Saturday, January 9, 2010

TUG (Inner Thigh) Flap Microsurgical Breast Reconstruction





 The following is an excerpt from a chapter I recently authored for an upcoming textbook.  It is written in medical lingo.  A version that uses more regular language more suitable for the general public will soon be posted on the Women's Plastic Surgery website.  All surgical photographs have been removed, as they may be upsetting to some readers; only diagrams are shown for educational purposes.  Read on to learn more about the TUG (inner thigh flap)!:


Introduction to the TUG Flap

            The inner thigh skin and fat based on the transverse upper gracilis musculocutaneous (TUG) flap blood supply provides an autologous donor area with several qualities complimentary to microvascular breast reconstruction.  The gracilis flap is an exciting alternative to abdominal, back or buttock tissue flaps for reconstruction of a natural looking and soft, shapely breast. 
            The gracilis muscle has a consistent and reliable blood supply, and has been well described (1, 2).  The transverse upper gracilis flap can be shaped to mimic a mastectomy specimen, providing excellent contour and projection to the breast reconstruction.  The characteristics and skin color of the TUG flap allow for immediate nipple-areola reconstruction in both immediate reconstruction following skin-sparing mastectomy and in delayed breast reconstruction alike.  TUG flap microvascular breast reconstruction is an excellent option for patients who desire autologous reconstruction and who do not have adequate abdominal donor tissue or who do not desire abdominal scars.



History
            Use of the transverse upper gracilis (TUG) myocutaneous flap for breast reconstruction was first described as a single breast reconstructive case in 1992 (3).  The cutaneous territory of the gracilis myocutaneous flap was demonstrated by anatomic and injection studies to lie perpendicular to the muscle in its proximal third, transverse and parallel to the medial groin crease.  Based on the direction of exit of cutaneous perforators in the superomedial thigh region, the transverse cutaneous skin paddle of the gracilis muscle has since been accepted as dominant, much like the lower transverse paddle of the rectus abdominis muscle (3).  Perforators extending through the gracilis muscle vascularize the area reaching from over the adductor magnus and sartorius muscle anteriorly to the midline of the thigh posteriorly (4).  
            Although the vertical paddle of the gracilis has been used for breast reconstruction (5), it is accepted as much less reliable (6), and has a more visible vertical scar.  We now offer inner thigh free flap reconstruction using the transverse skin paddle to patients without adequate abdominal donor tissue and to those patients that do not wish to have postoperative scars associated with abdominal tissue harvest. 
            The transverse upper gracilis flap technique is relatively straightforward, reliable and can be aesthetically superior to abdominal reconstruction in two significant ways:  1) it has the advantage of allowing for immediate nipple-areolar reconstruction, negating the need for secondary surgery and 2) coning of the flap into a projecting breast shape is simpler than for abdominal flaps.  By using a semi-lunar construction of the skin paddle, this flap provides excellent dimensions, good projection and can be contoured for immediate nipple areola reconstruction.  The aesthetics of this type of reconstruction can be excellent.
           
Transverse Upper Gracilis Flap Design
            The TUG flap is designed with a semi-lunar skin paddle transverse to the longitudinal axis of the gracilis muscle in the inner thigh (Figure 1)  The superior aspect of the flap is marked approximately one centimeter below the groin crease anteriorly and centrally, but extends well into the gluteal crease at the most posterior aspect.  Placement of the incision slightly below the crease avoids distortion of the labia majora with related symptoms, as can occur in medial thigh lift (7). 
            The anteroposterior length of the flap extends up to 28 centimeters.  The width of the flap is judged by pinching the inner thigh tissue with the thighs in adduction, using the maximum width that can be easily closed without tension.  The flap has been designed it as wide as 11 centimeters at the central axis over the gracilis muscle (Figure 6).  A pencil Doppler probe is used to confirm the location of perforating vessel(s) over the gracilis muscle and into the skin paddle (Figure 7). 
            The procedure is performed with the patient in the supine position, with the thigh abducted and the knee flexed.  The flap is harvested with the patient in well padded OB-GYN operative stirrups, which facilitates dissection and closure of the posterior aspect of the wound. 
            The anterior thigh incisions are made first.  The posterior branch of the saphenous vein is harvested with the flap (Figure 2), and any anterior venous branches are left in situ although they can be included in the skin paddle if needed.  Lymph nodes are avoided and are left in situ to avoid the risk of lower extremity lymphedema.


            Anterior flap dissection proceeds superficial to the muscular fascia until the medial/posterior edge of the adductor longus is encountered (Figure 3).  Beveling of subcutaneous adipose tissue is used to maximize the bulk taken with the flap.  The deep fascia is incised longitudinally and the space between the adductor longus and gracilis muscle is separated and the vascular pedicle to the gracilis is identified.  Pedicle dissection proceeds proximally to the origin from the superficial femoral artery.  Posterior dissection then continues superficial to the muscular fascia, entering the deep fascia at the posterior aspect of the gracilis.  Pedicle length ranges from 6 to 8 cm.


            The gracilis muscle is transected superiorly and inferiorly, commonly taking only a portion of muscle lying directly beneath the flap (Figure 4).  Additional inferior muscle length may be optionally included for enhanced flap volume.  Usual flap elevation time is approximately 45 minutes or less.


