Hutchins Jacob, Argenta Peter, Berg Aaron, Habeck Jason, Kaizer Alexander, Geller Melissa A
Department of Anesthesiology, University of Minnesota, Minneapolis, MN, USA.
Department of Obstetrics, Gynecology and Women's Health, Minneapolis, MN, USA.
J Pain Res. 2019 Jul 4;12:2087-2094. doi: 10.2147/JPR.S193872. eCollection 2019.
To determine if a transversus abdominis plane (TAP) block with liposomal bupivacaine reduces total postoperative opioid use in the first 72 hrs following laparoscopic or robotic hysterectomy compared to port-site infiltration with 0.25% bupivacaine.
Patients received either a true TAP block procedure with 266 mg liposomal bupivacaine and 50 mg of 0.25% bupivacaine and sham port infiltration or sham TAP block procedure with true port-site infiltration with 100-125 mg of 0.25% bupivacaine. All patients had a standardized, scheduled, non-opioid pain management plan. The primary outcome was total IV morphine equivalents used in the first 72 hrs following surgery. Secondary outcomes included assessment of postoperative pain over the study period and quality of recovery measures.
Patients undergoing TAP blockade required fewer total opioid equivalents during the observation period than patients allocated to infiltration (median 21 versus 25 mg IV Morphine equivalents, =0.03). Opioid use was highest in the first 24 hrs after surgery, with less difference between the groups during days 2 and 3 postoperatively. There were 5 in the TAP group and 0 in the infiltration group were opioid free at 72 hrs. Those in the TAP group had improved quality of recovery (QoR15) with no change in overall benefit of analgesia score.
TAP blockade reduced the requirement for opioid pain medication in the first 72 hrs after surgery, had more patients opioid free at 72 hrs, and improved patients' quality of their recovery.
与用0.25%布比卡因进行切口浸润相比,确定脂质体布比卡因腹横肌平面(TAP)阻滞是否能减少腹腔镜或机器人辅助子宫切除术后72小时内的术后阿片类药物总用量。
患者接受266mg脂质体布比卡因加50mg 0.25%布比卡因的真正TAP阻滞操作和假切口浸润,或接受100 - 125mg 0.25%布比卡因真正切口浸润的假TAP阻滞操作。所有患者均有标准化、预定的非阿片类疼痛管理计划。主要结局是术后72小时内使用的静脉注射吗啡等效物总量。次要结局包括研究期间术后疼痛评估和恢复质量指标。
在观察期内,接受TAP阻滞的患者所需的阿片类药物等效物总量少于接受浸润的患者(中位数为21mg静脉注射吗啡等效物对25mg,P = 0.03)。术后24小时内阿片类药物使用量最高,术后第2天和第3天两组之间差异较小。TAP组有5例患者在72小时时未使用阿片类药物,浸润组为0例。TAP组患者的恢复质量(QoR15)有所改善,镇痛评分的总体获益无变化。
TAP阻滞减少了术后72小时内阿片类止痛药物的需求,72小时时更多患者未使用阿片类药物,并改善了患者的恢复质量。