sleep during ivs

JennifersHope

New member
I have been on home IV's for six months now, now six infusions a day.. All on a gravity drip pump because that is all my insurance will pay for.

I usually do my Zyvox which I infuse over two hours right before I go to bed and half fall asleep until it is done... then in the morning.. I drift back to sleep while I start my morning infusions. I for sure sleep better at home.. for sure...but keeping up a crazy IV schedule at home is not easy.. Who knows though with my recent hearing loss I might be dropping some of the medications.
 

JennifersHope

New member
I have been on home IV's for six months now, now six infusions a day.. All on a gravity drip pump because that is all my insurance will pay for.

I usually do my Zyvox which I infuse over two hours right before I go to bed and half fall asleep until it is done... then in the morning.. I drift back to sleep while I start my morning infusions. I for sure sleep better at home.. for sure...but keeping up a crazy IV schedule at home is not easy.. Who knows though with my recent hearing loss I might be dropping some of the medications.
 
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witzersmom

Guest
i unserstand, especially when the nurses dont respond to the beeping for a while each time. my daughter makes up for it when home
 
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witzersmom

Guest
i unserstand, especially when the nurses dont respond to the beeping for a while each time. my daughter makes up for it when home
 

randomgirl

New member
When I'm on home iv's I can sleep for 18 hours a day easy but I try not to. Sometimes I take naps for at least 30 minutes but usually longer. When I'm in the hospital I have a very different schedule. I wake up at about 7 am because you have to order food within a specific time. But I always nap in the hospital anways.
 

randomgirl

New member
When I'm on home iv's I can sleep for 18 hours a day easy but I try not to. Sometimes I take naps for at least 30 minutes but usually longer. When I'm in the hospital I have a very different schedule. I wake up at about 7 am because you have to order food within a specific time. But I always nap in the hospital anways.
 

lilmac1177

New member
<div class="FTQUOTE"><begin quote><i>Originally posted by: <b>Incomudrox</b></i> It maybe soon enough, I am considering going to JH for a second opinion. <img src=""></end quote>
<span style="font-family: tahoma, arial, helvetica, sans-serif; font-size: small; color: #3366ff;">if it influences your decision at all, i cannot say enuff about Johns Hopkins Adult CF team! i absolutely love them all and to date they've never steered me wrong ... i don't know how your clinic works, but at Hopkins the adult team consists of four pulmonologists, two nurses, a nutritionist, a physical therapist and a social worker. i've only seen them since 2006 when i moved to the area, but i feel like they've known me my whole life!
<span style="font-family: tahoma, arial, helvetica, sans-serif; font-size: small; color: #3366ff;">i'm sure you have, or will, check them out before deciding whether to go, but here are a couple links to their program:
<a href="http://www.hopkinsmedicine.org/pulmonary/clinics/cystic_fibrosis.html">http://www.hopkinsmedicine.org/pulmonary/clinics/cystic_fibrosis.html</a>
<a href="http://www.hopkinscf.org/main/aboutus/index.html">http://www.hopkinscf.org/main/aboutus/index.html</a>
 

lilmac1177

New member
<div class="FTQUOTE"><begin quote><i>Originally posted by: <b>Incomudrox</b></i> It maybe soon enough, I am considering going to JH for a second opinion. <img src=""></end quote>
<span style="font-family: tahoma, arial, helvetica, sans-serif; font-size: small; color: #3366ff;">if it influences your decision at all, i cannot say enuff about Johns Hopkins Adult CF team! i absolutely love them all and to date they've never steered me wrong ... i don't know how your clinic works, but at Hopkins the adult team consists of four pulmonologists, two nurses, a nutritionist, a physical therapist and a social worker. i've only seen them since 2006 when i moved to the area, but i feel like they've known me my whole life!
<span style="font-family: tahoma, arial, helvetica, sans-serif; font-size: small; color: #3366ff;">i'm sure you have, or will, check them out before deciding whether to go, but here are a couple links to their program:
<a href="http://www.hopkinsmedicine.org/pulmonary/clinics/cystic_fibrosis.html">http://www.hopkinsmedicine.org/pulmonary/clinics/cystic_fibrosis.html</a>
<a href="http://www.hopkinscf.org/main/aboutus/index.html">http://www.hopkinscf.org/main/aboutus/index.html</a>
 

