Sudden Cardiac Death

心源性猝死
  • 文章类型: Case Reports
    心律失常性二尖瓣脱垂综合征(ARMV)是一种公认但未被诊断的疾病模式。ARMV的风险因素已经确定,但不是很清楚,结构异常与室性心律失常的关系尚不完全清楚。
    这里,我们介绍了一个年轻人的案例,他在两次幸存的心脏骤停后,在我们医院接受了射频导管消融和二尖瓣手术。我们讨论了所使用的诊断和治疗策略。我们揭示了ARMV的风险因素,以及为什么早期识别至关重要。我们讨论一级预防及其局限性的主题。最后,我们讨论了ARMV患者的不同治疗方式。
    对ARMV的更多了解至关重要。关于临床管理的共识是存在的,但一级预防前瞻性数据中的科学空白需要填补,需要更好地了解ARMV的发病机制.
    UNASSIGNED: Arrhythmic mitral valve prolapse syndrome (ARMV) is a recognized but underdiagnosed disease pattern. Risk factors for ARMV are established but not very well known, and the association of the structural abnormality with ventricular arrhythmias is incompletely understood.
    UNASSIGNED: Here, we present the case of a young man who presented at our hospital for radiofrequency catheter ablation and mitral valve surgery after two episodes of survived sudden cardiac arrest. We discuss the diagnostic and therapeutic strategies that were used. We shine light on the risk factors for ARMV and why early identification is crucial. We address the topic of primary prevention and its limitations. Finally, we discuss different treatment modalities for patients with ARMV.
    UNASSIGNED: More awareness for ARMV is crucial. A consensus statement on clinical management exists, but scientific gaps in prospective data for primary prevention need to be filled and there is a need for a better understanding of the pathogenesis of ARMV.
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  • 文章类型: Case Reports
    暂无摘要。
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  • 文章类型: Systematic Review
    背景:阿片类药物使用与室性心律失常(VA)风险之间的关联知之甚少。
    目的:本研究的目的是综合与阿片类药物使用相关的VA风险的证据。
    方法:我们系统地搜索了Cochrane库,Embase,MEDLINE,2022年7月和CINAHL数据库。使用Cochrane用于随机对照试验(RCTs)的偏倚风险工具和ROBINS-I用于观察性研究的偏倚风险进行评估。使用等级评估证据的确定性。
    结果:我们纳入了15项研究(12项观察性,对RCT进行2次事后分析,1RCT)。大多数研究集中在阿片类药物用于维持治疗(n=9),比较美沙酮与丁丙诺啡(n=13),并报告QTc延长(n=13)。六项观察性研究存在严重的偏倚风险,1例RCT存在高偏倚风险.两项研究无法纳入荟萃分析,因为它们报告了不同的结果并研究了阿片类药物拮抗剂。对13项研究的荟萃分析表明,与使用丁丙诺啡相比,使用美沙酮与VA风险增加相关。吗啡,安慰剂,或左乙酰美沙多(风险比[RR],2.39;95%CI,1.31-4.35;I2=60%)。观察性研究之间的汇总估计值差异很大(RR,2.12;95%CI,1.15-3.91;I2=62%)和RCT(RR,14.09;95%CI,1.52-130.61;I2=0%),但两者都表明风险增加。
    结论:在本系统综述和荟萃分析中,我们发现,美沙酮的使用与对照组相比,VA的风险是前者的两倍多.然而,鉴于现有证据的质量有限,我们的研究结果应谨慎解释.
    BACKGROUND: The association between opioid use and the risk of ventricular arrhythmias (VA) is poorly understood.
    OBJECTIVE: The objective of this study was to synthesize the evidence on the risk of VA associated with opioid use.
    METHODS: We systematically searched the Cochrane Library, Embase, MEDLINE, and CINAHL databases in July 2022. Risk of bias was assessed using the Cochrane risk for bias tool for randomized controlled trials (RCTs) and ROBINS-I for observational studies. Certainty of evidence was assessed using GRADE.
