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1.
Hernia ; 27(3): 671-676, 2023 06.
Article in English | MEDLINE | ID: mdl-37160504

ABSTRACT

INTRODUCTION: Over the past decade, an increase has been seen in robotics used for hernia repair, specifically robotic abdominal wall reconstruction (rAWR). However, the learning curve for rAWR can be steep and presently, little is understood regarding the optimal case volume required to achieve proficiency. The aim of our study was to review skill acquisition and describe the learning curve for rAWR. METHODS: A retrospective, single-surgeon case series of consecutive patients who underwent rAWR from 2018 to 2022. The primary outcome was operative time, obtained from console time identified through the MyIntutive application. A one-sided cumulative sum analysis (CUSUM) curve for the total operative time was derived based on the mean operative time of chronological procedures (207 min). RESULTS: 185 patients underwent rAWR between 2018 and 2022. These patients were more likely to be female, Caucasian, and have undergone two previous hernia repairs. ASA complexity increased over time with ASA 3 being predominant from 2020 onwards. The median hernia length was 15.0 cm and the median width was 7 cm. Average operative time was 207.8 min and decreased over time. The CUSUM analysis identified four phases of skill acquisition with the following case volumes: Initial Learning Curve (0-20), Stabilization Phase (21-55), Second Learning Curve (56-70), 4) Skill Proficiency (> 70). CONCLUSION: In the early learning curve of rAWR, operative time decreased consistently after 70 cases, with an initial inflection after 20 cases. We identified varying stages of skill acquisition that are likely typical of a surgeon as they would progress through the learning curve of advanced robotic surgery. Future studies are needed to confirm the optimal case volume for determining the skill level for the performance of rAWR.


Subject(s)
Abdominal Wall , Laparoscopy , Robotic Surgical Procedures , Humans , Female , Male , Abdominal Wall/surgery , Learning Curve , Retrospective Studies , Laparoscopy/methods , Herniorrhaphy , Robotic Surgical Procedures/methods , Operative Time
2.
Mucosal Immunol ; 8(3): 533-44, 2015 May.
Article in English | MEDLINE | ID: mdl-25249167

ABSTRACT

Despite the high prevalence of chronic gastritis caused by Helicobacter pylori, the gastric mucosa has received little investigative attention as a unique immune environment. Here, we analyzed whether retinoic acid (RA), an important homeostatic factor in the small intestinal mucosa, also contributes to gastric immune regulation. We report that human gastric tissue contains high levels of the RA precursor molecule retinol (ROL), and that gastric epithelial cells express both RA biosynthesis genes and RA response genes, indicative of active RA biosynthesis. Moreover, primary gastric epithelial cells cultured in the presence of ROL synthesized RA in vitro and induced RA biosynthesis in co-cultured monocytes through an RA-dependent mechanism, suggesting that gastric epithelial cells may also confer the ability to generate RA on gastric dendritic cells (DCs). Indeed, DCs purified from gastric mucosa had similar levels of aldehyde dehydrogenase activity and RA biosynthesis gene expression as small intestinal DCs, although gastric DCs lacked CD103. In H. pylori-infected gastric mucosa, gastric RA biosynthesis gene expression was severely disrupted, which may lead to reduced RA signaling and thus contribute to disease progression. Collectively, our results support a critical role for RA in human gastric immune regulation.


Subject(s)
Epithelial Cells/immunology , Gastric Mucosa/immunology , Helicobacter Infections/immunology , Helicobacter pylori/immunology , Tretinoin/immunology , Vitamin A/immunology , Aldehyde Dehydrogenase/immunology , Aldehyde Dehydrogenase/metabolism , Animals , Coculture Techniques , Epithelial Cells/microbiology , Female , Gastric Mucosa/microbiology , Helicobacter Infections/metabolism , Helicobacter Infections/microbiology , Helicobacter Infections/pathology , Helicobacter pylori/pathogenicity , Humans , Immunity, Mucosal , Mice , Mice, Inbred C57BL , Monocytes/immunology , Monocytes/microbiology , Primary Cell Culture , Tretinoin/metabolism , Vitamin A/metabolism
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