Subtype

亚型
  • 文章类型: Journal Article
    志贺毒素(Stx),产志贺毒素大肠杆菌(STEC)的主要毒力因子,最初是在痢疾志贺氏菌菌株中发现的。虽然有报道称其他几种细菌会产生Stx,STEC对人类健康构成最重大的风险,因为它在与人类群体密切接触的各种动物宿主中普遍存在。根据其生化和分子特性,志贺毒素可以分为两种类型,Stx1和Stx2,其中已在各种细菌和宿主物种中鉴定出多种变体和亚型。有趣的是,不同的Stx亚型似乎在其宿主分布特征和与之相关的疾病的严重程度上有所不同。因此,这篇综述提供了一个全面的概述,已经记录到具有stx基因的细菌物种,特别关注在STEC中发现的各种Stx亚型变体,它们在某些宿主物种中的流行,以及它们的疾病相关特征。这篇综述提供了对Stx亚型的更好理解,并强调需要快速准确的毒素亚型方法,以正确评估与志贺毒素相关的细菌性食品污染和人类感染相关的健康风险。
    Shiga toxin (Stx), the main virulence factor of Shiga-toxin-producing E. coli (STEC), was first discovered in Shigella dysenteriae strains. While several other bacterial species have since been reported to produce Stx, STEC poses the most significant risk to human health due to its widespread prevalence across various animal hosts that have close contact with human populations. Based on its biochemical and molecular characteristics, Shiga toxin can be grouped into two types, Stx1 and Stx2, among which a variety of variants and subtypes have been identified in various bacteria and host species. Interestingly, the different Stx subtypes appear to vary in their host distribution characteristics and in the severity of diseases that they are associated with. As such, this review provides a comprehensive overview on the bacterial species that have been recorded to possess stx genes to date, with a specific focus on the various Stx subtype variants discovered in STEC, their prevalence in certain host species, and their disease-related characteristics. This review provides a better understanding of the Stx subtypes and highlights the need for rapid and accurate approaches to toxin subtyping for the proper evaluation of the health risks associated with Shiga-toxin-related bacterial food contamination and human infections.
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  • 文章类型: Review
    神经退行性疾病与遗传学的异质性有关,病理学,和临床表现。了解这种异质性与临床预后和对患者进行疾病修饰治疗的分层特别相关。最近,基于神经影像学的数据驱动方法已被用于研究神经退行性疾病的亚型,有助于解开这种异质性。我们回顾了衰老和代表性神经退行性疾病中基于脑的亚型研究,包括老年痴呆症,轻度认知障碍,额颞叶痴呆,路易体痴呆,从2000年1月到2022年11月。我们总结了聚类方法,验证,鲁棒性,再现性,以及本研究中71项符合条件的研究的临床相关性。我们发现研究之间的方法存在巨大差异,包括十种神经成像模式,24个聚类算法,和41种簇数确定方法。通过总结临床测量的分析方法,评估了亚型研究的临床相关性,在目前的研究中显示出相对较低的临床效用。最后,我们得出结论,未来对神经退行性疾病异质性的研究应该集中在验证上,亚型方法之间的比较,并优先考虑临床效用。
    Neurodegenerative diseases are associated with heterogeneity in genetics, pathology, and clinical manifestation. Understanding this heterogeneity is particularly relevant for clinical prognosis and stratifying patients for disease modifying treatments. Recently, data-driven methods based on neuroimaging have been applied to investigate the subtyping of neurodegenerative disease, helping to disentangle this heterogeneity. We reviewed brain-based subtyping studies in aging and representative neurodegenerative diseases, including Alzheimer\'s disease, mild cognitive impairment, frontotemporal dementia, and Lewy body dementia, from January 2000 to November 2022. We summarized clustering methods, validation, robustness, reproducibility, and clinical relevance of 71 eligible studies in the present study. We found vast variations in approaches between studies, including ten neuroimaging modalities, 24 cluster algorithms, and 41 methods of cluster number determination. The clinical relevance of subtyping studies was evaluated by summarizing the analysis method of clinical measurements, showing a relatively low clinical utility in the current studies. Finally, we conclude that future studies of heterogeneity in neurodegenerative disease should focus on validation, comparison between subtyping approaches, and prioritise clinical utility.
