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<strong>Florida</strong> <strong>Family</strong> Physician<br />
Official Publication <strong>of</strong> the <strong>Florida</strong> <strong>Academy</strong> <strong>of</strong> <strong>Family</strong> Physicians Winter 2008<br />
<strong>Complementary</strong><br />
& <strong>Alternative</strong><br />
<strong>Medicine</strong>
<strong>Florida</strong> <strong>Academy</strong> <strong>of</strong> <strong>Family</strong> Physicians<br />
OFFICERS<br />
President<br />
Timothy Davlantes, MD, Jacksonville<br />
President-Elect<br />
Dennis Mayeaux, MD, Milton<br />
Vice President<br />
George A.W. Smith, MD, Pensacola<br />
Secretary-Treasurer<br />
Bruce Flareau, MD, Clearwater<br />
Board Chair<br />
Cyneetha Strong, MD, Tallahassee<br />
Directors<br />
TERMS EXPIRE 2009<br />
David Feller, MD, Gainesville<br />
John Gross, MD, St. Petersburg<br />
Robert Raspa, MD, Jacksonville<br />
Coy Irvin, MD, Gulf Breeze<br />
Caroline Van Sant-Crowle, MD, Palm Harbor<br />
TERMS EXPIRE 2010<br />
Marvin Dewar, MD, Gainesville<br />
Jennifer Keehbauch, MD, Orlando<br />
Martha Price, MD, Tampa<br />
Greg Sloan, MD, Chipley<br />
Anne Waldron, MD, Jacksonville<br />
TERMS EXPIRE 2011<br />
Gregg Gutowski, MD, Plant City<br />
Amber Isley, MD, Orange Park<br />
Ira Pearlstine, MD, Port St. Lucie<br />
Marc Rivo, MD, Miami Beach<br />
Bernd Wollschlaeger, MD, Miramar<br />
EX-OFFICIO DIRECTORS<br />
(<strong>Family</strong> <strong>Medicine</strong> Department Chairs)<br />
H. James Brownlee, MD, Tampa<br />
R. Whit Curry, MD, Gainesville<br />
E. Robert Schwartz, MD, Miami<br />
Daniel J. Van Durme, MD, Tallahassee<br />
RESIDENT DIRECTORS<br />
Carrie Vey, MD, President (Daytona Beach)<br />
Brooke Orr, MD, Vice President (Clearwater)<br />
Terreze Gamble, MD, Secretary-Treasurer<br />
(Tallahassee)<br />
STUDENT DIRECTORS<br />
Catherine Crawford (University <strong>of</strong> Miami)<br />
Raj Mehta (University <strong>of</strong> <strong>Florida</strong>)<br />
Coren Menendez (University <strong>of</strong> South <strong>Florida</strong>)<br />
Kim Plumitallo (<strong>Florida</strong> State University)<br />
DELEGATES/ALTERNATE DELEGATES<br />
Delegates<br />
Alma Littles, MD, Tallahassee<br />
Dennis Saver, MD, Vero Beach<br />
Alternate Delegates<br />
Amber Isley, MD, Orange Beach<br />
Donald Twiggs, MD, Callahan<br />
<strong>Florida</strong> <strong>Family</strong> Physician<br />
Volume 57 • Issue 2<br />
<strong>Florida</strong> <strong>Academy</strong> <strong>of</strong> <strong>Family</strong> Physicians<br />
6720 Atlantic Boulevard • Jacksonville, <strong>Florida</strong> 32211-8730<br />
(904) 726-0944 • (800) 223-3237 • Fax (904) 726-0923 • www.fafp.org<br />
FAFP Staff:<br />
Tad P. Fisher, Executive Vice President (tad@fafp.org)<br />
Camille Adams, Director <strong>of</strong> CME Programs and Exhibits (camille@fafp.org)<br />
Mary Jo Griseuk, Director <strong>of</strong> Membership Development (maryjo@fafp.org)<br />
Joyce Lowe, Comptroller & Executive Assistant to the EVP (joyce@fafp.org)<br />
Annelle McClean, Director <strong>of</strong> Meeting Planning<br />
& Director <strong>of</strong> Resident & Student Relations (amcclean@fafp.org)<br />
Kathy Short, Administrative Assistant (kathy@fafp.org)<br />
FAFP Consultants:<br />
Ed Shahady, MD, Director <strong>of</strong> Centers <strong>of</strong> Office Practice Excellence (eshahady@att.net)<br />
Jim Daughton, Metz, Husband & Daughton, Legislative Consultant (jim.daughton@metzlaw.com)<br />
Christine P. Fisher, Director <strong>of</strong> Public Affairs (cpf1219@aol.com)<br />
Amanda Fliger, Moore Consulting Group, Communications Consultants (amandaf@moore-pr.com)<br />
Ray Lowe, EHR Now! Project Director (ray_lowe@comcast.net)<br />
Guest Editor:<br />
Jan Larson, MD<br />
<strong>Florida</strong> <strong>Family</strong> Physician is printed on recycled paper with soy-based inks.<br />
The opinions expressed in this publication are not necessarily those <strong>of</strong> the <strong>Florida</strong> <strong>Academy</strong> <strong>of</strong> <strong>Family</strong> Physicians.<br />
<strong>Florida</strong> <strong>Family</strong> Physician Writing Guide<br />
The <strong>Florida</strong> <strong>Academy</strong> <strong>of</strong> <strong>Family</strong> Physicians is seeking contributors for its <strong>of</strong>ficial quarterly journal on such<br />
topics as practice management and physician community involvement, as well as clinical subjects.<br />
Articles can contain up to 900 words. Photos <strong>of</strong> authors are requested but are not required. Photos should<br />
be emailed as a JPG file scanned at 400 dpi. If you are unsure, e-mail us what you have and we will have<br />
our publisher evaluate it. We are also seeking cover photos that may accompany a feature article or simply<br />
an interesting photo with a two- or three-sentence description.<br />
The editor reserves the right to edit in a reasonable manner for grammar, spelling and punctuation. If there<br />
are any questions regarding content or if any major changes are necessary, the editor will contact the author.<br />
If you have questions, please contact Christine Fisher, Managing Editor, cpf1219@aol.com.<br />
2009 Editorial Calendar<br />
Spring issue (March) copy due to FAFP by January 31, 2009<br />
Summer issue (June) copy due to FAFP by April 30, 2009<br />
Fall issue (September) copy due to FAFP by July 31, 2009<br />
The theme <strong>of</strong> the winter issue <strong>of</strong> <strong>Florida</strong> <strong>Family</strong> Physician is “Emerging Crisis — Primary Care<br />
Physician Shortage.” Please contact the Managing Editor, Christine P. Fisher, at cpf1219@aol.com,<br />
if you would like to submit an article. Letters to the editor are accepted.<br />
Published December 2008<br />
FAFP FOUNDATION OFFICERS<br />
President<br />
Daniel B. Lestage, MD, Orange Park<br />
Vice President<br />
Dennis Saver, MD, Vero Beach<br />
Treasurer<br />
Bruce Flareau, MD, Clearwater<br />
Secretary<br />
Tad Fisher, Jacksonville<br />
Amber Isley, MD<br />
Communications Chair & Editor, Orange Park<br />
Carolyn Mayeaux<br />
Editorial Assistant<br />
Editorial Board<br />
Tad P. Fisher<br />
Executive Editor, Jacksonville<br />
Christine P. Fisher<br />
Managing Editor, Jacksonville
Contents<br />
Features<br />
Medical Acupuncture . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8<br />
To Herb or Not to Herb . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 12<br />
Menopause and Botanicals . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 14<br />
CAM Primer for <strong>Family</strong> Physicians. . . . . . . . . . . . . . . . . . . . . . . . . 18<br />
Treatment <strong>of</strong> Hypertension with Nutraceuticals, Vitamins,<br />
Antioxidants and Minerals . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 20<br />
The Root Doctor. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 28<br />
Extras<br />
FAFP New England and CME Cruise on the Jewel <strong>of</strong> the Seas . . . . . 7<br />
Multiple Sclerosis . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10<br />
Departments<br />
<strong>Family</strong> <strong>Medicine</strong> in the News . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6<br />
Your FAFP Foundation at Work . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6<br />
Calendar <strong>of</strong> Events . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7<br />
Residents’ & Students’ Corner . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 30<br />
<strong>Florida</strong> <strong>Family</strong> Physician is published by Innovative Publishing Ink.<br />
10629 Henning Way, Suite 8 • Louisville, Kentucky 40241 • Phone 502.423.7272 • Fax 502.423.7979<br />
Innovative Publishing Ink specializes in creating custom magazines for associations. Please direct all inquiries to Aran Jackson, ajackson@ipipublishing.com.<br />
5
F A M I L Y M E D I C I N E I N T H E<br />
N E W S<br />
AAFP Congress <strong>of</strong> Delegates in San Diego<br />
John M. Montgomery, MD, <strong>of</strong> Jacksonville<br />
was awarded the 2008 Robert Graham<br />
Physician Executive Award by the American<br />
<strong>Academy</strong> <strong>of</strong> <strong>Family</strong> Physicians at the AAFP<br />
annual meeting in San Diego in September.<br />
This award recognizes an outstanding family<br />
physician whose executive skills in<br />
health care organizations have contributed<br />
to excellence in the provision <strong>of</strong> high-quality<br />
health care. Dr. Montgomery is vice<br />
president for pr<strong>of</strong>essional relations at Blue<br />
Cross Blue Shield <strong>of</strong> <strong>Florida</strong>. He is the<br />
immediate past president <strong>of</strong> the Duval<br />
County Medical Society, secretary and<br />
board member <strong>of</strong> the <strong>Florida</strong> Patient Safety<br />
Attending the AAFP Congress <strong>of</strong> Delegates in San Diego: Tim Davlantes, MD, FAFP president; John<br />
Montgomery, MD; Tanya Anim (FSU College <strong>of</strong> <strong>Medicine</strong>), AAFP FMIG national coordinator; Donald<br />
Twiggs, MD, alternate delegate; Amber Isley, MD, alternate delegate; Dennis Saver, MD, delegate; Alma<br />
Littles, MD, delegate; and Cyneetha Strong, MD, FAFP Board chair<br />
John M. Montgomery, MD, MPH, FAAFP; and Jim<br />
King, MD, AAFP president<br />
Corporation and member <strong>of</strong> the board and<br />
executive committee <strong>of</strong> the <strong>Florida</strong> Division<br />
<strong>of</strong> the American Cancer Society. Dr.<br />
Montgomery is also a member <strong>of</strong> the<br />
Mayor’s Council <strong>of</strong> Wellness and Physical<br />
Fitness and serves as one <strong>of</strong> the commissioners<br />
<strong>of</strong> the AMA-NMA Commission to<br />
End Health Care Disparities. He is boardcertified<br />
in family practice, a fellow <strong>of</strong> the<br />
American <strong>Academy</strong> <strong>of</strong> <strong>Family</strong> Physicians<br />
and a member <strong>of</strong> the FAFP.<br />
Congratulations to You!<br />
At the 2008 AAFP Annual Leadership<br />
Forum, <strong>Florida</strong> received a second-place<br />
award for the Highest Percentage <strong>of</strong> Increase<br />
in the Active Category in 2007 for chapters<br />
with more than 1,000 active members.<br />
Y O U R F A F P F O U N D A T I O N A T W O R K<br />
Dr. Shahady Honored with National Award<br />
The American <strong>Academy</strong> <strong>of</strong> <strong>Family</strong> Physicians and the<br />
Society <strong>of</strong> Teachers <strong>of</strong> <strong>Family</strong> <strong>Medicine</strong> selected<br />
Fernandina Beach physician Edward Shahady, MD, honoring<br />
him as the national winner <strong>of</strong> the 2008 Medical<br />
Economics Award for Innovation in Practice<br />
Improvement. The award was given for his work in<br />
developing the Diabetes Master Clinician Program.<br />
Developed as a project <strong>of</strong> the FAFP Foundation, the goal<br />
<strong>of</strong> the DMCP is to help primary care physicians and<br />
their patients manage diabetes by implementing an<br />
Internet-based diabetes registry and improving the quality<br />
<strong>of</strong> care through group visits. Currently, 80 <strong>Florida</strong><br />
practices participate in the program, with 13,000<br />
patients in the registry. Dr. Shahady is the medical director<br />
<strong>of</strong> the DMCP and has more than 40 years <strong>of</strong> experience<br />
with advising on prevention and treatment <strong>of</strong> the<br />
disease. He is a member <strong>of</strong> the AAFP and the FAFP and<br />
is also a past president <strong>of</strong> both the Society <strong>of</strong> Teachers <strong>of</strong><br />
<strong>Family</strong> <strong>Medicine</strong> and its Foundation. He continues to be<br />
an active leader and innovator for family medicine. Dr.<br />
Shahady received his award at the AAFP Conference on<br />
Practice Improvement on December 6 in Savannah.
