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1.
Echocardiography ; 27(8): E77-9, 2010 Sep.
Artigo em Inglês | MEDLINE | ID: mdl-20849472

RESUMO

A 78-year-old male patient was referred cardiovascular risk evaluation before elective resection of a bronchial carcinoma. A myocardial infarction with a subsequent coronary artery bypass revascularization and a mitral prosthetic valve surgery were known. Left lateral decubitus (LLD) was permanently avoided because of significant trepopnea since several years. No signs of heart failure were found in the physical examination. A mitral valve prosthesis presented normal characteristics at examination. Left ventricular dimensions and function were normal. A severe tricuspid regurgitation could be documented during examination in the LLD, with changing characteristics in dorsal decubitus, when it could be graded as moderate. Trepopnea associated with severe paroxysmal tricuspid regurgitation was never described before in the literature. Sympathetic/parasympathetic modulation of papillary muscles of the tricuspid valve can be proposed as a probable cause of this dynamic valvular dysfunction.


Assuntos
Dispneia/diagnóstico por imagem , Dispneia/etiologia , Postura , Insuficiência da Valva Tricúspide/diagnóstico por imagem , Insuficiência da Valva Tricúspide/etiologia , Idoso , Diagnóstico Diferencial , Humanos , Masculino , Ultrassonografia
2.
J Zoo Wildl Med ; 40(4): 711-25, 2009 Dec.
Artigo em Inglês | MEDLINE | ID: mdl-20063818

RESUMO

As a result of the lack of basic microscopic anatomy of the elephants' foot, this study deals with the normal microscopic morphology of both the Asian (Elephas maximus) and African (Loxodonta africana) elephant foot with consideration of pathologic changes. A total of 727 histologic samples from defined locations of 24 hooves of both species (17 Asian and seven African species) were studied, measured, and evaluated. Minor differences between the feet and species are seen histologically. Poor horn quality in captive elephants' hooves and loci of minor resistance in captive and wild animals are detected. The thickness of the weight-bearing surface of the captive elephants' hooves is histologically measured as "very thin" (about 10 mm). The normal histologic findings provide a basis for assessing histopathologic changes and especially horn quality. The histologic findings might explain some of the foot problems, but they also give rise to questions about the quality and correctness of current husbandry techniques.


Assuntos
Elefantes/anatomia & histologia , Casco e Garras/anatomia & histologia , Microscopia/veterinária , Envelhecimento , Animais , Feminino , Membro Anterior , Membro Posterior , Masculino , Pele/anatomia & histologia
3.
Annu Int Conf IEEE Eng Med Biol Soc ; 2019: 6529-6532, 2019 Jul.
Artigo em Inglês | MEDLINE | ID: mdl-31947337

RESUMO

Recent breakthroughs in computer vision offer an exciting avenue to develop new remote, and non-intrusive patient monitoring techniques. A very challenging topic to address is the automated recognition of breathing disorders during sleep. Due to its complexity, this task has rarely been explored in the literature on real patients using such marker-free approaches. Here, we propose an approach based on deep learning architectures capable of classifying breathing disorders. The classification is performed on depth maps recorded with 3D cameras from 76 patients referred to a sleep laboratory that present a range of breathing disorders. Our system is capable of classifying individual breathing events as normal or abnormal with an accuracy of 61.8%, hence our results show that computer vision and deep learning are viable tools for assessing locally or remotely breathing quality during sleep.


Assuntos
Aprendizado Profundo , Respiração , Humanos , Sono
4.
Eur J Heart Fail ; 5(1): 55-62, 2003 Jan.
Artigo em Inglês | MEDLINE | ID: mdl-12559216

