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Clinical outcomes following shock team implementation for cardiogenic shock: a systematic review. 休克小组实施心源性休克后的临床结果:系统回顾。
Mohamed Abdelnabi, Ahmed Saad Elsaeidy, Aya Moustafa Aboutaleb, Amit Johanis, Ahmed K Ghanem, Hazem Rezq, Basel Abdelazeem

Background: Cardiogenic shock is a critical cardiac condition characterized by low cardiac output leading to end-organ hypoperfusion and associated with high in-hospital mortality rates. It can manifest following acute myocardial infarction or acute exacerbation of chronic heart failure. Despite advancements, mortality rates remain elevated, prompting interest in multidisciplinary approaches to improve outcomes. This manuscript presents a review focused on the concept of a cardiogenic shock team and its potential impact on patient management and outcomes.

Methods: A comprehensive search was performed on March 19, 2023, covering PubMed, Web of Science, Scopus, Embase, and Cochrane Library. We included primary studies (prospective and retrospective) only and evaluated their quality using the Newcastle-Ottawa Quality Scale. This review was registered in PROSPERO (CRD42023440354).

Results: Six relevant studies with 2066 cardiogenic shock patients were included, of which 1071 were managed by shock teams and 995 received standard care. Findings from the reviewed studies indicated the favorable outcomes associated with implementing cardiogenic shock teams. Patients managed by these teams exhibited higher 30-day and in-hospital survival rates compared to those without team intervention. The implementation of cardiogenic shock teams was linked to reduced in-hospital and intensive care unit mortality rates. Additionally, shock team involvement was associated with shorter door-to-balloon times.

Conclusion: The findings suggest that cardiogenic shock teams play a crucial role in improving patient outcomes through earlier detection and timely interventions. Despite challenges in team implementation, their potential to reduce mortality and improve efficiency in patient care warrants further research and greater integration of multidisciplinary strategies into clinical practice.

背景:心源性休克是一种以低心输出量导致终末器官灌注不足为特征的危重心脏疾病,与高住院死亡率相关。它可在急性心肌梗死或慢性心力衰竭急性加重后出现。尽管取得了进步,但死亡率仍然很高,这促使人们对多学科方法的兴趣,以改善结果。本文介绍了一篇综述,重点介绍了心源性休克小组的概念及其对患者管理和结果的潜在影响。方法:于2023年3月19日全面检索PubMed、Web of Science、Scopus、Embase、Cochrane Library。我们只纳入了初步研究(前瞻性和回顾性),并使用纽卡斯尔-渥太华质量量表评估了它们的质量。本综述已在PROSPERO注册(CRD42023440354)。结果:纳入6项相关研究共2066例心源性休克患者,其中1071例由休克小组管理,995例接受标准治疗。所回顾的研究结果表明,实施心源性休克小组相关的良好结果。与没有团队干预的患者相比,这些团队管理的患者表现出更高的30天和住院存活率。心源性休克小组的实施与降低住院和重症监护病房死亡率有关。此外,突击小组的参与缩短了门到气球的时间。结论:研究结果表明,心源性休克团队通过早期发现和及时干预,在改善患者预后方面发挥着至关重要的作用。尽管在团队实施方面存在挑战,但它们在降低死亡率和提高患者护理效率方面的潜力值得进一步研究,并将多学科策略更大程度地整合到临床实践中。
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引用次数: 0
Different phenotypes of hypertension and associated cardiovascular and all-cause mortality: a systematic review and meta-analysis. 不同表型的高血压和相关的心血管和全因死亡率:系统回顾和荟萃分析。
Jay Tewari, Khalid Ahmad Qidwai, Shubhajeet Roy, Mehul Saxena, Anadika Rana, Ajoy Tewari, Vineeta Tewari, Anuj Maheshwari

Background: Hypertension is a leading cause of premature mortality and morbidity. Recent guidelines advocate for out-of-office blood pressure monitoring, including ambulatory and home BP monitoring, to better identify hypertension phenotypes like masked hypertension, white coat hypertension, and sustained hypertension. However, clinical inertia persists due to a lack of robust evidence on the effectiveness of screening these phenotypes and their association with cardiovascular and all-cause mortality. This systematic review and meta-analysis aims to evaluate the relationship between various hypertension phenotypes and future cardiovascular events and all-cause mortality to support the broader implementation of out-of-office BP monitoring.

Main body: Following PRISMA, Cochrane, and MOOSE guidelines, we conducted a comprehensive search in Pubmed, OvidSP, and Cochrane Central databases up to October 17, 2023. Eligible studies reported associations between hypertension phenotypes and cardiovascular or all-cause mortality, with normotension as the reference group. Hazard ratios with 95% confidence intervals (CIs) were pooled using random-effects models. Eight studies with 15,327 participants were included. Masked hypertension was associated with increased cardiovascular mortality (pooled HR 2.05, 95% CI 1.69-2.48). Sustained hypertension also showed a higher risk (pooled HR 2.42, 95% CI 2.12-2.76). WCH did not significantly increase cardiovascular mortality risk (pooled HR 1.18, 95% CI 0.98-1.42). For all-cause mortality, neither masked hypertension (pooled HR 2.10, 95% CI 0.91-4.88) nor white coat hypertension (pooled HR 1.96, 95% CI 0.71-5.42) showed significant increases.

Conclusion: Masked hypertension and sustained hypertension are linked to higher cardiovascular mortality compared to normotension, highlighting the importance of out-of-office BP monitoring to identify and manage high-risk phenotypes effectively. Further high-quality studies are needed to generalize these findings and support policy changes.

