国际病毒学杂志
國際病毒學雜誌
국제병독학잡지
INTERNATIONAL JOURNAL OF VIROLOGY
2011年
2期
44-47
,共4页
马春涛%张桂云%裴丽健%刘波%张辉%肖瑶%郭晓黎%蒋岩
馬春濤%張桂雲%裴麗健%劉波%張輝%肖瑤%郭曉黎%蔣巖
마춘도%장계운%배려건%류파%장휘%초요%곽효려%장암
HIV/HCV%质量控制%实验室检测
HIV/HCV%質量控製%實驗室檢測
HIV/HCV%질량공제%실험실검측
HIV/HCV%laboratory quality control%testing
目的 分析山西某县开展HIV/HCV调查的实验室质量控制方法,探讨质控对调查准确性的影响.方法 在整个调查中对现场的HIV、HCV检测实施插入质控品及样本抽检的质控方案.根据预调查质控结果,通过增加人员培训、加强考核频次、提高抽检比例等手段调整质控方案用于主调查.结果 HIV感染预调查,现场的插入质控品检测和抽检结果与预期结果一致,预调查有效;在主调查中4份样本结果不一致,结合现场调查和质控记录,判定主调查有效.HCV感染预调查时现场HCV检测插入的质控品与预期结果符合率66.7%,抽检质控符合率95.1%,预调查无效;实施了检测人员HCV强化培训和能力验证考核后主调查HCV质控检测结果和预期结果一致,结果有效.结论 质控的实施有助于及时发现现场检测存在的问题、调整质控方案,从而保证调查数据的准确性和可靠性.
目的 分析山西某縣開展HIV/HCV調查的實驗室質量控製方法,探討質控對調查準確性的影響.方法 在整箇調查中對現場的HIV、HCV檢測實施插入質控品及樣本抽檢的質控方案.根據預調查質控結果,通過增加人員培訓、加彊攷覈頻次、提高抽檢比例等手段調整質控方案用于主調查.結果 HIV感染預調查,現場的插入質控品檢測和抽檢結果與預期結果一緻,預調查有效;在主調查中4份樣本結果不一緻,結閤現場調查和質控記錄,判定主調查有效.HCV感染預調查時現場HCV檢測插入的質控品與預期結果符閤率66.7%,抽檢質控符閤率95.1%,預調查無效;實施瞭檢測人員HCV彊化培訓和能力驗證攷覈後主調查HCV質控檢測結果和預期結果一緻,結果有效.結論 質控的實施有助于及時髮現現場檢測存在的問題、調整質控方案,從而保證調查數據的準確性和可靠性.
목적 분석산서모현개전HIV/HCV조사적실험실질량공제방법,탐토질공대조사준학성적영향.방법 재정개조사중대현장적HIV、HCV검측실시삽입질공품급양본추검적질공방안.근거예조사질공결과,통과증가인원배훈、가강고핵빈차、제고추검비례등수단조정질공방안용우주조사.결과 HIV감염예조사,현장적삽입질공품검측화추검결과여예기결과일치,예조사유효;재주조사중4빈양본결과불일치,결합현장조사화질공기록,판정주조사유효.HCV감염예조사시현장HCV검측삽입적질공품여예기결과부합솔66.7%,추검질공부합솔95.1%,예조사무효;실시료검측인원HCV강화배훈화능력험증고핵후주조사HCV질공검측결과화예기결과일치,결과유효.결론 질공적실시유조우급시발현현장검측존재적문제、조정질공방안,종이보증조사수거적준학성화가고성.
Objective The laboratory quality control,QC,for an epidemiological study of HIV/ HCV infection in Shanxi province of China was analyzed,so as to study the influence of laboratory QC measures upon the quality of epidemiological study result.Methods Laboratory QC measures,including laboratory QC samples testing and confirmatory testing on sampled specimens from the site laboratory were carried out during all phases of the epidemiological study.Strengthening measures,including more training for the testing personnel,more frequent testing proficiency evaluation and higher percentage of sampling of the site specimens for confirmatory testing were implemented in the main study.Results HIV specimens for quality control were congruent between the site and QC laboratory during the pilot study.During the main study,all 4 specimens with undetermined testing results were confirmed negative.With site testing procedure checked and quality record analyzed,the validity of all HIV testing results were obtained.During the pilot phase of HCV study,the site laboratory only obtained congruency rates of 66.7% and 95.1% on the QA samples and on the sampled specimens for confirmatory testing,respectively,resulting in the invalidity of all HCV testing results in the pilot study.With corrective QC measures in place,such as adequate personnel training and intensive testing proficiency evaluation,the congruency rate achieved 100% on the QA samples and on the sampling specimens for confirmatory testing during the HCV main study.Thus the validity of all HCV testing results in the main study was obtained.Conclusion Laboratory QC is especially important in timely identifying deficiencies in laboratory testing,adjusting and optimizing QC protocols,which further guarantee accuracy and reliability of the studies.