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Burkholderia pseudomallei in cystic fibrosis and treatment complications

机译:假伯克霍尔德氏菌在囊性纤维化中的作用及治疗并发症

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AbstractA healthy 29-year-old Australian man with cystic fibrosis (CF) grew Burkholderia pseudomallei on a routine sputum culture 1 month after returning from holiday in Thailand. He underwent a 12-month treatment regime with multiple antibiotics resulting in a number of adverse events. Sputum cultures were cleared of the pathogen and remain negative 8 years post-treatment. There were no clinical sequelae and no deterioration in lung function. Few reports have been published to date on melioidosis in CF patients. The proposed management for this infection includes multiple antibiotics regimens for prolonged periods of time, which may result in adverse events. Optimal treatment and length of treatment are currently determined on an individual basis.
机译:摘要一名健康的29岁澳大利亚男子患有囊性纤维化(CF),在泰国度假归来后1个月,通过常规的痰培养培养了Burkholderia pseudomallei。他接受了为期12个月的多种抗生素治疗方案,导致了许多不良事件。清除痰培养物中的病原体,并在治疗后8年保持阴性。没有临床后遗症,肺功能也没有恶化。迄今为止,很少有报道涉及CF患者的类黑斑病。对于这种感染的建议管理方法包括长时间使用多种抗生素方案,这可能会导致不良事件。目前,最佳治疗方法和治疗时间长短是由个体决定的。

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