Imaging
- CXR:
- Pneumonitis
- Pneumonias
- Pleural effusion
- Cardiomegaly
- ECG/echocardiogram
- CT chest:
- Pulmonary embolus
- Pulmonary hemorrhage
- Diffuse alveolar hemorrhage
- CT head for change in mental status or neurologic findings (lupus cerebritis is a diagnosis of exclusion)
Pregnancy Considerations
- Pregnancy is not recommended during active disease owing to the high risk of spontaneous abortion
- The effect of pregnancy on disease activity is variable
DIFFERENTIAL DIAGNOSIS
- Hypotension in the known lupus patient may be due to shock from a major flare-up, secondary to acute steroid withdrawal, or the result of sepsis
- Other autoimmune diseases:
- Rheumatic fever
- Rheumatoid arthritis
- Dermatomyositis
- Overlap syndromes
- Skin changes:
- Urticaria
- Erythema multiforme
- Idiopathic thrombocytopenic purpura
- Multiple sclerosis
- Epilepsy
TREATMENT
INITIAL STABILIZATION/THERAPY
ABCs
ED TREATMENT/PROCEDURES
- Mainstays include NSAIDs, corticosteroids, antimalarials, and immunosuppressive drugs
- Special attention must be given to CNS and renal involvement as well as infections; these are the main determinants of morbidity
- Mild flare-ups
—
arthralgias, myalgias, fatigue, and rash:
- NSAIDs (careful with lupus nephritis), acetyl salicylic acid (ASA), topical steroids for rash, sunscreen
- Topical steroids for most cutaneous manifestations
- If not sufficient, begin low-dose prednisone
- Major flare-ups
—
life- or organ-threatening:
- Methylprednisolone
- Anticoagulation for thrombosis; give blood products early if needed
- Psychotropics for neuropsychiatric symptoms
- Anticonvulsants for seizures
- If poor response, consult rheumatology before starting cytotoxic medications
- Chronically:
- Prednisone taper
- NSAIDs
- Rheumatologist initiated:
- Antimalarials: Quinacrine, chloroquine:
- Side effect is irreversible retinopathy
- Cyclophosphamide
- Azathioprine
- Methotrexate
- Belimumab (FDA approved for active, autoantibody positive disease in patients under active treatment)
- Hormonal therapy, mycophenolate mofetil, rituximab, and autologous marrow stem cell transplant are under investigation
MEDICATION
- Methylprednisolone: 15 mg/kg/d IV up to 1 g; consult rheumatologist for peds dosing
- Prednisone: 5–30 mg (peds: <0.5 mg/kg) PO daily for minor flare
- Prednisone: 1–2 mg/kg/d PO for major flares in adults
- Ibuprofen: 800 mg (peds: 5–10 mg/kg) PO TID
FOLLOW-UP
DISPOSITION
Admission Criteria
- Patients who have end-organ disease such as renal, cardiac, or CNS involvement
- Thrombocytopenia with hemorrhage, arterial or venous thrombosis
- Consider admission with pericarditis, myocarditis, pleural effusion or infiltrates, and evidence of vasculitis
- Those with severe end-organ or life-threatening manifestations should be admitted to the ICU
- Patients with lupus should be treated as immunocompromised and suspected or diagnosed infections should be treated aggressively
Discharge Criteria
- Patients may be discharged home with mild flare-ups if afebrile, well hydrated, and not ill appearing
- ESR should not be used as disposition criterion as it may be elevated long after a flare-up has subsided
Issues for Referral
Because lupus is a chronic disease, a rheumatologist or knowledgeable primary care physician (PCP) must follow the patient adequately
FOLLOW-UP RECOMMENDATIONS
PCPs must educate patients regarding sun protection, immunizations, and lowering risks of atherosclerosis
PEARLS AND PITFALLS
- The diagnosis of SLE is complicated and requires a thorough history and physical exam supported by appropriate lab testing
- Chronic steroid therapy leads to immunosuppression
- Renal involvement confers a poor prognosis
- Serum creatinine may be elevated, but is a poor indicator of the disease (urinalysis is more sensitive with proteinuria and/or red blood cell casts)
- All patients with SLE should be offered annual, seasonal influenza vaccinations and be sure that pneumococcal vaccination is up to date
- VDRL may be falsely positive
ADDITIONAL READING
- Buyon JP. Systemic lupus erythematosus: Clinical and laboratory features. In: Klippel JH, ed.
Primer on the Rheumatic Diseases
. 13th ed. Atlanta: Arthritis Foundation; 2008:303–318.
