Standard Document
Third Edition
Quality Management Systems

CLSI GP15

Cervicovaginal Cytology Based on the Papanicolaou Technique

This document provides essential guidelines for collecting cervicovaginal specimens, along with detailed steps for preparing, fixing, staining, and storing Papanicolau-stained cytology slides, perfect for ensuring accurate and reliable results. 

November 24, 2008
George Birdsong, MD

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Abstract

Clinical and Laboratory Standards Institute document GP15-A3—Cervicovaginal Cytology Based on the Papanicolaou Technique; Approved Guideline—Third Edition is intended for health care providers who are responsible for collecting cervicovaginal cytology specimens and preparing conventional Papanicolaou smears and liquid-based preparations. The guideline focuses on quality collection and processing of specimens, addressing all steps, including patient assessment, test requisition, specimen collection, specimen transport, and specimen receipt and processing. Illustrations of the techniques are described, and a specimen requisition form is also included.

Overview of Changes

This third edition has been updated to provide additional information on education of the patient, design of the requisition, and specimen collection. Additional information regarding the handling and processing of liquid-based Pap tests and ancillary studies is also provided. The nomenclature of the second edition of The Bethesda System is incorporated in this edition, and handling of cases in the context of an electronic health record is discussed.

Scope

This guideline provides the most current recommendations regarding standard precautions, patient assessment, test requisition, cervicovaginal specimen collection, specimen transport, specimen receipt, specimen processing, and storage of slides. Cytologic interpretation is outside the scope of this document and is not addressed. 

This guideline is useful to health care providers, laboratory directors, supervisors, and others who have responsibilities for quality control in cytopathology laboratories.

Product Details
GP15A3E
1-56238-679-4
52
Additional Details

This document is available in electronic format only.

This archived document is no longer being reviewed through the CLSI Consensus Document Development Process. However, this document is technically valid and because of its value to the laboratory community, it is being retained in CLSI’s library.

Authors
George Birdsong, MD
Mujtaba Husain, MD
Tremel Faison, SCT(ASCP)
Daron G. Ferris, MD
Barbara Fetterman, SCT(ASCP)
Lisa C. Flowers, MD, FACOG
Maria A. Friedlander, MPA, CT(ASCP)
MariBeth Gagnon, MS, CT(ASCP), HTL
Leza N. Gallo, MD
Gabriele Medley, AM, MB, BS, FRCPA, FIAC
Abstract

Clinical and Laboratory Standards Institute document GP15-A3—Cervicovaginal Cytology Based on the Papanicolaou Technique; Approved Guideline—Third Edition is intended for health care providers who are responsible for collecting cervicovaginal cytology specimens and preparing conventional Papanicolaou smears and liquid-based preparations. The guideline focuses on quality collection and processing of specimens, addressing all steps, including patient assessment, test requisition, specimen collection, specimen transport, and specimen receipt and processing. Illustrations of the techniques are described, and a specimen requisition form is also included.

Overview of Changes

This third edition has been updated to provide additional information on education of the patient, design of the requisition, and specimen collection. Additional information regarding the handling and processing of liquid-based Pap tests and ancillary studies is also provided. The nomenclature of the second edition of The Bethesda System is incorporated in this edition, and handling of cases in the context of an electronic health record is discussed.

Scope

This guideline provides the most current recommendations regarding standard precautions, patient assessment, test requisition, cervicovaginal specimen collection, specimen transport, specimen receipt, specimen processing, and storage of slides. Cytologic interpretation is outside the scope of this document and is not addressed. 

This guideline is useful to health care providers, laboratory directors, supervisors, and others who have responsibilities for quality control in cytopathology laboratories.

Additional Details

This document is available in electronic format only.

This archived document is no longer being reviewed through the CLSI Consensus Document Development Process. However, this document is technically valid and because of its value to the laboratory community, it is being retained in CLSI’s library.

Authors
George Birdsong, MD
Mujtaba Husain, MD
Tremel Faison, SCT(ASCP)
Daron G. Ferris, MD
Barbara Fetterman, SCT(ASCP)
Lisa C. Flowers, MD, FACOG
Maria A. Friedlander, MPA, CT(ASCP)
MariBeth Gagnon, MS, CT(ASCP), HTL
Leza N. Gallo, MD
Gabriele Medley, AM, MB, BS, FRCPA, FIAC