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  • 文章类型: English Abstract
    BACKGROUND: Hearing-impaired persons with asymmetric hearing loss and a unilateral indication for a cochlear implant (CI) generally benefit from a bimodal hearing solution. The influence of bimodal fitting on speech comprehension (SC) over time has not yet been sufficiently investigated. The present study examines the influence of bimodal fitting on SC in bimodally fitted CI users with postlingual deafness at least 36 months after implantation and analyzes possible influencing factors.
    METHODS: Included in this retrospective longitudinal study were 54 bimodally fitted speech-competent CI users with at least 36 months of CI experience. Audiometric data of these CI users at predefined timepoints were compared.
    RESULTS: The change in the results of the Freiburg monosyllabic test (FT) over 36 months was significant (p < 5%) for the deafness group at <10 years for both the 65 dB sound pressure level (SPL) and at 80 dB SPL and also significant for the deafness group ≥10 years for 65 dB SPL. In the Oldenburg sentence test (OlSa) there was a highly significant change (p < 0.1%) for S0, S0N0, and S0NCI configurations and a very significant change (p < 1%) for S0NHA (HA: hearing aid). Age at implantation as a possible influencing factor could not be confirmed in the FT. In contrast, the duration of deafness was a negative influencing factor for SC with CI in the FT, whereas a longer duration of deafness was associated with worse results in the FT. The degree of hearing loss in the ear fitted with an HA did not influence SC. The median bimodal benefit (here: difference in SC with bimodal fitting compared to unilateral HA fitting for FT at 65 dB SPL) was 10% over the total study period. For a median of 79% of the test subjects, the bimodal benefit was found over the entire period of 36 months.
    CONCLUSIONS: Over time, SC improves significantly with a CI for the bimodal test subjects. The investigated influencing factors (age, duration of deafness, and degree of hearing loss in the contralateral ear) support the indication for bimodal provision in accordance with the guideline in Germany for cochlear implantation-regardless of age, duration of deafness, and hearing ability of the contralateral ear.
    UNASSIGNED: HINTERGRUND: Hörgeschädigte Menschen mit asymmetrischem Hörverlust und einseitiger Indikation für ein Cochleaimplantat (CI) profitieren in aller Regel deutlich von einer bimodalen Hörversorgung. Der Einfluss dieser Versorgungsart auf das Sprachverstehen (SV) im zeitlichen Verlauf ist bislang nicht hinreichend untersucht. Die vorliegende Studie untersucht den Einfluss einer bimodalen Versorgung auf das SV postlingual ertaubter, bimodal versorgter CI-Träger:innen nach einer Tragedauer von mindestens 36 Monaten und analysiert dabei mögliche Einflussfaktoren.
    METHODS: Es wurden 54 bimodal versorgte lautsprachkompetente CI-Träger:innen mit einer CI-Erfahrung von mindestens 36 Monaten in diese retrospektive Längsschnittstudie eingeschlossen. Audiometrische Daten von diesen CI-Träger:innen wurden im zeitlichen Verlauf verglichen.
    UNASSIGNED: Die Veränderung der Ergebnisse im Freiburger Einsilbertest (FBE) im Verlauf der 36 Monate war für die Ertaubungsgruppe < 10 Jahre sowohl für den Pegel 65 dB „sound pressure level“ (SPL) als auch für 80 dB SPL signifikant und für die Ertaubungsgruppe ≥ 10 Jahre für 65 dB SPL signifikant (p < 5 %). Beim Oldenburger Satztest (OlSa) ergab sich für die Konfigurationen S0, S0N0 und S0NCI eine hochsignifikante Veränderung (p < 0,1 %). und für S0NHG (HG: Hörgerät) eine sehr signifikante Veränderung (p < 1 %). Das Alter bei Versorgung als möglicher Einflussfaktor konnte durch den FBE nicht bestätigt werden. Die Ertaubungsdauer stellte dagegen einen negativen Einflussfaktor für das SV mit dem CI dar, wobei eine längere Ertaubungsdauer mit schlechteren Ergebnissen beim FBE assoziiert ist. Der Grad der Schwerhörigkeit des mit HG versorgten Ohrs beeinflusste das SV nicht. Im Median betrug der bimodale Nutzen (Differenz aus dem SV mit bimodaler Versorgung gegenüber einseitiger HG-Versorgung beim FBE für 65 dB SPL) über die gesamte Untersuchungszeit 10 %. Für im Median 79 % der Versuchspersonen war der bimodale Nutzen über den gesamten Zeitverlauf von 36 Monaten nachweisbar.