            Following pedicle division, absorbable sutures are used to maintain flap coning and achieve projection (Figures 5 and 8).  The gracilis muscle may additionally be used to increase projection by securing it posteriorly behind the adipose tissue, with predictable postoperative muscle atrophy.  In immediate reconstructions, the mastectomy specimen is weighed and measured for comparison with the TUG flap, typically an appropriate match in terms of volume and dimensions.  Flap projection has often been greater than the native mastectomy specimen (Figure 9).



            The flap is deepithelialized except for an areolar circle in immediate reconstructions (Figure 9d and Figure 10), and completely deepithelialized in nipple-sparing mastectomy.  An areolar circle is created and accentuated by a circumareolar incision for delayed reconstructions, deepithelializing and burying of the superior flap beneath the native mastectomy skin (Figure 11).




            Microvascular anastomosis is usually to the internal mammary system beneath the third or fourth costal cartilage.  Following coning, the pedicle enters the undersurface at the center of the flap, enabling inset of the flap in any orientation desired (Figure 12).  Postoperative flap assessment includes clinical and external pencil Doppler monitoring if the flap is exposed, in addition to continuous implantable venous Doppler probe monitoring.



            The inner thigh donor area is closed with interrupted sutures in the deep fascia (7), interrupted deep dermal and continuous subcuticular skin sutures over a suction drain exiting from the superior aspect of the thigh wound.


            Immediate nipple-areolar reconstruction is performed by folding the semilunar flap and accentuating the apex of the resultant standing cone as the area of maximum projection using interrupted horizontal mattress sutures (Figure 10).  Care is taken not to create excessive suture tension to avoid circulatory compromise to the nipple reconstruction.  An areola circle is drawn, and skin surrounding this circle is deepithelialized and buried beneath the mastectomy flaps prior to microvascular anastomosis.  The naturally darker pigment of inner thigh defines the areolar reconstruction. 
            Patients are placed on post-operative aspirin as an anticoagulant for one month and allowed to ambulate at two to three days postoperatively.  Hospital stay averages five to seven days.











Discussion
            Autologous abdominal soft tissue reconstruction after mastectomy, although becoming more common, comprised less than a quarter of breast reconstructions performed in the United States in 2008 (8).  The deep inferior epigastric perforator (DIEP) free flap was performed in only 7.5% of reconstructions in that year. 
            The reason for the relative scarcity of soft tissue reconstructions relative to implant reconstructions is not clear; however the complexity of microsurgical reconstruction and the technical difficulty of perforator flap harvest may contribute to the lack of widespread acceptance.  Many patients do not need or desire abdominoplasty at the same time as having a breast reconstruction.  As such, the potential aesthetic perk (9) of abdominal perforator flap harvest may be considered a drawback.  In addition, abdominal flap scars are not insignificant, including the umbilical scar which is visible in currently fashionable low-cut jeans and swim suit bottoms.
            Advantages of gracilis muscle as a microvascular transplant include low donor-site morbidity, a concealed donor scar, constant anatomy with large-diameter vessels, and the potential for a neurosensory flap as well as a large skin paddle.  Anatomic studies (3, 6) have revealed the angiosome of the upper gracilis muscle to lie at right angles to the muscle, in a transverse direction.  As such, the generous size of the transverse skin island that can be harvested with the gracilis allows for shaping of the flap in a circular and cone-like fashion, more closely mimicking natural breast anatomy than the relatively flat projection of abdominal flaps (10).  The inner thigh flap also avoids the relatively visible scar on the lower abdomen together with a numb area below the umbilicus, sequelae of abdominal perforator flaps (11).  The quality of inner thigh tissue is soft and similar to abdominal flaps and breast tissue, unlike the firm, fibrous and stiffer texture of buttock flaps.  Some patients' body habitus clearly favors the inner thigh flap over abdominal flaps, based on their natural depostion of adipose tissue (Figure 13). 
            The conical apex at the central portion of the folded inner thigh flap constructs nipple projection using subdermal fixation sutures at the time of reconstruction.  The resulting nipple areola in our opinion can be aesthetically superior to those reconstructed with local flaps or skin grafts.  Inner thigh skin naturally has slightly darker pigmentation than the skin of the chest or torso, and when contracted and allowed to pucker slightly it can appear even darker.  This color difference with breast skin allows for a natural areolar reconstruction that can be later augmented using medical tattooing if desired (Figures 14 and 15). 
            Early reports of the TUG flap described coverage of defects in the head and neck, lower extremity and thoracic region (12).  Schoeller (13) described a ‘medial thigh lift free flap’ for bilateral autologous breast augmentation after bariatric surgery.  Arnez (14) reported 7 immediate TUG flap breast reconstructions, for ‘small’ or ‘moderate’-sized breasts with sufficient medial thigh tissue, who declined scars in other donor sites.  Wechselberger and Schoeller (15) performed 12 TUG flaps in 10 patients for immediate breast reconstruction.  Fansa (16) reported 32 flaps and Scheoller (11) published a large series of 154 flaps for breast reconstruction in immediate and delayed settings for breast reconstruction, without immediate nipple-areolar reconstruction.  For bilateral reconstructions, the transverse gracilis flap has been suggested to surpass the DIEP flap because of a better concealed donor scar and easier harvest (11).  We have also recently submitted our early data for publication (12). 

Inner Thigh Flap Donor Site          
            Although other autologous tissue reconstruction options are available to patients with previous abdominal tissue harvest or in very thin patients (18), in many of these patients, the inner thigh flap can be used.  Unlike loss of the rectus abdominis muscle, loss of the gracilis muscle is not associated with the risk of abdominal hernias, bulging or functional donor site complications.  The greatest drawback of the inner thigh flap is the inner thigh scar; yet its location near the groin crease is readily concealable in all clothing except swim suits or underwear (19) (Figure 16).







