Pub Date : 2022-06-08DOI: 10.1136/heartjnl-2022-321214
R. Alharethi, R. A. Butschek, Kismet Rasmusson, B. Whisenant
With recent advancements in the treatment of heart failure with reduced ejection fraction (HFrEF) including the addition of angiotensin receptor–neprilysin inhibitor, sodium–glucose cotransporter 2 inhibitors (SGLT2i) and transcatheter edgetoedge mitral valve repair (TEER), the treatment of patients with cardiomyopathy and secondary mitral regurgitation (SMR) has become increasingly complex and can lead to suboptimal utilisation of indicated therapies. Tanaka and colleagues have provided a realworld analysis of guidelinedirected medical therapy (GDMT) among HFREF patients with SMR and managed with TEER. Their findings reinforce the importance of engaging focused heart failure (HF) cardiologists and allied teams to optimise medical therapy before and after TEER. Consistent with the 2021 European Society of Cardiology guideline on HF management, the authors define GDMT as modulation of the renin–angiotensin–aldosterone and sympathetic nervous systems with triple therapy including renin–angiotensin system (RAS) inhibitors, betablockers (BBs) and mineralocorticoid receptor antagonists (MRAs) noting that SGLT2is were approved after study completion. Their results demonstrated the clinical benefits of maintaining triple therapy neuromodulation following TEER. They have thus provided a pragmatic and simple threshold of GDMT that will undoubtedly improve the care of patients with SMR undergoing TEER. Tanaka et al retrospectively divided patients with SMR and left ventricular ejection fraction (LVEF) <50% who underwent TEER into GDMT and nonGDMT cohorts. Local heart teams optimised medical therapy and decided when to perform TEER. As such, this is a realworld population of patients with SMR managed with TEER. GDMT was defined as patients who received triple therapy at the time of discharge with RAS inhibitors, BBs and MRAs of any doses. Nevertheless, among the GDMT cohort, only 21% of patients received target doses of BBs, and only 12% received target doses of RAS inhibitors. NonGDMT patients were prescribed optimal medical therapy per the local heart team consensus including BBs in 84% (16% with target doses), and RAS inhibitors in 60% (12% at target doses). While all GDMT patients were prescribed MRAs, only 22% of nonGDMT patients were prescribed MRAs. Among patients without GDMT, 42% had factors related to ineligibility (ie, systolic blood pressure <100 mm Hg, heart rate <60 bpm or estimated glomerular filtration rate <30 mL/min/m). This underscores the difference between relative ineligibility to a medication and the intolerance to this medication with the inherent complexity of providing detailed reasons for intolerance of GDMT, which were not recorded in this study. We are not sure if the lack of triple therapy in the nonGDMT cohort and the less than target doses of medications in both cohorts represents the absolute maximally tolerated medical therapy. Twoyear mortality was compared between groups after calculating propensity scores and performing
随着最近在治疗心力衰竭伴射血分数降低(HFrEF)方面的进展,包括血管紧张素受体- neprilysin抑制剂、钠-葡萄糖共转运蛋白2抑制剂(SGLT2i)和经导管边缘二尖瓣修复(TEER),心肌病和继发性二尖瓣反流(SMR)患者的治疗变得越来越复杂,并可能导致适应症治疗的次优利用。Tanaka及其同事对伴有SMR的HFREF患者的指导药物治疗(GDMT)进行了现实分析,并采用TEER进行管理。他们的研究结果强调了专注心力衰竭(HF)心脏病专家和相关团队在TEER前后优化药物治疗的重要性。与2021年欧洲心脏病学会心衰管理指南一致,作者将GDMT定义为通过包括肾素血管紧张素系统(RAS)抑制剂、β受体阻滞剂(BBs)和矿皮质激素受体拮抗剂(MRAs)在内的三联疗法调节肾素血管紧张素醛酮和交感神经系统,并指出SGLT2is在研究完成后获得批准。他们的结果证明了TEER后维持三联疗法神经调节的临床益处。因此,他们提供了一个实用而简单的GDMT阈值,这无疑将改善SMR患者接受TEER的护理。Tanaka等回顾性地将接受TEER的SMR和左室射血分数(LVEF) <50%的患者分为GDMT和非ongdmt两组。当地心脏团队优化了医疗治疗并决定了何时进行TEER。因此,这是一个用TEER治疗SMR患者的真实世界人群。GDMT被定义为在出院时接受任何剂量的RAS抑制剂、BBs和mra三联治疗的患者。然而,在GDMT队列中,只有21%的患者接受了目标剂量的BBs,只有12%的患者接受了目标剂量的RAS抑制剂。根据当地心脏团队共识,NonGDMT患者被处方最佳药物治疗,包括84%的bb(16%的目标剂量)和60%的RAS抑制剂(12%的目标剂量)。虽然所有GDMT患者都开了mra,但只有22%的非ongdmt患者开了mra。在没有GDMT的患者中,42%存在与不合格相关的因素(即收缩压<100 mm Hg,心率<60 bpm或估计肾小球滤过率<30 mL/min/m)。这强调了一种药物的相对不适宜性和对这种药物的不耐受之间的差异,提供GDMT不耐受的详细原因固有的复杂性,这在本研究中没有记录。我们不确定在nonGDMT队列中缺乏三联治疗以及两个队列中低于目标剂量的药物是否代表绝对最大耐受的药物治疗。在计算倾向得分并进行治疗加权逆概率(IPTW)分析后,比较两组之间的两年死亡率。三联治疗GDMT (BBs、RAS抑制剂和MRAs)出院的患者死亡率明显低于未治疗GDMT出院的患者(19.8% vs 31.1%, p=0.011)。与没有GDMT的患者相比,患有GDMT的患者在TEER后1年的左心室反向重构率同样更高。正如作者所指出的,这项研究必须在回顾性观察性研究的限制范围内进行解释。虽然作者试图通过使用IPTWadjusted方法来纠正选择偏差,但混杂因素可能会影响结果。耐受三联治疗GDMT的能力可能预示着良好的预后。三联治疗GDMT出院的患者年龄较小,肾功能较好,血液透析较少。然而,作者提出的明显结论是,优化RAS抑制剂、BBs和MRAs联合药物治疗对于改善因SMR接受TEER治疗的患者的临床结果至关重要。GDMT的工作定义为BBs、RAS抑制剂和MRAs的三重神经激素抑制,可作为考虑TEER的最低阈值,并作为TEER后出院的优先考虑。两组患者的靶剂量率相对较低,这强调了实现靶剂量的难度,以及让心衰专家参与HFrEF患者管理的重要性。在MitraClip经皮治疗心力衰竭合并功能性二尖瓣反流(COAPT)试验的患者心血管结局评估中,8.65%随机分组至TEER和GDMT的患者开始新的BB或将当前BB剂量增加100%,而仅随机分组至GDMT的患者为3.8% (p=0.01),这与TEER增加收缩压并促进强化药物治疗的常见临床观察一致。 重要的是,考虑到TEER后随访中GDMT剂量没有显著变化,Tanaka研究再次证明了纵向护理的必要性,并持续不断地尝试寻找最大耐受剂量的GDMT。这些TEER发现反映了其他几个关于HFrEF患者GDMT利用不足的研究结果。2018年,改变心力衰竭患者的管理,CHAMPSHF登记收集了社区心脏病学和初级保健实践中的GDMT率,揭示了HFrEF患者适当治疗的利用率惊人不足(如前所述,不到25%的患者接受了三联治疗,只有1%的患者接受了目标剂量)。在2021年通过患者和医院参与心力衰竭临床试验的护理优化中,CONNECTHF研究再次证实了GDMT优化方面的持续差距,该研究显示,尽管医院和出院后质量得到了改善,但GDMT率仍未达到最佳水平。植入式心律转复除颤器(ICD)和心脏再同步装置研究发现,在植入ICD/心脏再同步装置之前和之后,心衰药物治疗都是按照规定进行的,在心律装置治疗后,最佳药物治疗的患者生存率提高,心衰住院率降低。最近的HFrEF指南将“改进型LVEF”一词编入了美国犹他州默里市山间医学中心心脏病科的既往HFrEF患者
