Table 2 |
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Possible use of anti-infective chemoprophylaxis in primary systemic vasculitis patients |
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|
Infectious agent |
Prophylactic measure |
Appropriate clinical situation |
Level of evidence |
|
|
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|
Pneumocystis jiroveci |
Trimethoprim/sulfamethoxazole 960 mg thrice weekly. Alternative: monthly aerolized pentamidine (300 mg) |
Should be given to all patients receiving long term glucocorticoid >15 mg/day and additional intense immunosuppression |
B to C |
|
S. aureus |
Nasal mupirocin ointment three times daily for 7 consecutive days per month |
Might be given to patients with generalized SVV who are S. aureus carriers during induction of remission |
C |
|
Mycobacterium tuberculosis |
Isoniazid 5 mg/kg per day up to 300 mg plus pyridoxin (vitamin B6). Alternative: rifampin 10 mg/kg per day up to 600 mg |
If latent tuberculosis is detected and immunosuppression necessary, especially when infliximab is used |
C |
|
Varicella-zoster virus |
Aciclovir 2 × 800 mg per day |
Generally not recommended, but might be considered in very selected cases with several reactivations and ongoing need for intense immunosuppression |
C |
|
Zoster vaccine |
Not recommended |
C |
|
|
Cytomegalovirus |
Valganaciclovir 1 × 900 mg per day |
Not generally recommended, but might be considered in selected severe cases with earlier reactivations and ongoing need for intense immunosuppression |
C |
|
Aspergillus sp. |
For example, posaconazole |
Not recommended |
C |
|
Candida sp. |
Oral amphotericin B suspension, 4 × 1 ml (= 100 mg) per day |
Should be considered in patients with long term glucocorticoid therapy >15 mg/day |
C |
|
|
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Level of evidence: A = evidence from at least one properly performed randomized controlled trial or meta-analysis of several controlled trials; B = well-conducted clinical studies, but no randomized clinical trials - evidence may be extensive but essentially descriptive; C = evidence obtained from expert committee reports or opinions, and/or clinical experience of respected authorities. |
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Moosig et al. Arthritis Research & Therapy 2009 11:253 doi:10.1186/ar2826 |
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