Autocolheita vaginal versus colheita por profissional de saúde para rastreio do cancro do colo do útero: uma revisão sistemática com meta-análise de precisão e aceitabilidade

Authors

  • Mafalda Paula-Pinto Médica Interna de Medicina Geral e Familiar. USF Ramalde, ULS de Santo António. Porto, Portugal. https://orcid.org/0000-0003-0411-6601
  • Marta Amaral Especialista de Medicina Geral e Familiar. USF Ramalde, ULS de Santo António. Porto, Portugal.
  • Leonor Norton Médica Interna de Medicina Geral e Familiar. USF Ramalde, ULS de Santo António. Porto, Portugal.
  • Francisca Vilas-Boas Especialista de Medicina Geral e Familiar. USF Ramalde, ULS de Santo António. Porto, Portugal.
  • Inês Santos-Silva Especialista de Medicina Geral e Familiar. USF Ars Médica, ULS de Loures / Odivelas. Lisboa, Portugal.

DOI:

https://doi.org/10.32385/rpmgf.v41i1.13988

Keywords:

Papilomavírus humano, Cancro do colo do útero, Autocolheita, Rastreio, Teste diagnóstico, Aceitabilidade

Abstract

Introdução: Estratégias de autocolheita de DNA do papilomavírus humano (HPV) mostraram-se promissoras na deteção de doença; no entanto, não é clara a sua real potencialidade ou aceitabilidade pelas mulheres.

Objetivos: Como objetivo principal pretendeu-se determinar a precisão da deteção, estudo de não inferioridade, de HPV em amostras de autocolheita, comparativamente às colhidas por profissional de saúde. Secundariamente, pretendeu-se avaliar a aceitabilidade pelas mulheres.

Métodos: Realizou-se uma pesquisa sistemática maioritariamente em bases de dados eletrónicas (MEDLINE, CENTRAL e Scopus). Foram incluídos estudos que compararam os dois métodos de rastreio. A seleção dos estudos e extração de dados foi feita por dois autores de forma independente. Utilizou-se o QUADAS2 Tool e Cochrane Risk of Bias Tool para avaliar o risco de viés. A sensibilidade e a especificidade dos testes foram estimadas e elaboradas curvas SROC, utilizando o RevMan v. 5.4. e MetaDisc para a análise de dados. Foi também realizada uma análise de subgrupo e de sensibilidade.

Resultados: Foram incluídos 67 artigos (precisão 47 e aceitabilidade 36) com uma amostra total de 18.615 mulheres, com idades entre 15-80 anos. Demonstrou-se uma sensibilidade de 86,4% e uma especificidade de 91.8% Na análise de subgrupos não foram detetadas diferenças significativas relativas ao tipo de teste, dispositivo de autocolheita e respetivo transporte ou prevalência de HPV. Relativamente à aceitabilidade, as mulheres consideram a autocolheita fácil, confortável, privada e não constrangedora. 62,8% prefere a autocolheita.

Conclusão: Esta revisão sistemática e meta-análise demonstrou uma taxa de deteção de HPV não inferior à colheita por profissional de saúde e revelou ser um método com boa aceitabilidade pela maioria das mulheres. No entanto, ainda há poucas evidências sobre a sua viabilidade e aplicabilidade, pelo que futuramente a avaliação de custo-efetividade deste tipo de rastreio deve ser realizada a nível nacional e internacional.

Downloads

Download data is not yet available.

References

1. Arbyn M, Castellsagué X, de Sanjosé S, Bruni L, Saraiya M, Bray F, et al. Worldwide burden of cervical cancer in 2008. Ann Oncol. 2011;22(12):2675-86.

2. Ferlay J, Soerjomataram I, Dikshit R, Eser S, Mathers C, Rebelo M, et al. Cancer incidence and mortality worldwide: sources, methods and major patterns in GLOBOCAN 2012. Int J Cancer. 2015;136(5):E359-86.

