2014
DOI: 10.1177/1060028014557859
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Pharmacological Management of Obesity in Pediatric Patients

Abstract: Lifestyle interventions remain the treatment of choice in pediatric obesity, but concomitant pharmacotherapy may be beneficial in some patients. Orlistat should be considered as second-line therapy for pediatric obesity. Evidence suggests that other diabetes and antiepileptic medications may also provide weight-loss benefits, but safety should be further evaluated.

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Cited by 44 publications
(51 citation statements)
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“…The weight‐lowering drugs approved for use in the United States work by reducing appetite through enhanced neurotransmission in the central nervous system (i.e., the 5HT2C agonist lorcaserin, phentermine/topiramate extended release, and naltrexone/bupropion) or by decreasing intestinal fat absorption (orlistat) and should be used only as an adjunct to lifestyle interventions . Orlistat is also approved for pediatric patients . Compliance is reduced by gastrointestinal adverse effects and increased risk of nephrolithiasis and liver failure for orlistat; headache, dizziness, and increased risk of serotonin syndrome for lorcaserin; and insomnia, irritability, anxiety, and disturbance of attention for phentermine/topiramate; and nausea, constipation, xerostomia, amnesia, seizures, and hepatotoxicity for naltrexone/bupropion .…”
Section: Resultsmentioning
confidence: 99%
“…The weight‐lowering drugs approved for use in the United States work by reducing appetite through enhanced neurotransmission in the central nervous system (i.e., the 5HT2C agonist lorcaserin, phentermine/topiramate extended release, and naltrexone/bupropion) or by decreasing intestinal fat absorption (orlistat) and should be used only as an adjunct to lifestyle interventions . Orlistat is also approved for pediatric patients . Compliance is reduced by gastrointestinal adverse effects and increased risk of nephrolithiasis and liver failure for orlistat; headache, dizziness, and increased risk of serotonin syndrome for lorcaserin; and insomnia, irritability, anxiety, and disturbance of attention for phentermine/topiramate; and nausea, constipation, xerostomia, amnesia, seizures, and hepatotoxicity for naltrexone/bupropion .…”
Section: Resultsmentioning
confidence: 99%
“…Metformin is the first-line oral therapy for Type 2 Diabetes (T2D) [1], and is also approved for use or used off-label in a variety of other diseases, such as polycystic ovary syndrome [2], gestational diabetes [3], pediatric obesity [4] and cancer [5,6]. Side effects of metformin are mainly gastrointestinal in 20% to 30% of patients, and in very rare cases include lactic acidosis [7].…”
Section: Introductionmentioning
confidence: 99%
“…Compared to children with overweight or obesity, lifestyle approaches and standard behavioral interventions have been shown to be less effective; more intensive treatments are recommended to improve both obesity (e.g., BMI percentile) and health metrics (e.g., blood glucose) (Danielsson, Kowalski, Ekblom, & Marcus, 2012; Johnston et al, 2011). Traditionally, interventions for severe obesity have included intensive family-based treatment (sometimes as an inpatient) (Luca et al, 2015; Taylor, Peterson, Garland, & Hastings, 2016; van der Baan-Slootweg, Benninga, Beelen, et al, 2014), bariatric surgery (Nobili et al, 2015; Schmitt et al, 2016; Thakkar & Michalsky, 2015), medication (Boland, Harris, & Harris, 2015), and/or long-term treatment using a chronic care model (Rijks et al, 2015). Therefore, school-based interventions for children with severe obesity must be coupled with more intensive treatment to lead to clinically meaningful decreases in body measures.…”
Section: Discussionmentioning
confidence: 99%