cardiorenal syndrome

心肾综合征
  • 文章类型: Review
    该临床共识声明回顾了在晚期心力衰竭患者中使用正性肌力支持。当前的指南仅支持在有器官灌注不良或休克证据的急性失代偿性心力衰竭的情况下使用肌力药。然而,在其他没有急性严重失代偿的晚期心力衰竭患者中,正性肌力支持可能是合理的。回顾了支持在这些情况下使用肌力剂的临床证据。特别是,持续充血的患者,全身灌注不足,或需要缓解的晚期心力衰竭,并讨论了与植入左心室辅助装置或心脏移植有关的具体情况。讨论了具有正性肌力作用的传统和新型药物,并回顾了在正性肌力支持过程中指导治疗的使用。最后,描述了家庭正性肌力疗法,和姑息治疗和生命终结方面的审查与持续的正性肌力支持的管理(包括指导慢性正性肌力治疗支持的维持和撤机).本文受版权保护。保留所有权利。
    This clinical consensus statement reviews the use of inotropic support in patients with advanced heart failure. The current guidelines only support use of inotropes in the setting of acute decompensated heart failure with evidence of organ malperfusion or shock. However, inotropic support may be reasonable in other patients with advanced heart failure without acute severe decompensation. The clinical evidence supporting use of inotropes in these situations is reviewed. Particularly, patients with persistent congestion, systemic hypoperfusion, or advanced heart failure with need for palliation, and specific situations relevant to implantation of left ventricular assist devices or heart transplantation are discussed. Traditional and novel drugs with inotropic effects are discussed and use of guideline-directed therapy during inotropic support is reviewed. Finally, home inotropic therapy is described, and palliative care and end-of-life aspects are reviewed in relation to management of ongoing inotropic support (including guidance for maintenance and weaning of chronic inotropic therapy support).
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  • 文章类型: Journal Article
    慢性肾脏疾病和慢性心力衰竭综合征之间的广泛重叠意味着熟悉2021年欧洲心脏病学会指南对肾病学家很重要。这两种综合征的共同危险因素以及与慢性肾脏疾病相关的不良心脏结构重塑意味着许多肾脏疾病患者呼吸困难,属于指南中分类的心力衰竭表型。心力衰竭的管理正在迅速发展,导致最新指南迭代中的重大变化。2021年指南与2016年版本相比有所变化,首先更加注重识别心力衰竭的三种表型,以指导适当的循证管理。其次,一种新的简化的心力衰竭治疗算法,降低了射血分数,包括快速序贯启动和上调4个“支柱”的药物治疗-ACE抑制剂或血管紧张素-脑啡肽抑制剂,β受体阻滞剂,盐皮质激素受体拮抗剂,多亏了令人信服的试验数据,钠-葡萄糖协同转运蛋白-2抑制剂。第三,对于非缺血性心力衰竭患者的一级预防植入式心律转复除颤器治疗和左束支传导阻滞且QRS波持续时间<150ms的心脏再同步治疗的适应症,器械治疗指南已进行了降级建议.对于与非心血管合并症(包括慢性肾脏疾病)相关的心力衰竭,有更新的治疗计划。
    The wide overlap between the syndromes of chronic kidney disease (CKD) and chronic heart failure (HF) means that familiarity with the 2021 European Society of Cardiology guidelines is of importance to nephrologists. The common risk factors for the two syndromes together with the adverse cardiac structural remodelling associated with CKD means that many kidney disease patients experience breathlessness and fall within the HF phenotypes categorized in the guidelines. The management of HF is evolving rapidly leading to significant changes in the latest guideline iteration. The 2021 guidelines have changed from the 2016 version firstly by an increased focus on identifying the three phenotypes of HF to guide appropriate evidence-based management. Secondly, a new and simplified treatment algorithm for HF with reduced ejection fraction involving the rapid sequential initiation and up-titration of four \'pillars\' of drug treatment-angiotensin-converting enzyme inhibitors or angiotensin-neprilysin inhibitors, beta blockers, mineralocorticoid receptor antagonists and now, thanks to convincing trial data, sodium-glucose co-transporter 2 inhibitors. Thirdly, guidelines for device therapy have been changed with down-graded advice on indications for primary prevention implantable cardioverter defibrillator therapy for patients with non-ischaemic HF and for cardiac resynchronization therapy with left bundle branch block (LBBB) and a QRS duration <150 ms. There are updated treatment plans for HF associated with non-cardiovascular comorbidities including CKD.
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  • 文章类型: Journal Article
    即使使用严格的方法,共识会议的报告的价值通常也低于临床试验的报告。然而,有限的数据比较了这两种塑造临床实践方法的影响.
    比较共识会议和临床试验的出版影响。
    根据主题确定并分类了2002年至2017年急性疾病质量倡议(ADQI)的共识出版物。随机试验在同一发表年份和期刊上确定,从最高的影响因子开始。两种出版物类型都匹配,并使用谷歌学者确定每个人的总引用次数。二次分析比较了每种出版物类型的总成本。
    确定了17份ADQI共识会议报告和17项随机试验。ADQI报告收到的每篇论文引用次数相似(中位数,四分位数范围)与随机试验(132,54-228;vs.159,60-340,p=ns)。同样,10例(58.8%)ADQI报告和10例随机试验被引用>100次。平均而言,与临床试验相比,ADQI报告出现在影响因子较低的期刊上(5.4±4.6vs.25.4±27.1;p<0.01)。ADQI报告的每次引用成本中位数(2017年美元)为606.01美元,而这一数字几乎是这个数字的两倍。1,182.59美元,用于相同主题的临床试验(p=0.09)。尽管发表在影响因子较低的期刊上,关于重症监护肾脏病学主题的共识报告,收到了与同年发表的随机对照试验相似的引用.
    Reports of consensus conferences are usually valued less than reports of clinical trials even when rigorous methodology is used. However, limited data are available comparing the impact of these 2 methods of shaping clinical practice.
    Compare the publication impact of consensus conferences and clinical trials.
    Consensus publications from the Acute Disease Quality Initiative (ADQI) from 2002 through 2017 were identified and classified by subject matter. Randomized trials were identified in the same publication year and subject in journals, starting with the highest impact factor. Both publication types were matched, and total citations were determined for each using Google Scholar. A secondary analysis compared total costs for each publication type.
    Seventeen ADQI consensus conference reports and 17 randomized trials were identified. ADQI reports received a similar number of citations per paper (median, interquartile range) compared to randomized trials (132, 54-228; vs. 159, 60-340, p = ns). Similarly, 10 (58.8%) ADQI reports and 10 randomized trials were cited >100 times. On average, ADQI reports appeared in journals with lower impact factors compared to clinical trials (5.4 ± 4.6 vs. 25.4 ± 27.1; p < 0.01). The median cost per citation (USD 2017) for ADQI reports was USD 606.01 compared to almost twice this figure, USD 1,182.59, for clinical trials on the same topics (p = 0.09). Despite being published in lower impact factor journals, consensus reports on topics in critical care nephrology, received similar citations to randomized controlled trials published the same year.
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