            Tissue expanders and breast implants, latissimus muscle flaps with implants, the inferior gluteal artery free flap, and superior gluteal artery free flap have all been well described as alternatives to abdominal flaps, and the inner thigh flap presents an additional option to these choices.  It is inherent that all autologous soft tissue reconstructions require creation of a donor site and donor area scarring, to some degree.  Certainly, wound complications at the inner thigh donor site necessitating dressing changes are an annoyance for patients as are seromas, and although frequent, this complication is relatively minor.  Patients receive preoperative counseling and full informed consent about this possibility.  In all cases, our patients have been quite satisfied with the final results of their TUG flap reconstructions. 

Gracilis Perforator Flaps
            The inner thigh skin can be harvested as a perforator flap based on the vascular pedicle to the gracilis muscle (19-22).  However, donor site hernia and functional loss are not accepted complications of gracilis muscle flap harvest and are not compelling indications to spare the gracilis muscle.  Despite reports of successful transfer of gracilis perforator flaps, inclusion of the gracilis muscle in the TUG flap has been suggested to potentially provide more tissue volume, to increase safety of monitoring the skin paddle, and to allow rapid harvest with minimal functional donor site morbidity (15).  Anatomic studies of the proximal cutaneous perforator vessels of the gracilis muscle (23) suggest that it is safer to include the gracilis muscle for transfer of tissue in the TUG flap distribution. 
            Gracilis perforator flaps are smaller than the dimensions available for TUG flaps, unless an extended dissection including some gracilis muscle is performed (22).  These authors do not support a clear clinical advantage of preserving the gracilis muscle.  The clinical indication and advantage of the perforator flap is therefore a thin and pliable flap (22), perhaps better suited to extremity coverage.  Although safe applicability of gracilis perforator flaps have been demonstrated, the required longer and more tedious dissection should be weighed against the rapid, easy and routine dissection of a more bulky musculocutaneous gracilis flap. 
            Gracilis perforator dissection would potentially spare loss of donor muscle in the thigh, but functional advantages are not clear, and there may be increased risk to flap circulation as well as increased operating time.  Inclusion of gracilis muscle in TUG flap is suggested to provide more tissue volume, increase safety and allow rapid flap harvest with minimal functional donor site morbidity (23).  In addition, the gracilis muscle does add some bulk to the reconstruction, an advantage in patients with minimal thigh subcutaneous fat.  Certainly, harvesting this flap as a perforator flap is an option, but one that we do not currently see as advantageous. 
             It has been recommended that the saphenous cutaneous venous system be harvested with the perforator flap to enhance venous drainage (19), but we have only required the saphenous system for venous outflow in one patient that had poor internal mammary drainage.  This outflow may have been helpful in our other patient that developed some delayed venous insufficiency.  Nevertheless, saphenectomy can be a cause of morbidity (24) while the need for secondary venous drainage in this series has been rare. 

Summary
            The transverse upper gracilis flap can be used for microsurgical breast reconstruction in patients with previous abdominoplasty, inadequate abdominal tissue, or in patients that object to abdominal or buttock scars.  The inner thigh flap offers an autogenous tissue reconstructive option after mastectomy with excellent projection, the potential for immediate nipple-areolar complex reconstruction, and a favorable donor scar position and quality. 
            The TUG flap has significant advantages in addition to its pleasing final reconstructive appearance.  The gracilis muscle pedicle and harvest are extremely reliable and straightforward, and are familiar to most Microsurgeons.  No intraoperative repositioning is required as often for flaps from the buttocks or back, and a two-team approach is facilitated by dissection of the contralateral thigh during mastectomy.  Since TUG flap design allows immediate nipple areola reconstruction, the need for tattooing, local flaps or skin grafting may be obviated.  In some patients, the medial thigh lift may be considered an aesthetic perk of this procedure.  The inner thigh flap has become a favorite in our armamentarium of microvascular breast reconstruction choices. 
            Candidates for the inner thigh gracilis flap include patients desiring autologous breast reconstruction; those with sufficient superomedial thigh tissue; previous abdominoplasty or DIEP, SIEA or TRAM flap harvest; previous abdominal surgery precluding use of abdominal tissue for reconstruction; or very thin or athletic patients without sufficient abdominal or buttock donor tissue.



References (see full publication - to be posted)

How do you reconstruct a nipple and areola after breast cancer?


        I am scheduled to have nipple reconstruction in May, and know there are various options available. Can you comment on the differences in cosmetic outcome when utilizing tissue from another part of the body, skin from the flap itself or tattooing alone?

The nipple and areolar complex (NAC) reconstruction involves two components, the nipple prominence and the areolar circle.  Sometimes the nipple reconstruction is performed first, with the areola done at a later date; at other times, they are performed together.  NAC reconstruction is the finishing touch of a breast reconstruction, and is the "icing on the cake" to complete the breast! 

Nipple reconstruction usually involves a local flap procedure where wings of tissue (skin and fat) from the breast reconstruction itself are rotated in place to create a nipple prominence.  Some surgeons also add some additional tissue inside the local flaps (soft or firm) to try to improve projection of the nipple reconstruction.  After surgery, the nipple reconstruction is expected to shrink between 30% and 50%.  The ideal nipple prominence matches a natural nipple at rest.  It will not have the capacity to become erect with stimulation or cold temperature.



