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	<pubDate>Sat, 20 Mar 2010 10:03:01 +0000</pubDate>
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		<title>Combat Acne Naturally7 Ways to</title>
		<link>http://alliesowned.anthonyjansen.com/2010/03/20/combat-acne-naturally7-ways-to/</link>
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		<pubDate>Sat, 20 Mar 2010 10:03:01 +0000</pubDate>
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		<description><![CDATA[Acne is a skin ailment that affects people all over the world. Tons people are relying to heavily upon commercial and medical creams and treatments that simply are not getting the job done. Acne can actually be treated naturally from home with seven different simple remedies. Rather than allowing acne to affect your flavour forever, [...]]]></description>
			<content:encoded><![CDATA[<p>Acne is a skin ailment that affects people all over the world. Tons people are relying to heavily upon commercial and medical creams and treatments that simply are not getting the job done. Acne can actually be treated naturally from home with seven different simple remedies. Rather than allowing acne to affect your flavour forever, regard adopting some of these tonic methods for curing it. Don&#8217;t frustrate acne get the best of you; elect a candid remedy today to rid your body of acne. These seven home remedies are simple and easy to prepare, and really get rid of a punch.
<p>  1 - Honey    </p>
<p>  Apply natural honey with no added preservatives. Applying it directly to the area can significantly reduce the spots.    </p>
<p>  2 - Lemon and Cinnamon    </p>
<p>  Mix 1 teaspoon of cinnamon with lemon juice and apply it directly to the area to reduce acne exposure.     </p>
<p>  3 - Toothpaste    </p>
<p>  It has said that this particular remedy is a myth, but it truly isn&#8217;t. Apply toothpaste directly to the places where you have acne. Make sure that you are not applying toothpaste to areas where there is no acne, as this may dry your skin out. Toothpaste will dry the acne out and cause pimples to go away.    </p>
<p>  4 - Mint    </p>
<p>  Another excellent way to reduce acne is to concoct a face mask from fresh mint. Apply this mask before you go to bed if you want to have the best impact. This particular face mask is also useful for black heads. Mint has also proven itself useful for other skin conditions including eczema.     </p>
<p>  5 - Cotton
 </p>
<p>  If you have acne on your back or shoulders, you should choose cotton clothing rather than other materials. Cotton is one of the kindest possible materials that you can choose to wear.    </p>
<p>  6 - Washing    </p>
<p>  Figure out what level of washing is required for you to combat acne. For some people, washing your neck, back or face can have a positive result. For other people, increased washing can lead to drier skin, which can cause more conditions of the skin. Figure out what works for you by tweaking your washing schedule until you get it right.    </p>
<p>  7 - Lime and Rose Water    </p>
<p>  Try mixing lime water with rose water together. Apply this concoction directly to the areas where you are battling acne. This can help to clean up not only current pimples, but also areas where you tend to have a lot of acne.    </p>
<p>  Keep in mind when it comes to home remedies, that not everything will work for everyone. Try each of these home remedies out on your own. Make sure to test them on a small amount of skin until the desired results are achieved. If you try a remedy that is not producing results, try something else. Consider consulting a physician for more natural remedies or advice on what you are already trying.    </p>
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		<title>Gene Therapy, Cancer-Killing Viruses And New Drugs Highlight Novel Approaches To Cancer Treatment</title>
		<link>http://alliesowned.anthonyjansen.com/2010/03/17/gene-therapy-cancer-killing-viruses-and-new-drugs-highlight-novel-approaches-to-cancer-treatment/</link>
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		<pubDate>Wed, 17 Mar 2010 20:03:10 +0000</pubDate>
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		<description><![CDATA[Studies presented at the 2007 session of the American Association for Cancer Examine exposition how researchers are using the fashionable, as probably as the reasonable, to help design and test new drugs to treat cancer.
Owing lesson, researchers are marrying the latest technologies and drug map together to figure out if a drug is having a [...]]]></description>
			<content:encoded><![CDATA[<p>Studies presented at the 2007 session of the American Association for Cancer Examine exposition how researchers are using the fashionable, as probably as the reasonable, to help design and test new drugs to treat cancer.</p>
<p>Owing lesson, researchers are marrying the latest technologies and drug map together to figure out if a drug is having a biological contact, what the conclusion is, when it stops working and what can be done about it. They have &#8220;watched&#8221; as an conjectural angiogenesis inhibitor shrank deadly brain tumors and when it began to fall through. By reading blood proteins they discovered why that happened, and how a combination of therapies might work better.</p>
<p>Scientists are also turning to existing &#8220;natural&#8221; biological systems to help them delineate next age cancer therapies. Several research groups are making progress in turning viruses into smart search-and-destroy tumor busters that drive assign normal cells exclusively, and others are pronouncement that marijuana&#8217;s quick ingredient can tweak receptors on the most common form of lung cancer and slash cancer growth.</p>
<p>Eradication of unsubmissive prostate cancer by a novel gene therapy MO = &#8216;modus operandi&#8217;: Abstract 4182 </p>
<p>A research team at Columbia University has designed a novel viral-based gene therapy they say blasts including a portion, targeting both primary and distant tumors, while leaving normal cells untouched. In the 15 mice they tested, injections of the therapy in tumors on inseparable side of the mouse eliminated those cancers as doubtlessly as tumors on the other side of the animal&#8217;s body, producing a cure in all of the mice.</p>
<p>This study tested this &#8220;dual cancer-specific targeting strategy&#8221; with combative therapy resistant prostate cancer. The researchers have also shown it works in animals with teat, and melanoma tumors.</p>
<p>An earlier version of the therapy showed powerful effects in a phase I clinical contest, said Paul B. Fisher, M.Ph., Ph.D., professor clinical pathology at Columbia. This improved treatment appears to be a much &#8220;smarter shell with imminent of treating metastatic and therapy-resistant cancers,&#8221; he said.</p>
<p>&#8220;The looker of this make a proposal to is that two methods are being used to destroy a tumor,&#8221; said Devanand Sarkar, M.B.B.S, Ph.D., the study&#8217;s primary founder, associate delve into scientist at Columbia. &#8220;The virus we designed replicates within a tumor, and at the at any rate pro tempore produces a massive amount of a cancer killing compound. Either action alone is damaging and potentially deadly, but together they are lethal.&#8221;</p>
<p>Columbia researchers built the therapy around their earlier, significant unearthing of a cytokine (a signaling protein) called melanoma differentiation associated gene-7/interleukin-24 (mda-7/IL-24). A technology developed in the Fisher laboratory, &#8220;subtraction hybridization,&#8221; applied to human melanoma, induced the cancer to pick up again to a more rational state, allowing comparison of genes expressed in both states. They discovered mda-7/IL-24 was progressively down-regulated as melanoma developed. In its normal state, the cytokine may affect growth and immune modification, whereas shading at high levels kills cancer cells.</p>
<p>The investigators altered an adenovirus to carry the mda-7/IL-24 into tumors that normally did not express the gene, and based on celebrated animal studies, this cytokine was tested for safety in patients with advanced melanoma and other incontestable cancers. &#8220;Interestingly, this phase I clinical trial produced a significant clinical response,&#8221; Fisher said.</p>
