阻塞性呼吸道疾病影响遗传性出血性空脉切除症患者:数据库审查
Tristan Sinnatamby1, Jennifer LaBranche1,2, Maxine Farr-Jones1,3
1Department of Medicine (Pulmonary), University of Alberta.
PloS one
|September 25, 2025
概括
近19%的遗传性出血性长管切除症 (HHT) 患者患有阻塞性呼吸道疾病 (OAD),影响呼吸障碍的诊断和治疗. 识别这些重叠可以改善患者的护理.
科学领域:
- 肺部医学 肺部医学
- 遗传学 遗传学 是一个
- 心脏病学 心脏病学
背景情况:
- 呼吸不良是一种常见的症状,有多种不同的原因.
- 遗传性出血性长管iectasia (HHT) 可以通过肺动脉静脉形 (PAVMs) 和肺高血压 (PH) 引起呼吸障碍.
- 阻塞性呼吸道疾病 (OADs) 如喘,支气管切除症和COPD也会导致呼吸障碍,并且可以与HHT同时发生.
研究的目的:
- 确定与HHT患者同时发生的OADs的患病率.
- 改进HHT患者呼吸障碍的诊断和治疗,同时患有呼吸道疾病.
主要方法:
- 对来自埃德蒙顿HHT中心的132名患者病历进行了横截面审查.
- 经证实HHT诊断的患者被评估是否同时患有OAD (喘,支气管切除症,COPD).
主要成果:
- 在HHT患者中,有55.3%患有PAVMs.
- 28.0%的HHT患者有记录的OAD.
- 显著的18.9%的个体有与HHT相关的肺血管问题和OAD.
结论:
- 同时发生的OADs和HT相关的肺血管疾病是常见的.
- 识别患有这两种疾病的患者对于有效的呼吸障碍管理至关重要.
- 对于出现呼吸障碍的HHT患者,需要采用综合护理方法,以解决OAD和PAVM.
相关概念视频
Pulmonary Hypertension: Classification and Pathogenesis
576
Pulmonary hypertension (PH) is a severe health condition in which the mean pulmonary arterial pressure increases to 25 mmHg or more, even when the body is at rest. This high pressure in the blood vessels that transport blood from the heart to the lungs can cause various symptoms, including shortness of breath, can lead to right heart failure, and significantly affect the overall quality of life.
There are various classifications for PH, each relating to different underlying causes and also...
There are various classifications for PH, each relating to different underlying causes and also...
576
Esophageal Varices-I: Introduction
1.2K
Esophageal varices are dilated, tortuous veins which are found mainly in the submucosa of the lower esophagus but which may also appear higher up or extend into the stomach. They develop due to increased pressure in the portal venous system, often as a result of liver cirrhosis. This condition scars and damages the liver, impeding normal blood flow through the portal vein. To compensate, blood seeks alternative pathways, forming fragile new vessels (varices) in the esophagus and stomach. These...
1.2K
Disorders of Hemostasis
2.0K
Hemostasis, the process that stops bleeding after a blood vessel injury, is crucial for maintaining the integrity of the circulatory system. However, disorders of hemostasis can disrupt this delicate balance, leading to either excessive clotting or bleeding. These disorders can be broadly classified into thromboembolic disorders and bleeding disorders.
Thromboembolic Disorders
Two factors primarily cause thromboembolic conditions.
Thromboembolic Disorders
Two factors primarily cause thromboembolic conditions.
2.0K
Esophageal Varices-II: Clinical Features and Management
374
Esophageal varices often manifest as gastrointestinal bleeding episodes, presenting symptoms like hematemesis (vomiting of blood), hematochezia (passing fresh blood via the rectum), and melena (black, tarry stools). Other signs can include weight loss, anorexia, abdominal discomfort, jaundice, pruritus, altered mental status, and muscle cramps.
In the initial assessment, a thorough review of the patient's medical history is vital to identify risk factors such as liver disease, alcohol...
In the initial assessment, a thorough review of the patient's medical history is vital to identify risk factors such as liver disease, alcohol...
374
Treatment for Pulmonary Arterial Hypertension: Endothelin Receptor Antagonists
441
Endothelins (ETs) are potent vasoactive peptides critical in the human body's various physiological and pathological processes. One of the most promising therapeutic strategies for treating pulmonary arterial hypertension (PAH) involves counteracting the effects of these endothelins using a class of drugs known as endothelin receptor antagonists.
ETs are synthesized through a complex sequence of enzymatic steps, primarily involving an enzyme referred to as endothelin-converting enzyme...
ETs are synthesized through a complex sequence of enzymatic steps, primarily involving an enzyme referred to as endothelin-converting enzyme...
441
Cardiomyopathy III: Hypertrophic Cardiomyopathy
411
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...
411


