用 LED 光评估出生时皮肤成熟度及其与肺成熟度的关系临床试验的次要结果

Gabriela Silveira Neves, Z. Reis, Roberta Romanelli, James Batchelor
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引用次数: 0

摘要

由于全球范围内的不平等,临床医生在评估婴儿出生时的肺成熟度时面临障碍。然而,仅根据胎龄来预测呼吸窘迫综合征(RDS)可能性的检测策略并不能提供一种全面的方法来应对结果不确定的挑战。我们假设,对皮肤成熟度的无创评估可能预示着肺成熟度。 本研究旨在评估新生儿皮肤成熟度与 RDS 发生率之间的关联。 我们在一项前瞻性队列研究中进行了病例对照,这是一项多中心临床试验的次要终点。这项研究在巴西 5 个城市的高度复杂围产期护理参考中心进行。在队列研究的 781 名新生儿中,有 640 名被选中进行病例对照分析。患有 RDS 的新生儿为病例组,无 RDS 的新生儿为对照组。所有患有其他呼吸系统疾病的新生儿均被排除在外。新生儿足底皮肤成熟度的评估是通过一个光学装置进行的,该装置通过 LED 传感器获取反射信号。该设备已通过验证,可测量和记录皮肤反射率。与呼吸系统结果相关的临床数据来自新生儿 72 小时随访期间的医疗记录,或直至出院或死亡,以先发生者为准。主要结果测量是使用单变量和多变量二元逻辑回归分析皮肤反射率与 RDS 之间的关系。此外,我们还评估了皮肤反光与新生儿重症监护室(NICU)入院和呼吸支持需求等因素之间的联系。 在 604 名新生儿中,470 名(73.4%)来自 RDS 组,170 名(26.6%)来自对照组。与对照组相比,RDS 组新生儿的胎龄(31.6 周对 39.1 周,P<.001)和出生体重(1491 克对 3121 克,P<.001)均小于对照组。皮肤反射率与 RDS 相关(几率比 [OR] 0.982,95% CI 0.979-0.985,R2=0.632,P<.001)。经产前皮质类固醇和出生体重等辅助因子调整后,这一关系仍很明显(OR 0.994,95% CI 0.990-0.998,R2=0.843,P<.001)。次要结果还显示了皮肤反射率的差异。需要通气支持的新生儿与不需要通气支持的新生儿之间的平均差异为 0.219(95% CI 0.200-0.238),需要入住新生儿重症监护室的新生儿与不需要入住新生儿重症监护室的新生儿之间的平均差异为 0.223(95% CI 0.205-0.241)。皮肤反射率与通气支持相关(OR 0.996,95% CI 0.992-0.999,R2=0.814,P=.01),与入住新生儿重症监护室相关(OR 0.994,95% CI 0.990-0.998,R2=0.867,P=.004)。 我们的研究结果利用皮肤评估的间接方法提出了出生时肺部不成熟的潜在标志物。本研究利用 RDS 临床条件和医疗设备证明了肺和皮肤成熟度之间的同步性。 Registro Brasileiro de Ensaios Clínicos (ReBEC) RBR-3f5bm5; https://tinyurl.com/9fb7zrdb RR2-10.1136/bmjopen-2018-027442
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Assessment of Skin Maturity by LED Light at Birth and Its Association With Lung Maturity: Clinical Trial Secondary Outcomes
Clinicians face barriers when assessing lung maturity at birth due to global inequalities. Still, strategies for testing based solely on gestational age to predict the likelihood of respiratory distress syndrome (RDS) do not offer a comprehensive approach to addressing the challenge of uncertain outcomes. We hypothesize that a noninvasive assessment of skin maturity may indicate lung maturity. This study aimed to assess the association between a newborn’s skin maturity and RDS occurrence. We conducted a case-control nested in a prospective cohort study, a secondary endpoint of a multicenter clinical trial. The study was carried out in 5 Brazilian urban reference centers for highly complex perinatal care. Of 781 newborns from the cohort study, 640 were selected for the case-control analysis. Newborns with RDS formed the case group and newborns without RDS were the controls. All newborns with other diseases exhibiting respiratory manifestations were excluded. Skin maturity was assessed from the newborn's skin over the sole by an optical device that acquired a reflection signal through an LED sensor. The device, previously validated, measured and recorded skin reflectance. Clinical data related to respiratory outcomes were gathered from medical records during the 72-hour follow-up of the newborn, or until discharge or death, whichever occurred first. The main outcome measure was the association between skin reflectance and RDS using univariate and multivariate binary logistic regression. Additionally, we assessed the connection between skin reflectance and factors such as neonatal intensive care unit (NICU) admission and the need for ventilatory support. Out of 604 newborns, 470 (73.4%) were from the RDS group and 170 (26.6%) were from the control group. According to comparisons between the groups, newborns with RDS had a younger gestational age (31.6 vs 39.1 weeks, P<.001) and birth weight (1491 vs 3121 grams, P<.001) than controls. Skin reflectance was associated with RDS (odds ratio [OR] 0.982, 95% CI 0.979-0.985, R2=0.632, P<.001). This relationship remained significant when adjusted by the cofactors antenatal corticosteroid and birth weight (OR 0.994, 95% CI 0.990-0.998, R2=0.843, P<.001). Secondary outcomes also showed differences in skin reflectance. The mean difference was 0.219 (95% CI 0.200-0.238) between newborns that required ventilatory support versus those that did not and 0.223 (95% CI 0.205-0.241) between newborns that required NICU admission versus those that did not. Skin reflectance was associated with ventilatory support (OR 0.996, 95% CI 0.992-0.999, R2=0.814, P=.01) and with NICU admission (OR 0.994, 95% CI 0.990-0.998, R2=0.867, P=.004). Our findings present a potential marker of lung immaturity at birth using the indirect method of skin assessment. Using the RDS clinical condition and a medical device, this study demonstrated the synchrony between lung and skin maturity. Registro Brasileiro de Ensaios Clínicos (ReBEC) RBR-3f5bm5; https://tinyurl.com/9fb7zrdb RR2-10.1136/bmjopen-2018-027442
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