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  • 文章类型: Systematic Review
    外周T细胞淋巴瘤(PTCL)的总生存期令人沮丧。组蛋白去乙酰化酶(HDAC)抑制剂对PTCL患者具有良好的治疗效果。因此,这项工作旨在系统评估基于HDAC抑制剂的治疗对未治疗和复发/难治性(R/R)PTCL患者的治疗结果和安全性.
    在WebofScience上搜索了HDAC抑制剂治疗PTCL的前瞻性临床试验,PubMed,Embase,ClinicalTrials.gov,和Cochrane图书馆数据库。汇总的总体反应率,完全反应(CR)率,并测量部分反应率。评估不良事件的风险。此外,亚组分析用于评估不同HDAC抑制剂的疗效和不同PTCL亚型的疗效.
    对于未经处理的PTCL,参与了7项研究的502名患者,合并CR率为44%(95%CI,39-48%)。对于R/RPTCL患者,包括16项研究,CR率为14%(95%CI,11-16%)。与HDAC抑制剂单一疗法相比,基于HDAC抑制剂的联合疗法对R/RPTCL患者表现出更好的疗效(P=0.02)。此外,合并CR率为17%(95%CI,13-22%),10%(95%CI,5-15%),和10%(95%CI,5-15%)的罗米地辛,belinostat,和西达本胺单药治疗亚组,分别。在R/R血管免疫母细胞性T细胞淋巴瘤亚组中,合并的ORR为44%(95%CI,35-53%),高于其他亚型。共有18项研究参与治疗相关不良事件的安全性评估。血小板减少和恶心是最常见的血液学和非血液学不良事件。分别。
    这项荟萃分析表明,HDAC抑制剂是未经治疗和R/RPTCL患者的有效治疗选择。在R/RPTCL设置中,HDAC抑制剂和化学疗法的组合显示出优于HDAC抑制剂单一疗法的疗效。此外,基于HDAC抑制剂的治疗在血管免疫母细胞性T细胞淋巴瘤患者中的疗效高于其他亚型。
    UNASSIGNED: The overall survival of peripheral T-cell lymphoma (PTCL) is dismal. Histone deacetylase (HDAC) inhibitors have exhibited promising treatment outcomes for PTCL patients. Therefore, this work aims to systematically evaluate the treatment outcome and safety profile of HDAC inhibitor-based treatment for untreated and relapsed/refractory (R/R) PTCL patients.
    UNASSIGNED: The prospective clinical trials of HDAC inhibitors for the treatment of PTCL were searched on the Web of Science, PubMed, Embase, ClinicalTrials.gov, and Cochrane Library database. The pooled overall response rate, complete response (CR) rate, and partial response rate were measured. The risk of adverse events was evaluated. Moreover, the subgroup analysis was utilized to assess the efficacy among different HDAC inhibitors and efficacy in different PTCL subtypes.
    UNASSIGNED: For untreated PTCL, 502 patients in seven studies were involved, and the pooled CR rate was 44% (95% CI, 39-48%). For R/R PTCL patients, there were 16 studies included, and the CR rate was 14% (95% CI, 11-16%). The HDAC inhibitor-based combination therapy exhibited better efficacy when compared with HDAC inhibitor monotherapy for R/R PTCL patients (P = 0.02). In addition, the pooled CR rate was 17% (95% CI, 13-22%), 10% (95% CI, 5-15%), and 10% (95% CI, 5-15%) in the romidepsin, belinostat, and chidamide monotherapy subgroups, respectively. In the R/R angioimmunoblastic T-cell lymphoma subgroup, the pooled ORR was 44% (95% CI, 35-53%), higher than other subtypes. A total of 18 studies were involved in the safety assessment of treatment-related adverse events. Thrombocytopenia and nausea were the most common hematological and non-hematological adverse events, respectively.
    UNASSIGNED: This meta-analysis demonstrated that HDAC inhibitors were effective treatment options for untreated and R/R PTCL patients. The combination of HDAC inhibitor and chemotherapy exhibited superior efficacy to HDAC inhibitor monotherapy in the R/R PTCL setting. Additionally, HDAC inhibitor-based therapy had higher efficacy in angioimmunoblastic T-cell lymphoma patients than that in other subtypes.