    UNASSIGNED: Im zeitlichen Verlauf verbessert sich das SV mit dem CI der bimodalen Versuchspersonen signifikant. Die untersuchten Einflussfaktoren (Alter, Ertaubungsdauer und Grad der Schwerhörigkeit des Gegenohrs) unterstützen die leitliniengerechte Indikationsstellung einer bimodalen Versorgung in Deutschland – unabhängig von Alter, Ertaubungsdauer und Hörfähigkeit des Gegenohrs – eine Cochleaimplantation durchzuführen.
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  • 文章类型: Journal Article
    背景:氟喹诺酮类药物是最常用的抗生素。由于它们已知的驱动抗菌素耐药性的趋势,他们的处方模式需要更多的限制。本研究旨在描述氟喹诺酮类药物处方的临床实践,肾损害患者的剂量调整和细菌耐药性,最终提供循证建议,以优化当地人群的抗生素处方.
    方法:本回顾性研究,横断面研究在巴勒斯坦的An-Najah国立大学医院进行.数据收集自2021年7月至2023年6月接受环丙沙星或左氧氟沙星的住院患者。检查了来自各个医院部门的692名住院患者的数据(左氧氟沙星为409名,环丙沙星为283名)。统计分析是通过IBMSPSS23.0版进行的,以总结人口统计,临床,和流行病学数据。
    结果:社会人口统计学特征显示出不同的年龄分布,环丙沙星和左氧氟沙星的年龄在50岁以上的比例为25.4%和39%,分别。环丙沙星主要用于肿瘤科(28.2%),手术预防(22.6%)和发热或无发热性中性粒细胞减少(21.1%)是最常见的适应症。左氧氟沙星主要用于内科病房(45.7%),主要用于下呼吸道感染(58.8%)和预防骨髓移植(16.5%)。肠球菌和耐甲氧西林金黄色葡萄球菌是最常见的病原菌,62.5%的分离株对环丙沙星有耐药性。此外,产超广谱β-内酰胺酶的肠杆菌是最常见的病原菌,33.3%对左氧氟沙星耐药。统计分析显示,抗生素的选择与治疗方法之间存在显着关联。左氧氟沙星比环丙沙星更有可能用作经验性治疗(p<0.001)。而环丙沙星更可能用作靶向治疗(p<0.001)。
    结论:本研究调查了发展中国家一家大型医院的处方实践和对左氧氟沙星和环丙沙星的耐药性。根据细菌的耐药性,我们得出的结论是,医院部门需要对这些抗生素的使用施加更大的限制。为此,应开展针对氟喹诺酮类药物与现行治疗指南的临床疗效的进一步研究,以评估其适当性.
    BACKGROUND: Fluoroquinolones are the most commonly prescribed antibiotics. Because of their known tendency to drive antimicrobial resistance, their prescribing patterns need to be more restricted. This study aimed to describe the clinical practice of fluoroquinolone prescription, dose adjustments for renal impairment patients and bacterial resistance profiles, eventually providing evidence-based recommendations to optimize antibiotic prescribing practices in the local population.
    METHODS: This retrospective, cross-sectional study was conducted at An-Najah National University Hospital in Palestine. The data were collected from admitted patients who were given ciprofloxacin or levofloxacin from July 2021 to June 2023. Data from 692 inpatients across various hospital departments were examined (409 for levofloxacin and 283 for ciprofloxacin). Statistical analysis was performed via IBM SPSS version 23.0 to summarize the demographic, clinical, and epidemiological data.
