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Plastic Surgeon Dr. Michele Koo’s Blog | St. Louis | Kansas City 2009 July

Archive for July, 2009

LATISSE FOR LONG SEXY NATURAL EYELASHES - DR MICHELE KOO - MISSOURI - ILLINOIS - KANSAS

Saturday, July 18th, 2009

DR MICHELE KOO, MD, BOARD CERTIFIED PLASTIC SURGEON, ST LOUIS, MO has the latest newest skin products and procedures for skin care and eye lash growth.

Get ready for an innovation in eye lashes.LATISSE® (bimatoprost ophthalmic solution) 0.03% is the first and only prescription treatment approved by the FDA for inadequate or not having enough eyelashes, growing them longer, fuller and darker.

LATISSE® works effectively.LATISSE® makes lash growth possible because of its active ingredient: bimatoprost. Although the precise mechanism of action is not known, research suggests that the growth of eyelashes occurs by increasing the percent of hairs in, and the duration of, the anagen (or growth) phase. Lashes can grow longer, thicker and darker because bimatoprost can also prolong this growth phase.

Clinically proven results you can see over time.

LATISSE® is FDA approved and effective. It’s a once-a-day treatment you apply topically to the base of your upper eyelashes. Patients in a clinical trial saw results in as few as 8 weeks with full results after 12 to 16 weeks.

It’s an innovation backed by research.

While LATISSE® is a treatment for inadequate or not enough eyelashes, it was developed through years of research by Allergan, a pharmaceutical leader with over 60 years of expertise in prescription eye care products.

Ask DR MICHELE KOO, MD, BOARD CERTIFIED PLASTIC SURGEON, ST LOUIS, MISSOURI  if LATISSE® solution is right for you.

If you’re considering LATISSE® (bimatoprost ophthalmic solution) 0.03%, it’s important to get all the facts. You may have questions about how the treatment works, how soon you’ll see results and, of course, the safety of the product. This site was intended to give you a basic understanding of the product, but you should talk to your doctor to see if LATISSE® is right for you.

The first step: talk to DR MICHELE KOO, MD, BOARD CERTIFIED PLASTIC SURGEON, ST LOUIS, MISSOURI, 314-984-8331, www.drmichelekoo.com, bodybykoo@hotmail.com. While any doctor can prescribe LATISSE®, Dr Michele Koo, MD, is knowledgeable about this FDA-approved treatment. Dr Koo will evaluate your medical history to determine if you’re a good candidate for LATISSE®.

 

What are the side effects?

The most common side effects after using LATISSE® solution are an itching sensation in the eyes and/or eye redness, which were reported in approximately 4% of patients. These may occur immediately after use, but should usually last only for a short period of time. Eye itching and eye redness are not allergic reactions, and do not mean that your eyes are being harmed.

LATISSE® solution may cause other less common side effects, which typically occur on the skin close to where LATISSE® is applied, or in the eyes. These include eye irritation, dryness of the eyes, and redness of the eyelids. Skin darkening (or hyperpigmentation) is another less common side effect. This condition causes areas of skin to become darker than the surrounding skin color, but has been reported to be reversible after discontinuation of the product.

You should always only use the FDA-approved sterile applicators to apply LATISSE® directly to the base of your upper eyelashes. The applicators have been specially designed and manufactured to meet FDA standards, and help patients properly apply the product.

Could LATISSE® cause the color of my eyes to change?Increased brown iris pigmentation has occurred when similar medications were instilled directly into the eye to treat elevated intraocular pressure/glaucoma. Although iris pigmentation was not reported in clinical studies with LATISSE®, patients should be advised about the potential for increased brown iris pigmentation which is likely to be permanent.

Is LATISSE® safe?LATISSE® is an FDA-approved prescription treatment for hypotrichosis used to grow eyelashes, making them longer, thicker and darker. Hypotrichosis is another name for having inadequate or not enough eyelashes. The FDA reviewed clinical study results to verify the identity, potency, purity and stability of the ingredients, and demonstrated that the product is safe and effective for its intended use if used as prescribed. 

Tips for Success

Once you know how to apply LATISSE®, it’s important to understand a few simple tips to help you make your treatment as effective as possible.

Follow these guidelines for best results:

Think routineTry to incorporate LATISSE® into your nightly routine — for example, after you’ve washed your face and brushed your teeth.

Keep it handyStore the LATISSE® bottle near your other skin care products or toothbrush, so you won’t forget to apply it each night.

Have patienceLATISSE® (bimatoprost ophthalmic solution) 0.03% takes time to work. Only use it once a night, and don’t overuse it, as this may increase the chance of experiencing eye redness or itchiness.

