Evidence map›Paper›PMID 29609449›Full record

ArticleAnnals of pediatric endocrinology & metabolism2018

Design of the long-term observational cohort study with recombinant human growth hormone in Korean children: LG Growth Study.

Sochung Chung, Jae-Ho Yoo, Jin Ho Choi, Young-Jun Rhie, Hyun-Wook Chae, Jae Hyun Kim, Il Tae Hwang, Choong Ho Shin, Eun Young Kim, Kee-Hyoung Lee

Open access · diamondAbstract read
In one paragraph

Article in Annals of pediatric endocrinology & metabolism, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
1.3field-weighted citation impact, top 19% 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

21 citing papers in PubMed, 24 citations in OpenAlex.

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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

10 authors at 10 institutions in 1 country.

Sochung ChungDepartment of Pediatrics, Konkuk University Medical Center, Konkuk University School of Medicine, Seoul, Korea.
Jae-Ho YooDepartment of Pediatrics, Dong-A University College of Medicine, Busan, Korea.
Jin Ho ChoiDepartment of Pediatrics, Asan Medical Center, Seoul, Korea.
Young-Jun RhieDepartment of Pediatrics, Korea University Ansan Hospital, Korea University College of Medicine, Ansan, Korea.
Hyun-Wook ChaeDepartment of Pediatrics, Gangnam Severance Hospital, Seoul, Korea.
Jae Hyun KimDepartment of Pediatrics, Seoul National University Bundang Hospital , Seongnam , Korea.
Il Tae HwangDepartment of Pediatrics, Kangdong Sacred Heart Hospital, Hallym University College of Medicine, Seoul, Korea.
Choong Ho ShinDepartment of Pediatrics, Seoul National University College of Medicine, Seoul, Korea.
Eun Young KimLG Chem, Ltd., Seoul, Korea.
Kee-Hyoung LeeDepartment of Pediatrics, Korea University Anam Hospital, Seoul, Korea.ORCID 0000-0002-4319-9019
Asan Medical Center · KRDong-A University · KRHallym University · KRKonkuk University Medical Center · KRKorea University · KRKorea University Medical Center · KRLG (South Korea) · KRSeoul National University · KRSeoul National University Bundang Hospital · KRSeverance Hospital · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeRegarding recombinant human growth hormone (rhGH) use in the pediatric population, no long-term follow-up data are available for Korean patients. To fill in the gap of knowledge, a registry study (LG Growth Study) was initiated to assess the safety and effectiveness of four types of rhGH products in real-life settings.

methodsA total of 4,000 children will be registered and prospectively followed up at 6-month intervals until 2 years after epiphyseal closure to collect data on treatment and adverse events, with primary interest in malignancies and growth outcomes.

resultsAs of 22 March 2017, approximately 50% (2,024) of the target number of patients have been included in the analysis set: growth hormone deficiency, 1,297 (64.1%); idiopathic short stature, 315 (15.6%); small for gestational age, 206 (10.2%); Turner syndrome, 197 (9.7%); and chronic renal failure, 9 (0.4%). At baseline, median age (years) was 8 (interquartile range [IQR], 5-11); 52% (1,048) were boys; and the majority were at Tanner stage I (83% based on breast/external genitalia, 97% on pubic hair). Median height standard deviation score was -2.26 (IQR, -2.69 to -2.0), and median bone age delay (years) was -1.46 (IQR, -2.26 to -0.78).

conclusionsThis registry study will provide the opportunity to assess the risk of malignancies as well as the general safety data in Korean pediatric patients receiving rhGH. In addition, the long-term effectiveness of rhGH and comparative data between different disease entities will provide practical insight on the standard rhGH treatment.

Indexed as

Chronic renal failureGrowth hormone deficiencyIdiopathic short statureSmall for gestational ageTurner syndrome

Identifiers

PMID29609449
PMCPMC5894560
OpenAlexW2794868630

What OpenQuestion holds

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LicenceCC BY-NC
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Registered trials

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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.