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Interpretation of the Annual Report on Cardiovascular Health and Diseases in China 2021 2021中国心血管健康与疾病年度报告》解读
Pub Date : 2023-11-29 DOI: 10.1097/cd9.0000000000000107
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引用次数: 0
Thirty-day Outcomes of First-in-man Implantation of a Novel Transcatheter Edge-to-edge Mitral Repair System in Patients with Severe Mitral Regurgitation 在严重二尖瓣返流患者中首次植入新型经导管边缘到边缘二尖瓣修复系统的 30 天疗效观察
Pub Date : 2023-11-23 DOI: 10.1097/cd9.0000000000000112
Kai Xu, Yan Wang, Shaoliang Chen, X. Pan, Ben He, Ruiyan Zhang, Bin Wang, Junjie Zhang, Zhengbin Zhu, Bin Wang, D. Zhu, Yaling Han
The aim of this multicenter, prospective, single-arm pilot study (ClinicalTrials.gov number: NCT05040074) was to observe the procedural and 30-day results of the novel transcatheter mitral valve repair system, SQ-Kyrin®-M Clip (Shenqi Medical, Shanghai, China), in patients with severe mitral regurgitation (MR). The heart team considered patients from 5 centers in China with clinically significant functional mitral regurgitation ≥3+ despite optimal medical therapy or degenerative mitral regurgitation ≥3+ with high surgical risk as candidates for transcatheter repair. All patients received transcatheter edge-to-edge mitral valve repair under general anesthesia. The primary outcome was technical success, which included all of the following measured at the exit from the catheterization laboratory: (1) absence of procedural mortality; (2) successful access, delivery, and retrieval of the device delivery system; (3) successful deployment and correct positioning of the first intended device; and (4) no emergency surgery or reintervention related to the device or access procedure. The secondary outcomes included all-cause mortality, serious adverse events, device success, and procedural success 30 d after the intervention. From June 2021 to December 2021, 18 patients were enrolled in this study with age (75.7 ± 7.4) years. Fifteen (83.3%) patients had MR 4+, while 3 (16.7%) had MR 3+. Technical success was achieved in all patients, including 6 degenerative mitral regurgitation and 12 functional mitral regurgitation patients. There was no all-cause mortality at 30 d. One (5.6%) patient had single leaflet device attachment within 30 d, which was regarded as a serious adverse event, and the patient was successfully treated with reintervention by implanting another clip. Another patient’s transmitral gradient was 6 mmHg (>5 mmHg), with an effective orifice area of 2.57 cm2 after the procedure. Sixteen (88.9%) patients had device success and procedural success at 30 d postoperation. Fourteen (77.8%) patients had MR 1+, 3 (16.7%) had MR 2+, and only 1 (5.6%) patient had MR 3 + 30 d after the procedure. The results of this feasibility study showed the efficacy and safety of the SQ-Kyrin®-M device in the Chinese population with severe MR, laying a solid foundation for a subsequent large-scale confirmatory study.
