Migrant women and cervical cancer: Background of a prevention study

L. Mariani, A. Morrone, M. Preti, C. Sbiroli, F. Tomao, S. Tomao

Research output: Contribution to journalArticle

Abstract

The study was scheduled in order to organize a program of prevention against cervical cancer in female migrants in Rome, and therefore to facilitate access to appropriate preventive oncological facilities for discriminated women. Moreover, the study will also investigate the risk factors and social conditions (HPV-subtypes, sexual behavior, smoking habits) of such women since their migration to Italy. This is scientific and cultural background of a longitudinal, observational study on the cervical cancer risk in Roman migrant population. By means of a mother language questionnaire (with the presence of a cultural mediator) it will be possible to achieve data on social conditions and the new life-style. An HPV-testing (HC2) combined with Pap-test (with further genotype distribution) will be performed in all women enrolled in the study. Further diagnostic/therapeutic decisions will depend on the results of both tests. Scientific results are expected in the next two years, but an increasing of cancer prevention awareness among female migrant populations is expected from the beginning of the program. The present study was aimed at culturally appropriate intervention strategies to limit the disparities that migrants usually suffer in most of the developed Western nations in respect to the native counterparts.

Original languageEnglish
Pages (from-to)52-56
Number of pages5
JournalEuropean Journal of Gynaecological Oncology
Volume29
Issue number1
Publication statusPublished - 2008

Keywords

  • Cervical cancer
  • Health discrimination
  • Migrants
  • Prevention

ASJC Scopus subject areas

  • Obstetrics and Gynaecology
  • Oncology

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  • Cite this

    Mariani, L., Morrone, A., Preti, M., Sbiroli, C., Tomao, F., & Tomao, S. (2008). Migrant women and cervical cancer: Background of a prevention study. European Journal of Gynaecological Oncology, 29(1), 52-56.