Drugs clinical Flashcards

1
Q

TReatment of CA pneumonia

Home or admitted to hospital (but not severe, social/other admission with CAP, or no previous therapy)

A

Amoxicillin 0.5g-1.0g tds

OR Erythromycin

OR Clarithromycin

OR Doxycycline

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2
Q

TReatment of CA pneumonia NOT SEVERE

IN HOSPITAL

A

Amoxicillin 0.5-1g tds AND [Erythromycin OR Clarithromycin OR Doxycycline]

All oral because not severe

Note: Hospitals tend to use amox + doxycyline because macrolides promote MRSA by selection. Modify therapy if blood cultures etc positive.

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3
Q

SEVERE CAP

treated in HOSPITAL

A

•Co-amox 1.2g tdsIV

_AND _

Doxycycline orally OR [Erythromycin OR Clarithromycin] IV

Can ADD Rifampicin if severe Legionnaires’ disease OR Levofloxacin 0.5 g od plus Ben Pen 1.2 g qds

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4
Q

Early HAP or Aspiration pneumonia e.g. post-op chest infection/pneumonia

A

AS FOR CAP

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5
Q

Late HAP or Late Aspiration pneumonia

A

Piperacillin-tazobactam [‘Tazocin’],

plus dose of gentamicin if severe sepsis/shock

•Severely compromised patients - case by case management

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6
Q

ANTIBIOTICS: FIRST DOSE

typical meningo rash

Bacterial meningitis

A

2.4g Ben Pen IV 4 hrly

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7
Q

no typical rash & 18-50 y

ANTIBIOTICS: FIRST DOSE

bacterial maningitis

A

2g cefotaxime 6 hrly

OR

2 g ceftriaxone 12 hrly

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8
Q

Antibiotics first dose:

DELAYED LP or Pen-resistant Pneumococcis risk

bacterial meningitis

A

add vanc or rifamp to cephalosporin (d/w Micro)

>50 y

consider adding Ampicillin or Amox 2g 4 hrly

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9
Q

meningitis

ANTIBIOTISC FIRST DOSE IF

ANAPHYLAXIS TO BETA-LACTAMS

A

Chloramphenicol + vancomycin;

       **ADD ** *cotrimoxazole* for \> 50y
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10
Q

GANCICLOVIR mode of action

A

Active form phosphorylated (GCV-P)

CMV UL97 gene product >> GCV-P

GCV-P >> GCV-PPP by cell

oral absorption only 5%

with added valine ir increases to 60%

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11
Q

aciclovir mode of action

A

for VZV, herpes simplex

ACV-PPP inhibits viral DNA polymerase

ACV is selectively activated by thymidine kinase > it adds Pi: ACV-P

ACV-P >> ACV-PPP (phosphates added by cellular enzymes)

Nucleoside analogue
Active in triphosphate form
Requires viral thymidine kinase activity to addfirst PO4
2- group

Competitive substrate for viral DNA polymerase
Preferentially, irreversibly incorporated into growing DNA chain
Inhibits viral DNA polymerase
Obligatory chain terminator

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12
Q

issues with aciclovir

modified structure

resistance

A
  • Oral Bioavailability only 15 – 30% & Poor oral absorption
  • Plasma Half-life 3 hour
  • Frequent oral dosing required; 5 x per day
  • 85% of drug excreted unchanged in urine
  • Problem if renal impaired
  • Nephrotoxicity due to precipitation in renal tubules
  • CNS toxicity

added valine ester to aciclovir => VALACICLOVIR

1g tds of Valaciclovir comparable blood level as iv Aciclovir 5mg/kg tds

Common: Virus thymidine kinase absent
or
altered substrate specificity

Rarely: Virus DNA polymerase altered substrate specificity

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