3. Pan S, Wei W, Du X, Li Z, Tuo J, Zhang M, et al. Factors associated with persistence and clearance of HPV16/18 among rural Chinese women: a cohort study in Wufeng, Hubei province. Women Health. 2022;62(4):276-86.

4. Greibe Andersen J, Shrestha AD, Gyawali B, Neupane D, Kallestrup P. Barriers and facilitators to cervical cancer screening uptake among women in Nepal: a qualitative study. Women Health. 2020;60(9):963-74.

5. Rozemeijer K, de Kok IM, Naber SK, van Kemenade FJ, Penning C, van Rosmalen J, et al. Offering self-sampling to non-attendees of organized primary HPV screening: when do harms outweigh the benefits? Cancer Epidemiol Biomarkers Prev. 2015;24(5):773-82.

6. Koliopoulos G, Nyaga VN, Santesso N, Bryant A, Martin-Hirsch PP, Mustafa RA, et al. Cytology versus HPV testing for cervical cancer screening in the general population. Cochrane Database Syst Rev. 2017;8(8):CD008587.

7. Bertucci M, Bonnet E, Satger L, Kreiche A, Chappert JL, Loy-Morel S, et al. Acceptability of vaginal self-sampling with high-risk human papillomavirus testing for cervical cancer screening: a French questionnaire-based study. Women Health. 2021;61(1):83-94.

8. WHO Department for NCDs. Rapid assessment of service delivery for noncommunicable diseases (NCDs) during the COVID-19 pandemic: final results [homepage]. Geneva: WHO; 2020. Available from: https://www.who.int/publications/m/item/rapid-assessment-of-service-delivery-for-ncds-during-the-covid-19-pandemic

9. Lozar T, Nagvekar R, Rohrer C, Dube Mandishora RS, Ivanus U, Fitzpatrick MB. Cervical cancer screening postpandemic: self-sampling opportunities to accelerate the elimination of cervical cancer. Int J Womens Health. 2021;13:841-59.

10. Moher D, Liberati A, Tetzlaff J, Altman DG; PRISMA Group. Preferred reporting items for systematic reviews and meta-analyses: the PRISMA statement. BMJ. 2009;339:b2535.

11. Adedimeji A, Ajeh R, Dzudie A, Kendowo E, Fuhngwa N, Nsame D, et al. Cervical human papillomavirus DNA detection in women living with HIV and HIV-uninfected women living in Limbe, Cameroon. J Clin Virol. 2020;128:104445.

12. Saville M, Hawkes D, Keung M, Ip E, Silvers J, Sultana F, et al. Analytical performance of HPV assays on vaginal self-collected vs practitioner-collected cervical samples: the SCoPE study. J Clin Virol. 2020;127:104375.

13. Kuriakose S, Sabeena S, Binesh D, Abdulmajeed J, Ravishankar N, Ramachandran A, et al. Diagnostic accuracy of self-collected vaginal samples for HPV DNA detection in women from South India. Int J Gynaecol Obstet. 2020;149(2):219-24.

14. Satake H, Inaba N, Kanno K, Mihara M, Takagi Y, Kondo N, et al. Comparison study of self-sampled and physician-sampled specimens for high-risk human papillomavirus test and cytology. Acta Cytol. 2020;64(5):433-41.

15. Haguenoer K, Giraudeau B, Gaudy-Graffin C, de Pinieux I, Dubois F, Trignol-Viguier N, et al. Accuracy of dry vaginal self-sampling for detecting high-risk human papillomavirus infection in cervical cancer screening: a cross-sectional study. Gynecol Oncol. 2014;134(2):302-8.

16. Catarino R, Vassilakos P, Bilancioni A, Bougel S, Boukrid M, Meyer-Hamme U, et al. Accuracy of self-collected vaginal dry swabs using the Xpert human papillomavirus assay. PLoS One. 2017;12(7):e0181905.

17. Guan Y, Gravitt PE, Howard R, Eby YJ, Wang S, Li B, et al. Agreement for HPV genotyping detection between self-collected specimens on a FTA cartridge and clinician-collected specimens. J Virol Methods. 2013;189(1):167-71.

