期刊文献+

生长激素治疗儿童特发性矮小症疗效分析 被引量:17

Growth Hormone on Children with Idiopathic Short Stature
下载PDF
导出
摘要 目的:探讨生长激素治疗儿童特发性矮小症(ISS)对成年终身高的改善情况。方法:回顾性分析已确诊为ISS并使用生长激素治疗,且目前已达到成年终身高的86例患儿,其中男50例,女36例。根据用药时间分为长疗程组(≥1年) 65例和短疗程组(<1年) 21例。观察患儿身高标准差积分(HSDS)、基线身高标准差积分(BHSDS)、遗传靶身高(TH)、遗传靶身高标准差积分(THSDS)、接近成年终身高(NAH)、接近成年终身高标准差积分(NAHSDS)等指标。结果:长疗程组患儿NAHSDS大于短疗程组(P<0. 05);长疗程组患儿NAHSDS大于THSDS(P<0. 05);短疗程组患儿NAHSDS小于THSDS(P<0. 05); 75. 6%(65/86)的患儿最终身高达到正常身高,其中长疗程组中95. 2%患儿最终身高达到正常身高。结论:使用生长激素治疗ISS患儿,长疗程(≥1年)较适宜。 Objective:To probe into the improvement of growth hormone on near-adult height of children with idiopathic short stature(ISS).Methods:Retrospective analysis was performed on 86 children diagnosed with ISS and treated with growth hormone,who had reached the near-adult height,including 50 males and 36 females.According to the duration of medication,there were 65 patients in the long course group(≥1 year)and 21 patients in the short course group(<1 year).Height standard deviation scores(HSDS),baseline height standard deviation scores(BHSDS),genetic target height(TH),genetic target height standard deviation scores(THSDS),near-adult height(NAH),near-adult height standard deviation scores(NAHSDS)and other indicators of two groups were observed.Results:NAHSDS of the long course group was greater than that of the short course group(P<0.05).NAHSDS was greater than THSDS in the long course group(P<0.05).NAHSDS of short course group was less than THSDS(P<0.05).A total of 75.6%(65/86)of the children eventually reached the normal height,and 95.2%of the children in the long treatment group eventually reached the normal height.Conclusion:To set the course of treatment≥1 year in children with ISS with growth hormone therapy is suitable.
作者 陈倩 杨亭 张萱 程茜 Chen Qian;Yang Ting;Zhang Xuan;Cheng Qian(Children's Hospital of Chongqing Medical University,Chongqing Key Laboratory of Child Nutrition and Health,Ministry of Education Key Laboratory of Child Development and Disorders,China International Science and Technology Cooperation Base of Child Development and Critical Disorders,Chongqing Key Laboratory of Pediatrics,Chongqing 400014,China)
出处 《儿科药学杂志》 CAS 2019年第6期6-9,共4页 Journal of Pediatric Pharmacy
基金 重庆市卫生局科研计划面上项目 编号2013-2-054
关键词 生长激素 特发性矮小症 接近成年终身高 growth hormone idiopathic short stature near-adult height
  • 相关文献

参考文献5

二级参考文献57

  • 1中华医学会儿科学分会内分泌遗传代谢学组,王慕逖.矮身材儿童诊治指南[J].中华儿科杂志,2008(6):428-430. 被引量:487
  • 2杨美琳.国产基因重组人生长激素治疗特发性矮小患儿的疗效[J].实用儿科临床杂志,2005,20(6):521-522. 被引量:8
  • 3Rikken MB, Massa GG, Wit JM.Final height in a large cohort of Dutch patients with growth hormone deficiency treated with growth hormone.Horm Res, 1997, 48: 62-71.
  • 4Tanaka T, Cohen P, Clayton PE, et al.Diagnosis and management of growth hormone deficiency in childhood and adolescence.Part 2: Growth hormone treatment in growth hormone deficient children.Growth Horm IGF Res, 2002, 12: 323-341.
  • 5Longobardi S, Merole B, Pivonello R, et al.Reevaluation of GH secretionin 69 adults diagnosed as GH-deficient patients during childhood.J Clin Endocrinol Metab, 1996, 81: 1244-1247.
  • 6Tillmann V, Buckler JMH, Kibirige MS, et al.Biochemical test in the diagnosis of childhood growth hormone deficiency.J Clin Endocrinol Metab, 1997, 82: 531-535.
  • 7De Boer H, van der Veen EA.Editorial: why retest young adults with childhood-onset growth hormone deficiency?J Clin Endocrinol Metab, 1997, 82: 2032-2036.
  • 8Rosenfield R, Attie K, Frane J, et al.Growth hormone therapy of Turner syndrome: beneficial effect on adult final height.J Pediatr, 1998, 132: 319-324.
  • 9Care J, Mathivon L, Gendrel C, et al.Near normalization of final height with adapted doses of growth hormone in Turner syndrome.J Clin Endocrinol Metab, 1998, 83: 1462-1466.
  • 10Rosenfeld RG, Attie KM, Frane J, et al.Growth hormone therapy of Turner's syndrome: beneficial effect on adult height.J Pediatr, 1998, 132: 319-324.

共引文献115

同被引文献140

引证文献17

二级引证文献92

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部