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  • 文章类型: Journal Article
    基底细胞癌(BCC)是最常见的皮肤癌,尤其是皮肤白皙的成年人,在该人群中,其发病率的终生风险估计约为30%。我们提出了一项荟萃分析和系统综述,总结了BCC增长率的大小,也取决于它的亚型。
    要查找所有相关研究,在线医疗数据库,如PubMed,Scopus,Embase,WebofScience,搜索了谷歌学者关于BCC增长率的信息。
    本综述共纳入7项研究。五项研究包含有关基底细胞癌生长速率的数据。确定BCC长轴的平均生长速率为0.71mm/月(标准误差:0.22)。
    所提出的分析表明,BCC通常是一种生长缓慢的肿瘤,平均增长率约为0.7毫米/月。然而,事实证明,这种生长速率因BCC亚型而异。
    UNASSIGNED: Basal cell carcinoma (BCC) is the most common skin cancer, especially in fair-skinned adults, and the lifetime risk of its incidence in this population is estimated to be approximately 30%. We present a meta-analysis and systematic review summarizing the size of the growth rate in BCC, depending also on its subtypes.
    UNASSIGNED: To find all relevant studies, online medical databases such as PubMed, Scopus, Embase, Web of Science, and Google Scholar were searched regarding the growth rate of BCC.
    UNASSIGNED: A total of 7 studies were included in this review. Five studies contained data on the growth rate of basal cell carcinomas. The mean growth rate for the longer axis of the BCC was established to be 0.71 mm/month (standard error: 0.22).
    UNASSIGNED: The presented analysis shows that BCC is generally a slow-growing tumour, with a mean growth rate of about 0.7 mm/month. However, it was proven that this growth rate differs depending on the BCC subtype.
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  • 文章类型: Journal Article
    脑膜瘤是成人患者中最常见的颅内肿瘤。尽管大多数脑膜瘤被诊断为良性的,大约20%的病例是需要重大临床治疗的高级别肿瘤。中枢神经系统肿瘤分级的金标准来自世界卫生组织中枢神经系统肿瘤分类。治疗方案也取决于地点,成像,和肿瘤的组织病理学特征。这篇综述将涵盖脑膜瘤的诊断策略,包括2021年世界卫生组织脑膜瘤分级的更新。脑膜瘤治疗计划是可变的,并且高度依赖于肿瘤分级。这篇综述还将使读者了解脑膜瘤的治疗进展,包括手术,放射治疗和单克隆抗体治疗。
    Meningiomas are the most common intracranial tumors in adult patients. Although the majority of meningiomas are diagnosed as benign, approximately 20% of cases are high-grade tumors that require significant clinical treatment. The gold standard for grading central nervous system tumors comes from the World Health Organization Classification of Tumors of the central nervous system. Treatment options also depend on the location, imaging, and histopathological features of the tumor. This review will cover diagnostic strategies for meningiomas, including 2021 updates to the World Health Organization\'s grading of meningiomas. Meningioma treatment plans are variable and highly dependent on tumor grading. This review will also update the reader on developments in the treatment of meningiomas, including surgery, radiation therapy and monoclonal antibody treatment.
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  • 文章类型: Journal Article
    UNASSIGNED:本系统评价和荟萃分析评估了亚型囊胚菌。与伊朗的人类隔离。
    未经批准:囊胚。是一种厌氧肠原生动物,感染人类以及家畜和野生动物,即哺乳动物,两栖动物,爬行动物,和节肢动物.
    UNASSIGNED:利用英语和波斯语数据库对2022年4月之前发表的论文进行了全面搜索。在电子搜索中使用了以下MeSH关键字:(囊胚。)和(分子或亚型)和(流行或流行病学)和伊朗。对纳入研究的质量进行评价。此后,我们进行了一项随机效应荟萃分析,以估计纳入研究的合并患病率和比值比.
    UNASSIGNED:共有32项研究符合资格标准,包括5项病例对照研究和27项横断面研究。亚型囊胚的总体汇总患病率。在伊朗,估计为10%(95%置信区间:6%至15%)。囊胚的八种亚型。(ST1-ST7和ST9)在我们的研究中被确定,其中ST3是最常见的亚型(0.04);0.02-0.07)。在报告的研究中,两个病例组和对照组之间的亚型差异不显著,但病例中ST3感染的比值比(0.98;95%CI,0.30~3.20)较高.