{"title":"The synergy of myopathic valvular disease","authors":"R. Alharethi, R. A. Butschek, Kismet Rasmusson, B. Whisenant","doi":"10.1136/heartjnl-2022-321214","DOIUrl":"https://doi.org/10.1136/heartjnl-2022-321214","url":null,"abstract":"With recent advancements in the treatment of heart failure with reduced ejection fraction (HFrEF) including the addition of angiotensin receptor–neprilysin inhibitor, sodium–glucose cotransporter 2 inhibitors (SGLT2i) and transcatheter edgetoedge mitral valve repair (TEER), the treatment of patients with cardiomyopathy and secondary mitral regurgitation (SMR) has become increasingly complex and can lead to suboptimal utilisation of indicated therapies. Tanaka and colleagues have provided a realworld analysis of guidelinedirected medical therapy (GDMT) among HFREF patients with SMR and managed with TEER. Their findings reinforce the importance of engaging focused heart failure (HF) cardiologists and allied teams to optimise medical therapy before and after TEER. Consistent with the 2021 European Society of Cardiology guideline on HF management, the authors define GDMT as modulation of the renin–angiotensin–aldosterone and sympathetic nervous systems with triple therapy including renin–angiotensin system (RAS) inhibitors, betablockers (BBs) and mineralocorticoid receptor antagonists (MRAs) noting that SGLT2is were approved after study completion. Their results demonstrated the clinical benefits of maintaining triple therapy neuromodulation following TEER. They have thus provided a pragmatic and simple threshold of GDMT that will undoubtedly improve the care of patients with SMR undergoing TEER. Tanaka et al retrospectively divided patients with SMR and left ventricular ejection fraction (LVEF) <50% who underwent TEER into GDMT and nonGDMT cohorts. Local heart teams optimised medical therapy and decided when to perform TEER. As such, this is a realworld population of patients with SMR managed with TEER. GDMT was defined as patients who received triple therapy at the time of discharge with RAS inhibitors, BBs and MRAs of any doses. Nevertheless, among the GDMT cohort, only 21% of patients received target doses of BBs, and only 12% received target doses of RAS inhibitors. NonGDMT patients were prescribed optimal medical therapy per the local heart team consensus including BBs in 84% (16% with target doses), and RAS inhibitors in 60% (12% at target doses). While all GDMT patients were prescribed MRAs, only 22% of nonGDMT patients were prescribed MRAs. Among patients without GDMT, 42% had factors related to ineligibility (ie, systolic blood pressure <100 mm Hg, heart rate <60 bpm or estimated glomerular filtration rate <30 mL/min/m). This underscores the difference between relative ineligibility to a medication and the intolerance to this medication with the inherent complexity of providing detailed reasons for intolerance of GDMT, which were not recorded in this study. We are not sure if the lack of triple therapy in the nonGDMT cohort and the less than target doses of medications in both cohorts represents the absolute maximally tolerated medical therapy. Twoyear mortality was compared between groups after calculating propensity scores and performing ","PeriodicalId":9311,"journal":{"name":"British Heart Journal","volume":"108 1","pages":"1670 - 1671"},"PeriodicalIF":0.0,"publicationDate":"2022-06-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"44168303","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}
Pub Date : 2022-06-08DOI: 10.1136/heartjnl-2022-320831
A. Ioannou
20 Webb JG, Pate GE, Munt BI. Percutaneous closure of an aortic prosthetic paravalvular leak with an Amplatzer duct occluder. Catheter Cardiovasc Interv 2005;65:69–72. 21 Piéchaud JF. Percutaneous closure of mitral paravalvular leak. J Interv Cardiol 2003;16:153–5. 22 Sorajja P, Cabalka AK, Hagler DJ, et al. Percutaneous repair of paravalvular prosthetic regurgitation: acute and 30day outcomes in 115 patients. Circ Cardiovasc Interv 2011;4:314–21. 23 Ruiz CE, Jelnin V, Kronzon I, et al. Clinical outcomes in patients undergoing percutaneous closure of periprosthetic paravalvular leaks. J Am Coll Cardiol 2011;58:2210–7. 24 Millán X, Bouhout I, Nozza A, et al. Surgery Versus Transcatheter Interventions for Significant Paravalvular Prosthetic Leaks. JACC Cardiovasc Interv 2017;10:1959–69. 25 Sorajja P, Cabalka AK, Hagler DJ, et al. The learning curve in percutaneous repair of paravalvular prosthetic regurgitation: an analysis of 200 cases. JACC Cardiovasc Interv 2014;7:521–9. 26 Lancellotti P, Pibarot P, Chambers J, et al. Recommendations for the imaging assessment of prosthetic heart valves: a report from the European Association of Cardiovascular Imaging endorsed by the Chinese Society of Echocardiography, the InterAmerican Society of Echocardiography, and the Brazilian Department of Cardiovascular Imaging . Eur Heart J Cardiovasc Imaging 2016;17:589–90. 27 Hascoet S, Smolka G, Bagate F, et al. Multimodality imaging guidance for percutaneous paravalvular leak closure: insights from the multicentre FFPP register. Arch Cardiovasc Dis 2018;111:421–31. 28 Lesser JR, Han BK, Newell M, et al. Use of cardiac CT angiography to assist in the diagnosis and treatment of aortic prosthetic paravalvular leak: a practical guide. J Cardiovasc Comput Tomogr 2015;9:159–64. 29 Suh YJ, Hong GR, Han K, et al. Assessment of mitral paravalvular leakage after mitral valve replacement using cardiac computed tomography: comparison with surgical findings. Circ Cardiovasc Imaging 2016;9. 30 de Agustin JA, JimenezQuevedo P, NombelaFranco L, et al. Paravalvular mitral leak closure under EcoXray fusion guidance. Eur Heart J Cardiovasc Imaging 2018;19:586. 31 Faletra FF, Pozzoli A, Agricola E, et al. Echocardiographicfluoroscopic fusion imaging for transcatheter mitral valve repair guidance. Eur Heart J Cardiovasc Imaging 2018;19:715–26. 32 Gafoor S, Steinberg DH, Franke J, et al. Tools and techniques--clinical: paravalvular leak closure. EuroIntervention 2014;9:1359–63. 33 Calvert PA, Northridge DB, Malik IS, et al. Percutaneous device closure of paravalvular leak: combined experience from the United Kingdom and Ireland. Circulation 2016;134:934–44. 34 García E, Arzamendi D, JimenezQuevedo P, et al. Outcomes and predictors of success and complications for paravalvular leak closure: an analysis of the Spanish realworld paravalvular leaks closure (HOLE) registry. EuroIntervention 2017;12:1962–8. 35 AnguloLlanos R, SarnagoCebada F, Rivera AR, et al. Twoyear follow up after surgical
