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1.
目的 探讨新生儿病房患儿入院时即进行肠道病毒筛查的意义.方法 在2009年5月~2010年5月对每位新人患儿首先进行隔离,然后进行咽拭子及粪便采样,采样用RT-PCR方法检测肠道病毒通用型、肠道病毒71型、柯萨奇A16型.对采样检测阳性的个体及密切接触人群进行系统的流行病学研究.结果 新生儿存在肠道病毒宫内感染、产时感染和生后感染几种方式,感染率分别为2.72%、6.28%、15.76%.结论 预防新生儿肠道病毒感染在院前及院内同样重要.  相似文献   

2.
目的 探讨新生儿病房患儿入院时即进行肠道病毒筛查的意义.方法 在2009年5月~2010年5月对每位新人患儿首先进行隔离,然后进行咽拭子及粪便采样,采样用RT-PCR方法检测肠道病毒通用型、肠道病毒71型、柯萨奇A16型.对采样检测阳性的个体及密切接触人群进行系统的流行病学研究.结果 新生儿存在肠道病毒宫内感染、产时感染和生后感染几种方式,感染率分别为2.72%、6.28%、15.76%.结论 预防新生儿肠道病毒感染在院前及院内同样重要.  相似文献   

3.
Objective To evaluate the application value of UF-1000i automated urine formed elements analyzer in the diagnosis of urinary tract infection. Methods 150 urine specimens were analyzed using the UF-1000i in parallel with detection of leukocyte, yeast-like fungus, and bacteria. These detection results were collected for evaluation of urinary tract infection and scatter grams were recorded. At the same time, these samples were cultured for bacterial identification, which results were compared with that of the UF-1000i. The clinical diagnose criteria of the UTI was performed as golden standard. As compare with results obtained with UF-1000i, the sensitivity and specificity of UF-1000i for diagnosis of urinary tract infection were evaluated, and the consistency were analyzed among scatter grams, bacterial culture and final diagnosis. Results The statistical results from 146 specimens showed that the positive rate of UF-1000i was 32. 9% (48/146), the positive rate of urine culture is 28. 8% (42/146). There was no significant statistical difference found (χ2 = 1.79 ,P = 0. 18 )and Kappa test showed a considerable consistency (K = 0. 775 6). The UF-1000i detection results showed the sensitivity 76. 0% ( 38/50 ), specificity 89. 6% ( 86/96 ), positive predictive value 79. 2% ( 38/48 ) and negative predictive value 87. 8% ( 86/98 ), respectively. The distribution of coccus and bacilli obtained from the UF-1000i testing was basically in accordance with the results of bacterial culture. Conclusion The "UTI-information" of UF-1000i is very important for the diagnosis of urinary tract infections.  相似文献   

4.
Objective To evaluate the application value of UF-1000i automated urine formed elements analyzer in the diagnosis of urinary tract infection. Methods 150 urine specimens were analyzed using the UF-1000i in parallel with detection of leukocyte, yeast-like fungus, and bacteria. These detection results were collected for evaluation of urinary tract infection and scatter grams were recorded. At the same time, these samples were cultured for bacterial identification, which results were compared with that of the UF-1000i. The clinical diagnose criteria of the UTI was performed as golden standard. As compare with results obtained with UF-1000i, the sensitivity and specificity of UF-1000i for diagnosis of urinary tract infection were evaluated, and the consistency were analyzed among scatter grams, bacterial culture and final diagnosis. Results The statistical results from 146 specimens showed that the positive rate of UF-1000i was 32. 9% (48/146), the positive rate of urine culture is 28. 8% (42/146). There was no significant statistical difference found (χ2 = 1.79 ,P = 0. 18 )and Kappa test showed a considerable consistency (K = 0. 775 6). The UF-1000i detection results showed the sensitivity 76. 0% ( 38/50 ), specificity 89. 6% ( 86/96 ), positive predictive value 79. 2% ( 38/48 ) and negative predictive value 87. 8% ( 86/98 ), respectively. The distribution of coccus and bacilli obtained from the UF-1000i testing was basically in accordance with the results of bacterial culture. Conclusion The "UTI-information" of UF-1000i is very important for the diagnosis of urinary tract infections.  相似文献   

