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1.
Surg Laparosc Endosc Percutan Tech ; 34(2): 136-142, 2024 Apr 01.
Artigo em Inglês | MEDLINE | ID: mdl-38462904

RESUMO

OBJECTIVE: In this study, we aimed to evaluate the efficacy of the Magnetic Scope Guide Assist (ScopeGuide) in enhancing the procedural competence of endoscopists and reducing patient discomfort during colonoscopy. METHODS: This was a retrospective study with 88 trainee participants. The study participants were trained on patients who underwent colonoscopy without anesthesia. Both ScopeGuide-assisted training and conventional training (without ScopeGuide) were utilized for colonoscopy instruction. The outcomes of training were compared, with a particular emphasis on the competency of looping resolution. RESULTS: ScopeGuide-assisted training was superior to conventional training in multiple aspects, including looping resolution ( Z =-3.681, P <0.001), pain scores ( Z =-4.211, P <0.001), time to reach the cecum ( Z =-4.06, P <0.001), willingness to undergo repeat colonoscopy ( Z =-4.748, P <0.001), competence of positional changes ( Z =-4.079, P <0.001), and the effectiveness of assisted compression ( Z =-3.001, P =0.003). Further stratified analysis revealed that the ScopeGuide-assisted training mode was more beneficial for junior endoscopists ( P <0.05 in all parameters) but not for intermediate endoscopists ( P >0.05) and partially beneficial for senior endoscopists ( P <0.05 for all parameters except looping resolution). CONCLUSION: ScopeGuide-assisted training can significantly facilitate endoscopists in resolving loops and reducing patient pain, thereby enhancing their colonoscopy abilities.


Assuntos
Ceco , Colonoscopia , Humanos , Estudos Retrospectivos , Dor/etiologia , Dor/prevenção & controle , Competência Clínica
2.
Z Gastroenterol ; 61(4): 394-398, 2023 Apr.
Artigo em Inglês | MEDLINE | ID: mdl-35839794

RESUMO

BACKGROUND: Endoscopic submucosal dissection (ESD) is a method that can be used for en bloc resection, regardless of the size and form of the lesion. The special location of ileocecal tumors leads to insufficient counter-traction and poor field of vision, making ESD difficult. An S-O clip has been developed to simplify the attachment procedure, eliminating interference with the endoscope and improving accessibility. CASE PRESENTATION: The patient was a 70-year-old man who presented with abdominal pain and bloating. A colonoscopy revealed a flat-elevated-type lesion on the ileocecal valve, with the oral side of the lesion having progressed to the terminal ileum. The traction direction was adjusted from distal to proximal during the procedure using the S-O clip. Finally, with the help of the S-O clip, the tumor was safely removed and collected. CONCLUSION: The S-O clip was successful in ESD of a colorectal tumor. By removing and re-anchoring the loaded ring, the S-O clips allowed the adjustment of traction direction from distal to proximal during ESD.


Assuntos
Neoplasias Colorretais , Ressecção Endoscópica de Mucosa , Valva Ileocecal , Masculino , Humanos , Idoso , Ressecção Endoscópica de Mucosa/métodos , Tração/métodos , Resultado do Tratamento , Neoplasias Colorretais/cirurgia , Instrumentos Cirúrgicos
5.
Natl Med J India ; 34(1): 27-28, 2021.
Artigo em Inglês | MEDLINE | ID: mdl-34397001

RESUMO

Foreign bodies in the digestive tract are a common cause of patients presenting to emergency departments. A 3-year-old boy who had accidentally swallowed magnetic beads while playing was admitted to the hospital. After failed endoscopic removal, he underwent laparoscopic removal. We found that the stomach and jejunum were tightly bound together by the magnetic beads, and this had caused perforations. The perforations had then connected to form a tract resulting in a spontaneous gastrojejunostomy. During the operation, four magnetic beads were removed from the stomach and eight from the jejunum.


Assuntos
Corpos Estranhos , Derivação Gástrica , Laparoscopia , Criança , Pré-Escolar , Corpos Estranhos/diagnóstico por imagem , Corpos Estranhos/cirurgia , Derivação Gástrica/efeitos adversos , Humanos , Masculino , Estômago/diagnóstico por imagem , Estômago/cirurgia
6.
J Gastrointest Surg ; 24(8): 1869-1879, 2020 08.
Artigo em Inglês | MEDLINE | ID: mdl-32306226

