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Cannula With Long and Narrow Tubing vs Short Binasal Prongs for Noninvasive Ventilation in Preterm Infants: Noninferiority Randomized Clinical Trial

机译:套管长而狭窄的管道与早产儿的非侵入性通风的短二合一叉子:非事实体随机临床试验

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ImportanceUse of cannulas with long and narrow tubing (CLNT) has gained increasing popularity for applying noninvasive respiratory support for newborn infants thanks to ease of use, perceived patient comfort, and reduced nasal trauma. However, there is concern that this interface delivers reduced and suboptimal support.ObjectiveTo determine whether CLNT is noninferior to short binasal prongs and masks (SPM) when providing nasal intermittent positive pressure ventilation (NIPPV) in preterm infants.Design, Setting, and ParticipantsThis randomized controlled, unblinded, prospective noninferiority trial was conducted between December 2017 and December 2019 at 2 tertiary neonatal intensive care units. Preterm infants born between 24 weeks’ and 33 weeks and 6 days’ gestation were eligible if presented with respiratory distress syndrome with the need for noninvasive ventilatory support either as initial treatment after birth or after first extubation. Analysis was performed by intention to treat.InterventionsRandomization to NIPPV with either CLNT or SPM interface.Main Outcomes and MeasuresThe primary outcome was the need for intubation within 72 hours after NIPPV treatment began. Noninferiority margin was defined as 15% or less absolute difference.ResultsOverall, 166 infants were included in this analysis, and infant characteristics and clinical condition (including fraction of inspired oxygen, Pco_(2), and pH level) were comparable at recruitment in the CLNT group (n?=?83) and SPM group (n?=?83). The mean (SD) gestational age was 29.3 (2.2) weeks vs 29.2 (2.5) weeks, and the mean (SD) birth weight was 1237 (414) g vs 1254 (448) g in the CLNT and SPM groups, respectively. Intubation within 72 hours occurred in 12 of 83 infants (14%) in the CLNT group and in 15 of 83 infants (18%) in the SPM group (risk difference, ?3.6%; 95% CI, ?14.8 to 7.6 [within the noninferiority margin], χ~(2)?P?=?.53). Moderate to severe nasal trauma was significantly less common in the CLNT group compared with the SPM group (4 [5%] vs 14 [17%];P?=?.01). There were no differences in other adverse events or in the course during hospitalization.Conclusions and RelevanceIn this study, CLNT was noninferior to SPM in providing NIPPV for preterm infants, while causing significantly less nasal trauma.
机译:重要的是,由于使用方便,患者感觉舒适,并减少了鼻腔创伤,长窄管插管(CLNT)在新生儿无创呼吸支持方面的应用越来越受欢迎。然而,有人担心该接口提供的支持减少且不理想。目的确定在为早产儿提供鼻腔间歇正压通气(NIPPV)时,CLNT是否优于短双尖牙和口罩(SPM)。设计、设置和参与者该随机对照、非盲、前瞻性非劣效性试验于2017年12月至2019年12月在2个三级新生儿重症监护病房进行。如果在出生后或首次拔管后出现呼吸窘迫综合征,且需要无创通气支持作为初始治疗,则在妊娠24周至33周和6天之间出生的早产儿符合条件。按意向治疗进行分析。干预通过CLNT或SPM接口向NIPPV发送命令。主要结果和测量主要结果是NIPPV治疗开始后72小时内需要插管。非劣效性边缘被定义为15%或更小的绝对差异。结果总体而言,166名婴儿被纳入本分析,CLNT组(n?=?83)和SPM组(n?=?83)的婴儿特征和临床状况(包括吸入氧分数、Pco_2和pH水平)在招募时具有可比性。CLNT组和SPM组的平均(SD)胎龄分别为29.3(2.2)周和29.2(2.5)周,平均(SD)出生体重分别为1237(414)克和1254(448)克。CLNT组83名婴儿中有12名(14%)在72小时内插管,SPM组83名婴儿中有15名(18%)在72小时内插管(风险差异为3.6%;95%可信区间为14.8-7.6[在非劣效范围内],χ2)?P?=?。53). 与SPM组相比,CLNT组中重度鼻外伤的发生率显著降低(4[5%]比14[17%];P=0.01)。住院期间,其他不良事件或病程没有差异。结论和相关性在这项研究中,CLNT在为早产儿提供NIPPV方面并不比SPM差,同时造成的鼻损伤显著减少。

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