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Use of intraaortic balloon pump in cardiogenic shock patients. 在心源性休克患者中使用主动脉内球囊泵。
IF 1.5 4区 医学 Q2 MEDICINE, GENERAL & INTERNAL Pub Date : 2024-01-01 DOI: 10.4149/BLL_2024_81
Peter Misun, Marek Sramko, Josef Kautzner, Jiri Kettner, Michal Zelizko, Jan Mares, Allan Bohm, Marta Kollarova, Branislav Bezak, Michal Pazdernik

Background and objectives: The relevance of the use of intra-aortic balloon pump (IABP) in cardiogenic shock (CS) has been discussed over the past years. The aim of this study is to describe a single-centre 10-year experience with IABP and analyse the risk factors for 30-day mortality.

Methods: The data for this single-centre, observational, retrospective study were drawn from records dated from January 2012 to May 2022 pertaining to patients presenting with CS, treated with IABP and hospitalised at the Department of Acute Cardiology, Institute for Clinical and Experimental Medicine, Prague.

Results: Among the patients included in the study, 87% patients presented with newly developed heart failure. The leading cause of CS was acute myocardial infarction accounting for 86% of cases. Hospital mortality was recorded at 39% and the 30-day mortality reached 43%. Upon multi-variable analysis, only the vasoactive inotropic score on day 5 emerged as a statistically significant predictor for 30-day mortality (p=0.0055). Cox regression analysis revealed that the presence of mechanical complications was the only variable identified as yielding a statistically significant impact on the 30-day survival (Log-rank p=0.014, HR 2.19, 95% CI: 1.15‒4.15). There was no statistically significant difference in the 30-day mortality across the SCAI classes.

Conclusion: The main cause of CS was a newly developed acute heart failure secondary to acute myocardial infarction. Despite the implementation of mechanical circulatory support, both in-hospital and 30-day mortality rates remained high. Increased vasoactive inotropic score and presence of mechanical complications were identified as significant predictors the 30-day survival (Tab. 6, Fig. 1, Ref. 36). Text in PDF www.elis.sk Keywords: cardiogenic shock, IABP, risk factors, mortality, Czech Republic, AMICS.

背景和目的:在过去几年中,人们一直在讨论在心源性休克(CS)中使用主动脉内球囊反搏泵(IABP)的相关性。本研究旨在描述单中心使用 IABP 的 10 年经验,并分析 30 天死亡率的风险因素:这项单中心、观察性、回顾性研究的数据来自 2012 年 1 月至 2022 年 5 月的记录,这些记录涉及在布拉格临床与实验医学研究所急性心脏病学部住院的 CS 患者,他们都接受了 IABP 治疗:在纳入研究的患者中,87%的患者是新发心力衰竭。导致 CS 的主要原因是急性心肌梗死,占 86%。住院死亡率为 39%,30 天死亡率为 43%。经过多变量分析,只有第 5 天的血管活性肌力评分对 30 天死亡率的预测具有统计学意义(P=0.0055)。Cox 回归分析显示,机械并发症是唯一一个对 30 天存活率有显著统计学影响的变量(Log-rank p=0.014,HR 2.19,95% CI:1.15-4.15)。各SCAI级别的30天死亡率在统计学上没有明显差异:结论:CS的主要原因是继发于急性心肌梗死的新发急性心力衰竭。尽管实施了机械循环支持,但院内死亡率和 30 天死亡率仍然很高。血管活性肌力评分的增加和机械并发症的存在被认为是30天存活率的重要预测因素(表6,图1,参考文献36)。Text in PDF www.elis.sk 关键词:心源性休克、IABP、风险因素、死亡率、捷克共和国、AMICS。
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引用次数: 0
Overview of typical dental abnormalities in rare genetic syndromes occurring in the Czech Roma population. 典型的牙齿异常罕见的遗传综合征发生在捷克罗姆人的概述。
IF 1.5 4区 医学 Q2 MEDICINE, GENERAL & INTERNAL Pub Date : 2024-01-01 DOI: 10.4149/BLL_2024_124
Tatjana Dostalova, Marketa Havlovicova, Silvia Timkova, Diana Filipova, Hana Eliasova, Marketa Batkova, Petra Liskova, Milan Macek