18. Phoolcharoen N, Kantathavorn N, Krisorakun W, Sricharunrat T, Teerayathanakul N, Taepisitpong C, et al. Agreement of self- and physician-collected samples for detection of high-risk human papillomavirus infections in women attending a colposcopy clinic in Thailand. BMC Res Notes. 2018;11(1):136.

19. Dijkstra MG, Heideman DA, van Kemenade FJ, Hogewoning KJ, Hesselink AT, Verkuijten MC, et al. Brush-based self-sampling in combination with GP5+/6+-PCR-based hrHPV testing: high concordance with physician-taken cervical scrapes for HPV genotyping and detection of high-grade CIN. J Clin Virol. 2012;54(2):147-51.

20. McLarty JW, Williams DL, Loyd S, Hagensee ME. Cervical human papillomavirus testing with two home self-collection methods compared with a standard clinically collected sampling method. Sex Transm Dis. 2019;46(10):670-5.

21. Chang CC, Tseng CJ, Liu WW, Jain S, Horng SG, Soong YK, et al. Clinical evaluation of a new model of self-obtained method for the assessment of genital human papilloma virus infection in an underserved population. Chang Gung Med J. 2002;25(10):664-71.

22. Safaeian M, Kiddugavu M, Gravitt PE, Ssekasanvu J, Murokora D, Sklar M, et al. Comparability of self-collected vaginal swabs and physician-collected cervical swabs for detection of human papillomavirus infections in Rakai, Uganda. Sex Transm Dis. 2007;34(7):429-36.

23. Latiff LA, Ibrahim Z, Pei CP, Rahman SA, Akhtari-Zavare M. Comparative assessment of a self-sampling device and gynecologist sampling for cytology and HPV DNA detection in a rural and low resource setting: Malaysian experience. Asian Pac J Cancer Prev. 2015;16(18):8495-501.

24. Gage JC, Partridge EE, Rausa A, Gravitt PE, Wacholder S, Schiffman M, et al. Comparative performance of human papillomavirus DNA testing using novel sample collection methods. J Clin Microbiol. 2011;49(12):4185-9.

25. Bergengren L, Kaliff M, Larsson GL, Karlsson MG, Helenius G. Comparison between professional sampling and self-sampling for HPV-based cervical cancer screening among postmenopausal women. Int J Gynaecol Obstet. 2018;142(3):359-64.

26. Nutthachote P, Oranratanaphan S, Termrungruanglert W, Triratanachat S, Chaiwongkot A, Baedyananda F, et al. Comparison of detection rate of high risk HPV infection between self-collected HPV testing and clinician-collected HPV testing in cervical cancer screening. Taiwan J Obstet Gynecol. 2019;58(4):477-81.

27. Lack N, West B, Jeffries D, Ekpo G, Morison L, Soutter WP, et al. Comparison of non-invasive sampling methods for detection of HPV in rural African women. Sex Transm Infect. 2005;81(3):239-41.

28. Castle PE, Aftab A, Saint-Jean G, Mendez L. Detection of carcinogenic human papillomavirus in specimens collected with a novel self-sampling device. J Clin Microbiol. 2006;44(6):2158-9.

29. Chernesky M, Jang D, Gilchrist J, Elit L, Lytwyn A, Smieja M, et al. Evaluation of a new APTIMA specimen collection and transportation kit for high-risk human papillomavirus E6/E7 messenger RNA in cervical and vaginal samples. Sex Transm Dis. 2014;41(6):365-8.

30. Daponte A, Pournaras S, Mademtzis I, Hadjichristodoulou C, Kostopoulou E, Maniatis AN, et al. Evaluation of HPV 16 PCR detection in self- compared with clinician-collected samples in women referred for colposcopy. Gynecol Oncol. 2006;103(2):463-6.

31. Qin Y, Zhang H, Marlowe N, Fei M, Yu J, Lei X, et al. Evaluation of human papillomavirus detection by Abbott m2000 system on samples collected by FTA Elute™ Card in a Chinese HIV-1 positive population. J Clin Virol. 2016;85:80-5.

