Iwona Gorczyca, Beata Uziębło-Życzkowska, Anna Szpotowicz, Magdalena Chrapek, Paweł Krzesiński, Bernadetta Bielecka, Agnieszka Woronowicz-Chróściel, Paweł Wałek, Małgorzata Krzciuk, Beata Wożakowska-Kapłon
Background: Current guidelines recommend electrical cardioversion (ECV) in patients with atrial fibrillation (AF) after at least 3 weeks of adequate non-vitamin K antagonist oral anticoagulant (NOAC) treatment without prior transesophageal echocardiography (TEE). However, in clinical practice in some centres, TEE is performed before ECV in patients with AF. The aim of the study was to evaluate prevalence of thromboembolic and hemorrhagic complications in patients with AF treated with NOACs and undergoing ECV without prior TEE.
Methods: This observational, multicentre study included consecutive patients with AF treated with NOACs who were admitted for ECV without prior TEE. Thromboembolic events and major bleeding complications were investigated during a 30-day follow-up.
Results: In the study group there were 611 patients, mean age was 66.3 ± 9.2 years, 40% were women. 52 (8.5%) patients had a low thromboembolic risk, 148 (24.2%) patients had an intermediate thromboembolic risk and 411 (67.2%) patients had a high thromboembolic risk. In the study group 253 (41.4%) patients were treated with rivaroxaban, 252 (41.2%) patients were treated with dabigatran and 106 (17.3%) patients were treated with apixaban. Reduced doses of NOACs were administered to 113 (18.9%) patients. In the entire study group, there were no thromboembolic events or major bleeding complications during the in-hospital stay and the 30-day follow-up.
Conclusions: In this "real-world" study of AF patients treated with NOACs, it was proved that ECV is safe without a preceding TEE, regardless of the risk of thromboembolic complications and of the type of NOAC used.
{"title":"Elective cardioversion of atrial fibrillation is safe without transesophageal echocardiography in patients treated with non-vitamin K antagonist oral anticoagulants: Multicenter experience.","authors":"Iwona Gorczyca, Beata Uziębło-Życzkowska, Anna Szpotowicz, Magdalena Chrapek, Paweł Krzesiński, Bernadetta Bielecka, Agnieszka Woronowicz-Chróściel, Paweł Wałek, Małgorzata Krzciuk, Beata Wożakowska-Kapłon","doi":"10.5603/CJ.a2021.0010","DOIUrl":"https://doi.org/10.5603/CJ.a2021.0010","url":null,"abstract":"<p><strong>Background: </strong>Current guidelines recommend electrical cardioversion (ECV) in patients with atrial fibrillation (AF) after at least 3 weeks of adequate non-vitamin K antagonist oral anticoagulant (NOAC) treatment without prior transesophageal echocardiography (TEE). However, in clinical practice in some centres, TEE is performed before ECV in patients with AF. The aim of the study was to evaluate prevalence of thromboembolic and hemorrhagic complications in patients with AF treated with NOACs and undergoing ECV without prior TEE.</p><p><strong>Methods: </strong>This observational, multicentre study included consecutive patients with AF treated with NOACs who were admitted for ECV without prior TEE. Thromboembolic events and major bleeding complications were investigated during a 30-day follow-up.</p><p><strong>Results: </strong>In the study group there were 611 patients, mean age was 66.3 ± 9.2 years, 40% were women. 52 (8.5%) patients had a low thromboembolic risk, 148 (24.2%) patients had an intermediate thromboembolic risk and 411 (67.2%) patients had a high thromboembolic risk. In the study group 253 (41.4%) patients were treated with rivaroxaban, 252 (41.2%) patients were treated with dabigatran and 106 (17.3%) patients were treated with apixaban. Reduced doses of NOACs were administered to 113 (18.9%) patients. In the entire study group, there were no thromboembolic events or major bleeding complications during the in-hospital stay and the 30-day follow-up.</p><p><strong>Conclusions: </strong>In this \"real-world\" study of AF patients treated with NOACs, it was proved that ECV is safe without a preceding TEE, regardless of the risk of thromboembolic complications and of the type of NOAC used.</p>","PeriodicalId":9492,"journal":{"name":"Cardiology journal","volume":"30 2","pages":"228-236"},"PeriodicalIF":2.9,"publicationDate":"2023-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://ftp.ncbi.nlm.nih.gov/pub/pmc/oa_pdf/9f/ca/cardj-30-2-228.PMC10129268.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"9401255","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Juan Luis Gutiérrez-Chico, Carlos Cortés, Niels Ramsing Holm, Evald Høj Christiansen, Maciej Lesiak, Bernward Lauer, Sylvia Otto, Francesco Lavarra, Viktor Sasi, Yiannis S Chatzizisis, Sudhir Rathore, Kambis Mashayekhi
Percutaneous coronary intervention (PCI) of chronic total occlusions (CTO) in coronary bifurcation lesions (CBL) is undergoing substantial technical progress and standardization, paralleling the evolution of dedicated devices, tools, and techniques. A standard consensus to classify CTO-CBL might be instrumental to homogenize data collection and description of procedures for scientific and educational purposes. The Medina-CTO classification replicates the classical three digits in Medina classification for bifurcations, representing the proximal main vessel, distal main vessel, and side branch, respectively. Each digit can take a value of 1 if it concerns atherosclerosis and is anatomically stenosed, or 0 if it is not. In addition, the occluded segment(s) of the bifurcation are noted by a subscript, which describes key interventional features of the cap: t (tapered), b (blunt), or a (ambiguous). This approach results in 56 basic categories that can be grouped by means of different elements, depending on the specific needs of each study. Medina-CTO classification, consisting of adding a subscript describing the basic cap characteristics to the totally occluded segment(s) of the standard Medina triplet, might be a useful methodological tool to standardize percutaneous intervention of bifurcational CTO lesions, with interesting scientific and educational applications.
