surgical oncology

肿瘤外科
  • 文章类型: Letter
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  • 文章类型: Journal Article
    确定老年手术癌症患者术后体力活动恢复(PA)下降的风险,本研究评估术前放射性肌肉减少症(RS)是否与恢复至基线PA的能力降低相关.RS被定义为在椎骨L3水平的CT扫描上通过性别特异性截止值减少的腰大肌质量或密度。PA被评估为使用PA跟踪器测量的步骤/天,并且PA的恢复被定义为术后3个月时>90%的术前步骤/天。在44名65岁及以上接受肿瘤手术的患者中,18例(41%)患者显示RS。17名患者(39%)恢复到基线PA,其中8例患者有RS(47%)。RS与基线PA的恢复无关(OR:1.38,95CI0.39-4.92,p=0.61)。在这项探索性研究中,术前RS与术后PA恢复无相关性.
    To identify older surgical cancer patients at risk of decreased postoperative recovery of physical activity (PA), this study assesses whether preoperative radiological sarcopenia (RS) is associated with a decreased ability to return to baseline PA. RS was defined as decreased psoas muscle mass or -density by gender-specific cut-offs on CT-scans at level of vertebra L3. PA was assessed as steps/day measured with PA tracker and recovery of PA was defined as >90% of preoperative steps/day at 3 months postoperatively. Of 44 included patients aged 65 and over undergoing oncologic surgery, 18 patients (41%) showed RS. Seventeen patients (39%) returned to baseline PA, of which eight patients had RS (47%). RS was not associated with a return to baseline PA (OR: 1.38, 95%CI 0.39-4.92, p = 0.61). In this exploratory study, no association was found between preoperative RS and recovery of PA postoperatively.
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  • 文章类型: Journal Article
    BACKGROUND: The indication of preoperative prophylaxis in the insertion of indwelling tunneled central venous catheters (ITCVC) has a low level of evidence. Our objective was to assess risk factors of ITCVC-related early bacteremia in oncological pediatric patients and to determine the need for preoperative prophylaxis.
    METHODS: A univariate and multivariate retrospective analysis of patients in whom an ITCVC was placed from January 2020 to July 2023, according to whether they had ITCVC-related early bacteremia (EB) in the first 30 postoperative days, was carried out. Demographic variables, leukopenia, neutropenia, use of preoperative antibiotic prophylaxis, and history of central venous catheter (CVC) or bacteremia were collected. Calculations were carried out using the IBM SSPS29® software.
    RESULTS: 176 patients with a mean age of 7.6 years (SD: 4.82) were analyzed. 7 EB cases were identified, with a greater frequency of neutropenia (p= 0.2), history of CVC in the 48 hours before insertion (p= 0.08), and intraoperative CVC (p= 0.04). The presence of intraoperative CVC increased the risk of EB 9-fold [OR: 9.4 (95%CI: 1.288-69.712) (p= 0.027)]. The lack of preoperative prophylaxis did not increase the risk of EB [OR: 2.2 (CI: 0.383-12.669) (p= 0.3)]. The association with other variables was not significant.
    CONCLUSIONS: The intraoperative presence of CVC was a risk factor of EB in our patients. Preoperative prophylaxis had no impact on the risk of EB, which in our view does not support its use. However, further studies with a larger sample size are required. Leukopenia or neutropenia at diagnosis were not associated with a greater prevalence of infection.
    BACKGROUND: La indicación de profilaxis preoperatoria en la colocación de catéteres venosos centrales tunelizados permanentes (CVCTP) tiene bajo nivel de evidencia. Nuestro objetivo fue evaluar factores de riesgo de bacteriemia precoz asociada a CVCTP en pacientes pediátricos oncológicos y determinar la necesidad de profilaxis preoperatoria.
