RESUMO
BACKGROUND: Computed tomography aortic valve calcium (AVC) score has accepted value for diagnosing and predicting outcomes in aortic stenosis (AS). Multi-energy CT (MECT) allows virtual non-contrast (VNC) reconstructions from contrast scans. We aim to compare the VNC-AVC score to the true non-contrast (TNC)-AVC score for assessing AS severity. METHODS: We prospectively included patients undergoing a MECT for transcatheter aortic valve replacement (TAVR) planning. TNC-AVC was acquired before contrast, and VNC-AVC was derived from a retrospectively gated contrast-enhanced scan. The Agatston scoring method was used for quantification, and linear regression analysis to derive adjusted-VNC values. RESULTS: Among 109 patients (55% female) included, 43% had concordant severe and 14% concordant moderate AS. TNC scan median dose-length product was 116 âmGy∗cm. The median TNC-AVC was 2,107 AU (1,093-3,372), while VNC-AVC was 1,835 AU (1293-2,972) after applying the coefficient (1.46) and constant (743) terms. A strong correlation was demonstrated between methods (r â= â0.93; p â< â0.001). Using accepted thresholds (>1,300 AU for women and >2,000 AU for men), 65% (n â= â71) of patients had severe AS by TNC-AVC and 67% (n â= â73) by adjusted-VNC-AVC. After estimating thresholds for adjusted-VNC (>1,564 AU for women and >2,375 AU for men), 56% (n â= â61) had severe AS, demonstrating substantial agreement with TNC-AVC (κ â= â0.77). CONCLUSIONS: MECT-derived VNC-AVC showed a strong correlation with TNC-AVC. After adjustment, VNC-AVC demonstrated substantial agreement with TNC-AVC, potentially eliminating the requirement for an additional scan and enabling reductions in both radiation exposure and acquisition time.
Assuntos
Estenose da Valva Aórtica , Tomografia Computadorizada por Raios X , Masculino , Humanos , Feminino , Estudos Retrospectivos , Valor Preditivo dos Testes , Tomografia Computadorizada por Raios X/métodos , Estenose da Valva Aórtica/diagnóstico por imagem , Estenose da Valva Aórtica/cirurgia , Valva Aórtica/diagnóstico por imagem , Valva Aórtica/cirurgia , Constrição Patológica , CálcioRESUMO
Infiltrative cardiomyopathies comprise a broad spectrum of inherited or acquired conditions caused by deposition of abnormal substances within the myocardium. Increased wall thickness, inflammation, microvascular dysfunction, and fibrosis are the common pathological processes that lead to abnormal myocardial filling, chamber dilation, and disruption of conduction system. Advanced disease presents as heart failure and cardiac arrhythmias conferring poor prognosis. Infiltrative cardiomyopathies are often diagnosed late or misclassified as other more common conditions, such as hypertrophic cardiomyopathy, hypertensive heart disease, ischemic or other forms of nonischemic cardiomyopathies. Accurate diagnosis is also critical because clinical features, testing methodologies, and approach to treatment vary significantly even within the different types of infiltrative cardiomyopathies on the basis of the type of substance deposited. Substantial advances in noninvasive cardiac imaging have enabled accurate and early diagnosis. thereby eliminating the need for endomyocardial biopsy in most cases. This scientific statement discusses the role of contemporary multimodality imaging of infiltrative cardiomyopathies, including echocardiography, nuclear and cardiac magnetic resonance imaging in the diagnosis, prognostication, and assessment of response to treatment.
Assuntos
Cardiomiopatias , Insuficiência Cardíaca , Humanos , American Heart Association , Cardiomiopatias/diagnóstico por imagem , Cardiomiopatias/patologia , Coração , Miocárdio/patologia , Imageamento por Ressonância MagnéticaAssuntos
Cardiomiopatias/diagnóstico , Cistos/diagnóstico , Adulto , Cardiomiopatias/diagnóstico por imagem , Cardiomiopatias/patologia , Cistos/diagnóstico por imagem , Cistos/patologia , Ecocardiografia , Epitélio/diagnóstico por imagem , Epitélio/patologia , Feminino , Humanos , Miocárdio/patologia , Tomografia Computadorizada por Raios XAssuntos
Cardiopatias/diagnóstico por imagem , Septos Cardíacos/diagnóstico por imagem , Septos Cardíacos/patologia , Insuficiência da Valva Mitral/diagnóstico por imagem , Varizes/diagnóstico por imagem , Idoso , Procedimentos Cirúrgicos Cardíacos/métodos , Dispneia/diagnóstico , Dispneia/etiologia , Ecocardiografia Transesofagiana/métodos , Seguimentos , Átrios do Coração , Cardiopatias/cirurgia , Septos Cardíacos/cirurgia , Implante de Prótese de Valva Cardíaca/métodos , Humanos , Masculino , Insuficiência da Valva Mitral/cirurgia , Doenças Raras , Medição de Risco , Resultado do Tratamento , Varizes/patologia , Varizes/cirurgiaRESUMO
Bicuspid aortic valve (BAV) is the most common form of congenital heart disease, with 20% of asymptomatic adults with BAV presenting with significant valve insufficiency. Yet, limited data exist regarding surgical indications and outcomes when BAV is accompanied by left ventricular dilation, systolic dysfunction, or left ventricle non-compaction (LVNC) syndrome. We present a case of dilated cardiomyopathy due to severe BAV regurgitation and partial LVNC syndrome and the decision to undergo aortic valve replacement. Our patient represents the most extreme documented case of regurgitant BAV with dilated, dysfunctional, and partially non-compacted left ventricle. Yet, surgical intervention provided improvement in systolic performance and ventricular dimensions.
Assuntos
Insuficiência da Valva Aórtica/diagnóstico por imagem , Valva Aórtica/anormalidades , Doenças das Valvas Cardíacas/diagnóstico por imagem , Implante de Prótese de Valva Cardíaca , Adulto , Valva Aórtica/diagnóstico por imagem , Valva Aórtica/fisiopatologia , Valva Aórtica/cirurgia , Insuficiência da Valva Aórtica/fisiopatologia , Insuficiência da Valva Aórtica/cirurgia , Doença da Válvula Aórtica Bicúspide , Doenças das Valvas Cardíacas/fisiopatologia , Doenças das Valvas Cardíacas/cirurgia , Próteses Valvulares Cardíacas , Ventrículos do Coração/diagnóstico por imagem , Ventrículos do Coração/fisiopatologia , Ventrículos do Coração/cirurgia , Humanos , Masculino , Sístole , Resultado do Tratamento , Função Ventricular EsquerdaRESUMO
Asymptomatic carotid artery disease is relatively common and poses a challenge for internists as well as vascular specialists when deciding whether to pursue surgical endarterectomy, percutaneous stenting, or medical therapy alone. The authors review the management of asymptomatic carotid disease, reflecting the most current data.