My department philosophy has always been to record the detail which includes specific values, outputs etc. for a lot of certainly higher risk devices.
Infusion/Anaesthetics/Ventilators/Defibs would be a good example, for instance.
However lately we have had to try to 'tailor' our PPM regime (probably like mainy others have had to) slightly and refine what we do record in the interests of time saving/efficiency (call it what you will).
Overall i feel we still capture the relevant results and values and this has been commented on positively, in 'legal' cases that have occured in the past.
