唐氏综合征肺动脉高压的治疗

S. Herbert, Tulloh Rmr
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引用次数: 9

摘要

唐氏综合症(DS)是最常见的染色体异常,与多种合并症相关,包括先天性心脏病和呼吸道疾病,通常伴有气道阻塞。如果不及时治疗,这些合并症会在几个月内导致肺动脉高压(PAH)。因此,识别先天性异常以防止这些人的多环芳烃进展至关重要。由于与正常人群相比,退行性肺病患者发生多环芳烃的风险更高,因此必须监测他们的疾病症状,并根据世卫组织的功能分类进行积极治疗,以阻止或减缓疾病进程。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Treatment of Pulmonary Hypertension in Downs Syndrome
Down’s Syndrome(DS) is the most common chromosomal abnormality associated with multiple comorbidities including congenital heart disease and respiratory disease typically with airway obstruction. These comorbidities have been documented to contribute to pulmonary arterial hypertension (PAH) within months if left untreated. It is therefore of paramount importance to identify congenital abnormalities to prevent the progression of PAH in such people. Since people with DS have a higher risk of developing PAH in comparison to the normal population, they must be both monitored for symptoms of disease as categorized by WHO functional class and be actively treated in order to halt or slow the disease process.
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