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Research

Feasibility of self-collection of specimens for human papillomavirus testing in hard-to-reach women

Gina Ogilvie, Mel Krajden, Juanita Maginley, Judy Isaac-Renton, Greg Hislop, Ruth Elwood-Martin, Chris Sherlock, Darlene Taylor and Michael Rekart
CMAJ August 28, 2007 177 (5) 480-483; DOI: https://doi.org/10.1503/cmaj.070013
Gina Ogilvie MD MSc
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Mel Krajden MD
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Juanita Maginley RN
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Judy Isaac-Renton MD
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Greg Hislop MDCM MSc
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Ruth Elwood-Martin MD
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Chris Sherlock MB
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Darlene Taylor BSN
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Michael Rekart MD
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  • © 2007 Canadian Medical Association

Abstract

To study the feasibility of self-collected specimens for testing human papillomavirus (HPV) status among hard-to-reach women, outreach nurses recruited women in women's centres, shelters and alleys in Vancouver's Downtown Eastside. Of the 151 participants for whom samples were available, 43 (28.5%) tested positive for high-risk HPV. Outreach nurses were able to recontact 81.4% of the participants who tested positive and referred them for further testing. About 14% (21/151) of participants had never received a Papanicolaou smear in British Columbia, as compared with 8.3% (608/7336) of women in the BC general population (p < 0.05). This difference suggests that self-collection of specimens for HPV testing is a feasible method to reach women who have not previously participated in cervical cancer screening programs.

Despite the availability of cytology screening programs in developed countries, women who are of lower socioeconomic status may not make full use of these programs.1–3 As a result, these women experience higher rates of cervical cancer than women in the general population.4–6 Screening tests that use patient-collected samples may increase the rate of cervical cancer screening in populations that are historically underscreened.7,8 Unlike Papanicolaou smears, which require a clinician to collect the specimen, women can directly obtain a cervicovaginal sample by intravaginal insertion of a swab, tampon or cytobrush.9 These self-collected specimens can then be used to screen for the presence of human papillomavirus types of high oncogenic risk (herein referred to as high-risk HPV), and women whose test results are positive for high-risk HPV can then be encouraged to seek further testing (e.g., Pap smear, colposcopy). In order to examine the feasibility of self-collection of specimens for HPV testing as a part of cervical cancer screening, we offered self-collection of specimens to women in Vancouver's Downtown Eastside.

Methods

Study population

The study population included sexually active women over the age of 16 who were homeless or had unstable housing in Vancouver's Downtown Eastside (a region characterized by high rates of drug-related mortality and homelessness10), who were involved in the sex trade or who had a history of alcohol or drug abuse. Women were recruited to the study from November 2004 to October 2005 by outreach nurses using a standardized recruitment statement in women's centres, shelters and alleys. Self-collection of specimens for HPV testing is not a standard part of cervical cancer screening; thus, all women were advised to have a Pap smear within 1 year. Participants were given a diagram that illustrated how to obtain a cervicovaginal specimen. They were instructed to insert a Dacron swab intravaginally, rotate it 3 times and place it in a specimen tube containing specimen transport medium (Digene Corporation). Women were asked to collect the specimen immediately at the closest washroom or private location and to return it to the nurse. Samples were transported to the British Columbia Centre for Disease Control within 24 hours of collection. They were analyzed for the presence of high-risk HPV DNA using the Digene HPV test, as per manufacturer's instructions.

Ethical approval for the study was obtained from the Ethics Board at the University of British Columbia.

Data sources and analysis

We searched the database of the Cervical Cancer Screening Program at the British Columbia Cancer Agency (where all Pap smears in British Columbia are processed) in order to determine the recent cervical cancer screening practices of participants. In addition, we obtained self-reported data about the frequency of Pap smear testing in the general population of British Columbia from the Canadian Community Health Survey.11

Descriptive analysis of the study population included willingness to provide a self-collected specimen and whether nurses were able to recontact women who tested positive for high-risk HPV. We compared the rate of participation in cervical cancer screening programs among study participants and the general population of British Columbia using self-reported data from the Canadian Community Health Survey and aggregate data from the Cervical Cancer Screening Program. We also compared the frequency of Pap smear testing between participants and the general population of British Columbia. We determined the prevalence of high-risk HPV among participants and performed bivariate analyses of categorical variables by comparing the characteristics of women who tested positive with those who tested negative for high-risk HPV. Variables that were significant (p < 0.05) in the bivariate analysis were included in a multivariable model by means of a backward elimination logistic regression procedure to achieve a best-fit final model. We used this final model to calculate adjusted odds ratios to identify factors associated with positive high-risk HPV status.12 An odds ratio greater than 1 indicates characteristics that are associated with high-risk HPV infection.

