Necrotizing Pneumococcal Pneumonia With Bronchopleural Fistula Among Children in Taiwan

被引:54
作者
Hsieh, Yu Chia
Wang, Chih-Wei [2 ]
Lai, Shen-Hao
Lai, Jin-Yao [3 ]
Wong, Kin-Sun
Huang, Yhu-Chering
Chang, Kuang-Yi [4 ,5 ,6 ]
Chiu, Cheng-Hsun [1 ]
Lin, Tzou-Yien
机构
[1] Chang Gung Childrens Hosp, Dept Pediat, Div Pediat Infect Dis, Tao Yuan, Taiwan
[2] Chang Gung Univ, Coll Med, Chang Gung Mem Hosp, Chang Gung Childrens Hosp,Dept Anat Pathol, Tao Yuan, Taiwan
[3] Chang Gung Univ, Coll Med, Chang Gung Mem Hosp, Chang Gung Childrens Hosp,Dept Pediat Surg, Tao Yuan, Taiwan
[4] Natl Taiwan Univ, Coll Publ Hlth, Div Biostat, Taipei 10764, Taiwan
[5] Taipei Vet Gen Hosp, Dept Anesthesiol, Taipei, Taiwan
[6] Natl Yang Ming Univ, Sch Med, Taipei 112, Taiwan
关键词
pneumococcal pneumonia; bronchopleural fistula; serotype; 19A; pulmonary infarction; STREPTOCOCCUS-PNEUMONIAE; SEROTYPE; 19A; CLINICAL CHARACTERISTICS; CONJUGATE VACCINE; UNITED-STATES; IDENTIFICATION; COMPLICATION; EMERGENCE; DISEASE;
D O I
10.1097/INF.0b013e31821b10c3
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
071005 [微生物学]; 100108 [医学免疫学];
摘要
Background: Severe necrotizing pneumococcal pneumonia may progress to the development of bronchopleural fistula (BPF). The purpose of this study was to describe the clinical courses and identify risk factors for the development of bronchopleural fistula in children with pneumococcal pneumonia. Histopathologic features of children receiving surgical resections of the lung because of BPF were analyzed to explore the pathogenesis of destructive lung disease caused by Streptococcus pneumoniae. Methods: A total of 112 cases of culture-proven pneumococcal pneumonia were identified between January 2001 and March 2010 at Chang Gung Children's Hospital. The medical charts of all cases of culture-proven pneumococcal pneumonia were reviewed. Results: Pneumococcal pneumonia in 18 children (18/112, 16.1%) was complicated by BPF. As compared with children without BPF, children with BPF had significantly lower white blood cell counts at admission (P = 0.03) and significantly longer durations of fever and hospitalization (P < 0.001). Multivariate analysis revealed that acute respiratory failure (odds ratio = 8.9; 95% confidence interval = 2.6-30.9; P = 0.001) and serotype 19A infection (odds ratio = 5.0; 95% confidence interval = 1.2-22.1; P = 0.03) were risk factors for the development of BPF. Histopathologic analyses were available for 12 children who underwent surgical resections of the lung. Coagulative necrosis with pulmonary infarction was found in 11 of the 12 cases. Conclusions: Serotype 19A was strongly associated with BPF. Vaccines containing this serotype will be important for prevention.
引用
收藏
页码:740 / 744
页数:5
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