Health Care Reform And "unnecessary" Tests makes me a little concerned...
#1
Posted 02 November 2009 - 11:01 AM
I've been hearing a lot lately about how "cutting waste" from the health care system in the US is the way they are planning on paying for health care reform. Now, I'm all for reform, as I *have* insurance and still have racked up thousands of dollars in debt over the last couple of years trying to get the proper diagnosis. However, a lot of the chatter lately (news, pundits, etc) has been about how doctors run soooo many unnecessary tests. Well, if I had not pressured my doctors into "unnecessary" tests, I would still be very sick. The attitude that the doctor knows all and is in 100% control of your testing is dangerous, because they are not all as educated as we would hope. What about all the drugs that I was prescribed, paid for, and took unnecessarily because the proper tests were not done to begin with?
It is really unsettling to me that we could potentially be facing a system where we can't get the care we need simply because someone else thinks that the proper care is "wasteful." I still don't have an actual diagnosis even though I have been gluten free for 10 months and this makes me worry a little bit- if I were ever to be hospitalized, I hear getting gluten free food is very difficult, and I imagine it would be even harder without a "real" diagnosis.
Anyone else have opinions on this?
#2
Posted 02 November 2009 - 12:21 PM
knittygirl1014, on Nov 2 2009, 02:01 PM, said:
I've been hearing a lot lately about how "cutting waste" from the health care system in the US is the way they are planning on paying for health care reform. Now, I'm all for reform, as I *have* insurance and still have racked up thousands of dollars in debt over the last couple of years trying to get the proper diagnosis. However, a lot of the chatter lately (news, pundits, etc) has been about how doctors run soooo many unnecessary tests. Well, if I had not pressured my doctors into "unnecessary" tests, I would still be very sick. The attitude that the doctor knows all and is in 100% control of your testing is dangerous, because they are not all as educated as we would hope. What about all the drugs that I was prescribed, paid for, and took unnecessarily because the proper tests were not done to begin with?
It is really unsettling to me that we could potentially be facing a system where we can't get the care we need simply because someone else thinks that the proper care is "wasteful." I still don't have an actual diagnosis even though I have been gluten free for 10 months and this makes me worry a little bit- if I were ever to be hospitalized, I hear getting gluten free food is very difficult, and I imagine it would be even harder without a "real" diagnosis.
Anyone else have opinions on this?
I understand your concerns and if you know anything about socialized medicine, it gets downright scary, after what many Americans are used to here. However, there are many cases where unnecessary testing is done and I think this is what the government may try to address. I am not in favor at all of a government plan but I do think there have been a couple of ideas which sound sensible to me.
Pre-surgery testing has reached the ridiculous stage. All you need is a blood screen and a lung x-ray, like they used to do and now you have doctors who test for everything to cover their butts in case someone dies and there is the resultant lawsuit. Some people with multiple health problems may need to be screened a little more but many do not need all this testing and shouldn't have to undergo the majority of it.
We push physicals too often and do too many screening tests today. People have become so paranoid about their health and demand all these screening tests when they may not be warranted. Family history and other factors should be taken into consideration here and not have all members of the population undergo all of the same tests. It just isn't necessary and this could save millions of dollars. Medicine only got really expensive when all of this came into play. If you have symptoms which you are seeking answers for, then this is when testing is necessary. I doubt that many doctors will blow off tests if you come in with a complaint of diarrhea which is disrupting your life.
If the US models their plan after socialized medicine which exists in other countries, then it may be a problem. We have heard the complaints about long waits for tests and I hope this does not happen here. If a test can wait, fine, but if someone is sick and their lifestyle is impacted, no one should have to wait.
As for having Celiac, we are lucky in that we can always resort to a dietary trial for some answers. Do not be discouraged because you do not have a formal diagnosis. That can be a good thing, as far as insurance goes. People have been denied insurance because of Celiac Disease. I expect that to get worse.
As for being hospitalized, that shouldn't be an issue. You would tell them you need to eat gluten-free and refuse any food which isn't. Personally, I doubt I would eat hospital food anyway and have family members bring me something decent to eat from home. It isn't hard to cook up a gluten-free meal anywhere. You may not have any bread but it's easy to go without bread for a week or so. I do it all the time when I travel.
I also have good health insurance but have spend thousands on alternative care and testing because mainstream medicine is only so good. I think it's money well spent. It can be frustrating to not get the answers you want but if you have gone gluten-free and feel much better, then you know what the problem is. I paid for all my testing out of pocket and have my diagnosis but my insurance company has no copies of any testing...which I find very comforting! We will have to wait
and see what happens, I guess, but I am a little worried myself over how many more taxes we'll get hit with to pay for all of this!
