Implantable cardioverter-defibrillator

植入式心律转复除颤器
  • 文章类型: Case Reports
    我国合法药品的销售有所增加。这些物质之一是kratom。Kratom(Mitragynaspeciosa)是阿片类κ的部分激动剂,mu,和δ受体。它在低浓度时起到兴奋剂的作用,让用户感觉更有活力和欣快。它在较高剂量下具有镇静和抗伤害作用。
    一名18岁男子在足球训练中晕倒,需要心肺复苏;最初的心律是通过除颤控制的心室纤颤。实验室参数不显著。送去进行毒理学评估的血液样本对kratom和咖啡因呈阳性。超声心动图检查,冠状动脉计算机断层扫描血管造影,和心脏磁共振成像没有证实原因。基因检测未发现与家族性室颤相关的致病基因变异,但是在MYOM1中发现了一个未知意义的变体。鉴于这种情况,我们根据欧洲心脏病学会(ESC)的指南,在心源性猝死(SCD)二级预防中植入了植入式心律转复除颤器(ICD).通过对我们的患者进行动态ICD记忆检查,未报告室性心律失常复发。
    在某些国家/地区,kratom是免费提供和出售的植物,不是毒品。文献中仅描述了使用kratom后发生心室纤颤的情况。没有足够的科学证据将kratom与心室纤颤联系起来。这是绝对关键的这类病例报告,在世界类似情况下尚未出版。因此,心室纤颤的发展被认为是由于kratom的组合,咖啡因,和锻炼。kratom的安全性和作用应该是未来研究的主题。我们要强调,必须报告更多的病例系列,以获得更多的科学证据,从而增加一些国家对kratom的更严格供应和监管的压力,尤其是在非处方药的地方.
    UNASSIGNED: There is an increase in the sale of legal drugs in our country. One of these substances is kratom. Kratom (Mitragyna speciosa) is a partial agonist of the opioid kappa, mu, and delta receptors. It acts as a stimulant at low concentrations, making users feel more energetic and euphoric. It has sedative and antinociceptive effects at higher doses.
    UNASSIGNED: An 18-year-old man collapsed during football training and required cardiopulmonary resuscitation; the initial rhythm was ventricular fibrillation managed by defibrillation. Laboratory parameters were unremarkable. Blood samples sent for toxicological evaluation were positive for kratom and caffeine. Echocardiographic examination, coronary computed tomography angiography, and cardiac magnetic resonance imaging did not prove the cause. Genetic testing did not find a pathogenic gene variant associated with familial ventricular fibrillation, but a variant of unknown significance was found in MYOM1. Given this situation, we implanted an implantable cardioverter-defibrillator (ICD) from the secondary prevention of sudden cardiac death (SCD) according to the guidelines of the European Society of Cardiology (ESC). No recurrence of ventricular arrhythmia has been reported by ambulatory ICD memory checks on our patient.
    UNASSIGNED: In some country, kratom is freely available and sold as a plant, not a drug. Only incident cases of ventricular fibrillation after kratom use are described in the literature. There is insufficient scientific evidence linking kratom to ventricular fibrillation. This is an absolutely crucial case report of this type, which has not yet been published in similar circumstances in the world. Therefore, the development of ventricular fibrillation was assumed to be due to a combination of kratom, caffeine, and exercise. The safety profile and effects of kratom should be the subject of future research. We would like to stress the importance of reporting further case series for more scientific evidence and thus increasing the pressure for stricter availability and regulation of kratom in some countries, especially where it is over-the-counter.
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  • 文章类型: Case Reports
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  • 文章类型: Case Reports
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  • 文章类型: Journal Article
    2017年HRS关于导线管理和提取的专家共识文件并未表示优先提取或放弃升级后功能失调或多余的起搏或除颤器导线(进一步称为冗余导线)1。然而,目前还没有随机甚至非随机试验显示,拔牙后的患者结局更好.目前,许多有经验的中心建议患者在多年放弃后移除多余的导线,以防止更复杂的程序。但是根据文献,并非所有废弃的引线都需要提取,因为超过90%的引线将得到顺利的跟进。由于立即拔除多余导线的风险很小但很大,因此与将来有导线并发症的患者相比,这将在人群水平上产生更多的不良事件。即使当时考虑到更高的提取风险。铅的提取也仅限于专门的中心,通常需要昂贵的工具,相反,放弃引线可以由任何有经验的设备专家安全地执行,而无需额外费用。
    The 2017 HRS expert consensus paper on lead management and extraction did not express a preference for either extracting or abandoning pacing or defibrillator leads that are dysfunctional or superfluous after an upgrade (further referred to as redundant leads) 1. However, there are no randomized or even non-randomized trials that show a better patient outcome with extraction. Many experienced centers currently advise patients to have redundant leads removed to prevent more complicated procedures after years of abandonment. But according to the literature not all abandoned leads need to be extracted as more than 90% will have an uneventful follow-up. As immediate extraction of redundant leads has a small but significant risk this will generate more adverse events at population level than when extraction is limited to the patients with future lead complications, even considering a higher extraction risk at that time. Lead extraction is also limited to specialized centers and often necessitates expensive tools, in contrast to abandoning leads which can be safely performed by any experienced device specialist without additional cost.
