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Penicillin allergy management strategies relevant for clinical practice - a narrative review. 与临床实践相关的青霉素过敏管理策略-叙述性回顾。
IF 1.6 Q2 MEDICINE, GENERAL & INTERNAL Pub Date : 2025-03-31 eCollection Date: 2025-03-01 DOI: 10.2478/rjim-2024-0035
Ileana-Maria Ghiordanescu, Nicolas Molinari, Ana-Maria Forsea, Rik Schrijvers, Cyrille Hoarau, Pascal Demoly

Penicillin allergy is the most commonly reported drug allergy, with prevalence rates ranging from 6% to 31% across various populations and geographic areas. The penicillin allergy label is linked to higher mortality and morbidity rates, extended hospital stays, increased readmission rates, and a greater reliance on second-line antibiotics. Research indicates that nearly 99% of those labeled as penicillin-allergic can tolerate the drug. However, alternative antibiotics are often prescribed without confirming the allergy, largely due to legal concerns regarding re-exposure. Even when a negative challenge test is conducted, non-allergist providers may remain hesitant to reintroduce penicillins. To address the considerable gap between reported and actual penicillin allergies, as well as to ensure the prompt use of penicillins by non-allergists, various management strategies have emerged in recent years. Although several comprehensive reviews have examined these strategies, selecting and applying the most suitable for routine practice is difficult. This narrative review focuses on the most relevant data regarding the efficiency of key penicillin allergy risk-assessment tools, particularly those of clinical significance, and discusses their readiness for implementation in non-allergist settings.

青霉素过敏是最常见的药物过敏,在不同人群和地理区域的患病率从6%到31%不等。青霉素过敏标签与较高的死亡率和发病率、延长的住院时间、增加的再入院率以及对二线抗生素的更大依赖有关。研究表明,近99%被标记为青霉素过敏的人可以耐受这种药物。然而,替代抗生素通常在没有确认过敏的情况下开处方,这主要是由于法律上对再次暴露的担忧。即使进行了阴性激发试验,非过敏专科医生也可能对重新引入青霉素犹豫不决。为了解决报告和实际青霉素过敏之间的巨大差距,以及确保非过敏专科医生及时使用青霉素,近年来出现了各种管理策略。尽管对这些策略进行了几次全面的审查,但选择和应用最适合日常实践的策略是困难的。这篇叙述性综述的重点是关于关键青霉素过敏风险评估工具效率的最相关数据,特别是那些具有临床意义的数据,并讨论了它们在非过敏医师环境中实施的准备情况。
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引用次数: 0
Impact of smoking on microRNAs in significant coronary artery disease. 吸烟对重大冠状动脉疾病微RNA的影响
IF 1.6 Q2 MEDICINE, GENERAL & INTERNAL Pub Date : 2025-03-31 eCollection Date: 2025-03-01 DOI: 10.2478/rjim-2024-0031
Shokoufeh Hajsadeghi, Aida Iranpour, Shayan Mirshafiee, Reza Nekouian, Maryam Mollababaei, Hamed Motevalli, Seyyed Amir Yasin Ahmadi, Mohammad Sedigh Dakkali

Background: Given the importance of coronary artery disease (CAD) and the range of cardiovascular disease phenotypes in smokers, as well as the potential genetic and epigenetic factors, we were motivated to explore the impact of smoking on some selected microRNAs associated with significant CAD.

Methods: A total of 60 individuals were selected in four groups including non-smoker without significant CAD (S-A-), non-smokers with significant CAD (S-A+), smokers without significant CAD (S+A-) and smokers with significant CAD (S+A+). Micro-RNA expression was investigated using real-time PCR. General linear model was used to calculate fold change (FC) considering S-A- as the reference group.

Results: For mir-34a, down-regulation was observed in S+A- (FC =0.13, P =0.007) and S+A+ (FC =0.23, P =0.036) groups. For mir-126-3p, down-regulation was observed in S-A+ group (FC =0.05, P =0.024). For mir-199, up-regulation was observed for S+A- group (FC =9.38, P =0.007). The only significant interaction between pack-years of smoking and number of significantly narrowed vessels (≥75% stenosis) was for mir-199 which was in favor of down-regulation (P =0.006), while the main effects were in favor of up-regulation (P <0.05).

