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1.
Ann Pharmacother ; : 10600280221077158, 2022 Feb 15.
Artigo em Inglês | MEDLINE | ID: mdl-35168381

RESUMO

BACKGROUND: Recent guidelines suggest that, for venous thromboembolism (VTE), standard doses of apixaban are appropriate in patients with body mass index (BMI) >40 kg/m2 or >120 kg. Atrial fibrillation (AF) is excluded from this recommendation. OBJECTIVE: The goals of our study were to measure and describe anti-Xa levels of patients with a BMI ≥40 kg/m2 and/or a weight ≥120 kg with a clinical indication of AF or VTE who were treated with apixaban, and to determine whether BMI or weight are associated with anti-Xa levels in this population. METHODS: We conducted an observational cohort study at a single health care system in Oregon, USA. Patients meeting enrollment criteria were recruited and had peak and trough apixaban anti-Xa levels drawn. RESULTS: Of 55 patients enrolled, 5 (9%) had peak anti-Xa levels below the reference range and 3 (6%) had trough anti-Xa levels below the reference range. BMI did not significantly correlate with peak or trough anti-Xa levels (r = -0.10, p = 0.45 and r = -0.14, p = 0.31). Weight had a moderate, negative correlation with peak anti-Xa levels (r = -0.42, p = 0.002) and a weak, negative correlation with trough anti-Xa levels (r = -0.32, p = 0.02). CONCLUSIONS AND RELEVANCE: This study provides evidence that anti-Xa levels among obese patients are not substantially different from patients with nomral BMI and weight. This supports recent ISTH guidance for standard dosing of apixaban for VTE patients with BMI >40 kg/m2 or weight >120 kg and provides additional evidence that the standard dosing may also be appropriate in patients with AF.

2.
Int Semin Surg Oncol ; 4: 14, 2007 Jun 29.
Artigo em Inglês | MEDLINE | ID: mdl-17603895

RESUMO

BACKGROUND: We report a case of pulmonary sarcoma which is a rare cause of the common symptom of dyspnea. CASE PRESENTATION: A fifty-one year old previously healthy male presented to the emergency room with complaints of dyspnea on exertion. A cardiac workup including an exercise stress test was negative but an echocardiography showed pulmonary stenosis. Cardiac MRI showed a large mass extending from the pulmonic valve to both the right and left pulmonary arteries suggestive of sarcoma. A complete resection and repair of the pulmonary artery was done and adjuvant chemotherapy with doxorubicin and ifosfamide was recommended. The patient is currently disease free after eighteen months. CONCLUSION: Pulmonary artery sarcomas are a difficult diagnosis. The diagnosis may remain elusive for some time until the proper imaging techniques are utilized to make a diagnosis. Earlier and accurate diagnosis may lead to earlier interventions and improve survival.

3.
PLoS One ; 9(9): e104844, 2014.
Artigo em Inglês | MEDLINE | ID: mdl-25251403

RESUMO

AIMS: Cardiovascular magnetic resonance (MR) provides non-invasive assessment of early (24-hour) edema and injury following pulmonary vein isolation (by ablation) and subsequent scar formation. We hypothesize that 24-hours after ablation, cardiovascular MR would demonstrate a pattern of edema and injury due to ablation and the severity would correlate with subsequent scar. METHODS: Fifteen atrial fibrillation patients underwent cardiovascular MR prior to pulmonary vein isolation, 24-hours post (N = 11) and 30-days post (N = 7) ablation, with T2-weighted (T2W) and late gadolinium enhancement (LGE) imaging. Left atrial wall thickness, edema enhancement ratio and LGE enhancement were assessed at each time point. Volumes of LGE and edema enhancement were measured, and the circumferential presence of injury was assessed at 24-hours, including comparison with LGE enhancement at 30 days. RESULTS: Left atrial wall thickness was increased 24-hours post-ablation (10.7 ± 4.1 mm vs. 7.0 ± 1.8 mm pre-PVI, p<0.05). T2W enhancement at 24-hours showed increased edema enhancement ratio (1.5 ± 0.4 for post-ablation, vs. 0.9 ± 0.2 pre-ablation, p < 0.001). Edema and LGE volumes at 24-hours were correlated with 30-day LGE volume (R = 0.76, p = 0.04, and R = 0.74, p = 0.09, respectively). Using a 16 segment model for assessment, 24-hour T2W had sensitivity, specificity, and accuracy of 82%, 63%, and 79% respectively, for predicting 30-day LGE. 24-hour LGE had sensitivity, specificity, and accuracy of 91%, 47%, and 84%. CONCLUSIONS: Increased left atrial wall thickening and edema were characterized on cardiovascular MR early post-ablation, and found to correlate with 30-day LGE scar.


