Treatment outcome

治疗结果
  • 文章类型: Journal Article
    目前皮肤癌的诊断和治疗问题的相关性不仅取决于高发病率,但是传统方法在鉴别诊断和治疗方面存在困难。对于“不方便”治疗的基底细胞皮肤癌(BCSC)的定位,比如外耳道,耳廓,和鼻子的翅膀,治疗与某些困难和可能出现的美容缺陷有关,因此,在选择治疗方法时,这些器官的解剖特征被考虑在内。已经确定,鼻和耳廓原发性BCSC的治疗效果高于复发性BCSC,在各种治疗方法中,最有效和最彻底的是手术方法。通过手术方法以PR形式治疗BCSC的即时结果为86.7%,与其他类型的治疗相比具有统计学意义(p<0.05)。与其他方法相比,手术方法的长期治疗结果也更高(77%),这也是统计学上显著的(p<0.05)。
    The relevance of the problems of diagnosis and treatment of skin cancer is currently determined not only by the high incidence rate, but by the existing difficulties in differential diagnosis and treatment with traditional methods. For localizations of basal cell skin cancer (BCSC) that are \"inconvenient\" for treatment, such as the external auditory canal, auricle, and wing of the nose, treatment is associated with certain difficulties and the possible appearance of a cosmetic defect, therefore, when choosing a treatment method, the anatomical features of these organs are taken into account. It has been determined that the effectiveness of treatment for primary BCSC of the nose and auricles is higher than recurrent one, and among the various treatment methods, the most effective and radical is the surgical method. The immediate results of treatment of BCSC in the form of PR by surgical method were 86.7%, which is statistically significant compared with other types of treatment (p < 0.05). Long-term treatment results with the surgical method are also higher (77%) compared to other methods, which is also statistically significant (p < 0.05).
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    文章类型: Journal Article
    BACKGROUND: There has been an upsurge in the use of electrocautery in the treatment of benign prostatic hyperplasia (BPH) in our environment. Monopolar transurethral resection of the prostate (M-TURP) still remains the gold standard in the surgical management of BPH.
    OBJECTIVE: To present our experience and the clinical outcome of M-TURP in north-central Nigeria.
    METHODS: Data on demographics, indications, comorbidities, duration of surgery, weight of resected tissue, outcome of surgery, and complications were collected. International Prostate Symptom Score (IPSS) and Quality of Life (QoL) scores were assessed pre- and post-operatively. Results were analyzed using descriptive statistics. Student t-test was used for the comparison of continuous data while categorical data were compared by using Chi-square. P-value was considered significant if <0.05.
    RESULTS: In this retrospective study, out of 227 men who met the inclusion criteria, two patients\' procedures were converted to open surgery (conversion rate of 0.9%). The mean age of our patients was 65.2 + 7.5 years (44-90). The commonest indication for surgery was LUTS unresponsive to medical therapy (54.7%, n=123), followed by acute urinary retention (36.4%, n=82). The average weight of resected tissue was 36.5+12.1g (range 10-89) The weight of resected tissue correlated positively to prostate size measured by ultrasonography and it was also statistically significant (r = 0.568 and p-value <0.001). The early complications encountered were urinary tract infection (3.6%, n=8), clot retention (1.8%, n=4), and significant hematuria requiring blood transfusion (1.8%, n=4).
    CONCLUSIONS: In our setting, M-TURP demonstrates safety and efficacy in treating BPH. Skill and experience contribute to better outcomes, facilitating the management of larger prostates through refined techniques.
    BACKGROUND: Il y a eu une augmentation de l\'utilisation de l\'électrocautérisation dans le traitement de l\'hyperplasie bénigne de la prostate (HBP) dans notre environnement. La résection transurétrale monopolaire de la prostate (RTUP-M) reste néanmoins la référence en matière de gestion chirurgicale de l\'HBP.
    OBJECTIVE: Présenter notre expérience et les résultats cliniques de la RTUP-M dans le centre-nord du Nigéria.
