Low-dose inhaled nitric oxide in patients with acute lung injury - A randomized controlled trial

被引:333
作者
Taylor, RW
Zimmerman, JL
Dellinger, RP
Straube, RC
Criner, GJ
Davis, K
Kelly, KM
Smith, TC
Small, RJ
机构
[1] Univ Med & Dent New Jersey, Robert Wood Johnson Med Sch, Cooper Univ Hosp, Camden, NJ 08103 USA
[2] St Louis Univ, St Johns Mercy Med Ctr, St Louis, MO 63103 USA
[3] Baylor Coll Med, Dept Med, Houston, TX 77030 USA
[4] Ben Taub Gen Hosp, Houston, TX 77030 USA
[5] INO Therapeut Inc, Clinton, NJ USA
[6] Temple Univ Hosp & Med Sch, Temple Lung Ctr, Philadelphia, PA 19140 USA
[7] Univ Cincinnati, Med Ctr, Dept Surg, Cincinnati, OH 45267 USA
[8] Ortho Biotech, Dept Clin Res, Bridgewater, MA USA
[9] Albany Med Coll, Dept Pulm Med, Albany, NY 12208 USA
来源
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION | 2004年 / 291卷 / 13期
关键词
D O I
10.1001/jama.291.13.1603
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Context Inhaled nitric oxide has been shown to improve oxygenation in acute lung injury. Objective To evaluate the clinical efficacy of low-dose (5-ppm) inhaled nitric oxide in patients with acute lung injury. Design and Setting Multicenter, randomized, placebo-controlled study, with blinding of patients, caregivers, data collectors, assessors of outcomes, and data analysts (triple blind), conducted in the intensive care units of 46 hospitals in the United States. Patients were enrolled between March 1996 and September 1999. Patients Patients (n=385) with moderately severe acute lung injury, a modification of the American-European Consensus Conference definition of acute respiratory distress syndrome (ARDS) using a ratio of PaO2 to FiO(2) of less than or equal to250, were enrolled if the onset was within 72 hours of randomization, sepsis was not the cause of the lung injury, and the patient had no significant nonpulmonary organ system dysfunction at randomization. Interventions Patients were randomly assigned to placebo (nitrogen gas) or inhaled nitric oxide at 5 ppm until 28 days, discontinuation of assisted breathing, or death. Main Outcome Measures The primary end point was days alive and off assisted breathing. Secondary outcomes included mortality, days alive and meeting oxygenation criteria for extubation, and days patients were alive following a successful unassisted ventilation test. Results An intent-to-treat analysis revealed that inhaled nitric oxide at 5 ppm did not increase the number of days patients were alive and off assisted breathing (mean [SD], 10.6 [9.8] days in the placebo group and 10.7 [9.7] days in the inhaled nitric oxide group; P=.97; difference, -0.1 day [95% confidence interval, -2.0 to 1.9 days]). This lack of effect on clinical outcomes was seen despite a statistically significant increase in PaO2 that resolved by 48 hours. Mortality was similar between groups (20% placebo vs 23% nitric oxide; P=.54). Days patients were alive following a successful 2-hour unassisted ventilation trial were a mean (SD) of 11.9 (9.9) for placebo and 11.4 (9.8) for nitric oxide patients (P=.54). Days alive and meeting criteria for extubation were also similar: 17.0 placebo vs 16.7 nitric oxide (P=.89). Conclusion Inhaled nitric oxide at a dose of 5 ppm in patients with acute lung injury not due to sepsis and without evidence of nonpulmonary organ system dysfunction results in short-term oxygenation improvements but has no substantial impact on the duration of ventilatory support or mortality.
引用
收藏
页码:1603 / 1609
页数:7
相关论文
共 30 条
[1]  
[Anonymous], INTENSIVE CARE ME S1
[2]   REPORT OF THE AMERICAN-EUROPEAN CONSENSUS CONFERENCE ON ACUTE RESPIRATORY-DISTRESS SYNDROME - DEFINITIONS, MECHANISMS, RELEVANT OUTCOMES, AND CLINICAL-TRIAL COORDINATION [J].
BERNARD, GR ;
ARTIGAS, A ;
BRIGHAM, KL ;
CARLET, J ;
FALKE, K ;
HUDSON, L ;
LAMY, M ;
LEGALL, JR ;
MORRIS, A ;
SPRAGG, R ;
Cochin, B ;
Lanken, PN ;
Leeper, KV ;
Marini, J ;
Murray, JF ;
Oppenheimer, L ;
Pesenti, A ;
Reid, L ;
Rinaldo, J ;
Villar, J ;
van Asbeck, BS ;
Dhainaut, JF ;
Mancebo, J ;
Matthay, M ;
Meyrick, B ;
Payen, D ;
Perret, C ;
Fowler, AA ;
Schaller, MD ;
Hudson, LD ;
Hyers, T ;
Knaus, W ;
Matthay, R ;
Pinsky, M ;
Bone, RC ;
Bosken, C ;
Johanson, WG ;
Lewandowski, K ;
Repine, J ;
Rodriguez-Roisin, R ;
Roussos, C ;
Antonelli, MA ;
Beloucif, S ;
Bihari, D ;
Burchardi, H ;
LeMaire, F ;
Montravers, P ;
Petty, TL ;
Robotham, J ;
Zapol, W .