5.
Objective To evaluate the application value of UF-1000i automated urine formed elements analyzer in the diagnosis of urinary tract infection. Methods 150 urine specimens were analyzed using the UF-1000i in parallel with detection of leukocyte, yeast-like fungus, and bacteria. These detection results were collected for evaluation of urinary tract infection and scatter grams were recorded. At the same time, these samples were cultured for bacterial identification, which results were compared with that of the UF-1000i. The clinical diagnose criteria of the UTI was performed as golden standard. As compare with results obtained with UF-1000i, the sensitivity and specificity of UF-1000i for diagnosis of urinary tract infection were evaluated, and the consistency were analyzed among scatter grams, bacterial culture and final diagnosis. Results The statistical results from 146 specimens showed that the positive rate of UF-1000i was 32. 9% (48/146), the positive rate of urine culture is 28. 8% (42/146). There was no significant statistical difference found (χ2 = 1.79 ,P = 0. 18 )and Kappa test showed a considerable consistency (K = 0. 775 6). The UF-1000i detection results showed the sensitivity 76. 0% ( 38/50 ), specificity 89. 6% ( 86/96 ), positive predictive value 79. 2% ( 38/48 ) and negative predictive value 87. 8% ( 86/98 ), respectively. The distribution of coccus and bacilli obtained from the UF-1000i testing was basically in accordance with the results of bacterial culture. Conclusion The "UTI-information" of UF-1000i is very important for the diagnosis of urinary tract infections.  相似文献   

6.
Objective To evaluate the application value of UF-1000i automated urine formed elements analyzer in the diagnosis of urinary tract infection. Methods 150 urine specimens were analyzed using the UF-1000i in parallel with detection of leukocyte, yeast-like fungus, and bacteria. These detection results were collected for evaluation of urinary tract infection and scatter grams were recorded. At the same time, these samples were cultured for bacterial identification, which results were compared with that of the UF-1000i. The clinical diagnose criteria of the UTI was performed as golden standard. As compare with results obtained with UF-1000i, the sensitivity and specificity of UF-1000i for diagnosis of urinary tract infection were evaluated, and the consistency were analyzed among scatter grams, bacterial culture and final diagnosis. Results The statistical results from 146 specimens showed that the positive rate of UF-1000i was 32. 9% (48/146), the positive rate of urine culture is 28. 8% (42/146). There was no significant statistical difference found (χ2 = 1.79 ,P = 0. 18 )and Kappa test showed a considerable consistency (K = 0. 775 6). The UF-1000i detection results showed the sensitivity 76. 0% ( 38/50 ), specificity 89. 6% ( 86/96 ), positive predictive value 79. 2% ( 38/48 ) and negative predictive value 87. 8% ( 86/98 ), respectively. The distribution of coccus and bacilli obtained from the UF-1000i testing was basically in accordance with the results of bacterial culture. Conclusion The "UTI-information" of UF-1000i is very important for the diagnosis of urinary tract infections.  相似文献   

7.
Objective To evaluate the application value of UF-1000i automated urine formed elements analyzer in the diagnosis of urinary tract infection. Methods 150 urine specimens were analyzed using the UF-1000i in parallel with detection of leukocyte, yeast-like fungus, and bacteria. These detection results were collected for evaluation of urinary tract infection and scatter grams were recorded. At the same time, these samples were cultured for bacterial identification, which results were compared with that of the UF-1000i. The clinical diagnose criteria of the UTI was performed as golden standard. As compare with results obtained with UF-1000i, the sensitivity and specificity of UF-1000i for diagnosis of urinary tract infection were evaluated, and the consistency were analyzed among scatter grams, bacterial culture and final diagnosis. Results The statistical results from 146 specimens showed that the positive rate of UF-1000i was 32. 9% (48/146), the positive rate of urine culture is 28. 8% (42/146). There was no significant statistical difference found (χ2 = 1.79 ,P = 0. 18 )and Kappa test showed a considerable consistency (K = 0. 775 6). The UF-1000i detection results showed the sensitivity 76. 0% ( 38/50 ), specificity 89. 6% ( 86/96 ), positive predictive value 79. 2% ( 38/48 ) and negative predictive value 87. 8% ( 86/98 ), respectively. The distribution of coccus and bacilli obtained from the UF-1000i testing was basically in accordance with the results of bacterial culture. Conclusion The "UTI-information" of UF-1000i is very important for the diagnosis of urinary tract infections.  相似文献   

