Hypercapnic acidosis attenuates shock and lung injury in early and prolonged systemic sepsis

被引:71
作者
Costello, Joseph
Higgins, Brendan
Contreras, Maya
Chonghaile, Martina Ni
Hassett, Patrick
O'Toole, Daniel
Laffey, John G. [1 ]
机构
[1] Natl Univ Ireland, Inst Clin Sci, Dept Anaesthesia, Galway, Ireland
关键词
acute lung injury; hypercapnia acidosis; acute respiratory distress syndrome; shock; sepsis; RESPIRATORY-DISTRESS-SYNDROME; CARBON-DIOXIDE; THERAPEUTIC HYPERCAPNIA; ABDOMINAL INSUFFLATION; PROTECTIVE-VENTILATION; INFLAMMATORY RESPONSE; INCREASES SURVIVAL; INTRACELLULAR PH; PULMONARY; HYPOXIA;
D O I
10.1097/CCM.0b013e3181a385d3
中图分类号
R4 [临床医学];
学科分类号
1002 ; 100602 ;
摘要
Objective. To investigate whether acute hypercapnic acidosis-induced by adding CO2 to inspired gas-would protect against severe systemic sepsis-induced lung and systemic organ injury resulting from cecal ligation and puncture. Acute hypercapnic acidosis protects against lung injury after both nonseptic and early pneumonia-induced lung injury. In contrast, prolonged hypercapnia worsens pneumonia-induced lung injury. The effects of hypercapnia and acidosis in the setting of systemic sepsis remain to be determined. Design: Prospective randomized animal study. Setting: University research laboratory. Subjects: Adult male Sprague-Dawley rats. Interventions: In the early systemic sepsis series, post induction of anesthesia and tracheostomy placement, animals were randomized to normocapnia (FICO2 = 0.00, n = 12) or hypercapnic acidosis (FICO2 = 0.05, n = 12). Cecal ligation and puncture were performed and the animals were ventilated for 3 hrs. In the prolonged systemic sepsis series, rats were anesthetized, cecal ligation and puncture were performed, and the animals were allowed to recover. The animals were then randomized to housing under conditions of environmental normocapnia (FICO2 = 0.00, n = 20) or hypercapnia (FICO2 = 0.08, n = 20). After 96 hrs, the animals were reanesthetized, and the severity of lung and hemodynamic injury was assessed. Results: In early systemic sepsis, hypercapnic acidosis attenuated the development and severity of hypotension, and reduced lactate accumulation and the decrement in central venous oxyhemoglobin levels, compared with normocapnia. Hypercapnic acidosis reduced bronchoalveolar lavage neutrophil infiltration, and lung wet/ dry weight ratios. In prolonged systemic sepsis, hypercapnic acidosis reduced histologic indices of lung injury. There was no evidence that hypercapnia worsened prolonged systemic sepsis-induced lung injury. Hypercapnic acidosis did not alter lung or systemic bacterial loads in early or prolonged systemic sepsis. Conclusion. Hypercapnic acidosis exerts beneficial effects in early and prolonged cecal ligation and puncture-induced polymicrobial systemic sepsis. (Crit Care Med 2009; 37:2412-2420)
引用
收藏
页码:2412 / 2420
页数:9
相关论文
共 45 条
[1]  
Allen DB, 1997, ARCH SURG-CHICAGO, V132, P991
[2]   Effect of a protective-ventilation strategy on mortality in the acute respiratory distress syndrome [J].
Amato, MBP ;
Barbas, CSV ;
Medeiros, DM ;
Magaldi, RB ;
Schettino, GDP ;
Lorenzi, G ;
Kairalla, RA ;
Deheinzelin, D ;
Munoz, C ;
Oliveira, R ;
Takagaki, TY ;
Carvalho, CRR .
NEW ENGLAND JOURNAL OF MEDICINE, 1998, 338 (06) :347-354
[3]   LUNG MORPHOMETRY - A NEW-GENERATION OF TOOLS AND EXPERIMENTS FOR ORGAN, TISSUE, CELL, AND MOLECULAR-BIOLOGY [J].
BOLENDER, RP ;
HYDE, DM ;
DEHOFF, RT .
AMERICAN JOURNAL OF PHYSIOLOGY, 1993, 265 (06) :L521-L548
[4]   Protective effects of hypercapnic acidosis on ventilator-induced lung injury [J].
Broccard, AF ;
Hotchkiss, JR ;
Vannay, C ;
Markert, M ;
Sauty, A ;
Feihl, F ;
Schaller, MD .
AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE, 2001, 164 (05) :802-806
[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]   CO2 Pneumoperitoneum Prolongs Survival in an Animal Model of Peritonitis Compared to Laparotomy [J].
Chatzimavroudis, Grigoris ;
Pavlidis, Theodoros E. ;
Koutelidakis, Ioannis ;
Giamarrelos-Bourboulis, Evangelos J. ;
Atmatzidis, Stefanos ;
Kontopoulou, Konstantina ;
Marakis, Georgios ;
Atmatzidis, Konstantinos .
JOURNAL OF SURGICAL RESEARCH, 2009, 152 (01) :69-75
[7]   Hypercapnic acidosis attenuates severe acute bacterial pneumonia-induced lung injury by a neutrophil-independent mechanism [J].
Chonghaile, Martina Ni ;
Higgins, Brendan D. ;
Costello, Joseph F. ;
Laffey, John G. .
CRITICAL CARE MEDICINE, 2008, 36 (12) :3135-3144
[8]  
Coakley RJ, 2002, J LEUKOCYTE BIOL, V71, P603
[9]   Cytosolic pH and the inflammatory microenvironment modulate cell death in human neutrophils after phagocytosis [J].
Coakley, RJ ;
Taggart, C ;
McElvaney, NG ;
O'Neill, SJ .
BLOOD, 2002, 100 (09) :3383-3391
[10]   Preventing ventilator-associated pneumonia in adults - Sowing seeds of change [J].
Craven, Donald E. .
CHEST, 2006, 130 (01) :251-260