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#44189 11-10-2004 11:56 PM
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Dolores Offline OP
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Ken is almost through his third week of radiation and things are going as well as can be expected. Still chugging down the Boosts and only lost 1 pound last week. Some thrush and mouth sores have been causing him a great deal of pain, so his chemo doctor put him on a 25 mg. Fentanyl patch, with 1 tsp. Oxycodone as needed (usually 3-4 times a day.) He was doing well with this course; however, when we met with his radiation oncologist yesterday, he expressed concern with the amount of pain medication he was taking. He told Ken the pain would "increase greatly over the next few weeks" and if he were already taking strong meds, nothing would be able to help him with the pain further down the road. Any opinions or advice on this?


Sherry (Dolores is the name of my cat) Wife to Ken, starting chemo/radiation 10/25/04. Stage IV SCC of right tonsil, T2,N2A,MO
#44190 11-11-2004 12:28 AM
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My RO told me the same stuff. Ignore it. They can increase the patch to 300mg if necessary. 25 mg is a starter dose. Most people here are at 75-150mg. If he is taking too much oxycodone then they will increase the patch. Tell your RO to read the pain management guidelines on the NCCN site http://www.nccn.org/professionals/physician_gls/PDF/pain.pdf

Effective pain management is a basic patient right.

Keep that thrush under control. Talk to your doctor about Diflucan or Nystatin. Systemic thrush can have serious complications and can even be fatal.

My oncologist managed all of my medications and he was the most qualified.


Gary Allsebrook
***********************************
Dx 11/22/02, SCC, 6 x 3 cm Polypoid tumor, rt tonsil, Stage III/IVA, T3N0M0 G1/2
Tx 1/28/03 - 3/19/03, Cisplatin ct x2, IMRT, bilateral, with boost, x35(69.96Gy)
________________________________________________________
"You are a mist that appears for a little while and then vanishes" (James 4:14 NIV)
#44191 11-11-2004 07:26 AM
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Sherry,
I so agree with Gary. Dan also started out at 25 and ended up at 100 or 150. He also had Oxycodone for breakthru pain and probably one or two other meds. About the three week treatment time is when Dan really started having bowel trouble from the strong meds. Watch for that and there are different regimens to try. Dan suffered for a whole day practically on the floor in pain from not being able to go to the bathroom. It kind of happened suddenly and we were not given any instructions about that problem until he was in the middle of it.
Take care and God bless,
Debbie


Debbie - Caregiver for husband, Dan, diagnosed with tongue cancer 7/03. Partial gloss., mod. neck dissections, graft. Recurrence neck tumor 12/03. Radical left neck dissection 12/24/03-unable to get all the tumor. 8 weeks chemo/rad beginning 1/12/04.
#44192 11-11-2004 08:41 AM
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In my case the pain stayed about the same once it hit. So I wouldn't be to concerned about what is to come. The meds your on now should do, if you need more you can certainly obtain. The biggest issue to come as Debbie said is the constipation. I too had a very bad day about a week after the constipation started. I would talk to the doctor to give you the proper meds for that and have them on hand so you have them if you need them.


SCC R-Tonsil T2 NO MO Dec 2003. Completed IMRT Radiation only to tonsils(72Gy) and neck(55Gy)March 04. Detected at age 50.
#44193 11-11-2004 10:29 AM
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I took the hard narcotics. Don't worry about the addiction, just stay pain free. It was only moderately difficult to get off the Morphine.
Darrell


Stage 3, T3,N1,M0,SCC, Base of Tongue. No Surgery, Radiationx39, Chemo, Taxol & Carboplatin Weekly 8 Treatments 2004. Age 60. Recurrence 2/06, SCC, Chest & Neck (Sub clavean), Remission 8/06. Recurrence SCC 12/10/06 Chest.
#44194 11-11-2004 02:41 PM
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Hi Sherry,
My doctor told me to increase the fentanyl patches as needed to handle the pain most of the time and to use another drug (Roxicet - a mix of acetomenophen and oxycodeine) for breakthrough pain. She said it was important not to rely on the breakthrough pain drug too much but rather to add another 25 mg. patch anytime the pain was breaking through too frequently.
As Gary said, you can keep adding patches and get up to 300 mg. of fentanyl. and that most of us ended up in the 100-150 range. I would say not to worry about adding sufficient medication to handle the pain. You should pay attention to the constipating aspects of the narcotics, though, and start using Boost (or whatever) with fiber. You can also buy water soluble fiber and add it to his diet. I'd suggest starting to increase the fiber before the constipating effects really kick in.
Also, when treatments are over and the pain begins to diminish (usually a couple of weeks after treatment ends), you should carefully and slowly taper off the patches so that ending the narcotics will not create too much of a withdrawal effect. You can even go from a 25 mg. patch to smaller dosages by placing some clear plastic tape under part of the patch to prevent its absorption into the body.
Good luck with the treatments and remember that despite the pain and suffering of the radiation, it will pass with time and there will be better days ahead. Best, Sheldon


