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Current insights into the possible role of laboratory monitoring of effectiveness and safety of direct oral anticoagulants 目前对实验室监测直接口服抗凝剂的有效性和安全性的可能作用的见解
IF 0.2 Q4 CARDIAC & CARDIOVASCULAR SYSTEMS Pub Date : 2023-07-27 DOI: 10.20996/1819-6446-2023-2922
S. Gilyarevsky, N. Vereina, M. Golshmid
The article is devoted to the discussion of modern approaches to the use of laboratory methods to improve the tactics of using direct oral anticoagulants (DOACs) therapy. Clinical situations in which it may be reasonable to use data on the blood concentration of DOACs are given, including very old age, a marked deviation from the norm of body weight or impaired renal function. Data on the role of measuring the blood level of DOACs are considered in cases of the development of diseases or complications in which information is required on the preservation of the anticoagulant effect of DOACs, for example, in the development of severe bleeding or the need for urgent surgical intervention. The advantages and limitations of modern laboratory methods for assessing the blood concentration of DOACs are discussed. It is emphasized that one of the main advantages of using DOACs is the absence of the need to monitor laboratory parameters in most patients. Data from pharmacological studies are presented that may be useful in explaining the mechanisms that determine the higher safety of some DOACs compared to others. Promising methods for assessing the blood level of DOACs, as well as the possibility of using less specific reagents for assessing the concentration of DOACs, are considered. The possibility of using less specific, but more accessible methods for assessing the blood concentration of factor Xa inhibitors, in particular, a reagent for assessing the level of the antifactor, which is used to determine the blood level of heparin, is being considered. The opinions of experts on the role of assessing the blood level of DOACs and the possibility of tactics for selecting doses of DOACs based on laboratory analysis data are given.
本文致力于讨论使用实验室方法的现代方法,以改进使用直接口服抗凝剂(DOACs)治疗的策略。给出了可能合理使用doac血药浓度数据的临床情况,包括非常年老、明显偏离体重标准或肾功能受损。在发生疾病或并发症时,例如发生严重出血或需要紧急手术干预时,需要关于保持多氯乙酸甲酯抗凝作用的信息,则考虑测量血液中多氯乙酸甲酯水平作用的数据。讨论了评价DOACs血药浓度的现代实验室方法的优点和局限性。需要强调的是,使用doac的主要优点之一是大多数患者不需要监测实验室参数。药理学研究提供的数据可能有助于解释决定某些doac比其他doac安全性更高的机制。考虑了评估DOACs血液水平的有前途的方法,以及使用不太特异性的试剂来评估DOACs浓度的可能性。正在考虑使用特异性较低,但更容易获得的方法来评估Xa因子抑制剂血药浓度的可能性,特别是用于评估抗因子水平的试剂,用于确定肝素血药水平。对多氯乙酸血药浓度评估的作用及根据实验室分析数据选择多氯乙酸剂量的可能策略提出了专家意见。
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引用次数: 0
Biomarkers in assessing the vulnerability of atherosclerotic plaques: a narrative review 评估动脉粥样硬化斑块易损性的生物标志物:叙述性回顾
IF 0.2 Q4 CARDIAC & CARDIOVASCULAR SYSTEMS Pub Date : 2023-07-27 DOI: 10.20996/1819-6446-2023-2878
A. Kovalskaya, D. Duplyakov
Aim. To study the role of biomarkers in assessing the vulnerability of atherosclerotic plaques.Material and methods. A review of literature sources investigating the biomarker assessment of the vulnerability of atherosclerotic plaques published for the period 01.01.2016 to 31.12.2022 was carried out. Literature search was carried out in English and Russian in PubMed databases, in Google Academy, Elibrary.ru according to the following keywords: “biomarkers of plaque vulnerability”, “NLR and vulnerable plaque”, “CRP and vulnerable plaque”, ”MMP-9 and vulnerable plaque”, “TIMP-1 and vulnerable plaque”, ”galectin-3 and vulnerable plaque”, “NGAL and vulnerable plaque”. A total of 183 articles were found, of which 42 articles in full-text format containing original clinical studies were selected for the preparation of this review.Results. Numerous studies have shown that the vulnerability and rupture of the plaque, rather than its size and severity of stenosis, are the main cause of cardiovascular events in patients with coronary heart disease. Small plaques rich in lipids often become unstable due to an inflammatory reaction supported by the interaction between lipoproteins, monocytes, macrophages, T-lymphocytes and vascular wall cells. NLR, CRP, NGAL, Galectin-3, as well as markers of extracellular matrix degradation (MMP-9, TIMP-1) can play a special role in assessing the vulnerability of plaques.Conclusion. The development of acute coronary syndrome is based on the destabilization of the atherosclerotic plaque, which occurs not only due to changes in its lipid composition, but also infiltration by immuno-inflammatory cells, degradation of the extracellular matrix, as well as an active inflammatory reaction and neovascularization of the plaque. Therefore, traditional imaging methods that characterize the plaque by its appearance and size are not enough to predict the risk of rupture and the development of an acute thrombotic event. Thus, there is a need to identify new biomarkers that would correlate with the instability of plaque atheroma.