    RESULTS: We included 15 studies (12 observational, 2 post hoc analyses of RCTs, 1 RCT). Most studies focused on opioid use for maintenance therapy (n = 9), comparing methadone to buprenorphine (n = 13), and reported QTc prolongation (n = 13). Six observational studies had a critical risk of bias, and one RCT was at high risk of bias. Two studies could not be included in the meta-analysis as they reported a different outcome and studied an opioid antagonist. Meta-analysis of 13 studies indicated that the use of methadone was associated with an increased risk of VA compared to the use of buprenorphine, morphine, placebo, or levacetylmethadol (risk ratio [RR], 2.39; 95% CI, 1.31-4.35; I2 = 60%). The pooled estimate varied greatly between observational studies (RR, 2.12; 95% CI, 1.15-3.91; I2 = 62%) and RCTs (RR, 14.09; 95% CI, 1.52-130.61; I2 = 0%), but both indicated an increased risk.
    CONCLUSIONS: In this systematic review and meta-analysis, we found that methadone use is associated with more than twice the risk of VA compared to comparators. However, our findings should be interpreted cautiously given the limited quality of the available evidence.
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  • 文章类型: Journal Article
    目的:很少有报告显示心源性猝死(SCD)发生率和停搏前合并症的长期趋势。本研究旨在全面分析SCD发病趋势及其与逮捕前合并症的关系。
    方法:这项基于人群的队列研究分析了台湾的国民健康保险(NHI)研究数据库,并通过检查2011年至2018年所有急诊科就诊的数据来确定SCD事件。纳入标准为ICD-9:427.5或427.41,或ICD-10:I46.9、I46.8或I46.2。根据药物使用确认了先前存在的合并症。采用多变量logistic回归与年龄,性别,和预先存在的合并症。
    结果:这项研究回顾了总共184,164,969人年记录,并确定了92,138例SCD事件。从2011年到2018年,台湾每100,000名参与者的SCD发病率从36.3增加到55.4。前五大合并症稳定,而慢性肾脏病的患病率明显上升。与20-29岁的人群相比,年龄>65岁的参与者患SCD的几率明显更高(aOR:27.30,95%CI:26.05-28.61)。在癫痫发作的参与者中发现了更高的SCD几率(aOR:2.24,95%CI:2.12-2.38),帕金森病(AOR:1.81,95%CI:1.73-1.89),心理障碍(AOR:1.59,95%CI:1.56-1.62),糖尿病(aOR:1.44,95%CI:1.41-1.46),心脏病(aOR:1.41,95%CI:1.38-1.44)。
    结论:从2011年到2018年,台湾的SCD发病率稳步上升。高血压,糖尿病,心脏病,心理障碍,关节炎是停药前的主要合并症。年龄是SCD最重要的危险因素。除了亚洲人之外,还需要进一步进行大规模的基于人口的研究,以调查不同种族的国家。
    OBJECTIVE: Few reports have indicated the secular trend in the sudden cardiac death (SCD) incidence and pre-arrest comorbidities. This study aimed to comprehensively analyze the trend of SCD incidence and its association with pre-arrest comorbidities.
    METHODS: This population-based cohort study analyzed Taiwan\'s National Health Insurance (NHI) research database and identified SCD incidents by inspecting data from all emergency department visits from 2011 to 2018. The inclusion criteria were ICD-9:427.5 or 427.41, or ICD-10:I46.9, I46.8, or I46.2. Pre-existing comorbidities were confirmed based on medication use. Multivariable logistic regression was adopted with covariates age, sex, and pre-existing comorbidities.
    RESULTS: This study reviewed a total of 184,164,969 person-year records, and identified 92,138 SCD incidents. From 2011 to 2018, the SCD incidence rate increased from 36.3 to 55.4 per 100,000 enrollees in Taiwan. The top five pre-arrest comorbidities were stable, while the prevalence of chronic kidney disease rose significantly. Compared to those aged 20-29, enrollees aged >65 years had significantly higher odds of SCD (aOR:27.30, 95% CI:26.05-28.61). Higher odds of SCD were noted in the enrollees who had a seizure (aOR:2.24, 95% CI:2.12-2.38), parkinsonism (aOR:1.81, 95% CI:1.73-1.89), psychological disorders (aOR:1.59, 95% CI:1.56-1.62), diabetes mellitus (aOR:1.44, 95% CI:1.41-1.46), heart diseases (aOR:1.41, 95% CI:1.38-1.44).
