The Centers for Disease Control and Prevention (CDC) refers to itself as the nation's health protection agency. Among other things, they monitor infectious disease outbreaks (such as Zika, influenza or AIDS), and they issue recommendations for vaccines and immunizations.
There is a quiet epidemic in our country, and it is oral/throat cancer related to human papillomavirus (HPV) infection. We've known about HPV causing almost all cervical cancer for a long time, but the number of oropharyngeal cancers related to HPV infection has risen dramatically in recent years. Ever since actor Michael Douglas announced in 2013 that he suffered from HPV-related throat cancer, people realized HPV poses a threat not only to women, but to men as well.
HPV infection is very common. According to the CDC, 80 million people - about one in four - are currently infected in the United States. There are more than 150 related HPV viruses, but only a handful are responsible for causing most HPV-related cancers.
HPV is so common that nearly all sexually active men and women get it at some point in their lives. Most of the time, people get HPV from having vaginal and/or anal sex. Men and women can also get HPV from having oral sex or other sex play. Sometimes no symptoms develop, and 9 out of 10 infections go away on their own within a year or two. However, the more serious HPV types can cause the infected person to develop cancer.
The CDC states that HPV infections can cause cancers of the cervix, vagina, and vulva in women; cancers of the penis in men; and cancers of the anus and back of the throat, including the base of the tongue and tonsils (oropharynx), in both women and men. This year in the United States, HPV will have caused more than 30,000 cancers.
The good news is that there are vaccines against the most significant cancer-causing types of HPV. But for vaccination to be as effective as possible, it needs to be given at age 11-12, before teenagers become sexually active. This isn't about whether or not our kids have sex; it is about lifelong risks of routine sexual activity.
Rather than get hung up on (or deny) how HPV infection happens - and the unpleasant types of cancer it can cause - we should put into practice what the CDC recommends and the American Cancer Society endorses: vaccination of our boys and girls.
As noted above, routine HPV vaccination of all children should be initiated at age 11 or 12. The vaccination series can be started beginning as early as age 9 and up to age 26, though late vaccination is not as effective.
There are several available vaccines, but Gardasil 9 (the newest version) protects against 9 types of HPV that are responsible for about 90% of cancers related to HPV and is now the sole HPV vaccine available through government programs. Even if someone has already had sex, they should still get HPV vaccine. (Even though a person’s first HPV infection usually happens during one of the first few sexual experiences, a person might not be exposed to all of the HPV types that are covered by HPV vaccines.)
According to Debbie Saslow, PhD, Director of Cancer Control Intervention for HPV Vaccination and Women’s Cancers for the American Cancer Society, “HPV vaccination has the potential to prevent tens of thousands of cancers and hundreds of thousands of pre-cancers each year."
If you could prevent your child from getting cervical, vaginal, vulvar, anal, penile, and oropharyngeal cancer, why wouldn't you? HPV vaccination may be the best, long-term gift you can provide for your kids.
Columns are posted at https://www.angelinaradiation.com/blog along with additional information about Dr. Roberts.
Tuesday, December 6, 2016
Tuesday, November 1, 2016
History and Medicine in Angelina County
I recently came into possession of Angelina County Medical
Society meeting minutes dating back 80 years, from 1936 to 1954. These archives
were kept by Dr. W. D. Thames. A walk down medical memory lane with these
records is remarkable. Some facts are simply mundane. For example, dues in 1936
were $10.50 per member - $488 in today’s dollar. That makes our current County
Medical Society dues of $100 seem like a bargain.
More fascinating to me is that even though the practice of
medicine has changed profoundly over the last 80 years, little of the economics
and politics of being a physician has changed. For example, charity care issues
were documented back in 1937. We struggle with that today. The
physician-patient relationship – what today would be assessed by patient
satisfaction scores – was the topic of lectures in 1938.
The broad legislative issues on the table today are hardly
different than those in 1938 when a Legislative Committee was appointed. Scope
of practice issues with optometrists and chiropractors were discussed way back in
1941. In 1953, Dr. Arnett “encouraged members of our society to join the
American Association of Physicians and surgeons, which is a political
organization of doctors. Its purpose is to stop socialized medicine.” (What
would they say now?)