的目标。研究生物标志物在评估动脉粥样硬化斑块易损性中的作用。材料和方法。我们对2016年1月1日至2022年12月31日期间发表的研究动脉粥样硬化斑块易损性生物标志物评估的文献来源进行了回顾。在PubMed数据库、Google Academy、elibrarry .ru中,根据“斑块易损性生物标志物”、“NLR和易损性斑块”、“CRP和易损性斑块”、“MMP-9和易损性斑块”、“TIMP-1和易损性斑块”、“半乳糖凝集素-3和易损性斑块”、“NGAL和易损性斑块”等关键词,进行英文和俄语文献检索。共检索到183篇文献,其中选取了42篇包含原始临床研究的全文文献作为本综述的准备。大量研究表明,斑块的易碎性和破裂,而不是其狭窄的大小和严重程度,是冠心病患者心血管事件的主要原因。富含脂质的小斑块往往由于脂蛋白、单核细胞、巨噬细胞、t淋巴细胞和血管壁细胞相互作用所支持的炎症反应而变得不稳定。NLR、CRP、NGAL、Galectin-3以及细胞外基质降解标志物(MMP-9、TIMP-1)在斑块易感性评价中具有特殊作用。急性冠状动脉综合征的发生是基于动脉粥样硬化斑块的不稳定,这不仅是由于其脂质成分的改变,还包括免疫炎症细胞的浸润,细胞外基质的降解,以及活跃的炎症反应和斑块的新生血管。因此,通过斑块的外观和大小来描述斑块特征的传统成像方法不足以预测斑块破裂的风险和急性血栓事件的发展。因此,有必要确定与斑块粥样硬化不稳定性相关的新生物标志物。
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引用次数: 0
Polypharmacy: definition, impact on outcomes, need for correction 多药:定义,对结果的影响,需要纠正
IF 0.2 Q4 CARDIAC & CARDIOVASCULAR SYSTEMS Pub Date : 2023-07-27 DOI: 10.20996/1819-6446-2023-2924
S. Martsevich, N. Kutishenko, Y. Lukina, O. Drapkina
The review is devoted to a modern problem of polypharmacy. A universal definition and clear criteria for this concept have not yet been formed, but it is believed that this is the prescribing of at least 5 medications (M). The article discusses the frequency and main causes of polypharmacy, demonstrates its clear relationship with the age. The presence of overweight and obesity, multimorbidity, low physical activity, fragility are clearly associated with polypharmacy. Cognitive impairment, disability, long-term pain syndrome and malignant diseases also predispose to polypharmacy. The absence of a permanent attending physician, living in a nursing home, consulting with several specialists, poor management of medical records are associated with polypharmacy. It is believed that polypharmacy leads to a following number of adverse consequences: it increases the risk of falls, side effects of M, hospitalizations and even death. The main reason for this is the occurrence of various adverse interactions between M, including unpredictable ones, but the causal relationship of these phenomena with polypharmacy is not always proven. To study of adherence to prescribed therapy with polypharmacy is not an easy task, to date, there is no clear answer to the question whether polypharmacy affects adherence to drug therapy. The article presents in detail the problems of potentially irrational prescriptions, discusses the main methods of preventing and combating polypharmacy. Obviously, the most acceptable methods are the cancellation of drugs that are not indicated or contraindicated to the patient, and the prescribing of those drugs for which there are direct indications, but which the patient does not receive. The patient’s therapy should be individualized as much as possible, taking into account numerous factors related to the peculiarities of the disease course, the prognosis, the patient’s lifestyle, his physical and mental status.