FAFP New England and CME<br />
Cruise on the Jewel <strong>of</strong> the Seas<br />
FAFP Future Meetings<br />
March 27-29, 2009<br />
102nd <strong>Family</strong> <strong>Medicine</strong> Weekend<br />
Bay Point Marriott Golf Resort & Spa<br />
Panama City<br />
July 16-19, 2009<br />
2009 Summer Break Away<br />
Boca Raton Resort & Club<br />
C A L E N D A R O F E V E N T S<br />
November 13-15, 2009<br />
103rd <strong>Family</strong> <strong>Medicine</strong> Weekend<br />
Buena Vista Palace<br />
Lake Buena Vista<br />
<strong>Florida</strong> <strong>Family</strong> Physician 7
MEDICAL ACUPUNCTURE<br />
A COMPLEMENT TO YOUR PRACTICE<br />
by Kirksak Jay Poonkasem, MD, LMT, Administrative Fellow, University <strong>of</strong> South <strong>Florida</strong>/Morton Plant Mease <strong>Family</strong> <strong>Medicine</strong><br />
Residency, Integrative <strong>Medicine</strong> Fellow, University <strong>of</strong> Arizona College <strong>of</strong> <strong>Medicine</strong> – Center for Integrative <strong>Medicine</strong><br />
“Mrs. J, could you please tell me what food you have the most affinity for,<br />
given no restrictions at all What about your favorite color What time <strong>of</strong><br />
the year do you look forward to the most” These are not the standard<br />
types <strong>of</strong> questions that we ask patients in our primary care practices. I was<br />
not trained to ask such questions while I was in medical school, and most<br />
likely, you were not either. However, you will hear these questions being<br />
asked by practitioners trained in the Eastern philosophies <strong>of</strong> medicine.<br />
Several months ago, I embarked on a journey to explore other worlds and<br />
discover fresh ideas for treating my patients. To expand my mind and to<br />
look at medicine from a totally new perspective, I took part in a medical<br />
acupuncture course for physicians. Interestingly, I found physicians from<br />
all specialties <strong>of</strong> medicine participating in this course (family medicine,<br />
internal medicine, surgery, physical medicine and rehabilitation, sports<br />
medicine, anesthesiology, pain management, OB/GYN, etc.).<br />
Most physicians have heard about acupuncture but do not understand it.<br />
It can be difficult for us to understand the Eastern medical philosophies<br />
and accept them because they are so different from the philosophies our<br />
minds draw from when we see patients. To most <strong>of</strong> us, the concepts <strong>of</strong><br />
“energy,” and yin and yang are foreign and, at best, theoretical. With a little<br />
background information, you can begin to realize the intricacies and<br />
the foundations <strong>of</strong> this type <strong>of</strong> medicine. A full discussion <strong>of</strong> the theory <strong>of</strong><br />
acupuncture is beyond the scope <strong>of</strong> this article, but a simplified explanation<br />
will suffice.<br />
According to acupuncture theory, an energetic entity called Qi (pronounced<br />
“chee”) flows throughout the body. There are different types <strong>of</strong><br />
Qi, and each type has its own properties and functions. Qi flows throughout<br />
the body through a multitude <strong>of</strong> energy channels called meridians. In<br />
a balanced and disease-free state, the energy flow is smooth and uninterrupted.<br />
When minor symptoms occur or diagnosable diseases are present,<br />
it is said that the energetic system <strong>of</strong> the body is out <strong>of</strong> balance and/or that<br />
the Qi flow is impeded or blocked. With careful placement <strong>of</strong> acupuncture<br />
needles at points along the meridians, we strive to unblock and rebalance<br />
the energetic system <strong>of</strong> the body.<br />
My current medical acupuncture course has continued to open my eyes to<br />
ways we can use this to help our patients every day, either in a hospital or<br />
<strong>of</strong>fice setting. Can you imagine decreasing the length <strong>of</strong> a patient’s stay<br />
with post-operative ileus using acupuncture Or making a patient more<br />
comfortable post-operatively by managing pain with only a few acupuncture<br />
needles Helping a patient to quit smoking non-pharmacologically, to<br />
tolerate chemotherapy better or to finally be rid <strong>of</strong> that bothersome tennis<br />
elbow These are just some <strong>of</strong> the possibilities. Practitioners are using<br />
acupuncture to treat these and many other conditions all over the country<br />
and the world!<br />
Many people inquire about the safety <strong>of</strong> acupuncture. The needles that I,<br />
and most physicians, use in practice are sterile, disposable needles that are<br />
meant for one-time use. The standard acupuncture needles that I use for<br />
the body are 0.25 mm in diameter and 40 mm in length. These needles are<br />
Dr. Poonkasem treating a patient with lateral epicondylitis<br />
different from the hypodermic needles we are accustomed to using.<br />
They are solid, non-cored and non-beveled. Acupuncture needles<br />
separate tissue as they are inserted rather than cutting the tissue.<br />
There is also no need to be concerned with introducing the skin plug<br />
down to the deeper tissue levels.<br />
Complications from acupuncture are very few. Some patients may experience<br />
“needle shock,” which is a vaso-vagal reaction to being needled.<br />
Most contraindications are relative. Patients should be evaluated on a<br />
case-by-case basis to determine if acupuncture is right for them.<br />
There is abundant literature available describing many randomized,<br />
controlled trials on acupuncture. Due to the nature <strong>of</strong> the modality, it is<br />
challenging to design acupuncture studies. Every patient is evaluated separately,<br />
and treatments are highly individualized.<br />
From my experience thus far, belief (or disbelief) in acupuncture is not<br />
necessary for it to work. Acupuncture has even been performed on animals<br />
with positive results. <strong>Family</strong>, friends and patients whom I have<br />
treated with acupuncture embrace it because they see results. As I near<br />
the completion <strong>of</strong> my medical acupuncture program, I can see that it<br />
has transformed how I evaluate and treat patients while never neglecting<br />
the standard <strong>of</strong> care. Acupuncture has been a great adjunct to my<br />
current practices.<br />
The American <strong>Academy</strong> <strong>of</strong> Medical Acupuncture is an outstanding<br />
resource for more information about medical acupuncture. If<br />
you are interested in incorporating this into your practice, a list<br />
<strong>of</strong> training programs is available on their Web site, at<br />
http://www.medicalacupuncture.org. You may also contact me<br />
for more information at kirksak.poonkasem@baycare.org.<br />
8
The FAFP Partners with<br />
Atlantic Health Partners<br />
The <strong>Florida</strong> <strong>Academy</strong> <strong>of</strong> <strong>Family</strong> Physicians is pleased to announce a partnership with Atlantic<br />
Health Partners, a leading physician vaccine-purchasing program. With the increased burden<br />
you face providing a growing number <strong>of</strong> vaccines to your patients in a fiscally responsible<br />
manner, Atlantic may be able to help lower your costs and improve your purchasing terms.<br />
Advantages <strong>of</strong> Atlantic’s program include:<br />
• Favorable pricing for san<strong>of</strong>i pasteur and Merck vaccines<br />
• Improved purchasing terms, as you do not need to make large,<br />
multi-product orders<br />
• No fee to participate and enrollment is voluntary<br />
• Online or phone orders placed directly with san<strong>of</strong>i pasteur and Merck<br />
• Full spectrum <strong>of</strong> pediatric, adolescent, adult and travel vaccines<br />
• Reimbursement support provided by Atlantic<br />
We encourage you to contact Jeff Winokur at Atlantic Health Partners at (800) 741-2044 or jwinokur@atlantichealthpartners.com<br />
for more information and to determine how Atlantic can benefit your practice.
MULTIPLE<br />
SCLEROSIS<br />
by Megan W. Barrett,<br />
MSN, ARNP-c, Multiple<br />
Sclerosis Certified Nurse;<br />
Research Advocate, North<br />
<strong>Florida</strong> Chapter, National<br />
MS Society<br />
Important Information<br />
for the <strong>Family</strong> Physician<br />
Multiple sclerosis (MS) is a chronic, unpredictable,<br />
usually relapsing-remitting, demyelinating<br />
disease <strong>of</strong> the central nervous system.<br />
A specific cause has not been identified;<br />
however, the etiological associations include<br />
genetic predisposition, environmental triggers<br />
and autoimmunity. 1 MS is the most common<br />
neurological disease in people under the age <strong>of</strong> 40, and it<br />
afflicts more than 400,000 Americans. 2 Its diagnosis is one <strong>of</strong><br />
exclusion, and its symptomatology mimics that <strong>of</strong> many other conditions<br />
with which people present to their family physicians (FPs).<br />
The Institute for Healthcare Improvement, the Robert Wood Johnson<br />
Foundation, the U.S. Department <strong>of</strong> Health and Human Services and<br />
the World Health Organization recognize appropriate management<br />
<strong>of</strong> chronic illness as a problem in care delivery. The chronicity <strong>of</strong><br />
MS, coupled with the fact that the lifespan <strong>of</strong> people with the disease<br />
is similar to that <strong>of</strong> people without it, mandate the need for FPs<br />
to be familiar with the neurological aspects <strong>of</strong> the disease, as well as<br />
the primary care needs <strong>of</strong> people with it. 3, 4<br />
The most common comorbid conditions in people with MS are<br />
hypertension, hypercholesterolemia, arthritis, irritable bowel syndrome<br />
and chronic lung disaease. 5 Unfortunately, people with MS<br />
tend to lack knowledge about other chronic diseases, and may also<br />
dismiss the possibility <strong>of</strong> acquiring a second chronic illness. 6 The<br />
Approximately 85 percent <strong>of</strong> people with MS start out with a<br />
relapsing-remitting course, and about half <strong>of</strong> these people will<br />
experience secondary progressive disease after 10 years. Less<br />
common types <strong>of</strong> MS include primary progressive (10 percent)<br />
and progressive relapsing (5 percent). There are six available disease-modifying<br />
agents for MS: Avonex (interferon beta 1a),<br />
Betaseron (interferon beta 1b), Copaxone (glatiramir acetate);<br />
Rebif (interferon beta 1a, Novantrone (mitoxantrone) and Tysabri<br />
(natalizumab). 1 These medications require monitoring for adherence,<br />
site reactions and/or systemic side effects. The most common<br />
primary care needs <strong>of</strong> people with MS relate to bladder and bowel<br />
symptoms, fatigue, sexual dysfunction, depression, acute bacterial<br />
or viral illness and pseudoexacerbation related to the latter. A<br />
patient’s neurologist may be managing disease-modifying and<br />
symptomatic treatment; however, the FP should be well-versed in<br />
the drugs used to treat the common symptoms, as well as the monitoring<br />
required for the disease-modifying agents in order to ensure<br />
that essential elements <strong>of</strong> chronic illness care are provided.<br />
Collaboration between the neurologist and FP is vital in the care <strong>of</strong><br />
these patients in order to maintain their health and prevent the<br />
development <strong>of</strong> secondary conditions.<br />
10
influence <strong>of</strong> the FP is extremely important in these cases. Barriers<br />
to primary care, including physical barriers to access, patient frustration<br />
with lack <strong>of</strong> primary care provider familiarity or experience<br />
with MS and erroneous assumptions, have been identified in the literature<br />
as significant roadblocks to the receipt <strong>of</strong> recommended<br />
preventive screening in this population. 3, 7-10 The literature also suggests<br />
that recommended screening and counseling needs are not<br />
being met in the MS population. So what can a busy FP do to<br />
provide appropriate preventive care to this vulnerable population<br />
Primarily, consider the disability-friendliness <strong>of</strong> your <strong>of</strong>fice environment.<br />