The areolar circle can be made using either a medical tattoo or a skin graft.  Natural flesh-colored medical tattoo pigments (ranging from tan, to pink or brownish or black) are available and can be mixed together to very closely match a natural nipple and areola.  The nipple prominence is also tattooed to match the other side.  Tattooing can be done either in the operating room or in the office of your Surgeon under local anesthesia, and is usually done by the Plastic Surgeon or occasionally a specially-trained surgical Nurse. 

Skin grafting for areolar reconstruction involves taking a full-thickness graft (all the layers of the skin, requiring closure of the "donor site" with stitches) from another area of the body.  Common sites for harvest of a skin graft for areolar reconstruction include the groin, the other breast's areola (if a balancing breast reduction or a lift is also being done), or rarely, the labia (external genitalia).  Skin grafts may heal with either lighter or darker pigmentation than expected, and by definition, require creation of a scar at their donor location.  For this reason, I usually use a tattoo for the areolas I create.

Sunday, January 3, 2010

Constipation is very common after any surgery!



Any surgery that involves taking narcotic pain medication (intravenous or pills) and/or being under anesthesia can cause temporary constipation.

I advise each of my patients to expect some constipation after surgery and to start taking an over-the-counter stool softener immediately after surgery. An examples of a medication I often recommend is called Colace (Docusate).

Your local Pharmacist can recommend what is appropriate for you, given your specific medical history and current medications you are already taking.

You may not have a bowel movement for 3-5 days after surgery. This is not dangerous, just uncomfortable!



Start with one stool softener, and considering adding a natural laxative such as Senna (also over-the-counter) after a day or two if you have still not had a bowel movement.

Remember not to overdo it - "more" is not always better! Taking too much of any medication can create other serious problems.

Be patient - it will take some time for your body to recover and return to normal after surgery.

In addition, be sure to drink plenty of fluids and to continue a regular diet with good nutrition (including vitamins and minerals) and lots of fiber.

Karen M. Horton, M.D., M.Sc. F.R.C.S.C.

Monday, December 28, 2009

Personal beauty tip from a Plastic Surgeon: Keep it simple


The following is an except from an article I was interviewed for in Health Magazine:

Natural Cures - Anti Aging Solutions

The Best Anti-Aging Secrets
From Health magazine

We've all been there:

That moment midappointment when you catch yourself shamelessly staring at your hairdresser, dermatologist, or dentist and thinking, How the heck does she pull it off? What's the secret to her great hair, pore-free complexion, or flawless teeth? Well, we decided to go straight to the source and find out, once and for all, how to get that ageless look—naturally.

We asked the beauty industry's most-sought-after stylists, aestheticians, and MDs to divulge their tricks for stopping the clock. If there's no fountain of youth, their unexpectedly simple advice might be the next best thing.

MY ADVICE: Keep it simple!

"Because I'm a plastic surgeon, companies send me so many skin-care samples—and some of them have 10 different steps! But I'm realistic, so there's no way I'm going to sign up for some huge beauty system that costs hundreds of dollars and requires a commitment that I'm not willing to make.
Honestly, here's my daily skin-care routine: I go home, wash my face with a drugstore cleanser, put on a moisturizer, and fall into bed. I find that this simple regimen works well for me."
—Karen M. Horton, MD, Plastic Surgeon and Reconstructive Microsurgeon at the Women's Plastic Surgery Center, San Francisco
I would also add that a healthy, nutritious diet, regular exercise, lots of sleep and a healthy home and work environment are also very important in health overall, and to beautiful skin!

Sunday, December 20, 2009

You should be at your ideal weight and fitness level before a "mommy makeover"

Karen M. Horton, MD answers: Tummy Tuck for skin, fat, and stretch marks after pregnancy?

I'm 5'11 and 249 lbs. After pregnancy, I have a hanging mass of skin, fat, and stretch marks. I went from 186 lbs to 277 lbs. I have zero elasticity, and 1 week after I had my daughter, I had dropped from 277 lbs to 231 lbs. I am still overweight and currently trying to lose the weight, but I have this hanging mass on my stomach of stretch marks and fat. It's horrific. I want a tummy tuck and have done a lot of research, but how much will it cost me? How much do I need to lose before I should have the surgery? I don't accept blood at all, is that a concern?


By Karen M. Horton, MD - San Francisco Plastic Surgeon

For any Mom considering Plastic Surgery such as a "mommy makeover", I always advise women to achieve their weight loss goals prior to seriously considering surgery.

You should have lost as much weight as you feel is reasonably realistic, be physically fit, and have healthy nutrition as part of your lifestyle.

There should also be "calmness" in your personal and/or professional life. Chaos is never a good fit with surgery!

Most Moms seek a full abdominoplasty (tummy tuck), which removes excess lower abdominal skin and fat (including some stretch marks!), tightens the muscles of the abdominal wall back together, and decreases the waist line. Sometimes liposuction of the flanks and/or upper abdomen are added to the procedure, if needed.

For women who have not yet reached their ideal weight but who have a large overhang of skin and fat (a "pannus") in their lower abdominal region, it is possible as an interim procedure, to do a limited "panniculectomy". This will only remove the overhang but will not address the abdominal muscles or the upper abdomen.

Be sure to visit a Board-Certified Plastic Surgeon with a great deal of experience in these types of procedures!

Karen M. Horton, MD, MSc, FRCSC

Friday, December 11, 2009

Alloderm with the use of implants - is it safe?

