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泌尿生殖道支原体检测在临床抗菌治疗中的应用
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Abstract:
目的:调查分析2021~2023年泌尿生殖道支原体的感染情况,并探讨三年间的耐药率变迁,为临床合理使用抗菌药物提供科学参考。方法:选取2021年1月~2023年12月就诊于广西中医药大学附属瑞康医院妇科、男性科的首诊患者作研究对象,收集支原体的检测结果进行回顾性分析,比较不同性别、不同年龄段的支原体感染情况,同时分析不同年份耐药率的变迁。结果:共纳入11,103例病例,阳性结果4771例,总阳性率为42.97% (4771/11,103例),其中34.9%为单独解脲支原体感染,共计3871阳性例数,其次为UU + MH混合感染,7.2% (802/11,103例),以及单独人型支原体的0.9%感染率(98/11,103例),三种类型的感染率存在显著差异(P < 0.05)。同时,在不同年龄阶段,男性感染阳性率均明显低于女性患者,P < 0.05。不同年份间感染率无差异(P > 0.05),但耐药率有差异,其中,单独UU感染时,甲砜霉素、克林霉素及司帕沙星耐药率逐年增长,差异均有统计学意义(P < 0.05);单独MH感染时,强力霉素、交沙霉素为全敏感;而UU + MH混合感染者对四种大环内酯类抗菌药物耐药率皆超过90%,且克林霉素、司帕沙星及加替沙星耐药率有增长趋势(P < 0.05)。结论:泌尿生殖道支原体最常见为解脲支原体感染,且女性感染率显著高于男性。在抗菌药物的使用中,甲砜霉素、克林霉素、司帕沙星等均有增长趋势,需提高临床监控,进一步加强抗菌药物的合理使用。
Objective: To investigate and analyze the infection status of Mycoplasma in the urogenital tract from 2021 to 2023, and to explore the changes in drug resistance rates over the three years, providing a scientific reference for the rational clinical use of antibacterial drugs. Methods: First-visit patients who visited the Gynecology and Andrology Departments of Ruikang Hospital Affiliated to Guangxi University of Chinese Medicine from January 2021 to December 2023 were selected as the research subjects. The test results of mycoplasma were collected for retrospective analysis. The mycoplasma infection situations of different genders and age groups were compared, and the changes in drug resistance rates in different years were analyzed simultaneously. Result: A total of 11,103 cases were included, with 4771 positive results, and the total positive rate was 42.97% (4771/11,103 cases). Among them, 34.9% were isolated Ureaplasma urealyticum infections, with a total of 3871 positive cases. The second was mixed UU + MH infections, with 7.2% (802/11,103 cases). And the 0.9% infection rate of Mycoplasma hominis alone (98/11,103 cases), there were significant differences in the infection rates among the three types (P < 0.05). Meanwhile, at different age stages, the positive rate of infection in males was significantly lower than that in female patients, P < 0.05. There was no difference in the infection rate among different years (P > 0.05), but there were differences in the drug resistance rate. Among them, when UU was infected alone, the drug resistance rates of thiamphenicol, clindamycin and spafloxacin increased year by year, and the differences were
[1] | Kokkayil, P. and Dhawan, B. (2015) Ureaplasma: Current Perspectives. Indian Journal of Medical Microbiology, 33, 205-214. https://doi.org/10.4103/0255-0857.154850 |
[2] | O’leary, W.M. (1990) Ureaplasmas and Human Disease. Critical Reviews in Microbiology, 17, 161-168. https://doi.org/10.3109/10408419009105723 |
[3] | Stol, K., Jans, J., Ott de Bruin, L., Unger, W. and van Rossum, A. (2021) Perinatal Infections with Ureaplasma. Pediatric Infectious Disease Journal, 40, S26-S30. https://doi.org/10.1097/inf.0000000000002859 |
[4] | Sweeney, E.L., Dando, S.J., Kallapur, S.G. and Knox, C.L. (2017) The Human Ureaplasma Species as Causative Agents of Chorioamnionitis. Clinical Microbiology Reviews, 30, 349-379. https://doi.org/10.1128/cmr.00091-16 |
[5] | Silwedel, C., Laube, M., Speer, C.P. and Glaser, K. (2024) The Role of Ureaplasma Species in Prenatal and Postnatal Morbidity of Preterm Infants: Current Concepts. Neonatology, 121, 627-635. https://doi.org/10.1159/000539613 |
[6] | Fan, W., Wang, Q., Liang, Z., Wang, J. and Zhang, L. (2023) Efficacy of Azithromycin in Treating Ureaplasma urealyticum: A Systematic Review and Meta-Analysis. BMC Infectious Diseases, 23, Article No. 163. https://doi.org/10.1186/s12879-023-08102-5 |
[7] | Andrews, W.W., Hauth, J.C., Cliver, S.P., Savage, K. and Goldenberg, R.L. (2003) Randomized Clinical Trial of Extended Spectrum Antibiotic Prophylaxis with Coverage for Ureaplasma urealyticum to Reduce Post-Cesarean Delivery Endometritis. Obstetrics & Gynecology, 101, 1183-1189. https://doi.org/10.1097/00006250-200306000-00010 |
