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1.
Card Electrophysiol Clin ; 13(3): 531-542, 2021 09.
Artigo em Inglês | MEDLINE | ID: mdl-34330379

RESUMO

Atrial fibrillation (AF) is associated with adverse outcomes. Screening may lead to earlier recognition and treatment of asymptomatic AF. However, most evidence regarding AF applies to clinical AF, with symptoms or electrocardiographic diagnosis. Whether this evidence can be translated toward subclinical AF, without symptoms and detected by novel, more continuous screening devices is uncertain. The diagnostic yield of screening is determined by the screening population, tool, duration and frequency. Longer and more frequent screening in a higher risk population leads to more effective screening. New devices based on photoplethysmography and single-lead electrocardiography increase convenience and the likelihood of cost-effectiveness.


Assuntos
Fibrilação Atrial , Fibrilação Atrial/diagnóstico , Análise Custo-Benefício , Eletrocardiografia , Humanos , Programas de Rastreamento , Fatores de Risco
2.
JMIR Mhealth Uhealth ; 7(10): e12586, 2019 10 29.
Artigo em Inglês | MEDLINE | ID: mdl-31663862

RESUMO

BACKGROUND: Medical smartphone apps and mobile health devices are rapidly entering mainstream use because of the rising number of smartphone users. Consequently, a large amount of consumer-generated data is being collected. Technological advances in innovative sensory systems have enabled data connectivity and aggregation to become cornerstones in developing workable solutions for remote monitoring systems in clinical practice. However, few systems are currently available to handle such data, especially for clinical use. OBJECTIVE: The aim of this study was to develop and implement the digital health research platform for mobile health (DHARMA) that combines data saved in different formats from a variety of sources into a single integrated digital platform suitable for mobile remote monitoring studies. METHODS: DHARMA comprises a smartphone app, a Web-based platform, and custom middleware and has been developed to collect, store, process, and visualize data from different vendor-specific sensors. The middleware is a component-based system with independent building blocks for user authentication, study and patient administration, data handling, questionnaire management, patient files, and reporting. RESULTS: A prototype version of the research platform has been tested and deployed in multiple clinical studies. In this study, we used the platform for the follow-up of pregnant women at risk of developing pre-eclampsia. The patients' blood pressure, weight, and activity were semi-automatically captured at home using different devices. DHARMA automatically collected and stored data from each source and enabled data processing for the end users in terms of study-specific parameters, thresholds, and visualization. CONCLUSIONS: The increasing use of mobile health apps and connected medical devices is leading to a large amount of data for collection. There has been limited investment in handling and aggregating data from different sources for use in academic and clinical research focusing on remote monitoring studies. In this study, we created a modular mobile health research platform to collect and integrate data from a variety of third-party devices in several patient populations. The functionality of the platform was demonstrated in a real-life setting among women with high-risk pregnancies.


Assuntos
Ergonomia/normas , Aplicativos Móveis/normas , Monitorização Fisiológica/instrumentação , Humanos , Aplicativos Móveis/estatística & dados numéricos , Monitorização Fisiológica/métodos , Monitorização Fisiológica/normas , Portais do Paciente , Inquéritos e Questionários
3.
Eur J Emerg Med ; 24(6): 423-427, 2017 Dec.
Artigo em Inglês | MEDLINE | ID: mdl-27043771

RESUMO

BACKGROUND: It is important that patients with symptoms of acute coronary syndrome receive appropriate medical care as soon as possible. Little is known about the preadmission actions that patients with chest pain take before arrival at the Emergency Department (ED). OBJECTIVE: This study aimed to describe the actions of patients with chest pain or pressure after onset of symptoms. What is the first action following onset of symptoms? Who is the first lay or professional person to be contacted? Which steps are taken first? How is the patient transported to the hospital? METHODS: Consecutive patients, arriving at the ED of two large hospitals in Belgium, were asked additional questions during the initial assessment. RESULTS: Overall, 35% of 412 consecutive patients with chest pain admitted to the ED were diagnosed with acute coronary syndrome. A total of 57% contacted a GP between symptom onset and arrival at the ED. Only 32% of the patients were transported to the ED by ambulance, 16% drove themselves and 52% arrived by other means of transport (by family, neighbour, GP, public transport). CONCLUSION: In Belgium, the GP is still the first professional to be contacted for most patients. Other patients initially rely on their partner, family or friends when symptoms emerge. Too often, patients with chest pain rely on other transport to get to the ED instead of calling the Emergency Medical Services. This study included only patients who ultimately attended the ED.