Secondly, make sure that patients with MS are scheduled for<br />
preventive health screening visits. If a patient presents to the <strong>of</strong>fice<br />
for an acute illness, be sure to review screening history at the visit,<br />
and schedule testing and follow-up appointments if needed. Thirdly,<br />
be aware <strong>of</strong> your closest comprehensive MS center, local neurologists,<br />
rehabilitation and counseling services, and social and community<br />
services. Such information can be readily found on the National<br />
MS Society’s Web site, http://www.nationalmssociety.org.<br />
While a cure for MS has yet to be discovered, recent progress has<br />
been made in all <strong>of</strong> the proposed etiological areas contributing to the<br />
disease. Susceptibility genes have been reported, environmental risk<br />
factors identified, new therapies targeting autoimmunity and nerve<br />
protection are being studied, advanced rehabilitation techniques are<br />
being used, and advocacy for people with MS is on the rise.<br />
Encouraging healthy lifestyles and being the stimulus for preventive<br />
care in this population will increase the likelihood <strong>of</strong> a healthy life<br />
for people with MS.<br />
Disclosure: The author serves on speakers’ bureaus for Bayer, Biogen-Idec,<br />
Serono-Pfizer and Teva Neuroscience.<br />
References<br />
1. http://www.nationalmssociety.org<br />
2. Holland, N. Clinical bulletin: Information for health pr<strong>of</strong>essionals –<br />
Overview <strong>of</strong> multiple sclerosis. Retrieved September 7, 2008, from National<br />
MS Society Web site: http://www.nationalmssociety.org/for-pr<strong>of</strong>essionals/<br />
publications/clinicalbulletins/download.aspxid=161, 2006.<br />
3. Cheng, E., Myers, L., Wolf, S., Shatin, D., Cui, X., Ellison, G., et al.<br />
Mobility impairments and use <strong>of</strong> preventive services in women with multiple<br />
sclerosis: observational study. British Medical Journal, 2001; 323: 968-969.<br />
4. The National Coalition on Health Care, The Institute for Healthcare<br />
Improvement. Curing the system: Stories <strong>of</strong> change in chronic illness care.<br />
From http://www.ihi.org/IHI/Topics/ChronicConditions/<br />
AllConditions/Literature/ CuringthesystemStories <strong>of</strong>changeinchronicillness.htm<br />
5. Marie, R., Cutter, G., Tyry, T., Vollmer, T., & Campagnolo, D. Comorbid conditions<br />
are common in multiple sclerosis. Paper presented at the Consortium <strong>of</strong><br />
Multiple Sclerosis Centers, 2007.<br />
6. O’Connell, D. When the diagnosis is MS...& something else. InsideMS,<br />
2005; June-July: 50-53.<br />
7. Beatty, P., Hagglund, K., Neri, M., Dhont, K., Clark, M., & Hilton, S. Access<br />
to health care services among people with chronic or disabling conditions: patterns<br />
and predictors. Archives <strong>of</strong> Physical <strong>Medicine</strong> and Rehabilitation, 2003;<br />
84: 1417-1425.<br />
8. DeJong, G. An overview <strong>of</strong> the problem. American Journal <strong>of</strong> Physical<br />
<strong>Medicine</strong> & Rehabilitation, 1997; 76(3): 2-8.<br />
9. Tezzoni, L., McCarthy, E., Davis, R., Harris-Davis, L., & O’Day, B. Use <strong>of</strong><br />
screening and preventive services among women with disabilities. American<br />
Journal <strong>of</strong> Medical Quality, 2001; 16(4): 135-144.<br />
10. Nosek, M. H., B., Rintala, D., Young, M., & Chanpong, G. National study<br />
<strong>of</strong> women with physical disabilities: Final report. Sexuality and Disability,<br />
2001; 19(1): 5-39.<br />
<strong>Florida</strong> <strong>Family</strong> Physician 11
y Diego T. Torres II, MD,<br />
Ormond Beach<br />
To Herb<br />
or Not to Herb<br />
Herbal medicine use has increased approximately 380 percent since<br />
1990. Market sales have reached an estimated $3.4 billion annually. 1,2<br />
Eisenberg et al. recently reported that the use <strong>of</strong> complementary<br />
therapies was more common among women, middle-aged, collegeeducated<br />
and higher-income individuals. Almost one in five people in<br />
the survey taking herbs and/or high-dose vitamins were also taking<br />
prescribed medicines. 1 Another large national survey revealed that only<br />
one-third <strong>of</strong> the adults who reported using herbal supplements did so<br />
“in accordance with evidence-based indications.” 3 Surprisingly, a study<br />
by the Stanford University Center for Research in Disease Prevention<br />
showed that dissatisfaction with traditional allopathic medicine was<br />
NOT a predictor <strong>of</strong> herbal use. The most important variable was that<br />
alternative medicine parallels their own values and health philosophy.<br />
Poor health status, back pain, allergies and digestive and lung problems<br />
were also measures for the use <strong>of</strong> complementary treatments. 4 The purpose<br />
<strong>of</strong> this article is to emphasize this dynamic and review the riskbenefit<br />
pr<strong>of</strong>iles <strong>of</strong> a few <strong>of</strong> the top herbs based on reported use. I hope<br />
this will encourage dialogue between primary care physicians and their<br />
patients and raise awareness <strong>of</strong> not only potential benefits <strong>of</strong> herbal<br />
medicines in select populations, but also the potential drug-herb interactions<br />
that put an estimated 15 million adults at risk. 1<br />
Echinacea<br />
Echinacea is among the most popular herbal medicines used in North<br />
America, reaching annual sales <strong>of</strong> more than $300 million. 2,5 It is a member<br />
<strong>of</strong> the daisy family, and its potentially active compounds have<br />
immunostimulatory as well as anti-inflammatory, anesthetic, antiviral,<br />
antineoplastic and antioxidant activity. 6-9 It is used for the treatment and<br />
prophylaxis <strong>of</strong> upper respiratory infections. 5,6,8 Standard dosing is 250 to<br />
500 mg <strong>of</strong> the capsule form t.i.d. at the onset <strong>of</strong> symptoms. 8 In vitro,<br />
E. purpurea has been shown to increase TNF-α and interleukins, thus<br />
activating macrophages and increasing neutrophil phagocytosis. 5,7,9<br />
Experts, therefore, warn <strong>of</strong> its use in patients who may need immunosuppression,<br />
such as those awaiting organ transplantation and patients diagnosed<br />
with systemic illnesses such as TB, HIV/AIDS, multiple sclerosis<br />
and autoimmune disease. 6,8 However, it has been reported that long-term<br />
use (more than eight weeks) has been associated with immunosuppression<br />
and can, therefore, increase the risk <strong>of</strong> infection and cause poor<br />
wound healing. 6<br />
Due to the immunostimulatory effects <strong>of</strong> Echinacea, allergic reactions<br />
are the most commonly reported side effects. 6,7 Thus, caution should be<br />
taken in patients with a history <strong>of</strong> asthma and atopy. 6 An Australian<br />
Advisory Committee has reported cases <strong>of</strong> hepatitis, asthma, rash and<br />
anaphylaxis in conjunction with Echinacea use. 7 A small Canadian<br />
study published in 2000 was the first to prospectively study fetal safety<br />
after gestational use <strong>of</strong> Echinacea. Findings showed that “the rate <strong>of</strong><br />
major malformations between the study and control groups were not<br />
statistically significant.” 2<br />
Furthermore, a University <strong>of</strong> Washington study showed that<br />
Echinacea was not effective in 2- through 11-year olds treated for<br />
URI symptoms and it increased the risk <strong>of</strong> rash. 5 The PDR for<br />
Herbal <strong>Medicine</strong>s, Third Edition, reports reduced sperm motility<br />
and velocity after contact with donor sperm. Echinacea has also<br />
been shown to inhibit CYP 450 3A4, and caution is advised with coadministration<br />
<strong>of</strong> medications that act as substrates. 9<br />
Ginko Biloba<br />
Ginko Biloba is a fossil tree that has not changed in more than 200<br />
million years and has a high tolerance to pollution, insects and microorganisms.<br />
10 It has been marketed as a memory enhancer and is used in<br />
clinical practice for dementia, tinnitus and claudication. 7,11 It has also<br />
been used experimentally for macular degeneration (age-related), vertigo,<br />
erectile dysfunction and altitude sickness. 6,7 The most common<br />
dosage used clinically is 40 mg t.i.d. Sales reached approximately $151<br />
million in 1998. 7<br />
Active components, especially the ginkolides, antagonize platelet-activating<br />
factor (PAF). PAF causes platelet aggregation, promotes inflammation<br />
and contracts smooth muscle (including bronchial). 10 Studies show in<br />
vitro and in vivo actions against edema, hypoxia, free-radicals and platelet<br />
aggregation. 7 In addition to improving cerebral capillary blood flow, it has<br />
been observed that Ginko is an inhibitor <strong>of</strong> monoamine oxidase A and<br />
B. 10,11 Thus, its actions with respect to dementia are due to vasoregulation<br />
and neurotransmitter modulation. 6 High-quality studies suggest Ginko is<br />
12
more effective than placebo in slowing cognitive decline in dementia. The<br />
evidence for enhancing normal cognitive function is not as compelling. A<br />
review <strong>of</strong> clinical trials for its use in tinnitus showed a statistically significant<br />
effect on the perceived loudness <strong>of</strong> ringing after 12 weeks <strong>of</strong><br />
treatment. Furthermore, European studies have shown similarities in<br />
effectiveness between Ginko and pentoxifylline for claudication. 7<br />
The adverse effects <strong>of</strong> Ginko are usually mild and reversible, but serious<br />
bleeding events have been reported. Due to its antiplatelet effect, it may<br />
increase the action <strong>of</strong> warfarin. It is recommended to discontinue Ginko<br />
use at least 36 hours prior to surgery. Intracranial bleeding, seizures and<br />
post-operative bleeding have been reported. 6,7<br />
St. John’s Wort<br />
St. John’s Wort (Hypericum perferatum) grows as a common weed in the<br />
United States. 12 It is used almost exclusively now as an antidepressant,<br />
with clinical trials supporting its use in mild-to-moderate depression but<br />
not in major depression. 6,7,13 The dosage is 300 mg <strong>of</strong> extract t.i.d. 8,9 It is<br />
one <strong>of</strong> the most prescribed antidepressants in Europe, and U.S. sales<br />
reached $86 million in 2000. 12,14<br />
Many <strong>of</strong> the active compounds <strong>of</strong> Hypericum have been shown to inhibit<br />
the reuptake <strong>of</strong> serotonin, dopamine and norepinephrine. 6,7,12 It has been<br />
shown to be more effective than placebo and equivalent to imipramine,<br />
amitriptyline and fluoxetine in improving depression scores. 7,9 Anxiolytic<br />
effects have also been described most likely through Hypericum’s effects<br />
on L-glutamate and GABA. Reversal <strong>of</strong> this effect has been shown after<br />
administration <strong>of</strong> the benzodiazepine antagonist flumazenil. 9 Hypericin, a<br />
component <strong>of</strong> St. John’s Wort, inhibits colon cancer cells in vitro. Other<br />
reported effects include antioxidant, antiviral and antibacterial activity.<br />
Another fraction has shown activity against S. aureus (including MRSA)<br />
and H. pylori.<br />
References<br />
1. Eisenberg, D. et al. Trends in alternative medicine use in the United States, 1990-<br />
1997. JAMA. 1998: 280: 1569-1575.<br />
2. Gallo, M. et al. Pregnancy outcome following gestational exposure to Echinacea.<br />
Arch Intern Med. 2000: 160: 3141-3143.<br />
3. Bardia, A. et al. Use <strong>of</strong> herbs among adults based on evidence-based indications:<br />
Findings from the National Health Interview Survey. Mayo Clin Proc. 2007 May:<br />
82(5): 561-566.<br />
4. Astin, J. Why patients use alternative medicine. JAMA. 1998: 279: 1548-1553.<br />
5. Taylor, J. et al. Efficacy and safety <strong>of</strong> Echinacea in treating upper respiratory infections<br />
in children. JAMA. 2003: 290: 2824-2830.<br />
6. Ang-Lee, M. et al. Herbal medicines and perioperative care. JAMA.<br />
2001: 286: 208-216.<br />
7. Ernst, E. The risk-benefit pr<strong>of</strong>ile <strong>of</strong> commonly used herbal therapies:<br />
