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1.
Shock ; 24(2): 153-8, 2005 Aug.
Article in English | MEDLINE | ID: mdl-16044086

ABSTRACT

According to a previous study, a pathologically increased intraabdominal pressure (IAP) reduces cardiac output (CO) and results in medium- to high-grade organ damage in a porcine model of the abdominal compartment syndrome (ACS). The purpose of this study was to evaluate whether fluid resuscitation can preserve organ integrity together with CO. We examined 12 domestic pigs with a mean body weight of 48 kg. We used a CO2 pneumoperitoneum to increase the IAP to 30 mmHg in 6 animals, and the others served as control group. The investigation period was 24 h. In addition to a standard infusion regimen, Ringer's solution was infused to maintain CO at the level of control animals. Hemodynamic parameters (ITBV, EVLW, MAP, CVP), urine output, inspiratory pressure, as well as serum parameters (e.g., ALT, lipase, AP, lactate, creatinine) were recorded. In the end histological examination of liver, bowel, kidney, and lung was performed. CO, ITBV, EVLW, and urine output did not change when compared with control. Fluid intake was increased (P < 0.01) when compared with control (10,570 +/- 1,928 vs. 3,918 +/- 1,042 mL). CVP, MAP, and inspiratory pressure were increased. Serum parameters did not change. Acidosis occurred in the study group. Liver, bowel, kidney, and lung displayed mean- to high-grade damage (P < 0.01). Although extensive fluid resuscitation preserved CO, diuresis, and serum parameters in this previously described model of the ACS, organ damage occurred. In the clinical regard, these results support decompressive treatment in the presence of pathologically high IAP despite "normalized" parameters.


Subject(s)
Fluid Therapy/methods , Hypertension/pathology , Resuscitation/methods , Acidosis , Analysis of Variance , Animals , Arteries/pathology , Blood Pressure , Body Weight , Carbon Dioxide/pharmacology , Carbon Monoxide/chemistry , Cardiac Output , Hemodynamics , Intercellular Adhesion Molecule-1/biosynthesis , Kidney/pathology , Liver/pathology , Lung/pathology , Male , Pressure , Swine , Time Factors
2.
Crit Care Med ; 33(6): 1243-7, 2005 Jun.
Article in English | MEDLINE | ID: mdl-15942338

ABSTRACT

OBJECTIVE: To investigate factors that may influence the estimation of extravascular lung water (EVLW) with a single (cold) indicator compared with assessment using two indicators (thermo-dye dilution). DESIGN: Post hoc analysis of an electronic hemodynamic database. SETTING: Surgical intensive care unit of a university hospital. PATIENTS: Forty-eight critically ill patients monitored by the thermo-dye dilution technique in the postoperative period. INTERVENTIONS: None. MEASUREMENTS AND MAIN RESULTS: The EVLW was simultaneously assessed by the thermo-dye dilution technique (EVLWref) and estimated by transpulmonary thermodilution (EVLWest). EVLWref index ranged between 1 and 40 mL/kg (mean 10 +/- 7 mL/kg) and EVLWest between 2 and 39 mL/kg (mean 9 +/- 6 mL/kg). EVLWref was closely correlated (r = .96) with EVLWest. The mean difference (bias) between EVLWref and EVLWest was -0.5 +/- 1.9 mL/kg. The bias was not influenced by the weight, height, body surface area, body mass index, Pao2, intrathoracic blood volume, cardiac output, or dosage of vasoactive agents. In contrast, the bias was slightly but significantly influenced by EVLWref, Pao2/Fio2 ratio, tidal volume, and level of positive end-expiratory pressure. CONCLUSIONS: In our surgical intensive care unit population, the estimation of EVLW by transpulmonary thermodilution was influenced by the amount of EVLW, the Pao2/Fio2 ratio, the tidal volume, and the level of positive end-expiratory pressure. However, compared with the double indicator method, transpulmonary thermodilution estimation remained clinically acceptable even in patients with severe lung disease.


Subject(s)
Extravascular Lung Water , Pulmonary Edema/diagnosis , Thermodilution , Aged , Coloring Agents , Hemodynamics , Humans , Indocyanine Green , Intensive Care Units , Linear Models , Male , Positive-Pressure Respiration , Respiratory Mechanics
3.
Shock ; 18(4): 316-21, 2002 Oct.
Article in English | MEDLINE | ID: mdl-12392274

ABSTRACT

The purpose of this study was to investigate whether an intra-abdominal pressure (IAP) of 30 mmHg lasting 24 h in a porcine model will lead to a condition comparable with the abdominal compartment syndrome (ACS) in humans. We examined 12 intubated and anesthetized domestic pigs with a mean body weight of 52.5 +/- 4.9 kg. Using a CO2 pneumoperitoneum, the IAP was increased to 30 mmHg (study group, n = 6) for an investigation period of 24 h. In the control group, the IAP remained unchanged. Investigated parameters were cardiac output (CO), peak inspiratory pressure (PIP), urine output (UO), as well as serum alanine aminotransferase (ALT), lactate, lipase, and alkaline phosphatase (AP). Additionally, histopathological examinations were performed. In the study group, CO was significantly reduced compared with the control group. All animals of this group became anuric and their PIP exceeded 40 cm H2O. Furthermore, ALT, AP, lipase, and lactate were significantly increased. Histopathologically, high-grade atelectasis in the lower lobes of the lung together with medium grade liver necrosis, medium grade proximal tubular epithelial necrosis, and medium grade mucosal bowel damage were observed. In this porcine model, an intra-abdominal pressure of 30 mmHg led to a condition comparable with the ACS. Because function or integrity of additional organ systems was impaired, an IAP of 30 mmHg has to be considered a predisposition for the multi-organ dysfunction syndrome in this porcine model.


Subject(s)
Compartment Syndromes/physiopathology , Abdomen/physiopathology , Alanine Transaminase/blood , Alkaline Phosphatase/blood , Animals , Anuria/etiology , Carbon Monoxide/blood , Compartment Syndromes/complications , Compartment Syndromes/metabolism , Disease Models, Animal , Gastric Mucosa/pathology , Lactates/blood , Lipase/blood , Liver/pathology , Liver/physiology , Lung/pathology , Male , Pancreas/physiology , Pressure , Sus scrofa
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