Effect of tolvaptan on the prognosis of patients with hepatic ascites
Autor: | Hidemori Sakamoto, Shigeho Maenohara, Takazumi Yada, Osamu Kubozono, Seiichi Mawatari, Shuji Kanmura, Yukiko Inada, Akiko Saishoji, Takuya Hiwaki, Akio Ido, Hirofumi Uto, Yasunari Hiramine, Yasushi Imamura, Hirofumi Higashi |
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Rok vydání: | 2019 |
Předmět: |
medicine.medical_specialty
Hepatology Proportional hazards model business.industry Hazard ratio Tolvaptan Furosemide medicine.disease Gastroenterology 03 medical and health sciences chemistry.chemical_compound 0302 clinical medicine Infectious Diseases chemistry 030220 oncology & carcinogenesis Internal medicine Propensity score matching medicine Spironolactone 030211 gastroenterology & hepatology business Hyponatremia Survival rate medicine.drug |
Zdroj: | Hepatology Research. 49:765-777 |
ISSN: | 1872-034X 1386-6346 |
DOI: | 10.1111/hepr.13337 |
Popis: | AIM Despite accumulating evidence concerning the efficacy of tolvaptan in the treatment of body fluid retention or hyponatremia, the effect of tolvaptan on the prognosis of patients with hepatic ascites has not been fully investigated. METHODS A total of 628 patients with hepatic ascites who were treated with diuretics (furosemide, spironolactone, or tolvaptan) between 2007 and 2017 were enrolled and divided into two groups: those who received tolvaptan (original tolvaptan group, n = 278) and those who did not (original control group, n = 350). The cumulative survival rates between the groups were compared and the factors associated with survival in patients with hepatic ascites were identified using a Cox regression analysis. In addition, propensity score matching was applied in patients who started conventional diuretics for new-onset hepatic ascites after September 2013 (pre-matching tolvaptan group, n = 177; pre-matching control group, n = 63), and the cumulative survival rates were compared between the post-matching tolvaptan and control groups. RESULTS The survival rate was significantly higher in the tolvaptan group than the control group (P = 0.005), and tolvaptan therapy was identified as an independent factor associated with survival (hazard ratio 0.721 for death relative to control, P |
Databáze: | OpenAIRE |
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