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find Keyword "镇痛效果" 3 results
  • The Study of Postoperative Patients ’ Analgesic Effects Compared of Different Routes of Administration

    目的:探讨术后镇痛安全有效的用药最佳途径。方法:将我科住院需手术治疗的90例肝胆疾病患者随机分成3组,在术后采用不同的镇痛给药途径,Ⅰ组为肌肉注射、Ⅱ组为自控硬膜外镇痛(PCEA)、Ⅲ组为微量输液泵。分别于术后6 h、24 h、48 h采用视觉模拟评分法(VAS)观察镇痛效果和不良反应等指标。 结果:Ⅱ组自控硬膜外镇痛(PCEA)和Ⅲ组微量输液泵镇痛效果明显优于Ⅰ组肌肉注射(Plt;001),Ⅱ组自控硬膜外镇痛(PCEA)组并发症多于Ⅰ组肌肉注射和Ⅲ组微量输液泵(Plt;001)。结论:3种不同镇痛给药途径用于术后患者,经临床实践研究,其最佳给药途径为微量输液泵,因易操作、安全、不良反应少、可根据疼痛的程度及时调节有效剂量,患者易接受,是一种经济实用科学的镇痛方法。

    Release date:2016-08-26 02:21 Export PDF Favorites Scan
  • 隆乳术后使用静脉自控镇痛泵的镇痛效果调查分析

    目的对静脉自控镇痛泵(PCIA)用于隆乳术后疼痛的镇痛效果进行调查分析,为更好地选用PCIA提供参考。 方法从2013年1月-11月收治的隆乳术患者中随机抽取62例患者,根据患者是否同意使用镇痛泵,将患者分为观察组及对照组,采用视觉模拟评分(VAS)方法,对观察组及对照组的镇痛效果分别进行评分。 结果观察组术后各时点VAS评分均低于对照组,差异均有统计学意义(P<0.05),观察组各时段镇痛效果均优于对照组;观察组不良反应多于对照组,两组间不良反应发生率差异无统计学意义(P>0.05)。 结论镇痛泵对隆乳术后疼痛治疗相比传统止痛方法值得临床推广。

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  • Observation of analgesic efficacy of liposomal bupivacaine for local infiltration anesthesia in unicompartmental knee arthroplasty: a prospective randomized controlled study

    ObjectiveA prospective randomized controlled study was conducted to investigate the early postoperative analgesic effectiveness of using liposomal bupivacaine (LB) for local infiltration anesthesia (LIA) in unicompartmental knee arthroplasty (UKA). Methods Between January 2024 and July 2024, a total of 80 patients with knee osteoarthritis (KOA) who met the selection criteria were enrolled in the study. Patients were randomly assigned to either the LB group or the “cocktail” group in a 1∶1 ratio using a random number table, with 40 patients in each group. Baseline characteristics, including gender, age, body mass index, operated side, Kellgren-Lawrence grade, and preoperative American Society of Anesthesiologists (ASA) classification, Western Ontario and McMaster Universities Osteoarthritis Index (WOMAC) score, and knee joint range of motion, showed no significant difference between the two groups (P>0.05). Both groups received LIA and comprehensive pain management. The surgical duration, incision length, pain-related indicators [resting and activity visual analogue scale (VAS) scores, total dosage of oral morphine, WOMAC scores], knee joint range of motion, first ambulation time after operation, length of hospital stay, and postoperative adverse events. ResultsThere was no significant difference between the two groups in surgical duration, incision length, first ambulation time after operation, length of hospital stay, total dosage of oral morphine, and pre-discharge satisfaction with surgery and WOMAC scores (P>0.05). At 4, 12, and 24 hours after operation, the resting and activity VAS scores in the “cocktail” group were lower than those in the LB group; at 60 and 72 hours postoperatively, the resting VAS scores in the LB group were lower than those in the “cocktail” group, with the activity VAS scores also being lower at 60 hours; all showing significant differences (P<0.05). There was no significant difference in the above indicators between the two groups at other time points (P>0.05). On the second postoperative day, the sleep scores of the LB group were significantly higher than those of the “cocktail” group (P<0.05), while there was no significant difference in sleep scores on the day of surgery and the first postoperative day (P>0.05). Additionally, the incidence of complications showed no significant difference between the two groups (P>0.05). ConclusionThe use of LB for LIA in UKA can provide prolonged postoperative pain relief; however, it does not demonstrate a significant advantage over the “cocktail” method in terms of short-term analgesic effects or reducing opioid consumption and early functional recovery after UKA. Nevertheless, LB may help reduce postoperative sleep disturbances, making it a recommended option for UKA patients with cardiovascular diseases and insomnia or other mental health issues.

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