Buttock Augmentation in Arkansas

Buttock Augmentation in Arkansas section, includes general infrmation about Buttock Augmentation Procedure, Buttock Augmentation Arkansas Local News, Buttock Augmentation Arkansas Surgeon Locator and other Buttock Augmentation related material.


Buttock Augmentation Procedure


This surgical procedure also called gluteoplasty or buttock augmentation. It is design to reshape the size of your buttocks and create more firm and aesthetic appearance. The buttock area is not easily changed by weight reduction or exercise, therefore you may consider this operation to improve the look of your buttock. In general every person who wishes to undergo the operation and is in a good physical condition can do so.

Buttock augmentation is achieved using fat. The idea is to remove fat from your one body part and inject in into your buttocks. The big advantage of this technique is the fact that there is no rejection since the tissue used is taken from your one body. In addition this method can make your buttock look very natural. The fat is usually taken from areas of the body, which have extra fat, like the flank area, the thigh and the upper and lower buttock. The extra fat, which is removed from the above areas, can further reshape the buttock making it look like you've been through a butt lift. After the fat is removed is undergoes some special processing and then injected to your buttocks using a special cannula, which has a very small diameter therefore leaves minimal scars. The big challenge of the fat grafting is to cause the graft to survive in the new place, this can be achieved by injecting small amount of fat each time into different layers, above and below the butt muscles. This way better blood supply is accomplished and irregularities of the surface is minimized. The graft survival is unpredictable, some of the fat is absorbed causing you to loose the augmentation effect. It is generally believed that what's left after 3 month usually stays forever. After the procedure the buttock area usually don't heart, the pain is generally from the incisions make in the donor area. Those incisions are also very small, the same ones used for liposuction.

Every procedure has its risks, the risks for this one is minimal. The main risk of the procedure is fat absorption, occurring in approximately one-third of the patients. Bleeding, infection and scarring are rare.

You'll be able to go back to work after 3-5 days, but you'll have to wear special garment for 3-4 weeks. It may take up to one month until you feel normal, some swelling may appear, which will usually disappear after a couple of month.

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Buttock AugmentationLatest Forum Posts...

  • Yep, butt augmentation is so in these days. I was surprised when I found out that a friend of mine, which is a GUY, had butt implants. Hehe. I just never expected that he'd turn out to be vain after all this time.

Plastic Surgery News...

  • The Southwest Oncology Group Study 9626 has examined the efficacy of megesterol acetate (MA) in treating hot flushes in women with breast cancer. It involved 288 patients (2 ineligible) with T1-3, N0-1, M0 breast cancer who had completed surgery and chemotherapy and at least 4 months of tamoxifen (if prescribed). They had to have experienced at least 10 hot flushes of any severity or at least five severe episodes per week. Overall, 85% were on tamoxifen, 40% had over 63 hot flushes per week and 75% had vasomotor symptoms for 6 months or longer. They were randomised to receive placebo (n=101), MA 20 mg (n=92), or MA 40 mg (n=93) for 3 months. Success at 3 months was defined as completion of treatment with a 75% or greater reduction in hot flushes from baseline. Another 3 months of treatment was given in the same blinded arm if success was achieved, and in those who were not classified as successfully treated, open-label MA 20 mg was added to blinded study drug and continued for 3 months. Success at 3 months was reported in: • 14% on placebo • 65% on 20 mg (p < 0.0001 vs placebo) • 48% on 40 mg (p < 0.0001 vs placebo) In addition, most successes at 3 months were maintained at 6 months (77% on 20 mg and 81% on 40 mg). There was however no significant impact on other menopausal symptoms. In physicians’ assessment of toxicity experienced by patients up to and including the 3-month evaluation, oedema and weight gain was reported in the placebo arm; fatigue in the MA20 arm; and depression, fatigue, nausea, and weight gain in the MA40 arm. There were no statistically significant differences by treatment arm for any toxicities. The researchers concluded that MA at the preferred dose of 20mg was successful in alleviating vasomotor symptoms in breast cancer survivors with durable results at 6 months. They suggest that “this treatment could be considered in women refractory to non-hormonal therapies whose symptom status is impaired by the vasomotor symptoms and who have been informed of the risk and benefit of such treatment by their physician.”
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