小儿和青少年腹患者的亚临床心肌功能障碍:系统性审查和元分析
Elpida Emmanouilidou-Fotoulaki1, Maria Kavga2, Michail Delis3
11st Department of Pediatrics, School of Medicine, Aristotle University of Thessaloniki, 54642 Thessaloniki, Greece.
Children (Basel, Switzerland)
|May 1, 2025
概括
患有乳病的儿童可能有早期心肌功能障碍,可通过心声回声检测. 在这个系统性审查中,无质饮食并没有显著改善这些心脏标志物.
科学领域:
- 儿童心脏病学 儿童心脏病学
- 胃肠病学 胃肠病学
- 系统审查是系统的审查.
背景情况:
- 病是一种影响小肠的自身免疫性疾病.
- 早期检测子临床心肌功能障碍在儿科腹腔疾病中至关重要.
- 无质饮食对这些患者心脏功能的影响需要研究.
研究的目的:
- 系统地审查和元分析早期心肌功能回声学标记在儿童和青少年患有腹腔疾病.
- 为了比较乳患者和健康对照人群之间的心脏功能.
- 评估坚持无质饮食对心肌功能的影响.
主要方法:
- 在主要电子数据库中进行系统的文献搜索.
- 包括15项研究,涉及916名儿科乳病患者和569名健康对照.
- 分析传统和先进的心声回声学参数,包括分数缩短和心肌性能指数.
主要成果:
- 在各种心声学参数中,在乳病患者中观察到心肌功能下降的趋势.
- 在分数缩短和心肌性能指数中注意到统计学意义.
- 在坚持无质饮食后,没有发现这些心脏参数的显著改善.
结论:
- 使用心声扫描进行常规心血管检查,建议儿童患有腹腔疾病,以检测亚临床心肌功能障碍.
- 心肌性能指数显示出在这个人群中评估心脏功能的非侵入性标记物的潜力.
- 需要进一步的研究来证实心声学标志物的可靠性和临床适用性,并评估无质饮食遵守的长期影响.
相关概念视频
Myocarditis II: Clinical Features and Diagnostic Tests
497
Myocarditis is an inflammation of the heart muscle. The symptoms vary widely, encompassing asymptomatic presentations to severe, acute manifestations.Clinical PresentationAsymptomatic cases: In some instances, myocarditis may be asymptomatic, with the infection resolving without intervention. These cases often go undetected unless discovered incidentally through diagnostic imaging or tests conducted for other reasons.General Early Symptoms: Early symptoms of myocarditis are non-specific and can...
497
Cardiomyopathy I: Introduction and Classification
837
Cardiomyopathy, or CMP, is a group of diseases affecting the myocardial structure, impairing its ability to pump blood effectively. This condition can lead to arrhythmias, heart failure, or sudden cardiac death.Cardiomyopathies are classified into primary and secondary categories:Primary Cardiomyopathy refers to conditions involving only the heart muscle that are often idiopathic (of unknown cause) or genetic. They primarily affect the myocardium without the involvement of other systemic...
837
Cardiomyopathy II: Dilated Cardiomyopathy
802
Dilated cardiomyopathy, or DCM, is a progressive myocardial disorder characterized by ventricular chamber dilation and contractile dysfunction.EtiologyVarious factors can cause DCM, including hypertension and heavy alcohol intake, which contribute to the weakening and enlargement of the heart muscle. Viral infections, such as Coxsackievirus B, adenoviruses, and influenza, can lead to DCM by causing inflammation and damage to heart tissue. Certain chemotherapeutic agents, including daunorubicin,...
802
Cardiomyopathy III: Hypertrophic Cardiomyopathy
812
Hypertrophic cardiomyopathy, or HCM, is an autosomal dominant genetic disorder characterized by asymmetric left ventricular hypertrophy without ventricular dilation. It is more common in men and is typically diagnosed in young, athletic adults.EtiologyHCM is primarily genetic and is caused by mutations in genes encoding sarcomeric proteins. Researchers have identified over 1400 mutations across at least 11 different genes. Among these, the most frequently occurring mutations are found in the...
812


