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The Administration Of Oral Sucrose Solution

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Study Purpose The purpose of this study was to determine whether administration of oral sucrose solution would lower skin blood flow (SBF) and Neonatal Infant Pain Scale (NIPS) scores compared to a saline water placebo during a procedure during which blood was drawn from an infant’s heel. The infant’s response was to be measured at a baseline, immediately following the insertion of the lancet, and 5 minutes after the blood was collected. Type of Research (Quantitative or Qualitative) Quantitative Research Design Randomized double-blind trial in which participants were assigned to either the placebo group or the study group by computer randomization, and the sucrose and placebo were placed in identical plastic syringes, preventing the …show more content…

Each of the infants had taken nothing by mouth for 2 hours before the procedure. Prior to the procedure, each infant had a heel warmer placed on the heel from which the blood was drawn, eye shields were applied, monitors were applied to determine physiological changes, and a Laser Doppler Imager (LDI) scanner was positioned approximately 30 centimeters from the leg not being punctured. The LDI measured SBF. 0.5 milliliters of either the sucrose or the saline was given by syringe to the infant. The lancet was applied one minute after the solution as initially given, and an additional 1.5 milliliters of the solution was given throughout the procedure. HR, RR, SpO2, SBF, and NIPS scores were collected from each infant 10 minutes before the procedure, immediately after application of the lancet, and 5 minutes after completing the blood draw. Statistical Test Used 2-Factor General Linear Model, Bonferroni post hoc test, Kruskal-Wallis test, linear multiple regression model, SPSS Version 21.0 Results/Findings There was no statistically significant difference in SBF between the study group and the control group at baseline, after application of the lancet, or at the recovery point (5 minutes post procedure). There was no significant different in NIPS scores between the groups at baseline, but the study group did have statistically significant lower NIPS scores after application of the lancet than the control group. There was no difference

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