    UNASSIGNED: Des données sur la démographie, les indications, les comorbidités, la durée de la chirurgie, le poids du tissu réséqué, les résultats de la chirurgie et les complications ont été collectées. Les scores de l\'Indice International des Symptômes Prostatiques (IPSS) et de la Qualité de Vie (QoL) ont été évalués avant et après l\'opération. Les résultats ont été analysés à l\'aide de statistiques descriptives. Le test t de Student a été utilisé pour comparer les données continues tandis que les données catégorielles ont été comparées à l\'aide du test du Chi-carré. La valeur p était considérée comme significative si elle était inférieure à 0,05.
    UNASSIGNED: Dans cette étude rétrospective, sur 227 hommes répondant aux critères d\'inclusion, deux interventions ont été converties en chirurgie ouverte (taux de conversion de 0,9 %). L\'âge moyen de nos patients était de 65,2±7,5 ans (44-90). L\'indication la plus courante pour la chirurgie était les LUTS non réactifs au traitement médical (54,7 %, n =123), suivis de la rétention urinaire aiguë (36,4 %, n=82). Le poids moyen du tissu réséqué était de 36,5 ± 12,1 g (plage 10-89). Le poids du tissu réséqué était positivement corrélé à la taille de la prostate mesurée par échographie et était également statistiquement significatif (r=0,568 et p-value <0,001). Les complications précoces rencontrées étaient les infections des voies urinaires (3,6 %, n = 8), la rétention de caillot (1,8 %, n = 4) et une hématurie significative nécessitant une transfusion sanguine (1,8 %, n = 4).
    CONCLUSIONS: Dans notre cadre, la RTUP-M démontre sa sécurité et son efficacité dans le traitement de l\'HBP. La compétence et l\'expérience contribuent à de meilleurs résultats, facilitant la gestion de prostates plus grandes grâce à des techniques affinées.
    UNASSIGNED: Électrocautérisation; Référence; Hommes; Formation; Poids; Réséqué.
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  • 文章类型: Journal Article
    Brexpiprazole是来自多巴胺D2/D3受体部分激动剂的新型抗精神病药物。它代表了第二代抗精神病药的发展,并且是精神分裂症药物治疗选择的重要补充。本文的目的是介绍,以布立哌唑为例,新的抗精神病药物的药理特性的进步如何转化为精神分裂症治疗的改善结果,不仅在减轻症状方面,而且在功能改进方面。与阿立哌唑和卡利拉嗪相比,布雷哌唑的D2/D3受体的激活与阻断比率较低,这可能会降低静坐不能的风险。Brexpiprazole还具有更强的抗组胺活性,这可能与更强的镇静作用有关,静坐不能的风险较低,过度激动和失眠。Brexpiprazole符合抗精神病药物疗效的传统要求,即,与安慰剂相比,在短期研究中,它可以使精神分裂症症状减少,并在长期随访中防止精神分裂症复发。发现最高的抗精神病药效与最高的注册剂量(4mg/天)。除了减少阳性症状,brexiprazole治疗也导致减少阴性和抑郁症状,以及焦虑。它对患者的社会和个人功能以及生活质量也有积极的影响。药物的这种作用符合患者及其家人对有效治疗的期望。它不仅应该减轻症状,而且还可以恢复健康,即,一个州,除了最佳的健康和心理幸福感,也有可能保持适当的社会关系。
    Brexpiprazole is a new antipsychotic drug from the group of dopamine D2/D3 receptor partial agonists. It represents a development of the second-generation antipsychotics and is an important addition to the pharmacological treatment options for schizophrenia. The purpose of this article is to present, illustrated by the case of brexpiprazole, how advances in the pharmacological properties of new antipsychotics translate into improved results in the treatment of schizophrenia, not only in terms of symptom reduction, but also in terms of functional improvement. The ratio of activation to blocking of the D2/D3 receptor is lower for brexpiprazole than for aripiprazole and cariprazine, which may translate into a lower risk of akathisia. Brexpiprazole has also stronger antihistaminic activity, which is likely to be associated with a stronger sedative effect, a lower risk of akathisia, excessive agitation and insomnia. Brexpiprazole meets the traditional requirements for an antipsychotic drug\'s efficacy, i.e., compared to placebo, it brings a greater reduction in schizophrenia symptoms in short-term studies and prevents schizophrenia relapses in long-term follow-up. The highest antipsychotic efficacy was found with the highest registered dose (4 mg/day). In addition to reducing positive symptoms, brexpiprazole treatment also leads to a reduction in negative and depressive symptoms, as well as anxiety. It has also a positive effect on patients\' social and personal functioning and quality of life. This action of the drug is in line with the expectations of patients and their families regarding effective treatment. It should not only reduce symptoms, but also enable a return to health, i.e., a state that, in addition to optimal health and a sense of psychological well-being, also makes it possible to maintain proper social relations.