Some issues from the past seem frankly quaint today. In
1952, Dr. Arnett was to appoint a committee to investigate a physician who took
out an ad in the Lufkin Daily News, apparently quite the no-no at the time. The
next month’s minutes document how that physician “apologized and said it
wouldn’t happen again”. The Society even had a secret ballot to vote whether he
was guilty or not guilty of advertising. He was acquitted on a 9 to 2 vote.
Admirably, the Angelina County Medical Society minutes also
contain notable evidence of community involvement and civic leadership. In
January, 1940, the Society was holding joint meetings with city and county
officials and the Chamber of Commerce directors to discuss a federal aid program
for the building of a county hospital. It was these very discussions that spurred
local industry leaders to join together to build a new hospital. The legend we pass
down is that in 1941, Arthur Temple, Sr., President of Southern Pine Lumber
Company, W.C. Trout, President of Lufkin Foundry & Machine Company, E.L.
Kurth, President of Southland Paper Mills, and Col. Cal C. Chambers, President
of Texas Foundries, along with ten other businesses and industries, joined
resources, refused federal funds, and raised one million dollars to build the
non-profit Memorial Hospital (now CHI St. Luke’s Health Memorial). But we have
forgotten the groundwork was laid the previous year by the healthcare
community, the city and county leaders, and the Chamber of Commerce, all
working together. Such cooperation and leadership can still take place today.
Another more poignant event occurred in February, 1954. Then
President Dr. Gail Medford “read a letter from the Negro Chamber of Commerce
wanting help from the Angelina County Medical Society in their plan to improve
sanitary conditions in the colored community. Drs. Taylor and Spivey, City and
County health officers, were appointed to work with the colored organization.” We
cringe now, thinking about Jim Crow segregation and disparities in neighborhood
services and conditions. But do we recognize similar disparities in healthcare
today? Are we addressing the needs of the indigent, uninsured and underserved
populations among us? Is the medical community as approachable today as it apparently
was in the segregated 1950s?
Technology has revolutionized healthcare over the last
eighty years. But technology cannot replace the heart. Let us not forget our
calling, our oath, and our love for the patient. The practice of medicine should
never be just a job. It is a profession.
I invite everyone to the Salute to Healthcare banquet on
Thursday, November 10, 2016. Help us recognize and honor those in our community
who set the standard in healthcare and who are true to the calling – the
profession – of medicine. Call the Chamber at 634-6644 for ticket information.
Labels:
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CHI,
Ethics,
Healthcare,
Lufkin,
Medicine,
Memorial,
Politics,
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Tuesday, October 4, 2016
Empowered – and Inundated – by Pink
There is a minor malady that comes around every season. It
is characterized by a drop in energy, glazed eyes, and a strong desire just to
sit and do nothing. This condition usually strikes around mid-October and peaks
about the end of the month. Luckily, it doesn’t long. After a week or two of
wearing dark clothes and drinking Standpipe coffee, it resolves completely with
no lasting effects. I call it pink fatigue.
October has barely begun and I have already been interviewed
both for the City Hall Update about the upcoming Power of Pink! celebrations in
Lufkin and Livingston and by KICKS 105 about breast cancer for their website. I
have an on-air interview with Danny Merrell this morning. October 18th is the 5th
annual Power of Pink! event in Livingston, and October 20th is 24th
annual Power of Pink! in Lufkin. Nearly 500 women are expected in Livingston,
and an incredible 800 women in Lufkin. And even though it is not a breast
cancer-specific event, the American Cancer Society’s amazing Cattle Baron’s
Gala is October 15th. October is a busy – and very pink – month!
I jest about getting pink fatigue, but I hope it never, ever
happens. We cannot tire of fighting this disease. Breast cancer is the most
common cancer in women (246,660 new cases in the US anticipated this year) and
the second most common cause of cancer death in women (40, 450 deaths predicted
in 2016). Only lung cancer kills more women. The good news is that the cure
rate for breast cancer that is caught early is really quite high. Today, most
cases (61%) are diagnosed at a localized stage (no spread to lymph nodes,
nearby structures, or other locations outside the breast), for which the 5-year
survival is a stunning 99%.
The American Cancer Society reports that from 2003 to 2012,
breast cancer death rates decreased by 1.9% per year in white women and by 1.4%
per year in black women. Overall, breast cancer death rates declined by 36%
from 1989 to 2012 due to improvements in early detection and treatment,
translating to the avoidance of approximately 249,000 breast cancer deaths.
That is truly remarkable!
