Tanaka Toshiki, Minatoguchi Shingo, Yamada Yoshihisa, Kanamori Hiromitsu, Kawasaki Masanori, Nishigaki Kazuhiko, Minatoguchi Shinya
Department of Cardiology, Gifu University Graduate School of Medicine Gifu Japan.
Gifu Municipal Hospital Gifu Japan.
Circ Rep. 2018 Dec 12;1(1):35-41. doi: 10.1253/circrep.CR-18-0002.
Given that residual congestion is a predictor of poor outcome in patients with heart failure (HF), a therapeutic strategy for decongestion is required. Eighteen HF patients with fluid retention despite oral furosemide >20 mg/day, with chronic kidney disease (CKD; estimated glomerular filtration rate [eGFR], <59 mL/min/1.73 m) were enrolled. Patients were randomized into 2 groups: a tolvaptan group (tolvaptan, 7.5 mg/day, n=10) and a furosemide group (additional furosemide 20 mg/day, n=8), and followed up for 7 days. The urine volume significantly increased on day 3 in the tolvaptan group but not in the furosemide group. The body weight significantly decreased in the tolvaptan compared with the furosemide group on days 3 and 5. Although there was no difference in serum creatinine or eGFR in the 7 days between the 2 groups, serum cystatin C significantly decreased on day 7 in the tolvaptan group compared with the furosemide group. The residual congestion was more improved in the tolvaptan group than in the furosemide group. Adding tolvaptan but not furosemide significantly increased urine volume, decreased body weight and improved residual congestion without affecting the renal function or electrolytes in patients with HF with CKD under furosemide treatment.
鉴于残余充血是心力衰竭(HF)患者预后不良的预测指标,因此需要一种减轻充血的治疗策略。纳入了18例尽管口服呋塞米剂量>20mg/天仍有液体潴留且患有慢性肾脏病(CKD;估计肾小球滤过率[eGFR]<59mL/min/1.73m²)的HF患者。患者被随机分为两组:托伐普坦组(托伐普坦,7.5mg/天,n=10)和呋塞米组(额外给予呋塞米20mg/天,n=8),并随访7天。托伐普坦组在第3天尿量显著增加,而呋塞米组未增加。在第3天和第5天,托伐普坦组的体重相比呋塞米组显著下降。虽然两组在7天内血清肌酐或eGFR无差异,但与呋塞米组相比,托伐普坦组在第7天血清胱抑素C显著下降。托伐普坦组的残余充血情况比呋塞米组改善更明显。在接受呋塞米治疗的CKD合并HF患者中,加用托伐普坦而非呋塞米可显著增加尿量、降低体重并改善残余充血,且不影响肾功能或电解质。