这项多中心、前瞻性、单臂试验研究(ClinicalTrials.gov 编号:NCT05040074)旨在观察新型经导管二尖瓣修复系统 SQ-Kyrin®-M Clip(神麒医疗,中国上海)在重度二尖瓣反流(MR)患者中的手术和 30 天疗效。 心脏团队将来自中国 5 个中心的患者视为经导管修复的候选者,这些患者尽管接受了最佳药物治疗,但临床上仍存在功能性二尖瓣反流≥3+,或退行性二尖瓣反流≥3+,且手术风险较高。所有患者都在全身麻醉下接受了经导管边缘对边缘二尖瓣修复术。主要结果是技术成功,包括从导管室出来时测量的以下所有结果:(1) 无手术死亡率;(2) 成功接入、输送和取回装置输送系统;(3) 成功部署和正确定位第一个预定装置;(4) 无与装置或接入程序相关的急诊手术或再干预。次要结果包括干预 30 天后的全因死亡率、严重不良事件、装置成功率和程序成功率。 从 2021 年 6 月到 2021 年 12 月,18 名患者参与了这项研究,年龄为(75.7 ± 7.4)岁。15例(83.3%)患者患有MR 4+,3例(16.7%)患者患有MR 3+。所有患者都取得了技术成功,其中包括 6 名退行性二尖瓣反流患者和 12 名功能性二尖瓣反流患者。一名患者(5.6%)在 30 天内出现单瓣装置附着,这被视为严重不良事件,该患者通过植入另一个夹子重新介入治疗,并获得成功。另一名患者的透射阶差为 6 mmHg(>5 mmHg),术后有效孔面积为 2.57 平方厘米。16名患者(88.9%)在术后30 d时装置成功,手术成功。14名患者(77.8%)在术后 30 天出现 MR 1+,3 名患者(16.7%)出现 MR 2+,只有 1 名患者(5.6%)出现 MR 3+。 这项可行性研究的结果表明,SQ-Kyrin®-M 装置在中国重度 MR 患者中具有良好的疗效和安全性,为后续的大规模确证研究奠定了坚实的基础。
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引用次数: 0
Overview of the Association between Non-Alcoholic Fatty Liver Disease and Hypertension 非酒精性脂肪肝与高血压之间的关系概述
Pub Date : 2023-11-21 DOI: 10.1097/cd9.0000000000000113
Niki S. Kakouri, C. Thomopoulos, E. Siafi, A. Valatsou, Kyriakos Dimitriadis, Iliana P. Mani, S. Patsilinakos, Dimitrios M. Tousoulis, Konstantinos P. Tsioufis
Non-alcoholic fatty liver disease (NAFLD) is the most common chronic liver disease, and its prevalence is rising. NAFLD is closely associated with metabolic syndrome, with both conditions sharing common clinical characteristics such as obesity, insulin resistance, type 2 diabetes mellitus, hypertension, and hypertriglyceridemia. Several observational studies have evaluated the relationship between NAFLD and hypertension, with the overall evidence suggesting a bidirectional relationship. It is hypothesized that activation of the sympathetic nervous and renin-angiotensin systems, observed in NAFLD with or without insulin resistance promotes the development of hypertension. In patients with hypertension, activation of these systems can lead to hepatic fibrosis and progressive inflammation through increased oxidative stress and activation of hepatic stellate cells and Kupffer cells. The present review examines the pathophysiologic and clinical evidence supporting the bidirectional association between NAFLD and hypertension.
非酒精性脂肪肝(NAFLD)是最常见的慢性肝病,其发病率呈上升趋势。非酒精性脂肪肝与代谢综合征密切相关,这两种疾病具有共同的临床特征,如肥胖、胰岛素抵抗、2 型糖尿病、高血压和高甘油三酯血症。多项观察性研究评估了非酒精性脂肪肝与高血压之间的关系,总体证据表明两者之间存在双向关系。据推测,非酒精性脂肪肝伴有或不伴有胰岛素抵抗时,交感神经系统和肾素-血管紧张素系统的激活会促进高血压的发生。在高血压患者中,这些系统的激活可通过增加氧化应激和激活肝星状细胞和 Kupffer 细胞,导致肝纤维化和进行性炎症。本综述探讨了支持非酒精性脂肪肝与高血压之间双向关联的病理生理学和临床证据。
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引用次数: 0
Chronic Pulmonary Artery Stenosis: Time to Think as a Disease Entity 慢性肺动脉狭窄:是时候将其视为一种疾病实体了
Pub Date : 2023-11-08 DOI: 10.1097/cd9.0000000000000110
Wenjie Dong, Jingwen Zhang, Hongling Su, Yunshan Cao
Chronic pulmonary artery stenosis (CPAS) is characterized by a reduction or complete obstruction of the cross-sectional area of the pulmonary artery owing to various causes. The condition exhibits similar pathophysiological progress, leading to pulmonary hypertension (PH), reduced physical endurance, right heart failure, and death. Although CPAS is often regarded as a subgroup of PH, it can manifest independently for an extended duration before the onset of PH and can significantly impact patient quality of life. It may therefore be more appropriate to consider PH as pathophysiological progression of CPAS, thereby recognizing CPAS as a distinct disease entity.