    RESULTS: The sociodemographic profile revealed diverse age distributions, with 25.4% and 39% older than 50 years for ciprofloxacin and levofloxacin, respectively. Ciprofloxacin was predominantly used in the oncology department (28.2%), with surgical prophylaxis (22.6%) and febrile or afebrile neutropenia (21.1%) being the most common indications. Levofloxacin was predominantly used in the medical ward (45.7%), mainly for lower respiratory tract infection (58.8%) and prophylaxis for bone marrow transplantation (16.5%). Enterococcus and methicillin-resistant Staphylococcus aureus were the most commonly isolated pathogens, with 62.5% of the isolates demonstrating resistance to ciprofloxacin. Moreover, extended-spectrum beta-lactamase-producing Enterobacterales were the most common pathogen isolated, with 33.3% being resistant to levofloxacin. Statistical analysis revealed a significant association between the choice of antibiotic and the approach to therapy. Levofloxacin was significantly more likely than ciprofloxacin to be used as empiric therapy (p < 0.001), whereas ciprofloxacin was more likely to be used as targeted therapy (p < 0.001).
    CONCLUSIONS: This study investigated prescribing practices and resistance to levofloxacin and ciprofloxacin in a large hospital in a developing country. According to the bacterial resistance profiles, we conclude that there is a need for hospital departments to exercise greater restraint on the use of these antibiotics. To this end, further studies addressing the clinical efficacy of fluoroquinolones against the current treatment guidelines to evaluate their appropriateness should be carried out.
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  • 文章类型: Journal Article
    关于将创新药物纳入国家报销药物清单(NRDL)的年度中国国家谈判表明,越来越多的新药具有重叠的作用机制和类似的适应症。然而,目前尚不清楚竞争是否会影响报销决定。因此,我们探讨了竞争对中国癌症药物报销决策的影响.
    我们确定了2017年至2022年NRDL谈判中涉及的癌症药物,并专注于符合条件的新谈判药物的初始报销决定。根据其等效的生物学作用机制和批准的适应症,将药物归类为类别内竞争对手。包括已确定的和潜在的竞争对手。其他变量包括药物类型,临床效益和安全性,每月药费,和疾病发病率。我们采用传统的单变量和多变量Firth的惩罚逻辑回归来评估适应症和药物水平的报销决策与变量之间的关联。
    在2017年至2022年之间,研究了对应于141种适应症的102种癌症药物,NRDL中添加了66种药物(64.7%),涵盖95种适应症(67.4%)。已确定竞争的适应症的报销比例明显高于未确定竞争的适应症(84.6%vs52.6%,p<0.0001)。然而,有和没有潜在竞争的组之间的报销比例差异无统计学意义(66.7%vs68.3%,p=0.84)。Firth的惩罚逻辑回归显示,已识别的竞争与成功的NRDL纳入呈正相关,而潜在竞争对谈判结果没有显著影响.改善的总生存期或无进展生存期与NRDL纳入呈正相关,而疾病发病率对报销决定产生负面影响。
    改善的临床获益和确定的竞争与NRDL纳入呈正相关。在中国基于价值的谈判模式中,临床效益是癌症药物价格谈判的关键基础,和市场竞争帮助这些药物以更合理的价格进入NRDL。这对全球创新药物的报销决定以及可获得性和可负担性的改善具有重要意义。
    国家自然科学基金(编号:72104151)。
    UNASSIGNED: Annual Chinese National negotiations for including innovative drugs in the National Reimbursement Drug List (NRDL) reveal an increasing number of new drugs with overlapping action mechanisms of action and similar indications. Yet, it is unclear if competition affects reimbursement decisions. Thus, we explored the impact of competition on reimbursement decisions for cancer drugs in China.
    UNASSIGNED: We identified the cancer drugs involved in NRDL negotiations from 2017 to 2022 and focused on the initial reimbursement decision for eligible newly negotiated drugs. Drugs were classified as within-class competitors based on their equivalent biological mechanisms of action and approved indications, including identified and potential competitors. Other variables included drug type, clinical benefit and safety, monthly drug cost, and disease incidence rate. We employed traditional univariate and multivariate Firth\'s penalized logistic regression to assess the association between reimbursement decisions and variables at the indication and drug levels.
