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Antiplatelet agents for preventing pre-eclampsia and its complications. 预防先兆子痫及其并发症的抗血小板药物。
IF 8.8 Q2 Medicine Pub Date : 2019-10-30 DOI: 10.1002/14651858.CD004659.pub3
Lelia Duley, Shireen Meher, Kylie E Hunter, Anna Lene Seidler, Lisa M Askie
<p><strong>Background: </strong>Pre-eclampsia is associated with deficient intravascular production of prostacyclin, a vasodilator, and excessive production of thromboxane, a vasoconstrictor and stimulant of platelet aggregation. These observations led to the hypotheses that antiplatelet agents, low-dose aspirin in particular, might prevent or delay development of pre-eclampsia.</p><p><strong>Objectives: </strong>To assess the effectiveness and safety of antiplatelet agents, such as aspirin and dipyridamole, when given to women at risk of developing pre-eclampsia.</p><p><strong>Search methods: </strong>For this update, we searched Cochrane Pregnancy and Childbirth's Trials Register, ClinicalTrials.gov, the WHO International Clinical Trials Registry Platform (ICTRP) (30 March 2018), and reference lists of retrieved studies. We updated the search in September 2019 and added the results to the awaiting classification section of the review.</p><p><strong>Selection criteria: </strong>All randomised trials comparing antiplatelet agents with either placebo or no antiplatelet agent were included. Studies only published in abstract format were eligible for inclusion if sufficient information was available. We would have included cluster-randomised trials in the analyses along with individually-randomised trials, if any had been identified in our search strategy. Quasi-random studies were excluded. Participants were pregnant women at risk of developing pre-eclampsia. Interventions were administration of an antiplatelet agent (such as low-dose aspirin or dipyridamole), comparisons were either placebo or no antiplatelet.</p><p><strong>Data collection and analysis: </strong>Two review authors assessed trials for inclusion and extracted data independently. For binary outcomes, we calculated risk ratio (RR) and its 95% confidence interval (CI), on an intention-to-treat basis. For this update we incorporated individual participant data (IPD) from trials with this available, alongside aggregate data (AD) from trials where it was not, in order to enable reliable subgroup analyses and inclusion of two key new outcomes. We assessed risk of bias for included studies and created a 'Summary of findings' table using GRADE.</p><p><strong>Main results: </strong>Seventy-seven trials (40,249 women, and their babies) were included, although three trials (relating to 233 women) did not contribute data to the meta-analysis. Nine of the trials contributing data were large (> 1000 women recruited), accounting for 80% of women recruited. Although the trials took place in a wide range of countries, all of the nine large trials involved only women in high-income and/or upper middle-income countries. IPD were available for 36 trials (34,514 women), including all but one of the large trials. Low-dose aspirin alone was the intervention in all the large trials, and most trials overall. Dose in the large trials was 50 mg (1 trial, 1106 women), 60 mg (5 trials, 22,322 women), 75mg (1 tri