    METHODS: Realizamos un análisis retrospectivo univariante y multivariante de los pacientes con colocación de CVCTP entre enero 2020 y julio 2023, en función de si presentaron bacteriemia precoz (BP) relacionada con CVCTP en los primeros 30 días postoperatorios. Recogimos variables demográficas y otras como: leucopenia, neutropenia, uso de profilaxis antibiótica preoperatoria y antecedente de catéter venoso central (CVC) o bacteriemia. Los cálculos se realizaron mediante el software IBM SSPS29®.
    RESULTS: Analizamos 176 pacientes, con edad media de 7,6 años (SD 4,82). Identificamos 7 casos de BP, que presentaron mayor frecuencia de neutropenia (p=  0,2) y antecedente de CVC las 48h previas a la colocación (p=  0,08) y CVC intraoperatorio (p=  0,04). La presencia de CVC intraoperatorio aumentó 9 veces el riesgo de BP [OR 9,4 (IC 95% de 1,288-69,712) (p=  0,027)]. La falta de profilaxis prequirúrgica no aumentó el riesgo de BP [OR 2,2 (IC 0,383-12,669) (p=  0,3)]. La relación con otras variables no fue significativa.
    CONCLUSIONS: La presencia intraoperatoria de CVC fue factor de riesgo de BP en nuestros pacientes. La profilaxis preoperatoria no influyó sobre el riesgo de BP, por lo que creemos que su empleo no está justificado, aunque se necesitarían más estudios con mayor tamaño muestral. La leucopenia o neutropenia al momento diagnóstico no se relacionaron con mayor prevalencia de infección.
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  • 文章类型: Journal Article
    关于“观察和等待直肠癌”主题的前瞻性数据的缺乏促使Norwait的实施,一项基于人群的研究,包括新辅助治疗后的直肠癌患者。该研究的目的是评估临床完全缓解(cCR)的准确性并量化再生长率。Norwait是一项前瞻性的基于人群的观察性研究,在clinicaltrials.com(NTC03402477)注册了伦理批准(2017/935)。在7家医院完成放疗或放化疗后,经组织学证实为直肠癌的挪威居民符合资格。cCR是指肿瘤和任何溃疡的消失,有/没有出现先前肿瘤部位的变白和12周时通过直肠指检评估的毛细血管扩张,和内窥镜成像。该研究旨在包括100例以再生长率为主要终点的cCR患者。数据以粗略形式呈现。从2018年到2020年,研究终止时,有82名患者被纳入7家医院。五十一名病人被纳入六间医院,而在一家医院发现了违反协议的行为,其中纳入了31名(而不是方案估计的12名)患者。在31名患者中,只有2个有记录的cCR。在后者29例中,有16例患有溃疡或持续性肿瘤,和13,没有任何cCR文件。其中,23人接受了手术,延迟长达50周。在31例患者的中位54个月随访中,有77%的地方再生长(n=23),40%异时转移(n=12)和23%死亡(n=7)。在51例cCR患者的中位54个月随访中,有53%的地方再生长(n=27),14%的异时转移(n=7)和4%的死亡(n=2)。Norwait告诫一个警告,超越了一项基于人口的研究的不确定结果,该研究因严重违反协议和进行安全研究的立法而受到威胁。
    The paucity of prospective data on the subject of Watch and Wait for rectal cancer prompted the implementation of Norwait, a population-based study including rectal cancer patients after neoadjuvant therapy. The aim of the study was to assess the accuracy of clinical complete response (cCR) and quantify the regrowth rates. Norwait was a prospective population-based observational study with ethical approval (2017/935) registered at clinicaltrials.com (NTC03402477). Residents of Norway with histologically proven rectal cancer located within 15 cm from anal verge were eligible following completion of radiotherapy or chemoradiation at seven hospitals. cCR was the disappearance of tumour and of any ulcer with/without the appearance of whitening of prior tumour site and telangiectasia evaluated at 12 weeks by digital rectal exam, and endoscopic imaging. The study aimed to include 100 cCR patients with regrowth rates as primary endpoint. The data are presented in crude form. Eighty-two patients were included in seven hospitals from 2018 to 2020 when the study was terminated. Fifty-one patients were included in six hospitals, whereas protocol violations were identified in one hospital, where thirty-one (rather than protocol-estimated 12) patients were enrolled. Amongst the 31 patients, there were only 2 with documented cCR. Of the latter 29, there were 16 with ulcer or persistent tumour, and 13 without any documentation of cCR. Of these, 23 underwent surgery with a delay up to 50 weeks. At median 54-month follow-up of 31 patients, there were 77% local regrowths (n = 23), 40% metachronous metastases (n = 12) and 23% deaths (n = 7). At median 54-month follow-up of 51 cCR patients, there were 53% local regrowths (n = 27), 14% metachronous metastases (n = 7) and 4% deaths (n = 2). Norwait admonishes a word of caution reaching beyond the inconclusive results of a population-based study jeopardised by serious violation to protocol and legislation for conducting safe research.
