Mori Takefumi, Oba Ikuko, Koizumi Kenji, Kodama Mayumi, Shimanuki Miwako, Tanno Mizuho, Chida Makiko, Saito Mai, Kiyomoto Hideyasu, Miyazaki Mariko, Ogawa Susumu, Sato Hiroshi, Ito Sadayoshi
Division of Nephrology, Endocrinology and Vascular Medicine, Tohoku University Graduate School of Medicine, Sendai, Japan.
Adv Perit Dial. 2013;29:33-7.
The V2 receptor antagonist tolvaptan has been approved for volume control in heart-failure patients in Japan. Tolvaptan increases renal blood flow, and so the present study was designed to ascertain whether tolvaptan could be a useful diuretic for volume control without reducing residual renal function (RRF) in peritoneal dialysis (PD) patients. Tolvaptan was administered in 15 PD patients (15 mg daily). Urine volume, body weight, and blood pressure were monitored Urinary excretion of urea nitrogen Na+, the osmolality of plasma and urine, and peritoneal and renal Kt/V were analyzed before and after tolvaptan treatment. In 11 of 15 patients, urine volume increased to more than 400 mL daily. A significant increase in diluted urine was observed, as indicated by a reduction in the specific gravity or osmolality of urine (or both). Urinary excretion of urea nitrogen, and Na+ was significantly increased Increases in renal Kt/V were observed, but peritoneal Kt/V was unchanged. Singnificant increase in creatinine clearance was also observed These data suggest that tolvaptan not only stimulates water diuresis, but also natriuresis, without reducing RRF in PD patients. Hence, tolvaptan could be a beneficial tool for the control of body fluid and maintenance of RRF in PD patients.
血管加压素2(V2)受体拮抗剂托伐普坦已在日本被批准用于控制心力衰竭患者的血容量。托伐普坦可增加肾血流量,因此本研究旨在确定托伐普坦是否可作为一种有效的利尿剂来控制血容量,同时又不降低腹膜透析(PD)患者的残余肾功能(RRF)。对15例PD患者给予托伐普坦(每日15毫克)。监测尿量、体重和血压。分析托伐普坦治疗前后尿素氮、钠的尿排泄量、血浆和尿液的渗透压以及腹膜和肾脏的Kt/V。15例患者中有11例尿量增加至每日超过400毫升。观察到稀释尿显著增加,表现为尿比重或渗透压(或两者)降低。尿素氮和钠的尿排泄量显著增加。观察到肾脏Kt/V增加,但腹膜Kt/V未改变。肌酐清除率也显著增加。这些数据表明,托伐普坦不仅能刺激水利尿,还能促进利钠,且不降低PD患者的RRF。因此,托伐普坦可能是控制PD患者体液和维持RRF的有益手段。