DanaC |
08-17-2007 06:06 PM |
From the 193-page report, "Care Without Coverage: Too Little, Too Late"
as reported in USA Today 2002 : http://www.usatoday.com/news/health/...nce-deaths.htm
Quote:
the second in a planned series of six reports by the Institute of Medicine (IOM) examining the impact of the nation's fragmented health system. The IOM is a non-profit organization of experts that advises Congress on health issues.
Overall, the researchers say, 18,314 people die in the USA each year because they lack preventive services, a timely diagnosis or appropriate care.
The estimated death toll includes about 1,400 people with high blood pressure, 400 to 600 with breast cancer and 1,500 diagnosed with HIV.
"Our purpose is simply to deliver the facts, and the facts are unequivocal," says Reed Tuckson, an author of the report and vice president for consumer health at UnitedHealth Group in Minnetonka, Minn.
Among the study's findings is a comparison of the uninsured with the insured:
Uninsured people with colon or breast cancer face a 50% higher risk of death.
Uninsured trauma victims are less likely to be admitted to the hospital, receive the full range of needed services, and are 37% more likely to die of their injuries.
About 25% of adult diabetics without insurance for a year or more went without a checkup for two years. That boosts their risk of death, blindness and amputations resulting from poor circulation.
Being uninsured also magnifies the risk of death and disability for chronically sick and mentally ill patients, poor people and minorities, who disproportionately lack access to medical care, the landmark study states.
"The report documents the immense consequence of having 40 million uninsured people out there," says Ray Werntz, a consumer health expert with the Employee Benefit Research Institute. "We need to elevate the problem in the national conscience."
Calculating the cost in human suffering, he says, "is one way to get there."
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Presumably the people writing these reports and conducting these studies also live in America. You tell me you should know what it's like there. But who do I believe? You? The people conducting the studies? The President of the University of Michigan? You all live in America, you all know what the country is like. There does seem to be a great deal of evidence that the system fails a significant number of Americans. You all point at my healthcare system and say it limits access, yet I tell you I live in this country and have never had my access to medical care limited. And that's with several long term chronic conditions that I've had my whole life. My family haven't had their access limited. When my niece went into febrile convulsions and the local hospital saved her life, her parents weren't faced with a crippling bill afterwards. Most of my, and my family's and my friends' experiences of healthcare in the UK is positive.
There are exceptions. There is a drug which should be available and isn't and the consequence of which is that a friend of mine is losing her sight (we did eventually manage to persuade her to buy the treatment: she is a political activist, and ex member of parliament, who has campaigned all her life for the values expressed in the NHS. She used her situation to launch a campaign to try and make the drug available under the NHS for people with her condition. As someone who has fought against privatised medicine she did not feel in good conscience she could spend thousands on treatment that most could not afford.) There are a handful of drugs where such problems of access, or getting NICE to approve them are the case. Usually these are fought over for a while and eventually they get adopted. These are the exceptions, but they are numerous enough to make me realise that we have work to do to improve the system. It works for most people most of the time without creating financial hardship.
But you tell me that nobody is ever denied the treatment they need under your system?
Oh, as a side note, Alice was successful in her campaign to get the drug into the NHS. But, it will take a while for the Primary Care Trusts to finish wrangling over the details. There are already people receiving these injections. The campaign took about a year and a half and was related to a fairly new treatment for this condition.
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