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Clinical Decision Pathway for the Use of Fondaparinux in the Management of Acute Coronary Syndrome (ACS) in Hospitals with and Without Catheter Laboratories: An Expert Opinion from India. 在有和没有导管实验室的医院中使用Fondaparinux管理急性冠脉综合征(ACS)的临床决策途径:来自印度的专家意见。
IF 3.4 Q2 CARDIAC & CARDIOVASCULAR SYSTEMS Pub Date : 2023-06-01 DOI: 10.1007/s40119-023-00312-x
Saumitra Ray, Bharat Shivdasani, Jagdish Chander Mohan, V T Shah, Jagdish Hiremath, Rajiv Karnik, Bhupen Desai, Hemant Madan, Rajeev Garg, Johann Christopher

The current recommendations by Indian experts who are focused on the challenges in the management of patients with acute coronary syndrome (ACS) in rural areas, due to limited catheterization (CATH) lab facilities and interventional cardiologist coverage across the country, are described. 120 cardiologist experts drafted recommendations during ten advisory board meetings conducted from April to May 2022. Experts framed statements based on experience, collective clinical judgment from practical experience, and available scientific evidence regarding ACS. The consensus positioned fondaparinux as highly useful in non-CATH-lab-based hospitals for patients diagnosed with non-ST elevation acute coronary syndrome (NSTE-ACS) and ST elevation acute coronary syndrome (STE-ACS) patients who cannot be shifted to percutaneous coronary intervention (PCI)-capable centres, or for patients who are thrombolysed at peripheral centres.

由于全国范围内导管(CATH)实验室设施和介入心脏病专家覆盖范围有限,印度专家目前的建议主要集中在农村地区急性冠脉综合征(ACS)患者管理方面的挑战。在2022年4月至5月举行的10次咨询委员会会议上,120名心脏病专家起草了建议。专家们根据经验、来自实践经验的集体临床判断和有关ACS的现有科学证据制定了声明。共识是fondaparinux在非cat -实验室医院非常有用,用于诊断为非ST段抬高急性冠脉综合征(NSTE-ACS)和ST段抬高急性冠脉综合征(STE-ACS)的患者,这些患者不能转移到经皮冠状动脉介入治疗(PCI)中心,或在周围中心溶栓的患者。
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引用次数: 0
Effect of Obesity Duration and BMI Trajectories on Cardiovascular Disease: A Narrative Review. 肥胖持续时间和BMI轨迹对心血管疾病的影响:一项叙述性综述
IF 3.4 Q2 CARDIAC & CARDIOVASCULAR SYSTEMS Pub Date : 2023-06-01 DOI: 10.1007/s40119-023-00317-6
Reza Amani-Beni, Bahar Darouei, Hamidreza Zefreh, Erfan Sheikhbahaei, Masoumeh Sadeghi

Obesity is an important risk factor for cardiovascular diseases (CVDs). It is crucial to understand the impact of its duration due to the more extended exposure period and the higher frequency of overweight/obesity at younger ages. In the last decade, various studies have discovered that the duration of obesity, in addition to its severity, might have an impact. Therefore, this study aimed to summarize the current literature to investigate the effect of body mass index (BMI) trajectories and overweight/obesity duration on cardiovascular outcomes. To retrieve related articles, we searched PubMed, EMBASE, Google Scholar, Web of Science, Scopus, and Cochrane electronic databases. The duration of overweight/obesity is significantly associated with CVDs, especially heart failure and atrial fibrillation. However, there are contradictory results regarding the association between coronary heart disease and stroke with the duration of obesity. Additionally, no association with peripheral vascular disease has yet to be reported. The absence of this association may be brought on by covariates or various follow-up times. Nevertheless, it seems that both stable overweight and remarkably stable obesity increase the risk of CVDs, as does both stable overweight and notably stable obesity. Metrics showing both the severity and the duration of overweight/obesity are more effective than each alone, and it is recommended to be used for assessing the risk of various CVDs. There are few studies in these areas, and studies with more extended follow-up periods, with a wide age range, while adjusting for some specific covariates, are needed.