RESUMO

BACKGROUND: Studies indicate that low graft-to-recipient weight ratio (GRWR) affect graft survival in adult-to-adult living donor liver transplantation. However, the potential role of GRWR in the prognosis of patients following living donor liver transplantation according to patient characteristics remains controversial. This study aimed to update the role of GRWR in patients following living donor liver transplantation. METHODS: PubMed, Embase, and Cochrane Library were comprehensively searched for studies comparing low GRWR (< 0.8%) with normal GRWR (≥ 0.8%) in the prognosis following living donor liver transplantation from inception to March 2019. The 1-, 3-, and 5-year summary survival rates, small-for-size syndrome (SFSS), perioperative mortality, biliary complications, postoperative bleeding, and acute rejection were calculated using the random-effects model. RESULTS: Eighteen studies comprising 4001 patients were included. Patients with low GRWR were associated with lower 1-year and 3-year survival rates compared to patients with normal GRWR, while no significant difference was found in the association of 5-year survival rate with low and normal GRWRs. Moreover, the risk of SFSS significantly increased in patients with low GRWR. Finally, no significant differences were observed in the association of low and normal GRWRs with the risk of perioperative mortality, biliary complications, postoperative bleeding, and acute rejection. CONCLUSION: The results of this study indicated that low GRWR was associated with poor prognosis for patients following living donor liver transplantation, especially in terms of 1- and 3-year survival rates and SFSS.


Assuntos
Transplante de Fígado , Adulto , Sobrevivência de Enxerto , Humanos , Fígado , Transplante de Fígado/efeitos adversos , Doadores Vivos , Tamanho do Órgão , Prognóstico , Estudos Retrospectivos , Resultado do Tratamento
7.
Dig Dis Sci ; 65(9): 2619-2629, 2020 09.
Artigo em Inglês | MEDLINE | ID: mdl-32006210

RESUMO

BACKGROUND: Currently there is no consensus on the optimal management of small-for-size syndrome following liver transplantation. Here we describe a technique to alleviate portal hypertension and improve the hepatocyte reperfusion in small-for-size liver transplantation in a Lewis rat model. METHODS: The rats underwent trans-portal vein intra-hepatic portosystemic shunt using a self-developed porous conical tube (TPIPSS: Fig. 1) on small-for-size liver transplants (SFS) with right lobe graft. The treatment effect was evaluated by comparing hemodynamic parameters, morphological changes, serum parameters, ET-1 and eNOS expression, hepatocyte proliferation and apoptosis, CYP3A2 levels, postoperative complications, and survival between the two groups with SFS liver transplants. RESULTS: Porous conical prosthesis prolonged the filling time of small-for-size grafts. Moreover, grafts with TPIPSS showed a lower portal vein pressure, improved microcirculatory flow, alleviated histological changes, decreased ET-1 and increased eNOS expressions, and significantly less damage to liver function comparing to grafts without TPIPSS. Mean survival and overall 30-day survival were significantly higher in the TPIPSS group. CONCLUSIONS: These results demonstrate that porous conical tube as trans-portal vein intra-hepatic portosystemic shunt device is an effective way to alleviate portal vein hypertension and improve hepatocyte reperfusion after small-for-size liver transplantation.


Assuntos
Implante de Prótese Vascular/instrumentação , Prótese Vascular , Transplante de Fígado/efeitos adversos , Veia Porta/cirurgia , Complicações Pós-Operatórias/prevenção & controle , Veia Cava Inferior/cirurgia , Animais , Apoptose , Proliferação de Células , Citocromo P-450 CYP3A/metabolismo , Endotelina-1/metabolismo , Hemodinâmica , Circulação Hepática , Masculino , Óxido Nítrico Sintase Tipo III/metabolismo , Tamanho do Órgão , Porosidade , Veia Porta/fisiopatologia , Complicações Pós-Operatórias/metabolismo , Complicações Pós-Operatórias/patologia , Complicações Pós-Operatórias/fisiopatologia , Desenho de Prótese , Ratos Endogâmicos Lew , Síndrome , Veia Cava Inferior/fisiopatologia
8.
BMC Gastroenterol ; 20(1): 7, 2020 Jan 13.
Artigo em Inglês | MEDLINE | ID: mdl-31931737

RESUMO

BACKGROUND: The anti-immunological rejection therapy for small-for-size syndrome (SFSS) after live donor liver transplantation (LDLT) play a central role in keeping graft survival. The hepatocyte number and grafts function has undergone real-time changes with the proliferation and apoptosis of the grafts after reperfusion. Lacking an accurate and effective treatment regiments or indicators to guide the use of immunosuppressive drugs in SFS liver transplantation has made immunotherapy after SFS liver transplantation an urgent problem to be solved. Herein, we established small-for-size (SFS) and normal size liver transplantation model in rats to explore the effective indicators in guiding immunotherapy, to find an effective way for overcoming SFSS. METHODS: Lewis rats (donors) and BN rats (recipients) were used to mimic allograft liver transplantation and treated with tacrolimus. Local graft immune response was analyzed through haematoxylin and eosin and immunohistochemistry. Flow cytometry was used to assess the overall immune status of recipient. The pharmacokinetics mechanism of immunosuppressive drugs was explored through detecting CYP3A2 expression at mRNA level and protein levels. RESULTS: The results showed the local immune reaction of SFS grafts and systemic immune responses of recipient were significantly increased compared with those in normal size grafts and their recipient at four days after liver transplantation. Regression equation was used to regulate the tacrolimus dose which not only controlled tacrolimus serum concentration effectively but alleviated liver damage and improved survival rate. CONCLUSIONS: This study showed that AST level and tacrolimus serum concentrations are effective indicators in guiding immunotherapy. Regression equation (TD = - 0.494TC-0.0035AST + 260.487) based on AST and tacrolimus serum concentration can be used as a reference for adjustment of immunotherapy after SFS liver transplantation, which is applicable in clinical practice.


