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乙酰唑胺和呋塞米用于婴儿出血后脑室扩张的国际随机对照试验。国际出血后脑室扩张药物试验组

International randomised controlled trial of acetazolamide and furosemide in posthaemorrhagic ventricular dilatation in infancy. International PHVD Drug Trial Group.

出版信息

Lancet. 1998 Aug 8;352(9126):433-40.

PMID:9708751
Abstract

BACKGROUND

Furosemide and acetazolamide are widely used in the treatment of posthaemorrhagic ventricular dilatation (PHVD) in the hope of avoiding the need for surgical management, but this approach has not been evaluated in a controlled trial. This multicentre randomised controlled trial tested the hypothesis that these drugs would reduce the rate of shunt placement and increase disability-free survival at 1 year of age.

METHODS

Between 1992 and 1996, 177 infants aged less than 3 months past term, and with ventricular width more than 4 mm above 97th centile after intraventricular haemorrhage, were randomly assigned standard therapy alone or standard therapy plus treatment with acetazolamide (100 mg/kg daily) and furosemide (1 mg/kg daily). A minimisation algorithm ensured balance between groups with respect to both referral centre and the presence of a cerebral parenchymal lesion on cerebral ultrasonography at enrolment. The trial was stopped in September, 1996, because the data showed a clear advantage with standard therapy.

FINDINGS

We report outcomes for 151 infants whose expected date of delivery was before the end of 1995, with complete information at 1 year for 129 infants. The median gestational age was 28 weeks, mean birthweight 1299 g, and mean postnatal age at enrolment 25 days. 44% had a parenchymal lesion at randomisation. Death or shunt placement occurred in 49 of 75 infants allocated drugs plus standard therapy, compared with 35 of 76 allocated to standard therapy alone. The relative risk was 1.42 (95% CI 1.06-1.90; p=0.026), which is equivalent to one extra death or shunt placement for every five infants allocated drug therapy. 84% (52/62) of infants assigned drug therapy had died or were disabled or impaired at 1 year, compared with 60% (40/67) of those assigned standard therapy (relative risk 1.40 [1.12-1.76]; p=0.012).

INTERPRETATION

These preliminary results suggest that the use of acetazolamide and furosemide in preterm infants with PHVD is associated with a higher rate of shunt placement and increased neurological morbidity, and so cannot be recommended.

摘要

背景

呋塞米和乙酰唑胺被广泛用于治疗出血后脑室扩张(PHVD),以期避免手术治疗,但这种方法尚未在对照试验中得到评估。这项多中心随机对照试验检验了以下假设:这些药物将降低分流管置入率,并提高1岁时无残疾生存率。

方法

在1992年至1996年期间,177名孕龄超过3个月的婴儿,在脑室内出血后脑室宽度超过第97百分位数4毫米以上,被随机分配接受单纯标准治疗或标准治疗加乙酰唑胺(每日100mg/kg)和呋塞米(每日1mg/kg)治疗。一种最小化算法确保了两组在转诊中心和入组时脑超声检查发现脑实质病变方面的平衡。该试验于1996年9月停止,因为数据显示标准治疗具有明显优势。

结果

我们报告了151名预期分娩日期在1995年底之前的婴儿的结局,其中129名婴儿在1岁时获得了完整信息。中位胎龄为28周,平均出生体重1299g,入组时平均出生后年龄为25天。44%的婴儿在随机分组时有脑实质病变。在接受药物加标准治疗的75名婴儿中,49名发生了死亡或分流管置入,而在单纯接受标准治疗的76名婴儿中,这一数字为35名。相对风险为1.42(95%CI 1.06 - 1.90;p = 0.026),这相当于每5名接受药物治疗的婴儿中就有1名额外发生死亡或分流管置入。在接受药物治疗的婴儿中,84%(52/62)在1岁时死亡、残疾或有损伤,而接受标准治疗的婴儿中这一比例为60%(40/67)(相对风险1.40 [1.12 - 1.76];p = 0.012)。

解读

这些初步结果表明,在患有PHVD的早产儿中使用乙酰唑胺和呋塞米与更高的分流管置入率和增加的神经疾病发病率相关,因此不推荐使用。

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