Tumour necrosis factor-α inhibitors: Difference between revisions

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== Background ==
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* TNF-α is a cytokine involved in the inflammatory response to infection
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* Has soluble and transmembrane forms
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* Produced by macrophages, NK cells, granulocytes, fibroblasts, and T cells
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* Receptors for TNF-α (TNFR1 and TNFR2) are found on most human cells, and are involved in cell activation and proliferation, cytokine production, and granuloma formation
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== Medications ==
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* [[Adalimumab]]
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* [[Infliximab]]
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* [[Certolizumab pegol]]
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* [[Etanercept]]
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== Contraindications ==
 
== Contraindications ==
   
 
* Active bacterial infection, active tuberculosis or untreated LTBI, active herpes zoster infection, active invasive fungal infection, infected skin ulcers, acute hepatitis B or C, untreated chronic hepatitis B, or chronic hepatitis B or C with Child-Pugh B or C
 
* Active bacterial infection, active tuberculosis or untreated LTBI, active herpes zoster infection, active invasive fungal infection, infected skin ulcers, acute hepatitis B or C, untreated chronic hepatitis B, or chronic hepatitis B or C with Child-Pugh B or C
   
== Infections ==
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== Safety ==
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* Baseline [[TST]], ±CXR, prior to starting medications, with patients identified as having [[LTBI]] being offered prophylaxis
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** Cutoff for TST is 5 mm
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*Assess for [[hepatitis B prophylaxis]]
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=== Adverse Effects ===
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==== Infections ====
   
* Bacteria: [[septic arthritis]], [[Listeria monocytogenes]], [[Legionella species]], [[Nocardia species]], [[Actinomyces species]], [[Salmonella species]]
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* Bacteria: [[septic arthritis]], [[Listeria monocytogenes]], [[Legionella]], [[Nocardia]], [[Actinomyces]], [[Salmonella]]
* Mycobacteria: [[Mycobacterium tuberculosis]], [[Mycobacterium avium]], [[Mycobacterium bovis]], BCG
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* Mycobacteria: [[Mycobacterium tuberculosis|'''Mycobacterium tuberculosis''']], [[Mycobacterium avium]], [[Mycobacterium bovis]], BCG
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**Risk of TB is higher for [[infliximab]] and [[adalimumab]] compared to [[etanercept]]
* Fungi: [[Aspergillus fumigatus]], [[Histoplasma capsulatum]], [[Coccidioides species]], [[Cryptococcus neoformans]], [[Candida albicans]]
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* Fungi: [[Aspergillus fumigatus]], [[Histoplasma capsulatum|'''Histoplasma capsulatum''']], [[Coccidioides]], [[Cryptococcus neoformans]], [[Candida albicans]]
 
* Parasites: [[Toxoplasma gondii]]
 
* Parasites: [[Toxoplasma gondii]]
* Viruses: [[hepatitis B virus]], [[hepatitis C virus]], [[varicella-zoster virus]]
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* Viruses: [[hepatitis B virus|'''hepatitis B virus''']], [[hepatitis C virus]], [[varicella-zoster virus]]
 
* Screening prior to use should be done for [[LTBI]] (TST or IGRA), [[hepatitis B]], [[hepatitis C]], and [[HIV]]
 
* Screening prior to use should be done for [[LTBI]] (TST or IGRA), [[hepatitis B]], [[hepatitis C]], and [[HIV]]
   

Latest revision as of 20:40, 16 March 2022

Background

  • TNF-α is a cytokine involved in the inflammatory response to infection
  • Has soluble and transmembrane forms
  • Produced by macrophages, NK cells, granulocytes, fibroblasts, and T cells
  • Receptors for TNF-α (TNFR1 and TNFR2) are found on most human cells, and are involved in cell activation and proliferation, cytokine production, and granuloma formation

Medications

Contraindications

  • Active bacterial infection, active tuberculosis or untreated LTBI, active herpes zoster infection, active invasive fungal infection, infected skin ulcers, acute hepatitis B or C, untreated chronic hepatitis B, or chronic hepatitis B or C with Child-Pugh B or C

Safety

  • Baseline TST, ±CXR, prior to starting medications, with patients identified as having LTBI being offered prophylaxis
    • Cutoff for TST is 5 mm
  • Assess for hepatitis B prophylaxis

Adverse Effects

Infections