There is a diversity of surgical approaches for GISTs treatment. From our point of view, the main selection criteria for certain procedure are size, localization, growth type of the tumor and status of overlying mucosa. Nevertheless, due to relative rarity and heterogeneity of this pathology, individualization is necessary in each specific case. Laparoscopic and endoscopic surgery is proved to be safe and feasible for resection of the gastric GISTs, with a reasonable operation time, low blood loss, and an acceptable complication rate. Immediate results indicate that all interventions were performed radically without mortality or serious morbidity.
Evaluation of tissue perfusion at various stages of surgery is of great importance for the implementation of the concept of safe surgery, including operations on the abdominal organs. Currently, there is no accurate and reliable intraoperative method for assessing tissue perfusion that could help surgeons determine the risks of ischemia and improve outcomes. We propose novel method of intraoperative assessment of tissue perfusion using video camera synchronized with the electrocardiogram. The technique is referred to as imaging photoplethysmography (iPPG). It can be used continuously for monitoring blood supply to organs e.g., before and after anastomosis. In our study, we followed 14 different surgical cases (four stomach and ten colorectal cancers) requiring reconstruction of various organs with anastomosis. With iPPG, intraoperative blood perfusion was successfully visualized and quantified in all 14 patients under study. As most indicative, here we describe in detail two clinical demonstrations during gastrectomy for gastric cancer and right-sided hemicolectomy for cancer of the ascending colon. Feasibility of the iPPG system to assess blood perfusion in organs before and after anastomosis during open surgery was demonstrated for the first time.
Background. Infection caused by SARS-CoV-2 mostly affects the upper and lower respiratory tracts and causes symptoms ranging from the common cold to pneumonia with acute respiratory distress syndrome. Chemokines are deeply involved in the chemoattraction, proliferation, and activation of immune cells within inflammation. It is crucial to consider that mutations within the virion can potentially affect the clinical course of SARS-CoV-2 infection because disease severity and manifestation vary depending on the genetic variant. Our objective was to measure and assess the different concentrations of chemokines involved in COVID-19 caused by different variants of the virus. Methods. We used the blood plasma of patients infected with different variants of SARS-CoV-2, i.e., the ancestral Wuhan strain and the Alpha, Delta, and Omicron variants. We measured the concentrations of 11 chemokines in the samples: CCL2/MCP-1, CCL3/MIP-1α, CCL4/MIP-1β, CCL7/MCP-3, CCL11/Eotaxin, CCL22/MDC, CXCL1/GROα, CXCL8/IL-8, CXCL9/MIG, CXCL10/IP-10, and CX3CL1/Fractalkine. Results. We noted a statistically significant elevation in the concentrations of CCL2/MCP-1, CXCL8/IL-8, and CXCL1/IP-10 independently of the variant, and a drop in the CCL22/MDC concentrations. Conclusions. The chemokine concentrations varied significantly depending on the viral variant, leading us to infer that mutations in viral proteins play a role in the cellular and molecular mechanisms of immune responses.
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