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  • 文章类型: Journal Article
    本综述的目的是确定ICD患者中常见的情绪问题,并建议简短的心理筛查器对于早期发现和监测患者护理至关重要。
    回顾了可靠有效的心理评估工具,包括专门为ICD患者人群设计的那些。
    心理评估,结合心脏病护理标准,可以帮助克服与不良的植入式心脏复律除颤器(ICD)管理和相关心血管结局相关的许多障碍。ICD患者情绪问题的早期识别和治疗已被证明可以改善生活质量(QOL)和患者预后。此时,然而,后勤挑战和时间限制,除了了解适当的治疗计划或转诊方案外,仍然是提供一体化的核心障碍,以病人为中心的护理。最终,所有心脏病学诊所都将受益于一个协作护理团队,该团队包括一名心理健康顾问或内部心理学家,他们可以提供咨询或转诊服务.此外,所有到诊所就诊的患者都应完成主动筛查措施,作为常规护理的组成部分,以评估是否存在情绪问题,从而改善患者预后并帮助制定治疗计划.
    UNASSIGNED: The aim of this review is to identify common mood concerns in ICD patients and suggest brief psychological screeners essential for early detection and monitoring in patient care.
    UNASSIGNED: Reliable and valid psychological assessment tools are reviewed, including those specifically designed for ICD patient populations.
    UNASSIGNED: Psychological assessment, in combination with cardiologic standard of care, can help overcome many barriers associated with poor implantable cardioverter-defibrillator (ICD) management and related cardiovascular outcomes. Earlier identification and treatment of mood concerns in ICD patients has been shown to improve quality of life (QOL) and patient outcomes. At this time, however, logistical challenges and time restraints, in addition to knowledge of appropriate treatment plans or referral options, remain central barriers to providing integrated, patient-centered care. Ultimately, all cardiology clinics would benefit from a collaborative care team that includes a mental health consultant or in-house psychologists who can provide consultations or referral services. Additionally, all patients that come to the clinics should complete proactive screening measures as routine component of care to assess the presence of mood concerns to improve patient outcomes and aid in treatment planning.
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  • 文章类型: Comparative Study
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  • 文章类型: Journal Article
    先前的研究未能对符合二次植入心脏复律除颤器(ICD)植入条件的心力衰竭(HF)患者进行风险分层。我们旨在评估使用常规可用的临床数据进行基于机器学习的表型分析是否可以识别特征和预后不同的亚组。
    共包括389例植入ICD的慢性HF患者,并收集了44个基线变量.使用基于混合数据因子分析(FAMD)的分层k均值聚类进行现象映射。通过比较表型群体中首次适当休克和全因死亡的基线特征和结果,验证了表型定位的实用性。
    在中位随访2.7年的设备询问和5.1年的生存状态,142(36.5%)首次适当电击和113(29.0%)全因死亡。使用FAMD提取的前12个主成分,解释了总变异性的60.5%,被留下来进行表型分析。确定了三个相互排斥的表型群。表型组1包括年龄最大的缺血性心肌病患者;糖尿病比例最高,高血压,和高脂血症;在表型群中具有最有利的心脏结构和功能。Phenogroup2包括最年轻的患者,大多数是非缺血性心肌病患者,具有中等心脏尺寸和功能的人,和最少的合并症。表型群3具有最差的HF进展。Kaplan-Meier曲线显示,在表型组之间,第一次适当的休克(p=0.002)和全因死亡(p<0.001)存在显着差异。在Cox回归中调整药物后,与表型组1相比,表型组2和3显示了适当休克风险的分级增加(风险比[HR]1.54,95%置信区间[CI]1.03-2.28,p=0.033;HR2.21,95%CI1.42-3.43,p<0.001;趋势<0.001)。关于死亡风险,表型组3与风险增加相关(HR2.25,95%CI1.45-3.49,p<0.001)。相比之下,表型群2具有与表型群1相当的风险(p=0.124)。
    基于机器学习的表型分析可以识别临床异质性HF患者采用二级预防性ICD治疗的不同表型亚组。这种新策略可能有助于这些患者的个性化医疗。
    UNASSIGNED: Previous studies have failed to implement risk stratification in patients with heart failure (HF) who are eligible for secondary implantable cardioverter-defibrillator (ICD) implantation. We aimed to evaluate whether machine learning-based phenomapping using routinely available clinical data can identify subgroups that differ in characteristics and prognoses.