    UNASSIGNED: Between 2017 and 2022, 102 cancer drugs corresponding to 141 indications were studied, and 66 drugs (64.7%) covering 95 indications (67.4%) were added to the NRDL. The proportion of reimbursements for indications with identified competition was significantly higher than that for indications without identified competition (84.6% vs 52.6%, p < 0.0001). However, the difference in reimbursement proportions between groups with and without potential competition was not statistically significant (66.7% vs 68.3%, p = 0.84). Firth\'s penalized logistic regression showed that identified competition was positively correlated with successful NRDL inclusion, whereas potential competition had no significant effect on negotiation outcomes. Improved overall survival or progression-free survival were positively associated with NRDL inclusion, whereas disease incidence negatively impacted reimbursement decisions.
    UNASSIGNED: Improved clinical benefit and identified competition were positively correlated with NRDL inclusion. In China\'s value-based negotiation model, clinical benefits served as a crucial foundation of price negotiation for cancer drugs, and market competition helped these drugs enter the NRDL at more reasonable prices. This has important implications for reimbursement decisions and accessibility and affordability improvement for innovative drugs worldwide.
    UNASSIGNED: National Natural Science Foundation of China (No. 72104151).
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  • 文章类型: Journal Article
    对于无法诊断出各种实验室检查结果的患者,通常会考虑进行脑部活检。然而,医生倾向于对它们在可能的非肿瘤性脑部疾病中的应用犹豫不决,由于侵入性和风险。目的是确定病因不明的神经系统疾病的脑活检指征。我们回顾性评估了诊断准确性,实验室检查结果(包括恶性淋巴瘤的液体活检),磁共振成像(MRI)的特点和接受脑活检的患者的治疗后的结果不明病因的神经系统疾病。在新泻大学医院住院期间接受过脑部活检的患者的数据,在2011年至2024年之间,进行了审查。此外,我们比较了明确活检和非特异性活检诊断患者的实验室数据和MRI表现.二十六位病人接受了脑部活检,14例患者(53.8%)获得明确诊断。即使在做出非特异性诊断的情况下,活检结果有助于排除恶性肿瘤并指导临床诊断和治疗决策.对8例患者进行了恶性淋巴瘤的液体活检,一个人产生了积极的结果,符合原发性中枢神经系统淋巴瘤。液体活检的敏感性和特异性分别为0.5和1。磁共振成像中弥漫性对比皮质病变和肿块效应的存在,与明确的诊断显着相关,与非特异性诊断相比。总之,脑MRI和液体活检可以帮助确定病因不明的神经系统疾病的脑活检的适当指征。
    Brain biopsies are often considered for patients who cannot be diagnosed with various laboratory test results. However, physicians tend to be hesitant regarding their application in possibly non-neoplastic brain diseases, due to the invasiveness and risks. The aim was to determine the indications for brain biopsies in cases of neurological diseases of unknown etiology. We retrospectively evaluated diagnostic accuracy, laboratory findings (including a liquid biopsy for malignant lymphoma), magnetic resonance imaging (MRI) characteristics and the post-treatment outcomes of patients undergoing brain biopsies for neurological diseases of unknown etiology. The data of patients who had undergone a brain biopsy during their admission to Niigata University Hospital, between 2011 and 2024, were reviewed. Moreover, the laboratory data and MRI findings between patients with definitive and nonspecific biopsy diagnoses were compared. Twenty-six patients underwent a brain biopsy, and a definitive diagnosis was obtained in 14 patients (53.8%). Even in cases where a nonspecific diagnosis was made, biopsy findings helped rule out malignancy and guide clinical diagnosis and treatment decisions. The liquid biopsy for malignant lymphoma was performed in eight patients, with one yielding a positive result, consistent with primary central nervous system lymphoma. The sensitivity and specificity of liquid biopsy were 0.5 and 1, respectively. Diffusely contrasted cortical lesions and the presence of mass effects on MRI, were significantly associated with a definitive diagnosis, compared to a nonspecific diagnosis. In conclusion, brain MRI and liquid biopsies can assist in determining the appropriate indications for brain biopsies in neurological diseases of unknown etiology.
