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Global Walk To End World Hunger
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Research: Improving Treatment Of Patients With Heart Attack
When faced with patients suffering a heart attack, doctors have two choices: inject them with medication to dissolve the blood clot (fibrinolytic therapy) or insert a small balloon to open the blocked artery (primary percutaneous coronary intervention (PCI)). Guidelines for treating heart attacks are generally based on clinical trials that do not take "real-life" conditions into account. The latest study by Dr. Thao Huynh of the Research Institute of the MUHC analyses these gaps and provides potential solutions to improve treatment of heart attack. Her article was published in the June 23rd issue of Circulation.
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New Breast Implant Designed As Alternative To Silicone Gel

At a time when breast augmentation tops the list for U.S. cosmetic surgical procedures, women are still left choosing between either the safety of saline or the natural result of silicone gel. Plastic surgeons are now looking to offer the best features of both in the revolutionary new technology of the IDEAL IMPLANT® Saline-filled Breast Implant. A clinical trial is launching this month in select markets nationwide, giving some women the opportunity to be among the first to have this new implant. The first major new breast implant technology in over 20 years, the IDEAL IMPLANT is designed to offer the natural result of silicone gel, but with only saline inside to give peace of mind. Its novel yet simple design was developed by a noted plastic surgeon expert and consists of a series of implant shells of increasing size nested together. The internal perforated shells control saline movement to reduce "sloshing and bouncing." The IDEAL IMPLANT is also engineered to conform to the chest wall with the edge low, to minimize the unattractive wrinkling on the sides often associated with standard saline implants. Despite recent FDA approval of silicone gel implants, standard saline implants represent about 60 percent of all breast augmentations, reflecting women"s desire for the benefits and safety of saline. The IDEAL IMPLANT looks to provide natural results similar to silicone gel implants, but without the safety concerns, such as difficulty detecting silent ruptures requiring MRI scans, diffusion of small silicone compounds into the tissues, and possible long-term side effects. "With advances in healthcare technology and an awakening of environmental consciousness, Americans are more aware of what we put into our bodies than ever before - we eat organic food, avoid pesticides, and scrutinize labels," explains Dr. Robert S. Hamas, M.D., the plastic surgeon inventor of the IDEAL IMPLANT. "Women seeking breast augmentation are increasingly informed about the potential risks and benefits. I designed the IDEAL IMPLANT to meet the needs of today"s women, who want a natural result but prefer the safety of saline." The selected plastic surgeons in Atlanta, Dallas, Houston, Southeast Florida (Miami and Fort Lauderdale area), and Southern California (Los Angeles and Orange County area), will enroll a total of 500 women in the clinical trial, set to provide the FDA with the data needed to establish the safety and effectiveness of the IDEAL IMPLANT. The trial is open to healthy women who are undergoing a first breast augmentation or the replacement of their existing augmentation implants. Women interested in the IDEAL IMPLANT are encouraged to make a consultation appointment with one of the plastic surgeon investigators to get acquainted and learn about both the benefits and risks of breast augmentation. Ideal Implant Incorporated is offering a unique follow-up incentive plan to patients who complete all required follow-up visits for the trial. For a full list of participating surgeons and contact information, please see the "To Enroll" section of the Web site at http://www.idealimplant.com. Ideal Implant Incorporated


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