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从患有囊性纤维化的成年人中分离出的生物体。

Organisms isolated from adults with cystic fibrosis.

作者信息

McManus Terence E, McDowell Andrew, Moore John E, Elborn Stuart J

机构信息

Regional Adult Cystic Fibrosis Center, Belfast City Hospital, Belfast, Northern Ireland, BT9 7AB, UK.

出版信息

Ann Clin Microbiol Antimicrob. 2004 Dec 15;3:26. doi: 10.1186/1476-0711-3-26.

DOI:10.1186/1476-0711-3-26
PMID:15601468
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC544565/
Abstract

BACKGROUND

Patients with cystic fibrosis [CF] have frequent pulmonary exacerbations associated with the isolation of bacterial organisms from sputum samples. It is not clear however, if there are differences in the types of additional organisms isolated from patients who are infected with Burkholderia cepacia complex [BCC] or Pseudomonas aerugionsa [PA] in comparison to those who are not infected with either of these organisms [NI].

METHODS

Adult patients attending the regional CF unit were followed over a two year period and patients were assigned to three groups depending on whether they were known to be chronically infected with BCC, PA or NI. We compared the numbers and types of organisms which were isolated in each of these groups.

RESULTS

Information was available on a total of 79 patients; BCC 23, PA 30 and NI 26. Total numbers of organisms isolated, expressed as median and IQR for each group, [P = 0.045] and numbers of co-infecting organisms [P = 0.003] were significantly higher in the BCC group compared to PA, and in the PA group [P < 0.001, p = 0.007 respectively] compared to NI patients. The pattern of co-infecting organisms was similar in all three groups.

CONCLUSIONS

Total numbers of organisms isolated and numbers of co-infecting organisms were significantly higher in the BCC group compared to PA, and in the PA group compared to NI patients. Types of co-infecting organisms are similar in all groups of patients.

摘要

背景

囊性纤维化(CF)患者经常出现肺部病情加重,且痰标本中可分离出细菌。然而,与未感染洋葱伯克霍尔德菌复合体(BCC)或铜绿假单胞菌(PA)的患者相比,从感染这两种细菌的患者中分离出的其他生物体类型是否存在差异尚不清楚。

方法

对在地区CF治疗中心就诊的成年患者进行了为期两年的随访,并根据患者是否已知长期感染BCC、PA或未感染(NI)将其分为三组。我们比较了这三组中分离出的生物体数量和类型。

结果

共有79例患者的信息可供分析,其中BCC组23例,PA组30例,NI组26例。以每组的中位数和四分位间距表示的分离出的生物体总数,[P = 0.045]以及合并感染生物体的数量[P = 0.003],BCC组显著高于PA组,PA组与NI组患者相比也显著更高(分别为P < 0.001,p = 0.007)。所有三组中合并感染生物体的模式相似。

结论

与PA组相比,BCC组分离出的生物体总数和合并感染生物体数量显著更高,与NI组患者相比,PA组也显著更高。所有患者组中合并感染生物体的类型相似。

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本文引用的文献

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Risk factors for initial acquisition of Pseudomonas aeruginosa in children with cystic fibrosis identified by newborn screening.通过新生儿筛查确定的囊性纤维化患儿初次感染铜绿假单胞菌的危险因素。
Pediatr Pulmonol. 2003 Apr;35(4):257-62. doi: 10.1002/ppul.10230.
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Predictors of deterioration of lung function in cystic fibrosis.囊性纤维化患者肺功能恶化的预测因素
Pediatr Pulmonol. 2002 Jun;33(6):483-91. doi: 10.1002/ppul.10100.
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Outcome of Burkholderia cepacia colonisation in an adult cystic fibrosis centre.成年囊性纤维化中心洋葱伯克霍尔德菌定植的结果
Thorax. 2002 Feb;57(2):142-5. doi: 10.1136/thorax.57.2.142.
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Prophylactic antibiotics for cystic fibrosis.囊性纤维化的预防性抗生素治疗
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Wasting as an independent predictor of mortality in patients with cystic fibrosis.消瘦作为囊性纤维化患者死亡率的独立预测因素。
Thorax. 2001 Oct;56(10):746-50. doi: 10.1136/thorax.56.10.746.
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Fifteen-year follow-up of pulmonary function in individuals heterozygous for the cystic fibrosis phenylalanine-508 deletion.对携带囊性纤维化苯丙氨酸-508缺失杂合突变个体的肺功能进行的15年随访
J Allergy Clin Immunol. 2001 May;107(5):818-23. doi: 10.1067/mai.2001.114117.
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Clinical outcome after early Pseudomonas aeruginosa infection in cystic fibrosis.囊性纤维化患者早期铜绿假单胞菌感染后的临床结局
J Pediatr. 2001 May;138(5):699-704. doi: 10.1067/mpd.2001.112897.
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Cystic fibrosis: inflammatory response to infection with Burkholderia cepacia and Pseudomonas aeruginosa.囊性纤维化:对洋葱伯克霍尔德菌和铜绿假单胞菌感染的炎症反应。
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Severe viral respiratory infections in infants with cystic fibrosis.患有囊性纤维化的婴儿的严重病毒性呼吸道感染
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