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1.
Acta Cytol ; 41(6): 1690-6, 1997.
Artículo en Inglés | MEDLINE | ID: mdl-9390125

RESUMEN

OBJECTIVE: To determine the false negative fraction (FNF) at a small community hospital and its relation to the discovery of a significant error. STUDY DESIGN: All cervical cytologic smears (6,889) initially interpreted over a one-year period (1992) as "normal" or "near normal" were retrospectively rescreened and interpreted by outside institutions, without knowledge of the initial interpretation, to calculate yearly and quarterly FNFs. RESULTS: The overall FNF for 1992 was 12.3% and was 19.1%, 22.2%, 3.8% and 6.1% per successive quarters in 1992. A significant error was discovered at the start of the third quarter that subsequently received both local and national media attention. CONCLUSION: This study gives further proof that the FNF can be reduced to < 5% by motivated cytotechnologist/ pathologist teams, although it may not be possible to maintain this low an FNF.


Asunto(s)
Reacciones Falso Negativas , Displasia del Cuello del Útero/patología , Neoplasias del Cuello Uterino/patología , Frotis Vaginal/normas , Biopsia , Femenino , Hospitales Comunitarios , Humanos , Patología/normas , Reproducibilidad de los Resultados , Estudios Retrospectivos , Estados Unidos
2.
Lancet ; 1(8388): 1210-2, 1984 Jun 02.
Artículo en Inglés | MEDLINE | ID: mdl-6144925

RESUMEN

Hepatitis B surface antigen (HBsAg) was detected in 17% of adult males and 11% of mothers in Ovamboland , South West Africa/Namibia. Hepatitis B e antigen (HBeAg) was present in 15% of HBsAg-positive mothers. Only 1% of children less than 6 months of age were HBsAg-positive, compared with 13% of children over the age of 1 year. 27% of mothers who were HBsAg-positive had HBsAg-positive children, whereas the corresponding figure for mothers who were HBsAg-negative was 6%. 63% of mothers who were positive for both HBsAg and HBeAg had HBsAg-positive children. 37% of HBsAg-positive children had HBsAg-positive mothers, compared with 8% of HBsAg-negative children. Later "horizontal" rather than neonatal maternal-infant transmission of the hepatitis B virus (HBV) seems to be the more important mode of spread of this infection in Ovambo children. The difference in the pattern of transmission of this virus between the Far East and Africa seems to centre mainly on the differences in the HBeAg status of the mothers in these two regions.


Asunto(s)
Portador Sano/transmisión , Antígenos de Superficie de la Hepatitis B/análisis , Hepatitis B/transmisión , Adolescente , Adulto , Factores de Edad , Anciano , Población Negra , Niño , Preescolar , Asia Oriental , Femenino , Antígenos e de la Hepatitis B/análisis , Humanos , Lactante , Masculino , Intercambio Materno-Fetal , Persona de Mediana Edad , Namibia , Embarazo
3.
J Infect Dis ; 152(3): 566-71, 1985 Sep.
Artículo en Inglés | MEDLINE | ID: mdl-2411829

RESUMEN

We have examined serological markers of replicative and nonreplicative infection in 124 adult, black South African carriers of hepatitis B virus (HBV), in whom this infection is predominantly acquired in early childhood. The mean age of the group was 36 years. Antibody to hepatitis B e antigen (anti-HBe) was present in the serum of 93.5% of these carriers. Only 25.8% of the carriers were positive for HBV DNA in serum, and in the majority of these only trace amounts were detectable. IgM antibody to hepatitis B core antigen (IgM anti-HBc) was negative in 54% of the carriers, and only 26% had IgM anti-HBc in high titer. A significantly greater proportion of carriers who were positive for anti-HBe were positive for IgM anti-HBc (43.1%) than were positive for HBV DNA (24.5%). Serum aminotransferases were less than twofold elevated in 90.3% of the carriers. Only one carrier has thus far developed hepatocellular carcinoma. These results suggest that there is an inexorable progression to predominantly nonreplicative infection in the majority of southern African adult, black carriers, an occurrence that may take several decades. In areas endemic for HBV infection, antiviral agents effective against replicative HBV will have to be administered in childhood.


Asunto(s)
Portador Sano/microbiología , Virus de la Hepatitis B/fisiología , Hepatitis B/microbiología , Adulto , Alanina Transaminasa/sangre , ADN Viral/sangre , Femenino , Hepatitis B/sangre , Hepatitis B/epidemiología , Hepatitis B/inmunología , Anticuerpos contra la Hepatitis B/análisis , Antígenos del Núcleo de la Hepatitis B/inmunología , Antígenos de Superficie de la Hepatitis B/análisis , Antígenos e de la Hepatitis B/análisis , Antígenos e de la Hepatitis B/inmunología , Humanos , Inmunoglobulina M/análisis , Masculino , Persona de Mediana Edad , Sudáfrica , Replicación Viral , alfa-Fetoproteínas/análisis
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