    UNASSIGNED:当前的系统评价表明,除ST8和ST12外,所有人类囊胚菌属。世界上报道的亚型在伊朗的不同地区都有发现。
    UNASSIGNED: This systematic review and meta-analysis evaluated the subtyped Blastocystis sp. isolated from humans in Iran.
    UNASSIGNED: Blastocystis sp. is an anaerobic intestinal protozoan that infects humans as well as domestic and wild animals, i.e. mammals, amphibians, reptiles, and arthropods.
    UNASSIGNED: A comprehensive search for papers published before April 2022 was undertaken utilizing English and Persian databases. The following MeSH keywords were used in the electronic search: (Blastocystis sp.) AND (molecular OR subtype) AND (prevalence OR epidemiology) AND Iran. The quality of the included studies was evaluated. Thereafter, a random-effects meta-analysis was conducted to estimate the pooled prevalence and odds ratios regarding the included studies.
    UNASSIGNED: A total of 32 studies comprised of five case-control studies and 27 cross-sectional studies met the eligibility criteria. The overall pooled prevalence of subtyped Blastocystis sp. in Iran was estimated to be 10% (95% confidence interval: 6 to 15%). Eight subtypes of Blastocystis sp. (ST1- ST7 and ST9) were identified in our study, of which ST3 was the most common subtype (0.04); 0.02-0.07). The difference in subtypes between two case and control groups in reported studies was not significant, but the odds ratio of infection by ST3 (0.98; 95% CI, 0.30 to 3.20) was higher in cases.
    UNASSIGNED: The current systematic review showed that with the exception of ST8 and ST12, all human Blastocystis sp. subtypes reported in the world are found in different parts of Iran.
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  • 文章类型: Journal Article
    心力衰竭目前分为三种主要形式,HFrEF,HFpEF,和HFmrEF,但其病因多样且高度异质性。许多研究报道了心力衰竭患者中各种新的亚组,使用无监督机器学习方法。这个范围审查的目的是提供这些技术如何能够更快更好地诊断和管理HF的见解,从而为今后的研究提供方向,并促进其在临床实践中的常规使用。
    审查是根据PRISMA-SCR指南进行的。我们在PubMed数据库中搜索了符合条件的出版物。如果他们使用聚类分析方法在HF患者中定义新的亚组,并排除,如果它们是(1)评论,评注,或社论,(2)不是关于定义新的子类型的研究,或(3)不使用无监督算法的研究。所有研究筛选和数据提取均由两名研究者独立进行,并对纳入研究的数据进行叙事整合。
    在确定的498项研究中,47名被纳入分析。大多数研究(61.7%)是在2020年及以后发表的。来自美国的研究数量最多(46.8%),大多数研究都是在同一国家/地区撰写和收录的。最常用的机器学习方法是层次聚类分析(46.8%),最常用的集群变量类型是共病(61.7%),最少使用的簇变量类型是基因组学(12.8%)。大多数研究使用的数据集少于500名患者(48.9%),样本量与聚类变量数量呈负相关。大多数研究(85.1%)评估了聚类分组与至少一个结果之间的关联,死亡和住院是最常用的结局指标。
    本范围审查概述了最近提出基于聚类分析的新型HF亚群的研究。在研究设计中发现了差异,研究人群,聚类方法和变量,和利益的结果,我们提供了这些研究如何进行的见解,并确定了知识差距,以指导未来的研究。
    UNASSIGNED: Heart failure is currently divided into three main forms, HFrEF, HFpEF, and HFmrEF, but its etiology is diverse and highly heterogeneous. Many studies reported a variety of novel subgroups in heart failure patients, with unsupervised machine learning methods. The aim of this scoping review is to provide insights into how these techniques can diagnose and manage HF faster and better, thus providing direction for future research and facilitating its routine use in clinical practice.
    UNASSIGNED: The review was performed following PRISMA-SCR guideline. We searched the PubMed database for eligible publications. Studies were included if they defined new subgroups in HF patients using clustering analysis methods, and excluded if they are (1) Reviews, commentary, or editorials, (2) Studies not about defining new sub-types, or (3) Studies not using unsupervised algorithms. All study screening and data extraction were conducted independently by two investigators and narrative integration of data extracted from included studies was performed.
