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[Result survey analysis of prenatal chromosome karyotyping in an external quality assessment program].
Wang, Wei; Chen, Yuanyuan; Chen, Xi; Zhong, Kun; He, Falin; Zhang, Yan; Bao, Liming; Zou, Lin; Wang, Zhiguo.
Afiliação
  • Wang W; Chinese National Center for Clinical Laboratories, Beijing Hospital of the Ministry of Health, Beijing 100730, P.R. China. zhiguo_w@sina.com.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi ; 31(4): 483-6, 2014 Aug.
Article em Zh | MEDLINE | ID: mdl-25119916
ABSTRACT

OBJECTIVE:

To analyze the results of prenatal karyotype of the external quality assessment program in 2013 in order to provide references and recommendations for improving the capability and performances of karyotype analysis of prenatal screening laboratories.

METHODS:

Five lots of quality control cell photos were sent to 500 laboratories. The participants were asked to decide whether the photos have demonstrated any abnormal karyotype and determine the abnormal type. The results should be submitted before the deadline and compared with the standard results to evaluate the performances of the laboratory.

RESULTS:

One hundred forty three laboratories have returned their karyotype results for the survey. The standard answers were 7,XX,+18, 46,X,i(X)(q10), 46,XY,i(21)(q10) or 46,XY,+21,der(21;21)(q10;q10), 46,XY and 47,XY,+21 in sequential order, which were used to estimate the score of each participant. The pass rates for five lots were 97.9%, 97.2%, 95.8%, 100.0% and 97.9%, respectively. The total pass rate was 97.7%. The error rates were 2.1%, 2.8%, 4.2%, 0 and 2.1%, respectively. The total error rate was 2.3%.

CONCLUSION:

Some laboratories did not correctly identify the abnormal karyotypes, while some could not determine the right type of karyotype. The external quality assessment program of prenatal diagnosis of karyotype analysis should be conducted annually in order to improve the capability and performances of karyotype analysis of prenatal screening laboratories.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Diagnóstico Pré-Natal / Testes Genéticos / Cromossomos Humanos / Doenças Fetais / Cariotipagem Tipo de estudo: Diagnostic_studies / Guideline / Prognostic_studies Limite: Adult / Female / Humans / Male / Pregnancy Idioma: Zh Revista: Zhonghua Yi Xue Yi Chuan Xue Za Zhi Assunto da revista: GENETICA MEDICA Ano de publicação: 2014 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Diagnóstico Pré-Natal / Testes Genéticos / Cromossomos Humanos / Doenças Fetais / Cariotipagem Tipo de estudo: Diagnostic_studies / Guideline / Prognostic_studies Limite: Adult / Female / Humans / Male / Pregnancy Idioma: Zh Revista: Zhonghua Yi Xue Yi Chuan Xue Za Zhi Assunto da revista: GENETICA MEDICA Ano de publicação: 2014 Tipo de documento: Article