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4%艾考糊精溶液对哈特曼氏回纳术中粘连松解手术时间的影响:一项试点、多中心、随机对照试验(与乳酸林格氏液对比)

The effect of 4% icodextrin solution on adhesiolysis surgery time at the Hartmann's reversal: a pilot, multicentre, randomized control trial vs lactated Ringer's solution.

作者信息

Kössi J, Grönlund S, Uotila-Nieminen M, Crowe A, Knight A, Keränen U

机构信息

Department of Surgery, Päijät-Häme Central Hospital, Lahti, Finland.

出版信息

Colorectal Dis. 2009 Feb;11(2):168-72. doi: 10.1111/j.1463-1318.2008.01562.x. Epub 2008 May 3.

Abstract

OBJECTIVE

A pilot randomized controlled clinical multicentre trail was established to compare intraperitoneal 4% icodextrin (ID) solution with lactated Ringer's solution (LRS) on adhesion formation after Hartmann's procedure. The adhesiolysis surgery time during Hartman's reversal was used as a marker of the severity of adhesions.

METHOD

Patients scheduled for Hartmann's resection were randomized at surgery to either of the two study solutions used as an irrigant during the operation and instilled (1000 ml) at the end of surgery. During the reversal procedure, the time for small bowel adhesiolysis was recorded.

RESULTS

On completion of 17 eligible patients, an interim analysis was performed. There were no complications following the use of 4% ID solution. The mean (SD) total adhesiolysis times in patients treated with 4% ID solution and LRS were 30.8 (18.0) min and 47.6 (45.7) min, respectively. The mean reduction of 16.8 min, although greater than expected, was not statistically significant (P = 0.33) because of the large variance in adhesiolysis times. Further statistical analysis showed that to achieve significance for the observed differences and variance, a minimum of 240 patients in each group would be required.

CONCLUSION

Icodextrin treatment resulted in a decreasing trend in adhesiolysis time. The use of 4% ID solution in peritonitis patients seemed to be safe. Because of larger than expected variations in adhesiolysis times, this pilot study was underpowered to meet the study end-point and further statistical modelling estimated that significance cannot be reached within a reasonable time scale. Other models should be used to evaluate the efficacy of anti-adhesive agents.

摘要

目的

开展一项多中心随机对照临床试验试点,比较腹腔内注入4%艾考糊精(ID)溶液与乳酸林格氏液(LRS)对哈特曼手术(Hartmann's procedure)后粘连形成的影响。将哈特曼回纳术中粘连松解手术时间作为粘连严重程度的指标。

方法

计划接受哈特曼切除术的患者在手术时随机分为两组,术中使用两种研究溶液之一作为灌洗液,并在手术结束时注入(1000毫升)。在回纳手术过程中,记录小肠粘连松解时间。

结果

在17例符合条件的患者完成试验后,进行了中期分析。使用4%ID溶液后未出现并发症。接受4%ID溶液和LRS治疗的患者平均(标准差)总粘连松解时间分别为30.8(18.0)分钟和47.6(45.7)分钟。平均减少16.8分钟,尽管大于预期,但由于粘连松解时间差异较大,差异无统计学意义(P = 0.33)。进一步的统计分析表明,为使观察到的差异和方差具有统计学意义,每组至少需要240例患者。

结论

艾考糊精治疗使粘连松解时间呈下降趋势。在腹膜炎患者中使用4%ID溶液似乎是安全的。由于粘连松解时间的差异大于预期,该试点研究的效能不足以达到研究终点,进一步的统计模型估计在合理的时间范围内无法达到显著性。应使用其他模型来评估抗粘连剂的疗效。

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