Greece

希腊
  • 文章类型: Journal Article
    (1)背景和目标:这篇综述旨在确定有关双语对居住在希腊的自闭症谱系障碍(ASD)儿童的语言技能的可能影响的最新文献。(2)材料和方法:通过选择文章并回顾在同行评审期刊上发表的四项研究,在Scopus和PubMed的数据库中检索文献。本范围审查基于PRISMA范围审查建议的标准,而PCC框架被用作构建明确而有意义的目标和资格标准的指南。(3)结果:审查中包含的出版物涉及各种与语言相关的技能,包括形态学,语法-语用接口,叙事能力,以及接受和表达语言技能。(4)结论:四分之三的研究提供的证据表明,双语ASD儿童与单语同龄人相比并不处于不利地位,而是享受一些好处。在某种程度上,由于双语。然而,审查研究的数量以及研究本身的局限性使该结论具有暂定性。此外,这些发现为言语治疗师制定了指导方针,教育工作者,心理学家,希腊背景下的医生在治疗或教育患有ASD的双语儿童时需要遵循。
    (1) Background and Objectives: This review aims to identify the latest literature on the possible effect of bilingualism on the linguistic skills of children with autism spectrum disorder (ASD) residing in Greece. (2) Materials and Methods: The literature was searched in the databases of Scopus and PubMed by selecting articles and by reviewing four studies published in peer-reviewed journals. This Scoping Review is based on the standards of PRISMA recommendations for scoping reviews, while the PCC framework was used as a guide to construct clear and meaningful objectives and eligibility criteria. (3) Results: The publications included in the review addressed a variety of language-related skills, including morphology, the syntax-pragmatics interface, narrative ability, as well as both receptive and expressive language skills. (4) Conclusions: Three out of four studies provide evidence that bilingual ASD children are not disadvantaged compared to monolingual peers but rather enjoy some benefits, to a certain extent, due to bilingualism. However, the number of the reviewed studies as well as the limitations of the studies themselves render this conclusion tentative. Additionally, the findings set guidelines that speech therapists, educators, psychologists, and doctors in the Greek context need to follow when treating or educating bilingual children with ASD.
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  • 文章类型: Journal Article
    背景:来那度胺(Len)在多发性骨髓瘤(MM)的一线(1L)治疗中的使用越来越多,导致相当比例的患者在1L治疗后变得Len难治性。然而,关于1L治疗后Len难治性患者的治疗策略和结局的实际数据有限.
    方法:这项真实世界的回顾性队列研究分析了在希腊MM中心接受1LLen并开始二线(2L)治疗的Len难治性和非Len难治性患者。Len暴露队列(n=249)包括1L后55.4%的Len难治性患者。
    结果:与非难治性患者相比,难治性患者在诊断时更频繁地具有高风险的细胞遗传学和修订的国际分期系统-3疾病阶段,1L治疗后无进展生存期(PFS)较短。Len-难治性与非Len-难治性患者更频繁地接受三胞胎(59%vs.40%),抗CD38药物(20%vs.9%)和泊马度胺(22%vs.13%)。在2L治疗中,Len难治性患者的总有效率为53%,非Len难治性患者的总有效率为64%;中位PFS为10.7。18.3个月,分别。Len难治性患者的中位总生存期(OS)短于非Len难治性患者(23.8vs.53.6个月)。Len难治性是Len暴露患者PFS和OS的独立预后因素。
    结论:在这个真实世界的Len暴露队列中,接受1LLen治疗的Len难治性患者的生存结果低于非Len难治性患者,强调了这一患者群体中未满足的需求,这推动了新疗法的发展。
    BACKGROUND: The increasing use of lenalidomide (Len) in first-line (1L) therapy of multiple myeloma (MM) has led to a significant proportion of patients becoming Len-refractory following 1L treatment. However, there are limited real-world data on treatment strategies and outcomes of patients who become Len-refractory following 1L therapy.
    METHODS: This real-world retrospective cohort study analyzed Len-refractory and non-Len-refractory patients who received 1L Len and initiated second-line (2L) therapy at a Greek MM center. The Len-exposed cohort (n = 249) included 55.4% Len-refractory patients after 1L.