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  • 文章类型: Journal Article
    经食管超声心动图(TEE)是评价心脏结构和功能的重要影像学方法,在心血管疾病的临床管理中具有重要价值。与经胸超声心动图(TTE)不同,是非侵入性的,TEE涉及半侵入性腔内手术,导致人们越来越关注其安全性和潜在的并发症。特别是随着临床实践中对TEE应用的需求不断增加,以及使用TEE的设施数量的快速增长,TEE技术的标准化应用和安全运行变得尤为重要。本文将回顾文献并借鉴个人经验,从技术角度分析TEE检查的并发症和安全性。
    Transesophageal Echocardiography (TEE) is an important imaging method for the evaluation of cardiac structure and function, and it holds significant value in the clinical management of cardiovascular diseases. Unlike transthoracic echocardiography (TTE), which is non-invasive, TEE involves semi-invasive intracavity operations, leading to increasing attention to its safety and potential complications. Especially with the increasing demand for TEE applications in clinical practice and the rapid growth in the number of facilities utilizing it, the standardized application and safe operation of TEE technology have become particularly crucial. This article will review the literature and draw upon personal experience to analyze the complications and safety of TEE examinations from a technical perspective.
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  • 文章类型: Journal Article
    近年来,随着外科技术的进步和体外心脏辅助装置如体外膜氧合(ECMO)的广泛使用,ALCAPA(来自肺动脉的异常左冠状动脉)的治疗结果已证明显著改善.然而,ALCAPA的手术适应症和方法,特别是冠状动脉壁内ALCAPA的手术方法,是否同时治疗MR仍存在争议。长期预后仍然令人沮丧,同时,不同中心的结果存在显著差异。本审查具体解决了上述这些问题。本文综述了病理生理学和分类,诊断,适应症,ALCAPA的手术策略和预后。相信本综述将为今后的研究者提供一定的参考,为今后降低先天性心脏病患儿的不良预后提供新的思路。
    In recent years, with advancements in surgical techniques and the widespread utilization of extracorporeal cardiac assist devices such as extracorporeal membrane oxygenation (ECMO), the treatment outcomes for ALCAPA (Anomalous left coronary artery from the pulmonary artery) have demonstrated significant improvements. However, the surgical indications and methods of ALCAPA, especially the surgical methods of ALCAPA with intramural coronary artery, and whether to treat MR at the same time are still controversial. The long-term prognosis remain discouraging simultaneously, with significant variations in outcomes across different centers. The present review specifically addresses these aforementioned concerns. This article reviews the pathophysiology and classification, diagnosis, indications, surgical strategy and prognosis of ALCAPA. We believe that this review will provide some reference for future researchers and provide new ideas for reducing the adverse prognosis of children with congenital heart disease in future.
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  • 文章类型: Journal Article
    最近批准的药物的适应症明显少于多年前批准的药物。一个可能的原因可能是,控制自批准或启动以来的年数,最近批准的药物有较少的适应症(例如在上市时)。精准医疗和个性化医疗的作用越来越大,精准医学的目标是提供更精确的预防方法,疾病的诊断和治疗。具有较少适应症的药物可能比具有许多适应症的药物“更精确”。
    我们使用来自法国和美国两个国家的不同类型的数据来分析许多药物之间的关系,该药物的年份——即药物首次上市或批准的年份——以及它的年龄——它已经上市的年数。
    两国的所有证据都表明,控制药物年龄,与多年前批准的药物相比,最近批准的药物往往具有更少的适应症。在美国,年份的10年增长与所有药物的有效适应症数量下降10.7%有关,1989年后批准的药物的有效适应症数量下降了19.4%。在法国,药物年龄增加对适应症数量的积极影响被药物年份增加的负面影响所抵消。
    最近批准的药物与旧药物相比,不太可能是“通用技术”(甚至是多用途技术)。近几十年来,“精准医学”的相对重要性有所增加。具有较少适应症的药物可能比具有许多适应症的药物“更精确”。
    UNASSIGNED: More recently approved drugs have significantly fewer indications than drugs approved many years ago. One possible reason for this may be that, controlling for the number of years since approval or launch, more recently approved drugs have fewer indications (e.g. at the time of launch). The role of precision and personalised medicine has increased, and the goal of precision medicine is to provide a more precise approach for the prevention, diagnosis and treatment of disease. Drugs that have fewer indications may be \'more precise\' than drugs that have many indications.
    UNASSIGNED: We use different kinds of data from two countries - France and the U.S. - to analyze the relationship across many drugs between the number of indications of a drug, the drug\'s vintage - i.e. the year in which the drug was first marketed or approved - and its age - the number of years it has been marketed.