这篇评论专门讨论了一个现代的多药问题。这一概念尚未形成一个普遍的定义和明确的标准,但认为这是至少5种药物(M)的处方。本文讨论了多药的频率和主要原因,并论证了其与年龄的明确关系。超重和肥胖、多病、低体力活动、脆弱明显与多重用药相关。认知障碍、残疾、长期疼痛综合征和恶性疾病也易导致多重用药。缺少长期主治医生、住在养老院、咨询多名专家、医疗记录管理不善,这些都与综合药房有关。据信,多种用药会导致以下一系列不良后果:它增加了跌倒的风险、M的副作用、住院甚至死亡。其主要原因是M之间发生了各种不良相互作用,包括不可预测的相互作用,但这些现象与多药的因果关系并不总是得到证实。研究复方药物对处方治疗的依从性并不是一件容易的事情,迄今为止,复方药物是否影响药物治疗的依从性这个问题还没有明确的答案。文章详细介绍了可能存在的不合理处方问题,探讨了预防和打击多药的主要方法。显然,最可接受的方法是取消对患者没有指征或禁忌症的药物,以及开那些有直接指征但患者没有接受的药物。患者的治疗应尽可能个体化,考虑到与病程特点、预后、患者的生活方式、身体和精神状态有关的许多因素。
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引用次数: 0
Ventricular tachycardia and myocardial infarction during antiarrhythmic therapy: a case report 抗心律失常治疗期间室性心动过速和心肌梗死1例报告
IF 0.2 Q4 CARDIAC & CARDIOVASCULAR SYSTEMS Pub Date : 2023-07-27 DOI: 10.20996/1819-6446-2023-2914
A. Gurbanova, K. Pereverzeva, S. Yakushin, I. V. Budanova
The article analyzes the case of the development of ventricular tachycardia and type 2 myocardial infarction (MI) in an 80-year-old patient with a history of coronary artery disease, MI and chronic heart failure. In 2020, the patient was diagnosed with ventricular extrasystole and started antiarrhythmic therapy with diethylamino propionylethoxycarbonylaminophenothiazine 150 mg per day and sotalol 160 mg per day. In 2022, the patient had an episode of clinical death due to ventricular tachycardia with successful resuscitation. A diagnosis of non-ST-elevation acute coronary syndrome was made, coronary angiography was performed, which did not reveal significant coronary stenosis. Upon further examination, the dynamics of biomarkers of myocardial necrosis confirmed the diagnosis of acute MI. In the analyzed case, the development of ventricular tachycardia and MI is most likely associated with the intake of diethylaminopropionylethoxycarbonylaminophenothiazine in combination with sotalol, prescribed in the presence of contraindications to their use.
