Eating Disorders

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Anorexia
Loss of appetite and/or inability to eat
Associated with: Cancer, HIV, GI problems, depression, infections, medication side effects, etc.
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Anorexia Nervosa
Eating disorder (a psychiatric disorder)
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Anorexia Nervosa DSM-5
Significantly low body weight (< minimally expected) in relation to age, sex, development, and physical health
Intense fear of gaining weight
Disturbance in the way one’s body weight/shape is experienced and denial of the seriousness of the current low body weight
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Atypical Anorexia DSM-5
Intense fear of gaining weight
Disturbance in the way one’s body weight/shape is experienced and denial of the seriousness of the current low body weight

Same as for anorexia nervosa but without a low body weight
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Psychiatric Symptoms for Anorexia Nervosa
Fear of gaining weight
Preoccupation with food, cooking, and nutrition
Social isolation/withdrawal
Restlessness
Irritability
Ritualistic behaviors
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Food-related behaviors with anorexia nervosa
Cutting food into small pieces
Avoiding meals
Switching to vegetarian/vegan diet
Calorie counting or restricting
Water loading
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GI symptoms of AN
Delayed gastric emptying, slowed motility, constipation, abdominal pain
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Endocrine symptoms of AN
Cold intolerance, decreased metabolic rate, lethargy, brittle nails, dry skin
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Dermatological symptoms of AN
Lanugo(fine hairs), hypercarotenemia (yellowed skin)
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Electrolyte symptoms of AN
Refeeding syndrome, hypoglycemia, low serum Cl, Na, K, Ca, Mg
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Reproductive symptoms of AN
Hypoestrogenic state, decreased FSH and LH, amenorrhea, infertility, premature births, risk for miscarriage
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Cariac symptoms of AN
Cardiac muscle atrophy, decreased contractile force and output, bradycardia, hypotension, arrhythmias
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Bone symptoms of AN
Osteopenia/osteoporosis
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Risk factors of AN
Genetics
Female youth with type 1 diabetes
OCD personality class
Unhealthy family dynamics
trauma/life stressors
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Peak onset of AN
early to mid-adolescence
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average episode duration AN
8 months
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average duration of illness AN
9-15 years
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First-line treatment of AN
Nutritional Rehabilitation
Psychotherapy
Pharmacologic symptom relief (pro-motility agents) during refeeding
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Second line treatment of AN
Pharmacologic treatment of depression, anxiety, or obsessive compulsive symptoms, with SSRIs and psychotherapy, but avoid bupropion due to seizures
SGAs for severe, unremitting resistance to weight gain, severe obsessional thinking and denial that assumes delusional properties. Not appropriate solely for weight gain.
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When do you need to keep an AN patient inpatient?
Continued weight loss despite outpatient treatment, SBP <80 mmHg, arrhythmia, Na+ <125mmol/L, K+ <3 mmol/L, suicidal ideation, active self-harm
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Inpatient treatment intensity
24 hours/day, 7 days/week
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Inpatient treatment focus
Treatment of acute risks (suicidality, severe electrolyte abnormalities, cardiac irregularities)
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Outpatient treatment intensity
8-10 hours/day, 5-7 days/week
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Outpatient treatment focus
Treatment of chronic symptoms and relapse prevention
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Refeeding syndrome
May occur as a result of fluid and electrolyte shift during aggressive nutritional rehabilitation, may be fatal (most deaths from CV complications)
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Clinical features of refeeding syndrome
Hypophosphatemia (predominant cause of refeeding syndrome): Carbohydrate intake causes release of insulin which triggers cellular uptake of phosphate, leads to hypoxia, myocardial dysfunction, and respiratory failure
Hypokalemia
Congestive heart failure
Peripheral edema
Rhabdomyolysis
Seizures
Hemolysis
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Pharmacological treatment for malnutrition
daily multivitamin
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Pharmacological treatment for constipation
Bulk-forming laxatives (polyethylene glycol), stool softeners (docusate sodium), preferred over stimulant laxatives
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Pharmacological treatment for Abdominal bloating/pain
Metoclopramide 10 mg 30 min before meals (avoid long term)
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Pharmacological treatment for Amenorrhea
Not recommended to induce menstruation pharmacologically. Typically resolves as weight normalizes.