Conclusion: Mir-34a expression may be affected by smoking, whereas mir-126-3p expression may be affected by atherosclerosis, the most common reason of CAD. The significant down-regulation of mir-199 for the interaction of smoking dose and severity of CAD was a notable finding showing the harmful consequence of this interaction. Further studies are needed for this micro-RNA.

背景:鉴于冠状动脉疾病(CAD)的重要性和吸烟者心血管疾病表型的范围,以及潜在的遗传和表观遗传因素,我们有动机探索吸烟对某些与明显CAD相关的microRNA的影响:方法: 我们共选取了 60 人,分为四组,包括无明显 CAD 的非吸烟者(S-A-)、有明显 CAD 的非吸烟者(S-A+)、无明显 CAD 的吸烟者(S+A-)和有明显 CAD 的吸烟者(S+A+)。使用实时 PCR 检测微 RNA 表达。以SA-为参照组,使用一般线性模型计算折叠变化(FC):结果:mir-34a在S+A-组(FC =0.13,P =0.007)和S+A+组(FC =0.23,P =0.036)出现下调。对于 mir-126-3p,在 S-A+ 组观察到下调(FC =0.05,P =0.024)。对于 mir-199,在 S+A- 组观察到上调(FC =9.38,P =0.007)。吸烟包年与明显狭窄血管(狭窄程度≥75%)数量之间的唯一显着交互作用是对 mir-199 的交互作用,该交互作用有利于下调(P =0.006),而主效应则有利于上调(P 结论:Mir-34a 的表达可能受 S+A- 组的影响(FC =9.38,P =0.007):Mir-34a 的表达可能受到吸烟的影响,而 mir-126-3p 的表达可能受到动脉粥样硬化的影响,动脉粥样硬化是导致 CAD 的最常见原因。值得注意的是,mir-199 在吸烟剂量和 CAD 严重程度的交互作用下明显下调,这表明这种交互作用会产生有害后果。对这种微RNA还需要进一步研究。
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引用次数: 0
Extremely elevated erythrocyte sedimentation rates: Associations with patients' diagnoses and clinical characteristics. 红细胞沉降率异常升高:与患者诊断和临床特征的关系
IF 1.6 Q2 MEDICINE, GENERAL & INTERNAL Pub Date : 2025-03-31 eCollection Date: 2025-03-01 DOI: 10.2478/rjim-2024-0034
Esen Nur Holoğlu, Mehmet Uzunlulu, Cundullah Torun

Introduction: The aim of the study was to assess the etiological distribution of patients with an erythrocyte sedimentation rate (ESR) over 100 mm/hour and to evaluate differences in demographic, comorbidity, laboratory characteristics, and clinical outcomes.

Methods: This retrospective observational clinical study included patients aged 18 years and older who were admitted to the internal medicine inpatient clinic between May 1, 2015 and June 1, 2021 and had ESR values above 100 mm/h. Demographic data, comorbidities, laboratory parameters, imaging studies, histopathological findings, microbiological and serological data, along with in-hospital and post-discharge mortality, were collected from the hospital's electronic database. Two independent clinicians evaluated the data to identify diagnoses associated with elevated ESR. Patients were divided into six categories based on the most likely diagnosis.

Results: The study included 441 patients, 52.6% of whom were female, and the mean age was 72.6 years. The etiological distribution was as follows: infectious diseases (34%), malignancies (31.5%), undiagnosed cases (15.9%), renal diseases (9.8%), other causes (5%), and rheumatologic diseases (3.8%). Etiological distributions did not differ by gender, age, or ESR ranges. The in-hospital mortality rate was 3.6%, and the overall mortality rate from hospitalization to the data collection date was 64.4%. Mortality was higher in patients with malignancies (81.3%) compared to other etiologies (p<0.001). Patients who died had higher mean age, ferritin levels, having diabetes mellitus, heart failure, or malignancy, and lower hemoglobin and lymphocyte levels compared to survivors (p<0.05 for all).