本文分析了一例80岁冠心病、心肌梗死和慢性心力衰竭患者室性心动过速和2型心肌梗死(MI)的发展情况。2020年,患者被诊断为室性早搏,并开始使用二乙胺丙炔乙氧羰基氨基吩噻嗪150 mg /天、索他洛尔160 mg /天的抗心律失常治疗。2022年,患者因室性心动过速发生临床死亡,复苏成功。诊断为非st段抬高急性冠状动脉综合征,行冠状动脉造影,未见明显冠状动脉狭窄。进一步检查后,心肌坏死生物标志物的动态变化证实了急性心肌梗死的诊断。在所分析的病例中,室性心动过速和心肌梗死的发生很可能与二乙基氨基丙酰乙氧羰基氨基吩噻嗪与索他洛尔的联合使用有关,在存在使用禁忌的情况下开具处方。
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引用次数: 1
Plasma branched-chain amino acid concentrations in individuals without cardiovascular diseases versus patients diagnosed with hypertension and coronary artery disease 无心血管疾病个体与诊断为高血压和冠状动脉疾病患者的血浆支链氨基酸浓度
IF 0.2 Q4 CARDIAC & CARDIOVASCULAR SYSTEMS Pub Date : 2023-07-27 DOI: 10.20996/1819-6446-2023-2894
M. Kozhevnikova, E. O. Korobkova, A. V. Krivova, A. Kukharenko, N. Moskaleva, K. Shestakova, N. Mesonzhnik, A. Ageev, A. A. Boldin, A. Brito, S. Appolonova, E. Privalova, Y. Belenkov
Aim. Branched-chain amino acids (BCAAs) have been postulated as potential indicators of cardiovascular risk. The objective of this study was to explore the relationship between plasma BCAAs and different stages of cardiovascular disorders.Material and methods. In our cross-sectional study, plasma BCAAs (valine, leucine and isoleucine) in individuals without cardiovascular diseases (CVDs) (nonCVD group, total n=27, with n=16 healthy, but with metabolic disorders) were compared to patients diagnosed with CVDs [CVD group, total n=109, being n=61 hypertension (n=31 with signs of beginning of myocardial remodeling) and n=48 patients with coronary artery disease (CAD)].Results. The plasma concentration of BCAAs was significantly higher in the group of patients with cardiovascular disease compared with the healthy group (p<0.05 for all amino acids tested): valine concentration was 238.7 [219.6; 267.0] μM in the non-CVD group and 261.2 [233.8; 298.7] μM in the CVD group; leucine concentration was 134.8 [122.4; 153.2] μM and 146.8 [129.0; 166.6] μM, respectively; and isoleucine 72.7 [65.3; 84.4] μM and 81.7 [68.0; 96.2] μM, respectively. Leucine and isoleucine concentration levels were minimal in the healthy participant subgroup and maximal in the IBS patient subgroup. No statistically significant differences in BCAAs concentrations were found in the subgroups without CAD. Significant increases in concentrations were observed in the subgroups of patients with CAD as follows: valine concentration was 256.3 [219.0; 297.9] μM in hypertension group and 261.7 [236.5; 307.5] μM in CAD group; leucine concentration was 141.8 [123.5; 166.6] μM and 154.1 [134.7; 172.7] μM, respectively, and isoleucine 72.8 [65.7; 94.0] μM and 85.7 [74.9; 101.7] μM, respectively. BCAAs profiles in all participants with metabolic disorders had “good” diagnostic accuracy with area under the receiver operating characteristics curve being 0.72, 0.70 and 0.70 for valine, leucine and isoleucine, respectively.Conclusion. BCAAs concentrations are elevated with higher severity of the cardiovascular disorder and exhibit potential as early independent indicators of coronary artery disease.
的目标。支链氨基酸(BCAAs)被认为是心血管风险的潜在指标。本研究的目的是探讨血浆支链氨基酸与不同阶段心血管疾病的关系。材料和方法。在我们的横断面研究中,将无心血管疾病(CVD)个体(非CVD组,总n=27,健康但有代谢障碍的n=16)的血浆BCAAs(缬氨酸、亮氨酸和异亮氨酸)与诊断为CVD的患者(CVD组,总n=109,其中n=61高血压(n=31有心肌重构开始的体征)和n=48有冠状动脉疾病(CAD)的患者)进行比较。结果。心血管疾病患者血浆BCAAs浓度显著高于健康组(各氨基酸检测值p<0.05):缬氨酸浓度为238.7 [219.6;非cvd组267.0]m, 261.2 [233.8] m;298.7] μM在CVD组;亮氨酸浓度为134.8 [122.4;153.2] μM和146.8 [129.0;166.6] μM;异亮氨酸72.7 [65.3;84.4] μM和81.7 [68.0];96.2] μM。亮氨酸和异亮氨酸浓度水平在健康参与者亚组中最低,在肠易激综合征患者亚组中最高。在没有CAD的亚组中,BCAAs浓度无统计学差异。在CAD患者亚组中观察到的浓度显著升高如下:缬氨酸浓度为256.3 [219.0;高血压组297.9 μM, 261.7 μM [236.5];307.5] μM CAD组;亮氨酸浓度为141.8 [123.5;166.6] μM和154.1 [134.7];172.7] μM,异亮氨酸72.8 [65.7;94.0] μM和85.7 [74.9];101.7] μM。所有代谢紊乱患者的BCAAs谱具有“良好”的诊断准确性,缬氨酸、亮氨酸和异亮氨酸的受试者工作特征曲线下面积分别为0.72、0.70和0.70。BCAAs浓度随着心血管疾病严重程度的升高而升高,并表现出作为冠状动脉疾病早期独立指标的潜力。
