一个中心的小儿囊性纤维化急性肺部恶化门诊治疗指南》。

IF 1.7 Q2 PEDIATRICS Clinical Medicine Insights-Pediatrics Pub Date : 2016-07-12 eCollection Date: 2016-01-01 DOI:10.4137/CMPed.S38336
Corinne A Muirhead, Jillian N Sanford, Benjamin G McCullar, Dawn Nolt, Kelvin D MacDonald
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引用次数: 0

摘要

囊性纤维化(CF)是一种慢性疾病,以急性肺部恶化为特征,包括咳嗽加重、胸部充血、粘液分泌增多、呼吸急促、体重减轻和疲劳。通常情况下,病情严重的患者需要住院治疗,包括静脉注射抗菌素、气道清理疗法和营养支持。病情较轻的患儿通常可在门诊接受口服抗菌药物和在家加强气道通畅治疗,而无需前往 CF 专科中心开始治疗。特定抗菌药的选择取决于监测培养中发现的病原体、抗菌药在 CF 患者体内的活性以及这些患者的独特生理机能。在这篇儿科综述中,我们介绍了我们在以下方面的做法:定义急性肺部恶化、决定治疗地点、亲自或远程开始治疗、确定气道清理频率、选择抗菌药物治疗、建议复诊时间以及识别和处理治疗失败。
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One Center's Guide to Outpatient Management of Pediatric Cystic Fibrosis Acute Pulmonary Exacerbation.

Cystic fibrosis (CF) is a chronic disorder characterized by acute pulmonary exacerbations that comprise increased cough, chest congestion, increased mucus production, shortness of breath, weight loss, and fatigue. Typically, severe episodes are treated in the inpatient setting and include intravenous antimicrobials, airway clearance therapy, and nutritional support. Children with less-severe findings can often be managed as outpatients with oral antimicrobials and increased airway clearance therapy at home without visiting the specialty CF center to begin treatment. Selection of specific antimicrobial agents is dependent on pathogens found in surveillance culture, activity of an agent in patients with CF, and the unique physiology of these patients. In this pediatric review, we present our practice for defining acute pulmonary exacerbation, deciding treatment location, initiating treatment either in-person or remotely, determining the frequency of airway clearance, selecting antimicrobial therapy, recommending timing for follow-up visit, and recognizing and managing treatment failures.

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