Conclusion: Most patients with an ESR over 100 mm/hour had significant underlying medical conditions, with infectious diseases and malignancies comprising two-thirds of the cases.

本研究的目的是评估红细胞沉降率(ESR)超过100 mm/小时的患者的病因分布,并评估人口统计学、合并症、实验室特征和临床结果的差异。方法:本回顾性观察性临床研究纳入2015年5月1日至2021年6月1日在内科住院部就诊且ESR值大于100 mm/h的18岁及以上患者。从医院的电子数据库中收集了人口统计数据、合并症、实验室参数、影像学检查、组织病理学发现、微生物学和血清学数据以及院内和出院后死亡率。两名独立的临床医生对数据进行评估,以确定与ESR升高相关的诊断。根据最可能的诊断将患者分为六类。结果:纳入441例患者,女性占52.6%,平均年龄72.6岁。病因分布如下:传染病(34%)、恶性肿瘤(31.5%)、未确诊病例(15.9%)、肾脏疾病(9.8%)、其他原因(5%)和风湿病(3.8%)。病因分布不因性别、年龄或ESR范围而异。住院死亡率为3.6%,住院至数据收集日的总死亡率为64.4%。与其他病因相比,恶性肿瘤患者的死亡率更高(81.3%)(结论:大多数ESR超过100 mm/小时的患者有明显的潜在疾病,其中感染性疾病和恶性肿瘤占三分之二的病例。
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引用次数: 0
Epidemiology of kidney biopsy from regional referral center in Romania: 10-year review. 罗马尼亚地区转诊中心肾活检流行病学:10年回顾。
IF 1.6 Q2 MEDICINE, GENERAL & INTERNAL Pub Date : 2025-03-31 eCollection Date: 2025-03-01 DOI: 10.2478/rjim-2024-0032
Yuriy Maslyennikov, Crina Claudia Rusu, Diana Moldovan, Alina Potra, Dacian Tirinescu, Maria Ticala, Andrada Barar, Urs Alexandra, Cosmina Ioana Bondor, Ina Kacso

Purpose: To provide epidemiologic data on kidney biopsy from Romania.

Methods: Retrospective observational study of kidney biopsy records for adult patients from a referral center in the north-western part of Romania, reported for 2014-2023.

Results: 556 biopsies were performed, corresponding to an incidence of 12 biopsies/m person-year with over 50% increase over the last reported year. Optimal core for optic microscopy was available in 81.4%, immunofluorescence was performed in 86.3%, and electron microscopy in 35.2% of patients. The mean age at biopsy was 47.12 years, and 53.8% were males. Indications for kidney biopsy were nephrotic syndrome in 63.1% of patients, nephritic in 25.9% of patients, asymptomatic urinary abnormalities in 2.9%, acute kidney injury/ rapid progressive renal failure in 3.6%, and chronic kidney disease in 1.4%. The most frequent diagnostic categories were membranous nephritis (14.7%), IgA nephropathy (13.9%), focal segmental glomerulosclerosis (11,1%), minimal change disease (12,2%), lupus nephritis (10,9%), vasculitis (7.6%), and membranoproliferative glomerulonephritis (8%). The age of diagnosis increased for IgA Nephropathy over time while it decreased for membranous nephritis.

Conclusions: Our study adds data for the completion of the kidney biopsy map in our region.