The following is an excerpt from questions submitted by the Young Survival Coalition. I have been asked to answer questions on breast reconstruction as an expert.


How safe is the use of cadaver tissue (Alloderm) in breast reconstruction with implants?


Alloderm is one brand name product of human cadaver (donated by dead people) dermis, which is the bottom strength layer of skin. It is sometimes used in reconstructive surgery to potentially add another layer of tissue to thicken the mastectomy skin, to help hold submuscular implants in place, or to decrease rippling of implants.


Alloderm is a "graft", which by definition does not have a blood supply. This is in contrast to a "flap", which has a blood supply and may be either attached to a muscle ("pedicled"), or "free", which involves microsurgery to disconnect and then reconnect tiny blood vessels under the microscope.


If the breast skin has been radiated already, the use of Alloderm adds the additional risks of infection, wound healing problems, and/or the need for implant or Alloderm removal. This is because the radiation interferes with blood vessels growing into the product, and slows the rate of incorporation of the product.


I unfortunately have removed much more Alloderm (inserted by other surgeons) in my patients that I have ever put in myself. I personally do not use this product, but understand that many surgeons do.

Monday, December 7, 2009

Template for a Letter Regarding Cosmetic Surgery Tax ("BoTax")

The Aesthetic Society and all of organized Plastic Surgery present a united front to fight the unfair Cosmetic Surgery Tax!

The Society leadership strongly disagrees with this discriminatory tax and is very concerned with the role of the surgeon as tax collector. Additionally, we see potentially devastating consequences to patient safety, as some may choose to have surgery abroad, seeing physicians who may not have comparable training certification or surgical site standards up to those of ABMS Board-certified Plastic Surgeons.

The following is the template for a letter that patients can use to express their opinion and dissent toward the proposed cosmetic surgery tax:


You can find your elected representative by clicking here: http://www.senate.gov/general/contact_information/senators_cfm.cfm



Dear Senator ______,


HEALTHCARE PLAN IN THE SENATE WILL UNFAIRLY DISCRIMATE AGAINST US!


I am writing you today about an issue that affects everyone who utilizes plastic surgery services for anything from Botox to Tummy Tucks.


The healthcare bill approved by the US Senate this weekend, Page 2045 Sec. 9017, Excise Tax on Elective Cosmetic Medical Procedures included in the “Patient Protection and Affordable Care Act.


This dense legalese translates to a tax on all cosmetic procedures as partial payment for the healthcare overhaul our current administration is attempting to implement.


The problem is that we would be paying this tax, the FIRST time this country has levied a tax on patients for medical procedures. This Bill is objectionable in many ways, including:

· This is a discriminatory tax. According to the Aesthetic Society Annual Statistics, 91% of all cosmetic procedures are requested by women

· This will not have considerable consequences on the wealthiest patients but, as usual, affects the middle class. We working women, soccer moms, and scores of others who carefully save and budget to improve our appearance and self esteem will be penalized for doing so.

· Procedures such as breast reduction that have been cited in the literature for improving self esteem and quality of life would be taxed as well.

· Our doctor as tax collector: This provision places physicians in the role of tax collector and holds physicians liable should an individual fail or refuse to pay the tax. That is not the relationship we want with our medical provider!

Please, do not allow this portion of the tax bill to pass!


Sincerely,


______________________

Saturday, November 21, 2009

Federal Health Care Reform - Concerns of the California Medical Association


November 21, 2009

Special Alert: Federal Health Reform

Today the United States Senate will vote on “cloture” to begin debate on health reform. CMA is opposed to the proposal currently before the Senate and has communicated our position and concerns to both California Senators. I and Immediate Past-President Dr. Dev GnanaDev will speak directly to Senators Feinstein and Boxer on Monday to make clear our concerns with the current proposal. In CMA’s view the current version does not improve patient care and could in fact, substantially harm the doctor-patient relationship. CMA is committed to working with our Congressional Delegation to substantially improve this legislation.

It is our hope that we will be able to support a final product that protects what currently works well for patients and fixes what is broken. The CMA Executive Committee and Board of Trustees will review any final legislative agreement and, with input from CMA member physicians, make a decision as to our final position.

Please stay tuned for more updates; CMA will provide a more detailed summary of our concerns shortly.

J. Brennan Cassidy, M.D.
CMA President

Monday, November 16, 2009

Research, Stem Cells and Microsurgery - Working toward growing breast tissue in the lab

The following describes exciting new research on "growing" breast tissue in the lab, using stem cells, tissue engineering and technology!

Breast 'regrowth' trial planned



Researchers in Australia plan to test a medical "scaffold" designed to stimulate natural breast tissue to regrow following surgery.

Doctors from the Bernard O'Brien Institute of Microsurgery in Melbourne, will test the technique next year in a trial involving six patients.

The team say that the permanent fat found in breasts can be grown inside this contoured scaffold. They claim to have successfully tested the device in pigs.

The results of that experiment were presented at a plastic surgery conference in Sydney. The researchers recently announced on the institute's website that they had received funding from the Australian government to carry out the human trial.

If this is successful, they hope to develop it into a breast reconstruction technique that avoids using silicone.

Breast scaffold

The teams says that when the "empty chamber" is implanted, fat tissue will naturally fill it to form a new breast.

It's at such an early stage, it is not yet clear whether it will work in people - Dr. Lesley Walker, Cancer Research UK.

