Gabrielli Liliana, Pavoni Matteo, Monari Francesca, Baiesi Pillastrini Federico, Bonasoni Maria Paola, Locatelli Chiara, Bisulli Maria, Vancini Alessandra, Cataneo Ilaria, Ortalli Margherita, Piccirilli Giulia, Cantiani Alessia, Ambretti Simone, Facchinetti Fabio, Lazzarotto Tiziana
Microbiology Unit, IRCCS Azienda Ospedaliero-Universitaria di Bologna, 40138 Bologna, Italy.
Microbiology, Department of Medical and Surgical Sciences, University of Bologna, 40138 Bologna, Italy.
Microorganisms. 2025 Jan 2;13(1):71. doi: 10.3390/microorganisms13010071.
Although several conditions and specific risk factors have been associated with stillbirth (SB), in most of the cases it is difficult to identify the definitive etiopathology and cause of death. Specifically, the role of infections in SB is still debated. Our aim was to study maternal, placental, and fetal tissues in cases of SB in order to define the causative link between infections and fetal death, through a multidisciplinary clinical audit.
Between 2014 and 2022, microbiological investigations on maternal, placental and fetal samples of SB cases were performed according to a standardized protocol including serology, cultures, and molecular biology. Autopsies and placental examination were mandatory in all SB cases.
A total of 182 cases of SB were investigated. Bacteria were detected in 22.2% of vaginal swabs, 65% of placental biopsies, 29% of fetal blood, and 14.1% of oropharyngeal swabs. Vaginal and oropharyngeal swabs were positive for urogenital mycoplasmas in 25.2% and 8.6%, respectively. Positive results of microbiological investigations, in association with histological features suggestive of infection, were observed in six cases, indicating that fetal death was likely related to a bacterial infection. In one case, a high SARS-CoV-2 load was found in the placenta of a SB due to placental abruption.
Infections were likely associated with fetal death in 3.8% of cases. Thus, in developed countries, an infection, defined when positive microbiological findings are associated with histological evidence of organ damage, is a minor contributory factor in SB.
尽管几种情况和特定风险因素与死产(SB)相关,但在大多数情况下,很难确定确切的病因病理和死亡原因。具体而言,感染在死产中的作用仍存在争议。我们的目的是通过多学科临床审计研究死产病例中的母体、胎盘和胎儿组织,以确定感染与胎儿死亡之间的因果关系。
2014年至2022年期间,根据包括血清学、培养和分子生物学在内的标准化方案,对死产病例的母体、胎盘和胎儿样本进行了微生物学调查。所有死产病例均必须进行尸检和胎盘检查。
共调查了182例死产病例。在22.2%的阴道拭子、65%的胎盘活检组织、29%的胎儿血液和14.1%的咽拭子中检测到细菌。阴道拭子和咽拭子中泌尿生殖道支原体阳性率分别为25.2%和8.6%。6例观察到微生物学调查阳性结果,并伴有提示感染的组织学特征,表明胎儿死亡可能与细菌感染有关。1例因胎盘早剥导致死产的病例中,在胎盘中发现了高载量的严重急性呼吸综合征冠状病毒2(SARS-CoV-2)。
在3.8%的病例中,感染可能与胎儿死亡有关。因此,在发达国家,当微生物学阳性结果与器官损伤的组织学证据相关时所定义的感染,是死产中的一个次要促成因素。