    CONCLUSIONS: The incidence of SCD steadily increased in Taiwan from 2011 to 2018. Hypertension, diabetes mellitus, heart disease, psychological disorders, and arthritis were major pre-arrest comorbidities. Age is the most important risk factor for SCD. Further large-scaled population-based study that investigated in diverse ethnicities from countries in addition to Asians would be warranted.
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  • 文章类型: Journal Article
    背景:(非)侵入性程序心室刺激(NIPS)预测室性心动过速(VT)复发的预后价值正在讨论中。室性心动过速消融的最佳终点没有明确定义,NIPS的最佳时间点未知。本研究的目的是评估室性心动过速消融术(PVS)和室性心动过速消融术后NIPS程序刺激的能力,以确定室性心动过速复发的高危患者。
    方法:2016年1月至2022年2月,纳入了接受首次VT消融和连续NIPS的室性心动过速和结构性心脏病患者。总的来说,138名患者被包括在内。所有患者在消融后的中位时间3(1-5)天(至少2个驱动周期长度(500和400ms)和最多4个右心室刺激外直至难治性)后,通过植入ICD进行NIPS。通过与自发性VT发作的12导联心电图和存储的ICD电描记图进行比较来定义临床VT。随访患者的中位数为37(13-61)个月。
    结果:在138例患者中,104为非诱导型(75%),非临床VT可诱导27例(20%),临床室性心动过速为7(5%)。在107名患者(78%)中,观察到PVS和NIPS的结果一致。37±20个月后,任何室性心律失常的复发率为40%(正常NIPS29%vs.NIPS期间的可诱导VT为66%;log-rankp=0.001),临床VT为3%(正常NIPS为1%NIPS期间的诱导型VT为9%;对数秩p=0.045)。与PVS相比,NIPS的阳性预测值(PPV)和阴性预测值(NPV)更高(PPV:65%vs.46%和NPV:68%与61%)。NIPS显示在ICM和LVEF>35%的患者中NPV最高。在NIPS期间患有诱导型VT的患者的VT复发率和总死亡率最高。PVS和NIPS均阴性的患者的VT复发率最低,为32%。初次住院期间复发性VT患者的早期再消融是可行的,但并未显示出更好的长期无VT生存率。
    结论:在室性心动过速消融和结构性心脏病后的患者中,NIPS对室性心动过速复发的风险分层优于消融后PVS。第3天的NIPS的PPV和NPV优于手术结束时的PVS,以预测复发性VT。尤其是ICM患者。
    BACKGROUND: The prognostic value of (non)-invasive programmed ventricular stimulation (NIPS) to predict recurrences of ventricular tachycardia (VT) is under discussion. Optimal endpoints of VT ablation are not well defined, and optimal timepoint of NIPS is unknown. The goal of this study was to evaluate the ability of programmed ventricular stimulation at the end of the VT ablation procedure (PVS) and NIPS after VT ablation to identify patients at high risk for VT recurrence.
    METHODS: Between January 2016 and February 2022, consecutive patients with VT and structural heart disease undergoing first VT ablation and consecutive NIPS were included. In total, 138 patients were included. All patients underwent NIPS through their implanted ICDs after a median of 3 (1-5) days after ablation (at least 2 drive cycle lengths (500 and 400 ms) and up to four right ventricular extrastimuli until refractoriness). Clinical VT was defined by comparison with 12-lead electrocardiograms and stored ICD electrograms from spontaneous VT episodes. Patients were followed for a median of 37 (13-61) months.
    RESULTS: Of the 138 patients, 104 were non-inducible (75%), 27 were inducible for non-clinical VTs (20%), and 7 for clinical VT (5%). In 107 patients (78%), concordant results of PVS and NIPS were observed. After 37 ± 20 months, the recurrence rate for any ventricular arrhythmia was 40% (normal NIPS 29% vs. inducible VT during NIPS 66%; log-rank p = 0.001) and for clinical VT was 3% (normal NIPS 1% vs. inducible VT during NIPS 9%; log-rank p = 0.045). Positive predictive value (PPV) and negative predictive value (NPV) of NIPS were higher compared to PVS (PPV: 65% vs. 46% and NPV: 68% vs. 61%). NIPS revealed the highest NPV among patients with ICM and LVEF > 35%. Patients with inducible VT during NIPS had the highest VT recurrences and overall mortality. Patients with both negative PVS and NIPS had the lowest any VT recurrence rates with 32%. Early re-ablation of patients with recurrent VTs during index hospitalization was feasible but did not reveal better long-term VT-free survival.
