4 48 80 0 D espite 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.
4-6Screening 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 populationThe 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 homelessness 10 ), 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 highrisk 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. 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 ...