慢性肺动脉狭窄(Chronic pulmonary artery stenosis, CPAS)的特点是由于各种原因导致肺动脉横截面积减少或完全阻塞。这种疾病表现出类似的病理生理过程,导致肺动脉高压(PH)、身体耐力降低、右心衰和死亡。虽然CPAS通常被认为是PH的一个亚组,但它可以在PH发病前的较长时间内独立表现,并且可以显著影响患者的生活质量。因此,将PH视为CPAS的病理生理进展可能更合适,从而认识到CPAS是一种独特的疾病实体。
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引用次数: 0
What Is New in the 2023 European Society of Cardiology Guidelines for the Management of Acute Coronary Syndromes 2023年欧洲心脏病学会急性冠状动脉综合征管理指南有什么新内容
Pub Date : 2023-11-07 DOI: 10.1097/cd9.0000000000000106
Marco Roffi
For the first time, European Society of Cardiology (ESC) guidelines have aggregated in 1 single document recommendations for the management of patients with non-ST-segment elevation acute coronary syndromes (NSTE-ACS) and ST-elevation myocardial infarction (STEMI). From a clinical perspective, this is coherent, as the spectrum of clinical presentations in acute coronary syndromes (ACS) may range from new onset or progressive troponin-negative angina to STEMI, cardiogenic shock, or cardiac arrest. In addition, the management pathways of NSTE-ACS and STEMI patients are widely similar. Compared with previous editions of the guidelines, the extensive document is improved also from a graphic perspective, containing several appealing and easy-to-understand figures. New or modified recommendations include, among others, the topics of diagnostic work-up, timing of invasive strategy, revascularization in multi-vessel disease, intravascular imaging, cardiac arrest, cardiogenic shock, and antithrombotic treatment. For the first time in the field of ACS, ESC guidelines have incorporated a section on patient perspectives with dedicated recommendations. Some of the most relevant changes in recommendations impacting clinical practice are discussed in this article.
欧洲心脏病学会(ESC)指南首次将非st段抬高型急性冠状动脉综合征(NSTE-ACS)和st段抬高型心肌梗死(STEMI)患者的治疗建议汇总为1篇文献。从临床角度来看,这是一致的,因为急性冠状动脉综合征(ACS)的临床表现范围可能从新发或进行性肌钙蛋白阴性心绞痛到STEMI、心源性休克或心脏骤停。此外,NSTE-ACS和STEMI患者的管理途径非常相似。与以前版本的指南相比,这份内容广泛的文件也从图形的角度进行了改进,包含了几个吸引人且易于理解的数字。新的或修改的建议包括,除其他外,诊断检查、侵入策略的时机、多血管疾病的血运重建、血管内成像、心脏骤停、心源性休克和抗血栓治疗等主题。在ACS领域,ESC指南首次纳入了一个关于患者观点的章节,并提供了专门的建议。本文讨论了影响临床实践的建议中一些最相关的变化。
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引用次数: 0
Invasive Hemodynamic and Vasoreactivity Testing with Inhaled Iloprost in Children with Pulmonary Arterial Hypertension Associated with Congenital Heart Defects 吸入依洛前列素对先天性心脏缺陷肺动脉高压患儿有创血流动力学和血管反应性的检测
Pub Date : 2023-11-02 DOI: 10.1097/cd9.0000000000000109
Qiangqiang Li, Yuan He, Chen Zhang, Hong Gu
Objective: Invasive hemodynamic evaluation and acute vasoreactivity testing are recommended in the diagnosis of pulmonary arterial hypertension (PAH), but their clinical role in children with PAH associated with congenital heart defects (CHD) is unclear. This study aims to investigate acute hemodynamic responses to inhaled iloprost, and its role in prognosis in children with PAH-CHD. Methods: A retrospective analysis was conducted on 83 pediatric patients with PAH-CHD in whom invasive hemodynamics were evaluated before and after a single inhaled dose of iloprost at a single center between 2010 and 2022. Details of the CHD corrective operation, medical treatment, and outcome for each patient were obtained via medical records or telephone contact. A composite endpoint of all-cause death, admission for worsening heart failure during follow-up, and event-free survival was defined, and risk factors associated with this composite endpoint were analyzed. Results: The average patient age was (11.3 ± 4.6) years, and 60 (72.3%) were female. Fifty-nine (71.1%) patients were diagnosed with Eisenmenger syndrome. After iloprost inhalation, mean pulmonary artery pressure decreased from (78.2 ± 11.5) to (72.3 ± 13.2) mmHg ( P < 0.001), and pulmonary vascular resistance index (PVRI) decreased from (18.0 ± 7.9) to (14.5 ± 8.1) WU·m 2 ( P < 0.001). A total of 38 (45.8%) patients had a positive response, defined as a PVRI decrease >25% with stable systemic pressure. Thirty-seven (44.6%) patients underwent a corrective CHD operation at a median of 24 d after hemodynamic evaluation. Nine patients died, and 15 met the composite endpoint during a follow-up period of 5.4 (3.8, 8.8) years. Five-year event-free survival estimates were 96.7% (95% confidence interval: 90.3%–100%) in patients with a positive response, and 82.8% (95% confidence interval: 71.7%–94.5%) in patients with a non-positive response (log-rank P = 0.012). A positive PVRI response and higher pulmonary arterial oxygen saturation after iloprost inhalation, lower baseline brain natriuretic peptide, and PAH-targeted therapy at follow-up were significantly associated with a favorable clinical outcome. A positive acute vasoreactivity testing response and PAH-targeted therapy at follow-up were independent predictors of outcome in multivariate Cox analysis. Conclusions: Acute inhalation of iloprost can lead to a significant decrease in hemodynamic parameters. Responsiveness to inhaled iloprost is associated with better outcomes and can be a valuable predictor of outcomes.
