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[一组身材矮小变异儿童中三种身高预测方法的准确性]

[Accuracy of three methods of height prediction in a group of variant short stature children].

作者信息

Bueno Lozano G, Ruibal Francisco J L, Reverte Blanc F, Casado de Frías E

机构信息

Departamento de Pediatría, Hospital Universitario San Carlos, Universidad Complutense, Madrid.

出版信息

An Esp Pediatr. 1998 Jul;49(1):27-32.

PMID:9718763
Abstract

OBJECTIVE

The objective of this study was to determine how accurately three methods of height prediction estimate adult height in a group of 27 boys and 16 girls with untreated short stature who have reached adult height. Twenty of the patients were considered to have familial short stature, 8 constitutional delay of growth and puberty, 12 a combination of both conditions and 3 idiopathic short stature.

PATIENTS AND METHODS

Height predictions at various chronological ages were retrospectively compared to final adult height according to the Tanner-Whitehouse Mark I, Bayley-Pinneau and Roche-Wainer-Thisen methods. Heights were expressed as centimeters and standard deviation scores (SDS) and related to Tanner standardized curves.

RESULTS

The final heights reached were significantly below the target height [-2.0 (0.5) SDS versus -1.6 (0.6), p < 0.01]. The three methods over-estimated adult height. The Bayley-Pinneau method was especially accurate in girls and in familial short stature. The Tanner and Bayley-Pinneau predictions were similar in constitutional delay of growth and puberty. The Roche method gave the greatest errors in all groups.

CONCLUSIONS

  1. Thee groups of normal variant short stature patients reached an adult height in the lower normal range. 2) The three method of height prediction over-estimated final height. 3) As in some pathological conditions, the Bayley-Pinneau was the most reliable method of height prediction in children with short stature. 4) These children may be considered as a historical group to evaluate the effect of growth-promoting therapies.
摘要

目的

本研究的目的是确定三种身高预测方法在一组27名男孩和16名已达到成人身高的未经治疗的身材矮小的女孩中对成人身高的估计准确性。其中20名患者被认为患有家族性身材矮小,8名生长和青春期体质性延迟,12名两者兼而有之,3名特发性身材矮小。

患者与方法

根据坦纳-怀特豪斯I型、贝利-皮诺和罗氏-韦纳-西森方法,回顾性比较不同实足年龄时的身高预测值与最终成人身高。身高以厘米和标准差分数(SDS)表示,并与坦纳标准化曲线相关。

结果

最终达到 heights were significantly below the target height [-2.0 (0.5) SDS versus -1.6 (0.6), p < 0.01]。这三种方法高估了成人身高。贝利-皮诺方法在女孩和家族性身材矮小患者中尤其准确。在生长和青春期体质性延迟患者中,坦纳和贝利-皮诺预测值相似。罗氏方法在所有组中误差最大。

结论

1)三组正常变异型身材矮小患者的成人身高处于正常范围下限。2)三种身高预测方法高估了最终身高。3)与某些病理情况一样,贝利-皮诺方法是身材矮小儿童中最可靠的身高预测方法。4)这些儿童可被视为一个历史组,以评估生长促进疗法的效果。

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