    UNASSIGNED: A total of 389 patients with chronic HF implanted with an ICD were included, and forty-four baseline variables were collected. Phenomapping was performed using hierarchical k-means clustering based on factor analysis of mixed data (FAMD). The utility of phenomapping was validated by comparing the baseline features and outcomes of the first appropriate shock and all-cause death among the phenogroups.
    UNASSIGNED: During a median follow-up of 2.7 years for device interrogation and 5.1 years for survival status, 142 (36.5%) first appropriate shocks and 113 (29.0%) all-cause deaths occurred. The first 12 principal components extracted using the FAMD, explaining 60.5% of the total variability, were left for phenomapping. Three mutually exclusive phenogroups were identified. Phenogroup 1 comprised the oldest patients with ischemic cardiomyopathy; had the highest proportion of diabetes mellitus, hypertension, and hyperlipidemia; and had the most favorable cardiac structure and function among the phenogroups. Phenogroup 2 included the youngest patients, mostly those with non-ischemic cardiomyopathy, who had intermediate heart dimensions and function, and the fewest comorbidities. Phenogroup 3 had the worst HF progression. Kaplan-Meier curves revealed significant differences in the first appropriate shock (p = 0.002) and all-cause death (p < 0.001) across the phenogroups. After adjusting for medications in Cox regression, phenogroups 2 and 3 displayed a graded increase in appropriate shock risk (hazard ratio [HR] 1.54, 95% confidence interval [CI] 1.03-2.28, p = 0.033; HR 2.21, 95% CI 1.42-3.43, p < 0.001, respectively; p for trend < 0.001) compared to phenogroup 1. Regarding mortality risk, phenogroup 3 was associated with an increased risk (HR 2.25, 95% CI 1.45-3.49, p < 0.001). In contrast, phenogroup 2 had a risk (p = 0.124) comparable with phenogroup 1.
    UNASSIGNED: Machine-learning-based phenomapping can identify distinct phenotype subgroups in patients with clinically heterogeneous HF with secondary prophylactic ICD therapy. This novel strategy may aid personalized medicine for these patients.
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  • 文章类型: Journal Article
    开发了一种可植入的心脏复律除颤器(ICD),以防止心脏猝死。尽管能有效终止室性心律失常,随着时间的推移,传统的经静脉ICD在血管通路的需要和循环系统内异物的存在(即导线故障和感染)方面似乎存在一定的局限性.开发了一种皮下植入式心脏复律除颤器(S-ICD),以克服这些局限性,并预防心血管系统外部的心源性猝死。这种现代治疗方法的应用在世界范围内不断增加,新的中心将该系统的植入纳入其投资组合。这篇综述旨在介绍与S-ICD植入手术相关的最相关问题。基于作者的经验和广泛的文献检索。
    An implantable cardioverter-defibrillator (ICD) was developed to provide protection against sudden cardiac death. Despite being effective in terminating ventricular arrhythmias, traditional transvenous ICDs appeared over time to have certain limitations related to the need for vascular access and the presence of foreign material inside the circulatory system (namely lead failure and infections). A subcutaneous implantable cardioverter-defibrillator (S-ICD) was developed to overcome those limitations and to provide prevention against sudden cardiac death from outside the cardiovascular system. Utilization of that modern method of treatment is constantly increasing worldwide, and new centers incorporate implantation of that system in their portfolio. This review aims to present the most relevant issues related to S-ICD implantation procedure, based on experience of the authors and an extensive literature search.
