Department of Nephrology and Hypertension, Rabin Medical Center, Petah-Tikva, and the Sackler School of Medicine, Tel Aviv University, Tel-Aviv, Israel.
Am J Kidney Dis. 2010 Aug;56(2):325-37. doi: 10.1053/j.ajkd.2010.01.013. Epub 2010 Jun 9.
In patients with euvolemic and hypervolemic hyponatremia, the effect of vasopressin antagonists is yet undefined.
Systematic review and meta-analysis of randomized controlled trials (RCTs).
SETTING & POPULATION: In- and outpatients with euvolemic or hypervolemic hyponatremia.
We included all RCTs regardless of publication status or language.
Vasopressin antagonists with or without fluid restriction versus placebo or no treatment with or without fluid restriction.
Response rate defined as normalization of serum sodium level or significant increase in serum sodium level at 3-7 days (primary) and later, change from baseline serum sodium level at 3-7 days and later, adverse events, rate of rapid sodium level correction, and rate of hypernatremia.
15 RCTs were identified. Vasopressin antagonist treatment significantly increased response rate both early (RR, 3.15; 95% CI, 2.27-4.37; 11 trials) and late (RR, 2.27; 95% CI, 1.79-2.89; 4 trials). Response rates were high in trials assessing mostly euvolemic patients and those assessing mostly hypervolemic patients, with greater effect estimate in the former. Change from baseline serum sodium level was significantly increased both early (weighted mean difference, 5.27 mEq/L; 95% CI, 4.27-6.26, 13 trials) and late (weighted mean difference, 3.49 mEq/L; 95% CI, 2.56-4.41, 8 trials). Although there was an increased rate of rapid sodium correction (RR, 2.52; 95% CI, 1.26-5.08, 8 trials) with vasopressin antagonists, hypernatremia rates were not significantly higher (RR, 2.21; 95% CI, 0.61-7.96; 5 trials), adverse events were not increased, and there were no reports of osmotic demyelination syndrome.
Significant heterogeneity in the primary outcome.
Vasopressin antagonists are effective for the treatment of hypervolemic and euvolemic hyponatremia.
在血容量正常和血容量过多性低钠血症患者中,血管加压素拮抗剂的作用尚不清楚。
系统评价和随机对照试验(RCT)的荟萃分析。
血容量正常或血容量过多性低钠血症的门诊和住院患者。
我们纳入了所有 RCT,无论其发表状态或语言如何。
血管加压素拮抗剂联合或不联合液体限制与安慰剂或不治疗联合或不联合液体限制。
以血清钠水平正常或血清钠水平在 3-7 天内显著升高(主要)和以后为定义的反应率,3-7 天内和以后的血清钠水平从基线的变化,不良事件,血清钠水平快速纠正的速度,以及高钠血症的速度。
确定了 15 项 RCT。血管加压素拮抗剂治疗在早期(RR,3.15;95%CI,2.27-4.37;11 项试验)和晚期(RR,2.27;95%CI,1.79-2.89;4 项试验)均显著提高了反应率。在评估大多数血容量正常患者和大多数血容量过多患者的试验中,反应率较高,前者的估计效果更大。早期(加权均数差,5.27mEq/L;95%CI,4.27-6.26,13 项试验)和晚期(加权均数差,3.49mEq/L;95%CI,2.56-4.41,8 项试验)的血清钠水平从基线的变化均显著增加。虽然血管加压素拮抗剂治疗时快速纠正钠的速度增加(RR,2.52;95%CI,1.26-5.08,8 项试验),但高钠血症的发生率并没有显著升高(RR,2.21;95%CI,0.61-7.96;5 项试验),不良事件没有增加,也没有报告出现渗透性脱髓鞘综合征。
主要结局存在显著异质性。
血管加压素拮抗剂对治疗血容量过多和血容量正常性低钠血症有效。