Lee Jane, Hamidi Oksana, Simon Emily, Mirfakhraee Sasan
University of Texas Southwestern Medical Center, Division of Endocrinology and Metabolism, Dallas, Texas.
University of Texas Southwestern Medical Center, Division of Endocrinology and Metabolism, Dallas, Texas.
Endocr Pract. 2025 Aug;31(8):987-994. doi: 10.1016/j.eprac.2025.05.004. Epub 2025 May 13.
Diminished subjective health status and increased mortality have been reported in people with adrenal insufficiency (pwAI) receiving conventional glucocorticoid replacement therapy. Continuous subcutaneous hydrocortisone infusion (CSHI) permits individualized glucocorticoid delivery and mimics a more physiologic cortisol pattern compared with oral glucocorticoid therapy. However, data are limited regarding patient selection for CSHI, optimal dosing of CSHI, and CSHI impact on relevant clinical outcomes.
We performed a single-center, retrospective longitudinal cohort study in 33 consecutive pwAI offered a therapeutic trial of CSHI due to persistent AI symptoms.
Our cohort comprised of 33 pwAI (82% women). Nine (27.3%) had primary adrenal insufficiency, 16 (48.5%) had secondary AI, and 8 (24.2%) had glucocorticoid-induced AI. The median total daily dose of glucocorticoid (in hydrocortisone equivalent) decreased from 30 mg/d (range, 15-180 mg) before CSHI to 26.7 mg/d (P = .013) at CSHI initiation and 26.6 mg/d (P = .023) at last encounter. The median number of ED visits/year due to adrenal crisis decreased from 0.5 (range, 0-3.4) to 0 (P = .002) and median number of hospitalization days/y decreased from 0.2 (range, 0-18) to 0 (P = .019) after switching to CSHI. There was a numerical increase in subjective health scores (SF-36 survey) following CSHI use. No significant differences were noted for change in weight, blood pressure, diabetes, cardiovascular/cerebrovascular events, total cholesterol, LDL, and/or triglyceride concentrations pre and post CSHI. At study conclusion, most patients (84.8%) remained on CSHI based on personal preference and tolerability.
CSHI is a safe and effective means of delivering individualized glucocorticoid therapy to pwAI.
据报道,接受传统糖皮质激素替代治疗的肾上腺功能不全患者(pwAI)主观健康状况下降,死亡率增加。与口服糖皮质激素治疗相比,持续皮下注射氢化可的松(CSHI)可实现个体化糖皮质激素给药,并模拟更符合生理的皮质醇模式。然而,关于CSHI的患者选择、CSHI的最佳剂量以及CSHI对相关临床结局的影响的数据有限。
我们对33例因持续性肾上腺皮质功能减退症状而接受CSHI治疗试验的连续pwAI患者进行了单中心回顾性纵向队列研究。
我们的队列包括33例pwAI患者(82%为女性)。9例(27.3%)患有原发性肾上腺功能不全,16例(48.5%)患有继发性肾上腺皮质功能减退,8例(24.2%)患有糖皮质激素诱导的肾上腺皮质功能减退。糖皮质激素的每日总剂量中位数(以氢化可的松当量计)从CSHI治疗前的30mg/d(范围为15 - 180mg)降至CSHI开始时的26.7mg/d(P = 0.013),末次随访时为26.6mg/d(P = 0.023)。转换为CSHI治疗后,每年因肾上腺危象导致的急诊就诊次数中位数从0.5次(范围为0 - 3.4次)降至0次(P = 0.002),每年住院天数中位数从0.2天(范围为0 - 18天)降至0天(P = 0.019)。使用CSHI后主观健康评分(SF - 36调查)有数值上的增加。CSHI治疗前后体重、血压、糖尿病、心血管/脑血管事件、总胆固醇、低密度脂蛋白和/或甘油三酯浓度的变化无显著差异。在研究结束时,大多数患者(84.8%)基于个人偏好和耐受性仍在接受CSHI治疗。
CSHI是一种向pwAI患者提供个体化糖皮质激素治疗的安全有效方法。