That's what our prof said. Also, doesn't it depend on the severity of the infection? Like, if an elderly woman comes in with raging bilateral pneumonia, wouldn't we want to do 20mg/kg and then see whàt happens? And then adjust accordingly with trough levels?
EDIT: what I mean is, if it is a real severe infection or a bone infection, wouldn't you choose the higher dosing in the range (20mg/kg vs 15mg/kg) depending on the CrCl?
The initial dose isn't really that important because its a usually shot in the dark. It's just based on what you want the trough before the next dose to be. There are some instances where a lower dose given q8 is advantageous to a higher dose given q12. You have to do the math on paper, using a good dosing chart (which is probably the easiest to use), or on a computer (what I'd do) and play around with the numbers to see what gives you the best hypothetical result.
The two ranges you'd shoot for based on "severity" are defined as a trough of 10-15 and 15-20...depending on the diagnosis...and under no circumstance less than 10.
I hate that word "severity."
If the infection is likely to exhibit a higher MIC or if it would likely require deeper tissue penetration...or if you just want to be aggressive because its septic or something...yeah, then you'd go for a trough of 15-20.
But anyway, the important thing is how you deal with this initial estimate after you get your data from the trough.
In the real world, it gets pretty complicated sometimes even though the math is relatively easy. They will give it late...or take the trough early...or somehow the bag will start leaking during administration...the patients renal function will magically improve overnight...etc etc...
One time we had an obese midget with renal stents...that were getting taken out halfway through the vanc regimen...
One of the all-time great WTFDID moments...
If you are really interested in it, go to the ID Society's website and read the guideline paper. It is spelled out clearly and in depth what you need to do.