    UNASSIGNED: Of the 498 studies identified, 47 were included in the analysis. Most studies (61.7%) were published in 2020 and later. The largest number of studies (46.8%) coming from the United States, and most of the studies were authored and included in the same country. The most commonly used machine learning method was hierarchical cluster analysis (46.8%), the most commonly used cluster variable type was comorbidity (61.7%), and the least used cluster variable type was genomics (12.8%). Most of the studies used data sets of less than 500 patients (48.9%), and the sample size had negative correlation with the number of clustering variables. The majority of studies (85.1%) assessed the association between cluster grouping and at least one outcomes, with death and hospitalization being the most commonly used outcome measures.
    UNASSIGNED: This scoping review provides an overview of recent studies proposing novel HF subgroups based on clustering analysis. Differences were found in study design, study population, clustering methods and variables, and outcomes of interests, and we provided insights into how these studies were conducted and identify the knowledge gaps to guide future research.
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  • 文章类型: Journal Article
    乳腺癌是女性最常见的恶性肿瘤。虽然大多数癌症被归类为浸润性癌,无特殊类型(NST),一组具有不同病理和临床特征的不同肿瘤也被认识到,发病率从相对较常见到罕见。所谓的“特殊组织学类型”肿瘤显示90%以上的特异性,独特的组织学模式,而在唾液腺中经常遇到的一系列肿瘤也可能出现在乳房中。化生性癌会带来诊断挑战。一些不常见的肿瘤有病理性遗传改变。本文概述了这组不同病变的关键诊断点和鉴别诊断,以及每个实体的显着临床特征。
    Breast cancer is the most common malignant tumor in females. While most carcinomas are categorized as invasive carcinoma, no special type (NST), a diverse group of tumors with distinct pathologic and clinical features is also recognized, ranging in incidence from relatively more common to rare. So-called \"special histologic type\" tumors display more than 90% of a specific, distinctive histologic pattern, while a spectrum of tumors more often encountered in the salivary gland may also arise in the breast. Metaplastic carcinomas can present diagnostic challenges. Some uncommon tumors harbor pathognomonic genetic alterations. This article provides an overview of the key diagnostic points and differential diagnoses for this group of disparate lesions, as well as the salient clinical characteristics of each entity.
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  • 文章类型: Case Reports
    甲状舌管囊肿(TDC)通常发生在舌骨下方的颈部。已记录了TDC的不常见站点,其中,甲状腺内的位置非常罕见。我们报告了这种罕见的甲状腺内TDC(ITTDC),最初是通过超声检查确定的,是一名59岁的男性原发性甲状旁腺功能亢进症患者甲状腺左叶的偶然甲状腺成像报告和数据系统(TI-RADS)三个病变。甲状旁腺腺瘤。甲状腺病变的术前超声引导下细针穿刺活检(US-FNAB)细胞学检查被解释为BethesdaIII(意义不明的非典型性或意义不明的滤泡性病变)。进行了左半甲状腺切除术和左上甲状旁腺切除术。术后组织学显示甲状腺病变为ITTDC。组织学上还发现了偶然的甲状腺乳头状微小癌。术后2.5年随访顺利。基于文献检索,临床特征,细针穿刺活检(FNAB)细胞学,组织学,鉴别诊断,治疗,并对ITTDC的后续行动进行了审查和讨论。提出了将ITTDC分类为两个解剖位置亚型的建议。强调了由于稀有和缺乏形态特异性,ITTDC在FNAB细胞学上被误解的可能性。
    Thyroglossal duct cyst (TDC) commonly occurs in the neck just below the hyoid bone. Uncommon sites of TDC have been documented, and of these, an intra-thyroid location is very rare. We report such a rare intra-thyroid TDC (ITTDC) initially identified by ultrasound examination as an incidental thyroid imaging reporting and data system (TI-RADS) three lesion in the left thyroid lobe of a 59-year-old male patient with primary hyperparathyroidism due to a parathyroid adenoma. The preoperative ultrasound-guided fine-needle aspiration biopsy (US-FNAB) cytology of the thyroid lesion was interpreted as Bethesda III (atypia of undetermined significance or follicular lesion of undetermined significance). A left hemithyroidectomy and left superior parathyroidectomy were performed. The postoperative histology revealed the thyroid lesion to be an ITTDC. An incidental papillary thyroid microcarcinoma was also histologically revealed. The 2.5-year postoperative follow-up was uneventful. Based on literature searches, the clinical features, fine-needle aspiration biopsy (FNAB) cytology, histology, differential diagnosis, treatment, and follow-up of ITTDC were reviewed and discussed. A proposal to categorize ITTDC into two anatomical location subtypes is made. The liability of ITTDC to be misinterpreted on FNAB cytology due to rarity and lack of morphological specificity is emphasized.
