Pub Date : 2024-03-12DOI: 10.1016/j.recesp.2024.03.002
In Spain, 33% of adults aged 30 to 79 years (10 million) were hypertensive in 2019. Among them, 68% were diagnosed, 57% received drug therapy, and effective therapeutic coverage (control) reached 33%. Both diagnosis and control show geographical and social disparities. Approximately 46 000 cardiovascular deaths per year are attributable to hypertension. In recent decades, the control of hypertension has increased, due to improvements in lifestyle measures and increased use of polytherapy, coinciding with a reduction in stroke mortality. There are several modifiable determinants of the lack of hypertension control: a) white-coat phenomenon affects 22% to 33% of treated individuals, partly due to the limited availability of ambulatory blood pressure monitoring (ABPM) (49%) and self-measured BP (SMBP) (78%); b) inadequate patient adherence to medication and healthy lifestyles (weight loss, the most effective measure, is the least used, ≈40%); and c) insufficient use of polytherapy (≈55%). The remaining challenges include: a) technological aspects, such as measuring BP with more accurate techniques (ABPM, SMBP) and using cardiovascular-risk estimation tools (eg, SCORE); b) clinical challenges, such as reducing therapeutic inertia (≈59%), involving patients in their own management (medication adherence, ≈62%) and effectively implementing clinical guidelines); and c) public health challenges, such as reducing the burden of obesity (≈24%), monitoring progress with updated surveys, and setting national BP control targets.
{"title":"Cifras e impacto de la hipertensión arterial en España","authors":"","doi":"10.1016/j.recesp.2024.03.002","DOIUrl":"10.1016/j.recesp.2024.03.002","url":null,"abstract":"<div><p>In Spain, 33% of adults aged 30 to 79 years (10 million) were hypertensive in 2019. Among them, 68% were diagnosed, 57% received drug therapy, and effective therapeutic coverage (control) reached 33%. Both diagnosis and control show geographical and social disparities. Approximately 46 000 cardiovascular deaths per year are attributable to hypertension. In recent decades, the control of hypertension has increased, due to improvements in lifestyle measures and increased use of polytherapy, coinciding with a reduction in stroke mortality. There are several modifiable determinants of the lack of hypertension control: <em>a)</em> white-coat phenomenon affects 22% to 33% of treated individuals, partly due to the limited availability of ambulatory blood pressure monitoring (ABPM) (49%) and self-measured BP (SMBP) (78%); <em>b)</em> inadequate patient adherence to medication and healthy lifestyles (weight loss, the most effective measure, is the least used, ≈40%); and <em>c)</em> insufficient use of polytherapy (≈55%). The remaining challenges include: <em>a)</em> technological aspects, such as measuring BP with more accurate techniques (ABPM, SMBP) and using cardiovascular-risk estimation tools (eg, SCORE); <em>b)</em> clinical challenges, such as reducing therapeutic inertia (≈59%), involving patients in their own management (medication adherence, ≈62%) and effectively implementing clinical guidelines); and <em>c)</em> public health challenges, such as reducing the burden of obesity (≈24%), monitoring progress with updated surveys, and setting national BP control targets.</p></div>","PeriodicalId":21299,"journal":{"name":"Revista espanola de cardiologia","volume":"77 9","pages":"Pages 767-778"},"PeriodicalIF":5.9,"publicationDate":"2024-03-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.sciencedirect.com/science/article/pii/S0300893224001076/pdfft?md5=68cf2c42fae107001f8d17b455f1b568&pid=1-s2.0-S0300893224001076-main.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"140271556","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2024-03-07DOI: 10.1016/j.recesp.2024.02.020
Introduction and objectives
Cardiac resynchronization therapy (CRT) is an effective treatment for patients with nonischemic dilated cardiomyopathy associated with left bundle branch block (LBBB). In these patients, the device can normalize left ventricular ejection fraction (LVEF). Nevertheless, it remains unclear whether CRT responders still require neurohormonal blockers. The aim of this study is to determine the long-term safety of withdrawing drug therapy in these patients.
