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1.
Langenbecks Arch Surg ; 409(1): 112, 2024 Apr 08.
Article in English | MEDLINE | ID: mdl-38587671

ABSTRACT

INTRODUCTION: Either extracorporeal anastomosis (EA) or intracorporeal anastomosis (IA) could be selected for digestive reconstruction in laparoscopic right hemicolectomy (LRH). However, whether LRH with IA is feasible and beneficial for overweight right-side colon cancer (RCC) is unclear. This study aims to investigate the feasibility and advantage of IA in LRH for overweight RCC. METHODS: Forty-eight consecutive overweight RCC patients undergoing LRH with IA were matched with 48 consecutive cases undergoing LRH with EA. Both clinical and surgical data were collected and analyzed. RESULTS: The incidence of postoperative complications was 20.8% (10/48) in the EA group and 14.6% (7/48) in the IA group respectively, with no statistical difference. Compared to the EA group, patients in the IA group revealed faster gas (40.2 + 7.8 h vs. 45.6 + 7.9 h, P = 0.001) and stool discharge (4.0 + 1.2 d vs. 4.5 + 1.1 d, P = 0.040), shorter assisted incision (5.3 + 1.3 cm vs. 7.5 + 1.2 cm, P = 0.000), and less analgesic used (3.3 + 1.3 d vs. 4.0 + 1.3 d, P = 0.012). There were no significant differences in operation time, blood loss, or postoperative hospital stays. In the IA group, the first one third of cases presented longer operation time (228.4 + 29.3 min) compared to the middle (191.0 + 35.0 min, P = 0.003) and the last one third of patients (182.2 + 20.7 min, P = 0.000). CONCLUSION: LRH with IA is feasible and safe for overweight RCC, with faster bowel function recovery and less pain. Accumulation of certain cases of LRH with IA will facilitate surgical procedures and reduce operation time.


Subject(s)
Carcinoma, Renal Cell , Colonic Neoplasms , Kidney Neoplasms , Laparoscopy , Humans , Case-Control Studies , Overweight , Colonic Neoplasms/surgery , Colectomy , Anastomosis, Surgical
2.
BMC Surg ; 23(1): 110, 2023 May 06.
Article in English | MEDLINE | ID: mdl-37149588

ABSTRACT

AIM: The incidence and risk factors of low anterior resection syndrome (LARS) largely variate in different studies. In addition, there is lack of study on how patients evaluate the therapeutic effect of LARS. This single-center retrospective study aims to investigate the status of LARS in Chinese patients undergoing laparoscopic low anterior resection (LAR). METHODS: Consequent patients undergoing laparoscopic LAR and free from disease recurrence from January 2015 to May 2021 were issued with both LARS questionnaire and satisfaction survey. Related data were collected and analyzed. RESULTS: Both LARS questionnaires and self-made satisfaction survey were received from 261 eligible patients. The overall incidence of LARS was 47.1% (minor in 19.5%, major in 27.6%), decreased with the passage of postoperative time (64.7% within 12 months, and 41.7% within 12-36 months), and became stable 36 months later (39.7%). The most common symptoms were defecation clustering (n = 107/261, 41.0%) and defecation urgency (n = 101/261, 38.7%). According to the multivariable regression analysis, risk factors of major LARS were: 1 year increase in age (OR 1.035, 95% CI 1.004-1.068), protective stoma (OR 2.656, 95% CI 1.233-5.724) and T3 - 4 stage (OR 2.449, 95% CI 1.137-5.273). Most patients complained defecation disorder (87.3%) to doctors and 84.5% got suggestions or treatments for it. However, only 36.8% patients thought the treatments worked for them. CONCLUSIONS: LARS frequently occurs after laparoscopic LAR, while the therapeutic effect is not satisfying. Elder, advanced T-stage and protective stoma were risk factors for postoperative major LARS.