{"title":"Plasma branched-chain amino acid concentrations in individuals without cardiovascular diseases versus patients diagnosed with hypertension and coronary artery disease","authors":"M. Kozhevnikova, E. O. Korobkova, A. V. Krivova, A. Kukharenko, N. Moskaleva, K. Shestakova, N. Mesonzhnik, A. Ageev, A. A. Boldin, A. Brito, S. Appolonova, E. Privalova, Y. Belenkov","doi":"10.20996/1819-6446-2023-2894","DOIUrl":"https://doi.org/10.20996/1819-6446-2023-2894","url":null,"abstract":"Aim. Branched-chain amino acids (BCAAs) have been postulated as potential indicators of cardiovascular risk. The objective of this study was to explore the relationship between plasma BCAAs and different stages of cardiovascular disorders.Material and methods. In our cross-sectional study, plasma BCAAs (valine, leucine and isoleucine) in individuals without cardiovascular diseases (CVDs) (nonCVD group, total n=27, with n=16 healthy, but with metabolic disorders) were compared to patients diagnosed with CVDs [CVD group, total n=109, being n=61 hypertension (n=31 with signs of beginning of myocardial remodeling) and n=48 patients with coronary artery disease (CAD)].Results. The plasma concentration of BCAAs was significantly higher in the group of patients with cardiovascular disease compared with the healthy group (p<0.05 for all amino acids tested): valine concentration was 238.7 [219.6; 267.0] μM in the non-CVD group and 261.2 [233.8; 298.7] μM in the CVD group; leucine concentration was 134.8 [122.4; 153.2] μM and 146.8 [129.0; 166.6] μM, respectively; and isoleucine 72.7 [65.3; 84.4] μM and 81.7 [68.0; 96.2] μM, respectively. Leucine and isoleucine concentration levels were minimal in the healthy participant subgroup and maximal in the IBS patient subgroup. No statistically significant differences in BCAAs concentrations were found in the subgroups without CAD. Significant increases in concentrations were observed in the subgroups of patients with CAD as follows: valine concentration was 256.3 [219.0; 297.9] μM in hypertension group and 261.7 [236.5; 307.5] μM in CAD group; leucine concentration was 141.8 [123.5; 166.6] μM and 154.1 [134.7; 172.7] μM, respectively, and isoleucine 72.8 [65.7; 94.0] μM and 85.7 [74.9; 101.7] μM, respectively. BCAAs profiles in all participants with metabolic disorders had “good” diagnostic accuracy with area under the receiver operating characteristics curve being 0.72, 0.70 and 0.70 for valine, leucine and isoleucine, respectively.Conclusion. BCAAs concentrations are elevated with higher severity of the cardiovascular disorder and exhibit potential as early independent indicators of coronary artery disease.","PeriodicalId":20812,"journal":{"name":"Rational Pharmacotherapy in Cardiology","volume":"12 1","pages":""},"PeriodicalIF":0.2,"publicationDate":"2023-07-27","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"84950715","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
Intractable complicated course of tricuspid valve infective endocarditis due to non-compliance of treatment with clinical guidelines with a decisive role of molecular biological study in etiological diagnosis: a case report 顽固性三尖瓣感染性心内膜炎因治疗不符合临床指南导致病程复杂,分子生物学研究在病因诊断中起决定性作用1例
IF 0.2 Q4 CARDIAC & CARDIOVASCULAR SYSTEMS Pub Date : 2023-07-27 DOI: 10.20996/1819-6446-2023-2689
E. Kotova, A. Moiseeva, E. Domonova, O. Y. Silveytrova, A. Pisaryuk, P. V. Kakhktsyan, J. I. Babukhina, Z. Kobalava
A clinical observation of the treatment non-compliance consequences with clinical guidelines and principles of empirical therapy selection in a female patient with intravenous drug abuse, viral hepatitis C and HIV infection, with a history of a COVID-19 and the development of uncontrolled staphylococcal infective endocarditis (IE) of the tricuspid valve, complicated recurrence of early prosthetic IE is presented. Successful treatment was achieved only by a combination of tricuspid valve replacement and the appointment of etiotropic therapy for S. aureus (MSSA). The typical clinical scenario was not accompanied by the choice of adequate empirical antibiotic therapy, despite the high suspicion of association with MSSA, which determined the complicated course of IE. Only the polymerase chain reaction of the heart valve tissue played a key role in the etiological diagnosis. The use of valve tissue polymerase chain reaction in addition to traditional microbiological methods is a valuable diagnostic study.
