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假性甲状旁腺功能减退症:意大利共同医疗路径的应用,实现同质化的临床诊疗方法和共同的随访。

Pseudohypoparathyroidism: application of the Italian common healthcare-pathway for a homogeneous clinical approach and a shared follow up.

机构信息

Department of Pediatric Endocrinology, Regina Margherita Children's Hospital - Health and Science City, Turin, Italy.

Department of Public Health and Pediatrics, University of Turin, Piazza Polonia 94, 10126, Torino (TO), Italy.

出版信息

Ital J Pediatr. 2021 Mar 4;47(1):48. doi: 10.1186/s13052-021-01000-z.

Abstract

BACKGROUND

Pseudohypoparathyroidism (PHP) represents a heterogeneous group of rare endocrine disorders caused by (epi) genetic abnormalities affecting the GNAS locus. It is mainly characterized by resistance to PTH and TSH, and by peculiar clinical features such as short stature, obesity, cognitive impairment, subcutaneous ossifications and brachydactyly. Delayed puberty, GHRH and calcitonin resistances have also been described. The healthcare-pathway recently proposed by the Italian Society of Pediatric Endocrinology and Diabetology (ISPED) has provided a standardized clinical approach to these conditions. The purpose of the present study was to evaluate its application in clinical practice, and to collect data for setting future specific studies.

METHODS

Through a semi-structured survey, based on the indications of the care-pathway, data on PHP clinical management were collected. The compilation of each data in the survey was read as an index of the adoption of the healthcare-pathway in clinical practice.

RESULTS

In addition to the proposing Center, 4 Centers joined the study, thus obtaining a large collection of data on 48 PHP patients. Highest rates in the completion of data were obtained for diagnostic history, auxological measurements and subcutaneous ossifications evaluation. As expected, the availability of data for the other investigated fields was lower, coming from recent research studies. More information has been obtained on hormonal resistance classically involved in PHP (PTH, TSH, GHRH and GnRH) and on cognitive impairment, while a few data has been collected on bone mineral status, calcitonin levels and glucolipid metabolism.

CONCLUSIONS

The presented data show that the ISPED healthcare-pathway could represent a valid tool both to confirm the clinical approach to PHP patients and to allow homogeneous data collection; however, it has not yet been fully adopted. The strengthening of the network among the major Italian Endocrine Centers will contribute to improve its application in clinical practice, optimizing the follow-up of these patients and increasing knowledge on PHP.

摘要

背景

假性甲状旁腺功能减退症(PHP)代表了一组由影响 GNAS 基因座的(外显子)遗传异常引起的罕见内分泌疾病。其主要特征为对 PTH 和 TSH 的抵抗,以及身材矮小、肥胖、认知障碍、皮下骨化和短指(趾)等特殊的临床特征。此外,还描述了青春期延迟、GHRH 和降钙素抵抗。意大利儿科内分泌学会(ISPED)最近提出的医疗保健路径为这些疾病提供了一种标准化的临床方法。本研究的目的是评估其在临床实践中的应用,并收集数据以进行未来的具体研究。

方法

通过基于医疗保健路径指示的半结构化调查,收集 PHP 临床管理的数据。调查中每个数据的编制都被视为医疗保健路径在临床实践中应用的指标。

结果

除了提出中心外,还有 4 个中心参与了这项研究,从而获得了 48 名 PHP 患者的大量数据。在完成数据方面,最高的是诊断史、生长测量和皮下骨化评估。正如预期的那样,其他调查领域的数据可用性较低,来自于最近的研究。获得了更多关于 PHP 中涉及的经典激素抵抗(PTH、TSH、GHRH 和 GnRH)和认知障碍的信息,而关于骨矿物质状态、降钙素水平和糖脂代谢的信息则较少。

结论

所提供的数据表明,ISPED 医疗保健路径不仅可以作为确认 PHP 患者临床方法的有效工具,还可以允许进行同质的数据收集;然而,它尚未得到充分应用。加强意大利主要内分泌中心之间的网络将有助于改善其在临床实践中的应用,优化这些患者的随访,并增加对 PHP 的了解。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0ef6/7934261/50d53181b53c/13052_2021_1000_Fig1_HTML.jpg

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