背景:先兆子痫与血管内前列环素(一种血管扩张剂)分泌不足和血栓素(一种血管收缩剂和血小板聚集刺激剂)分泌过量有关。这些观察结果导致假设抗血小板药物,特别是低剂量阿司匹林,可能预防或延缓先兆子痫的发展。目的评价抗血小板药物(如阿司匹林和双嘧达莫)用于有先兆子痫风险的妇女的有效性和安全性。检索方法:在本次更新中,我们检索了Cochrane妊娠与分娩试验注册、ClinicalTrials.gov、WHO国际临床试验注册平台(ICTRP)(2018年3月30日)和检索研究的参考文献列表。我们在2019年9月更新了检索,并将结果添加到综述的等待分类部分。选择标准:所有比较抗血小板药物与安慰剂或无抗血小板药物的随机试验均纳入研究。如果有足够的信息,只有以摘要形式发表的研究才有资格纳入。如果在我们的搜索策略中发现了任何随机试验,我们将在分析中包括集群随机试验和个体随机试验。排除了准随机研究。参与者是有先兆子痫风险的孕妇。干预措施是给予抗血小板药物(如低剂量阿司匹林或双嘧达莫),比较是安慰剂或无抗血小板药物。数据收集和分析两位综述作者独立评估试验纳入和提取数据。对于二元结果,我们在意向治疗的基础上计算风险比(RR)及其95%置信区间(CI)。在本次更新中,我们纳入了来自可获得该数据的试验的个体参与者数据(IPD),以及来自未获得该数据的试验的总体数据(AD),以便进行可靠的亚组分析并纳入两个关键的新结果。我们评估了纳入研究的偏倚风险,并使用GRADE创建了“结果摘要”表。主要结果77项试验(40249名妇女及其婴儿)被纳入,尽管3项试验(233名妇女)没有为meta分析提供数据。提供数据的试验中有9项是大型试验(招募了超过1000名女性),占招募女性的80%。虽然试验在许多国家进行,但所有9项大型试验均仅涉及高收入和/或中高收入国家的妇女。IPD可用于36项试验(34,514名妇女),包括除一项大型试验外的所有试验。在所有大型试验和大多数试验中,单独使用低剂量阿司匹林是一种干预措施。大型试验的剂量为50毫克(1项试验,1106名妇女),60毫克(5项试验,22,322名妇女),75毫克(1项试验,3697名妇女),100毫克(1项试验,3294名妇女)和150毫克(1项试验,1776名妇女)。大多数研究要么偏倚风险低,要么偏倚风险不明确;大型试验都是低风险的。抗血小板药物与安慰剂/无治疗相比,使用抗血小板药物可使蛋白尿先兆子痫的风险降低18%(36,716名妇女,60项试验,RR 0.82, 95% CI 0.77 ~ 0.88;高质量证据),一名妇女受益(NNTB)需要治疗的人数为61 (95% CI 45 - 92)。早产500毫升(23,769名妇女,19项试验;RR 1.06, 95% CI 1.00 ~ 1.12;中等质量的证据(由于临床异质性),它们可能会略微增加胎盘早剥的风险,尽管对于这个结果,证据被降级了,因为有很宽的置信区间,包括没有影响的可能性(30,775名妇女;29日试验;RR 1.21, 95% CI 0.95 ~ 1.54;moderate-quality证据)。两项评估18个月大儿童的大型试验(包括来自5000多名儿童的结果)的数据没有发现两组儿童在发育方面的明显差异。作者的结论:给孕妇服用低剂量阿司匹林可以带来小到中等的益处,包括减少先兆子痫(每1000名接受治疗的妇女减少16名)、早产(每1000名接受治疗的妇女减少16名)、出生时胎龄较小的婴儿(每1000名接受治疗的妇女减少7名)和胎儿或新生儿死亡(每1000名接受治疗的妇女减少5名)。总的来说,对1000名妇女使用抗血小板药物导致了20例发生严重不良后果的妊娠。所有这些结果的证据质量都很高。阿司匹林可能会轻微增加产后出血超过500毫升的风险,然而,由于考虑到失血量的临床异质性,这一结果的证据质量降至中等。抗血小板药物可能会轻微增加胎盘早剥,但由于事件数量少,证据质量降至中等,因此95% CI较宽。 背景:子痫前期与血管内前列环素(一种血管扩张剂)分泌不足和血栓素(一种血管收缩剂和血小板聚集刺激剂)分泌过多有关。这些观察结果提出了一个假设,即抗血小板药物,尤其是小剂量阿司匹林,可以预防或延缓先兆子痫的发生:目的:评估阿司匹林和双嘧达莫等抗血小板药物对有先兆子痫风险的妇女的有效性和安全性:在本次更新中,我们检索了Cochrane妊娠与分娩试验登记册、ClinicalTrials.gov、WHO国际临床试验登记平台(ICTRP)(2018年3月30日)以及检索到的研究的参考文献列表。我们于2019年9月更新了检索,并将结果添加到综述的等待分类部分:纳入所有比较抗血小板药物与安慰剂或无抗血小板药物的随机试验。如果有足够的信息,仅以摘要形式发表的研究也可纳入。如果在搜索策略中发现了分组随机试验和单独随机试验,我们也会将其纳入分析。准随机研究除外。参与者为有先兆子痫风险的孕妇。干预措施为服用抗血小板药物(如小剂量阿司匹林或双嘧达莫),对比试验为服用安慰剂或不服用抗血小板药物:两位综述作者独立评估试验的纳入情况并提取数据。对于二元结果,我们在意向治疗的基础上计算风险比 (RR) 及其 95% 置信区间 (CI)。在本次更新中,我们纳入了可获得的试验的个体参与者数据(IPD),以及不可获得的试验的总体数据(AD),以便进行可靠的亚组分析,并纳入两个关键的新结果。我们评估了纳入研究的偏倚风险,并使用 GRADE 编制了 "研究结果摘要 "表:共纳入了 77 项试验(40249 名妇女及其婴儿),但有三项试验(涉及 233 名妇女)未为荟萃分析提供数据。在提供数据的试验中,有九项试验规模较大(招募的妇女人数超过 1000 人),占招募妇女人数的 80%。虽然这些试验在多个国家进行,但所有九项大型试验都只涉及高收入和/或中上收入国家的妇女。有 36 项试验(34,514 名妇女)提供了 IPD,其中包括除一项大型试验外的所有试验。在所有大型试验和大多数试验中,仅小剂量阿司匹林是干预措施。大型试验的剂量分别为 50 毫克(1 项试验,1106 名妇女)、60 毫克(5 项试验,22322 名妇女)、75 毫克(1 项试验,3697 名妇女)、100 毫克(1 项试验,3294 名妇女)和 150 毫克(1 项试验,1776 名妇女)。大多数研究的偏倚风险较低或偏倚风险不明确;大型试验的基本风险均较低。抗血小板药物与安慰剂/不治疗 抗血小板药物可将蛋白尿先兆子痫的风险降低 18%(36716 名妇女,60 项试验,RR 0.82,95% CI 0.77 至 0.88;高质量证据),一名妇女获益所需的治疗人数(NNTB)为 61(95% CI 45 至 92)。早产 500 mL 的 RR 有小幅(9%)下降(23,769 名妇女,19 项试验;RR 1.06,95% CI 1.00 至 1.12;由于临床异质性,为中度质量证据),而且可能会略微增加胎盘早剥的风险,但由于置信区间较宽,包括可能没有影响(30,775 名妇女,29 项试验;RR 1.21,95% CI 0.95 至 1.54;中度质量证据),因此该结果的证据等级被降低。两项大型
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引用次数: 0
Statin adherence and persistence on secondary prevention of cardiovascular disease in Taiwan. 台湾地区他汀类药物在心血管疾病二级预防中的坚持与坚持
Q2 Medicine Pub Date : 2019-09-02 eCollection Date: 2019-01-01 DOI: 10.1136/heartasia-2018-011176
Wen-Yi Shau, Chao-Lun Lai, Shih-Ting Huang, Shu-Ting Chen, Jim Z Li, Selwyn Fung, Vicki C Tse, Mei-Shu Lai