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  • 文章类型: Journal Article
    背景:脊髓肿瘤的微创治疗很常见。这项研究的目的是比较经微内镜微创手术-通过自制管状牵开器(MIS-TR)和显微全椎板切除术(开放手术)治疗的胸髓外脊柱肿瘤(TEST)患者的围手术期结果。
    方法:2016年2月至2021年2月,纳入了51例TEST患者。根据他们的临床数据,将患者分为MIS-TR组(n=30)和开放手术组(n=21)并进行评估.
    结果:在两组中,平均手术时间,围手术期ASIA评分的变化,和改良的Macnab评分具有可比性。MIS-TR组术后平均住院时间明显短于开放手术组(p<0.0001)。MIS-TR组的平均失血量明显低于开放手术组(p=0.001)。MIS-TR组围手术期并发症发生率明显低于开放手术组(p<0.0001)。在3个月的随访中,两组间Oswestry残疾指数(ODI)评分改善无显著差异.尽管如此,在12个月的随访中,MIS-TR组的平均ODI显著低于开放手术组(p=0.023).术后完全恢复的主要影响因素为术前ASIA评分(OR7.848,P=0.002),手术并发症(OR0.017,P=0.008)和年龄(OR0.974,P=0.393)。
    结论:MIS-TR比开放手术治疗TEST更安全有效,但MIS-TR的长期恢复并不比开放手术好。
    BACKGROUND: Minimally invasive treatments for spinal cord tumours are common. The aim of this study was to compare the perioperative outcomes of patients with thoracic extramedullary spinal tumours (TEST) treated by microendoscopic minimally invasive surgery-hemilaminectomy through a homemade tubular retractor (MIS-TR) and microscopic full laminectomy (open surgery).
    METHODS: Between February 2016 and February 2021, 51 patients with TEST were included. According to their clinical data, patients were classified into the MIS-TR group (n = 30) and the open surgery group (n = 21) and assessed.
    RESULTS: In both groups, the mean operation time, change in perioperative ASIA score, and modified Macnab score were comparable. The average postoperative hospital stay in the MIS-TR group was substantially shorter than that in the open surgery group (p < 0.0001). The mean blood loss volume in the MIS-TR group was substantially lower than that in the open surgery group (p = 0.001). The perioperative complication rate in the MIS-TR group was considerably lower than that in the open surgery group (p < 0.0001). At the 3-month follow-up, there was no substantial difference in the Oswestry Disability Index (ODI) score improvement between the two groups. Nonetheless, at the 12-month follow-up, the average ODI in the MIS-TR group was considerably lower than that in the open surgery group (p = 0.023). The main influencing factors for complete postoperative recovery were preoperative ASIA score (OR 7.848, P = 0.002), surgical complications (OR 0.017, P = 0.008) and age (OR 0.974, P = 0.393).
    CONCLUSIONS: MIS-TR is safer and more effective than open surgery for treating TEST, but the long-term recovery of MIS-TR is not better than that of open surgery.