背景:高血压是导致过早死亡和发病的主要原因。最近的指南提倡在办公室外进行血压监测,包括门诊和家庭血压监测,以更好地识别高血压表型,如隐匿性高血压、白大褂高血压和持续性高血压。然而,由于缺乏关于筛查这些表型的有效性及其与心血管和全因死亡率的关联的有力证据,临床惰性仍然存在。本系统综述和荟萃分析旨在评估各种高血压表型与未来心血管事件和全因死亡率之间的关系,以支持更广泛地实施办公室外血压监测。正文:遵循PRISMA、Cochrane和MOOSE指南,我们在Pubmed、OvidSP和Cochrane Central数据库中进行了全面检索,检索时间截止到2023年10月17日。符合条件的研究报告了高血压表型与心血管或全因死亡率之间的关联,血压正常者作为参照组。采用随机效应模型汇总95%置信区间的风险比。包括8项研究,15327名参与者。隐匿性高血压与心血管死亡率增加相关(总危险比2.05,95%可信区间1.69-2.48)。持续高血压也显示出更高的风险(总危险度2.42,95% CI 2.12-2.76)。WCH没有显著增加心血管死亡风险(合并HR 1.18, 95% CI 0.98-1.42)。对于全因死亡率,隐匿性高血压(总危险比2.10,95% CI 0.91-4.88)和白大衣高血压(总危险比1.96,95% CI 0.71-5.42)均未显示显著增加。结论:与血压正常相比,隐匿性高血压和持续性高血压与更高的心血管死亡率相关,强调了办公室外血压监测对有效识别和管理高危表型的重要性。需要进一步的高质量研究来概括这些发现并支持政策变化。
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引用次数: 0
Concurrent acute myocardial infarction and acute ischemic stroke in a diabetic patient undergoing chemotherapy for non-Hodgkin lymphoma: Should I administer thrombolytic therapy? A case report. 1例接受非霍奇金淋巴瘤化疗的糖尿病患者并发急性心肌梗死和急性缺血性卒中:我应该给予溶栓治疗吗?一份病例报告。
Sigfrid Casmir Shayo, Khuzeima Khanbai, Yona Gandye, Flora Lwakatare, Nakigunda Kiroga, Tatizo Waane, Peter Kisenge

Background: Concurrent ST-elevation myocardial infarction (STEMI) and acute ischemic stroke (AIS) are extremely rare, and their management remains perplexing due to the absence of high-quality evidence and limited resources. For the first time, we report a rare, preventable, and suboptimally managed case of concurrent AIS and STEMI in a patient with non-Hodgkin lymphoma (NHL) who received cyclophosphamide, doxorubicin, vincristine, and prednisolone (CHOP) chemotherapy.

Case presentation: A 59-year-old postmenopausal woman of African origin with a background history of type 2 diabetes mellitus presented to the Jakaya Kikwete Cardiac Institute with sudden onset of left-sided weakness and typical ischemic chest pain for 3 days. The patient was recently diagnosed with NHL and started CHOP chemotherapy 3 weeks prior. Physical examination revealed left-sided hemiplegia. Emergency brain computed tomography and 12-lead echocardiography (ECG) revealed AIS and STEMI, respectively. A diagnosis of concurrent AIS and STEMI was reached, and the patient was loaded with dual antiplatelets and heparin and rushed for emergency coronary angiography (GAG) and percutaneous coronary intervention (PCI). CAG revealed massive thrombotic occlusion of the mid-segment of the left anterior descending coronary artery (mLAD) and proximal segment of the right coronary artery. Revascularization was achieved in both vessels with a resultant TIMI flow grade of 3. The post-PCI period was marked by significant improvement in chest pain and resolution of ST-elevation, as revealed by 12-lead ECG. However, the patient remained hemiplegic.

Conclusion: We have described a rare case of concurrent AIS and STEMI in a postmenopausal woman who had a significant risk of thromboembolism. The patient had uncontrolled type 2 diabetes and received CHOP chemotherapy for NHL, which was diagnosed 3 weeks prior. This case underscores the need for thromboembolic prophylaxis for selected cancer patients receiving chemotherapy. The need to individualize management is also emphasized, as both PCI and thrombolysis carry the risk of serious repercussions. In our patient, if thrombolysis was attempted it would have caused myocardial rupture and immediate death. The patient would have benefited from endovascular mechanical embolectomy for AIS; however, this practice is lacking at our institution. This calls for the establishment and strengthening of neurointerventional practices in our tertiary healthcare facilities.