But we must not succumb to pink fatigue until ALL women who
need mammograms are getting them. Our minority communities, for example, still
fall behind when it comes to getting mammograms and other screening tests.
The American Cancer Society recommends that women at average
risk of developing breast cancer should have the choice to start annual breast
cancer screening with mammograms beginning age 40 to 44. Women age 45 to 54
should get mammograms every year. Women age 55 and older should switch to
mammograms every 2 years, or have the choice to continue yearly screening.
Always, the risks of screening as well as the potential benefits should be
considered.
These guidelines are for women at average risk for breast
cancer. Women with a personal history of breast cancer, a family history of
breast cancer, a genetic mutation known to increase risk of breast cancer (such
as BRCA), and women who had radiation therapy to the chest before the age of 30
are at higher risk for breast cancer, not average-risk, and should talk to
their doctor about appropriate screening. If in doubt, or you just can’t
remember, get a mammogram every year. It is just easier that way.
Please don’t get pink fatigue! Support cancer research for
prevention, early detection, and curative treatment for all by participating in
something pink this month. Contact Lindsey Mott at 639-7613 for tickets to
Power of Pink! Contact the American Cancer Society at 634-2940 for tickets to
Cattle Baron’s Gala! Or go online to www.CHIStLukesHealthMemorial.org
and click the link to purchase a pink flamingo for $15. Put it in your yard or
at your office to show support for breast cancer awareness. All flamingo
proceeds go to support patients in need right here at the Temple Cancer Center.
Go pink! #BC4TheBirds
Tuesday, September 6, 2016
Prostate Cancer Screening Saves Lives
Over the last 30 years, I have been witness to a remarkable change in how we diagnose and treat prostate cancer. Prior to the mid-1980s, prostate cancer was detected most often when symptoms of advanced prostate cancer were present, such as bone pain from metastatic disease. Very few patients were diagnosed at a curable stage.
The PSA (prostate-specific antigen) blood test came into wide use around 1986 when the FDA approved it for monitoring known prostate cancer. In the early 1990s, physicians started ordering it to detect early, asymptomatic prostate cancer. A spike in prostate cancer diagnosis happened. This wave of patients was a boon to treating physicians, primarily urologists who operate on prostate cancer, but also for radiation oncologists who treat cancer with various types of radiation. More early diagnoses also led to more clinical trials about how best to treat prostate cancer.
We learned a lot. Techniques for removing the prostate got better with the advent of robotic-assisted prostatectomy, as did precision and dose of radiation delivery with intensity modulated radiation treatment. The 15-year relative survival rate for prostate cancer is now an astounding 95%.
But we also learned that not every man with prostate cancer needs treatment.
How can we say this? How can we diagnose someone with cancer and then say, “Oh, by the way, you don't need to do anything about it”? Add to this confusion the 2012 US Preventive Services Task Force recommendation to do away with screening altogether because of the risk of over-diagnosis and harm. In my opinion, that is a dangerous step backward for many of us guys who will get prostate cancer.
Granted, we are too aggressive about treating some prostate cancers. It is easy to vilify doctors who are incentivized to treat rather than watch and wait. But I think a big part of the problem in the US is that patients don't want to be told they have cancer and nothing needs to be done about it, especially when all this wonderful technology exists and insurance will pay for it.
What’s the solution?
We have very good tools now for determining aggressiveness of an individual patient's prostate cancer. That, along with evaluation of a patient's age and overall health status, helps us predict quite well whether or not a particular patient's prostate cancer will ever be a problem for them without treatment. Over treatment can be just as much of an error as under treatment or the wrong treatment. Know all your options for treatment if you need it; no single treatment is right for everyone. Get a second opinion if you haven’t gotten a good explanation about your need for treatment and what your full options are. And, yes, don’t even get screened for prostate cancer if your age and health status are such that you wouldn’t benefit from treatment anyway.
In the near future, there are certain pathologies that we call cancer now that we will no longer label as malignant, as they simply don't act like cancer. (It is a lot easier to say we don't need to treat a condition if we don't call it cancer.) In addition, genetic testing may add to our ability to individualize decision-making based on aggressiveness and risk of spread and progression of disease.
The American Cancer Society continues to support screening for prostate cancer, because they know that screening saves lives. If you are 50 or older – 45 for African American men – and are likely to live for ten years or more, get a PSA blood test. Do it regularly. Go to www.cancer.org for more information. Man up; take charge of your health.
