生长激素缺乏症患儿替代治疗的不良事件

M. Aryayev, L. Senkivska
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摘要

背景。目的是根据体格检查、生命体征评估、实验室参数和随访结果,分析和总结生长激素缺乏症(GHD)儿童使用重组人生长激素(rhGH)治疗的累积短期和长期安全性数据。材料和方法。该研究于2012年至2022年在敖德萨地区儿童临床医院进行,92名儿童使用平均剂量为0.033 mg/kg/天的rhGH治疗GHD。对该疗法安全性的评估是基于对不良事件(ae)作为医疗护理的负面后果的发生率的评估。我们分析了短期和长期的结果。结果。在根据体格检查资料研究rhGH治疗的短期安全性时,18例(19.57%)儿童出现不良反应,包括颅内高压症(1例)、关节痛(1例)、青春期前男性乳房发育症(1例)、贫血(3例)、表现为潜伏性肾上腺功能不全(3例)、潜伏性甲状腺功能不全(2例)、糖耐量受损(7)。20.6 (7.0 ÷ 34.2%) %的患者无法接受rhGH治疗,而接受rhGH治疗的儿童中有4.3 (-1.6 ÷ 10.2) %的患者报告注射时疼痛(χ2 = 5.15;= 0.02)。所有患儿均未发生严重不良事件,如脊柱侧凸进展、股骨头骨骺滑动、水肿和生命功能受损。血液学和生化参数方面的ae通常是短暂的,通常与并发疾病合并,与rhGH无关。在长期安全性方面,rhGH治疗与癌症、心脑血管疾病的风险之间没有关联。尽管如此,仍有3名儿童(3.26%)患有2型糖尿病,其中1例超重,2例肥胖。结论。总的来说,在短期内,促生长激素治疗儿童GHD是安全的。注射部位的疼痛是临床显著的AE,是坚持rhGH治疗的认知情绪障碍。从rhGH治疗的长期安全性的角度来看,在3例(3.26%)体重增加和肥胖的儿童中检测到2型糖尿病是必不可少的。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Adverse events of replacement therapy in children with growth hormone deficiency
Background. The purpose was to analyze and summarize the accumulated short-term and long-term safety data in children with growth hormone deficiency (GHD) treated using recombіnant human growth hormone (rhGH) based on the results of a physical examination, assessment of vital signs, laboratory parameters, and follow-up. Materials and methods. The study was conducted at the Odesa Regional Children’s Clinical Hospital from 2012 to 2022, with 92 children treated for GHD using rhGH at an average dose of 0.033 mg/kg/day. The evaluation of the safety of this therapy was based on assessing the incidence of adverse events (AEs) as a negative consequence of medical care. We analyzed both short-term and long-term outcomes. Results. When studying the short-term safety of rhGH therapy according to physical examination data, AEs were found in 18 (19.57 %) children, including intracranial hypertension (1), arthralgia (1), prepubertal gynecomastia (1), anemia (3), manifestation of latent adrenal insufficiency (3), latent thyroid insufficiency (2), impaired glucose tolerance (7). 20.6 (7.0 ÷ 34.2) % of patients with unacceptable adherence to rhGH therapy reported painful injections compared to 4.3 (–1.6 ÷ 10.2) % of children with acceptable compliance (χ2 = 5.15; р = 0.02). None of the children experienced serious adverse events such as scoliosis progression, slipped capital femoral epiphysis, edema, and impaired vital functions. AEs in terms of hematological and biochemical parameters were usually transient, often in combination with intercurrent diseases, and were not associated with rhGH. In long-term safety, there was no association between rhGH therapy and the risk of cancer, cardiac, and cerebrovascular diseases. Still, three children (3.26 %) had type 2 diabetes, with overweight in one case and obesity in two. Conclusions. In general, in the short-term context, rhGH therapy for children with GHD is safe. The pain at the injection site is a clinically significant AE as a cognitive emotional barrier to the adherence to rhGH therapy. From the point of view of the long-term safety of rhGH therapy, the fact that type 2 diabetes was detected in 3 (3.26 %) children with increased body weight and obesity is essential.
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