Acute rheumatic fever: Difference between revisions
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==Management== |
==Management== |
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===Acute |
===Acute Management=== |
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*Supportive care |
*Supportive care |
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*Decolonization, achieved by treating as streptococcal pharyngitis with either benzathine [[penicillin]] G 1.2 MU IM once or [[amoxicillin]] 500 mg PO bid for 10 days |
*Decolonization, achieved by treating as streptococcal pharyngitis with either benzathine [[penicillin]] G 1.2 MU IM once or [[amoxicillin]] 500 mg PO bid for 10 days |
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===Secondary |
===Secondary Prevention=== |
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*Needed to prevent further infections with [[Streptococcus pyogenes]], which most commonly manifests as [[pharyngitis]] or [[pyoderma]] |
*Needed to prevent further infections with [[Streptococcus pyogenes]], which most commonly manifests as [[pharyngitis]] or [[pyoderma]] |
Latest revision as of 01:01, 22 August 2020
Background
- Post-infectious complication of Streptococcus pyogenes infection
- Caused by certain serotypes of M protein
Clinical Manifestation
- Presents 1 to 5 weeks following a streptococcal infection
- Clinical syndrome characterized by fever, carditis, polyarticular arthritis, subcutaneous nodules, Sydenham chorea, and erythema marginatum
- Diagnosed using the Modified Jones criteria
- Patients with a history of acute rheumatic fever or rheumatic heart disease may have recurrences with subsequent reinfection with Streptococcus pyogenes
- Recurrences do not require as many criteria to diagnose
- Still need to exclude other possibilities
Differential Diagnosis
Arthritis
- Septic arthritis including gonococcal arthritis
- Connective tissue disease or other autoimmune diseases include juvenile idiopathic arthritis
- Viral arthropathy
- Reactive arthropathy
- Lyme disease
- Sickle cell anemia
- Infective endocarditis
- Leukemia or lymphoma
- Gout or pseudogout
- Post-streptococcal reactive arthritis
- Henoch-Schonlein purpura
Carditis
- Physiological mitral valve regurgitation
- Mitral valve prolapse
- Myxomatous mitral valve
- Fibroelastoma
- Congenital mitral valve disease
- Congenital aortic valve disease
- Infective endocarditis
- Cardiomyopathy
- Myocarditis (including viral and idiopathic)
- Kawasaki disease
Chorea
- Drug intoxication
- Wilson disease
- Tic disorder
- Choreoathetoid cerebral palsy
- Encephalitis
- Familial chorea, including Huntington disease
- Intracranial tumour
- Lyme disease
- Hormonal
- Metabolic, including Lesch-Nyhan, hyperalaninemia, ataxia-telangiectasia
- Antiphospholipid antibody syndrome
- Systemic lupus erythematosus
- Vasculitis
- Sarcoidosis
- Hyperthyroidism
Diagnosis
- Acute rheumatic fever is diagnosed using the modified Jones criteria
Management
Acute Management
- Supportive care
- Arthritis: NSAID, such as aspirin, ibuprofen, or naproxen, until all joint symptoms are resolved
- Fever: acetaminophen, if desired
- Heart failure: diuretics if mild or moderate; add ACE inhibitor if severe
- Atrial fibrillation: digoxin
- Chorea: if moderate, can use carbamazepine or valproate; if severe, can add risperidone, haloperidol, or diazepam; and if persistent or very severe, can add prednisone or methylprednisolone
- Decolonization, achieved by treating as streptococcal pharyngitis with either benzathine penicillin G 1.2 MU IM once or amoxicillin 500 mg PO bid for 10 days
Secondary Prevention
- Needed to prevent further infections with Streptococcus pyogenes, which most commonly manifests as pharyngitis or pyoderma
- Choice of antibiotic:
- The best evidence is benzathine penicillin G 1.2 MU every 2 to 4 weeks (for adults and children ≥20 kg) or 600 KU (for children <20 kg)
- Although every 2 weeks provides the best protection, every 3 to 4 weeks is still good (and more common, since it is more acceptable to patients)
- Can, for example, suggest patients get their injection every full moon
- Alternatively, can use oral penicillin V 250 mg PO bid
- If allergy, can use any alternative antibiotic, though they are inferior to penicillin
- The best evidence is benzathine penicillin G 1.2 MU every 2 to 4 weeks (for adults and children ≥20 kg) or 600 KU (for children <20 kg)
- Duration, per Australian guidelines:
- Possible: 12 months, then reassess
- Probable: for at least 5 years and until at least 21 years of age
- Definite, without carditis: for at least 5 years and until at least 21 years of age
- Definite, with carditis:
- Mild RHD: for at least 10 years (or 5 years if no preceding ARF) and until at least 21 years of age
- Moderate RHD: for at least 10 years (or 5 years if no preceding ARF) and until at least 35 years of age
- Severe RHD: for at least 10 years (or 5 years if no preceding ARF) and until at least 40 years of age
Further Reading
- The 2020 Australian guideline for prevention, diagnosis and management of acute rheumatic fever and rheumatic heart disease (3rd edition). 2020. Available online.
- Excellent resource with clear, evidence-based guidance.
- Revision of the Jones Criteria for the Diagnosis of Acute Rheumatic Fever in the Era of Doppler Echocardiography. Circulation. 2015;131:1806-1818. doi: 10.1161/CIR.0000000000000205