Appetite Stimulant for Elderly Patients
For elderly patients with appetite loss and concurrent depression, use mirtazapine 7.5 mg at bedtime as first-line therapy; for those without depression, use megestrol acetate 400-800 mg daily; however, avoid all appetite stimulants entirely in patients with dementia who do not have depression. 1, 2, 3
Clinical Decision Algorithm
Step 1: Assess for Depression
If depression is present:
- Start mirtazapine 7.5 mg at bedtime 1, 3
- This addresses both appetite loss and depression simultaneously with beneficial side effects including improved sleep 1
- Titrate to maximum 30 mg at bedtime based on response 1, 3
- Expected outcomes: mean weight gain of 1.9 kg at 3 months and 2.1 kg at 6 months, with approximately 80% experiencing some weight gain 1, 4
- Allow 4-8 weeks for full therapeutic trial 1
If no depression:
- Use megestrol acetate 400-800 mg daily 1, 3, 5
- Approximately 1 in 4 patients will have increased appetite and 1 in 12 will gain weight 1
- In clinical trials, 64% of patients on 800 mg gained ≥5 pounds over 12 weeks with mean weight gain of 7.8 pounds 5
Step 2: Screen for Dementia
Critical caveat: If dementia is present without depression, do NOT use appetite stimulants 2, 3
- The American Gastroenterological Association and Clinical Nutrition guidelines (89% consensus) recommend against appetite stimulants in dementia due to very limited evidence and potentially harmful side effects that outweigh uncertain benefits 2
- Studies testing megestrol acetate included only 41% with dementia, making the evidence inadequate for this population 2
- In older hospitalized patients with functional decline, megestrol acetate 800 mg daily actually attenuated beneficial effects of resistance training, causing deterioration in muscle strength and functional performance 2
Exception: Mirtazapine may be used in dementia patients ONLY if concurrent depression requires treatment 2, 3
Safety Monitoring
For Mirtazapine:
- Monitor for somnolence (occurs in 54% of patients) 6
- Check for QTc prolongation, especially in patients with cardiovascular disease or family history of QT prolongation 6
- Monitor cholesterol (15% develop increases ≥20% above normal) and triglycerides (6% develop levels ≥500 mg/dL) 6
- Reassess at weeks 1,2,4,8, and 12 1, 3
- After 9 months, consider dosage reduction to reassess need for continued medication 1
- Discontinue over 10-14 days to limit withdrawal symptoms 1
For Megestrol Acetate:
- Critical safety concerns: thromboembolic events, edema, vaginal spotting, and adrenal suppression 1, 5
- One Cochrane review found higher rates of deaths in the megestrol acetate group compared to placebo 1
- Monitor for respiratory infections (increased risk with long-term use) 5
- May interact with warfarin and increase INR—closely monitor if co-prescribed 5
Non-Pharmacological Interventions (Prioritize First)
Before initiating pharmacotherapy, implement these evidence-based strategies:
- Medication review: Identify and temporarily discontinue non-essential medications contributing to poor appetite (iron supplements, multiple medications before meals) 1, 3
- Fortified foods and oral nutritional supplements: Offer when dietary intake falls to 50-75% of usual intake 1, 3
- Social interventions: Encourage shared meals with family or other patients 1, 3
- Dietary modifications: Provide smaller, more frequent meals with favorite foods and energy-dense options 1
- Screen for treatable causes: Dental problems, swallowing difficulties, depression 1
Medications NOT Recommended
Cannabinoids (dronabinol): Multiple guidelines conclude insufficient evidence for routine use 1, 3
- Three small placebo-controlled trials in dementia patients found no significant effect on body weight, BMI, or energy intake 1, 3
Common Pitfalls to Avoid
- Using appetite stimulants in dementia without depression—this is explicitly contraindicated by major guidelines with 89% consensus 2
- Failing to assess for depression first—this determines which medication to use 1, 3
- Not monitoring for thromboembolic events with megestrol acetate—these can be fatal 1, 5
- Inadequate trial duration—mirtazapine requires 4-8 weeks for full effect 1
- Ignoring non-pharmacological interventions—these should always be implemented first 1, 3