Dx 1/29/04, SCC, T2N0M0
Tx 2/12/04 Surgery, 4/15/04 66 Gy. radiation (36 sessions)
Dx 3/15/2016, SCC, pT1NX
Tx 3/29/16 Surgery
#44195 11-11-2004 03:32 PM
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Sherry - one little tidbit to everyone's post - if you increase the patch by huge doses - Ed went from 25mcg at onset of radiation to 75mcg not too far after onset then straight to 150mcg be sure you're with them or someone with them for at least 24 hours. Ed had the tendancy to get VERY light headed and nearly passed out more times than I can remember, behaved (more) oddly, and actually had a near migraine headache for about 1 week. His pain got out of control really quickly and we used liquid Tylenol 3 (only thing we used his PEG for) for breakthrough pain. Don't forget to include senna or some vegetable stool softener like Sheldon said. FYI - watch for perimiter burning. Ed got a batch that were (we later found out) recalled. We told the pharmacy and doctor about it - it burned his flesh just on the outer edge of where the adhesive was - at first we thought it was like an allergy to tape/sticky stuff...

Like I tell everyone for radiation burn - get Domeboro Soak. Best $4 you could ever spend for relief! Been 'round since the 30's for good reason.

Good luck! Every treatment down is one less left on the list! smile

Susan


Caregiver to Uptown/Ed, SCC Stage IV, Base of tongue - Completed Chemo (Cisplatnin/5FU) and 45 days' simultaneous Radiation 10/08/03
#44196 11-11-2004 11:57 PM
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Dolores Offline OP
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When we met with Ken's chemo oncologist yesterday, he basically told me what Gary said in his post, which was to ignore the radiation oncologist. The chemo doctor said the doses Ken is on are low and can be increased quite a bit if the pain worsens. I think I will listen to the chemo guy from now on--he is much more cheerful and I like his advice better!
By the way, the Fentanyl makes Ken pretty goofy and spacey. Does that lessen as his body adjusts to it?


Sherry (Dolores is the name of my cat) Wife to Ken, starting chemo/radiation 10/25/04. Stage IV SCC of right tonsil, T2,N2A,MO
#44197 11-15-2004 08:14 AM
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Dolores' mom :rolleyes: ,

As the body adjusts to the Fentanyl, Ken will hardly know it is there other than not feeling the intense pain. I drove to work 400 miles away with 150 on and even drove back in the middle of the night without scaring myself or anyone else, that I know of eek . My work was accounting and I was able to perform my duties fine, too.

I used liquid morphine for the breakthrough towards the end and it did more to make me loopy than anything.

Ed


SCC Stage IV, BOT, T2N2bM0
Cisplatin/5FU x 3, 40 days radiation
Diagnosis 07/21/03 tx completed 10/08/03
Post Radiation Lower Motor Neuron Syndrome 3/08.
Cervical Spinal Stenosis 01/11
Cervical Myelitis 09/12
Thoracic Paraplegia 10/12
Dysautonomia 11/12
Hospice care 09/12-01/13.
COPD 01/14
Intermittent CHF 6/15
Feeding tube NPO 03/16
VFI 12/2016
ORN 12/2017
Cardiac Event 06/2018
Bilateral VFI 01/2021
Thoracotomy Bilobectomy 01/2022
Bilateral VFI 05/2022
Total Laryngectomy 01/2023
#44198 11-16-2004 04:37 PM
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Sherry-
Don't you listen to him! It wasn't the morphine that made him loopy, it was the NASTY dexamethasone! :p I swear those doctors wanting to administer anti-nausea drugs and any other kind kept on like Eve to Adam - "Here! Take this...it will make it feel/work better". Dex made him act like he had brain mets. The liquid morphine made him VERY short tempered more than disoriented.

The Fentanyl patches are one of the best ways to curb the major pain and still let the patient be/feel productive. There are a bunch of articles out there written by the palliative teams supporting oncologists whose patients were incapacitated because of the other/ancillary side effects of other pain meds; one in Time Magazine sticks out in my mind because it was just about the time Ed started needing them. Through the use of the duragsic patch, people with extreme pain actually have a chance at some "normal" routine.

What kind of kitty is Dolores? smile

Susan


Caregiver to Uptown/Ed, SCC Stage IV, Base of tongue - Completed Chemo (Cisplatnin/5FU) and 45 days' simultaneous Radiation 10/08/03
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