    RESULTS: Compared to non-Len-refractory patients, Len-refractory patients more frequently had high-risk cytogenetics and Revised-International Staging System-3 disease stage at diagnosis, and had shorter progression-free survival (PFS) following 1L therapy. Len-refractory versus non-Len-refractory patients more frequently received triplets (59% vs. 40%), anti-CD38 agents (20% vs. 9%) and pomalidomide (22% vs. 13%). The overall response rate was 53% for Len-refractory patients and 64% for non-Len-refractory patients in 2L therapy; median PFS was 10.7 vs. 18.3 months, respectively. Median overall survival (OS) was shorter for Len-refractory patients vs non-Len-refractory patients (23.8 vs. 53.6 months). Len refractoriness was an independent prognostic factor for both PFS and OS in Len-exposed patients.
    CONCLUSIONS: In this real-world Len-exposed cohort, Len-refractory patients receiving 1L Len experienced poorer survival outcomes than non-Len-refractory patients, highlighting the unmet need in this patient population which has driven the development of novel therapies.
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  • 文章类型: Systematic Review
    暂无摘要。
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  • 文章类型: Journal Article
    背景:据推测,营养可能会影响皮肤黑色素瘤(CM)的风险;因此,我们旨在评估希腊人群中食物组和个体营养素摄入量与CM的关联。
    方法:在本病例对照研究中,151例经组织学证实的CM,在“Laikon”大学医院肿瘤科(雅典,希腊),和居住在雅典都会区的151名年龄和性别匹配的健康个体,在参与者中招募进行常规健康检查,包括在内。所有参与者都填写了一份包含人体测量的问卷,社会人口统计学,生活方式,和健康相关变量。一个经过验证的,半定量食物频率问卷用于评估发病前12个月内136种食物的平均消费量.使用多变量条件回归模型得出9种食物组和7种常量营养素与CM之间关联的比值比(OR),置信区间为95%(95%CI)。
    结果:发现与CM具有统计学意义的正相关,能量摄入(OR:1.67,95%CI:1.22-2.30)和饱和脂肪酸摄入(OR:2.28,95%CI:1.00-5.28),在调整了对太阳的敏感度之后,抑郁症病史,酒精摄入量。与更高的牛奶和乳制品摄入量的反向关联(OR:0.65,95%CI:0.48-0.88),水果(OR:0.68,95%CI:0.51-0.90),添加脂质(OR:0.65,95%CI:0.47-0.91),还观察到糖和糖浆(OR:0.70,95%CI:0.53-0.93)。
    结论:除了内在风险因素,我们的结果支持CM与多种食物和营养素的关联;如果通过前瞻性研究证实,这些发现可以进一步了解这种致命的癌症。
    BACKGROUND: It has been postulated that nutrition may influence the risk for cutaneous melanoma (CM); therefore, we aimed to assess the associations of food groups and individual nutrient intakes with CM in a Greek population.
    METHODS: In this case-control study, 151 patients with histologically confirmed CM, newly diagnosed and treated in the Oncology Department of the \"Laikon\" University Hospital (Athens, Greece), and 151 age- and sex-matched healthy individuals residing in the Athens metropolitan area, recruited among participants for routine health examinations, were included. All participants completed a questionnaire comprising anthropometric measurements, sociodemographic, lifestyle, and health-related variables. A validated, semiquantitative food frequency questionnaire was used to assess average consumption of 136 food items during the 12 months preceding the onset of disease. Multivariate conditional regression models were used to derive odds ratios (ORs) with 95% confidence intervals (95% CI) regarding the association of nine food groups and seven macronutrients with CM.
    RESULTS: Statistically significant positive associations with CM were found with higher energy intake (OR: 1.67, 95% CI: 1.22-2.30) and intake of saturated fatty acids (OR: 2.28, 95% CI: 1.00-5.28), after adjusting for sun sensitivity, major depression history, and alcohol intake. Inverse associations with higher intake of milk and dairy products (OR: 0.65, 95% CI: 0.48-0.88), fruits (OR: 0.68, 95% CI: 0.51-0.90), added lipids (OR: 0.65, 95% CI: 0.47-0.91), and sugars and syrups (OR: 0.70, 95% CI: 0.53-0.93) were also observed.
