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1.
JACC Case Rep ; 29(2): 102148, 2024 Jan 17.
Article in English | MEDLINE | ID: mdl-38264303

ABSTRACT

We report the case of a 50-year-old woman with secondary oxalosis following bowel resection resulting in restrictive cardiomyopathy and a diagnosis of cardiac amyloidosis based on the initial workup. The case documented findings by cardiac magnetic resonance imaging and technetium Tc 99m-labeled pyrophosphate scan in patients with cardiac oxalosis, which can mimic findings in cardiac amyloidosis, expanding the differential diagnosis.

2.
Cureus ; 15(9): e45341, 2023 Sep.
Article in English | MEDLINE | ID: mdl-37720134

ABSTRACT

Regular electrocardiogram (ECG) monitoring in patients with endocarditis of the aortic region is a simple yet effective approach to help evaluate for the development of aortic abscess. It is important to recognize this condition as it carries a high morbidity and mortality. We report a case of a 62-year-old Caucasian female diagnosed with methicillin-sensitive Staphylococcus aureus (MSSA) bacteremia with mitral and aortic endocarditis. Progressive PR prolongation prompted re-evaluation, ultimately finding the progression of a new aortic abscess, changing the patient's care pathway. With a standardized approach of obtaining regular ECGs in patients with aortic endocarditis, it is possible to identify the progression of aortic valve endocarditis, thereby lowering the risk of morbidity and mortality.

3.
Heart Vessels ; 37(8): 1373-1379, 2022 Aug.
Article in English | MEDLINE | ID: mdl-35178605

ABSTRACT

BACKGROUND: Worsening heart failure (WHF) is defined as persistent or worsening symptoms of heart failure that require an escalation in intravenous therapy or initiation of mechanical and ventilatory support during hospitalization. We assessed a simplified version of WHF called diuretic failure (DF), defined as an escalation of loop diuretic dosing after 48 h, and assessed its effects on mortality and rehospitalizations at 60-days. METHODS: We conducted a multicenter retrospective study between December 1, 2017 and January 1, 2020. We identified 1389 patients of which 6.4% experienced DF. RESULTS: There was a significant relationship between DF and cumulative rates of 60-day mortality and 60-day rehospitalizations (p = 0.0002 and p = 0.0214). After multivariate adjustment, DF was associated with longer hospital stay (p < 0.0001), increased rate of 60-day mortality (p = 0.026), 60-day rehospitalizations (p = 0.036), and a composite outcome of 60-day mortality and 60-day cardiac rehospitalizations (p = 0.018). CONCLUSIONS: DF has a strong relationship with adverse heart failure outcomes suggesting it is a simple yet robust prognostic indicator which can be used in real time to identify high-risk patients during hospitalization and beyond.


Subject(s)
Diuretics , Heart Failure , Acute Disease , Disease Progression , Diuretics/therapeutic use , Heart Failure/diagnosis , Hospitalization , Humans , Prognosis , Retrospective Studies
4.
J Nucl Cardiol ; 25(4): 1247-1256, 2018 08.
Article in English | MEDLINE | ID: mdl-28050864

ABSTRACT

BACKGROUND: Quantitative uptake of Technetium 99 m-pyrophosphate (TcPYP) is sensitive and specific for diagnosing transthyretin cardiac amyloidosis (ATTR). We sought to examine the association between TcPYP uptake intensity and echocardiographic measures of disease severity and clinical outcomes. METHODS AND RESULTS: A retrospective analysis was performed of 75 patients who underwent TcPYP scintigraphy. Planar images were evaluated semiquantitatively and using heart-to-contralateral lung (H/CL) ratio. The associations between H/CL ratio and echocardiographic parameters and outcomes were evaluated using linear regression and Cox models, respectively. There were 48 patients diagnosed with ATTR with mean H/CL ratio 1.58 ± 0.22 (vs 1.08 ± 0.09 if semiquantitative score = 0). The H/CL ratio was not associated with any measured echocardiographic parameter. Both semiquantitative uptake grade and H/CL ratio were associated with all-cause mortality (P = 0.009 and 0.007, respectively) and all-cause mortality or heart failure hospitalization (P = 0.001 and 0.020, respectively); however, neither were associated with outcomes when limited to patients with confirmed ATTR (P = 0.18 and 0.465, respectively). CONCLUSION: In patients with suspected ATTR, quantitative and semiquantitative uptake intensity of TcPYP is associated with all-cause mortality as well as all-cause mortality or heart failure hospitalization. However, in those with confirmed ATTR, there is no association with echocardiographic disease severity or outcomes.


