Shoaf Susan E, Bricmont Patricia, Dandurand Ann
Otsuka Pharmaceutical Development & Commercialization, Inc., Princeton, NJ, USA.
, 2440 Research Blvd, Rockville, MD, 20850, USA.
Eur J Clin Pharmacol. 2017 Nov;73(11):1399-1408. doi: 10.1007/s00228-017-2302-7. Epub 2017 Aug 12.
Tolvaptan (TLV) is indicated to treat hyponatremia due to syndrome of inappropriate diuretic hormone (SIADH) in Europe. Treatment is to be initiated at 15 mg QD but post-approval reporting indicates increasing use of 7.5 mg as the starting dose. Physicians believe 7.5 mg is effective and has a lower incidence of overly rapid correction of serum sodium.
Single TLV doses of 3.75, 7.5, and 15 mg were administered to 14 healthy adults in a crossover design and to 29 subjects ≥18 years with SIADH and serum sodium between 120 and 133 mmol/L in a parallel-group design. Pharmacodynamics and TLV plasma concentrations were assessed for 24 h post-dose.
In SIADH subjects, corrections of serum sodium (Δ of ≥8 mmol/L in the first 8 h or ≥12 mmol/L in the first 24 h) were observed in one, one, and two subjects in the 3.75-, 7.5-, and 15-mg dose groups. Fluid balance (FB) for 0-6 h post-dose was correlated (r = 0.37) with maximum increases in serum sodium; subjects with large corrections had large (~1 L) negative FB. Compared to healthy adults, subjects with SIADH did not drink in response to their negative FB and had larger increases in serum sodium at 24 h. Median time of maximum increase in healthy adults was 6 h, with no rapid corrections, and FB was near 0 mL by 24 h.
Starting titration with 7.5 mg TLV will not eliminate the risk of rapid corrections in serum sodium. Monitoring FB may indicate that a subject is at risk for over correction.
在欧洲,托伐普坦(TLV)被用于治疗抗利尿激素分泌失调综合征(SIADH)所致的低钠血症。治疗起始剂量为15毫克每日一次,但批准后报告显示,越来越多的人开始使用7.5毫克作为起始剂量。医生认为7.5毫克有效,且血清钠过度快速纠正的发生率较低。
采用交叉设计,对14名健康成年人给予3.75、7.5和15毫克的单剂量TLV;采用平行组设计,对29名年龄≥18岁、患有SIADH且血清钠在120至133毫摩尔/升之间的受试者给予上述剂量。给药后24小时评估药效学和TLV血浆浓度。
在SIADH受试者中,3.75毫克、7.5毫克和15毫克剂量组分别有1名、1名和2名受试者的血清钠出现纠正(最初8小时内≥8毫摩尔/升或最初24小时内≥12毫摩尔/升)。给药后0至6小时的液体平衡(FB)与血清钠的最大升高值相关(r = 0.37);血清钠纠正幅度大的受试者FB为大幅负值(约1升)。与健康成年人相比,SIADH受试者不会因FB为负而饮水,且24小时时血清钠升高幅度更大。健康成年人血清钠最大升高的中位时间为6小时,无快速纠正情况,且到24小时时FB接近0毫升。
以7.5毫克TLV开始滴定不会消除血清钠快速纠正的风险。监测FB可能表明受试者存在过度纠正的风险。