Division of Pulmonary and Critical Care Medicine, Eastern Virginia Medical School, Norfolk, Virginia 23507, USA.
Pharmacotherapy. 2013 Jan;33(1):51-5. doi: 10.1002/phar.1169.
To determine the natremic response of a single 20-mg bolus dose of conivaptan, an arginine vasopressin antagonist, in hyponatremic neurosurgical patients with the syndrome of inappropriate antidiuretic hormone secretion (SIADH).
Retrospective medical record review.
Neurosurgical intensive care unit of a tertiary care referral hospital.
Thirty-two hyponatremic patients with SIADH who were admitted to the neurosurgical intensive care unit and received a single 20-mg bolus dose of conivaptan between January and December 2011.
Each patient's natremic response over 48 hours was determined. The primary end point was an increase in serum sodium level of 4 mEq/L or greater over the first 24 hours. The mean ± SD baseline serum sodium level was 129.8 ± 3.4 mEq/L, which increased to 133.1 ± 3.2 mEq/L at 6 hours after administration of the bolus dose of conivaptan. The serum sodium level at 24 hours was 134.2 ± 3.2 mEq/L, indicating a 24-hour natremic response of 4.3 ± 2.6 mEq/L (range 1-13 mEq/L) from baseline (p<0.001). Eighteen patients (56%) met the primary end point. The mean ± SD fluid balance over the first 24 hours was -783 ± 440 ml. The mean ± SD change in serum sodium level from 24 to 48 hours was 0.5 ± 1.3 mEq/L. No adverse effects or injection-site reactions were noted. The patients who failed to reach the primary end point were treated with repeated doses of conivaptan plus other agents.
We recommend a single 20-mg dose of conivaptan as the preferred initial approach to treating patients with SIADH who are in the neurosurgical intensive care unit. The 24-hour natremic response should then dictate whether additional doses of conivaptan or other therapeutic interventions are required. We believe that such an approach is safe and will result in a controlled and predictable increase in the serum sodium concentration.
确定 20mg 单剂量盐酸可替洛肽(一种血管加压素拮抗剂)对伴有抗利尿激素分泌不当综合征(SIADH)的低钠血症神经外科患者的血钠反应。
回顾性病历分析。
三级转诊医院神经外科重症监护病房。
2011 年 1 月至 12 月期间入住神经外科重症监护病房并接受 20mg 单剂量盐酸可替洛肽治疗的 32 例伴有 SIADH 的低钠血症患者。
确定每位患者在 48 小时内的血钠反应。主要终点是 24 小时内血清钠水平升高 4mEq/L 或以上。平均±SD 基线血清钠水平为 129.8±3.4mEq/L,在给予盐酸可替洛肽推注后 6 小时增加至 133.1±3.2mEq/L。24 小时血清钠水平为 134.2±3.2mEq/L,表明从基线开始 24 小时血钠反应为 4.3±2.6mEq/L(范围 1-13mEq/L)(p<0.001)。18 名患者(56%)达到主要终点。24 小时内的平均±SD 液体平衡为-783±440ml。24 至 48 小时血清钠水平的平均±SD 变化为 0.5±1.3mEq/L。未观察到不良反应或注射部位反应。未达到主要终点的患者接受了盐酸可替洛肽重复剂量加其他药物治疗。
我们建议对神经外科重症监护病房中伴有 SIADH 的患者,采用单剂量 20mg 盐酸可替洛肽作为首选初始治疗方法。然后,24 小时的血钠反应应决定是否需要额外剂量的盐酸可替洛肽或其他治疗干预。我们相信,这种方法是安全的,并且会导致血清钠浓度的受控和可预测增加。