32. Chen Q, Du H, Zhang R, Zhao JH, Hu QC, Wang C, et al. Evaluation of novel assays for the detection of human papilloma virus in self-collected samples for cervical cancer screening. Genet Mol Res. 2016;15(2).

33. Toliman PJ, Kaldor JM, Badman SG, Phillips S, Tan G, Brotherton JML, et al. Evaluation of self-collected vaginal specimens for the detection of high-risk human papillomavirus infection and the prediction of high-grade cervical intraepithelial lesions in a high-burden, low-resource setting. Clin Microbiol Infect. 2019;25(4):496-503.

34. Wong EL, Chan PK, Chor JS, Cheung AW, Huang F, Wong SY. Evaluation of the impact of human papillomavirus DNA self-sampling on the uptake of cervical cancer screening. Cancer Nurs. 2016;39(1):E1-E11.

35. Bonilla-Osma LJ, Amaya-Guio J, Olaya-García P, Bonilla-Bula L. Evaluation of the usefulness of a device for human papilloma virus DNA collection and preservation in self-collected cervicovaginal samples stored dry in women with cervical dysplasia, Bogotá, Colombia. Rev Colomb Obstet Ginecol. 2018;69(3):179-88.

36. Chen K, Ouyang Y, Hillemanns P, Jentschke M. Excellent analytical and clinical performance of a dry self-sampling device for human papillomavirus detection in an urban Chinese referral population. J Obstet Gynaecol Res. 2016;42(12):1839-45.

37. Esber A, Norris A, Jumbe E, Kandodo J, Nampandeni P, Reese PC, et al. Feasibility, validity and acceptability of self-collected samples for human papillomavirus (HPV) testing in rural Malawi. Malawi Med J. 2018;30(2):61-6.

38. Campos KL, Machado AP, Almeida FG, Bonin CM, Prata TT, Almeida LZ, et al. Good agreements between self and clinician-collected specimens for the detection of human papillomavirus in Brazilian patients. Mem Inst Oswaldo Cruz. 2014;109(3):352-5.

39. Tranberg M, Jensen JS, Bech BH, Blaakær J, Svanholm H, Andersen B. Good concordance of HPV detection between cervico-vaginal self-samples and general practitioner-collected samples using the Cobas 4800 HPV DNA test. BMC Infect Dis. 2018;18(1):348.

40. Ketelaars PJ, Bosgraaf RP, Siebers AG, Massuger LF, van der Linden JC, Wauters CA, et al. High-risk human papillomavirus detection in self-sampling compared to physician-taken smear in a responder population of the Dutch cervical screening: results of the VERA study. Prev Med. 2017;101:96-101.

41. Castle PE, Gage JC, Partridge EE, Rausa A, Gravitt PE, Scarinci IC. Human papillomavirus genotypes detected in clinician-collected and self-collected specimens from women living in the Mississippi Delta. BMC Infect Dis. 2013;13:5.

42. Wang R, Lee K, Gaydos CA, Anderson J, Keller J, Coleman J. Performance and acceptability of self-collected human papillomavirus testing among women living with HIV. Int J Infect Dis. 2020;99:452-7.

43. Igidbashian S, Boveri S, Radice D, Casadio C, Spolti N, Sandri MT, et al. Performance of self-sampled HPV test in comparison with liquid based cytology. Eur J Obstet Gynecol Reprod Biol. 2014;177:72-6.

44. Dannecker C, Siebert U, Thaler CJ, Kiermeir D, Hepp H, Hillemanns P. Primary cervical cancer screening by self-sampling of human papillomavirus DNA in internal medicine outpatient clinics. Ann Oncol. 2004;15(6):863-9.

45. Holanda F Jr, Castelo A, Veras TM, de Almeida FM, Lins MZ, Dores GB. Primary screening for cervical cancer through self sampling. Int J Gynaecol Obstet. 2006;95(2):179-84.

