The problem is that the I/O data from every device is proprietary.
That's because many (most) of them were designed before the likes of HL-7 arrived on the scene.
In short - there
has to be an interface.
Only now we seem to be moving on from "every manufacturer doing their own thing" to "every hospital doing their own thing". OK as far as it goes, perhaps ... until a few years down the road when hospitals amalgamate, kit gets sold ... or yet another Standard gets imposed from Those On High.
But before going further, can anyone take a step back and remind me just
why all the kit has to be connected (data-wise)? Is the aim "just" to record settings, performance, timings
etc. on some sort of central system (that can then send out messages to the Smart Devices in medics' pockets ... or whatever) - or is it to enable equipment to talk to one-another. In either case, why?
If it's all aimed at the EMR (Electronic Patient Record), what data actually needs to be recorded there? The serial (asset) number of the pump, the drug(s) infused, flow-rates, timings - or what, exactly? Surely such "protocols" (requirements) shall vary from hospital to hospital. What's wrong with the Written Patient Record?
If all equipment data is to be recorded in real time (more or less); how much is enough? How long is it to be kept (how many stacks of hard-drives will we need)? And - more importantly - who is going to analyze it all?
If the reason is for recalling histories in the event of "incidents" - well, most (all modern) infusion pumps (the most likely culprit) already do all that, surely?
Yes, it's interesting technically ... but is it just more "gee-whiz" technology (and expense) - or is there a Real Need?
As I've said many times before, just because technology allows us to do things, it doesn't necessarily follow that we all have to do them. In the UK, at least, the money involved could undoubtedly be better spent elsewhere within healthcare. Please discuss!