Did I put my question about - how to get staff to "hear" my son's irritability as they reduce sedation not as pain (thus a need for more pain meds and let's not forget the restraints), but rather communicating to stop the sedation - in the wrong community?
I asked him if he has pain, he clearly shook his head no with his eyes open while squeezing my hand.
I have arranged to be there almost all the time so I can insert myself as needed to be sure he is "heard." Please help me do that effectively. Don't let me make the rookie mistakes, please? Thank you.
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MamaFern
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They were sedating him because he would become agitated when they reduced the dosage. No one used the d-word with me and he'd only been there a few days at that point. They reduced the dose during a particularly restless night to see if that would help him relax and he became so agitated trying to get free of everything, he self-extubated! We were *incredibly* lucky and it turned out well. He's okay, maintaining healthy oxygenation with O2 support through a nasal cannula. Today, the foley came out and he sailed his maiden voyage on a bedpan. We're battling sepsis and I think he's going to hate me tomorrow when I push him to use his spirometer, but it sure beats the alternative.
that all sounds very positive although sepsis is no fun that’s for sure.
I’d forgotten about the spirometer, doing everything in ICU was exhausting, so I resented anyone trying to get me to do anything. I was particularly waspish with a physio who was helping me regain use of my hands and fingers. ‘suctioning the lungs’ remains one of the worst things in ICU for me.
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