    CONCLUSIONS: In patients after VT ablation and structural heart disease, NIPS is superior to post-ablation PVS to stratify the risk of VT recurrences. The PPV and NPV of NIPS at day 3 were superior compared to PVS at the end of the procedure to predict recurrent VT, especially in patients with ICM.
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  • 文章类型: Journal Article
    在过去几年中,心脏病基因检测的适应症和临床影响显着增加。这项以医生为基础的EHRA调查的目的是评估ESC国家/地区当前的临床实践和对心脏病的基因检测,并评估对2022年EHRA/HRS/APHRS/LAHRS基因检测专家共识声明的遵守情况。由28个问题组成的在线问卷已提交给EHRA研究网络和欧洲参考网络GUARD-Heart医疗保健合作伙伴,并通过专门的社交媒体渠道进行推广。来自69个国家的357名受访者,40%的人在医院工作,拥有心脏遗传服务和/或专注于遗传性心脏病的专门诊所,27%的人在现场遗传实验室工作。39%的受访者没有宣布基因检测或低年率(<10/y)。大多数受访者(78%)在临床实践中宣称基因检测存在问题或局限性。不提供或有限获得基因检测的主要原因是没有专门的单位或基因实验室(35%)或报销问题(25%)。最常报告的基因检测适应症是诊断目的(55%)。大多数受访者(92%)宣布提供基因检测,然后进行遗传咨询,42%的人定期对心脏遗传病患者进行多学科评估。基因检测在诊断中的感知价值,预后,和治疗评估是可变的(67%,39%,29%,分别)和主要基于特定的遗传疾病。大多数受访者建议在先证者中存在致病性/可能致病性(P/LP)变异的情况下,对一级家庭成员进行级联基因检测。这项调查强调了遗传检测的获取和提供以及归因于专用单位/遗传实验室和报销的问题的显着异质性。然而,在有心脏病的患者中,我们观察到了对目前基因检测建议中适应症的充分遵守.
    Indications and clinical impact of genetic testing for cardiac diseases have increased significantly over the past years. The aim of this physician-based EHRA survey was to assess current clinical practice and access to genetic testing for cardiac diseases across ESC countries and to evaluate adherence to the 2022 EHRA/HRS/APHRS/LAHRS Expert Consensus Statement on genetic testing. An online questionnaire composed of 28 questions was submitted to the EHRA Research Network and European Reference Network GUARD-Heart healthcare partners and promoted via dedicated social media channels. There were 357 respondents from 69 countries, 40% working in a hospital setting with a cardiac genetic service and/or a dedicated clinic focusing on inherited cardiac diseases and 27% with an onsite genetic laboratory. No genetic testing or low annual rate (<10/y) was declared by 39% of respondents. The majority of respondents (78%) declared issues or limitations to genetic testing access in their clinical practice. The main reasons for not providing or limited access to genetic testing were no availability of dedicated unit or genetic laboratory (35%) or reimbursement issues (25%). The most frequently reported indication for genetic testing was diagnostic purpose (55%). Most respondents (92%) declared offering genetic testing preceded by genetic counselling and 42% regular multidisciplinary evaluations for patients with cardiac genetic diseases. The perceived value of genetic testing in the diagnostic, prognostic, and therapeutic assessment was variable (67%, 39%, and 29%, respectively) and primarily based on the specific inherited disease. The majority of respondents recommended cascade genetic testing for the first-degree family members in case of pathogenic/likely pathogenic (P/LP) variant in the proband. This survey highlights a significant heterogeneity of genetic testing access and provision and issues attributable to the availability of dedicated unit/genetic laboratory and reimbursement. However, adequate adherence to indications in the current recommendations for genetic testing in patients with cardiac diseases was observed.