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  • 文章类型: Journal Article
    本研究旨在评估心力衰竭和射血分数降低(HFrEF)患者对指南指导的最佳药物治疗(OMT)的依从性及其与早期植入式心脏复律除颤器(ICD)激活的相关性。
    收集并分析了2011年至2017年进行ICD植入以进行一级预防的307例患者的回顾性数据。
    在研究参与者中,只有23.8%的人在ICD植入前接受了最大耐受剂量的OMT,59.0%接受所有三个OMT药物组。缺血性心肌病(ICM)与非缺血性扩张型心肌病(DCM)患者的OMT依从性无明显差异。然而,DCM患者在诊断时接受ICD的频率高于ICM患者(13.8%vs.0.7%)。早期ICD激活(3个月内)仅发生在一名未接受适当OMT的患者中。占所有ICM患者的0.7%。此外,在接受OMT的患者中,早期激活也很少发生(2.9%的ICM患者和2.6%的DCM患者).超声心动图随访数据显示,在ICD植入前未接受OMT的ICM患者中有20.4%和29.8%的DCM患者显示左心室射血分数(EF)改善至35%或更多。
    本研究发现HFrEF患者在ICD植入前对OMT的依从性欠佳。结果显示早期ICD激活在所有患者组中都是罕见的,特别是那些没有收到规定的3个月的OMT。需要更多的研究来调查更长的等待时间,以评估潜在的EF改善,并更好地评估HFrEF患者ICD的资格。目前的发现对临床实践和患者预后有潜在的影响。
    UNASSIGNED: This study was conducted to evaluate compliance with guideline-directed optimal medical therapy (OMT) and its association with early implantable cardioverter-defibrillator (ICD) activation in patients with heart failure and reduced ejection fraction (HFrEF).
    UNASSIGNED: Retrospective data from 307 patients who underwent ICD implantation for primary prevention from 2011 to 2017 were collected and analyzed.
    UNASSIGNED: Among the study participants, only 23.8% received the maximum tolerated dose of OMT prior to ICD implantation, with 59.0% receiving all three OMT medication groups. No significant difference in OMT compliance was found between patients with ischemic cardiomyopathy (ICM) and those with non-ischemic dilated cardiomyopathy (DCM). However, DCM patients received ICDs more frequently at the time of diagnosis than ICM patients (13.8% vs. 0.7%). Early ICD activation (within 3 months) occurred in only one patient who had not received appropriate OMT, representing 0.7% of all ICM patients. Furthermore, early activation was also infrequent in patients who received OMT (2.9% of ICM patients and 2.6% of DCM patients). Echocardiography follow-up data revealed that 20.4% of ICM patients and 29.8% of DCM patients who did not receive OMT before ICD implantation showed improvement in the left ventricular ejection fraction (EF) to 35% or more.
    UNASSIGNED: This study found suboptimal compliance with OMT prior to ICD implantation in HFrEF patients. The results showed that early ICD activation was rare in all patient groups, especially those who did not receive the prescribed 3 months of OMT. More research is needed to investigate longer waiting periods for the evaluation of potential EF improvement, and to better evaluate the eligibility of HFrEF patients for ICD. The current findings have potential implications for clinical practice and patient outcomes.
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  • 文章类型: Journal Article
    植入式心脏装置是治疗心动过速/缓慢心律失常和心力衰竭并伴有传导疾病的重要治疗选择。近年来,这些设备变得越来越复杂,具有较高的植入成功率和寿命。然而,这些设备并非没有风险和并发症,这需要在植入前仔细考虑。在一个快速发展的心脏设备治疗的时代,这篇综述文章将提供最新的文献,并概述一些旨在最大限度地提高可植入装置效率和减少并发症的新兴技术。我们讨论新的起搏技术,包括抗心动过缓和双心室起搏的替代起搏部位,以及围绕无引线设备技术和可植入设备治疗的患者选择的最新证据。
    Implantable cardiac devices are a vital treatment option in the management of tachy/brady-arrhythmias and heart failure with conduction disease. In the recent years, these devices have become increasingly sophisticated, with high implantation success rates and longevity. However, these devices are not without risks and complications, which need to be carefully considered before implantation. In an era of rapidly evolving cardiac device therapies, this review article will provide an update on the literature and outline some of the emerging technologies that aim to maximise the efficiency of implantable devices and reduce complications. We discuss novel pacing techniques, including alternative pacing sites in anti-bradycardia and biventricular pacing, as well as the latest evidence surrounding leadless device technologies and patient selection for implantable device therapies.
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