8.
Objective To evaluate the application value of UF-1000i automated urine formed elements analyzer in the diagnosis of urinary tract infection. Methods 150 urine specimens were analyzed using the UF-1000i in parallel with detection of leukocyte, yeast-like fungus, and bacteria. These detection results were collected for evaluation of urinary tract infection and scatter grams were recorded. At the same time, these samples were cultured for bacterial identification, which results were compared with that of the UF-1000i. The clinical diagnose criteria of the UTI was performed as golden standard. As compare with results obtained with UF-1000i, the sensitivity and specificity of UF-1000i for diagnosis of urinary tract infection were evaluated, and the consistency were analyzed among scatter grams, bacterial culture and final diagnosis. Results The statistical results from 146 specimens showed that the positive rate of UF-1000i was 32. 9% (48/146), the positive rate of urine culture is 28. 8% (42/146). There was no significant statistical difference found (χ2 = 1.79 ,P = 0. 18 )and Kappa test showed a considerable consistency (K = 0. 775 6). The UF-1000i detection results showed the sensitivity 76. 0% ( 38/50 ), specificity 89. 6% ( 86/96 ), positive predictive value 79. 2% ( 38/48 ) and negative predictive value 87. 8% ( 86/98 ), respectively. The distribution of coccus and bacilli obtained from the UF-1000i testing was basically in accordance with the results of bacterial culture. Conclusion The "UTI-information" of UF-1000i is very important for the diagnosis of urinary tract infections.  相似文献   

9.
Objective To evaluate the application value of UF-1000i automated urine formed elements analyzer in the diagnosis of urinary tract infection. Methods 150 urine specimens were analyzed using the UF-1000i in parallel with detection of leukocyte, yeast-like fungus, and bacteria. These detection results were collected for evaluation of urinary tract infection and scatter grams were recorded. At the same time, these samples were cultured for bacterial identification, which results were compared with that of the UF-1000i. The clinical diagnose criteria of the UTI was performed as golden standard. As compare with results obtained with UF-1000i, the sensitivity and specificity of UF-1000i for diagnosis of urinary tract infection were evaluated, and the consistency were analyzed among scatter grams, bacterial culture and final diagnosis. Results The statistical results from 146 specimens showed that the positive rate of UF-1000i was 32. 9% (48/146), the positive rate of urine culture is 28. 8% (42/146). There was no significant statistical difference found (χ2 = 1.79 ,P = 0. 18 )and Kappa test showed a considerable consistency (K = 0. 775 6). The UF-1000i detection results showed the sensitivity 76. 0% ( 38/50 ), specificity 89. 6% ( 86/96 ), positive predictive value 79. 2% ( 38/48 ) and negative predictive value 87. 8% ( 86/98 ), respectively. The distribution of coccus and bacilli obtained from the UF-1000i testing was basically in accordance with the results of bacterial culture. Conclusion The "UTI-information" of UF-1000i is very important for the diagnosis of urinary tract infections.  相似文献   

10.
Objective To evaluate the application value of UF-1000i automated urine formed elements analyzer in the diagnosis of urinary tract infection. Methods 150 urine specimens were analyzed using the UF-1000i in parallel with detection of leukocyte, yeast-like fungus, and bacteria. These detection results were collected for evaluation of urinary tract infection and scatter grams were recorded. At the same time, these samples were cultured for bacterial identification, which results were compared with that of the UF-1000i. The clinical diagnose criteria of the UTI was performed as golden standard. As compare with results obtained with UF-1000i, the sensitivity and specificity of UF-1000i for diagnosis of urinary tract infection were evaluated, and the consistency were analyzed among scatter grams, bacterial culture and final diagnosis. Results The statistical results from 146 specimens showed that the positive rate of UF-1000i was 32. 9% (48/146), the positive rate of urine culture is 28. 8% (42/146). There was no significant statistical difference found (χ2 = 1.79 ,P = 0. 18 )and Kappa test showed a considerable consistency (K = 0. 775 6). The UF-1000i detection results showed the sensitivity 76. 0% ( 38/50 ), specificity 89. 6% ( 86/96 ), positive predictive value 79. 2% ( 38/48 ) and negative predictive value 87. 8% ( 86/98 ), respectively. The distribution of coccus and bacilli obtained from the UF-1000i testing was basically in accordance with the results of bacterial culture. Conclusion The "UTI-information" of UF-1000i is very important for the diagnosis of urinary tract infections.  相似文献   