目的:有创血流动力学评价和急性血管反应性试验被推荐用于肺动脉高压(PAH)的诊断,但它们在PAH合并先天性心脏缺陷(CHD)患儿中的临床作用尚不清楚。本研究旨在探讨吸入伊洛前列素对PAH-CHD患儿的急性血流动力学反应及其在预后中的作用。方法:回顾性分析2010年至2022年在单中心单次吸入伊洛前列素前后83例PAH-CHD患儿的有创血流动力学。通过医疗记录或电话联系获得每位患者的冠心病矫正手术、医疗和结果的详细信息。定义了全因死亡、随访期间因心力衰竭恶化入院和无事件生存的综合终点,并分析了与该综合终点相关的危险因素。结果:患者平均年龄(11.3±4.6)岁,女性60例(72.3%)。59例(71.1%)诊断为艾森曼格综合征。吸入伊洛前列素后,平均肺动脉压由(78.2±11.5)降至(72.3±13.2)mmHg (P <肺血管阻力指数(PVRI)由(18.0±7.9)降至(14.5±8.1)WU·m2 (P <0.001)。共有38例(45.8%)患者出现阳性反应,定义为PVRI下降25%,体压稳定。37例(44.6%)患者在血流动力学评估后平均24天内接受了冠心病矫正手术。在5.4(3.8,8.8)年的随访期间,9例患者死亡,15例达到复合终点。阳性反应患者的5年无事件生存率估计为96.7%(95%置信区间:90.3%-100%),非阳性反应患者的5年无事件生存率估计为82.8%(95%置信区间:71.7%-94.5%)(log-rank P = 0.012)。吸入伊洛前列素后PVRI阳性反应和较高的肺动脉氧饱和度,较低的基线脑利钠肽,以及随访时pah靶向治疗与良好的临床结果显著相关。在多变量Cox分析中,急性血管反应试验阳性反应和随访时多环芳烃靶向治疗是预后的独立预测因素。结论:急性吸入伊洛前列素可导致血流动力学参数显著降低。对吸入伊洛前列素的反应性与更好的预后相关,可以作为预后的有价值的预测指标。
{"title":"Invasive Hemodynamic and Vasoreactivity Testing with Inhaled Iloprost in Children with Pulmonary Arterial Hypertension Associated with Congenital Heart Defects","authors":"Qiangqiang Li, Yuan He, Chen Zhang, Hong Gu","doi":"10.1097/cd9.0000000000000109","DOIUrl":"https://doi.org/10.1097/cd9.0000000000000109","url":null,"abstract":"Objective: Invasive hemodynamic evaluation and acute vasoreactivity testing are recommended in the diagnosis of pulmonary arterial hypertension (PAH), but their clinical role in children with PAH associated with congenital heart defects (CHD) is unclear. This study aims to investigate acute hemodynamic responses to inhaled iloprost, and its role in prognosis in children with PAH-CHD. Methods: A retrospective analysis was conducted on 83 pediatric patients with PAH-CHD in whom invasive hemodynamics were evaluated before and after a single inhaled dose of iloprost at a single center between 2010 and 2022. Details of the CHD corrective operation, medical treatment, and outcome for each patient were obtained via medical records or telephone contact. A composite endpoint of all-cause death, admission for worsening heart failure during follow-up, and event-free survival was defined, and risk factors associated with this composite endpoint were analyzed. Results: The average patient age was (11.3 ± 4.6) years, and 60 (72.3%) were female. Fifty-nine (71.1%) patients were diagnosed with Eisenmenger syndrome. After iloprost inhalation, mean pulmonary artery pressure decreased from (78.2 ± 11.5) to (72.3 ± 13.2) mmHg ( P < 0.001), and pulmonary vascular resistance index (PVRI) decreased from (18.0 ± 7.9) to (14.5 ± 8.1) WU·m 2 ( P < 0.001). A total of 38 (45.8%) patients had a positive response, defined as a PVRI decrease >25% with stable systemic pressure. Thirty-seven (44.6%) patients underwent a corrective CHD operation at a median of 24 d after hemodynamic evaluation. Nine patients died, and 15 met the composite endpoint during a follow-up period of 5.4 (3.8, 8.8) years. Five-year event-free survival estimates were 96.7% (95% confidence interval: 90.3%–100%) in patients with a positive response, and 82.8% (95% confidence interval: 71.7%–94.5%) in patients with a non-positive response (log-rank P = 0.012). A positive PVRI response and higher pulmonary arterial oxygen saturation after iloprost inhalation, lower baseline brain natriuretic peptide, and PAH-targeted therapy at follow-up were significantly associated with a favorable clinical outcome. A positive acute vasoreactivity testing response and PAH-targeted therapy at follow-up were independent predictors of outcome in multivariate Cox analysis. Conclusions: Acute inhalation of iloprost can lead to a significant decrease in hemodynamic parameters. Responsiveness to inhaled iloprost is associated with better outcomes and can be a valuable predictor of outcomes.","PeriodicalId":72524,"journal":{"name":"Cardiology discovery","volume":"23 7","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"2023-11-02","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"135876626","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Chinese Expert Consensus on Microvascular Protection Strategy during Emergency Percutaneous Coronary Intervention Therapy in Patients with ST-elevation Myocardial Infarction st段抬高型心肌梗死急诊经皮冠状动脉介入治疗中微血管保护策略的专家共识
