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  • 1
    ISSN: 1432-1238
    Keywords: Trauma-sepsis ; Inflammatory response ; Soluble adhesion molecules ; Endothelium Tissue damage ; Neutrophils
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract Objective The time course of circulating adhesion molecules was monitored in traumatized and sepsis patients. Design Prospective, descriptive. Setting A surgical intensive care unit of a university hospital. Patients A total of 30 consecutive critically ill patients suffering either from trauma (n=15) or postoperative sepsis (n=15). Interventions All patients were on continuous analgo-sedation and mechanical ventilation. Measurements and results From arterial blood samples, plasma levels of soluble adhesion molecules [endothelial leukocyte adhesion molecules (sELAM-1), intercellular adhesion molecule-1 (sICAM-1)], and vascular cell adhesion molecule-1 (sVCAM-1) were measured on the day of admission (trauma patients) or on the day of diagnosis of sepsis (=baseline values), and during the following 5 days. In the trauma group,sELAM-1 (57.9±11.0 ng/ml) andsVCAM-1 (698±93 ng/ml) were within normal ranges at baseline, whereas they were markedly elevated in the sepsis group (sELAM-1: 340±95 ng/ml;sVCAM-1; 1,042±449 ng/ml). In the sepsis patients,sELAM-1 significantly decreased andsVCAM-1 increased, but remained almost unchanged in the trauma patients. Non-survivors showed markedly elevated plasma levels ofsELAM-1 andsVCAM-1.sICAM-1 was elevated in both groups at baseline and was higher in the sepsis group (1,266±261 ng/ml) than in the trauma group. In the septic patients,sICAM-1 increased further (2,022±609 ng/ml) and remained unchanged in the trauma group. All non-survivors showedsICAM-1 plasma levels of 〉800 ng/ml. Conclusion Endothelial damage may result in multiple-organ dysfunction syndrome. Adhesion molecules are considered to be a cornerstone in this process. Trauma patients showed lower plasma levels of circulating adhesion molecules than did sepsis patients indicating more pronounced (inflammatory related) endothelial activation or damage in sepsis. Therapeutic modulation of circulating adhesion molecules may be of benefit to the patients outcome and therefore warrants further study.
    Type of Medium: Electronic Resource
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  • 2
    ISSN: 1432-1238
    Keywords: Continuous hemofiltration ; Renal failure Inflammatory response ; Soluble adhesion molecules ; Endothelial leukocyte adhesion molecules [sELAM-1] ; Vascular cell adhesion molecule-1 [sVCAM-1] ; Intercellular adhesion molecule-1 [sICAM-1] ; Granule membrane protein 140 [sGMP-140] ; Neutrophils ; Endothelium
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract Objective Circulating adhesion molecules appear to be excellent markers of endothelial activation in critically ill patients. Pentoxifylline (PTX) may limit sequelae of inflammation and subsequent endothelial activation by various mechanisms. The influence of PTX on the plasma levels of soluble adhesion molecules in critically ill patients undergoing continuous veno-venous hemofiltration (CVVH) was studied. Design Prospective, randomized, blinded study. Setting Clinical investigation in the surgical intensive care unit of a university hospital. Patients and participants Fourteen consecutive patients suffering from acute renal failure (ARF) with postoperative complications who received continuous pentoxifylline (CVVH-PTX) i.v. were compared with 14 patients with ARF who did not receive PTX (CVVH control group). Interventions Pump-driven CVVH was carried out with a blood flow ranging from 120 to 150 ml/min. All patients received fentanyl and midazolam continuously and were on mechanical ventilation. PTX (300 mg) was given as a loading dose, followed by continuous infusion of 1.2 mg/kg per h for the next 5 days. Measurements and results From arterial blood samples, plasma levels of soluble adhesion molecules (endothelial leukocyte adhesion molecules [sELAM-1], and intercellular adhesion molecule-1 [sICAM-1], vascular cell adhesion molecule-1 [sVCAM-1], and P-selectin granule membrane protein [sGMP-140] were measured using enzyme-linked immuno-sorbent assays (ELISA). Measurements were carried out before the start of CVVH to establish baseline values and continued during the next 5 days. Main results Eleven of the CVVH-PTX patients and 8 of the CVVH control patients survived during the investigation period. In the CVVH-PTX patients 2.4±0.3 g/day of PTX was given. At baseline, plasma levels of sELAM-1, sICAM-1, and sVCAM-1 were markedly higher than normal in both groups. In the CVVH control patients, all measured soluble adhesion molecules increased further during the study period (sELAM-1 from 90±22 to 134±30 ng/ml; sICAM-1 from 958±173 to 1460±209 ng/ml; sVCAM-1 from 1100±188 to 1804 ng/ml; sGM-140 from 499±102 to 688±121 ng/ml) (p〈0.05), whereas in the PTX-treated CVVH patients, plasma levels of all soluble adhesion molecules remained almost unchanged. The PaO2/FIO2 increased in the PTX-treated patients (from 209±67 to 282±58 mmHg) and remained almost unchanged in the CVVH control patients. Conclusion Leukocyte/endothelial interactions play an important role in the inflammatory process. Circulating adhesion molecules may serve as markers of the extent of inflammation. Continuous i.v. administration of PTX was successful in blunting the increase of soluble adhesion molecules in critically ill patients undergoing CVVH. Whether these effects result from improved circulation at the microcirculatory level or from (direct or indirect) beneficial effects on endothelial cells warrants further controlled studies.
