A Randomized Clinical Trial of Hydroxymethylglutaryl-Coenzyme A Reductase Inhibition for Acute Lung Injury (The HARP Study)

被引:163
作者
Craig, Thelma R. [1 ,2 ]
Duffy, Martin J. [1 ,2 ]
Shyamsundar, Murali [1 ,2 ]
McDowell, Cliona [3 ]
O'Kane, Cecilia M. [1 ]
Elborn, J. Stuart [1 ]
McAuley, Daniel F. [1 ,2 ]
机构
[1] Queens Univ Belfast, Ctr Infect & Immun, Belfast BT9 7BL, Antrim, North Ireland
[2] Royal Victoria Hosp, Reg Intens Care Unit, Belfast BT12 6BA, Antrim, North Ireland
[3] Royal Victoria Hosp, Clin Res Support Ctr, Belfast BT12 6BA, Antrim, North Ireland
关键词
simvastatin; acute lung injury; acute respiratory distress syndrome; INFLAMMATION; PULMONARY; OUTCOMES; MORTALITY; SPACE;
D O I
10.1164/rccm.201003-0423OC
中图分类号
R4 [临床医学];
学科分类号
1002 ; 100602 ;
摘要
Rationale There is no effective pharmacological treatment for acute lung injury (All). Statins are a potential new therapy because they modify many of the underlying processes important in ALI. Objectives: To test whether simvastatin improves physiological and biological outcomes in ALI. Methods: We conducted a randomized, double-blinded, placebo-controlled trial in patients with ALL Patients received 80 mg simvastatin or placebo until cessation of mechanical ventilation or up to 14 days. Extravascular lung water was measured using thermodilution. Measures of pulmonary and nonpulmonary organ function were assessed daily. Pulmonary and systemic inflammation was assessed by bronchoalveolar lavage fluid and plasma cytokines. Systemic inflammation was also measured by plasma C-reactive protein. Measurements and Main Results: Sixty patients were recruited. Baseline characteristics, including demographics and severity of illness scores, were similar in both groups. At Day 7, there was no difference in extravascular lung water. By Day 14, the simvastatin-treated group had improvements in nonpulmonary organ dysfunction. Oxygenation and respiratory mechanics improved, although these parameters failed to reach statistical significance. Intensive care unit mortality was 30% in both groups. Simvastatin was well tolerated, with no increase in adverse events. Simvastatin decreased bronchoalveolar lavage IL-8 by 2.5-fold (P = 0.04). Plasma C-reactive protein decreased in both groups but failed to achieve significance in the placebo-treated group. Conclusions: Treatment with simvastatin appears to be safe and may be associated with an improvement in organ dysfunction in ALI. These clinical effects may be mediated by a reduction in pulmonary and systemic inflammation.
引用
收藏
页码:620 / 626
页数:7
相关论文
共 28 条
[1]  
Ando H, 2000, J PHARMACOL EXP THER, V294, P1043
[2]  
[Anonymous], 2004, COCHRANE DB SYST REV
[3]  
Banta EM, 2010, AM J RESP CRIT CARE, V181
[4]   THE AMERICAN-EUROPEAN CONSENSUS CONFERENCE ON ARDS - 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 ;
VANASBECK, 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 ;
RODRIGUEZROISIN, R ;
ROUSSOS, C ;
ANTONELLI, MA ;
BELOUCIF, S ;
BIHARI, D ;
BURCHARDI, H ;
LEMAIRE, F ;
MONTRAVERS, P ;
PETTY, TL ;
ROBOTHAM, J ;
ZAPOL, W .
AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE, 1994, 149 (03) :818-824
[5]   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
[6]  
Craig T, 2007, POTENTIAL MECH STATI, P276
[7]   SIMVASTATIN REDUCES INFLAMMATION AND IMPROVES CLINICAL OUTCOMES IN ALI: RESULTS OF THE HARP STUDY [J].
Craig, T. R. ;
Duffy, M. J. ;
Shyamsundar, M. ;
O'Kane, C. ;
Elborn, J. S. ;
McAuley, D. F. .
THORAX, 2009, 64 :A2-A2
[8]  
Drage SM, 2009, J INTENSIVE CARE SOC, V10, P61
[9]  
HONGWEI Y, 2006, CLIN EXP PHARM PHYSL, V33, P793
[10]   Acute lung injury and the acute respiratory distress syndrome in Ireland: a prospective audit of epidemiology and management [J].
Sheridan, M. ;
Donnelly, M. ;
Bailie, R. ;
Power, M. ;
Seigne, P. ;
Austin, S. ;
Marsh, B. ;
Motherway, C. ;
Scully, M. ;
Fagan, C. ;
Benson, P. ;
McAuley, D. ;
Trinder, J. ;
Bates, J. ;
Bailie, K. .
CRITICAL CARE, 2008, 12 (01)