本文报道1例静脉药物滥用、病毒性丙型肝炎和HIV感染女性患者的治疗不符合临床指南和经验治疗选择原则的临床观察,该患者具有COVID-19病史,并发三尖瓣葡萄球菌性感染性心内膜炎(IE),并发早期假体IE复发。成功的治疗仅通过联合三尖瓣置换术和预约金黄色葡萄球菌(MSSA)的致病因治疗来实现。尽管高度怀疑与MSSA相关,但典型的临床情况并未伴随适当的经经验抗生素治疗的选择,这决定了IE的复杂病程。只有心脏瓣膜组织的聚合酶链反应在病因诊断中起关键作用。除了传统的微生物学方法外,使用瓣膜组织聚合酶链反应是一项有价值的诊断研究。
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引用次数: 0
Effect of long-term nicorandil therapy on myocardial perfusion parameters according to triphosadenine stress-volume computed tomography in a patient with non-obstructive coronary artery disease: a care report 非阻塞性冠状动脉疾病患者长期服用尼可地尔对三磷腺嘌呤应激容积计算机断层扫描心肌灌注参数的影响:护理报告
IF 0.2 Q4 CARDIAC & CARDIOVASCULAR SYSTEMS Pub Date : 2023-07-11 DOI: 10.20996/1819-6446-2023-2913
O. F. Egorkina, G. N. Soboleva, S. Gaman, Y. A. Karpov, S. Ternovoy
A case of a patient with myocardial perfusion improvement according to volume computed tomography (VCT) of the heart with triphosadenine infusion against the background of optimal therapy, including nicorandil for 3,5 years, is presented. In a patient with an established diagnosis of non-obstructive coronary artery disease (CAD) in 2019, stress-induced myocardial ischemia of left ventricular (LV) septal and lateral area was detected. Repeated investigation 3,5 years later against the background of optimal therapy showed an ischemia decrease in the form of the disappearance of previously detected defects in the basal segments of the anteriorlateral and inferior-lateral walls and the middle segments of the anterior-septal and inferior-lateral walls of the LV.