Background: Evidence and treatment guidelines support the use of statins in patients with established atherosclerotic cardiovascular disease (ASCVD) for secondary prevention of subsequent cardiovascular (CV) event. However, treatment adherence and persistence are still a concern.

Methods: We constructed a retrospective population-based cohort of patients, who initiated statin treatment within 90 days after discharge from hospital for ASCVD using the claims database of Taiwan National Health Insurance. Proportion of days covered (PDC) was used to measure statin adherence, and PDC ≥80% was defined as good adherence. The study outcomes were subsequent rehospitalisation or in-hospital death due to composite ASCVD, myocardial infarction or ischaemic stroke. Their associations with statin prescription adherence or persistence were analysed using time-dependent Cox proportional hazards model.

Results: The study cohort included 185 252 postdischarge statin initiators. There were 50 015 subsequent ASCVD rehospitalisations including 2858 in-hospital death during 7 years of study period. Good adherence was significantly associated with lower risk of ASCVD rehospitalisation (adjusted HR (aHR) 0.90; 95% CI 0.87 to 0.92) and significantly lower risk of in-hospital death (aHR 0.59; 95% CI 0.53 to 0.65). Compared with constant use of statin, patients in the three less persistent states (recent stop, non-persistence and intermittent use) were associated with higher risk of subsequent ASCVD rehospitalisation, aHRs were 1.16, 1.13 and 1.26, respectively (all p<0.05). The increased risks were consistent with specific outcome of acute myocardial infarction and ischaemic stroke. Also, patients in the recent stop period had significantly higher risk for fatal CV event.

Conclusions: Good adherence and persistence to statin therapy are significantly associated with lower risk of secondary ASCVD rehospitalisation and in-hospital death.

