诊断和治疗肺炎,一种常见的导致呼吸衰竭的神经肌肉疾病患者。

Q3 Medicine Acta Myologica Pub Date : 2021-09-30 eCollection Date: 2021-09-01 DOI:10.36185/2532-1900-053
Novella Carannante, Anna Annunziata, Antonietta Coppola, Francesca Simioli, Antonella Marotta, Mariano Bernardo, Eugenio Piscitelli, Pasquale Imitazione, Giuseppe Fiorentino
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引用次数: 3

摘要

神经肌肉疾病患者在患病期间,由于易感因素,更容易发生呼吸道感染。无效的咳嗽、肺不张、呼吸不足、吞咽困难和流口水是发生呼吸道感染和致命呼吸衰竭的危险因素。急性呼吸衰竭的呼吸道感染是最常见的住院原因,肺炎是世界范围内发病率和死亡率的主要原因之一。获得性肺炎的环境严重影响诊断和治疗选择。我们将重点关注这些受试者的病原发生、肺炎的诊断和治疗,特别是考虑到疾病的严重程度、抗生素耐药性和可能的并发症。在这种情况下,强烈建议咨询专业医生。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Diagnosis and treatment of pneumonia, a common cause of respiratory failure in patients with neuromuscular disorders.

Patients with neuromuscular diseases, during their illness are more susceptible to respiratory infections due to predisposing factors. Ineffective cough and the presence of atelectasis and hypoventilation, dysphagia and drooling can represent risk factors for the development of respiratory infection and fatal respiratory failure. Infections of respiratory tract with acute respiratory failure are the most common reason for hospitalizations, and pneumonia is among the leading causes of morbidity and mortality worldwide. The setting in which pneumonia is acquired heavily influences diagnostic and therapeutic choices. We will focus on aetiopathogenesis, diagnosis and treatment of pneumonia in these subjects, particularly considering the disease severity, rates of antibiotic resistance and the possible complications. In this case consultations with specialized physicians are strongly recommended.

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来源期刊
Acta Myologica
Acta Myologica Medicine-Cardiology and Cardiovascular Medicine
CiteScore
3.70
自引率
0.00%
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0
期刊最新文献
PROCEEDINGS OF THE XXIII CONGRESS OF THE ITALIAN ASSOCIATION OF MYOLOGY: PadovaJune 8-10, 2023. Year 2023: a new look for Acta Myologica. Experience with telemedicine in neuromuscular clinic during COVID-19 pandemic. VCP-related myopathy: a case series and a review of literature. Xp21 contiguous gene deletion syndrome presenting as Duchenne muscular dystrophy and glycerol kinase deficiency associated with intellectual disability: case report and review literature.
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