本文介绍了一例患者在接受了包括尼可地尔在内的3.5年最佳治疗的背景下,通过输注三磷腺嘌呤进行心脏容积计算机断层扫描(VCT)发现心肌灌注改善的病例。在一名于 2019 年确诊为非阻塞性冠状动脉疾病(CAD)的患者身上,发现了应激诱发的左心室(LV)室间隔和外侧心肌缺血。3.5 年后,在最佳治疗背景下进行的重复检查显示,缺血程度有所减轻,之前在左心室前外侧壁和下外侧壁基底段以及前隔壁和下外侧壁中间段发现的缺损消失了。
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引用次数: 0
Paradigm shift on the role of mineralocorticoid receptor antagonists in hypertension therapy 矿物质皮质激素受体拮抗剂在高血压治疗中的作用范式转变
IF 0.2 Q4 CARDIAC & CARDIOVASCULAR SYSTEMS Pub Date : 2023-07-11 DOI: 10.20996/10.20996/1819-6446-2023-2918
S. Gilyarevsky, D. O. Ladygina
The literature review is devoted to modern ideas about the role of hyperaldosteronism as one of the important pathophysiological links in hypertension (HTN) development. Data are presented on aldosterone synthesis mechanisms both in healthy and sick people, in particular in primary aldosteronism (PA), as well as in some cases of secondary aldosteronism. The results of modern studies are discussed, which established autonomous formation of aldosterone in elderly and senile people even without formal criteria for PA. The most important stages of studying and solving the hyperaldosteronism problem using surgical or conservative methods areconsidered. Data are presented on target organ damage caused by an increased blood concentration of aldosterone. The influence of the interaction between increased dietary sodium intake and the severity of cardiovascular damage is discussed. Separately, the role of subclinical hyperaldosteronism in the development of hypertension is considered, as well as the possibility of target organ damage in such cases, despite the normal blood pressure level. Modern data on the role of mineralocorticoid receptor antagonists (MRAs), in particular spironolactone, in the treatment of hyperaldosteronism and resistant hypertension are presented. The limitations of MRA use, which are mainly due to reduced kidney function, are considered. In particular, the results of the most important clinical studies are discussed, which became the basis for higher prescription rate of MRAs in the treatment of hypertensive patients.
这篇文献综述探讨了高醛固酮增多症作为高血压(HTN)发病的重要病理生理环节之一的现代观点。文章介绍了健康人和病人的醛固酮合成机制,特别是原发性醛固酮增多症(PA)和一些继发性醛固酮增多症病例的醛固酮合成机制。讨论了现代研究的结果,这些结果确定了老年人和老龄人体内醛固酮的自主形成,即使没有 PA 的正式标准。考虑了使用手术或保守方法研究和解决高醛固酮症问题的最重要阶段。介绍了血液中醛固酮浓度升高对靶器官造成损害的数据。讨论了膳食钠摄入量增加与心血管损害严重程度之间相互作用的影响。另外,还考虑了亚临床高醛固酮血症在高血压发病中的作用,以及在这种情况下,尽管血压水平正常,但仍有可能造成靶器官损害。介绍了有关矿质皮质激素受体拮抗剂(MRA),特别是螺内酯在治疗高醛固酮症和抵抗性高血压中的作用的现代数据。还考虑了使用 MRA 的局限性,这主要是由于肾功能减退造成的。特别讨论了最重要的临床研究结果,这些研究结果是提高 MRAs 治疗高血压患者处方率的基础。
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引用次数: 0
Outpatient Practice of Lipid-Lowering Therapy Prescription (According to the ARGO-3 Study) 降脂治疗处方的门诊实践(根据ARGO-3研究)
IF 0.2 Q4 CARDIAC & CARDIOVASCULAR SYSTEMS Pub Date : 2023-05-17 DOI: 10.20996/1819-6446-2023-04-04
M. Ezhov, N. Akhmedzhanov, T. E. Kolmakova, A. Tyurina, A. Martynov
Aim. To study the frequency of prescriptions of various types of lipid-lowering therapy and their effectiveness in outpatient clinical practice based on the results of a questionnaire of primary care physicians.Material and methods. The study was performed in 2022 in 75 constituent entities of the Russian Federation with the participation of 1117 doctors working in outpatient clinics. Most of the doctors had work experience of 10-20 years or more. Doctors of polyclinics (therapists and cardiologists, etc.) before the start of the study received instructions, questionnaires for filling out, developed by the National Atherosclerosis Society. The frequency of prescriptions by primary care physicians of various types of lipid-lowering therapy and their effectiveness in terms of the frequency of achieving target levels of low-density lipoprotein cholesterol (LDL-C) was studied based on the results of a questionnaire.Results. Monotherapy with statins was prescribed in 55.2% of cases, free combination of rosuvastatin with ezetimibe – in 17.2%, single pill combination of rosuvastatin with ezetimibe – in 23.2%, combination therapy with PCSK9 inhibitors – in 4.1% of cases. Target levels of LDL-C ˂ 1.8 mmol/l and ˂ 1.4 mmol/l were achieved with statin monotherapy in 42.6% and 28.2% of cases, respectively, free combination of rosuvastatin with ezetimibe – in 61.7% and 39 .5%, a fixed combination of rosuvastatin with ezetimibe – in 67.8% and 48.5%, combination therapy with PCSK9 inhibitors – in 96.8% and 92.8% of cases.Conclusion. The single pill combination of rosuvastatin with ezetimibe is more effective in achieving target levels of LDL-C compared with statin monotherapy and therapy with free combination of statin with ezetimibe. Despite the fact that the target values of LDL-C when prescribing a combination with PCSK9 inhibitors were achieved in 96.8% and 92.8% of cases, they were used quite rarely at the outpatient stage of treatment in the Russian Federation.