Background: The Roma population is a genetically isolated population with a shared origin, totaling between 10 to 14 million individuals worldwide, stemming from a limited number of "genetic founders". Roma individuals exhibit specific hereditary diseases, often stemming from recessive genetic variants due to a higher degree of consanguinity, with recent molecular-genetic investigations shedding light on several conditions prevalent within the Czech Roma population. However, an overview of stomatological issues in diagnosing such diseases proves challenging, leading to frequent underdiagnosis or misdiagnosis.

Methods: The contribution monitors the clinical description, typical symptoms and treatment options including dental abnormalities in rare genetic diseases in the Roma population which are treated in ERN CRANIO centre at Motol University Hospital in Prague.

Results: Our research provides examples of autosomal recessive diseases, which can be molecularly confirmed, and prevalent within the Roma community. These include congenital cataract syndrome, facial dysmorphism and demyelinating neuropathy, non-syndromic prelingual e.g. deafness with GJB2 gene impairment, and myasthenic syndrome.

Conclusion: Our report aimed to provide a systematic review of dental phenotypes which can relate to Czech Roma's rare genetic disorders therapy including dental treatment. Understanding is important for preventing unterdiagnosis or treatment for the patients affected review of observed (Fig. 6, Ref. 27).

背景:罗姆人是一个遗传上孤立的群体,拥有共同的起源,全世界共有1000万至1400万人,源于数量有限的“遗传创始人”。罗姆人表现出特定的遗传性疾病,通常是由于较高的血缘关系造成的隐性遗传变异,最近的分子遗传学调查揭示了捷克罗姆人口中普遍存在的几种疾病。然而,在诊断这些疾病的口腔问题的概述证明具有挑战性,导致经常漏诊或误诊。方法:捐款监测在布拉格Motol大学医院ERN CRANIO中心治疗的罗姆人罕见遗传病的临床描述、典型症状和治疗方案,包括牙齿异常。结果:我们的研究提供了常染色体隐性遗传病的例子,这可以在分子上得到证实,并在罗姆社区流行。这些包括先天性白内障综合征、面部畸形和脱髓鞘神经病变、非综合征性语前病变,如GJB2基因损伤的耳聋和肌无力综合征。结论:我们的报告旨在提供一个系统的牙齿表型,这可能涉及捷克罗姆人的罕见遗传疾病治疗,包括牙科治疗。了解是重要的,以防止漏诊或治疗受影响的患者回顾观察(图6,参考文献27)。
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引用次数: 0
The founding of the UPJS Faculty of Medicine from the memories of the first dean Prof. MUDr. Jan Knazovicky. 75th anniversary of the UPJS Faculty of Medicine in Kosice. UPJS医学院的成立源于首任院长MUDr教授的回忆。Jan Knazovicky,科希策UPJS医学院成立75周年。
IF 1.1 4区 医学 Q2 MEDICINE, GENERAL & INTERNAL Pub Date : 2024-01-01 DOI: 10.4149/BLL_2024_001
Milos Knazovicky
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引用次数: 0
Genetic factors affecting susceptibility to dental caries. 影响龋齿易感性的遗传因素。
IF 1.5 4区 医学 Q2 MEDICINE, GENERAL & INTERNAL Pub Date : 2024-01-01 DOI: 10.4149/BLL_2024_98
Ladislava Slobodnikova, Andrej Ivan Halasa, Sarah Kalmanova, Bruno Calkovsky, Rastislav Juricek, Igor Malachovsky, Vanda Repiska, Maria Skerenova, Maria Janickova