    UNASSIGNED: All the evidence from both countries indicates that, controlling for drug age, more recently approved drugs tend to have fewer indications than drugs approved many years ago. In the U.S., a 10-year increase in vintage is associated with a 10.7% decline in the effective number of indications of all drugs, and a 19.4% decline in the effective number of indications of drugs approved after 1989. In France, the positive effect on the number of indications of the increase in drug age was more than offset by the negative effect of the increase in drug vintage.
    UNASSIGNED: More recently approved drugs are less likely to be \'general-purpose technologies\' (or even multi-purpose technologies) than older drugs. The relative importance of \'precision medicine\' has increased in recent decades. Drugs that have fewer indications may be \'more precise\' than drugs that have many indications.
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  • 文章类型: Journal Article
    由于中央骨赘上方的薄覆盖关节软骨不足以支撑UKA后的负重功能,因此外侧隔室中存在中央骨赘的患者可能是内侧膝关节炎的单室膝关节置换术(UKA)的不良候选人。因此,应尝试检测中枢骨赘,以确认UKA的适用性。
    Patients with central osteophytes in the lateral compartment may be poor candidates for unicompartmental knee arthroplasty (UKA) for medial knee arthritis given the thin overlying articular cartilage above the central osteophytes that is inadequate for supporting weight-bearing after UKA. Therefore, attempts should be made to detect central osteophytes to confirm suitability for UKA.
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  • 文章类型: Journal Article
    支气管内超声引导下经支气管针吸活检术(EBUS-TBNA)是一种用于肺活检的微创技术,实时超声引导下的肺周组织和淋巴结活检。它用于良性和恶性肺部和非肺部疾病的诊断和/或分期。我们的研究是基于大样本,在多元化的人群中,这提供了一个代表性的真实世界队列进行分析。
    在2019年9月至2022年8月期间接受EBUS-TBNA手术的患者被纳入这项回顾性研究。对于EBUS-TBNA诊断为良性和未分类病变的病例,最终诊断是通过进一步侵入性手术或联合治疗和临床随访至少6个月确定的.
    共有618名患者被纳入研究,包括182名女性(29.4%)和436名男性(70.6%)。所有患者的平均年龄为61.9±10.5岁。这些患者通过EBUS-TBNA成功穿刺以获得病理结果。将EBUS-TBNA的病理诊断结果与最终临床诊断结果进行比较,结果为良性病变133例(21.5%),恶性病变485例(78.5%)。其中,546例(88.3%)(464个恶性病变和82个良性病变)患者通过EBUS-TBNA获得病理诊断,而EBUS-TBNA在72例患者中无法明确诊断(11.6%).20/72非诊断性EBUS-TBNA为真阴性。整体诊断灵敏度,特异性,正预测值,负预测值,EBUS-TBNA的准确率为91.3%,100%,100%,27.8%,和91.6%[95%置信区间(CI):89.1-93.6%],分别。在这项研究中,只有1例患者在EBUS-TBNA手术期间出现活动性出血,无严重并发症.
    鉴于其低侵入性,诊断准确率高,和安全,EBUS-TBNA在胸部病变中值得推广。
    UNASSIGNED: Endobronchial ultrasound-guided transbronchial needle aspiration (EBUS-TBNA) is a minimally invasive technique for biopsy of lung, peri-pulmonary tissue and lymph nodes under real-time ultrasound-guided biopsy. It is used in the diagnosis and/or staging of benign and malignant pulmonary and non-pulmonary diseases. Our study is based on a large sample size, in a diversified population which provides a representative real-world cohort for analysis.
    UNASSIGNED: Patients who underwent EBUS-TBNA procedure between September 2019 and August 2022 were included in this retrospective study. For cases diagnosed as benign and unclassified lesions by EBUS-TBNA, the final diagnosis was determined by further invasive surgery or a combination of therapy and clinical follow-up for at least 6 months.