    CONCLUSIONS: Beyond intrinsic risk factors, our results support associations of CM with multiple food groups and nutrients; if confirmed by prospective studies, these findings can add further knowledge about this fatal cancer.
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  • 文章类型: Journal Article
    在过去的30年中,儿童和青少年骨肉瘤的5年总体生存率一直处于平稳状态。本系统综述(1976-2023年)和荟萃分析旨在探讨与儿童和年轻成人高级别骨肉瘤预后有关的因素。分析了包括≤30岁的患者和涉及≤14岁儿童的全国儿童血液恶性肿瘤和实体瘤注册(NARECHEM-ST)数据(2010-2021年)的原始研究。个体参与者数据(IPD)和汇总估计用于评估n年生存率,以及危险因素与总生存期(OS)和无事件生存期(EFS)的关系。使用Kaplan-Meier和Cox回归模型汇总IPD和n年生存率,和随机效应模型,分别。8412名患者的数据,包括46种出版物,NARECHEM-ST数据,分析了10项研究的277项IPD。总结5年OS率为64%[95%置信区间(95CI):62%-66%,37项研究,6661例患者],EFS为52%(95CI:49%-56%,30项研究,5010名患者)。在预先指定的亚组中,生存率通常不同。肢体抢救手术显示5年OS率(69%)高于截肢手术(47%)。良好反应者在3年(94%)和5年(81%)的OS率较高,与3年时反应不佳的人(66%)相比,5年(56%)。转移性疾病患者的死亡风险更高[危险比(HR):3.60,95CI:2.52,5.15,11项研究]。性别对EFS没有影响(HR女性/男性:0.90,95CI:0.54,1.48,3项研究),而年龄>18岁似乎会对EFS产生不利影响(HR18+/<10年:1.36,95CI:1.09,1.86,3项研究)。我们的结果总结了儿童和年轻人中高级别骨肉瘤预后因素的集体经验。诊断时对新辅助化疗反应差和转移性疾病被证实是预后差的主要危险因素。骨肉瘤研究小组的国际合作对于提高生存率至关重要。
    The 5-year overall survival of children and adolescents with osteosarcoma has been in plateau during the last 30 years. The present systematic review (1976-2023) and meta-analysis aimed to explore factors implicated in the prognosis of children and young adults with high-grade osteosarcoma. Original studies including patients ≤30 years and the Nationwide Registry for Childhood Hematological Malignancies and Solid Tumors (NARECHEM-ST) data (2010-2021) referred to children ≤14 years were analysed. Individual participant data (IPD) and summary estimates were used to assess the n-year survival rates, as well as the association of risk factors with overall survival (OS) and event-free survival (EFS). IPD and the n-year survival rates were pooled using Kaplan-Meier and Cox regression models, and random effects models, respectively. Data from 8412 patients, including 46 publications, NARECHEM-ST data, and 277 IPD from 10 studies were analysed. The summary 5-year OS rate was 64% [95% confidence interval (95%CI): 62%-66%, 37 studies, 6661 patients] and the EFS was 52% (95%CI: 49%-56%, 30 studies, 5010 patients). The survival rates generally differed in the pre-specified subgroups. Limb-salvage surgery showed a higher 5-year OS rate (69%) versus amputation (47%). Good responders had higher OS rates at 3 years (94%) and 5 years (81%), compared to poor responders at 3 years (66%), and 5 years (56%). Patients with metastatic disease had a higher risk of death [Hazard Ratio (HR): 3.60, 95%CI: 2.52, 5.15, 11 studies]. Sex did not have an impact on EFS (HR females/males: 0.90, 95%CI: 0.54, 1.48, 3 studies), whereas age>18 years seems to adversely affect EFS (HR 18+/<10 years: 1.36, 95%CI: 1.09, 1.86, 3 studies). Our results summarize the collective experience on prognostic factors of high-grade osteosarcoma among children and young adults. Poor response to neoadjuvant chemotherapy and metastatic disease at diagnosis were confirmed as primary risk factors of poor outcome. International collaboration of osteosarcoma study groups is essential to improve survival.