Assuntos
Fibrilação Atrial/terapia , Ablação por Cateter/métodos , Cicatriz/diagnóstico , Imageamento por Ressonância Magnética/métodos , Veias Pulmonares/patologia , Adulto , Sistema Cardiovascular/diagnóstico por imagem , Sistema Cardiovascular/patologia , Ablação por Cateter/efeitos adversos , Cicatriz/diagnóstico por imagem , Cicatriz/etiologia , Meios de Contraste , Edema/diagnóstico , Edema/diagnóstico por imagem , Edema/etiologia , Feminino , Gadolínio DTPA , Humanos , Aumento da Imagem/métodos , Modelos Lineares , Masculino , Pessoa de Meia-Idade , Estudos Prospectivos , Veias Pulmonares/diagnóstico por imagem , Radiografia , Reprodutibilidade dos Testes , Sensibilidade e Especificidade , Fatores de Tempo
4.
Circ Arrhythm Electrophysiol ; 4(6): 851-7, 2011 Dec.
Artigo em Inglês | MEDLINE | ID: mdl-21956038

RESUMO

BACKGROUND: For patients with symptomatic New York Heart Association class III or IV, ejection fraction ≤ 35%, and QRS ≥ 130 ms, cardiac resynchronization therapy (CRT) has become an established treatment option. However, use of these implant criteria fails to result in clinical or echocardiographic improvement in 30% to 45% of CRT patients. METHODS AND RESULTS: The Predictors of Response to CRT (PROSPECT)-ECG is a substudy of the prospective observational PROSPECT trial. ECGs collected before, during, and after CRT implantation were analyzed. Primary outcomes were improvement in clinical composite score (CCS) and reduction of left ventricular end systolic volume (LVESV) of >15% after 6 months. Age, sex, cause of cardiomyopathy, myocardial infarction location, right ventricular function, mitral regurgitation, preimplantation QRS width, preimplantation PR interval, preimplantation right ventricular-paced QRS width, preimplantation axis categories, LV-paced QRS width, postimplantation axis categories, difference between biventricular (Bi-V) pacing and preimplantation QRS width, and QRS bundle branch morphological features were analyzed univariably in logistic regression models to predict outcomes. All significant predictors (α=0.1), age, and sex were used for multivariable analyses. Cardiomyopathy cause interaction and subanalyses were also performed. In multivariable analyses, only QRS left bundle branch morphological features predicted both CCS (odds ratio [OR]=2.46, P=0.02) and LVESV (OR=2.89, P=0.048) response. The difference between Bi-V and preimplantation QRS width predicted CCS improvement (OR=0.89, P=0.04). LV-paced QRS width predicted LVESV reduction (OR=0.86, P=0.01). Specifically, an LV-paced QRS width of ≤ 200 ms was predictive of nonischemic LVESV reduction (OR=5.12, P=0.01). CONCLUSIONS: Baseline left bundle branch QRS morphological features, LV-paced QRS width, and the difference between Bi-V and preimplantation QRS width can predict positive outcomes after CRT and may represent a novel intraprocedural method to optimize coronary sinus lead placement. CLINICAL TRIAL REGISTRATION: URL: http://www.clinicaltrials.gov. Unique identifier: NCT00253357.


