de Vries Friso, Lobatto Daniel J, Bakker Leontine E H, van Furth Wouter R, Biermasz Nienke R, Pereira Alberto M
Department of Medicine, Division of Endocrinology, Leiden University Medical Centre, Leiden, The Netherlands.
Center for Endocrine Tumors Leiden (CETL), Center for Pituitary Care, Leiden University Medical Center, Leiden, The Netherlands.
Endocrine. 2020 Jan;67(1):161-171. doi: 10.1007/s12020-019-02094-6. Epub 2019 Sep 25.
To assess the reliability and safety of a postsurgical evaluation strategy of adrenal function using CRH stimulation and basal cortisol concentrations after transsphenoidal pituitary surgery.
Retrospective cohort study of all patients undergoing endoscopic transsphenoidal surgery from 2010 to 2017, in whom early postoperative basal cortisol and/or CRH-stimulated cortisol secretion were available, including confirmation of adrenal function during follow-up. Patients with Cushing's disease were excluded. Optimal test performances were assessed using ROC analysis.
A total of 156 patients were included. Sensitivity and specificity of the CRH test were 78% and 90%, respectively, and 86% and 92% for basal cortisol, respectively, using an optimal cutoff of 220 nmol/L. Eight patients had false-negative test results with the CRH test (normal test but adrenal insufficient at follow-up), and six patients with basal cortisol, the majority of which had multiple pituitary hormone deficiencies and fluid imbalances. No clinical adverse events occurred in patients with false-negative test results. The diagnostic performance of a single basal cortisol measurement was superior to the CRH test.
The early postoperative basal cortisol is a safe and simple measurement to guide (dis)continuation of hydrocortisone replacement. However, disturbing factors, e.g., sodium balance disorders, contraceptives, untreated hypopituitarism, and illness impact the interpretation and in those cases this measure is unreliable. We propose an algorithm in which hydrocortisone replacement at discharge is based on basal cortisol <220 nmol/L on postoperative day 2 or 3 in a stable condition.
评估经蝶窦垂体手术后使用促肾上腺皮质激素释放激素(CRH)刺激试验和基础皮质醇浓度进行肾上腺功能术后评估策略的可靠性和安全性。
对2010年至2017年接受内镜经蝶窦手术的所有患者进行回顾性队列研究,这些患者术后早期可获得基础皮质醇和/或CRH刺激后的皮质醇分泌情况,包括随访期间肾上腺功能的确认。库欣病患者被排除。使用ROC分析评估最佳测试性能。
共纳入156例患者。CRH试验的敏感性和特异性分别为78%和90%,基础皮质醇的敏感性和特异性分别为86%和92%,最佳截断值为220 nmol/L。8例患者CRH试验结果为假阴性(试验正常但随访时肾上腺功能不全),6例患者基础皮质醇试验结果为假阴性,其中大多数患者存在多种垂体激素缺乏和液体平衡失调。假阴性试验结果的患者未发生临床不良事件。单次基础皮质醇测量的诊断性能优于CRH试验。
术后早期基础皮质醇是指导氢化可的松替代治疗(停用)的安全、简单的测量方法。然而,干扰因素,如钠平衡紊乱、避孕药、未治疗的垂体功能减退和疾病会影响结果解读,在这些情况下该测量方法不可靠。我们提出一种算法,即出院时氢化可的松替代治疗基于术后第2天或第3天病情稳定时基础皮质醇<220 nmol/L。