ginko, St. John’s Wort, Ginseng, Echinacea, Saw Palmetto, and Kava. Ann<br />
Intern Med. 2002: 136: 42-53.<br />
8. Debusk, R. and Treadwell, P. Herbs as <strong>Medicine</strong>. What You Should Know. 2000.<br />
Debusk Communications, Tallahassee, <strong>Florida</strong>, USA.<br />
9. PDR for Herbal <strong>Medicine</strong>s, Third Edition. 2004. Thomson PDR, Montvale, NJ.<br />
10Oken, B. et al. The efficacy <strong>of</strong> Ginko biloba on cognitive function in Alzheimer<br />
disease. Arch Neurol. 1998: 55: 1409-1415.<br />
11. Palacioz, K. Ginko for memory. Prescriber’s Letter detail-document #180926.<br />
Sept. 2002; Vol 18: #180926.<br />
12. Gaster, B. and Holroyd, J. St. John’s Wort for depression. Arch Intern Med.<br />
2000: 160: 152-156.<br />
13. Markowitz, J. et al. Effect <strong>of</strong> St. John’s Wort on drug metabolism by induction<br />
<strong>of</strong> cytochrome P450 3A4 enzyme. JAMA. 2003: 290: 1500-1504.<br />
14. Lecrubier, Y. et al. Efficacy <strong>of</strong> St. John’s Wort extract WS 5570 in major<br />
depression: A double-blind, placebo-controlled trial. Am J Psychiatry. 2002:<br />
159: 1361-1366.<br />
The most common side effects are nausea, rash and photosensitivity. 7-9,12<br />
The suggested mechanism for herb-drug interactions is by induction <strong>of</strong><br />
CYP 450 3A4 and the P-glycoprotein drug efflux transporter. Therefore,<br />
St. John’s Wort can significantly increase the metabolism <strong>of</strong> many drugs,<br />
causing reduced levels <strong>of</strong> such medicines as amiodarone, digoxin,<br />
cyclosporine, anti-retrovirals, anticoagulants, ß-blockers and calcium<br />
channel blockers. 6,7,9,13 Blood levels <strong>of</strong> oral contraceptives may also be<br />
reduced, resulting in unwanted pregnancy. 9,13 Expert opinion also concurs<br />
with a theoretical possibility <strong>of</strong> serotonin syndrome in conjunction with<br />
SSRIs and MAOIs. 6-9 Mania and hypomania have also been reported. St.<br />
John’s Wort is contraindicated in pregnancy, and in vitro studies showed<br />
mutagenicity in sperm cells.<br />
In conclusion, the Dietary Supplement Health and Educations Act <strong>of</strong> 1994<br />
exempts herbal supplements from safety and efficacy requirements, such<br />
as those regulating prescription drugs. 3,6 The herbal industry claims it cannot<br />
sustain the costs <strong>of</strong> long-term studies, but retail sales prove otherwise. 7<br />
Healthy patients who lack polypharmacy may indeed find benefit from<br />
herbal supplements. Unfortunately, the public perceives herbal medicines<br />
as safe when there are not many high-quality studies supporting their indications.<br />
Furthermore, potency and pesticide, herbicide and heavy-metal<br />
content <strong>of</strong> herbal products is controversial. 7 I fear that the use <strong>of</strong> herbal supplements<br />
is severely underreported, as most sample populations do not<br />
include non-English-speaking minorities. 4 It is our duty to promote safety<br />
and encourage discussions with our patients. The clinical importance <strong>of</strong><br />
this dialogue is magnified not only by the potential for drug-herb interactions,<br />
but also by large population surveys that suggest that only one-third<br />
<strong>of</strong> patients may be using herbs for their evidence-based indications. 3
y Kathy D. Sella, MD,<br />
PGY-2, Mayo <strong>Family</strong><br />
<strong>Medicine</strong> Residency,<br />
Jacksonville<br />
Menopause and<br />
The term menopause is derived<br />
from two Greek words:<br />
“meno,” which translates into<br />
“month,” and “pausis,” which<br />
means “cessation.” Together,<br />
they literally mean “last menstruation.”<br />
A modern definition<br />
<strong>of</strong> the term has defined it as the<br />
absence <strong>of</strong> menses for a full<br />
year and does not differentiate<br />
the underlying mechanism. It is<br />
during this average four-year 1<br />
period leading up to menopause<br />
that women may experience a<br />
variety <strong>of</strong> symptoms related to<br />
fluctuating hormonal levels,<br />
notably decreasing levels <strong>of</strong><br />
estrogen and progesterone. 2<br />
Perimenopausal symptoms include vasomotor<br />
symptoms, urinary incontinence, vaginal<br />
atrophy, disrupted sleep, sexual dysfunction<br />
and mood disorders. The most dominant <strong>of</strong><br />
these symptoms include vasomotor symptoms,<br />
including hot flashes and night<br />
sweats. Hot flashes occur in as many as 75<br />
percent <strong>of</strong> Western females over the age <strong>of</strong><br />
50 years old, but rates vary with age and<br />
ethnicity. 3 The SWAN study showed that<br />
presentation <strong>of</strong> symptoms varies between<br />
racial groups, with white American women<br />
experiencing higher rates <strong>of</strong> psychomotor<br />
symptoms than other ethic/racial groups,<br />
and African-Americans experiencing more<br />
vasomotor symptoms. 4<br />
Women <strong>of</strong>ten seek treatment for perimenopausal<br />
symptoms. Traditionally, hormone<br />
replacement therapy (HRT) was used<br />
for symptomatic relief. However, the<br />
Women’s Heath Initiative questioned the<br />
safety <strong>of</strong> this therapy, and many women<br />
began to seek out alternatives, leading to<br />
increased research in botanical and dietary<br />
supplements. Studies have shown that 44 to<br />
66 percent <strong>of</strong> menopausal women use botanical<br />
dietary supplements, <strong>of</strong>ten in addition<br />
to hormone replacement therapy. 5,6 Often,<br />
women do not receive advice from their<br />
health care providers, nor do they make<br />
records <strong>of</strong> their use <strong>of</strong> botanicals. Vashisht,<br />
Domoney, Cronje and Studd 6 concluded that<br />
physicians were the primary source <strong>of</strong><br />
information regarding botanicals for<br />
menopausal women less than 20 percent <strong>of</strong><br />
the time. Fortunately, a University <strong>of</strong><br />
Chicago study found that health care<br />
providers were willing to increase their<br />
knowledge and usage regarding these<br />
alternative treatments. 7 The most commonly<br />
used botanicals for menopausal symptoms<br />
include black cohosh, evening<br />
primrose oil, red clover, dong quai and soy<br />
is<strong>of</strong>lavones. Numerous studies have evaluated<br />
the effectiveness, safety and side<br />
effects <strong>of</strong> these botanicals.<br />
Black cohosh is a native North American<br />
plant that has been studied for many years.<br />
A common preparation <strong>of</strong> this herb is<br />
Remifemin, with daily dosing recommendations<br />
between 40 to 80mg/day. It has<br />
been the target <strong>of</strong> clinical trials that generally<br />
show supportive evidence for the<br />
treatment <strong>of</strong> menopausal symptoms such<br />
as hot flashes, pr<strong>of</strong>use sweating, insomnia<br />
and anxiety. However, many studies have<br />
been limited by methodology, and further<br />
evaluation is needed. 8<br />
The herb is noted to have minor transient<br />
side effects, including nausea, vomiting,<br />
headaches, dizziness, mastalgia and weight<br />
gain. There have been case reports <strong>of</strong> hepatotoxicity<br />
associated with black cohosh, but<br />
direct correlation has not been demonstrated,<br />
and previous safety trials on the herb<br />
have shown it to be safe for daily usage.<br />
However, the U.S. Pharmacopecia Council<br />
<strong>of</strong> Experts recently reviewed reports <strong>of</strong><br />
liver damage possibly connected to black<br />
cohosh and concluded that, while all<br />
reports <strong>of</strong> “liver damage were assigned<br />
possible causality, none were probable<br />
or cer tain causality.” 9 The Dietar y<br />
Supplemental Expert committee did conclude<br />
that black cohosh products should<br />
bear a warning label.<br />
The mechanism <strong>of</strong> action <strong>of</strong> black cohosh is<br />
poorly understood, but a small 2007 study<br />
from Columbia University on postmenopausal<br />
women showed the herb to<br />
have central nervous system effects,<br />
specifically on the mu receptors with up<br />
regulation and down regulation in different<br />
parts <strong>of</strong> the brain. However, this effect had<br />
also been seen in placebos in prior studies. 10<br />
The study was able to conclude that black<br />
cohosh did not have an estrogen-like effect<br />
on the opiod activity restoration. 10 The<br />
HALT study also concluded that black<br />
cohosh, when taken for vasomotor symptoms,<br />
after one year <strong>of</strong> use had no effect on<br />
vaginal cytology or reproductive hormones,<br />
notably follicle stimulating hormone<br />
(FSH), luteinizing hormone or estradiol. 11<br />
Perimenopausal women with a history <strong>of</strong><br />
breast cancer may have another benefit.<br />
Some evidence shows that black cohosh<br />
is safe for this subset <strong>of</strong> the population<br />
and may even have some tumor-growthinhibiting<br />
properties. 12<br />
14
Botanicals<br />
Evening primrose oil is another North<br />
American plant with high levels <strong>of</strong> linoleic<br />
and gamma linolenic acid. Daily dosing recommendations<br />
vary from 3 to 6 grams/day<br />
with some preparations containing Vitamin<br />
E as a natural stabilizer. Mild side effects<br />
noted included bloating, nausea, flatulence<br />
and diarrhea. 8 A small, randomized trial <strong>of</strong><br />
56 females in menopause (with only 35<br />
completing the study) were given either 2<br />
grams <strong>of</strong> evening primrose oil per day or a<br />
placebo. The only significant difference was<br />
a reduced number <strong>of</strong> nighttime flushes over<br />
baseline (P
with Shanghai Endometrial Cancer Study<br />
found that postmenopausal women did not<br />
have an increased risk <strong>of</strong> endometrial cancer<br />
with consumption <strong>of</strong> soy is<strong>of</strong>lavones<br />
whether or not at least one A allele<br />
<strong>of</strong> the rs605059 polymorphism <strong>of</strong> the<br />
17Éß-hydroxysteroid dehydrogenase type I<br />
(17Éß-HSD1) gene was present. 19 17Éß-<br />
HSD1 is the final step <strong>of</strong> the estrogen pathway,<br />
converting estrone (E1) to the more<br />
biologically active estradiol (E2). 19<br />
Soy is<strong>of</strong>lavones do appear to have an effect<br />
on breast tissue in a biphasic manner,<br />
dependent on estrogen levels. In a recent<br />
in-vitro study by Imh<strong>of</strong>, Imh<strong>of</strong> and Molzer,<br />
in MCF-7 (ER +) breast cancer cells<br />
showing unphysiologically low levels <strong>of</strong><br />
estrogen (
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<strong>Florida</strong> <strong>Family</strong> Physician 17
y David B. Feller, MD,<br />
Clinical Associate<br />
Pr<strong>of</strong>essor, University <strong>of</strong><br />
<strong>Florida</strong> College <strong>of</strong><br />
<strong>Medicine</strong>, Gainesville<br />
CAM<br />
Primer for <strong>Family</strong><br />
Physicians<br />
<strong>Complementary</strong> and alternative medicine (CAM) represents a broad range <strong>of</strong> healing philosophies, approaches and<br />
therapies. In general, CAM has been defined as treatments and health care practices not taught widely in medical<br />
schools, nor used in hospitals or usually reimbursed by medical insurance companies. What is considered CAM<br />
versus a standard therapy may change depending upon the historical period, the particular culture or the politically<br />
dominant health system. Common examples include homeopathy, herbal medicine, TCM (traditional Chinese<br />
medicine, which includes acupuncture, herbals and energy therapies), chiropractic manipulation, Ayurvedic medicine,<br />
chelation therapy, mind-body medicine and therapeutic touch.<br />
Despite the fact that most physicians have minimal formal training<br />
with these modalities, our patients commonly use them. Eisenberg’s<br />
(JAMA, 1998. 280(18):1569-75) highly publicized survey demonstrated<br />
that more than 42 percent <strong>of</strong> patients used some type <strong>of</strong> alternative<br />
therapy. More recent studies have suggested that nearly 50<br />
percent <strong>of</strong> patients (including physicians themselves) used CAM at<br />