<p>To make the treatment more potent, they then paired the mda-7/IL-24 gene with a &#8220;replication competent&#8221; adenovirus, a virus that can multiply within cells. After such a microzoon enters a cell, it can reproduce and cause the cubicle to burst, releasing more viral particles. During replication, the mda/IL-24 gene is also reproduced and then expressed, delivering huge quantities of active mda/IL-24 locally and systemically.</p>
<p>Definitely, the researchers worked doused a plan to ensure that the loaded virus would only replicate within cancer cells. They manipulated the viral genome again, and substituted its healthy promoter (E1A) with a promoter (PEG-3) that they discovered could no greater than be activated by transcription factors found in cancer cells. That means that if the virus may participate in a normal cell, it won&#8217;t replicate and the cubicle resolve not die, the researchers about. It also suggests that the therapy will go well in a genre of cancers &#8220;because virtually all cancers we drink tested contain the needed transcription factors that galvanize the PEG-3 promoter,&#8221; Fisher said.</p>
<p>When the viral gene therapy was injected into tumors growing in the mice, the virus replicated and produced mda-7/IL-24, which then killed the tumors, releasing millions of newly produced, prejudicial viral particles from the beginning to the end of the blood circulation to settle into distant tumors where the process was repeated. It also worked on prostate cancer unmanageable to other cure because the two-pronged attack &#8220;overwhelmed their defense mechanisms,&#8221; Sarker said.</p>
<p>Although Sarkar and Fisher speak the results are exciting, they stress that additional research is needed preceding to testing the therapy in humans, including experiment in mice with an intact immune system. While a inform immune methodology return against the virus may eliminate some of the loaded particles, the researchers say that the mda-7/IL-24 when one pleases odds-on amplify a secondary therapeutic unaffected response, offering a much stronger cancer-killing potential.</p>
<p> AZD2171, a pan-VEGF receptor tyrosine kinase inhibitor, normalizes tumor vasculature and alleviates edema in glioblastoma patients: Abstract 2118 </p>
<p>A development II clinical trial of an angiogenesis inhibitor to treat glioblastoma has shown betoken in a majority of patients tested, say researchers at Massachusetts Popular Hospital and Harvard Medical School. But they also say that the novel imaging and biomarker studies they performed as treatment was underway have revealed why the treatment, AZD2171, in the end failed, and what authority increase the answer.</p>
<p>The imaging studies, which used expressly adapted Magnetic Resonance Imaging (MRI) scans, exposed a &#8220;window&#8221; during which the blood technique feeding the tumor reverted to a more normal nation, previously morphing again into the leaky, dilated vessels that perceive sedative treatment difficult.</p>
<p>The blood biomarker studies showed that as tumors stopped relying on vascular endothelial growth factors (VEGF) to pump up blood flow to them -and VEGF is what AZD2171 targets-they started using two other growth factors, neither of which had previously been recognized as important for woman tumor blood vessel growth.</p>
<p>The study is unique because it is the win initially to test AZD2171 in glioblastoma patients, and to turn up that it &#8220;offered rosy benefits such as tumor shrinkage and reduction of wit protrusion,&#8221; said Tracy Batchelor, M.D., chief of neuro-oncology at Massachusetts Universal Convalescent home.</p>
<p>Of 31 patients who participated, more than half master tumor shrinkage of 50 percent or more, and median one of these days to tumor regrowth was 111 days. &#8220;This was not a randomized swat, but compared to real benchmarks, in which response to standard therapies is approximately 10 percent and progression is usually 63 days, these results are encouraging,&#8221; Dr. Batchelor said.</p>
<p>The agent, which has been tested in other tumor types but is not even so approved, also reduced edema, or swelling, in the knowledge, he said. Because of that, some patients were able to termination using steroids, which can well-spring debilitating side effects.</p>
<p>The clinical trial also provided insights into how AZD2171 functions and how the remedial programme might be improved, the researchers say. MRI scans charmed before, during, and after treatment provided a timeline depiction of AZD2171&#8217;s effectiveness, and then loss of concern as tumors began to resist the intermediary.</p>
<p>&#8220;This was bonny,&#8221; said Rakesh Jain, Ph.D., professor of tumor biology at Harvard Medical School. &#8220;We were gifted to see changes within 24 hours of bewitching a single administer.&#8221;</p>
<p>Jain and his colleagues suffer with gone years documenting how developing cancers promote blood proliferation factor signaling, which causes blood vessel architecture to go truly awry: vessels loop back on each other, send blood in the wrong direction, and enhance enlarged as positively as leaky due to holes that emerge. They have found regions in solid tumors in which blood flows briskly, and others in which there is petite or not anyone. &#8220;If we try to deliver drugs to those latter areas, they do not arrive,&#8221; Jain said.</p>
<p>Still, cancer cells are alive in those hypoxic regions, and, in low-down, they morph into much more martial cells, he said. It is also in these areas where cancer come cells might hide. &#8220;Buried deep in this cold environment are the cells responsible for raid and metastasis,&#8221; Jain said.</p>
<p>The blood biomarker studies allowed them to track what was incident in the tumors. The researchers discovered that as expression of VEGF proteins decreased, levels of two other proteins increased as the tumor switched to other pathways. At one of these proteins, fibroblast growth consideration (FGF), was thought to be interested in angiogenesis, but the other, chemokine stroma-room-derived factor 1 alpha (SDF1 alpha), was a novel conception, Jain said. &#8220;We threw a ultimate up with the biomarker studies and found the involvement of FGF, which had never been documented in patients, and SDF1 alpha, which was not known to be one of dissimilar dozen pro-angiogenic molecules identified so besotted in such studies.&#8221;</p>
<p>&#8220;We all detect that what we basic to do now is incorporate this therapy with other types of treatments, either existing or to be developed, and to express these drug combinations during the window we eat identified,&#8221; Dr. Batchelor said. &#8220;This might help us manage patients much more effectively.&#8221;</p>
<p>Delta Tetrahydrocannabinol inhibits intumescence and metastasis of lung cancer: Non-representational 4749 </p>
<p>The vigorous ingredient in marijuana cuts tumor development in common lung cancer in half and significantly reduces the ability of the cancer to spread, say researchers at Harvard University who tested the chemical in both lab and mouse studies.</p>
<p>They say this is the premier set of experiments to exhibit that the merging, Delta-tetrahydrocannabinol (THC), inhibits EGF-induced nurturing and migration in epidermal growth factor receptor (EGFR) expressing non-small chamber lung cancer cell lines. Lung cancers that throughout-express EGFR are usually highly aggressive and resistant to chemotherapy.</p>
<p>THC that targets cannabinoid receptors CB1 and CB2 is equivalent in function to endocannabinoids, which are cannabinoids that are naturally produced in the body and activate these receptors. The researchers suggest that THC or other plotter agents that stimulate these receptors might be used in a targeted fashion to treat lung cancer.</p>
<p>&#8220;The beauty of this study is that we are showing that a resources of abuse, if used prudently, may furnish a new road to analysis against lung cancer,&#8221; said Anju Preet, Ph.D., a researcher in the Division of Experimental Pharmaceutical.</p>
<p>Acting auspices of cannabinoid receptors CB1 and CB2, endocannabinoids (as well as THC) are vision to play a capacity in variety of biological functions, including pest and solicitude mastery, and inflammation. Although a medical derivative of THC, known as Marinol, has been approved for deplete as an zest urge over the extent of cancer patients, and a small hundred of U.S. states allow squander of medical marijuana to treat the same side effect, few studies possess shown that THC sway prepare anti-tumor activity, Preet says. The only clinical trial testing THC as a treatment against cancer growth was a recently completed British pilot study in sympathetic glioblastoma.</p>
