PRE HOSPITAL
- Ensure safety of patient and providers
- Understand local laws for involuntary commitment to hospital
INITIAL STABILIZATION/THERAPY
- Safety: Assess risk of suicide, violence
- General medical evaluation
- Management:
- 1-to-1 observation and suicide precautions when appropriate
- Work up potential medical causes
ED TREATMENT/PROCEDURES
- Psychological management:
- Listen empathically to understand context and relevant stressors
- Reassurance and education (e.g., depression is a treatable condition)
- Initiate medications:
- Antidepressant medication may be initiated for some patients with clear diagnosis and established follow-up
- Usually takes weeks for antidepressant medications to resolve major depression
- Low-dose benzodiazepines or neuroleptics may be used for associated agitation, insomnia, or psychosis
- Choice of drug determined by:
- Indications, efficacy
- Side-effect profile and risks
- Convenience, cost, availability
- Selective serotonin reuptake inhibitors (SSRIs: fluoxetine, paroxetine, sertraline, citalopram, escitalopram):
- Well tolerated
- Side effects may include:
- Mild nausea
- Headache
- Anxiety, restlessness, insomnia
- Somnolence
- Sexual dysfunction
- Weight gain
- Minimal overdose risk
- Serotonin norepinephrine reuptake inhibitors (SNRIs: venlafaxine, duloxetine):
- Well tolerated
- May be helpful for some pain syndromes
- Side effects similar to SSRIs
- Dopamine norepinephrine reuptake inhibitor (bupropion):
- Agitation, insomnia
- Tremor
- Decreased seizure threshold
- Well-tolerated; no sexual side effects
- Norepinephrine serotonin modulator (mirtazapine):
- Weight gain
- Sedation
- Orthostasis
- Constipation
- Tricyclic antidepressants (amitriptyline, imipramine, nortriptyline, clomipramine):
- Anticholinergic effects
- Weight gain
- Postural hypotension
- Sedation
- Decreased seizure threshold
- Cardiac risk; overdose can be fatal
- Nortriptyline is best tolerated
- Monoamine oxidase inhibitors (phenelzine, tranylcypromine, selegiline transdermal):
- Dietary and other medication restrictions to avoid hypertensive crisis
- Dangerous in overdose
MEDICATION
Medication dosage ranges are for adults.
Dose may be titrated over weeks as indicated.
- Amitriptyline: Initial 25–50 mg/d PO
- Bupropion: 75–400 mg/d PO
- Citalopram: 20–40 mg/d PO
- Desvenlafaxine: 50 mg/d PO
- Duloxetine: 30–120 mg/d PO
- Escitalopram: 10–20 mg/d PO
- Fluoxetine: 20–60 mg/d PO
- Imipramine: Initial 25–50 mg/d PO
- Mirtazapine: 15–45 mg/d PO
- Nortriptyline: Initial 25 mg/d PO
- Paroxetine: 20–40 mg/d PO
- Phenelzine: 15–90 mg/d PO
- Sertraline: 50–200 mg/d PO
- Tranylcypromine: 10–60 mg/d PO
- Venlafaxine: 75–300 mg/d PO
First Line
SSRIs, SNRIs, bupropion, mirtazapine
Second Line
- Tricyclics and monoamine oxidase inhibitors
- Use with caution in geriatric or medically ill
- Consider ECT for severe or treatment-resistant depression, psychotic depression, or catatonia
Geriatric Considerations
- Older patients may require lower dose; pay careful attention to potential drug interactions
- Caution with orthostatic hypotension and cholinergic blockade
Pediatric Considerations
FDA “Black box” warning: Antidepressants may increase risk of suicidal thinking and behavior in some children, adolescents, or young adults with depression
Pregnancy Considerations
In pregnant or breast-feeding women pay special attention to risks and benefits of medication treatments—consider consultation with a specialist in perinatal psychiatry
FOLLOW-UP
DISPOSITION
Admission Criteria
- Patient is suicidal or at high risk for suicide. See “Suicide, Risk Evaluation”
- Minimal or unreliable social supports
- Symptoms so severe that continual observation or nursing supportive care is required
- Psychotic features
- Civil commitment
for psychiatric hospitalization is necessary if the patient is refusing treatment and is at risk to harm self or others