This chamber will also contain a gel made using the patients' muscle cells to "induce fat tissue production".

Professor Anthony Hollander, an expert in tissue engineering from the University of Bristol in the UK, said the attractions of this approach were its simplicity and the fact that the tissue growth occurred inside the body.

"At the time of implanting the cells the surgeon redirects the vasculature of the body which keeps a good blood supply to the implant. That is in itself nothing new, but combining it with a cell implant is an interesting step," he said.

He said that the technological advance was the use of a biomaterial cage used to trap the cells in the right place.

In future, the team plan to make this cage biodegradable so it does not have to be removed.
"If it's tried and it works that will be a really nice approach," Professor Hollander said.
But he cautioned that there was "still some way to go".

"This procedure is first likely to be used on cancer patients," he said. "[The team will] have to be able to demonstrate a technique that guarantees that all the cancerous cells are removed and none are grown up in the process, so there is still some way to go."

Dr Lesley Walker, director of cancer information at Cancer Research UK, said: "We know that having a mastectomy can be a very difficult experience for many women and so research to try to improve breast reconstruction after surgery is important.

"[But] it's at such an early stage, it is not yet clear whether it will work in people. Even if this surgery proves to be effective, it will be a number of years before it can be used in the clinic."

Wednesday, November 11, 2009

The Jakarta Post Article - The Brave New World of Plastic Surgery


I was recently interviewed by San Francisco freelance writer, May-lee Chai, for an article in the Jakarta Post, Indonesia.

Click on the images for a full-size version of this article on Plastic Surgery.

Saturday, November 7, 2009

Local Heroes in Medicine: Women Pioneers that Shaped Medicine in San Francisco

The following is an article from the September 2009 San Francisco Medicine publication:

www.sfms.org


Local Heroes in Medicine


Pioneers that Shaped Medicine in San Francisco
by Nancy Thomson, MD

“Women should not be expected to write or fight or build or compose scores. She does all by inspiring men to do all.” —Ralph Waldo Emerson (1802–1882)

In 1948, when I started college at Stanford University, my physician father discouraged me from preparing for medical school, saying that I would take a man’s place, then marry and never practice. Lois Scully, MD, a San Francisco internist, Stanford graduate, and 1979 president of the American Women’s Medical Association, ran into the same bias at about the same time when the
Stanford physician who interviewed her told her to go home, marry, and have five children.

In the early 19th century, Lucy Stone (1818–1893) wanted a good education, but the only college in the world that accepted women at that time was in Brazil. Luckily, Oberlin University was founded in 1835 in Ohio, the first U.S. college to accept both women and African-American students. Stone enrolled and graduated in 1847. However, when it came time to seek a profession, the only field open to women was teaching. In 1849 (the year Elizabeth Blackwell graduated from Geneva Medical College in New York), Lucy Stone wrote, “We believe that if the system of educating females for physicians be generally adopted, a great amount of suffering and death will be saved.”

In fact, the number of female medical school graduates rose steadily from 1849 to 1900. By 1900 in Boston, women represented 18 percent of practicing physicians. However, by 1903 women’s participation in medicine began to decline, as most of the women’s medical schools established in the previous 50 years were closed or merged with male dominated schools, which continued to reject women applicants. This situation generally prevailed until the 1970s, when the feminist movement and antibias legislation brought about an increase in women attending medical schools.

In 1970, female admissions to medical schools were at 9.2 percent; in 1980 they had risen to 27.9 percent, and they are at almost 50 percent today. The decline in economic potential for physicians (which was historically one of the foremost motivations for male medical students) is given comparatively little importance by female students, who cite longtime interest in medicine and science, the desire to help others, and dissatisfaction with other types of work among
their reasons for choosing medicine.

The following time line highlights women’s place in the medical history of San Francisco.

Historical Time Line

From the time of landing at Plymouth Rock, women as well as men practice medicine in New England, often after an apprenticeship with a practicing physician. However, when American medical schools are established, they follow the European pattern of barring women from
seeking medical degrees.

1863
Elizabeth Pfeifer Stone, the first woman to practice medicine in California, settles in San Francisco. Probably German-born and -trained, she previously practiced in New York.

1873
University of California acquires Toland Medical School in San Francisco, and since U.C. is already coeducational, Lucy Maria Field Wanzer, a thirty-three year-old teacher, is accepted as its first female medical student. However, the dean suggests to her fellow students that they “make it so uncomfortable for her that she cannot stay.”

1874
Charlotte Blake Brown applies to the San Francisco Medical Society for admission. Some members of the membership committee feel strongly that females are mentally, physically, and morally unfit to study medicine, let alone practice the profession. On advice of mentors, Brown
withdraws her application.

1875
Following the model of Elizabeth Blackwell’s New York Infirmary for Indigent Women, Pacific Dispensary for Women and Children is founded by three women, all educated on the East Coast: Charlotte Blake Brown, Martha Bucknall, and Sarah E. Browne. This outpatient clinic, initially located at 510 Taylor Street, is intended to provide opportunities for women physicians to obtain internship experience.

1876
San Francisco Medical College of the Pacific accepts its first female student, Alice Boyle Higgins, who graduates in 1877.

1877
Having been admitted to the California Medical Society along with four other women in 1876, Lucy Wanzer becomes the first female member of the San Francisco Medical Society.

1880
Founders of Pacific Dispensary create the first nursing school west of the Rockies. Its one-year course becomes a two-year curriculum in 1882.