Results

Overall, 296 women were invited to participate in the study from November 2004 to October 2005. Of these, 152 (51.4%) agreed to participate. Participants had a median age of 39 years as compared with a median age of 40 years for women who participated in the provincial cervical cancer screening program.13

All of the participants provided a self-collected specimen for analysis of HPV status; 1 specimen was lost during accession and analysis, leaving 151 for analysis. Of the 151 participants with specimens available for analysis, 43 tested positive for high-risk HPV (28.5%, 95% confidence interval [CI] 21.2%–35.4%). In univariate and bivariate analyses, women who tested positive for high-risk HPV were significantly younger, less educated and reported having had more sex-trade partners than women who tested negative (p < 0.05, Table 1). In logistic regression modelling that included these 3 variables, women who were younger were less likely to be infected with high-risk HPV (adjusted OR 0.96, 95%CI 0.92–0.99). After HPV status was determined, the outreach team was able to recontact 81.4% (35/43) of the participants who tested positive for high-risk HPV. These women were referred for further testing.

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Table 1.

Compared with the general population, significantly more women in the study group had never had a Pap smear in British Columbia (13.9% v. 8.3%, p < 0.05, Table 2). Of the participants, 53.6% (81/151) had received a Pap smear within the 36 months before study recruitment. This was significantly lower than both the rates in the BC general population, as determined from the self-reported survey data, and the data from the Cervical Cancer Screening Program13 (Table 2).

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Table 2.

Interpretation

We found that self-collection of specimens for HPV testing was feasible in women who did not participate in the provincial cervical cancer screening program. Over 50% of the women who were invited to participate in the study agreed to do so, which is similar to the participation rate of other studies in Vancouver's Downtown Eastside.14 Study participants were significantly less likely than women in the general population to have ever had a Pap smear or to have had a Pap smear in the 3 years before recruitment, which suggests that this specimen-collection method is a feasible way to reach women who do not receive routine cervical cancer screening. In addition, the prevalence of high-risk HPV in our study was more than double that in the general BC population recently reported by the Cervical Cancer Screening Program (28.3% v. 13.9%), despite the fact that median age in the 2 groups was similar. This suggests that self-collection of specimens is feasible for women who are at high risk of cervical cancer.15 Self-collected specimens may not possess the same degree of diagnostic accuracy as clinician-collected specimens9; however, this limitation is outweighed by the increased uptake of HPV testing among hard-to-reach women.

Recent studies of the HPV vaccine confirm the need for ongoing cytology screening programs.16 Our findings suggest that women who do not participate in cervical cancer screening programs may be willing to provide a self-collected specimen.17 Future studies should include an examination of the rate of follow-up testing among women found to be positive for high-risk HPV. In addition, improved methods are necessary to enhance uptake of follow-up interventions.18 As well, given the high incidence of this preventable cancer in developing countries,19 self-collection of specimens for HPV screening could be offered as a component of reproductive health programs and could be administered by health care workers to improve access to cervical cancer screening. Follow-up using screen-and-treat methods could then be used to offer definitive treatment for women at risk for cervical cancer.20,21

@ See related articles pages 456, 462, 464, 469 and 484

Footnotes

  • Une version française de ce résumé est disponible à l'adresse www.cmaj.ca/cgi/content/full/177/5/480/DC1

    This article has been peer reviewed.

    Contributors: Gina Ogilvie conceived the study (with assistance from Mel Krajden and Darlene Taylor) and its design (with assistance from all of the coauthors). She also supervised the study, conducted the data analysis (with Greg Hislop and Darlene Taylor) and prepared the manuscript. Mel Krajden supervised laboratory testing (with Judy Isaac-Renton). Juanita Maginley supervised the outreach team and specimen collection. Darlene Taylor assisted in coordinating the study. All of the authors revised the manuscript and approved the final version submitted for publication.

    Acknowledgement: This study was funded by the Reducing Health Disparities Strategic Initiative of the Canadian Institutes of Health Research.

    Competing interests: None declared.