11.
2007-2008年北京地区儿童手足口病的病原学分析   总被引:8,自引:0,他引:8  
目的 通过病毒分离和鉴定了解2007-2008年春夏北京地区手足口病的病原学特征,为手足口病防治工作提供科学依据.方法 分别于2007年4-8月及2008年5-9月收集256例手足口病患儿的咽拭子和疱疹液标本共356份,其中咽拭子255份(包括10份重症患儿标本),疱疹液标本101份.将所有标本接种Vero细胞进行病毒分离,分离阳性的毒株用RT-PCR进行鉴定;对10份重症患儿标本除病毒分离外,还直接进行RT-PCR检测病毒核酸.结果 256例被检测患儿中188例为肠道病毒阳性,阳性率为73.4%.356份标本中共分离到239株肠道病毒,总阳性率为67.1%.其中疱疹液标本分离阳性率为75.2%(76/101),咽拭子标本分离阳性率63.9%(163/255),但两种标本接种细胞后出现病变的速度没有差别.重症患儿标本病毒分离阳性率50%(5/10).2007年的45例病毒分离株经肠道病毒通用引物PCR检测均为阳性,分型PCR显示,其中CA16占95.6%(43/45),EV71占4.4%(2/45);而2008年的143例病毒分离株经肠道病毒通用引物PCR检测142例为阳性,PCR分型显示,EV71占82.4%(117/142),CA16占16.8%(24/142).10份重症患儿标本直接分型检测结果均为EV71.结论 北京儿童手足口病病原体以EV71和CAV16为主,2007年与2008年流行的优势型别不同,2007年主要为CA16,而2008年主要为EV71.本组重症手足口病患儿的病原均为EV71.  相似文献   

12.
目的 通过病毒分离和鉴定了解2007-2008年春夏北京地区手足口病的病原学特征,为手足口病防治工作提供科学依据.方法 分别于2007年4-8月及2008年5-9月收集256例手足口病患儿的咽拭子和疱疹液标本共356份,其中咽拭子255份(包括10份重症患儿标本),疱疹液标本101份.将所有标本接种Vero细胞进行病毒分离,分离阳性的毒株用RT-PCR进行鉴定;对10份重症患儿标本除病毒分离外,还直接进行RT-PCR检测病毒核酸.结果 256例被检测患儿中188例为肠道病毒阳性,阳性率为73.4%.356份标本中共分离到239株肠道病毒,总阳性率为67.1%.其中疱疹液标本分离阳性率为75.2%(76/101),咽拭子标本分离阳性率63.9%(163/255),但两种标本接种细胞后出现病变的速度没有差别.重症患儿标本病毒分离阳性率50%(5/10).2007年的45例病毒分离株经肠道病毒通用引物PCR检测均为阳性,分型PCR显示,其中CA16占95.6%(43/45),EV71占4.4%(2/45);而2008年的143例病毒分离株经肠道病毒通用引物PCR检测142例为阳性,PCR分型显示,EV71占82.4%(117/142),CA16占16.8%(24/142).10份重症患儿标本直接分型检测结果均为EV71.结论 北京儿童手足口病病原体以EV71和CAV16为主,2007年与2008年流行的优势型别不同,2007年主要为CA16,而2008年主要为EV71.本组重症手足口病患儿的病原均为EV71.  相似文献   

13.
目的 分析西安地区2010年引起手足口病(HFMD)的肠道病毒血清型和调查HFMD高发的6月、7月健康儿童携带肠道病毒核酸情况,为HFMD防治提供依据.方法 2010年4至9月,在西安市所属13个区县,每月采集临床诊断HFMD患儿的肛拭子标本,同时,在西安市儿童医院采集临床诊断为重症、危重症HFMD病例标本,以及采集高发的6月和7月健康儿童肛拭子标本进行病原学分析,研究西安地区2010年HFMD病原构成和健康儿童病原携带情况.结果 2010年西安地区共报告HFMD 23439例,病原EV71占24.81%、CA16占55.04%、非EV71和非CA16的其它肠道病毒占20.16%;EV71 7、8月所占比例增高;EV71占重症病例病原的75.71%;农村、城市健康儿童肠道病毒核酸阳性率分别为9.68%和3.51%.结论 2010年西安地区HFMD病例数较2009年增加,病原以CA16为主,重症病例主要由EV71引起,农村健康儿童携带肠道病毒与城市儿童差异无统计学意义.  相似文献   

