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如今哪些人接受生长激素治疗?卡比国际生长研究执行科学委员会。

Who is treated with growth hormone today? The Executive Scientific Committee of the Kabi International Growth Study.

作者信息

Vanderschueren-Lodeweyckx M

机构信息

Department of Paediatric and Adolescent Endocrinology, University Hospital, Leuven, Belgium.

出版信息

Acta Paediatr Scand Suppl. 1990;370:107-13; discussion 114.

PMID:2260448
Abstract

The present demographic data from the Kabi International Growth Study (KIGS) database are summarized. Of the 2580 patients included, 85% have growth hormone deficiency (GHD) and 15% have other causes of growth failure. Idiopathic GHD is present in 78.5% of the patients, the remaining 21.5% have organic GHD. Isolated GHD is common in idiopathic GHD whereas multiple pituitary hormone deficiencies occur in at least 50% of the organic GHD patients. A preponderance of boys is observed in most groups of patients. Median chronological age (CA) at start of treatment is 10 years and median duration of therapy is 2.3 years. However, a wide range is observed. In most cases growth retardation is severe. In most patients with GHD height SDS for chronological age at start of therapy is at or below -3. The median difference between idiopathic and organic GHD is 1 SDS. Most patients have 6 or 7 injections of growth hormone (GH) per week. The median total weekly dose is approximately 0.5 IU/kg/week, but it is lower in older patients. It is concluded that steadily increasing numbers of patients with idiopathic and organic GHD are being treated with human GH (hGH). In addition, many patients with other growth disorders not necessarily associated with GHD receive hGH therapy. Chronological age at start of treatment still appears to be (too) high in most patients and growth retardation severe. The frequency of hGH injections has been increased to nearly daily administration. However, the total weekly dose appears to be low, especially in the older patients.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

本文总结了卡比国际生长研究(KIGS)数据库中的现有人口统计学数据。纳入的2580例患者中,85%患有生长激素缺乏症(GHD),15%有其他导致生长障碍的原因。特发性GHD患者占78.5%,其余21.5%为器质性GHD。孤立性GHD在特发性GHD中常见,而至少50%的器质性GHD患者存在多种垂体激素缺乏。大多数患者组中男孩占优势。治疗开始时的中位实足年龄(CA)为10岁,中位治疗持续时间为2.3年。然而,观察到范围很广。在大多数情况下,生长迟缓严重。大多数GHD患者治疗开始时按实足年龄计算的身高标准差评分处于或低于-3。特发性和器质性GHD之间的中位差异为1个标准差。大多数患者每周注射生长激素(GH)6或7次。每周总剂量中位数约为0.5 IU/kg/周,但老年患者较低。结论是,接受重组人生长激素(hGH)治疗的特发性和器质性GHD患者数量在稳步增加。此外,许多不一定与GHD相关的其他生长障碍患者也接受hGH治疗。大多数患者治疗开始时的实足年龄似乎仍然(过高),生长迟缓严重。hGH注射频率已增加到几乎每日给药。然而,每周总剂量似乎较低,尤其是老年患者。(摘要截选至250字)

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Acta Paediatr Scand Suppl. 1990;370:107-13; discussion 114.
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