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54 Cards in this Set
- Front
- Back
3 classes of anti viral agents
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unclassified
chain terminators neuramidase inhibitors |
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herpes simplex virus involves
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mucotaneous surfaces, cns, and occasionally visceral organs
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dna of hsv 1&2
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- linear, double stranded dna virus
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what happens after initail infxn of hsv 1&2
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- goes to latent stage w/ minimal replication until reactivated by some cz
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hsv 1&2 are infection only during
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- pts are infectious at all stages, atlhough the highest viral shedding is at reactivation
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pathway of herpes infection
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herpes enters the body--> herpes virus lies formant in the nerves --> herpes is reactivated causing another outbreak
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hsv 1 affects what areas of the body more
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facial
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hsv 2 affects what areas of the body more
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genital
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herpes simplex virus potential triggers
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- uv light
- stress -fatigue -trauma - chapped lips - menses -pregnancy -food allergies |
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herpes simplex virus presentation
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- itching, tingling, numbnes in the area. area will become red and look like a pimples
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hsv type 1&2 otc tx
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1) entry inhibitors
-abreva 2) non-antiviral - pain relievers, l-lysine - skin moisturizers, zinc oxide 3) denavir (penciclovir) cream 4) acyclovir (zovirax) cream |
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hsv type 1 &2 otc ppx
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- avoid triggers
- sunscreen -zinc oxide |
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varicella zoster aka
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chicken pox
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herpes zoster is aka
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shingles
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pathogenesis of vsv
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primary infection- via inhalation seeding in the nasopharynx leading to viremia
- viremia results in dissemination to the skin w/ resultant lesions -recurrent infection- reactivation of chicken pox |
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chicken pox is spread easily ?
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yes, very contagious
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age group most at risk for vzv
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children 5-9
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chicken pox incubation period
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10-21days
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syx of chicken pox
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- rash, low grade fever, malaise
- skin lesions- evolve frm maculopapular to vesicles in hrs to days - risk of superinfection w/ staph and strep |
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clinical manifestations of zoster (shingles)
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-can occurs at all ages but predominatly affects elderly >60 yo and immunocompromised
- charac by unilateral vesicular eruption of dermatomes - post herpetic neuralgia- continum of pain |
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anti herpetics
chain terminators agents |
- acyclovir
- valacyclovir -famciclovir |
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chain terminators moa
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- all mimic guanine, replace guanine when it would be used in dna chain, but do not allow the nxt nucleic acid to join
- need to be triphos in vivo - longer intracellular half life than extracellular |
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acyclovir
a) formulation b) se |
a) iv, po
b) possible kidney damage, keep hydrated |
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when do you use iv acyclovir
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cns herpes
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valacyclovir
a) formulation b) indication c) comp vs acyclovir |
a) only po
b) po indicated for immunocompromised |
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famciclovir
a) formulation b) indications |
-prodrug of penciclovir
a) only avail oral b) limited indications |
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which of the chain terminators need renal adjustment
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- all should be dose adjusted
agents: acyclovir, valacyclovir, famciclovir |
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hpv is what kind of virus
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dna virus
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hpv cz what
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warts
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how is hpv spread
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direct contact from a wart to skin
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hpv warts develop
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3-4 m (6wks -2 yrs)
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hpv warts start in
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the basal cells of the epidermis
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tx of hpv
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-caustic agent: salicyclic acid
-cryotherapy (freezing) -surgical excision - drugs: -antivirals- cidofovir -immune modulators- imiquimod - laser/electrosurgery |
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cmv stands for
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cytomegalovirus
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cmv cz
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common infection that is usually controlled by the immune system
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cmv causes
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retinitis, gi infections, pneumonitis in immunocompromised pts
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pts at risk for cmv
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advanced hiv and transplant most commonly
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hiv pts w/ cmv have cd4 count
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<100
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how do transplant pts get cmv
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highest risk are people who are cmv - and receive cmv+ organ
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clinical presentation of cmv
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- retinitis, colitis, esophagitis, pneumonia, encephalitis
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hiv pts w/ cmv usually presents as
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retinitis
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syx of retinitis
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unilateral visual field loss
dec visual acuity floaters flashes blind spots fever/wt loss |
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dx of cmv
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-fundoscopic examination- cottge cheese on catsup
- viral culture of urine, blood or biopsy |
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cmv tx for immediately site threatening dz
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-gancyclovir intravitreal inserts and valgancyclovir 900 mg po qd
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gancyclovir intravitreal inserts are dosed for cmv
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1 insert every 6-8m
decreased visual acuity at 1st, risk of retinal detachment |
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tx for cmv peripheral lesions
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- valgancyclovir 900 mg po bid 14-21 d then valgancyclovir 900 mg po qd
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cmv alternative txs
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-all are 14-21 days, follow with valgancyclovir as maintenance
- gancyclovir iv - foscarnet iv -cidofovir iv |
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cmv
-ganciclovir a) moa b) ae |
a) guanine analogue
- results in chain termination - poor oral absorption b) ae - primary bone marrow suppression - use w/ caution w/ azt - poor gi tolerance if given po |
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cmv
-valganciclovir a) moa b) dose |
a) prodrug of gcv
-metabolized to gcv after absorption - allows better absorption through the gi tract tract dose -induction: 900 mg po bid for 21 days w/ food -maintenance: 900 mg po qd w/ food - dose adj for renal dysfxn |
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cmv
-foscarnet a) ae |
- nephrotoxicity
-can be severe, watch bun &scr -adjust dose based on changing renal fxn electrolyte abnormalities (ca, k, mg, phos) - foscarnet is in triphosphate form - loose phosphate cz problems -penile ulcerations -irritation from drug in urine - proper hygiene -rash -neutropenia |
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cidofovir
a) ae |
- nephrotoxicity: dose depend, probenecid helps protect proximal kidney cells
- neutropenia - ocular hypotony - iritis -check cbc and scr w/ in 24 hrs before dose -hold if anc <750 or scr> 1.5 |
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cmv
primary ppx for |
- no primary ppx in hiv
- induction then 3m of maintenance in medium and high risk transplant pts |
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cmv secondary ppx
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- valganciclovir 900 mg po bid
- foscarnet 90-120 mg iv qd - cidofovir 5 mg/kg qoweek: with 2 gm probenecid po 3hrs before dose and 1 gm po at 2 hrs & 8 hrs post-dose |
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common viruses
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- picornaviridae
-rhinovirueses ( common cold, sore throat) and enteroviruses ( gi syx usually in infants) |