Pub Date : 2023-11-01 DOI: 10.1097/cd9.0000000000000104
Microcirculatory dysfunction (CMD) typically occurs in patients with acute ST-segment elevation myocardial infarction during percutaneous coronary intervention, which is associated with more severe myocardial injury and a worse prognosis. With the advancement of intracoronary physiology and imaging technology, the prevention and therapeutic interventions of CMD have attracted more attention. However, relevant guidelines or consensus on CMD are lacking in China. The current consensus summarizes the prevention and diagnostic strategies of emergency percutaneous coronary intervention-related CMD and gives suggestions to improve the prognosis of ST-segment elevation myocardial infarction patients based on evidence from recent clinical studies, guidelines, and consensus from international sources.
微循环功能障碍(CMD)通常发生在急性st段抬高型心肌梗死患者经皮冠状动脉介入治疗期间,其心肌损伤更严重,预后更差。随着冠状动脉内生理学和影像学技术的进步,对CMD的预防和治疗干预越来越受到重视。然而,中国缺乏相关的指导方针或共识。目前的共识总结了急诊经皮冠状动脉介入相关CMD的预防和诊断策略,并根据最近的临床研究证据、指南和国际共识,提出了改善st段抬高型心肌梗死患者预后的建议。
{"title":"Chinese Expert Consensus on Microvascular Protection Strategy during Emergency Percutaneous Coronary Intervention Therapy in Patients with ST-elevation Myocardial Infarction","authors":"","doi":"10.1097/cd9.0000000000000104","DOIUrl":"https://doi.org/10.1097/cd9.0000000000000104","url":null,"abstract":"Microcirculatory dysfunction (CMD) typically occurs in patients with acute ST-segment elevation myocardial infarction during percutaneous coronary intervention, which is associated with more severe myocardial injury and a worse prognosis. With the advancement of intracoronary physiology and imaging technology, the prevention and therapeutic interventions of CMD have attracted more attention. However, relevant guidelines or consensus on CMD are lacking in China. The current consensus summarizes the prevention and diagnostic strategies of emergency percutaneous coronary intervention-related CMD and gives suggestions to improve the prognosis of ST-segment elevation myocardial infarction patients based on evidence from recent clinical studies, guidelines, and consensus from international sources.","PeriodicalId":72524,"journal":{"name":"Cardiology discovery","volume":"187 3","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"2023-11-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"135371574","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Emergency Treatment of Acute Decompensated Severe Aortic Stenosis with Transcatheter Aortic Valve Implantation Under the Coplane View Using J-Tipped Wires Fluoroscopy j头线共面透视下经导管主动脉瓣置入术急诊治疗急性失代偿性重度主动脉瓣狭窄
Pub Date : 2023-11-01 DOI: 10.1097/cd9.0000000000000111
Xian Liu, Yingdong Wang, Yuhe Sheng, Bin Wang, Kai Xu
Patients experiencing severe aortic stenosis with acute decompensation often face elevated surgical aortic valve replacement risks, leading to high postoperative mortality rates. However, for some patients eligible for transcatheter aortic valve implantation (TAVI), computed tomography angiography for assessing the aortic root and coronary artery might be challenging before the TAVI procedure. This case highlights a patient who underwent emergency TAVI guided by coplane view generated using J-tipped wires fluoroscopy without computed tomography evaluation before the TAVI. This approach reduces contrast usage during the TAVI procedure, significantly mitigating the risks of renal injury and heart function deterioration.
