A multicenter, randomized trial comparing synthetic surfactant with modified bovine surfactant extract in the treatment of neonatal respiratory distress syndrome

被引:1
作者
Arnold, C
Adams, E
Vollman, J
Giebner, D
Maurer, M
Dreyer, G
Bailey, L
Anderson, M
Mefford, L
Beaumont, E
Sutton, D
Puppala, B
Mangurten, HH
Secrest, J
Lewis, WJ
Carteaux, P
Bednarek, F
Welsberger, S
Gosselin, R
Pantoja, AF
Belenky, A
Campbell, P
Patole, S
Duenas, M
Kelly, M
Alejo, W
Lewallen, P
DeanLieber, S
Hanft, M
Ferlauto, J
Newell, RW
Bagwell, J
Levine, D
Lipp, RW
Harkavy, K
Vasa, R
Birenbaum, H
Broderick, KA
Santos, AQ
Long, BA
Gulrajani, M
Stern, M
Hopgood, G
Hegyi, T
Alba, J
Christmas, L
McQueen, M
Nichols, N
Brown, M
Quissell, BJ
机构
[1] UNIV VERMONT,COLL MED,DEPT PEDIAT,BURLINGTON,VT 05405
[2] ST JOHNS MERCY MED CTR,ST LOUIS,MO 63141
[3] GOOD SAMARITAN HOSP,CINCINNATI,OH
[4] PLANTAT GEN HOSP,PLANTATION,FL 33317
[5] NEONATAL RES & TECHNOL ASSESSMENT INC,DATA COORDINATING CTR,BURLINGTON,VT
[6] DARTMOUTH COLL,HANOVER,NH 03755
[7] COOK FT WORTH CHILDRENS MED CTR,FT WORTH,TX
[8] HARRIS METHODIST HOSP,FT WORTH,TX
[9] UNIV TENNESSEE,MED CTR,KNOXVILLE,TN
[10] UNIV TENNESSEE,MEMPHIS,TN
[11] DEVOS CHILDRENS HOSP,GRAND RAPIDS,MI
[12] LUTHERAN GEN HOSP,PARK RIDGE,IL 60068
[13] PARKVIEW MEM HOSP,FT WAYNE,IN
[14] MED CTR CENT MASSACHUSETTS MEM,WORCESTER,MA
[15] ST JOSEPH HOSP,DENVER,CO
[16] ROYAL HOSP WOMEN,NEWBORN MED CTR,SYDNEY,NSW,AUSTRALIA
[17] CHILDRENS HOSP,MED CTR,AKRON,OH
[18] ST JOHN HOSP & MED CTR,DETROIT,MI
[19] EMANUEL CHILDRENS HOSP,PORTLAND,OR
[20] CHILDRENS HOSP,GREENVILLE MEM MED CTR,GREENVILLE,SC
[21] COLUMBIA HOSP WOMEN,WASHINGTON,DC
[22] MERCY HOSP & MED CTR,CHICAGO,IL
[23] ST AGNES HOSP,BALTIMORE,MD
[24] BROOKLYN HOSP CTR,BROOKLYN,NY
[25] MEM HOSP,HOLLYWOOD,FL
[26] ST PETERS MED CTR,NEW BRUNSWICK,NJ
[27] PHOENIX CHILDRENS HOSP,PHOENIX,AZ
[28] RUSH PRESBYTERIAN ST LUKES MED CTR,DENVER,CO
[29] PENN STATE UNIV HOSP,MILTON S HERSHEY MED CTR,HERSHEY,PA 17033
[30] MARSHFIELD CLIN FDN MED RES & EDUC,MARSHFIELD,WI
[31] GREATER BALTIMORE MED CTR,BALTIMORE,MD 21204
[32] KENNESTONE HOSP,MARIETTA,GA
[33] SUNRISE CHILDRENS HOSP,LAS VEGAS,NV
[34] ARNOT OGDEN MED CTR,ELMIRA,NY
[35] HENRICO DOCTORS HOSP,RICHMOND,VA
[36] AULTMAN HOSP,CANTON,OH
[37] MT SINAI MED CTR,CLEVELAND,OH 44106
[38] FITZGERALD MERCY HOSP,DARBY,PA
[39] FLETCHER ALLEN HLTH CARE,BURLINGTON,VT
[40] NORTHSIDE HOSP,ATLANTA,GA
[41] CARDINAL GLENNON CHILDRENS HOSP,ST LOUIS,MO
[42] HUNTSVILLE DIST MEM HOSP,HUNTSVILLE,AL
[43] ST VINCENTS MED CTR,TOLEDO,OH
关键词
newborn; clinical trials; respiratory distress syndrome; pulmonary surfactant;
D O I
暂无
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
Objective. To compare the efficacy of a synthetic surfactant (Exosurf Neonatal, Burroughs-Wellcome Co) and a modified bovine surfactant extract (Survanta, Ross Laboratories) in the treatment of neonatal respiratory distress syndrome (RDS). Design. Multicenter, randomized trial. Setting. Thirty-eight neonatal intensive fare units participating in the Vermont-Oxford Neonatal Network. Patients. Premature infants (n = 1296) weighing 501 to 1500 g with RDS requiring assisted ventilation with 30% oxygen or more were enrolled within 6 hours of birth. Interventions. Infants were randomly assigned to receive up to four intratracheal doses of the synthetic surfactant (Exosurf Neonatal, n = 644) or the modified bovine surfactant extract (Survanta, n = 652). Main Outcome Measure. The primary outcome measure was the occurrence of death or chronic lung disease 28 days after birth. Results. Death or chronic lung disease occurred in 57% of the infants treated with Exosurf Neonatal and in 54% of those infants treated with Survanta (relative risk [RR], 0.95; 95% confidence interval [CI], 0.86 to 1.04). Infants with birth weights of 1001 to 1500 g who received Survanta had a significantly lower risk of chronic lung disease or death at 28 days (Survanta, 27% vs Exosurf, 34%; RR, 0.78; 95% CI, 0.60 to 0.99). Treatment with Survanta led to significant improvement in several secondary outcome measures. Survanta-treated infants received less supplemental oxygen and had lower mean airway pressure 6 and 72 hours after treatment. Survanta-treated infants had significantly fewer pneumothoraces (Survanta, 9% vs Exosurf, 15%; RR, 0.60; 95% CI, 0.44 to 0.81). There were no differences between the groups in the incidence of other neonatal complications. Conclusion. Although no differences were noted between Survanta- and Exosurf-treated infants regarding the primary outcome of death or chronic lung disease at 28 days of age, the significant improvement in secondary clinical outcomes suggests that Survanta is more effective than Exosurf Neonatal in the treatment of established RDS.
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页码:1 / 6
页数:6
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