Division of Obstetrics and Gynecology, University of Western Australia, Crawley, Western Australia, Australia; Center for Perinatal and Neonatal Medicine, Tohoku University Hospital, Sendai, Miyagi, Japan.
Center for Perinatal and Neonatal Medicine, Tohoku University Hospital, Sendai, Miyagi, Japan.
Am J Obstet Gynecol. 2019 Jul;221(1):69.e1-69.e17. doi: 10.1016/j.ajog.2019.03.001. Epub 2019 Mar 7.
Ex vivo uterine environment therapy is an experimental life support platform designed to reduce the risk of morbidity and mortality for extremely preterm infants born at the border of viability (21-24 weeks' gestation). To spare the functionally immature lung, this platform performs gas exchange via a membranous oxygenator connected to the umbilical vessels, and the fetus is submerged in a protective bath of artificial amniotic fluid. We and others have demonstrated the feasibility of extended survival with ex vivo uterine environment therapy therapy in late preterm fetuses; however, there is presently no evidence to show that the use of such a platform can support extremely preterm fetuses, the eventual translational target for therapy of this nature.
The objective of the study was to use our ex vivo uterine environment therapy platform to support the healthy maintenance of 600-700 g/95 days gestational age (equivalent to 24 weeks of human gestation) sheep fetuses. Primary outcome measures were as follows: (1) maintenance of key physiological variables; (2) absence of infection; (3) absence of brain injury; and (4) growth and cardiovascular function patterns matching that of noninstrumented, age-matched in utero controls.
Singleton fetuses from 8 ewes underwent surgical delivery at 95 days' gestation (term, 150 days). Fetuses were adapted to ex vivo uterine environment therapy and maintained for 120 hours with real-time monitoring of key physiological variables. Umbilical artery blood samples were regularly collected to assess blood gas data, differential counts, inflammation, and microbial load to exclude infection. Brain injury was evaluated by gross anatomical and histopathological approaches after euthanasia. Nine pregnant control animals were euthanized at 100 days' gestation to allow comparative postmortem analyses. Data were tested for mean differences with an analysis of variance.
Seven of 8 ex vivo uterine environment group fetuses (87.5%) completed 120 hours of therapy with key parameters maintained in a normal physiological range. There were no significant intergroup differences (P > .05) in final weight, crown-rump length, and body weight-normalized lung and brain weights at euthanasia compared with controls. There were no biologically significant differences in hematological parameters (total or differential leucocyte counts and plasma concentration of tumor necrosis factor-α and monocyte chemoattractant protein 1) (P > .05). Daily blood cultures were negative for aerobic and anaerobic growth in all ex vivo uterine environment animals. There was no difference in airspace consolidation between control and ex vivo uterine environment animals, and there was no increase in the number of lung cells staining positive for the T-cell marker CD3. There were no increases in interleukin-1, interleukin-6, interleukin-8, tumor necrosis factor-α, and monocyte chemoattractant protein 1 mRNA expression in lung tissues compared with the control group. No cases of intraventricular hemorrhage were observed, and white matter injury was identified in only 1 ex vivo uterine environment fetus.
For several decades, there has been little improvement in outcomes of extremely preterm infants born at the border of viability. In the present study, we report the use of artificial placenta technology to support, for the first time, extremely preterm ovine fetuses (equivalent to 24 weeks of human gestation) in a stable, growth-normal state for 120 hours. With additional refinement, the data generated by this study may inform a treatment option to improve outcomes for extremely preterm infants.
子宫外环境治疗是一种旨在降低极早产儿(21-24 孕周)出生时发病率和死亡率的实验性生命支持平台。为了避免功能不成熟的肺部受损,该平台通过连接脐带血管的膜式氧合器进行气体交换,胎儿则浸没在人工羊水的保护浴中。我们和其他人已经证明了晚期早产儿在子宫外环境治疗中延长生存的可行性;然而,目前尚无证据表明这种平台的使用可以支持极早产儿,这是这种治疗的最终转化目标。
本研究的目的是使用我们的子宫外环境治疗平台来支持 600-700g/95 天胎龄(相当于 24 周人类妊娠)绵羊胎儿的健康维持。主要观察指标如下:(1)维持关键生理变量;(2)无感染;(3)无脑损伤;(4)生长和心血管功能模式与非器械、年龄匹配的宫内对照组相匹配。
8 只母羊的单胎胎儿在 95 天胎龄(足月,150 天)行剖宫产术。胎儿适应子宫外环境治疗,并在实时监测关键生理参数的情况下维持 120 小时。定期采集脐动脉血样,评估血气数据、差异计数、炎症和微生物负荷,以排除感染。安乐死后通过大体解剖和组织病理学方法评估脑损伤。9 只妊娠对照动物在 100 天胎龄时安乐死,以便进行比较性死后分析。数据采用方差分析进行均值差异检验。
8 只子宫外环境组胎儿中有 7 只(87.5%)完成了 120 小时的治疗,关键参数维持在正常生理范围内。与对照组相比,最终体重、头臀长以及安乐死后体重归一化的肺和脑重量无显著组间差异(P>.05)。血液学参数(总或差异白细胞计数以及肿瘤坏死因子-α和单核细胞趋化蛋白 1 的血浆浓度)(P>.05)无生物学显著差异。每日血培养均为阴性,未检出需氧和厌氧生长。对照组和子宫外环境组的气腔实变无差异,并且 T 细胞标记物 CD3 染色阳性的肺细胞数量也无增加。与对照组相比,肺组织中白细胞介素-1、白细胞介素-6、白细胞介素-8、肿瘤坏死因子-α和单核细胞趋化蛋白 1mRNA 表达无增加。未观察到脑室出血,仅 1 只子宫外环境胎儿有白质损伤。
几十年来,极早产儿(出生于 24 周界限)的生存结局几乎没有改善。在本研究中,我们首次报告使用人工胎盘技术支持极早产儿(相当于 24 周人类妊娠)在稳定、生长正常的状态下维持 120 小时。通过进一步改进,本研究产生的数据可能为改善极早产儿的预后提供一种治疗选择。