hypercapnia
Does anyone on here suffer with hypercapnia? My husband has advanced copd and stage iv lung cancer and has gone into respiratory distress twice since September of this year. Actually it has happened since he was diagnosed with cancer. The hospital wanted him to wear a bipap but he refused. Are there any other options out there to keep this from happening that anyone knows of? Thank you.
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Oh, yes, Denise...our husbands are the same. Both are 68, Both have been using drugs from their early days, trading drugs, and finding out where us wives hiding places are of theirs or our drugs, etc. Drives me Nuts. Our drs took Jimmy off zannys and lowed his Oxy dose down to 5 mg once he started experiencing hypercapnia as that represses your system. However, he didn't have enough meds in his system to cause Hypercapnia. His blood tests would come back showing zero Benzos and zero Opioids. It was all due to his Cancer in his throat and what it was effecting his body. Plus as you age, your system can't accept a high dose of either; but we know our husbands and they will take enough to get high. I take Xanax because of living with him (LOL). That is true to a point, but I've high anxiety, high blood pressure and the xanax does wonders for my BP. And, of course he knows I have them and bugs me for them or gets mad. Anyway, He grew up in Provincetown, MA and I moved to Cape Cod, MA in 1980. I grew up in a suburb of Fall River, MA. Married in 1990. Hubs and 1st wife had a baby boy in 1975; and we had a baby girl in 1991. I'll be 65 and on Medicare in August! LOL. I still feel like in my late 30's and work out as much as I can BEFORE summer comes. I really hope your husband rethinks the feeding tube. It is so easy. It doesn't have to be a life time event. I assume he sees a Speech Pathologist and a dietician that the hospital sets you up with. They do in MA; I'd assume in PA. My husband was a cook for years and also installed floors did roofing an siding. He always made dinner..was the best cook! That he misses but he's gotton over it after 17 months with feeding tube. Now, it's his lack of a voicebox that depresses him. It's hard and real quiet in the house. He's got a great sense of humor which even though he can't speak it, his facial expressions or charades or writing it out helps his sense of being. He does not want to die. He is doing what the doctors tell him. He also has a great support system made up of family and close friends, plus his many doctors who liked him as they got to really know him and his ways (drugs included) and made them all laugh. I used to tell him that if I knew him when I was 18, I'd stay away from him cuz he was a trouble-maker. He's got a long record but none that involve the worse of the worse. The only trouble he got in when with me since 1983 was being pulled over 3 times for drunk driving. We are both alcoholics but have been "Free" for me going on 14 years, and my hubs 10 years. You should read this to your husband. I'm hoping it might give him the gumption he needs to stop saying NO to foods he's offered...cripes he's lucky he can still eat! The Feeding tube will actually give him more calories if he's weighing under 100 lbs. My husband was told he can eat by mouth since having the trach and then the laryngectomy, but during the operation, they found a section in way back of his tongue had cancer so had to cut that out and he now only drinks coffee, a Wendy's Choc Frosty, and his Nestle IsoSource which is same as Boost or Ensure but is by prescription. It's helping my husband slowly, but surely put on some weight. I'll try and be better at checking messages on this platform now that I started. I am very glad we met and have a lot of common problems; namely....Husband! LOL Peace, Betsc
Hi. Yes it sounds like our husbands would have made good friends. Well, Joe has decided that he no longer wants to take chemo. He will meet with the oncologist on Jan. 23, to see what his options are. He is trying to eat more, and he is doing a little better. He did vomit once last night, but so far today it has not happened. I did not give him any nausea pills because I forgot and he didnt ask for them, so I never mentioned it. I just bought him two new pairs of joggers, size medium and they are just hanging on him. I guess I will return them and get a small. I had also ordered two chemo shirts that have top flaps that open for easy access to the port. Guess I will be sending them back also. Today he wanted shrimp scampi over rice. I only had long grain and I guess I did not cook it to his satifaction because he yelled and said why don't you must buy minute rice? Was mad because I burnt the first batch and he had to wait another 20 minutes to eat. I wanted to say-screw you. But I didn't. I had set the table but he came into the kitchen, grabbed a plate, put a litte food on it and went back to the living room. He sits in the living room in his recliner and he wants something, he yells my name. He is so picky. Usually, it is, get me some pepsi with 1 ice cube and half glass. I accidently put 2 ice cubes into it yesterday and he complained. He just told me that when he yells my name, I am just to automatically go in and see what he needs. I saluted him. Yes, I am being a smart ass, but he seems to be getting ruder and more demanding. I also have xanax, and start using them more than I have been. I don't want to be mean to him, but my nerves are growing thin. I won't sit in the living room with him because he controls the tv and always watches american pickers and pawn stars -24/7. So I sit in the dining room where I have my computer and watch youtube videos, etc. But this is nothing new. Last night, I did watch a movie with him. He has not been a pleasant man to be around. He is smart and won't let me forget it. He is the type of person who answers your questions with a question of his own. I am 69 and should do what you do. Start working out before summer gets here because I have gained some weight. I weigh 156 and would like to be 145. LOL I have weighed around 156 for a year now. You can tell that I have not used my walking tapes or my weight lifting tapes. I only ever lifted 2,5,and 8 pounds. One time I was lifting 5,8 and 10. Guess I have been depressed and don't feel like doing anything. OK, enough of my venting. We have boost but he won't drink it. So, I do. Last week I ordered ginger and peppermint tea because I read that it helps settle the stomach. I told him about that and he said I DON'T LIIKE TEA! So, luckily for me, I do drink hot tea so I guess I will be drinking the tea, too. I suggested a feeding tube and he said, NO. I am tired of fighting with him. Can your husband still drive or go to the store? My husband is too weak that he can't do much of anything. But at least your husband still has a sense of humor. Thanks for writing and it was nice meeting you, also. I check this site daily and I always try to respond to anyones comments. Have a great day!
