The last 20 years have offered the slimming market a number of different scientific procedures for combating obesity – gastric bypass and band included. Yet despite the 2006 directive which required all Centers to have experienced staff and equipment, these types of weight loss surgeries are still life threatening.
Even following recent modifcations wherecomplication rates have fallen from 12.2% of patients to 10%, and the 30 day mortality rate has shrunk from 0.28% to 0.20% – these improvements are not enough when you factor in the thousands of individuals who undergo these procedures every single year…
Yet, hope could be on the horizon for obese patients if the ReShape’s double balloon meets the approval of the Food and Drug Administration.
Designed to help slimmer’s who are just below or above eligibility guidelines for gastric bypass and laparoscopic gastric band placements surgeries, or who are too young for such critical surgeries; the double-balloon mechanism could easily cater for this excluded niche.
How does it work?
As it stands, the dual action balloon mechanism is inserted into a slimmer’s throat using thin tubing before being filled with saline. As these 2 balloons are filled, slimmer’s will start tofeel full and will begin to lose weight.
And, once patients attain their weight loss goal, this double balloon system can easily by deflated and removed from the stomach without risk.
As we speak, this dual action balloon is meant to complete its first clinical studyat the start of April where 30 volunteers across three cosmetic centers will be inserted with this device. Should it be found to be safe, this study will be extended to 350 volunteers across ten medical centers and eventually will be shown to the Food and Drug Administration for permission to be used.
Is it dangerous?
It is undisputable that this double balloon mechanism could essentially help hundreds of slimmers who are either under 18 or suffer from diabetes, heart disease and muscle problems to lose those excess lbs, however this double balloon system has got far to travelbefore it is recommended.
Back in 1984 a similar single balloon system was created by Garren-Edwards and was implanted into patients. However, with no backup membrane to protect it, this device was prone to bursting and entering into the small intestine where it caused serious blockages. Consequently, this device was quickly removed from the market.
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