Stevens D C, Schreiner R L, Bull M J, Bryson C Q, Lemons J A, Gresham E L, Grosfeld J L, Weber T R
J Pediatr Surg. 1980 Dec;15(6):964-70. doi: 10.1016/s0022-3468(80)80311-3.
There were 47 seriously-ill neonates with medical causes of respiratory distress and 10 infants with severe respiratory distress secondary to a congenital diaphragmatic hernia treated with tolazoline according to a strict protocol designed to manage persistent fetal circulation (PFC). Of the 47 infants, 28 (60%) had a positive response defined as an increase in the pO2 greater than or equal to 24 mm Hg within 4 hr of beginning the drug. Of 7 infants, 4 with congenital diaphragmatic hernia had a positive response. The mean increase in the pO2 for the 47 infants was statistically significant (p less than .05). Of the 47 infants with medical disorders, 27 survived (survival 57%), whereas only 2 of the 10 infants with congenital diaphragmatic hernia and severe persistent fetal circulation survived (survival 28%). Erythema (60%), hematest positive gastric aspirates (55%), thrombocytopenia (45%), hyponatremia (40%) and increased gastric aspirates (36%) were the most common adverse effects occurring during tolazoline infusion. Hypotension occurred in nine cases, but was transient. Of the 27 survivors, 20 with medical causes of persistent fetal circulation were evaluated at age 1 yr. Eighty percent of these infants studied were considered normal as defined by an MDI and PI of the Bayley Scales of greater than or equal to 70. These data suggest that tolazoline is a useful adjunct in the management of neonates with PFC. In addition, tolazoline was more effective in mechanically ventilated neonates treated with respiratory paralytic agents. Although tolazoline resulted in a significant improvement in the paO2 in 4 infants with congenital diaphragmatic hernia, it did not appear to improve mortality in these infants.
有47名因医学原因导致呼吸窘迫的重症新生儿和10名因先天性膈疝继发严重呼吸窘迫的婴儿,根据旨在处理持续性胎儿循环(PFC)的严格方案接受妥拉唑啉治疗。在这47名婴儿中,28名(60%)有阳性反应,定义为开始用药后4小时内动脉血氧分压(pO2)升高大于或等于24 mmHg。在7名患有先天性膈疝的婴儿中,4名有阳性反应。47名婴儿的pO2平均升高具有统计学意义(p<0.05)。在47名患有医学疾病的婴儿中,27名存活(存活率57%),而10名患有先天性膈疝和严重持续性胎儿循环的婴儿中只有2名存活(存活率28%)。红斑(60%)、胃液潜血阳性(55%)、血小板减少(45%)、低钠血症(40%)和胃液增多(36%)是妥拉唑啉输注期间最常见的不良反应。9例出现低血压,但为一过性。在27名存活者中,对20名因医学原因导致持续性胎儿循环的婴儿在1岁时进行了评估。根据贝利婴幼儿发育量表的心理发育指数(MDI)和运动发育指数(PI)大于或等于70的定义,这些接受研究的婴儿中有80%被认为正常。这些数据表明,妥拉唑啉在治疗患有PFC的新生儿中是一种有用的辅助药物。此外,妥拉唑啉在接受呼吸麻痹剂治疗的机械通气新生儿中更有效。虽然妥拉唑啉使4名患有先天性膈疝的婴儿的动脉血氧分压(paO2)有显著改善,但似乎并未改善这些婴儿的死亡率。