quadrant

象限
  • 文章类型: Journal Article
    对于需要腹腔镜胃癌根治术的患者,淋巴结清扫术(LND)和外科手术的优化尤为重要。本研究介绍了顺时针模块化D2LND中的“象限三明治”方法,并评估了该方法的优点和安全性。
    回顾性分析2019年1月至2022年1月郑州大学附属肿瘤医院收治的108例腹腔镜全胃切除术患者的临床资料。基于不同的LND流程,55例患者被分配到观察组,使用“象限三明治法”进行顺时针模块化LND,53例患者被分配到对照组,经历了传统的LND。该方法在操作时间方面的有效性和安全性,失血,淋巴结产量,观察两组患者术后恢复情况及术后并发症发生情况。
    两组的基线数据之间没有统计学差异。关于手术,观察组手术时间为227.0±48.5分钟,术中出血100.0mL[四分位数间距(IQR),30.0-200.0mL],对照组手术时间为247±41.5分钟,术中出血180.0mL(IQR,130.0-245.0mL)。两组手术时间、术中出血量比较差异均有统计学意义(P=0.001,P=0.020)。关于LND,两组在每个分区的淋巴结总数方面没有统计学上的显著差异,和阳性淋巴结的数量。关于术后结果,两组术后病理分期差异无统计学意义,术后第一次口服喂养,术后住院时间,和术后并发症。
    使用“象限夹心法”顺时针模块化D2LND在腹腔镜全胃切除术中潜在安全可行。它不仅确保了LND的彻底性,而且还确保了高效和快速的手术过程,缩短手术时间,减少术中出血量。
    UNASSIGNED: For patients who need laparoscopic radical gastrectomy, lymph node dissection (LND) and optimization of surgical procedures are particularly important. This study introduces the \"quadrant-sandwich\" method in clockwise modular D2 LND and evaluates the advantages and safety of this method.
    UNASSIGNED: The clinical data of 108 laparoscopic total gastrectomy patients admitted to the Affiliated Cancer Hospital of Zhengzhou University from January 2019 to January 2022 were retrospectively analyzed. Based on the different LND processes, 55 patients were allocated to the observation group, which underwent clockwise modular LND using the \"quadrant-sandwich method\", and 53 patients were allocated to the control group, which underwent traditional LND. The effectiveness and safety of the approach in terms of operation time, blood loss, lymph node yield, postoperative recovery and postoperative complications were observed in the two groups.
    UNASSIGNED: There was no statistical difference between the baseline data of the two groups. In relation to the surgery, the observation group had an operation time of 227.0±48.5 minutes, and intraoperative bleeding of 100.0 mL [inter-quartile range (IQR), 30.0-200.0 mL], while the control group had an operation time of 247±41.5 minutes, and intraoperative bleeding of 180.0 mL (IQR, 130.0-245.0 mL). There were statistically significant differences between the two groups in terms of the operation time and intraoperative bleeding (P=0.001, P=0.020). In relation to the LND, there were no statistically significant differences between the two groups in terms of the total number of lymph nodes in each division, and the number of positive lymph nodes. In relation to the post-operative results, there were no statistically significant differences between the two groups in terms of the post-operative pathological stage, first postoperative oral feeding, post-operative hospitalization time, and post-operative complications.
    UNASSIGNED: Clockwise modular D2 LND using the \"quadrant-sandwich method\" is potentially safe and feasible in laparoscopic total gastrectomy. It not only ensures the thoroughness of the LND, but also ensures and efficient and fast surgical process, shortens the operation time, and reduces the amount of intraoperative bleeding.
    导出

    更多引用

    收藏

    翻译标题摘要

    我要上传

       PDF(Pubmed)