Assuntos
Síndrome Coronariana Aguda/prevenção & controle , Dor no Peito/diagnóstico , Dor no Peito/mortalidade , Serviço Hospitalar de Emergência/estatística & dados numéricos , Inquéritos e Questionários , Síndrome Coronariana Aguda/mortalidade , Fatores Etários , Idoso , Bélgica , Dor no Peito/terapia , Estudos Transversais , Progressão da Doença , Diagnóstico Precoce , Medicina de Emergência/métodos , Feminino , Clínicos Gerais/estatística & dados numéricos , Acessibilidade aos Serviços de Saúde/organização & administração , Humanos , Masculino , Pessoa de Meia-Idade , Qualidade da Assistência à Saúde , Encaminhamento e Consulta/estatística & dados numéricos , Medição de Risco , Fatores Sexuais , Taxa de Sobrevida , Tempo para o Tratamento
4.
Eur J Prev Cardiol ; 23(7): 674-82, 2016 May.
Artigo em Inglês | MEDLINE | ID: mdl-26289723

RESUMO

BACKGROUND: Notwithstanding the cardiovascular disease epidemic, current budgetary constraints do not allow for budget expansion of conventional cardiac rehabilitation programmes. Consequently, there is an increasing need for cost-effectiveness studies of alternative strategies such as telerehabilitation. The present study evaluated the cost-effectiveness of a comprehensive cardiac telerehabilitation programme. DESIGN AND METHODS: This multi-centre randomized controlled trial comprised 140 cardiac rehabilitation patients, randomized (1:1) to a 24-week telerehabilitation programme in addition to conventional cardiac rehabilitation (intervention group) or to conventional cardiac rehabilitation alone (control group). The incremental cost-effectiveness ratio was calculated based on intervention and health care costs (incremental cost), and the differential incremental quality adjusted life years (QALYs) gained. RESULTS: The total average cost per patient was significantly lower in the intervention group (€2156 ± €126) than in the control group (€2720 ± €276) (p = 0.01) with an overall incremental cost of €-564.40. Dividing this incremental cost by the baseline adjusted differential incremental QALYs (0.026 QALYs) yielded an incremental cost-effectiveness ratio of €-21,707/QALY. The number of days lost due to cardiovascular rehospitalizations in the intervention group (0.33 ± 0.15) was significantly lower than in the control group (0.79 ± 0.20) (p = 0.037). CONCLUSIONS: This paper shows the addition of cardiac telerehabilitation to conventional centre-based cardiac rehabilitation to be more effective and efficient than centre-based cardiac rehabilitation alone. These results are useful for policy makers charged with deciding how limited health care resources should best be allocated in the era of exploding need.


Assuntos
Reabilitação Cardíaca/economia , Doenças Cardiovasculares/terapia , Custos de Cuidados de Saúde/tendências , Readmissão do Paciente/tendências , Qualidade de Vida , Anos de Vida Ajustados por Qualidade de Vida , Telerreabilitação/economia , Idoso , Doenças Cardiovasculares/economia , Análise Custo-Benefício , Feminino , Seguimentos , Humanos , Masculino , Pessoa de Meia-Idade , Readmissão do Paciente/economia , Estudos Prospectivos , Centros de Reabilitação , Fatores de Tempo
5.
Echocardiography ; 32(3): 557-64, 2015 Mar.
Artigo em Inglês | MEDLINE | ID: mdl-25048733

RESUMO

PURPOSE: Echocardiography is increasingly important in the guidance and follow-up of percutaneous transcatheter device closures. It was recently shown that the Amplatzer left atrial appendage occluder frequently presents as a figure-of-eight artifact due to interaction of device mesh and ultrasound waves. It remains unknown whether this can be translated to other types of disc occluders. Furthermore, the morphology of this figure-of-eight artifact appears to be different in the transesophageal and transthoracic image of the same device. The aim of this study was to evaluate the echocardiographic appearance of different types of disc occluders, and to clarify differences in morphology of the figure-of-eight artifact. METHODS: A mathematical model of an epitrochoid curve was used for numerical simulation of disc occluder appearance at various imaging depths. In addition, an in vitro setup was used for echocardiographic analysis of different types of disc occluders at adjustable imaging depth and position. RESULTS: Mathematically, decreasing the imaging depth resulted in a more asymmetric figure-of-eight, i.e. with small upper part and wide lower part. In vitro results were in close agreement with the mathematical results. In addition, in vitro a figure-of-eight artifact was obtained in all different types of disc occluder devices. CONCLUSIONS: Different types of percutaneous disc occluders all present as a figure-of-eight artifact on echocardiography when imaged from a coronal imaging position. The morphology of the artifact depends on the imaging depth, with a more asymmetric figure-of-eight morphology at smaller probe-to-device distance. This clarifies the differences observed between transesophageal and transthoracic imaging.


Assuntos
Artefatos , Ecocardiografia/instrumentação , Ecocardiografia/métodos , Dispositivo para Oclusão Septal , Análise de Falha de Equipamento , Imagens de Fantasmas , Desenho de Prótese , Reprodutibilidade dos Testes , Sensibilidade e Especificidade
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