#3
Posted 02 November 2009 - 12:28 PM
Health care reform isn't going to eliminate insurance companies, they're going to still be there, but they are going to set rules about who they can refuse and stop all the nonsense like recission. There's also the potential for a government run option. I don't hear too many seniors or vets complaining about their government run health care. Besides, if we don't like the health care we end up with we can always kick people out of office until they fix it. Hard to do that with private companies...
And of course, people don't get all the tests they want with private insurance either. I suspect things won't change a whole lot and that gluten issues will still be self-diagnosed fairly often like it currently is. Just so long as I can continue to utilize companies like Enterolab to do my own testing, I'll be fine with that.
#4
Posted 02 November 2009 - 01:48 PM
I'm also not contesting the fact that there are a ton of unnecessary tests being done- especially to avoid malpractice suits- but in the future WHO is going to decide what is unnecessary? I'd like to say I hope it's left up to the medical professionals and not someone sitting behind a desk doing pre-approvals, but I don't have a whole lot of confidence in that either! Especially with some of the doctors I've seen...
It would be great to hear from some international people who have government health care too!
#5
Posted 03 November 2009 - 08:47 AM
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I didn't have a lot of tests run in years past because no one wanted to do anything other than an upper GI and ultrasound. I went for Celiac symptoms starting 25 years ago, before endoscopies were in existence. There is no paper trail. I went to a private physician and paid out of pocket and got much better health care.
I am not saying that this particular aspect of health care doesn't need fixing (pre-existing conditions) but the current system we have is not bad, if you find the right doctor. Also, I think that part will go away and private companies will not be allowed to do so because everyone has a pre-existing condition. Americans are in bad health and there are so few people who can boast they are 100% healthy with no issues. They'll go out of business all on their own if they refuse to cover that many people.
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Actually, I hear lots of people complain about Medicare. You also have to have supplemental insurance because Medicare doesn't cover everything. Many doctors around where I live no longer accept Medicare because they don't get paid enough money to make it worth their while. I don't blame them either. Doctors are highly skilled and go to school for many years to become doctors. When I go, I want to see the best and will pay for that. That will become a huge problem in future if there is a public option.....access to good doctors will be restricted. You will not be able to see better doctors and go to better hospitals or it will be very hard to do so....you may have to wait a long time.
I live in Massachusetts and we are the model state for the national health care bill. It is not a distinction I am proud of. We are one of the highest taxed states in the nation. Ever since we were mandated to pay for health care for those without it, the run on the border has been unreal. Lots of illegals flocking here for their free health care, at the working families expense. We are being nickeled and dimed and squeezed hard by our government because now there is no money for anything else. The cost of living here has gone dramatically up due to all the new fee's and taxes.
A huge chunk of that goes to health care for everyone. I am in no way opposed to helping out my fellow American citizens at all but I will not pay for people who do not belong here. I honestly do not think most people have really thought this out and what it will mean to their paychecks.
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I am in the camp where I now have a good doctor who runs any test I want but I am not overly demanding of tests that really do not need to be done. If I am feeling really good, which I am, there is no need to screen the hell out of me just because I am older. I base my screenings on common sense, like we used to, and not by age. That is one way to save some money. Let them screen those with strong family histories of certain diseases or insure more Americans on the money saved.
Whatever ends up happening, Americans have to think long and hard if they want to lose 15% of their paychecks and have increased taxes and fees to pay for it all. The money has to come from somewhere and if they want the same kind of care we are used to in this county, in blanket form for everyone, it's going to have a huge price tag, which will be felt. That scares me more than anything because I work for a living and it gets hard to save for retirement when your paycheck keeps shrinking.
#6
Posted 03 November 2009 - 09:09 AM
knittygirl1014, on Nov 2 2009, 01:48 PM, said:
But doctors are CURRENTLY encourage to run fewer tests, because insurance companies - as they stand - do not want to pay for them, and will sometimes deny them (even for random reasons). There are still instances, however, of doctors just running ridiculous tests - and a celiac blood test if you've got GI issues isn't ridiculous. A head CT if you've got GI issues (well, certainly without *ANY* symptoms suggesting for one - and I'll grant you that celiac could well cause those symptoms) would be something they might try to eliminate.
There is a LOT that is done in the medical community for no other reason than to cover someones behind. (This is becoming only more apparent to me as I go through my pregnancy. The OB world is FULL of things done for no other reason than to have data to justify decisions in case the data is needed in a lawsuit.) That wouldn't be such a bad thing to get rid of. (Yes, I'm deliberately ignoring the "well, why don't we... instead" argument. Not a politics thread.)
