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首页> 外文期刊>The journal of clinical endocrinology and metabolism >Safety Outcomes During Pediatric GH Therapy: Final Results From the Prospective GeNeSIS Observational Program
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Safety Outcomes During Pediatric GH Therapy: Final Results From the Prospective GeNeSIS Observational Program

机译:小儿GH治疗期间的安全性结果:前瞻性GeNeSIS观察计划的最终结果

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Context Safety concerns have been raised regarding premature mortality, diabetes, neoplasia, and cerebrovascular disease in association with GH therapy. Objective To assess incidence of key safety outcomes. Design Prospective, multinational, observational study (1999 to 2015). Setting A total of 22,311 GH-treated children from 827 investigative sites in 30 countries. Patients Children with growth disorders. Interventions GH treatment. Main outcome measures Standardized mortality ratio (SMR) and standardized incidence ratio (SIR) with 95% CIs for mortality, diabetes, and primary cancer using general population registries. Results Predominant short stature diagnoses were GH deficiency (63%), idiopathic short stature (13%), and Turner syndrome (8%), with mean ± SD follow-up of 4.2 ± 3.2 years (~92,000 person-years [PY]). Forty-two deaths occurred in patients with follow-up, with an SMR (95% CI) of 0.61 (0.44, 0.82); the SMR was elevated for patients with cancer-related organic GH deficiency [5.87 (3.21, 9.85)]. Based on 18 cases, type 2 diabetes mellitus (T2DM) risk was elevated [SIR: 3.77 (2.24, 5.96)], but 72% had risk factors. In patients without cancer history, 14 primary cancers were observed [SIR: 0.71 (0.39, 1.20)]. Second neoplasms occurred in 31 of 622 cancer survivors [5.0%; 10.7 (7.5, 15.2) cases/1000 PY] and intracranial tumor recurrences in 67 of 823 tumor survivors [8.1%; 16.9 (13.3, 21.5) cases/1000 PY]. All three hemorrhagic stroke cases had risk factors. Conclusions GeNeSIS (Genetics and Neuroendocrinology of Short Stature International Study) data support the favorable safety profile of pediatric GH treatment. Overall risk of death or primary cancer was not elevated in GH-treated children, and no hemorrhagic strokes occurred in patients without risk factors. T2DM incidence was elevated compared with the general population, but most cases had diabetes risk factors. Safety of GH therapy was assessed in a pediatric observational study. Death and primary cancer rates were not higher than in the general population; T2DM rate was higher owing to risk factors.
机译:背景与GH疗法相关的早产,糖尿病,瘤形成和脑血管疾病引起了人们对安全性的关注。目的评估关键安全结果的发生率。设计前瞻性,跨国观察研究(1999年至2015年)。在30个国家/地区的827个研究地点设置了总计22,311名接受GH治疗的儿童。患者儿童有生长障碍。干预GH治疗。主要结局指标使用一般人群登记表,死亡率,糖尿病和原发性癌症的标准化死亡率(SMR)和标准化发生率(SIR)以及95%的CI。结果主要的矮小身材诊断为生长激素缺乏症(63%),特发性矮小身材(13%)和特纳综合征(8%),平均±SD随访时间为4.2±3.2年(〜92,000人年[PY]) )。随访患者中有42例死亡,SMR(95%CI)为0.61(0.44,0.82);癌症相关的器质性GH缺乏症患者的SMR升高[5.87(3.21,9.85)]。基于18例病例,2型糖尿病(T2DM)的危险性升高[SIR:3.77(2.24,5.96)],但72%的人具有危险因素。在没有癌症病史的患者中,观察到14例原发癌[SIR:0.71(0.39,1.20)]。 622名癌症幸存者中有31名发生了第二肿瘤[5.0%; [10.7(7.5,15.2)例/ 1000 PY]和823例肿瘤幸存者中颅内肿瘤复发[8.1%; 16.9(13.3,21.5)例/ 1000 PY]。三例出血性中风病例均具有危险因素。结论GeNeSIS(国际矮身病遗传学和神经内分泌学)数据支持儿童GH治疗的良好安全性。在接受GH治疗的儿童中,死亡或原发性癌症的总体风险并未升高,并且在没有危险因素的患者中未发生出血性中风。与普通人群相比,T2DM发病率升高,但是大多数病例具有糖尿病危险因素。儿科观察性研究评估了GH治疗的安全性。死亡率和原发癌率均不高于一般人群。由于危险因素,T2DM发生率较高。

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