{"title":"An interesting case of fever and left ventricular systolic dysfunction","authors":"A. Ioannou","doi":"10.1136/heartjnl-2022-320831","DOIUrl":"https://doi.org/10.1136/heartjnl-2022-320831","url":null,"abstract":"20 Webb JG, Pate GE, Munt BI. Percutaneous closure of an aortic prosthetic paravalvular leak with an Amplatzer duct occluder. Catheter Cardiovasc Interv 2005;65:69–72. 21 Piéchaud JF. Percutaneous closure of mitral paravalvular leak. J Interv Cardiol 2003;16:153–5. 22 Sorajja P, Cabalka AK, Hagler DJ, et al. Percutaneous repair of paravalvular prosthetic regurgitation: acute and 30day outcomes in 115 patients. Circ Cardiovasc Interv 2011;4:314–21. 23 Ruiz CE, Jelnin V, Kronzon I, et al. Clinical outcomes in patients undergoing percutaneous closure of periprosthetic paravalvular leaks. J Am Coll Cardiol 2011;58:2210–7. 24 Millán X, Bouhout I, Nozza A, et al. Surgery Versus Transcatheter Interventions for Significant Paravalvular Prosthetic Leaks. JACC Cardiovasc Interv 2017;10:1959–69. 25 Sorajja P, Cabalka AK, Hagler DJ, et al. The learning curve in percutaneous repair of paravalvular prosthetic regurgitation: an analysis of 200 cases. JACC Cardiovasc Interv 2014;7:521–9. 26 Lancellotti P, Pibarot P, Chambers J, et al. Recommendations for the imaging assessment of prosthetic heart valves: a report from the European Association of Cardiovascular Imaging endorsed by the Chinese Society of Echocardiography, the InterAmerican Society of Echocardiography, and the Brazilian Department of Cardiovascular Imaging . Eur Heart J Cardiovasc Imaging 2016;17:589–90. 27 Hascoet S, Smolka G, Bagate F, et al. Multimodality imaging guidance for percutaneous paravalvular leak closure: insights from the multicentre FFPP register. Arch Cardiovasc Dis 2018;111:421–31. 28 Lesser JR, Han BK, Newell M, et al. Use of cardiac CT angiography to assist in the diagnosis and treatment of aortic prosthetic paravalvular leak: a practical guide. J Cardiovasc Comput Tomogr 2015;9:159–64. 29 Suh YJ, Hong GR, Han K, et al. Assessment of mitral paravalvular leakage after mitral valve replacement using cardiac computed tomography: comparison with surgical findings. Circ Cardiovasc Imaging 2016;9. 30 de Agustin JA, JimenezQuevedo P, NombelaFranco L, et al. Paravalvular mitral leak closure under EcoXray fusion guidance. Eur Heart J Cardiovasc Imaging 2018;19:586. 31 Faletra FF, Pozzoli A, Agricola E, et al. Echocardiographicfluoroscopic fusion imaging for transcatheter mitral valve repair guidance. Eur Heart J Cardiovasc Imaging 2018;19:715–26. 32 Gafoor S, Steinberg DH, Franke J, et al. Tools and techniques--clinical: paravalvular leak closure. EuroIntervention 2014;9:1359–63. 33 Calvert PA, Northridge DB, Malik IS, et al. Percutaneous device closure of paravalvular leak: combined experience from the United Kingdom and Ireland. Circulation 2016;134:934–44. 34 García E, Arzamendi D, JimenezQuevedo P, et al. Outcomes and predictors of success and complications for paravalvular leak closure: an analysis of the Spanish realworld paravalvular leaks closure (HOLE) registry. EuroIntervention 2017;12:1962–8. 35 AnguloLlanos R, SarnagoCebada F, Rivera AR, et al. Twoyear follow up after surgical","PeriodicalId":9311,"journal":{"name":"British Heart Journal","volume":"108 1","pages":"1011 - 1074"},"PeriodicalIF":0.0,"publicationDate":"2022-06-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"43925789","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}
Pub Date : 2022-06-07DOI: 10.1136/heartjnl-2022-320826
Tetsu Tanaka, R. Kavsur, M. Spieker, C. Iliadis, C. Metze, Birthe M Brachtendorf, P. Horn, C. Zachoval, A. Sugiura, M. Kelm, S. Baldus, G. Nickenig, R. Westenfeld, R. Pfister, M. Becher
Objective A sizeable proportion of patients with secondary mitral regurgitation (SMR) do not receive guideline-directed medical therapy (GDMT) for heart failure (HF). We investigated the association between the use of GDMT and mortality in patients with SMR who underwent transcatheter edge-to-edge repair (TEER). Methods We retrospectively analysed patients with SMR and a left ventricular ejection fraction of <50% who underwent TEER at three centres. According to current HF guidelines, GDMT was defined as triple therapy consisting of beta-blockers, renin–angiotensin system (RAS) inhibitors and mineralocorticoid receptor antagonists (MRAs). Patients were divided into two groups: GDMT and non-GDMT groups. We calculated the propensity scores and carried out inverse probability of treatment weighting (IPTW) analyses to compare 2-year mortality between the two groups. Results Of 463 patients, 228 (49.2%) were treated with GDMT upon discharge. IPTW-adjusted Kaplan-Meier curve showed patients with GDMT had a lower incidence of mortality than those without GDMT (19.8% vs 31.1%, p=0.011). In IPTW-adjusted Cox proportional hazards analysis, GDMT was associated with a reduced risk of 2-year mortality (HR: 0.58; 95% CI: 0.35 to 0.95; p=0.030), which was consistent among clinical subgroups. Moreover, patients with GDMT had a higher rate of left ventricular reverse remodelling at 1 year after TEER than those without GDMT. Conclusion GDMT, defined as triple therapy consisting of beta-blockers, RAS inhibitors and MRAs, was associated with a reduced risk of 2-year mortality after TEER for SMR. Optimisation of medical therapy is crucial to improve clinical outcomes in patients undergoing TEER for SMR.
目的相当大比例的继发性二尖瓣返流(SMR)患者未接受心力衰竭(HF)的指导药物治疗(GDMT)。我们调查了接受经导管边缘到边缘修复(TEER)的SMR患者使用GDMT与死亡率之间的关系。方法我们回顾性分析了在三个中心接受TEER治疗的SMR和左心室射血分数<50%的患者。根据目前的HF指南,GDMT被定义为由β受体阻滞剂、肾素-血管紧张素系统(RAS)抑制剂和矿皮质激素受体拮抗剂(MRAs)组成的三联疗法。患者分为GDMT组和非GDMT组。我们计算倾向得分,并进行治疗加权逆概率(IPTW)分析,比较两组的2年死亡率。结果463例患者中,228例(49.2%)在出院时接受了GDMT治疗。经iptw校正的Kaplan-Meier曲线显示,GDMT患者的死亡率低于未GDMT患者(19.8% vs 31.1%, p=0.011)。在iptw校正的Cox比例风险分析中,GDMT与2年死亡风险降低相关(HR: 0.58;95% CI: 0.35 ~ 0.95;P =0.030),这在临床亚组中是一致的。此外,与没有GDMT的患者相比,有GDMT的患者在TEER后1年的左心室反向重构率更高。结论GDMT,定义为由β受体阻滞剂、RAS抑制剂和MRAs组成的三联疗法,与SMR患者TEER后2年死亡率降低相关。优化药物治疗对于改善因SMR而接受TEER治疗的患者的临床结果至关重要。