14.
目的探讨小儿肠道病毒(EV)中枢神经系统感染病毒基因VP1序列的分子分型的临床意义。方法采用逆转录聚合酶链反应(RTPCR)方法.应用通用引物和VP1段分子分型引物检测77例临床诊断为无菌性脑膜炎病儿(其中急性期63例.恢复期14例)脑脊液(CSF)的EVRNA,并对VP1分型引物扩增阳性片段进行克隆、测序及分型研究。结果77例无菌性脑膜炎病儿CSF中,采用通用引物经两次PCR在急性期共获得阳性结果47例(占急性期的74.6%),恢复期3例(占恢复期的21.4%)。将EVRNA阳性的50例标本应用分型引物经两次PCR共获得阳性结果31例(占62.0%)。随机抽取27条阳性片段进行克隆测序,测序结果通过BLAST软件与GenBankEV标准毒株进行同源性对比分析,相关序列同源性均在97%以上。结论采用分型引物扩增VP1部分序列并测序.将EV的VP1部分序列与GenBank中的EV标准毒株进行对比,根据基因序列的同源性可以对EV进行型别鉴定.为EV的分型研究提供了新的方法和思路。  相似文献   

15.
孙宝昌  卢姝姝  吴矛矛  陈栋 《疾病监测》2019,34(12):1096-1099
目的研究流感病毒检测阴性的流感样病例(ILI)中肠道病毒(EV)的病原谱及其主要流行病毒型,为其防治提供基础科学依据。方法收集2017 — 2018年温州市ILI,利用荧光定量PCR技术检测流感病毒甲型和乙型,流感阴性病例进行EV检测;利用反转录–聚合酶链式反应(RT-PCR)扩增EV的VP1区序列,扩增产物进行基因测序和基因分型。 对结果进行统计学分析,P<0.05为差异有统计学意义。结果共调查病例2 298例,流感病毒检测阳性488例(21.23%),流感病毒阴性 1 810例(78.76%),其中,EV检测阳性254例(14.03%)。 EV感染全年均有发生,流行高峰为4 — 7月(70.47%)。 254例EV阳性标本中,测序成功并经基因序列比对获得基因分型的135例,可分为包含EV-A、EV-B和EV-C型的13个EV亚型,主要感染型别为柯萨奇病毒 A 组 6 型 (Cox A6)、Cox A2和Cox A10,分别占24.44%、22.22%和13.33%。 不同年份、月份、性别和年龄EV阳性率差异有统计学意义(χ2=9.399、329.380、4.311、29.246,均P<0.05)。结论流感病毒检测阴性的ILI中EV是主要病原体之一,其病原谱复杂。 应重点加强低年龄组病例的诊断和监测。  相似文献   

16.
17.
目的了解江苏省徐州地区2009-2010年儿童手足口病流行的病原学特征。方法 2009年3-8月和2010年1-12月共采集徐州儿童医院门诊、住院及常规监测的511例疑似手足口病(HFMD)儿童患者的咽拭、肛拭标本,提取病毒RNA,用实时荧光定量PCR(real-time PCR)方法同时进行肠道病毒(EV),肠道病毒71型(EV71)和柯萨奇病毒A16(Cox A16)的特异性基因检测。结果 511例疑似手足口病患儿的标本中,总肠道病毒阳性288例,占56.36%;288个肠道病毒核酸阳性病例中,EV71核酸阳性202例,Cox A16核酸阳性55例,构成比分别为70.14%和19.10%。≤5岁儿童感染的肠道病毒有EV71型、Cox A16型及非EV71非Cox A16的其他肠道病毒感染,>5岁儿童则只有EV71感染病例。结论 2009-2010年徐州地区儿童手足口病患儿以1~3岁儿童为主,其主要病原是肠道病毒EV71型,其次是Cox A16型。  相似文献   

18.
目的 探讨杭州市手足口病病原谱构成及其肠道病毒71型(human enterovirus 71,EV71)的分子特征。 方法 采集210例疑似手足口病感染者的粪便标本及其相关临床资料,采用实时荧光定量反转录聚合酶链反应(real time RT-PCR)方法进行初步检测,利用RT-PCR扩增部分EV71和柯萨奇病毒A组16型(coxsackievirus A16, Cox A16)阳性样本VP1基因区并测序分析。 结果 荧光定量RT-PCR检测表明,210例疑似感染者的粪便中, EV71、Cox A16 和其他肠道病毒的阳性率分别为60.95%(128/210)、21.43%(45/210)和9.05%(19/210)。10株EV71病毒VP1区核酸序列与JX509922、JX509924、JX509926、JX509927、 JX509928和 JX509929的同源性最高为95.7%~98.0%,且均属于EV71中 C4a亚型。 结论 EV71和Cox A16是杭州市儿童手足口病的主要病原体。因此加强EV71和Cox A16的监测特别是EV71的检测,有助于更好地预防和控制手足口病。  相似文献   

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