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  • 文章类型: Clinical Trial Protocol
    背景:数字化减肥计划可以提供方便,可能更便宜,以及可能需要减肥的人的可扩展治疗选择。然而,从长期来看,结果通常不如面对面干预.该试验将使用多相优化策略(MOST)框架中的原则来测试它是否可以提高商业数字行为减肥计划的有效性。该试验旨在确定四种干预成分的优化组合,以在24周内增强体重减轻。我们还将探讨哪些组件有助于改善参与者的保留和参与该计划。
    方法:将招募约1400名BMI>21kg/m2的成年人,并随机分配到24因子聚类设计中的16个实验条件之一。该试验将测试四个干预组件:与健康教练的介绍性视频通话,与健康教练进行网络聊天,目标设定声明,和食物日记审查和反馈。所有参与者将获得核心数字行为减肥计划和最多四个新的干预组件。参与试验将持续24周。主要结果是16周时的体重变化。其他成果,在4、16和24周测量,包括程序退出和参与(与三个主要应用程序功能的交互次数)。保真度和可接受性将使用组件依从性数据和自我报告问卷进行评估。增强计划的决策将基于至少有助于减轻体重的最小改善的组成部分,定义为≥0.75kg,单独或与其他组件组合。
    结论:析因设计是测试单独行为成分功效的有效方法,或组合,提高数字化减肥方案的效果。该试验将测试MOST框架在行业环境中的实施情况,使用常规收集的数据,这可以提供一种更好的方法来完善和评估这些类型的干预措施,以持续服务改进的模型。
    背景:试用注册:ISRCTN,ISRCTN14407868。注册日期为2024年1月5日,10.1186/ISRCTN14407868。
    BACKGROUND: Digitally delivered weight loss programmes can provide a convenient, potentially cheaper, and scalable treatment option for people who may need to lose weight. However, outcomes are often inferior to in-person interventions in the long-term. This trial will use principles from the Multiphase Optimisation Strategy (MOST) framework to test whether it can enhance the effectiveness of a commercial digital behavioural weight loss programme. This trial aims to identify an optimised combination of four intervention components to enhance weight loss over a 24-week period. We will also explore which components contribute to improvements in participant retention and engagement with the programme.
    METHODS: Approximately 1400 adults with a BMI > 21 kg/m2 will be enrolled and randomised to one of 16 experimental conditions in a 24 factorial cluster design. The trial will test four intervention components: an introductory video call with the health coach, drop-in webchat sessions with the health coach, goal setting statements, and food diary review and feedback. All participants will receive the core digital behavioural weight loss programme and up to four new intervention components. Participation in the trial will last for 24 weeks. The primary outcome will be weight change at 16 weeks. Other outcomes, measured at 4, 16, and 24 weeks, include programme drop-out and engagement (number of interactions with the three main app functions). Fidelity and acceptability will be assessed using data on component adherence and self-report questionnaires. Decision-making for the enhanced programme will be based on components that contribute to at least a minimal improvement in weight loss, defined as ≥ 0.75kg, alone or in combination with other components.
    CONCLUSIONS: The factorial design is an efficient way to test the efficacy of behavioural components alone, or in combination, to improve the effectiveness of digital weight loss programmes. This trial will test the implementation of the MOST framework in an industry setting, using routinely collected data, which may provide a better way to refine and evaluate these types of interventions in a model of continuous service improvement.
    BACKGROUND: Trial registration: ISRCTN, ISRCTN14407868. Registered 5 January 2024, 10.1186/ISRCTN14407868.