Dental caries remains the most prevalent chronic, oral biofilm-associated disease affecting majority of the globe's population in all age categories. Despite enormous and revolutionary progress in omics technologies, it´s aetiology is not fully understood. The interest of current research is primarily focused on the identification and understanding of the crosstalk between main players such as host cell genome, oral microbiome´s genome, factors of immune response, saliva content and nutrition. For accurate, multi-omix analyses, it is essential to know which patient´s genes enter into crucial interactions. Identifying genes and understanding the mechanism of their action is the key for deeper understanding of their involvement in the pathogenesis of this disease. Serious alterations of these genes should be consequently used as markers to determine the extent of genetic predisposition to dental caries and identify susceptible patients. That should significantly improve the prevention, diagnostic and therapy of the disease with an individual approach and provide more efficient and effective implementation of newer preventive measures and novel therapeutic approaches in the management of the disease. This review focuses on contemporary evidence on genetics factors affecting dental caries and to provide an up-to-date comprehensive description and classification of the genes and their alterations influencing the disease. It also aims to delineate and discuss evidence gaps and potential novel applications of genetics in the context of recent advances (Tab. 2, Ref. 113). Text in PDF www.elis.sk Keywords: dental caries, candidate gene, genetic variation, multifactorial disease.

龋齿仍然是最普遍的口腔生物膜相关慢性疾病,影响着全球各年龄段的大多数人口。尽管全息技术取得了巨大的革命性进展,但人们对其病因仍不完全了解。目前的研究兴趣主要集中在识别和了解宿主细胞基因组、口腔微生物组基因组、免疫反应因素、唾液含量和营养等主要因素之间的相互影响。要进行准确的多混合分析,就必须知道哪些患者基因参与了关键的相互作用。确定基因并了解其作用机制是深入了解其参与该疾病发病机制的关键。因此,这些基因的严重改变应被用作确定龋齿遗传易感性程度和识别易感患者的标记。这将大大提高龋齿的预防、诊断和治疗水平,并为龋齿的治疗提供更有效的预防措施和新的治疗方法。这篇综述重点关注影响龋齿的遗传因素的当代证据,并对影响龋齿的基因及其改变进行最新的全面描述和分类。本综述还旨在结合最新进展,划分并讨论证据差距和遗传学的潜在新应用(参考文献113,表2)。Text in PDF www.elis.sk Keywords: dental caries, candidate gene, genetic variation, multifactorial disease.
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引用次数: 0
Invasive and metastatic hydatidiform moles in Slovakia in 1993‒2022. 1993-2022 年斯洛伐克的侵袭性和转移性水瘤。
IF 1.5 4区 医学 Q2 MEDICINE, GENERAL & INTERNAL Pub Date : 2024-01-01 DOI: 10.4149/BLL_2024_65
Liam McCullough, Ludovit Danihel, Jozef Sufliarsky, Michaela Kubickova, Zuzana Niznanska, Adam Adamec, Miroslav Korbel

Objective: A retrospective analysis of invasive and metastatic hydatidiform moles (HM) in the Slovak Republic (SR)‒epidemiology, patient characteristics and treatment outcomes.

Backround: Invasive and metastatic mole is a highly curable type of gestational trophoblastic neoplasia. Both invasive and metastatic HM may be cured by hysterectomy without adjuvant chemotherapy.

Methods: Nineteen cases of histopathologically confirmed HM (10 invasive and 9 metastatic) were treated in SR from 1993 to 2022. Patients were divided into two groups according to treatment modality (hysterectomy only ‒ 8; hysterectomy and chemotherapy ‒ 11). The parameters included in the analysis were patient age, antecedent pregnancy, human chorionic gonadotropin level, tumor size and time to remission.