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  • 文章类型: Meta-Analysis
    在低至极低疟疾传播地区,大多数感染可能发生在特定的群体中,这些群体的行为或职业使他们感染的风险增加。如果这些感染占感染库的很大一部分,针对这些群体的干预措施可以减少人口层面的传播.我们进行了系统评价,以评估向疟疾风险增加的人群提供抗疟药的影响,这些人群的感染被认为占当地感染库的很大比例(靶向药物施用[TDA])。文献检索于2021年3月进行,并于2022年4月进行了更新。两名审稿人筛选了标题,摘要,和全文记录。建议评估的分级,使用开发和评估方法对每个结果的证据确定性(CoE)进行评分。在2563条记录中,我们确定了5项纳入研究:乌干达和肯尼亚的2项集群随机对照试验(cRCT);加纳的1项前后对照研究;斯里兰卡和希腊的2项前后对照研究.与没有干预相比,TDA在人群水平上的感染率几乎没有差异(风险比[RR]:0.85,95%CI:0.73-1.00;一个cRCT,高CoE),尽管TDA可能导致干预目标人群的患病率大幅下降(RR:0.15,95%CI:0.06-0.38;两个cRCT,中度CoE)。尽管TDA可以减轻接受抗疟药的人的疟疾负担,我们没有发现任何证据表明它能减少人群的传播.
    In low- to very low-malaria transmission areas, most infections may be accrued within specific groups whose behaviors or occupations put them at increased risk of infection. If these infections comprise a large proportion of the reservoir of infection, targeting interventions to these groups could reduce transmission at the population level. We conducted a systematic review to assess the impact of providing antimalarials to groups of individuals at increased risk of malaria whose infections were considered to comprise a large proportion of the local reservoir of infections (targeted drug administration [TDA]). A literature search was conducted in March 2021 and updated in April 2022. Two reviewers screened titles, abstracts, and full-text records. The Grading of Recommendations Assessment, Development and Evaluation approach was used to rate the certainty of the evidence (CoE) for each outcome. Out of 2,563 records, we identified five studies for inclusion: two cluster-randomized controlled trials (cRCTs) in Uganda and Kenya; one controlled before-after study in Ghana; and two uncontrolled before-after studies in Sri Lanka and Greece. Compared with no intervention, TDA resulted in little to no difference in the prevalence of infection at the population level (risk ratio [RR]: 0.85, 95% CI: 0.73-1.00; one cRCT, high CoE), although TDA likely resulted in a large reduction in prevalence among those targeted by the intervention (RR: 0.15, 95% CI: 0.06-0.38; two cRCTs, moderate CoE). Although TDA may reduce the burden of malaria among those receiving antimalarials, we found no evidence that it reduces transmission at the population level.
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  • 文章类型: Multicenter Study
    这项研究的主要目的是在2015年1月1日至2018年1月1日(指数期)期间,在免疫肿瘤学(IO)或靶向治疗(TT)基础上开始的晚期(不可切除的III期/转移性)皮肤黑色素瘤患者的概况和一线治疗(1LT)模式的真实世界证据(RWE)。在希腊的常规环境中。这是一个多中心,回顾性图表回顾研究。符合条件的同意(除非死者,医院放弃了同意)的患者连续被六个肿瘤科诊所纳入。回顾期从知情同意或死亡延长到最初的黑色素瘤诊断。在2021年6月9日至2022年2月9日之间,包括225名符合条件的患者(所有高加索人;60.4%男性;35.6%被诊断为从头晚期黑色素瘤)。在1LT启动时,中位年龄为62.6岁;2.7/6.7/90.7%的患者患有IIIB/IIIC/IV期疾病,9.3%的患者未切除.最常见的转移部位是肺(46.7%),非区域节点(33.8%),和肝脏(20.9%)。在患者中,98.2%有单原发黑色素瘤,45.6%的疾病位于躯干上,63.6%为BRAF突变体。在患者中,45.3%启动了基于IO的1LT,53.3%采用基于TT的方案,3名患者(1.3%)接受了基于TT的治疗,然后是基于IO的治疗,反之亦然。最常见的1LT模式(频率≥10%)为BRAFi/MEKi组合(31.6%),抗PD-1单药治疗(25.3%),BRAFi单药治疗(21.8%),和抗CTLA-4单药治疗(17.8%)。最常见的方案是Dabrafenib+Trametinib,占25.3%,在23.6/17.8/11.1/10.7%的患者中,使用Pembrolizumab/Ipilimumab/Vemurafenib/Dabrafenib的单一疗法,分别。SUMMER提供了RWE的1LT策略以及在3年指标期内在希腊开始基于1LIO或TT治疗的患者的概况。
