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1.
J Trauma ; 61(1): 185-91, 2006 Jul.
Article in English | MEDLINE | ID: mdl-16832269

ABSTRACT

BACKGROUND: This study evaluates the effects of early rapid control of multiple bowel perforations on cardiovascular and pulmonary function in high-energy traumatic shock compared with conventional small bowel resection anastomosis. METHODS: Fifteen anesthetized pigs, 10 to 12 weeks old, were exposed to a reproducible high-energy trauma and were divided into two groups. In the first group, the resection anastomosis group (RA, n = 8), small-bowel injuries were treated with resection and anastomosis; in the second group, the multiple bowel ligation group (BL, n = 7), small-bowel injuries were treated by resection and ligation. Repeated measurement analysis of variance was used to study the within group change overtime, the between group difference, and the interaction between them. Mean outcome measures were intravascular pressures, cardiac output, vascular resistance, lactic acid, and blood gases. RESULTS: The high-energy injuries caused traumatic shock in both groups with reduced cardiac output (p < 0.001) and lactic acidemia (p < 0.001). The BL group had a trend for higher cardiac output (p = 0.06). The rise in systemic and pulmonary vascular resistance was significantly reduced in the BL group compared with the RA group (p < 0.05). The BL group had a strong trend for higher oxygen extraction ratio (p = 0.06). There was a trend for less oxygen consumption in the BL group (p = 0.07). There was no difference in the lactic acidemia between the two groups. CONCLUSIONS: Early rapid control of multiple bowel perforations after high-energy trauma resulted in less impairment of cardiovascular function than conventional resection anastomosis of the bowel.


Subject(s)
Intestinal Perforation/surgery , Multiple Trauma/surgery , Wounds, Gunshot/surgery , Acidosis, Lactic , Anastomosis, Surgical , Animals , Cardiac Output , Intestinal Perforation/complications , Multiple Trauma/complications , Shock, Traumatic/etiology , Shock, Traumatic/surgery , Swine , Vascular Resistance , Wounds, Gunshot/complications
2.
Microvasc Res ; 67(2): 192-6, 2004 Mar.
Article in English | MEDLINE | ID: mdl-15020210

ABSTRACT

Nonspecific vasodilatation during iontophoresis is an important confounding factor in experimental pharmacology. In this investigation, we studied the involvement of sensory nerves and histamine-related reactions in causing nonspecific vasodilatation in a model of anodal and cathodal iontophoresis of sodium chloride. Firstly, we applied a mixture of local anesthetic (EMLA) cream to confirm its suppressive effect on nonspecific vasodilatation and to measure its efficacy in three different dosages (duration: 1, 2, and 3 h). We then investigated the role of histamine in nonspecific vasodilatation by giving an oral antihistamine drug (cetirizine) to subjects who had and had not been given EMLA. We found substantial suppression of the nonspecific vasodilatation in all EMLA-treated groups (all dosages) compared with untreated controls (with suppression rates of 60-65%). Dosage had no significant effect. A further suppression of nonspecific vasodilatation was seen after oral cetirizine during anodal and cathodal iontophoresis in both EMLA-treated and untreated groups. The antihistamine effect was most pronounced during anodal iontophoresis. These results suggest a histaminergic increase in perfusion that may be independent of neurogenic mechanisms and depend on polarity (anode or cathode). Local nerve blocks (EMLA) together with cetirizine may therefore be used to reduce nonspecific vasodilatation in both anodal and cathodal iontophoresis.


Subject(s)
Histamine Release , Iontophoresis , Vasodilation , Administration, Oral , Adult , Anesthetics, Local/pharmacology , Cetirizine/pharmacology , Confounding Factors, Epidemiologic , Histamine H1 Antagonists, Non-Sedating/pharmacology , Histamine Release/drug effects , Humans , Iontophoresis/methods , Lidocaine/pharmacology , Lidocaine, Prilocaine Drug Combination , Neurons, Afferent/drug effects , Neurons, Afferent/physiology , Prilocaine/pharmacology , Sodium Chloride/administration & dosage , Sodium Chloride/pharmacology , Vasodilation/drug effects , Vasodilation/physiology
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