Results: The incidence of invasive and metastatic HM in the SR was 1:121,253 pregnancies, or 1:86,589 live births. The overall cure rate was 100%, without recurrence. Hysterectomy was performed as first-line therapy in 14 patients, with a cure rate of 57.1%. 4 out of 8 patients (50%) with metastatic moles, who underwent first-line hysterectomy, were cured without chemotherapy. There was no statistically significant difference between the two groups in all selected parameters.

Conclusion: First-line hysterectomy may lead to remission without adjuvant chemotherapy or reduce the number of chemotherapies in invasive and metastatic HM (Tab. 4, Fig. 2, Ref. 21).

目的:对斯洛伐克共和国(SR)的侵袭性和转移性水瘤(HM)--流行病学、患者特征和治疗效果进行回顾性分析:对斯洛伐克共和国(SR)的浸润性和转移性水滴状痣(HM)--流行病学、患者特征和治疗结果--进行回顾性分析:背景:浸润性和转移性水瘤是一种高度可治愈的妊娠滋养细胞肿瘤。浸润性和转移性痣均可通过子宫切除术治愈,无需辅助化疗:方法:1993 年至 2022 年期间,19 例经组织病理学证实的 HM(10 例浸润性和 9 例转移性)在 SR 接受了治疗。根据治疗方式将患者分为两组(仅子宫切除术--8 例;子宫切除术和化疗--11 例)。分析参数包括患者年龄、先兆妊娠、人绒毛膜促性腺激素水平、肿瘤大小和缓解时间:SR中浸润性和转移性HM的发病率为1:121,253,即1:86,589。总体治愈率为 100%,无复发。有 14 名患者接受了子宫切除术作为一线治疗,治愈率为 57.1%。在 8 名接受一线子宫切除术的转移痣患者中,有 4 人(50%)无需化疗即可治愈。两组患者在所有选定参数上的差异均无统计学意义:结论:一线子宫切除术可使浸润性和转移性 HM 患者在不进行辅助化疗的情况下获得缓解,或减少化疗次数(表 4,图 2,参考文献 21)。
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引用次数: 0
Can atypical response in endothelial dysfunction-related genes and microRNAs arise from low hydrogen peroxide exposure? 低过氧化氢暴露会导致内皮功能障碍相关基因和 microRNA 的非典型反应吗?
IF 1.5 4区 医学 Q2 Medicine Pub Date : 2024-01-01 DOI: 10.4149/BLL_2024_021
Meral Urhan-Kucuk, Menderes Yusuf Terzi

Objective: Vascular endothelium is a tissue in which several vasoactive substances are produced and secreted. Reactive oxygen species can cause endothelial dysfunction (ED). miRNAs can be implicated in the oxidative stress-related ED during vascular disease pathogeneses. Our aim is to investigate effect of H2O2-induced oxidative stress on expression levels of genes and miRNAs that are key players in ED.

Methods: H2O2 effect on cell viability of human umbilical-vein endothelial cells (HUVEC) at 24-hour was measured with MTT. Low sub-cytotoxic H2O2 concentrations (25, 50 µM) were selected to analyze their oxidative stress-inducing capacities with MDA assay and their effects on EDN1, NOS3, VCAM1, SERPINE1, miR21, miR22, miR126, and miR146a levels with RT-qPCR.

Results: Each tested H2O2 concentration reduced HUVEC cell viability. Fifty µM H2O2 augmented cellular MDA levels. Intriguingly, EDN1, VCAM1, and SERPINE1 and all analyzed miRNAs' levels attenuated upon H2O2 treatment whereas there was no change in NOS3 levels compared to control. There was a positive correlation between miR-21 and VCAM1.

Conclusion: Rather than individual alterations in analyzed parameters, consistent changes in our findings i.e., parallel decreases in EDN1, VCAM1, SERPINE1 mRNA levels as well as miRNAs, suggests that H2O2 concentration-dependent modulation of expression patterns can bring about various impacts on ED (Tab. 1, Fig. 5, Ref. 63).