的目标。目的:通过对基层医师的问卷调查,了解各类降脂治疗药物在门诊临床使用的频次及效果。材料和方法。该研究于2022年在俄罗斯联邦的75个组成实体中进行,有1117名在门诊诊所工作的医生参与。大部分医生都有10-20年以上的工作经验。综合诊所的医生(治疗师和心脏病专家等)在研究开始前收到指示,填写由国家动脉粥样硬化协会制定的调查问卷。根据问卷调查的结果,研究了基层医生使用各类降脂疗法的频率及其在低密度脂蛋白胆固醇(LDL-C)达标频率方面的有效性。他汀类药物单药治疗占55.2%,瑞舒伐他汀与依泽替米布自由联合治疗占17.2%,瑞舒伐他汀与依泽替米布单药联合治疗占23.2%,PCSK9抑制剂联合治疗占4.1%。他汀类药物单药治疗达到LDL-C小于1.8 mmol/l和小于1.4 mmol/l的目标水平分别为42.6%和28.2%,瑞舒伐他汀与依泽替米比自由联合治疗分别为61.7%和39.5%,瑞舒伐他汀与依泽替米比固定联合治疗分别为67.8%和48.5%,与PCSK9抑制剂联合治疗分别为96.8%和92.8%。瑞舒伐他汀单片联合依泽替米比他汀单药和他汀与依泽替米自由联合治疗更有效地达到LDL-C目标水平。尽管在处方联合PCSK9抑制剂时,LDL-C的目标值在96.8%和92.8%的病例中达到,但在俄罗斯联邦的门诊治疗阶段,它们很少被使用。
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引用次数: 0
Vasotoxic Effects of Anticancer Therapy: a Review of Current Data 抗癌治疗的血管毒性作用:对当前数据的回顾
IF 0.2 Q4 CARDIAC & CARDIOVASCULAR SYSTEMS Pub Date : 2023-05-12 DOI: 10.20996/1819-6446-2023-03-03
Y. Vasyuk, E. Shupenina, A. G. Nosova, E. Novosel, D. Vyzhigin
Cardiovascular and oncological diseases are the leading causes of adult death in the world. Despite proven efficacy, anticancer drugs can cause severe cardiovascular complications. Recently, data have appeared on the possible vasotoxic effects of chemotherapy drugs, which can manifest themselves as the progression of arterial hypertension and atherosclerosis, the development of myocardial ischemia and acute coronary syndrome, the formation of venous and arterial thrombosis. The key mechanism for the development of vasotoxicity is endothelial dysfunction, and anticancer drugs can also affect the processes of thrombosis. The review presents the results of 12 selected observational retro- and prospective studies involving cancer patients receiving presumably vasotoxic therapy. Data on the frequency of occurrence and possibilities for the prevention of vasotoxicity are presented. 
心血管和肿瘤疾病是世界上成年人死亡的主要原因。尽管抗癌药物已被证明有效,但它可能导致严重的心血管并发症。近年来,有资料显示化疗药物可能存在血管毒性作用,表现为动脉高血压和动脉粥样硬化的进展,心肌缺血和急性冠状动脉综合征的发展,静脉和动脉血栓的形成。血管毒性发展的关键机制是内皮功能障碍,抗癌药物也可以影响血栓形成的过程。本综述介绍了12项选择性观察性回顾性和前瞻性研究的结果,这些研究涉及可能接受血管毒性治疗的癌症患者。资料的发生频率和预防血管毒性的可能性提出。
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引用次数: 0
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Rational Pharmacotherapy in Cardiology
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