背景证据和治疗指南支持在已确诊的动脉粥样硬化性心血管疾病(ASCVD)患者中使用他汀类药物二级预防随后的心血管(CV)事件。然而,治疗的依从性和持久性仍然是一个问题。方法采用台湾国民健康保险理赔数据库,对ASCVD患者在出院后90天内开始他汀类药物治疗,构建了一个基于人群的回顾性队列。使用覆盖天数比例(PDC)来衡量他汀类药物的依从性,PDC≥80%被定义为良好的依从性。研究结果是由于复合ASCVD、心肌梗死或缺血性卒中导致的再住院或院内死亡。使用时间相关的Cox比例风险模型分析其与他汀类药物处方依从性或持久性的关系。结果研究队列包括185 252名出院后他汀类药物起始者。在7年的研究期间,有5015例ASCVD再住院,其中2858例院内死亡。良好的依从性与较低的ASCVD再住院风险显著相关(调整HR (aHR) 0.90;95% CI 0.87 ~ 0.92),院内死亡风险显著降低(aHR 0.59;95% CI 0.53 ~ 0.65)。与持续使用他汀类药物相比,持续时间较短的三种状态(近期停药、非持续使用和间歇使用)患者随后ASCVD再住院的风险较高,ahr分别为1.16、1.13和1.26(均p<0.05)。增加的风险与急性心肌梗死和缺血性脑卒中的特定结果一致。此外,最近停药期的患者发生致命性心血管事件的风险显著增加。结论:良好的依从性和坚持他汀类药物治疗与继发性ASCVD再住院和院内死亡风险降低显著相关。
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引用次数: 0
Association of school hours with outcomes of out-of-hospital cardiac arrest in schoolchildren 学龄儿童院外心脏骤停与上课时间的关系
Q2 Medicine Pub Date : 2019-08-01 DOI: 10.1136/heartasia-2019-011236
A. Yamashita, Hisanori Kurosaki, Kohei Takada, Yoshio Tanaka, Yoshitaka Hamada, Tetsuya Ishita, Minoru Kubo, H. Inaba
Objective To investigate the association of school hours with outcomes of schoolchildren with out-of-hospital cardiac arrest (OHCA). Methods From the 2005–2014 nationwide databases, we extracted the data for 1660 schoolchildren (6–17 years) with bystander-witnessed OHCA. Univariate analyses followed by propensity-matching procedures and stepwise logistic regression analyses were applied. School hours were defined as 08:00 to 18:00. Results The neurologically favourable 1-month survival rate during school hours was better than that during non-school hours only on school days: 18.4% and 10.5%, respectively. During school hours on school days, patients with OHCA more frequently received bystander cardiopulmonary resuscitation (CPR) and public access defibrillation (PAD), and had a shockable initial rhythm and presumed cardiac aetiology. The neurologically favourable 1-month survival rate did not significantly differ between school hours on school days and all other times of day after propensity score matching: 16.4% vs 16.1% (unadjusted OR 1.02; 95% CI 0.69 to 1.51). Stepwise logistic regression analysis during school hours on school days revealed that shockable initial rhythm (adjusted OR 2.44; 95% CI 1.12 to 5.42), PAD (adjusted OR 3.32; 95% CI 1.23 to 9.10), non-exogenous causes (adjusted OR 5.88; 95% CI 1.85 to 20.0) and a shorter emergency medical service (EMS) response time (adjusted OR 1.15; 95% CI 1.02 to 1.32) and witness-to-first CPR interval (adjusted OR 1.08; 95% CI 1.01 to 1.15) were major factors associated with an improved neurologically favourable 1-month survival rate. Conclusions School hours are not an independent factor associated with improved outcomes of OHCA in schoolchildren. The time delays in CPR and EMS arrival were independently associated with poor outcomes during school hours on school days.
目的探讨学时与院外心脏骤停(OHCA)预后的关系。方法从2005-2014年全国数据库中提取1660名6-17岁儿童旁观者目击OHCA的数据。采用单变量分析、倾向匹配程序和逐步逻辑回归分析。上课时间定为08:00至18:00。结果上学期间神经系统良好的1个月生存率分别为18.4%和10.5%,优于非上学期间的1个月生存率。在上课时间,OHCA患者更频繁地接受旁观者心肺复苏(CPR)和公共场所除颤(PAD),并且具有休克性初始节律和假定的心脏病因。倾向评分匹配后,上学日上课时间和一天中其他时间的1个月生存率无显著差异:16.4% vs 16.1%(未调整OR 1.02;95% CI 0.69 ~ 1.51)。逐步逻辑回归分析显示,在上学日的上课时间,休克初始节律(调整OR为2.44;95% CI 1.12 - 5.42), PAD(调整OR 3.32;95% CI 1.23 - 9.10),非外源性原因(调整OR 5.88;95% CI 1.85 - 20.0)和更短的紧急医疗服务(EMS)响应时间(调整OR 1.15;95% CI 1.02 - 1.32)和证人到第一名CPR间隔(调整OR 1.08;95% CI 1.01 ~ 1.15)是改善神经系统有利的1个月生存率的主要因素。结论:学时并不是与学童OHCA改善结果相关的独立因素。CPR和EMS到达的时间延迟与上学时间的不良结果独立相关。
{"title":"Association of school hours with outcomes of out-of-hospital cardiac arrest in schoolchildren","authors":"A. Yamashita, Hisanori Kurosaki, Kohei Takada, Yoshio Tanaka, Yoshitaka Hamada, Tetsuya Ishita, Minoru Kubo, H. Inaba","doi":"10.1136/heartasia-2019-011236","DOIUrl":"https://doi.org/10.1136/heartasia-2019-011236","url":null,"abstract":"Objective To investigate the association of school hours with outcomes of schoolchildren with out-of-hospital cardiac arrest (OHCA). Methods From the 2005–2014 nationwide databases, we extracted the data for 1660 schoolchildren (6–17 years) with bystander-witnessed OHCA. Univariate analyses followed by propensity-matching procedures and stepwise logistic regression analyses were applied. School hours were defined as 08:00 to 18:00. Results The neurologically favourable 1-month survival rate during school hours was better than that during non-school hours only on school days: 18.4% and 10.5%, respectively. During school hours on school days, patients with OHCA more frequently received bystander cardiopulmonary resuscitation (CPR) and public access defibrillation (PAD), and had a shockable initial rhythm and presumed cardiac aetiology. The neurologically favourable 1-month survival rate did not significantly differ between school hours on school days and all other times of day after propensity score matching: 16.4% vs 16.1% (unadjusted OR 1.02; 95% CI 0.69 to 1.51). Stepwise logistic regression analysis during school hours on school days revealed that shockable initial rhythm (adjusted OR 2.44; 95% CI 1.12 to 5.42), PAD (adjusted OR 3.32; 95% CI 1.23 to 9.10), non-exogenous causes (adjusted OR 5.88; 95% CI 1.85 to 20.0) and a shorter emergency medical service (EMS) response time (adjusted OR 1.15; 95% CI 1.02 to 1.32) and witness-to-first CPR interval (adjusted OR 1.08; 95% CI 1.01 to 1.15) were major factors associated with an improved neurologically favourable 1-month survival rate. Conclusions School hours are not an independent factor associated with improved outcomes of OHCA in schoolchildren. The time delays in CPR and EMS arrival were independently associated with poor outcomes during school hours on school days.","PeriodicalId":12858,"journal":{"name":"Heart Asia","volume":" ","pages":""},"PeriodicalIF":0.0,"publicationDate":"2019-08-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1136/heartasia-2019-011236","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"45555960","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: 4