目的:血管内皮是产生和分泌多种血管活性物质的组织。在血管疾病的发病过程中,miRNAs 可能与氧化应激相关的内皮功能障碍(ED)有关。我们的目的是研究 H2O2 诱导的氧化应激对 ED 中起关键作用的基因和 miRNAs 表达水平的影响。方法:用 MTT 测定 24 小时内 H2O2 对人脐静脉内皮细胞(HUVEC)活力的影响,选择低亚毒性 H2O2 浓度(25、50 µM),用 MDA 分析其氧化应激诱导能力,用 RT-qPCR 分析其对 EDN1、NOS3、VCAM1、SERPINE1、miR21、miR22、miR126 和 miR146a 水平的影响:每种测试的 H2O2 浓度都会降低 HUVEC 细胞的活力。50 µM H2O2 会增加细胞的 MDA 水平。耐人寻味的是,H2O2 处理后,EDN1、VCAM1 和 SERPINE1 以及所有分析的 miRNA 水平都有所降低,而 NOS3 水平与对照组相比没有变化。miR-21 与 VCAM1 呈正相关:结论:我们的研究发现,EDN1、VCAM1、SERPINE1 mRNA 和 miRNA 水平的平行下降表明,H2O2 浓度依赖性表达模式的调节可对 ED 产生各种影响(表 1,图 5,参考文献 63)。
{"title":"Can atypical response in endothelial dysfunction-related genes and microRNAs arise from low hydrogen peroxide exposure?","authors":"Meral Urhan-Kucuk, Menderes Yusuf Terzi","doi":"10.4149/BLL_2024_021","DOIUrl":"https://doi.org/10.4149/BLL_2024_021","url":null,"abstract":"<p><strong>Objective: </strong>Vascular endothelium is a tissue in which several vasoactive substances are produced and secreted. Reactive oxygen species can cause endothelial dysfunction (ED). miRNAs can be implicated in the oxidative stress-related ED during vascular disease pathogeneses. Our aim is to investigate effect of H2O2-induced oxidative stress on expression levels of genes and miRNAs that are key players in ED.</p><p><strong>Methods: </strong>H2O2 effect on cell viability of human umbilical-vein endothelial cells (HUVEC) at 24-hour was measured with MTT. Low sub-cytotoxic H2O2 concentrations (25, 50 µM) were selected to analyze their oxidative stress-inducing capacities with MDA assay and their effects on EDN1, NOS3, VCAM1, SERPINE1, miR21, miR22, miR126, and miR146a levels with RT-qPCR.</p><p><strong>Results: </strong>Each tested H2O2 concentration reduced HUVEC cell viability. Fifty µM H2O2 augmented cellular MDA levels. Intriguingly, EDN1, VCAM1, and SERPINE1 and all analyzed miRNAs' levels attenuated upon H2O2 treatment whereas there was no change in NOS3 levels compared to control. There was a positive correlation between miR-21 and VCAM1.</p><p><strong>Conclusion: </strong>Rather than individual alterations in analyzed parameters, consistent changes in our findings i.e., parallel decreases in EDN1, VCAM1, SERPINE1 mRNA levels as well as miRNAs, suggests that H2O2 concentration-dependent modulation of expression patterns can bring about various impacts on ED (Tab. 1, Fig. 5, Ref. 63).</p>","PeriodicalId":55328,"journal":{"name":"Bratislava Medical Journal-Bratislavske Lekarske Listy","volume":"124 2","pages":"125-132"},"PeriodicalIF":1.5,"publicationDate":"2024-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"139467353","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Binary fire hawks optimizer with deep learning driven non-invasive diabetes detection and classification. 二元火鹰优化器与深度学习驱动的无创糖尿病检测和分类。
IF 1.5 4区 医学 Q2 Medicine Pub Date : 2024-01-01 DOI: 10.4149/BLL_2024_020
Namakkal Ramasamy Periasamy

