CORRELACIÓN ENTRE VULVOVAGINITIS RECURRENTE E INFECCIONES DE TRANSMISIÓN SEXUAL
DOI:
https://doi.org/10.54620/cadesp.v18i1.1939Palabras clave:
Infecciones de Transmisión Sexual, Vaginosis Bacteriana, Candidiasis Vulvovaginal, Reacción en Cadena de la Polimerasa MultiplexResumen
El objetivo de este estudio fue correlacionar la vulvovaginitis recurrente y las Infecciones de Transmisión Sexual (ITS) y analizar la importancia de agregar la prueba de Reacción en Cadena de la Polimerasa (PCR) para ITS al estudio diagnóstico de la vulvovaginitis recurrente. Se adoptó el método de investigación descriptivo, transver-sal, observacional y retrospectivo. Se evaluaron las historias clínicas de 115 pacientes atendidas en un consulto-rio ginecológico, quienes tuvieron pruebas PCR positivas para ITS con algún microorganismo desde agosto de 2021 hasta octubre de 2023. Un gran número de estas pacientes, correspondiente al 26%, tuvieron secreciones vaginales recurrentes y Se demostró que al menos el 50% de ellas se curaron de estas secreciones después del tratamiento de las ITS. Parece que puede haber una relación entre la vulvovaginitis recurrente y las ITS, sin em-bargo, es importante ampliar este tema de investigación, ya que el estudio tiene limitaciones.
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Linhares IM, Amaral RL, Robial R, Eleutério Junior J. Vaginites e vaginoses. São Paulo: Federação Brasileira das Associações de Ginecologia e Obstetrícia (Febrasgo), 2018. (Protoco-lo Febrasgo – Ginecologia, nº 24/ Comissão Nacional Especializada em Doenças Infectoconta-giosas).
Protocolo Clínico e Diretrizes Terapêuticas para Atenção Integral às Pessoas com Infecções Sexualmente Transmissíveis – IST [recurso eletrônico] / Ministério da Saúde, Secretaria de Vigilância em Saúde, Departamento de Doenças de Condições Crônicas e Infecções Sexual-mente Transmissíveis. – Brasília : Ministério da Saúde, 2022.
Yuk YS, Choi JE, Kim JK. Age and sex trends of Gardnerella vaginalis infection in patients with sexually transmitted infections in Korea. Iranian Journal of Microbiology. 2021 Dec 22; DOI: https://doi.org/10.18502/ijm.v13i6.8079
Baek J-C, Jo H-C, Lee S-M, Park J-E, Cho I-A, Sung J-H. Prevalence of Pathogens and Other Microorganisms in Premenopausal and Postmenopausal Women with Vulvovaginal Symptoms: A Retrospective Study in a Single Institute in South Korea. Medicina. 2021 Jun 4;57(6):577. DOI: https://doi.org/10.3390/medicina57060577
Nardis C, Mosca L, Mastromarino P. Vaginal microbiota and viral sexually transmitted dis-eases. Ann Ig. 2013 Sep-Oct;25(5):443-56.
Faught BM, Reyes S. Characterization and Treatment of Recurrent Bacterial Vaginosis. Journal of Women’s Health. 2019 Sep 1;28(9):1218–26. DOI: https://doi.org/10.1089/jwh.2018.7383
Freitas F, Carlos Henrique Menke, Waldemar Augusto Rivoire, Eduardo Pandolfi Passos, Al E. Rotinas em ginecologia. Porto Alegre Artmed Editora; 2011.
