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Identifying and measuring the biochemical effects of procedural pain in infants is a continuing challenge for clinicians. To address this issue we evaluated the relationship between procedural pain, ATP utilization (hypoxanthine and uric acid), and oxidative stress (MDA and allantoin) in premature infants. Through these studies we found that 1) a single heel-lance significantly increases plasma uric acid in rabbit kits, 2) tape removal increases MDA and prevents a decrease in uric acid in the plasma of premature infants, and 3) a single dose of oral sucrose before a heel-lance is sufficient to significantly increase plasma markers of ATP utilization and oxidative stress. These studies indicate that, in premature infants, ATP utilization and oxidative stress are altered by procedural pain and that oral sucrose, a common analgesia, may increase ATP breakdown. Next, we examined clinical factors that need to be considered when using the urinary concentrations of hypoxanthine, xanthine, uric acid, and allantoin to evaluate the biochemical effects of procedural pain. Specifically, we determined the effects of gestational age, weight for gestational age, and neonatal morbidity on the urinary concentration of purines and allantoin. We found infants born at earlier gestational ages had significantly higher urinary purine and allantoin concentrations compared to infants born at later gestations, after 31 weeks. Weight for gestational age also altered the urinary concentration of purines with small for gestational age infants having significantly lower urinary hypoxanthine compared to appropriate and large for gestational age infants. In addition, respiratory morbidity significantly increased urinary purines, but not allantoin, within the late preterm population. These data suggest that gestational age, weight for gestational age, and neonatal morbidity alter the urinary concentration of purine metabolites. Allantoin was also found to be significantly altered by gestational ag

Identifying and measuring the biochemical effects of procedural pain in infants is a continuing challenge for clinicians. To address this issue we evaluated the relationship between procedural pain, ATP utilization (hypoxanthine and uric acid), and oxidative stress (MDA and allantoin) in premature infants. Through these studies we found that 1) a single heel-lance significantly increases plasma uric acid in rabbit kits, 2) tape removal increases MDA and prevents a decrease in uric acid in the plasma of premature infants, and 3) a single dose of oral sucrose before a heel-lance is sufficient to significantly increase plasma markers of ATP utilization and oxidative stress. These studies indicate that, in premature infants, ATP utilization and oxidative stress are altered by procedural pain and that oral sucrose, a common analgesia, may increase ATP breakdown. Next, we examined clinical factors that need to be considered when using the urinary concentrations of hypoxanthine, xanthine, uric acid, and allantoin to evaluate the biochemical effects of procedural pain. Specifically, we determined the effects of gestational age, weight for gestational age, and neonatal morbidity on the urinary concentration of purines and allantoin. We found infants born at earlier gestational ages had significantly higher urinary purine and allantoin concentrations compared to infants born at later gestations, after 31 weeks. Weight for gestational age also altered the urinary concentration of purines with small for gestational age infants having significantly lower urinary hypoxanthine compared to appropriate and large for gestational age infants. In addition, respiratory morbidity significantly increased urinary purines, but not allantoin, within the late preterm population. These data suggest that gestational age, weight for gestational age, and neonatal morbidity alter the urinary concentration of purine metabolites. Allantoin was also found to be significantly altered by gestational ag