Methods
The REMOVE trial is a prospective, multicenter, open-label and randomized 1:1 study designed to assess the effect of withdrawing neurohormonal blockers in patients with nonischemic dilated cardiomyopathy associated with left bundle branch block who recovered LVEF after CRT. The study will include a 12-month follow-up with the option to continue into the follow-up extension phase for up to 24 months. The primary endpoint is the recurrence of cardiomyopathy defined as any of the following criteria: a) a reduction in LVEF > 10% (provided the LVEF is < 50%); b) a reduction in LVEF > 10% accompanied by an increase > 15% in the indexed end-systolic volume relative to the previous value and in a range higher than the normal values, or c) decompensated heart failure requiring intravenous diuretic administration. In patients meeting the primary endpoint, drug therapy will be restarted.
Conclusions
The results of this study will help to enhance our understanding of CRT superresponders, a specific group of patients. Registred at ClinicalTrials.gov (Identifier: NCT05151861).
{"title":"Retirada del tratamiento farmacológico en pacientes respondedores a terapia de resincronización cardiaca: justificación y diseño del ensayo clínico REMOVE","authors":"","doi":"10.1016/j.recesp.2024.02.020","DOIUrl":"10.1016/j.recesp.2024.02.020","url":null,"abstract":"<div><h3>Introduction and objectives</h3><div>Cardiac resynchronization therapy (CRT) is an effective treatment for patients with nonischemic dilated cardiomyopathy associated with left bundle branch block (LBBB). In these patients, the device can normalize left ventricular ejection fraction (LVEF). Nevertheless, it remains unclear whether CRT responders still require neurohormonal blockers. The aim of this study is to determine the long-term safety of withdrawing drug therapy in these patients.</div></div><div><h3>Methods</h3><div>The REMOVE trial is a prospective, multicenter, open-label and randomized 1:1 study designed to assess the effect of withdrawing neurohormonal blockers in patients with nonischemic dilated cardiomyopathy associated with left bundle branch block who recovered LVEF after CRT. The study will include a 12-month follow-up with the option to continue into the follow-up extension phase for up to 24 months. The primary endpoint is the recurrence of cardiomyopathy defined as any of the following criteria: <em>a)</em> a reduction in LVEF ><!--> <!-->10% (provided the LVEF is <<!--> <!-->50%); <em>b)</em> a reduction in LVEF ><!--> <!-->10% accompanied by an increase ><!--> <!-->15% in the indexed end-systolic volume relative to the previous value and in a range higher than the normal values, or <em>c)</em> decompensated heart failure requiring intravenous diuretic administration. In patients meeting the primary endpoint, drug therapy will be restarted.</div></div><div><h3>Conclusions</h3><div>The results of this study will help to enhance our understanding of CRT superresponders, a specific group of patients. Registred at ClinicalTrials.gov (Identifier: <span><span>NCT05151861</span><svg><path></path></svg></span>).</div></div>","PeriodicalId":21299,"journal":{"name":"Revista espanola de cardiologia","volume":"77 10","pages":"Pages 851-858"},"PeriodicalIF":5.9,"publicationDate":"2024-03-07","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"140278980","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2024-03-07DOI: 10.1016/j.recesp.2023.11.002
Jorge Nuche , Julien Ternacle , Marisa Avvedimento , Asim N. Cheema , Gabriela Veiga-Fernández , Antonio J. Muñoz-García , Victoria Vilalta , Ander Regueiro , Luis Asmarats , María del Trigo , Vicenç Serra , Guillaume Bonnet , Melchior Jonveaux , Giovanni Esposito , Effat Rezaei , José M. de la Torre-Hernández , Eduard Fernández-Nofrerías , Pablo Vidal , Lola Gutiérrez-Alonso , Juan Francisco Oteo , Josep Rodés-Cabau
Introduction and objectives
There are scarce data on the factors associated with impaired functional status after transcatheter aortic valve replacement (TAVR) and its clinical impact. This study aimed to determine the incidence, predictors, and prognostic implications of impaired functional class (NYHA class III-IV) following TAVR.