{"title":"Guideline-directed medical therapy after transcatheter edge-to-edge mitral valve repair","authors":"Tetsu Tanaka, R. Kavsur, M. Spieker, C. Iliadis, C. Metze, Birthe M Brachtendorf, P. Horn, C. Zachoval, A. Sugiura, M. Kelm, S. Baldus, G. Nickenig, R. Westenfeld, R. Pfister, M. Becher","doi":"10.1136/heartjnl-2022-320826","DOIUrl":"https://doi.org/10.1136/heartjnl-2022-320826","url":null,"abstract":"Objective A sizeable proportion of patients with secondary mitral regurgitation (SMR) do not receive guideline-directed medical therapy (GDMT) for heart failure (HF). We investigated the association between the use of GDMT and mortality in patients with SMR who underwent transcatheter edge-to-edge repair (TEER). Methods We retrospectively analysed patients with SMR and a left ventricular ejection fraction of <50% who underwent TEER at three centres. According to current HF guidelines, GDMT was defined as triple therapy consisting of beta-blockers, renin–angiotensin system (RAS) inhibitors and mineralocorticoid receptor antagonists (MRAs). Patients were divided into two groups: GDMT and non-GDMT groups. We calculated the propensity scores and carried out inverse probability of treatment weighting (IPTW) analyses to compare 2-year mortality between the two groups. Results Of 463 patients, 228 (49.2%) were treated with GDMT upon discharge. IPTW-adjusted Kaplan-Meier curve showed patients with GDMT had a lower incidence of mortality than those without GDMT (19.8% vs 31.1%, p=0.011). In IPTW-adjusted Cox proportional hazards analysis, GDMT was associated with a reduced risk of 2-year mortality (HR: 0.58; 95% CI: 0.35 to 0.95; p=0.030), which was consistent among clinical subgroups. Moreover, patients with GDMT had a higher rate of left ventricular reverse remodelling at 1 year after TEER than those without GDMT. Conclusion GDMT, defined as triple therapy consisting of beta-blockers, RAS inhibitors and MRAs, was associated with a reduced risk of 2-year mortality after TEER for SMR. Optimisation of medical therapy is crucial to improve clinical outcomes in patients undergoing TEER for SMR.","PeriodicalId":9311,"journal":{"name":"British Heart Journal","volume":"108 1","pages":"1722 - 1728"},"PeriodicalIF":0.0,"publicationDate":"2022-06-07","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"48787144","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}
Pub Date : 2022-06-01DOI: 10.1136/heartjnl-2022-321056
Janet I Ma, D. Defaria Yeh, Ada C. Stefanescu Schmidt
While global maternal mortality has decreased in the last three decades, pregnancyrelated deaths remain prevalent in the USA, even after accounting for possible overreporting based on changes in death certificates. In 2017, approximately 17 US mothers per 100 000 live births died due to complications related to pregnancy or childbirth; in contrast, only 7 UK mothers per 100 000 live births died that year. Up to twothirds of US maternal deaths may have been preventable. Cardiovascular disease has emerged as the driving cause of current maternal mortality rates, causing or related to over onethird of US maternal deaths, with most deaths occurring during or after delivery. Recent studies worldwide have also begun to elucidate the longterm consequences of pregnancyrelated cardiovascular conditions such as gestational hypertension or preeclampsia 6 ; for instance, a largescale population study in the UK found hypertensive disorders of pregnancy increased risk across a multitude of cardiovascular disorders with the impact starting soon after pregnancy. In the USA, preeclampsiarelated deaths have decreased in the last two decades, while deaths associated with or due to chronic hypertension have been increasing. However, one striking difference between the USA and similarly wealthy countries, which may contribute to rising maternal mortality, is its fragmented insurance coverage. Marschner et al give readers a revealing snapshot of the intersection between cardiovascular maternal health and insurance coverage in an important and unique US demographic, pregnant women covered under Medicaid. As the US public insurance programme aimed to improve access to basic healthcare for those otherwise cannot afford it, Medicaid plays a pivotal role in supporting pregnant women living in poverty and currently provides coverage for half of all US births. Marschner et al take a deeper dive into the Medicaid population by exploring pregnancyrelated cardiovascular conditions and early postnatal adverse outcomes among Medicaidinsured pregnant women in three states in the USA between 2015 and 2019. They found that a striking onefourth of these women were diagnosed with a pregnancyrelated cardiometabolic condition, including hypertensive disorders of pregnancy and gestational or preexisting diabetes. Furthermore, between pregnancy and 60 days after delivery, over onetenth of these women were found to have a severe cardiovascular outcome, including heart failure, pulmonary embolism, stroke, cardiac arrest and myocardial infarction. Their study concluded that any type of pregnancyrelated cardiometabolic condition is associated with a threefold higher risk of a severe cardiovascular outcome. Marschner et al point out that current literature suggests the Medicaid population is at much higher risk of pregnancyrelated cardiometabolic conditions compared with those who have private insurance. Their analysis is based on claims data submitted to one Medicaid management company (the m