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  • 文章类型: Journal Article
    目的:开发一种术前工具来评估原发性减瘤手术围手术期红细胞输注的风险。
    方法:我们回顾性回顾了一个机构数据库,以确定在2001年1月1日至2019年5月31日期间在单个中心接受卵巢癌原发性减瘤手术的患者。计算接收器工作特征曲线和接收器工作特征曲线下面积(AUC)。将五折交叉验证应用于多变量模型。如果存在,则将重要变量分配为“血液”(卵巢癌膨胀手术的血液输血)评分为+1。计算每位患者的总血液评分,并对每个评分确定接受输血的几率.
    结果:总体而言,1566例患者符合资格标准;800例(51%)接受了围手术期输血。美国麻醉医师协会评分为3分和4分的赔率比(OR)具有统计学意义(OR1.34,95%置信区间(95%CI)1.09至1.63),术前癌症抗原125(CA125)水平(OR2.43,95%CI1.98至2.99),血小板(OR1.59,95%CI1.45至1.74),肥胖(OR0.76,95%CI0.60至0.96),存在癌病(OR2.45,95%CI1.93至3.11),上腹部大部疾病(OR2.86,95%CI2.32至3.54),术前血清白蛋白水平(OR0.31,95%CI0.24至0.40),术前血红蛋白水平(OR0.56,95%CI0.51至0.61)。校正的AUC为0.748(95%CI0.693至0.804)。血液得分为0分和5分,分别对应11%和73%的赔率,分别,接受围手术期输血.
    结论:我们开发了一种通用的术前评分系统,血液分数,以帮助识别卵巢癌患者谁将受益于手术计划和血液节约技术。血液评分与美国麻醉医师协会的评分成正比,上腹部疾病的存在,癌,CA125水平,和血小板水平。我们相信该模型可以帮助医生制定手术计划,并有利于患者的预后。
    OBJECTIVE: To develop a pre-operative tool to estimate the risk of peri-operative packed red blood cell transfusion in primary debulking surgery.
    METHODS: We retrospectively reviewed an institutional database to identify patients who underwent primary debulking surgery for ovarian cancer at a single center between January 1, 2001 and May 31, 2019. Receiver operating characteristic curve and area under the receiver operating characteristic curve (AUC) were calculated. Five-fold cross-validation was applied to the multivariate model. Significant variables were assigned a \'BLOODS\' (BLood transfusion Over an Ovarian cancer Debulking Surgery) score of +1 if present. A total BLOODS score was calculated for each patient, and the odds of receiving a transfusion was determined for each score.
    RESULTS: Overall, 1566 patients met eligibility criteria; 800 (51%) underwent a peri-operative blood transfusion. Odds ratios (OR) were statistically significant for American Society of Anesthesiologists scores of 3 and 4 (OR 1.34, 95% confidence interval (95% CI) 1.09 to 1.63), pre-operative levels of cancer antigen 125 (CA125) (OR 2.43, 95% CI 1.98 to 2.99), platelets (OR 1.59, 95% CI 1.45 to 1.74), obesity (OR 0.76, 95% CI 0.60 to 0.96), presence of carcinomatosis (OR 2.45, 95% CI 1.93 to 3.11), bulky upper abdominal disease (OR 2.86, 95% CI 2.32 to 3.54), pre-operative serum albumin level (OR 0.31, 95% CI 0.24 to 0.40), and pre-operative hemoglobin level (OR 0.56, 95% CI 0.51 to 0.61). The corrected AUC was 0.748 (95% CI 0.693 to 0.804). BLOODS scores of 0 and 5 corresponded to 11% and 73% odds, respectively, of receiving a peri-operative blood transfusion.