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Pharmacological treatment for Osteopenia
Calcium 1500 mg daily + vitamin D 400 units daily
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AN mild severity
BMI > or equal to 17
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AN moderate severity
BMI 16-16.99
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AN severe severity
BMI 15-15.99
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AN Extreme severity
BMI <15
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Bulimia Nervosa DSM-5
1. Recurrent episodes of binge eating*
2. Recurrent, inappropriate compensatory behavior to prevent weight gain
Self-induced vomiting
Misuse of laxatives, diuretics, enemas
Fasting
Excessive exercise
3. These behaviors occur > or equal to 1 time per week for > or equal to 3 months
4. Self-evaluation is disproportionately influenced by body shape/weight
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Mild BN
1-3 episodes per week
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Moderate BN
4-7 episodes per week
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Severe BN
8-13 episodes per week
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Extreme BN
> or equal to 14 episodes per week
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Psychiatric signs and symptoms of BN
Depression
Impulsivity
Mood lability
Personality disorders
Substance use disorders
Anxiety disorders
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Food related signs and symptoms of BN
Self-induced vomiting
Laxative/diuretic abuse
Fasting
Compulsive exercising
Over evaluation of shape/size
Eating preoccupations
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GI symptoms BN
Loss of dental enamel, dental cavities, parotid gland enlargement, gastric rupture
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endocrine symptoms BN
Lethargy, fluctuations in metabolic rate
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Dermatological symptoms BN
Russel's sign (calluses on back of knuckles due to inducing gag reflex)
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electrolyte symptoms of BN
Low serum Cl, Na, K, Ca, Mg; metabolic alkalosis (high CO2), metabolic acidosis
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Reproductive symptoms BN
Amenorrhea
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Cardiac symptoms BN
Orthostatic hypotension, bradycardia, prolonged QTc, arrhythmias
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Bone symptoms BN
Osteopenia/osteoporosis
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Risk factors for BN
genetic
trauma/life stressors
Personality Traits/Disorders
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BN peak onset
16-20 years
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BN average episode duration
3 months
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BN average duration of illness
7-12 years
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First-line treatment of BN
Nutritional Rehabilitation, develop structured meal plan
Psychotherapy: cognitive behavioral therapy (CBT), family therapy
Pharmacotherapy: SSRIs, May require higher doses than required for antidepressant effect, Fluoxetine has greatest efficacy data over placebo (60 mg daily)
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Second-line treatment of BN
Alternative types of psychotherapy: Interpersonal Therapy (IPT)
Alternative antidepressants depending on comorbid psychiatric illnesses
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malnutrition treatment BN
Daily multivitamin
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constipation treatment BN
Bulk-forming laxatives (polyethylene glycol), stool softeners (docusate sodium)
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excessive vomiting treatment BN
Replete electrolytes and fluids
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excessive laxitive use treatment BN
Replete electrolytes and fluids
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poor dentition treatment BN
Implement routine dental care (dental erosion)
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Binge eating disorder DSM-5
Recurrent binge eating without compensatory behavior to prevent weight gain
Patients feel a lack of control during these periods
Associated with >3 of the following:
• Eating rapidly
• Eating until uncomfortably full
• Eating large amounts when not hungry
• Eating alone out of embarrassment
• Feeling disgusted, depressed, or guilty after eating
These behaviors occur at least > or equal to 1 time per week for >greater than or equal to 3 months
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Mild BED
1-3 episodes per week
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moderate BED
4-7 episodes per week
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severe BED
8-13 episodes per week
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Extreme BED
> or equal to 14 episodes per week
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BED psychiatric symptoms
Emotional stress
Impulsivity/loss of control
Feelings of guilt
Co-occurring anxiety or depressive disorders
Impulse control disorders
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BED food symptoms
Eating rapidly
Eating until uncomfortably full
Eating large amounts when not hungry
Eating alone out of embarrassment
Feeling disgusted, depressed, or guilty after eating
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GI symptoms BED
GERD, acute gastric dilation and rupture
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Endocrine symptoms BED
Elevated BMI, lethargy, fluctuation in metabolic rate, hyperlipidemia, hyperglycemia
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Dermatological symptoms BED
striae distensae (stretch marks)
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Electrolyte symptoms BED
Abnormalities not typical without compensatory behaviors
Gallbladder disease
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Cardiac symptoms BED
Hypertension, cardiovascular disease
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BED risk factors
genetics
patients with BED at high risk for Generalized anxiety disorder, Panic attacks, MDD and suicidality
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Peak onset of BED
18-20 years
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Yo-yo dieting
seen in many BED patients, period of weight gain followed by weight loss
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First-line treatment BED
Nutrition Counseling
Psychotherapy: Cognitive behavioral therapy (CBT), IPT
Pharmacotherapy:
SSRIs (sertraline, citalopram, escitalopram preferred), Some guidelines include orlistat or topiramate
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Second-line treatment BED
Psychotherapy: Alternative types of psychotherapy, IPT and dialectal behavior therapy (DBT)
