Aly Hany, Lotfy Wael, Badrawi Nadia, Ghawas Mohamed, Abdel-Meguid Iman Ehsan, Hammad Tarek A
Newborn Services Department, The George Washington University Hospital, Washington, District of Columbia 20037, USA.
Am J Perinatol. 2007 May;24(5):267-70. doi: 10.1055/s-2007-976550. Epub 2007 May 4.
The purpose of this study was to evaluate the feasibility of the use oral ibuprofen suspension (OIS) in the treatment of patent ductus arteriosus (PDA) in premature infants. Premature infants (</= 35 weeks) age 2 to 7 days who suffered from respiratory distress and had been diagnosed with PDA were included in this study. Color Doppler echocardiography (ECHO) was used to measure the internal ductal diameter, pressure gradient, and the ratio of left atrial to aortic root diameters (La/Ao). Infants were randomly assigned to one of two groups: group I received three doses of intravenous (IV) indomethacin (0.2 mg/kg at 12-hour intervals) and group O received an initial dose of OIS (10 mg/kg), followed by two doses of 5 mg/kg each, after 24 and 48 hours. A follow-up ECHO was done after treatment by the same pediatric cardiologist who was blinded to the assignment of the study groups. Changes in blood platelet count, hematocrit, blood urea nitrogen, and creatinine were compared between groups. In total, 78 premature infants were screened: 21 had been diagnosed with PDA. Infants in group I (n = 9) and group O (n = 12) did not differ in birthweight (1884 +/- 485 versus 1521 +/- 398 g [mean +/- SD]; P = 0.13), gestational age (32.9 +/- 1.6 versus 31.2 +/- 2.5 weeks; P = 0.07), internal diameter of PDA (2.3 +/- 0.5 versus 2.1 +/- 0.5 mm; P = 0.34), pressure gradient across PDA (12.83 +/- 6.46 versus 11.11 +/- 4.5 mm Hg; P = 0.48), and La/Ao ratio (1.26 +/- 0.21 versus 1.17 +/- 0.12; P = 0.25). Closure of PDA was achieved in 78% (seven of nine) of infants in group I and in 83% (10 of 12) of infants in group O. Comparisons of laboratory changes following treatment in group I and group O were as follows: decrease in hematocrit (-6.5 +/- 6.6 versus -1.2 +/- 4.2; P = 0.04) and in platelet count (-54 +/- 67 versus -1 +/- 53 x 10 (3)/muL; P = 0.24), and increase in blood urea nitrogen (16.4 +/- 16.4 versus 2.1 +/- 17.4 mg/dL; P = 0.06) and serum creatinine (0.12 +/- 0.22 versus -0.06 +/- 0.19 mg/dL; P = 0.13). Two infants in group I had severe pulmonary hemorrhage, whereas there were none in the group O. Oral ibuprofen could be an easy-to-administer and efficacious alternative in the treatment of PDA.
本研究的目的是评估口服布洛芬混悬液(OIS)用于治疗早产儿动脉导管未闭(PDA)的可行性。本研究纳入了年龄为2至7天、患有呼吸窘迫且已诊断为PDA的早产儿(≤35周)。采用彩色多普勒超声心动图(ECHO)测量动脉导管内径、压力阶差以及左心房与主动脉根部直径之比(La/Ao)。婴儿被随机分为两组:I组接受三剂静脉注射吲哚美辛(0.2mg/kg,间隔12小时),O组接受初始剂量的OIS(10mg/kg),随后在24小时和48小时后各接受两剂5mg/kg。由对研究组分配情况不知情的同一位儿科心脏病专家在治疗后进行随访ECHO检查。比较两组之间血小板计数、血细胞比容、血尿素氮和肌酐的变化。总共筛查了78名早产儿:21名被诊断为PDA。I组(n = 9)和O组(n = 12)婴儿在出生体重(1884±485对1521±398g[平均值±标准差];P = 0.13)、胎龄(32.9±1.6对31.2±2.5周;P = 0.07)、PDA内径(2.3±0.5对2.1±0.5mm;P = 0.34)、PDA压力阶差(12.83±6.46对11.11±4.5mmHg;P = 0.48)以及La/Ao比值(1.26±0.21对1.17±0.12;P = 0.25)方面无差异。I组78%(9名中的7名)婴儿和O组83%(12名中的10名)婴儿的PDA实现闭合。I组和O组治疗后实验室变化的比较如下:血细胞比容下降(-6.5±6.6对-1.2±4.2;P = 0.04)和血小板计数下降(-54±67对-1±53×10³/μL;P = 0.24),血尿素氮升高(16.4±16.4对2.1±17.4mg/dL;P = 0.06)和血清肌酐升高(0.12±0.22对-0.06±0.19mg/dL;P = 0.13)。I组有两名婴儿发生严重肺出血,而O组无。口服布洛芬可能是治疗PDA的一种易于给药且有效的替代方法。