摘要
目的分析涂阳培阴及涂阳培养污染的原因分析,为了解决降低涂阳培阴率及涂阳培养污染率提出更合理的操作流程。方法 2013年8月-2014年12月实验室共接收各区实验室耐多药可疑患肺结核涂阳的痰标本和本单位的门诊及住院确诊肺结核病人涂阳的痰标本共819份,进行分离培养。对分离培养阴性及污染结果进行分析。结果 819份痰涂片阳性标本分离培养结果:分离培养阳性709份,占86.57%(709/819);培养阴性77份,占9.47%(77/819);培养污染33份,占4.03%(33/819);总涂阳培阴77份痰标本中:1条-8条23份占29.87%(23/77);1+42份占54.54%(42/77);2+10份占12.98%(10/77);3+1份占1.29%(1/77);4+1份占1.29%(1/77)。结论涂阳培阴标本涂片痰菌量分布在1+>8和条>2+之间,B组比A组患者痰标本出现涂阳培阴率和污染率高,应注意各个步骤操作流程细节。
Objective To analyze the causes of smear-panning and smear-culture pollution, and to propose a more reasonable operation procedure in order to reduce the smear-positive rate and smear-culture pollution rate.Methods From August 2013 to December 2014, the laboratory received a total of 819 specimens from the smear-positive tuberculosis of the multi-drug-susceptible tuberculosis in the laboratory and 819 specimens of the smear-positive smearpositive tuberculosis patients in the unit.The negative culture and contamination results were analyzed. Results A total of 819 smear-positive specimens were isolated and cultured: 709 copies were positive for culture, accounting for 86.57%(709/819); 77 were negative for culture, accounting for 9.47%(77/819); 33 cultures were contaminated, accounting for4.03%(33/819); total of 77 samples of sputum sputum negative: 1-8 articles 23 copies accounted for 29.87%(23/77); 1+42 copies accounted for 54.54%(42/77); 2+10 shares accounted for 12.98%(10/77); 3+1 shares accounted for 1.29%(1/77);4+1 shares accounted for 1.29%(1/77). Conclusion The distribution of sputum in smear of smear-coated smear specimens is between 1+>8 and 2+2+. The sputum specimens of group B have higher smear-positive rate and higher contamination rate than sputum specimens.
引文
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