1887
The Pacific Dispensary moves to a new two-story building at California and Maple Streets and becomes Children’s Hospital. Interns and residents can be either male or female, but there are no men allowed on the medical staff.

1895
Citizens of San Francisco raise money to build the Little Jim Building for pediatrics at Children’s Hospital.

1896
One year after X-rays are discovered, Elizabeth Fleischman-Aschheim, an engineer, opens the first X-ray laboratory in California, at 611 Sutter Street.

1896
William Randolph Hearst leads the campaign for the Eye and Ear Pavilion at Children’s Hospital.

1904
Dr. Charlotte Blake Brown dies at age fifty-eight. Her daughter, Adelaide Brown, MD (1868–1933), carries on her mother’s work at Children’s Hospital but also serves on the Stanford faculty at Lane Hospital. She fights locally and nationally for clean milk, sanitary garbage disposal, maternal and child welfare, visiting nurse services, and clinics offering cardiac care and birth control.

1906
The San Francisco earthquake forces the demolition of the 1887 Children’s Hospital building.

1911
A new, four-story brick Children’s Hospital building opens at California and Cherry Streets.

1912
The Contagious Disease Pavilion opens at Children’s Hospital, with money donated by William Randolph Hearst, to care for diphtheria, scarlet fever, measles, TB, and, later, polio.

1915
Children’s Hospital affiliates with the University of California for the teaching of medical students.

1915
The American Medical Association admits its first female member.

1916
Henries Hagar Duggan, MD, becomes a pioneering medical anesthesiologist. She works at various hospitals but settles at Children’s for twenty-five years, retiring after the end of World War II.

1938
UCSF pediatricians Mary Olney and Ellen Simpson found summer camps for children with diabetes.

1946
Marian Yueh Mei Li arrives in San Francisco, having completed medical school in Shanghai. She eventually opens a private practice and becomes the first Chinese female ophthalmologist to practice in Chinatown.

1952
Pediatrician Hulda Thelander establishes the Child Development Center at Children’s Hospital for children with cerebral palsy, developmental delays, and congenital defects.

1960
Internist Roberta Fenlon, MD, becomes the first female president of the San Francisco Medical Society.

1971
Dr. Roberta Fenlon becomes the first female president of the California Medical Association.

1977
Linda Hawes Clever, MD, MPH, founds (and chairs) the Department of Occupational Health at California Pacific Medical Center. She is also the first female editor of the Western Journal of
Medicine and is the founder of RENEW, an organization to help fight professional exhaustion and dissatisfaction.

1980
Children’s Hospital acquires St. Joseph’s Hospital.

1988
Marshall Hale Hospital, formerly Hahnemann Homeopathic Hospital, merges with Children’s Hospital.

1991
Children’s Hospital and Pacific-Presbyterian Medical Center merge to create California Pacific Medical Center (CPMC). CPMC joins the Sutter Health chain.

1995
Judith M. Mates, MD (ob-gyn), becomes the second female president of the San Francisco Medical Society.

1996
Toni J. Brayer, MD (internist), becomes third female president of SFMS and, in 1990, the first female chief of staff at California Pacific Medical Center.

2003
Rita Melkonian, MD, FACOG (obgyn), becomes the fourth female president of the San Francisco Medical Society, with E. Ann Myers, MD (endocrinology), as the president-elect.

In closing, it’s interesting to note that in 1868, while debating the admission of women, the American Medical Association recorded this statement by Dr. Alfred Stille, prominent teacher of pathology:

“Another disease has become epidemic. The woman question in relation to medicine is only one of the forms in which the pestis mulieribus vexes the world. In other shapes it attacks the bar, wriggles in the jury box, and clearly means to mount upon the bench; it strives thus far in vain to serve at the altar and thunder from the pulpit; it raves at political meetings, harangues in the lecture room, infects the masses with its poison, and even pierces the triple brass that surrounds the politician.”

If only Dr. Stille could see us today. We’ve sure come a long way.

Nancy Thomson, MD, was a practicing anesthesiologist at Children’s Hospital from 1963 to 1985. In 1988 she received her master’s in public health from the University of California at Berkeley. From 1991 to 2000 she worked as the infectious disease officer and staff physician at San Quentin State Prison. Dr. Thomson currently serves on the editorial board for San Francisco Medicine and is the magazine’s obituarist.

Friday, November 6, 2009

All About Labiaplasty - Labia Minora Reduction

WHAT IS LABIAPLASTY?


Labiaplasty is a surgical procedure which corrects excessively long, enlarged or redundant labia minora. Women who seek this surgical procedure may be self-conscious about hanging labial tissue, they may have asymmetric labias, or they may have pain or discomfort during sex, with exercise or sometimes just walking!


The purpose of labiaplasty is to surgically reduce excessive large labia minorae, to create symmetry when it is lacking, and to make the labia appear more cosmetically appealing. Occasionally excess tissue around the clitoral hood is also carefully trimmed, without any injury to the nerves that provide sexual stimulation.


Labiaplasty only addresses the labia minora (inner lips of the external genitalia of women). It does not generally affect the labia majora (outer lips), nor does it alter the vagina.


HOW IS LABIAPLASTY PERFORMED?


In order to ensure complete comfort and relaxation, we perform labiaplasty in the operating room, under a short and safe general anesthesia. Surgical loupes (microscope glasses) are always used to ensure the most meticulous possible repair.


