The effect of ultrasound-guided lung recruitment maneuvers on atelectasis in lung-healthy patients undergoing laparoscopic gynecologic surgery: a randomized controlled trial

医学 肺不张 气腹 麻醉 潮气量 超声波 Pacu公司 随机对照试验 麻醉学 腹腔镜手术 入射(几何) 外科 腹腔镜检查 呼吸系统 放射科 内科学 物理 光学
作者
Yi Liu,Jingyu Wang,Geng Yuan,Yiran Zhang,Hang Su,Yujiao Yang
出处
期刊:BMC Anesthesiology [BioMed Central]
卷期号:22 (1) 被引量:12
标识
DOI:10.1186/s12871-022-01742-1
摘要

Abstract Background Atelectasis is the primary cause of hypoxemia during general anesthesia. This study aimed to evaluate the impact of the combination of recruitment maneuvers (RM) and positive end-expiratory pressure (PEEP) on the incidence of atelectasis in adult women undergoing gynecologic laparoscopic surgery using pulmonary ultrasound. Methods In this study, 42 patients with healthy lungs undergoing laparoscopic gynecologic surgery were randomly divided into the recruitment maneuver group (RM group; 6 cm H 2 O PEEP and RM) or the control group (C group; 6 cm H 2 O PEEP and no RM), 21 patients in each group. Volume-controlled ventilation was used in all selected patients, with a tidal volume of 6–8 mL·kg −1 of ideal body weight. When atelectasis was detected, patients in the RM group received ultrasound-guided RM, while those in the C group received no intervention. The incidence and severity of atelectasis were determined using lung ultrasound scores. Results A total of 41 patients were investigated. The incidence of atelectasis was lower in the RM group (40%) than in the C group (80%) 15 min after arrival in the post-anesthesia care unit (PACU). Meanwhile, lung ultrasound scores (LUSs) were lower in the RM group compared to the C group. In addition, the differences in the LUS between the two groups were mainly due to the differences in lung ultrasound scores in the posterior regions. However, this difference did not persist after 24 h of surgery. Conclusions In conclusion, the combination of RM and PEEP could reduce the incidence of atelectasis in patients with healthy lungs 15 min after arrival at the PACU; however, it disappeared within 24 h after surgery. Trial registration (Prospectively registered): ChiCTR2000033529 . Registered on 4/6/2020.
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