<p>In the dole out inquiry, the researchers first demonstrated that two different lung cancer room lines as well as patient lung tumor samples express CB1 and CB2, and that non-toxic doses of THC reserved growth and spread in the apartment lines. &#8220;When the cells are pretreated with THC, they have less EGFR stimulated attack as measured by various in-vitro assays,&#8221; Preet said.</p>
<p>Then, for three weeks, researchers injected rod doses of THC into mice that had been implanted with somebody lung cancer cells, and found that tumors were reduced in gauge and weight by all round 50 percent in treated animals compared to a hold sway over group. There was also nearby a 60 percent reduction in cancer lesions on the lungs in these mice as well as a significant reduction in protein markers associated with cancer progression, Preet says.</p>
<p>Although the researchers do not know why THC inhibits tumor excrescence, they whisper the substance could be activating molecules that catch the room cycle. They speculate that THC may also interfere with angiogenesis and vascularization, which promotes cancer expansion.</p>
<p>Preet says much work is needed to illuminate the pathway by which THC functions, and cautions that some animal studies have shown that THC can stimulate some cancers. &#8220;THC offers some promise, but we attired in b be committed to a long way to go beforehand we know what its potential is,&#8221; she said.</p>
<p>Targeted release of oncolytic measles virus by blood outgrowth endothelial cells in situ inhibits orthotopic gliomas: Non-representational 4185 </p>
<p>Researchers in Germany have hidden vaccine-grade measles virus inside artificially generated blood cells in require to bestow a search-and-bring therapy for human percipience cancer that can&#8217;t be &#8220;seen&#8221; by the safe system.</p>
<p>They say their mouse experiments may be seen a tough of code that this non-pathogenic virus can attack glioma by getting within tumor cells and replicating, destroying the cliched brain tumors from the inside out. This and other so-called &#8220;oncolytic&#8221; viruses are already being tested in clinical trials, but their effectiveness has been limited by an unthinking child immune response, the researchers say.</p>
<p>&#8220;In an vaccinated-competent long-suffering, the immune system will bout the virus, and most adults are immune against measles since they have been vaccinated against the disease in puberty or have had measles,&#8221; said Christian Beltinger, M.D., an associate professor at the University Children&#8217;s Hospital in Ulm. &#8220;Although cancer patients are immune-compromised by their affliction or because of therapy, they still may mount a enough attack against vaccine measles virus.&#8221;</p>
<p>To trick this immune surveillance, the researchers generated blood outgrowth endothelial cells (BOECs), which are produced outside of the body using human blood bathed in a cocktail of growth factors. &#8220;They do not naturally suggest itself to in the blood, but they are derived from endothelial precursor cells, rare cells that are produced in the bone marrow and doff into the blood,&#8221; Dr. Beltinger said.</p>
<p>These cells are in good shape suited for cancer therapy to two reasons, he said. If a vaccine measles virus is tucked within them, it can&#8217;t be reached by the immune system&#8217;s neutralizing antibodies. Also, they are endothelial forerunner cells, which are recruited in the body wherever late-model blood vessels are formed.</p>
<p>&#8220;Tumors need vessels to thicken, hence they enrol these blood progenitor cells,&#8221; Dr. Beltinger said. &#8220;That makes them home to the tumors.&#8221;</p>
<p>BOECs have been inured to for other gene therapeutic approaches, such as for hemophilia, but this is the original moment they have been adapted to delight a win vaccine measles virus, he said.</p>
<p>To test how well they functioned as a cancer group therapy, the researchers injected U87 cells (the most commonly used human glioma cancer cell line) into the brains of immune-compromised mice. Sporadically the tumors were established, BOECs recently infected with vaccine measles virus were injected thither, but not into, the knowledge tumor. These loaded blood cells navigated past common brain tissue to the tumor mass, and in one go inside, the BOECs released the virus into surrounding tumor cells. It then spread to other tumor cells.</p>
<p>Eventually the blood cells died. This set back of death, however, was adequate to add the infected cells to expert in to the tumor and release the virus, the researchers bruit about.</p>
<p>They ground that mice treated with BOECs survived significantly longer than mice receiving due unused blood cells or &#8220;naked&#8221; measles virus. But the researchers say that all mice in the final analysis died, showing that the therapy could not entirely eradicate the tumors.</p>
<p>&#8220;While these modified blood cells carrying vaccine measles virus look like a promising novel therapy for gliomas, it is still a preclinical hypothetical approach,&#8221; Dr. Beltinger said. &#8220;Potentially it could be inured to on most malignant gliomas, including glioblastomas, because the targeting of the virus can be genetically modified.&#8221;</p>
<p>&#8212;&#8212;&#8212;&#8212;&#8212;&#8212;&#8212;&#8212;&#8212;-<br />Article adapted by Medical News Today from queer fish press release.<br />&#8212;&#8212;&#8212;&#8212;&#8212;&#8212;&#8212;&#8212;&#8212;-</p>
<p>The business of the American League for Cancer Research is to check and restore to health cancer. Founded in 1907, AACR is the world&#8217;s oldest and largest able organization dedicated to advancing cancer investigation. The membership includes more than 25,000 basic, translational, and clinical researchers; health care professionals; and cancer survivors and advocates in the United States and more than 70 other countries. AACR marshals the robust spectrum of expertise from the cancer community to accelerate promotion in the mitigation, diagnosis and treatment of cancer through high-calibre well-ordered and educational programs. It funds innovative, honourable into grants. The AACR Annual Meeting attracts once again 17,000 participants who share the latest discoveries and developments in the field. Extra Conferences throughout the year hand-out narrative data across a wide variety of topics in cancer research, diagnosis and treatment. AACR publishes five worst peer-reviewed journals: Cancer Research; Clinical Cancer Research; Molecular Cancer Therapeutics; Molecular Cancer Research; and Cancer Epidemiology, Biomarkers &amp; Blocking. Its most recent publication, CR, is a magazine someone is concerned cancer survivors, acquiescent advocates, their families, physicians, and scientists. It provides a forum benefit of sharing essential, support-based information and perspectives on progress in cancer scrutiny, survivorship and advocacy.</p>
<p>Contact: Staci Vernick Goldberg<br />
<br />
American Association for the purpose Cancer Research</p>
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		<title>Reaction To Expansion Of Wal-Mart Generic Prescription Drug Discount Program Mixed</title>
		<link>http://alliesowned.anthonyjansen.com/2010/03/14/reaction-to-expansion-of-wal-mart-generic-prescription-drug-discount-program-mixed/</link>
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		<pubDate>Sun, 14 Mar 2010 21:03:12 +0000</pubDate>
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		<description><![CDATA[The expansion of a Wal-Mart Stores generic preparation drug discount program to 12 additional states on Thursday &#8220;will likely provide honorarium relief quest of the uninsured, a quick undulate in sales and matching deals from other large retailers&#8221; in those areas, the Baltimore Sun reports (Salganik, Baltimore Bronze knick-knacks, 10/27).  Wal-Mart last month announced [...]]]></description>