目的:提供罗马尼亚肾活检的流行病学资料。方法:回顾性观察研究2014-2023年罗马尼亚西北部转诊中心成年患者肾活检记录。结果:共行活组织检查556例,发病率为12例/m人/年,较上一报告年度增加50%以上。81.4%的患者在光学显微镜下获得最佳核心,86.3%的患者在免疫荧光下获得最佳核心,35.2%的患者在电子显微镜下获得最佳核心。活检时的平均年龄为47.12岁,53.8%为男性。肾活检的适应症为肾病综合征(63.1%)、肾病(25.9%)、无症状尿路异常(2.9%)、急性肾损伤/快速进行性肾衰竭(3.6%)和慢性肾病(1.4%)。最常见的诊断类型是膜性肾炎(14.7%)、IgA肾病(13.9%)、局灶节段性肾小球硬化(11.1%)、微小病变(12.2%)、狼疮性肾炎(10.9%)、血管炎(7.6%)和膜性增生性肾小球肾炎(8%)。随着时间的推移,IgA肾病的诊断年龄增加,而膜性肾炎的诊断年龄减少。结论:我们的研究为完成本地区的肾活检图谱增加了数据。
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引用次数: 0
The Association between DNA Methylation Status and Epstein-Barr Virus Infection in Laryngeal Carcinomas. 喉癌中DNA甲基化状态与eb病毒感染的关系
IF 1.6 Q2 MEDICINE, GENERAL & INTERNAL Pub Date : 2025-03-21 eCollection Date: 2025-06-01 DOI: 10.2478/rjim-2025-0005
Irina Elisaveta Hotoboc, Alina Fudulu, Irina Huica, Iulia Virginia Iancu, Raluca Grigore, Șerban Vifor Gabriel Bertesteanu, Coralia Bleotu, Gabriela Anton, Anca Botezatu

Introduction: Infection with Epstein-Barr virus is a known risk factor for laryngeal carcinogenesis; it might influence DNA methylation acting as an epigenetic driver in this type of malignancy.

Methods: Paired laryngeal tissues (neoplastic and peri-neoplastic) harvested from 24 patients were included in the study. Eleven patients expressing latent/lytic EBV genes were considered positive. 5-mC% was determined using ELISA technique and TSGs (PDLIM4, WIF1, DAPK1) promoters' methylation percentages were quantified by qMS-PCR. DNMTs (DNMT1 and DNMT3B) expression levels were quantified in qRT-PCR.

Results: Overall, in laryngeal neoplastic samples vs peri-neoplastic ones, lower 5mC% (p=0.004) and higher TSGs promoters hypermethylation were found (p<0.0001). Significant correlation between PDLIM4 and DAPK1 promoter methylation and 5-mC% (PDLIM4 p=0.0186; DAPK1 p=0.0259) was noted. Higher 5-mC% (p=0.0041), lower PDLIM4 gene promoter methylation (p=0.0017) and overexpression of DNMTs (DNMT1: p=0.0018, respectively DNMT3B: p=0.0017) were associated with EBV infection. Also, significant differences between EBV-positive and EBV-negative cases based on tumor stage (T) were noted for 5mC% in both T1/T2 (p=0.0364) and T3/T4 stages (p=0.0275), and for PDLIM4 promoter methylation in T1/T2 stages (p=0.0121).

Conclusion: Future studies are needed to more effectively illustrate the interplay between EBV infection and these epigenetic mechanisms. Notably, our study highlighted a correlation between EBV and epigenetic changes in laryngeal carcinoma.