背景:并发st段抬高型心肌梗死(STEMI)和急性缺血性卒中(AIS)极为罕见,由于缺乏高质量证据和资源有限,其治疗仍然令人困惑。我们首次报道了一例罕见的、可预防的、管理不理想的同时发生AIS和STEMI的非霍奇金淋巴瘤(NHL)患者,该患者接受了环磷酰胺、阿霉素、长春新碱和泼尼松龙(CHOP)化疗。病例介绍:一名59岁的非洲裔绝经后妇女,有2型糖尿病的背景病史,因突然发作的左侧无力和典型的缺血性胸痛3天来到Jakaya Kikwete心脏研究所。该患者最近被诊断为NHL,并在3周前开始CHOP化疗。体检发现左侧偏瘫。急诊脑ct和12导联超声心动图(ECG)分别显示AIS和STEMI。诊断为并发AIS和STEMI,患者被加载双重抗血小板和肝素,并紧急进行急诊冠状动脉造影(GAG)和经皮冠状动脉介入治疗(PCI)。CAG显示左冠状动脉前降支中段和右冠状动脉近段大量血栓闭塞。两条血管都实现了血运重建,TIMI血流等级为3级。12导联心电图显示,pci术后胸痛明显改善,st段抬高缓解。然而,病人仍然处于偏瘫状态。结论:我们报道了一例罕见的并发AIS和STEMI的绝经后妇女,她有明显的血栓栓塞风险。患者患有不受控制的2型糖尿病,3周前诊断为NHL,接受CHOP化疗。本病例强调了对接受化疗的癌症患者进行血栓栓塞预防的必要性。个性化治疗的必要性也被强调,因为PCI和溶栓都有严重不良反应的风险。在我们的病人中,如果尝试溶栓会导致心肌破裂和立即死亡。患者将受益于血管内机械栓塞切除术治疗AIS;然而,这种做法在我们的机构是缺乏的。这就要求在我们的三级医疗机构中建立和加强神经介入实践。
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引用次数: 0
Retrieval of patent ductus arteriosus device embolization using hybrid approach: a case report. 混合入路恢复动脉导管未闭装置栓塞1例。
Uma Devi Karuru, Sadanand Reddy Tummala, T Naveen, Sai Kumar Mysore, Kiran Kumar Kanjerla

Background: Patent ductus arteriosus (PDA) is a congenital heart defect that requires closure to prevent complications like heart failure and pulmonary hypertension. Catheter-based closure using devices such as the Amplatzer duct occluder is the preferred method due to its minimally invasive nature. However, device embolization is a rare but recognized complication, particularly in small children or high-flow PDAs.

Case presentation: We report a rare and complex case of spontaneous embolization of a PDA closure device into the descending aorta in an 11-month-old female. The patient, with a history of recurrent lower respiratory tract infections and poor weight gain, underwent a PDA closure procedure after a thorough assessment. During the procedure, the Amplatzer Duct Occluder I device unexpectedly migrated into the descending aorta. Despite initial attempts at percutaneous retrieval using a goose neck snare, the device lodged in the left common iliac artery due to size discrepancy. Further snaring was abandoned to prevent the risk of artery dissection. The patient was then taken for emergency surgical exploration. The cardiovascular surgical team successfully retrieved the device through a left supra-inguinal incision, with no complications post-surgery. The patient showed improved limb perfusion and was discharged one week later.

Conclusions: This case underscores the importance of meticulous procedural planning, multidisciplinary collaboration, and adaptive decision-making in managing rare and challenging complications during PDA device closure. The successful outcome, despite the complex nature of the complication, highlights the effectiveness of combining percutaneous and surgical approaches in pediatric cardiology.

背景:动脉导管未闭(PDA)是一种先天性心脏缺陷,需要关闭以防止心力衰竭和肺动脉高压等并发症。由于其微创性,使用诸如Amplatzer导管闭塞器之类的导管闭合装置是首选的方法。然而,器械栓塞是一种罕见但公认的并发症,特别是在小孩或高流量pda中。病例介绍:我们报告一个罕见的和复杂的情况下,自发栓塞PDA关闭装置进入降主动脉在一个11个月大的女性。患者有复发性下呼吸道感染史和体重增加不佳,在彻底评估后接受了PDA闭合手术。在手术过程中,Amplatzer导管闭塞器I意外移动到降主动脉。尽管最初尝试使用鹅颈圈套经皮取出,但由于尺寸差异,该装置卡在了左侧髂总动脉中。为了防止动脉夹层的危险,放弃了进一步的圈套。患者随即接受紧急手术探查。心血管外科团队通过左侧腹股沟上切口成功取出该装置,术后无并发症。患者四肢灌注改善,1周后出院。结论:该病例强调了细致的手术计划、多学科合作和适应性决策在处理PDA设备关闭过程中罕见和具有挑战性的并发症中的重要性。尽管并发症的复杂性,但成功的结果突出了经皮和手术相结合的方法在儿科心脏病学中的有效性。
{"title":"Retrieval of patent ductus arteriosus device embolization using hybrid approach: a case report.","authors":"Uma Devi Karuru, Sadanand Reddy Tummala, T Naveen, Sai Kumar Mysore, Kiran Kumar Kanjerla","doi":"10.1186/s43044-024-00595-y","DOIUrl":"10.1186/s43044-024-00595-y","url":null,"abstract":"<p><strong>Background: </strong>Patent ductus arteriosus (PDA) is a congenital heart defect that requires closure to prevent complications like heart failure and pulmonary hypertension. Catheter-based closure using devices such as the Amplatzer duct occluder is the preferred method due to its minimally invasive nature. However, device embolization is a rare but recognized complication, particularly in small children or high-flow PDAs.</p><p><strong>Case presentation: </strong>We report a rare and complex case of spontaneous embolization of a PDA closure device into the descending aorta in an 11-month-old female. The patient, with a history of recurrent lower respiratory tract infections and poor weight gain, underwent a PDA closure procedure after a thorough assessment. During the procedure, the Amplatzer Duct Occluder I device unexpectedly migrated into the descending aorta. Despite initial attempts at percutaneous retrieval using a goose neck snare, the device lodged in the left common iliac artery due to size discrepancy. Further snaring was abandoned to prevent the risk of artery dissection. The patient was then taken for emergency surgical exploration. The cardiovascular surgical team successfully retrieved the device through a left supra-inguinal incision, with no complications post-surgery. The patient showed improved limb perfusion and was discharged one week later.</p><p><strong>Conclusions: </strong>This case underscores the importance of meticulous procedural planning, multidisciplinary collaboration, and adaptive decision-making in managing rare and challenging complications during PDA device closure. The successful outcome, despite the complex nature of the complication, highlights the effectiveness of combining percutaneous and surgical approaches in pediatric cardiology.</p>","PeriodicalId":74993,"journal":{"name":"The Egyptian heart journal : (EHJ) : official bulletin of the Egyptian Society of Cardiology","volume":"76 1","pages":"160"},"PeriodicalIF":0.0,"publicationDate":"2024-12-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11662123/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142866462","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
Finerenone: a breakthrough mineralocorticoid receptor antagonist for heart failure, diabetes and chronic kidney disease. 非格列酮:治疗心力衰竭、糖尿病和慢性肾病的突破性矿物皮质激素受体拮抗剂。
Akshyaya Pradhan, Umesh Chandra Tripathi