    CONCLUSIONS: We developed a universal pre-operative scoring system, the BLOODS score, to help identify patients with ovarian cancer who would benefit from surgical planning and blood-saving techniques. The BLOODS score was directly proportional to the American Society of Anesthesiologists score, presence of upper abdominal disease, carcinomatosis, CA125 level, and platelets level. We believe this model can help physicians with surgical planning and can benefit patient outcomes.
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  • 文章类型: Journal Article
    背景:筋膜平面阻滞(FPB)被广泛用于腹部手术,假设脂质体布比卡因(LB)比标准布比卡因(SB)更有效。
    方法:这是一项单机构的回顾性队列研究,研究对象是给予FPB与LB或SB+混合物(地塞米松/右美托咪定)用于开腹手术的患者。倾向评分匹配产生2:1(LB:SB)匹配的队列。阿片类药物使用(mg口服吗啡当量,比较了OME)和严重疼痛(24小时内≥3疼痛评分≥7)。
    结果:在19.9%(29/146)LB和16.4%(12/73)SB患者中,阿片类药物的使用>150mgOME(p=0.586)。44%(64/146)LB和53%(39/73)SB患者经历了严重疼痛(p=0.198)。在多变量分析中,SB与LB选择与高阿片类药物量>150毫克或严重疼痛无关。
    结论:与脂质体布比卡因相比,使用标准布比卡因的FPB与更高的72小时阿片类药物使用或更严重的疼痛无关。
    BACKGROUND: Fascial plane blocks (FPBs) are widely used for abdominal surgery with the assumption that liposomal bupivacaine (LB) is more effective than standard bupivacaine (SB).
    METHODS: This was a single-institution retrospective cohort study of patients administered FPBs with LB or SB ​+ ​admixtures (dexamethasone/dexmedetomidine) for open abdominal cancer surgery. Propensity score matching generated a 2:1 (LB:SB) matched cohort. Opioid use (mg oral morphine equivalents, OME) and severe pain (≥3 pain scores ≥7 in a 24-h period) were compared.
    RESULTS: Opioid use was >150 ​mg OME in 19.9 ​% (29/146) LB and 16.4 ​% (12/73) SB patients (p ​= ​0.586). Severe pain was experienced by 44 ​% (64/146) LB and 53 ​% (39/73) SB patients (p ​= ​0.198). On multivariable analysis, SB vs LB choice was not associated with high opioid volume >150 ​mg or severe pain.
    CONCLUSIONS: FPBs with standard bupivacaine were not associated with higher 72-h opioid use or more severe pain compared to liposomal bupivacaine.
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  • 文章类型: Journal Article
    背景:日间手术正在发展,其普及程度越来越高,原因有多种:经济限制,专业实践的变化,患者的附着力更大。在外科手术进步的时代,如果由经验丰富的团队计划和管理,带蒂穿支皮瓣可以减少供体部位的发病率并避免微吻合,可以在Day手术中占据一席之地。
    方法:在2019年1月至2021年1月期间,我们在门诊环境中进行了穿支皮瓣覆盖软组织。回顾性纳入患者,并通过回顾病历收集数据。记录主要和次要并发症。
    结果:回顾性队列包括32例患者的32例外科手术。在所有情况下,穿支皮瓣用于肿瘤皮肤科手术后修复软组织缺损(84.3%),软组织肉瘤手术(12.5%),浸润性导管乳腺癌(3.1%)。需要手术翻修的主要并发症克服了3/32倍(9.4%)。在这些情况下,一次需要从襟翼上放下的故障克服了一次。平均伤口愈合时间为33天(15-90),平均随访时间为9.6个月(1-22)。
    结论:我们系列的低并发症率表明,在门诊手术中首次使用穿支皮瓣的经验在安全性和可行性方面是有希望的。日间手术可能是这种类型的外科手术的实用选择,避免了常规部门的饱和,并允许提供适当的手术护理。
    BACKGROUND: Day surgery is developing and its popularity is increasing for a variety of reasons: economic constraints, changes in professional practices, a greater adhesion of the patient. In an era of progress in surgical procedures, pedicled-perforator flaps reducing donor site morbidity and avoiding micro-anastomosis could take their place in Day surgery if planned and managed by an experienced team.