Subject(s)
Rectal Neoplasms , Humans , Aged , Rectal Neoplasms/surgery , Low Anterior Resection Syndrome , Retrospective Studies , Postoperative Complications/epidemiology , Postoperative Complications/etiology , Neoplasm Recurrence, Local , Quality of Life
3.
Bioorg Med Chem Lett ; 28(11): 2091-2097, 2018 06 15.
Article in English | MEDLINE | ID: mdl-29724588

ABSTRACT

A new concise and facile method was explored to synthesize a series of novel chalcone derivatives containing a purine and benzenesulfonamide moiety and their antiviral properties were evaluated against TMV and CMV. Biological assays indicated that several of the derivatives exhibited significant anti-TMV and anti-CMV activities in vivo. In particular, compound d2 displayed excellent inactivating activity against TMV, with the EC50 value of 51.65 µg/mL, which was better than that of ribavirin (150.45 µg/mL). Molecular docking showed that there are four hydrogen bonds between compound d2 and TMV coat protein (TMV-CP). Compound d2 demonstrated strong binding capacity to TMV-CP with Ka = 1.58 × 105 L/mol and Kd = 12.16 µM. These findings indicated that chalcone derivatives are worthy of further research and development as templates for new antiviral agents.


Subject(s)
Antiviral Agents/pharmacology , Chalcone/pharmacology , Cucumovirus/drug effects , Purines/pharmacology , Sulfonamides/pharmacology , Tobacco Mosaic Virus/drug effects , Antiviral Agents/chemical synthesis , Antiviral Agents/chemistry , Chalcone/chemical synthesis , Chalcone/chemistry , Dose-Response Relationship, Drug , Microbial Sensitivity Tests , Molecular Structure , Purines/chemistry , Structure-Activity Relationship , Sulfonamides/chemistry , Benzenesulfonamides
4.
Molecules ; 22(4)2017 Apr 21.
Article in English | MEDLINE | ID: mdl-28430149

ABSTRACT

1,4-Pentadien-3-one derivatives derived from curcumin possess excellent inhibitory activity against plant viruses. On the basis of this finding, a series of novel 1,4-pentadien-3-one derivatives containing a 1,3,4-thiadiazole moiety were designed and synthesized, and their structures confirmed by IR, ¹H-NMR, and 13C-NMR spectroscopy and elemental analysis. The antiviral activities of the title compounds were evaluated against tobacco mosaic virus (TMV) and cucumber mosaic virus (CMV) in vivo. The assay results showed that most of compounds had remarkable antiviral activities against TMV and CMV, among which compounds 4b, 4h, 4i, 4k, 4o, and 4q exhibited good curative, protection, and inactivation activity against TMV. Compounds 4h, 4i, 4k, 4l, 4o, and 4q exhibited excellent protection activity against TMV, with EC50 values of 105.01, 254.77, 135.38, 297.40, 248.18, and 129.87 µg/mL, respectively, which were superior to that of ribavirin (457.25 µg/mL). In addition, preliminary SARs indicated that small electron-withdrawing groups on the aromatic ring were favorable for anti-TMV activity. This finding suggests that 1,4-pentadien-3-one derivatives containing a 1,3,4-thiadiazole moiety may be considered as potential lead structures for discovering new antiviral agents.


Subject(s)
Antiviral Agents/chemical synthesis , Antiviral Agents/pharmacology , Cucumovirus/drug effects , Pentanones/chemical synthesis , Pentanones/pharmacology , Thiadiazoles/chemical synthesis , Thiadiazoles/pharmacology , Tobacco Mosaic Virus/drug effects , Antiviral Agents/chemistry , Dose-Response Relationship, Drug , Drug Design , Magnetic Resonance Spectroscopy , Microbial Sensitivity Tests , Molecular Structure , Pentanones/chemistry , Ribavirin/pharmacology , Structure-Activity Relationship , Thiadiazoles/chemistry , Tobacco Mosaic Virus/metabolism
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