N-acetylcysteine does not prevent bronchopulmonary dysplasia in immature infants:: A randomized controlled trial

被引:102
作者
Ahola, T
Lapatto, R
Raivio, KO
Selander, B
Stigson, L
Jonsson, B
Jonsbo, F
Esberg, G
Stövring, S
Kjartansson, S
Stiris, T
Lossius, K
Virkola, K
Fellman, V
机构
[1] Univ Helsinki, Cent Hosp, Hosp Children & Adolescents, Helsinki 00029, Finland
[2] Univ Hosp, Gothenburg, Sweden
[3] Univ Lund Hosp, S-22185 Lund, Sweden
[4] Univ Hosp, Stockholm, Sweden
[5] Univ Copenhagen Hosp, DK-2100 Copenhagen, Denmark
[6] Aarhus Univ Hosp, DK-8000 Aarhus, Denmark
[7] Univ Hosp, Aalborg, Denmark
[8] Univ Hosp, Reykjavik, Iceland
[9] Univ Hosp, Oslo, Norway
[10] Univ Trondheim Hosp, Trondheim, Norway
关键词
D O I
10.1067/S0022-3476(03)00419-0
中图分类号
R72 [儿科学];
学科分类号
100202 [儿科学];
摘要
Objective To evaluate whether N-acetyleysteine (NAC) infusion during the first week of life reduces the risk of death or bronchopulmonary dysplasia (BPD in infants with extremely low birth weight. Study design In a Nordic multicenter, double-blind trial, infants (n = 391) weighing 500 to 999 g and on ventilator or nasal continuous positive airway pressure were randomized before the age of 36 hours to receive NAC 16 to 32 mg/kg/d (n = 194) or placebo (n = 197) intravenously for 6 days. Primary end points were death or BPD, defined as supplementary oxygen requirement at 36 weeks' gestational age. Results There was no difference in the combined incidence of the primary end points death or BPD, 51% vs. 49%, between the NAC group and control group. Also similar was the incidence of BPD in survivors at 36 weeks' gestational age, 40% vs. 40%, and the mean oxygen requirement at the age of 28 days, 31.2% vs. 30.7%, respectively. The severity of BPD was similar in both groups. Conclusions A 6-day course of intravenous N-acetylcysteine at the dosage used does not prevent BPD or death in infants with extremely low birth weight.
引用
收藏
页码:713 / 719
页数:7
相关论文
共 38 条
[1]
Pharmacokinetics of intravenous N-acetylcysteine in pre-term new-born infants [J].
Ahola, T ;
Fellman, V ;
Laaksonen, R ;
Laitila, J ;
Lapatto, R ;
Neuvonen, PJ ;
Raivio, KO .
EUROPEAN JOURNAL OF CLINICAL PHARMACOLOGY, 1999, 55 (09) :645-650
[2]
N-ACETYLCYSTEINE IN COMBINATION WITH NITROGLYCERIN AND STREPTOKINASE FOR THE TREATMENT OF EVOLVING ACUTE MYOCARDIAL-INFARCTION - SAFETY AND BIOCHEMICAL EFFECTS [J].
ARSTALL, MA ;
YANG, JF ;
STAFFORD, I ;
BETTS, WH ;
HOROWITZ, JD .
CIRCULATION, 1995, 92 (10) :2855-2862
[3]
THE ANTIOXIDANT ACTION OF N-ACETYLCYSTEINE - ITS REACTION WITH HYDROGEN-PEROXIDE, HYDROXYL RADICAL, SUPEROXIDE, AND HYPOCHLOROUS ACID [J].
ARUOMA, OI ;
HALLIWELL, B ;
HOEY, BM ;
BUTLER, J .
FREE RADICAL BIOLOGY AND MEDICINE, 1989, 6 (06) :593-597
[4]
Expression and developmental profile of antioxidant enzymes in human lung and liver [J].
Asikainen, TM ;
Raivio, KO ;
Saksela, M ;
Kinnula, VL .
AMERICAN JOURNAL OF RESPIRATORY CELL AND MOLECULAR BIOLOGY, 1998, 19 (06) :942-949
[5]
NEONATAL NECROTIZING ENTEROCOLITIS - THERAPEUTIC DECISIONS BASED UPON CLINICAL STAGING [J].
BELL, MJ ;
TERNBERG, JL ;
FEIGIN, RD ;
KEATING, JP ;
MARSHALL, R ;
BARTON, L ;
BROTHERTON, T .
ANNALS OF SURGERY, 1978, 187 (01) :1-7
[6]
A trial of antioxidants N-acetylcysteine and procysteine in ARDS [J].
Bernard, GR ;
Wheeler, AP ;
Arons, MM ;
Morris, PE ;
Paz, HL ;
Russell, JA ;
Wright, PE ;
Bernard, GR ;
Arons, MM ;
Wheeler, AP ;
Carmichael, LC ;
Morris, PE ;
Higgins, SB ;
Dupont, WD ;
Edens, TR ;
Swindell, BB ;
Russell, JA ;
Paz, HL ;
Wright, PE ;
Steinberg, KP .
CHEST, 1997, 112 (01) :164-172
[7]
THE METABOLISM OF N-ACETYLCYSTEINE BY HUMAN ENDOTHELIAL-CELLS [J].
COTGREAVE, I ;
MOLDEUS, P ;
SCHUPPE, I .
BIOCHEMICAL PHARMACOLOGY, 1991, 42 (01) :13-16
[8]
Cotgreave I A, 1997, Adv Pharmacol, V38, P205
[9]
METHODOLOGIES FOR THE APPLICATION OF MONOBROMOBIMANE TO THE SIMULTANEOUS ANALYSIS OF SOLUBLE AND PROTEIN THIOL COMPONENTS OF BIOLOGICAL-SYSTEMS [J].
COTGREAVE, IA ;
MOLDEUS, P .
JOURNAL OF BIOCHEMICAL AND BIOPHYSICAL METHODS, 1986, 13 (4-5) :231-249
[10]
DARLOW BA, 2002, VITAMIN A SUPPLEMENT