Assuntos
Estimulação Cardíaca Artificial , Terapia de Ressincronização Cardíaca , Eletrocardiografia , Técnicas Eletrofisiológicas Cardíacas , Insuficiência Cardíaca/diagnóstico , Insuficiência Cardíaca/terapia , Função Ventricular Esquerda , Terapia de Ressincronização Cardíaca/efeitos adversos , Europa (Continente) , Feminino , Insuficiência Cardíaca/fisiopatologia , Hong Kong , Humanos , Modelos Logísticos , Masculino , Razão de Chances , Seleção de Pacientes , Valor Preditivo dos Testes , Estudos Prospectivos , Recuperação de Função Fisiológica , Medição de Risco , Fatores de Risco , Volume Sistólico , Fatores de Tempo , Resultado do Tratamento , Estados Unidos
5.
Heart Rhythm ; 7(4): 489-96, 2010 Apr.
Artigo em Inglês | MEDLINE | ID: mdl-20122877

RESUMO

BACKGROUND: Radiofrequency (RF) ablation of the left atrium (LA) in patients with atrial fibrillation (AF) is guided by electroanatomic mapping systems. The cardiovascular magnetic resonance (CMR) late gadolinium enhancement (LGE) technique can detect scar after ablation. Direct comparisons between the locations of intended RF ablation sites and locations of scar formation in the LA have not been performed. OBJECTIVE: This study sought to develop and use a method for comparing the sites of RF application with the sites of post-procedural scar formation in the LA. METHODS: A method for rigid registration of CMR LGE images with electroanatomic mapping data (Carto data), visualization of the registered data sets, and quantification of the correlations was developed and used in 19 studies of patients with AF. The distance between the Carto points and the CMR LA surface was measured as the mean integration error. The distance between each Carto ablation and the nearest scar was measured. The gaps in sites of LGE and in Carto ablation were also assessed qualitatively, in 6 sectors of each PV. RESULTS: The custom registration method provided a mean integration error between Carto and CMR of 2.7 +/- 0.7 mm. The average distance between Carto and LGE scar was 3.6 +/- 1.3 mm. Qualitatively, 20% of sectors with sites of Carto ablation showed no evidence of LGE. CONCLUSION: There was a visual and quantitative correspondence between Carto ablation sites and LGE scar, but for 20% of Carto ablation sites there was no visible corresponding LGE.


Assuntos
Fibrilação Atrial/cirurgia , Ablação por Cateter , Cicatriz/diagnóstico por imagem , Imageamento por Ressonância Magnética , Idoso , Mapeamento Potencial de Superfície Corporal , Feminino , Gadolínio , Átrios do Coração/diagnóstico por imagem , Humanos , Masculino , Pessoa de Meia-Idade , Cintilografia , Compostos Radiofarmacêuticos
6.
Eur J Heart Fail ; 12(8): 889-92, 2010 Aug.
Artigo em Inglês | MEDLINE | ID: mdl-20494924

RESUMO

Low-flow, low-gradient aortic stenosis is a heterogeneous entity that encompasses truly severe aortic stenosis as well as mild-to-moderate aortic stenosis in which aortic valve orifice area is severely reduced primarily due to left ventricular (LV) contractile dysfunction. Under such circumstances the capacity of the LV to generate stroke-work is severely compromised. In this case report, we describe a patient with severe LV dysfunction and ventricular dyssynchrony due to right ventricular pacing who presented with decompensated heart failure in the setting of low-flow, low-gradient aortic stenosis. We discuss the management of this high-operative-risk patient, who ultimately underwent upgrading of his dual chamber pacemaker to a biventricular pacemaker with significant echocardiographic, haemodynamic, and clinical improvement.


Assuntos
Estenose da Valva Aórtica/terapia , Estimulação Cardíaca Artificial , Contração Miocárdica , Marca-Passo Artificial , Valva Aórtica/patologia , Progressão da Doença , Evolução Fatal , Insuficiência Cardíaca/patologia , Ventrículos do Coração/patologia , Humanos , Masculino , Índice de Gravidade de Doença , Disfunção Ventricular Esquerda/patologia , Obstrução do Fluxo Ventricular Externo
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