NEW TECHNOLOGIES IN HYPERTENSION CONTROL– EVALUATION OF A NEW CUFF-LESS DEVICE IN CLINICAL SETTING

Detalhes bibliográficos
Autor(a) principal: Tomás Xufre, Mikael
Data de Publicação: 2022
Outros Autores: Castelo-Branco, Miguel
Tipo de documento: Artigo
Idioma: por
Título da fonte: Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
Texto Completo: https://doi.org/10.58043/rphrc.20
Resumo: Introduction: Known as the most prevalent cardiovascular risk factor, hypertension, or High Blood Pressure (HBP), affects up to 1.13 billion people worldwide. It is responsible for up to 45% of deaths from cardiovascular disease and 51% of deaths from stroke. It is currently known that one of the reasons is that patients with hypertension are at greater risk of developing Atrial Fibrillation (AF) and consequent arterial thromboembolism to the cerebral circulation. It has been showed that reducing and maintaining blood pressure (BP) in hypertensive patients at levels considered ideal has a significant impact in reducing associated morbidity and mortality. Thus, the control of hypertension becomes essential. In addition to patient involvement, some technologies have showed potential in improving this control, such as telemonitoring and AF detection algorithms in BP monitoring devices. New devices have attempted to combine these technologies with a greater ease of use such as smartwatches or other wrist meters with or without a cuff, however, most failed to obtain certification and clinical validation. In this study, a new portable cuff-less BP meter, which includes heart rate measurement, telemonitoring and detection of suspected AF rhythms is evaluated. The measurements are carried out in about 10 seconds at the wrist level and the device has the advantage of being already certified and clinically validated by the European Society of Hypertension. Objetives: Evaluate the opinion of a group of patients with hypertension about a new portable and cuffless BP meter (FreeScan®, Maisense) after using it for 1 month through a questionnaire and evaluate the number of recommended measurements performed. Méthods: Patients being followed at HBP consultation who had access to a smartphone (necessary for telemonitoring) were invited to participate in the study. A Freescan® device was provided, it was demonstrated how it works and the calibration with a digital BP meter (with arm cuff, Rossmax X5®) was made. For follow-up, participants were asked to take 2 consecutive measurements in the morning before taking medication for HBP and 2 consecutive measurements at the end of the day, preferably before dinner. After 4 weeks, a meeting was arranged to collect the device and to deliver a questionnaire, in order to assess the participant’s opinion on different aspects of the Freescan® device. Results: We obtained a final sample of 20 participants. The mean age was 57.15 (standard deviation (SD) 9.88) years. The average number of days with at least 1 measurement was 23,05 (SD 8,80) corresponding to 82,32% of the 28 days. The average number of recommended measurements taken was 61,80 (SD 36,05) corresponding to 55,18% of the total, 112. In the questionnaires, 95% answered that it was easy to learn how to use the device (answer 4 “I agree” or 5 “I totally agree”), 80% that it was easy to take BP measurements (4 or 5), 70% that they trusted the BP values (4 or 5), 100% that it was easy to telemonitor the data (4 or 5), 100% gave great importance to the doctor constantly receiving the data (4 or 5) and 70% preferred the Freescan® over cuff-based BP monitors. During the study, 7 cases of non-controlled hypertension and 3 cases with at least one suspected AF measurement were reported to the responsible physician. The number of recommended measurements taken was not influenced by age or sex. Conclusion: In this prospective study of hypertensive patients followed up in hospital hypertension consultations, most participants preferred Freescan® over cuff-based BP monitors and there was a good adaptation to the new technology as well as a good adherence to the number of measurements recommended, independently of age or sex. That leads us to conclude that these new devices may have an important role in the follow-up of patients with hypertension, in order to increase control and decrease the morbidity and mortality associated with this condition.