Subject(s)
Amyloid Neuropathies, Familial/diagnostic imaging , Cardiomyopathies/diagnostic imaging , Echocardiography/methods , Technetium Tc 99m Pyrophosphate , Aged , Aged, 80 and over , Amyloid Neuropathies, Familial/mortality , Cardiomyopathies/mortality , Female , Heart/diagnostic imaging , Humans , Lung/diagnostic imaging , Male , Proportional Hazards Models , Retrospective Studies
5.
JACC Cardiovasc Imaging ; 11(2 Pt 1): 234-242, 2018 02.
Article in English | MEDLINE | ID: mdl-28917675

ABSTRACT

OBJECTIVES: This study sought to investigate the regional uptake of technetium 99m-pyrophosphate (TcPYP) in transthyretin cardiac amyloidosis (ATTR) and its association with mortality. BACKGROUND: TcPYP nuclear scintigraphy is a diagnostic and prognostic tool in ATTR. Echocardiography has identified a pattern of regional variation in longitudinal strain (LS) with a gradient of improved strain from base to apex in ATTR. METHODS: Consecutive patients with ATTR were evaluated who underwent TcPYP nuclear scintigraphy with planar and attenuation corrected single-photon emission computed tomography (SPECT). Heart-to-contralateral lung (H/CL) ratio was calculated on planar images, and left ventricular (LV) uptake was determined in each of the 17 segments using SPECT. A measure of apical-sparing of myocardial TcPYP uptake, termed the apical-sparing ratio (ASR), was calculated as basal + mid / apical counts. RESULTS: Overall, 54 patients with ATTR (age 78 ± 9 years, 76% male, 31% hereditary ATTR) were analyzed. There was increased TcPYP uptake in basal and mid relative to apical LV segments, and an apical-sparing LS pattern on echocardiography. The right ventricle similarly showed greater uptake in basal segments. There were 26 deaths over 1.8 years median follow-up. The ASR of TcPYP uptake was associated with age-adjusted all-cause mortality (p = 0.013) with worse prognosis seen at levels <2.75. Global LS was also prognostic (p = 0.01), whereas H/CL ratio and total LV uptake indexed to blood pool were not (p = 0.772 and p = 0.850, respectively). The prognostic utility of the ASR persisted in multivariable modeling (p = 0.003), whereas global LS did not. CONCLUSIONS: There is decreased TcPYP uptake in apical as compared to mid and basal segments in the LV, mimicking apical-sparing LS seen on echocardiography. Regional distribution of LV TcPYP uptake is associated with mortality, whereas overall amount of uptake as measured by H/CL ratio and indexed LV SPECT uptake is not.


Subject(s)
Amyloid Neuropathies, Familial/diagnostic imaging , Cardiomyopathies/diagnostic imaging , Heart Ventricles/diagnostic imaging , Radiopharmaceuticals/administration & dosage , Technetium Tc 99m Pyrophosphate/administration & dosage , Tomography, Emission-Computed, Single-Photon , Aged , Aged, 80 and over , Amyloid Neuropathies, Familial/mortality , Amyloid Neuropathies, Familial/physiopathology , Cardiomyopathies/mortality , Cardiomyopathies/physiopathology , Female , Heart Ventricles/physiopathology , Humans , Male , Predictive Value of Tests , Prognosis , Reproducibility of Results , Retrospective Studies , Ventricular Function, Left , Ventricular Function, Right
6.
J Am Coll Cardiol ; 67(25): 2941-8, 2016 06 28.
Article in English | MEDLINE | ID: mdl-27339491

ABSTRACT

BACKGROUND: Light-chain amyloidosis (AL) with cardiac involvement carries a poor prognosis; median untreated survival is <6 months. Three-drug therapy with bortezomib, dexamethasone, and an alkylating agent (BDex+AA) is associated with improved biomarker response rates in AL amyloidosis. OBJECTIVES: This study sought to evaluate the effect of BDex+AA as a first-line treatment strategy on mortality in patients with symptomatic heart failure from AL cardiac amyloidosis. METHODS: Patients newly diagnosed with symptomatic New York Heart Association (NYHA) functional class ≥II heart failure due to AL amyloidosis were retrospectively studied. Initial treatment strategy was adjudicated and propensity score analysis was used to adjust for the nonrandomized allocation of treatments. Survival was assessed using a Cox proportional hazards model after adjusting for the propensity score for receiving treatment, age, NYHA functional class, and ejection fraction. RESULTS: Among 106 treated patients (age 64.6 ± 11.3 years, 63% male, 76% lambda subtype), 40 received the 3-drug regimen and 66 received other regimens. Mortality was 65% overall, 48% in the BDex+AA cohort (median survival time 821 days), and 76% in patients who received other regimens (median survival time 223 days). Initial treatment with BDex+AA was associated with decreased mortality after multivariable adjustment (hazard ratio: 0.209; 95% confidence interval: 0.069 to 0.636; p = 0.006). This association remained after further adjustment for components of the Mayo Stage. CONCLUSIONS: Use of BDex+AA in the treatment of AL amyloidosis in patients presenting with symptomatic heart failure is associated with improved survival after adjusting for clinical variables.


