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首页> 外文期刊>World Journal of Surgery: Official Journal of the Societe Internationale de Chirurgie, Collegium Internationale Chirurgiae Digestivae, and of the International Association of Endocrine Surgeons >Clinical benefits after the implementation of a protocol of restricted perioperative intravenous crystalloid fluids in major abdominal operations.
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Clinical benefits after the implementation of a protocol of restricted perioperative intravenous crystalloid fluids in major abdominal operations.

机译:在大型腹部手术中实施围手术期限制性静脉注射晶体液方案后的临床益处。

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BACKGROUND: Perioperative fluid replacement is a challenging issue in surgical care. The purpose of the present study was to investigate the effect of two different perioperative hydration protocols on the outcome in patients undergoing major abdominal operations. METHODS: This was a prospective study involving 61 patients (42 men/19 women; mean age: 52 years; age range: 18-81 years) who underwent major abdominal operations. The study had two distinct phases: before (conventional group; administered 30-50 ml/kg per day of crystalloid fluids; n = 33) and after the implementation of a protocol of restricted use of intravenous fluids (restricted group; administered less than 30 ml/kg per day of crystalloid fluids; n = 28). The total volume of intravenous crystalloid fluids infused was recorded until postoperative day (POD) 4. Morbidity, mortality, and the length of postoperative hospital stay were the main clinical variables. RESULTS: Mortality was 4.9% (p > 0.05 between groups). Intravenous therapy in the restricted group was terminated earlier (p < 0.001) and the patients received 2.4 l less crystalloid fluid than did those in the conventional group from POD 1 through POD 4 (p < 0.001). The adoption of the restricted protocol shortened the postoperative hospital stay by 2 days (p = 0.02) and diminished the morbidity by 25% (p = 0.04). CONCLUSIONS: Restriction of perioperative intravenous crystalloid fluid is associated with reductions in morbidity and length of postoperative hospital stay after major abdominal operations.
机译:背景:围手术期补液是外科护理中一个具有挑战性的问题。本研究的目的是研究两种不同的围手术期水化方案对进行大腹部手术的患者预后的影响。方法:这是一项前瞻性研究,涉及61例行大腹部手术的患者(42例男性/ 19例女性;平均年龄:52岁;年龄范围:18-81岁)。该研究分为两个不同的阶段:之前(常规组;每天服用30-50 ml / kg的晶体液; n = 33);以及在实施了限制使用静脉液的规程之后(受限组;给药量少于30每天每毫升晶体液ml / kg; n = 28)。直到术后第4天才记录静脉注射的晶体液的总体积。发病率,死亡率和术后住院时间是主要的临床变量。结果:死亡率为4.9%(两组间p> 0.05)。限制组的静脉治疗提前终止(p <0.001),并且从POD 1到POD 4的患者比常规组的患者接受的晶体液少2.4 l(p <0.001)。采用限制方案可将术后住院时间缩短2天(p = 0.02),并将发病率降低25%(p = 0.04)。结论:围手术期静脉内晶体液的限制与腹部大手术后发病率的降低和术后住院时间的缩短有关。

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