The PSA (prostate-specific antigen) blood test came into wide use around 1986 when the FDA approved it for monitoring known prostate cancer. In the early 1990s, physicians started ordering it to detect early, asymptomatic prostate cancer. A spike in prostate cancer diagnosis happened. This wave of patients was a boon to treating physicians, primarily urologists who operate on prostate cancer, but also for radiation oncologists who treat cancer with various types of radiation. More early diagnoses also led to more clinical trials about how best to treat prostate cancer.
We learned a lot. Techniques for removing the prostate got better with the advent of robotic-assisted prostatectomy, as did precision and dose of radiation delivery with intensity modulated radiation treatment. The 15-year relative survival rate for prostate cancer is now an astounding 95%.
But we also learned that not every man with prostate cancer needs treatment.
How can we say this? How can we diagnose someone with cancer and then say, “Oh, by the way, you don't need to do anything about it”? Add to this confusion the 2012 US Preventive Services Task Force recommendation to do away with screening altogether because of the risk of over-diagnosis and harm. In my opinion, that is a dangerous step backward for many of us guys who will get prostate cancer.
Granted, we are too aggressive about treating some prostate cancers. It is easy to vilify doctors who are incentivized to treat rather than watch and wait. But I think a big part of the problem in the US is that patients don't want to be told they have cancer and nothing needs to be done about it, especially when all this wonderful technology exists and insurance will pay for it.
What’s the solution?
We have very good tools now for determining aggressiveness of an individual patient's prostate cancer. That, along with evaluation of a patient's age and overall health status, helps us predict quite well whether or not a particular patient's prostate cancer will ever be a problem for them without treatment. Over treatment can be just as much of an error as under treatment or the wrong treatment. Know all your options for treatment if you need it; no single treatment is right for everyone. Get a second opinion if you haven’t gotten a good explanation about your need for treatment and what your full options are. And, yes, don’t even get screened for prostate cancer if your age and health status are such that you wouldn’t benefit from treatment anyway.
In the near future, there are certain pathologies that we call cancer now that we will no longer label as malignant, as they simply don't act like cancer. (It is a lot easier to say we don't need to treat a condition if we don't call it cancer.) In addition, genetic testing may add to our ability to individualize decision-making based on aggressiveness and risk of spread and progression of disease.
The American Cancer Society continues to support screening for prostate cancer, because they know that screening saves lives. If you are 50 or older – 45 for African American men – and are likely to live for ten years or more, get a PSA blood test. Do it regularly. Go to www.cancer.org for more information. Man up; take charge of your health.
Tuesday, August 2, 2016
Colorectal Cancer Screening: 80% by 2018
Katie Couric has raised awareness of colorectal cancer ever
since her husband died of the disease in 1998. Yet colorectal cancer remains
the second leading cause of cancer death in the United States, only surpassed
by lung cancer. Both are preventable: lung cancer by not smoking, and
colorectal cancer by screening for and removing precancerous polyps.
The American Cancer Society has teamed up with the CDC (the
Centers for Disease Control and Prevention) and other organizations to set an
ambitious goal of screening 80% of eligible people for colorectal cancer by the
year 2018. Screening for colorectal cancer is incredibly important because
removing precancerous polyps actually prevents colorectal cancer. Across the
nation, if 80% of the eligible population gets screened, it would prevent
277,000 new cases of colorectal cancer and 203,000 deaths (270 of those in
Angelina County!) within 20 years. Those are staggering numbers.
Why so high? Because one in three adults in the United
States between ages 50 and 75 – about 23 million people – are not getting
tested as recommended. In Texas in 2016, there will be 9,680 new cases of
colorectal cancer and 3,520 deaths. This translates in Angelina County to about
36 new cases and 14 deaths this year alone. Remember, these are preventable
deaths.
How are we going to achieve this screening goal locally?
The Angelina County & Cities Health District, CHI St.
Luke’s Health Memorial, the Temple Cancer Center and our local gastroenterologists
have teamed up with the American Cancer Society and CPRIT – the state-funded
Cancer Prevention Research Institute of Texas – to educate our area population
and screen eligible patients for colorectal cancer through a cooperative grant headed
by UT Tyler. Most insurances cover routine screening, but this group stands
ready to make sure that any eligible patient, whether insured or not, has access
to life-saving screening and, if a cancer is found, treatment as well.