My husband has not had another attack of the respiratory distress which caused his two hospital stays. The first time it happened in September was because he od on his oxycodones and who knows what else. I don't know what caused the second one. Probably the same thing but I don't think he took as many. I had him 4 oxycodones each morning but I hear him in the kitchen getting more. I am at the point where I don't care how many he takes. If he doesn't find where I put them, he will just get them from someone else. But so far, it has been almost a month since he was admitted on Dec. 15. He is happy now because there is a football game on now. I don't know if the steelers play or not. I am not a sports fan. Of course, I hope the steelers win, but whether they do or not makes no difference to me. But football will keep him happy tonight. 🙂
I think there May be some confusion if you are talking about a pulse oximeter, a small apparatus that you place on the tip end of one's finger, preferably the ring or middle finger on the left hand. Those devices measure O2 levels not CO2. The reading to the small window on the left measures SpO2, on the right is PRbpm (Pulse Rate-beats per minute0). The SpO2 level should remain 88% and above. The only way to measure the CO2 level is through lab work. Maybe this is why you have made so many trips to the ER and ended up in the ICU. Please call the physicians office tomorrow first thing and see if there is a nurse, or even the PCP to instruct you on the readings of the pulse oximeters.
Ok, thanks.
The only way to check for hypercapnia is a blood test.
Pulse oximeters, the little gadgets we put on a finger, measure oxygen and pulse rate.
My husband had to have many arterial blood gas tests which are very painful as they need to take it from an artery vein in your wrist. He would be "out of it" so didn't feel it. The test was done for respiratory diseases that affect lungs and determines if oxygen therapy (C-pap/Bi-pap would be effective for him as he has COPD. His test results showed a c-pap / bi-pap would not help him. I answered this in another "comment" on this post that he was given a non-invasive Ventilator. It was great because when used only at night to sleep, it would give readings to Adapt, the company that supplied machine and they were able to tell us if any problems arised. In the long run, he now uses nothing to sleep because he's had a full laryngectomy to rid of Cancer.
@kndaustin71. What I have is an oxymeter. Each time you go to your doctors they do your vitals and put this oxymeter on your "pointer" finger. It measures your blood oxygen level which should be close to "100" meaning you don't have any problems. My husbands would read in the 50's or 40's at times and start acting all "wonky" and not making sense. Just as Denise96 said of her husband. I don't know anything about the pulse but my oxymeter has since broke so not sure if there was another number. Thank you.
@denise96 - We should live next door to each other and be besties. I also use 5 - 8's and 10's in weights LOL . The TV part is funny. I use the TV in the bedroom cuz my hubs watches American Pickers and Pawn Stars too. Also, he's into WWII and probably could win a whole column on Jeopardy about any war! All his medical equipment is in Livingroom so he got dibs on the bigger TV. He does drive, but I need to be with him so I can speak. He also shovels, does as much as he can without over doing it. He, at times, will have the attitude that he has no illness which is when we get along the best. It's when he has to face the fact that he has no voice that bothers him the most; and I don't blame him. Our husbands are weakened and fighting for their lives. It is very frustrating for both partners when in this situation. It's hard to deal with. Hugs to you girl🤗
It is so sad that your husband can't speak. Can't they do something like putting in a mechanical voicebox or whatever it is called? My girlfriends husband had throat cancer and they were able to put that in and he can speak. In fact, I did not notice any difference in his speech. Sometimes people sound mechanical when they speak, but I guess it depends on the person and how bad the cancer was. You two will have to learn sign language. Yes, it would be nice to live next to someone who is fighting this battle. Is your husband's cancer in remission? It is funny that they watch the same type of shows on tv. ONly my husband is not interested in WWII shows. I never was much of a TV person. I would rather read a book, but every now and then, I would like to watch something that I like. Well, he did not have a good night. Said he did have the dry heaves again, but the food did not come up. (I know it is nasty talking about vomit), said his feet are not as swollen but they are still swollen. The oncologist comes in at 9 and I will be calling then. My mom wants to go and get new shoes later this morning and she always buys lunch since I drive her. It is a shame that where we live, so many department stores have closed. Pittsburgh is only an hour away but I wont drive there. First of all, I don't know my way around there and second of all, I hate all the traffic. I am a country girl and for us to go anywhere it is at least a half hour drive. There are grocery stores closer but no clothing or shoe stores. We drive to Indiana, Pa which is 30 minutes. They have a jc penneys, Kohls, Maurices and I believe that is it. There is a shoe store in this mall. They used to have BonTon, but it went out of business. I order a lot online. Oh, and of course, there is a walmart. I hate walmart. lol But sometimes you have no choice but to go there. My mom is 92 and is pretty good health for her age, but she doesn't drive much. I worked full time for 30 years at our public assistance office and retired at 58. The year after I retired (2013) I had a heart attack and had to have a double bypass. But have been fine ever since. Six months after the attack, I began working part time. I have worked at several part time jobs since then. In July last year I started working as a cashier at a grocery store, but I had to quit as Joe became weaker and weaker, He is more dependent on me than he was and I did not want to be at work if he needed me. AFter this is all over, I may go back, but we will just have to wait and see. HOw many children do you have? I have two boys, one is 46 and the other is 40. No grandchildren because neither of the boys wanted children. My oldest son is married to an oncology nurse and she has been a great help to me in explaining what certain medical terms mean. Whenever I Have a question, I call her-sometimes before the doctor. Ok, I have written your ear off, so I will end this with prayers for your husband and you. Talk at you later. Have a great day!