肥胖是心血管疾病的重要危险因素。至关重要的是要了解其持续时间的影响,因为接触时间越长,超重/肥胖的频率越高。在过去的十年里,各种各样的研究发现,除了肥胖的严重程度之外,持续的时间可能也会产生影响。因此,本研究旨在总结现有文献,探讨体重指数(BMI)轨迹和超重/肥胖持续时间对心血管结局的影响。为了检索相关文章,我们检索了PubMed、EMBASE、Google Scholar、Web of Science、Scopus和Cochrane电子数据库。超重/肥胖的持续时间与心血管疾病,特别是心力衰竭和心房纤颤显著相关。然而,关于冠心病和中风与肥胖持续时间之间的关系,有相互矛盾的结果。此外,未见与周围血管疾病相关的报道。这种关联的缺失可能是由协变量或各种随访时间引起的。然而,稳定的超重和非常稳定的肥胖似乎都增加了心血管疾病的风险,稳定的超重和明显稳定的肥胖也是如此。显示超重/肥胖严重程度和持续时间的指标比单独使用更有效,建议用于评估各种心血管疾病的风险。在这些领域的研究很少,需要更长的随访期,更大的年龄范围,同时调整一些特定协变量的研究。
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引用次数: 0
Impact of Intraprocedural Pressure Changes on Hemodynamic Outcome During Self-Expanding TAVR. 术中压力变化对自扩张TAVR血流动力学结果的影响。
IF 3.4 Q2 CARDIAC & CARDIOVASCULAR SYSTEMS Pub Date : 2023-06-01 DOI: 10.1007/s40119-023-00307-8
Jouni Pykäri, Tuija Vasankari, Antti Ylitalo, Pekka Porela, Tuomas Paana, Markus Malmberg, Sanna Laurila, Juho Koskinen, Tero Koivisto, Mikko Savontaus

Introduction: During the transcatheter aortic valve replacement (TAVR) procedure, hemodynamic measurements can be used to evaluate transcatheter heart valve (THV) performance. We hypothesized that the occurrence of a significant decrease in invasive aortic pressure immediately after annular contact by a self-expanding THV indicates effective annular sealing. This phenomenon could thus be used as a marker for the occurrence of paravalvular leak (PVL).

Methods: Thirty-eight patients undergoing TAVR procedure with a self-expandable Evolut R or Evolut Pro (Medtronic) valve prosthesis were included in the study. Drop in aortic pressure during valve expansion was defined as a decrease in systolic pressure of 30 mmHg immediately after annular contact. The primary endpoint was the occurrence of more than mild PVL immediately after valve implantation.

Results: A pressure drop was seen in 60.5% (23/38) of patients. More than mild PVL requiring balloon post-dilatation (BPD) was significantly more frequent in patients who did not have a systolic pressure decrease > 30 mmHg during valve implantation (46.7% [7/15] vs. 13.0% [3/23], respectively; p = 0.03). Patients without a systolic pressure decrease > 30 mmHg also had a lower mean cover index on computed tomography analysis (16.2% vs. 13.3%; p = 0.016). The 30-day outcomes were similar between the two groups, and echocardiography at 30 days demonstrated more than none/trace PVL in 21.1% (8/38) of patients, with no difference between the two groups.

Conclusion: A decrease in aortic pressure after annular contact is associated with an increased probability of good hemodynamic outcome after self-expanding TAVR implantation. In addition to other methods, this parameter could be used as an additional marker for optimal valve positioning and hemodynamic outcome during the implantation procedure.