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  • 文章类型: Journal Article
    背景:本研究旨在比较原发性高级别神经胶质瘤(HGG)患者的生存结果和副作用,这些患者单独接受碳离子放疗(CIRT)或作为光子放疗后的增强策略(光子+CIRTboost)。
    方法:三十四(34)例经组织学证实的HGG患者,并单独接受CIRT或光子CIRTboost,在2020.03-2023.08期间在武威市肿瘤医院和研究所同时使用替莫唑胺,对中国进行了回顾性审查。总生存期(OS),无进展生存期(PFS),并对急性毒性和晚期毒性进行了分析和比较。
    结果:8名WHO3级和26名4级患者被纳入分析。对于所有HGG病例,单独CIRT组和光子CIRTboost组的中位PFS分别为15个月和19个月,4级病例分别为15个月和17.5个月。对于所有HGG病例,单独CIRT组和光子CIRTboost组的中位OS分别为28个月和31个月,4级病例分别为21个月和19个月。在单独的CIRT和光子+CIRTboost组之间没有观察到这些生存结果的显著差异。仅在单独的CIRT和光子CIRTboost组中观察到1级急性毒性。与光子+CIRTboost相比,单纯CIRT组的急性毒性比率显著降低(3/18vs.9/16,p=0.03)。没有观察到晚期毒性的显著差异。
    结论:单独使用BothCIRT和光子+CIRTboost同时使用替莫唑胺是安全的,HGG患者的PFS和OS无显著差异。在未来的随机试验中,探讨CIRTboost的剂量递增是否可以改善HGG患者的生存结果是有意义的。
    BACKGROUND: This study aimed to compare the survival outcome and side effects in patients with primary high-grade glioma (HGG) who received carbon ion radiotherapy (CIRT) alone or as a boost strategy after photon radiation (photon + CIRTboost).
    METHODS: Thirty-four (34) patients with histologically confirmed HGG and received CIRT alone or Photon + CIRTboost, with concurrent temozolomide between 2020.03-2023.08 in Wuwei Cancer Hospital & Institute, China were retrospectively reviewed. Overall survival (OS), progression-free survival (PFS), and acute and late toxicities were analyzed and compared.
    RESULTS: Eight WHO grade 3 and 26 grade 4 patients were included in the analysis. The median PFS in the CIRT alone and Photon + CIRTboost groups were 15 and 19 months respectively for all HGG cases, and 15 and 17.5 months respectively for grade 4 cases. The median OS in the CIRT alone and Photon + CIRTboost groups were 28 and 31 months respectively for all HGG cases, and 21 and 19 months respectively for grade 4 cases. No significant difference in these survival outcomes was observed between the CIRT alone and Photon + CIRTboost groups. Only grade 1 acute toxicities were observed in CIRT alone and Photon + CIRTboost groups. CIRT alone group had a significantly lower ratio of acute toxicities compared to Photon + CIRTboost (3/18 vs. 9/16, p = 0.03). No significant difference in late toxicities was observed.
    CONCLUSIONS: Both CIRT alone and Photon + CIRTboost with concurrent temozolomide are safe, without significant differences in PFS and OS in HGG patients. It is meaningful to explore whether dose escalation of CIRTboost might improve survival outcomes of HGG patients in future randomized trials.
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  • 文章类型: Journal Article
    背景:本研究通过评估术后早期结果,研究了在成人心脏手术中,与传统血液心脏停搏液相比,DelNido心脏停搏液的疗效。
    方法:共119例接受单纯常规冠状动脉旁路移植术的患者,根据使用的心脏停搏液类型分为两组(DelNido心脏停搏液组[n=36]和血液心脏停搏液组[n=50])。本研究比较了术前特点,术中数据,和术后早期结果。对高危患者组进行了进一步的亚组分析。
    结果:两组间30天死亡率和发病率无显著差异。delNido心脏停搏液组表现出有利的心肌保护结果,手术后肌钙蛋白I水平的升高明显较小(2.8[-0.4;4.2]vs.4.5[2.9;7.4]ng/mL,p=0.004),体外循环断奶期间的除颤尝试较少(0.0±0.2vs.0.4±1.1倍,与血液心脏停搏液组相比,p=0.011)。此外,delNido组减少了手术时间,主动脉交叉钳夹时间减少(64.0[55.5;75.5]vs.77.5[65.0;91.0]分钟,p=0.001)和总手术时间(287.5[270.0;305.0]vs.315.0[285.0;365.0]min,p=0.008)。亚组分析一致表明,在所有亚组中,delNido心脏停搏组的术后肌钙蛋白I水平增加明显较小(p<0.05)。
    结论:delNido心脏停搏液与血液心脏停搏液相比可提供心肌保护和良好的术后早期结局,使其成为常规冠状动脉旁路移植术的可行选择。需要就成人手术中DelNido心脏停搏液的给药方案达成共识。
    BACKGROUND: This study examined the efficacy of del Nido cardioplegia compared with traditional blood cardioplegia in adult cardiac surgery for isolated coronary artery bypass grafting by evaluating the early postoperative outcomes.
