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      Perioperative outcomes and safety of valveless insufflation system in minimally invasive urological surgery: a systematic review and meta-analysis

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          Abstract

          Background:

          With the rapid development of laparoscopic and robot-assisted surgery, many technological innovations and improvements have emerged to optimize minimally invasive surgery and ensure minimal patient risk. Although AirSeal has been widely reported in the field of urology, its perioperative outcomes and safety in minimally invasive urological surgery remain unclear because of inconsistent levels of evidence.

          Objectives:

          The authors performed this meta-analysis to evaluate the perioperative outcomes and safety of the valveless insufflation system (VIS) in minimally invasive urological surgery compared with the conventional insufflation system (CIS).

          Methods:

          The authors comprehensively searched PubMed, Web of Science, Cochrane Library, and Embase databases to identify eligible studies published up to January 2024. Review Manager software (version 5.3.0) was used for the statistical analysis. Eligible studies were randomized controlled trials (RCTs) or non-RCTs of minimally invasive urological surgery with VIS vs CIS. The study outcomes included perioperative outcomes and safety. The authors excluded publication types, including letters, reviews, case reports, and animal and pediatric studies.

          Results:

          The authors finally identified five RCTs and eight non-RCTs in this meta-analysis. The meta- analysis indicated that the operative time was comparable between the groups ( P=0.57, I 2=91%). However, a VIS may increase blood loss ( P=0.0004, I 2=45%) and shorten hospital stays ( P<0.00001, I 2=90%). Due to the high heterogeneity of the results, the authors carefully evaluated all included studies and discovered that the studies by Bucur and Ferroni may be the sources of heterogeneity. When these two studies were excluded, heterogeneity was significantly reduced, and the operative time for VIS was significantly shorter than that for CIS ( P=0.0002). Adjusted blood loss showed no difference between the VIS and CIS groups ( P=0.10). In terms of safety, the pooled results revealed that the incidence of Clavien–Dindo III–IV complications in the VIS group was significantly lower than that in the CIS group ( P=0.02, I 2=0%). Moreover, VIS significantly reduced general pain ( P=0.02, I 2=15%) and shoulder pain ( P=0.001, I 2=0%) 12–24 h postoperatively. No significant differences were observed in total complications ( P=0.06, I 2=0%), blood transfusion ( P=0.14, I 2=0%), and subcutaneous emphysema ( P=0.96, I 2=63%) between the two groups.

          Conclusions:

          Our meta-analysis revealed additional perioperative advantages of the VIS in minimally invasive urological surgery. Moreover, VIS is superior to CIS owing to less severe complication rates, general pain, and shoulder pain.

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          Most cited references25

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          AMSTAR 2: a critical appraisal tool for systematic reviews that include randomised or non-randomised studies of healthcare interventions, or both

          The number of published systematic reviews of studies of healthcare interventions has increased rapidly and these are used extensively for clinical and policy decisions. Systematic reviews are subject to a range of biases and increasingly include non-randomised studies of interventions. It is important that users can distinguish high quality reviews. Many instruments have been designed to evaluate different aspects of reviews, but there are few comprehensive critical appraisal instruments. AMSTAR was developed to evaluate systematic reviews of randomised trials. In this paper, we report on the updating of AMSTAR and its adaptation to enable more detailed assessment of systematic reviews that include randomised or non-randomised studies of healthcare interventions, or both. With moves to base more decisions on real world observational evidence we believe that AMSTAR 2 will assist decision makers in the identification of high quality systematic reviews, including those based on non-randomised studies of healthcare interventions.
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            The PRISMA 2020 statement: An updated guideline for reporting systematic reviews

            The Preferred Reporting Items for Systematic reviews and Meta-Analyses (PRISMA) statement, published in 2009, was designed to help systematic reviewers transparently report why the review was done, what the authors did, and what they found. Over the past decade, advances in systematic review methodology and terminology have necessitated an update to the guideline. The PRISMA 2020 statement replaces the 2009 statement and includes new reporting guidance that reflects advances in methods to identify, select, appraise, and synthesise studies. The structure and presentation of the items have been modified to facilitate implementation. In this article, we present the PRISMA 2020 27-item checklist, an expanded checklist that details reporting recommendations for each item, the PRISMA 2020 abstract checklist, and the revised flow diagrams for original and updated reviews.
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              Methodological index for non-randomized studies (minors): development and validation of a new instrument.

              Because of specific methodological difficulties in conducting randomized trials, surgical research remains dependent predominantly on observational or non-randomized studies. Few validated instruments are available to determine the methodological quality of such studies either from the reader's perspective or for the purpose of meta-analysis. The aim of the present study was to develop and validate such an instrument. After an initial conceptualization phase of a methodological index for non-randomized studies (MINORS), a list of 12 potential items was sent to 100 experts from different surgical specialties for evaluation and was also assessed by 10 clinical methodologists. Subsequent testing involved the assessment of inter-reviewer agreement, test-retest reliability at 2 months, internal consistency reliability and external validity. The final version of MINORS contained 12 items, the first eight being specifically for non-comparative studies. Reliability was established on the basis of good inter-reviewer agreement, high test-retest reliability by the kappa-coefficient and good internal consistency by a high Cronbach's alpha-coefficient. External validity was established in terms of the ability of MINORS to identify excellent trials. MINORS is a valid instrument designed to assess the methodological quality of non-randomized surgical studies, whether comparative or non-comparative. The next step will be to determine its external validity when used in a large number of studies and to compare it with other existing instruments.

                Author and article information

                Contributors
                Journal
                Int J Surg
                Int J Surg
                JS9
                International Journal of Surgery (London, England)
                Lippincott Williams & Wilkins (Hagerstown, MD )
                1743-9191
                1743-9159
                September 2024
                23 May 2024
                : 110
                : 9
                : 5763-5770
                Affiliations
                [a ]Department of Urology, The Affiliated Yantai Yuhuangding Hospital of Qingdao University, Yantai
                [b ]Department of Urology, Qingdao Municipal Hospital, Qingdao University, Qingdao
                [c ]Department of Endocrinology, Yantai Municipal Government Hospital, Yantai, Shandong, People’s Republic of China
                Author notes
                [* ]Corresponding author. Address: Department of Endocrinology, Yantai Municipal Government Hospital, NO. 16 West Yuhuangding Road, Yantai 264000, Shandong, People’s Republic of China. Tel.: +18 61 595 66 69. E-mail: 719981127@ 123456qq.com (Q. Li); Department of Urology, Qingdao Municipal Hospital, Qingdao University, NO. 1 Jiaozhou Road, Qingdao 266000, Shandong, People’s Republic of China. Tel.: +183 639 382 96. E-mail: jiangboqdy@ 123456126.com (B. Jiang).
                Article
                IJS-D-24-01158 00044
                10.1097/JS9.0000000000001634
                11392197
                38781046
                279d68f8-dcd7-4abb-a3aa-f91946ec99df
                Copyright © 2024 The Author(s). Published by Wolters Kluwer Health, Inc.

                This is an open access article distributed under the terms of the Creative Commons Attribution-Non Commercial-No Derivatives License 4.0 (CCBY-NC-ND), where it is permissible to download and share the work provided it is properly cited. The work cannot be changed in any way or used commercially without permission from the journal. http://creativecommons.org/licenses/by-nc-nd/4.0/

                History
                : 27 March 2024
                : 6 May 2024
                Categories
                Reviews
                Custom metadata
                TRUE
                T

                Surgery
                airseal,meta-analysis,postoperative pain,urological surgery,valveless insufflation system
                Surgery
                airseal, meta-analysis, postoperative pain, urological surgery, valveless insufflation system

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