Inconclusive Blood Tests, Positive Dietary Results, No Endoscopy
G.F. - September 2003; C.F. - July 2004
Hiker, Yoga Teacher, Engineer, Painter, Be-er of Me
Bellevue, WA
#7
Posted 05 November 2009 - 02:42 PM
As for there not being a paper trail, the only way that is possible is if you gave them a fake name when you went for your procedures. I suppose it's possible that those records won't make it to another doctor or to the insurance company, but if you don't tell them and they find out later, you can be sued for fraud.
I absolutely agree that I don't want my taxes going sky high, and yes the money has to come from somewhere. I just don't want the cost-saving to go to the opposite extreme and have doctors be penalized for running too many tests. Because then the patient is penalized too. I'm probably being overly worried, but it's just hard to find information about what's going on in "reform" right now, and I'm so busy!
#8
Posted 05 November 2009 - 03:44 PM
Now let me tell you what health care is like in New Zealand, and I assure you you are not going to end up with this!!! We have a public socialized health system, and a parallel private system with often the same doctors in both. In other words, the doctors work for the public system but operate a private specialty practice on the side. You can choose your own GP, but need a referral to see a specialist (and there are not very many of them, although GP's are becoming scarce now as the old ones retire and the newly minted doctors see that you make lots more money as a specialist). GP visits costs about $40 (subsidized), prescriptions of PHARMAC-approved drugs cost $3, lab tests, x-rays, hospitalizations are free. Now the rub really comes in when you need to see a specialist, especially if it is for a condition for which you are likely to need surgery. You can "go private" (where you don't need a referral) and pay the $75-150 for the visit, and any lab work and x-rays will be covered, but then you are stuck if you need surgery. Then you have to go back and wait for an "official" visit to be evaluated under the public system. And at this evaluation you are awarded points toward qualifying for the medical procedure, whatever it is. Points are awarded based on degree of pain, disability, whether you are working or not, whether you are a primary caregiver, and I don't know all the other criteria. If you earn enough points you are put on a waiting list, and these lists used to be endless. Now they will only put you on the waiting list if you can be treated within six months (i.e., you need more points now to get on the list). Needless to say, if you are 80 years old and need surgery for cataracts, can still see well enough to do your daily chores (without chopping your finger off while cutting carrots) and have a partner who can drive you places, you will not score very high on the list.
There is also a private insurance system for which the premiums used to be relatively inexpensive, but which have gone up astronomically in the last ten years (commensurate with the difficulty of getting on the public list). There are several private hospitals, and if you are lucky enough to be able to afford the private insurance or got in before you had any pre-existing conditions it operates pretty much the way the U.S. system does. There is no employer-based health insurance, except that provided by the ACC (Accident Compensation Corporation--workers' comp with a twist). If you can afford it, you can have your cataract surgery done at a private hospital, probably by the same doctor who would do it in the public system.
ACC is funded by employers, by automobile registration, by sporting bodies (professional) and maybe some other source I can't think of at the moment. It works this way because we have no fault auto insurance, and injuries of any type, whether automobile, cutting your finger off while chopping carrots
This may help explain why my husband and I, even though we live nine months of the year in New Zealand, maintain our (former) employer-based Medicare supplemental insurance and pay our Medicare premiums, and visit the U.S. every summer for three months. Everyone in New Zealand thinks we are going off for a lovely holiday in the sun, but our time is mostly spent taking care of our health
So anyway, someone asked for some international experience--that's mine.
This is not meant to be a cautionary tale for you, but just to demonstrate that this is not the kind of system you are going to end up with after "health care reform."
"Everything that can be counted does not necessarily count; everything that counts cannot necessarily be counted." - Albert Einstein
"Life is not weathering the storm; it is learning to dance in the rain"
"Whatever the question, the answer is always chocolate." Nigella Lawson
------------
Caffeine free 1973
Lactose free 1990
(Mis)diagnosed IBS, fibromyalgia '80's and '90's
Diagnosed psoriatic arthritis 2004
Self-diagnosed gluten intolerant, gluten-free Nov. 2007
Soy free March 2008
Nightshade free Feb 2009
Citric acid free June 2009
Potato starch free July 2009
(Totally) corn free Nov. 2009
Legume free March 2010
Now tolerant of lactose
Celiac.com - Celiac Disease Board Moderator
#9
Posted 05 November 2009 - 11:24 PM
And I'd kill for ANY kind of health care plan at this point. I'm not picky, just give me something I can afford that will allow me to sign up inspite of my medical history. I'd be thrilled beyond words to have ANY option.
as long as you put it back where you got it when you're done with it."