Non-invasive diabetes detection refers to the utilization and development of technologies and methods that can monitor and diagnose diabetes without requiring invasive procedures, namely invasive glucose monitoring or blood sampling. The objective is to provide a more convenient and less burdensome approach to screening and management of diabetes. It is noteworthy that while non-invasive method offers promising avenues for diabetes detection, they frequently require validation through clinical studies and might have limitation in terms of reliability and accuracy than classical invasive approaches. In recent times, deep learning (DL) and feature selection (FS) are used to monitor and diagnose diabetes accurately without requiring invasive procedures. This technique combines the FS method with the DL algorithm for making accurate predictions and extracting relevant features from non-invasive data. This article introduces a new Binary Fire Hawks Optimizer with Deep Learning-Driven Non-Invasive Diabetes Detection and Classification (BFHODL-NIDDC) technique. The major intention of the BFHODL-NIDDC technique focuses on the involvement of non-invasive procedures for the detection of diabetes. In the BFHODL-NIDDC technique, data preprocessing is initially performed to preprocess the input data. Next, the BFHO algorithm chooses an optimal subset of features and improves the classifier results. For the identification of diabetes, multichannel convolutional bidirectional long short-term memory (MC-BLSTM) model is used. At last, the beetle antenna search (BAS) algorithm is used for the hyperparameter selection of the MC-BLSTM method which in turn enhances the detection performance of the MC-BLSTM model. A series of simulations were conducted on the diabetes dataset to assess the diabetes detection performance of the BFHODL-NIDDC technique. The experimental outcomes illustrated better performance of the BFHODL-NIDDC method over other recent approaches in terms of different metrics (Tab. 4, Fig. 9, Ref. 23). Keywords: diabetes, non-invasive detection, binary fire hawks optimizer, deep learning, hyperparameter tuning.

无创糖尿病检测是指利用和开发无需侵入性程序(即侵入性葡萄糖监测或血液采样)即可监测和诊断糖尿病的技术和方法。其目的是提供一种更方便、负担更轻的糖尿病筛查和管理方法。值得注意的是,虽然非侵入性方法为糖尿病检测提供了前景广阔的途径,但它们往往需要通过临床研究进行验证,而且与传统侵入性方法相比,在可靠性和准确性方面可能存在局限性。近来,深度学习(DL)和特征选择(FS)被用于在无需侵入性程序的情况下准确监测和诊断糖尿病。该技术将 FS 方法与 DL 算法相结合,可从非侵入性数据中进行准确预测并提取相关特征。本文介绍了一种新的二元火鹰优化器与深度学习驱动的无创糖尿病检测和分类(BFHODL-NIDDC)技术。BFHODL-NIDDC 技术的主要意图在于利用无创程序检测糖尿病。在 BFHODL-NIDDC 技术中,首先对输入数据进行预处理。接下来,BFHO 算法选择最佳特征子集,改进分类器结果。对于糖尿病的识别,采用了多通道卷积双向长短期记忆(MC-BLSTM)模型。最后,在 MC-BLSTM 方法的超参数选择中使用了甲虫天线搜索(BAS)算法,从而提高了 MC-BLSTM 模型的检测性能。为了评估 BFHODL-NIDDC 技术的糖尿病检测性能,对糖尿病数据集进行了一系列模拟。实验结果表明,就不同指标而言,BFHODL-NIDDC 方法的性能优于其他最新方法(表 4,图 9,参考文献 23)。关键词:糖尿病;无创检测;二元火鹰优化器;深度学习;超参数调整。
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引用次数: 0
Medication adherence: measurement methods and approaches. 坚持用药:测量方法和途径。
IF 1.5 4区 医学 Q2 Medicine Pub Date : 2024-01-01 DOI: 10.4149/BLL_2024_40
Patricia Schnorrerova, Petra Matalova, Martin Wawruch