    METHODS: In the period January 2019 to January 2021, we performed perforator flaps for soft tissue coverage in ambulatory setting. The patients were included retrospectively and data were collected by reviewing the medical records. Major and minor complications were recorded.
    RESULTS: The retrospective cohort included 32 surgical procedures in 32 patients. In all cases, perforator flaps were realized for resurfacing soft tissue defects consequent to oncodermatology surgery (84.3%), soft tissue sarcoma surgery (12.5%), invasive ductal breast carcinoma (3.1%). Major complications needing a surgical revision overcame 3/32 times (9.4%). In these cases, a failure requiring the drop off the flap overcame once. The average wound healing time was of 33 days (15-90) and the mean duration of follow-up was 9.6 months (1-22).
    CONCLUSIONS: The low complication rate in our series suggests that this first experience on perforator flaps in outpatient surgery is promising in terms of safety and feasibility. Day surgery could be a practical option for this type of surgical procedures avoiding the conventional department\'s saturation and allowing the delivery of proper surgical cares.
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  • 文章类型: Journal Article
    背景:酪氨酸激酶抑制剂(TKIs)在早期和转移性癌基因驱动的非小细胞肺癌(NSCLC)中的作用已确立,但在局部晚期疾病中,如何最好地将TKIs与同步放化疗(cCRT)相结合仍是未知的。2期ASCENT试验评估了阿法替尼和cCRT伴或不伴手术治疗局部晚期表皮生长因子受体(EGFR)突变NSCLC的疗效和安全性。
    方法:在MassGeneral和Dana-Farber/Brigham癌症中心招募了经组织学证实的III期(AJCC第7版)非小细胞肺癌患者,波士顿,马萨诸塞州。患者每天接受阿法替尼40mg诱导,持续2个月,然后顺铂75mg/m2和培美曲塞500mg/m2在RT(确定性或新辅助给药)期间每3周静脉注射一次。患有可切除疾病的患者接受了手术。所有患者均接受阿法替尼巩固治疗2年。主要终点是诱导TKI的客观反应率(ORR)。次要终点是安全性,转换为可操作性,无进展生存期(PFS),总生存率(OS)。对意向治疗人群进行了分析。
    结果:纳入了19例患者(中位年龄56岁;74%为女性)。诱导阿法替尼的ORR为63%。17例患者接受cCRT;2/9以前不可切除的患者变为可切除。10人接受了手术;6人出现重大或完全病理反应。十三人接受了阿法替尼巩固治疗。中位随访时间为5.0年,中位PFS和OS分别为2.6(95%CI,1.4-3.1)和5.8年(2.9-NR),分别。16例复发或死亡;CNS分离出6例复发。停止巩固TKI后的中位进展时间为2.9个月(95%CI,1.1-7.2)。4人发展为2级肺炎。没有治疗相关的死亡。
    结论:我们探讨了TKI联合cCRT在癌基因驱动的非小细胞肺癌中的疗效。诱导TKI不影响随后接受多模式治疗。PFS很有希望,但是TKI停药后仅中枢神经系统复发和快速进展的患病率说明了在测量和根除微转移性疾病方面未满足的需求。
    BACKGROUND: The role of tyrosine kinase inhibitors (TKIs) in early-stage and metastatic oncogene-driven non-small cell lung cancer (NSCLC) is established, but it remains unknown how best to integrate TKIs with concurrent chemoradiotherapy (cCRT) in locally advanced disease. The phase 2 ASCENT trial assessed the efficacy and safety of afatinib and cCRT with or without surgery in locally advanced epidermal growth factor receptor (EGFR)-mutant NSCLC.