RESUMO

OBJECTIVES: This prospective study was performed to analyse whether routine clinical follow-up investigations at 12+/-6 months add to risk stratification and improve survival rates in patients with a first diagnosis of dilated cardiomyopathy (DCM). METHODS: Four hundred and eighty consecutive patients (mean age 53.4+/-12.3 years, 369 males, mean NYHA class 2.4+/-0.8) with invasively confirmed DCM were included and followed for 3.9+/-3.5 years. Patients were requested to adhere to a follow up investigation within 6-18 months either at the referring physicians or at our out patient department. Two hundred and eighty-one of the 480 patients presented for follow up which consisted of a detailed evaluation of symptoms, standardized physical examination, 12-lead-electrocardiogram recording and echocardiography. Seventeen patients were lost for follow up, 182 did not seek specialized medical follow up. Patients outcome was assessed by structured telephone interviews. RESULTS: Independent predictors of death or transplantation at initial diagnosis were LV-ejection fraction <30% (P=0.0001, risk ratio 2.25), LV-end diastolic pressure >or=15 mmHg (P=0.002, risk ratio 2.0), age >or=54 years, (P=0.04, risk ratio 1.55), and presence of left bundle branch block (P=0.046, risk ratio 1.53). On follow up investigations only deterioration of clinical status by at least one NYHA-class (P=0.001, risk ratio 2.6) and new onset or worsening of mitral regurgitation (P=0.02, risk ratio 1.8), remained independent prognostic factors for cardiac death. Patients who presented for routine follow up revealed significant better 5-year survival rates (n=281, 70%) than those who did not (n=153, 55%, P=0.005). CONCLUSIONS: Routine clinical follow up investigations within 6-18 months after first diagnosis of DCM adds to risk stratification and improves survival rates.


Assuntos
Cardiomiopatia Dilatada/diagnóstico , Adulto , Idoso , Assistência Ambulatorial , Inibidores da Enzima Conversora de Angiotensina/uso terapêutico , Procedimentos Cirúrgicos Cardíacos , Cardiomiopatia Dilatada/mortalidade , Cardiomiopatia Dilatada/terapia , Método Duplo-Cego , Eletrocardiografia , Saúde da Família , Feminino , Seguimentos , Alemanha , Humanos , Masculino , Pessoa de Meia-Idade , Análise Multivariada , Cooperação do Paciente , Valor Preditivo dos Testes , Prognóstico , Estudos Prospectivos , Pressão Propulsora Pulmonar/fisiologia , Volume Sistólico/fisiologia , Análise de Sobrevida , Resultado do Tratamento
5.
Int J Cardiol ; 84(2-3): 179-85, 2002 Aug.
Artigo em Inglês | MEDLINE | ID: mdl-12127370

RESUMO

BACKGROUND: Due to its higher diagnostic accuracy stress echocardiography (SE) has been advocated as a substitute for stress ECG to detect coronary heart disease (CAD). However, its contribution to clinical decision-making in unselected patients presenting to the ambulatory care centre for known or suspected coronary artery disease is unclear. METHODS: To evaluate the clinical value of SE in unselected patients, we prospectively obtained SE and stress ECG in 221 consecutive patients (142 males; mean age 58+/-12 years) presenting to the ambulatory care centre with known or suspected CAD. Patients with acute coronary syndrome were not included. RESULTS: Results of stress ECG and SE were concordant in 181 (82%) and discordant in 40 patients (18%). The clinical decision to recommend or to currently withhold coronary angiography was possible solely on the basis of clinical criteria and stress ECG findings in 191 (86.4%) patients but was guided by the results of SE in 30 patients (13.6%). Left heart catheterization and coronary angiography were conducted in 61 patients. In this population SE was more accurate (82.6%) than stress ECG (65.6%) in indicating significant coronary artery stenosis. CONCLUSION: Despite its higher accuracy, SE adds little to the information derived from dynamic stress ECG and symptom evaluation in unselected outpatients with known or suspected CAD. Thus, SE should not in general replace stress ECG as a screening method for detecting significant coronary artery disease, for both clinical and economic reasons.


Assuntos
Doença da Artéria Coronariana/diagnóstico , Tomada de Decisões , Ecocardiografia sob Estresse , Adulto , Idoso , Idoso de 80 Anos ou mais , Pressão Sanguínea/fisiologia , Angiografia Coronária , Doença da Artéria Coronariana/fisiopatologia , Eletrocardiografia Ambulatorial , Teste de Esforço , Reações Falso-Positivas , Feminino , Sistema de Condução Cardíaco/fisiopatologia , Frequência Cardíaca/fisiologia , Humanos , Masculino , Pessoa de Meia-Idade , Estudos Prospectivos , Sensibilidade e Especificidade
6.
J Heart Lung Transplant ; 27(1): 66-71, 2008 Jan.
Artigo em Inglês | MEDLINE | ID: mdl-18187089