Methods
This multicenter study included 3462 transarterial TAVR patients receiving newer generation devices. The patients were compared according to their NYHA class at 1 month of follow-up (NYHA I-II vs NYHA III-IV). A multivariate logistic regression was performed to identify the predictors of 30-day NYHA class III-IV. Patient survival was compared with the Kaplan-Meier method and factors associated with decreased survival were identified with Cox regression analysis.
Results
The mean age of the study population was 80.3 ± 7.3 years, with 47% of women, and a median Society of Thoracic Surgeons score of 3.8% [IQR, 2.5-5.8]. A total of 208 patients (6%) were in NYHA class III-IV 1 month after TAVR. Predictors of 30-day NYHA class III-IV were baseline NYHA class III-IV (OR, 1.76; 95%CI, 1.08-2.89; P = .02), chronic pulmonary obstructive disease (OR, 1.80; 95%CI, 1.13-2.83; P = .01), and post-TAVR severe mitral regurgitation (OR, 2.00; 95%CI, 1.21-3.31; P < .01). Patients in NYHA class III-IV 1 month after TAVR were at higher risk of death (HR, 3.68; 95%CI, 2.39-5.70; P < .01) and heart failure-related hospitalization (HR, 6.00; 95%CI, 3.76-9.60; P < .01) at 1-year follow-up.
Conclusions
Up to 6% of contemporary TAVR patients exhibited an impaired functional status following TAVR. Worse baseline NYHA class, chronic pulmonary obstructive disease, and severe mitral regurgitation predicted 30-day NYHA class III/IV, and this determined a higher risk of mortality and heart failure hospitalization at 1-year follow-up. Further studies on the prevention and treatment optimization of patients with impaired functional status after TAVR are needed.
{"title":"Incidencia, predictores e impacto pronóstico de una clase funcional disminuida inmediatamente después de un implante percutáneo de válvula aórtica","authors":"Jorge Nuche , Julien Ternacle , Marisa Avvedimento , Asim N. Cheema , Gabriela Veiga-Fernández , Antonio J. Muñoz-García , Victoria Vilalta , Ander Regueiro , Luis Asmarats , María del Trigo , Vicenç Serra , Guillaume Bonnet , Melchior Jonveaux , Giovanni Esposito , Effat Rezaei , José M. de la Torre-Hernández , Eduard Fernández-Nofrerías , Pablo Vidal , Lola Gutiérrez-Alonso , Juan Francisco Oteo , Josep Rodés-Cabau","doi":"10.1016/j.recesp.2023.11.002","DOIUrl":"10.1016/j.recesp.2023.11.002","url":null,"abstract":"<div><h3>Introduction and objectives</h3><p>There are scarce data on the factors associated with impaired functional status after transcatheter aortic valve replacement (TAVR) and its clinical impact. This study aimed to determine the incidence, predictors, and prognostic implications of impaired functional class (NYHA class III-IV) following TAVR.</p></div><div><h3>Methods</h3><p>This multicenter study included 3462 transarterial TAVR patients receiving newer generation devices. The patients were compared according to their NYHA class at 1 month of follow-up (NYHA I-II vs NYHA III-IV). A multivariate logistic regression was performed to identify the predictors of 30-day NYHA class III-IV. Patient survival was compared with the Kaplan-Meier method and factors associated with decreased survival were identified with Cox regression analysis.</p></div><div><h3>Results</h3><p>The mean age of the study population was 80.3<!--> <!-->±<!--> <!-->7.3 years, with 47% of women, and a median Society of Thoracic Surgeons score of 3.8% [IQR, 2.5-5.8]. A total of 208 patients (6%) were in NYHA class III-IV 1 month after TAVR. Predictors of 30-day NYHA class III-IV were baseline NYHA class III-IV (OR, 1.76; 95%CI, 1.08-2.89; <em>P</em> <!