跳至主要内容
临床试验/NCT02915380
NCT02915380Unknown不适用

Pituitary Dysfunction After Aneurysmal Subarachnoid Hemorrhage

Dr. Rita Bertuetti0 个研究点目标入组 50 人开始时间: 2017年1月最近更新:
适应症

试验速览

阶段
不适用
发起方
入组人数
50
主要终点
Incidence of thyroid disfunction

研究概览

简要总结

Recently, the occurrence and potential impact of pituitary dysfunction after aSAH has gained increasing interest. Several studies have demonstrated pituitary dysfunction after SAH suggesting that pituitary dysfunction may be a contributing factor for residual symptoms after SAH. This is an observational multicentric study aimed to test the prevalence of thyroid abnormalities, other neuroendocrinological dysfunction and their influence on outcome of patients affected by aSAH.

详细描述

The incidence of aneurysmal subarachnoid hemorrhage (aSAH) varies between 6 to 10/100,000 subjects per year and it is a major cause of death and disability. The mortality rate ranges from 40 to 50%, and those who do survive SAH have high rates of functional limitations that could lead to impaired quality of life, including fatigue, depression, and loss of motivation.

Because aSAH affects patients in their most productive years of life, the disease has important social, and economic implications, and early prediction of long-term outcome is based on multiple factors including the primary injury secondary insults as well as neurorehabilitation interventions.

Recently, the occurrence and potential impact of pituitary dysfunction after aSAH has gained increasing interest. Several studies have demonstrated pituitary dysfunction after SAH suggesting that pituitary dysfunction may be a contributing factor for residual symptoms after SAH. However, questions remain about the real prevalence and impact of such dysfunction on patients' outcome both in the acute and chronic phase after these events.

In two recent metanalysis, the prevalence of total pituitary dysfunction was found with pooled frequencies of 0.31 (95% confidence interval CI: 0.22-0.43) [Can et a.] and 49.3.0% (95% CI 41.6%-56.9%) [Robba et al] during the acute phase (< 6 months from aSAH) and decreasing in the chronic phase to 0.25 (95% CI: 0.16-0.36) [Can et al.] and 25.6% (95% CI 18.0%-35.1%) [Robba et al]. However, the authors found high heterogenicity and different results between the available literature; many differences were found in the in the choice of time of pituitary function assessment and SAH, of diagnostic criteria and units of measurement used to establish the diagnosis of hypopituitarism after SAH.

Finally, it is not clear which is the hormone axis more likely to be affected after aSAH.

研究设计

研究类型
Observational
观察模型
Cohort
时间视角
Prospective

入排标准

年龄范围
18 Years 至 70 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • patients with acute aneurysmal SAH aged between 18 and 70 years of age who could be subjected to endocrine evaluation within 10 days of ictus and at follow-up.

排除标准

  • be major depression, psychiatric premorbidity, pituitary adenoma or perisellar lesion,preexisting hypopituitarism of any degree, previous hormonal substitution, patients in moribund state, pregnancy, glucocorticoid medication on admission to hospital or during treatment, prior pituitary insufficiency, and unsalvageable aSAH.

结局指标

主要结局

Incidence of thyroid disfunction

时间窗: 12 months after aSAH

Thyroid-stimulating hormone (TSH), free thyroxin (fT4), free triiodothyronine (fT3).

次要结局

  • Incidence of pituitary- sexual hormones disfunction(At 2 weeks, and at follow up at 3, 6 and 12 months.)
  • Survival(At 2 weeks, and at follow up at 3, 6 and 12 months)
  • Incidence of pituitary-adrenal axis disfunction(At 2 weeks, and at follow up at 3, 6 and 12 months.)
  • Incidence of growth hormone insufficiency(At 2 weeks, and at follow up at 3, 6 and 12 months)
  • Incidence of language disorders(At 2 weeks, and at follow up at 3, 6 and 12 months)
  • Incidence of memory disorders(At 2 weeks, and at follow up at 3, 6 and 12 months)
  • Incidence of attention disorders(At 2 weeks, and at follow up at 3, 6 and 12 months)

研究者

发起方
Dr. Rita Bertuetti
申办方类型
Other
责任方
Sponsor Investigator
主要研究者

Dr. Rita Bertuetti

Medical Doctor

Cambridge University Hospitals NHS Foundation Trust

相似试验