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Published on: January 13, 2018
Effects of midazolam and nitrous oxide on endocrine and metabolic measurements in children
Kerstin Ekbom1, Sigridur Kalman, Jan Jakobsson
1Division of Anaesthesiology, Department of Clinical Science, Intervention and Technology, Karolinska Institute, Stockholm, Sweden. kerstin.ekbom@karolinska.se
Insights
Procedural sedation with nitrous oxide (N2O) or midazolam impacts glucose and stress hormone levels differently in children undergoing intravenous access. Understanding these variations is crucial for accurate clinical interpretation and diagnosis.
Area of Science:
- Pediatric Endocrinology
- Anesthesiology
- Metabolic Research
Background:
- Pain and stress significantly influence metabolic and endocrine measurements in children.
- Procedural sedation is often necessary for interventions like intravenous access in pediatric patients.
- Obesity and growth retardation can further complicate physiological responses to stress and sedation.
Purpose of the Study:
- To investigate the effects of procedural sedation using nitrous oxide (N2O) or midazolam on glucose and stress hormone release in obese and lean children.
- To compare the impact of different sedation methods on endocrine and metabolic parameters during intravenous access procedures.
- To correlate children's subjective pain and procedure experience with objective hormonal and metabolic changes.
Main Methods:
- A prospective, double-blind, randomized study involving 90 children (5-18 years) randomized to midazolam, 50% N2O, or 10% N2O.
- Blood samples were collected at multiple time points to measure cortisol, growth hormone, and glucose levels.
- Children's pain and procedure evaluations were correlated with hormonal and glucose measurements. Control groups (n=60) without sedation were included for comparison.
Main Results:
- Midazolam resulted in significantly lower cortisol levels compared to both N2O groups and unstressed controls.
- Growth hormone levels decreased over time with midazolam, whereas they increased with N2O.
- Glucose levels increased in growth-retarded children but decreased in obese children regardless of sedation. Significant correlations were found between subjective experience and hormone levels with 10% N2O.
Conclusions:
- Sedation with N2O or midazolam differentially affects glucose and stress hormone levels in children.
- Insufficient sedation during intravenous access can lead to pain and stress, altering hormone values.
- These distinct hormonal responses must be considered for accurate diagnosis and clinical decision-making in pediatric care.
Objective:
Pain, stress as well as drugs may affect metabolic and endocrine measurements, especially in stressed children. The aim was to study how release of glucose and stress hormones are affected when procedural sedation with nitrous oxide or midazolam are used for establishing intravenous access in obese and lean children.
Methods:
In a prospective, double-blind, randomized study 90 children, 60 obese and 30 growth-retarded (GR), aged 5-18 years, with reported anxiety or difficulties connected with i.v. access, were randomized to 1 of 3 groups: oral midazolam (0.3 mg/kg, max. 15 mg), 50% nitrous oxide (N(2)O), and 10% N(2)O. In addition, all children received anesthesia cream (EMLA®) locally 1 h before i.v. access. Blood samples were drawn at 4 time points during 30 min after establishing venous access and, when feasible, after 24 h. The 24-hour sample was regarded as obtained during unstressed condition. The effect of procedural sedation was analyzed. Children's evaluations of pain (Numeric Rating Scale) and procedure (Likert Scale) were correlated with mean values of cortisol and glucose after i.v. access. For the metabolic and hormone control measurements, 60 children aged 4-18 years (40 obese and 20 GR) served as controls. These children underwent a 24-hour blood sampling and did not receive sedation. The control samples were drawn 10-12 h after i.v. access.
Results:
After midazolam, significantly lower cortisol levels were found compared to both 50% N(2)O and 10% N(2)O and to unstressed controls. The growth hormone levels decreased with time in the midazolam group compared to 50 and 10% N(2)O, where the effect of time was reversed. Glucose levels among GR children increased from 0 to 30 min, whereas the opposite was found in obese children regardless of treatment. A post hoc analysis demonstrated significant correlations between children's evaluations of the procedure and mean values of cortisol (r = -0.53), growth hormone (r = -0.52), and norepinephrine (r = -0.5) in children treated with a very low dose of N(2)O (10%).
Conclusions:
When sedation is insufficient during i.v. access, and blood sampling pain and stress affect hormone values, treatment with N(2)O or midazolam influence the glucose and stress hormone levels differently. These differences need to be accounted for when results are used for diagnosis and clinical decisions.
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