Drugs clinical Flashcards
TReatment of CA pneumonia
Home or admitted to hospital (but not severe, social/other admission with CAP, or no previous therapy)
Amoxicillin 0.5g-1.0g tds
OR Erythromycin
OR Clarithromycin
OR Doxycycline
TReatment of CA pneumonia NOT SEVERE
IN HOSPITAL
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.
SEVERE CAP
treated in HOSPITAL
•Co-amox 1.2g tds… IV
_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
Early HAP or Aspiration pneumonia e.g. post-op chest infection/pneumonia
AS FOR CAP
Late HAP or Late Aspiration pneumonia
Piperacillin-tazobactam [‘Tazocin’],
plus dose of gentamicin if severe sepsis/shock
•Severely compromised patients - case by case management
ANTIBIOTICS: FIRST DOSE
typical meningo rash
Bacterial meningitis
2.4g Ben Pen IV 4 hrly
no typical rash & 18-50 y
ANTIBIOTICS: FIRST DOSE
bacterial maningitis
2g cefotaxime 6 hrly
OR
2 g ceftriaxone 12 hrly
Antibiotics first dose:
DELAYED LP or Pen-resistant Pneumococcis risk
bacterial meningitis
add vanc or rifamp to cephalosporin (d/w Micro)
>50 y
consider adding Ampicillin or Amox 2g 4 hrly
meningitis
ANTIBIOTISC FIRST DOSE IF
ANAPHYLAXIS TO BETA-LACTAMS
Chloramphenicol + vancomycin;
**ADD ** *cotrimoxazole* for \> 50y
GANCICLOVIR mode of action
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%
aciclovir mode of action
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
issues with aciclovir
modified structure
resistance
- 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