Chiruvella Sunil, Donthu Balaji, Nallam Srinivasa Rao, Salla Dora Babu
Department of Anaesthesiology and Critical Care, RIMS, Kadapa, Andhra Pradesh, India.
Anesth Essays Res. 2018 Jan-Mar;12(1):103-108. doi: 10.4103/aer.AER_207_17.
Anesthesia for total abdominal hysterectomies is not only concerned with relieving pain during intraoperative period but also during the postoperative period. We compared clonidine and dexmedetomidine as an adjuvant to levobupivacaine for epidural analgesia with respect to onset and duration of sensory block, duration of analgesia, and adverse effects.
A total of 80 individuals between the age of 45 and 65 years of American Society of Anesthesiologists (ASA) physical status Classes I and II who underwent total abdominal hysterectomies were randomly allocated into two groups, comprising 40 patients in each group. Group LC received 10 ml of 0.125% levobupivacaine and 2 μg/kg of clonidine while Group LD received 10 ml of 0.125% levobupivacaine and 1 μg/kg of dexmedetomidine through the epidural catheter. Onset of analgesia, time of peak effect, duration of analgesia, cardiorespiratory parameters, side effects, and need of rescue intravenous (IV) analgesics were observed. The data analysis was carried out with Z-test and Chi-square test.
The demographic profile and ASA physical classes were comparable between the groups. Group LD had early onset, early peak effect, prolonged duration, and stable cardiorespiratory parameters when compared with Group LC. Less number of patients (42.5%) in Group LD required IV rescue analgesics when compared to Group LC (70%) and was statistically significant. The side effects' profile was also comparable.
Dexmedetomidine is a better neuraxial adjuvant compared with clonidine for providing early onset and prolonged postoperative analgesia and stable cardiorespiratory parameters.
全腹子宫切除术的麻醉不仅关乎术中止痛,还涉及术后止痛。我们比较了可乐定和右美托咪定作为左旋布比卡因硬膜外镇痛辅助药物时,在感觉阻滞起效时间和持续时间、镇痛持续时间及不良反应方面的差异。
选取80例年龄在45至65岁之间、美国麻醉医师协会(ASA)身体状况分级为I级和II级且接受全腹子宫切除术的患者,随机分为两组,每组40例。LC组通过硬膜外导管接受10毫升0.125%左旋布比卡因和2微克/千克可乐定,而LD组接受10毫升0.125%左旋布比卡因和1微克/千克右美托咪定。观察镇痛起效时间、峰值效应时间、镇痛持续时间、心肺参数、副作用以及静脉注射(IV)急救镇痛药的需求情况。数据分析采用Z检验和卡方检验。
两组间的人口统计学特征和ASA身体分级具有可比性。与LC组相比,LD组起效早、峰值效应早、持续时间延长且心肺参数稳定。与LC组(70%)相比,LD组需要静脉注射急救镇痛药的患者较少(42.5%),且具有统计学意义。副作用情况也具有可比性。
与可乐定相比,右美托咪定作为神经轴辅助药物能提供更早起效、更长时间的术后镇痛以及稳定的心肺参数。