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spelling NEW TECHNOLOGIES IN HYPERTENSION CONTROL– EVALUATION OF A NEW CUFF-LESS DEVICE IN CLINICAL SETTINGNOVAS TECNOLOGIAS NO CONTROLO DA HIPERTENSÃO – AVALIAÇÃO DE UM NOVO DISPOSITIVO SEM BRAÇADEIRA EM CONTEXTO CLÍNICOIntroduction: Known as the most prevalent cardiovascular risk factor, hypertension, or High Blood Pressure (HBP), affects up to 1.13 billion people worldwide. It is responsible for up to 45% of deaths from cardiovascular disease and 51% of deaths from stroke. It is currently known that one of the reasons is that patients with hypertension are at greater risk of developing Atrial Fibrillation (AF) and consequent arterial thromboembolism to the cerebral circulation. It has been showed that reducing and maintaining blood pressure (BP) in hypertensive patients at levels considered ideal has a significant impact in reducing associated morbidity and mortality. Thus, the control of hypertension becomes essential. In addition to patient involvement, some technologies have showed potential in improving this control, such as telemonitoring and AF detection algorithms in BP monitoring devices. New devices have attempted to combine these technologies with a greater ease of use such as smartwatches or other wrist meters with or without a cuff, however, most failed to obtain certification and clinical validation. In this study, a new portable cuff-less BP meter, which includes heart rate measurement, telemonitoring and detection of suspected AF rhythms is evaluated. The measurements are carried out in about 10 seconds at the wrist level and the device has the advantage of being already certified and clinically validated by the European Society of Hypertension. Objetives: Evaluate the opinion of a group of patients with hypertension about a new portable and cuffless BP meter (FreeScan®, Maisense) after using it for 1 month through a questionnaire and evaluate the number of recommended measurements performed. Méthods: Patients being followed at HBP consultation who had access to a smartphone (necessary for telemonitoring) were invited to participate in the study. A Freescan® device was provided, it was demonstrated how it works and the calibration with a digital BP meter (with arm cuff, Rossmax X5®) was made. For follow-up, participants were asked to take 2 consecutive measurements in the morning before taking medication for HBP and 2 consecutive measurements at the end of the day, preferably before dinner. After 4 weeks, a meeting was arranged to collect the device and to deliver a questionnaire, in order to assess the participant’s opinion on different aspects of the Freescan® device. Results: We obtained a final sample of 20 participants. The mean age was 57.15 (standard deviation (SD) 9.88) years. The average number of days with at least 1 measurement was 23,05 (SD 8,80) corresponding to 82,32% of the 28 days. The average number of recommended measurements taken was 61,80 (SD 36,05) corresponding to 55,18% of the total, 112. In the questionnaires, 95% answered that it was easy to learn how to use the device (answer 4 “I agree” or 5 “I totally agree”), 80% that it was easy to take BP measurements (4 or 5), 70% that they trusted the BP values (4 or 5), 100% that it was easy to telemonitor the data (4 or 5), 100% gave great importance to the doctor constantly receiving the data (4 or 5) and 70% preferred the Freescan® over cuff-based BP monitors. During the study, 7 cases of non-controlled hypertension and 3 cases with at least one suspected AF measurement were reported to the responsible physician. The number of recommended measurements taken was not influenced by age or sex. Conclusion: In this prospective study of hypertensive patients followed up in hospital hypertension consultations, most participants preferred Freescan® over cuff-based BP monitors and there was a good adaptation to the new technology as well as a good adherence to the number of measurements recommended, independently of age or sex. That leads us to conclude that these new devices may have an important role in the follow-up of patients with hypertension, in order to increase control and decrease the morbidity and mortality associated with this condition.Introdução: Conhecido como fator de risco cardiovascular mais prevalente, a Hipertensão arterial (HTA) afeta cerca de 1,13 mil milhões de pessoas em todo o mundo. É apontada como causa em até 45% das mortes por doença cardiovascular e 51% das mortes por Acidente Vascular Cerebral (AVC). Sabe-se atualmente que uma das razões é o facto dos doentes com HTA terem maior risco de desenvolver Fibrilhação Auricular (FA) e consequente embolização de trombos auriculares para a circulação cerebral. Foi demonstrado que reduzir e manter a pressão arterial (PA) de doentes hipertensos em níveis considerados ideais tem um impacto significativo na redução da mortalidade e morbilidade associada. Assim, o controlo da doença hipertensiva torna-se fundamental. Além