Inhaled nitric oxide versus conventional therapy - Effect on oxygenation in ARDS

被引:179
作者
Michael, JR
Barton, RG
Saffle, JR
Mone, M
Markewitz, BA
Hillier, K
Elstad, MR
Campbell, EJ
Troyer, BE
Whatley, RE
Liou, TG
Samuelson, WM
Carveth, HJ
Hinson, DM
Morris, SE
Davis, BL
Day, RW
机构
[1] Univ Utah, Div Resp Crit Care & Occupat Pulm Med, Sch Med, Dept Med, Salt Lake City, UT 84132 USA
[2] Univ Utah, Dept Surg, Sch Med, Salt Lake City, UT 84132 USA
[3] Univ Utah, Dept Pediat, Sch Med, Salt Lake City, UT 84132 USA
[4] Salt Lake City Adm Med Ctr, Salt Lake City, UT USA
[5] Univ Utah, Utah Supercomp Ctr, Salt Lake City, UT USA
关键词
D O I
10.1164/ajrccm.157.5.96-10089
中图分类号
R4 [临床医学];
学科分类号
1002 ; 100602 ;
摘要
A randomized, controlled clinical trial was performed with patients with acute respiratory distress syndrome (ARDS) to compare the effect of conventional therapy or inhaled nitric oxide (iNO) on oxygenation. Patients were randomized to either conventional therapy or conventional therapy plus iNO for 72 h. We tested the following hypotheses: (1) that iNO would improve oxygenation during the 72 h after randomization, as compared with conventional therapy; and (2) that iNO would increase the likelihood that patients would improve to the extent that the Fi(O2) could be decreased by greater than or equal to 0.15 within 72 h after randomization. There were two major findings. First, That iNO as compared with conventional therapy increased Pa-O2/Fi(O2) at 1 h, 12 h, and possibly 24 h. Beyond 24 h, the two groups had an equivalent improvement in Pa-O2/Fi(O2). Second, that patients treated with iNO therapy were no more likely to improve so that they could be managed with a persistent decrease in Fi(O2) greater than or equal to 0.15 during the 72 h following randomization (11 of 20 patients with iNO versus 9 of 20 patients with conventional therapy, p = 0.55). In patients with severe ARDS, our results indicate that iNO does not lead to a sustained improvement in oxygenation as compared with conventional therapy.
引用
收藏
页码:1372 / 1380
页数:9
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共 50 条
[1]   EFFICACY AND SAFETY OF MONOCLONAL-ANTIBODY TO HUMAN TUMOR-NECROSIS-FACTOR-ALPHA IN PATIENTS WITH SEPSIS SYNDROME - A RANDOMIZED, CONTROLLED, DOUBLE-BLIND, MULTICENTER CLINICAL-TRIAL [J].
ABRAHAM, E ;
WUNDERINK, R ;
SILVERMAN, H ;
PERL, TM ;
NASRAWAY, S ;
LEVY, H ;
BONE, R ;
WENZEL, RP ;
BALK, R ;
ALLRED, R ;
PENNINGTON, JE ;
WHERRY, JC .
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 1995, 273 (12) :934-941
[2]   MUTAGENICITY OF NITRIC-OXIDE AND ITS INHIBITION BY ANTIOXIDANTS [J].
ARROYO, PL ;
HATCHPIGOTT, V ;
MOWER, HF ;
COONEY, RV .
MUTATION RESEARCH, 1992, 281 (03) :193-202
[3]   INHALED NITRIC-OXIDE LOWERS PULMONARY CAPILLARY-PRESSURE AND CHANGES LONGITUDINAL DISTRIBUTION OF PULMONARY VASCULAR-RESISTANCE IN PATIENTS WITH ACUTE LUNG INJURY [J].
BENZING, A ;
GEIGER, K .
ACTA ANAESTHESIOLOGICA SCANDINAVICA, 1994, 38 (07) :640-645
[4]   INHALED NITRIC-OXIDE REDUCES PULMONARY TRANSVASCULAR ALBUMIN FLUX IN PATIENTS WITH ACUTE LUNG INJURY [J].
BENZING, A ;
BRAUTIGAM, P ;
GEIGER, K ;
LOOP, T ;
BEYER, U ;
MOSER, E .
ANESTHESIOLOGY, 1995, 83 (06) :1153-1161
[5]   Effect of inhaled nitric oxide on venous admixture depends on cardiac output in patients with acute lung injury and acute respiratory distress syndrome [J].
Benzing, A ;
Loop, T ;
Mols, G ;
Geiger, K .
ACTA ANAESTHESIOLOGICA SCANDINAVICA, 1996, 40 (04) :466-474
[6]   NITRIC-OXIDE AS A MEDIATOR OF OXIDANT LUNG INJURY DUE TO PARAQUAT [J].
BERISHA, HI ;
PAKBAZ, H ;
ABSOOD, A ;
SAID, SI .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1994, 91 (16) :7445-7449
[7]   PROLONGED INHALATION OF LOW CONCENTRATIONS OF NITRIC-OXIDE IN PATIENTS WITH SEVERE ADULT-RESPIRATORY-DISTRESS-SYNDROME - EFFECTS ON PULMONARY HEMODYNAMICS AND OXYGENATION [J].
BIGATELLO, LM ;
HURFORD, WE ;
KACMAREK, RM ;
ROBERTS, JD ;
ZAPOL, WM .
ANESTHESIOLOGY, 1994, 80 (04) :761-770
[8]   DEFINITIONS FOR SEPSIS AND ORGAN FAILURE AND GUIDELINES FOR THE USE OF INNOVATIVE THERAPIES IN SEPSIS [J].
BONE, RC ;
BALK, RA ;
CERRA, FB ;
DELLINGER, RP ;
FEIN, AM ;
KNAUS, WA ;
SCHEIN, RMH ;
SIBBALD, WJ .
CHEST, 1992, 101 (06) :1644-1655
[9]  
BROWN BW, 1997, STAT BIOMEDICAL INTR, P119
[10]   Nitric oxide donor prevents hydrogen peroxide-mediated endothelial cell injury [J].
Chang, J ;
Rao, NV ;
Markewitz, BA ;
Hoidal, JR ;
Michael, JR .
AMERICAN JOURNAL OF PHYSIOLOGY-LUNG CELLULAR AND MOLECULAR PHYSIOLOGY, 1996, 270 (06) :L931-L940