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患者自控镇痛联合昂丹司琼或昂丹司琼加氯丙嗪用于控制腹部手术患者的疼痛及恶心呕吐。

Patient-controlled analgesia combined with either ondansetron or ondansetron plus prochlorperazine for control of pain and nausea and vomiting in patients undergoing abdominal surgery.

作者信息

Jellish W Scott, Owen Kevin, Fluder Elaine, Sawicki Kristina, Sinacore James

机构信息

Department of Anesthesiology, Loyola University Medical Center, Maywood, IL 60153, USA.

出版信息

J Clin Anesth. 2008 Dec;20(8):594-600. doi: 10.1016/j.jclinane.2008.06.008.

Abstract

STUDY OBJECTIVE

To compare ondansetron with ondansetron plus prochlorperazine, added to a patient-controlled analgesia (PCA) solution for control of postoperative nausea and vomiting (PONV).

DESIGN

Prospective, randomized, double-blinded study.

SETTING

University hospital.

PATIENTS

150 ASA physical status I, II, and III patients undergoing abdominal surgery.

INTERVENTIONS

Patients were given a PCA morphine solution containing either 30 mg of ondansetron (Group O), 30 mg of ondansetron plus 20 mg of prochlorperazine (Group OP), or no antiemetic (Group C; control group).

MEASUREMENTS

Demographic data were recorded, along with anesthetic and surgical time, total fluid intake, frequency of Postanesthesia Care Unit (PACU) PONV, discharge time and length of stay, frequency of PONV while on the hospital floor, highest nausea scores, total PCA morphine use, and PCA utilization times.

MAIN RESULTS

Demographic and intraoperative variables were similar in all groups. In the first 24 hours after surgery, nausea was higher in Group C than Group OP. Emesis in Group C was twice that of either Group O or Group OP. No differences were noted between groups in PACU PONV. Patients receiving ondansetron plus prochlorperazine when on the hospital floor had a lower frequency of nausea, while patients receiving ondansetron alone had a lower frequency of vomiting than did the control group. The adjusted odds of vomiting doubled for every 12 hours for Group C patients when receiving PCA.

CONCLUSIONS

Combination antiemetics added to PCA reduced emetic symptoms after abdominal surgery.

摘要

研究目的

比较昂丹司琼与昂丹司琼联合异丙嗪添加到患者自控镇痛(PCA)溶液中用于控制术后恶心呕吐(PONV)的效果。

设计

前瞻性、随机、双盲研究。

地点

大学医院。

患者

150例美国麻醉医师协会(ASA)身体状况为I、II和III级的接受腹部手术的患者。

干预措施

给予患者含30毫克昂丹司琼的PCA吗啡溶液(O组)、30毫克昂丹司琼加20毫克异丙嗪的PCA吗啡溶液(OP组)或不含止吐药的PCA吗啡溶液(C组;对照组)。

测量指标

记录人口统计学数据,以及麻醉和手术时间、总液体摄入量、麻醉后护理单元(PACU)发生PONV的频率、出院时间和住院时间、在病房时PONV的频率、最高恶心评分、PCA吗啡的总用量以及PCA使用时间。

主要结果

所有组的人口统计学和术中变量相似。术后头24小时内,C组的恶心程度高于OP组。C组的呕吐发生率是O组或OP组的两倍。各组在PACU发生PONV的情况无差异。在病房时接受昂丹司琼联合异丙嗪的患者恶心发生率较低,而单独接受昂丹司琼的患者呕吐发生率低于对照组。C组患者接受PCA时,每12小时呕吐的调整比值增加一倍。

结论

PCA中添加联合止吐药可减轻腹部手术后的呕吐症状。

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