone a confirmatory test following positive newborn screening and 55% had imaging at diagnosis, but only 50% were identified as having the etiology identified. Thyroid withdrawal challenge testing was the choice method for re-evaluating thyroid function, but the approach varied. Clinician and parent responses to education and genetic counseling also differed. Clinicians report face-to-face education as the most common method, with less than 50% providing handouts to patients. Only 14% of patients were referred to a genetics counselor. Of parents reporting on their educational experience, 86% received face-to-face education from a pediatric endocrinologist and 4% received education from a genetic counselor. Only 65%, however, were satisfied with their education. These survey data suggest a lack of a standardized approach to diagnosis, follow-up, education, and genetic counseling. This collaborative effort provides insight into developing three-year follow-up, education and genetic counseling guidelines for children diagnosed with CH.

Indexed as

congenital hypothyroidismneonatalnewbornscreeningthyroid

Identifiers

PMID33072941
PMCPMC7548898

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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.