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1.
Int J Surg ; 110(4): 2253-2262, 2024 Apr 01.
Article in English | MEDLINE | ID: mdl-38320088

ABSTRACT

BACKGROUND: Roux-en-Y reconstruction is a common anastomosis technique during gastrectomy in gastric cancer. There is a lack of studies on gallstones after Roux-en-Y reconstruction gastrectomy. This study investigated the incidence and potential risk factors associated with gallstones after Roux-en-Y reconstructive gastrectomy in gastric cancer. METHODS: The study analyzed data from gastric cancer who underwent radical gastrectomy and Roux-en-Y reconstruction at two hospitals between January 2014 and December 2020. The patients fall into distal and total gastrectomy groups based on the extent of gastrectomy. The cumulative event probability curve was plotted using the Kaplan-Meier, and differences in gallstone between groups were evaluated using the Log-Rank. Propensity score matching was applied to construct a balanced total versus distal gastrectomies cohort. A Cox regression was employed to analyze the risk factors for gallstones after Roux-en-Y reconstructive gastrectomy in gastric cancer. Further subgroup analysis was performed. RESULTS: Five hundred thirty-one patients were included in this study, 201 in the distal gastrectomy group and 330 in the total gastrectomy. During the follow-up, gallstones occurred in 170 cases after gastrectomy, of which 145 cases accounted for 85.29% of all stones in the first two years after surgery. Then, to reduce the impact of bias, a 1:1 propensity score matching analysis was performed on the two groups of patients. A total of 344 patients were evaluated, with each subgroup comprising 172 patients. In the matched population, the Cox regression analysis revealed that females, BMI ≥23 kg/m 2 , total gastrectomy, No.12 lymph node dissection, and adjuvant chemotherapy were risk factors for gallstones after Roux-en-Y reconstructive gastrectomy. Subgroup analysis showed that open surgery further increased the risk of gallstones after total gastrectomy. CONCLUSION: The incidence of gallstones increased significantly within 2years after Roux-en-Y reconstructive gastrectomy for gastric cancer. Patients with these risk factors should be followed closely after gastrectomy to avoid symptomatic gallstones.


Subject(s)
Anastomosis, Roux-en-Y , Gallstones , Gastrectomy , Postoperative Complications , Stomach Neoplasms , Humans , Stomach Neoplasms/surgery , Gastrectomy/adverse effects , Gastrectomy/methods , Female , Male , Middle Aged , Gallstones/surgery , Gallstones/epidemiology , Gallstones/etiology , Incidence , Anastomosis, Roux-en-Y/adverse effects , Aged , Risk Factors , Postoperative Complications/epidemiology , Postoperative Complications/etiology , Retrospective Studies , Propensity Score , Cohort Studies , Adult
2.
Biotechnol Lett ; 32(10): 1487-95, 2010 Oct.
Article in English | MEDLINE | ID: mdl-20495943

ABSTRACT

The morphological effects of CF66I, an antifungal compound produced by Burkholderia cepacia, on growing hyphae of Fusarium oxysporum were studied by fluorescence microscopy (FM) and transmission electron microscopy (TEM). At 20 µg/ml, CF66I strongly inhibited growth and induced significant changes of the hyphal morphology. These changes included swelling of hyphae with considerable thickening cell wall and abnormal chitin deposition, which was indicative of the alterations in cell wall structure. Furthermore, fluorescein diacetate (FDA) staining indicated the loss of intracellular esterase activity. CF66I probably inhibits fungal growth by interfering with the cell metabolic pathways. At 120 µg/ml, CF66I killed F. oxysporum (accompanied by propidium iodide permeation, intracellular cytoplasm leakage and crushing of hyphal tips), probably by direct damage to the cell membrane. Thus, there are two different antifungal mechanisms of CF66I, depending on its concentration, and further studies on this compound might be useful for us to develop a new class of antifungal agents.


Subject(s)
Amides/pharmacology , Antifungal Agents/pharmacology , Burkholderia cepacia/chemistry , Fusarium/drug effects , Hyphae/drug effects , Amides/isolation & purification , Antifungal Agents/isolation & purification , Cell Wall/chemistry , Cell Wall/ultrastructure , Chitin/analysis , Esterases/analysis , Fusarium/chemistry , Fusarium/ultrastructure , Hyphae/chemistry , Hyphae/ultrastructure , Microbial Viability/drug effects , Microscopy, Electron, Transmission , Microscopy, Fluorescence
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