Anaesthesia use in catheter ablation for atrial fibrillation: a systematic review and meta-analysis of observational studies 麻醉在房颤导管消融中的应用:观察性研究的系统回顾和荟萃分析
Q2 Medicine Pub Date : 2019-08-01 DOI: 10.1136/heartasia-2018-011155
K. H. C. Li, T. Sang, C. Chan, M. Gong, Yingzhi Liu, A. Jesuthasan, Guangping Li, Tong Liu, M. H. S. Lam, William K. K. Wu, M. Chan, Fang-zhou Liu, Cheng Chen, J. Ho, Yunlong Xia, G. Tse
Objectives This meta-analysis and systematic review seeks to compare both characteristic parameters and procedural outcomes of atrial fibrillation (AF) catheter ablation in patients under general anaesthesia (GA)/deep sedation and mild/moderate sedation. Background Catheter ablation has become a widely applied intervention for treating symptomatic AF and arrhythmias that are refractory to medical therapy. It can be conducted through from mild sedation to GA. Methods PubMed and Embase were searched up to July 2018 for randomised controlled trials, cohort and observational studies that assessed the outcomes of catheter ablation under GA/deep sedation or mild/moderate sedation. Nine studies were included in this meta-analysis after screening with the inclusion and exclusion criteria. Heterogeneity between studies and publication bias was evaluated by I2 index and Egger’s regression, respectively. Results Our meta-analysis found catheter AF ablation with GA/deep sedation to be associated with reduced risk of recurrence (RR: 0.79, 95% CI 0.56 to 1.13, p=0.20) and complications (RR: 0.95, 95% CI 0.64 to 1.42, p=0.82), though statistically insignificant. In terms of procedural parameters, there was no significant difference between the two groups for both procedural time (SMD: −0.13, 95% CI −0.90 to 0.63, p=0.74) and fluoroscopy time (SMD: −0.41, 95% CI −1.40 to 0.58, p=0.41). Univariate meta-regression did not reveal any covariates as a moderating factor for complication and recurrence risk. Conclusion Apart from an increased likelihood of procedural success, ablation by GA/deep sedation was found to be non-significantly different from the mild/moderate sedation approach in both procedural parameters and outcome measures.
目的本荟萃分析和系统综述旨在比较全麻(GA)/深度镇静和轻度/中度镇静患者心房颤动(AF)导管消融的特征参数和手术结果。背景导管消融术已成为一种广泛应用的干预措施,用于治疗药物治疗难治的症状性房颤和心律失常。它可以从轻度镇静到GA进行。方法截至2018年7月,检索PubMed和Embase的随机对照试验、队列和观察性研究,评估GA/深度镇静或轻度/中度镇静下导管消融的结果。根据纳入和排除标准进行筛选后,9项研究被纳入该荟萃分析。研究和发表偏倚之间的异质性分别通过I2指数和Egger回归进行评估。结果我们的荟萃分析发现,采用GA/深度镇静的导管房颤消融与复发风险(RR:0.79,95%CI 0.56-1.13,p=0.020)和并发症风险(RR=0.95,95%CI 0.64-1.42,p=0.082)的降低有关,尽管在统计学上不显著。就手术参数而言,两组在手术时间(SMD:−0.13,95%CI−0.90至0.63,p=0.74)和荧光检查时间(SMD:−0.41,95%CI–1.40至0.58,p=0.41)方面均无显著差异。单变量元回归未发现任何协变量作为并发症和复发风险的调节因素。结论除了增加手术成功的可能性外,GA/深度镇静消融在手术参数和结果测量方面与轻度/中度镇静方法没有显著差异。
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引用次数: 8
Clinical consequences of poor adherence to lipid-lowering therapy in patients with cardiovascular disease: can we do better? 心血管疾病患者降脂治疗依从性差的临床后果:我们能做得更好吗?
Q2 Medicine Pub Date : 2019-08-01 DOI: 10.1136/heartasia-2019-011200
H. Klimis, C. Chow
There is high-quality evidence demonstrating that early initiation of statin use following an acute coronary syndrome (ACS) and persistent use thereafter reduces the risk of major adverse cardiovascular events (MACE) including mortality. However, despite the overwhelming evidence, adherence remains suboptimal and the medications frequently discontinued.1 Here we discuss the data on lipid-lowering therapy among patients with cardiovascular disease and discuss some potential interventions that address the gap.Among those with established atherosclerotic cardiovascular disease (ASCVD), poor statin adherence has been reported to be 47.2% in real-world registry data.2 Discontinuation rates have been reported ranging from 14%3 to 26.5%4 at 12 months in both large multicentre randomised clinical trial (RCT) data and national registries, with long-term discontinuation being 51% after 7 years in a large-scale RCT involving 39 countries.3 In a systematic review including 28 studies (5 nested case–control and 22 cohort studies), adherence to statin use in patients at high risk of ASCVD and those with established ASCVD was associated with a reduction in subsequent cardiovascular events (OR 1.22–5.26) and improved survival (OR 1.79–5.00).5 The US National Cardiovascular data Registry’s PINNACLE database (data collected at the point of care at cardiology practices) was used in a large study that showed that in 1 029 633 adults with known ASCVD, 27.9% did not receive any lipid-lowering medication.6 Similarly, other registries demonstrate high proportions of patients not receiving lipid-lowering therapy within the first year following an ACS in Australia7 and New Zealand8—22% and 25% respectively.Prescription of statins at the time of discharge after ACS is associated with continued use,7 and a range of data demonstrates significant gaps in use of lipid-lowering drugs among patients with cardiovascular disease. In the CONCORDANCE trial, failure to discharge patients on guideline-recommended therapies was 10 …
有高质量的证据表明,急性冠状动脉综合征(ACS)后早期开始使用他汀类药物并在此后持续使用可降低包括死亡率在内的主要心血管不良事件(MACE)的风险。然而,尽管有压倒性的证据,依从性仍然不理想,药物经常停用。1在这里,我们讨论了心血管疾病患者的降脂治疗数据,并讨论了一些解决这一差距的潜在干预措施。在那些患有动脉粥样硬化性心血管疾病(ASCVD)的患者中,据报道,在现实世界的注册数据中,他汀类药物依从性差的比例为47.2%。2在大型多中心随机临床试验(RCT)数据和国家注册中,12个月时的停药率从14%3到26.5%4不等,在一项涉及39个国家的大规模随机对照试验中,7年后长期停药的比例为51%。3在一项包括28项研究(5项嵌套病例对照和22项队列研究)的系统综述中,ASCVD高危患者和已确诊ASCVD患者坚持使用他汀类药物与随后心血管事件的减少(OR 1.22–5.26)和生存率的提高(OR 1.79–5.00)相关。5美国国家心血管数据注册中心的PINNACLE数据库(在心脏病学实践的护理点收集的数据)用于一项大型研究,该研究表明633名患有已知ASCVD的成年人,27.9%没有接受任何降脂药物治疗。6同样,其他登记处显示,澳大利亚7和新西兰8在ACS后的第一年内没有接受降脂治疗的患者比例很高,分别为22%和25%。ACS后出院时他汀类药物的处方与持续使用有关,7一系列数据表明,心血管疾病患者在降脂药物的使用方面存在显著差距。在CONCORDANCE试验中,未能按照指南推荐的治疗方法让患者出院的人数为10…
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引用次数: 4
Cardioprotective medication adherence among patients with coronary heart disease in China: a systematic review. 中国冠心病患者的心脏保护药物依从性:一项系统综述。
Q2 Medicine Pub Date : 2019-06-24 eCollection Date: 2019-01-01 DOI: 10.1136/heartasia-2018-011173
Zhao Ni, Latefa Dardas, Bei Wu, Ryan Shaw

