Obesity Clinical Trial
Official title:
Effects of Obstructive Sleep Apnea Syndrome and Obesity on Morphine Pharmacokinetics in Children
Adenotonsillectomy (AT) is one of the most common pediatric surgeries performed, and is
estimated to comprise 530,000 procedures in children under 15 years of age. Historically, the
leading cause for these procedures was recurrent infections; however, more recently surgical
indications include sleep disordered breathing and obstructive sleep apnea (OSAS).
Pre-operative polysomnography (PSG) is recommended for all children with suspected OSAS prior
to undergoing AT, although it is unclear whether sleep disordered breathing characteristics
predict post-operative outcomes or complications.
Obesity has become an epidemic in the pediatric population. More recently, an increased
population of obese children are presenting for AT with upper airway obstruction with or
without tonsillar hypertrophy, which is similar to the adult etiology of OSAS. Obesity is a
multisystem disease, causing fatty liver and cardiac disease, defects in glucose metabolism,
insulin resistance, leptin resistance, and creates a state of chronic inflammation. Markers
for inflammation, including tumor necrosis factor (TNF)-α, C-reactive protein (CRP), leptin,
interleukin (IL)-6 and IL-10, are abnormal in obese patients and have also been linked to
more severe OSAS disease in children even after controlling for BMI.
In pediatrics, medication dosing is based on an actual body-weight calculation, however,
recent reports suggest that this dosing method is over-dosing patients with obesity.
Therefore, increased respiratory complications after surgery may be related to inappropriate
intra-operative opioid dosing.
Specific Aim 1 (SA1): To compare morphine pharmacokinetics in normal children <=12 years of
age, non-obese children with severe OSAS, and obese children with severe OSAS. The
investigators hypothesize that obesity independently enhances morphine pharmacokinetics.
Specific Aim 2 (SA2): To determine whether biomarkers related to obesity, chronic
inflammation, and OSAS predict changes to morphine pharmacokinetics. The investigators
hypothesize that inflammatory and obesity-related biomarkers are elevated in overweight
children with OSAS, more so in obese children with OSA, compared to lean children with OSAS.
In addition, the investigators hypothesizes that leptin independently is linked to altered
morphine pharmacokinetics.
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