Reproductive Medicine, Instituto Valenciano de Infertilidad-RMA Global Headquarters Madrid, Madrid, Spain.
Reproductive Medicine, Instituto Valenciano de Infertilidad-RMA Global Headquarters Madrid, Madrid, Spain.
Fertil Steril. 2023 Apr;119(4):618-623. doi: 10.1016/j.fertnstert.2022.12.022. Epub 2022 Dec 17.
To assess whether vaccination or the type of vaccine against SARS-CoV-2 affects ovarian function in an assisted reproduction treatment.
A retrospective and observational study.
University-affiliated private in vitro fertilization (IVF) center.
PATIENT(S): Five hundred one patients who had received the complete vaccination schedule.
INTERVENTION(S): Treatment before and after vaccination.
MAIN OUTCOME MEASURE(S): Parameters for both reproductive outcomes and IVF results in patients vaccinated RESULT(S): We included 510 patients, distributed as follows: 13.5% (n = 69) received a viral vector vaccine, either the adenovirus serotype 26 vector vaccine (Ad26.CoV2.S; Janssen; n = 31) or the chimpanzee adenovirus vector vaccine (ChAdOx; AstraZeneca; n = 38). The remaining 86.5% (n = 441) received an messenger RNA vaccine from either Pfizer-BioNTech (n = 336) or Moderna (n = 105). Sample size for the unexposed women was n = 1190. No differences were found in any of the evaluated parameters for both reproductive outcomes and IVF results in patients vaccinated with any adenovirus or messenger RNA vaccine. When we compared the results after vaccination with different types of vaccines between the exposed and unexposed groups, and similar results were obtained in the days of stimulation or the doses of administered follicle stimulating hormone. Finally, the numbers of oocytes were as follows: Johnson & Johnson (9.2 ± 2.6), AstraZeneca (7.7 ± 1.2), Moderna (11.3 ± 1.8), Pfizer (12.6 ± 1.0), and the unvaccinated group (10.2 ± 1.5), P=0.057.
CONCLUSION(S): These early results suggest no measurable detrimental effect on reproductive outcomes, regardless of the type of vaccine received.
评估 SARS-CoV-2 疫苗接种或疫苗类型是否会影响辅助生殖治疗中的卵巢功能。
回顾性和观察性研究。
大学附属私立体外受精(IVF)中心。
接受完整疫苗接种计划的 501 名患者。
接种疫苗前后的治疗。
接种疫苗患者的生殖结局和 IVF 结果参数。
我们纳入了 510 名患者,分布如下:13.5%(n=69)接种了病毒载体疫苗,分别为腺病毒血清型 26 载体疫苗(Ad26.CoV2.S;Janssen;n=31)或黑猩猩腺病毒载体疫苗(ChAdOx;阿斯利康;n=38)。其余 86.5%(n=441)接种了来自辉瑞-生物技术(n=336)或 Moderna(n=105)的信使 RNA 疫苗。未接种疫苗女性的样本量为 n=1190。接种任何腺病毒或信使 RNA 疫苗的患者在生殖结局和 IVF 结果的所有评估参数方面均无差异。当我们比较暴露组和未暴露组之间接种不同类型疫苗后的结果时,在刺激天数或给予的卵泡刺激素剂量方面也得到了类似的结果。最后,获得的卵母细胞数量如下:强生(9.2±2.6)、阿斯利康(7.7±1.2)、Moderna(11.3±1.8)、辉瑞(12.6±1.0)和未接种疫苗组(10.2±1.5),P=0.057。
这些早期结果表明,无论接种何种疫苗,都不会对生殖结局产生可衡量的不利影响。