托伐普坦长期治疗韩国常染色体显性多囊肾病。

Q3 Medicine
Electrolyte and Blood Pressure Pub Date : 2018-12-01 Epub Date: 2018-12-31 DOI:10.5049/EBP.2018.16.2.23
Ha Yeon Kim, Seung Jin Lee, Byung Ki Kim, Minah Kim, Eun Hui Bae, Seong Kwon Ma, Soo Wan Kim
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引用次数: 0

摘要

一位22岁男性患者被诊断为常染色体显性多囊肾病(ADPKD)。他接受了血管紧张素转换酶抑制剂的保守治疗。两年后,开始口服治疗,每天服用60mg托伐普坦。与高度调整后的肾脏总体积相比,自托伐普坦治疗开始以来,肾脏的年增长率从7.33%显著下降到0.66%。肝酶谱、血清钠水平和渗透压均在正常范围内。在韩国,这是第一例接受托伐普坦治疗超过1年的ADPKD患者。该病例表明,长期托伐普坦治疗对ADPKD是安全、耐受性良好和有效的。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Long-term Tolvaptan Treatment of Autosomal Dominant Polycystic Kidney Disease in Korea.

Long-term Tolvaptan Treatment of Autosomal Dominant Polycystic Kidney Disease in Korea.

Long-term Tolvaptan Treatment of Autosomal Dominant Polycystic Kidney Disease in Korea.

Long-term Tolvaptan Treatment of Autosomal Dominant Polycystic Kidney Disease in Korea.

A 22-year-old male patient was diagnosed with autosomal dominant polycystic kidney disease (ADPKD). He received conservative treatment with an angiotensin-converting enzyme inhibitor. Two years later, oral therapy, consisting of 60 mg tolvaptan per day, was initiated. Compared with height-adjusted total kidney volume, the rate of kidney growth reduced significantly from 7.33% to 0.66% annually, since commencement of the tolvaptan therapy. The liver enzyme profile and serum sodium level and osmolality were constantly within normal ranges. In Korea, this is the first reported case of a patient with ADPKD who received tolvaptan treatment for more than 1 year. This case demonstrates that long-term tolvaptan treatment appears to be safe, well tolerated, and effective for ADPKD.

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来源期刊
Electrolyte and Blood Pressure
Electrolyte and Blood Pressure Medicine-Internal Medicine
CiteScore
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