do envolvimento do doente, que é fulcral, algumas tecnologias têm-se mostrado promissoras no sentido de melhorar esse controlo como a telemonitorização e os algoritmos de deteção de FA nos medidores de PA. Novos dispositivos têm tentado combinar estas tecnologias com uma maior facilidade de utilização, como smartwatches ou outros medidores de pulso com ou sem braçadeira, no entanto, a maioria falha em obter certificação e validação clínica. Neste estudo é avaliado a opinião dos utilizadores de um novo medidor de PA portátil, sem braçadeira, que engloba também medição da frequência cardíaca, telemonitorização e deteção de ritmos suspeitos de FA. A medição é realizada em cerca de 10 segundos ao nível do pulso e tem a vantagem de estar já certificado e clinicamente validado pela Sociedade Europeia de Hipertensão. Objetivos: Avaliar a opinião de doentes com HTA na utilização de um novo dispositivo portátil sem braçadeira (Freescan®, Maisense) após 1 mês de utilização, através de questionário, e ainda avaliar o número de medições recomendadas realizadas. Métodos: Foram recrutados doentes seguidos em consulta de HTA que tivessem acesso a um smartphone (necessário para telemonitorização) e interesse em participar. Foi fornecido um dispositivo Freescan®, demostrado o seu funcionamento e feito a calibração com um medidor de PA digital com braçadeira (Rossmax X5®). Para o seguimento foi pedido aos participantes que efetuassem 2 medições consecutivas de manhã antes de tomar a medicação para a HTA e 2 medições consecutivas ao fim do dia, preferencialmente antes de jantar. Após 4 semanas marcou-se um encontro para recolher o dispositivo e para responderem a um questionário, de forma a avaliar a opinião do participante sobre diferentes aspetos do Freescan®. Resultados: Obteve-se uma amostra final de 20 participantes. A média de idade foi de 57,15 (desvio padrão (DP) 9,88) anos. A média de dias com pelo menos 1 medição foi de 23,05 (DP 8,60), correspondendo a 82,32% dos 28 dias. A média do número de medições recomendadas realizadas foi de 61,80 (DP 36,05), correspondendo a 55,18% do total de medições recomendadas, 112. Aos questionários, 95% respondeu ser fácil aprender a utilizar o Freescan® (Resposta 4 “Concordo” ou 5 “Concordo totalmente”), 80% ser fácil realizar medições (4 ou 5), 70% confiam nos valores de PA (4 ou 5), 100% que foi fácil telemonitorizar os dados (4 ou 5), 100% acham importante o envio dos dados para o médico (4 ou 5) e 70% prefere o Freescan® aos medidores com braçadeira. Durante o estudo foram ainda sinalizados ao médico responsável 7 casos de HTA não controlada e 3 casos com pelo menos uma medição suspeita de FA. O número de medições realizadas não foi significativamente diferente entre os diferentes sexos e idades. Conclusão: No estudo prospetivo em doentes hipertensos acompanhados em consulta hospitalar de Hipertensão, a maioria dos participantes preferiu o Freescan® aos medidores com braçadeira e houve uma boa adaptação à nova tecnologia, verificando-se uma boa adesão ao número de medições recomendadas realizadas independentemente da idade e do sexo. Assim, a preferência dos participantes por este dispositivo aliado às tecnologias de telemonitorização e deteção de FA leva-nos a concluir que estes novos dispositivos poderão ter um papel importante no seguimento dos doentes com HTA, com potencial para aumentar o controlo da HTA e diminuir a mortalidade e morbilidade associadas a esta doença.Revista Portuguesa de Hipertensão e Risco Cardiovascular2022-05-28info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleapplication/pdfhttps://doi.org/10.58043/rphrc.20https://doi.org/10.58043/rphrc.20Revista Portuguesa de Hipertensão e Risco Cardiovascular; N.º 85 (2021): Setembro / Outubro; 8-191646-8287reponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)instname:Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãoinstacron:RCAAPporhttps://revistahipertensao.pt/index.php/rh/article/view/20https://revistahipertensao.pt/index.php/rh/article/view/20/20Tomás Xufre, MikaelCastelo-Branco, Miguelinfo:eu-repo/semantics/openAccess2024-02-03T07:36:24Zoai:ojs.revistahipertensao.pt:article/20Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireopendoar:71602024-03-19T16:05:07.688554Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) - Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãofalse
dc.title.none.fl_str_mv NEW TECHNOLOGIES IN HYPERTENSION CONTROL– EVALUATION OF A NEW CUFF-LESS DEVICE IN CLINICAL SETTING
NOVAS TECNOLOGIAS NO CONTROLO DA HIPERTENSÃO – AVALIAÇÃO DE UM NOVO DISPOSITIVO SEM BRAÇADEIRA EM CONTEXTO CLÍNICO
title NEW TECHNOLOGIES IN HYPERTENSION CONTROL– EVALUATION OF A NEW CUFF-LESS DEVICE IN CLINICAL SETTING
spellingShingle NEW TECHNOLOGIES IN HYPERTENSION CONTROL– EVALUATION OF A NEW CUFF-LESS DEVICE IN CLINICAL SETTING
Tomás Xufre, Mikael
title_short NEW TECHNOLOGIES IN HYPERTENSION CONTROL– EVALUATION OF A NEW CUFF-LESS DEVICE IN CLINICAL SETTING