Start freshIf your eye makeup remover leaves an oily residue on your eyelids, wipe off any excess oils with soap and water to ensure a clean surface before you apply LATISSE®.

Follow the rulesAlways use the sterile, disposable FDA-approved applicator provided in the kit. Don’t try to apply LATISSE® with a cotton swab. The LATISSE® applicator is specially designed to hold a drop and release a drop.

Don’t play catch upIf you miss a dose one night, don’t apply more just to catch up. Simply apply LATISSE® the next evening and stay on schedule.

Beware of germsDon’t let the tip of the bottle or applicator contact your fingers or any other unintended surface, in order to avoid contamination.

Chart your progressWhen you start using LATISSE® solution, be sure to mark your calendar and take pictures throughout weeks (0, 4, 8, 12, 16), so you can have your own “Before & After Gallery.”

Talk to DR MICHELE KOO, MD, ST LOUIS, MO, for some additional tips for success.

WHAT TO EXPECT 

Great eyelashes don’t just happen overnight. That’s why it’s important to note that LATISSE® (bimatoprost ophthalmic solution) 0.03% works gradually and remarkably — with full results after 12 to 16 weeks. Once you begin treatment, you must continue applying the topical solution each night and follow the directions for best results. Remember results are gradual over time.
Your eyelashes will experience real measurable growth.
LATISSE® works from the inside out. As the treatment progresses, you’ll begin to see changes in length, thickness and darkness gradually. After week 16, you’ll see the full effect of LATISSE® — and so will others.
There are possible side effects.
Throughout clinical trials, some users did experience itchy eyes and eye redness. However, some users found that these irritations went away once they became accustomed to the product or began applying it properly. As with any prescription treatment, always consult with your doctor for information and proper usage of LATISSE® solution.
In the clinical study, 78% of participants experienced a significant increase in overall eyelash prominence (including elements of length, fullness, and darkness) at week 16.

 

 

 

BOTOX 911 - WAR AGAINST WRINKLES - JUVEDERM - DR MICHELE KOO - ST LOUIS - KANSAS CITY - MISSOURI - ILLINOIS

Thursday, July 16th, 2009

 

 

 

 

 

Before BOTOXAfter BOTOX

 

 

 

 

 

 

 

Dr Michele Koo, MD, St Louis, Missouri, is a Board Certified Plastic Surgeon who treats facial wrinkles including crows feet, glabellar frowns (11’s between eyebrows), forehead creases, peri-oral (lip wrinkles), and platysmal bands (neck bands) with BOTOX. She also treats nasolabial grooves, chin creases, thin lips, and downturned lips with various fillers including JUVEDERM, RESTYLANE, AND EVOLENCE.

 

If you’ve been feeling tired and people keep asking you if you are sad or disinterested, then perhaps it’s time to refresh your face with some filling out of the creases and hollows to make you look softer, fuller and more alive.  

 

BOTOX along with filler and a simple skin care regimen can make a significant difference in the appearance of your face in very little time in the office of Dr Koo. You will have very little if any recovery time and you can do it on a Friday and be ready to go out the next night.

Dr Michele Koo feels that the following information will be helpful in educating you about BOTOX and its safety. She feels if you understand its actions and chemistry that you will feel much more comfortable and understand that BOTOX is very safe used by trained personnel such as Dr Michele Koo, MD, of St Louis, Missouri, 314-984-8331.

 

Inactivation of the orbicularis oculi muscle by chemodenervation with botulinum toxin type A (Botox, Allergan, Inc., Irvine, Calif.) as a sole procedure or in conjunction with blepharoplasty has proved to be a reliable method to improve the appearance of the periocular area. Botox has the unique and ideal characteristic in that, with repeated use, there is potential for a prolonged clinical effect with smaller dosages. In addition, if a complication does arise—while not aesthetically acceptable and potentially untoward—it is time-limited, and the anatomical area will eventually return to its pretreatment baseline status.

The eradication of facial wrinkles has traditionally been approached with facelifts, blepharoplasties, and various surgical interventions of soft-tissue augmentation, and resurfacing methods. Facial wrinkles are a result of a combination of basic chronologic aging compounded by sun damage and smoking.

 

Facial wrinkles can be categorized as dynamic (accentuated with animation) or static (present regardless of facial expression) in nature. An example of dynamic facial wrinkles are the crow’s feet wrinkles. These facial creases  are primarily a consequence of hyperkinetic activity of the orbicularis oculi muscle that encircles the eye. With animation, there is hypertrophy of the lateral muscle fibers. Treatment, therefore, should ideally be aimed at the underlying muscular component. One of the most recent advances in the aesthetic arena has been the expanded use of the botulinum type A neurotoxin (Botox, Allergan, Inc., Irvine, Calif.) to improve the appearance of dynamic facial wrinkles.

