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1.
J Pediatr Surg ; 30(7): 1072-5; discussion 1075-6, 1995 Jul.
Article in English | MEDLINE | ID: mdl-7472935

ABSTRACT

Three data sets describe the pattern of gunshot injuries to children from 1960 to 1993: The Harlem Hospital pediatric trauma registry (HHPTR), the northern Manhattan injury surveillance system (NMISS) a population-based study, and the National Pediatric Trauma Registry (NPTR). A small case-control study compares the characteristics of injured children with a control group. Before 1970 gunshot injuries to Harlem children were rare. In 1971 an initial rise in pediatric gunshot admissions occurred, and by 1988 pediatric gunshot injuries at Harlem Hospital had peaked at 33. Population-based data through NMISS showed that the gunshot rate for Central Harlem children 10 to 16 years of age rose from 64.6 per 100,000 in 1986 to 267.6 per 100,000 in 1987, a 400% increase. The case fatality for children admitted to Harlem Hospital (1960 to 1993) was 3%, usually because of brain injury, but the majority of deaths occurred before hospitalization. During the same period, felony drug arrests in Harlem increased by 163%. The neighboring South Bronx experienced the same increase in gunshot wound admissions and felony arrests from 1986 to 1993. The NPTR showed a similar injury pattern for other communities in the United States. In a case-control analysis. Harlem adolescents who had sustained gunshot wounds were more likely to have dropped out of school, to have lived in a household without a biological parent, to have experienced parental death, and to have known of a relative or friend who had been shot than community adolescents treated for other medical or surgical problems.(ABSTRACT TRUNCATED AT 250 WORDS)


Subject(s)
Wounds, Gunshot/epidemiology , Adolescent , Brain Injuries/epidemiology , Brain Injuries/mortality , Case-Control Studies , Child , Child, Preschool , Community Networks , Crime/statistics & numerical data , Death , Drug and Narcotic Control , Family , Female , Humans , Illicit Drugs , Incidence , Infant , Life Change Events , Male , New York City/epidemiology , Population Surveillance , Registries , Student Dropouts/statistics & numerical data , United States/epidemiology , Wounds, Gunshot/mortality , Wounds, Gunshot/prevention & control
2.
J Trauma ; 38(5): 767-75, 1995 May.
Article in English | MEDLINE | ID: mdl-7760407

ABSTRACT

It has been suggested that septic shock is a disorder of microvascular autoregulation. Tissue blood flow is modulated by the state of activation of upstream endothelial receptors controlling the vascular smooth muscle tone. Because vascular receptor populations vary between organs, it should be expected that vasoactive drugs affect tissue oxygenation differently in different organs. We studied the effects of dopexamine HCl (a novel inotrope) and septic shock on oxygen delivery as well as tissue Po2 in gut, liver, and skeletal muscle in anesthetized rabbits. Employing the thermodilution technique, cardiac output was measured across the pulmonary bed and used to calculate oxygen delivery. Three eight-channel Mehrdraht Dortmund Oberfläche oxygen electrodes were placed on gut serosa, liver, and skeletal muscle surfaces, respectively, and sufficient readings were obtained to calculate tissue Po2 distributions. During septic shock mean arterial pressure, cardiac output, oxygen delivery, and mean tissue Po2 decreased in all organs. Our results suggest that the observed changes in tissue oxygenation during septic shock were caused by defective regulation of microvascular blood flow. In conclusion, during baseline conditions dopexamine HCl caused no statistically significant changes in tissue oxygenation in any organ, except in skeletal muscle at 10 micrograms/kg/min when tissue Po2 increased. During septic shock, however, dopexamine HCl improved oxygenation in all three organs in a dose-dependent manner.


Subject(s)
Dopamine/analogs & derivatives , Intestinal Mucosa/metabolism , Liver/metabolism , Muscle, Skeletal/metabolism , Oxygen/metabolism , Shock, Septic/metabolism , Vasodilator Agents/pharmacology , Animals , Blood Pressure/drug effects , Cardiac Output/drug effects , Dopamine/pharmacology , Dose-Response Relationship, Drug , Heart Rate/drug effects , Oxygen/blood , Rabbits , Shock, Septic/physiopathology
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