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首页> 外文期刊>Clinical hemorheology and microcirculation >Vasopressor support vs. liberal fluid administration in deep inferior epigastric perforator (DIEP) free flap breast reconstruction – a randomized controlled trial
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Vasopressor support vs. liberal fluid administration in deep inferior epigastric perforator (DIEP) free flap breast reconstruction – a randomized controlled trial

机译:VasoPressor支持与自由流体管理在深劣等外延穿孔(Diep)免费襟翼乳房重建 - 随机对照试验

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BACKGROUND:Perioperatively, patients hemodynamics are modulated predominantly by intravenous fluid administration and vasoactive pharmacological support. Vasopressor agents are suspected to be detrimental on free flap survival by the cause of vasoconstriction of the pedicle with consecutive reduced overall flap perfusion and by aggravation of flap dissection. OBJECTIVE:A novel, standardized fluid restrictive perioperative hemodynamic management was assessed for its feasibility in clinical practice in free flap patients undergoing breast reconstruction. METHODS:Patients were randomized to two perioperative regimens with different fluid and vasopressor limits. The primary endpoint regarded flap survival. Secondary endpoints included surgery times, time of patient ambulation and length of hospital stay. RESULTS:There was one total flap failure with liberal fluid administration (LFA). No total or partial flap failure was noted in the fluid restrictive regimen with norepinephrine administration up to 0.04糶/kg/min (FRV). No delay regarding operation time (p=0.217), patient mobilization (p=0.550) or hospital discharge (p=0.662) was registered in the FRV study subpopulation compared to LFA. CONCLUSIONS:The results of this prospective interventional trial could not detect any negative impact of vasopressors, neither for the primary endpoint of flap survival nor for the overall patient outcome. The fear of vasopressor associated flap complications has led to a traditional liberal fluid administration, which failed to demonstrate any benefits when compared to a fluid restrictive vasopressor strategy.
机译:背景:围手术期,患者血流动力学通过静脉内流体给药和血管活性药理学载体主要调节。怀疑血管加压剂剂因椎弓根的血管收割机的自由皮瓣存活而有害,连续减少整个皮瓣灌注和襟翼分析的加重。目的:评估一种新的标准化流体限制性围手术化血液动力学管理,可用于其在接受乳房重建的自由皮瓣患者中的临床实践中的可行性。方法:患者随机与不同的流体和血管加压器极限随机分配给两个围手术期方案。主要终点被认为皮瓣存活。次要终点包括手术时间,患者手臂的时间和住院时间的时间。结果:具有自由液施用(LFA)的总皮瓣失效。在流体限制性方案中没有全面或部分皮瓣衰竭,Norepinephrine施用高达0.04×kg / min(FRV)。无延迟有关操作时间(P = 0.217),与LFA相比,在FRV研究亚ppopulation中登记患者动员(P = 0.550)或医院放电(P = 0.662)。结论:这一前瞻性介入试验的结果无法检测到血管加药物的任何负面影响,既不是皮瓣存活的主要终点,也没有针对整体患者结果。对血管加压器相关的皮瓣并发症的恐惧导致了传统的自由流体给药,这与流体限制性血管加压液策略相比,未能证明任何益处。

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