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  <title>ONCE-WEEKLY SOMAPACITAN AS AN ALTERNATIVE MANAGEMENT OF GROWTH HORMONE DEFICIENCY IN PREPUBERTAL CHILDREN:</title>
  <subTitle>A SYSTEMATIC REVIEW AND META-ANALYSIS OF RANDOMIZED CONTROLLED TRIAL</subTitle>
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  <namePart>Ghina Tsurayya</namePart>
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   <roleTerm type="text">Primary Author</roleTerm>
  </role>
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  <place>
   <placeTerm type="text">Banda Aceh</placeTerm>
   <publisher>Fakultas Kedokteran</publisher>
   <dateIssued>2024</dateIssued>
  </place>
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 <note>Growth hormone treatment has effectively restored normal growth in children with growth&#13;
hormone deficiency (GHD); however, it poses challenges in compliance with a daily growth hormone&#13;
injection regimen, leading to low adherence and persistence rates. Once-weekly Somapacitan is&#13;
a potential alternative for treating children with GHD. This study aimed to evaluate the efficacy,&#13;
safety, and adherence of once-weekly subcutaneous Somapacitan compared to daily growth hormone&#13;
injection in prepubertal children with GHD. A search for the published records was carried out on&#13;
17 October 2023 utilizing the searching feature available on PubMed, Embase, and Scopus. Primary&#13;
study outcomes included (1) efficacy, measured by height velocity (HV), standard deviation score&#13;
(SDs), height SDs, insulin-like growth factor-SDs (IGF-I SDs), and bone age vs. chronological age&#13;
ratio (BA vs. CA); (2) safety, assessed through adverse events and injection site reactions; and&#13;
(3) adherence, determined by the percentage of the sample completing treatments. Secondary&#13;
outcomes evaluated disease burden scores, divided into three subgroup domains: emotional well-&#13;
being, physical functional, and social well-being scores. We retrieved 6 studies that were eligible&#13;
for the systematic review (417 versus 186 for intervention and control, respectively). Only 2 of&#13;
the total included studies were eligible for pooled analysis (175 versus 82 for intervention and&#13;
control, respectively). The efficacy profile of Somapacitan was similar to daily growth hormones,&#13;
indicated by HV (mean difference (MD = 0.04; p = 0.96), HV SDs (MD = −0.71; p = 0.09), height&#13;
SDs (MD = 0.11; p = 0.69), IGF-I SDs (MD = 0.06; p = 0.70), and CA vs. BA (MD = 0.67; p = 0.70)),&#13;
demonstrated similar and non-inferior outcomes. Treatment adherence is 3 times higher in the&#13;
Somapacitan group as compared to control (OR = 3.02; p = 0.03) with adherence rates reaching 95%&#13;
and 88% for Somapacitan and Norditropin®, respectively. The disease burden measurement is similar&#13;
in Somapacitan and daily growth hormones (MD = −0.62; p = 0.83), as indicated by the Growth&#13;
Hormone Deficiency–Child Impact Measure. In almost all outcomes, the level of confidence is strong.&#13;
The confidence level in the data is generally strong, but for CA vs. BA and the subgroup of severe&#13;
adverse events with heterogeneity &gt;50%, the confidence level is moderate. Although the efficacy&#13;
and safety profiles of Somapacitan were found to be similar to those of daily growth hormones, a&#13;
reduced frequency of once-weekly Somapacitan injections led to increased adherence. PROSPERO&#13;
registration: CRD42023473209.</note>
 <note type="statement of responsibility"></note>
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  <physicalLocation>ELECTRONIC THESES AND DISSERTATION Universitas Syiah Kuala</physicalLocation>
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