My 15 year old son has had the vest since he was 4. It has never really caused him to cough up anything even though his CT scans show lots of mucus in his airways. Recently, while hospitalized, he tried the IPV machine. Right away he began coughing up stuff. My doctor then ordered a machine for him, but my insurance refused to pay for it because they already bought the vest (11 years ago!). Do any of you use this machine? I know it may be considered outdated. Does anyone have an old one that they don't use and would be willing to sell? Any ideas on how I could get financial assistance to buy one of these machines?
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IPV machine
- Thread starter marla
- Start date
My 15 year old son has had the vest since he was 4. It has never really caused him to cough up anything even though his CT scans show lots of mucus in his airways. Recently, while hospitalized, he tried the IPV machine. Right away he began coughing up stuff. My doctor then ordered a machine for him, but my insurance refused to pay for it because they already bought the vest (11 years ago!). Do any of you use this machine? I know it may be considered outdated. Does anyone have an old one that they don't use and would be willing to sell? Any ideas on how I could get financial assistance to buy one of these machines?
My 15 year old son has had the vest since he was 4. It has never really caused him to cough up anything even though his CT scans show lots of mucus in his airways. Recently, while hospitalized, he tried the IPV machine. Right away he began coughing up stuff. My doctor then ordered a machine for him, but my insurance refused to pay for it because they already bought the vest (11 years ago!). Do any of you use this machine? I know it may be considered outdated. Does anyone have an old one that they don't use and would be willing to sell? Any ideas on how I could get financial assistance to buy one of these machines?
My 15 year old son has had the vest since he was 4. It has never really caused him to cough up anything even though his CT scans show lots of mucus in his airways. Recently, while hospitalized, he tried the IPV machine. Right away he began coughing up stuff. My doctor then ordered a machine for him, but my insurance refused to pay for it because they already bought the vest (11 years ago!). Do any of you use this machine? I know it may be considered outdated. Does anyone have an old one that they don't use and would be willing to sell? Any ideas on how I could get financial assistance to buy one of these machines?
My 15 year old son has had the vest since he was 4. It has never really caused him to cough up anything even though his CT scans show lots of mucus in his airways. Recently, while hospitalized, he tried the IPV machine. Right away he began coughing up stuff. My doctor then ordered a machine for him, but my insurance refused to pay for it because they already bought the vest (11 years ago!). Do any of you use this machine? I know it may be considered outdated. Does anyone have an old one that they don't use and would be willing to sell? Any ideas on how I could get financial assistance to buy one of these machines?
debs2girls
New member
Respitory was just in here so I asked her about it..she doesnt know what it is. She said she may know it by another name....she is going to check into it for me. Chey is the same way with her vest.
debs2girls
New member
Respitory was just in here so I asked her about it..she doesnt know what it is. She said she may know it by another name....she is going to check into it for me. Chey is the same way with her vest.
debs2girls
New member
Respitory was just in here so I asked her about it..she doesnt know what it is. She said she may know it by another name....she is going to check into it for me. Chey is the same way with her vest.
debs2girls
New member
Respitory was just in here so I asked her about it..she doesnt know what it is. She said she may know it by another name....she is going to check into it for me. Chey is the same way with her vest.
debs2girls
New member
Respitory was just in here so I asked her about it..she doesnt know what it is. She said she may know it by another name....she is going to check into it for me. Chey is the same way with her vest.
NYCLawGirl
New member
I used the IPV all through college and for a couple years after, although I have since switched back to the vest. The IPV is similar to a large nebulizer and shoots salt water into the lungs, as you probably know. Most RTs have limited experience with it but my understanding is that it is considered an "intense" CPT -- not really recommended for those with histories of pneumothorax or serious bleeding. It worked wonders for me.
My insurance covered the IPV, although not sure if we had a co-pay since I was in high school at the time and covered by my parent's policies. I do know they bought it for us outright and we have never had to return it. I still occasionally use it to "mix it up" a little, so unfortunately I can't offer it to sell, but I do know that these machines are still used and they are not all that rare. My advice would be to keep pushing -- get your doctor to write another letter about why this machine is needed and why the vest is not an acceptable substitute, and go through an appeal with your insurance. Denial is common, but sometimes you just have to fight the system. Good luck!
