| Literature DB >> 34297343 |
Shanna Tucker1, Carolyn Bramante2,3, Molly Conroy4, Angela Fitch5, Adam Gilden6,7, Sandra Wittleder1, Melanie Jay8,9.
Abstract
PURPOSE OF REVIEW: While obesity-related comorbidities are frequently addressed and treated in primary care (PC), obesity itself is undertreated. We review the current treatments for obesity and provide potential provider and system-level strategies for integrating weight management and improving longer term obesity care within PC settings. RECENTEntities:
Keywords: Challenges/barriers; Obesity; Primary care; Shared decision making; Weight management
Mesh:
Year: 2021 PMID: 34297343 PMCID: PMC8300078 DOI: 10.1007/s13679-021-00444-y
Source DB: PubMed Journal: Curr Obes Rep ISSN: 2162-4968
Weight-loss medications used in primary care
| Medication | Mechanism, adverse effects | Contraindications | Dosing | Monitoring/cautions |
|---|---|---|---|---|
| FDA-approved medications | ||||
| Orlistat | Intestinal lipase inhibitor. SEs: GI side effects — diarrhea, fecal urgency, decreased absorption of fat-soluble vitamins | Malabsorption disorder, cholecystitis | 60-mg TID or 120-mg TID with meals | Consider checking levels of fat-soluble vitamins, when indicated |
| Phentermine (FDA-approved duration varies by state) | Norepinephrine reuptake inhibitor SEs: elevated BP, tachycardia, insomnia, dry mouth, serotonin syndrome | Uncontrolled hypertension, cardiovascular disease, congestive heart failure, seizures glaucoma, MAOI use. | Once daily dosing: 8mg; 15mg; 30mg; 37.5mg | Check BP and HR monthly for 3 months, then every 3 months after patient loses 5% of body weight |
| Phentermine-topiramate | See separate sections for phentermine and topiramate | Phentermine 3.75 mg/topiramate 23 mg, phentermine 7.5 mg/topiramate 46 mg, phentermine 11.25mg/topiramate 69mg, phentermine 15 mg/topiramate 92 mg | ||
| Naltrexone-bupropion | Naltrexone is a μ-opioid receptor antagonist. Bupropion is a dopamine and norepinephrine reuptake inhibitor. SEs: nausea, which usually subsides, headache, vomiting, dizziness, insomnia, and dry mouth, elevated BP, HR | Uncontrolled hypertension, seizures, regular opioid use, opiate withdrawal, recent abrupt discontinuation of alcohol, MAOIs | Week 1: 1 tab in AM Week 2: 1 tab in AM and 1 tab in PM Week 3: 2 tabs in the AM, 1 tab in the PM Week 4: 2 tabs in AM 2 tabs in the PM | Monitor BP, HR, suicidal ideation, neuropsychiatric symptoms, signs of withdrawal. Medication reconciliation (opioids medications) and MAOIs. Careful social history for current and recent opioid and alcohol use |
| Liraglutide 3.0 mg | GLP-1 receptor agonist. SEs: nausea, diarrhea, and constipation, usually avoidable with slow dose increases Other SEs: cholecystitis and pancreatitis | Personal or family history of medullary thyroid cancer or multiple endocrine neoplasia type 2, or chronic pancreatitis | 0.6 mg daily for 1 week; increase by 0.6 mg at 1- to 2-week intervals to 3mg daily. Efficacy has not been established for<3 mg/day but consider using highest tolerated dose. | Patients currently on insulin and being started on a this GLP-1 agonist should be monitored for hypoglycemia and must be given clear and direct guidelines on how to titrate their insulin down accordingly. |
| Semaglutide 2.4mg | Same as above | Same as above | Initiate at 0.25 mg once weekly for 4 weeks, then increase the dose every 4 weeks (0.5 mg, 1 mg, then 1.7 mg) until maintenance dose of 2.4 mg weekly in reached. If patients do not tolerate the maintenance 2.4 mg dose, the dose can be temporarily decreased to 1.7 mg weekly for a maximum of 4 weeks and then increase to 2.4 mg weekly. | Same as above |
| Off-label medications for weight loss (not FDA approved for obesity treatment) | ||||
| Metformin | Anti-diabetic agent, biguanide Decreases hepatic glucose production, decreases intestinal absorption of glucose, and improves insulin sensitivity by increasing peripheral glucose uptake and utilization. SEs: nausea, loose stools, abdominal discomfort. | Acute or chronic renal dysfunction (eGFR<30 mL/min). | Start 500mg daily IR (immediate release) or ER (extended release). Increase to max dose tolerated (up to 2500mg daily). IR is taken across divided doses. ER may be taken as once or divided doses. | Basic metabolic panel at initiation to assess GFR. About 10–20% of individuals will experience loose stool, GI upset. It will usually go away and will be decreased by having metformin at the end of a meal or by using the ER form. |
| Topiramate | Carbonic anhydrase inhibitor. SEs: paresthesias, dysgeusia, cognitive dysfunction (poor concentration, psychomotor slowing), suicidal ideation, kidney stones, and hypokalemia. | Women of child-bearing age (must be on contraception), glaucoma, MAOI use, and hyperthyroidism | 25mg BID Can increase AM or PM dose as needed) | Use with caution in women of child-bearing age, as topiramate is teratogenic. Ensure they are on contraception. |
*SE Side effects, GI gastrointestinal, BP blood pressure, HR heart rate, TID three times daily, BID twice daily, MOAIs monoamine oxidase inhibitors
Fig. 1Obesity treatment pyramid developed by Angela Fitch, MD
Recommendations to potentially improve patient treatment success
| • Diagnose obesity as class I, II, or III to identify appropriate treatment intensity. | |
| • Aim for a 5–10% weight loss for class I and/or if the goal is to prevent diabetes and/or promote remission of a mild–moderate complication (e.g., hypertension, dyslipidemia) [ | |
| • Aim for a 10–20% weight loss for patients with class II or III and/or a moderate complication (e.g., nonalcoholic fatty liver disease [ | |
| • Aim for a | |
| • Create and document an obesity treatment plan. | |
| • Develop a system for routine follow-up at a minimum of every 3 months (more frequent if possible) during the “core” weight loss phase, increasing interval follow-up during the “maintenance” phase (every 6–12 months). |