机器人手术系统辅助解剖性与非解剖性肝切除术的围手术期疗效分析

Perioperative efficacy analysis of robotic surgical system assisted anatomic and non-anatomic hepatectomy

  • 摘要:
    目的 探讨机器人手术系统辅助解剖性与非解剖性肝切除术的围手术期疗效。
    方法 采用倾向评分匹配及回顾性队列研究方法。收集2016年3月至2021年12月浙江大学医学院附属邵逸夫医院收治的103例行机器人手术系统辅助肝切除术患者的临床资料;男54例,女49例;年龄为56(44~64)岁。103例患者中,55例行机器人手术系统辅助解剖性肝切除术设为解剖组;48例行机器人手术系统辅助非解剖性肝切除术设为非解剖组。观察指标:(1)倾向评分匹配情况及匹配后两组患者一般资料比较。(2)术中情况。(3)围手术期并发症情况。倾向评分匹配按1∶1最近邻匹配法匹配。正态分布的计量资料以x±s表示,组间比较采用t检验;偏态分布的计量资料以M(范围)表示,组间比较采用Mann‑Whitney U检验。计数资料用绝对数及百分比表示,组间比较采用χ²检验或Fisher确切概率法。等级资料比较采用秩和检验。
    结果 (1)倾向评分匹配情况及匹配后两组患者一般资料比较。103例患者中,94例配对成功,解剖组和非解剖组各47例。倾向评分匹配消除术前体质量指数、术前血小板、术前白蛋白因素混杂偏倚,具有可比性。(2)术中情况。倾向评分匹配后,解剖组患者手术时间、术中出血量分别为175(120~240)min、50(50~100)mL,非解剖组患者上述指标分别为155(105~190)min、100(50~200)mL,两组患者上述指标比较,差异均有统计学意义(Z=1.97,2.49,P<0.05)。(3)围手术期并发症情况。倾向评分匹配后,解剖组患者胸腔积液和(或)腹水、胆瘘、血栓、腹腔感染、切口感染分别为11、1、2、4、1例,非解剖组上述指标分别为12、0、4、1、0例,两组患者上述指标比较,差异均无统计学意义(P>0.05);解剖组患者Clavien‑Dindo分级(Ⅰ级、Ⅱ级、Ⅲ级、Ⅵ级)分别为33、14、0、0例,非解剖组上述指标分别为28、14、3、2例,两组患者上述指标比较,差异无统计学意义(Z=-1.38,P>0.05)。
    结论 机器人手术系统辅助解剖性肝切除术与机器人手术系统辅助非解剖性肝切除术临床应用均安全可行。与机器人手术系统辅助非解剖性肝切除术比较,机器人手术系统辅助解剖性肝切除术手术时间延长,术中出血量更少。

     

    Abstract:
    Objective To investigate the perioperative efficacy of robot surgical system assisted anatomic and non‑anatomic hepatectomy.
    Methods The propensity score matching and retrospective cohort study was conducted. The clinical data of 103 patients who underwent robot surgical system assisted hepatectomy in Sir Run Run Shaw Hospital, Affiliated with the Zhejiang University School of Medicine from March 2016 to December 2021 were collected. There were 54 males and 49 females, aged 56(range, 44‒64)years. Of the 103 patients, 55 cases undergoing robot surgical system assisted anatomic hepatectomy were divided into the anatomic group, and 48 cases undergoing robot surgical system assisted non-anatomic hepatectomy were divided into the non-anatomic group. Observation indicators: (1) propensity score matching and comparison of general data of patients between the two groups after matching; (2) intraoperative conditions; (3) perioperative complications. Propensity score matching was done by the 1:1 nearest neighbor matching method. Measurement data with normal distribution were represented as Mean±SD, and comparison between groups was conducted using the t test. Measurement data with skewed distribution were expressed as M(range), and comparison between groups was conducted using the Mann‑Whitney U test. Count data were described as absolute numbers or percentages, and comparison between groups was conducted using the chi‑square test or Fisher exact probability. Comparison of ordinal data was conducted using the rank sum test.
    Results (1) Propensity score matching and compari-son of general data of patients between the two groups after matching. Of the 103 patients, 94 cases were successfully matched, including 47 cases in the anatomic group and 47 cases in the non-anatomic group. The elimination of preoperative body mass index, preoperative platelet and preoperative albumin confounding bias ensured comparability between the two groups after propensity score matching. (2) Intraoperative conditions. After propensity score matching, the operation time and volume of intraoperative blood loss were 175(range, 120‒240)minutes and 50(range, 50‒100)mL in patients of the anatomic group, versus 155(range, 105‒190)minutes and 100(range, 50‒200)mL in patients of the non‑anatomic group, showing significant differences in the above indicators between the two groups (Z=1.97, 2.49, P<0.05). (3) Perioperative complications. After propensity score matching, cases with pleural fluid and/or ascites, case with biliary fistula, case with thrombosis, case with peritoneal infection, case with incision infection were 11, 1, 2, 4, 1 in patients of the anatomic group, versus 12, 0, 4, 1, 0 in patients of the non‑anatomic group, showing no significant difference in the above indicators between the two groups (P>0.05). Cases with complications classified as grade Ⅰ, grade Ⅱ, grade Ⅲ, grade Ⅳ of the Clavien‑Dindo classification were 33, 14, 0, 0 in patients of the anatomic group, versus 28, 14, 3, 2 in patients of the non‑anatomic group, showing no significant difference in the above indicators between the two groups (Z=‒1.38, P>0.05).
    Conclusions Robotic surgical system assisted anatomic and non-anatomic hepatectomy are safe and feasible for clinical application. Compared with robot surgical system assisted non‑anatomic hepatectomy, patients under-going robot surgical system assisted anatomic hepatectomy have long operation time and less volume of intraoperative blood loss.

     

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