    METHODS: A total of 119 patients who underwent isolated conventional coronary artery bypass grafting were enrolled and divided into two groups (del Nido cardioplegia group [n = 36] and blood cardioplegia group [n = 50]) based on the type of cardioplegia used. This study compared the preoperative characteristics, intraoperative data, and early postoperative outcomes. Further subgroup analyses were conducted for high-risk patient groups.
    RESULTS: The 30-day mortality and morbidity rates were not significantly different between groups. The del Nido cardioplegia group exhibited advantageous myocardial protection outcomes, demonstrated by a significantly smaller rise in Troponin I levels post-surgery (2.8 [-0.4; 4.2] vs. 4.5 [2.9; 7.4] ng/mL, p = 0.004) and fewer defibrillation attempts during weaning off of cardiopulmonary bypass (0.0 ± 0.2 vs. 0.4 ± 1.1 times, p = 0.011) when compared to the blood cardioplegia group. Additionally, the del Nido group achieved a reduction in surgery duration, as evidenced by the reduced aortic cross-clamping time (64.0 [55.5; 75.5] vs. 77.5 [65.0; 91.0] min, p = 0.001) and total operative time (287.5 [270.0; 305.0] vs. 315.0 [285.0; 365.0] min, p = 0.008). Subgroup analyses consistently demonstrated that the del Nido cardioplegia group had a significantly smaller postoperative increase in Troponin I levels across all subgroups (p < 0.05).
    CONCLUSIONS: del Nido cardioplegia provided myocardial protection and favorable early postoperative outcomes compared to blood cardioplegia, making it a viable option for conventional coronary artery bypass grafting. Establishing a consensus on the protocol for Del Nido cardioplegia administration in adult surgeries is needed.
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  • 文章类型: Journal Article
    背景:国家综合癌症网络(NCCN)指南建议考虑将每周一次的顺铂作为头颈部癌症患者接受确定性放化疗的替代选择。然而,在最近的III期试验(ConCERT)中,20%的患者每周顺铂治疗不能总共接受200mg/m2,低依从性与每周顺铂和癌症控制结果的关系仍不清楚。为了填补这一知识空白,我们对接受每周一次顺铂确定性放化疗的头颈部癌患者进行了一项观察性队列研究.
    方法:我们的机构数据库查询了2007年11月至2023年4月期间接受每周顺铂(40mg/m2)确定性放化疗的非转移性头颈癌患者。坚持每周顺铂定义为接受至少5个周期,总累积剂量为200mg/m2。使用Kaplan-Meier方法评估生存结果,对数秩测试,Cox比例风险多变量(MVA)分析。进行LogisticMVA以确定与每周顺铂依从性低相关的变量。进行Fine-GrayMVA分析以死亡为竞争性事件的失败结果。
    结果:在符合我们标准的119名患者中,51例患者(42.9%)每周顺铂依从性低。中位随访时间为19.8个月(四分位距8.8-65.6)。对每周顺铂的低依从性与较差的总生存期(校正风险比[aHR]2.94,95%置信区间[CI]1.58-5.47,p<0.001)和无进展生存期(aHR2.32,95%CI1.29-4.17,p=0.005)相关。它还与更严重的远处衰竭相关(aHR4.55,95%CI1.19-17.3,p=0.03),但不是局部失败(aHR1.61,95%CI0.46-5.58,p=0.46)。KPS<90是与每周顺铂依从性低相关的唯一变量(调整后比值比[aOR]2.67,95%CI1.10-6.65,p=0.03)。
    结论:我们的研究表明,超过40%的患者接受少于5个每周顺铂周期,并且每周顺铂依从性低是独立的,不良预后因素生存和远处失败的结果。那些每周顺铂依从性降低的人更有可能表现不佳。需要进一步的研究来提高对化疗的依从性和预后。
    BACKGROUND: The National Comprehensive Cancer Network (NCCN) guideline recommends consideration of weekly cisplatin as an alternative option for patients with head and neck cancer undergoing definitive chemoradiation. However, in a recent phase III trial (ConCERT), 20% of patients treated with weekly cisplatin could not receive a total of 200 mg/m2, and the association of low adherence to weekly cisplatin and cancer control outcomes remains unclear. To fill this knowledge gap, we performed an observational cohort study of patients with head and neck cancer undergoing definitive chemoradiation with weekly cisplatin.
