RESUMEN
The method for the diagnostic value evaluation of preparations, based on the calculation of the accuracy of test results and taking into account the spread of the diagnosed disease (the comparison of the PCR test systems for the diagnostics of hepatitis B and ureaplasmosis) is proposed. As shown in this work, evaluations obtained with the use of this method coincide with those obtained on the basis of prognostic value, but are more convenient in use and provide additional information.
Asunto(s)
Hepatitis B/diagnóstico , Reacción en Cadena de la Polimerasa/normas , Infecciones por Ureaplasma/diagnóstico , ADN Bacteriano/análisis , ADN Viral/análisis , Virus de la Hepatitis B/genética , Humanos , Control de Calidad , Sensibilidad y Especificidad , Ureaplasma/genéticaRESUMEN
The test system developed at the Central Research Institute of Epidemiology, Ministry of Health of the Russian Federation for identification of hepatitis C virus RNA was studied. The sensitivity of the test system which the rate of similar results was 100% with its 5-fold reproduction was evaluated. That was 5 x 103 genomic equivalents (or international units) per ml of a sample. A scheme for evaluation of the reproductibility of test systems based on the polymerase chain reaction (PCR) by using model samples is proposed. Whether it can be used for intra- and extra-laboratory assessment of the quality of PCR analyses is discussed.
Asunto(s)
Hepacivirus/aislamiento & purificación , Hepatitis C/diagnóstico , Reacción en Cadena de la Polimerasa/normas , ARN Viral/sangre , Hepacivirus/genética , Hepatitis C/virología , Reproducibilidad de los Resultados , Sensibilidad y EspecificidadRESUMEN
The stability of hepatitis C virus (HPC) RNA concentration in 5 human plasma samples after storage at +22 degrees C for two months, at -20 degrees C, and +4 degrees C for six months after 10 freezing-unfreezing cycles was evaluated. In this study, the concentration of HCV RNA in the samples was stable after six months of storage at -20 degrees C. The concentration of HCV RNA decreased on the average of 92% after 2-month storage at +22 degrees C. After six months of storage at +4 degrees C and after 10 freezing-unfreezing cycles, that decreased by 28 and 42%, respectively. Based on their own findings, the authors developed a HCV-RNA panel containing 5 positive human plasma samples with RNA levels of 103-105 IU/ml. The panel may be recommended both for the standardization of PCR kits and for the intra- and interlaboratory quality control of PCR laboratories.