Background: Aldosterone is categorized as a mineralocorticoid hormone produced in the zona glomerulosa of the adrenal cortex. Aldosterone has considerable action in sodium and water retention along with cardiac remodeling, promoting fibrosis and these detrimental effects have been counteracted by mineralocorticoid receptors antagonists over time. Spironolactone, a non-selective steroidal MRA used extensively is potent but has serious adverse effects like gynecomastia and hyperkalemia. Eplerenone another second generation MRA, though non-steroidal and selective causes hyperkalemia and adversely effecting renal functions.

Main body: Recently Finerenone- a novel MRA has been introduced which is as potent like spironolactone with less adverse effects and improved cardiovascular outcomes particularly in chronic kidney failure with diabetes. The article reviews the physical and chemical properties of Finerenone and compares it with MRAs already in use, and then about the patient specific uses of Finerenone and future avenues of it. Finerenone is non-steroidal selective MRA, with promising results in improving the deterioration of renal functions in CKD with DM, reducing albuminuria with less hyperkalemia along with improvement in cardiovascular outcomes by reducing heart failure events.

Conclusion: Mineralocorticoid receptor antagonists have a proven role in preventing the adverse effects of RAAS pathway on heart, kidneys and blood vessels. Non-selective steroidal MRAs have potent action but by virtue of their non-selectivity associated with adverse effects like gynecomastia, hirsutism along with hyperkalemia Finerenone is novel non-steroidal & highly selective MRA, with promising results in halting the deterioration of renal functions in CKD with DM, reducing albuminuria, improvement in cardiovascular outcomes by reducing heart failure events albeit with less hyperkalemia. More randomized studies in dedicated HF patients are ongoing with Finerenone to prove it is worth in this sector with huge unmet need despite GDMT. Finerenone alleviates the risk of adverse renal and cardiac outcomes in patients with diabetes and CKD despite baseline medical therapy.

背景:醛固酮是肾上腺皮质肾小球区产生的一种矿质皮质激素。醛固酮在钠和水潴留、心脏重塑、促进纤维化等方面具有相当大的作用,这些有害影响已逐渐被矿物皮质激素受体拮抗剂所抵消。螺内酯(Spironolactone)是一种广泛使用的非选择性类固醇 MRA,具有强效作用,但有严重的不良反应,如妇科炎症和高钾血症。另一种第二代 MRA--依普利酮(Eplerenone)虽然是非类固醇和选择性的,但会导致高钾血症并对肾功能产生不良影响:最近推出的新型 MRA 非格列酮(Finerenone-)与螺内酯(spironolactone)的药效相同,但不良反应较少,可改善心血管预后,尤其是对慢性肾衰竭合并糖尿病患者的预后。文章回顾了非奈酮的物理和化学特性,并将其与已在使用的 MRA 进行了比较,然后介绍了非奈酮的患者特定用途及其未来的发展方向。非奈瑞酮是一种非甾体类选择性 MRA,在改善慢性肾功能衰竭合并 DM 患者的肾功能恶化、减少白蛋白尿和高钾血症方面具有良好效果,同时还能通过减少心衰事件改善心血管预后:结论:矿物质皮质激素受体拮抗剂在预防 RAAS 通路对心脏、肾脏和血管的不良影响方面发挥着公认的作用。非选择性类固醇 MRA 具有强效作用,但由于其非选择性,会产生妇科炎症、多毛症和高钾血症等不良反应,而菲尼酮是一种新型的非类固醇和高选择性 MRA,在阻止慢性肾功能衰竭合并糖尿病患者的肾功能恶化、减少白蛋白尿、通过减少心力衰竭事件改善心血管预后(尽管高钾血症较少)方面具有良好效果。目前正在对专门的心力衰竭患者进行更多的非奈酮随机研究,以证明它在这一领域的价值,尽管有 GDMT,但仍有大量需求未得到满足。尽管已接受了基线药物治疗,但非奈酮仍能减轻糖尿病和慢性肾功能衰竭患者的肾脏和心脏不良预后风险。
{"title":"Finerenone: a breakthrough mineralocorticoid receptor antagonist for heart failure, diabetes and chronic kidney disease.","authors":"Akshyaya Pradhan, Umesh Chandra Tripathi","doi":"10.1186/s43044-024-00586-z","DOIUrl":"10.1186/s43044-024-00586-z","url":null,"abstract":"<p><strong>Background: </strong>Aldosterone is categorized as a mineralocorticoid hormone produced in the zona glomerulosa of the adrenal cortex. Aldosterone has considerable action in sodium and water retention along with cardiac remodeling, promoting fibrosis and these detrimental effects have been counteracted by mineralocorticoid receptors antagonists over time. Spironolactone, a non-selective steroidal MRA used extensively is potent but has serious adverse effects like gynecomastia and hyperkalemia. Eplerenone another second generation MRA, though non-steroidal and selective causes hyperkalemia and adversely effecting renal functions.</p><p><strong>Main body: </strong>Recently Finerenone- a novel MRA has been introduced which is as potent like spironolactone with less adverse effects and improved cardiovascular outcomes particularly in chronic kidney failure with diabetes. The article reviews the physical and chemical properties of Finerenone and compares it with MRAs already in use, and then about the patient specific uses of Finerenone and future avenues of it. Finerenone is non-steroidal selective MRA, with promising results in improving the deterioration of renal functions in CKD with DM, reducing albuminuria with less hyperkalemia along with improvement in cardiovascular outcomes by reducing heart failure events.</p><p><strong>Conclusion: </strong>Mineralocorticoid receptor antagonists have a proven role in preventing the adverse effects of RAAS pathway on heart, kidneys and blood vessels. Non-selective steroidal MRAs have potent action but by virtue of their non-selectivity associated with adverse effects like gynecomastia, hirsutism along with hyperkalemia Finerenone is novel non-steroidal & highly selective MRA, with promising results in halting the deterioration of renal functions in CKD with DM, reducing albuminuria, improvement in cardiovascular outcomes by reducing heart failure events albeit with less hyperkalemia. More randomized studies in dedicated HF patients are ongoing with Finerenone to prove it is worth in this sector with huge unmet need despite GDMT. Finerenone alleviates the risk of adverse renal and cardiac outcomes in patients with diabetes and CKD despite baseline medical therapy.</p>","PeriodicalId":74993,"journal":{"name":"The Egyptian heart journal : (EHJ) : official bulletin of the Egyptian Society of Cardiology","volume":"76 1","pages":"159"},"PeriodicalIF":0.0,"publicationDate":"2024-12-16","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11649598/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142831164","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
sST2 levels and 3D speckle tracking as predictors of CAD severity in chronic coronary syndrome. 预测慢性冠状动脉综合征中 CAD 严重程度的 sST2 水平和 3D斑点追踪技术。
Amr Setouhi, K Maghraby, Nasser Taha, M Abdelsayed, Mohammed H Hassan, Hossam Eldin M Mahmoud

