Utilize este identificador para referenciar este registo: https://hdl.handle.net/1822/67919

Título100% rapid rescreening for quality assurance in a quality control program in a public health cytologic laboratory
Autor(es)Ferraz, Maria da Gloria Mattosinho de Castro
Dall' Agnol, Miria
di Loreto, Celso
Pirani, Wiliam M.
Utagawa, Maria Lúcia
Pereira, Sonia Maria Miranda
Sakai, Yuriko Ito
Feres, Camilo Lelis
Shih, Lai W. S.
Yamamoto, Luzia Setuko
Rodrigues, Rosemeire O. L.
Shirata, Neuza Kasumi
Longatto, Adhemar
Palavras-chaveBrazil
Cervical Intraepithelial Neoplasia
Cytodiagnosis
Female
Humans
Laboratories
Mass Screening
Medical Audit
Public Health Practice
Quality Assurance, Health Care
Sensitivity and Specificity
Uterine Cervical Dysplasia
Uterine Cervical Neoplasms
Vaginal Smears
Papanicolaou smear
Cervical cancer
Health care quality assurance
Quality control
Rapid rescreening
Data2005
EditoraKarger Publishers
RevistaActa Cytologica
CitaçãoMattosinho, G. D. C. F. M., Dall, M. A., Pirani, W. M., Utagawa, M. L., et. al.(2005). 100% rapid rescreening for quality assurance in a quality control program in a public health cytologic laboratory. Acta cytologica, 49(6), 639-643
Resumo(s)To verij5 the efficacy of the quality control (QC) program in a cytologic laboratwy with a rapid rescreening (RR) protocol. To verij5 the efficacy of the quality control (QC) program in a cytologic laboratwy with a rapid rescreening (RR) protocol.RR, according to the Turret RR method, of all samples initially screened as negative at the Laboratory of Cytology, Adolfo Lutz Institute, was performed. The slides were reviewed for 60 seconds. Suspect smears were fully checked by 2 reviewers to determine the final diagnoses. A total of 2954 sequential cytologic results were considered in this study. Of the 2954, 2568 (86.9%) were considered initially negative according to our internal QC, and these cases underwent RR. Also, 10% were randomly selected from these negative cases for full reviewing. The internal QC in our laboratory includes review of cases selected according to clinical and cytomorphologic criteria.Among the 2954 total cases, QC detected 386 (13%) atypias with final diagnoses reported according to The Bethesda System 2001 as follows: 82 (2.18%) low grade squamous intraepithelial lesions (LSILs), 35 (1.18%) high grade squamous intraepithelial lesions (HSILs), 2 (0.06%) squamous cell carcinomas, 105 (3.5%) atypical cells of undetermined significance (ASC-US), 4 (0.12%) atypical endocervical cells (AECs) and 158 (5.3%) unsatisfactory samples. RR of 2568 smears initially considered negative selected 194 (7.5%) slides. Of the 194, 146 (75.3%) were negative, 28 (14.4%) ASC-US, 5 (2.6%) AEC, 1 (0.5%) LSIL and 14 (7.2%) unsatisfactory. Full review of a 10% random fraction of the 2568 cases interpreted as negative did not detect lesions but did detect 5 (1.95%) unsatisfactory samples.Internal QC used in our laboratory based on clinical and cytomorphologic criteria to select cases for review proved to be an efficient method of detecting HSIL and cervical cancer. The consensus basis of this program strongly limits the false positive and false negative rates and also provides subjects with continuing education. One hundred percent RR is more efficient than 10% full reviewing in detecting cervical abnormalities.
TipoArtigo
URIhttps://hdl.handle.net/1822/67919
DOI10.1159/000326252
ISSN0001-5547
e-ISSN1938-2650
Versão da editorahttps://www.karger.com/Article/Abstract/326252
Arbitragem científicayes
AcessoAcesso aberto
Aparece nas coleções:ICVS - Artigos em revistas internacionais / Papers in international journals

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