Author name: mozarb31@gmail.com

Amiloidose Cardíaca por Transtirretina

CLEOPATTRA Analisar os efeitos do tratamento com Coramitug (NNC6019-0001) em pacientes com insuficiência cardíaca devido à amiloidose ATTR. Regional: Bahia e PernambucoInvestigador Principal: Dr. Tonnison de Oliveira (BA) e Dr. Carlos Eduardo Lucena Montenegro (PE)Informações: Núcleo de Captação – (11) 94257-9076Clinical Trial: NCT07207811https://clinicaltrials.gov/study/NCT07207811?term=cleopattrA&viewType=Card&rank=1 Perfil de paciente Critérios de Inclusão: Valor de NT-proBNP > 1.000 pg/mL […]

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Posicionamento Brasileiro sobre o Uso da Multimodalidadede Imagens na Cardio-Oncologia – 2021

Brazilian Position Statement on the Use Of Multimodality Imaging in Cardio-Oncology – 2021Realização: Departamento de Imagem Cardiovascular (DIC) da Sociedade Brasileira de Cardiologia (SBC) eendossado pela Sociedad Interamericanana de Imágenes Cardiovasculares (SiSIAC) da Sociedad Interamericanade Cardiología (SIAC)Conselho de Normatizações e Diretrizes (2020-2021): Brivaldo Markman Filho, Antonio Carlos Sobral Sousa,Aurora Felice Castro Issa, Bruno Ramos Nascimento,

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Posicionamento do Departamento de Imagem Cardiovascularda Sociedade Brasileira de Cardiologia sobre o Uso do StrainMiocárdico na Rotina do Cardiologista – 2023

Position Statement on the Use of Myocardial Strain in Cardiology Routines by the BrazilianSociety of Cardiology’s Department Of Cardiovascular Imaging – 2023Realização: Departamento de Imagem Cardiovascular da Sociedade Brasileira de Cardiologia (DIC/SBC) Almeida ALC, Melo MDT, Bihan DCSL, Vieira MLC, Pena JLB, Castillo JMD, Abensur H, et al. Posicionamento do Departamento de Imagem Cardiovascular da

Posicionamento do Departamento de Imagem Cardiovascularda Sociedade Brasileira de Cardiologia sobre o Uso do StrainMiocárdico na Rotina do Cardiologista – 2023 Read More »

Cardiac Amyloidosis: Is It Truly a Hypertrophic PhenotypeCardiomyopathy?

Cardiac amyloidosis is a classic example of an infiltrativedisease whose predominant phenotype is characterized by ahypertrophic pattern of myocardial involvement.¹,² The mostrelevant studies—both those focused on the development ofdisease-modifying therapies and cohorts evaluating diagnostictools—have used increased ventricular wall thickness as akey criterion for suspecting cardiac amyloidosis.1-6 Based onthis concept, several diagnostic algorithms have proposedventricular wall

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Relative apical sparing of longitudinal strain usingtwo-dimensional speckle-tracking echocardiographyis both sensitive and specific for the diagnosis ofcardiac amyloidosis

Background The diagnosis of cardiac amyloidosis (CA) ischallenging owing to vague symptomatology and nonspecific echocardiographic findings.Objective To describe regional patterns in longitudinalstrain (LS) using two-dimensional speckle-trackingechocardiography in CA and to test the hypothesis thatregional differences would help differentiate CA fromother causes of increased left ventricular (LV) wallthickness.Methods and results 55 consecutive patients with CAwere compared

Relative apical sparing of longitudinal strain usingtwo-dimensional speckle-tracking echocardiographyis both sensitive and specific for the diagnosis ofcardiac amyloidosis Read More »

Evaluation and management of recent onsetcardiomyopathy in the current era of heartfailure therapeutics: a clinical consensusstatement of the Heart Failure Associationof the ESC

Recent-onset cardiomyopathy represents a clinically dynamic and potentially reversible clinical framework of non-ischaemiccardiomyopathy, characterized by high variability in left ventricular (LV) function and arrhythmic risk. This clinical consensusstatement provides a structured diagnostic and therapeutic approach based on two prognostic axes: the potential for LV reverse remodelling (LVRR) and the risk of sudden cardiac death (SCD).

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Non-Invasive Diagnostic Algorithm in Transthyretin CardiacAmyloidosis: Is Bone Scintigraphy Always Enough?

Technetium-99m bone scintigraphy has revolutionized the non-invasive diagnosis oftransthyretin cardiac amyloidosis (ATTR-CM) and markedly increased disease recognition.Although this technique should ideally be applied in patients with a high pre-test probability of ATTR-CM, its use in other clinical settings may reveal incidental pathologicalmyocardial uptake that prompts referral to specialized centers even in the absence of typicalred

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The Last Decade in Cardiac Amyloidosis

Cardiac amyloidosis represents a unique disease process characterized by amyloid fibril deposition within the myocardialextracellular space. Advances in multimodality cardiac imaging enable accurate diagnosis and facilitate prompt initiationof disease-modifying therapies. Furthermore, rapid advances in multimodality imaging have enriched understanding ofthe underlying pathogenesis, enhanced prognostication, and resulted in the development of imaging-based markers thatreflect the amyloid

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Long-term efficacy of tafamidis in patientswith transthyretin amyloid cardiomyopathyby National Amyloidosis Centre stage

Aims Tafamidis is an approved treatment for patients with transthyretin amyloid cardiomyopathy (ATTR-CM) basedon the 30-month Tafamidis in Transthyretin Cardiomyopathy Clinical Trial (ATTR-ACT). This post-hoc analysisevaluated outcomes in ATTR-ACT and its long-term extension study (LTE) by baseline National AmyloidosisCentre (NAC) stage. …………………………………………………………………………………………………………………………………………………Methodsand resultsPatients received either the approved dose of tafamidis 80 mg or placebo in

Long-term efficacy of tafamidis in patientswith transthyretin amyloid cardiomyopathyby National Amyloidosis Centre stage Read More »

Long-Term Durability of Acoramidis Efficacy in TransthyretinAmyloid CardiomyopathyOpen-Label Extension of the ATTRibute-CM Randomized Clinical Trial

IMPORTANCE Transthyretin amyloid cardiomyopathy (ATTR-CM) is a progressive disordercaused by destabilization of serum transthyretin (sTTR). Acoramidis, an approved therapythat achieves near-complete (90%) sTTR stabilization, demonstrated clinical benefitthrough month 30 in ATTRibute-CM, which was incremental through month 42 in theopen-label extension (OLE); however, the longer-term durability of outcomes has not beenreported.OBJECTIVE To evaluate the long-term efficacy

Long-Term Durability of Acoramidis Efficacy in TransthyretinAmyloid CardiomyopathyOpen-Label Extension of the ATTRibute-CM Randomized Clinical Trial Read More »