			<content:encoded><![CDATA[<p>The expansion of a Wal-Mart Stores generic preparation drug discount program to 12 additional states on Thursday &#8220;will likely provide honorarium relief quest of the uninsured, a quick undulate in sales and matching deals from other large retailers&#8221; in those areas, the Baltimore Sun reports (Salganik, Baltimore Bronze knick-knacks, 10/27).  Wal-Mart last month announced that the program &#8212; under which some company pharmacies would sell 30-day prescriptions of indisputable generic medications for the benefit of $4 &#8212; would initially include 65 Wal-Mart, Sam&#8217;s Club and Neighborhood Market pharmacies in the Tampa, Fla., square and would expand statewide in early 2007 and possibly to other states in the future.  This month, Wal-Mart has expanded the program statewide in Florida and to 26 additional states (Kaiser Daily Healthfulness Policy Report, 10/26).  According to Wal-Mart, the program, which includes 143 different generic medications in a total of 314 dosages, represents not quite one-fourth of all prescriptions sold in pharmacies nationwide.  However, a rota of the 20 most commonly prescribed medications prepared by IMS Robustness includes only two of the generic treatments offered through the program (Feldstein, St. Louis Post-Dispatch, 10/27).  CMS spokesperson Julie Bookhart said that the program is &#8220;good statement since seniors&#8221; and &#8220;shows that struggle is a good thing&#8221; (Karash, Kansas See Name, 10/27).  Officials for the American Pharmacists Intimacy said that the gathering supports more affordable medications but cautioned patients to consult their physicians in front they switch to generic treatments included in the program.  Kristina Lunner, acting vice president of regulation and communications for the purpose APA, said that the program &#8220;starts to send a message that drugs are by the skin of one&#8217;s teeth another commodity,&#8221; adding that they are &#8220;very different&#8221; (Mui/Wiggins, Washington List inform, 10/27).  Charlie Sewell, senior degradation president of guidance affairs for the sake of the National Community Pharmacists Association, said that Wal-Mart is &#8220;misleading patients into thinking they&#8217;re wealthy to imply cheap drugs&#8221; (St. Louis Delivery-Rapidity, 10/27).  </p>
<p>&#8220;Reprinted with permission from http://www.kaisernetwork.org. You can view the entire Kaiser Daily Trim Way Description, search the archives, or sign up for email childbirth at http://www.kaisernetwork.org/dailyreports/healthpolicy. The Kaiser Habitually Health Policy Report is published for kaisernetwork.org, a free service of The Henry J. Kaiser Family Foundation . &copy; 2005 Warning Directors South African private limited company and Kaiser Family Foundation. All rights reserved.</p>
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		<title>Scientists enticed back to Australia to tackle major health challenges</title>
		<link>http://alliesowned.anthonyjansen.com/2010/03/11/scientists-enticed-back-to-australia-to-tackle-major-health-challenges/</link>
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		<pubDate>Fri, 12 Mar 2010 00:23:19 +0000</pubDate>
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		<description><![CDATA[CSIRO and the Queensland Government are attracting leading abroad-based Australian scientists to return to work on foremost health challenges at the e-health Research Mid-point in Brisbane.
Gary Morgan, CEO of the Centre, today announced the appointment of two more distinguished Australian scientists, Dr David Hansen, a leader in the fast growing field of bioinformatics which deals [...]]]></description>
			<content:encoded><![CDATA[<p>CSIRO and the Queensland Government are attracting leading abroad-based Australian scientists to return to work on foremost health challenges at the e-health Research Mid-point in Brisbane.<br />
<P>Gary Morgan, CEO of the Centre, today announced the appointment of two more distinguished Australian scientists, Dr David Hansen, a leader in the fast growing field of bioinformatics which deals with the management and analysis of vast biological data collections, and Dr Craig Kennedy, an expert in the implementation of e-health technologies.</P><br />
<P>&#8220;The e-Health Centre&#8217;s research is about applying information and communication technologies (ICT) to national health challenges,&#8221; says Mr Morgan.</P><br />
<P>&#8220;We&#8217;ve been very successful at attracting some fantastically talented people to the Centre. We have also successfully bid to host the prestigious international Medical Image Computing and Computer-Assisted Intervention (MICCAI) conference in 2007,&#8221; says Mr Morgan.</P><br />
<P>&#8220;This international conference on medical image computing, computer-assisted intervention and medical robotics will bring many of the world&#8217;s leading clinicians, computer scientists and other researchers to Brisbane.&#8221;</P><br />
<P>Queensland Minister for State Development and Innovation, Tony McGrady welcomed the appointments and the successful bid to host the MICCAI conference.</P><br />
<P>&#8220;I&#8217;m delighted at the e-Health Research Centre&#8217;s success in attracting these two talented researchers home to Queensland,&#8221; Mr McGrady said.</P><br />
<P>&#8220;This is proof once again that the Queensland Government&#8217;s Smart State Strategy is working. Queensland is quickly becoming a location of choice for people wanting both scientific careers and great lifestyle opportunities.</P><br />
<P>&#8220;It&#8217;s particularly timely that these appointments are being announced this week, with thousands of researchers descending on Brisbane for AusBiotech 2004 this week.&#8221;</P><br />
<P>The Minister said AusBiotech is Australia&#8217;s largest biotechnology business meeting and would feature a key session on bioinformatics, a main focus of Dr Hansen&#8217;s research.</P><br />
<P>Dr David Hansen was educated at the University of Queensland and the Australian National University, and has returned from the UK where he was head of development at LION bioscience. David led research and development of the company&#8217;s genomic data integration tools.</P><br />
<P>David will lead Health Data Integration research at the e Health Research Centre, which will focus on making health data more available for research while preserving patient privacy. Initially this will involve working with Queensland Health to integrate patient cancer data and provide more information on treatment to clinicians and researchers.</P><br />
<P>&#8220;Better access to population health data is vital for research into a host of diseases,&#8221; says Dr Hansen. &#8220;Our work at the Centre will deliver this access without compromising the equally important principles of patient confidentiality.&#8221;</P><br />
<P>Dr Craig Kennedy obtained his PhD from the University of Queensland and has been involved in the implementation of e-health technologies since 1995 when he was a manager of the Queensland Telemedicine Network, which introduced tele-psychiatry in Queensland. Most recently he has been a Senior Research Fellow at University College and Moorfields Eye Hospital, London, where he has been researching and implementing e-health technologies to support eye practitioners in Ghana, Tanzania, The Gambia, and South Africa.</P><br />
<P>&#8220;Queensland is uniquely placed to benefit from advances in telemedicine,&#8221; says Dr Kennedy. &#8220;The work we do in improving service delivery to remote communities at the e Health Research Centre will be applicable across Australia and the world.&#8221;</P><br />
<P>The e-Health Research Centre, a $15 million joint venture between CSIRO and the Queensland Government, is at the forefront of e-health innovation in Australia and globally, and will revolutionise the way Queensland&#8217;s health sector delivers services in the future.</P><br />
<P>Its world-class researchers conduct trials on e-health solutions in Queensland and undertake R&amp;D into critical health conditions such as cancer and stroke, with the aim of building knowledge on how the next generation of information and communication technologies can improve the delivery of patient centred health care.</P><br />
<P>http://www.csiro.com.au/ </P></p>
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		<title>Colorado Children Without Private Insurance Have Higher Mortality Rate</title>
		<link>http://alliesowned.anthonyjansen.com/2010/03/08/colorado-children-without-private-insurance-have-higher-mortality-rate/</link>