title_full NEW TECHNOLOGIES IN HYPERTENSION CONTROL– EVALUATION OF A NEW CUFF-LESS DEVICE IN CLINICAL SETTING
title_fullStr NEW TECHNOLOGIES IN HYPERTENSION CONTROL– EVALUATION OF A NEW CUFF-LESS DEVICE IN CLINICAL SETTING
title_full_unstemmed NEW TECHNOLOGIES IN HYPERTENSION CONTROL– EVALUATION OF A NEW CUFF-LESS DEVICE IN CLINICAL SETTING
title_sort NEW TECHNOLOGIES IN HYPERTENSION CONTROL– EVALUATION OF A NEW CUFF-LESS DEVICE IN CLINICAL SETTING
author Tomás Xufre, Mikael
author_facet Tomás Xufre, Mikael
Castelo-Branco, Miguel
author_role author
author2 Castelo-Branco, Miguel
author2_role author
dc.contributor.author.fl_str_mv Tomás Xufre, Mikael
Castelo-Branco, Miguel
description Introduction: Known as the most prevalent cardiovascular risk factor, hypertension, or High Blood Pressure (HBP), affects up to 1.13 billion people worldwide. It is responsible for up to 45% of deaths from cardiovascular disease and 51% of deaths from stroke. It is currently known that one of the reasons is that patients with hypertension are at greater risk of developing Atrial Fibrillation (AF) and consequent arterial thromboembolism to the cerebral circulation. It has been showed that reducing and maintaining blood pressure (BP) in hypertensive patients at levels considered ideal has a significant impact in reducing associated morbidity and mortality. Thus, the control of hypertension becomes essential. In addition to patient involvement, some technologies have showed potential in improving this control, such as telemonitoring and AF detection algorithms in BP monitoring devices. New devices have attempted to combine these technologies with a greater ease of use such as smartwatches or other wrist meters with or without a cuff, however, most failed to obtain certification and clinical validation. In this study, a new portable cuff-less BP meter, which includes heart rate measurement, telemonitoring and detection of suspected AF rhythms is evaluated. The measurements are carried out in about 10 seconds at the wrist level and the device has the advantage of being already certified and clinically validated by the European Society of Hypertension. Objetives: Evaluate the opinion of a group of patients with hypertension about a new portable and cuffless BP meter (FreeScan®, Maisense) after using it for 1 month through a questionnaire and evaluate the number of recommended measurements performed. Méthods: Patients being followed at HBP consultation who had access to a smartphone (necessary for telemonitoring) were invited to participate in the study. A Freescan® device was provided, it was demonstrated how it works and the calibration with a digital BP meter (with arm cuff, Rossmax X5®) was made. For follow-up, participants were asked to take 2 consecutive measurements in the morning before taking medication for HBP and 2 consecutive measurements at the end of the day, preferably before dinner. After 4 weeks, a meeting was arranged to collect the device and to deliver a questionnaire, in order to assess the participant’s opinion on different aspects of the Freescan® device. Results: We obtained a final sample of 20 participants. The mean age was 57.15 (standard deviation (SD) 9.88) years. The average number of days with at least 1 measurement was 23,05 (SD 8,80) corresponding to 82,32% of the 28 days. The average number of recommended measurements taken was 61,80 (SD 36,05) corresponding to 55,18% of the total, 112. In the questionnaires, 95% answered that it was easy to learn how to use the device (answer 4 “I agree” or 5 “I totally agree”), 80% that it was easy to take BP measurements (4 or 5), 70% that they trusted the BP values (4 or 5), 100% that it was easy to telemonitor the data (4 or 5), 100% gave great importance to the doctor constantly receiving the data (4 or 5) and 70% preferred the Freescan® over cuff-based BP monitors. During the study, 7 cases of non-controlled hypertension and 3 cases with at least one suspected AF measurement were reported to the responsible physician. The number of recommended measurements taken was not influenced by age or sex. Conclusion: In this prospective study of hypertensive patients followed up in hospital hypertension consultations, most participants preferred Freescan® over cuff-based BP monitors and there was a good adaptation to the new technology as well as a good adherence to the number of measurements recommended, independently of age or sex. That leads us to conclude that these new devices may have an important role in the follow-up of patients with hypertension, in order to increase control and decrease the morbidity and mortality associated with this condition.
publishDate 2022
dc.date.none.fl_str_mv 2022-05-28
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publisher.none.fl_str_mv Revista Portuguesa de Hipertensão e Risco Cardiovascular
dc.source.none.fl_str_mv Revista Portuguesa de Hipertensão e Risco Cardiovascular; N.º 85 (2021): Setembro / Outubro; 8-19
1646-8287
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