Update on pubertal development in France. PROSPEL - Observational study. Preliminary feasibility study

被引:1
作者
Mazzarino, J. [1 ]
Puel, O. [2 ]
Jesuran-Perelroizen, M. [3 ]
机构
[1] Univ Bordeaux, Fac Med, 146 Rue Leo Saignat, F-33076 Bordeaux, France
[2] Cabinet Pediat, 88 Ave Pasteur, F-33600 Pessac, France
[3] Cabinet Endocrinol Pediat, 14 Rue Rempart St Etienne, F-31000 Toulouse, France
来源
ARCHIVES DE PEDIATRIE | 2019年 / 26卷 / 02期
关键词
Puberty; Feasibility; Growth and development; Secular trend; Tanner staging; Training; SECONDARY SEXUAL CHARACTERISTICS; BREAST DEVELOPMENT; PEDIATRIC RESEARCH; SECULAR TRENDS; DANISH BOYS; AGE; COPENHAGEN; MENARCHE; PATTERN; HEALTH;
D O I
10.1016/j.arcped.2018.11.009
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
Introduction: Recent publications report a decrease in the age of onset of pubertal changes in the United States and Europe. The PROSPEL study (PRemier Observatoire des Stades Pubertaire en Liberal) will provide the first French data on the age at which pubertal signs appear. Before considering this work at the national level, we wanted to assess its feasibility. Materials and methods: Private pediatricians and general practitioners were recruited in Bordeaux and Toulouse. Before participating in the study, they had been trained in pubertal assessment and then evaluated. Each physician completed 1-4 weeks of inclusion during which children aged 5-18 years seen in consultation were included, except children who were adopted or had a chronic condition. Pubertal stages were assessed according to Tanner's classification and using an orchidometer for testicular volume. The causes of non-realization were documented where appropriate. Inter-individual reproducibility was analyzed by a double examination for a number of children who had previously given their consent. Results: In total, 63 physicians participated in the study (35 pediatricians and 28 general practitioners). All were certified at the end of the training session. A total of 2646 children were included (1318 girls, 1328 boys) with a homogeneous age distribution. The study was carried out in 83.5% of cases. The main reason for non-realization was that physicians did not propose the study to patients who met the criteria (10.1%). Lack of time was the main reason. Inter-individual reproducibility was excellent. Discussion and conclusion: Our results attest to the good feasibility of the PROSPEL study. They allowed us to validate our methodology, the training and certification of the participating physicians, and to consider extending the study to the national level. (C) 2018 Elsevier Masson SAS. All rights reserved.
引用
收藏
页码:108 / 114
页数:7
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