在经导管主动脉瓣置换术(TAVR)过程中,血流动力学测量可用于评估经导管心脏瓣膜(THV)的性能。我们假设,自扩式THV接触环后,有创主动脉压立即显著降低,表明环密封有效。因此,这种现象可以作为发生瓣旁漏(PVL)的标志。方法:38例采用自膨胀Evolut R或Evolut Pro(美敦力)瓣膜假体行TAVR手术的患者为研究对象。瓣膜扩张期间主动脉压下降的定义是在环接触后立即收缩压下降30 mmHg。主要终点是瓣膜植入后立即出现轻度以上的PVL。结果:60.5%(23/38)患者出现血压下降。在瓣膜植入期间收缩压下降不> 30 mmHg的患者中,需要球囊扩张(BPD)的轻度以上PVL更为常见(分别为46.7%[7/15]和13.0% [3/23];p = 0.03)。收缩压降低不大于30 mmHg的患者在计算机断层扫描分析中的平均覆盖指数也较低(16.2% vs 13.3%;p = 0.016)。两组30天的结果相似,30天的超声心动图显示21.1%(8/38)的患者超过无/微量PVL,两组之间无差异。结论:自扩式TAVR植入后,环形接触后主动脉压降低与良好血流动力学结果的可能性增加有关。除其他方法外,该参数可作为植入过程中最佳瓣膜定位和血流动力学结果的附加标记。
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引用次数: 0
TAVI in Patient Suffering from Niemann-Pick Disease (Acid Sphingomyelinase Deficiency) with Concomitant Situs Inversus and Dextrocardia. 尼曼-匹克病(酸性鞘磷脂酶缺乏症)并发倒位和右心的TAVI。
IF 3.4 Q2 CARDIAC & CARDIOVASCULAR SYSTEMS Pub Date : 2023-06-01 DOI: 10.1007/s40119-023-00308-7
Daniele De Feo, Anna D'Anzi, Vincenzo Pestrichella, Pietro Scicchitano, Carlo Lafranceschina, Vito Caragnano, Fabio Tiecco, Antonella Scialpi, Giuliana Laronga, Marco Matteo Ciccone, Sabino Iliceto

Acid sphingomyelinase deficiency (ASMD)-also known as Niemann-Pick (NP) disease-is a rare, autosomal recessive disorder which is characterized by deficiency of the lysosomal enzyme acid sphingomyelinase (ASM), resulting in excessive storage of lipids in organs (i.e., spleen, liver, lung, bone marrow, lymph nodes, and vascular system). Only a few cases of moderate-to-severe valvular heart disease due to ASMD are described in the literature, mostly in adulthood. We report here the case of a patient with NP disease subtype B that was diagnosed during adulthood. NP disease in this patient was found to be associated with situs inversus. Specifically, a severe, symptomatic aortic stenosis was identified, and the need for surgical or percutaneous intervention was discussed. The heart team chose transcatheter aortic valvular implantation (TAVI), which was successfully performed with no complications on follow-up.

酸性鞘磷脂酶缺乏症(ASMD),也被称为尼曼-匹克病(NP),是一种罕见的常染色体隐性遗传病,其特征是溶酶体酶酸性鞘磷脂酶(ASM)缺乏,导致脂质在器官(即脾、肝、肺、骨髓、淋巴结和血管系统)中过度储存。文献中仅描述了少数由ASMD引起的中度至重度瓣膜性心脏病病例,主要发生在成年期。我们在此报告一例在成年期被诊断为NP病B亚型的患者。发现该患者的NP疾病与倒位有关。具体来说,一个严重的,有症状的主动脉狭窄被确定,并需要手术或经皮介入讨论。心脏科选择经导管主动脉瓣植入术(TAVI),手术成功,随访无并发症。
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引用次数: 0
Efficacy and Safety of Evolocumab in Chinese Patients with Primary Hypercholesterolemia and Mixed Dyslipidemia: 12-Week Primary Results of the HUA TUO Randomized Clinical Trial. Evolocumab在中国原发性高胆固醇血症和混合性血脂异常患者中的疗效和安全性:华拓随机临床试验的12周初步结果
IF 3.4 Q2 CARDIAC & CARDIOVASCULAR SYSTEMS Pub Date : 2023-06-01 DOI: 10.1007/s40119-023-00304-x
Hong Tan, Weimin Li, Zhouqing Huang, Yajun Han, Xuecheng Huang, Dongye Li, Xiaochun Xing, Maria Laura Monsalvo, You Wu, Jackie Mao, Lily Xin, Jiyan Chen

Introduction: Evolocumab, a fully human proprotein convertase/subtilisin kexin type 9 inhibitor antibody, significantly lowers low-density lipoprotein cholesterol (LDL-C) in patients with type 2 diabetes mellitus and hyperlipidemia and mixed dyslipidemia. This 12-week study evaluated the efficacy and safety of evolocumab in Chinese patients with primary hypercholesterolemia and mixed dyslipidemia at different levels of cardiovascular disease risk.