Background: Previous studies on the relation of sST2 with atherosclerotic disease mostly focused on the predictive value of sST2 for heart failure. However, there is no definite conclusion about the correlation between sST2 level and a complex coronary lesion morphology detected with coronary angiography (CAG). The purpose of this work was to know sST2 level and 3D speckle-tracking echocardiography as predictor of coronary artery disease (CAD) severity in chronic coronary syndrome (CCS) individuals using Gensini score. This prospective cohort work was performed on 90 participants aging from 18 to 80 years old, both sexes, with stable angina pectoris. Participants had been categorized into three groups: Group I (n = 30): control group scheduled by normal coronary angiography and group II (n = 60): case group which subdivided according to Gensini score into two equal subgroups: IIa: simple lesion (Gensini score < 20) and group IIb: complex lesion (Gensini score of ≥ 20). Plasma sST2 levels were measured in all participants using ELISA technique.

Results: GLS, GAS, GCS and ST2 can significantly predict severity of CAD in CCS, respectively (P < 0.001 and AUC (95% CI) = 0.949(0.881-0.984), 0.980(0.925 to 0.998), 0.908(0.828 to 0.959) and 0.702(0.597 to 0.794)) at cutoff ≥ - 10, - 21, - 12 and ≥ 10 with 96.67% (82.8% to 99.9%), 96.67% (82.8 to 99.9), 86.67% (69.3 to 96.2) and 63.33% (43.9 to 80.1) sensitivity (95% CI), 76.67% (64.0% to 86.6%), 85.0% (73.4 to 92.9), 73.33% (60.3 to 83.9) and 65.0% (51.6 to 76.9) specificity (95% CI), 67.44%, 76.32%, 61.90% and 47.50% PPV and 97.87%, 98.08%, 91.67% and 78.00%, NPV with accuracy of 83.33%, 88.89%, 77.78% and 64.44%.

Conclusions: sST2 level, GLS, GAS and GCS can significantly predict severity of CAD in CCS.