导言:感染爱泼斯坦-巴氏病毒是喉癌发生的一个已知风险因素;它可能会影响 DNA 甲基化,成为此类恶性肿瘤的表观遗传驱动因素:研究包括从 24 名患者身上采集的配对喉组织(肿瘤和肿瘤周围)。11例表达潜伏/溶解性EBV基因的患者被视为阳性。采用 ELISA 技术测定 5-mC% ,并通过 qMS-PCR 定量 TSGs(PDLIM4、WIF1、DAPK1)启动子的甲基化百分比。qRT-PCR 定量了 DNMTs(DNMT1 和 DNMT3B)的表达水平:结果:总体而言,在喉肿瘤样本与肿瘤周围样本中,发现了较低的 5mC% (p=0.004) 和较高的 TSGs 启动子高甲基化水平(pC):未来的研究需要更有效地说明 EBV 感染与这些表观遗传机制之间的相互作用。值得注意的是,我们的研究强调了喉癌中 EBV 与表观遗传学变化之间的相关性。
{"title":"The Association between DNA Methylation Status and Epstein-Barr Virus Infection in Laryngeal Carcinomas.","authors":"Irina Elisaveta Hotoboc, Alina Fudulu, Irina Huica, Iulia Virginia Iancu, Raluca Grigore, Șerban Vifor Gabriel Bertesteanu, Coralia Bleotu, Gabriela Anton, Anca Botezatu","doi":"10.2478/rjim-2025-0005","DOIUrl":"10.2478/rjim-2025-0005","url":null,"abstract":"<p><strong>Introduction: </strong>Infection with Epstein-Barr virus is a known risk factor for laryngeal carcinogenesis; it might influence DNA methylation acting as an epigenetic driver in this type of malignancy.</p><p><strong>Methods: </strong>Paired laryngeal tissues (neoplastic and peri-neoplastic) harvested from 24 patients were included in the study. Eleven patients expressing latent/lytic EBV genes were considered positive. 5-mC% was determined using ELISA technique and TSGs (PDLIM4, WIF1, DAPK1) promoters' methylation percentages were quantified by qMS-PCR. DNMTs (DNMT1 and DNMT3B) expression levels were quantified in qRT-PCR.</p><p><strong>Results: </strong>Overall, in laryngeal neoplastic samples vs peri-neoplastic ones, lower 5mC% (p=0.004) and higher TSGs promoters hypermethylation were found (p<0.0001). Significant correlation between PDLIM4 and DAPK1 promoter methylation and 5-mC% (PDLIM4 p=0.0186; DAPK1 p=0.0259) was noted. Higher 5-mC% (p=0.0041), lower PDLIM4 gene promoter methylation (p=0.0017) and overexpression of DNMTs (DNMT1: p=0.0018, respectively DNMT3B: p=0.0017) were associated with EBV infection. Also, significant differences between EBV-positive and EBV-negative cases based on tumor stage (T) were noted for 5mC% in both T1/T2 (p=0.0364) and T3/T4 stages (p=0.0275), and for PDLIM4 promoter methylation in T1/T2 stages (p=0.0121).</p><p><strong>Conclusion: </strong>Future studies are needed to more effectively illustrate the interplay between EBV infection and these epigenetic mechanisms. Notably, our study highlighted a correlation between EBV and epigenetic changes in laryngeal carcinoma.</p>","PeriodicalId":21463,"journal":{"name":"Romanian Journal of Internal Medicine","volume":" ","pages":"152-162"},"PeriodicalIF":1.6,"publicationDate":"2025-03-21","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143674592","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Silent Strike: Stroke in Context of Endocarditis - Brain Imaging as a Catalyst for Diagnosis. 无声中风:心内膜炎背景下的中风——脑成像作为诊断的催化剂。
IF 1.6 Q2 MEDICINE, GENERAL & INTERNAL Pub Date : 2025-02-27 eCollection Date: 2025-06-01 DOI: 10.2478/rjim-2025-0003
Iulia-Cosmina Stoican, Dorin Dragoș, Atena Papagheorghe, Suzana Maria Guberna, Sorin Tuta, Maria Mirabela Manea

Introduction: Endocarditis is a pathology which is rarely encountered in clinical practice that presents itself in various manners, thus posing a great challenge for the clinician in the process of formulating a timely diagnosis, especially given its potentially lethal evolution. The diagnosis of infective endocarditis is based on Modified Duke Criteria. A wide array of complications may accompany endocarditis, including septic or thrombotic emboli to various territories - those occluding branches of cerebral arteries result in ischemic strokes, which may be demonstrated by brain imaging and the symptoms which may range from mild mental status alteration to deep coma.

Objective: Assessment of brain imaging as a diagnostic tool for bacterial endocarditis.

Materials and methods: This is a nested case-control study, in which 84 patients with ischemic stroke were enrolled, half of them having endocarditis related stroke (cases), and the other half stroke due to cardioembolism from other sources or to large-artery atherosclerosis (controls).