{"title":"Anatomical classification of chronic total occlusions in coronary bifurcations.","authors":"Juan Luis Gutiérrez-Chico, Carlos Cortés, Niels Ramsing Holm, Evald Høj Christiansen, Maciej Lesiak, Bernward Lauer, Sylvia Otto, Francesco Lavarra, Viktor Sasi, Yiannis S Chatzizisis, Sudhir Rathore, Kambis Mashayekhi","doi":"10.5603/CJ.a2022.0115","DOIUrl":"https://doi.org/10.5603/CJ.a2022.0115","url":null,"abstract":"<p><p>Percutaneous coronary intervention (PCI) of chronic total occlusions (CTO) in coronary bifurcation lesions (CBL) is undergoing substantial technical progress and standardization, paralleling the evolution of dedicated devices, tools, and techniques. A standard consensus to classify CTO-CBL might be instrumental to homogenize data collection and description of procedures for scientific and educational purposes. The Medina-CTO classification replicates the classical three digits in Medina classification for bifurcations, representing the proximal main vessel, distal main vessel, and side branch, respectively. Each digit can take a value of 1 if it concerns atherosclerosis and is anatomically stenosed, or 0 if it is not. In addition, the occluded segment(s) of the bifurcation are noted by a subscript, which describes key interventional features of the cap: t (tapered), b (blunt), or a (ambiguous). This approach results in 56 basic categories that can be grouped by means of different elements, depending on the specific needs of each study. Medina-CTO classification, consisting of adding a subscript describing the basic cap characteristics to the totally occluded segment(s) of the standard Medina triplet, might be a useful methodological tool to standardize percutaneous intervention of bifurcational CTO lesions, with interesting scientific and educational applications.</p>","PeriodicalId":9492,"journal":{"name":"Cardiology journal","volume":"30 1","pages":"6-11"},"PeriodicalIF":2.9,"publicationDate":"2023-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://ftp.ncbi.nlm.nih.gov/pub/pmc/oa_pdf/59/8c/cardj-30-1-6.PMC9987547.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"9418590","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Jan-Erik Guelker, Christian Blockhaus, Alexander Bufe, Knut Kroeger, Julian Kürvers, Dimitrios Ilousis, Kambis Mashayekhi
Background: With the advent of novel recanalization techniques and emerging devices, percutaneous coronary intervention (PCI) has become a promising leading treatment option for patients with chronic total occlusions (CTO). The present study aims to evaluate the acute outcomes of PCI in previously failed re-attempted vs. first-attempted CTO-lesions.
Methods: Between 2012 and 2019, 619 patients were included and treated with PCI of at least one CTO. 253 patients were re-attempted lesions, while 366 were initially attempted lesions.
Results: Re-attempted lesions were more complex, including higher Japanese-CTO (J-CTO) score and the need for a retrograde approach. The procedure time and fluoroscopy time were longer in this group. Nevertheless, overall success rates were comparable between both groups of patients. In-hospital events were rare and without significant differences.
Conclusions: Re-attempted CTO lesions are more complex than first-attempt lesions and are associated with longer procedural times. However, they can be safely intervened by experienced operators with a similar success rate.