严重主动脉狭窄伴急性失代偿的患者往往面临手术主动脉瓣置换术风险升高,导致术后死亡率高。然而,对于一些有资格接受经导管主动脉瓣植入术(TAVI)的患者,在进行TAVI手术之前,评估主动脉根和冠状动脉的计算机断层血管造影可能具有挑战性。本病例强调了一名患者接受急诊TAVI,在TAVI前没有进行计算机断层扫描评估的情况下,使用j头线透视生成的共面视图。这种方法减少了TAVI手术期间造影剂的使用,显著降低了肾损伤和心功能恶化的风险。
{"title":"Emergency Treatment of Acute Decompensated Severe Aortic Stenosis with Transcatheter Aortic Valve Implantation Under the Coplane View Using J-Tipped Wires Fluoroscopy","authors":"Xian Liu, Yingdong Wang, Yuhe Sheng, Bin Wang, Kai Xu","doi":"10.1097/cd9.0000000000000111","DOIUrl":"https://doi.org/10.1097/cd9.0000000000000111","url":null,"abstract":"Patients experiencing severe aortic stenosis with acute decompensation often face elevated surgical aortic valve replacement risks, leading to high postoperative mortality rates. However, for some patients eligible for transcatheter aortic valve implantation (TAVI), computed tomography angiography for assessing the aortic root and coronary artery might be challenging before the TAVI procedure. This case highlights a patient who underwent emergency TAVI guided by coplane view generated using J-tipped wires fluoroscopy without computed tomography evaluation before the TAVI. This approach reduces contrast usage during the TAVI procedure, significantly mitigating the risks of renal injury and heart function deterioration.","PeriodicalId":72524,"journal":{"name":"Cardiology discovery","volume":"6 1","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"2023-11-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"135222653","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
A Network Meta-analysis of the Efficacy and Safety of Targeted Drug Combinations in the Treatment of Pulmonary Arterial Hypertension 靶向药物联合治疗肺动脉高压疗效和安全性的网络meta分析
Pub Date : 2023-11-01 DOI: 10.1097/cd9.0000000000000105
Rui Wang, Meng Wei, Jie Wang, Xiang Huang, Qianzhi Yan, Shichao Wang, Yun Wu
Objective: This network meta-analysis aims to compare the efficacy and safety of different targeted drug combination treatment for pulmonary arterial hypertension (PAH). Methods: Searches were conducted in Cochrane, PubMed, EMBASE, China National Knowledge Infrastructure, China Biomedical Literature Database, Wanfang Database, and VIP Chinese Science and Technology Journal Data to identify both published and unpublished randomized controlled trials from inception until January 1, 2022. The risk of bias in the included studies was assessed in accordance with the Cochrane Handbook for Systematic Reviews of Interventions. A network meta-analysis was performed using Stata 16.0 software. The efficacy and safety of different targeted drugs combined treatment for PAH were evaluated based on forest plot, funnel plot, and surface under the cumulative ranking. Results: A total of 29 randomized controlled trails with 4,448 patients treated with 10 different types of targeted drug combinations were included in this study. The results of the surface under the cumulative ranking showed that the combination regimen was the best clinical option to improve symptoms and delay progression in patients with pulmonary artery hypertension compared with monotherapy. Sildenafil in combination with ambrisentan significantly improved the 6-minute walk distance and reduced N-terminal pro-brain natriuretic peptide levels. Bosentan in combination with sildenafil significantly reduced mean pulmonary artery pressure, whereas bosentan in combination with epoprostenol was more effective than other combinations in reducing pulmonary vascular resistance. Bosentan in combination with tadalafil significantly improved the Borg dyspnea score, and bosentan in combination with iloprost was the best combination for improving World Health Organization functional class/New York Heart Association functional class. In terms of safety, there was no significant reduction in the incidence of adverse events, hospitalizations, or all-cause mortality for combination therapy compared with monotherapy. Bosentan combined with sildenafil significantly reduced the risk of serious adverse events, but the risk of discontinuation due to an adverse event was higher than monotherapy. Sildenafil combined with epoprostenol reduced the risk of clinical worsening in patients with PAH. Conclusion: Compared with monotherapy, targeted drug combinations for PAH significantly improves exercise tolerance, pulmonary hemodynamic parameters, and reduces the risk of serious adverse events and clinical worsening in patients. Bosentan in combination with sildenafil and bosentan in combination with iloprost are combinations of targeted agents with significant efficacy and better safety profile than monotherapy for the treatment of PAH. Sildenafil in combination with epoprostenol has a low risk of clinical worsening in PAH.