In China, poor cardioprotective medication adherence is a key reason for the high mortality rate of coronary heart disease (CHD). The aims of this systematic review are to (1) describe and synthesise factors that influence medication adherence among Chinese people with CHD, (2) evaluate the current status of intervention studies, and (3) discuss directions of future research to improve medication adherence. A comprehensive search using PubMed, Cumulative Index to Nursing and Allied Health Literature, Embase, Scopus, Global Health and PsycINFO was undertaken to describe poor adherence in China. Thirty-three eligible articles were included in the study. The review shows that there are multiple contributing factors to poor medication adherence, including patients' sociodemographic characteristics, health status and medication characteristics. In addition, from patients' perspective, lack of medication-related knowledge, such as the name, function, dosage and frequency, contributes to poor adherence. From physicians' perspective, a gap exists between CHD secondary prevention guidelines and clinical practice in China. Follow-up phone calls, educational lectures, booklets and reminder cards were common methods found to be effective in improving medication adherence. This systematic review indicates that cardioprotective medications were commonly prescribed as secondary prevention medication to patients with CHD in China, but adherence to these medications gradually decreased during a follow-up period. Therefore, more research should be conducted on how to establish high-quality health educational programmes aimed at increasing patients' medication adherence.

在中国,心脏保护药物依从性差是导致冠心病死亡率高的主要原因。本系统综述的目的是(1)描述和综合影响中国冠心病患者药物依从性的因素,(2)评估干预研究的现状,以及(3)讨论未来提高药物依从性研究的方向。使用PubMed、护理累积指数和相关健康文献、Embase、Scopus、Global Health和PsycINFO进行了全面搜索,以描述中国依从性差的情况。33篇符合条件的文章被纳入研究。综述表明,导致药物依从性差的因素有多种,包括患者的社会人口学特征、健康状况和药物特征。此外,从患者的角度来看,缺乏药物相关知识,如名称、功能、剂量和频率,导致依从性差。从医生的角度来看,中国冠心病二级预防指南与临床实践之间存在差距。随访电话、教育讲座、小册子和提醒卡是提高药物依从性的常用方法。这项系统综述表明,在中国,心脏保护药物通常是CHD患者的二级预防药物,但在随访期间,对这些药物的依从性逐渐降低。因此,应该对如何建立高质量的健康教育计划进行更多的研究,以提高患者的药物依从性。
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引用次数: 18
The influence of frailty under direct oral anticoagulant use in patients with atrial fibrillation. 房颤患者直接口服抗凝剂对衰弱的影响。
Q2 Medicine Pub Date : 2019-06-21 eCollection Date: 2019-01-01 DOI: 10.1136/heartasia-2019-011212
Takashi Yamamoto, Kentaro Yamashita, Kiichi Miyamae, Yuichiro Koyama, Masataka Izumimoto, Yoshihiro Kamimura, Satoko Hayakawa, Kazutaka Mori, Takaaki Yamada, Yasushi Tomita, Toyoaki Murohara

Background: Frailty is a prognostic factor in patients with atrial fibrillation (AF). However, there is no report on the associations between frailty and clinical adverse events in patients with AF taking direct oral anticoagulants (DOAC). The factors related to the occurrence of clinical adverse events are still under discussion. Therefore, we examined the associations between frailty and clinical adverse events in patients with AF taking DOAC in daily clinical practice.

Methods: We retrospectively evaluated 240 consecutive patients with AF who had been newly prescribed DOAC in our hospital from April 2016 through May 2017. Data collected included Clinical Frailty Scale (CFS) scores, laboratory results and basic demographic information.

Results: During the mean follow-up period of 13.4 months, 20 patients died (7.6 per 100 person-years), stroke or systemic embolism occurred in seven patients (2.6 per 100 person-years) and major bleeding occurred in 11 patients (4.2 per 100 person-years). We defined these adverse events as composite end points, and we estimated adjusted HRs and 95% CIs for risk factors using the Cox proportional hazard regression model. Frailty (defined as a CFS score of 5 or more; HR: 3.71; 95% CI: 1.59 to 8.65), female sex (HR: 3.49; 95% CI: 1.73 to 7.07), serum albumin level (HR: 0.47; 95% CI: 0.28 to 0.79) and malignancy (HR: 4.02; 95% CI: 1.83 to 8.84) were independent predictors of the composite end points.

Conclusions: Frailty, female sex, hypoalbuminaemia and malignancy were associated with clinical adverse events in patients with AF who were prescribed DOAC.