CFkitty

New member
I feel more tired when my infections are more severe, but being in the hospital makes it difficult to sleep for decent periods of time. At my previous clinic, where we had a dedicated CF floor or wing, the nurses would just hook up my meds whether I am awake or not - I had learned to sleep in positions so that whatever arm my PICC line is in, is accessible. However, in my current hospital, I can end up on any floor with nurses who might see one CF patient a year and not "get it", so they wake me up.

The bigger problem is the frequency of people coming into my room - the floor doctor, the pulmonary team, infectious disease/internal medicine, the pharmacist, respiratory therapy, the social worker/patient advocate, the glucose checks (they don't let me do it myself), and vitals at the beginning and end of every shift (even the 4 hour shifts!). Of course, the right person never comes in when you have an important question!

Another issue is that my blood pressure often plummets when I am sick (especially at night), and the nurse/CNA is coming in constantly to monitor it. And, of course, the stupid electronic infusers that beep and say "Occlusion" when there is one teeny bubble in the line, and it takes an hour for them to come clear it out. That certainly makes it tough to nap through!

If I am inpatient for the entire two weeks (which thankfully hasn't been for a few years), as I start feeling better towards the end, I don't need as much monitoring and am able to request six hours of uninterrupted time at night.

Doing IVs at home is convenient, but when you have to do them yourself, you might only have 4-6 hours in between infusions, and that's not a lot of time to get into a deep sleep. You really have to be awake to make sure you sanitize, flush, hook up, flush, and detach (close the line or the blood will pool in the line...eeeww). My hubby will sometimes run my very late or early morning infusions, but we have to plan it because of his work responsibilities. My family outside of my hubby don't help at all, so it's just us.
 

CFkitty

New member
I feel more tired when my infections are more severe, but being in the hospital makes it difficult to sleep for decent periods of time. At my previous clinic, where we had a dedicated CF floor or wing, the nurses would just hook up my meds whether I am awake or not - I had learned to sleep in positions so that whatever arm my PICC line is in, is accessible. However, in my current hospital, I can end up on any floor with nurses who might see one CF patient a year and not "get it", so they wake me up.

The bigger problem is the frequency of people coming into my room - the floor doctor, the pulmonary team, infectious disease/internal medicine, the pharmacist, respiratory therapy, the social worker/patient advocate, the glucose checks (they don't let me do it myself), and vitals at the beginning and end of every shift (even the 4 hour shifts!). Of course, the right person never comes in when you have an important question!

Another issue is that my blood pressure often plummets when I am sick (especially at night), and the nurse/CNA is coming in constantly to monitor it. And, of course, the stupid electronic infusers that beep and say "Occlusion" when there is one teeny bubble in the line, and it takes an hour for them to come clear it out. That certainly makes it tough to nap through!

If I am inpatient for the entire two weeks (which thankfully hasn't been for a few years), as I start feeling better towards the end, I don't need as much monitoring and am able to request six hours of uninterrupted time at night.

