Published
To prevent clotting, I suppose. We switch all meds that can to PO to oral forms. If there's one that can't, (like Gent for a ROS) we'll run D5 1:1 hep at 1.2ml. That's usually only for a day or so. I don't see many kids with long-term IV only meds who are on full feeds. We try to get our PICCs out as soon as humanly possible, so we may even go to a saline lock PIV at that point if it's going to be a while. Very rarely (I've seen in once in 2+ years) they'll put in a Portacath if there's an intermittent thing - bisphosphonate for an osteogenesis imperfecta kid, the time I saw it.
The unit where I work, the protocol is flush 0.5 to 1ml every 6hrs of NS + heparin 2units/ml. I actually am not sure the dilutent anymore, we recently changed to these premixed syringes and I think it's NS but I'm not sure.
Those HL'd PICC's do tend to clot off pretty frequently. I could see not keeping one. It just seems the minute we take one out, the kit will need it for something.
RN4Little1s
113 Posts
Your baby's PICC is capped and clamped.
1) What is routine care (flushes) if you are not giving anything through it?
2) How do you flush with frequent intermittent meds? NS? Hep NS?
We have scheduled hep NS flushes TID. Then when there are intermittent meds between and with those, people flush differently.