46. Harper DM, Noll WW, Belloni DR, Cole BF. Randomized clinical trial of PCR-determined human papillomavirus detection methods: self-sampling versus clinician-directed – biologic concordance and women's preferences. Am J Obstet Gynecol. 2002;186(3):365-73.

47. Leinonen MK, Schee K, Jonassen CM, Lie AK, Nystrand CF, Rangberg A, et al. Safety and acceptability of human papillomavirus testing of self-collected specimens: a methodologic study of the impact of collection devices and HPV assays on sensitivity for cervical cancer and high-grade lesions. J Clin Virol. 2018;99-100:22-30.

48. Obiri-Yeboah D, Adu-Sarkodie Y, Djigma F, Hayfron-Benjamin A, Abdul L, Simpore J, et al. Self-collected vaginal sampling for the detection of genital human papillomavirus (HPV) using care HPV among Ghanaian women. BMC Womens Health. 2017;17(1):86.

49. Surriabre P, Allende G, Prado M, Cáceres L, Bellot D, Torrico A, et al. Self-sampling for human papillomavirus DNA detection: a preliminary study of compliance and feasibility in Bolivia. BMC Womens Health. 2017;17(1):135.

50. De Alba I, Anton-Culver H, Hubbell FA, Ziogas A, Hess JR, Bracho A, et al. Self-sampling for human papillomavirus in a community setting: feasibility in Hispanic women. Cancer Epidemiol Biomarkers Prev. 2008;17(8):2163-8.

51. Lim LM, Chan MF, Win PP, Shen L, Arunachalam I, Ng SY, et al. Self-sampling HPV DNA test for cervical cancer screening in Singapore: a prospective study. Ann Acad Med Singap. 2022;51(11):733-5.

52. Petignat P, Hankins C, Walmsley S, Money D, Provencher D, Pourreaux K, et al. Self-sampling is associated with increased detection of human papillomavirus DNA in the genital tract of HIV-seropositive women. Clin Infect Dis. 2005;41(4):527-34.

53. Agorastos T, Dinas K, Lloveras B, Font R, Kornegay JR, Bontis J, et al. Self-sampling versus physician-sampling for human papillomavirus testing. Int J STD AIDS. 2005;16(11):727-9.

54. Asciutto KC, Ernstson A, Forslund O, Borgfeldt C. Self-sampling with HPV mRNA analyses from vagina and urine compared with cervical samples. J Clin Virol. 2018;101:69-73.

55. Jentschke M, Chen K, Arbyn M, Hertel B, Noskowicz M, Soergel P, et al. Direct comparison of two vaginal self-sampling devices for the detection of human papillomavirus infections. J Clin Virol. 2016;82:46-50.

56. Asciutto KC, Henningsson AJ, Borgfeldt H, Darlin L, Borgfeldt C. Vaginal and urine self-sampling compared to cervical sampling for HPV-testing with the Cobas 4800 HPV test. Anticancer Res. 2017;37(8):4183-7.

57. Boggan JC, Walmer DK, Henderson G, Chakhtoura N, McCarthy SH, Beauvais HJ, et al. Vaginal self-sampling for human papillomavirus infection as a primary cervical cancer screening tool in a Haitian population. Sex Transm Dis. 2015;42(11):655-9.

58. Islam JY, Mutua MM, Kabare E, Manguro G, Hudgens MG, Poole C, et al. High-risk human papillomavirus messenger RNA testing in wet and dry self-collected specimens for high-grade cervical lesion detection in Mombasa, Kenya. Sex Transm Dis. 2020;47(7):464-72.

59. Karwalajtys T, Howard M, Sellors JW, Kaczorowski J. Vaginal self sampling versus physician cervical sampling for HPV among younger and older women. Sex Transm Infect. 2006;82(4):337-9.

60. Rosenbaum AJ, Gage JC, Alfaro KM, Ditzian LR, Maza M, Scarinci IC, et al. Acceptability of self-collected versus provider-collected sampling for HPV DNA testing among women in rural El Salvador. Int J Gynaecol Obstet. 2014;126(2):156-60.

