Department of Gynecologic Oncology, Mugla Sıtkı Kocman University Education and Research Hospital, Mugla, Turkey.
Department of Gynecologic Oncology, Kanuni Sultan Suleyman Education and Research Hospital, Istanbul, Turkey.
J Gynecol Oncol. 2018 Nov;29(6):e92. doi: 10.3802/jgo.2018.29.e92.
To evaluate the effectiveness of the pulmonary recruitment maneuver (PRM) at the end of the operation to decrease laparoscopy-induced abdominal or shoulder pain after gynecological oncologic surgery.
In total, 113 women undergoing laparoscopic surgery for malignant or premalignant gynecological lesions were assigned randomly to two groups: the PRM group (the patient was placed in the Trendelenburg position (30°) and the PRM, consisting of two manual pulmonary inflations to a maximum pressure of 40 cmH₂O) (n=54) and the control group (n=52). Postoperative shoulder and abdominal pain was assessed 12, 24, and 48 hours later using a visual analog scale (0-10). In addition, the incidence of post-discharge nausea and vomiting was recorded until 48 hours after discharge.
Postoperative shoulder pain at 12 and 24 hours was significantly less severe in the PRM group (2.2±0.5 and 2.0±0.4) than in the control group (4.0±0.5 and 3.9±0.4; both p<0.001). The PRM significantly reduced the severity of upper abdominal pain at 12 and 24 h compared with the control group (3.1±0.4 and 2.9±0.4 vs. 5.9±0.5 and 4.9±0.5; both p<0.001). The analgesic requirement during the postoperative period was similar in the two groups (control group, 78.8%; PRM group, 75.9%; p=0.719).
The PRM effectively and safely reduced postoperative shoulder and upper abdominal pain levels in patients undergoing laparoscopic gynecological oncologic surgery. Trial registry at ClinicalTrials.gov, NCT01940042.
评价肺复张手法(PRM)在手术结束时对降低妇科恶性或癌前病变腹腔镜手术后腹部或肩部疼痛的效果。
共有 113 名接受腹腔镜手术治疗妇科恶性或癌前病变的患者被随机分为两组:PRM 组(患者置于头高脚低位(30°),PRM 由两次手动肺充气组成,最大压力为 40 cmH₂O)(n=54)和对照组(n=52)。术后 12、24 和 48 小时采用视觉模拟评分法(0-10)评估肩部和腹部疼痛。此外,还记录了出院后 48 小时内恶心和呕吐的发生率。
PRM 组术后 12 小时和 24 小时肩部疼痛明显轻于对照组(2.2±0.5 和 2.0±0.4 比 4.0±0.5 和 3.9±0.4;均 p<0.001)。与对照组相比,PRM 组术后 12 小时和 24 小时上腹部疼痛明显减轻(3.1±0.4 和 2.9±0.4 比 5.9±0.5 和 4.9±0.5;均 p<0.001)。两组术后镇痛需求相似(对照组 78.8%;PRM 组 75.9%;p=0.719)。
PRM 可有效、安全地降低行腹腔镜妇科恶性肿瘤手术患者术后肩部和上腹部疼痛程度。临床试验注册于 ClinicalTrials.gov,NCT01940042。