-->=<!--> <!-->.02), chronic pulmonary obstructive disease (OR, 1.80; 95%CI, 1.13-2.83; <em>P</em> <!-->=<!--> <!-->.01), and post-TAVR severe mitral regurgitation (OR, 2.00; 95%CI, 1.21-3.31; <em>P</em> <!--><<!--> <!-->.01). Patients in NYHA class III-IV 1 month after TAVR were at higher risk of death (HR, 3.68; 95%CI, 2.39-5.70; <em>P</em> <!--><<!--> <!-->.01) and heart failure-related hospitalization (HR, 6.00; 95%CI, 3.76-9.60; <em>P</em> <!--><<!--> <!-->.01) at 1-year follow-up.</p></div><div><h3>Conclusions</h3><p>Up to 6% of contemporary TAVR patients exhibited an impaired functional status following TAVR. Worse baseline NYHA class, chronic pulmonary obstructive disease, and severe mitral regurgitation predicted 30-day NYHA class III/IV, and this determined a higher risk of mortality and heart failure hospitalization at 1-year follow-up. Further studies on the prevention and treatment optimization of patients with impaired functional status after TAVR are needed.</p></div>","PeriodicalId":21299,"journal":{"name":"Revista espanola de cardiologia","volume":"77 5","pages":"Pages 396-407"},"PeriodicalIF":5.9,"publicationDate":"2024-03-07","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"140278508","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2024-03-07DOI: 10.1016/j.recesp.2024.02.019
{"title":"Predicción del desarrollo de insuficiencia cardiaca en pacientes con fibrilación auricular","authors":"","doi":"10.1016/j.recesp.2024.02.019","DOIUrl":"10.1016/j.recesp.2024.02.019","url":null,"abstract":"","PeriodicalId":21299,"journal":{"name":"Revista espanola de cardiologia","volume":"77 9","pages":"Pages 720-722"},"PeriodicalIF":5.9,"publicationDate":"2024-03-07","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"140268540","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2024-02-29DOI: 10.1016/j.recesp.2024.02.015
Introduction and objectives
Exposure to secondhand smoke (SHS) causes cardiovascular disease, respiratory disease, and cancer. The aim of this study was to estimate the mortality attributed to SHS in people aged ≥ 35 years in Spain and its autonomous communities (AC) by sex from 2016 to 2021.
Methods
Estimates of SHS-attributable mortality were calculated by applying the prevalence-dependent method where SHS exposure was derived from the adjustment of small-area models and based on the calculation of population-attributed fractions. Sex, age group, AC, and cause of death (ischemic heart disease and lung cancer) were included. The estimates of attributed mortality are presented with their 95% confidence interval (95%CI). Crude and age-standardized rates were estimated for each sex and AC.
Results
From 2016 to 2021, SHS exposure caused 4,970 (95%CI, 4,787-5,387) deaths, representing 1.6% of total mortality for ischemic heart disease and lung cancer. The burden of attributed mortality differed widely among the AC, with Andalusia having the highest burden of attributed mortality (crude rate: 46.6 deaths per 100 000 population in men and 17.0/100 000 in women). In all the AC, the main cause of death in both sexes was ischemic heart disease. The highest burden of mortality was observed in nonsmokers.
Conclusions
The burden of SHS-attributable mortality was high and varied geographically. The results of this study should be considered to advance tobacco control legislation in Spain.