some point. Even with CAM’s increasing popularity, patients are<br />
<strong>of</strong>ten hesitant to tell their physicians they are using it. Surveys<br />
demonstrate patients only volunteer the information about CAM use<br />
about one-third <strong>of</strong> the time, so direct questioning is essential.<br />
So why do our patients use CAM Well, modern Western medicine<br />
just doesn’t hold all the answers to many <strong>of</strong> our common medical<br />
problems. In addition, many <strong>of</strong> our patients perceive significant risk<br />
with our usual allopathic therapies (recall the hype associated with<br />
the recall <strong>of</strong> Baycol and Vioxx and the recent estrogen “scare”). It’s<br />
not surprising, then, that our patients look for other modalities that<br />
are perceived as either safer or more effective. Unfortunately, this<br />
perception that CAM is either safer or better than traditional therapies<br />
can be faulty. It, therefore, becomes important that physicians<br />
become familiar with CAM modalities enough to provide<br />
reasonable guidance to our patients. Any therapy (traditional or not)<br />
prescribed to our patients involves a personalized risk/benefit<br />
analysis. CAM therapies should be no different and foster the same<br />
scrutiny as any other therapy. In doing this analysis, safety (which<br />
includes interactions with concomitant therapies) should be <strong>of</strong><br />
highest concern, followed by efficacy (objective or perceived) and<br />
cost. Data quantity and quality vary greatly between the CAM<br />
therapies, so one should judge the specific therapy, not all CAM as<br />
a single entity.<br />
One <strong>of</strong> the best sources <strong>of</strong> non-biased CAM information is from the<br />
National Center for <strong>Complementary</strong> and <strong>Alternative</strong> <strong>Medicine</strong><br />
(NCCAM), http://nccam.nih.gov/. This section <strong>of</strong> the National<br />
Institute <strong>of</strong> Health (NIH) functions as both a clearinghouse for CAM<br />
information and as a funding source for CAM research. Although<br />
research in many areas <strong>of</strong> CAM is still lacking, much more information<br />
is available than in previous years.<br />
The following is a quick summary <strong>of</strong> some common CAM therapies:<br />
Acupuncture<br />
Typically, acupuncture is performed by stimulating specific points along<br />
the body either with needling (most commonly), laser, manual pressure or<br />
moxibustion. It is thought that stimulating specific points helps return the<br />
internal balance <strong>of</strong> energy that is blocked in the diseased state. To date,<br />
these energy fields have not been validated, but regional effects on neurotransmitter<br />
expression have been demonstrated. From a safety standpoint,<br />
acupuncture is actually quite safe, and very few complications have been<br />
reported to the FDA. However, if not practiced appropriately, acupuncture<br />
has been associated (rarely) with cellulitis, Hepatitis B transmission,<br />
pneumothorax and even cardiac trauma. Osteoarthritis <strong>of</strong> the knee,<br />
headache, post-operative nausea and vomiting, chemotherapy-induced<br />
nausea and vomiting and post-operative dental pain all have reasonable<br />
data demonstrating a positive clinical effect from acupuncture.<br />
Homeopathy<br />
Homeopathic medicine is based on the principle <strong>of</strong> similars, and remedies<br />
are <strong>of</strong>ten prescribed in high dilutions <strong>of</strong> materials thought to induce the<br />
signs or symptoms one is treating. In most cases, the dilutions are so high<br />
that they may not contain any molecules <strong>of</strong> the original agents at all. As a<br />
consequence, homoeopathic remedies cannot act by typical pharmacological<br />
means. Theories for a mechanism <strong>of</strong> action invoke the homeopathic<br />
solution and postulate that information is actually stored in the dilution<br />
process by some physical means. In general, homeopathic solutions have<br />
been found to be safe but, despite much anecdotal success, are not felt to<br />
demonstrate any clinical efficacy in randomized trials over placebo.<br />
Ayurvedic <strong>Medicine</strong><br />
With a similar philosophy to traditional Chinese medicine, Ayruveda aims<br />
to balance the mind, body and spirit. This is done through a variety <strong>of</strong><br />
practices and products, including herbal mixtures, meditation, diet and<br />
lifestyle. Unfortunately, there have been safety concerns with the mixtures.<br />
For example, a random survey <strong>of</strong> OTC-purchased remedies
evealed clinically significant heavy-metal contamination (lead, mercury<br />
and arsenic) in more than 20 percent. Few good trials have been done to<br />
assess the safety and efficacy <strong>of</strong> Ayurveda, so one should use caution in<br />
recommending this therapy, given its unknown efficacy and documented<br />
problems with herbal contamination. At the same time, some Ayurvedic<br />
herbals have been shown to exhibit pharmacologic activity and deserve<br />
further evaluation (e.g., guggul has lipid-lowering properties).<br />
Chiropractic Manipulation<br />
Central to chiropractic care is physical manipulation <strong>of</strong> the spine. It is theorized<br />
that misalignments <strong>of</strong> the spine interfere with the energy flow that<br />
normally supports good health. The goal then is to realign the spine to<br />
regain appropriate energy flow. Chiropractic care is unique in that most<br />
insurance companies reimburse for it, and it is generally considered the<br />
least “alternative” <strong>of</strong> the CAM therapies. In general, spinal manipulation<br />
is considered safe, with serious complications quite rare. Controlled trials<br />
indicate that spinal manipulation is an equally effective alternative to conventional<br />
therapies for mild to moderate low-back pain.<br />
Chelation Therapy<br />
This therapy involves using chelating agents, usually intravenous EDTA<br />
(ethylene diamine tetra-acetic acid), to treat CAD. EDTA is thought to<br />
work by removing calcium from coronary plaque, which then results in<br />
dissolution <strong>of</strong> the plaque. Others postulate that EDTA exhibits<br />
anti-inflammatory and anti-oxidant effects on the endothelium, which<br />
result in improved endothelial function. Both safety and efficacy are indeterminate,<br />
since most data is anecdotal. Randomized trials that have been<br />
published have so few patients that it is unwise to conclude anything. The<br />
NCCAM is currently enrolling patients into a large multicenter trial to try<br />
to answer safety and efficacy issues more scientifically.<br />
Herbal Therapy<br />
Plants/herbals provide the backbone for the modern pharmaceutical<br />
industry, so herbals typically represent the most commonly used form<br />
<strong>of</strong> CAM. The safety, efficacy and utility depend upon the specific herb<br />
in question and the source from which it is acquired. Examples include:<br />
• Saw Palmetto appears very safe, has few interactions with other medications<br />
or herbals and appears at least modestly effective for mild to<br />
moderate BPH.<br />
• St. Johns Wort is relatively safe but has numerous drug-herb interactions.<br />
Studies also suggest it may be as effective as SSRIs for mild to<br />
moderate depression with potentially fewer side effects.<br />
• Ephedra was removed from the market because <strong>of</strong> concerns <strong>of</strong> severe<br />
toxicity, including death. Although this was usually associated with<br />
excessive doses, significant toxicity was reported even at typical<br />
doses. Most clinical trials found minimal clinical efficacy for congestion<br />
or weight loss.<br />
In summary, it’s important to be familiar with CAM, since many <strong>of</strong> our<br />
patients are using these therapies, and some do appear to provide safe and<br />
effective alternatives to standard therapies. As further studies are done,<br />
evidence, rather than anecdote, can fuel our recommendations.<br />
Regardless <strong>of</strong> popularity, CAM should be evaluated to the same degree as<br />
any traditional therapy.<br />
<strong>Florida</strong> <strong>Family</strong> Physician 19
TREATMENT OF<br />
HYPERTENSION<br />
by Mark C. Houston, MS,<br />
MS, FACP, FAHA<br />
Abstract<br />
Hypertension is the most common reason for visits to<br />
physicians’ <strong>of</strong>fices and the number-one reason for prescription<br />
drug use. The target organ damage associated<br />
with hypertension, such as stroke, myocardial infarction,<br />
congestive heart failure, renal disease and large artery<br />
disease, can be mitigated by aggressive non-drug and drug therapies.<br />
Hypertension is a syndrome <strong>of</strong> various metabolic, functional and structure abnormalities<br />
that must be viewed in a more global setting <strong>of</strong> cardiovascular risk.<br />
Aggressive detection, evaluation and treatment <strong>of</strong> the “blood vessel health” are<br />
mandatory to modern hypertensive care. Lifestyle modifications in conjunction<br />
with vitamins, minerals, antioxidants, nutraceutical supplements, optimal nutrition<br />
and drug therapy will prevent and treat hypertension and its sequelae while<br />
addressing global cardiovascular risk, vascular biology, endothelial dysfunction<br />
and overall vascular health.<br />
Introduction<br />
New and future treatment guidelines for lower target blood pressure (BP) levels in<br />
the general hypertensive population, as well as in specific populations <strong>of</strong> hypertensive<br />
patients with diseases such as diabetes mellitus, renal disease or coronary heart<br />
disease, will demand a combination <strong>of</strong> nonpharmacologic (lifestyle modifications)<br />
and pharmacologic therapy. 1, 2, 3, 4, 5 Lower recommended target BP goals <strong>of</strong> 130/80<br />
mm Hg or perhaps 110/70 mm Hg cannot be attained without aggressive use <strong>of</strong> balanced<br />
drug and non-drug treatments. Nutrition, dietary supplements, nutraceuticals,<br />
vitamins, antioxidants, minerals, achieving ideal body weight, exercise (aerobic and<br />
resistance training), restriction <strong>of</strong> caffeine and alcohol and cessation <strong>of</strong> all tobacco<br />
products are crucial ingredients <strong>of</strong> this combination approach, if BP and subsequent<br />
target organ damage (TOD) are to be reduced.<br />
Hypertension (HTN) is a consequence <strong>of</strong> the interaction <strong>of</strong> our environment and<br />
genetics. Macronutrients and micronutrients are crucial in the regulation <strong>of</strong> BP, subsequent<br />
TOD and atherosclerosis (AS). Nutrient-gene interactions, oxidative stress<br />
and subsequent gene expression have either positive or negative influences on vascular<br />
biology (VB) in humans. Endothelial dysfunction (ED) and vascular smooth<br />
muscle (VSM) dysfunction are the initiating and perpetuating factors in essential<br />
<strong>Florida</strong> <strong>Family</strong> Physician 21
HTN. The correct combination <strong>of</strong> macronutrients<br />
and micronutrients will significantly influence<br />
the prevention and treatment <strong>of</strong> HTN and<br />
subsequent vascular complications.<br />
Nutrition Trials and<br />
Hypertension<br />
Reductions in BP, as well as reductions in CV<br />
morbidity and mortality, have been demonstrated<br />
in numerous short- and long-term clinical<br />
HTN nutritional trials. 6, 7, 8, 9, 10, 11, 12, 13, 14 Even mild<br />
increases in BP may increase TOD, such that<br />
more aggressive and earlier treatment may be<br />
needed to decrease CV risk. Combined<br />
nutrients present in food, especially fruits and<br />
vegetables, as well as single and combined<br />
nutraceutical, nutrient or dietary supplementation,<br />
have been demonstrated to reduce BP. 15<br />
The combined low-sodium DASH II diet 10<br />
reduced blood pressure 11.5/6.8 mm Hg<br />
within two weeks, maintained this BP for<br />
the duration <strong>of</strong> the two-month study and<br />
improved quality <strong>of</strong> life. This level <strong>of</strong> BP<br />
reduction is equivalent to that achieved with<br />
pharmacologic monotherapy.<br />
Nutraceuticals, Vitamins,<br />
Antioxidants and Minerals<br />