    METHODS: Adults ≥18 years with histologically confirmed stage III (AJCC 7th edition) NSCLC with activating EGFR mutations were enrolled at Mass General and Dana-Farber/Brigham Cancer Centers, Boston, Massachusetts. Patients received induction afatinib 40 mg daily for 2 months, then cisplatin 75 mg/m2 and pemetrexed 500 mg/m2 IV every 3 weeks during RT (definitive or neoadjuvant dosing). Patients with resectable disease underwent surgery. All patients were offered consolidation afatinib for 2 years. The primary endpoint was the objective response rate (ORR) to induction TKI. Secondary endpoints were safety, conversion to operability, progression-free survival (PFS), and overall survival (OS). Analyses were performed on the intention-to-treat population.
    RESULTS: Nineteen patients (median age 56 years; 74% female) were enrolled. ORR to induction afatinib was 63%. Seventeen patients received cCRT; 2/9 previously unresectable became resectable. Ten underwent surgery; 6 had a major or complete pathological response. Thirteen received consolidation afatinib. With a median follow-up of 5.0 years, median PFS and OS were 2.6 (95% CI, 1.4-3.1) and 5.8 years (2.9-NR), respectively. Sixteen recurred or died; 6 recurrences were isolated to CNS. The median time to progression after stopping consolidation TKI was 2.9 months (95% CI, 1.1-7.2). Four developed grade 2 pneumonitis. There were no treatment-related deaths.
    CONCLUSIONS: We explored the efficacy of combining TKI with cCRT in oncogene-driven NSCLC. Induction TKI did not compromise subsequent receipt of multimodality therapy. PFS was promising, but the prevalence of CNS-only recurrences and rapid progression after TKI discontinuation speak to unmet needs in measuring and eradicating micrometastatic disease.
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  • 文章类型: Journal Article
    目的:评估妇科肿瘤和泌尿外科联合手术对妇科肿瘤患者健康影响的社会决定因素。
    方法:我们使用国际疾病分类-10代码在国家住院患者样本中确定了2016年至2019年接受妇科肿瘤手术的患者。人口统计,包括种族和保险状况,比较了仅接受妇科肿瘤学手术(肿瘤学)和并发失禁或盆腔器官脱垂手术(妇科-肿瘤学)的患者。逻辑回归模型在对其他相关变量进行调整后评估了感兴趣的变量。
    结果:从2016年到2019年,全国住院患者样本数据库包含389例(1.14%)妇科肿瘤病例和33796例(98.9%)肿瘤病例。泌尿妇科-肿瘤患者不太可能是白人(62.1%vs68.8%,p=0.02),年龄较大(中位数为67岁vs62岁,p<0.001)比肿瘤患者。妇科-肿瘤队列不太可能将私人保险作为他们的主要保险(31.9%vs38.9%,p=0.01),并且更有可能获得医疗保险(52.2%对42.8%,p=0.01)。经过多变量分析,黑人(校正比值比(aOR)1.41,95%CI1.05~1.89,p=0.02)和西班牙裔患者(aOR1.53,95%CI1.11~2.10,p=0.02)仍更有可能接受妇科-肿瘤手术,但两组的主要预期付款人不再有显著差异(p=0.95).入院时的年龄,患者住所,两组之间的教学地点仍然存在显着差异。
    结论:在对大型住院患者数据库的分析中,我们发现接受泌尿外科-肿瘤和肿瘤手术的患者队列之间存在显著的种族和地理差异。
    OBJECTIVE: To assess social determinants of health impacting patients undergoing gynecologic oncology versus combined gynecologic oncology and urogynecology surgeries.