Medication adherence is crucial for optimal treatment outcomes, yet many patients struggle to follow their prescribed regimens, impacting patients, families, and healthcare systems. Measurement of adherence is vital for effective care planning and intervention. This review explores medication adherence challenges and measurement methods, including therapeutic drug monitoring (TDM), medication event monitoring system (MEMS), analysis of adherence in insurance/pharmacy database, pill counts, and self-reports, each with its advantages and limitations.This review advocates a partnership-based approach to adherence, stressing standardized reporting and team-based care. Adherence is influenced by many factors such as complex regimens, packaging, patient perspectives, side effects. Effectively addressing these factors is crucial for improving patient outcomes. In summary, medication adherence is vital but complex. The article covers various adherence measurement methods to promote medication adherence as an important matter (Tab. 5, Fig. 2, Ref. 91). Text in PDF www.elis.sk Keywords: medication adherence, adherence barriers, primary non-adherence, medication event monitoring system, pill count, self-report.

坚持用药对于获得最佳治疗效果至关重要,然而许多患者却难以坚持按处方用药,这对患者、家庭和医疗系统都造成了影响。对用药依从性的测量对于有效的护理计划和干预至关重要。本综述探讨了用药依从性面临的挑战和测量方法,包括治疗药物监测(TDM)、用药事件监测系统(MEMS)、保险/药房数据库中的依从性分析、药片计数和自我报告,每种方法都有其优势和局限性。服药依从性受许多因素的影响,如复杂的治疗方案、包装、患者观点、副作用等。有效解决这些因素对于改善患者的治疗效果至关重要。总之,坚持用药至关重要,但也很复杂。文章介绍了各种用药依从性测量方法,以促进用药依从性这一重要事项(表 5,图 2,参考文献 91)。Text in PDF www.elis.sk Keywords: medication adherence, adherence barriers, primary non-adherence, medication event monitoring system, pill count, self-report.
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引用次数: 0
The first kidney transplantation in an HIV positive recipient in Slovakia. 斯洛伐克首例HIV阳性患者的肾脏移植手术。
IF 1.5 4区 医学 Q2 MEDICINE, GENERAL & INTERNAL Pub Date : 2024-01-01 DOI: 10.4149/BLL_2024_121
Katarina Stefancikova, Jan Breza Jr, Michaela Javorkova, Andrea Bystricanova, Martina Cirbusova, Marcela Cvoligova, Martin Chrastina, Juraj Maris, Janka Otavkova, Igor Tibensky, Zuzana Zilinska

Patients infected with human immunodeficiency virus (HIV) have long been considered unsuitable candidates for solid organ transplantation due to their poor prognosis. After the introduction of combination antiretroviral therapy, the survival of this group of patients improved significantly. HIV positive patients had been successfully transplanted for the last 18 years. HIV positive patients encounter very specific issues after transplantation, specifically related to drug interactions and higher rejection rates. Despite that, HIV positive patients have similar results to HIV negative patients post transplantation. We present the case of the first kidney transplantation in an HIV positive patient in Slovakia. The procedure was possible due to a change in legislation, as HIV positivity was an absolute contraindication for transplantation in Slovakia until October 2023. The aim of our case report is to draw attention to the possibility of kidney transplantation in an HIV positive patient and to the specific problems related to the preparation of an HIV positive patient for transplantation, post-transplant complications and the possibilities of their management (Fig. 6, Ref. 37). Keywords: kidney transplantation, HIV, human immunodeficiency virus, acute rejection, HAART, drug interaction.