背景:以往关于sST2与动脉粥样硬化性疾病关系的研究多集中在sST2对心力衰竭的预测价值上。然而,关于sST2水平与冠状动脉造影(CAG)检测到的复杂冠状动脉病变形态之间的相关性尚无明确的结论。本研究的目的是利用Gensini评分了解sST2水平和3D斑点跟踪超声心动图作为慢性冠脉综合征(CCS)患者冠状动脉疾病(CAD)严重程度的预测因子。这项前瞻性队列研究对90名年龄在18岁至80岁之间的稳定型心绞痛患者进行了研究。将参与者分为三组:I组(n = 30):正常冠状动脉造影对照组;II组(n = 60):病例组,根据Gensini评分再细分为两个相同的亚组:IIa:单纯病变(Gensini评分)结果:GLS、GAS、GCS和ST2分别可显著预测CCS中CAD的严重程度(P)结论:sST2水平、GLS、GAS和GCS可显著预测CCS中CAD的严重程度。
{"title":"sST2 levels and 3D speckle tracking as predictors of CAD severity in chronic coronary syndrome.","authors":"Amr Setouhi, K Maghraby, Nasser Taha, M Abdelsayed, Mohammed H Hassan, Hossam Eldin M Mahmoud","doi":"10.1186/s43044-024-00588-x","DOIUrl":"10.1186/s43044-024-00588-x","url":null,"abstract":"<p><strong>Background: </strong>Previous studies on the relation of sST2 with atherosclerotic disease mostly focused on the predictive value of sST2 for heart failure. However, there is no definite conclusion about the correlation between sST2 level and a complex coronary lesion morphology detected with coronary angiography (CAG). The purpose of this work was to know sST2 level and 3D speckle-tracking echocardiography as predictor of coronary artery disease (CAD) severity in chronic coronary syndrome (CCS) individuals using Gensini score. This prospective cohort work was performed on 90 participants aging from 18 to 80 years old, both sexes, with stable angina pectoris. Participants had been categorized into three groups: Group I (n = 30): control group scheduled by normal coronary angiography and group II (n = 60): case group which subdivided according to Gensini score into two equal subgroups: IIa: simple lesion (Gensini score < 20) and group IIb: complex lesion (Gensini score of ≥ 20). Plasma sST2 levels were measured in all participants using ELISA technique.</p><p><strong>Results: </strong>GLS, GAS, GCS and ST2 can significantly predict severity of CAD in CCS, respectively (P < 0.001 and AUC (95% CI) = 0.949(0.881-0.984), 0.980(0.925 to 0.998), 0.908(0.828 to 0.959) and 0.702(0.597 to 0.794)) at cutoff ≥ - 10, - 21, - 12 and ≥ 10 with 96.67% (82.8% to 99.9%), 96.67% (82.8 to 99.9), 86.67% (69.3 to 96.2) and 63.33% (43.9 to 80.1) sensitivity (95% CI), 76.67% (64.0% to 86.6%), 85.0% (73.4 to 92.9), 73.33% (60.3 to 83.9) and 65.0% (51.6 to 76.9) specificity (95% CI), 67.44%, 76.32%, 61.90% and 47.50% PPV and 97.87%, 98.08%, 91.67% and 78.00%, NPV with accuracy of 83.33%, 88.89%, 77.78% and 64.44%.</p><p><strong>Conclusions: </strong>sST2 level, GLS, GAS and GCS can significantly predict severity of CAD in CCS.</p>","PeriodicalId":74993,"journal":{"name":"The Egyptian heart journal : (EHJ) : official bulletin of the Egyptian Society of Cardiology","volume":"76 1","pages":"158"},"PeriodicalIF":0.0,"publicationDate":"2024-12-16","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11649605/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142831166","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
Permanent pacemaker implantation for atrioventricular block secondary to acute pancreatitis in a patient affected by panhypopituitarism. 永久性起搏器植入治疗全垂体功能低下患者继发于急性胰腺炎的房室传导阻滞。
Jacopo Giovacchini, Silvia Menale, Irene Merilli, Valentina Scheggi

Background: Hypopituitarism may trigger the development of acute pancreatitis (AP) through multiple mechanisms. AP may alter normal intracardiac conduction leading to an atrioventricular block. Due to the lack of similar cases, the correct timing and indication for pacemaker implantation in such a setting are unknown.

Case presentation: A 22-year-old woman with a history of sub-total excision of frontal astrocytoma with residual panhypopituitarism in replacement therapy was admitted to the emergency department with AP and peripancreatic necrosis, complicated by hypotension, sinus bradycardia with 2:1 atrioventricular block, and severe acute respiratory distress syndrome deserving intubation and mechanical ventilation. During the in-hospital course, the patient developed a systemic inflammatory response syndrome and acute kidney failure and was treated with intravenous dopamine, diuretics, and liquids. While she gradually recovered, advanced atrioventricular block persisted after the resolution of AP; therefore, a permanent pacemaker was implanted. During the follow-up, appropriate device interventions were detected.

Conclusions: No other cases of high-grade atrioventricular block in panhypopituitarism-induced AP have been reported in the literature. Our case suggests a pacemaker is necessary if the atrioventricular block does not recover with AP resolution. Further evidence is required to improve the management of rhythm disturbances in hypopituitarism patients who develop AP.

