Acute rheumatic fever: Difference between revisions

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==Background==
* Post-infectious complication of [[Streptococcus pyogenes]] infection

* Caused by certain serotypes of M protein
*Post-infectious complication of [[Streptococcus pyogenes]] infection
* Presents 1 to 5 weeks following a streptococcal infection
*Caused by certain serotypes of M protein
* Diagnosed using the [[Modified Jones criteria]]

==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]]
*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. [https://www.rhdaustralia.org.au/arf-rhd-guideline 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: [https://doi.org/10.1161/CIR.0000000000000205 10.1161/CIR.0000000000000205]

[[Category:Infectious diseases]]

Latest revision as of 01:01, 22 August 2020

Background

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
  • 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

Carditis

Chorea

Diagnosis

Management

Acute Management

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
  • 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