Subject(s)
Alkylating Agents/therapeutic use , Amyloidosis/complications , Amyloidosis/drug therapy , Bortezomib/therapeutic use , Dexamethasone/therapeutic use , Heart Diseases/complications , Heart Diseases/drug therapy , Heart Failure/etiology , Heart Failure/mortality , Aged , Drug Therapy, Combination , Female , Heart Failure/diagnosis , Humans , Male , Middle Aged , Retrospective Studies , Survival Rate , Treatment Outcome
7.
Int J Cardiol ; 214: 477-81, 2016 Jul 01.
Article in English | MEDLINE | ID: mdl-27093686

ABSTRACT

BACKGROUND: Low voltage electrocardiography (ECG) coupled with increased ventricular wall thickness is the hallmark of cardiac amyloidosis. However, patient characteristics influencing voltage in the general population, including bundle branch block, have not been evaluated in amyloid heart disease. METHODS: A retrospective analysis was performed of patients with newly diagnosed cardiac amyloidosis from 2002 to 2014. ECG voltage was calculated using limb (sum of QRS complex in leads I, II and III) and precordial (Sokolow: S in V1 plus R in V5-V6) criteria. The associations between voltage and clinical variables were tested using multivariable linear regression. A Cox model assessed the association of voltage with mortality. RESULTS: In 389 subjects (transthyretin ATTR 186, light chain AL 203), 30% had conduction delay (QRS >120ms). In those with narrow QRS, 68% met low limb, 72% low Sokolow and 57% both criteria, with lower voltages found in AL vs ATTR. LV mass index as well as other typical factors that impact voltage (age, sex, race, hypertension, BSA, and smoking) in the general population were not associated with voltage in this cardiac amyloidosis cohort. Patients with LBBB and IVCD had similar voltages when compared to those with narrow QRS. Voltage was significantly associated with mortality (p<0.001 for both criteria) after multivariable adjustment. CONCLUSION: Classic predictors of ECG voltage in the general population are not valid in cardiac amyloidosis. In this cohort, the prevalence estimates of ventricular conduction delay and low voltage are higher than previously reported. Voltage predicts mortality after multivariable adjustment.


Subject(s)
Amyloidosis/complications , Electrocardiography/methods , Heart Diseases/diagnosis , Aged , Aged, 80 and over , Female , Heart Diseases/physiopathology , Humans , Male , Middle Aged , Proportional Hazards Models , Retrospective Studies , Risk Factors
9.
J Am Heart Assoc ; 5(3): e002877, 2016 Mar 24.
Article in English | MEDLINE | ID: mdl-27013539

ABSTRACT

BACKGROUND: Light chain (AL) and transthyretin (ATTR) amyloidosis have a similar effect on myocardial function but very different disease trajectories and survival. However, limited data are available evaluating subtype-specific predictors of outcomes in a large contemporary cohort. METHODS AND RESULTS: We retrospectively investigated 360 patients at the time of initial diagnosis of cardiac amyloidosis (191 AL and 169 ATTR) from 2002 to 2014. Clinical, laboratory, electrical, and morphologic covariates were evaluated based upon amyloid subtype. ATTR etiology was associated with older age, more chronic medical conditions, and the use of standard heart failure medical therapy. Left ventricular mass index and electrocardiographic voltage were higher in ATTR, while there was no difference in ejection fraction or markers of diastology between subtypes. A multivariable Cox model was generated using previously identified predictors of negative outcomes in cardiac amyloidosis and analyzed after stratification for subsequent amyloid-specific treatment. An AL etiology was the most predictive variable (hazard ratio 3.143, P<0.001) of 3-year all-cause mortality. The only covariate that showed a significantly greater magnitude of effect on mortality in 1 amyloid subtype versus the other was amyloid-specific treatment in AL (P=0.015). The magnitude of effect of other variables on mortality did not significantly differ between subtypes. CONCLUSIONS: Clinical, morphological, electrical, and biomarker data do not significantly interact with amyloid subtype in its association with mortality, despite the fact that the prognosis in each subtype differs greatly. This suggests an additional factor or factors (such as light chain toxicity) contributing to poorer outcomes in AL amyloid.