 

BOTOX, temporarily prevents these dynamic muscles from working by inducing chemodenervation by preventing release of acetylcholine at the neuromuscular junction of striated muscles. The result is muscle-fiber atrophy and subsequent clinical flaccid paralysis, thereby smoothing out an area that once had facial wrinkles.

 

This form of therapy is particularly well suited to the muscles of the upper one-third of the face: the vertical midline glabellar groove (corrugator supercilii, procerus, and medial fibers of the orbicularis oculi muscles), the horizontal forehead lines (frontalis muscle), and the crow’s feet (lateral fibers of the orbicularis oculi muscle).

 

Botox is received in crystallized form (25°C) in a vial containing 100 units of toxin, 0.9 mg sodium chloride, and 0.5 mg human albumin. The toxin is reconstituted with preserved or unpreserved normal saline yielding various concentrations for the obliteration of facial and neck wrinkles. Dr Koo dilutes the BOTOX depending on the location of the muscle and how deep the wrinkles are and how hypertrophied the muscles are and whether this is a first or repeat injection, and when the last injection of BOTOX was.

 

The toxin is reportedly quite labile and readily denatured; therefore, Dr Koo  prepares the solution immediately before use and prefers to use it within 24 hours. Contingent upon the degree of orbicularis oculi muscle hypertrophy, Dr Michele Koo, St Louis, Missouri, typically uses an average of 7.5 to 15.0 U per side. The patient is asked to perform an exaggerated smile (squint), and equal divided aliquots of 2.5 U (0.05 ml) of Botox are injected into the raised folds of the skin corresponding to the presumed muscle pattern.

 

Three or four injections are spaced at 1.0- to 1.5-cm intervals, beginning immediately beneath the lateral edge of the eyebrow down to the lateral infraorbital rim. Because there is an inherent spread of Botox both in between and within muscle fibers, it is injected 1.0 to 1.5 cm (a fingerbreadth) from the lateral orbital rim to prevent its migration into adjacent periocular muscles.

 

Dr Koo performs the injections in the office in 15 minutes and the patient is ready to return to the office or out for the day immediately afterwards. The onset of action, with the loss of muscle activity and rhytids, can be rapid in this area, and although some improvement may be noted 48 to 72 hours after injection, the full effect may take 3-5 days.

 

Wrinkles in the crowsfeet area can be one of the earliest signs of aging. In large part, they are the result of muscle hypertrophy of the fibers of the orbicularis oculi that encircle the eye. Consequently, blepharoplasty, soft-tissue augmentation, and resurfacing of any depth are only partially effective in reducing their appearance, and muscular inactivation would therefore be the optimal treatment modality. However, given the muscle’s size and the critical function of tightly closing the eyelid, weakening of the muscle with BOTOX is an ideal and preferable method to diminish and eradicate the creases around the eyes.

 

Perhaps the most common untoward event that occurs when the crow’s feet are treated is bruising which Dr Koo minimizes by holding pressure for a minutes after the injection. This can also be minimized with superficial injections, because the relatively thin orbicularis oculi muscle seems to be satisfactorily affected when the toxin is injected into the subcutaneous space overlying the muscle. This not only reduces the chance of bruising but may prevent intravascular injection and hemodilution, which can affect potency. Furthermore, injection into the subcutaneous compartment may allow for more local and even diffusion over the targeted muscle and provide an additional safety barrier to structures deep to the muscle.

 

Botulinum type A neurotoxin physiologically denervates mimetic muscles, thereby eliminating the pull on the skin and the appearance of superimposed wrinkles. The improvement in the appearance of crow’s feet can be profound. Botox does not, however, address other stigmata of aging of the eye, such as fat-pad herniation and excess skin, both of which require surgical intervention. Botox injections and blepharoplasty should not be viewed as mutually exclusive but rather as potentially complementary procedures. Dr Michele Koo, MD, FACS, Board Certified Plastic Surgeon, St Louis, Missouri, will advise you as to the best approach for your complaints regarding your wrinkles and the excess skin around your eyes depending on your desires and your anatomy.

 

Currently available injection suggestions for the periocular area are general and primarily include a safety zone of approximately 1.0 cm (one  fingerbreadth) from the orbital rim in an arclike pattern. To reduce the temporary yet disfiguring risks of periocular Botox injections alone or in concert with blepharoplasty or facial surgery, Dr Michele Koo performs  precise identification of the muscular anatomy and needle placement.

 

 


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