Assuntos
Rejeição de Enxerto/tratamento farmacológico , Sobrevivência de Enxerto/imunologia , Imunossupressores/uso terapêutico , Transplante de Fígado/efeitos adversos , Tacrolimo/uso terapêutico , Animais , Aspartato Aminotransferases/sangue , Imunossupressores/sangue , Fígado/imunologia , Transplante de Fígado/métodos , Doadores Vivos , Tamanho do Órgão/imunologia , Ratos , Ratos Endogâmicos BN , Ratos Endogâmicos Lew , Tacrolimo/sangue , Transplantes/imunologia , Resultado do Tratamento
9.
Int J Oncol ; 52(4): 1081-1094, 2018 Apr.
Artigo em Inglês | MEDLINE | ID: mdl-29484374

RESUMO

SUMOylation is a reversible post-translational modification which has emerged as a crucial molecular regulatory mechanism, involved in the regulation of DNA damage repair, immune responses, carcinogenesis, cell cycle progression and apoptosis. Four SUMO isoforms have been identified, which are SUMO1, SUMO2/3 and SUMO4. The small ubiquitin-like modifier (SUMO) pathway is conserved in all eukaryotes and plays pivotal roles in the regulation of gene expression, cellular signaling and the maintenance of genomic integrity. The SUMO catalytic cycle includes maturation, activation, conjugation, ligation and de-modification. The dysregulation of the SUMO system is associated with a number of diseases, particularly cancer. SUMOylation is widely involved in carcinogenesis, DNA damage response, cancer cell proliferation, metastasis and apoptosis. SUMO can be used as a potential therapeutic target for cancer. In this review, we briefly outline the basic concepts of the SUMO system and summarize the involvement of SUMO proteins in cancer cells in order to better understand the role of SUMO in human disease.


Assuntos
Neoplasias , Processamento de Proteína Pós-Traducional/fisiologia , Proteínas Modificadoras Pequenas Relacionadas à Ubiquitina/metabolismo , Sumoilação/fisiologia , Animais , Humanos
10.
Mediators Inflamm ; 2012: 751629, 2012.
Artigo em Inglês | MEDLINE | ID: mdl-23125487

RESUMO

BACKGROUND: Free radicals and proinflammatory cytokines have been shown to play a critical role in the pathogenesis of ulcerative colitis (UC). Picroliv, a Picrorhiza kurroa derivative, has been demonstrated to have antioxidant and anti-inflammatory effect. The purpose of the study was to investigate the effects of picroliv on experimental model of UC in mice. MATERIALS AND METHODS: Picroliv was administrated orally by gavage to mice with colitis induced by dextran sulfate sodium (DSS). Disease activity index (DAI), colon length, and histology score were observed. Myeloperoxidase (MPO) activity, and SOD, MDA concentrations were measured by enzyme-linked immunosorbent assay (ELISA) while the expression of cytokine mRNAs was studied by real-time-quantitative polymerase chain reaction and also ELISA. The expression of NF-κB p65 was observed by immunohistochemistry staining and western blotting. RESULTS: A significant improvement was observed in DAI and histological score in mice treated with picroliv, and incerased MPO activity, MDA concentrations, and the expression of IL-1ß, TNF-α, and NF-κB p65 in mice with DSS-induced colitis were significantly reduced while decreased SOD level increased following administration of picroliv. CONCLUSION: The administration of picroliv leads to an amelioration of DSS-induced colitis, suggesting administration of picroliv may provide a therapeutic approach for UC.


Assuntos
Cinamatos/uso terapêutico , Colite/induzido quimicamente , Colite/tratamento farmacológico , Sulfato de Dextrana/toxicidade , Glicosídeos/uso terapêutico , Picrorhiza/química , Ácido Vanílico/uso terapêutico , Animais , Colo/efeitos dos fármacos , Colo/patologia , Feminino , Camundongos , Camundongos Endogâmicos BALB C , Reação em Cadeia da Polimerase Via Transcriptase Reversa
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