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髋关节置换术后患者自控镇痛与患者自控镇痛联合持续输注的比较。

Patient-controlled analgesia versus patient-controlled analgesia plus continuous infusion after hip replacement surgery.

作者信息

Smythe M A, O'Donnell M P, Schad R F, Dmuchowski C F

机构信息

Department of Pharmacy Practice, Wayne State University, Detroit, MI 48202, USA.

出版信息

Ann Pharmacother. 1996 Mar;30(3):224-7. doi: 10.1177/106002809603000302.

Abstract

OBJECTIVE

To compare the efficacy and adverse effect profile of patient-controlled analgesia (PCA) versus PCA plus continuous infusion (PCACI) after hip replacement surgery.

DESIGN

Prospective, randomized, open pilot study.

SETTING

Large teaching institution.

PARTICIPANTS

Thirty-four patients undergoing hip replacement or revision of hip replacement surgery.

INTERVENTIONS

Patients were randomized to receive PCA morphine: 1 mg with 6-minute lockout, or PCACI, using the same dose, with a 0.5-1 mg/h continuous infusion. Pain intensity, sedation, narcotic use, injection/attempt ratio (I/A), and adverse effects were assessed.

RESULTS

No significant differences in pain intensity were identified. Morphine use was not different between groups: PCA 61.8 +/- 35.0 and PCACI 74.2 +/- 54.9 mg (p =0.394). A trend toward an increased 12-hour I/A ratio was evident in the PCACI group: PCA 0.73 +/- 0.18 and PCACI 0.86 +/- 0.17 (p =0.073). Patient-reported adverse effects, sedation, and inability to sleep secondary to pain occurred similarly. Eight of 18 PCACI patients required discontinuation of either the continuous infusion mode or of PCA therapy entirely secondary to adverse effects.

CONCLUSIONS

When compared with PCA therapy, PCACI was not associated with improved pain control and more patients receiving PCACI required discontinuation of therapy secondary to adverse effects.

摘要

目的

比较髋关节置换术后患者自控镇痛(PCA)与PCA联合持续输注(PCACI)的疗效和不良反应情况。

设计

前瞻性、随机、开放试点研究。

地点

大型教学机构。

参与者

34例行髋关节置换术或髋关节置换翻修术的患者。

干预措施

患者被随机分为两组,分别接受PCA吗啡:1mg,锁定时间6分钟;或PCACI,使用相同剂量,持续输注速度为0.5 - 1mg/h。评估疼痛强度、镇静程度、麻醉药物使用情况、注射/尝试比值(I/A)和不良反应。

结果

未发现疼痛强度有显著差异。两组间吗啡使用量无差异:PCA组为61.8±35.0mg,PCACI组为74.2±54.9mg(p = 0.394)。PCACI组12小时I/A比值有升高趋势:PCA组为0.73±0.18,PCACI组为0.86±0.17(p = 0.073)。患者报告的不良反应、镇静情况以及因疼痛导致的睡眠障碍发生率相似。18例接受PCACI治疗的患者中有8例因不良反应需要完全停止持续输注模式或PCA治疗。

结论

与PCA治疗相比,PCACI并不能改善疼痛控制,且更多接受PCACI治疗的患者因不良反应需要停止治疗。

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