罕见心血管疾病和障碍临床分类:2018年更新

P. Podolec, G. Kopeć, P. Rubis, J. Stępniewski, J. Podolec, M. Komar, L. Tomkiewicz-Pajak, A. Leśniak‑Sobelga, A. Kabłak-Ziembicka, P. Matusik
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引用次数: 9

摘要

罕见病和失调是重要的临床问题。在规划这样一个异质患者群体的诊断和治疗过程时,医生有许多顾虑。这些关切不仅源于病例稀少,而且源于对罕见疾病和疾患患者管理知识方面的多重空白。在一般人口中,普遍接受的罕见疾病和失调患病率为每2 000人中有1人或更少。偶然流行和多重合并症导致无法在任何一个中心收集足够的经验。因此,合作和思想交流对罕见病患者的管理是重要的。罕见心血管疾病和障碍的分类对于扩大罕见心血管疾病和障碍领域的知识至关重要。它包括RCDD的概述,促进对患者的临床方法,并使注册表和数据库的创建更容易。我们希望最新的RCDD分类将通过对诊断和治疗进步的贡献来帮助医疗实践。它还总结了RCDD领域的科学成果。没有特定疾病的分组,很难创建诊断和治疗算法。RCDD的分类于2013年首次发表在Journal of Rare Cardiovascular Diseases (JRCD)上[1]。在阿姆斯特丹举行的2013年欧洲心脏病学会大会(www.crcd.eu/?p=2800)和国际期刊上讨论了RCDD分类,包括最近出版的《欧洲心脏杂志》[2,3]。RCDD的临床分类考虑了主要的临床症状和病理,并以共同的临床和/或解剖特征为基础。
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Clinical Classification of Rare Cardiovascular Diseases and Disorders: 2018 Update
Rare diseases and disorders constitute important clinical problems. There are many concerns among physicians while planning the diagnostic and treatment process of such a heterogenous group of patients. These concerns arise not only from the rarity of cases, but also from multiple gaps in knowledge on the management of patients with rare diseases and disorders. The commonly accepted prevalence of rare diseases and disorders is 1 per 2 000 in the general population or less. Incidental prevalence and multiplicity of comorbidities result in an inability to gather enough experience at any single centre. Thus, cooperation and the exchange of ideas is important for the management of patients with rare diseases. Classification of rare cardiovascular diseases and disorders (RCDD) is crucial for expanding knowledge in the field of RCDD. It consists of an overview of RCDD, facilitates clinical approaches to patients and makes the creation of registries and databases easier. We hope that the updated RCDD classification will aid medical practice through the contribution to progress in diagnostics and therapy. It also serves as a summary of scientific achievements in the field of RCDD. Without the grouping of specific disorders, it is very difficult to create diagnostic and therapeutic algorithms. The Classification of RCDD was published for the first time in the Journal of Rare Cardiovascular Diseases (JRCD) in 2013 [1]. RCDD classification was discussed during the 2013 European Society of Cardiology Congress held in Amsterdam (www.crcd.eu/?p=2800) and in international journals, including a recent publication of the European Heart Journal [2, 3]. Clinical classification of RCDD takes into account major clinical symptoms and pathologies and is based on common clinical and/or anatomical features.
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来源期刊
Journal of Rare Cardiovascular Diseases
Journal of Rare Cardiovascular Diseases Medicine-Cardiology and Cardiovascular Medicine
自引率
0.00%
发文量
0
审稿时长
23 weeks
期刊介绍: Journal of Rare Cardiovascular Diseases (JRCD) is an international, quarterly issued, peer-reviewed, open access, online journal that keeps cardiologists and non-cardiologists up-to-date with rare disorders of the heart and vessels. The Journal publishes fine quality review articles, original, basic and clinical sciences research papers, either positive or negative, case reports and articles on public health issues in the field of rare cardiovascular diseases and orphan cardiovascular drugs. Topics of interest include, but are not limited to the following areas: (1) rare diseases of systemic circulation (2) rare diseases of pulmonary circulation (3) rare diseases of the heart (cardiomyopathies) (4) rare congenital cardiovascular diseases (5) rare arrhythmogenic disorders (6) cardiac tumors and cardiovascular diseases in malignancy (7) cardiovascular diseases in pregnancy (8) basic science (9) quality of life
期刊最新文献
Association of fibrinogen and D‑dimer levels with severity of acute coronary syndromes Journal of Rare Cardiovascular Diseases in EuroPub database An Extremely Rare Congenital Association: Uni- cuspid Aortic Valve with Left Ventricular Noncom- paction (RCD code: III-5A.1.o) Survival analysis of time to develop cardiovascular complications and its predictors among hypertensive patients treated in the Ayder Comprehensive Specialized Hospital, Ethiopia: a retrospective cohort study (RCD code: VIII) Autoimmune hepatitis induced by bosentan in a patient with pulmonary arterial hypertension (RCD code: II‐1A.1; VIII)
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