检验医学与临床
檢驗醫學與臨床
검험의학여림상
JOURNAL OF LABORATORY MEDICINE AND CLINICAL SCIENCES
2014年
19期
2696-2697,2700
,共3页
殷琳%喻华%黄湘宁%乔宁%张凯%刘鑫
慇琳%喻華%黃湘寧%喬寧%張凱%劉鑫
은림%유화%황상저%교저%장개%류흠
无菌体液%血培养瓶法%直接接种法
無菌體液%血培養瓶法%直接接種法
무균체액%혈배양병법%직접접충법
aseptic humoral%blood culture bottle enrichment method%direct inoculation method
目的:探讨血培养瓶法在无菌体液病原菌培养中的应用。方法收集2013年3~9月四川省人民医院共321份无菌体液标本,通过双瓶血培养瓶法和直接接种法培养分离病原菌,通过与传统的直接接种法比较对其进行评价。结果321份标本中,通过血培养瓶法108份标本培养出细菌,阳性率为33.6%;直接接种法55份标本培养出细菌,阳性率为17.1%,差异有统计学意义( P<0.01)。血培养增菌后80%细菌在24~48 h内检出,而直接接种法90%细菌在24 h检出,检出时间直接接种法更具优势。两种方法检出细菌前3位均为屎肠球菌、大肠埃希菌和肺炎克雷伯菌,而凝固酶阴性葡萄球菌、草绿色链球菌等在血培养法中检出率明显高于直接法。血培养瓶法的敏感性为89.7%,阴性符合率为95.3%,直接接种法分别为43.2%和76.3%,而阳性符合率直接法略高于血培养瓶法。导致培养结果假阴性的细菌主要为凝固酶阴性葡萄球菌、棒状杆菌和微球菌。结论血培养法的敏感性明显高于直接接种法,可提高病原菌检出率,与直接接种法同时培养可缩短检出时间并防止漏检,特别是对链球菌群、厌氧菌和真菌的检出具有显著优势,但需注意严格无菌操作,减少污染环节。
目的:探討血培養瓶法在無菌體液病原菌培養中的應用。方法收集2013年3~9月四川省人民醫院共321份無菌體液標本,通過雙瓶血培養瓶法和直接接種法培養分離病原菌,通過與傳統的直接接種法比較對其進行評價。結果321份標本中,通過血培養瓶法108份標本培養齣細菌,暘性率為33.6%;直接接種法55份標本培養齣細菌,暘性率為17.1%,差異有統計學意義( P<0.01)。血培養增菌後80%細菌在24~48 h內檢齣,而直接接種法90%細菌在24 h檢齣,檢齣時間直接接種法更具優勢。兩種方法檢齣細菌前3位均為屎腸毬菌、大腸埃希菌和肺炎剋雷伯菌,而凝固酶陰性葡萄毬菌、草綠色鏈毬菌等在血培養法中檢齣率明顯高于直接法。血培養瓶法的敏感性為89.7%,陰性符閤率為95.3%,直接接種法分彆為43.2%和76.3%,而暘性符閤率直接法略高于血培養瓶法。導緻培養結果假陰性的細菌主要為凝固酶陰性葡萄毬菌、棒狀桿菌和微毬菌。結論血培養法的敏感性明顯高于直接接種法,可提高病原菌檢齣率,與直接接種法同時培養可縮短檢齣時間併防止漏檢,特彆是對鏈毬菌群、厭氧菌和真菌的檢齣具有顯著優勢,但需註意嚴格無菌操作,減少汙染環節。
목적:탐토혈배양병법재무균체액병원균배양중적응용。방법수집2013년3~9월사천성인민의원공321빈무균체액표본,통과쌍병혈배양병법화직접접충법배양분리병원균,통과여전통적직접접충법비교대기진행평개。결과321빈표본중,통과혈배양병법108빈표본배양출세균,양성솔위33.6%;직접접충법55빈표본배양출세균,양성솔위17.1%,차이유통계학의의( P<0.01)。혈배양증균후80%세균재24~48 h내검출,이직접접충법90%세균재24 h검출,검출시간직접접충법경구우세。량충방법검출세균전3위균위시장구균、대장애희균화폐염극뢰백균,이응고매음성포도구균、초록색련구균등재혈배양법중검출솔명현고우직접법。혈배양병법적민감성위89.7%,음성부합솔위95.3%,직접접충법분별위43.2%화76.3%,이양성부합솔직접법략고우혈배양병법。도치배양결과가음성적세균주요위응고매음성포도구균、봉상간균화미구균。결론혈배양법적민감성명현고우직접접충법,가제고병원균검출솔,여직접접충법동시배양가축단검출시간병방지루검,특별시대련구균군、염양균화진균적검출구유현저우세,단수주의엄격무균조작,감소오염배절。
Objective To assess the application of blood culture bottle method for pathogenic bacteria culture with aseptic humoral .Methods A total of 321 aseptic humoral specimens were collected in hospital from March to September in 2013 .All specimens were detected by double blood culture bottles method and direct inoculation meth-od .The comparison between the two methods was analyzed .Results The positive rate of the blood culture bottle method was 33 .6% (108/321) ,while 17 .1% (55/321) as the direct inoculation method ,and the difference between the two methodsv was statistically significant (P< 0 .01) .For the blood culture bottle method ,80% bacteria were checked out within 24 to 48 hours ;for the direct inoculation method ,90% bacteria were checked out within 24 h .The top three detected bacteria were Enterococcus faecium ,Escherichia coli and Klebsiella pneumoniae for both methods . However ,for the Coagulase negative staphylococcus ,Streptococcus viridans ,Rod bacillus ,Micrococcus ,Anaerobic bacteria and fungi ,the positive rates of the blood culture bottle method were significant higher than that of the direct inoculation method .The sensitivity and negative coincidence rate of blood culture bottle method were 89 .7% and 95 .3% respectively ,while 43 .2% and 76 .3% as the direct inoculation method .The positive coincidence rate of the direct inoculation method was slightly higher than that of the blood culture bottle method .Coagulase negative staphy-lococcus ,corynebacterium and micrococcus were the mainly false negative bacteria .Conclusion The sensitivity of the blood culture bottle enrichment method was higher than that of the direct inoculation method for pathogenic bacteria culture with aseptic humoral ,it could increase the positive rate of pathogen detection ,especially for the streptococcus group ,anaerobic bacteria and fungi .