Ten year analysis of the clinic profile of the tertiary paediatric endocrine service in Western Australia

Nadya Birdus, M. Grant, P. Stevenson, C. Choong, A. Siafarikas
{"title":"Ten year analysis of the clinic profile of the tertiary paediatric endocrine service in Western Australia","authors":"Nadya Birdus, M. Grant, P. Stevenson, C. Choong, A. Siafarikas","doi":"10.1515/jpem-2022-0055","DOIUrl":null,"url":null,"abstract":"Abstract Objectives There is a paucity of information regarding the profile of entire paediatric endocrine clinics and how they are changing. This study aimed to analyse the clinic profile of the Western Australian tertiary paediatric endocrine outpatient service over 10 years and compare to national and international data. Methods Retrospective analysis of the Western Australian Paediatric Endocrine Database (WAPED) between 2007 and 2017 looking at the frequency, proportion and longitudinal change of diagnosis categories, specific diagnoses, and gender breakdown. Results In total, 2,791 endocrine diagnoses were recorded for 2,312 patients. The most frequent reason for referral (22.1% of patients), was for evaluation of abnormalities in thyroid function. The most common diagnosis being hypothyroidism (76.7%). Evaluation of short stature was the reason for referral in 19.2% of patients, 14.6% of whom were diagnosed with growth hormone deficiency. Evaluation of puberty disorders, syndromes with endocrine features and disorders of calcium and phosphate metabolism were other common reasons for clinic referral, seen in 11.3, 9.8 and 8.2% of patients respectively. Between 2007 and 2017, the odds ratio of a thyroid diagnosis increased by 1.07 per year (95% CI: 1.02–1.12), whilst the odds ratio of a short stature diagnosis decreased by 0.91 per year (95% CI: 0.87–0.95). Conclusions The profile of the WAPED is similar to previously published national and international data. The analysis of the profile of diagnoses and its longitudinal change over a ten-year period offer a unique opportunity to guide clinic planning, resource allocation and future research.","PeriodicalId":16746,"journal":{"name":"Journal of Pediatric Endocrinology and Metabolism","volume":"72 1","pages":"785 - 794"},"PeriodicalIF":0.0000,"publicationDate":"2022-05-05","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Pediatric Endocrinology and Metabolism","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1515/jpem-2022-0055","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

Abstract

Abstract Objectives There is a paucity of information regarding the profile of entire paediatric endocrine clinics and how they are changing. This study aimed to analyse the clinic profile of the Western Australian tertiary paediatric endocrine outpatient service over 10 years and compare to national and international data. Methods Retrospective analysis of the Western Australian Paediatric Endocrine Database (WAPED) between 2007 and 2017 looking at the frequency, proportion and longitudinal change of diagnosis categories, specific diagnoses, and gender breakdown. Results In total, 2,791 endocrine diagnoses were recorded for 2,312 patients. The most frequent reason for referral (22.1% of patients), was for evaluation of abnormalities in thyroid function. The most common diagnosis being hypothyroidism (76.7%). Evaluation of short stature was the reason for referral in 19.2% of patients, 14.6% of whom were diagnosed with growth hormone deficiency. Evaluation of puberty disorders, syndromes with endocrine features and disorders of calcium and phosphate metabolism were other common reasons for clinic referral, seen in 11.3, 9.8 and 8.2% of patients respectively. Between 2007 and 2017, the odds ratio of a thyroid diagnosis increased by 1.07 per year (95% CI: 1.02–1.12), whilst the odds ratio of a short stature diagnosis decreased by 0.91 per year (95% CI: 0.87–0.95). Conclusions The profile of the WAPED is similar to previously published national and international data. The analysis of the profile of diagnoses and its longitudinal change over a ten-year period offer a unique opportunity to guide clinic planning, resource allocation and future research.
查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
西澳大利亚州三级儿科内分泌服务的十年临床分析
摘要目的关于整个儿科内分泌诊所的概况及其变化的信息缺乏。本研究旨在分析西澳大利亚州三级儿科内分泌门诊服务10年来的临床概况,并与国内和国际数据进行比较。方法回顾性分析2007年至2017年西澳大利亚儿科内分泌数据库(wape)的诊断类别、具体诊断和性别细分的频率、比例和纵向变化。结果2312例患者共记录内分泌诊断2791例。最常见的转诊原因(22.1%的患者)是甲状腺功能异常的评估。最常见的诊断是甲状腺功能减退(76.7%)。19.2%的患者因身材矮小而转诊,其中14.6%的患者被诊断为生长激素缺乏症。评估青春期障碍、内分泌特征综合征和钙磷酸盐代谢障碍是其他常见的临床转诊原因,分别占11.3、9.8和8.2%。2007年至2017年间,甲状腺诊断的优势比每年增加1.07 (95% CI: 1.02-1.12),而身材矮小诊断的优势比每年下降0.91 (95% CI: 0.87-0.95)。结论:wape的概况与以前发表的国家和国际数据相似。对十年来诊断概况及其纵向变化的分析为指导临床计划、资源分配和未来研究提供了独特的机会。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 去求助
来源期刊
自引率
0.00%
发文量
0
期刊最新文献
A rare case of skeletal dysplasia: biallelic variant in ACAN gene. Premature ovarian insufficiency in pediatric cancer patients: a 10 year Rady Children's hospital experience. Mineralocorticoid receptor antagonist monotherapy in pediatric non-classical 11β-hydroxylase deficiency. Estrogen-insensitivity syndrome (EIS) in a female adolescent patient - a case report. Alterations in optical coherence tomography and optical coherence tomography angiography findings in children with partial biotinidase deficiency.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1