{"title":"Disparities in cardiovascular maternal health","authors":"Janet I Ma, D. Defaria Yeh, Ada C. Stefanescu Schmidt","doi":"10.1136/heartjnl-2022-321056","DOIUrl":"https://doi.org/10.1136/heartjnl-2022-321056","url":null,"abstract":"While global maternal mortality has decreased in the last three decades, pregnancyrelated deaths remain prevalent in the USA, even after accounting for possible overreporting based on changes in death certificates. In 2017, approximately 17 US mothers per 100 000 live births died due to complications related to pregnancy or childbirth; in contrast, only 7 UK mothers per 100 000 live births died that year. Up to twothirds of US maternal deaths may have been preventable. Cardiovascular disease has emerged as the driving cause of current maternal mortality rates, causing or related to over onethird of US maternal deaths, with most deaths occurring during or after delivery. Recent studies worldwide have also begun to elucidate the longterm consequences of pregnancyrelated cardiovascular conditions such as gestational hypertension or preeclampsia 6 ; for instance, a largescale population study in the UK found hypertensive disorders of pregnancy increased risk across a multitude of cardiovascular disorders with the impact starting soon after pregnancy. In the USA, preeclampsiarelated deaths have decreased in the last two decades, while deaths associated with or due to chronic hypertension have been increasing. However, one striking difference between the USA and similarly wealthy countries, which may contribute to rising maternal mortality, is its fragmented insurance coverage. Marschner et al give readers a revealing snapshot of the intersection between cardiovascular maternal health and insurance coverage in an important and unique US demographic, pregnant women covered under Medicaid. As the US public insurance programme aimed to improve access to basic healthcare for those otherwise cannot afford it, Medicaid plays a pivotal role in supporting pregnant women living in poverty and currently provides coverage for half of all US births. Marschner et al take a deeper dive into the Medicaid population by exploring pregnancyrelated cardiovascular conditions and early postnatal adverse outcomes among Medicaidinsured pregnant women in three states in the USA between 2015 and 2019. They found that a striking onefourth of these women were diagnosed with a pregnancyrelated cardiometabolic condition, including hypertensive disorders of pregnancy and gestational or preexisting diabetes. Furthermore, between pregnancy and 60 days after delivery, over onetenth of these women were found to have a severe cardiovascular outcome, including heart failure, pulmonary embolism, stroke, cardiac arrest and myocardial infarction. Their study concluded that any type of pregnancyrelated cardiometabolic condition is associated with a threefold higher risk of a severe cardiovascular outcome. Marschner et al point out that current literature suggests the Medicaid population is at much higher risk of pregnancyrelated cardiometabolic conditions compared with those who have private insurance. Their analysis is based on claims data submitted to one Medicaid management company (the m","PeriodicalId":9311,"journal":{"name":"British Heart Journal","volume":"108 1","pages":"1504 - 1505"},"PeriodicalIF":0.0,"publicationDate":"2022-06-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"41915736","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}
Pub Date : 2022-05-31DOI: 10.1136/heartjnl-2021-320652
R. Citro, K. Chan, M. Miglioranza, C. Laroche, R. Benvenga, S. Furnaz, J. Magne, C. Olmos, B. Paelinck, A. Pasquet, C. Piper, A. Salsano, A. Savouré, S. Park, P. Szymański, P. Tattevin, N. Vallejo Camazón, P. Lancellotti, G. Habib
Aims Purpose of this study is to compare the clinical course and outcome of patients with recurrent versus first-episode infective endocarditis (IE). Methods Patients with recurrent and first-episode IE enrolled in the EUROpean ENDOcarditis (EURO-ENDO) registry including 156 centres were identified and compared using propensity score matching. Recurrent IE was classified as relapse when IE occurred ≤6 months after a previous episode or reinfection when IE occurred >6 months after the prior episode. Results 3106 patients were enrolled: 2839 (91.4%) patients with first-episode IE (mean age 59.4 (±18.1); 68.3% male) and 267 (8.6%) patients with recurrent IE (mean age 58.1 (±17.7); 74.9% male). Among patients with recurrent IE, 13.2% were intravenous drug users (IVDUs), 66.4% had a repaired or replaced valve with the tricuspid valve being more frequently involved compared with patients with first-episode IE (20.3% vs 14.1%; p=0.012). In patients with a first episode of IE, the aortic valve was more frequently involved (45.6% vs 39.5%; p=0.061). Recurrent relapse and reinfection were 20.6% and 79.4%, respectively. Staphylococcus aureus was the microorganism most frequently observed in both groups (p=0.207). There were no differences in in-hospital and post-hospitalisation mortality between recurrent and first-episode IE. In patients with recurrent IE, in-hospital mortality was higher in IVDU patients. Independent predictors of poorer in-hospital and 1-year outcome, including the occurrence of cardiogenic and septic shock, valvular disease severity and failure to undertake surgery when indicated, were similar for recurrent and first-episode IE. Conclusions In-hospital and 1-year mortality was similar in patients with recurrent and first-episode IE who shared similar predictors of poor outcome.