背景:垂体功能低下可能通过多种机制引发急性胰腺炎(AP)的发展。AP可改变正常的心内传导,导致房室传导阻滞。由于缺乏类似的病例,在这种情况下植入起搏器的正确时机和指征尚不清楚。病例介绍:一名22岁女性,在替代治疗中行额叶星形细胞瘤次全切除并残留垂体功能减退症,因AP和胰周坏死,并发低血压,窦性心动过缓伴2:1房室传导阻滞,严重急性呼吸窘迫综合征,需要插管和机械通气而入住急诊科。在住院期间,患者出现全身炎症反应综合征和急性肾衰竭,静脉注射多巴胺、利尿剂和液体治疗。虽然她逐渐恢复,但AP消退后仍持续存在晚期房室传导阻滞;因此,植入了一个永久性起搏器。在随访期间,检测到适当的设备干预。结论:文献中未见其他高级别房室传导阻滞的报道。本病例提示,如果房室传导阻滞不随AP消退而恢复,则必须使用起搏器。需要进一步的证据来改善垂体功能低下患者并发AP的节律障碍管理。
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引用次数: 0
Obstructive hypertrophic cardiomyopathy: from genetic insights to a multimodal therapeutic approach with mavacamten, aficamten, and beyond. 梗阻性肥厚性心肌病:从遗传学的见解到多模式的治疗方法与马伐卡坦,阿菲卡坦,和超越。
Khadija Sarwer, Saeeda Lashari, Nida Rafaqat, Maher, Abdul Raheem, Muneeb Ur Rehman, Syed Muhammad Iraj Abbas
<p><strong>Background: </strong>A cardiac condition marked by excessive growth of heart muscle cells, hypertrophic cardiomyopathy (HCM) is a complex genetic disorder characterized by left ventricular hypertrophy, microvascular ischemia, myocardial fibrosis, and diastolic dysfunction. Obstructive hypertrophic cardiomyopathy (oHCM), a subset of HCM, involves significant obstruction in the left ventricular outflow tract (LVOT), leading to symptoms like dyspnea, fatigue, and potentially life-threatening cardiac events. With advancements in genetic understanding and the introduction of novel pharmacologic agents, including cardiac myosin inhibitors like mavacamten and aficamten, there is a paradigm shift in the therapeutic approach to oHCM.</p><p><strong>Main body: </strong>The underlying mechanisms of HCM are closely tied to genetic mutations affecting sarcomere proteins, particularly those encoded by the MYH7 and MYBPC3 genes. These mutations lead to disrupted sarcomere function, resulting in hypertrophic changes and LVOT obstruction. While genetic heterogeneity is a hallmark of HCM, clinical diagnosis relies heavily on imaging techniques such as Echocardiography and cardiac magnetic resonance imaging to assess the extent of hypertrophy and obstruction. Current pharmacological management of obstructive HCM (oHCM) focuses on alleviating symptoms rather than modifying disease progression. Beta-blockers and calcium channel blockers are primary treatment options, although their effectiveness varies among patients. Recent clinical trials have highlighted the potential of novel cardiac myosin inhibitors, including mavacamten and aficamten, in enhancing exercise capacity, reducing LVOT obstruction, and improving overall cardiac function. These innovative agents represent a significant breakthrough in targeting the fundamental pathophysiological mechanisms driving oHCM. A comprehensive literature review was conducted, utilizing top-tier databases such as PubMed, Scopus, and Google Scholar, to compile an authoritative and up-to-date overview of the current advancements in the field. This review sheds light on the updated 2024 American Heart Association (AHA) guidelines for HCM management, emphasizing the treatment cascade and tailored management for each stage of oHCM. By introducing a new paradigm for personalized medicine in oHCM, this research leverages advanced genomics, biomarkers, and imaging techniques to optimize treatment strategies.</p><p><strong>Conclusions: </strong>The introduction of cardiac myosin inhibitors heralds a new era in the management of oHCM. By directly targeting the molecular mechanisms underpinning the disease, these novel therapies offer improved symptom relief and functional outcomes. Ongoing research into the genetic basis of HCM and the development of targeted treatments holds promise for further enhancing patient care. Future studies should continue to refine these therapeutic strategies and explore their long-term benefits a
背景:肥厚性心肌病(HCM)是一种以心肌细胞过度生长为特征的心脏疾病,是一种复杂的遗传性疾病,其特征为左心室肥厚、微血管缺血、心肌纤维化和舒张功能障碍。梗阻性肥厚性心肌病(oHCM)是HCM的一个亚型,涉及左心室流出道(LVOT)的严重阻塞,导致呼吸困难、疲劳和潜在的危及生命的心脏事件等症状。随着遗传学理解的进步和新型药物的引入,包括心脏肌球蛋白抑制剂如马伐camten和阿非卡坦,oHCM的治疗方法发生了范式转变。正文:HCM的潜在机制与影响肌瘤蛋白的基因突变密切相关,特别是那些由MYH7和MYBPC3基因编码的基因突变。这些突变导致肌节功能破坏,导致肥厚改变和LVOT阻塞。虽然遗传异质性是HCM的标志,但临床诊断在很大程度上依赖于超声心动图和心脏磁共振成像等成像技术来评估肥厚和梗阻的程度。目前梗阻性HCM (oHCM)的药理学治疗侧重于减轻症状,而不是改变疾病进展。受体阻滞剂和钙通道阻滞剂是主要的治疗选择,尽管它们的效果因患者而异。最近的临床试验强调了新型心肌肌球蛋白抑制剂的潜力,包括马伐卡坦和阿非卡坦,在增强运动能力,减少左心室静脉阻塞和改善整体心功能方面。这些创新药物在针对驱动oHCM的基本病理生理机制方面取得了重大突破。利用PubMed、Scopus和谷歌Scholar等顶级数据库,进行了全面的文献综述,编制了该领域当前进展的权威和最新概述。这篇综述阐明了更新的2024年美国心脏协会(AHA) HCM管理指南,强调了oHCM每个阶段的治疗级联和量身定制的管理。通过在oHCM中引入个性化医疗的新范例,本研究利用先进的基因组学、生物标志物和成像技术来优化治疗策略。结论:心肌肌球蛋白抑制剂的引入预示着oHCM治疗的新时代。通过直接靶向支持疾病的分子机制,这些新疗法可以改善症状缓解和功能结果。正在进行的HCM遗传基础研究和靶向治疗的发展有望进一步加强患者护理。未来的研究应该继续完善这些治疗策略,并探索它们在不同患者群体中的长期效益和潜力。本综述综合了最新的美国心脏协会指南,强调了量身定制的管理策略在优化oHCM患者预后方面的关键作用,并促进了尖端基因组学和成像模式的结合,以加强个性化护理,对该领域做出了重大贡献。
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引用次数: 0
Contrast-induced encephalopathy with visual and auditory hallucinations triggered by coronary angiography with iodixanol: a case report. 碘沙醇冠脉造影诱发造影剂诱导脑病伴视、听幻觉1例。
Michał Kuzemczak, Sławomir Gołębiewski

Background: Contrast-induced encephalopathy (CIE) is a rare complication of coronary angiography posing a significant diagnostic challenge. Its incidence has substantially declined with the introduction of nonionic low-osmolar contrast media and, in most cases, it manifests with transient cortical blindness. Concomitant visual and auditory hallucinations in the course of CIE have never been reported.