Discharge Criteria
- Low suicide risk
- Adequate social support
- Close follow-up available
Issues for Referral
- Outpatient mental health appointments and/or partial (day) hospital for patients not admitted
- Insurance carrier may determine inpatient disposition and options for other levels of care
- Case management or social services in ED may be helpful for disposition issues
- Communicate and coordinate care with other providers including primary care
FOLLOW-UP RECOMMENDATIONS
Follow-up depends on severity of illness and risk:
- If not admitted, patients with significant symptoms should follow up in 1–2 wk
- When medication is initiated, patient should be seen in follow-up in 1–2 wk
- More stable patients or those with minor symptoms may be seen with less urgency
PEARLS AND PITFALLS
- Patients with depression experience significant morbidity and may present a risk of self-harm
- Consider other conditions that mimic depression; also coexisting psychiatric and medical conditions, substance use
- Know hospitalization and involuntary commitment criteria in your area
ADDITIONAL READING
- American Psychiatric Association. Practice guideline for the treatment of patients with major depressive disorder, third edition.
Am J Psychiatry
. 2010;167(suppl 10):1–152.
- Belmaker RH, Agam G. Major depressive disorder.
N Engl J Med
. 2008;358:55–68.
- Cassem NH. Mood disordered patients. In: Stern TA, Fricchione GL, Cassem NH, eds.
MGH Handbook of General Hospital Psychiatry
. 6th ed. St. Louis, MO: Mosby; 2010.
- Stewart DE. Clinical practice. Depression during pregnancy.
N Engl J Med
. 2011;365:1605–1611.
See Also (Topic, Algorithm, Electronic Media Element)
- Bipolar Disorder
- Psychosis, Medical vs. Psychiatric
- Psychiatric Commitment
- Suicide, Risk Evaluation
CODES
ICD9
- 296.20 Major depressive affective disorder, single episode, unspecified
- 296.24 Major depressive affective disorder, single episode, severe, specified as with psychotic behavior
- 296.30 Major depressive disorder, recurrent episode, unspecified degree
ICD10
- F32.3 Major depressv disord, single epsd, severe w psych features
- F32.9 Major depressive disorder, single episode, unspecified
- F33.9 Major depressive disorder, recurrent, unspecified
DERMATOMYOSITIS/POLYMYOSITIS
Sean-Xavier Neath
BASICS
DESCRIPTION
- Dermatomyositis (DM) and polymyositis (PM) are systemic inflammatory myopathies, which represent the largest group of acquired and potentially treatable causes of skeletal muscle weakness
- Patients experience a marked progression of muscle weakness over weeks to months
- Can lead to respiratory insufficiency from respiratory muscle weakness
- Aspiration pneumonia can occur owing to a weak cough mechanism, pharyngeal muscle dysfunction, and esophageal dysmotility
- Cardiac manifestations include myocarditis, conduction defects, cardiomyopathy, and congestive heart failure (CHF)
- Arthralgias of the hands, wrists, knees, and shoulders
- Ocular muscles are not involved but facial muscle weakness may be seen in advanced cases
ETIOLOGY
- The exact cause is unknown, although autoimmune mechanisms are thought to be largely responsible
- Incidence ∼1:100,000 with a female preponderance
- Association with HLA-B8 and HLA-DR3
- There may be an association between PM and certain viral, bacterial, and parasitic infections
- DM/PM occurs with collagen vascular disease about 20% of the time
- In DM, humoral immune mechanisms are implicated, resulting in a microangiopathy and muscle ischemia
- In PM, a mechanism of T-cell–mediated cytotoxicity is posited. CD8 T cells, along with macrophages surround and destroy healthy, non-necrotic muscle fibers that aberrantly express class I major histocompatibility complex (MHC) molecules
- Deposition of complement is the earliest and most specific lesion, followed by inflammation, ischemia, microinfarcts, necrosis, and destruction of the muscle fibers