61. Waller J, McCaffery K, Forrest S, Szarewski A, Cadman L, Austin J, et al. Acceptability of unsupervised HPV self-sampling using written instructions. J Med Screen. 2006;13(4):208-13.

62. El-Zein M, Bouten S, Louvanto K, Gilbert L, Gotlieb W, Hemmings R, et al. Validation of a new HPV self-sampling device for cervical cancer screening: the Cervical and Self-Sample In Screening (CASSIS) study. Gynecol Oncol. 2018;149(3):491-7.

63. Oranratanaphan S, Termrungruanglert W, Khemapech N. Acceptability of self-sampling HPV testing among Thai women for cervical cancer screening. Asian Pac J Cancer Prev. 2014;15(17):7437-41.

64. Bakiewicz A, Rasch V, Mwaiselage J, Linde DS. "The best thing is that you are doing it for yourself" – Perspectives on acceptability and feasibility of HPV self-sampling among cervical cancer screening clients in Tanzania: a qualitative pilot study. BMC Womens Health. 2020;20(1):65.

65. Guan Y, Castle PE, Wang S, Li B, Feng C, Ci P, et al. A cross-sectional study on the acceptability of self-collection for HPV testing among women in rural China. Sex Transm Infect. 2012;88(7):490-4.

66. Khoo SP, Lim WT, Rajasuriar R, Nasir NH, Gravitt P, Woo YL. The acceptability and preference of vaginal self-sampling for human papillomavirus (HPV) testing among a multi-ethnic Asian female population. Cancer Prev Res. 2021;14(1):105-12.

67. Taku O, Meiring TL, Gustavsson I, Phohlo K, Garcia-Jardon M, Mbulawa ZZ, et al. Acceptability of self-collection for human papillomavirus detection in the Eastern Cape, South Africa. PLoS One. 2020;15(11):e0241781.

68. Anhang R, Nelson JA, Telerant R, Chiasson MA, Wright TC Jr. Acceptability of self-collection of specimens for HPV DNA testing in an urban population. J Womens Health. 2005;14(8):721-8.

69. Phoolcharoen N, Kantathavorn N, Krisorakun W, Taepisitpong C, Krongthong W, Saeloo S. Acceptability of self-sample human papillomavirus testing among Thai women visiting a colposcopy clinic. J Community Health. 2018;43(3):611-5.

70. Kohler RE, Elliott T, Monare B, Moshashane N, Ramontshonyana K, Chatterjee P, et al. HPV self-sampling acceptability and preferences among women living with HIV in Botswana. Int J Gynaecol Obstet. 2019;147(3):332-8.

71. Berner A, Hassel SB, Tebeu PM, Untiet S, Kengne-Fosso G, Navarria I, et al. Human papillomavirus self-sampling in Cameroon: women's uncertainties over the reliability of the method are barriers to acceptance. J Low Genit Tract Dis. 2013;17(3):235-41.

72. Szarewski A, Cadman L, Mallett S, Austin J, Londesborough P, Waller J, et al. Human papillomavirus testing by self-sampling: assessment of accuracy in an unsupervised clinical setting. J Med Screen. 2007;14(1):34-42.

73. Manguro GO, Masese LN, Mandaliya K, Graham SM, McClelland RS, Smith JS. Preference of specimen collection methods for human papillomavirus detection for cervical cancer screening: a cross-sectional study of high-risk women in Mombasa, Kenya. Reprod Health. 2018;15(1):206.

74. Igidbashian S, Boveri S, Spolti N, Radice D, Sandri MT, Sideri M. Self-collected human papillomavirus testing acceptability: comparison of two self-sampling modalities. J Womens Health. 2011;20(3):397-402.

75. Saidu R, Moodley J, Tergas A, Momberg M, Boa R, Wright T, et al. South African women's perspectives on self-sampling for cervical cancer screening: a mixed-methods study. S Afr Med J. 2018;109(1):47-52.

76. Dzuba IG, Díaz EY, Allen B, Leonard YF, Lazcano Ponce EC, Shah KV, et al. The acceptability of self-collected samples for HPV testing vs. the pap test as alternatives in cervical cancer screening. J Womens Health Gend Based Med. 2002;11(3):265-75.