Sodium<br />
A reduction in sodium intake to 2,400 mg per<br />
day may reduce the incidence <strong>of</strong> hypertension<br />
and lowers BP an average <strong>of</strong> 4 to 6 mm Hg systolic<br />
and 2 to 3 mm Hg diastolic BP, especially<br />
in salt-sensitive hypertensive patients. 16<br />
Reduced sodium intake also reduces renal<br />
dysfunction, proteinuria, CHF, CVA, vascular<br />
hypertrophy, diastolic dysfunction and left ventricular<br />
hypertrophy (LVH). 15 Further reductions<br />
<strong>of</strong> BP can be achieved with progressive<br />
restriction from 150 mmol to 100 mmol to 50<br />
mmol <strong>of</strong> dietary sodium per day in the DASH<br />
II diet. 10 A low-sodium diet combined with<br />
increased potassium and magnesium is even<br />
more effective. 16<br />
Potassium<br />
The magnitude <strong>of</strong> BP reduction with dietary<br />
supplementation <strong>of</strong> 60 to 120 mEq per day <strong>of</strong><br />
potassium is 4.4 mm Hg systolic and 2.5 mm<br />
16, 17<br />
Hg diastolic BP in hypertensive patients.<br />
In addition, potassium may reduce CV events<br />
and CVA independent <strong>of</strong> BP and reduce the<br />
risk <strong>of</strong> cardiac arrhythmias. 15 The recommended<br />
dietary intake is a K+/Na+ ratio <strong>of</strong><br />
5:1. 4,15 Potassium reduces vascular smooth<br />
muscle hypertrophy and vasoconstriction,<br />
induces natriuresis and blunts the effects <strong>of</strong><br />
15, 16, 17<br />
A-II and catecholamines.<br />
Magnesium<br />
Magnesium supplementation in the range <strong>of</strong><br />
500 to 1,000 mg per day reduces systolic BP 2.7<br />
mm Hg and diastolic BP 3.4 mm Hg. 18<br />
Magnesium lowers systemic vascular resistance<br />
(SVR) and reduces arrhythmias. The mechanism<br />
is blockade <strong>of</strong> calcium influx into VSM<br />
cells (calcium channel blocker-like effect) and<br />
increased levels <strong>of</strong> the vasodilating<br />
prostaglandin E1(PGE1). 15<br />
Calcium<br />
A recent meta-analysis <strong>of</strong> the effect <strong>of</strong> calcium<br />
supplementation in hypertensive patients<br />
demonstrated a reduction in systolic BP <strong>of</strong> 4.3<br />
mm Hg and diastolic BP <strong>of</strong> 1.5 mm Hg. 19<br />
Calcium is particularly effective in patients<br />
with a high sodium intake and when given in a<br />
natural form with potassium and magnesium.<br />
20, 21, 22 Blacks, elderly, diabetic, salt-sensitive,<br />
pregnant and postmenopausal women<br />
and low-renin hypertensives have the best<br />
response. 15 Vitamin D may be intimately<br />
involved in the role <strong>of</strong> calcium in hypertension<br />
15, 20, 21, 22<br />
through effects on rennin.<br />
22
Table 1<br />
Natural Antihypertensive Compounds<br />
Categorized by Antihypertensive Class<br />
Intervention<br />
Diuretics<br />
1. Hawthorne berry<br />
2. Vitamin B-6 (Pyridoxine)<br />
3. Taurine<br />
4. Celery<br />
5. GLA<br />
6. Vitamin C (Ascorbic Acid)<br />
7. K +<br />
8. Mg ++<br />
9. Ca ++<br />
10. Protein<br />
11. Fiber<br />
12. Co-Enzyme Q-10<br />
13. L-Carnitine<br />
15. Celery<br />
16. ALA (Alpha Lipoic Acid)<br />
Calcium Channel Blockers (CCB)<br />
1. Alpha Lipoic Acid (ALA<br />
2. Vitamin C (Ascorbic Acid)<br />
3. Vitamin B-6 (Pyridoxine)<br />
4. Magnesium (Mg ++ )<br />
5. N-Acetyl Cysteine (NAC)<br />
6. Vitamin E<br />
7. Hawthorne berry<br />
8. Celery<br />
9. Omega-3 fatty acids (EPA and DHA)<br />
10. Calcium<br />
11. Garlic<br />
Beta-Blockers (BB)<br />
1. Hawthorne berry<br />
Central Alpha Agonists (CAA)<br />
1. Taurine<br />
2. K +<br />
3. Zinc<br />
4. Na + Restriction<br />
5. Protein<br />
6. Fiber<br />
7. Vitamin C<br />
8. Vitamin B-6<br />
9. Co Enzyme Q-10<br />
10. Celery<br />
11. GLA/DGLA<br />
12. Garlic<br />
Direct Vasodilators<br />
1. Omega-3 FA<br />
2. MUFA (Omega-9 FA)<br />
3. K +<br />
4. Mg ++<br />
5. Ca ++<br />
6. Soy<br />
7. Fiber<br />
8. Garlic<br />
9. Flavonoids<br />
10. Vitamin C<br />
11. Vitamin E<br />
12. Co-Enzyme Q-10<br />
13. L-Arginine<br />
14. Taurine<br />
Angiotensin Converting Enzyme Inhibitors (ACEI)<br />
1. Garlic<br />
2. Seaweed – various (wakame, etc.)<br />
3. Tuna protein/muscle<br />
4. Sardine protein/muscle<br />
5. Hawthorne berry<br />
6. Bonito fish (dried)<br />
7. Pycnogenol<br />
8. Casein<br />
9. Hydrolyzed whey protein<br />
10. Sour milk<br />
11. Gelatin<br />
12. Sake<br />
13. Essential fatty acids (Omega-3 FA)<br />
14. Chicken egg yolks<br />
15. Zein<br />
16. Dried salted fish<br />
17. Fish sauce<br />
18. Zinc<br />
19. Hydrolyzed wheat germ isolate<br />
Angiotensin Receptor Blockers (ARBs)<br />
1. Potassium (K + )<br />
2. Fiber<br />
3. Garlic<br />
4. Vitamin C<br />
5. Vitamin B-6 (pyridoxine)<br />
6. Co-Enzyme Q-10<br />
7. Celery<br />
8. Gamma Linolenic Acid (GLA) and DGLA
Protein<br />
High intake <strong>of</strong> non-animal protein (1<br />
g/kg/day) (Intersalt Study, Intermap Study) is<br />
associated with a lower BP. 15, 16, 23 Hydrolyzed<br />
whey protein 24 and sardine muscle extract 25<br />
significantly lower BP in humans through an<br />
angiotensin-converting enzyme inhibitor<br />
(ACEI) mechanism. Animal protein with<br />
reduced fat content may <strong>of</strong>fer the same antihypertensive<br />
15, 16, 23, 24<br />
benefit.<br />
Fats<br />
Consumption <strong>of</strong> omega-3 fatty acids (polyunsaturated<br />
fatty acids — PUFA), such as EPA<br />
(eicosapentaenoic acid) and DHA (docosahexanoic<br />
acid), significantly reduce mean BP in<br />
humans by 5.8 to 8.1 mm Hg. 26, 27, 28, 29 This,<br />
combined with omega-9 fatty acids (olive oil)<br />
(monounsaturated, oleic acid), low saturated fat,<br />
elimination <strong>of</strong> trans-fatty acids and increased<br />
GLA (gamma linolenic acid), may have dramatic<br />
effects on BP, VB and AS. The omega-3<br />
to omega-6 fatty acid ratio should be 1:1 to 4:1<br />
with consumption <strong>of</strong> cold-water fish (cod, tuna,<br />
mackerel, salmon) or EPA/DHA supplements<br />
(3 to 4 grams per day).<br />
The omega-3 fatty acids increase nitric oxide,<br />
decrease leukotrienes and throboxane A2,<br />
improve insulin sensitivity and membrane fluidity,<br />
have PPAR gamma activity, reduce calcium<br />
influx, decrease plasma norepinephrine and<br />
26, 27, 28, 29<br />
improve endothelial dysfunction.<br />
The omega-9 fatty acids lower BP about 8/5<br />
mm Hg, reduce LDL oxidation, improve nitric<br />
oxide bioavailability, reduce oxidative stress<br />
and improve endothelial dysfunction. 30<br />
There are concerns about mercury and other<br />
toxic metals in fish. For this reason, high-potency-certified<br />
fish oil capsules may be substituted<br />
or used with fish consumption. The olive oil<br />
dose is 40 grams <strong>of</strong> extra-virgin olive oil per<br />
day (4 tablespoons). 30<br />
Garlic<br />
The prospective placebo-controlled studies utilizing<br />
the correct form (wild garlic is best) and<br />
dose <strong>of</strong> garlic demonstrate only minimal<br />
decreases in systolic BP <strong>of</strong> 5 to 8 mm Hg or a<br />
mean BP <strong>of</strong> 2 to 3 mm Hg. 31,32,33 However, garlic<br />
may have numerous other beneficial vascular<br />
effects, as it is a natural ACEI and calcium<br />
15, 31, 32, 33, 34<br />
channel blocker (CCB).<br />
Seaweed<br />
Wakame seaweed in doses <strong>of</strong> 3.3 grams per day<br />
significantly lowered BP in hypertensive<br />
humans within four weeks, due to its ACEI<br />
activity and high mineral content. 35 The average<br />
reduction in BP was 14/5 mm Hg. Long-term<br />
15, 35<br />
use in Japan appears to be safe.<br />
Fiber<br />
Clinical trials with various types <strong>of</strong> fiber to<br />
reduce BP have been inconsistent. 16, 36 The average<br />
BP reduction in prospective studies using<br />
60 grams per day <strong>of</strong> oatmeal fiber (3 grams <strong>of</strong><br />
betaglucan per day, glucomannan or 7 grams <strong>of</strong><br />
psyllium per day) is 7.5 mm Hg/5.5 mm Hg, 15,<br />
16, 36<br />
but retrospective, epidemiologic studies and<br />
meta-analysis suggest lower reductions in BP.<br />
Vitamin C<br />
Vitamin C at doses <strong>of</strong> 250 to 500 mg BID lowers<br />
BP, especially in hypertensive patients with<br />
37, 38, 39<br />
initially low plasma ascorbate levels.<br />
Vitamin C improves ED, improves aortic compliance,<br />
increases nitric oxide levels, is a potent<br />
antioxidant, decreases SVR and BP falls an<br />
average <strong>of</strong> 7/4 mm Hg. The greater the initial<br />
BP and the lower the plasma ascorbate level, the<br />
greater the response. Combinations with other<br />
antioxidants and vitamins may have synergistic<br />
antihypertensive effects.<br />
Vitamin B-6<br />
Supplemental vitamin B-6 at 5 mg/kg/day<br />
reduced BP 14/10 mm Hg over four weeks. 40<br />
Vitamin B-6 reduces central sympathetic nervous<br />
system activity and acts as a central alpha<br />
agonist (i.e., Clonidine), a CCB and a diuretic.<br />
Pyridoxine also improves insulin sensitivity and<br />
carbohydrate metabolism, which improves BP.<br />
Daily doses should probably not exceed 200 mg<br />
to avoid peripheral neuropathy. 15<br />
Lycopene<br />
Paran et al 41 evaluated 30 subjects with<br />
grade I hypertension given tomato lycopene<br />
extract for eight weeks. The BP fell 9/7 mm<br />
Hg within eight weeks. Lycopene is found<br />
in high concentrations in tomatoes, tomato<br />
products, guava, pink grapefruit, watermelon,<br />
papaya and apricots. 15<br />
Co-Enzyme Q-10 (Ubiquinone)<br />
Enzymatic assays show a deficiency <strong>of</strong> Co-<br />
Enzyme Q-10 (Co-Q-10) in 39 percent <strong>of</strong><br />
essential hypertensive patients versus only a 6<br />
percent deficiency in controls. 15, 42 Human studies<br />
demonstrate significant and consistent<br />
reductions in BP averaging 15/10 mm Hg in all<br />
43, 44, 45, 46, 47, 48<br />
reported prospective clinical trials.<br />
Doses <strong>of</strong> 100 to 225 mg per day (1 to 2<br />
mg/kg/day) to achieve a therapeutic plasma<br />
level <strong>of</strong> more than 3 micrograms/ml are effective<br />
within four to eight weeks in reducing BP.<br />
The BP remains steady at this level and returns<br />
to baseline at two weeks following discontinuation<br />
<strong>of</strong> Co-Q-10. Co-Q-10 reduces SVR, catecholamine<br />
and aldosterone levels, improves<br />
insulin sensitivity and endothelial function and<br />
increases nitric oxide levels. 43, 44, 47 No adverse<br />
effects have been noted at these doses with<br />
chronic use. Patients have been able to stop or<br />
reduce the number <strong>of</strong> antihypertensive drugs by<br />
one to three with chronic ingestion <strong>of</strong> Co-<br />
Enzyme Q-10. A reputable, certified<br />
absorbable form, with excellent bioavailability<br />
and measurement plasma levels, is an important<br />
clinical consideration.<br />
L-Arginine<br />
L-arginine is the natural predominant precursor<br />
for vascular nitric oxide. Administration <strong>of</strong> 10<br />
grams orally per day in food and/or as a supple-<br />
24
Table 2<br />
Recommendations<br />
Nutrition........................................................................Daily Intake<br />
1. DASH I and DASH II-Na + diets<br />
2. Sodium restriction ................................................50 to 100 mmol<br />
3. Potassium ................................................................60 to 100 mEq<br />
4. Potassium/Sodium ratio > 5:1 ........................................................<br />
5. Magnesium ......................................................................1,000 mg<br />
6. Calcium ............................................................................1,000 mg<br />
7. Zinc ........................................................................................25 mg<br />
8. Protein: total intake<br />
(30 percent total calories) ................................1.0 to 1.5 grams/kg<br />
A. Non-animal sources preferred, but lean or wild animal protein<br />
in moderation is acceptable<br />
B. Hydrolyzed whey protein ............................................30 grams<br />
C. Soy protein (fermented is best)....................................30 grams<br />
D. Hydrolyzed wheat germ isolate..............................2 to 4 grams<br />
E. Sardine muscle concentrate extract ....................................3 mg<br />