  • 文章类型: Randomized Controlled Trial
    缺乏比较数字和常规记录对静态咬合间配准的准确性的临床研究。因此,这项临床研究的目的是评估全足弓和象限足弓条件下数字咬合间配准与传统配准相比的精度。
    本研究招募了9名具有完全自然牙列的个体。每个参与者都接受了数字扫描,传统印象,并根据以下组进行静态咬合记录:DF组,使用Mediti700口内扫描仪(IOS)进行全足弓数字扫描和双侧颊扫描;DQ组,使用Mediti700IOS进行象限拱数字扫描和单侧颊扫描;CF组,全弓聚乙烯基硅氧烷(PVS)印象和PVS咬合记录;CQ组,象限弓PVS印象和PVS咬合间记录。对于CF组和CQ组,留下的印象,用硅胶咬合安装,用实验室扫描仪扫描,并与实验室扫描仪的口腔扫描几乎相连。在每一组中,每位参与者接受3个咬合间记录,重复虚拟关节3次,关节模型保存为STL文件.将STL文件导入到3D处理软件中以使用最佳拟合对齐方法计算重复测量之间的差异。研究组之间的显著性用双尾配对t检验计算,P<0.05。
    对于全拱,与CF组的204±81µm相比,DF组显示出明显更好的精确度,平均值为31±19µm(P=0.0003).同样,对于象限拱,与CQ组的255±136µm相比,DQ组显示出明显更好的精度,平均值为18±6µm(P=0.0009)。使用数字或常规方法时,象限弓和完整弓之间的精度没有显着差异。
    在全拱和象限拱情况下,与常规方法相比,数字方法在静态咬合间配准方面具有更好的精度。本临床试验于2022年7月6日在泛非临床试验注册数据库中注册。注册表的编号是PACTR202207648490275。
    Clinical studies comparing the accuracy of digital and conventional records for static interocclusal registration are lacking. Therefore, the purpose of this clinical study was to assess the precision of digital interocclusal registration compared to conventional registration for full arch and quadrant arch conditions.
    Nine individuals with complete natural dentition were enrolled in this study. Each participant received digital scans, conventional impressions, and static interocclusal records according to the following groups: group DF, full arch digital scans and bilateral buccal scans with Medit i700 intraoral scanner (IOS); group DQ, quadrant arch digital scans and unilateral buccal scans with Medit i700 IOS; group CF, full arch polyvinyl siloxane (PVS) impressions and PVS interocclusal records; group CQ, quadrant arch PVS impressions and PVS interocclusal records. For group CF and group CQ, the impressions were poured, mounted with the silicone bites, scanned with a laboratory scanner, and articulated virtually with buccal scans with the laboratory scanner. In each group, each participant received three interocclusal records to repeat the virtual articulation three times and the articulated models were saved as STL files. The STL files were imported into a 3D-processing software to calculate the discrepancies between repeated measures using best-fit-alignment method. The significance between the study groups was calculated with two-tailed paired t-test at P < 0.05.
    For full arch, group DF showed significantly better precision with a mean value of 31 ± 19 µm compared to 204 ± 81 µm for group CF (P = 0.0003). Similarly, for quadrant arch, group DQ showed significantly better precision with a mean value of 18 ± 6 µm compared to 255 ± 136 µm for group CQ (P = 0.0009). No significant difference in precision was found between quadrant arch and full arch when the digital or the conventional method was used.
    The digital approach had significantly better precision for static interocclusal registration compared to the conventional method in both full and quadrant arch situations. Trial Registry This clinical trial was registered on 06/07/2022 in the Pan African Clinical Trial Registry database, the number for the registry is PACTR202207648490275.
    导出

    更多引用

    收藏

    翻译标题摘要

    我要上传

    求助全文

  • 文章类型: Journal Article
    目的:在全口非手术治疗(FM-SRP)后24小时出现中度急性期反应。这项研究的目的是比较象限缩放(Q-SRP)和FM-SRP后的急性期(24小时)和中期(3个月)炎症。
    方法:38名受牙周炎影响的受试者在基线访视后随机分配到FM-SRP或Q-SRP。在基线和3个月时收集牙周和人体测量参数。在基线时抽取血清样本,治疗后1、7和90天。进行了炎症和内皮测定的高灵敏度测定。
    结果:FM-SRP在24小时后产生了更大的急性期反应[C反应蛋白(CRP)增加了三倍,白细胞介素(IL-6)增加两倍,肿瘤坏死因子略有增加]。在任何后续随访中,组间没有发现系统性生物标志物的差异。两种牙周治疗方法均可在临床牙周参数方面产生可比的改善,而组间没有差异。治疗时间与CRP(R=0.5,p<0.001)和IL-6(R=0.5,p=0.002)的相对24h升高呈正相关,而较深(>6mm)口袋的数量仅预测IL-6的相对增加(R=0.4,p<0.05)。
    结论:与Q-SRP相比,FM-SRP可触发24小时的中度急性期反应。需要进一步的研究来评估这些发现对血管事件风险的最终影响。(ClinicalTrials.govNCT01857804)。
    OBJECTIVE: A moderate acute-phase response occurs 24-h following full-mouth non-surgical treatment (FM-SRP). The aim of this study was to compare acute-phase (24-h) and medium-term (3 months) inflammation after quadrant scaling (Q-SRP) versus FM-SRP.
    METHODS: Thirty-eight periodontitis-affected subjects were randomly allocated to FM-SRP or Q-SRP after a baseline visit. Periodontal and anthropometric parameters were collected at baseline and 3 months. Serum samples were drawn at baseline, 1, 7, and 90 days after treatment. High-sensitivity assays of inflammation and endothelial assays were performed.
    RESULTS: FM-SRP produced a greater acute-phase response after 24 h [threefold increase in C-reactive protein (CRP), twofold increase in interleukin (IL-6), and a slight increase in tumour necrosis factor]. No differences in systemic biomarkers were noted between groups at any later follow-ups. Both periodontal treatments produced a comparable improvement in clinical periodontal parameters with no between-group differences. Treatment time was positively associated with the relative 24-h increase in CRP (R = 0.5, p < 0.001) and IL-6 (R = 0.5, p = 0.002), while the number of deeper (>6 mm) pockets predicted only the relative increase in IL-6 (R = 0.4, p < 0.05).
    CONCLUSIONS: FM-SRP triggers a moderate acute-phase response of 24 h duration compared to Q-SRP. Further research is needed to assess the eventual impact of such findings on the risk of vascular events is advocated. (ClinicalTrials.gov NCT01857804).
    导出

    更多引用

    收藏

    翻译标题摘要

    我要上传

    求助全文

公众号