    METHODS: Our institutional database was queried for patients with non-metastatic head and neck cancer who underwent definitive chemoradiation with weekly cisplatin (40 mg/m2) between November 2007 and April 2023. Adherence to weekly cisplatin was defined as receiving at least 5 cycles with a total cumulative dose of 200 mg/m2. Survival outcomes were evaluated using Kaplan-Meier method, log-rank tests, Cox proportional hazard multivariable (MVA) analyses. Logistic MVA was performed to identify variables associated with low adherence to weekly cisplatin. Fine-Gray MVA was performed to analyze failure outcomes with death as a competing event.
    RESULTS: Among 119 patients who met our criteria, 51 patients (42.9%) had low adherence to weekly cisplatin. Median follow up was 19.8 months (interquartile range 8.8-65.6). Low adherence to weekly cisplatin was associated with worse overall survival (adjusted hazards ratio [aHR] 2.94, 95% confidence interval [CI] 1.58-5.47, p < 0.001) and progression-free survival (aHR 2.32, 95% CI 1.29-4.17, p = 0.005). It was also associated with worse distant failure (aHR 4.55, 95% CI 1.19-17.3, p = 0.03), but not locoregional failure (aHR 1.61, 95% CI 0.46-5.58, p = 0.46). KPS < 90 was the only variable associated with low adherence to weekly cisplatin (adjusted odds ratio [aOR] 2.67, 95% CI 1.10-6.65, p = 0.03).
    CONCLUSIONS: Our study suggested that over 40% of patients underwent fewer than 5 weekly cisplatin cycles and that low adherence to weekly cisplatin was an independent, adverse prognostic factor for worse survival and distant failure outcomes. Those with reduced adherence to weekly cisplatin were more likely to have poor performance status. Further studies are warranted to improve the adherence to chemotherapy and outcomes.
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  • 文章类型: Journal Article
    即使在腹腔镜检查可能存在解剖挑战的情况下,机器人方法也提高了微创结肠切除术的可行性。在评估机器人结肠切除术的相对益处时,需要考虑使用这种新技术完成结肠切除术的失败是否与更糟糕的后果有关。这项研究的目的是评估机器人和腹腔镜结肠切除术后转换为开腹手术的比率,以及两种技术后转换后的结果是否有所不同,因为这尚未得到很好的研究。来自美国外科医生学院(ACS)-国家外科质量改进计划(NSQIP)(2015-2016),我们确定了接受择期微创结肠切除术的患者.将转换后的机器人与患者人口统计学的腹腔镜手术进行了比较,合并症;主要程序和诊断,延长手术时间和术后并发症。在36,046例结肠切除术中,30,808(85.5%)进行了腹腔镜检查,而5238(14.5%)是机器人辅助的。有3271例(9.1%)转换为开放手术(腹腔镜:2959[9.6%];机器人:312[6%])。术后30天手术部位感染,吻合口漏,肠梗阻,脓毒症,需要输血的出血,尿路感染,再次手术;肺性,肾,心/脑血管并发症;再入院,住院,和死亡率,两组之间相似。然而,机器人转换后深静脉血栓/肺栓塞发生率更高(4.5%vs.2.2%,p=0.01)。与腹腔镜结肠切除术相比,机器人术后的转化率较低。转换后的患者具有相似的结果,除了机器人手术后静脉血栓栓塞较高。机器人技术似乎提高了微创手术的可行性,即使需要转换也不会对安全性和有效性产生负面影响。
    The robotic approach improves the feasibility of minimally invasive colectomy even where there may be an anatomic challenge with laparoscopy. Whether a failure in completing colectomy with this newer technology is associated with worse consequences needs to be considered when evaluating the relative benefit of robotic colectomy. The aim of this study is to evaluate rates of conversion to open surgery after robotic and laparoscopic colectomy and whether outcomes after conversion vary after the two techniques since this has not been well studied. From the American College of Surgeons (ACS) - National