- Coca A, Sanz I. Updates on B-cell immunotherapies for systemic lupus erythematosus and Sjogren’s syndrome.
Curr Opin Rheumatol
. 2012;24:451–456.
- Lehrmann J, Sercombe CT. Systemic lupus erythematosus and the vasculitides.
Rosen’s Emergency Medicine.
7th ed. Philadelphia, PA: Mosby Elsevier; 2010.
- Schur PH, Wallace DJ. Overview of the therapy and prognosis of systemic lupus erythematosus in adults.
UptoDate.com
. Available at
http://utdol.com/
.
CODES
ICD9
- 420.0 Acute pericarditis in diseases classified elsewhere
- 583.81 Nephritis and nephropathy, not specified as acute or chronic, in diseases classified elsewhere
- 710.0 Systemic lupus erythematosus
ICD10
- M32.9 Systemic lupus erythematosus, unspecified
- M32.12 Pericarditis in systemic lupus erythematosus
- M32.14 Glomerular disease in systemic lupus erythematosus
TACHYDYSRHYTHMIAS
James G. Adams
•
Matthew S. Patton
BASICS
DESCRIPTION
- Any disturbance of the heart’s rhythm resulting in a rate >100 bpm
- Sinus tachycardia:
- Narrow complex regular rhythm at a rate of 100–150 bpm
- Max. rate typically 220 minus age
- Functional response to physiologic stress caused by increased catecholamine tone or decreased vagal stimulation
- Supraventricular tachycardia (SVT):
- A narrow complex tachycardia that originates above the His bundle
- Regular SVT:
- Atrial tachycardia
- Junctional tachycardia:
- Regular tachycardia without preceding depolarization waves
- Irregular SVT:
- Atrial fibrillation (AF)
- Atrial flutter
- Multifocal atrial tachycardia
- Ventricular tachycardia (VT):
- ≥3 consecutive ventricular ectopic beats at a rate of 100 bpm
- Most common initiating rhythm in sudden death in patients with previous MI
- Torsades de pointes:
- Paroxysmal form of VT with undulating axis and prolonged baseline QT interval
- Secondary to either congenital or acquired abnormalities of ventricular repolarization
- Often the result of drug therapy or electrolyte disturbances
- VF:
- Oscillations without evidence of discrete QRST morphology
- Accounts for 80–85% of sudden cardiac deaths
- Frequently results from degeneration of sustained VT
ETIOLOGY
- Sinus tachycardia:
- Acute MI
- Anemia
- Anxiety
- CHF
- Drug intoxication
- Hyperthyroidism
- Hypovolemia
- Hypoxia
- Infection
- Pain
- Pericardial tamponade
- Pulmonary embolus
- Atrial tachycardia:
- Precipitated by a premature atrial or ventricular contraction
- Electrolyte disturbances
- Drug toxicity
- Hypoxia
- Junctional tachycardia:
- AV nodal re-entry
- Myocardial ischemia
- Structural heart disease
- Pre-excitation syndromes
- Drug and alcohol toxicity
- AF:
- HTN
- Coronary artery disease
- Hyper-/Hypothyroidism
- Alcohol intake
- Mitral valve disease
- Chronic obstructive pulmonary disease
- Pulmonary embolus
- Wolf–Parkinson–White (WPW) syndrome
- Hypoxia
- Digoxin toxicity
- Chronic pericarditis
- Idiopathic AF
- Atrial flutter:
- Ischemic heart disease
- Valvular heart disease
- CHF
- Myocarditis
- Cardiomyopathies
- Pulmonary embolus
- Electrolyte abnormalities
- Recent cardiac surgery
- Multifocal atrial tachycardia:
- Hypoxic effects of chronic lung disease
- Theophylline toxicity
- VT:
- Dilated cardiomyopathy
- Cardiac ischemia
- Hypoxia
- Cardiac scarring/fibrosis
- After cardiac surgery or congenital anomaly repair
- Digoxin toxicity
- Long QT syndrome
- Electrolyte abnormalities
- Torsades de pointes:
- Drug toxicity (antiarrhythmic class IA and III agents, antipsychotics, antibiotics, etc.)
- Hypokalemia
- Hypomagnesemia
- Congenital QT prolongation
- VF:
- Acute MI (most common)
- Chronic ischemic heart disease
- Hypoxia
- Acidosis
- Anaphylaxis
- Electrocution
- Shock
- Hypokalemia
- Initiation of quinidine therapy
- Massive hemorrhage