Case report: We present the first reported case of CIE with concomitant visual and auditory hallucinations following coronary angiography in an 80-year-old female patient. The procedure was elective and performed via right radial approach. During the procedure, significant difficulties in crossing a tortuous and calcified brachiocephalic trunk were encountered. The patient lost awareness of time and place, became agitated and started having aphasia. Periprocedural stroke was suspected as a consequence of atherosclerotic plaque mobilization and dislodging atheromatous material to the cerebral vasculature. The patient became fully oriented without aphasia within 24 h, but started having auditory and visual hallucinations. Stroke was excluded by an urgent MRI, and ultimately CIE was diagnosed. A supportive therapy with sedation and intravenous hydration was used with subsequent commencement of quetiapine treatment for hallucinations. The symptoms resolved after 5 days, and quetiapine was successfully discontinued.

Conclusions: Based on the unique case report, CIE may manifest with concomitant visual and auditory hallucinations. In some instances, the clinical entity may mimic stroke; therefore, it is crucial to rule out this acute neurological condition and prevent patients from receiving a potentially harmful treatment.

背景:造影剂诱发的脑病(CIE)是冠状动脉造影中一种罕见的并发症,对诊断提出了重大挑战。随着非离子型低渗透性造影剂的使用,其发病率大大下降,在大多数情况下,它表现为短暂性皮质失明。CIE过程中伴随的视、听幻觉尚未见报道。病例报告:我们报告了首例冠状动脉造影后伴有视觉和听觉幻觉的CIE病例,患者为80岁的女性患者。手术是选择性的,通过右桡骨入路进行。在手术过程中,在穿过弯曲和钙化的头臂躯干时遇到了很大的困难。病人失去了时间和地点的意识,变得焦躁不安,开始失语。围手术期卒中被怀疑是动脉粥样硬化斑块动员和动脉粥样硬化物质转移到脑血管系统的结果。患者在24小时内完全定向,无失语,但开始出现听觉和视觉幻觉。通过紧急MRI排除卒中,最终确诊为CIE。支持治疗镇静和静脉水合使用,随后开始喹硫平治疗幻觉。5天后症状消失,并成功停用喹硫平。结论:根据独特的病例报告,CIE可能伴有视觉和听觉幻觉。在某些情况下,临床实体可能模仿中风;因此,排除这种急性神经系统疾病并防止患者接受可能有害的治疗是至关重要的。
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引用次数: 0
Thrombus aspiration in primary percutaneous coronary intervention in acute ST-elevation myocardial infarction patients with high thrombus burden: one-year outcomes in a tertiary healthcare center in Ho Chi Minh City. 高血栓负担急性st段抬高型心肌梗死患者经皮冠状动脉介入治疗中血栓吸出:胡志明市三级医疗中心的一年结果
Duy Cao Phuong Le, Giang Thai Pham, Quan Duy Vo

Background: Primary percutaneous coronary intervention (PCI) can dislodge atherosclerotic debris, risking microvascular embolism. Thrombus aspiration (TA) before stenting in ST-segment elevation myocardial infarction (STEMI) patients has been linked to reduced mortality, lower recurrence of heart attacks, and improved cardiac function. However, limited research exists on the effectiveness of TA in Vietnam, underscoring the need for further studies to enhance cardiovascular care. This prospective observational study was conducted to evaluate the role of TA in STEMI patients admitted with a substantial thrombus burden at Nguyen Tri Phuong Hospital.

Results: Out of 92 participants, 68 underwent TA treatment. Post-treatment, the TA group exhibited better TIMI and TMP flow grades and a higher rate of ST-segment normalization, with no significant difference in major adverse cardiac events (MACEs) at 30-day and 12-month follow-ups compared to those untreated.

Conclusions: TA during PCI enhances ST-segment normalization and TIMI and TMP scores in STEMI patients, improving myocardial perfusion. No difference in MACE occurrence was noted between groups after 30 days and 12 months, suggesting TA's potential benefits without increasing adverse outcomes.

背景:初级经皮冠状动脉介入治疗(PCI)可以清除动脉粥样硬化碎片,有微血管栓塞的风险。st段抬高型心肌梗死(STEMI)患者支架植入术前血栓抽吸(TA)与降低死亡率、降低心脏病发作复发率和改善心功能有关。然而,关于TA在越南的有效性的研究有限,强调需要进一步研究以加强心血管护理。这项前瞻性观察性研究旨在评估TA在Nguyen Tri Phuong医院住院的具有大量血栓负担的STEMI患者中的作用。结果:92名参与者中,68名接受了TA治疗。治疗后,TA组表现出更好的TIMI和TMP血流等级和更高的st段正常化率,在30天和12个月的随访中,与未治疗组相比,主要不良心脏事件(mace)无显著差异。结论:PCI时TA可增强STEMI患者st段正常化及TIMI、TMP评分,改善心肌灌注。30天和12个月后,两组间MACE的发生率没有差异,这表明TA的潜在益处不会增加不良后果。
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引用次数: 0
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The Egyptian heart journal : (EHJ) : official bulletin of the Egyptian Society of Cardiology
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