F. Cold water fish, fowl, poultry ....................3 servings per week<br />
9. Fats: ..........................................................30 percent total calories<br />
A. Omega-3 fatty acids (30 percent) PUFA ..............3 to 4 grams<br />
(DHA, EPA, cold water fish)<br />
B. Omega-6 fatty acids (10 percent) PUFA ........................1 gram<br />
(GLA, canola oil nuts)<br />
C. Omega-9 fatty acids (30%) MUFA......................4 tablespoons<br />
(olive oil – extra virgin)<br />
D. Saturated FA<br />
(lean, wild animal meat) (30%)<br />
E. P/S ratio<br />
(polyunsaturated/saturated) fats > 2.0<br />
F. Omega-3/Omega-6 PUFA, ratio 2:1 – 4:1<br />
G. No trans-fatty acids<br />
H. (hydrogenated margarines, vegetable oils)<br />
I. Nuts: almonds, walnuts, hazelnuts, etc.<br />
10. Carbohydrates (40 percent total calories)<br />
A. Reduce or eliminate refined sugars and simple carbohydrates<br />
B. Increase complex carbohydrates and whole grain fiber<br />
(oat, barley, wheat), vegetables, beans, legumes<br />
Oatmeal ..............................................................................60 grams<br />
Oatbran (dry)......................................................................40 grams<br />
Beta-glucan ..........................................................................3 grams<br />
Psyllium ................................................................................7 grams<br />
11. Garlic..................................................................4 cloves/4 grams<br />
12. Wakame seaweed (dried) ..................................3.0 to 3.5 grams<br />
13. Celery<br />
Celery sticks ........................................................................4 sticks<br />
Celery juice ..........................................................8 teaspoons TID<br />
Celery seed extract ..................................................1,000 mg BID<br />
Celery oil (tincture)............................................to 1 teaspoon TID<br />
14. Lycopene<br />
Tomatoes and tomato products, guava, watermelon, apricots,<br />
pink grapefruit, papaya<br />
Exercise....................................................................seven days/week<br />
• Aerobically at 60 to 80 percent MHR<br />
60 minutes daily<br />
4,200 KJ/week<br />
• Resistance training ..........................................three days per week<br />
Weight Loss<br />
• To LBW (lean body weight)<br />
• Lose 1 to 2 pounds/week<br />
• BMI < 25<br />
• Waist circumference<br />
< 35 inches in female<br />
< 40 inches in male<br />
• Total body fat<br />
< 16 percent in males<br />
< 22 percent in females<br />
• Increased lean muscle mass<br />
• Reduce WHR to below 0.9<br />
Alcohol Restriction..................................................< 20 grams/day<br />
Wine < 10 ounces<br />
Beer < 24 ounces<br />
Liquor < 2 ounces (100-pro<strong>of</strong> whiskey)<br />
Caffeine Restriction ..................................................< 100 mg/day<br />
Tobacco and Smoking ............................................................STOP<br />
Avoid drugs and interactions that increase BP<br />
Vitamins, Antioxidants and Nutraceutical Supplements<br />
1. Vitamin C........................................................250 to 500 mg BID<br />
2. Vitamin B-6 ................................................................100 mg BID<br />
3. Co-Enzyme Q-10 ..........................................100 mg QD to BID<br />
4. L-Arginine (supplement) plus lentils,<br />
hazelnuts, walnuts, peanuts ......................................5 grams BID<br />
5. Taurine ................................................................2 to 3 grams BID<br />
6. Pycnogenol ..................................................................200 mg QD
ment significantly reduces BP in human subjects<br />
by 6.2/6.8 mm Hg and improves ED and<br />
49, 50<br />
blood flow.<br />
Taurine<br />
Taurine, a sulfonic beta-amino acid, is significantly<br />
reduced in the urine <strong>of</strong> essential hypertensive<br />
patients. 51 Administration <strong>of</strong> six grams<br />
<strong>of</strong> taurine per day lowers BP 9/4 mm Hg. 52<br />
Taurine induces a sodium-water diuresis and<br />
vasodilation, increases atrial natriuretic factor<br />
(ANF), reduces sympathetic nervous system<br />
activity and aldosterone levels, improves insulin<br />
sensitivity and reduces homocysteine levels.<br />
Celery<br />
Celery has antihypertensive properties due<br />
to 3-N-butyl phthalide, apigenin and other<br />
substances that act like ACEI or CCB blockers.<br />
Four large celery sticks per day or the<br />
equivalent in celery juice, celery oil or<br />
celery-seed extract reduces BP in animals<br />
53, 54, 55, 56, 57<br />
and humans.<br />
Pycnogenol<br />
Pycnogenol, a bark extract from the French<br />
maritime pine, is a mixture <strong>of</strong> bi<strong>of</strong>lavonoids<br />
with antioxidant and antihypertensive properties.<br />
58 A dose <strong>of</strong> 200 mg per day significantly (p<br />
< 0.05) reduced systolic BP in a small study <strong>of</strong><br />
eleven hypertensive patients during an eightweek<br />
period. 58<br />
Combinations<br />
Combinations <strong>of</strong> various nutraceutical or<br />
dietary supplements, vitamins and antioxidants<br />
may further enhance BP reduction, reduce<br />
oxidative stress and improve vascular function<br />
and structure. 59 Optimal doses and combinations<br />
are yet to be determined, but future<br />
research will provide important data.<br />
Natural Antihypertensive<br />
Compounds Categorized by<br />
Antihypertensive Class<br />
As has been discussed previously, many <strong>of</strong> the<br />
natural compounds such as food, nutraceutical<br />
and dietary supplements, vitamins, antioxidants<br />
or minerals function in a similar fashion to a<br />
specific class <strong>of</strong> antihypertensive drugs (Table<br />
1). 15 Although the potency <strong>of</strong> these natural compounds<br />
may be less than or equal to the antihypertensive<br />
drug and the onset <strong>of</strong> action slower<br />
when used in combination, the antihypertensive<br />
effect is magnified. In addition, many <strong>of</strong> these<br />
natural compounds have varied, additive or synergistic<br />
antihypertensive mechanisms.<br />
Conclusion<br />
Individuals with pre-hypertension and Stage I<br />
hypertension can incorporate numerous<br />
lifestyle changes, including the selective use<br />
<strong>of</strong> nutraceuticals, vitamins, antioxidants and<br />
minerals to achieve a normal blood pressure<br />
and improve vascular structure, function and<br />
health. This will achieve improved reductions<br />
in TOD. Specific recommendations are shown<br />
in Table 2. The combinations <strong>of</strong> natural remedies<br />
and lifestyle changes are most likely<br />
additive to the antihypertensive effects <strong>of</strong><br />
pharmacologic agents. Utilization <strong>of</strong> different<br />
“classes” <strong>of</strong> natural antihypertensive compounds<br />
are likely to have similar, but smaller,<br />
effects on BP, based on the known or previous<br />
response to pharmacologic drugs(s).<br />
Mark C. Houston, MS, MS, FACP, FAHA<br />
Associate Clinical Pr<strong>of</strong>essor <strong>of</strong> <strong>Medicine</strong><br />
Vanderbilt University School <strong>of</strong> <strong>Medicine</strong><br />
Director, Hypertension Institute and<br />
Vascular Biology<br />
Medical Director, Division <strong>of</strong> Nutrition<br />
Saint Thomas Medical Group,<br />
Saint Thomas Hospital<br />
4230 Harding Road, Suite 400<br />
Nashville, Tennessee 37205<br />
Phone: 615.297.5551<br />
Fax: 615.467.0365<br />
E-mail: mhoustonhisth@yahoo.com<br />
26
References<br />
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29. Frisco D, Paniccia R, Bandinelli B, et al. Effect <strong>of</strong><br />
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3 polyunsaturated fatty acids on blood pressure in mild<br />
hypertensive patients. Thromb. Res. 91, 105-112 (1998).<br />
30. Ferrara LA, Raimondi S, d’Episcopa I, et al. Olive oil<br />
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32. Silagy CA, Neil AN. A meta-analysis <strong>of</strong> the<br />
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33. Ackermann RT, Muldow CD, Ramirez G. Garlic<br />
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36. He J, Welton PK. Effect <strong>of</strong> dietary fiber and protein<br />
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Clin. Exp. Hypertens. 21, 785-796 (1999).<br />
37. Duffy SJ, Gokce N, Holbrook, M, et al.<br />
Treatment <strong>of</strong> hypertension with ascorbic acid. Lancet<br />
354, 2048-2049 (1999).<br />
38. Fotherby MD, Williams JC, Forster LA, et al. Effect <strong>of</strong><br />
vitamin C on ambulatory blood pressure and plasma lipids<br />
in older persons. J. Hypertens. 18, 411-415 (2000).<br />
39. Ness AR, Chee D, Elliot P. Vitamin C and blood<br />
pressure – an overview. J. Hum. Hypertens. 11, 343-<br />
350 (1997).<br />
40. Aybak M, Sermet A, Ayyildiz MO, Karakilcik AZ.<br />
Effect <strong>of</strong> oral pyridoxine hydrochloride supplementation<br />
on arterial blood pressure in patients with essential hypertension.<br />
Arzneimittelforschung 45, 1271-1273 (1995).<br />
41. Paran E, Engelhard Y. Effect <strong>of</strong> tomato’s<br />
lycopene on blood pressure, serum lipoproteins,<br />
plasma homocysteine and oxidative stress markers in<br />
grade I hypertensive patients. Am. J. Hypertens. 14,<br />
141A (2001). Abstract p-333.<br />
42. Khosh F. Hypertension and co-enzyme Q10. Altern.<br />
Med. Rev. I(3), 171-174 (1996).<br />
43. Digiesi V, Cantini F, Bisi G, et al. Mechanism <strong>of</strong> action<br />
<strong>of</strong> coenzyme Q10 in essential hypertension. Curr. Ther.<br />
Res. 51, 668-672 (1992).<br />
44. Digiesi V, Cantini F, Brodbeck B. Effect <strong>of</strong> coenzyme<br />
Q10 on essential hypertension. Curr. Ther. Res. 47, 841-<br />
845 (1990).<br />
45. Digiesi V, Cantini F, Oradei A, et al. Coenzyme Q-10<br />
in essential hypertension. Mol. Aspects Med. 15, 8257-<br />
8263 (1994).<br />
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disease control: an update on vitamins and conditionally<br />
essential nutrients. Prog. Cardiovasc.<br />
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48. Burke BE, Neuenschwander R, Olson RD.<br />
Randomized, double-blind, placebo-controlled trial <strong>of</strong><br />
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49. Kelly JJ, Williamson P, Martin A, Whitworth JA.<br />
Effects <strong>of</strong> oral L-arginine on plasma nitrate and<br />
blood pressure in cortisol-treated humans. J.<br />
Hypertens. 19, 263-268 (2001).<br />
50. Siani A, Pagano E, Iacone R, et al. Blood pressure and<br />
metabolic changes during dietary L-arginine supplementation<br />
in humans. Am. J. Hypertens. 13, 547-551 (2000).<br />
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significance <strong>of</strong> taurine in hypertension. Nippon Rinsho 50,<br />
374-381 (1992).<br />
52. Fujita T, Ando K, Noda H, et al. Effects <strong>of</strong><br />
increased adrenomedullary activity and taurine in<br />
young patients with borderline hypertension.<br />
Circulation 75, 525-532 (1987).<br />
53. Castleman M. The Healing Herbs: The Ultimate<br />
Guide to the Curative Power <strong>of</strong> Nature’s <strong>Medicine</strong>s.<br />
Rodale Press, Emmaus, Pennsylvania, 105-107 (1991).<br />
54. Duke JA. The Green Pharmacy Herbal Handbook.<br />
Rodale Press, Emmaus, Pennsylvania, 68-69 (2000).<br />
55. Heinerman J. Heinerman’s New Encyclopedia <strong>of</strong><br />
Fruits and Vegetables. Prentice Hall, Paramus, New Jersey,<br />
93-95 (1995).<br />
56. Le OT, Elliott WJ. Dose response relationship <strong>of</strong> blood<br />
pressure and serum cholesterol to 3-N-butyl phthalide, a<br />
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(1991). Abstract.<br />
57. Le OT, Elliott WJ. Mechanisms <strong>of</strong> the hypotensive<br />
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oil. J. Am. Hypertens. 40, 326A (1992). Abstract.<br />
58. Hosseini S, Lee J, Sepulveda RT, et al. A randomized,<br />
double-blind, placebo-controlled, prospective, 16 week<br />
crossover study to determine the role <strong>of</strong> pycnogenol in<br />
modifying blood pressure in mildly hypertensive patients.<br />
Nutrition Research 21, 1251-1260 (2001).<br />