Doing IVs at home is convenient, but when you have to do them yourself, you might only have 4-6 hours in between infusions, and that's not a lot of time to get into a deep sleep. You really have to be awake to make sure you sanitize, flush, hook up, flush, and detach (close the line or the blood will pool in the line...eeeww). My hubby will sometimes run my very late or early morning infusions, but we have to plan it because of his work responsibilities. My family outside of my hubby don't help at all, so it's just us.
 

biz

New member
it really upsets me how bad my sons sleeping is when hes on iv. ugh the hospital is a nightmare. in those 4 or five days were there it caos. the shift changes and having to review everything all over again with the nurses. his machine beeping all the time. waiting for them to unhook him cause hes been done for twenty minutes. then getting hooked right back up. they throw the lights on at 6am. food drop off and pick up. its a mess. so not only does he not sleep neither do I. its so hard for me to function and remember what weve talked about with his doctors. or what i want to talk about. i am so fuzzy tired. then when we do get home waking him so much to flush and hook up meds. he never sleeps good. and i feel so guilty sending him to school cause i know hes tired. this was our first year in full day school with picc line so it was a learning experience. im trying to be ready for the next one as much as i can
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Elizabeth
mommy to Aidan 6 w/cf
 

biz

New member
it really upsets me how bad my sons sleeping is when hes on iv. ugh the hospital is a nightmare. in those 4 or five days were there it caos. the shift changes and having to review everything all over again with the nurses. his machine beeping all the time. waiting for them to unhook him cause hes been done for twenty minutes. then getting hooked right back up. they throw the lights on at 6am. food drop off and pick up. its a mess. so not only does he not sleep neither do I. its so hard for me to function and remember what weve talked about with his doctors. or what i want to talk about. i am so fuzzy tired. then when we do get home waking him so much to flush and hook up meds. he never sleeps good. and i feel so guilty sending him to school cause i know hes tired. this was our first year in full day school with picc line so it was a learning experience. im trying to be ready for the next one as much as i can
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Elizabeth
mommy to Aidan 6 w/cf
 
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witzersmom

Guest
I am so glad its not just us. I was refusing hospitalizations as I felt they were not a time of healing at all. Disorganization, waiting days for meds from pharmacy, constant intrusions. Here is what our clinic did for us. We agreed we would never go straight from clinic appointment. We would discuss the need and go home for a day or two to prepare. The staff then set up a pre hospital game plan for us and discuss it with the nurse manager. It includes us coming straight in for the picc line on arrival, and having meds ordered and on the floor, knowing ahead what antibiotics were trying first, and THE SAME NURSES AS OFTEN AS POSSIBLE, ( these nurses carry on the future visits.) We also set up a daily schedule so respiratory and meals arent clashing. respiratory followed her wishes kindly. We also refused psychologist visits and what not, as we can see a therapist near our home, and the hospital room is your home for two weeks. Would you ever relax at home if you had to fake smile and be polite for people all day long. We also put a sign on the door almost always that read " not feeling well, do not enter if you are not our nurse or respiratory. period."

I hope this may help anyone. This helped her heal. This last stay we hit the ground running. The nurse floor manager kept checking to see if we needed to fine tune things. I hope you can get your staff to do the same.
 
W

witzersmom

Guest
I am so glad its not just us. I was refusing hospitalizations as I felt they were not a time of healing at all. Disorganization, waiting days for meds from pharmacy, constant intrusions. Here is what our clinic did for us. We agreed we would never go straight from clinic appointment. We would discuss the need and go home for a day or two to prepare. The staff then set up a pre hospital game plan for us and discuss it with the nurse manager. It includes us coming straight in for the picc line on arrival, and having meds ordered and on the floor, knowing ahead what antibiotics were trying first, and THE SAME NURSES AS OFTEN AS POSSIBLE, ( these nurses carry on the future visits.) We also set up a daily schedule so respiratory and meals arent clashing. respiratory followed her wishes kindly. We also refused psychologist visits and what not, as we can see a therapist near our home, and the hospital room is your home for two weeks. Would you ever relax at home if you had to fake smile and be polite for people all day long. We also put a sign on the door almost always that read " not feeling well, do not enter if you are not our nurse or respiratory. period."

I hope this may help anyone. This helped her heal. This last stay we hit the ground running. The nurse floor manager kept checking to see if we needed to fine tune things. I hope you can get your staff to do the same.
 
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