{"title":"In-hospital outcome of re-attempted percutaneous coronary interventions for chronic total occlusion.","authors":"Jan-Erik Guelker, Christian Blockhaus, Alexander Bufe, Knut Kroeger, Julian Kürvers, Dimitrios Ilousis, Kambis Mashayekhi","doi":"10.5603/CJ.a2021.0012","DOIUrl":"https://doi.org/10.5603/CJ.a2021.0012","url":null,"abstract":"<p><strong>Background: </strong>With the advent of novel recanalization techniques and emerging devices, percutaneous coronary intervention (PCI) has become a promising leading treatment option for patients with chronic total occlusions (CTO). The present study aims to evaluate the acute outcomes of PCI in previously failed re-attempted vs. first-attempted CTO-lesions.</p><p><strong>Methods: </strong>Between 2012 and 2019, 619 patients were included and treated with PCI of at least one CTO. 253 patients were re-attempted lesions, while 366 were initially attempted lesions.</p><p><strong>Results: </strong>Re-attempted lesions were more complex, including higher Japanese-CTO (J-CTO) score and the need for a retrograde approach. The procedure time and fluoroscopy time were longer in this group. Nevertheless, overall success rates were comparable between both groups of patients. In-hospital events were rare and without significant differences.</p><p><strong>Conclusions: </strong>Re-attempted CTO lesions are more complex than first-attempt lesions and are associated with longer procedural times. However, they can be safely intervened by experienced operators with a similar success rate.</p>","PeriodicalId":9492,"journal":{"name":"Cardiology journal","volume":"30 1","pages":"44-50"},"PeriodicalIF":2.9,"publicationDate":"2023-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://ftp.ncbi.nlm.nih.gov/pub/pmc/oa_pdf/8e/89/cardj-30-1-44.PMC9987543.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"10847027","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Yong Hoon Kim, Ae-Young Her, Scot Garg, Eun-Seok Shin
Background: Previous work has highlighted the importance of the neutrophil-to-lymphocyte ratio (NLR) and the difference in the ward-to-catheterization laboratory systolic blood pressure (ΔSBP) in prognostic stratification after acute coronary syndrome. However, there is paucity of data regarding the added value of combining these two variables to predict 5-year major clinical outcomes after percutaneous coronary intervention.
Methods: A total of 1188 patients were classified into four groups according to the NLR andΔSBP (high vs. low) using cutoffs derived from an analysis of receiver operating characteristic curves. A NLR > 3.0 and aΔSBP > 25 mmHg were considered high values. The primary endpoint was the composite of all-cause death, cardiac death, and non-fatal myocardial infarction. The secondary endpoint was the composite of target lesion revascularization, target vessel revascularization, and incidence of cerebrovascular accidents.
Results: The incidence of the primary endpoint was significantly higher in the high NLR and ΔSBP group than in the other three groups (2.2% vs. 4.7% vs. 4.3% vs. 13.2%, p < 0.001). The incidence of the secondary endpoint was similar among the four groups. Incorporation of high NLR and high ΔSBP into a model with conventional and meaningful clinical and procedural risk factors increased the C-statistics in predicting the primary endpoint (0.575 to 0.635, p = 0.002).
Conclusions: The power to predict the primary endpoint after drug-eluting stent implantation at the 5-year follow-up was improved by combining NLR and ΔSBP.
背景:先前的研究强调了中性粒细胞与淋巴细胞比值(NLR)和病房与导管实验室收缩压(ΔSBP)的差异在急性冠状动脉综合征后预后分层中的重要性。然而,关于结合这两个变量预测经皮冠状动脉介入治疗后5年主要临床结果的附加价值的数据缺乏。方法:共1188例患者根据NLR andΔSBP(高与低)分为四组,采用由受试者工作特征曲线分析得出的截止值。NLR > 3.0和aΔSBP > 25 mmHg被认为是高值。主要终点为全因死亡、心源性死亡和非致死性心肌梗死。次要终点是靶病变血运重建、靶血管血运重建和脑血管意外发生率的综合结果。结果:高NLR组和ΔSBP组的主要终点发生率显著高于其他三组(2.2% vs. 4.7% vs. 4.3% vs. 13.2%, p < 0.001)。次要终点的发生率在四组之间相似。将高NLR和高ΔSBP纳入具有常规和有意义的临床和程序危险因素的模型中,可提高预测主要终点的c统计量(0.575至0.635,p = 0.002)。结论:NLR和ΔSBP联合应用可提高5年随访时药物洗脱支架植入术后主要终点的预测能力。
