GEMHEP multicenter quality control study of PCR detection of GB virus C hepatitis G virus RNA in serum

被引:22
作者
Bogard, M
BuffetJanvresse, C
Cantaloube, JF
Biagini, P
Duverlie, G
Castelain, S
Izopet, J
Dubois, M
Defer, C
Lepot, I
Coste, J
Marcellin, P
MartinotPeignoux, M
Halfon, P
Gerolami, V
Franguel, L
Pawlotsky, JM
RoudotThoraval, F
Dussaix, E
Loiseau, P
Ravera, N
Lewin, P
Lamoril, J
Lerable, J
Bouchardeau, F
Laperche, S
Mariotti, M
Lefrere, JJ
Nicot, T
Denis, F
Gassain, M
Merel, P
Trepo, C
Thiers, V
Brechot, C
Ferec, C
Mercier, B
StollKeller, F
Palmer, P
Lebon, P
机构
[1] INST NATL TRANSFUS SANGUINE, F-75012 PARIS, FRANCE
[2] CHU ROUEN, ROUEN, FRANCE
[3] CTR HOSP, MEAUX, FRANCE
[4] ETAB TRANSFUS SANGUINE, MARSEILLE, FRANCE
[5] LAB ALPHABIO, MARSEILLE, FRANCE
[6] HOP CONCEPTION, MARSEILLE, FRANCE
[7] CHU AMIENS, AMIENS, FRANCE
[8] CHU TOULOUSE, TOULOUSE, FRANCE
[9] ETS, LILLE, FRANCE
[10] ETS, MONTPELLIER, FRANCE
[11] HOP BEAUJON, CLICHY, FRANCE
[12] CHU PITIE SALPETRIERE, PARIS, FRANCE
[13] ASSISTANCE PUBL HOP PARIS, ETS, PARIS, FRANCE
[14] CHU NECKER, PARIS, FRANCE
[15] HOP ST VINCENT DE PAUL, F-75674 PARIS, FRANCE
[16] CHU HENRI MONDOR, F-94010 CRETEIL, FRANCE
[17] HOP PAUL BROUSSE, VILLEJUIF, FRANCE
[18] LAB CERBA, CERGY, FRANCE
[19] HOP LOUIS MOURIER, F-92701 COLOMBES, FRANCE
[20] CHU LIMOGES, LIMOGES, FRANCE
[21] CHU NANTES, F-44035 NANTES 01, FRANCE
[22] ETS, BORDEAUX, FRANCE
[23] HOP HOTEL DIEU, LYON, FRANCE
[24] ETS BRETAGNE OCCIDENTALE, BREST, BELARUS
[25] CHU STRASBOURG, F-67000 STRASBOURG, FRANCE
关键词
D O I
10.1128/JCM.35.12.3298-3300.1997
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
PCR is, to date, the only available tool for the detection of GB virus C (GBV-C) and hepatitis G virus (HGV) RNAs. Twenty-two French laboratories participated in a quality control study to assess the sensitivity and specificity of their procedures. The panel included 13 positive controls and 7 negative controls. The laboratories used either in-house PCR techniques adapted from the literature or partly standardized commercial tests, Three laboratories performed faultlessly with the entire panel. Most laboratories had excellent specificity (100% in 20 of 22 laboratories), Sensitivity was acceptable (85 to 100%) in 15 centers and insufficient (38 to 77%) in 7, As with nonstandardized in-house PCR, the commercial assays gave discrepant performances in different laboratories. These results suggest that laboratories willing to use PCR for detection of GBV-C/HGV RNA for research or diagnostic purposes should participate in multicenter quality control trials.
引用
收藏
页码:3298 / 3300
页数:3
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