    This study primarily aimed to generate real-world evidence (RWE) on the profile and first-line treatment (1LT) patterns of patients with advanced (unresectable Stage III/metastatic) cutaneous melanoma initiated on immuno-oncology (IO)- or targeted therapy (TT)-based 1LT between 1 January 2015 and 1 January 2018 (index period), in routine settings of Greece. This was a multicenter, retrospective chart review study. Eligible consented (unless deceased, for whom consent was waived by the hospital) patients were consecutively included by six oncology clinics. The look-back period extended from informed consent or death to initial melanoma diagnosis. Between 9 Junuary 2021 and 9 February 2022, 225 eligible patients (all Caucasians; 60.4% male; 35.6% diagnosed with de novo advanced melanoma) were included. At 1LT initiation, median age was 62.6 years; 2.7/6.7/90.7% of the patients had Stage IIIB/IIIC/IV disease and 9.3% were unresected. Most frequent metastatic sites were the lung (46.7%), non-regional nodes (33.8%), and liver (20.9%). Among patients, 98.2% had single primary melanoma, 45.6% had disease localized on the trunk, and 63.6% were BRAF-mutant. Of the patients, 45.3% initiated 1LT with an IO-based, 53.3% with a TT-based regimen, and three patients (1.3%) received TT-based followed by IO-based or vice versa. Most common 1LT patterns (frequency ≥10%) were BRAFi/MEKi combination (31.6%), anti-PD-1 monotherapy (25.3%), BRAFi monotherapy (21.8%), and anti-CTLA-4 monotherapy (17.8%). Most frequent regimens were Dabrafenib+Trametinib in 25.3%, and monotherapies with Pembrolizumab/Ipilimumab/Vemurafenib/Dabrafenib in 23.6/17.8/11.1/10.7% of patients, respectively. SUMMER provides RWE on 1LT strategies and profile of patients initiated 1L IO- or TT-based therapy in Greece during the 3-year index period.
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  • 文章类型: Review
    腹股沟疝是一种广泛的疾病,负责大量的急腹症病例。通常,间接,而不是直接,疝气导致并发症,由于它们狭窄的疝性缺陷。我们报告了一名71岁的男性患者,在塞萨洛尼基的一家大学综合医院的左腹股沟区出现急性疼痛,该患者的直嵌顿疝发生率相当罕见,希腊,在2017年。经临床检查,触诊了一个不可还原的腹股沟肿块。因此,怀疑存在复杂的疝气。病人接受了紧急修复,在此期间,确定疝气是直接和嵌顿的,并且其囊包含缺血性表皮附件。疝用网片修复成功,病人顺利康复,五天后出院。尽管复杂的腹股沟直疝罕见,应始终将它们包括在不可减少的腹股沟肿块的鉴别诊断中,因为它们会增加严重的并发症。
    Inguinal hernias are a widespread condition, responsible for a large number of acute abdomen cases. Typically, indirect, rather than direct, hernias lead to complications, as a consequence of their narrower hernial defect. We report a 71-year-old male patient with a rather rare incidence of a direct incarcerated hernia who presented with acute pain in the left inguinal area at a university general hospital in Thessaloniki, Greece, in 2017. Upon clinical examination, an irreducible inguinal mass was palpated. Therefore, the existence of a complicated hernia was suspected. The patient underwent an emergency repair, during which it was established that the hernia was direct and incarcerated and that its sac contained an ischaemic epiploic appendage. The hernia was successfully repaired with mesh, the patient recovered uneventfully and was discharged five days later. Despite the rarity of complicated direct inguinal hernias, they should always be included in the differential diagnosis of irreducible groin masses as they can increase severe complications.