Methods: HUA TUO was a 12-week randomized, double-blind, placebo-controlled study. Chinese patients aged 18 years or older on stable optimized statin therapy were randomized 2:2:1:1 to receive evolocumab 140 mg every 2 weeks (Q2W), evolocumab 420 mg monthly (QM), or a matching placebo. The coprimary endpoints were percent change from baseline in LDL-C at the mean of weeks 10 and 12 and at week 12.

Results: Overall, 241 randomized patients (mean [standard deviation] age, 60.2 [10.3] years) received evolocumab 140 mg Q2W (n = 79), evolocumab 420 mg QM (n = 80), placebo Q2W (n = 41), or placebo QM (n = 41). At weeks 10 and 12, the placebo-adjusted least-squares mean percent change from baseline in LDL-C for the evolocumab 140 mg Q2W group was - 70.7% (95% CI - 78.0% to - 63.5%); - 69.7% (95% CI - 76.5% to - 63.0%) for the evolocumab 420 mg QM group. Significant improvements in all other lipid parameters were observed with evolocumab. The patient incidence of treatment-emergent adverse events was similar between the treatment groups and across dosing regimens.

Conclusion: In Chinese patients with primary hypercholesterolemia and mixed dyslipidemia, 12-week treatment with evolocumab significantly lowered LDL-C and other lipids, and was safe and well tolerated (NCT03433755).