{"title":"Incremental predictive value of the combined use of the neutrophil-to-lymphocyte ratio and systolic blood pressure difference after successful drug-eluting stent implantation.","authors":"Yong Hoon Kim, Ae-Young Her, Scot Garg, Eun-Seok Shin","doi":"10.5603/CJ.a2021.0004","DOIUrl":"https://doi.org/10.5603/CJ.a2021.0004","url":null,"abstract":"<p><strong>Background: </strong>Previous work has highlighted the importance of the neutrophil-to-lymphocyte ratio (NLR) and the difference in the ward-to-catheterization laboratory systolic blood pressure (ΔSBP) in prognostic stratification after acute coronary syndrome. However, there is paucity of data regarding the added value of combining these two variables to predict 5-year major clinical outcomes after percutaneous coronary intervention.</p><p><strong>Methods: </strong>A total of 1188 patients were classified into four groups according to the NLR andΔSBP (high vs. low) using cutoffs derived from an analysis of receiver operating characteristic curves. A NLR > 3.0 and aΔSBP > 25 mmHg were considered high values. The primary endpoint was the composite of all-cause death, cardiac death, and non-fatal myocardial infarction. The secondary endpoint was the composite of target lesion revascularization, target vessel revascularization, and incidence of cerebrovascular accidents.</p><p><strong>Results: </strong>The incidence of the primary endpoint was significantly higher in the high NLR and ΔSBP group than in the other three groups (2.2% vs. 4.7% vs. 4.3% vs. 13.2%, p < 0.001). The incidence of the secondary endpoint was similar among the four groups. Incorporation of high NLR and high ΔSBP into a model with conventional and meaningful clinical and procedural risk factors increased the C-statistics in predicting the primary endpoint (0.575 to 0.635, p = 0.002).</p><p><strong>Conclusions: </strong>The power to predict the primary endpoint after drug-eluting stent implantation at the 5-year follow-up was improved by combining NLR and ΔSBP.</p>","PeriodicalId":9492,"journal":{"name":"Cardiology journal","volume":"30 1","pages":"91-104"},"PeriodicalIF":2.9,"publicationDate":"2023-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://ftp.ncbi.nlm.nih.gov/pub/pmc/oa_pdf/e1/0b/cardj-30-1-91.PMC9987556.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"10850976","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Damian Hudziak, Radosław Targoński, Wojciech Wańha, Radosław Gocoł, Adrianna Hajder, Radosław Parma, Tomasz Figatowski, Tomasz Darocha, Marek A Deja, Wojciech Wojakowski, Dariusz Jagielak
Background: The purpose of this study was to compare the safety and clinical outcomes of transcarotid (TC) and transapical access (TA) transcatheter aortic valve implantation (TAVI) patients whom the transfemoral approach (TF) was not feasible.
Methods: The analysis included consecutive patients with severe symptomatic aortic stenosis treated from 2017 to 2020 with TC-TAVI or TA-TAVI in two high-volume TAVI centers. The approach was selected by multidisciplinary heart teams after analyzing multislice computed tomography of the heart, aorta and peripheral arteries, transthoracic echocardiography and coronary angiography.
Results: One hundred and two patients were treated with alternative TAVI accesses (TC; n = 49 and TA; n = 53) in our centers. The groups were similar regarding age, gender, New York Heart Association class, and echocardiography parameters. Patients treated with TC-TAVI had significantly higher surgical risk. The procedural success rate was similar in both groups (TC-TAVI 98%; TA-TAVI 98.1%; p = 0.95). The rate of Valve Academic Research Consortium-2 defined clinical events was low in both groups. The percentage of new-onset rhythm disturbances and permanent pacemaker implantation was similar in TC and TA TAVI (4.1% vs. 11.3%; p = 0.17 and 10.2% vs. 5.7%; p = 0.39, respectively). In the TA-TAVI group, significantly more cases of pneumonia and blood transfusions were observed (11% vs. 0%; p = 0.01 and 30.2% vs. 12.2%; p = 0.03). The 30-day mortality was similar in TC and TA groups (4.1% vs. 5.7%; p = 0.71, respectively).
Conclusions: Both TC and TA TAVI are safe procedures in appropriately selected patients and are associated with a low risk of complications.