    Type of Medium: Electronic Resource
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  • 3
    ISSN: 1432-1238
    Keywords: Key words Continuous hemofiltration ; Renal failure ; Inflammatory response ; Soluble adhesion molecules ; Endothelial leukocyte adhesion molecules [sELAM-1] ; Vascular cell adhesion molecule-1 [sVCAM-1] ; Intercellular adhesion molecule-1 [sICAM-1] ; Granule membrane protein 140 [sGMP-140] ; Neutrophils ; Endothelium
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract Objective: Circulating adhesion molecules appear to be excellent markers of endothelial activation in critically ill patients. Pentoxifylline (PTX) may limit sequelae of inflammation and subsequent endothelial activation by various mechanisms. The influence of PTX on the plasma levels of soluble adhesion molecules in critically ill patients undergoing continuous veno-venous hemofiltration (CVVH) was studied. Design: Prospective, randomized, blinded study. Setting: Clinical investigation in the surgical intensive care unit of a university hospital. Patients and participants: Fourteen consecutive patients suffering from acute renal failure (ARF) with postoperative complications who received continuous pentoxifylline (CVVH-PTX) i.v. were compared with 14 patients with ARF who did not receive PTX (CVVH control group). Interventions: Pump-driven CVVH was carried out with a blood flow ranging from 120 to 150 ml/min. All patients received fentanyl and midazolam continuously and were on mechanical ventilation. PTX (300 mg) was given as a loading dose, followed by continuous infusion of 1.2 mg/kg per h for the next 5 days. Measurements and results: From arterial blood samples, plasma levels of soluble adhesion molecules (endothelial leukocyte adhesion molecules [sELAM-1], and intercellular adhesion molecule-1 [sICAM-1], vascular cell adhesion molecule-1 [sVCAM-1], and P-selectin granule membrane protein [sGMP-140] were measured using enzyme-linked immuno-sorbent assays (ELISA). Measurements were carried out before the start of CVVH to establish baseline values and continued during the next 5 days. Main results: Eleven of the CVVH-PTX patients and 8 of the CVVH control patients survived during the investigation period. In the CVVH-PTX patients 2.4±0.3 g/day of PTX was given. At baseline, plasma levels of sELAM-1, sICAM-1, and sVCAM-1 were markedly higher than normal in both groups. In the CVVH control patients, all measured soluble adhesion molecules increased further during the study period (sELAM-1 from 90±22 to 134±30 ng/ml; sICAM-1 from 958±173 to 1460±209 ng/ml; sVCAM-1 from 1100±188 to 1804 ng/ml; sGM-140 from 499±102 to 688±121 ng/ml) (p〈0.05), whereas in the PTX-treated CVVH patients, plasma levels of all soluble adhesion molecules remained almost unchanged. The PaO2/FIO2 increased in the PTX-treated patients (from 209±67 to 282±58 mmHg) and remained almost unchanged in the CVVH control patients. Conclusion: Leukocyte/endothelial interactions play an important role in the inflammatory process. Circulating adhesion molecules may serve as markers of the extent of inflammation. Continuous i.v. administration of PTX was successful in blunting the increase of soluble adhesion molecules in critically ill patients undergoing CVVH. Whether these effects result from improved circulation at the microcirculatory level or from (direct or indirect) beneficial effects on endothelial cells warrants further controlled studies.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
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