Evolocumab是一种全人源蛋白转化酶/枯草杆菌素9型抑制剂抗体,可显著降低2型糖尿病合并高脂血症和混合性血脂异常患者的低密度脂蛋白胆固醇(LDL-C)。这项为期12周的研究评估了evolocumab在中国不同心血管疾病风险水平的原发性高胆固醇血症和混合性血脂异常患者中的疗效和安全性。方法:华佗是一项为期12周的随机、双盲、安慰剂对照研究。接受稳定优化他汀类药物治疗的18岁或以上的中国患者以2:2:1:1随机分组,接受evolocumab 140 mg / 2周(Q2W)、evolocumab 420 mg /月(QM)或匹配的安慰剂。主要终点是第10周、第12周和第12周LDL-C相对基线的平均变化百分比。结果:总体而言,241名随机患者(平均[标准差]年龄,60.2[10.3]岁)接受了evolocumab 140 mg Q2W (n = 79), evolocumab 420 mg QM (n = 80),安慰剂Q2W (n = 41)或安慰剂QM (n = 41)。在第10周和第12周,evolocumab 140 mg Q2W组LDL-C与基线相比经安慰剂调整的最小二乘平均百分比变化为- 70.7% (95% CI - 78.0%至- 63.5%);evolocumab 420mg QM组- 69.7% (95% CI - 76.5% - 63.0%)。evolocumab可显著改善所有其他脂质参数。在治疗组和不同给药方案之间,患者治疗后出现的不良事件的发生率相似。结论:在中国原发性高胆固醇血症和混合性血脂异常患者中,evolocumab治疗12周可显著降低LDL-C和其他脂质,且安全且耐受性良好(NCT03433755)。
{"title":"Efficacy and Safety of Evolocumab in Chinese Patients with Primary Hypercholesterolemia and Mixed Dyslipidemia: 12-Week Primary Results of the HUA TUO Randomized Clinical Trial.","authors":"Hong Tan,&nbsp;Weimin Li,&nbsp;Zhouqing Huang,&nbsp;Yajun Han,&nbsp;Xuecheng Huang,&nbsp;Dongye Li,&nbsp;Xiaochun Xing,&nbsp;Maria Laura Monsalvo,&nbsp;You Wu,&nbsp;Jackie Mao,&nbsp;Lily Xin,&nbsp;Jiyan Chen","doi":"10.1007/s40119-023-00304-x","DOIUrl":"https://doi.org/10.1007/s40119-023-00304-x","url":null,"abstract":"<p><strong>Introduction: </strong>Evolocumab, a fully human proprotein convertase/subtilisin kexin type 9 inhibitor antibody, significantly lowers low-density lipoprotein cholesterol (LDL-C) in patients with type 2 diabetes mellitus and hyperlipidemia and mixed dyslipidemia. This 12-week study evaluated the efficacy and safety of evolocumab in Chinese patients with primary hypercholesterolemia and mixed dyslipidemia at different levels of cardiovascular disease risk.</p><p><strong>Methods: </strong>HUA TUO was a 12-week randomized, double-blind, placebo-controlled study. Chinese patients aged 18 years or older on stable optimized statin therapy were randomized 2:2:1:1 to receive evolocumab 140 mg every 2 weeks (Q2W), evolocumab 420 mg monthly (QM), or a matching placebo. The coprimary endpoints were percent change from baseline in LDL-C at the mean of weeks 10 and 12 and at week 12.</p><p><strong>Results: </strong>Overall, 241 randomized patients (mean [standard deviation] age, 60.2 [10.3] years) received evolocumab 140 mg Q2W (n = 79), evolocumab 420 mg QM (n = 80), placebo Q2W (n = 41), or placebo QM (n = 41). At weeks 10 and 12, the placebo-adjusted least-squares mean percent change from baseline in LDL-C for the evolocumab 140 mg Q2W group was - 70.7% (95% CI - 78.0% to - 63.5%); - 69.7% (95% CI - 76.5% to - 63.0%) for the evolocumab 420 mg QM group. Significant improvements in all other lipid parameters were observed with evolocumab. The patient incidence of treatment-emergent adverse events was similar between the treatment groups and across dosing regimens.</p><p><strong>Conclusion: </strong>In Chinese patients with primary hypercholesterolemia and mixed dyslipidemia, 12-week treatment with evolocumab significantly lowered LDL-C and other lipids, and was safe and well tolerated (NCT03433755).</p>","PeriodicalId":9561,"journal":{"name":"Cardiology and Therapy","volume":"12 2","pages":"341-359"},"PeriodicalIF":3.4,"publicationDate":"2023-06-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://ftp.ncbi.nlm.nih.gov/pub/pmc/oa_pdf/86/0f/40119_2023_Article_304.PMC9942644.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"9506377","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Guideline LDL-C Threshold Achievement in Acute Myocardial Infarction Patients: A Real-World Evidence Study Demonstrating the Impact of Treatment Intensification with PCSK9i. 急性心肌梗死患者LDL-C阈值达到:一项证明PCSK9i强化治疗影响的真实世界证据研究
IF 3.4 Q2 CARDIAC & CARDIOVASCULAR SYSTEMS Pub Date : 2023-06-01 DOI: 10.1007/s40119-022-00300-7
Erin S Mackinnon, Bryan Har, Salimah Champsi, Rajvi J Wani, Lee Geyer, Eileen Shaw, Megan S Farris, Todd J Anderson

Introduction: A high proportion of Canadian patients with acute myocardial infarction (AMI) do not achieve the threshold low-density lipoprotein cholesterol (LDL-C) levels recommended by the Canadian Cardiovascular Society in 2021. This increases the risk of subsequent atherosclerotic cardiovascular disease (ASCVD) events. Here, we assess LDL-C levels and threshold achievement among patients by lipid-lowering therapies (LLT) received post-AMI.

Methods: A retrospective cohort study of patients identified with AMI between 2015 and 2019 was conducted using administrative health databases in Alberta, Canada. Patients were grouped by their highest-intensity LLT post-AMI (proprotein convertase subtilisin/kexin type 9 inhibitors (PCSK9i) + another LLT; PCSK9i alone; ezetimibe + statin; statins (high, moderate, low intensity); or ezetimibe alone), and available LDL-C levels were examined in the year before and after LLT dispense date.