Results: Brain imaging revealed statistically significant differences between the two cohorts, endocarditis related stroke being more strongly associated with multiple territories involvement, multiple lesions coexistence, watershed lesions, and a greater extent of ischemia all these may serve as valuable diagnostic clues. Among these findings, the presence of multiple lesions has been the most sensitive tool (Sn = 0.786, Sp = 0.857, LR+ = 5.497, LR- = 0.25), while the involvement of multiple arterial territories had the highest specificity and positive likelihood ratio for endocarditis-related stroke (Sn = 0.738, Sp = 0.929, LR+ = 10.394, LR- = 0.282). A larger ischemic lesion as quantified by pc-ASPECTS score (more than by the ASPECTS score) also increases the likelihood of endocarditis as the cause of ischemic stroke, with an AUROC of 0.7361 (95% CI 0.629-0.843).

Conclusions: Early brain imaging could play a crucial role in endocarditis, helping the clinician to suspect this diagnosis. Further studies are needed to understand the role of early brain imaging when Modified Duke Criteria fail to establish the diagnosis.

心内膜炎是一种罕见的病理,在临床实践中表现形式多样,因此对临床医生在制定及时诊断的过程中提出了很大的挑战,特别是考虑到其潜在的致命演变。感染性心内膜炎的诊断是基于修改的杜克标准。心内膜炎可伴有多种并发症,包括脓毒性或血栓性栓塞到不同部位——脑动脉分支闭塞可导致缺血性中风,这可通过脑成像证实,症状可从轻度精神状态改变到深度昏迷。目的:评价脑成像对细菌性心内膜炎的诊断价值。材料与方法:本研究为巢式病例对照研究,纳入84例缺血性卒中患者,其中一半为心内膜炎相关卒中(病例),另一半为其他来源的心脏栓塞或大动脉粥样硬化所致卒中(对照组)。结果:脑显像显示两组间差异有统计学意义,心内膜炎相关脑卒中与多区域受累、多病变共存、分水岭病变、较大程度缺血的相关性更强,这些可能是有价值的诊断线索。其中,多发病变的存在是最敏感的工具(Sn = 0.786, Sp = 0.857, LR+ = 5.497, LR- = 0.25),而累及多动脉区域对心内膜相关卒中的特异性和阳性似然比最高(Sn = 0.738, Sp = 0.929, LR+ = 10.394, LR- = 0.282)。pc-ASPECTS评分量化的较大的缺血性病变(大于ASPECTS评分)也增加了心内膜炎作为缺血性卒中原因的可能性,AUROC为0.7361 (95% CI为0.629-0.843)。结论:早期脑成像可在心内膜炎中发挥关键作用,帮助临床医生怀疑这种诊断。当修改后的杜克标准不能确定诊断时,需要进一步的研究来了解早期脑成像的作用。
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引用次数: 0
Evaluation of Nutritional Recommendations Provided by the ChatGPT Language Model to Bariatric Surgery Patients. ChatGPT语言模型对减肥手术患者营养建议的评价
IF 1.6 Q2 MEDICINE, GENERAL & INTERNAL Pub Date : 2025-02-27 eCollection Date: 2025-06-01 DOI: 10.2478/rjim-2025-0004
Merve Kumru Yildirim, Hikmet Bayam, Nida Yildiz, Fatma Kahraman Gök, Nazli Batar
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引用次数: 0
Clinical Skills Learning Through Medical Students' Lenses, During and After a Pandemic - A Qualitative Study. 在大流行期间和之后,通过医学生的镜头学习临床技能-一项定性研究。
IF 1.6 Q2 MEDICINE, GENERAL & INTERNAL Pub Date : 2025-02-27 eCollection Date: 2025-06-01 DOI: 10.2478/rjim-2025-0002
Laura Elena Marin, Andreea Maila Măgdălin, Cristian Băicuș

The Coronavirus disease of 2019 (COVID-19) pandemic caused significant disruptions in medical education, particularly in clinical training, as students were restricted from direct patient interactions. This study explores medical students' experiences in learning semiology remotely and their perspectives on the role of online education in medical training. We conducted interviews with 16 medical students in their last year of study. Interviews were audio-recorded and the transcription was verbatim. Thematic analysis was performed. We identified four main themes: "Acquiring clinical skills during pandemic times", "Students' perception about semiology", "Mapping the role of online learning in medicine", and "Future perspectives for a better semiology learning". Students reported significant anxiety and fear regarding direct patient interactions, alongside a perceived deficiency in clinical skills. They mostly managed to overcome them during the following years. They considered that their teachers offered them as much as possible when it comes to the process of learning, giving the pandemic context. They were able to identify different traits of online learning when it comes to medical subjects except semiology. In some cases, they experienced a lack of understanding from their tutors in regard to their inadequate clinical skills. Programs should be implemented in order to consolidate COVID-19 students' clinical knowledge through residency. Online learning cannot be implemented for medical semiology, given the fact that hands-on procedures cannot be substituted.