目的:本网络荟萃分析旨在比较不同靶向药物联合治疗肺动脉高压(PAH)的疗效和安全性。方法:检索Cochrane、PubMed、EMBASE、中国国家知识基础设施、中国生物医学文献数据库、万方数据库和VIP中国科技期刊数据,确定从开始到2022年1月1日已发表和未发表的随机对照试验。纳入研究的偏倚风险按照Cochrane干预措施系统评价手册进行评估。采用Stata 16.0软件进行网络meta分析。在累积排序下,采用森林图、漏斗图、面法评价不同靶向药物联合治疗多环芳烃的疗效和安全性。结果:本研究共纳入29条随机对照试验,共4448例患者接受10种不同类型的靶向药物联合治疗。累积排名下的表面结果显示,与单药治疗相比,联合治疗方案是改善肺动脉高压患者症状和延缓病情进展的最佳临床选择。西地那非联合安布里森坦可显著改善6分钟步行距离,降低n端前脑利钠肽水平。波生坦联合西地那非显著降低平均肺动脉压,而波生坦联合丙烯醇在降低肺血管阻力方面比其他联合更有效。波生坦联合他达拉非可显著改善Borg呼吸困难评分,而波生坦联合伊洛前列素是改善世界卫生组织功能分级/纽约心脏协会功能分级的最佳组合。在安全性方面,与单一治疗相比,联合治疗的不良事件发生率、住院率或全因死亡率没有显著降低。波生坦联合西地那非显著降低了严重不良事件的风险,但因不良事件而停药的风险高于单药治疗。西地那非联合丙烯醇可降低PAH患者临床恶化的风险。结论:与单药治疗相比,靶向药物联合治疗PAH可显著提高患者的运动耐量、肺血流动力学参数,降低患者发生严重不良事件和临床恶化的风险。波生坦联合西地那非和波生坦联合伊洛前列素是治疗多环芳烃的靶向药物组合,其疗效显著,安全性优于单药治疗。西地那非联合丙烯醇在PAH中临床恶化的风险较低。
{"title":"A Network Meta-analysis of the Efficacy and Safety of Targeted Drug Combinations in the Treatment of Pulmonary Arterial Hypertension","authors":"Rui Wang, Meng Wei, Jie Wang, Xiang Huang, Qianzhi Yan, Shichao Wang, Yun Wu","doi":"10.1097/cd9.0000000000000105","DOIUrl":"https://doi.org/10.1097/cd9.0000000000000105","url":null,"abstract":"Objective: This network meta-analysis aims to compare the efficacy and safety of different targeted drug combination treatment for pulmonary arterial hypertension (PAH). Methods: Searches were conducted in Cochrane, PubMed, EMBASE, China National Knowledge Infrastructure, China Biomedical Literature Database, Wanfang Database, and VIP Chinese Science and Technology Journal Data to identify both published and unpublished randomized controlled trials from inception until January 1, 2022. The risk of bias in the included studies was assessed in accordance with the Cochrane Handbook for Systematic Reviews of Interventions. A network meta-analysis was performed using Stata 16.0 software. The efficacy and safety of different targeted drugs combined treatment for PAH were evaluated based on forest plot, funnel plot, and surface under the cumulative ranking. Results: A total of 29 randomized controlled trails with 4,448 patients treated with 10 different types of targeted drug combinations were included in this study. The results of the surface under the cumulative ranking showed that the combination regimen was the best clinical option to improve symptoms and delay progression in patients with pulmonary artery hypertension compared with monotherapy. Sildenafil in combination with ambrisentan significantly improved the 6-minute walk distance and reduced N-terminal pro-brain natriuretic peptide levels. Bosentan in combination with sildenafil significantly reduced mean pulmonary artery pressure, whereas bosentan in combination with epoprostenol was more effective than other combinations in reducing pulmonary vascular resistance. Bosentan in combination with tadalafil significantly improved the Borg dyspnea score, and bosentan in combination with iloprost was the best combination for improving World Health Organization functional class/New York Heart Association functional class. In terms of safety, there was no significant reduction in the incidence of adverse events, hospitalizations, or all-cause mortality for combination therapy compared with monotherapy. Bosentan combined with sildenafil significantly reduced the risk of serious adverse events, but the risk of discontinuation due to an adverse event was higher than monotherapy. Sildenafil combined with epoprostenol reduced the risk of clinical worsening in patients with PAH. Conclusion: Compared with monotherapy, targeted drug combinations for PAH significantly improves exercise tolerance, pulmonary hemodynamic parameters, and reduces the risk of serious adverse events and clinical worsening in patients. Bosentan in combination with sildenafil and bosentan in combination with iloprost are combinations of targeted agents with significant