Subject(s)
Amyloid Neuropathies, Familial/diagnosis , Amyloid/analysis , Amyloidosis/diagnosis , Cardiomyopathies/diagnosis , Action Potentials , Aged , Amyloid Neuropathies, Familial/classification , Amyloid Neuropathies, Familial/metabolism , Amyloid Neuropathies, Familial/mortality , Amyloid Neuropathies, Familial/physiopathology , Amyloid Neuropathies, Familial/therapy , Amyloidosis/classification , Amyloidosis/metabolism , Amyloidosis/mortality , Amyloidosis/physiopathology , Amyloidosis/therapy , Biomarkers/analysis , Biopsy , Cardiomyopathies/classification , Cardiomyopathies/metabolism , Cardiomyopathies/mortality , Cardiomyopathies/physiopathology , Cardiomyopathies/therapy , Chi-Square Distribution , Echocardiography, Doppler , Electrocardiography , Female , Heart Rate , Humans , Magnetic Resonance Imaging , Male , Middle Aged , Multivariate Analysis , Predictive Value of Tests , Prognosis , Proportional Hazards Models , Retrospective Studies , Risk Assessment , Risk Factors , Stroke Volume , Ventricular Function, Left
11.
Curr Cardiol Rep ; 17(11): 100, 2015 Nov.
Article in English | MEDLINE | ID: mdl-26374453

ABSTRACT

Amyloidosis is a disease in which proteins misfold, aggregate into fibrils, and deposit extracellularly disrupting organ architecture and function. There are two main types which affect the heart: light chain (AL) amyloidosis and transthyretin cardiac amyloidosis (ATTR). There is a misconception that cardiac amyloidosis has no effective treatment options. However, over the past decade, there has been extensive research and drug development. Outcomes are improving in AL amyloidosis with evolving chemotherapeutic regimens and novel monoclonal antibodies. In ATTR, therapies that decrease protein production, prevent dissociation, and promote clearance have the potential to slow or even halt a disease which is uniformly fatal. Selected patients may be candidates for heart and/or stem cell transplant and should be promptly referred to an experienced amyloid program. Herein, we discuss the emerging advances for the treatment of cardiac amyloidosis.


Subject(s)
Amyloidosis/therapy , Cardiomyopathies/therapy , Amyloid Neuropathies, Familial/therapy , Bortezomib/therapeutic use , Glucocorticoids/therapeutic use , Heart Transplantation , Humans , Immunoglobulin Light Chains/analysis , Stem Cell Transplantation/methods
12.
Am J Cardiol ; 111(7): 991-5, 2013 Apr 01.
Article in English | MEDLINE | ID: mdl-23340029

ABSTRACT

Obesity demonstrates a direct relation with cardiovascular risk and all-cause mortality, while cardiorespiratory fitness demonstrates an inverse relation. In clinical practice, several cardiometabolic (CM) risk factors are commonly measured to gauge cardiovascular risk, but the interaction between fitness and obesity with regard to CM risk has not been fully explored. In this study, 2,634 Brazilian adults referred for employer-sponsored heath exams were assessed. Obesity was defined as body mass index >30 kg/m(2) or waist circumference >102 cm in men or >88 cm in women when body mass index was 25 to 30 kg/m(2). Fitness was quantified by stage achieved on an Ellestad treadmill stress test, with those completing stage 4 considered fit. Hepatic steatosis was determined by ultrasound. CM risk factors were compared after stratifying patients into 4 groups: fit and normal weight, fit and obese, unfit and normal weight, and unfit and obese. Approximately 22% of patients were obese; 12% were unfit. Fitness and obesity were moderately correlated (ρ = 0.38 to 0.50). The sample included 6.5% unfit and normal-weight subjects and 16% fit and obese subjects. In overweight and obese patients, fitness was negatively associated with CM risk (p <0.01 for all values). In fit patients, increasing body mass index was positively associated with CM risk (p <0.01 for all values). In instances of discordance between fitness and obesity, obesity was the stronger determinant of CM risk. In conclusion, fitness and obesity are independently associated with CM risk. The effects of fitness and obesity are additive, but obesity is more strongly associated with CM risk when fitness and obesity are discordant. These findings underscore the need for weight loss in obese patients and suggest an unmeasured benefit of fitness.


Subject(s)
Cardiovascular Diseases/physiopathology , Obesity/physiopathology , Physical Fitness/physiology , Adult , Analysis of Variance , Biomarkers/blood , Body Mass Index , Brazil/epidemiology , Cardiovascular Diseases/mortality , Cause of Death , Chi-Square Distribution , Exercise Test , Fatty Liver/diagnostic imaging , Female , Humans , Male , Risk Factors , Statistics, Nonparametric , Ultrasonography
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