Guest guest Posted September 30, 2006 Report Posted September 30, 2006 Analysis: Develop antibiotics or pay? By ED SUSMAN Science Daily (press release) http://www.sciencedaily.com/upi/index.php?feed=Science & article=UPI-1- 20060929-16034900-bc-us-antibiotics-analysis-crn.xml SAN FRANCISCO, Sept. 29 (UPI) -- Researchers decried Thursday a lack of research that can fight an epidemic of microbes that have gained resistance against virtually everything that doctors have in their pharmaceutical arsenal. In fact, some are even suggesting that drug companies who refuse to rise to the new microbial challenge should face a financial penalty. " Pharmaceutical companies have made billions of dollars turning human beings into toxic waste dumps, " charged Louis Rice, chief of medicine services at the Louis Stokes Veterans Affairs Medical Center in Cleveland, at an infectious disease meeting sponsored by the American Society for Microbiology. Rice said that the overuse of antibiotics due in part to over- prescribing by medical professionals has created biologically resistant microbes that cannot be killed off by drugs now available - - especially for bugs known as Gram-negative pathogens. While the Gram-negative bugs were not considered as important or as dangerous as so-called Gram-positive bugs such as staphylococci or streptococci, he said that 25 percent of infections with klebsiella - - which causes pneumonia, urinary-tract infections and wound infections -- do not respond to anything clinicians can thrown at it. " I don't blame the pharmaceutical companies for resistant bacteria any more than I blame doctors for overprescribing the drugs, " Rice said. " But the pharmaceutical companies made so much money developing the antibiotics they have a responsibility to contribute financially to finding treatments. " Yet there is a dwindling number of pharmaceutical companies that are willing to commit funds to developing drugs to overcome resistance, he said, noting that many companies are merging or are leaving the development arena. To those companies that shy away from the challenge, Rice suggested they should be taxed to finance the work of other companies willing to find the compounds needed to treat patients with the antibiotic- created resistant pathogens. Rice also suggested that studies -- probably under the aegis of the National Institutes of Health -- should undertake studies to determine whether it is really necessary for people to take antibiotics for full courses of treatment. He pointed out that the recommendations for taking drugs for a full course was based on clinical trials with set timeframes, not on whether a person was feeling better. He said that taking antibiotics longer than necessary only contributes to creating more powerful, resistant bugs. " Gram-negative bacteria have a thicker cell wall that prevents drugs from penetrating and killing it, " Bush, distinguished research fellow at & Pharmaceutical Research and Development in Raritan, N.J., told United Press International at the 46th annual Interscience Conference on Antimicrobial Agents and Chemotherapy in San Francisco. " There are now multi-drug resistant acinetobacter strains -- including those brought back to the U.S. from troops and personnel in Iraq -- that don't respond to any classical treatment, " Bush said during a news briefing. , a consultant to pharmaceutical companies from Flintshire, Wales, United Kingdom, said, " It's a real challenge to find a wide spectrum Gram-negative antibiotic. " In another news briefing at ICAAC, a meeting that has attracted 16,000 scientists, researchers and allied healthcare providers, doctors looked at treatments for fungal infections -- illnesses that emerged among patients with suppressed immune systems or who are treated for extended times in intensive care units, attached to various devices and catheters. " We now have a number of ways of treating these patients, " said Elias Anaissie, professor of medicine at the University of Arkansas for Medical Sciences in Little Rock. For years the mainstay of fungal infection treatment was use of toxic, intravenous amphotericin B. Since then, equally effective but more convenient oral medications have been approved. " Now the question is whether we can treat those patients by combining medicines in these groups, " he told UPI. The problem is that, what looks good in test tube doesn't necessarily work in patients, and what looks good may work in treating one infection but not another. The need for clinical trials in this area, said Johan Mouton, professor of medicine at Canisius Wilhelmina Hospital, Nijmegen, the Netherlands, has intensified because there are more patients now who are at risk of these infections: Transplant patients, cancer patients, AIDS patients and long-term trauma patients. Quote
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