Opportunistic Infections Flashcards
Secondary prophylaxis- Definition and duration in HIV
Maintenance therapy which aims to prevent relapse
Stopped when CD4>200 on ART
Organisms causing bacterial pneumonia in HIV+
S. Pneumoniae H. Influenzae S. Aureus Klebsiella Atypical bacteria
Management of candidiasis
Limited to oral cavity or vagina - topical therapy
Refractory course or esophageal involvement - fluconazole
Fluconazole drug characteristics
Excellent oral bioavailability
Long half life
Penetrates CSF well
Renally excreted
Weak CYT p450 inhibitor
Active against yeasts- crypto and candida
Well tolerated - can lead to skin rash and hepatitis rarely
Management of PCP and complications of management
High dose cotrimoxazole for 21/7 - risks associated: high risk of severe hypersensitivity reaction (SJS/TEN, hepatitis); Prolonged use –> BM suppression
Adjunctive corticosteroids- indicated in all hypoxia patients
Cotrimoxazole drug characteristics
Indicated in PCP treatment
Used as primary prophylaxis
- indications: WHO stage 3/4, CD4
TB primary prophylaxis
6/12 isoniazid is standard regimen
Longer therapy is TST positive and if on ART
Screening for and management of cryptococcal infections
Look for cryptococcal antigen (CrAg) in all HIV + adults with CD4
MOA fluconazole
Causes the formation and accumulation of toxic sterols in the cell membrane
Amphotericin B drug characteristics
MOA: causes leak of intracellular proteins and cations
Drug of choice: invasive fungal infections- most active, little resistance, broad spectrum
Toxicity: nephrotoxic - dose-related,reversible, causes major loss of K and Mg
Route: slow IV - associated with fevers and rigors, managed with paracetamol or corticosteroids; prolonged use less to anemia and LOW
Clinical use of acyclovir
In immunocompetent: need to start rx early for effect-
Acyclovir drug characteristics
MOA: purine nucleoside analogue –> inhibits herpes DNA polymerase
Very well tolerated
Active against HSV and VZV (need higher doses)
PK: poor oral bioavailability, short plasma half life but long intracellular , excreted via kidneys
Resistance: uncommon, more often in immunocompromised, associated with extent of exposure
Shingles in HIV and management
Very common with moderate immunosuppression (CD4 around 350)
Tends to have longer duration, affect >1 dermatome and cause more severe pain with increased risk of post-herpetic neuralgia
Management: high dose acyclovir, pain mx, PHN rx with analgesia and adjuvant (eg amitriptyline)
CMV in HIV and management
AIDS-defining if outside RES/liver - MC sites are retina, GIT, lungs and CNS
Occurs at CD4
Management of TB
Intensive phase:
- 2/12
- rifampicin, isoniazid, ethambutol, pyrazinamide
Continuation phase:
- 4/12
- rifampicin, isoniazid
Main complication: isoniazid causes peripheral neuropathy - treat with prophylactic pyridine in high risk px.