2019年冠状病毒病(COVID-19)大流行严重扰乱了医学教育,特别是临床培训,因为学生被限制与患者直接接触。本研究探讨医学生远程学习符号学的经验,以及他们对在线教育在医学培训中的作用的看法。我们采访了16名医学院学生在他们最后一年的学习。采访录音,并逐字抄写。进行了专题分析。我们确定了四个主题:“在大流行时期获得临床技能”、“学生对符号学的看法”、“绘制在线学习在医学中的作用”和“更好的符号学学习的未来展望”。学生们报告了与患者直接互动的显著焦虑和恐惧,以及临床技能的明显不足。在接下来的几年里,他们大多成功地克服了这些困难。他们认为,在大流行的背景下,他们的老师在学习过程中尽可能多地为他们提供了知识。除了符号学之外,他们能够识别出在线学习的不同特征。在某些情况下,他们的导师对他们临床技能的不足缺乏理解。实施项目,通过实习巩固新冠肺炎学生的临床知识。在线学习不能用于医学符号学,因为实际操作程序无法替代。
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引用次数: 0
Evaluation of different scoring systems for repeating Transarterial Chemoembolization in Egyptian patients with Hepatocellular Carcinoma. 对埃及肝细胞癌患者重复经动脉化疗栓塞术的不同评分系统进行评估。
IF 1.6 Q2 MEDICINE, GENERAL & INTERNAL Pub Date : 2024-08-29 Print Date: 2024-12-01 DOI: 10.2478/rjim-2024-0028
Omkolsoum Alhaddad, Asmaa Gomaa, Merhan El Shamandy, Mohamed Kohla, Ahmed Edrees, Reham Ashour

Background: Hepatocellular carcinoma (HCC) patients undergoing transarterial chemoembolization (TACE) have a diverse range of outcomes due to their high degree of heterogeneity. Therefore, different predictive scoring systems have been created to assist in decision-making regarding retreatment with TACE. We compared the predictive capabilities of different scoring systems, such as ART, ABCR, and SNACOR, for prediction of the outcome of subsequent TACE in HCC patients.

Method: In this retrospective study, the three scoring systems were compared for their capability of predicting the outcome of repeating TACE in 149 HCC patients treated at the National Liver Institute, Egypt, between January 2017 and December 2019. We used the likelihood ratio to select the model with the highest predictive capability for overall survival (OS).

Results: According to our data, the amount of tumor, the change in Barcelona Clinic Liver Cancer (BCLC) stage following TACE, and the SNACOR score (with a 95% confidence range for HR 1.0305-1.256 and p-value = 0.0106) were the most predictive variables. It was also shown that the ABCR score was a good predictor of survival (90 patients had an ABCR score ≤ 0 with a P- value <0.0001, 56 patients had 0 < ABCR < 4 with a P-value <0.0001, and the ART score was not useful in predicting OS (P-value = 0.18).

Conclusion: The SNACOR score is the most predictive score for OS and would be the most helpful scoring system in decision-making regarding retreatment with TACE.

