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1.
J Cardiothorac Vasc Anesth ; 33(2): 274-289, 2019 02.
Artigo em Inglês | MEDLINE | ID: mdl-30149983

RESUMO

Chronic mitral regurgitation (MR) is the most prevalent valvular lesion in the adult US population. Appropriate patient selection for mitral intervention and selection of the appropriate interventional strategy and optimal periprocedural management rely on thorough clinical evaluation, accurate echocardiographic input, and in-depth understanding of chronic MR pathophysiology on the part of the cardiac anesthesiologist. The recently published Expert Consensus Decision Pathway on the management of MR was designed to provide tools to help the clinician with broad clinical decision-making, including patient referral, and the present review focuses and elaborates on the key aspects relevant to the cardiac anesthesiologist in the peri-interventional setting.


Assuntos
Anestesiologia , Cardiologia , Consenso , Tomada de Decisões , Gerenciamento Clínico , Implante de Prótese de Valva Cardíaca/normas , Insuficiência da Valva Mitral/cirurgia , Cateterismo Cardíaco , Humanos
2.
J Am Coll Cardiol ; 75(17): 2236-2270, 2020 05 05.
Artigo em Inglês | MEDLINE | ID: mdl-32068084

RESUMO

Mitral regurgitation (MR) is a complex valve lesion that can pose significant management challenges. This expert consensus decision pathway emphasizes that recognition of MR should prompt an assessment of its etiology, mechanism, and severity, as well as consideration of the indications for treatment. The document is a focused update of the 2017 ACC Expert Consensus Decision Pathway on the Management of Mitral Regurgitation, with some sections updated and others added in light of the publication of new trial data related to secondary MR, among other developments. A structured approach to evaluation based on clinical findings, accurate echocardiographic imaging, and, when necessary, adjunctive testing can help clarify decision making. Treatment goals include timely intervention by an experienced multidisciplinary heart team to prevent left ventricular dysfunction, heart failure, reduced quality of life, and premature death.


Assuntos
Comitês Consultivos/normas , Cardiologia/normas , Consenso , Gerenciamento Clínico , Insuficiência da Valva Mitral/terapia , Relatório de Pesquisa/normas , Cateterismo Cardíaco/métodos , Cateterismo Cardíaco/normas , Cardiologia/métodos , Implante de Prótese de Valva Cardíaca/métodos , Implante de Prótese de Valva Cardíaca/normas , Humanos , Insuficiência da Valva Mitral/diagnóstico por imagem , Insuficiência da Valva Mitral/epidemiologia , Estados Unidos/epidemiologia
3.
J Am Coll Cardiol ; 76(20): 2391-2411, 2020 11 17.
Artigo em Inglês | MEDLINE | ID: mdl-33190683

RESUMO

Consensus regarding a reasonable strategy to manage cardiac conduction disturbances after transcatheter aortic valve replacement (TAVR) has been elusive. This is due to the absence of adequately powered, randomized controlled trials; the often transient nature of the conduction disturbances; evolving technologies; and the interplay of cardiology subspecialties involved. In the absence of high-quality trials, numerous practice styles have been developed, and prolonged observation, electrophysiological testing, and pre-emptive pacemaker implantation have been described. Although the 2013 European Society of Cardiology guidelines address pacing post-TAVR, they do not provide in-depth discussion of this topic. Furthermore, a summary and proposed strategy for this problem have not been published by cardiovascular societies in the United States, despite an interest in establishing best practices in TAVR, valvular heart disease, and cardiovascular implantable electrical devices. This document reviews existing data and experience regarding the management of conduction disturbances after TAVR and proposes an evidence-based expert consensus decision pathway for their management. Where evidence is lacking or insufficient, the recommendations herein are based on expert opinion.


