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1.
Chinese Journal of Contemporary Pediatrics ; (12): 1204-1209, 2015.
Article in Chinese | WPRIM | ID: wpr-279940

ABSTRACT

<p><b>OBJECTIVE</b>To investigate the distribution and drug sensitivity of pathogens and risk factors for ventilator-associated pneumonia (VAP) in children with congenial heart disease (CAD) after surgery.</p><p><b>METHODS</b>According to the occurrence of VAP, 312 children with CAD who received mechanical ventilation after surgery for 48 hours or longer between January 2012 and December 2014 were classified into VAP (n=53) and non-VAP groups (n=259). Sputum samples were collected and cultured for pathogens in children with VAP. The drug sensitivity of pathogens was analyzed. The risk factors for postoperative VAP were identified by multiple logistic regression analysis.</p><p><b>RESULTS</b>The sputum cultures were positive in 51 out of 53 children with VAP, and a total of 63 positive strains were cultured, including 49 strains of Gram-negative bacteria (78%), 9 strains of Gram-positive bacteria (14%) and 5 strains of funqi (8%). The drug sensitivity test showed that Gram-negative bacteria were resistant to amoxicillin, piperacillin, cefotaxime and ceftazidime, with a resistance rate of above 74%, and demonstrated a sensitivity to amikacin, polymyxin and meropenem (resistance rate of 19%-32%). Single factor analysis showed albumin levels, preoperative use of antibiotics, duration of mechanical ventilation, times of tracheal intubation, duration of anesthesia agent use, duration of acrdiopulmonary bypass, duration of aortic occlusion and use of histamin2-receptor blockade were significantly different between the VAP and non-VAP groups (P<0.05). The multiple logistic regression showed albumin levels (<35 g/L), duration of mechanical ventilation (≥ 7 d), times of tracheal intubation (≥ 3), duration of acrdiopulmonary bypass (≥ 100 minutes) and duation of aortic occlusion (≥ 60 minutes) were independent risk factors for VAP in children with CAD after surgery.</p><p><b>CONCLUSIONS</b>Gram-nagative bacteria are main pathogens for VAP in children with CAD after surgery. The antibiotics should be used based on the distribution of pathogens and drug sensitivity test results of pathogens. The effective measures for prevention of VAP should be taken according to the related risk factors for VAP to reduce the morbidity of VAP in children with CAD after surgery.</p>


Subject(s)
Humans , Anti-Bacterial Agents , Pharmacology , Gram-Negative Bacteria , Heart Defects, Congenital , General Surgery , Logistic Models , Microbial Sensitivity Tests , Pneumonia, Ventilator-Associated , Risk Factors , Sputum , Microbiology
2.
Chinese Journal of Contemporary Pediatrics ; (12): 389-392, 2009.
Article in Chinese | WPRIM | ID: wpr-347907

ABSTRACT

<p><b>OBJECTIVE</b>Some research has shown that p38 mitogen-activated protein kinase (p38MAPK) plays important roles in lung injuries induced by various factors. Its expression and role in hyperoxia-induced lung injury remains unknown. This study investigated the expression and role of p38MAPK in hyperoxia-induced lung injury juvenile rat model.</p><p><b>METHODS</b>Hyperoxia-induced lung injury rat model was prepared by 90% O(2) exposure. The location and expression of p38MAPK in lung tissues were detected by immunohistochemistry and Western blot respectively. Apoptosis index of lung was evaluated by TUNEL technique. The effect of SB203580, a p38MAPK inhibitor, on the apoptosis index of lung was observed.</p><p><b>RESULTS</b>The expression of phosphor-p38MAPK increased obviously after hyperoxia. Positive phosphor-p38MAPK cells were mainly distributed in the alveolar, airway epithelial cells, pulmonary vascular endothelium cells and infiltrative inflammatory cells. The apoptosis index of lung also significantly elevated. SB203580 inhibited the activation of p38MAPK, and reduced the apoptosis index of lung.</p><p><b>CONCLUSIONS</b>The phosphor-p38MAPK increased and was expressed in many kinds of lung cells in lung injury rat model. It may play a role in the induction of apoptosis in hyperoxia-induced lung injury.</p>


Subject(s)
Animals , Female , Male , Rats , Apoptosis , Disease Models, Animal , Hyperoxia , Imidazoles , Therapeutic Uses , Immunoblotting , Lung Injury , Drug Therapy , MAP Kinase Signaling System , Phosphorylation , Pyridines , Therapeutic Uses , Rats, Wistar , p38 Mitogen-Activated Protein Kinases , Physiology
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