背景:虚弱是心房颤动(AF)患者的预后因素。然而,没有关于直接口服抗凝剂(DOAC)的房颤患者虚弱和临床不良事件之间关联的报道。临床不良事件发生的相关因素仍在讨论中。因此,我们研究了在日常临床实践中服用DOAC的房颤患者虚弱和临床不良事件之间的关系。方法:回顾性评估我院2016年4月至2017年5月连续240例新开DOAC的房颤患者。收集的数据包括临床虚弱量表(CFS)评分、实验室结果和基本人口统计信息。结果:在平均13.4个月的随访期间,20例患者死亡(7.6例/ 100人年),7例患者发生脑卒中或全身性栓塞(2.6例/ 100人年),11例患者发生大出血(4.2例/ 100人年)。我们将这些不良事件定义为复合终点,并使用Cox比例风险回归模型估计危险因素的调整hr和95% ci。虚弱(定义为CFS评分在5分或以上;人力资源:3.71;95% CI: 1.59 ~ 8.65),女性(HR: 3.49;95% CI: 1.73 ~ 7.07),血清白蛋白水平(HR: 0.47;95% CI: 0.28 ~ 0.79)和恶性肿瘤(HR: 4.02;95% CI: 1.83 ~ 8.84)是复合终点的独立预测因子。结论:虚弱、女性、低白蛋白血症和恶性肿瘤与服用DOAC的房颤患者的临床不良事件相关。
{"title":"The influence of frailty under direct oral anticoagulant use in patients with atrial fibrillation.","authors":"Takashi Yamamoto,&nbsp;Kentaro Yamashita,&nbsp;Kiichi Miyamae,&nbsp;Yuichiro Koyama,&nbsp;Masataka Izumimoto,&nbsp;Yoshihiro Kamimura,&nbsp;Satoko Hayakawa,&nbsp;Kazutaka Mori,&nbsp;Takaaki Yamada,&nbsp;Yasushi Tomita,&nbsp;Toyoaki Murohara","doi":"10.1136/heartasia-2019-011212","DOIUrl":"https://doi.org/10.1136/heartasia-2019-011212","url":null,"abstract":"<p><strong>Background: </strong>Frailty is a prognostic factor in patients with atrial fibrillation (AF). However, there is no report on the associations between frailty and clinical adverse events in patients with AF taking direct oral anticoagulants (DOAC). The factors related to the occurrence of clinical adverse events are still under discussion. Therefore, we examined the associations between frailty and clinical adverse events in patients with AF taking DOAC in daily clinical practice.</p><p><strong>Methods: </strong>We retrospectively evaluated 240 consecutive patients with AF who had been newly prescribed DOAC in our hospital from April 2016 through May 2017. Data collected included Clinical Frailty Scale (CFS) scores, laboratory results and basic demographic information.</p><p><strong>Results: </strong>During the mean follow-up period of 13.4 months, 20 patients died (7.6 per 100 person-years), stroke or systemic embolism occurred in seven patients (2.6 per 100 person-years) and major bleeding occurred in 11 patients (4.2 per 100 person-years). We defined these adverse events as composite end points, and we estimated adjusted HRs and 95% CIs for risk factors using the Cox proportional hazard regression model. Frailty (defined as a CFS score of 5 or more; HR: 3.71; 95% CI: 1.59 to 8.65), female sex (HR: 3.49; 95% CI: 1.73 to 7.07), serum albumin level (HR: 0.47; 95% CI: 0.28 to 0.79) and malignancy (HR: 4.02; 95% CI: 1.83 to 8.84) were independent predictors of the composite end points.</p><p><strong>Conclusions: </strong>Frailty, female sex, hypoalbuminaemia and malignancy were associated with clinical adverse events in patients with AF who were prescribed DOAC.</p>","PeriodicalId":12858,"journal":{"name":"Heart Asia","volume":" ","pages":"e011212"},"PeriodicalIF":0.0,"publicationDate":"2019-06-21","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1136/heartasia-2019-011212","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"37411279","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: 11
Severe adverse events following benzathine penicillin G injection for rheumatic heart disease prophylaxis: cardiac compromise more likely than anaphylaxis. 注射苄星青霉素G预防风湿性心脏病后的严重不良事件:心脏损害比过敏反应更容易发生。
Q2 Medicine Pub Date : 2019-06-20 eCollection Date: 2019-01-01 DOI: 10.1136/heartasia-2019-011191
Shannon Marantelli, Robert Hand, Jonathan Carapetis, Andrea Beaton, Rosemary Wyber

Objective: Secondary prophylaxis through long-term antibiotic administration is essential to prevent the progression of acute rheumatic fever to rheumatic heart disease (RHD). Benzathine penicillin G (BPG) has been shown to be the most efficacious antibiotic for this purpose; however, adverse events associated with BPG administration have been anecdotally reported. This study therefore aimed to collate case reports of adverse events associated with BPG administration for RHD prophylaxis.

Study design: A literature review was used to explore reported adverse reactions to BPG and inform development of a case report questionnaire. This questionnaire was circulated through professional networks to solicit retrospective reports of adverse events from treating physicians. Returned surveys were tabulated and thematically analysed. Reactions were assessed using the Brighton Collaboration case definition to identity potential anaphylaxis.

Results: We obtained 10 case reports from various locations, with patients ranging in age from early-teens to adults. All patients had clinical or echocardiogram-obtained evidence of valvular disease. The majority of patients (80%) had received BPG prior to the event with no previous adverse reaction. In eight cases, the reaction was fatal; in one case resuscitation was successful and in one case treatment was not required. Only three cases met Level 1 Brighton criteria consistent with anaphylaxis.

Conclusion: These results indicate that anaphylaxis is not a major cause of adverse reactions to BPG. An alternative mechanism for sudden death following BPG administration in people with severe RHD is proposed.

目的:二级预防通过长期抗生素给药是必不可少的,以防止急性风湿热发展为风湿性心脏病(RHD)。苄星青霉素G (BPG)已被证明是最有效的抗生素;然而,与BPG给药相关的不良事件有轶事报道。因此,本研究旨在整理与BPG预防RHD相关的不良事件的病例报告。研究设计:通过文献回顾来探讨BPG的不良反应报告,并为病例报告问卷的编制提供信息。该问卷通过专业网络分发,以征求治疗医生对不良事件的回顾性报告。返回的调查结果被制成表格并按主题进行分析。使用布莱顿合作病例定义评估反应,以确定潜在的过敏反应。结果:我们获得了来自不同地区的10例病例报告,患者年龄从青少年早期到成人不等。所有患者均有临床或超声心动图证实有瓣膜疾病。大多数患者(80%)在事件发生前接受过BPG治疗,既往无不良反应。在8个病例中,反应是致命的;1例复苏成功,1例不需要治疗。只有3例符合与过敏反应一致的1级布莱顿标准。结论:这些结果表明过敏反应不是BPG不良反应的主要原因。提出了严重RHD患者服用BPG后猝死的另一种机制。
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引用次数: 14
Effects of heat stroke on surface ECG: a study on clinical outcomes. 中暑对体表心电图的影响:临床结果研究。
Q2 Medicine Pub Date : 2019-06-19 eCollection Date: 2019-01-01 DOI: 10.1136/heartasia-2019-011221
Amal Paul, Reginald Alex, John Roshan Jacob, Bijesh Yadav

Aims: Classic heat stroke is associated with high in-hospital mortality and morbidity. The relation between the ECG findings in heat stroke and the clinical outcomes of these patients has not been studied. The aim of this study was to describe the electrocardiographic features in patients with classic heat stroke and to determine if there is any correlation of ECG findings with in-hospital outcomes.