REFERENCES

  1. 1.↵
    Katz SJ, Hofer TP. Socioeconomic disparities in preventive care persist despite universal coverage. Breast and cervical cancer screening in Ontario and the United States. JAMA 1994;272:530-4.
    OpenUrlCrossRefPubMed
  2. 2.
    Snider JA, Beauvais JE. Pap smear utilization in Canada: estimates after adjusting the eligible population for hysterectomy status. Chronic Dis Can 1998;19:19-24.
    OpenUrlPubMed
  3. 3.↵
    Snider J, Beauvais J, Levy I, et al. Trends in mammography and Pap smear utilization in Canada. Chronic Dis Can 1996;17:108-17.
    OpenUrlPubMed
  4. 4.↵
    Archibald CP, Coldman A, Wong FL, et al. The incidence of cervical cancer among Chinese and Caucasians in British Columbia. Can J Public Health 1993;84:283-5.
    OpenUrlPubMed
  5. 5.
    Hislop TG, Deschamps M, Band PR, et al. Participation in the British Columbia Cervical Cytology Screening Programme by Native Indian women. Can J Public Health 1992;83:344-5.
    OpenUrlPubMed
  6. 6.↵
    Band PR, Gallagher RP, Threlfall WJ, et al. Rate of death from cervical cancer among native Indian women in British Columbia. CMAJ 1992;147:1802-4.
    OpenUrlAbstract
  7. 7.↵
    Walboomers JM, Jacobs MV, Manos MM, et al. Human papillomavirus is a necessary cause of invasive cervical cancer worldwide. J Pathol 1999;189:12-9.
    OpenUrlCrossRefPubMed
  8. 8.↵
    Farley M, Golding JM, Minkoff JR. Is a history of trauma associated with a reduced likelihood of cervical cancer screening? J Fam Pract 2002;51:827-31.
    OpenUrlPubMed
  9. 9.↵
    Ogilvie GS, Patrick DM, Schulzer M, et al. Diagnostic accuracy of self obtained HPV cervicovaginal samples vs clinician obtained samples: a systematic review. Sex Transm Infect 2005;81:207-12.
    OpenUrlAbstract/FREE Full Text
  10. 10.↵
    Patrick DM, Rekart ML, Jolly A, et al. Heterosexual outbreak of infectious syphilis: epidemiological and ethnographic analysis and implications for control. Sex Transm Infect 2002;78(Suppl 1):i164-9.
  11. 11.↵
    Statistics Canada. Canadian Community Health Survey (CCHS): cycle 1.1: extending the wealth of health data in Canada. Ottawa: Statistics Canada; 2003. Available: www.statcan.ca/english/concepts/health/cchsinfo.htm#cont (accessed 2007 July 26).
  12. 12.↵
    Rosner B. Fundamentals of biostatistics. 5th ed. Pacific Grove (CA): Duxbury; 2000. p. 612–25.
  13. 13.↵
    British Columbia Cancer Agency. 2005 annual report: Cervical Cancer Screening Program. Vancouver: The Agency; 2005. Available: www.bccancer.bc.ca/NR/rdonlyres/34F5A494-73CD-4A7C-908A-D34F9E7B1F09/15237/2005ccsp_annual_reportFINAL.pdf (accessed 2007 June 25).
  14. 14.↵
    Sajan A, Corneil T, Grzybowski S. The street value of prescription drugs. CMAJ 1998;159:139-42.
    OpenUrlAbstract/FREE Full Text
  15. 15.↵
    Moore RA FD, Moravan V, Amirabbasi-Biek M, et al. HPV type distribution in North America — a population based study of 5000 British Columbia women. 23rd International Papillomavirus Conference and Clinical Workshop; 2006 September 1–7; Prague, Czech Republic. Prague: The Institute of Hematology and Blood Transfusion; 2006. p. 295.
  16. 16.↵
    The Future II Study Group. Quadrivalent vaccine against human papillomavirus to prevent high grade cervical lesions. N Engl J Med 2007;356:1915-27.
    OpenUrlCrossRefPubMed
  17. 17.↵
    Flores Y, Bishai D, Lazcano E, et al. Improving cervical cancer screening in Mexico: results from the Morelos HPV Study. Salud Publica Mex 2003;45(Suppl 3): S388-98.
  18. 18.↵
    Ogilvie GS, Shaw EA, Lusk S, et al. Access to colposcopy for at risk Canadian women: Can we do better? Can J Public Health 2004;95:346-51.
    OpenUrlPubMed
  19. 19.↵
    Parkin DM, Bray F, Ferlay J, et al. Global cancer statistics, 2002. CA Cancer J Clin 2005;55:74-108.
    OpenUrlCrossRefPubMed
  20. 20.↵
    Kuhn L, Denny L, Pollack A, et al. Human papillomavirus DNA testing for cervical cancer screening in low-resource settings. J Natl Cancer Inst 2000;92:818-25.
    OpenUrlAbstract/FREE Full Text
  21. 21.↵
    Denny L, Kuhn L, De Souza M, et al. Screen-and-treat approaches for cervical cancer prevention in low-resource settings: a randomized controlled trial. JAMA 2005;294:2173-81.
    OpenUrlCrossRefPubMed
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Canadian Medical Association Journal: 177 (5)
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Feasibility of self-collection of specimens for human papillomavirus testing in hard-to-reach women
Gina Ogilvie, Mel Krajden, Juanita Maginley, Judy Isaac-Renton, Greg Hislop, Ruth Elwood-Martin, Chris Sherlock, Darlene Taylor, Michael Rekart
CMAJ Aug 2007, 177 (5) 480-483; DOI: 10.1503/cmaj.070013

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Feasibility of self-collection of specimens for human papillomavirus testing in hard-to-reach women
Gina Ogilvie, Mel Krajden, Juanita Maginley, Judy Isaac-Renton, Greg Hislop, Ruth Elwood-Martin, Chris Sherlock, Darlene Taylor, Michael Rekart
CMAJ Aug 2007, 177 (5) 480-483; DOI: 10.1503/cmaj.070013
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