中华临床医师杂志(电子版)
中華臨床醫師雜誌(電子版)
중화림상의사잡지(전자판)
CHINESE JOURNAL OF CLINICIANS(ELECTRONIC VERSION)
2013年
20期
9056-9058
,共3页
吴军%蒋理%谢而付%张巧娣%倪芳
吳軍%蔣理%謝而付%張巧娣%倪芳
오군%장리%사이부%장교제%예방
肝炎抗体,丙型%酶联免疫吸附测定%化学发光测定法
肝炎抗體,丙型%酶聯免疫吸附測定%化學髮光測定法
간염항체,병형%매련면역흡부측정%화학발광측정법
Hepatitis C antibodies%Enzyme-linked immunosorbent assay%Chemiluminescent measurements
目的:探讨A、B和C三种不同国产酶联免疫吸附试验(ELISA)试剂检测丙型肝炎病毒抗体(抗-HCV)结果的差异性,并将检测结果与电化学发光法检测结果进行比较。方法随机挑选临床检测样本94例。所有样本再使用B、C和Roche电化学发光法试剂盒进行检测。ELISA试剂都使用各自的试剂盒S/CO值进行阴阳性判断,电化学发光检测结果判断以仪器的COI作为判断标准,结果>1为检测有反应性。结果 A、B、C和电化学发光检测的阳性率分别为84.04%(79/94)、35.11%(33/94)、25.53%(24/94)和39.36%(37/94),A试剂显著高于电化学发光法,而C试剂显著低于电化学发光法。A、B、C和电化学发光检测的结果一致性分别为55.32%(52/94)、95.74%(90/94)和86.17%(81/94)。将 A 试剂盒检测的结果分为阴性组(<1)、弱阳性组(1~8)、阳性组(>8)三个组,阴性和阳性组四种试剂检测结果符合率较好,而弱阳性组符合率较低。结论3种国产试剂对阴性和阳性标本与 Roche 电化学发光法检测符合率很高,弱阳性标本符合率则存在差异,对于弱阳性标本建议使用确诊试验。
目的:探討A、B和C三種不同國產酶聯免疫吸附試驗(ELISA)試劑檢測丙型肝炎病毒抗體(抗-HCV)結果的差異性,併將檢測結果與電化學髮光法檢測結果進行比較。方法隨機挑選臨床檢測樣本94例。所有樣本再使用B、C和Roche電化學髮光法試劑盒進行檢測。ELISA試劑都使用各自的試劑盒S/CO值進行陰暘性判斷,電化學髮光檢測結果判斷以儀器的COI作為判斷標準,結果>1為檢測有反應性。結果 A、B、C和電化學髮光檢測的暘性率分彆為84.04%(79/94)、35.11%(33/94)、25.53%(24/94)和39.36%(37/94),A試劑顯著高于電化學髮光法,而C試劑顯著低于電化學髮光法。A、B、C和電化學髮光檢測的結果一緻性分彆為55.32%(52/94)、95.74%(90/94)和86.17%(81/94)。將 A 試劑盒檢測的結果分為陰性組(<1)、弱暘性組(1~8)、暘性組(>8)三箇組,陰性和暘性組四種試劑檢測結果符閤率較好,而弱暘性組符閤率較低。結論3種國產試劑對陰性和暘性標本與 Roche 電化學髮光法檢測符閤率很高,弱暘性標本符閤率則存在差異,對于弱暘性標本建議使用確診試驗。
목적:탐토A、B화C삼충불동국산매련면역흡부시험(ELISA)시제검측병형간염병독항체(항-HCV)결과적차이성,병장검측결과여전화학발광법검측결과진행비교。방법수궤도선림상검측양본94례。소유양본재사용B、C화Roche전화학발광법시제합진행검측。ELISA시제도사용각자적시제합S/CO치진행음양성판단,전화학발광검측결과판단이의기적COI작위판단표준,결과>1위검측유반응성。결과 A、B、C화전화학발광검측적양성솔분별위84.04%(79/94)、35.11%(33/94)、25.53%(24/94)화39.36%(37/94),A시제현저고우전화학발광법,이C시제현저저우전화학발광법。A、B、C화전화학발광검측적결과일치성분별위55.32%(52/94)、95.74%(90/94)화86.17%(81/94)。장 A 시제합검측적결과분위음성조(<1)、약양성조(1~8)、양성조(>8)삼개조,음성화양성조사충시제검측결과부합솔교호,이약양성조부합솔교저。결론3충국산시제대음성화양성표본여 Roche 전화학발광법검측부합솔흔고,약양성표본부합솔칙존재차이,대우약양성표본건의사용학진시험。
Objective To investigate the difference of results based three commercially anti-HCV antibody ELISA kits(A, B and C) used in routine laboratory in China. We also compare the results with the results based chemiluminescence immune assay(CIA) methods. Methods Ninety four samples of sera were collected from inpatients. All sera were analysed using three different ELISA kits and Cobas e 601 anti-HCV CIA systems. All of the assays were performed and S/CO or COI were gained according to the manufacturers' instructions. If the S/CO or COI>1 the results were considered reactive. Results Total anti-HCV positive rate for the 94 serum samples to the three different ELISA tests and CIA systems were 84.04%(79/94), 35.11%(33/94), 25.53%(24/94) and 39.36%(37/94). The positive rate of A ELISA test kits was statistically higher than the rate of CIA systems, but C ELISA test kits was lower than CIA systems. No difference was between B ELISA test kits and CIA systems. The total coincidence rates between three ELISA kits and CIA systems were 55.32%(52/94), 95.74%(90/94) and 86.17%(81/94). According to the results based A ELISA kits, the samples were divided into three groups:negative group(<1), weak positive group(1-8) and positive group(>8). In the negative group and positive group, the results had good coincidence rate based four reagents, but weakly positive group, the coincidence rate was low. Conclusion In the negative group and positive group, the results have good coincidence rate based three ELISA kits, but weakly positive group, the coincidence rate is low, so the confirm tests is recommended.