Methods: We performed a retrospective study on 50 patients with classic heat stroke during summer months of 2016-2018. All 12-lead electrocardiographic recordings obtained from these patients were subjected to in-depth analysis. Statistical analysis was done to determine the correlation of electrocardiographic findings with in-hospital outcomes.

Results: 37 patients were in sinus rhythm, while supraventricular arrhythmias including atrial fibrillation (n=6), ectopic atrial tachycardia (n=4) and atrial flutter (n=2) were observed in the rest. There was a high prevalence of QTc prolongation, low voltage P waves, conduction defects like incomplete right bundle branch block and repolarisation abnormalities. The ratio of QRS voltage in the limb leads to that in precordial leads was ≤0.5 in nearly three-fourths of the patients. Among the observed electrocardiographic features, low P-wave voltage (<0.01 mV) in lead II was found to have statistically significant correlation with adverse in-hospital outcome (OR 8.93, p=0.04), after adjustment for clinical covariates.

Conclusion: There was high incidence of atrial arrhythmias in patients with classic heat stroke. A low P-wave voltage (<0.01 mV) in lead II was predictive of adverse in-hospital outcome in this cohort of patients.

目的:典型中暑与高住院死亡率和发病率相关。中暑患者的心电图表现与临床预后之间的关系尚未得到研究。本研究的目的是描述典型中暑患者的心电图特征,并确定心电图结果与住院预后是否存在相关性。方法:对2016-2018年夏季50例典型中暑患者进行回顾性研究。从这些患者获得的所有12导联心电图记录都进行了深入分析。统计分析确定心电图结果与住院结果的相关性。结果:窦性心律37例,室上性心律失常包括房颤(n=6)、异位房速(n=4)、心房扑动(n=2)。QTc延长、低电压P波、不完全性右束支阻滞等传导缺陷和复极异常发生率高。近四分之三的患者肢体导联与心前导联QRS电压之比≤0.5。观察到的心电图特征中,p波电压低(结论:经典中暑患者心房心律失常发生率高。低p波电压(
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引用次数: 8
Safety of performing transoesophageal echocardiography in patients with oesophageal varices. 经食管超声心动图检查食管静脉曲张患者的安全性。
Q2 Medicine Pub Date : 2019-06-12 eCollection Date: 2019-01-01 DOI: 10.1136/heartasia-2019-011223
Dania Hudhud, Haytham Allaham, Mohammad Eniezat, Tariq Enezate

Introduction: Oesophageal varices (EV) are one of the complications of liver cirrhosis that carries a risk of rupture and bleeding. The safety of performing transesophageal echocardiography (TEE) in patients with pre-existing EV is not well described in literature. Therefore, this retrospective study has been conducted to evaluate the safety of preforming TEE in this group of patients.

Methods: The study population was extracted from the 2016 Nationwide Readmissions Data using International Classification of Diseases, Tenth Revision, Clinical Modification/Procedure Coding System for EV, TEE and in-hospital outcomes. Study endpoints included in-hospital all-cause mortality, hospital length of stay, postprocedural gastrointestinal bleeding and oesophageal perforation.

Results: A total of 81 328 discharges with a diagnosis of EV were identified, among which 242 had a TEE performed during the index hospitalisation. Mean age was 58.3 years, 36.6% female. In comparison to the no-TEE group, the TEE group was associated with comparable in-hospital all-cause mortality (7.0% vs 6.7%, p=0.86) and bleeding (0.9% vs 1.1%, p=0.75); however, TEE group was associated with longer hospital stay (14.9 days vs 6.9 days, p<0.01). There were no reported oesophageal perforations.

Conclusions: TEE is not a common procedure performed in patients with pre-existing EV. TEE seems to be a safe diagnostic tool for evaluation of heart diseases in this group of patients.

简介:食管静脉曲张(EV)是肝硬化的并发症之一,有破裂和出血的危险。经食管超声心动图(TEE)的安全性在已有EV的患者中没有很好的文献描述。因此,本回顾性研究旨在评估在这组患者中预TEE的安全性。方法:采用国际疾病分类第十版、EV、TEE和院内结局的临床修改/程序编码系统,从2016年全国再入院数据中提取研究人群。研究终点包括院内全因死亡率、住院时间、术后消化道出血和食管穿孔。结果:共鉴定出81 328例诊断为EV的出院患者,其中242例在指数住院期间进行TEE检查。平均年龄58.3岁,女性占36.6%。与非TEE组相比,TEE组与相当的院内全因死亡率(7.0% vs 6.7%, p=0.86)和出血(0.9% vs 1.1%, p=0.75)相关;然而,TEE组与更长的住院时间相关(14.9天vs 6.9天)。结论:TEE不是预先存在的EV患者的常见手术。TEE似乎是评估这类患者心脏病的一种安全的诊断工具。
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引用次数: 5
期刊
Heart Asia
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