efficacy and better safety profile than monotherapy for the treatment of PAH. Sildenafil in combination with epoprostenol has a low risk of clinical worsening in PAH.","PeriodicalId":72524,"journal":{"name":"Cardiology discovery","volume":"187 12","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"2023-11-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"135371572","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Real-time Three-dimensional Echocardiography: A Feasible and Accurate Method for Measuring Right Ventricular Function in Pulmonary Hypertension 实时三维超声心动图:一种测量肺动脉高压患者右心室功能的可行而准确的方法
Pub Date : 2023-10-31 DOI: 10.1097/cd9.0000000000000108
Ashfaq Ahmad, Yifan Zou, Peng Zhang, Lingling Li, Xiaoyu Wang, Ahmed Ali Mohsen, Yousen Wang, Fenling Fan
Right ventricular function is independently associated with poor clinical outcomes in patients with various cardiovascular diseases including pulmonary hypertension (PH). The complex geometry and mode of contractility means the right ventricle (RV) inlet and outlet are not in line; hence, 2-dimensional echocardiography fails to accurately quantify RV volumes and function in such patients. Three-dimensional echocardiography (3DE) allows for reliable and reproducible quantification of RV volumes and function by overcoming these limitations of conventional echocardiography. This review focuses on the 3DE assessment of RV function in patients with PH and discusses the following points: (1) acquiring an RV data set for 3DE imaging, including details of all available 3DE systems and software utilized in daily practice; (2) the reliability and feasibility of RV remodeling measured with 3DE with different modalities in patients with PH; and (3) the prognostic value of 3DE-derived RV function in such patients.
在包括肺动脉高压(PH)在内的各种心血管疾病患者中,右心室功能与不良临床结果独立相关。右心室复杂的几何形状和收缩模式导致右心室进出口不成直线;因此,二维超声心动图无法准确量化此类患者的右心室体积和功能。三维超声心动图(3DE)通过克服传统超声心动图的这些局限性,可以可靠和可重复地量化右心室体积和功能。本文综述了PH患者右心室功能的3DE评估,并讨论了以下几点:(1)获取用于3DE成像的右心室数据集,包括日常实践中使用的所有可用3DE系统和软件的详细信息;(2)不同方式3DE测量PH患者RV重构的可靠性和可行性;(3) 3de源性右心室功能对此类患者的预后价值。
{"title":"Real-time Three-dimensional Echocardiography: A Feasible and Accurate Method for Measuring Right Ventricular Function in Pulmonary Hypertension","authors":"Ashfaq Ahmad, Yifan Zou, Peng Zhang, Lingling Li, Xiaoyu Wang, Ahmed Ali Mohsen, Yousen Wang, Fenling Fan","doi":"10.1097/cd9.0000000000000108","DOIUrl":"https://doi.org/10.1097/cd9.0000000000000108","url":null,"abstract":"Right ventricular function is independently associated with poor clinical outcomes in patients with various cardiovascular diseases including pulmonary hypertension (PH). The complex geometry and mode of contractility means the right ventricle (RV) inlet and outlet are not in line; hence, 2-dimensional echocardiography fails to accurately quantify RV volumes and function in such patients. Three-dimensional echocardiography (3DE) allows for reliable and reproducible quantification of RV volumes and function by overcoming these limitations of conventional echocardiography. This review focuses on the 3DE assessment of RV function in patients with PH and discusses the following points: (1) acquiring an RV data set for 3DE imaging, including details of all available 3DE systems and software utilized in daily practice; (2) the reliability and feasibility of RV remodeling measured with 3DE with different modalities in patients with PH; and (3) the prognostic value of 3DE-derived RV function in such patients.","PeriodicalId":72524,"journal":{"name":"Cardiology discovery","volume":"298 9","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"2023-10-31","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"135815020","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
期刊
Cardiology discovery
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