Results: The cohort included 15,283 patients. In patients on PCSK9i + LLT, the median [95% confidence interval (CI)] LDL-C levels decreased from 2.7 (2.3-3.4) before to 0.9 (0.5-1.2) mmol/l after treatment, the largest decrease among treatment groups. In the ezetimibe + statin and high-intensity statin groups, median (95% CI) values after treatment were 1.5 (1.5-1.6) and 1.4 (1.4-1.4) mmol/l, respectively. The proportion of patients below the 1.8 mmol/l threshold increased by 77.7% in the PSCK9i + LLT group after treatment, compared to 45.4 and 32.4% in the ezetimibe + statin and high-intensity statin groups, respectively.

Conclusions: Intensification with PCSK9i in AMI patients results in a greater proportion of patients achieving below the recommended LDL-C threshold versus statins and or ezetimibe alone. Increased focus on achieving below the LDL-C thresholds with additional LLT as required may benefit patient cardiovascular outcomes.

加拿大急性心肌梗死(AMI)患者中有很大比例未达到加拿大心血管协会2021年推荐的低密度脂蛋白胆固醇(LDL-C)阈值。这增加了随后发生动脉粥样硬化性心血管疾病(ASCVD)事件的风险。在这里,我们评估了ami后接受降脂治疗(LLT)的患者的LDL-C水平和阈值。方法:利用加拿大艾伯塔省的行政卫生数据库,对2015年至2019年确诊为AMI的患者进行回顾性队列研究。患者按ami后最高强度LLT分组(蛋白转化酶枯草杆菌素/酮素9型抑制剂(PCSK9i) +另一种LLT;PCSK9i孤独;依折麦布+他汀类药物;他汀类药物(高、中、低强度);或单独依折可布),并在LLT配药日期前后一年检测可用LDL-C水平。结果:该队列包括15283例患者。在接受PCSK9i + LLT治疗的患者中,LDL-C水平中位数[95%置信区间(CI)]从治疗前的2.7 (2.3-3.4)mmol/l下降到治疗后的0.9 (0.5-1.2)mmol/l,是治疗组中下降幅度最大的。依zetimibe +他汀和高强度他汀组治疗后的中位(95% CI)值分别为1.5(1.5-1.6)和1.4 (1.4-1.4)mmol/l。治疗后,PSCK9i + LLT组低于1.8 mmol/l阈值的患者比例增加了77.7%,而依zetimibe +他汀和高强度他汀组分别为45.4和32.4%。结论:与单独使用他汀类药物和/或依折麦比相比,AMI患者使用PCSK9i强化可使更大比例的患者达到低于推荐的LDL-C阈值。增加对达到低于LDL-C阈值的关注,并根据需要进行额外的LLT,可能有利于患者的心血管预后。
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引用次数: 0
Evaluating the Performance of High-Dimensional Propensity Scores Compared with Standard Propensity Scores for Comparing Antihypertensive Therapies in the CPRD GOLD Database. 评价CPRD GOLD数据库中高维度倾向评分与标准倾向评分在比较降压治疗中的表现
IF 3.4 Q2 CARDIAC & CARDIOVASCULAR SYSTEMS Pub Date : 2023-06-01 DOI: 10.1007/s40119-023-00316-7
Virginie Simon, Jade Vadel

Introduction: Propensity score (PS) matching is widely used in medical record studies to create balanced treatment groups, but relies on prior knowledge of confounding factors. High-dimensional PS (hdPS) is a semi-automated algorithm that selects variables with the highest potential for confounding from medical databases. The objective of this study was to evaluate performance of hdPS and PS when used to compare antihypertensive therapies in the UK clinical practice research datalink (CPRD) GOLD database.

Methods: Patients initiating antihypertensive treatment with either monotherapy or bitherapy were extracted from the CPRD GOLD database. Simulated datasets were generated using plasmode simulations with a marginal hazard ratio (HRm) of 1.29 for bitherapy versus monotherapy for reaching blood pressure control at 3 months. Either 16 or 36 known covariates were forced into the PS and hdPS models, and 200 additional variables were automatically selected for hdPS. Sensitivity analyses were conducted to assess the impact of removing known confounders from the database on hdPS performance.