    METHODS: We identified patients who underwent gynecologic oncology surgeries from 2016 to 2019 in the National Inpatient Sample using the International Classification of Diseases-10 codes. Demographics, including race and insurance status, were compared for patients who underwent gynecologic oncology procedures only (Oncologic) and those who underwent concurrent incontinence or pelvic organ prolapse procedures (Urogynecologic-Oncologic). A logistic regression model assessed variables of interest after adjustment for other relevant variables.
    RESULTS: From 2016 to 2019 the National Inpatient Sample database contained 389 (1.14%) Urogynecologic-Oncologic cases and 33 796 (98.9%) Oncologic cases. Urogynecologic-Oncologic patients were less likely to be white (62.1% vs 68.8%, p=0.02) and were older (median 67 vs 62 years, p<0.001) than Oncologic patients. The Urogynecologic-Oncologic cohort was less likely to have private insurance as their primary insurance (31.9% vs 38.9%, p=0.01) and was more likely to have Medicare (52.2% vs 42.8%, p=0.01). After multivariable analysis, black (adjusted odds ratio (aOR) 1.41, 95% CI 1.05 to 1.89, p=0.02) and Hispanic patients (aOR 1.53, 95% CI 1.11 to 2.10, p=0.02) remained more likely to undergo Urogynecologic-Oncologic surgeries but the primary expected payer no longer differed significantly between the two groups (p=0.95). Age at admission, patient residence, and teaching location remained significantly different between the groups.
    CONCLUSIONS: In this analysis of a large inpatient database we identified notable racial and geographical differences between the cohorts of patients who underwent Urogynecologic-Oncologic and Oncologic procedures.
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  • 文章类型: Journal Article
    背景:肉瘤切除术后立即血管化重建可以减少初次闭合中常见的伤口并发症,但是以前的研究是相互矛盾的。本研究分析了伤口并发症的发生率,并比较了直接血管化重建与初次闭合之间与伤口相关的结果。
    方法:从2010年至2020年在斯德哥尔摩肉瘤中心接受有治愈意向的初次手术的患者中收集患者的患者的患者和肿瘤特征。在医疗记录的自由文本中寻求临床结果。主要结果指标是早期(<30天)伤口并发症。次要结局指标包括晚期(30天至2年)伤口并发症,伤口愈合的时间,根据ClavienDindo的30天术后并发症,和医疗保健消费。
    结果:共纳入482例患者,其中69人立即进行了血管化重建。初次闭合重建手术的早期并发症的比较显示,第一组的并发症发生率明显更高(59.4%vs29.8%,p<0.01)。两组术后第一年和第二年的医疗保健消费相当。深入分析确定BMI>25,吸烟和高级别病变是对伤口愈合产生不利影响的因素。
    结论:肉瘤患者伤口并发症发生率高,消耗大量的医疗资源。重建个体比初次闭合的受试者更容易发生此类并发症。
    BACKGROUND: Immediate vascularized reconstruction after sarcoma resection may reduce wound complications common in primary closure, but previous research is conflicting. The present study analysed wound complication rates and compared wound-related outcomes among immediate vascularized reconstruction with primary closure.
    METHODS: Patient- and tumour characteristics were collected from patients who received primary surgery with curative intent between 2010 and 2020 at the Stockholm Sarcoma Centre. Clinical outcomes were sought in free text in medical records. The primary outcome measures were early (<30 days) wound complications. Secondary outcome measures included late (30-day to 2-year) wound complications, time to wound healing, 30-day postoperative complications according to Clavien Dindo, and health care consumption.
    RESULTS: A total of 482 patients were included, of whom 69 had immediate vascularized reconstruction. Comparison of early complications for reconstructive surgery with primary closure revealed a significantly higher complication rate for the first group (59.4 % vs 29.8 %, p < 0.01). The groups had comparable health care consumption the first and second postoperative years. In-depth analyses identified BMI >25, smoking and high-grade lesions as factors with adverse effects on wound healing.
    CONCLUSIONS: Sarcoma patients experience high rates of wound complications and consume considerable health care resources. Reconstructed individuals were more susceptible to such complications than were subjects with primary closure.
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