背景:本研究的目的是比较经颈动脉(TC)和经根尖通道(TA)经导管主动脉瓣植入术(TAVI)的安全性和临床结果,经股动脉入路(TF)是不可行的。方法:纳入2017年至2020年在两个大容量TAVI中心连续接受TC-TAVI或TA-TAVI治疗的严重症状性主动脉瓣狭窄患者。该方法是由多学科心脏团队在分析心脏、主动脉和外周动脉的多层计算机断层扫描、经胸超声心动图和冠状动脉造影后选择的。结果:102例患者采用TAVI替代通路(TC;n = 49, TA;N = 53)。各组在年龄、性别、纽约心脏协会分类和超声心动图参数方面相似。接受TC-TAVI治疗的患者手术风险明显较高。两组手术成功率相似(TC-TAVI 98%;TA-TAVI 98.1%;P = 0.95)。瓣膜学术研究协会-2定义的临床事件发生率在两组中均较低。TC组和TA组新发心律失常和永久起搏器植入的比例相似(4.1% vs. 11.3%;P = 0.17和10.2% vs. 5.7%;P = 0.39)。在TA-TAVI组中,观察到的肺炎和输血病例明显更多(11% vs 0%;P = 0.01, 30.2% vs. 12.2%;P = 0.03)。TC组和TA组的30天死亡率相似(4.1% vs. 5.7%;P = 0.71)。结论:在适当选择的患者中,TC和TA TAVI都是安全的手术,且并发症风险较低。
{"title":"Comparison of transcarotid versus transapical transcatheter aortic valve implantation outcomes in patients with severe aortic stenosis and contraindications for transfemoral access.","authors":"Damian Hudziak, Radosław Targoński, Wojciech Wańha, Radosław Gocoł, Adrianna Hajder, Radosław Parma, Tomasz Figatowski, Tomasz Darocha, Marek A Deja, Wojciech Wojakowski, Dariusz Jagielak","doi":"10.5603/CJ.a2021.0071","DOIUrl":"https://doi.org/10.5603/CJ.a2021.0071","url":null,"abstract":"<p><strong>Background: </strong>The purpose of this study was to compare the safety and clinical outcomes of transcarotid (TC) and transapical access (TA) transcatheter aortic valve implantation (TAVI) patients whom the transfemoral approach (TF) was not feasible.</p><p><strong>Methods: </strong>The analysis included consecutive patients with severe symptomatic aortic stenosis treated from 2017 to 2020 with TC-TAVI or TA-TAVI in two high-volume TAVI centers. The approach was selected by multidisciplinary heart teams after analyzing multislice computed tomography of the heart, aorta and peripheral arteries, transthoracic echocardiography and coronary angiography.</p><p><strong>Results: </strong>One hundred and two patients were treated with alternative TAVI accesses (TC; n = 49 and TA; n = 53) in our centers. The groups were similar regarding age, gender, New York Heart Association class, and echocardiography parameters. Patients treated with TC-TAVI had significantly higher surgical risk. The procedural success rate was similar in both groups (TC-TAVI 98%; TA-TAVI 98.1%; p = 0.95). The rate of Valve Academic Research Consortium-2 defined clinical events was low in both groups. The percentage of new-onset rhythm disturbances and permanent pacemaker implantation was similar in TC and TA TAVI (4.1% vs. 11.3%; p = 0.17 and 10.2% vs. 5.7%; p = 0.39, respectively). In the TA-TAVI group, significantly more cases of pneumonia and blood transfusions were observed (11% vs. 0%; p = 0.01 and 30.2% vs. 12.2%; p = 0.03). The 30-day mortality was similar in TC and TA groups (4.1% vs. 5.7%; p = 0.71, respectively).</p><p><strong>Conclusions: </strong>Both TC and TA TAVI are safe procedures in appropriately selected patients and are associated with a low risk of complications.</p>","PeriodicalId":9492,"journal":{"name":"Cardiology journal","volume":"30 2","pages":"188-195"},"PeriodicalIF":2.9,"publicationDate":"2023-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://ftp.ncbi.nlm.nih.gov/pub/pmc/oa_pdf/4f/93/cardj-30-2-188.PMC10129253.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"9400955","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Markus Jäckel, Simon Keller, Eric Peter Prager, Dawid Leander Staudacher, Christopher Schlett, Manfred Zehender, Fabian Bamberg, Christoph Bode, Constantin von Zur Mühlen, Peter Stachon
Background: Severe aortic valve stenosis inhibits renal perfusion, thereby potentially worsening renal function, in particular in elderly patients most often assigned to transcatheter aortic valve implantation (TAVI). Pre-TAVI diagnostics and the procedure itself may adversely impact renal function, however renal perfusion and function may also improve post-procedure. This study aimed to clarify the impact of TAVI planning and procedure on kidney function METHODS: In this retrospective study, kidney function of patients who underwent transfemoral TAVI at a tertiary university hospital between 2016 and 2019 was analyzed. The present study investigated kidney function at baseline, after computed tomography (CT) was performed for evaluation of TAVI, after TAVI, at discharge and at follow-up.
Results: Among 366 patients, the prevalence of acute kidney injury (AKI) was 14.5% after TAVI. Independent predictors of AKI were arterial hypertension, baseline creatinine, AKI post CT and coronary intervention during pre-procedural diagnostics. At discharge and follow-up, 2.1% and 3.4%, respectively had sustained relevant impairment of kidney function (defined as creatinine/baseline creatinine > 1.5 or renal replacement therapy). Patients with known chronic kidney disease showed no higher rates of short- and long-term impairment, but higher rates of improvement of renal function after TAVI.