Pharmacotherapy:
Topiramate (+/- phentermine)
Imipramine and other TCAs
Naltrexone
Atomoxetine
Lisdexamfetamine
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Use of pharmacotherapy in BED
Implemented as an adjunct to a dietary plan and increased physical activity
Discontinue treatment if no improvement in binge eating behaviors or not providing > 5% weight loss at 12 weeks
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Atomoxetine (Strattera®) MOA
NE reuptake inhibitor indicated for ADHD
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Atomoxetine (Strattera®) efficacy
May decrease binge eating, obsessive features of BED, hunger, and body weight (1 small study, N=40)
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Atomoxetine (Strattera®) Intended duration
10-12 weeks
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Atomoxetine (Strattera®) adverse effects
Dry mouth, nausea, nervousness, insomnia, headache, constipation
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Atomoxetine (Strattera®) monitoring
BP, HR, changes in mood or behavior
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Lisdexamfetamine (Vyvanse®) MOA
Prodrug, converted to dextroamphetamine
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Lisdexamfetamine (Vyvanse®) administration
Take in the morning, high fat meals can delay onset of action
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Lisdexamfetamine (Vyvanse®) efficacy
Decreases number of binge days per week
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Lisdexamfetamine (Vyvanse®) intended duration
12 weeks
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Lisdexamfetamine (Vyvanse®) adverse effects
Dry mouth, insomnia, decreased appetite, tachycardia, constipation, anxiety
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Lisdexamfetamine (Vyvanse®) monitoring
Signs of misuse/abuse, baseline EKG, HR, weight, waist circumference, BP, psychosis
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Lisdexamfetamine (Vyvanse®) DEA class
CII
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Orlistat (Xenical® Rx, Alli® OTC) MOA
Decreases absorption of dietary fats by 30% by forming covalent bond with gastric and pancreatic lipases within stomach and small intestine, unavailable to hydrolyze dietary triglycerides
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Orlistat (Xenical® Rx, Alli® OTC) administration
Take with meal or up to 1 hour after eating
Must be used with a low fat diet plan (max 30% kcal from fat)
Separate from cyclosporine and levothyroxine by at least 3 hrs
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Orlistat (Xenical® Rx, Alli® OTC) PK
Minimal systemic absorption (~83% excreted unchanged in feces)
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Orlistat (Xenical® Rx, Alli® OTC) intended duration
24 weeks
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Orlistat (Xenical® Rx, Alli® OTC) adverse effects
GI (flatus with discharge), fecal urgency, fatty stool, severe liver injury
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Orlistat (Xenical® Rx, Alli® OTC) contraindications
Pregnancy, chronic malabsorption syndrome, cholestasis
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Orlistat (Xenical® Rx, Alli® OTC) monitoring
Weight, liver function tests
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Phentermine/Topiramate (Qsymia®) MOA
P: Stimulant that increases norepinephrine levels
T: Increases satiety and decreases appetite via GABA / glutamate modulation and / or carbonic anhydrase inhibition
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Phentermine/Topiramate (Qsymia®) PK
P: Absorption unaffected by food, excreted in urine
T: Absorption unaffected by food, 15-41% protein bound, minimal hepatic metabolism, 70-80% excreted unchanged by kidneys
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Phentermine/Topiramate (Qsymia®) DEA class
CIV
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Phentermine/Topiramate (Qsymia®) intended duration
12 weeks
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Phentermine/Topiramate (Qsymia®) adverse effects
Anxiety, depression, suicidal thoughts, tachycardia, headache, cognitive impairment, constipation, dry mouth, insomnia, paresthesias, increased SCr
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Phentermine/Topiramate (Qsymia®) contraindications
Hyperthyroidism, glaucoma, pregnancy (REMS), lactation
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Phentermine/Topiramate (Qsymia®) monitoring
Weight, HR, BP, mood, pregnancy test, electrolytes
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Lorcaserin (Belviq®) MOA
Serotonin 5-HT2C receptor agonist, stimulates hypothalamus resulting in satiety and decreased food intake
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Lorcaserin (Belviq®) PK
70% protein bound, extensive hepatic metabolism
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Lorcaserin (Belviq®) DEA class
CIV
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Lorcaserin (Belviq®) intended duration
12 weeks
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Lorcaserin (Belviq®) adverse effects
Headaches, dizziness, fatigue, nausea, dry mouth, constipation, hypoglycemia, valvular heart disease, suicide risk, priapism, serotonin syndrome, increased prolactin, decreased blood counts (WBC, RBC), CNS effects
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Lorcaserin (Belviq®) contraindications
Pregnancy (Category X)
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Lorcaserin (Belviq®) monitoring
Weight, waist circumference, CBC, prolactin, mood, EKG
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Bupropion/Naltrexone (Contrave®) MOA
B: inhibits DA and NE reuptake
N: Opioid receptor antagonist
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Bupropion/Naltrexone (Contrave®) administration
Do not take with fatty meals (increases absorption), swallow whole
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Bupropion/Naltrexone (Contrave®) pk
N: Significant first-pass metabolism, 53% to 79% excreted by kidneys
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Bupropion/Naltrexone (Contrave®) intended duration
12 weeks
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Bupropion/Naltrexone (Contrave®) adverse effects
N/V, constipation, headache, dizziness, dry mouth, insomnia, tachycardia, htn
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Bupropion/Naltrexone (Contrave®) contraindications
Chronic opioid use or acute withdrawal and previously discussed contraindications to bupropion
Will block the effects of opioids and buprenorphine, must wait 7 to 10 days after opioid discontinuation prior to initiation of bupropion/naltrexone
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Bupropion/Naltrexone (Contrave®) monitoring
BP, HR, weight, BMI, mood
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