<?xml version="1.1" encoding="utf-8"?>
<article xsi:noNamespaceSchemaLocation="http://jats.nlm.nih.gov/publishing/1.1/xsd/JATS-journalpublishing1-mathml3.xsd" dtd-version="1.1" xmlns:xlink="http://www.w3.org/1999/xlink" xmlns:mml="http://www.w3.org/1998/Math/MathML" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance"><front><journal-meta><journal-id journal-id-type="publisher-id">JCNR</journal-id><journal-title-group><journal-title>Journal of Clinical and Nursing Research</journal-title></journal-title-group><issn>2208-3685</issn><eissn>2208-3693</eissn><publisher><publisher-name>Bio-Byword Scientific Publishing Pty. Ltd.</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="doi">10.26689/jcnr.v9i4.10377</article-id><article-categories><subj-group subj-group-type="heading"><subject>Article</subject></subj-group></article-categories><title>Real-world Clinical Study of Recombinant Human Growth Hormone in the Treatment of Idiopathic Short Stature</title><url>https://artdesignp.com/journal/JCNR/9/4/10.26689/jcnr.v9i4.10377</url><author>LiuJianhua,ShiJin</author><pub-date pub-type="publication-year"><year>2025</year></pub-date><volume>9</volume><issue>4</issue><history><date date-type="pub"><published-time>2025-04-29</published-time></date></history><abstract>Objective: To investigate the clinical efficacy and safety evaluation of Polyethylene Glycol Recombinant Human Growth Hormone Injection (PEG-rhGH) in the treatment of idiopathic short stature. Methods: A total of 1402 patients were enrolled from March 21, 2024 to January 13, 2025, including 778 males and 624 females, with ages mainly ranging from 5 to 13 years old. Follow-up visits were completed by 488 patients for the first time, 174 patients for the second time, and 81 patients for the third time. All patients were treated with PEG-rhGH (Jin Sai Zeng) as the main therapy after admission. The changes in height information, IGF-1, and thyroid examination results of each patient at the initial diagnosis, 6, 9, and 12 months after treatment were observed and analyzed. Results: There was no statistical difference between the baseline and the initial diagnosis, as well as the second follow-up visit (P &amp;lt; 0.05), while there was a statistical difference between the baseline and the first and third follow-up visits (P &amp;gt; 0.05). There was a statistically significant difference in IGF-1 between the initial diagnosis and the first follow-up visit (P &amp;lt; 0.05), but no statistical difference between the first, second, and third follow-up visits (P &amp;gt; 0.05). Additionally, IGF-1 levels increased with time. There was no statistical difference in TSH between the initial diagnosis and the first, second, and third follow-up visits (P &amp;gt; 0.05). There was a statistical difference in free T3 between the initial diagnosis and the first and second follow-up visits (P&amp;lt;0.05), but no statistical difference between the second and third follow-up visits (P&amp;gt;0.05). There was no statistical difference in free T4 between the initial diagnosis and the first and second follow-up visits (P &amp;gt; 0.05), but there was a statistical difference between the second and third follow-up visits (P &amp;lt; 0.05). Conclusion: PEG-rhGH (Jin Sai Zeng) is significantly effective in improving height and IGF-1 levels in patients with idiopathic short stature.</abstract><keywords/></article-meta></front><body/><back><ref-list><ref id="B1" content-type="article"><label>1</label><element-citation publication-type="journal"><p>Ge L, Zhao C, Xu F, et al., 2023, Research Progress on Polyethylene Glycol Recombinant Human Growth Hormone in the Treatment of Idiopathic Short Stature in Children. Modern Clinical Medicine, 49(2): 128–130.</p><pub-id pub-id-type="doi"/></element-citation></ref><ref id="B2" content-type="article"><label>2</label><element-citation publication-type="journal"><p>Wang X, Deng Q, Li M, et al., 2024, Clinical Study on the Effect of PEG-rhGH in the Treatment of Children with Idiopathic Short Stature on Growth Rate. 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