My insurance covered the IPV, although not sure if we had a co-pay since I was in high school at the time and covered by my parent's policies. I do know they bought it for us outright and we have never had to return it. I still occasionally use it to "mix it up" a little, so unfortunately I can't offer it to sell, but I do know that these machines are still used and they are not all that rare. My advice would be to keep pushing -- get your doctor to write another letter about why this machine is needed and why the vest is not an acceptable substitute, and go through an appeal with your insurance. Denial is common, but sometimes you just have to fight the system. Good luck!
NYCLawGirl
New member
I used the IPV all through college and for a couple years after, although I have since switched back to the vest. The IPV is similar to a large nebulizer and shoots salt water into the lungs, as you probably know. Most RTs have limited experience with it but my understanding is that it is considered an "intense" CPT -- not really recommended for those with histories of pneumothorax or serious bleeding. It worked wonders for me.
My insurance covered the IPV, although not sure if we had a co-pay since I was in high school at the time and covered by my parent's policies. I do know they bought it for us outright and we have never had to return it. I still occasionally use it to "mix it up" a little, so unfortunately I can't offer it to sell, but I do know that these machines are still used and they are not all that rare. My advice would be to keep pushing -- get your doctor to write another letter about why this machine is needed and why the vest is not an acceptable substitute, and go through an appeal with your insurance. Denial is common, but sometimes you just have to fight the system. Good luck!
My insurance covered the IPV, although not sure if we had a co-pay since I was in high school at the time and covered by my parent's policies. I do know they bought it for us outright and we have never had to return it. I still occasionally use it to "mix it up" a little, so unfortunately I can't offer it to sell, but I do know that these machines are still used and they are not all that rare. My advice would be to keep pushing -- get your doctor to write another letter about why this machine is needed and why the vest is not an acceptable substitute, and go through an appeal with your insurance. Denial is common, but sometimes you just have to fight the system. Good luck!
NYCLawGirl
New member
I used the IPV all through college and for a couple years after, although I have since switched back to the vest. The IPV is similar to a large nebulizer and shoots salt water into the lungs, as you probably know. Most RTs have limited experience with it but my understanding is that it is considered an "intense" CPT -- not really recommended for those with histories of pneumothorax or serious bleeding. It worked wonders for me.
My insurance covered the IPV, although not sure if we had a co-pay since I was in high school at the time and covered by my parent's policies. I do know they bought it for us outright and we have never had to return it. I still occasionally use it to "mix it up" a little, so unfortunately I can't offer it to sell, but I do know that these machines are still used and they are not all that rare. My advice would be to keep pushing -- get your doctor to write another letter about why this machine is needed and why the vest is not an acceptable substitute, and go through an appeal with your insurance. Denial is common, but sometimes you just have to fight the system. Good luck!
My insurance covered the IPV, although not sure if we had a co-pay since I was in high school at the time and covered by my parent's policies. I do know they bought it for us outright and we have never had to return it. I still occasionally use it to "mix it up" a little, so unfortunately I can't offer it to sell, but I do know that these machines are still used and they are not all that rare. My advice would be to keep pushing -- get your doctor to write another letter about why this machine is needed and why the vest is not an acceptable substitute, and go through an appeal with your insurance. Denial is common, but sometimes you just have to fight the system. Good luck!
NYCLawGirl
New member
I used the IPV all through college and for a couple years after, although I have since switched back to the vest. The IPV is similar to a large nebulizer and shoots salt water into the lungs, as you probably know. Most RTs have limited experience with it but my understanding is that it is considered an "intense" CPT -- not really recommended for those with histories of pneumothorax or serious bleeding. It worked wonders for me.
My insurance covered the IPV, although not sure if we had a co-pay since I was in high school at the time and covered by my parent's policies. I do know they bought it for us outright and we have never had to return it. I still occasionally use it to "mix it up" a little, so unfortunately I can't offer it to sell, but I do know that these machines are still used and they are not all that rare. My advice would be to keep pushing -- get your doctor to write another letter about why this machine is needed and why the vest is not an acceptable substitute, and go through an appeal with your insurance. Denial is common, but sometimes you just have to fight the system. Good luck!