Assuntos
Valvopatia Aórtica/cirurgia , Doença do Sistema de Condução Cardíaco/terapia , Complicações Pós-Operatórias/terapia , Substituição da Valva Aórtica Transcateter , Técnicas de Apoio para a Decisão , Humanos
9.
J Am Coll Cardiol ; 70(19): 2421-2449, 2017 Nov 07.
Artigo em Inglês | MEDLINE | ID: mdl-29055505

RESUMO

Mitral regurgitation (MR) is a complex valve lesion that can pose significant management challenges for the cardiovascular clinician. This Expert Consensus Document emphasizes that recognition of MR should prompt an assessment of its etiology, mechanism, and severity, as well as indications for treatment. A structured approach to evaluation based on clinical findings, precise echocardiographic imaging, and when necessary, adjunctive testing, can help clarify decision making. Treatment goals include timely intervention by an experienced heart team to prevent left ventricular dysfunction, heart failure, reduced quality of life, and premature death.


Assuntos
Comitês Consultivos/normas , Cardiologia/normas , Tomada de Decisão Clínica , Gerenciamento Clínico , Insuficiência da Valva Mitral/terapia , Relatório de Pesquisa/normas , Cardiologia/métodos , Tomada de Decisão Clínica/métodos , Consenso , Humanos , Estados Unidos
11.
J Am Coll Cardiol ; 70(14): 1785-1822, 2017 Oct 03.
Artigo em Inglês | MEDLINE | ID: mdl-28886926

RESUMO

In 2016, the American College of Cardiology published the first expert consensus decision pathway (ECDP) on the role of non-statin therapies for low-density lipoprotein (LDL)-cholesterol lowering in the management of atherosclerotic cardiovascular disease (ASCVD) risk. Since the publication of that document, additional evidence and perspectives have emerged from randomized clinical trials and other sources, particularly considering the longer-term efficacy and safety of proprotein convertase subtilisin/kexin 9 (PCSK9) inhibitors in secondary prevention of ASCVD. Most notably, the FOURIER (Further Cardiovascular Outcomes Research with PCSK9 Inhibition in Subjects with Elevated Risk) trial and SPIRE-1 and -2 (Studies of PCSK9 Inhibition and the Reduction of Vascular Events), assessing evolocumab and bococizumab, respectively, have published final results of cardiovascular outcomes trials in patients with clinical ASCVD and in a smaller number of high-risk primary prevention patients. In addition, further evidence on the types of patients most likely to benefit from the use of ezetimibe in addition to statin therapy after acute coronary syndrome has been published. Based on results from these important analyses, the ECDP writing committee judged that it would be desirable to provide a focused update to help guide clinicians more clearly on decision making regarding the use of ezetimibe and PCSK9 inhibitors in patients with clinical ASCVD with or without comorbidities. In the following summary table, changes from the 2016 ECDP to the 2017 ECDP Focused Update are highlighted, and a brief rationale is provided. The content of the full document has been changed accordingly, with more extensive and detailed guidance regarding decision making provided both in the text and in the updated algorithms. Revised recommendations are provided for patients with clinical ASCVD with or without comorbidities on statin therapy for secondary prevention. The ECDP writing committee judged that these new data did not warrant changes to the decision pathways and algorithms regarding the use of ezetimibe or PCSK9 inhibitors in primary prevention patients with LDL-C <190 mg/dL with or without diabetes mellitus or patients without ASCVD and LDL-C ≥190 mg/dL not due to secondary causes. Based on feedback and further deliberation, the ECDP writing committee down-graded recommendations regarding bile acid sequestrant use, recommending bile acid sequestrants only as optional secondary agents for consideration in patients intolerant to ezetimibe. For clarification, the writing committee has also included new information on diagnostic categories of heterozygous and homozygous familial hypercholesterolemia, based on clinical criteria with and without genetic testing. Other changes to the original document were kept to a minimum to provide consistent guidance to clinicians, unless there was a compelling reason or new evidence, in which case justification is provided.


Assuntos
Anticolesterolemiantes/farmacologia , Cardiologia/métodos , Doença da Artéria Coronariana/prevenção & controle , Ezetimiba/farmacologia , Hipercolesterolemia/tratamento farmacológico , Conduta do Tratamento Medicamentoso/organização & administração , Quimioprevenção/métodos , LDL-Colesterol/análise , Consenso , Inibidores Enzimáticos/farmacologia , Humanos , Hipercolesterolemia/diagnóstico , Sequestrantes/farmacologia , Estados Unidos
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