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首页> 外文期刊>Journal of clinical gastroenterology >The effects of treatment with octreotide, diuretics, or both on portal hemodynamics in nonazotemic cirrhotic patients with ascites.
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The effects of treatment with octreotide, diuretics, or both on portal hemodynamics in nonazotemic cirrhotic patients with ascites.

机译:奥曲肽,利尿剂或同时使用这两种药物对非固氮性肝硬化腹水患者门脉血流动力学的影响。

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摘要

GOALS: To evaluate the effects of diuretic treatment, octreotide, or both on portal hemodynamics in nonazotemic cirrhotic patients with ascites. BACKGROUND: Diuretics and octreotide have been associated with a decrease in portal pressure in cirrhotic patients, suggested to be mediated by plasma volume depletion and splanchnic vasoconstriction, respectively. However, liver cirrhosis is characterized by activation of the renin-angiotensin-aldosterone axis, which increases hepatic vascular resistance and is augmented or suppressed by diuretics or octreotide, respectively. STUDY: Twenty nonazotemic cirrhotic patients with ascites were treated with furosemide and spironolactone. Of them, 10 (group 1) discontinued diuretic treatment for 7 days. Thereafter for 5 days, each patient received subcutaneous octreotide, 300 microg twice per day; ten of them (group 2) received the octreotide in addition to their usual diuretic treatment. Portal and systemic hemodynamics with Doppler ultrasound and endogenous vasoactive systems were evaluated while the patients received diuretics (both groups), after discontinuation of diuretics (group 1), and after octreotide administration (both groups). RESULTS: The withdrawal of diuretics did not alter portal hemodynamics, but it impaired systemic hemodynamics and suppressed the renin-aldosterone axis. The addition of octreotide to diuretic treatment but not octreotide alone improved portal and systemic hemodynamics. In both groups the initiation of octreotide administration suppressed the renin-aldosterone axis and plasma glucagon levels. CONCLUSIONS: In nonazotemic cirrhotic patients with ascites, the combination of diuretics and octreotide improves systemic hemodynamics and inhibits the diuretic-related component of the activated renin-aldosterone axis, which in turn augments the portal hypotensive effect of diuretic-induced plasma volume depletion.
机译:目标:评估利尿剂,奥曲肽或两者对非固氮性肝硬化腹水患者门脉血流动力学的影响。背景:利尿剂和奥曲肽已与肝硬化患者门脉压力降低相关,提示分别由血浆容量减少和内脏血管收缩介导。然而,肝硬化的特征在于肾素-血管紧张素-醛固酮轴的激活,这增加了肝血管阻力,并分别由利尿剂或奥曲肽增强或抑制。研究:用速尿和螺内酯治疗20例非固氮性肝硬化腹水患者。其中,有10名(第1组)停用利尿剂治疗7天。此后5天,每位患者每天两次皮下注射奥曲肽,每次300微克。他们中的十个(第2组)除常规利尿剂治疗外还接受了奥曲肽。在患者接受利尿剂治疗(两组),停用利尿剂后(第1组)和服用奥曲肽后(两组),评估了多普勒超声和内源性血管活性系统的门脉和全身血流动力学。结果:停用利尿剂不会改变门静脉血流动力学,但会损害全身血流动力学并抑制肾素-醛固酮轴线。在利尿剂治疗中加入奥曲肽,但未单独使用奥曲肽可改善门静脉和全身血流动力学。在两组中,开始使用奥曲肽均抑制了肾素-醛固酮轴和血浆胰高血糖素的水平。结论:在非固氮型肝硬化腹水患者中,利尿剂和奥曲肽的组合可改善全身血流动力学,并抑制激活的肾素-醛固酮轴的利尿剂相关成分,进而增加利尿剂引起的血浆容量消耗的门脉降压作用。

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