    UNASSIGNED: A total of 618 patients were included in the study, including 182 females (29.4%) and 436 males (70.6%). The mean age of all patients was 61.9 ± 10.5 years. These patients were successfully punctured by EBUS-TBNA to obtain pathological results. The pathological diagnosis results of EBUS-TBNA were compared with the final clinical diagnosis results as follows: 133 cases (21.5%) of benign lesions and 485 cases (78.5%) of malignant lesions were finally diagnosed. Among them, the pathological diagnosis was obtained by EBUS-TBNA in 546 patients (88.3%) (464 malignant lesions and 82 benign conditions), while EBUS-TBNA was unable to define diagnosis in 72 patients (11.6%). 20/72 non-diagnostic EBUS-TBNA were true negative. The overall diagnostic sensitivity, specificity, positive predictive value, negative predictive value, and accuracy of EBUS-TBNA were 91.3%, 100%, 100%, 27.8%, and 91.6% [95% confidence interval (CI): 89.1-93.6%], respectively. In this study, only one case had active bleeding without serious complications during the EBUS-TBNA procedure.
    UNASSIGNED: Given its low invasiveness, high diagnostic accuracy, and safety, EBUS-TBNA is worth promoting in thoracic lesions.
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  • 文章类型: Journal Article
    背景:与开腹手术相关的死亡率是患者和医疗保健提供者的重要关注点。在非洲,由于劳动力资源稀缺和用于检测出现并发症的患者的生理恶化的预警系统不足,这尤其令人担忧。
    方法:这项前瞻性队列研究旨在随访在乌干达Lacor医院接受急诊或择期腹部手术的患者。参与者是4月27日在医院接受腹部手术的患者,2019年7月07日,2021年。训练有素的研究人员使用标准化表格收集数据,其中包括人口统计信息(年龄,性别,电话联系,和位置),手术适应症,外科手术,术前健康状况,术后发病率和死亡率,和住院时间。
    结果:本研究涉及124例患者,大部分是男性,平均年龄35岁,表现为腹痛和不同的潜在合并症。择期病例占总数的60.2%。急诊和择期手术的常见原因分别为胃十二指肠穿孔和胆石症。并发症发生率为17.7%,手术部位感染最常见。死亡率为7.3%,和几个因素如术前低血压,肾功能紊乱,术后使用血管加压药,术后辅助通气与之相关。择期和急诊手术患者的生存率(P值=0.41)或住院时间(P值=0.17)没有显着差异。然而,发病率有显著差异(p<0.001)。
    结论:胆石症和胃十二指肠穿孔是关键的手术指征,术后通气和肾上腺素输注等因素与死亡率有关。急诊手术并发症发生率较高,特别是手术部位感染,尽管与择期手术相比,住院时间和死亡率相似。
    BACKGROUND: The mortality rate associated with open abdominal surgery is a significant concern for patients and healthcare providers. This is particularly worrisome in Africa due to scarce workforce resources and poor early warning systems for detecting physiological deterioration in patients who develop complications.
    METHODS: This prospective cohort study aimed to follow patients who underwent emergency or elective abdominal surgery at Lacor Hospital in Uganda. The participants were patients who underwent abdominal surgery at the hospital between April 27th, 2019 and July 07th, 2021. Trained research staff collected data using standardized forms, which included demographic information (age, gender, telephone contact, and location), surgical indications, surgical procedures, preoperative health status, postoperative morbidity and mortality, and length of hospital stay.
    RESULTS: The present study involved 124 patients, mostly male, with an average age of 35 years, who presented with abdominal pain and varying underlying comorbidities. Elective cases constituted 60.2% of the total. The common reasons for emergency and elective surgery were gastroduodenal perforation and cholelithiasis respectively. The complication rate was 17.7%, with surgical site infections being the most frequent. The mortality rate was 7.3%, and several factors such as preoperative hypotension, deranged renal function, postoperative use of vasopressors, and postoperative assisted ventilation were associated with it. Elective and emergency-operated patients showed no significant difference in survival (P-value = 0.41) or length of hospital stay (P-value = 0.17). However, there was a significant difference in morbidity (p < 0.001).
    CONCLUSIONS: Cholelithiasis and gastroduodenal perforation were key surgical indications, with factors like postoperative ventilation and adrenaline infusion linked to mortality. Emergency surgeries had higher complication rates, particularly surgical site infections, despite similar hospital stay and mortality rates compared to elective surgeries.
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