Cervical cytology specimen adequacy: patient management guidelines and optimizing specimen collection

J Low Genit Tract Dis. 2008 Apr;12(2):71-81. doi: 10.1097/LGT.0b013e3181585b9b.

Abstract

Objective: To provide updated management guidelines according to cervical cytology specimen adequacy and techniques to optimize adequacy based on literature review and expert opinion.

Materials and methods: Selected members of the American Society for Colposcopy and Cervical Pathology committee and invited experts conducted a literature review and discussed appropriate management and areas for future research emphasis.

Results: The guidelines recommend a repeat Pap test in a short interval of 2 to 4 months for most women when the cytology result is unsatisfactory. The preferred follow-up for women with a negative cytology result lacking an endocervical/transformation zone component or showing other quality indicators is a repeat Pap test in 12 months. Indications for an early repeat Pap test in 6 months are provided, and the influence of human papillomavirus testing results on management is discussed. Techniques for optimizing specimen adequacy are provided in detail.

Conclusion: The specimen adequacy management guidelines will help promote uniform and optimal follow-up of patients receiving cervical cytology screening. The topics for future research emphasis will be helpful in promoting studies in needed areas.

Publication types

  • Review

MeSH terms

  • Female
  • Humans
  • Mass Screening / methods
  • Mass Screening / standards*
  • Practice Guidelines as Topic*
  • Quality Indicators, Health Care / standards*
  • Specimen Handling / standards*
  • Uterine Cervical Neoplasms / prevention & control*
  • Vaginal Smears / standards*