Results: With 36 known covariates, the estimated HRm (RMSE) was 1.31 (0.05) for hdPS and 1.30 (0.04) for PS matching; the crude HR was 0.68 (0.61). Using 16 known covariates, the estimated HRm (RMSE) was 1.23 (0.10) and 1.09 (0.20) for hdPS and PS, respectively. Performance of hdPS was not compromised when known confounders were removed from the database.

Results on real data: With 49 investigator-selected covariates, the HR was 1.18 (95% CI 1.10; 1.26) for PS and 1.33 (95% CI 1.22; 1.46) for hdPS. Both methods yielded the same conclusion, suggesting superiority of bitherapy over monotherapy for time to blood pressure control.

Conclusion: HdPS can identify proxies for missing confounders, thereby having an advantage over PS in case of unobserved covariates. Both PS and hdPS showed superiority of bitherapy over monotherapy for reaching blood pressure control.

简介:倾向评分(PS)匹配广泛应用于病历研究,以创建平衡的治疗组,但依赖于混杂因素的先验知识。高维PS (hdPS)是一种半自动算法,它从医学数据库中选择最有可能混淆的变量。本研究的目的是评估hdPS和PS在英国临床实践研究数据链(CPRD) GOLD数据库中用于比较降压治疗的性能。方法:从CPRD GOLD数据库中提取开始接受单药或双药降压治疗的患者。利用等离子体模型模拟生成模拟数据集,生物疗法与单一疗法在3个月达到血压控制的边际风险比(HRm)为1.29。将16或36个已知协变量强制纳入PS和hdPS模型,并自动为hdPS选择200个额外变量。进行敏感性分析以评估从数据库中删除已知混杂因素对hdPS性能的影响。结果:在已知36个协变量的情况下,hdPS的估计HRm (RMSE)为1.31 (0.05),PS匹配的估计HRm (RMSE)为1.30 (0.04);粗HR为0.68(0.61)。使用16个已知协变量,hdPS和PS的估计HRm (RMSE)分别为1.23(0.10)和1.09(0.20)。当从数据库中删除已知的混杂因素时,hdPS的性能不会受到影响。真实数据的结果:在49个研究者选择的协变量中,风险比为1.18 (95% CI 1.10;PS为1.26),1.33 (95% CI 1.22;1.46)的hdPS。两种方法都得出了相同的结论,表明生物疗法在时间上优于单一疗法来控制血压。结论:HdPS可以识别缺失混杂因素的代理,因此在未观察到的协变量情况下比PS具有优势。PS和hdPS在达到血压控制方面均显示出生物疗法优于单一疗法。
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引用次数: 0
Pediatric Myocarditis. 小儿心肌炎。
IF 3.4 Q2 CARDIAC & CARDIOVASCULAR SYSTEMS Pub Date : 2023-06-01 DOI: 10.1007/s40119-023-00309-6
Jason L Williams, Hannah M Jacobs, Simon Lee

Myocarditis is a condition caused by acute or chronic inflammation of the cardiac myocytes, resulting in associated myocardial edema and myocardial injury or necrosis. The exact incidence is unknown, but is likely underestimated, with more mild cases going unreported. Diagnosis and appropriate management are paramount in pediatric myocarditis, as it remains a recognized cause of sudden cardiac death in children and athletes. Myocarditis in children is most often caused by a viral or infectious etiology. In addition, there are now two highly recognized etiologies related to Coronavirus disease of 2019 (COVID-19) infection and the COVID-19 mRNA vaccine. The clinic presentation of children with myocarditis can range from asymptomatic to critically ill. Related to severe acute respiratory syndrome-Coronavirus 2 (SARs-CoV-2), children are at greater risk of developing myocarditis secondary to COVID-19 compared to the mRNA COVID-19 vaccine. Diagnosis of myocarditis typically includes laboratory testing, electrocardiography (ECG), chest X-ray, and additional non-invasive imaging studies with echocardiogram typically being the first-line imaging modality. While the reference standard for diagnosing myocarditis was previously endomyocardial biopsy, with the new revised Lake Louise Criteria, cardiac magnetic resonance (CMR) has emerged as an integral non-invasive imaging tool to assist in the diagnosis. CMR remains critical, as it allows for assessment of ventricular function and tissue characterization, with newer techniques, such as myocardial strain, to help guide management both acutely and long term.