Surgical Quality Improvement Program (NSQIP) (2015-2016), patients who underwent elective minimally invasive colectomy were identified. Converted robotic were compared to laparoscopic procedures for patient demographics, co-morbidities; primary procedure and diagnosis, prolonged operation and postoperative complications. Of 36,046 colectomy procedures, 30,808 (85.5%) were laparoscopic, while 5238 (14.5%) were robotic-assisted. There were 3271 (9.1%) conversions to open surgery (laparoscopic: 2959 [9.6%]; robotic: 312 [6%]). Thirty-day postoperative surgical site infection, anastomotic leak, ileus, sepsis, bleeding requiring transfusion, urinary tract infection, reoperation; pulmonary, renal, cardiac/cerebrovascular complications; readmission, hospital stay, and mortality, were similar between the two groups. However, deep vein thrombosis/pulmonary embolism was higher after robotic conversion (4.5% vs. 2.2%, p = 0.01). Conversion was lower after robotic when compared to laparoscopic colectomy. Converted patients had similar outcomes except for vein thromboembolism which was higher after robotic surgery. Robotic technology seems to improve the feasibility of minimally invasive surgery without negatively affecting safety and efficacy even when conversion is required.
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  • 文章类型: Journal Article
    目的:介绍我们对小儿腹股沟疝(PIH)单切口腹腔镜经皮腹膜外腹股沟环(IIR)闭合术(SILPEC)的技术改进。
    方法:对2016年至2023年在我中心接受SILPEC的所有诊断为PIH的儿童进行前瞻性收集的数据进行回顾,并分为两组进行结果比较:A组:之前和B组:实施完全修改后。我们的修改包括使用不可吸收的单丝缝合线,在腹股沟内环(IIR)造成腹膜热损伤,使用套管确保IIR处的缝合线仅连接腹膜,在选定的情况下进行IIR的双重结扎。
    结果:纳入A组和B组(1个月至14岁)的1755例患者。两组之间的基线患者特征没有显着差异。中位随访40个月,A组的CIH和皮下缝合肉芽肿(SSG)的复发率分别为2.3%和1.5%。B组分别为0%和0%(p<0.001)。没有鞘膜积液,没有上升或萎缩的睾丸。
    结论:我们的SILPEC技术修改可以实现PIH的零复发和零SSG。
    OBJECTIVE: To present our technical modifications of single incision laparoscopic percutaneous extraperitoneal closure (SILPEC) of the internal inguinal ring (IIR) for pediatric inguinal hernia (PIH).
    METHODS: The prospectively collected data of all children diagnosed with PIH undergoing SILPEC at our center from 2016 to 2023 were reviewed and divided into two groups for result comparison: Group A: before and Group B: after the implementation of full modifications. Our modifications included using a nonabsorbable monofilament suture, creating a peritoneal thermal injury at the internal inguinal ring (IIR), employing a cannula to ensure the suture at the IIR ligates only the peritoneum, and double ligation of the IIR in selected cases.
    RESULTS: 1755 patients in group A and in group B (1 month to 14 years old) were enrolled. There were no significant differences regarding baseline patient characteristics between the two groups. At a median follow-up of 40 months, the rate of recurrent CIH and subcutaneous stitch granuloma (SSG) was 2.3% and 1.5% in group A vs. 0% and 0% in group B (p < 0.001). There were no hydroceles, no ascended or atrophic testis.
    CONCLUSIONS: Our SILPEC technical modifications can achieve zero recurrence and zero SSG for PIH.
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