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Opposition builds to Zambian economist who challenges the liberal aid establishment By William Wallis in London, May 23 2009

Ms Moyo argues that [Aid] has fostered dependency and perpetuated poor governance.

A swell of opposition is building in the aid world to a new protagonist who has thrown down a strident challenge to the rock stars and liberal economists who have long dominated debate over foreign assistance to developing countries.

Galled by the ease with which Dambisa Moyo, the Zambian economist and former investment banker, has suddenly risen to prominence this year, activists are circulating detailed critiques of her ideas and mass mailing African non-government organisations to mobilise support against her.

Yet it is proving hard to suppress the hyper-active graduate of Oxford and Harvard, who pops up weekly in a new capital to promote her book Dead Aid - the title itself an affront to rock star Bob Geldof's Live Aid campaigns.

The former Goldman Sachs strategist has become something of a phenomenon. In April, she hit the New York Times bestseller list, this month she was named on Time Magazine's list of the 100 most influential people, and she has been appointed to the board of brewer SAB Miller.

Within days of reading about her, Paul Kagame, Rwanda's president, flew Ms Moyo out to address his government. This month, Col Muammar Gadaffi, the Libyan leader, invited her to Tripoli.

Broadly, Ms Moyo argues that official development assistance has fostered dependency and perpetuated poor governance. She proposes a blend of commercial debt, microfinance, fairer trade and investment in its place. . .

"It is ludicrous because we now have leaders like President Kagame supporting the anti-aid campaign. . . despite the clear successes of aid in promoting Rwanda's growth," he told the Financial Times. But Ms Moyo has struck a chord in Africa.

"The aid establishment is scared to death of the public relations disaster that a growing movement of independent critical African professionals would be," said William Easterly, the US academic.

Read more . . .

  Aid does not Improve Growth or Innovation, it only Fosters Dependency and Destroys hope.

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Where is the lowest mortality for Coronary Artery Bypass?

Coronary Artery Bypass Graft (CABG) Surgery in Ontario and Select US States by Michael Walker, Nadeem Esmail, Maureen Hazel, February 9, 2009 

The purpose of this study is threefold: first, to ascertain whether there are differences between mortality rates associated with coronary artery bypass graft (CABG) surgery in Ontario hospitals that perform such surgeries; second, to test whether the aggregate CABG mortality rate in Ontario is changing; and, third, to test whether the aggregate CABG mortality rate in Ontario is different than the aggregate CABG mortality rate in US states for which comparative data are available.

We find considerable hospital-by-hospital variation in risk-adjusted mortality rates in Ontario. Over the period of 2002/2003 to 2004/2005, the University of Ottawa Heart Institute and St. Mary's General Hospital were found to have the lowest risk-adjusted mortality rates in Ontario, while Sunnybrook and Women's College Health Sciences Centre and Anonymous Hospital 104 were found to have the highest rates in Ontario. According to the comparison of mortality rates associated with CABG in Ontario and 32 US states, patients seeking to minimize risk of death would be better off having surgery in all but five of the 32 identified US states in preference to Ontario in 2004.

www.fraserinstitute.org/researchandpublications/publications/6487.aspx

Canadian Medicare does not give access to first class health care, it only gives access to a second class waiting list.

--Canadian Supreme Court Decision 2005 SCC 35, [2005] 1 S.C.R. 791

http://scc.lexum.umontreal.ca/en/2005/2005scc35/2005scc35.html    


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Quality is an Unknown Political Issue

This health care 'reform' will kill thousands. --Karol Sikora, Tuesday, May. 12, 2009

One of the more unproductive elements of President Obama's stimulus bill is the $1.1 billion allotted for "comparative effectiveness research" to assess all new health treatments to determine whether they are cost-effective. It sounds great, but in Britain we have had a similar system since 1999, and it has cost lives and kept the country in a kind of medical time warp.  As a practicing oncologist, I am forced to give patients older, cheaper medicines. The real cost of this penny-pinching is premature death for thousands of patients - and higher overall health costs than if they had been treated properly: Sick people are expensive.  It is easy to see the superficial attraction for the United States. Health-care costs are rising as an aging population consumes ever-greater quantities of new medical technologies, particularly for long-term, chronic conditions, such as cancer.

As the government takes increasing control of the health sector with schemes such as Medicare and SCHIP (State Children's Health-care Insurance Program), it is under pressure to control expenditures. Some American health-policy experts have looked favorably at Britain, which uses its National Institute for Clinical Excellence (NICE) to appraise the cost-benefit of new treatments before they can be used in the public system.

If NICE concludes that a new drug gives insufficient bang for the buck, it will not be available through our public National Health Service, which provides care for the majority of Britons.  There is a good reason NICE has attracted interest from U.S. policymakers: It has proved highly effective at keeping expensive new medicines out of the state formulary. Recent research by Sweden's Karolinska Institute shows that Britain uses far fewer innovative cancer drugs than its European neighbors. Compared to France, Britain only uses a tenth of the drugs marketed in the last two years.

Partly as a result of these restrictions on new medicines, British patients die earlier. In Sweden, 60.3 percent of men and 61.7 percent of women survive a cancer diagnosis. In Britain the figure ranges between 40.2 to 48.1 percent for men and 48 to 54.1 percent for women. We are stuck with Soviet-quality care, in spite of the government massively increasing health spending since 2000 to bring the United Kingdom into line with other European countries.  Having a centralized "comparative effectiveness research" agency would also hand politicians inappropriate levels of control over clinical decisions, a fact which should alarm Americans as government takes ever more responsibility for delivering health care - already 45 cents in every health-care dollar. In Britain, NICE is nominally independent of government, but politicians frequently intervene when they are faced with negative headlines generated by dissenting terminal patients.

For years, NICE tried to block the approval of the breast cancer drug Herceptin. Outraged patient groups, including many terminally ill women, took to the streets to demonstrate. In 2006, the then-health minister suddenly announced the drug would be available to women with early stages of the disease, even though it had not fully gone through the NICE approval process.  A more recent example was the refusal to allow the use of Sutent for kidney cancer. In January, NICE made a U-turn because of pressure on politicians from patients and doctors. Twenty-six professors of cancer medicine signed a protest letter to a national newspaper - a unique event.  And yet this drug has been available in all Western European countries for nearly two years.  In Britain, the reality is that life-and-death decisions are driven by electoral politics rather than clinical need. Diseases with less vocal lobby groups, such as strokes and mental health, get neglected at the expense of those that can shout louder. This is a principle that could soon be exported to America.

Ironically, rationing medicines doesn't help the government's finances in the long run. We are entering a period of rapid scientific progress that will convert previous killers such as heart disease, stroke and cancer into chronic, controllable conditions. In cancer treatment, my specialty, the next generation of medicines could eliminate the need for time-consuming, expensive and unpleasant chemo and radiotherapy. These treatments mean less would have to be spent later on expensive hospitalization and surgery.

The risks of America's move toward British-style drug evaluation are clear: In Britain it has harmed patients. This is one British import Americans should refuse.

Karol Sikora, a practicing oncologist, is professor of cancer medicine at Imperial College School of Medicine, London, and former head of cancer control at the World Health Organization

Read the entire article and the Blog responses . . .

The NHS does not give timely access to modern health care, it only gives access to a waiting list.

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