		<comments>http://alliesowned.anthonyjansen.com/2010/03/08/colorado-children-without-private-insurance-have-higher-mortality-rate/#comments</comments>
		<pubDate>Tue, 09 Mar 2010 04:48:22 +0000</pubDate>
		<dc:creator>alliesowned</dc:creator>
		
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		<description><![CDATA[In Colorado, uninsured children and children enrolled in Medicaid who are hospitalized at Children&#8217;s Hospital in Denver are twice as tenable as those with hermitical guarantee to die after hospitalization, according to a bone up on published in the journal Pediatrics, the Denver Callous Mountain News reports. Destined for the study, two physicians at the [...]]]></description>
			<content:encoded><![CDATA[<p>In Colorado, uninsured children and children enrolled in Medicaid who are hospitalized at Children&#8217;s Hospital in Denver are twice as tenable as those with hermitical guarantee to die after hospitalization, according to a bone up on published in the journal Pediatrics, the Denver Callous Mountain News reports. Destined for the study, two physicians at the hospital looked at hospitalization rates per 100,000 children ages six months to 18 years. The swatting finds that children enrolled in Medicaid are twice as likely as those with ungregarious insurance to be hospitalized for vaccine-preventable illnesses, complications of diabetes and asthma, and ruptured appendices (Brand, Denver Unemotional Mountain News, 8/7). Well-ordered preventive care visits by uninsured children and children enrolled in Medicaid would salvage Colorado $46 million, according to the read. The study also finds that the many of Colorado pediatricians who are willing to shepherd a see to Medicaid beneficiaries fell from 41.4% in 2000 to 23.9% in 2003. Eighty-three percent of Colorado pediatricians in 2003 said Medicaid reimbursements did not overlie the cost of office visits (Auge, Denver Post, 8/7). Stephen Berman, leading position of general pediatrics at Children&#8217;s Sickbay and co-prime mover of the con, said, &#8220;The assignment, for the first time, provides the observations that show there are huge potential savings in caring for these kids.&#8221; Berman added, &#8220;The mortality rates are higher for children on Medicaid. They are higher because they are sicker, and they didn&#8217;t get their primary care&#8221; (Denver Rocky Mountain News, 8/7).</p>
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An condensation of the study is on tap online.  </p>
<p>&#8220;Reprinted with allowance from http://www.kaisernetwork.org. You can view the express Kaiser Day after day Health Practice Record, search the archives, or sign up for email delivery at http://www.kaisernetwork.org/dailyreports/healthpolicy. The Kaiser Daily Health Scheme Report is published as a remedy for kaisernetwork.org, a free military talents of The Henry J. Kaiser Family Foundation . &copy; 2005 Admonitory Trustees Company and Kaiser Family Foundation. All rights withdrawn.</p>
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		<title>5 Physical and Mental Health Problems Men Should Know</title>
		<link>http://alliesowned.anthonyjansen.com/2010/03/07/5-physical-and-mental-health-problems-men-should-know/</link>
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		<pubDate>Sun, 07 Mar 2010 10:53:23 +0000</pubDate>
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		<description><![CDATA[Every gentleman&#8217;s gentleman, in order to ensure their tangible and mental trim, should separate more about the &#8220;invisible killer&#8221; around them, which should be of sufficient importance to every man!
  1. Tension     
  A 10-year study Of the 4,000 people of various occupations by has confirmed, heart disease, is [...]]]></description>
			<content:encoded><![CDATA[<p>Every gentleman&#8217;s gentleman, in order to ensure their tangible and mental trim, should separate more about the &#8220;invisible killer&#8221; around them, which should be of sufficient importance to every man!
<p>  1. Tension     </p>
<p>  A 10-year study Of the 4,000 people of various occupations by has confirmed, heart disease, is mainly from emotional tension. Experts believe that: &#8220;When a person living in the tension in the day, the more susceptible to hypertension.&#8221; There are mainly two kind of tension: the environmental and psychological. The development of good interpersonal relationships, you can eliminate the unnecessary worries. To deal with the psychological tension is the wisdom of thinking and bio-feedback.    </p>
<p>  2. Smoking     </p>
<p>  Long-term smokers, the incidence of lung cancer is 10 times -20 times higher than non-smokers, the incidence of laryngeal cancer is 6 times -10 times and the incidence of coronary heart is disease -3 times 2 times. Smoking can damage sperm deformity and its DNA, which will cause premature birth and birth defects. Some studies found that The children of a smoking men have a higher risk of cancer. Smoking also reduces sperm and reduce the inflow of blood to the penis, which will lead to impotence. The issue of low fertility are more common among smokers.    </p>
<p>  3. Alcohol     </p>
<p>  Alcohol will injure liver. Human liver is the most important organ of detoxification, but also synthesis of bile, the glycogen storage element, excessive alcohol is bound to lead to fat digestion and absorption of liver dysfunction and decreased immune function, so that the body resistance of various diseases will reduce. Alcohol can damage the brain, memory, intelligence and judgment will significantly reduce. Frequent drunkenness can lead to vascular spasm, respiratory muscle paralysis. Long-term alcohol abuse will result in myocardial injury in cardiac function and fat, induced hypertension, coronary heart disease. Medical research has shown that: a lot of alcohol has a fatal &#8220;blow&#8221; and injuries on sperm and the fetus.    </p>
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<p>  4. Stay up all night     </p>
<p>  Stay up all night will significantly reduce sleep time, have no time to rest the brain and organs. This will lead to serious health hazards. Sleep is the the most important approach to rest body. Scientists suggested that the long-term lack of sleep will cause weakened sense, slow thinking, coordination dysfunction, risk of accidents, and personal injury. Long-term lack of sleep, will bring you direct physical damage, cause loss of appetite, dyspepsia, decrease immune function, trigger or aggravate insomnia, neurosis, ulcer disease, hypertension, diabetes, cerebrovascular disease and so on. Therefore, the long-term lack of sleep, Have not only a lack of sleep, but also can cause a variety of important problems. To sum up, nightlife or night work, should be in moderation, often stay up all night, is bound to have adverse health consequences.
 </p>
<p>  5. Excessive or lack of exercise     </p>
<p>  Appropriate degree of movement as a unanimous recommendation of many doctors. Some people just after 50 start to do exercise, it will cause some problems if have not appropriate amount of exercise. Experts suggest that the best dual-sport is to wear outdoor shoes to walk for half an hour, it will be able to strengthen your muscles, make your heart speed up and make your breathing smooth. Of course, if lack of appropriate exercise, it will also cause a lot of diseases such as chronic diseases, shortness of breath, obesity, dyspepsia, headache, back pain, anxiety, muscle weakness and atrophy, and accelerate the aging.    </p>
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		<title>Low Testosterone May Cause Health Problems That Lead To Erectile Dysfunction</title>
		<link>http://alliesowned.anthonyjansen.com/2010/03/04/low-testosterone-may-cause-health-problems-that-lead-to-erectile-dysfunction/</link>
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		<pubDate>Fri, 05 Mar 2010 04:53:23 +0000</pubDate>
		<dc:creator>alliesowned</dc:creator>
		
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		<description><![CDATA[Men with erectile dysfunction should be examined for testosterone deficiency and the metabolic syndrome, because these conditions commonly occur together, a new enquiry shows. The results will be presented at The Endocrine Society&#8217;s 90th Annual Meeting in San Francisco.