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  • 文章类型: Journal Article
    提出了一种罕见的先天性心脏病的心电图,以突出诊断的独特发现及其临床意义和预测价值。
    An electrocardiogram of an uncommon congenital heart disease is presented to highlight the unique findings in diagnosis with its clinical implications and predictive value.
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  • 文章类型: Journal Article
    与二尖瓣脱垂(MVP)相关的室性心律失常以及引起心源性猝死(SCD)的能力,称为“恶性MVP”,越来越被认可,虽然罕见,现象。SCD可在无显著二尖瓣反流的情况下发生,暗示影响二尖瓣装置和左心室的机械紊乱之间的相互作用。这些心律失常的风险分层是重要的临床和公共卫生问题,以提供精确和有针对性的管理。评估需要患者和家族史,体格检查以及基于电生理和成像的模式。我们提供了致心律失常MVP的综述,探索其流行病学,人口统计,临床表现,将MVP链接到SCD的机制,疾病严重程度的标记,测试方式和管理,并讨论了风险分层的重要性。即使最近有了更好的理解,如何最好地衡量临床的预后重要性仍然具有挑战性,影像学和电生理数据,以确定明确的高危心律失常发生情况,其中ICD应用于SCD的一级预防。
    Ventricular arrhythmias associated with mitral valve prolapse (MVP) and the capacity to cause sudden cardiac death (SCD), referred to as \'malignant MVP\', are an increasingly recognised, albeit rare, phenomenon. SCD can occur without significant mitral regurgitation, implying an interaction between mechanical derangements affecting the mitral valve apparatus and left ventricle. Risk stratification of these arrhythmias is an important clinical and public health issue to provide precise and targeted management. Evaluation requires patient and family history, physical examination and electrophysiological and imaging-based modalities. We provide a review of arrhythmogenic MVP, exploring its epidemiology, demographics, clinical presentation, mechanisms linking MVP to SCD, markers of disease severity, testing modalities and management, and discuss the importance of risk stratification. Even with recently improved understanding, it remains challenging how best to weight the prognostic importance of clinical, imaging and electrophysiological data to determine a clear high-risk arrhythmogenic profile in which an ICD should be used for the primary prevention of SCD.
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  • 文章类型: Journal Article
    这项描述性回顾性研究使用魁北克验尸官局的数据,分析了2006年1月至2019年12月在体育和娱乐中自然死亡的建议。
    有建议的报告按性别进行了分析,年龄组,死因,context,和活动。使用基于公共卫生的模型评估建议的性质。主题分析是按照四个阶段的方法进行的,其中强调了所开发的主题,并将其与现有文献进一步联系起来。
    涉及18-24岁个人的报告和与冰球相关的报告更有可能包含建议。与≥45岁的个人有关的报告,或与骑自行车或狩猎有关的死亡频率更高,但推荐率相对较低。大多数建议与基于公共卫生的模型一致,但很少指定实施时间框架(11.7%)。近60%的验尸官的建议集中在自动体外除颤器的实施,交付和培训。
    降低≥45岁个体心脏骤停风险,及时治疗危及生命的心律失常,特别是在偏远地区进行的活动,并规定实施时间范围被确定为改善领域.国际复苏联络委员会在2022年制定的加强公众获取除颤的多方面方法解决了验尸官重复出现的主题,并有可能为循证决策提供信息。
    UNASSIGNED: This descriptive retrospective study analyzed coronial recommendations for natural deaths in sport and recreation from January 2006 to December 2019 using data from the Bureau du coroner du Québec.
    UNASSIGNED: Reports with recommendations were analyzed by sex, age group, cause of death, context, and activity. The nature of recommendations was assessed using a public health-based model. Thematic analysis was conducted following a four-phase approach in which themes developed were emphasized and further connected with existing literature.
    UNASSIGNED: Reports involving individuals aged 18-24 and reports related to ice hockey were significantly more likely to contain recommendations. Reports related to individuals ≥45 years old, or related to cycling or hunting had higher death frequencies, but relatively low recommendation rates. Most recommendations aligned with the public health-based model but specifying implementation time frames was rare (11.7%). Nearly 60% of coroner\'s recommendations focused on automated external defibrillator implementation, delivery and training.