77. Van Baars R, Bosgraaf RP, ter Harmsel BW, Melchers WJ, Quint WG, Bekkers RL. Dry storage and transport of a cervicovaginal self-sample by use of the Evalyn Brush, providing reliable human papillomavirus detection combined with comfort for women. J Clin Microbiol. 2012;50(12):3937-43.

78. Serrano B, Ibáñez R, Robles C, Peremiquel-Trillas P, de Sanjosé S, Bruni L. Worldwide use of HPV self-sampling for cervical cancer screening. Prev Med. 2022;154:106900.

79. Nelson EJ, Maynard BR, Loux T, Fatla J, Gordon R, Arnold LD. The acceptability of self-sampled screening for HPV DNA: a systematic review and meta-analysis. Sex Transm Infect. 2017;93(1):56-61.

80. Cho HW, Shim SR, Lee JK, Hong JH. Accuracy of human papillomavirus tests on self-collected urine versus clinician-collected samples for the detection of cervical precancer: a systematic review and meta-analysis. J Gynecol Oncol. 2022;33(1):e4.

81. Racey CS, Withrow DR, Gesink D. Self-collected HPV testing improves participation in cervical cancer screening: a systematic review and meta-analysis. Can J Public Health. 2013;104(2):e159-66.

82. Giorgi Rossi P, Marsili LM, Camilloni L, Iossa A, Lattanzi A, Sani C, et al. The effect of self-sampled HPV testing on participation to cervical cancer screening in Italy: a randomised controlled trial (ISRCTN96071600). Br J Cancer. 2011;104(2):248-54.

83. Lam JU, Rebolj M, Møller Ejegod D, Pedersen H, Rygaard C, Lynge E, et al. Human papillomavirus self-sampling for screening nonattenders: opt-in pilot implementation with electronic communication platforms. Int J Cancer. 2017;140(10):2212-9.

84. Yeh PT, Kennedy CE, de Vuyst H, Narasimhan M. Self-sampling for human papillomavirus (HPV) testing: a systematic review and meta-analysis. BMJ Glob Health. 2019;4(3):e001351.

85. McCaffery K, Waller J, Nazroo J, Wardle J. Social and psychological impact of HPV testing in cervical screening: a qualitative study. Sex Transm Infect. 2006;82(2):169-74.

86. Arbyn M, Smith SB, Temin S, Sultana F, Castle P. Detecting cervical precancer and reaching underscreened women by using HPV testing on self samples: updated meta-analyses. BMJ. 2018;363:k4823.

87. Klischke L, von Ehr J, Kohls F, Kampers J, Hülse F, Schmitz M, et al. Performance of a six-methylation-marker assay on self-collected cervical samples: a feasibility study. J Virol Methods. 2021;295:114219.

88. Daponte A, Michail G, Daponte AI, Daponte N, Valasoulis G. Urine HPV in the context of genital and cervical cancer screening: an update of current literature. Cancers. 2021;13(7):1640.

89. Wentzensen N, von Knebel Doeberitz M. Biomarkers in cervical cancer screening. Dis Markers. 2007;23(4):315-30.

90. Cho HW, Hong JH, Lee JK. Detection of high-risk human papillomavirus infection and treatment of high-grade vaginal intraepithelial neoplasia: a single-institution study. Int J Gynaecol Obstet. 2021;154(2):227-32.

91. World Health Organization. Global strategy to accelerate the elimination of cervical cancer as a public health concern [homepage]. Geneva: WHO; 2020. Available from: https://www.who.int/publications/i/item/9789240014107

Published

2025-03-05

How to Cite

Autocolheita vaginal versus colheita por profissional de saúde para rastreio do cancro do colo do útero: uma revisão sistemática com meta-análise de precisão e aceitabilidade. (2025). Portuguese Journal of Family Medicine and General Practice, 41(1), 52-64. https://doi.org/10.32385/rpmgf.v41i1.13988