人类免疫缺陷病毒(HIV)感染患者由于预后差,长期以来被认为不适合进行实体器官移植。在引入抗逆转录病毒联合治疗后,该组患者的生存率明显提高。在过去的18年里,HIV阳性患者都成功地进行了移植。HIV阳性患者在移植后会遇到非常特殊的问题,特别是与药物相互作用和更高的排异率有关。尽管如此,HIV阳性患者移植后的结果与HIV阴性患者相似。我们提出的情况下,第一个肾移植在斯洛伐克艾滋病毒阳性患者。由于立法的改变,这一手术成为可能,因为直到2023年10月,艾滋病毒阳性是斯洛伐克移植的绝对禁忌症。我们病例报告的目的是引起人们对HIV阳性患者进行肾移植的可能性的关注,以及与HIV阳性患者移植准备、移植后并发症及其管理可能性相关的具体问题(图6,参考文献37)。关键词:肾移植,HIV,人类免疫缺陷病毒,急性排斥反应,HAART,药物相互作用
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引用次数: 0
The sodium-glucose cotransporter-2 inhibitors in patients with chronic kidney disease with or without kidney transplantation - a single centre study. 钠-葡萄糖共转运蛋白-2抑制剂在伴或不伴肾移植的慢性肾病患者中的应用——一项单中心研究
IF 1.5 4区 医学 Q2 MEDICINE, GENERAL & INTERNAL Pub Date : 2024-01-01 DOI: 10.4149/BLL_2024_116
Patricia Kleinova, Karol Granak, Matej Vnucak, Monika Beliancinova, Timea Blichova, Ivana Dedinska

Introduction:  The sodium-glucose cotransporter-2 inhibitors (SGLT2i) represent the first-line treatment for chronic kidney disease. The question remains of their benefit and safety for patients after kidney transplantation. The study aimed to show the renoprotective effect and safety of use in patients with chronic kidney disease with or without kidney transplantation.

Material:  This is a prospective monocentric study of the Transplant-Nephrology Department in Martin in which patients with chronic kidney disease with or without kidney transplant in therapy with dapagliflozin were included (n=79). The changes in glomerular filtration rate, albuminuria and side effects associated with SGLT2i were studied in patients with chronic kidney disease with or without kidney transplantation and in patients with or without diabetes mellitus.

Results:  Patients without diabetes mellitus achieved a significantly higher decrease in albuminuria at the time of the third month of follow-up (p=0.0396), with the continuation of the decrease until the average follow-up (10.9 months) (p=0.7866) than patients with diabetes mellitus. During the observed period, we recorded the cessation of the primary decrease in glomerular filtration with a return to the baseline values. In our group, we did not confirm a significant occurrence of adverse effects associated with dapagliflozin.

Conclusion:  SGLT2i significantly reduces albuminuria and stabilizes glomerular filtration in patients with chronic kidney disease. Based on our analysis, treatment with gliflozins is effective and safe for patients after kidney transplantation (Tab. 4, Fig. 6, Ref. 16).

钠-葡萄糖共转运蛋白-2抑制剂(SGLT2i)是慢性肾脏疾病的一线治疗药物。它们对肾移植后患者的益处和安全性仍然是一个问题。该研究旨在显示慢性肾病伴或不伴肾移植患者使用该药物的肾保护作用和安全性。材料:这是马丁市移植肾内科的一项前瞻性单中心研究,纳入了接受或不接受达格列净治疗的慢性肾病患者(n=79)。研究了伴有或不伴有肾移植的慢性肾病患者以及伴有或不伴有糖尿病的患者的肾小球滤过率、蛋白尿和SGLT2i相关副作用的变化。结果:非糖尿病患者在随访第3个月时尿白蛋白下降幅度明显高于糖尿病患者(p=0.0396),并持续下降至平均随访时间(10.9个月)(p=0.7866)。在观察期间,我们记录了原发性肾小球滤过减少的停止,并恢复到基线值。在我们的组中,我们没有确认与达格列净相关的显著不良反应的发生。结论:SGLT2i可显著降低慢性肾病患者蛋白尿并稳定肾小球滤过。根据我们的分析,格列净治疗肾移植后患者是有效且安全的(表4,图6,文献16)。
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引用次数: 0
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Bratislava Medical Journal-Bratislavske Lekarske Listy
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