RESUMO

BACKGROUND: Even after successful single-lung transplantation (SLTx) or bilateral lung transplantation (BLTx), patients continue to have peripheral muscle weakness and exercise impairment. After SLTx, exercise limitation is also attributed to persistent or recurrent pulmonary vascular abnormalities with elevated pulmonary arterial pressures at rest or during exercise. Therefore, the aim of this study was to evaluate systolic pulmonary artery pressures (PASPs) at rest and during supine bicycle exercise, exercise capacity and cardiopulmonary function in post-BLTx patients. METHODS: Nine patients underwent BLTx due to end-stage pulmonary arterial hypertension (PAH) and 37 age- and gender-matched control subjects underwent a physical examination, electrocardiographic (ECG) test, a 6-minute walk test, a lung function test, a cardiopulmonary exercise test and echocardiographic assessment at rest and during exercise. RESULTS: Exercise capacity was significantly reduced in the BLTx group, with an impaired 6-minute walk test and maximal oxygen uptake and workload. Ventilatory factors did not appear to limit exercise capacity. Right and left ventricular size and pump function and PASP values at rest were normal in both groups, but exceeded 40 mm Hg in 3 of 9 BLTx recipients and in 1 of 37 controls during exercise at low workloads. Mean PASP during exercise was only slightly higher in the BLTx group (40 +/- 5 vs 36 +/- 4 mm Hg, p = not statistically significant). CONCLUSIONS: Reduced exercise capacity of patients after BLTx due to end-stage pulmonary hypertension is not attributed to persistent or recurrent manifest pulmonary hypertension or cardiopulmonary dysfunction. Nevertheless, latent pulmonary hypertension with exaggerated pulmonary artery pressures during exercise may occur in some patients.


Assuntos
Ecocardiografia Doppler/métodos , Ecocardiografia sob Estresse/métodos , Hipertensão Pulmonar/cirurgia , Transplante de Pulmão/métodos , Artéria Pulmonar/diagnóstico por imagem , Pressão Propulsora Pulmonar/fisiologia , Adulto , Teste de Esforço , Tolerância ao Exercício/fisiologia , Feminino , Seguimentos , Humanos , Hipertensão Pulmonar/fisiopatologia , Masculino , Prognóstico , Artéria Pulmonar/fisiopatologia , Testes de Função Respiratória , Índice de Gravidade de Doença
7.
Respiration ; 74(5): 498-502, 2007.
Artigo em Inglês | MEDLINE | ID: mdl-17449958

RESUMO

BACKGROUND: Iloprost is a stable prostacyclin analogue that is associated with a longer duration of vasodilatation and has been approved for inhalative use with 6 or 9 inhalations during the daytime and a night pause. It is not known if during the night pause rebound pulmonary hypertension occurs. The aim of this study was to assess the hemodynamics in iloprost-treated patients during the daytime and at night. METHODS: We enrolled 5 adult patients (aged 45 +/- 10 years) with idiopathic pulmonary arterial hypertension (IPAH) and chronic inhaled iloprost therapy for at least 12 months. Further medication remained unchanged during the study period. Hemodynamics were monitored by right heart catheterization. RESULTS: After 30-60 min of nebulized iloprost, mean pulmonary arterial pressures (PAP) decreased from 68 +/- 15 to 51 +/- 18 mm Hg (p = 0.004). After 6 h off-medication sleeping time, mean PAP initially increased until 2 a.m. and decreased subsequently until wake-up time at 6 a.m. Mean PAP, cardiac index and pulmonary vascular resistance at night were not significantly different from the values during the day. CONCLUSIONS: In this study, patients with IPAH and chronic nebulized iloprost therapy did not reveal a rebound pulmonary hypertension during off-medication sleeping time.


Assuntos
Hipertensão Pulmonar/fisiopatologia , Iloprosta/administração & dosagem , Adolescente , Adulto , Pressão Sanguínea/efeitos dos fármacos , Feminino , Humanos , Masculino , Pessoa de Meia-Idade , Resistência Vascular/efeitos dos fármacos
8.
J Am Soc Echocardiogr ; 18(6): 693, 2005 Jun.
Artigo em Inglês | MEDLINE | ID: mdl-15947775

RESUMO

Isolated noncompaction of the left ventricular (LV) myocardium is a rare congenital disorder resulting from an arrest of the compaction process of the myocardial trabeculae during normal embryogenesis. It is characterized by the presence of prominent LV myocardial trabeculations and deep intertrabecular recesses that are in continuity with the LV cavity. The most common clinical presentation includes progressive LV dysfunction, life-threatening tachyarrhythmias, and the risk for severe cardioembolic events. We describe a case where isolated noncompaction of the LV myocardium was diagnosed after an embolic occlusion of the superior mesenteric artery in a 40-year-old Caucasian woman.