&#8220;Erectile dysfunction is a portal into men&#8217;s health,&#8221; said the study&#8217;s senior novelist, Aksam Yassin, MD, PhD, [...]]]></description>
			<content:encoded><![CDATA[<p>Men with erectile dysfunction should be examined for testosterone deficiency and the metabolic syndrome, because these conditions commonly occur together, a new enquiry shows. The results will be presented at The Endocrine Society&#8217;s 90th Annual Meeting in San Francisco.</p>
<p>&#8220;Erectile dysfunction is a portal into men&#8217;s health,&#8221; said the study&#8217;s senior novelist, Aksam Yassin, MD, PhD, of the Clinic for Urology and Andrology of the Segeberger Clinics in Norderstedt, Germany. &#8220;It is fashionable clear that obesity, diabetes, high blood on, cholesterol problems and erectile difficulties are intertwined, and a common denominator is testosterone deficiency.&#8221;</p>
<p>Yassin&#8217;s research, performed with scientists from The Netherlands, Germany and the Combined Arab Emirates, aimed to condition in men with erectile dysfunction (ED) the prevalence of hypogonadism, the meticulous term after testosterone deficiency.</p>
<p>Over and above a two-year time the investigators studied 771 patients who sought treatment for ED. Their undistinguished age was 56. The patients received a comprehensive screening for low testosterone and indicators of the metabolic syndrome, a cluster of jeopardize factors that spread the chances of developing heart and vascular disease and type 2 diabetes. Having three of the following five risk factors establishes the diagnosis of this syndrome: increased waist circumference (abdominal fat), coarse HDL (&#8221;good&#8221;) cholesterol, high triglycerides (fats in the blood), altered consciousness blood pressure, and intoxication blood sugar.</p>
<p>Among the 771 men, 18.3 percent of the men (141 men) had testosterone deficiency, which had once been undetected, the authors found. The prevalence of hypogonadism in the general population of men age 45 and older is alongside 12 percent, Yassin said.</p>
<p>Of all the men in the study, 270 (35 percent) had type 1 or pattern 2 diabetes; in eight of the men, diabetes was a new diagnosis, according to think over statistics. High blood adversity was develop in 239 men (31 percent), and 12 of these men had been incognizant of it. Among the 162 men (21 percent) who had dyslipidemia perverse cholesterol or triglycerides nine of them had not previously been diagnosed. And 108 men, or 14 percent, had varying degrees of coronary heart disease. Five of them received this diagnosis since the from the start leisure, Yassin said.</p>
<p>Men with ED especially older men should thus give entree ranking not only for ED but also for testosterone deficiency and any underlying signs of the metabolic syndrome, he advised.</p>
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<p>
Yassin disclosed that he is on the speakers&#8217; bureau for Bayer Schering, which makes a make of testosterone.</p>
<p>Founded in 1916, The Endocrine Society is the world&#8217;s oldest, largest, and most active organization devoted to research on hormones, and the clinical practice of endocrinology. Today, The Endocrine Society&#8217;s membership consists of through 14,000 scientists, physicians, educators, nurses and students in more than 80 countries. Together, these members represent all basic, applied, and clinical interests in endocrinology. The Endocrine Society is based in Chevy Court, Maryland. To learn more about the Society, and the field of endocrinology, visit our trap position at http://www.endo-society.org.</p>
<p>Endocrine Companionship<br />
8401 Connecticut Ave., Ste 900<br />
Chevy Woo, MD 20815<br />
In agreement States<br />
http://www.endo-society.org</p>
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		<title>Physicians Hail Arkansas Court Victory Against Baptist Health - Patient-physician Relationship Entitled To &#8220;exceptional Protections&#8221;</title>
		<link>http://alliesowned.anthonyjansen.com/2010/03/02/physicians-hail-arkansas-court-victory-against-baptist-health-patient-physician-relationship-entitled-to-exceptional-protections/</link>
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		<pubDate>Tue, 02 Mar 2010 07:28:38 +0000</pubDate>
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		<description><![CDATA[LITTLE ROCK, Ark., USA - In a rightful victory that preserves the patient-physician relationship and promotes struggle, an Arkansas state of affairs court ruled today that Baptist Fettle, Arkansas&#8217; largest hospital system, acted improperly by inappropriately restricting hospital admitting privileges and interfering with the continuity of self-possessed attend to. 
The ruling in Baptist v. Murphy [...]]]></description>
			<content:encoded><![CDATA[<p>LITTLE ROCK, Ark., USA - In a rightful victory that preserves the patient-physician relationship and promotes struggle, an Arkansas state of affairs court ruled today that Baptist Fettle, Arkansas&#8217; largest hospital system, acted improperly by inappropriately restricting hospital admitting privileges and interfering with the continuity of self-possessed attend to. </p>
<p>The ruling in Baptist v. Murphy permanently prohibits an profitable credentialing game plan adopted by Baptist Health in 2003, which would have allowed the hospital approach to interfere in the patient-physician relationship by denying hospital-admitting privileges to medical staff members based on financial concerns. </p>
<p>As the court observed, &#8220;The affection of this proves is the submissive-physician relationship. The relationship is entitled to unusual protection.&#8221; The court went on to say, &#8220;Strong patient-physician relationships are the underpinning of good medicine, and it was uncontroverted at trial that patients who be dressed protracted term relationships with their doctors induce better outcomes.&#8221; </p>
<p>The American Medical Federation (AMA) and the Arkansas Medical Society (AMS) successfully challenged the unfair hospital policy by arguing that the ranking backer in credentialing physicians should be competency, not solvent factors unrelated to quality. </p>
<p>&#8220;Hospital admitting privileges have want been considered an indispensable component of a medical practice,&#8221; said Rebecca Patchin, M.D., chair-elect of the AMA Lodge. &#8220;Baptist Health took advantage of this fact to coerce physicians and squash competition from other medical facilities.&#8221; </p>
<p>&#8220;Patients benefit when their physicians have staff privileges at multiple facilities, because the patient has a choice of facilities to chosen from that best suits their needs in terms of costs, quality and convenience,&#8221; said AMS President David Jacks, M.D.  </p>
<p>&#8220;This important court victory demonstrates that commercial policies that restrict physician credentialing are really intended to prevent patients from choosing medical facilities that might compete with large hospitals,&#8221; said Dr. Patchin. &#8220;Hospitals cannot end their economic interest to warrant policies that interfere with patients&#8217; health care choices.&#8221; </p>
<p>&#8220;Hospitals must apply oneself to the monetary realities of the health care environment toe novelty and fair competition, rather than relying on unfair policies that restrict patient appropriate and spike the continuity of care,&#8221; said Dr. Jacks. </p>
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<p>The combined resources of organized medicine were brought to bear on this case through the Legal remedy Center of the AMA and State Medical Societies, which provided substantial fiscal support and, along with the Arkansas Medical Society, worked in encouragement of the physicians who were subjected to Baptists&#8217; inappropriate credentialing policies. </p>
<p>&#8220;This case shows besides again that when doctors gather the help of organized drug, the best outcome in the interest of patients and doctors can be achieved,&#8221; said Dr. Patchin. </p>
<p>A ape of the court&#8217;s decision is available here.</p>
<p>American Medical Association<br />
515 North Body politic St. <br />
Chicago, IL 60610<br />
United States<br />
http://www.ama-assn.org</p>
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		<title>Meeting Highlights From The Committee For Medicinal Products For Human Use, 16-18 October 2006</title>
		<link>http://alliesowned.anthonyjansen.com/2010/02/27/meeting-highlights-from-the-committee-for-medicinal-products-for-human-use-16-18-october-2006/</link>
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		<pubDate>Sat, 27 Feb 2010 17:23:41 +0000</pubDate>
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		<description><![CDATA[The Committee fit Curative Products fit Human Use (CHMP) concluded the review of non-selective non-steroidal anti-fiery drugs (NSAIDs), which was initiated during the September 2006 meeting. A statement will be issued on Tuesday 24 October at 10h00 (London time).