{"title":"Mortalidad atribuida a la exposición al humo ambiental de tabaco en las comunidades autónomas de España","authors":"","doi":"10.1016/j.recesp.2024.02.015","DOIUrl":"10.1016/j.recesp.2024.02.015","url":null,"abstract":"<div><h3>Introduction and objectives</h3><div>Exposure to secondhand smoke (SHS) causes cardiovascular disease, respiratory disease, and cancer. The aim of this study was to estimate the mortality attributed to SHS in people aged ≥ 35 years in Spain and its autonomous communities (AC) by sex from 2016 to 2021.</div></div><div><h3>Methods</h3><div>Estimates of SHS-attributable mortality were calculated by applying the prevalence-dependent method where SHS exposure was derived from the adjustment of small-area models and based on the calculation of population-attributed fractions. Sex, age group, AC, and cause of death (ischemic heart disease and lung cancer) were included. The estimates of attributed mortality are presented with their 95% confidence interval (95%CI). Crude and age-standardized rates were estimated for each sex and AC.</div></div><div><h3>Results</h3><div>From 2016 to 2021, SHS exposure caused 4,970 (95%CI, 4,787-5,387) deaths, representing 1.6% of total mortality for ischemic heart disease and lung cancer. The burden of attributed mortality differed widely among the AC, with Andalusia having the highest burden of attributed mortality (crude rate: 46.6 deaths per 100 000 population in men and 17.0/100 000 in women). In all the AC, the main cause of death in both sexes was ischemic heart disease. The highest burden of mortality was observed in nonsmokers.</div></div><div><h3>Conclusions</h3><div>The burden of SHS-attributable mortality was high and varied geographically. The results of this study should be considered to advance tobacco control legislation in Spain.</div></div>","PeriodicalId":21299,"journal":{"name":"Revista espanola de cardiologia","volume":"77 11","pages":"Pages 912-918"},"PeriodicalIF":5.9,"publicationDate":"2024-02-29","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"140463043","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2024-02-22DOI: 10.1016/j.recesp.2023.12.010
Pablo Corredoira , Victoria Marco-Benedi , Ana Cenarro , Sonia Peribáñez , Salvador Olmos , Fernando Civeira
Introduction and objectives
Tendon xanthomas (TX) are lipid deposits highly specific to familial hypercholesterolemia (FH). However, there is significant variability in their presentation among FH patients, primarily due to largely unknown causes. Lipoprotein(a) is a well-established independent risk factor for atherosclerotic cardiovascular disease in the general population as well as in FH. Given the wide variability of lipoprotein(a) among FH individuals and the likelihood that TX may result from a proatherogenic and proinflammatory condition, the objective of this study was to analyze the size of TX in the Achilles tendons of FH participants and the variables associated with their presence, including lipoprotein(a) concentration.
Methods
A cross-sectional study was conducted on 377 participants with a molecular diagnosis of heterozygous FH. Achilles tendon maximum thickness (ATMT) was measured using ultrasonography with standardized equipment and procedures. Demographic variables and lipid profiles were collected. A multivariate linear regression model using a log-Gaussian approach was used to predict TX size. Classical cardiovascular risk factors and lipoprotein(a) were included as explanatory variables.
Results
The mean low-density lipoprotein cholesterol level was 277 mg/dL without lipid-lowering treatment, and the median ATMT was 5.50 mm. We demonstrated that age, sex, low-density lipoprotein cholesterol, and lipoprotein(a) were independently associated with ATMT. However, these 4 variables did not account for most the interindividual variability observed (R2 = 0.205).
Conclusions
TX, a characteristic hallmark of FH, exhibit heterogeneity in their presentation. Interindividual variability can partially be explained by age, male sex, low-density lipoprotein cholesterol, and lipoprotein(a) but these factors account for only 20% of this heterogeneity.