    UNASSIGNED: Mitigation of sudden cardiac arrest risk for individuals ≥45 years old, timely treatment of life-threatening arrhythmias especially for activity practiced in remote regions and specifying implementation time frames were identified as improvement areas. The multi-faceted approach to enhancing public access defibrillation developed by the International Liaison Committee on Resuscitation in 2022 addresses recurrent themes covered by coroners and holds the potential to inform evidence-based decision making.
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  • 文章类型: Journal Article
    目的:评估左心室(LV)整体纵向应变(GLS)源自心血管磁共振(CMR),与(i)进行性心力衰竭(HF)有关,和(ii)扩张型心肌病患者的心源性猝死(SCD),射血分数(DCMmrEF)轻度降低。
    结果:我们进行了一项前瞻性观察性队列研究,对CMR评估的DCM和LV射血分数(LVEF)≥40%的患者,包括功能跟踪以评估LVGLS和晚期钆增强(LGE)。长期裁定的随访包括(i)HF住院,LV辅助装置植入或HF死亡,和(Ii)SCD或中止SCD(aSCD)。在355名DCMmrEF患者中(中位年龄54岁[四分位距43-64],216名男性[60.8%],LVEF中位数49%[46-54])随访中位数7.8年(5.2-9.4),32例(9%)患者出现HF事件,19例(5%)患者突然死亡或出现aSCD。在多变量模型中,LVGLS与HF事件相关(按%风险比[HR]1.10,95%置信区间[CI]1.00-1.21,p=0.045)或二分变量(LVGLS>-15.4%:HR2.70,95%CI1.30-5.94,p=0.008)。LGE的存在与HF事件无关(HR1.49,95%CI0.73-3.01,p=0.270)。相反,LVGLS与SCD/aSCD无关(每%HR1.07,95%CI0.95-1.22,p=0.257),而LGE存在(HR3.58,95%CI1.39-9.23,p=0.008)。LVEF与HF事件和SCD/aSCD无关。
    结论:多参数CMR可用于DCMmrEF患者的精确预后分层。LVGLS对进行性HF的风险进行分层,而LGE对SCD风险进行分层。
    OBJECTIVE: To assess whether left ventricular (LV) global longitudinal strain (GLS), derived from cardiovascular magnetic resonance (CMR), is associated with (i) progressive heart failure (HF), and (ii) sudden cardiac death (SCD) in patients with dilated cardiomyopathy with mildly reduced ejection fraction (DCMmrEF).
    RESULTS: We conducted a prospective observational cohort study of patients with DCM and LV ejection fraction (LVEF) ≥40% assessed by CMR, including feature-tracking to assess LV GLS and late gadolinium enhancement (LGE). Long-term adjudicated follow-up included (i) HF hospitalization, LV assist device implantation or HF death, and (ii) SCD or aborted SCD (aSCD). Of 355 patients with DCMmrEF (median age 54 years [interquartile range 43-64], 216 men [60.8%], median LVEF 49% [46-54]) followed up for a median 7.8 years (5.2-9.4), 32 patients (9%) experienced HF events and 19 (5%) died suddenly or experienced aSCD. LV GLS was associated with HF events in a multivariable model when considered as either a continuous (per % hazard ratio [HR] 1.10, 95% confidence interval [CI] 1.00-1.21, p = 0.045) or dichotomized variable (LV GLS > -15.4%: HR 2.70, 95% CI 1.30-5.94, p = 0.008). LGE presence was not associated with HF events (HR 1.49, 95% CI 0.73-3.01, p = 0.270). Conversely, LV GLS was not associated with SCD/aSCD (per % HR 1.07, 95% CI 0.95-1.22, p = 0.257), whereas LGE presence was (HR 3.58, 95% CI 1.39-9.23, p = 0.008). LVEF was neither associated with HF events nor SCD/aSCD.
    CONCLUSIONS: Multi-parametric CMR has utility for precision prognostic stratification of patients with DCMmrEF. LV GLS stratifies risk of progressive HF, while LGE stratifies SCD risk.
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