Assuntos
Arteriopatias Oclusivas/diagnóstico por imagem , Embolia/diagnóstico por imagem , Ventrículos do Coração/anormalidades , Ventrículos do Coração/diagnóstico por imagem , Artéria Mesentérica Superior/diagnóstico por imagem , Disfunção Ventricular Esquerda/congênito , Disfunção Ventricular Esquerda/diagnóstico por imagem , Adulto , Arteriopatias Oclusivas/etiologia , Embolia/etiologia , Feminino , Humanos , Hipertrofia Ventricular Esquerda/complicações , Hipertrofia Ventricular Esquerda/congênito , Hipertrofia Ventricular Esquerda/diagnóstico por imagem , Ultrassonografia , Disfunção Ventricular Esquerda/complicações
9.
Int J Cardiovasc Imaging ; 19(2): 117-28, 2003 Apr.
Artigo em Inglês | MEDLINE | ID: mdl-12749392

RESUMO

AIMS: Objective methods for evaluating myocardial contrast echocardiography (MCE) are not yet widely available. We applied a Fourier analysis to myocardial contrast echocardiograms to identify myocardial perfusion defects. METHODS: Harmonic power-Doppler contrast echocardiograms were performed in 21 patients undergoing Tl-201-SPECT imaging and in 13 controls. Images were transformed using Fourier analysis to obtain phase of the first harmonic sinusoidal curve displayed as color coded sequence of myocardial intensity changes. Means and standard deviations of regional phase angles were measured. The method was validated in an in vitro model. A contrast filled latex balloon was imaged at different gain settings mimicking defined time-intensity curves. An intraoperative porcine infarction model served to prove feasibility of Fourier transformation to analyze real-time pulse inversion contrast echocardiography. RESULTS: In patients, phase imaging and intensity analysis showed focal areas with marked phase shifts (106 +/- 90 degrees) and heterogeneous distribution of phase angles (SD 66 +/- 17 degrees), correctly identifying 13/14 perfusion defects. The in vitro validation yielded increasing phase angles with increasing beta-values. This method was successfully applied to real-time MCE, identifying all infarction areas during occlusion of the left anterior descending artery. CONCLUSION: Phase analysis can be used to display dynamics of myocardial opacification.


Assuntos
Ecocardiografia/métodos , Infarto do Miocárdio/diagnóstico por imagem , Idoso , Animais , Estudos de Casos e Controles , Ecocardiografia Doppler , Feminino , Análise de Fourier , Coração/diagnóstico por imagem , Humanos , Processamento de Imagem Assistida por Computador , Masculino , Processamento de Sinais Assistido por Computador , Suínos , Radioisótopos de Tálio , Tomografia Computadorizada de Emissão de Fóton Único
10.
Pediatr Res ; 56(4): 571-8, 2004 Oct.
Artigo em Inglês | MEDLINE | ID: mdl-15295086

RESUMO

Mutations of the bone morphogenetic protein receptor II (BMPR2) gene on chromosome 2q33 can cause familial primary pulmonary hypertension (PPH) and may occur in 26% adult patients with sporadic disease. Other disease-related genes have been localized to chromosomes 2q31 (PPH2) and 12q13 (ALK1). The genetic background in affected children remains unclear. Thirteen children (age at diagnosis, 6 mo to 13 y; mean, 5.6 +/- 3.9 y) with invasively confirmed PPH were screened for BMPR2 mutations using denaturing HPLC and sequence analysis. In addition, all children were scanned for BMPR2 deletions by Southern blot analysis. Pulmonary artery pressure was assessed using echocardiography at rest and during exercise in 57 family members of six infants. The six families were subjected to linkage analysis. None of the 13 children had a BMPR2 mutation or deletion. Linkage to chromosome 2 or 12 could not be confirmed in any of the families investigated. In all assessed families, both parents of the index patient and/or members of both branches revealed an abnormal pulmonary artery systolic pressure (PASP)-response to exercise. PPH in children may have a different genetic background than in adults. We postulate a recessive mode of inheritance in a proportion of infantile cases.


Assuntos
Ligação Genética , Hipertensão Pulmonar/genética , Proteínas Serina-Treonina Quinases/genética , Adolescente , Adulto , Pressão Sanguínea , Receptores de Proteínas Morfogenéticas Ósseas Tipo II , Criança , Pré-Escolar , Ecocardiografia , Família , Feminino , Haplótipos , Humanos , Hipertensão Pulmonar/diagnóstico por imagem , Lactente , Masculino , Linhagem , Fenótipo
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