Comparison of LISA technique and INSURE technique in the treatment of respiratory distress syndrome in premature infants
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摘要:
目的 探讨微创肺表面活性物质给药(less invasive surfactant administration,LISA)技术相较于插管-肺表面活性物质给药-拔管(intubate-surfactant-extubate, INSURE)技术在早产儿呼吸窘迫综合征(respiratory distress syndrome,RDS)中的应用疗效及对早产儿住院期间并发症的影响。 方法 选取2019年8月—2020年4月期间安徽省8所新生儿重症监护病房(NICU)收治的20例符合入组条件的患儿作为微创肺表面活性物质给药组(LISA组),采用LISA技术完成肺泡表面活性物质(PS)给药。另选取自2017年1月—2020年1月期间在安徽省立医院收治的36例患儿作为INSURE组,采用INSURE技术完成PS给药。收集并比较2组患儿及母亲的基本信息、给药前后的动脉血气值、给药时的副反应及住院期间的并发症和用氧情况。 结果 LISA组给药后的pH值较给药前升高(P<0.001),给药后的PaCO2值较给药前降低(P=0.005),但给药前后PaO2差异无统计学意义;INSURE组患儿在给药前后的pH值、PaCO2值及PaO2值均无明显改变。LISA组在给药24内的pH值在正常范围内的例数较INSURE组多[38.89%(7/18)vs. 23.33%(7/30),P=0.009];在给药过程中血氧饱和度下降情况2组差异有统计学意义[0(0.00%)vs. 3(15.00%),P=0.041];2组支气管肺发育不良(BPD)的发生率、无创失败率及无创辅助通气时间差异无统计学意义(均P>0.05)。 结论 LISA技术可以在有自主呼吸的患儿中进行,可明显改善肺泡通气,且不会增加并发症的发生率。 -
关键词:
- 微创肺表面活性物质给药技术 /
- 插管-肺表面活性物质给药-拔管技术 /
- 新生儿呼吸窘迫综合征 /
- 支气管肺发育不良
Abstract:Objective To compare the outcomes and side effects between the less invasive surfactant administration (LISA) and the intubate surfactant extubate (INSURE) method in premature infants with respiratory distress syndrome. Methods In the experimental group, 20 children who met the inclusion criteria were recruited from eight neonatal intensive care units in Anhui Province from August 2019 to April 2020 to complete pulmonary surfactant (PS) administration by LISA technology. In the control group, 36 children were recruited from Anhui Provincial Hospital from January 2017 to January 2020 to complete PS administration by INSURE technology. The basic information of children and mothers, arterial blood gas values before and after administration, oxygen saturation and heart rate during administration, complications and oxygen use during hospitalisation were collected and compered. Results The pH value of the LISA group after administration was significantly higher than that before administration (P < 0.001). The PCO2 value in the LISA group after administration was significantly lower than that before administration (P=0.005). The PO2 changes in the LISA group before and after administration were not statistically significant. The pH, PCO2 and PO2 values of the INSURE group showed no significant changes before and after administration. The LISA group tended to have a normal pH range compared with the INSURE group (P=0.009). The decrease of blood oxygen saturation during the administration was statistically significant between the two groups (P=0.041). No statistically significant difference was observed in the incidence of bronchopulmonary dysplasia (BPD), noninvasive failure rate and time of noninvasive ventilation between the two groups. Conclusion LISA technology can be performed in infants with spontaneous breathing, and it can significantly improve alveolar ventilation without increasing the incidence of complications such as BPD. -
表 1 2组呼吸窘迫综合征早产儿基本资料比较
组别 例数 性别[例(%)] 胎龄(x ±s,周) 出生体重(x ±s,g) 多胎[例(%)] 试管婴儿[例(%)] Apgar评分≤3分[例(%)] 孕母年龄(x ±s,岁) 孕母妊娠期糖尿病[例(%)] 孕母产前激素[例(%)] 男性 女性 INSURE组 36 18(50.00) 18(50.00) 29.17±0.54 1280±198 6(16.67) 3(8.33) 3(8.33) 31.83±5.06 6(16.67) 27(75.00) LISA组 20 10(50.00) 10(50.00) 29.13±0.57 1254±193 0(0.00) 0(0.00) 1(5.00) 30.20±4.41 5(25.00) 14(70.00) 统计量 0.279a 0.462a 0.006c 1.209a 0.566c 0.164c P值 0.781 0.646 0.078b 0.545b 0.938 0.232 0.452 0.686 注:a为t值,b为采用Fisher精确检验,c为χ2值。 表 2 2组早产儿给药后的血气分析正常情况比较
[例(%)] 分组 例数 pH PaCO2 PaO2 INSURE组 30 7(23.33) 10(33.33) 25(83.33) LISA组 18 7(38.89) 7(38.89) 16(88.89) 统计量 6.850a 3.527a P值 0.009 0.060 0.696b 注:a为χ2值,b为采用Fisher精确检验。 表 3 LISA组早产儿给药前后的血气分析值变化(x ±s)
时间 例数 pH PaCO2(mm Hg) PaO2(mm Hg) 给药前 18 7.26±0.08 50.26±11.03 80.78±36.34 给药后 18 7.40±0.12 40.91±10.59 80.17±33.22 t值 -4.716 2.372 0.057 P值 <0.001 0.030 0.955 表 4 INSURE组早产儿给药前后的血气分析值变化(x ±s)
时间 例数 pH PaCO2(mm Hg) PaO2(mm Hg) 给药前 30 7.26±0.08 48.36±16.07 65.50±17.39 给药后 30 7.29±0.06 45.95±7.02 68.87±20.48 t值 -0.775 0.400 -0.374 P值 0.464 0.701 0.719 表 5 2组早产儿治疗后各种并发症情况及NIV时间比较
组别 例数 无创失败数[例(%)] BPD [例(%)] 颅内出血[例(%)] ROP [例(%)] NEC [例(%)] NIV时间(x ±s,d) INSURE组 36 8(22.22) 17(47.22) 6(16.67) 7(19.44) 1(2.78) 9.03±6.20 LISA组 20 4(20.00) 8(40.00) 5(25.00) 3(15.00) 3(15.00) 11.95±9.52 统计量 0.021a 0.271a 0.566a 0.003a 1.346a -1.390b P值 0.884 0.602 0.452 0.959 0.246 0.170 注:a为χ2值,b为t值。 表 6 2组早产儿给药过程中的不良反应比较
[例(%)] 分组 例数 心率下降 SpO2波动 INSURE组 36 0(0.00) 0(0.00) LISA组 20 1(5.00) 3(15.00) P值 0.368 0.041 注:均使用Fisher精确检验。 -
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