Conclusions: In most cases TAVI does not worsen renal function. A sustained impairment after TAVI was found in only a few cases. This was independent of reduced baseline kidney function. Transfemoral TAVI can thus be planned and performed even in patients with higher stages of chronic kidney disease.
{"title":"The impact of transcatheter aortic valve implantation planning and procedure on acute and chronic renal failure.","authors":"Markus Jäckel, Simon Keller, Eric Peter Prager, Dawid Leander Staudacher, Christopher Schlett, Manfred Zehender, Fabian Bamberg, Christoph Bode, Constantin von Zur Mühlen, Peter Stachon","doi":"10.5603/CJ.a2021.0057","DOIUrl":"https://doi.org/10.5603/CJ.a2021.0057","url":null,"abstract":"<p><strong>Background: </strong>Severe aortic valve stenosis inhibits renal perfusion, thereby potentially worsening renal function, in particular in elderly patients most often assigned to transcatheter aortic valve implantation (TAVI). Pre-TAVI diagnostics and the procedure itself may adversely impact renal function, however renal perfusion and function may also improve post-procedure. This study aimed to clarify the impact of TAVI planning and procedure on kidney function METHODS: In this retrospective study, kidney function of patients who underwent transfemoral TAVI at a tertiary university hospital between 2016 and 2019 was analyzed. The present study investigated kidney function at baseline, after computed tomography (CT) was performed for evaluation of TAVI, after TAVI, at discharge and at follow-up.</p><p><strong>Results: </strong>Among 366 patients, the prevalence of acute kidney injury (AKI) was 14.5% after TAVI. Independent predictors of AKI were arterial hypertension, baseline creatinine, AKI post CT and coronary intervention during pre-procedural diagnostics. At discharge and follow-up, 2.1% and 3.4%, respectively had sustained relevant impairment of kidney function (defined as creatinine/baseline creatinine > 1.5 or renal replacement therapy). Patients with known chronic kidney disease showed no higher rates of short- and long-term impairment, but higher rates of improvement of renal function after TAVI.</p><p><strong>Conclusions: </strong>In most cases TAVI does not worsen renal function. A sustained impairment after TAVI was found in only a few cases. This was independent of reduced baseline kidney function. Transfemoral TAVI can thus be planned and performed even in patients with higher stages of chronic kidney disease.</p>","PeriodicalId":9492,"journal":{"name":"Cardiology journal","volume":"30 2","pages":"247-255"},"PeriodicalIF":2.9,"publicationDate":"2023-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://ftp.ncbi.nlm.nih.gov/pub/pmc/oa_pdf/16/50/cardj-30-2-247.PMC10129259.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"9407261","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2023-01-01Epub Date: 2022-08-01DOI: 10.5603/CJ.a2022.0071
Yan Han, Xiaohang Yuan, Xin Hu, Yan Fang, Mengting Jiang, Huanhuan Feng, Lei Gao
Background: To date, it has not been ascertained whether shortening the duration of dual antiplatelet therapy (DAPT) can benefit high bleeding risk (HBR) patients. This systematic review and meta-analysis was performed to investigate the safety and efficacy of short (≤ 3 months) DAPT in HBR patients after percutaneous coronary intervention (PCI).
Methods: The PubMed, Embase, and Clinical Trials databases were searched from inception until November 2021 to identify studies that evaluated the safety and efficacy of short DAPT in HBR patients implanted with new-generation drug-eluting stents (DES). Primary endpoints included major bleeding, definite or probable stent thrombosis (ST), and myocardial infarction (MI), while secondary endpoints included all-cause death and ischemic stroke. Based on the fixed and random effect model, the risk ratio (RR) and 95% confidence interval of each endpoint were measured.
Results: Five observational studies and one randomized controlled trial were included, involving 15,432 HBR patients. Short DAPT for HBR patients undergoing PCI had a lower incidence of major bleeding in comparison with standard (> 3 months) DAPT (2.3% vs. 3.2%, RR 0.64 [0.44, 0.95], p = 0.03), while short DAPT was comparable to standard DAPT with regard to definite or probable ST (0.4% vs. 0.3%, RR 1.31 [0.77, 2.23], p = 0.32) and MI (2.4% vs. 2.0%, RR 1.17 [0.95, 1.45], p = 0.14).
Conclusions: Among HBR patients implanted with new-generation DES, short DAPT was associated with reduced risk of major bleeding without significantly increasing the risk of definite or probable ST and MI in comparison with standard DAPT.
