1) Nasopharyngeal swab
鼻咽拭子
1.
Methods Acquisition 393 cases of in-patient and out-patient pneumonia were orgnized for infusion in neonatal department of hospital,and their nasopharyngeal swab specimens were collected and ino-culated them into the monolayer McCoy cell.
方法收集本院新生儿科及门诊393例肺炎患儿鼻咽拭子标本进行CT组织培养检测,并参照Dille文献经计算机软件辅助设计4条质粒基因探针,地高辛和生物素标记,取鼻咽拭子标本应用以上引物进行Gap-LCR,产物进行聚丙烯酰胺凝胶电泳(PAGE)和ELISA检测;对Gap-LCR阳性而TC阴性的患者,应用主要外膜蛋白基因omp1引物进行PCR证实,并比较不同年龄、不同分娩方式间CT感染率。
2) Oropharyngeal swabs
咽拭子
1.
Analysis of pathogenic bacteria with Oropharyngeal swabs in acute respiratory infection in children:a 328-case report;
儿童急性呼吸道感染咽拭子培养328例分析
2.
METHODS Oropharyngeal swabs among 709 cases of respiratory infection neonates were investigated by the routine methods and drug resistance was analyzed by K-B method.
方法对709例新生儿上呼吸道感染患儿咽拭子进行常规细菌培养鉴定,用K-B法测定病原菌耐药性。
3) Throat swab
咽拭子
1.
Analysis the result of throat swab culture taking from 209 hospitalized neonatus
209例新生儿入院时咽拭子培养结果分析探讨
4) nasal swab
鼻拭子
1.
A nested polymerase chain reaction(N-PCR) assay for direct detection of toxigenic Pasteurella multocida(T+ Pm) in nasal swab specimens collected from pigs was developed using 2 pairs of primers that were designed according to the published sequences of T+ Pm toxA,The size of amplicons were 864 and 447 bp,respectively.
根据产毒素多杀性巴氏杆菌的toxA基因序列,设计了2对特异性引物,扩增的片段大小分别为864和447 bp,从而建立了一种能直接从猪鼻拭子中快速检测产毒素多杀性巴氏杆菌的巢氏PCR方法。
5) throat swab cultures
咽拭子培养
1.
Objects: To observe the significance of throat swab cultures in children with acute tonsillitis.
目的:研究儿童急性扁桃体炎咽拭子培养结果及药物敏感情况,探讨其临床价值。
6) pharynx-mop sample
咽拭
1.
Objective: To analyze of the pathogens composition and resistance of pharynx-mop and non- pharynx-mop sample from in-patients in chest-cardio surgery ward at Shanghai Chest Hospital, we explored the clinical meaning of pharynx-mop and non- pharynx-mop sample analyzing.
目的:通过对胸心外科住院病人咽拭与非咽拭标本细菌及药敏结果分析，探讨咽拭与非咽拭标本细菌及药敏结果的临床意义。
补充资料：湔拭
1.洗擦。引申指除去过错。
说明：补充资料仅用于学习参考，请勿用于其它任何用途。
参考词条