{"title":"Clinical profile and outcome of recurrent infective endocarditis","authors":"R. Citro, K. Chan, M. Miglioranza, C. Laroche, R. Benvenga, S. Furnaz, J. Magne, C. Olmos, B. Paelinck, A. Pasquet, C. Piper, A. Salsano, A. Savouré, S. Park, P. Szymański, P. Tattevin, N. Vallejo Camazón, P. Lancellotti, G. Habib","doi":"10.1136/heartjnl-2021-320652","DOIUrl":"https://doi.org/10.1136/heartjnl-2021-320652","url":null,"abstract":"Aims Purpose of this study is to compare the clinical course and outcome of patients with recurrent versus first-episode infective endocarditis (IE). Methods Patients with recurrent and first-episode IE enrolled in the EUROpean ENDOcarditis (EURO-ENDO) registry including 156 centres were identified and compared using propensity score matching. Recurrent IE was classified as relapse when IE occurred ≤6 months after a previous episode or reinfection when IE occurred >6 months after the prior episode. Results 3106 patients were enrolled: 2839 (91.4%) patients with first-episode IE (mean age 59.4 (±18.1); 68.3% male) and 267 (8.6%) patients with recurrent IE (mean age 58.1 (±17.7); 74.9% male). Among patients with recurrent IE, 13.2% were intravenous drug users (IVDUs), 66.4% had a repaired or replaced valve with the tricuspid valve being more frequently involved compared with patients with first-episode IE (20.3% vs 14.1%; p=0.012). In patients with a first episode of IE, the aortic valve was more frequently involved (45.6% vs 39.5%; p=0.061). Recurrent relapse and reinfection were 20.6% and 79.4%, respectively. Staphylococcus aureus was the microorganism most frequently observed in both groups (p=0.207). There were no differences in in-hospital and post-hospitalisation mortality between recurrent and first-episode IE. In patients with recurrent IE, in-hospital mortality was higher in IVDU patients. Independent predictors of poorer in-hospital and 1-year outcome, including the occurrence of cardiogenic and septic shock, valvular disease severity and failure to undertake surgery when indicated, were similar for recurrent and first-episode IE. Conclusions In-hospital and 1-year mortality was similar in patients with recurrent and first-episode IE who shared similar predictors of poor outcome.","PeriodicalId":9311,"journal":{"name":"British Heart Journal","volume":"108 1","pages":"1729 - 1736"},"PeriodicalIF":0.0,"publicationDate":"2022-05-31","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"49278776","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}
Pub Date : 2022-05-31DOI: 10.1136/heartjnl-2022-321136
R. Graham
Spontaneous coronary artery dissection (SCAD) is an infrequent but increasingly recognised cause of acute coronary syndrome (ACS) that predominantly affects relatively young women aged 45–52 years and may even occur in association with pregnancy, where it is the most common cause of a myocardial infarction. 2 In contrast to ACS due to atherosclerotic disease, SCAD sufferers have few traditional risk factors apart from hypertension, and the pathophysiology involves impaired coronary flow, not due to plaque rupture, plaque erosion or thrombus formation associated with a calcific nodule, as is the case for atherosclerotic disease, but to the spontaneous formation of an intramural haematoma (IMH) that causes dissection of the vessel wall medial layer. The IHM is likely due to vasa vasorum rupture with or without an intimal tear. As the IMH expands, it compresses the ipsilateral coronary artery wall against the contralateral wall, thereby occluding the coronary lumen and results in ischaemia or infarction of the subtended myocardium. While much has been learnt about the clinical presentation and sequelae of SCAD from studies of retrospective and ambispective registries, metaanalyses and prospective cohorts, major gaps in our understanding of disease mechanisms, management and outcomes persist, with little prospective data from large cohorts and lack of data from randomised control studies. GarciaGuimaraes and colleagues report on the treatment and clinical outcomes of SCAD determined in a cohort of 389 patients assembled from The Spanish Registry on SCAD involving subjects from 34 hospitals. Although the study uses a nonrandomised observational design, particular strengths are its prospective nature, the reasonably large size of the cohort assembled, its careful documentation of SCAD diagnosis by a central angiography reading group and the use of an independent clinical events committee to evaluate adverse outcomes. Moreover, although the study has limitations, as duly acknowledged by the authors, and sheds little new light on the optimal management of SCAD, it does yield important new hypothesisgenerating findings that warranted confirmation in future controlled studies. The study confirms that for those patients who survive to hospital admission, the overall prognosis is favourable, with a survival at discharge of 98%, and 6% suffering a major inhospital adverse cardiovascular event (MAE), mainly driven by reinfarction or unplanned revascularisation and 13% developing a major adverse cardiovascular or cerebrovascular event (MACCE) over a median followup of 2 years. Of course, the outcomes of SCAD sufferers prior to hospitalisation remains unknown, and undoubtedly, some succumb to the disorder. Although the inhospital outcomes reported by GarciaGuimaraes et al are confirmatory, if not better than those reported by others, the MAEs and MACCEs reported did not include the considerable psychosocial burden associated with SCAD, including insomnia, anxiet
{"title":"Adverse events after spontaneous coronary artery dissection","authors":"R. Graham","doi":"10.1136/heartjnl-2022-321136","DOIUrl":"https://doi.org/10.1136/heartjnl-2022-321136","url":null,"abstract":"Spontaneous coronary artery dissection (SCAD) is an infrequent but increasingly recognised cause of acute coronary syndrome (ACS) that predominantly affects relatively young women aged 45–52 years and may even occur in association with pregnancy, where it is the most common cause of a myocardial infarction. 