{"title":"Dual antiplatelet therapy after percutaneous coronary intervention in patients at high bleeding risk: A systematic review and meta-analysis.","authors":"Yan Han, Xiaohang Yuan, Xin Hu, Yan Fang, Mengting Jiang, Huanhuan Feng, Lei Gao","doi":"10.5603/CJ.a2022.0071","DOIUrl":"10.5603/CJ.a2022.0071","url":null,"abstract":"<p><strong>Background: </strong>To date, it has not been ascertained whether shortening the duration of dual antiplatelet therapy (DAPT) can benefit high bleeding risk (HBR) patients. This systematic review and meta-analysis was performed to investigate the safety and efficacy of short (≤ 3 months) DAPT in HBR patients after percutaneous coronary intervention (PCI).</p><p><strong>Methods: </strong>The PubMed, Embase, and Clinical Trials databases were searched from inception until November 2021 to identify studies that evaluated the safety and efficacy of short DAPT in HBR patients implanted with new-generation drug-eluting stents (DES). Primary endpoints included major bleeding, definite or probable stent thrombosis (ST), and myocardial infarction (MI), while secondary endpoints included all-cause death and ischemic stroke. Based on the fixed and random effect model, the risk ratio (RR) and 95% confidence interval of each endpoint were measured.</p><p><strong>Results: </strong>Five observational studies and one randomized controlled trial were included, involving 15,432 HBR patients. Short DAPT for HBR patients undergoing PCI had a lower incidence of major bleeding in comparison with standard (> 3 months) DAPT (2.3% vs. 3.2%, RR 0.64 [0.44, 0.95], p = 0.03), while short DAPT was comparable to standard DAPT with regard to definite or probable ST (0.4% vs. 0.3%, RR 1.31 [0.77, 2.23], p = 0.32) and MI (2.4% vs. 2.0%, RR 1.17 [0.95, 1.45], p = 0.14).</p><p><strong>Conclusions: </strong>Among HBR patients implanted with new-generation DES, short DAPT was associated with reduced risk of major bleeding without significantly increasing the risk of definite or probable ST and MI in comparison with standard DAPT.</p>","PeriodicalId":9492,"journal":{"name":"Cardiology journal","volume":"30 4","pages":"556-566"},"PeriodicalIF":2.9,"publicationDate":"2023-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://ftp.ncbi.nlm.nih.gov/pub/pmc/oa_pdf/6e/73/cardj-30-4-556.PMC10508065.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"10572657","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Eun-Seok Shin, Eun Jung Jun, Jung-Kyu Han, Min Gyu Kong, Jeehoon Kang, Chengbin Zheng, Scot Garg, Young Jin Choi, Jang-Whan Bae, Kook-Jin Chun, Doo-Il Kim, Seung-Woon Rha, Sung Yun Lee, Jay Young Rhew, Seong-Ill Woo, Han Cheol Lee, Jin-Ok Jeong, Han-Mo Yang, Kyung Woo Park, Hyun-Jae Kang, Bon-Kwon Koo, In-Ho Chae, Hyo-Soo Kim
Background: The contribution of sex and initial clinical presentation to the long-term outcomes in patients undergoing percutaneous coronary intervention (PCI) is still debated.
Methods: Individual patient data from 5 Korean-multicenter drug-eluting stent (DES) registries (The GRAND-DES) were pooled. A total of 17,286 patients completed 3-year follow-up (5216 women and 12,070 men). The median follow-up duration was 1125 days (interquartile range 1097-1140 days), and the primary endpoint was cardiac death at 3 years.
Results: The clinical indication for PCI was stable angina pectoris (SAP) in 36.8%, unstable angina pectoris (UAP) or non-ST-segment elevation myocardial infarction (NSTEMI) in 47.4%, and ST-segment elevation myocardial (STEMI) in 15.8%. In all groups, women were older and had a higher proportion of hypertension and diabetes mellitus compared with men. Women presenting with STEMI were older than women with SAP, with the opposite seen in men. There was no sex difference in cardiac death for SAP or UAP/NSTEMI. In STEMI patients, the incidence of cardiac death (7.9% vs. 4.4%, p = 0.001), all-cause mortality (11.1% vs. 6.9%, p = 0.001), and minor bleeding (2.2% vs. 1.2%, p = 0.043) was significantly higher in women. After multivariable adjustment, cardiac death was lower in women for UAP/NSTEMI (HR 0.69, 95% CI 0.53-0.89, p = 0.005), while it was similar for STEMI (HR 0.97, 95% CI 0.65-1.44, p = 0.884).
Conclusions: There was no sex difference in cardiac death after PCI with DES for SAP and UAP/NSTEMI patients. In STEMI patients, women had worse outcomes compared with men; however, after the adjustment of confounders, female sex was not an independent predictor of mortality.