心肌炎是由心肌细胞急性或慢性炎症引起的一种疾病,可导致心肌水肿和心肌损伤或坏死。确切的发病率尚不清楚,但很可能被低估了,更多轻微的病例没有报告。小儿心肌炎的诊断和适当的管理是至关重要的,因为它仍然是儿童和运动员心脏性猝死的公认原因。儿童心肌炎最常由病毒或感染性病因引起。此外,目前有两种高度认可的与2019年冠状病毒病(COVID-19)感染和COVID-19 mRNA疫苗相关的病因。小儿心肌炎的临床表现可以从无症状到危重。与严重急性呼吸综合征-冠状病毒2 (SARs-CoV-2)相关,与mRNA COVID-19疫苗相比,儿童患COVID-19继发性心肌炎的风险更高。心肌炎的诊断通常包括实验室检查、心电图(ECG)、胸部x线检查和额外的无创成像检查,超声心动图通常是一线成像方式。虽然以前诊断心肌炎的参考标准是心内膜活检,但随着新修订的路易斯湖标准,心脏磁共振(CMR)已成为辅助诊断的整体非侵入性成像工具。CMR仍然至关重要,因为它允许评估心室功能和组织特征,使用新的技术,如心肌应变,帮助指导急性和长期治疗。
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引用次数: 4
Correction to: Guideline LDL-C Threshold Achievement in Acute Myocardial Infarction Patients: A Real-World Evidence Study Demonstrating the Impact of Treatment Intensification with PCSK9i. 急性心肌梗死患者LDL-C阈值达到指南:一项证明PCSK9i强化治疗影响的真实世界证据研究。
IF 3.4 Q2 CARDIAC & CARDIOVASCULAR SYSTEMS Pub Date : 2023-06-01 DOI: 10.1007/s40119-023-00310-z
Erin S Mackinnon, Bryan Har, Salimah Champsi, Rajvi J Wani, Lee Geyer, Eileen Shaw, Megan S Farris, Todd J Anderson
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引用次数: 0
Risk and Management of Patients with Cancer and Heart Disease. 癌症和心脏病患者的风险与管理。
IF 3.4 Q2 CARDIAC & CARDIOVASCULAR SYSTEMS Pub Date : 2023-06-01 Epub Date: 2023-02-09 DOI: 10.1007/s40119-023-00305-w
Loreena Hill, Bruno Delgado, Ekaterini Lambrinou, Tara Mannion, Mark Harbinson, Claire McCune

Cancer and cardiovascular disease are two of the leading causes of global mortality and morbidity. Medical research has generated powerful lifesaving treatments for patients with cancer; however, such treatments may sometimes be at the expense of the patient's myocardium, leading to heart failure. Anti-cancer drugs, including anthracyclines, can result in deleterious cardiac effects, significantly impacting patients' functional capacity, mental well-being, and quality of life. Recognizing this, recent international guidelines and expert papers published recommendations on risk stratification and care delivery, including that of cardio-oncology services. This review will summarize key evidence with a focus on anthracycline therapy, providing clinical guidance for the non-oncology professional caring for a patient with cancer and heart failure.

癌症和心血管疾病是全球死亡率和发病率的两个主要原因。医学研究为癌症患者提供了强有力的救生治疗;然而,这种治疗有时可能以牺牲患者心肌为代价,导致心力衰竭。抗癌药物,包括蒽环类药物,会导致有害的心脏效应,严重影响患者的功能能力、心理健康和生活质量。认识到这一点,最近的国际指南和专家论文发表了关于风险分层和护理提供的建议,包括心脏肿瘤服务的建议。这篇综述将总结重点关注蒽环类药物治疗的关键证据,为癌症和心力衰竭患者的非肿瘤专业护理提供临床指导。
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引用次数: 0
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Cardiology and Therapy
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