2 In contrast to ACS due to atherosclerotic disease, SCAD sufferers have few traditional risk factors apart from hypertension, and the pathophysiology involves impaired coronary flow, not due to plaque rupture, plaque erosion or thrombus formation associated with a calcific nodule, as is the case for atherosclerotic disease, but to the spontaneous formation of an intramural haematoma (IMH) that causes dissection of the vessel wall medial layer. The IHM is likely due to vasa vasorum rupture with or without an intimal tear. As the IMH expands, it compresses the ipsilateral coronary artery wall against the contralateral wall, thereby occluding the coronary lumen and results in ischaemia or infarction of the subtended myocardium. While much has been learnt about the clinical presentation and sequelae of SCAD from studies of retrospective and ambispective registries, metaanalyses and prospective cohorts, major gaps in our understanding of disease mechanisms, management and outcomes persist, with little prospective data from large cohorts and lack of data from randomised control studies. GarciaGuimaraes and colleagues report on the treatment and clinical outcomes of SCAD determined in a cohort of 389 patients assembled from The Spanish Registry on SCAD involving subjects from 34 hospitals. Although the study uses a nonrandomised observational design, particular strengths are its prospective nature, the reasonably large size of the cohort assembled, its careful documentation of SCAD diagnosis by a central angiography reading group and the use of an independent clinical events committee to evaluate adverse outcomes. Moreover, although the study has limitations, as duly acknowledged by the authors, and sheds little new light on the optimal management of SCAD, it does yield important new hypothesisgenerating findings that warranted confirmation in future controlled studies. The study confirms that for those patients who survive to hospital admission, the overall prognosis is favourable, with a survival at discharge of 98%, and 6% suffering a major inhospital adverse cardiovascular event (MAE), mainly driven by reinfarction or unplanned revascularisation and 13% developing a major adverse cardiovascular or cerebrovascular event (MACCE) over a median followup of 2 years. Of course, the outcomes of SCAD sufferers prior to hospitalisation remains unknown, and undoubtedly, some succumb to the disorder. Although the inhospital outcomes reported by GarciaGuimaraes et al are confirmatory, if not better than those reported by others, the MAEs and MACCEs reported did not include the considerable psychosocial burden associated with SCAD, including insomnia, anxiet","PeriodicalId":9311,"journal":{"name":"British Heart Journal","volume":"108 1","pages":"1506 - 1507"},"PeriodicalIF":0.0,"publicationDate":"2022-05-31","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"46720459","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}
Pub Date : 2022-05-30DOI: 10.1136/heartjnl-2022-321009
E. Hulten, V. Murthy
Kelion et 1 report a cross- sectional study of the incidence of non- cardiac incidental findings on 4340 clinically indicated coronary CT angiography (CCTA). The first and most significant finding is that 15.8% of CCTA examinations contained an incidental finding, although 23.6% were previously known (12.1% newly recognised incidental findings). A large proportion of these findings, 43%, were pulmonary nodules or cysts of unclear clinical significance. While these incidentals would not otherwise have been diag-nosed by screening criteria, their identification often does impose a burden on patients and medical systems without prognostic benefit. Second, most incidentals, but not all, could be identified on a cardiac field of view (FOV) image, without a need for a wide FOV reconstruction as per routine at many centres. The authors suggest this finding could support a rationale to more expeditiously evaluate only the cardiac FOV dataset in resource- limited settings, given the added time and cost burden of requiring a radiologist to review the full FOV scan for incidentals. Currently, as Kelion et al have noted, the minimum recommendation evaluate the cardiac Society Cardiovascular 1 4 could be detected on limited cardiac FOV vs on wide FOV
{"title":"Thinking outside the box: clinical and economic implications of extracardiac findings on cardiac computed tomography angiography","authors":"E. Hulten, V. Murthy","doi":"10.1136/heartjnl-2022-321009","DOIUrl":"https://doi.org/10.1136/heartjnl-2022-321009","url":null,"abstract":"Kelion et 1 report a cross- sectional study of the incidence of non- cardiac incidental findings on 4340 clinically indicated coronary CT angiography (CCTA). The first and most significant finding is that 15.8% of CCTA examinations contained an incidental finding, although 23.6% were previously known (12.1% newly recognised incidental findings). A large proportion of these findings, 43%, were pulmonary nodules or cysts of unclear clinical significance. While these incidentals would not otherwise have been diag-nosed by screening criteria, their identification often does impose a burden on patients and medical systems without prognostic benefit. Second, most incidentals, but not all, could be identified on a cardiac field of view (FOV) image, without a need for a wide FOV reconstruction as per routine at many centres. The authors suggest this finding could support a rationale to more expeditiously evaluate only the cardiac FOV dataset in resource- limited settings, given the added time and cost burden of requiring a radiologist to review the full FOV scan for incidentals. Currently, as Kelion et al have noted, the minimum recommendation evaluate the cardiac Society Cardiovascular 1 4 could be detected on limited cardiac FOV vs on wide FOV","PeriodicalId":9311,"journal":{"name":"British Heart Journal","volume":"108 1","pages":"1426 - 1427"},"PeriodicalIF":0.0,"publicationDate":"2022-05-30","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"48906950","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}
Pub Date : 2022-05-25DOI: 10.1136/heartjnl-2022-320910
Akhmetzhan Galimzhanov, Yersyn Sabitov, Erhan Tenekecioglu, Han Naung Tun, Mirvat Alasnag, Mamas A Mamas
Objectives: The nature of the relationship between baseline platelet count and clinical outcomes following percutaneous coronary intervention (PCI) is unclear. We undertook dose-response and pairwise meta-analyses to better describe the prognostic value of the initial platelet count and clinical endpoints in patients after PCI.
