首页> 美国卫生研究院文献>Europace >European Heart Rhythm Association (EHRA) international consensus document on how to prevent diagnose and treat cardiac implantable electronic device infections—endorsed by the Heart Rhythm Society (HRS) the Asia Pacific Heart Rhythm Society (APHRS) the Latin American Heart Rhythm Society (LAHRS) International Society for Cardiovascular Infectious Diseases (ISCVID) and the European Society of Clinical Microbiology and Infectious Diseases (ESCMID) in collaboration with the European Association for Cardio-Thoracic Surgery (EACTS)
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European Heart Rhythm Association (EHRA) international consensus document on how to prevent diagnose and treat cardiac implantable electronic device infections—endorsed by the Heart Rhythm Society (HRS) the Asia Pacific Heart Rhythm Society (APHRS) the Latin American Heart Rhythm Society (LAHRS) International Society for Cardiovascular Infectious Diseases (ISCVID) and the European Society of Clinical Microbiology and Infectious Diseases (ESCMID) in collaboration with the European Association for Cardio-Thoracic Surgery (EACTS)

机译:欧洲心律协会(EHRA)关于如何预防诊断和治疗心脏植入式电子设备感染的国际共识文件得到了心律协会(HRS)亚太心律协会(APHRS)和拉丁美洲心律的认可协会(LAHRS)国际心血管传染病学会(ISCVID)和欧洲临床微生物学和传染病学会(ESCMID)与欧洲心胸外科协会(EACTS)合作

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摘要

Pacemakers, implantable cardiac defibrillators, and cardiac resynchronization therapy devices are potentially life-saving treatments for a number of cardiac conditions, but are not without risk. Most concerning is the risk of a cardiac implantable electronic device (CIED) infection, which is associated with significant morbidity, increased hospitalizations, reduced survival, and increased healthcare costs. Recommended preventive strategies such as administration of intravenous antibiotics before implantation are well recognized. Uncertainties have remained about the role of various preventive, diagnostic, and treatment measures such as skin antiseptics, pocket antibiotic solutions, anti-bacterial envelopes, prolonged antibiotics post-implantation, and others. Guidance on whether to use novel device alternatives expected to be less prone to infections and novel oral anticoagulants is also limited, as are definitions on minimum quality requirements for centres and operators and volumes. Moreover, an international consensus document on management of CIED infections is lacking. The recognition of these issues, the dissemination of results from important randomized trials focusing on prevention of CIED infections, and observed divergences in managing device-related infections as found in an European Heart Rhythm Association worldwide survey, provided a strong incentive for a 2019 International State-of-the-art Consensus document on risk assessment, prevention, diagnosis, and treatment of CIED infections.
机译:起搏器,植入式心脏除颤器和心脏再同步治疗设备可能会挽救许多心脏疾病的生命,但并非没有风险。最令人担忧的是心脏植入式电子设备(CIED)感染的风险,这与明显的发病率,住院增加,生存减少和医疗费用增加有关。推荐的预防策略,如在植入前静脉注射抗生素,已广为人知。各种预防,诊断和治疗措施的作用仍然不确定,例如皮肤防腐剂,袋装抗生素溶液,抗菌包膜,植入后长时间使用抗生素等。关于是否使用不那么容易感染的新型设备替代品和新型口服抗凝剂的指导也受到了限制,对中心和操作员的最低质量要求的定义和数量也受到限制。而且,缺乏关于CIED感染管理的国际共识文件。对这些问题的认识,对重点在于预防CIED感染的重要随机试验的结果传播以及在欧洲心律协会全球调查中观察到的与设备相关的感染管理上的差异,为2019年国际会议提供了强大动力有关CIED感染的风险评估,预防,诊断和治疗的最新共识文件。

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