The area to be trimmed is marked, and local anesthetic containing epinephrine (adrenaline) is injected to prevent bleeding and bruising during surgery, and to keep the area numb for many hours after surgery. Next, excess tissue is trimmed. A multiple-layer closure is then done (usually 2-3 layers of stitches) using all dissolving (absorbable) sutures. Antibiotic ointment is applied, and mesh panties with an absorbable pad are placed.


On average, surgery takes around an hour and a half to two hours. It is outpatient surgery - women can go home in a couple of hours, when they are awake and alert, without nausea and when they are eating and drinking well.


WHAT IS THE RECOVERY FOLLOWING LABIAPLASTY?


You can expect some mild discomfort requiring oral pain medication such as Tylenol or occasionally something stronger (Vicodin or Percocet) for a few days. Aspirin or Ibuprofen (Advil, Motrin) should be avoided as these can increase bruising or bleeding.


There will be some swelling and possibly bruising of the genital region. You can shower the next day, and will be advised to apply antibiotic ointment daily and wear a thin pad in your underwear in case of any spotting or bleeding.


If you have your period, use a pad instead of a tampon for your first 1-2 menstrual cycles to avoid irritation of the incisions while they are healing.


Most women take at least a few days off of work, or work from home during the first few days after surgery, when they are swollen and tender.


Sexual intercourse should be avoided for 3-6 weeks, or until the area is no longer swollen and tender. Aggressive physical activity should also be avoided for at least a week, as increasing your heart rate and blood pressure will bring more blood flow to the area and create more discomfort or swelling.


Some women describe intense itching (due to histamine release during healing), while others have very little discomfort at all after surgery. Keeping a small pillow in your purse can cushion the area if you are sitting on a hard surface during healing.


Like any incision, it takes at least 3-4 weeks for initial healing, and 6 months up to a year for the results to be absolutely final. Incisions are hidden in the natural crease. The area of surgery will eventually be very difficult to see, and there is usually very little scarring, as it involves a mucosal membrane (think about cuts to the inside of your mouth or gums, and how they have healed).


You will be seen back at your surgeon's office within a few days of surgery for an initial checkup, and then usually at 2-3 weeks, 6 weeks, 6 months and one year. All follow-up visits are covered by your surgery fees.

Most women find this operation liberating and are very satisfied with the results.


POTENTIAL RISKS AND COMPLICATIONS OF LABIAPLASTY:


Any surgical procedure carries with it potential risks of anesthesia (nausea, headache, etc), the potential for bleeding, infection and wound healing problems. There will be temporary pain or tenderness, swelling, bruising, and numbness of the area.


Bleeding is controlled during surgery by a cautery pen that coagulates any blood vessels that are encountered. You likely be given a few days of prophylactic (preventative) antibiotics to help prevent infection. You should shower daily and ensure the area is kept clean after surgery.


Your labia may not be completely symmetric - this is the norm for most women. You can have temporary change in pigmentation (lighter or darker) while you are healing.


WHO SEEKS LABIAPLASTY SURGERY?


Women of all backgrounds, shapes and sizes, professions (including stay-at-home moms) and cultures seek labiaplasty! Many women are born with asymmetric or redundant labial tissue, which is normal for them! Sometimes after childbearing, labial tissue can become stretched, and following menopause, the area can droop more.


Labiaplasty is a private procedure that should not be viewed with embarrassment or shame! It is often an empowering experience that can improve a woman's body image and self-esteem.


WHAT IS THE COST OF LABIAPLASTY?


Any surgical procedure includes a surgical fee, operating room or facility fee, and anesthesia-related fees. On average, the total cost can range between $4000 and $8000, depending on the complexity of the surgery, time needed for surgery, and other details specific to your unique anatomy.


Insurance does not usually cover labiaplasty. You can inquire with your insurance carrier about this benefit, but labiaplasty is usually viewed as cosmetic.


HOW SHOULD I PREPARE FOR MY LABIAPLASTY PROCEDURE?


Smoking should be stopped for at least 6 weeks before any operation. Other health problems such as diabetes, heart disease, high blood pressure, or autoimmune disorders should be well-controlled before considering any surgery.


You should be cleared by your primary care physician for surgery, and have had routine preoperative tests (bloodwork, EKG), as appropriate based on your age and medical history. You should not be pregnant, and should not undergo surgery immediately before a major life event (give yourself at least 4-6 weeks to heal before a vacation, etc).


Avoid medications and herbs or nutritional supplements that can increase the risk of bleeding or bruising with surgery (aspirin, anti-inflammatories, vitamin E, fish oil, etc) - your surgeon will give you a comprehensive list of what types of things to avoid and for how long before and after surgery.

Sunday, November 1, 2009

Research pays off when choosing a breast implant surgeon

When you are considering breast augmentation, be sure to research both the procedure and your surgeon extensively.

Learn as much as you can about the procedure using online sources (visit reputable websites such as the American Society of Plastic Surgeons (ASPS) or the ASAPS website) that do not feature only one surgeon, and that provide data on national statistics and safety issues.

Visit a surgeon who is experienced with breast augmentation, and is Board-Certified by either the American Board of Medical Specialties or the Royal College of Physicians and Surgeons of Canada (these are the only two Boards recognized by the American Societies for Plastic Surgery and Aesthetic Plastic Surgery).

Write your questions down for your surgeon, and ask to see before-and-after photographs of typical (not just the best) patient results. Ask to speak to patients who have had the procedure before.

Do your homework! Ensure you have found a good fit with the surgeon in terms of personality, office environment, and aesthetic goals for the procedure.