[8] | 严丽, 管湘玉. 泌尿生殖道支原体感染现状及其耐药性调查[J]. 中国消毒学杂志, 2023, 40(7): 519-521. |
[9] | Taylor‐Robinson, D. and Lamont, R. (2010) Mycoplasmas in Pregnancy. BJOG: An International Journal of Obstetrics & Gynaecology, 118, 164-174. https://doi.org/10.1111/j.1471-0528.2010.02766.x |
[10] | Gimenes, F., Souza, R.P., Bento, J.C., Teixeira, J.J.V., Maria-Engler, S.S., Bonini, M.G., et al. (2014) Male Infertility: A Public Health Issue Caused by Sexually Transmitted Pathogens. Nature Reviews Urology, 11, 672-687. https://doi.org/10.1038/nrurol.2014.285 |
[11] | Zhu, X., Li, M., Cao, H., Yang, X. and Zhang, C. (2016) Epidemiology of Ureaplasma urealyticum and Mycoplasma Hominis in the Semen of Male Outpatients with Reproductive Disorders. Experimental and Therapeutic Medicine, 12, 1165-1170. https://doi.org/10.3892/etm.2016.3409 |
[12] | Bai, S., Li, Y., Hu, M., Wu, L., Shui, L., Wang, X., et al. (2022) Association of Sexually Transmitted Infection with Semen Quality in Men from Couples with Primary and Secondary Infertility. Asian Journal of Andrology, 24, 317-322. https://doi.org/10.4103/aja202164 |
[13] | Liu, K., Mao, X., Pan, F. and An, R.F. (2021) Effect and Mechanisms of Reproductive Tract Infection on Oxidative Stress Parameters, Sperm DNA Fragmentation, and Semen Quality in Infertile Males. Reproductive Biology and Endocrinology, 19, Article No. 97. https://doi.org/10.1186/s12958-021-00781-6 |
[14] | Viscardi, R.M. (2013) Ureaplasma Species: Role in Neonatal Morbidities and Outcomes. Archives of Disease in Childhood-Fetal and Neonatal Edition, 99, F87-F92. https://doi.org/10.1136/archdischild-2012-303351 |
[15] | Yoon, B.H., Romero, R., Lim, J., Shim, S., Hong, J., Shim, J., et al. (2003) The Clinical Significance of Detecting Ureaplasma urealyticum by the Polymerase Chain Reaction in the Amniotic Fluid of Patients with Preterm Labor. American Journal of Obstetrics and Gynecology, 189, 919-924. https://doi.org/10.1067/s0002-9378(03)00839-1 |
[16] | Horowitz, S., Mazor, M., Horowitz, J., Porath, A. and Glezerman, M. (1995) Antibodies to Ureaplasma urealyticum in Women with Intraamniotic Infection and Adverse Pregnancy Outcome. Acta Obstetricia et Gynecologica Scandinavica, 74, 132-136. https://doi.org/10.3109/00016349509008922 |
[17] | Oeser, C., Pond, M., Butcher, P., Bedford Russell, A., Henneke, P., Laing, K., et al. (2020) PCR for the Detection of Pathogens in Neonatal Early Onset Sepsis. PLOS ONE, 15, e0226817. https://doi.org/10.1371/journal.pone.0226817 |
[18] | Chu, A., de St. Maurice, A., Sim, M.S. and Kallapur, S.G. (2020) Neonatal Mycoplasma and Ureaplasma Infections. Pediatric Annals, 49, e305-e12. https://doi.org/10.3928/19382359-20200625-01 |
[19] | Gerber, S., Vial, Y., Hohlfeld, P. and Witkin, S.S. (2003) Detection of Ureaplasma urealyticum in Second‐Trimester Amniotic Fluid by Polymerase Chain Reaction Correlates with Subsequent Preterm Labor and Delivery. The Journal of Infectious Diseases, 187, 518-521. https://doi.org/10.1086/368205 |
[20] | Glaser, K., Gradzka-Luczewska, A., Szymankiewicz-Breborowicz, M., Kawczynska-Leda, N., Henrich, B., Waaga-Gasser, A.M., et al. (2019) Perinatal Ureaplasma Exposure Is Associated with Increased Risk of Late Onset Sepsis and Imbalanced Inflammation in Preterm Infants and May Add to Lung Injury. Frontiers in Cellular and Infection Microbiology, 9, Article No. 68. https://doi.org/10.3389/fcimb.2019.00068 |
[21] | Chen, X., Huang, X., Zhou, Q., Kang, H., Qiu, H., Shi, L., et al. (2024) Association between Ureaplasma urealyticum Colonization and Bronchopulmonary Dysplasia in Preterm Infants: A Systematic Review and Meta-Analysis. Frontiers in Pediatrics, 12, Article ID: 1436568. https://doi.org/10.3389/fped.2024.1436568 |