Full English text available from:www.revespcardiol.org/en
{"title":"Factores asociados a la presencia de xantomas tendinosos en la hipercolesterolemia familiar","authors":"Pablo Corredoira , Victoria Marco-Benedi , Ana Cenarro , Sonia Peribáñez , Salvador Olmos , Fernando Civeira","doi":"10.1016/j.recesp.2023.12.010","DOIUrl":"10.1016/j.recesp.2023.12.010","url":null,"abstract":"<div><h3>Introduction and objectives</h3><p>Tendon xanthomas (TX) are lipid deposits highly specific to familial hypercholesterolemia (FH). However, there is significant variability in their presentation among FH patients, primarily due to largely unknown causes. Lipoprotein(a) is a well-established independent risk factor for atherosclerotic cardiovascular disease in the general population as well as in FH. Given the wide variability of lipoprotein(a) among FH individuals and the likelihood that TX may result from a proatherogenic and proinflammatory condition, the objective of this study was to analyze the size of TX in the Achilles tendons of FH participants and the variables associated with their presence, including lipoprotein(a) concentration.</p></div><div><h3>Methods</h3><p>A cross-sectional study was conducted on 377 participants with a molecular diagnosis of heterozygous FH. Achilles tendon maximum thickness (ATMT) was measured using ultrasonography with standardized equipment and procedures. Demographic variables and lipid profiles were collected. A multivariate linear regression model using a log-Gaussian approach was used to predict TX size. Classical cardiovascular risk factors and lipoprotein(a) were included as explanatory variables.</p></div><div><h3>Results</h3><p>The mean low-density lipoprotein cholesterol level was 277<!--> <!-->mg/dL without lipid-lowering treatment, and the median ATMT was 5.50<!--> <!-->mm. We demonstrated that age, sex, low-density lipoprotein cholesterol, and lipoprotein(a) were independently associated with ATMT. However, these 4 variables did not account for most the interindividual variability observed (R<sup>2</sup> <!-->=<!--> <!-->0.205).</p></div><div><h3>Conclusions</h3><p>TX, a characteristic hallmark of FH, exhibit heterogeneity in their presentation. Interindividual variability can partially be explained by age, male sex, low-density lipoprotein cholesterol, and lipoprotein(a) but these factors account for only 20% of this heterogeneity.</p><p><em>Full English text available from</em>:<span>www.revespcardiol.org/en</span><svg><path></path></svg></p></div>","PeriodicalId":21299,"journal":{"name":"Revista espanola de cardiologia","volume":"77 6","pages":"Pages 462-470"},"PeriodicalIF":5.9,"publicationDate":"2024-02-22","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"140468618","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2024-02-22DOI: 10.1016/j.recesp.2023.10.021
Grupo de Trabajo de la SEC para la actualización 2023 de la guía ESC 2021 sobre el diagnóstico y tratamiento de la insuficiencia cardiaca aguda y crónica y Comité de Guías de la SEC
{"title":"Comentarios a la actualización 2023 de la guía ESC 2021 sobre el diagnóstico y tratamiento de la insuficiencia cardiaca aguda y crónica","authors":"Grupo de Trabajo de la SEC para la actualización 2023 de la guía ESC 2021 sobre el diagnóstico y tratamiento de la insuficiencia cardiaca aguda y crónica y Comité de Guías de la SEC","doi":"10.1016/j.recesp.2023.10.021","DOIUrl":"https://doi.org/10.1016/j.recesp.2023.10.021","url":null,"abstract":"","PeriodicalId":21299,"journal":{"name":"Revista espanola de cardiologia","volume":"77 4","pages":"Pages 281-284"},"PeriodicalIF":5.9,"publicationDate":"2024-02-22","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"140296363","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2024-02-19DOI: 10.1016/j.recesp.2023.11.016
Mihnea Casian , Ruxandra Jurcut
{"title":"Amiloidosis por transtirretina diagnosticada en pacientes con una miocardiopatía previa - oportunidades y preguntas abiertas","authors":"Mihnea Casian , Ruxandra Jurcut","doi":"10.1016/j.recesp.2023.11.016","DOIUrl":"10.1016/j.recesp.2023.11.016","url":null,"abstract":"","PeriodicalId":21299,"journal":{"name":"Revista espanola de cardiologia","volume":"77 6","pages":"Pages 504-505"},"PeriodicalIF":5.9,"publicationDate":"2024-02-19","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"140463027","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2024-02-19DOI: 10.1016/j.recesp.2023.11.012
M. Rosa Dalmau Llorca , Carina Aguilar Martín , Noèlia Carrasco-Querol , Zojaina Hernández Rojas , Dolores Rodríguez Cumplido , Elisabet Castro Blanco , Alessandra Queiroga Gonçalves , José Fernández-Sáez , Julián Pérez-Villacastín
Introduction and objectives
The management of atrial fibrillation is complex and requires improvement at strategic points, such as in the control of patients treated with vitamin K antagonists. The aim of this study was to evaluate the impact on health outcomes of a nonvalvular atrial fibrillation decision support tool based on visualization of the time in therapeutic range in primary care.