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  • 文章类型: Journal Article
    大规模的人口流动改变了接收难民的国家头癣(TC)的流行病学。定期监测局部病原体谱可以作为选择适当的经验性抗真菌治疗和实施预防措施的基础。因此,我们调查了自2015年以来希腊前所未有的移民潮对TC流行病学趋势的影响.所有在2012-2019年期间在雅典的皮肤科疾病转诊学术医院确诊的微生物确诊的TC病例,希腊,进行回顾性审查。共记录583例患者,348(60%)是男性,547(94%)是儿童,160(27%)是来自巴尔干的移民,中东,亚洲和非洲国家。TC的总体年发病率为0.49,多年来显著增加(p=0.007)。犬分枝杆菌是主要的病原体(74%),其次是紫罗兰(12%),T.tonsurans(7%)和其他稀有皮肤癣菌(7%)。犬分枝杆菌患病率从2014年到2019年下降(84%到67%,p=0.021)与紫罗兰草率增加三倍(10%至32%,p=0.002)。随着向嗜人性毛癣菌的转移,TC的发病率增加。在希腊,可能与来自不同社会经济背景的移民流有关。
    Mass population movements have altered the epidemiology of tinea capitis (TC) in countries receiving refugees. Periodic monitoring of the local pathogen profiles may serve as a basis for both the selection of appropriate empirical antifungal therapy and the implementation of preventive actions. Therefore, we investigated the impact of an unprecedented immigration wave occurring in Greece since 2015 on the epidemiological trends of TC. All microbiologically confirmed TC cases diagnosed during the period 2012-2019 in a referral academic hospital for dermatological disorders in Athens, Greece, were retrospectively reviewed. A total of 583 patients were recorded, where 348 (60%) were male, 547 (94%) were children and 160 (27%) were immigrants from Balkan, Middle Eastern, Asian as well as African countries. The overall annual incidence of TC was 0.49, with a significant increase over the years (p = 0.007). M. canis was the predominant causative agent (74%), followed by T. violaceum (12%), T. tonsurans (7%) and other rare dermatophyte species (7%). M. canis prevalence decreased from 2014 to 2019 (84% to 67%, p = 0.021) in parallel with a three-fold increase in T. violaceum plus T. tonsurans rates (10% to 32%, p = 0.002). An increasing incidence of TC with a shift towards anthropophilic Trichophyton spp. in Greece could be linked to the immigration flows from different socioeconomic backgrounds.
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  • 文章类型: Review
    本评论文章介绍了由希腊Euboea岛的儿科病毒学研究所组织的第八届儿科病毒学研讨会的主要信息。研讨会期间涵盖的主要主题如下:i)针对巨细胞病毒的抗病毒剂和疫苗的新进展;ii)儿童汉坦病毒肾病;iii)需要儿科重症监护的儿童中人鼻病毒感染;iv)人类腺病毒感染的并发症和管理;v)儿童和青少年中2019年冠状病毒病(COVID19综合征)的挑战;vi)涉及中枢神经系统的病毒感染的胎儿磁共振成像。COVID-19时代需要更密集的,战略,临床和实验室的全球科学努力,专注于诊断,新生儿和儿童病毒感染的管理和预防。
    The present review article presents the key messages of the 8th Workshop on Paediatric Virology organised virtually by the Institute of Paediatric Virology based on the island of Euboea in Greece. The major topics covered during the workshop were the following: i) New advances in antiviral agents and vaccines against cytomegalovirus; ii) hantavirus nephropathy in children; iii) human rhinovirus infections in children requiring paediatric intensive care; iv) complications and management of human adenovirus infections; v) challenges of post‑coronavirus disease 2019 (COVID‑19) syndrome in children and adolescents; and vi) foetal magnetic resonance imaging in viral infections involving the central nervous system. The COVID‑19 era requires a more intensive, strategic, global scientific effort in the clinic and in the laboratory, focusing on the diagnosis, management and prevention of viral infections in neonates and children.
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