#10
Posted 06 November 2009 - 01:00 AM
VioletBlue, on Nov 6 2009, 08:24 PM, said:
Unfortunately, one of the biggest expenses in the US health care system are the obscene profits made by undetected fraud, especially in Medicare and Medicaid. Fraud exists everywhere, but it seems especially prevalent in the government health care programs (and, might I add, in the financial sector. too--which has impacted the whole world
"Everything that can be counted does not necessarily count; everything that counts cannot necessarily be counted." - Albert Einstein
"Life is not weathering the storm; it is learning to dance in the rain"
"Whatever the question, the answer is always chocolate." Nigella Lawson
------------
Caffeine free 1973
Lactose free 1990
(Mis)diagnosed IBS, fibromyalgia '80's and '90's
Diagnosed psoriatic arthritis 2004
Self-diagnosed gluten intolerant, gluten-free Nov. 2007
Soy free March 2008
Nightshade free Feb 2009
Citric acid free June 2009
Potato starch free July 2009
(Totally) corn free Nov. 2009
Legume free March 2010
Now tolerant of lactose
Celiac.com - Celiac Disease Board Moderator
#11
Posted 06 November 2009 - 04:45 AM
mushroom, on Nov 6 2009, 01:00 AM, said:
I agree. This drives up malpractice insurance, increases the number of unnecessary tests, and drives physicians away from high (sue-) risk specialties, like obstetrics. My PCP told me that 1/3 of her salary goes straight to malpractice insurance. When you factor in medical school debt, it takes a while before an MD is even earning a livable wage. And they are, what, 30? by the time they get their first real job?
Makes you wonder why anyone would choose the profession.
- James Watson
My sources are unreliable, but their information is fascinating.
- Ashleigh Brilliant
Leap, and the net will appear.
Celiac.com - Celiac Disease Board Moderator
#12
Posted 08 November 2009 - 08:36 PM
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There will not be any paper trail if a person pays for all testing and appointments in cash and keeps copies of the testing out of a PCP's hands. I went to a private doctor who does not use a computer for her patients records....she is not an HMO physician so isn't in the network. I had all my Celiac testing done this way and it was due to the lack of being able to get a timely appointment with a specialist
and nothing to do with having my insurance company find out. I was diagnosed through blood work and refused the biopsy....there was no need to do one.
They cannot sue you either if they cannot prove you have Celiac Disease. If you are healthy and following a strict gluten-free diet, anything else that may happen would not be linked to Celiac. At this point, if I were to be tested, everything would be negative as I've been gluten-free for so long. They can't prove I follow a gluten-free diet either. In today's world, you have to be selective about what you tell a doctor and what tests you agree to as we all know these can be held against you.
The other bright spot is I am in a group plan through my employer. Insurance companies in the US cannot refuse you coverage if you are in a group plan....that is how mine works. Obtaining insurance on my own might be another problem, if they knew I was a Celiac. I am also vested into the plan, which means they will have to cover me when I retire under their group plan. However, who knows what will happen if the government gets their hands into it.
#13
Posted 09 November 2009 - 04:34 AM
#14
Posted 09 November 2009 - 06:13 PM
We will also eventually havee a government run system. If the insurance companies continue to be villified, Congress will make sure they won't make enough profit to attract capital. They will die, and the government will step into the void. Then health care will be rationed by politics instead of insurance money. And with US budget deficits at record levels, service levels will be sacrificed for DMV-like efficiencies.
Doctor shortages and political rationing are a recipe for disaster. Yes, I'm pessimistic.
Gluten-free since 03/09 (and manic about it)
Looking forward to a better life since 03/09
#15
Posted 09 November 2009 - 06:35 PM
We have no for-profit HMOs that decide who gets cared for, and who doesn't, based on a profit motive.
We don't worry about "pre-existing conditions." Everybody is covered to exactly the same extent. The 80-year-old with a heart attack will get the same treatment as a 35-year-old.
Not everything is covered. Drugs are not, whether prescribed or over-the-counter. Dental care is not covered. Routine eye care is not covered, nor are the glasses you may need. For all of these, private insurance is available. But again, the insurers may not disallow a claim due to a "pre-existing condition" (trip cancellation insurance is an exception).
If a test is covered by the public plan (and most are), then it will be done if your doctor deems it necessary. There is no prior review by an insurance administrator--it just gets done.
Drugs are still sold by pharmaceutical companies at a profit, so there is still money to be made by researching and developing new drugs. Private, for-profit, companies make and sell medical supplies and equipment. They are still thriving.
There are waits for many procedures. But I will take that in a moment over not being able to get them at all because I don't have insurance, or because my diabetes or celiac disease is a "pre-existing condition."
Diagnosis by biopsy of practically non-existent villi; gluten-free since July 2000.
Type 1 (autoimmune) diabetes diagnosed in March 1986
Markham, Ontario (borders on Toronto)
Celiac.com - Celiac Disease Board Moderator

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