Methods
The present randomized clinical trial was conducted in 2018 with a 1-year follow-up in 325 primary care centers in Catalonia. In the intervention centers, the decision support tool was installed to control the time in therapeutic range of patients treated with vitamin K antagonists. The tool was not visualized in the control group.
Results
In total, 44 556 patients were studied. The intervention protected against admission for stroke (adjusted odds ratio [OR], 0.70; 95% confidence interval [95%CI], 0.55-0.88). The number needed to treat was 3502 (95%CI, 3305-3725) while the number of admissions for stroke avoided was 12.63 (95%CI, 11.88-13.38). The intervention also protected against mortality (adjusted OR, 0.78; 95%CI, 0.67-0.90), with a number needed to treat of 13 687 (95%CI, 10 789-18 714) and number of deaths avoided of 3.23 (95%CI, 2.36-4.10).
Conclusions
The decision support tool was associated with slight reductions in the numbers of admissions for ischemic stroke and mortality. Although the follow-up time was short and the effect of the intervention was small, the results are valuable and could improve implementation of the tool.
This clinical trial was registered with ClinicalTrials.gov (NCT03367325).
Full English text available from:www.revespcardiol.org/en
{"title":"Valor clínico de una herramienta de anticoagulación oral en fibrilación auricular no valvular en atención primaria. Ensayo clínico aleatorizado","authors":"M. Rosa Dalmau Llorca , Carina Aguilar Martín , Noèlia Carrasco-Querol , Zojaina Hernández Rojas , Dolores Rodríguez Cumplido , Elisabet Castro Blanco , Alessandra Queiroga Gonçalves , José Fernández-Sáez , Julián Pérez-Villacastín","doi":"10.1016/j.recesp.2023.11.012","DOIUrl":"10.1016/j.recesp.2023.11.012","url":null,"abstract":"<div><h3>Introduction and objectives</h3><p>The management of atrial fibrillation is complex and requires improvement at strategic points, such as in the control of patients treated with vitamin K antagonists. The aim of this study was to evaluate the impact on health outcomes of a nonvalvular atrial fibrillation decision support tool based on visualization of the time in therapeutic range in primary care.</p></div><div><h3>Methods</h3><p>The present randomized clinical trial was conducted in 2018 with a 1-year follow-up in 325 primary care centers in Catalonia. In the intervention centers, the decision support tool was installed to control the time in therapeutic range of patients treated with vitamin K antagonists. The tool was not visualized in the control group.</p></div><div><h3>Results</h3><p>In total, 44 556 patients were studied. The intervention protected against admission for stroke (adjusted odds ratio [OR], 0.70; 95% confidence interval [95%CI], 0.55-0.88). The number needed to treat was 3502 (95%CI, 3305-3725) while the number of admissions for stroke avoided was 12.63 (95%CI, 11.88-13.38). The intervention also protected against mortality (adjusted OR, 0.78; 95%CI, 0.67-0.90), with a number needed to treat of 13 687 (95%CI, 10 789-18 714) and number of deaths avoided of 3.23 (95%CI, 2.36-4.10).</p></div><div><h3>Conclusions</h3><p>The decision support tool was associated with slight reductions in the numbers of admissions for ischemic stroke and mortality. Although the follow-up time was short and the effect of the intervention was small, the results are valuable and could improve implementation of the tool.</p><p>This clinical trial was registered with ClinicalTrials.gov (<span>NCT03367325</span><svg><path></path></svg>).</p><p><em>Full English text available from</em>:<span>www.revespcardiol.org/en</span><svg><path></path></svg></p></div>","PeriodicalId":21299,"journal":{"name":"Revista espanola de cardiologia","volume":"77 6","pages":"Pages 471-480"},"PeriodicalIF":5.9,"publicationDate":"2024-02-19","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.sciencedirect.com/science/article/pii/S0300893223005201/pdfft?md5=5f1b5fe471da3d8adc093b02307efe88&pid=1-s2.0-S0300893223005201-main.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"139966095","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}