My insurance covered the IPV, although not sure if we had a co-pay since I was in high school at the time and covered by my parent's policies. I do know they bought it for us outright and we have never had to return it. I still occasionally use it to "mix it up" a little, so unfortunately I can't offer it to sell, but I do know that these machines are still used and they are not all that rare. My advice would be to keep pushing -- get your doctor to write another letter about why this machine is needed and why the vest is not an acceptable substitute, and go through an appeal with your insurance. Denial is common, but sometimes you just have to fight the system. Good luck!
NYCLawGirl
New member
I used the IPV all through college and for a couple years after, although I have since switched back to the vest. The IPV is similar to a large nebulizer and shoots salt water into the lungs, as you probably know. Most RTs have limited experience with it but my understanding is that it is considered an "intense" CPT -- not really recommended for those with histories of pneumothorax or serious bleeding. It worked wonders for me.
<br />
<br />My insurance covered the IPV, although not sure if we had a co-pay since I was in high school at the time and covered by my parent's policies. I do know they bought it for us outright and we have never had to return it. I still occasionally use it to "mix it up" a little, so unfortunately I can't offer it to sell, but I do know that these machines are still used and they are not all that rare. My advice would be to keep pushing -- get your doctor to write another letter about why this machine is needed and why the vest is not an acceptable substitute, and go through an appeal with your insurance. Denial is common, but sometimes you just have to fight the system. Good luck!
<br />
<br />My insurance covered the IPV, although not sure if we had a co-pay since I was in high school at the time and covered by my parent's policies. I do know they bought it for us outright and we have never had to return it. I still occasionally use it to "mix it up" a little, so unfortunately I can't offer it to sell, but I do know that these machines are still used and they are not all that rare. My advice would be to keep pushing -- get your doctor to write another letter about why this machine is needed and why the vest is not an acceptable substitute, and go through an appeal with your insurance. Denial is common, but sometimes you just have to fight the system. Good luck!
Ready2Dance
New member
I use the IPV and LOVE it!! What it took for my insurance to cover it was a strong letter from my doctor. I think we had to get the social worker involved too... but I can't remember. I've had my machine for about 5 years and am having a hard time thinking of the specifics. My parents did most of that battle for me. I would fight as hard as you can to get it, but that is due to me having such luck with it. Especially when I am sick, I can feel all sorts of stuff moving in there!! If I come up with anything new, I'll be sure to let you know!
Ready2Dance
New member
I use the IPV and LOVE it!! What it took for my insurance to cover it was a strong letter from my doctor. I think we had to get the social worker involved too... but I can't remember. I've had my machine for about 5 years and am having a hard time thinking of the specifics. My parents did most of that battle for me. I would fight as hard as you can to get it, but that is due to me having such luck with it. Especially when I am sick, I can feel all sorts of stuff moving in there!! If I come up with anything new, I'll be sure to let you know!
Ready2Dance
New member
I use the IPV and LOVE it!! What it took for my insurance to cover it was a strong letter from my doctor. I think we had to get the social worker involved too... but I can't remember. I've had my machine for about 5 years and am having a hard time thinking of the specifics. My parents did most of that battle for me. I would fight as hard as you can to get it, but that is due to me having such luck with it. Especially when I am sick, I can feel all sorts of stuff moving in there!! If I come up with anything new, I'll be sure to let you know!
Ready2Dance
New member
I use the IPV and LOVE it!! What it took for my insurance to cover it was a strong letter from my doctor. I think we had to get the social worker involved too... but I can't remember. I've had my machine for about 5 years and am having a hard time thinking of the specifics. My parents did most of that battle for me. I would fight as hard as you can to get it, but that is due to me having such luck with it. Especially when I am sick, I can feel all sorts of stuff moving in there!! If I come up with anything new, I'll be sure to let you know!
Ready2Dance
New member
I use the IPV and LOVE it!! What it took for my insurance to cover it was a strong letter from my doctor. I think we had to get the social worker involved too... but I can't remember. I've had my machine for about 5 years and am having a hard time thinking of the specifics. My parents did most of that battle for me. I would fight as hard as you can to get it, but that is due to me having such luck with it. Especially when I am sick, I can feel all sorts of stuff moving in there!! If I come up with anything new, I'll be sure to let you know!