Prime marketing authorisation applications
The Committee gave four positive opinions on approve marketing authorisation applications, including two opinions [...]]]></description>
			<content:encoded><![CDATA[<p>The Committee fit Curative Products fit Human Use (CHMP) concluded the review of non-selective non-steroidal anti-fiery drugs (NSAIDs), which was initiated during the September 2006 meeting. A statement will be issued on Tuesday 24 October at 10h00 (London time).</p>
<p>Prime marketing authorisation applications</p>
<p>The Committee gave four positive opinions on approve marketing authorisation applications, including two opinions by reason of medicinal products that are intended for the treatment of patients suffering from rare diseases:</p>
<p>&#8211; The Body recommended the granting of a conditional marketing authorisation in the interest Diacomit (stiripentol), from Laboratoires Biocodex, appropriate for the treatment of severe myoclonic epilepsy in infants in conjunction with clobazam and valproate. Conditional marketing authorisation has been recommended on the acclimate that further evidence on the subject of efficacy of stiripentol in combination with summit safe doses of clobazam and valproate, and on the bioavailability of Diacomit sachets compared to capsules is provided at a later fake. The EMEA wish re-assess Diacomit annually to confirm that the benefit-risk balance remains peremptory. Diacomit is the 32nd orphan medicinal product to come into a positive CHMP thought. EMEA review began on 18 May 2005 with an quick review time of 201 days.</p>
<p>&#8211; The Committee recommended the granting of a marketing authorisation under exceptional circumstances for Elaprase (idursulfase), from Shire Human Genetics Therapies AB, for the long-stretch treatment of patients with Tracker syndrome (Mucopolysaccharidosis II, MPS II). Elaprase is the 33rd orphan curative by-product to receive a positive CHMP opinion. EMEA review began on 28 December 2006 with an spry review every so often old-fashioned of 207 days. Marketing authorisation high exceptional circumstances may be granted participant to certain specific obligations, to be reviewed annually. In the case of Elaprase, this relates to the fact that the indication applied in requital for is so rare that the applicant cannot reasonably be expected to provide extensive data on the shelter and efficacy of the healing product.</p>
<p>&#8211; Tandemact (pioglitazone hydrochloride/glimepiride), from Takeda Europe R &amp; D Centre Ltd, is recommended for the treatment of patients with type-2 diabetes mellitus who be conspicuous narrow-mindedness to metformine or for whom metformin is contraindicated and who are already treated with a composition of pioglitazone and glimepiride. EMEA over again began on 17 August 2005 with an <a href="http://learnedwork.starblog.com/index.php?p=96">active review</a> ease of 196 days. </p>
<p>&#8211; Adrovance (alendronic acid and colecalciferol), from Merck Calculating &amp; Dohme Ltd, is recommended for the treatment of postmenopausal osteoporosis in patients at risk of vitamin D insufficiency. Adrovance is the same medicinal product as Fosavance, also from Merck Sharp &amp; Dohme Ltd, which is already authorised in the European Togetherness. EMEA review began on 21 July 2006 with an effective reconsideration time of 89 days.</p>
<p>Lifting of conditional marketing authorisation</p>
<p>The Committee recommended to inducement the conditional marketing authorisation for Sutent (sunitinib malate), from Pfizer Ltd. Sutent was the first iatrical product to be granted a conditional marketing authorisation in the European Coherence. It is currently indicated after the treatment of unresectable and/or metastatic malignant gastrointestinal stromal tumours after failure of imatinib mesylate treatment scheduled to resisters or intolerance, and advanced and/or metastatic renal cell carcinoma (MRCC) after deterioration of interferon alfa or interleukin-2 therapy.<br />
The marketing authorisation was granted under the condition that the marketing authorisation holder would provide in addition comprehensive data on Sutent&#8217;s aftermath in terms of relevant clinical endpoints such as progression unengaged survival in patients with MRCC.</p>
<p>Following evaluation of clinical text submitted by the marketing authorisation holder, the Committee recommended a swap from the conditional marketing authorisation to a buxom marketing authorisation. It also recommended to extend the clues to blue ribbon-stripe treatment of  advanced and/or metastatic renal cell carcinoma (MRCC). </p>
<p>Extension of forewarning</p>
<p>In reckoning to the extension of indication for Sutent, the Committee gave pragmatical opinions championing applications for extensions of indication, adding up to date treatment options for the following at one time approved medicines:</p>
<p>&#8211; Aldara (imiquimod), from Laboratoires 3M Santé, received a satisfied conviction to catalogue superficial treatment of clinically typical, nonhyperkeratotic, nonhypertrophic actinic keratosis in adults. Aldara was essential granted a marketing authorisation in the European Conjunction on 18 September 1998 and is currently indicated for the up to date treatment of external genital and perianal warts and miserly superficial basal cell carcinomas in adults.</p>
<p>&#8211; Glivec (imatinib mesylate), from Novartis Europharm Ltd, received two positive opinions to subsume treatment of myelodysplastic syndromes and myeloproliferative diseases (MDS/MPD) as indeed as treatment of of age patients with hypereosinophilic syndrome and inveterate eosinophilic leukaemia (HES/CEL). Glivec was first granted a marketing authorisation in the European Union on 7 November 2001 and is currently indicated for the treatment of adult and paediatric patients with Philadelphia chromosome (bcr-abl) positive dyed in the wool myeloid leukaemia, adult patients with Philadelphia chromosome pontifical acute lymphoblastic leukaemia (Ph+ ALL), adult patients with Kit (CD 117) positive unresectable and/or metastatic malignant gastrointestinal stromal tumours (GIST) and full-grown patients with dermatofibrosarcoma protuberans (DFSP).</p>
<p>&#8211; Hycamtin (topotecan), from SmithKline Beecham Plc, received a positive opinion to include treatment, in combination with cisplatin, of patients with carcinoma of the cervix regular after radiotherapy and for patients with Stage IVB disease. Patients with until revealing to cisplatin make a incessant treatment-unbind interval to justify treatment with the combination. Hycamtin was first granted a marketing authorisation in the European Union on 12 November 1996 and is currently indicated as monotherapy for relocate-line treatment of patients with metastatic carcinoma of the ovary and patients with relapsed small-scale apartment lung cancer. </p>
<p>&#8211; Rotarix (live Good Samaritan rotavirus RIX4414), an word-of-mouth vaccine from GlaxoSmithKline Biologicals, received a sure opinion to extend the therapeutic indication to categorize stylish information that shelter against rotavirus serotypes G4P[8] and G22P[4] has also been demonstrated. Rotarix was first granted a marketing authorisation in the European Union on 21 February 2001 and indicated due to the fact that the prevention of gastro-enteritis caused by Rotavirus of types G1P[8], G3P[8] and G9P[8].</p>
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<p>
New contraindications</p>
<p>The Committee recommended adding new contraindications for four medicinal products that stifle duloxetine as <a href="http://endurebiased.dateredheadz.com/index.php?p=86">active substance</a>. With a view all four products, namely Ariclaim and Xeristar, from Boehringer Ingelheim International GmbH, and Yentreve and Cymbalta, from Eli Lilly Nederland, the Committee recommended that treatment should not be initiated in patients with uncontrolled hypertension that could expose patients to a potential risk of hypertensive crisis.<br />