Methods: A search of PubMed, Scopus and Web of Science (up to 9 October 2021) was performed to identify studies that evaluated the association between platelet count and clinical outcomes following PCI. The primary outcomes of interest were all-cause mortality, major adverse cardiovascular events (MACE) and major bleeding. We performed random-effects pairwise and one-stage dose-response meta-analyses by calculating HRs and 95% CIs.
Results: The meta-analysis included 19 studies with 217 459 patients. We report a J-shaped relationship between baseline thrombocyte counts and all-cause death, MACE and major bleeding at follow-up. The risk of haemorrhagic events exceeded the risk of thrombotic events at low platelet counts (<175×109/L), while a predominant ischaemic risk was observed at high platelet counts (>250×109/L). Pairwise meta-analyses revealed a robust link between initial platelet counts and the risk of postdischarge all-cause mortality, major bleeding (for thrombocytopenia: HR 1.39, 95% CI 1.30 to 1.49; HR 1.51, 95% CI 1.15 to 2.00, respectively) and future death from any cause and MACE (thrombocytosis: HR 1.60, 95% CI 1.29 to 1.98; HR 1.47, 95% CI 1.22 to 1.78, respectively).
Conclusion: Low platelet counts were associated with the predominant bleeding risk, while high platelet counts were only associated with the ischaemic events.
Prospero registration number: CRD42021283270.
目的:目前尚不清楚经皮冠状动脉介入治疗(PCI)后基线血小板计数与临床预后之间的关系。我们进行了剂量-反应和两两荟萃分析,以更好地描述PCI术后患者初始血小板计数和临床终点的预后价值。方法检索PubMed, Scopus和Web of Science(截至2021年10月9日),以确定评估血小板计数与PCI术后临床结果之间关系的研究。主要结局为全因死亡率、主要不良心血管事件(MACE)和大出血。我们通过计算hr和95% ci进行了随机效应两两和一期剂量-反应荟萃分析。结果meta分析纳入19项研究,217459例患者。我们报告了基线血小板计数与随访时全因死亡、MACE和大出血之间的j型关系。在低血小板计数(250×109/L)时,出血事件的风险超过血栓形成事件的风险。两两荟萃分析显示,初始血小板计数与出院后全因死亡、大出血(血小板减少:HR 1.39, 95% CI 1.30 ~ 1.49;HR 1.51, 95% CI分别为1.15至2.00)和未来因任何原因死亡和MACE(血小板增多:HR 1.60, 95% CI 1.29至1.98;HR 1.47, 95% CI 1.22 ~ 1.78)。结论血小板计数低与主要出血风险相关,而血小板计数高仅与缺血性事件相关。普洛斯彼罗注册号CRD42021283270。
{"title":"Baseline platelet count in percutaneous coronary intervention: a dose-response meta-analysis.","authors":"Akhmetzhan Galimzhanov, Yersyn Sabitov, Erhan Tenekecioglu, Han Naung Tun, Mirvat Alasnag, Mamas A Mamas","doi":"10.1136/heartjnl-2022-320910","DOIUrl":"10.1136/heartjnl-2022-320910","url":null,"abstract":"<p><strong>Objectives: </strong>The nature of the relationship between baseline platelet count and clinical outcomes following percutaneous coronary intervention (PCI) is unclear. We undertook dose-response and pairwise meta-analyses to better describe the prognostic value of the initial platelet count and clinical endpoints in patients after PCI.</p><p><strong>Methods: </strong>A search of PubMed, Scopus and Web of Science (up to 9 October 2021) was performed to identify studies that evaluated the association between platelet count and clinical outcomes following PCI. The primary outcomes of interest were all-cause mortality, major adverse cardiovascular events (MACE) and major bleeding. We performed random-effects pairwise and one-stage dose-response meta-analyses by calculating HRs and 95% CIs.</p><p><strong>Results: </strong>The meta-analysis included 19 studies with 217 459 patients. We report a J-shaped relationship between baseline thrombocyte counts and all-cause death, MACE and major bleeding at follow-up. The risk of haemorrhagic events exceeded the risk of thrombotic events at low platelet counts (<175×10<sup>9</sup>/L), while a predominant ischaemic risk was observed at high platelet counts (>250×10<sup>9</sup>/L). Pairwise meta-analyses revealed a robust link between initial platelet counts and the risk of postdischarge all-cause mortality, major bleeding (for thrombocytopenia: HR 1.39, 95% CI 1.30 to 1.49; HR 1.51, 95% CI 1.15 to 2.00, respectively) and future death from any cause and MACE (thrombocytosis: HR 1.60, 95% CI 1.29 to 1.98; HR 1.47, 95% CI 1.22 to 1.78, respectively).</p><p><strong>Conclusion: </strong>Low platelet counts were associated with the predominant bleeding risk, while high platelet counts were only associated with the ischaemic events.</p><p><strong>Prospero registration number: </strong>CRD42021283270.</p>","PeriodicalId":9311,"journal":{"name":"British Heart Journal","volume":"108 1","pages":""},"PeriodicalIF":0.0,"publicationDate":"2022-05-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"46120096","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}