59. Galley HF, Thornton J, Howdle PD, et al. Combination<br />
oral antioxidant supplementation reduces blood pressure.<br />
Clin. Sci. 92, 361-365 (1997).<br />
<strong>Florida</strong> <strong>Family</strong> Physician 27
y Russ Hostetler, MD<br />
Plant City<br />
The Root Doctor<br />
And other Musings on Being a <strong>Family</strong> Doctor<br />
As soon as I walked into the exam room, she started crying. She did not look away for<br />
even a second. She just stared at me, following my every movement with apprehension<br />
on her tearful face. Her mother, leaning on the exam table just behind her, started<br />
to rub her back gently and told her everything was going to be all right.<br />
I would have expected such behavior from a 2-year-old. At that age,<br />
having had the experience <strong>of</strong> immunization shots, kids just assume<br />
you are going to try to kill them, and they cling to their mothers and<br />
fathers like pups to the belly <strong>of</strong> a possum. But even though she was<br />
tiny for her age, this girl was nearly 7 years old, and we had met<br />
before, years earlier. I thought she’d remember me, but her memory<br />
was clouded by the experiences <strong>of</strong> the intervening two years, and it<br />
was clear that she was afraid. I tried to console her.<br />
“It’s OK, LaTeesha. Don’t you remember me” I reached out and<br />
gently touched her knee. She withdrew, scrunching up closer to her<br />
mother. I looked to the mother for help.<br />
“LaTeesha, you be ahrye. Dis doctah ain’t gonna hurcha,” she consoled.<br />
“Let him zamen you so wees can figger out whatta do.” She<br />
gently pushed her daughter back to the end <strong>of</strong> the exam table. The<br />
tears continued but with a more quiet sob.<br />
“Of what is she so afraid” I asked s<strong>of</strong>tly.<br />
“Teesha, tell da doctah whuh you so ’fraid uh.” The mother was gentle<br />
and encouraging, not demanding or forceful.<br />
The little girl whimpered a bit more, sniffed, drew a finger under her<br />
nose and wiped it on her jeans, then looked up from a bowed head<br />
and asked, “You gonna pee on the ground an make mud”<br />
“What” came out <strong>of</strong> my mouth before I could think, and my tone<br />
implying incredulousness was not mistaken by the mother. She<br />
looked at my white face with a look that said she understood my lack<br />
<strong>of</strong> understanding, my cultural ignorance.<br />
“Huh daddy tuhk huh tuh ah root doctah. Fuh a treatmen, dey tuhk<br />
huh intuh duh woods at nye by duh full moon ’til he foun duh rye<br />
kindduh red clay duht. Den he pissed awn duh duht tuh make mud.<br />
Den he strip huh naked an make huh lay down innit an pack duh mud<br />
aroun’ huh neck an huh knees an huh elbahs.”<br />
LaTeesha’s crying intensified. The memory <strong>of</strong> the trips to the woods,<br />
the malodorous mud and the nakedness overwhelmed her. She<br />
crawled up into her mother’s lap. Her mother did not refuse her.<br />
I was dumbfounded. Three minutes is a long time during which to<br />
say nothing and do nothing, except allow this youngster to experience<br />
the warmth <strong>of</strong> her mother’s protective embrace, but that’s what<br />
we did. I had to pull my handkerchief from my pocket to dab my<br />
eyes. Finally, I spoke.<br />
“LaTeesha, that other doctor’s treatment isn’t anything like what<br />
modern medical treatment has to <strong>of</strong>fer. Let me examine you so we<br />
can figure out what might help you feel better. I promise I’ll try not<br />
to hurt you. If any part <strong>of</strong> my exam hurts, just let me know, and I’ll<br />
stop right away, OK”<br />
She peered out from her mother’s chest. Her mother gently pushed<br />
her back onto the exam table. I got out my stethoscope and started<br />
listening to LaTeesha’s mother’s upper arm. “See, it doesn’t hurt,<br />
does it, Mom” I asked rhetorically.<br />
Mom cooperated nicely, “Ih doan huht, Teesha.”<br />
I examined LaTeesha carefully. I found a grade 2 systolic heart murmur,<br />
but no rub. It didn’t appear to be hemodynamically significant<br />
at that point, but I wondered if she had some dilatation <strong>of</strong> her aortic<br />
root left over from the pericarditis she had when I first met her. I<br />
28
couldn’t see any eye problems with the hand-held ophthalmoscope,<br />
especially no anterior chamber changes with the scope dialed into<br />
the higher black numbers, but one knee and the contralateral ankle<br />
and elbow were tender and a bit red and swollen. I had LaTeesha<br />
walk around the room. Her gait was antalgic.<br />
Two years earlier, she had presented with fever, swollen joints, a s<strong>of</strong>t<br />
pericardial rub and photophobia. X-rays, labs (ANA+ but RF-) and<br />
a visit to the ophthalmologist confirmed what used to be eponymously<br />
called Still’s onset juvenile rheumatoid arthritis and now is<br />
called pauciarticular JRA, one <strong>of</strong> the three ways JRA presents — the<br />
others being polyarticular (five or more joints) and systemic. The<br />
ophthalmologist started her on some steroid drops for a mild uveitis,<br />
a finding that goes along with the positive ANA in young females<br />
with JRA. I sent her to a pediatric cardiologist, too, and had heard<br />
that he had overridden my ibupr<strong>of</strong>en prescription and started IV and<br />
then oral steroid treatment; however, as so <strong>of</strong>ten happened, she did<br />
not come back to me. To my shame, I did not follow up with<br />
inquiries about how she was doing, either. Looking back, a busy<br />
practice was not a good excuse for a primary care physician not to<br />
follow up on a patient’s significant and chronic disease.<br />
“Ih come down tuh thuh sheriff’s depuhtee pullin’ awn one ahm an<br />
huh daddy pullin’ awn thuh uhthuh. When LaTeesha scream, day bo’<br />
stop pullin’ an look at each uhthuh. Finuhly, huh daddy leh go an<br />
stomp back intuh he house. Dat wuh two week ago, an ah ain’t huhd<br />
from him since. I wen tuh duh county an got huh awn Med-caid an<br />
heeuh we awh.”<br />
We did get her on ibupr<strong>of</strong>en, and she did well. Still’s does abate<br />
(permanent remission) in some patients, and if there wasn’t too much<br />
damage done before such a blessed development, they can lead fairly<br />
normal lives. Seeing LaTeesha run up to my <strong>of</strong>fice from her mother’s<br />
parked car led me to hope for such an outcome for LaTeesha.<br />
The mother ultimately moved to Detroit, where she was promised a<br />
job with relatives. I imagined that LaTeesha had a good chance <strong>of</strong><br />
being cared for by a black doctor in the Detroit area, and I wondered<br />
if he or she would take LaTeesha’s history in stride or if he or she<br />
would have to pick his or her jaw up <strong>of</strong>f the floor after hearing the<br />
story <strong>of</strong> this child’s potentially dangerous encounter with alternative<br />
medicine in the form <strong>of</strong> a root doctor.<br />
I asked her mother what had happened after we sent her to the cardiologist.<br />
She reported that they went there a couple <strong>of</strong> times, but the<br />
copays imposed by their insurance for doctor visits and medications<br />
was a burden. Her ex-husband, LaTeesha’s father, had complained,<br />
but when she told him there was no alternative and that he’d have to<br />
change his lifestyle to accommodate their child’s medical needs, he<br />
came up with an alternative.<br />
To my shame, I did not follow up with<br />
inquiries about how she was doing, either.<br />
Looking back, a busy practice was not a<br />
good excuse for a primary care physician<br />
not to follow up on a patient’s significant<br />
and chronic disease.<br />
At first, she didn’t object, because she thought he had as much right to<br />
make decisions about LaTeesha’s health care as she did, and a trusted<br />
aunt advised her to let the root doctor have a chance to help the child.<br />
Additionally, she didn’t have any money for a lawyer, so when he<br />
assumed custody <strong>of</strong> LaTeesha, she felt powerless to fight him. But after<br />
a few months, she could tell that LaTeesha was much worse, that she<br />
had stopped growing and that her joint pains were crippling her. It took<br />
more than eight months to finally get LaTeesha back from her father’s<br />
house and bring her to me to restart medical treatments.<br />
<strong>Florida</strong> <strong>Family</strong> Physician 29
R E S I D E N T S ’ & S T U D E N T S ’<br />
by Terreze Gamble, MD, PGY-3, Tallahassee<br />
Memorial <strong>Family</strong> <strong>Medicine</strong> Residency<br />
C O R N E R<br />
Mind-Body <strong>Medicine</strong><br />
Many residency programs have implemented<br />
various aspects <strong>of</strong> complementary<br />
and alternative medicine, including an<br />
acupuncture specialist at Morton Plant and<br />
the initiation <strong>of</strong> a mind-body medicine<br />
grant in Tallahassee. Mind-body medicine<br />
enhances the mind’s capacity to affect bodily<br />
function and symptoms. It includes but<br />
is not limited to meditation, prayer, music,<br />
art and dance therapy.<br />
One key theory <strong>of</strong> mind-body medicine is bi<strong>of</strong>eedback research.<br />
This concept has shown that individuals can learn to control<br />
brainwave activity, cardiovascular and respiratory functioning. By<br />
focusing in on one’s “core” or wherever the individual finds that<br />
calm place, he or she can obtain a more variable brainwave activity<br />
similar to what we see on a fetal monitoring strip, which, as you will<br />
recall, is reassuring. This in turn invokes a sustainable lower heart<br />
rate. Deep breathing is one <strong>of</strong> the methods used to create that sense<br />
<strong>of</strong> calmness. The idea is that persons experiencing anxiety can, at<br />
any time, come back to their core.<br />
Mind-body medicine focuses on the interactions among the brain,<br />
mind, body and behavior. The emotional, mental, social, spiritual<br />
and behavioral factors intertwine in a dynamic way, which directly<br />
affects health. This field uses a variety <strong>of</strong> techniques: relaxation,<br />
hypnosis, meditation, yoga and concepts essential to conventional<br />
medicine, such as cognitive-behavioral therapies and group support.<br />
Mind-body medicine has provided considerable evidence that psychological<br />
factors can play a significant role in the development and<br />
progression <strong>of</strong> certain disease states. These techniques have even<br />
been employed in the treatment <strong>of</strong> various types <strong>of</strong> pain.<br />
Mind-body medicine approaches have potential benefits and advantages.<br />
The physical and emotional risks <strong>of</strong> using these interventions<br />
are minimal. Future research focusing on basic mind-body mechanisms<br />
and individual differences in responses is likely to yield new<br />
insights that may enhance the effectiveness and individual tailoring<br />
<strong>of</strong> mind-body interventions.<br />
30
Elected legislators make decisions about your financial survival and providing a medical home for your patients. These decisions are<br />
made in the chambers <strong>of</strong> the <strong>Florida</strong> House and Senate, not in the exam room. <strong>Florida</strong>'s <strong>Family</strong>MedPAC wants to elect people who are<br />
friendly to family physicians’ needs. To accomplish this goal, your <strong>Family</strong>MedPAC needs your help.<br />
<strong>Family</strong>MedPAC is an investment in your pr<strong>of</strong>ession. You invest in your home, family, food, clothing and transportation. You also invest<br />
in your education and pr<strong>of</strong>ession merit planned investment. Make your voice strong by supporting <strong>Family</strong>MedPAC.<br />
YES, count me in — I want to help family medicine speak with a<br />
stronger voice in Tallahassee!<br />
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AMERICAN EXPRESS # ____________________________________<br />
EXPIRATION DATE ________________________________________
<strong>Florida</strong> <strong>Academy</strong> <strong>of</strong> <strong>Family</strong> Physicians<br />
6720 Atlantic Boulevard<br />
Jacksonville, <strong>Florida</strong> 32211<br />
PRSRT STD<br />
US POSTAGE<br />
PAID<br />
LITTLE ROCK, AR<br />
PERMIT NO. 2437