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加巴喷丁预防导管相关性膀胱不适疗效的评估:一项前瞻性、随机、安慰剂对照、双盲研究。

An evaluation of the efficacy of gabapentin for prevention of catheter-related bladder discomfort: a prospective, randomized, placebo-controlled, double-blind study.

作者信息

Agarwal Anil, Dhiraaj Sanjay, Pawar Sandeep, Kapoor Rakesh, Gupta Devendra, Singh Prabhat K

机构信息

Department of Anesthesia, Sanjay Gandhi Post Graduate Institute of Medical Sciences, Lucknow, India.

出版信息

Anesth Analg. 2007 Nov;105(5):1454-7, table of contents. doi: 10.1213/01.ane.0000281154.03887.2b.

DOI:10.1213/01.ane.0000281154.03887.2b
PMID:17959982
Abstract

BACKGROUND

Catheter-related bladder discomfort (CRBD) secondary to catheterization of urinary bladder is distressing. In the present study, we evaluated gabapentin for preventing CRBD.

METHODS

One-hundred and eight consecutive adult patients, ASA physical status I and II, of either sex, undergoing elective percutaneous nephrolithotomy were randomized into two groups of 54 each. Group control: placebo and group G gabapentin: gabapentin 600 mg. Drugs were administered orally 1 h before surgery. After induction of anesthesia, patients were catheterized with a 16F Foley catheter and the balloon was inflated with 10 mL normal saline. In the postanesthesia care unit, the incidence and severity (mild, moderate, and severe) of CRBD were assessed on arrival (0) and at 1, 2, and 6 h.

RESULTS

Gabapentin reduced the incidence of CRBD to 50% (27 of 54) compared with 80% (43 of 54) observed in the control group (P < 0.05). Gabapentin also reduced the severity of CRBD and postoperative pain as observed by a reduction in the number of patients requiring any fentanyl and the total fentanyl consumption postoperatively (P < 0.05).

CONCLUSION

Gabapentin (600 mg) administered orally 1 h before surgery reduced the incidence and severity of CRBD, postoperative pain, number of patients requiring fentanyl and postoperative total fentanyl requirement.

摘要

背景

膀胱插管继发的导管相关膀胱不适(CRBD)令人痛苦。在本研究中,我们评估了加巴喷丁预防CRBD的效果。

方法

108例连续接受择期经皮肾镜取石术的成年患者,ASA身体状况分级为I级和II级,性别不限,随机分为两组,每组54例。对照组:安慰剂;G组:加巴喷丁600mg。术前1小时口服给药。麻醉诱导后,用16F Foley导管为患者插管,气囊用10mL生理盐水充盈。在麻醉后护理单元,在患者到达时(0小时)以及术后1、2和6小时评估CRBD的发生率和严重程度(轻度、中度和重度)。

结果

加巴喷丁组CRBD的发生率降至50%(54例中的27例),而对照组为80%(54例中的43例)(P<0.05)。加巴喷丁还减轻了CRBD的严重程度和术后疼痛,表现为术后需要使用芬太尼的患者数量减少以及芬太尼总消耗量降低(P<0.05)。

结论

术前1小时口服加巴喷丁(600mg)可降低CRBD发生率和严重程度、术后疼痛、需要芬太尼的患者数量以及术后芬太尼总需求量。

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