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  • 文章类型: Journal Article
    机器学习(ML)越来越多地用于子类型定义和风险预测的研究,尤其是心血管疾病。没有现有的ML模型常规用于心血管疾病管理,他们的临床应用阶段是未知的,部分原因是缺乏明确的标准。我们评估了ML的亚型定义和心力衰竭(HF)的风险预测,急性冠状动脉综合征(ACS)和心房颤动(AF)。
    对于亚型定义和风险预测的ML研究,我们对HF进行了系统的审查,ACS和AF,使用PubMed,MEDLINE和WebofScience从2000年1月到2019年12月。通过调整已发布的诊断和预后研究标准,我们开发了一个七域,ML特定的检查表。
    在确定的5918项研究中,97包括在内。在亚型定义(n=40)和风险预测(n=57)的研究中,数据源有变化,人口规模(中位数606和中位数6769),临床设置(门诊,住院,不同部门),协变量数(中位数19和中位数48)和ML方法。所有研究都是单一疾病,大多数是北美(n=61/97),只有14项研究结合了定义和风险预测.亚型定义和风险预测研究在发展中分别存在局限性(例如,15.0%和78.9%的研究与患者受益相关;15.0%和15.8%的患者选择偏倚较低),验证(12.5%和5.3%外部验证)和影响(32.5%和91.2%改善了结果预测;没有有效性或成本效益评估).
    HF中ML的研究,ACS和AF受包含协变量的数量和类型的限制,ML方法,人口规模,国家,临床设置和关注单一疾病,不重叠或多浊度。临床效用和实施依赖于开发的改进,验证和影响,由简单的清单促进。在心血管疾病和其他疾病领域的临床实践中安全实施机器学习之前,我们提供了明确的步骤。
    Machine learning (ML) is increasingly used in research for subtype definition and risk prediction, particularly in cardiovascular diseases. No existing ML models are routinely used for cardiovascular disease management, and their phase of clinical utility is unknown, partly due to a lack of clear criteria. We evaluated ML for subtype definition and risk prediction in heart failure (HF), acute coronary syndromes (ACS) and atrial fibrillation (AF).
    For ML studies of subtype definition and risk prediction, we conducted a systematic review in HF, ACS and AF, using PubMed, MEDLINE and Web of Science from January 2000 until December 2019. By adapting published criteria for diagnostic and prognostic studies, we developed a seven-domain, ML-specific checklist.
    Of 5918 studies identified, 97 were included. Across studies for subtype definition (n = 40) and risk prediction (n = 57), there was variation in data source, population size (median 606 and median 6769), clinical setting (outpatient, inpatient, different departments), number of covariates (median 19 and median 48) and ML methods. All studies were single disease, most were North American (n = 61/97) and only 14 studies combined definition and risk prediction. Subtype definition and risk prediction studies respectively had limitations in development (e.g. 15.0% and 78.9% of studies related to patient benefit; 15.0% and 15.8% had low patient selection bias), validation (12.5% and 5.3% externally validated) and impact (32.5% and 91.2% improved outcome prediction; no effectiveness or cost-effectiveness evaluations).
    Studies of ML in HF, ACS and AF are limited by number and type of included covariates, ML methods, population size, country, clinical setting and focus on single diseases, not overlap or multimorbidity. Clinical utility and implementation rely on improvements in development, validation and impact, facilitated by simple checklists. We provide clear steps prior to safe implementation of machine learning in clinical practice for cardiovascular diseases and other disease areas.
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