背景:性别和初始临床表现对经皮冠状动脉介入治疗(PCI)患者长期预后的影响仍有争议。方法:对来自5个韩国多中心药物洗脱支架(DES)注册中心(GRAND-DES)的个体患者数据进行汇总。共有17286名患者完成了为期3年的随访(5216名女性和12070名男性)。中位随访时间为1125天(四分位数间距1097-1140天),主要终点为3年时心脏性死亡。结果:PCI的临床指征为稳定性心绞痛(SAP)占36.8%,不稳定性心绞痛(UAP)或非st段抬高型心肌梗死(NSTEMI)占47.4%,st段抬高型心肌(STEMI)占15.8%。在所有组中,女性年龄较大,患高血压和糖尿病的比例高于男性。患有STEMI的女性比患有SAP的女性年龄大,而男性则相反。SAP或UAP/NSTEMI的心脏死亡没有性别差异。在STEMI患者中,女性心脏死亡(7.9% vs. 4.4%, p = 0.001)、全因死亡率(11.1% vs. 6.9%, p = 0.001)和轻微出血(2.2% vs. 1.2%, p = 0.043)的发生率明显更高。多变量调整后,UAP/NSTEMI患者的心脏死亡率较低(HR 0.69, 95% CI 0.53-0.89, p = 0.005),而STEMI患者的心脏死亡率相似(HR 0.97, 95% CI 0.65-1.44, p = 0.884)。结论:SAP和UAP/NSTEMI患者PCI合并DES后心脏死亡无性别差异。在STEMI患者中,女性的预后比男性差;然而,在调整混杂因素后,女性性别并不是死亡率的独立预测因子。
{"title":"Sex-related impact on clinical outcomes of patients treated with drug-eluting stents according to clinical presentation: Patient-level pooled analysis from the GRAND-DES registry.","authors":"Eun-Seok Shin, Eun Jung Jun, Jung-Kyu Han, Min Gyu Kong, Jeehoon Kang, Chengbin Zheng, Scot Garg, Young Jin Choi, Jang-Whan Bae, Kook-Jin Chun, Doo-Il Kim, Seung-Woon Rha, Sung Yun Lee, Jay Young Rhew, Seong-Ill Woo, Han Cheol Lee, Jin-Ok Jeong, Han-Mo Yang, Kyung Woo Park, Hyun-Jae Kang, Bon-Kwon Koo, In-Ho Chae, Hyo-Soo Kim","doi":"10.5603/CJ.a2021.0008","DOIUrl":"https://doi.org/10.5603/CJ.a2021.0008","url":null,"abstract":"<p><strong>Background: </strong>The contribution of sex and initial clinical presentation to the long-term outcomes in patients undergoing percutaneous coronary intervention (PCI) is still debated.</p><p><strong>Methods: </strong>Individual patient data from 5 Korean-multicenter drug-eluting stent (DES) registries (The GRAND-DES) were pooled. A total of 17,286 patients completed 3-year follow-up (5216 women and 12,070 men). The median follow-up duration was 1125 days (interquartile range 1097-1140 days), and the primary endpoint was cardiac death at 3 years.</p><p><strong>Results: </strong>The clinical indication for PCI was stable angina pectoris (SAP) in 36.8%, unstable angina pectoris (UAP) or non-ST-segment elevation myocardial infarction (NSTEMI) in 47.4%, and ST-segment elevation myocardial (STEMI) in 15.8%. In all groups, women were older and had a higher proportion of hypertension and diabetes mellitus compared with men. Women presenting with STEMI were older than women with SAP, with the opposite seen in men. There was no sex difference in cardiac death for SAP or UAP/NSTEMI. In STEMI patients, the incidence of cardiac death (7.9% vs. 4.4%, p = 0.001), all-cause mortality (11.1% vs. 6.9%, p = 0.001), and minor bleeding (2.2% vs. 1.2%, p = 0.043) was significantly higher in women. After multivariable adjustment, cardiac death was lower in women for UAP/NSTEMI (HR 0.69, 95% CI 0.53-0.89, p = 0.005), while it was similar for STEMI (HR 0.97, 95% CI 0.65-1.44, p = 0.884).</p><p><strong>Conclusions: </strong>There was no sex difference in cardiac death after PCI with DES for SAP and UAP/NSTEMI patients. In STEMI patients, women had worse outcomes compared with men; however, after the adjustment of confounders, female sex was not an independent predictor of mortality.</p>","PeriodicalId":9492,"journal":{"name":"Cardiology journal","volume":"30 1","pages":"105-116"},"PeriodicalIF":2.9,"publicationDate":"2023-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://ftp.ncbi.nlm.nih.gov/pub/pmc/oa_pdf/58/8e/cardj-30-1-105.PMC9987552.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"10847028","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}