Rosati D, Bruno M, Jaeger M, ten Oever J, Netea MG. Recurrent Vulvovaginal Candidia-sis: An Immunological Perspective. Microorganisms. 2020 Jan 21;8(2):144. DOI: https://doi.org/10.3390/microorganisms8020144
Lewis FMT, Bernstein KT, Aral SO. Vaginal Microbiome and Its Relationship to Behavior, Sexual Health, and Sexually Transmitted Diseases. Obstetrics & Gynecology [Internet]. 2017 Apr;129(4):643–54. DOI: https://doi.org/10.1097/AOG.0000000000001932
Van Houdt R, Ma B, Bruisten SM, Speksnijder AGCL, Ravel J, de Vries HJC. Lactobacil-lus iners-dominated vaginal microbiota is associated with increased susceptibility to Chlamyd-ia trachomatis infection in Dutch women: a case–control study. Sexually Transmitted Infec-tions. 2017 Sep 25;94(2):117–23. DOI: https://doi.org/10.1136/sextrans-2017-053133
Bardin MG, Giraldo PC, Benetti-Pinto CL, Sanches JM, Araujo CC de, Amaral RLG do. Habits of Genital Hygiene and Sexual Activity among Women with Bacterial Vaginosis and/or Vulvovaginal Candidiasis. Revista Brasileira de Ginecologia e Obstetrícia [Internet]. 2022 Apr 8;44:169–77 DOI: https://doi.org/10.1055/s-0041-1741536
Kebbi-Beghdadi C, Aeby S, Baud D, Greub G. Evaluation of a Multiplex Real-Time PCR Assay for Detecting Chlamydia trachomatis in Vaginal Samples. Diagnostics. 2022 May 4;12(5):1141. DOI: https://doi.org/10.3390/diagnostics12051141
Lima L deMiranda, Hoelzle CR, Simões RT, Lima MI de M, Fradico JRB, Mateo ECC, et al. Sexually Transmitted Infections Detected by Multiplex Real Time PCR in Asymptomatic Women and Association with Cervical Intraepithelial Neoplasia. Revista Brasileira de Gineco-logia e Obstetrícia [Internet]. 2018 Sep 1 [cited 2022 Nov 17];40:540–6 DOI: https://doi.org/10.1055/s-0038-1669994
Lins dos Santos R, Tonin Beneli Fontanezi C, da Silva Negreiros FD, Maria Correia Pequeno A. PERFIL CLÍNICO-EPIDEMIOLÓGICO DE PACIENTES ATENDIDOS EM UMA CLÍNICA ESCOLA DE UM CENTRO UNIVERSITÁRIO DE FORTALEZA. Cadernos ESP [Internet]. 29º de junho de 2020;14(1):30-7.
Marconi C, El-Zein M, Ravel J, Ma B, Lima MD, Carvalho NS, et al. Characterization of the vaginal microbiome in women of reproductive age from five regions in Brazil. Sexually Transmitted Diseases. 2020 Jun 8;Publish Ahead of Print. DOI: https://doi.org/10.1097/OLQ.0000000000001204
Ravel J, Gajer P, Abdo Z, Schneider GM, Koenig SSK, McCulle SL, et al. Vaginal microbiome of reproductive-age women. Proceedings of the National Academy of Sciences [Internet]. 2010 Jun 3;108(Supplement_1):4680–7. DOI: https://doi.org/10.1073/pnas.1002611107
Choe HS, Lee DS, Lee SJ, Hong SH, Park DC, Lee MK, et al. Performance of Any-plexTM II multiplex real-time PCR for the diagnosis of seven sexually transmitted infections: comparison with currently available methods. International Journal of Infectious Diseases. 2013 Dec;17(12):e1134–40. DOI: https://doi.org/10.1016/j.ijid.2013.07.011
Tamarelle J, Thiébaut ACM, de Barbeyrac B, Bébéar C, Ravel J, Delarocque-Astagneau E. The vaginal microbiota and its association with human papillomavirus, Chlamydia tracho-matis, Neisseria gonorrhoeae and Mycoplasma genitalium infections: a systematic review and meta-analysis. Clinical Microbiology and Infection. 2019 Jan;25(1):35–47. DOI: https://doi.org/10.1016/j.cmi.2018.04.019
Jonduo ME, Vallely LM, Wand H, Sweeney EL, Egli-Gany D, Kaldor J, et al. Adverse pregnancy and birth outcomes associated hominis, Ureaplasma urealyticum and Ureaplasma parvum: a systematic review and meta-analysis. BMJ Open. 2022 Aug;12(8):e062990. DOI: https://doi.org/10.1136/bmjopen-2022-062990
Xu Y, Hu J, Huang Y, Shi L. Maternal Ureaplasma exposure during pregnancy and the risk of preterm birth and BPD: a meta-analysis. Archives of Gynecology and Obstetrics. 2022 Mar 12;306(6):1863–72. DOI: https://doi.org/10.1007/s00404-022-06491-7
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Derechos de autor 2024 Cadernos ESP
Esta obra está bajo una licencia internacional Creative Commons Atribución 4.0.
Aceptado 2024-07-12
Publicado 2024-08-01