JOURNAL OF CRITICAL CARE, 1994, 9 (01) :72-81
[3]   Ventilation with lower tidal volumes as compared with traditional tidal volumes for acute lung injury and the acute respiratory distress syndrome. [J].
Brower, RG ;
Matthay, MA ;
Morris, A ;
Schoenfeld, D ;
Thompson, BT ;
Wheeler, A ;
Wiedemann, HP ;
Arroliga, AC ;
Fisher, CJ ;
Komara, JJ ;
Perez-Trepichio, P ;
Parsons, PE ;
Wolkin, R ;
Welsh, C ;
Fulkerson, WJ ;
MacIntyre, N ;
Mallatratt, L ;
Sebastian, M ;
McConnell, R ;
Wilcox, C ;
Govert, J ;
Thompson, D ;
Clemmer, T ;
Davis, R ;
Orme, J ;
Weaver, L ;
Grissom, C ;
Eskelson, M ;
Young, M ;
Gooder, V ;
McBride, K ;
Lawton, C ;
d'Hulst, J ;
Peerless, JR ;
Smith, C ;
Brownlee, J ;
Pluss, W ;
Kallet, R ;
Luce, JM ;
Gottlieb, J ;
Elmer, M ;
Girod, A ;
Park, P ;
Daniel, B ;
Gropper, M ;
Abraham, E ;
Piedalue, F ;
Glodowski, J ;
Lockrem, J ;
McIntyre, R .
NEW ENGLAND JOURNAL OF MEDICINE, 2000, 342 (18) :1301-1308
[4]   Low-dose nitric oxide therapy for persistent pulmonary hypertension of the newborn. [J].
Clark, RH ;
Kueser, TJ ;
Walker, MW ;
Southgate, WM ;
Huckaby, JL ;
Perez, JA ;
Roy, BJ ;
Keszler, M ;
Kinsella, JP .
NEW ENGLAND JOURNAL OF MEDICINE, 2000, 342 (07) :469-474
[5]   Safety of inhaled nitric oxide after lung transplantation [J].
Cornfield, DN ;
Milla, CE ;
Haddad, IY ;
Barbato, JE ;
Park, SJ .
JOURNAL OF HEART AND LUNG TRANSPLANTATION, 2003, 22 (08) :903-907
[6]   Effects of inhaled nitric oxide in patients with acute respiratory distress syndrome: Results of a randomized phase II trial [J].
Dellinger, RP ;
Zimmerman, JL ;
Taylor, RW ;
Straube, RC ;
Hauser, DL ;
Criner, GJ ;
Davis, K ;
Hyers, TM ;
Papadakos, P .
CRITICAL CARE MEDICINE, 1998, 26 (01) :15-23
[7]   A COMPARISON OF 4 METHODS OF WEANING PATIENTS FROM MECHANICAL VENTILATION [J].
ESTEBAN, A ;
FRUTOS, F ;
TOBIN, MJ ;
ALIA, I ;
SOLSONA, JF ;
VALVERDU, I ;
FERNANDEZ, R ;
DELACAL, MA ;
BENITO, S ;
TOMAS, R ;
CARRIEDO, D ;
MACIAS, S ;
BLANCO, J .
NEW ENGLAND JOURNAL OF MEDICINE, 1995, 332 (06) :345-350
[8]   INHALED NITRIC-OXIDE - A SELECTIVE PULMONARY VASODILATOR REVERSING HYPOXIC PULMONARY VASOCONSTRICTION [J].
FROSTELL, C ;
FRATACCI, MD ;
WAIN, JC ;
JONES, R ;
ZAPOL, WM .
CIRCULATION, 1991, 83 (06) :2038-2047
[9]   INHALED NITRIC-OXIDE SELECTIVELY REVERSES HUMAN HYPOXIC PULMONARY VASOCONSTRICTION WITHOUT CAUSING SYSTEMIC VASODILATION [J].
FROSTELL, CG ;
BLOMQVIST, H ;
HEDENSTIERNA, G ;
LUNDBERG, J ;
ZAPOL, WM .
ANESTHESIOLOGY, 1993, 78 (03) :427-435
[10]   Intravenous almitrine combined with inhaled nitric oxide for acute respiratory distress syndrome [J].
Gallart, L ;
Lu, Q ;
Puybasset, L ;
Rao, GSU ;
Coriat, P ;
Rouby, JJ .
AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE, 1998, 158 (06) :1770-1777