背景:接受经动脉化疗栓塞术(TACE)治疗的肝细胞癌(HCC)患者因其高度异质性而有不同的治疗结果。因此,人们建立了不同的预测评分系统,以协助TACE再治疗的决策。我们比较了 ART、ABCR 和 SNACOR 等不同评分系统对 HCC 患者后续 TACE 治疗结果的预测能力:在这项回顾性研究中,我们对 2017 年 1 月至 2019 年 12 月期间在埃及国家肝脏研究所接受治疗的 149 例 HCC 患者中,三种评分系统预测重复 TACE 结果的能力进行了比较。我们使用似然比来选择对总生存期(OS)预测能力最强的模型:根据我们的数据,肿瘤数量、TACE后巴塞罗那临床肝癌(BCLC)分期的变化以及SNACOR评分(HR的95%置信区间为1.0305-1.256,P值=0.0106)是预测能力最强的变量。研究还表明,ABCR 评分是预测生存率的良好指标(90 名患者的 ABCR 评分≤0,P 值为 结论:ABCR 评分是预测生存率的重要指标:SNACOR 评分是最能预测患者生存率的评分,也是对 TACE 再治疗决策最有帮助的评分系统。
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引用次数: 0
Fabry disease phenotyping in women from the complete Romanian cohort - time for early diagnostic awareness. 从完整的罗马尼亚队列中对妇女进行法布里病表型分析--是时候提高早期诊断意识了。
IF 1.6 Q2 MEDICINE, GENERAL & INTERNAL Pub Date : 2024-08-21 Print Date: 2024-12-01 DOI: 10.2478/rjim-2024-0027
Adriana Mursă, Sebastian Militaru, Elena Rusu, Sebastian Onciul, Gabriela Neculae, Robert Adam, Lucia Ciobotaru, Vlad Stefănescu, Adriana Dulămea, Viorica Rădoi, Bogdan Alexandru Popescu, Gener Ismail, Ruxandra Jurcuţ

Fabry disease (FD) is an X-linked rare disorder caused by mutations in the GLA gene. Women with FD have been less enrolled in studies and less treated compared with men. The aim of the present study is to describe the complete phenotype of the women cohort with FD diagnosed and evaluated in Romania and compare it to the male population. This study included all consecutive patients diagnosed with FD referred to the Expert Center for Rare Genetic Cardiovascular Diseases between 2014-2023 which included 73 consecutive Romanian FD patients: 41 women (56.2%) and 32 men (43.8%) from 33 unrelated families. Women with FD were diagnosed later and had a later symptom onset. Comparing with men, women were less often symptomatic, but with similar symptom severity. They had similar ophthalmologic and ENT involvement, but less angiokeratomas. Both women and men had similar heart failure symptoms, which were usually mild to moderate, with no difference between the age of developing of the heart failure symptoms. There were also similar rates of acroparesthesia and stroke between sexes, but women presented less renal involvement, with less requirement for renal transplant. This study demonstrates that women with Fabry disease are not just carriers of the disease, they can present symptoms as severe as men, and they have less or later access to pathogenic therapy. Further studies with more female participations are needed to better understand the burden of Fabry disease in women.

法布里病(FD)是一种由 GLA 基因突变引起的 X 连锁罕见疾病。与男性相比,女性法布里病患者参与研究和接受治疗的人数较少。本研究旨在描述罗马尼亚诊断和评估的女性法布里病患者的完整表型,并与男性患者进行比较。本研究纳入了2014-2023年间转诊至罕见遗传性心血管疾病专家中心的所有连续确诊的FD患者,其中包括73名连续的罗马尼亚FD患者:其中包括 73 名罗马尼亚 FD 连续患者:41 名女性(56.2%)和 32 名男性(43.8%),他们来自 33 个无血缘关系的家庭。女性FD患者确诊时间较晚,症状出现也较晚。与男性患者相比,女性患者较少出现症状,但症状严重程度相似。她们的眼科和耳鼻喉科受累情况相似,但血管角化瘤较少。女性和男性的心力衰竭症状相似,通常为轻度至中度,心力衰竭症状的出现年龄没有差异。男性和女性的尖锐湿疣和中风发病率也相似,但女性的肾脏受累较少,需要进行肾移植的情况也较少。这项研究表明,患有法布里病的女性不仅是该病的携带者,她们也可能出现与男性一样严重的症状,而且她们接受病理治疗的机会较少或较晚。为了更好地了解法布里病给女性带来的负担,还需要进行更多女性参与的研究。
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Romanian Journal of Internal Medicine
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