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Double-blind developmental evaluation at 1-year corrected age of 597 premature infants with birth weights from 500 to 1350 grams enrolled in three placebo-controlled trials of prophylactic synthetic surfactant. American Exosurf Neonatal Study Group I.

作者信息

Corbet A, Long W, Schumacher R, Gerdes J, Cotton R

机构信息

Department of Pediatrics, Baylor College of Medicine, Houston, Texas, USA.

出版信息

J Pediatr. 1995 May;126(5 Pt 2):S5-12. doi: 10.1016/s0022-3476(95)70002-1.

DOI:10.1016/s0022-3476(95)70002-1
PMID:7745511
Abstract

Infants enrolled in three clinical trials of prophylactic treatment for respiratory distress syndrome with a single dose of synthetic surfactant (Exosurf Neonatal) or air placebo were monitored through 1-year adjusted age. A total of 1046 infants with birth weights from 500 to 1350 gm were enrolled in the three trials; of the 735 infants who survived to 1 year of age, follow-up evaluations were completed for 597 (80%, air placebo group; 82%, synthetic surfactant group). Infants in the air placebo and synthetic surfactant treatment groups had no differences in general health, growth, or nerodevelopmental outcomes or impairments. These follow-up results at 1-year adjusted age for infants who received a single dose of synthetic surfactant indicate that a single dose of synthetic surfactant reduces mortality without increasing the absolute number or proportion of infants with impairments at 1 year of age.

摘要

相似文献

1
Double-blind developmental evaluation at 1-year corrected age of 597 premature infants with birth weights from 500 to 1350 grams enrolled in three placebo-controlled trials of prophylactic synthetic surfactant. American Exosurf Neonatal Study Group I.
J Pediatr. 1995 May;126(5 Pt 2):S5-12. doi: 10.1016/s0022-3476(95)70002-1.
2
One-year follow-up of 273 infants with birth weights of 700 to 1100 grams after prophylactic treatment of respiratory distress syndrome with synthetic surfactant or air placebo. American Exosurf Neonatal Study Group I.对273名出生体重700至1100克的婴儿采用合成表面活性剂或空气安慰剂预防性治疗呼吸窘迫综合征后的一年随访。美国外源性表面活性物质新生儿研究组I。
J Pediatr. 1995 May;126(5 Pt 2):S20-5. doi: 10.1016/s0022-3476(95)70004-8.
3
One-year follow-up of 66 premature infants weighing 500 to 699 grams treated with a single dose of synthetic surfactant or air placebo at birth: results of a double-blind trial. American Exosurf Neonatal Study Group I.对66例出生时接受单剂量合成表面活性剂或空气安慰剂治疗的体重500至699克的早产儿进行的一年随访:一项双盲试验的结果。美国外源性表面活性剂新生儿研究组I。
J Pediatr. 1995 May;126(5 Pt 2):S13-9. doi: 10.1016/s0022-3476(95)70003-x.
4
One-year outcome in 232 premature infants with birth weights of 750 to 1249 grams and respiratory distress syndrome randomized to rescue treatment with two doses of synthetic surfactant or air placebo. Canadian Exosurf Neonatal Study Group.232例出生体重750至1249克且患有呼吸窘迫综合征的早产儿被随机分为两组,分别接受两剂合成表面活性剂或空气安慰剂的抢救治疗,随访一年。加拿大外源性表面活性物质新生儿研究组。
J Pediatr. 1995 May;126(5 Pt 2):S61-7. doi: 10.1016/s0022-3476(95)70009-9.
5
One-year follow-up evaluation of 260 premature infants with respiratory distress syndrome and birth weights of 700 to 1350 grams randomized to two rescue doses of synthetic surfactant or air placebo. American Exosurf Neonatal Study Group I.对260名呼吸窘迫综合征且出生体重在700至1350克之间的早产儿进行为期一年的随访评估,这些早产儿被随机分为接受两剂合成表面活性剂或空气安慰剂治疗组。美国外源性表面活性物质新生儿研究组I。
J Pediatr. 1995 May;126(5 Pt 2):S68-74. doi: 10.1016/s0022-3476(95)70010-2.
6
Double-blind 1-year follow-up of 1540 infants with respiratory distress syndrome randomized to rescue treatment with two doses of synthetic surfactant or air in four clinical trials. American and Canadian Exosurf Neonatal Study Groups.在四项临床试验中,对1540例患有呼吸窘迫综合征的婴儿进行双盲1年随访,这些婴儿被随机分配接受两剂合成表面活性剂或空气的抢救治疗。美国和加拿大外源性表面活性物质新生儿研究组。
J Pediatr. 1995 May;126(5 Pt 2):S43-52. doi: 10.1016/s0022-3476(95)70007-2.
7
One-year follow-up of 89 infants with birth weights of 500 to 749 grams and respiratory distress syndrome randomized to two rescue doses of synthetic surfactant or air placebo. Canadian Exosurf Neonatal Study Group. Canadian Exosurf Neonatal Follow-Up Group.对89名出生体重在500至749克之间且患有呼吸窘迫综合征的婴儿进行了为期一年的随访,这些婴儿被随机分配接受两剂合成表面活性剂或空气安慰剂治疗。加拿大外源性表面活性物质新生儿研究组。加拿大外源性表面活性物质新生儿随访组。
J Pediatr. 1995 May;126(5 Pt 2):S53-60. doi: 10.1016/s0022-3476(95)70008-0.
8
Health and neurodevelopmental outcome at 1-year adjusted age in 508 infants weighing 700 to 1100 grams who received prophylaxis with one versus three doses of synthetic surfactant. American Exosurf Neonatal Study Groups I and II.508名体重700至1100克的婴儿接受一剂与三剂合成表面活性剂预防治疗后,在1岁校正年龄时的健康和神经发育结局。美国外源性表面活性物质新生儿研究组I和II。
J Pediatr. 1995 May;126(5 Pt 2):S26-32. doi: 10.1016/s0022-3476(95)70005-6.
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J Pediatr. 1995 May;126(5 Pt 2):S33-42. doi: 10.1016/s0022-3476(95)70006-4.
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Controlled trial of a single dose of synthetic surfactant at birth in premature infants weighing 500 to 699 grams. The American Exosurf Neonatal Study Group I.对出生时体重500至699克的早产儿单剂量合成表面活性剂的对照试验。美国外源性表面活性物质新生儿研究组I。
J Pediatr. 1992 Feb;120(2 Pt 2):S3-12. doi: 10.1016/s0022-3476(05)81226-0.

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