In joining, as a replacement for Ariclaim and Yentreve, the Board also recommended that these two products should not be used in patients with plain renal enfeeblement. This contraindication is already included in the offshoot poop for Cymbalta and Xeristar.</p>
<p>Ariclaim and Yentreve were first granted marketing authorisations on 11 August 2004 and are currently authorised since the treatment of unexcessive to severe stress urinary incontinence in women. Cymbalta and Xeristar were word go granted marketing authorisations on 17 December 2004 and are currently authorised for the treatment of major depressive episodes and the treatment of diabetic unimportant neuropathic pain in adults.</p>
<p>Summaries of opinions, including more complicated message on the further indications or contraindications for all products mentioned above are at and can be found here www.emea.europa.eu/htms/human/opinion/opinion.htm.</p>
<p>Referral procedures concluded</p>
<p>The Committee concluded a referral procedure for Alendros 70 (alendronate sodium trihydricum), from Zentiva a.s., intended for the treatment of osteoporosis in postmenopausal women. The CHMP recommended the refusal of a marketing authorisation in the troubled Associate States and a expulsion of the marketing authorisation for Alendros 70 mg tablets in the reference Associate State because bioequivalence with the reference product (Fosamax 70 mg tablets) has not been demonstrated. The forth was initiated under Article 29 of the Community code on human medicinal products (Directive 2001/83/EC as amended) by the Czech Republic because of disagreement among the Member States in the structure of the mutual recognition procedure.</p>
<p>The Body concluded a referral procedure recommending the suspension of a generic medicinal product called Simvastatine (simvastatine), from Neo Pharma Ltd, because of non-compliance with tolerable clinical vocation (GCP) in the lead of the lucubrate utilized to demonstrate bioequivalence with the originator upshot. The procedure was initiated by the Netherlands under Article 36 of the Community unwritten law&#8217; on human therapeutic products (Directive 2001/83/EC as amended). These procedures are initiated where a Member State considers that there are public health concerns relating to a consequence that may require regulatory action in all Member States where the artifact is authorised. </p>
<p>Referral procedures started</p>
<p>The Board started referral procedures respecting two generic medicinal products included Article 29 of the Community code on woman medicinal products (Directive 2001/83/EC as amended) because of disagreement surrounded by the Member States in the structure of the mutual recognition forge ahead:</p>
<p>&#8211; The referral for Cefuroximaxetil 125 omhulde tabletten 125 mg, Cefuroximaxetil 250 omhulde tabletten 250 mg, Cefuroximaxetil 500 omhulde tabletten 500 mg, (cefuroxim (as axetil)), from Sandoz B.V., was initiated because of disagreements on whether the medicinal effect should be indicated for the treatment of uncomplicated gonorrhoea (urethritis and cervicitis).</p>
<p>&#8211; The referral for Fexofenadinhydrochlorid &#8220;Teva&#8221; 120 mg and 180 mg film-coated tablets (fexofenadine hydrochloride), from Teva UK Ltd, was initiated because of disagreements concerning bioequivalence with the originator product.</p>
<p>A more detailed CHMP meeting scrutinize purposefulness be published shortly.</p>
<p>http://www.emea.europa.eu</p>
<p>Watch numb information on Aldara; Cymbalta; Elaprase.</p>
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		<title>Modification of O&#8217;Connor&#8217;s technique for the treatment of vesico-vaginal fistula repair described</title>
		<link>http://alliesowned.anthonyjansen.com/2010/02/25/modification-of-oconnors-technique-for-the-treatment-of-vesico-vaginal-fistula-repair-described/</link>
		<comments>http://alliesowned.anthonyjansen.com/2010/02/25/modification-of-oconnors-technique-for-the-treatment-of-vesico-vaginal-fistula-repair-described/#comments</comments>
		<pubDate>Thu, 25 Feb 2010 16:18:39 +0000</pubDate>
		<dc:creator>alliesowned</dc:creator>
		
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		<guid isPermaLink="false">http://alliesowned.anthonyjansen.com/2010/02/25/modification-of-oconnors-technique-for-the-treatment-of-vesico-vaginal-fistula-repair-described/</guid>
		<description><![CDATA[Vesicovaginal fistula (VVF) is a distressing disease with common, aseptic, and psychosexual consequences.
In third world countries, obstetric etiologies prevail, while in the west, 90% of cases are caused by inadvertent bladder trauma during surgery with hysterectomy being the most common procedure (75% of cases). 
The transabdominal Oâ€™Connorâ€™s operation has been the most accepted method of [...]]]></description>
			<content:encoded><![CDATA[<p>Vesicovaginal fistula (VVF) is a distressing disease with common, aseptic, and psychosexual consequences.<br />
<P>In third world countries, obstetric etiologies prevail, while in the west, 90% of cases are caused by inadvertent bladder trauma during surgery with hysterectomy being the most common procedure (75% of cases). </P><br />
<P>The transabdominal Oâ€™Connorâ€™s operation has been the most accepted method of repair of supratrigonal fistula to date. The traditional Oâ€™Connor operation utilizes suprapubic access for extraperitoneal dissection of the retropubic space to dissect the bladder, followed by long sagittal cystotomy (bivalving the bladder) until the fistula is reached. The fistulous tract is excised, flowed by two-layer closure after tissue transposition between the bladder and vaginal walls. </P></p>
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<p>A recent review by D. Dalela and colleagues from Lucknow, India, describes a transperitoneal modification of the Oâ€™Connor procedure which decreases the amount of bladder dissection and operative time. It also is postulated to decrease the post-operative voiding dysfunction and detrussor overactivity the goes with a larger and more involved cystotomy and vesical dissection. The study is published in the March, 2006 issue of European Urology. </P><br />
<P>The modification involves a smaller, posterior cystotomy that is carried toward the edge of the fistula. The fistula tract is excised, and the bladder defect is closed by advancing the flap that is created. The closure is completed in a single, running, locking layer of monocryl suture. An omental flap is utilized in all cases where the omentum is able to reach this far. </P><br />
<P>In the series of 26 cases reported, the mean fistula size was 2.8 cm. The mean age of the patient was 21.4 years with 22 patients having obstructed labor as the cause for their fistulas. Nine patients had had a prior attempt at repair elsewhere. Mean operative time was 104 minutes and blood loss was insignificant. Three patients required ureteroneocystotomy. In 24 cases, the greater omentum was able to be mobilized to interpose between the bladder and vaginal closures. In 2 patients, a paravesical peritoneal flap was utilized. Suprapubic and urethral catheters were utilized for two weeks post-operatively. All patients had a successful repair of the fistula after 2 or 3 weeks of catheter drainage. </P><br />
<P>The paper provided some illustrations to better describe the technique which appears to be less involved than the classic description from Oâ€™Connor. One would only suppose that less bladder dissection would mean less post-operative lower urinary tract symptoms. The avoidance of the retropubic space also is an advantage as it leaves this space undisturbed for stress incontinence procedures that may be needed later in life. </P></p>
<p><P>Reference: </P><br />
<P>Eur Urol. 2006 Mar; 49(3):551-56 </P><br />
<P>http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&amp;db=pubmed&amp;dopt=Abstract&amp;list_uids=16413101&amp;query_hl=3&amp;itool=pubmed_docsum</P><br />
<P>Dalela D, Ranjan P, Sankhwar PL, Sankhwar SN, Naja V, Goel A</P><br />
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