There are many ways to be screened, but I want to focus on
the two most available. These two -
colonoscopy and FIT testing – are also funded under the CPRIT grant and by
almost all insurances. Having a colonoscopy is the best test, in my opinion,
because if any polyps are found they can be removed right then and there. If
the colonoscopy is negative, nothing else needs to be done for 10 years! My
wife and I had ours done the year we turned 50, and it really is not a big
deal. Yes, you have to do a bowel prep to clean out your colon, but that is a
small price to pay for peace of mind for 10 years.
The second test covered under the CPRIT grant – and the one
that will be done most often at the Health District – is the FIT (fecal
immunochemical) test. It is a test for hidden blood in the stool, which can be
an early sign of colon cancer. This test is done at home by using a small brush
to collect some stool and place it on a test card. The test kit is then mailed
back to the clinic for processing. The FIT test must be done every year, as
opposed to the colonoscopy every 10 years, but it is cheaper and doesn’t
require a bowel prep. If the FIT test is positive, a colonoscopy is then
necessary.
If you are between the ages of 50 and 75 and have not had a
colonoscopy in the last 10 years or had an annual FIT test, ask your doctor to
schedule you for one. If you do not have insurance, call Angelina County
Connects at (936) 633-1442 and ask the eligibility specialists if you qualify to
be screened under the CPRIT grant. Let’s work together to prevent cancer and
get to 80% by 2018!
Tuesday, July 5, 2016
The Significance of an Ethical Foundation
Last month, I wrote about the role of the hospital Ethics
Committee and commented that open and honest communication between healthcare
professionals, patients and family solves most ethical dilemmas. That assumes
we are speaking the same ethical language and have a common ethical foundation,
both in medicine and in society at large. In our increasingly pluralistic
society, that is no longer a safe assumption. The recent Orlando attack on a
gay nightclub showed us that people can do terrible things when ostensibly motivated
by a perverse ethic or belief system.
Ethics, at its core, is simply a set of moral principles or
values which guide an individual’s – or a religion’s or a government’s –
actions. In the United States, that governing set of principles has been rooted,
sometimes more and, regretfully, sometimes less, in a Judeo-Christian ethic
based on the inherent (and, according to the Declaration of Independence,
Creator-endowed) equal value of every individual. In medical ethics, the two related
guiding principles date much further back, to Hippocrates around 400 BC: the
sanctity of human life and the concept of “first do no harm”.
Modern medical ethics rests on four major pillars: Autonomy
(the patient decides), Beneficence (does it help), Non-maleficence (don’t harm),
and Justice (is it fair or impartial). In other words, do our medical
recommendations and interventions respect the rights of the individual patient,
are they helpful, do they not do harm, and are they fairly and equally available.
It is a tall order to keep these broad principles in mind, especially when
trying to balance competing interests with limited resources.
American history in general – and medicine in particular –
has tended to elevate Autonomy over and above her sister principles. We are a
pioneering, individualistic “I did it my way” society. The winds appear to be
changing, both in healthcare (with the move toward universal healthcare) and in
political discourse. The traditional emphasis on the individual’s responsibility
in his or her own pursuit of happiness is taking a back seat to the notion that
it is the government’s role somehow to guarantee equal outcomes, seemingly
regardless of effort, for all. For example, we just completed a groundbreaking
primary season where an avowed socialist garnered significant support on a
platform of income redistribution.
Amidst this sea change of process, of roles and
responsibilities, can we agree on a common ethic to guide us?
I firmly believe that regardless of who we elect and within
whatever system of healthcare delivery we end up with, a Judeo-Christian emphasis
on the inherent, God-given value of each and every individual (whether black or
white, gay or straight, handicapped or not, born or unborn) is uniquely
protective of both the individual and society as a whole. Mass shootings and
terrorist acts demonstrate that our moral ethic (or lack thereof) determines our
behavior. To paraphrase a Dostoevsky character in The Brothers Karamazov: If
God does not exist, all things are permissible. A disturbing corollary appears
to be: If my moral ethic condones and encourages killing lots of people, why
not do it?
Motivational speaker Zig Ziglar once said, “Since belief
determines behavior, doesn't it make sense that we should be teaching ethical,
moral values in every home and in every school in America?” Whose values? All
belief systems are not equal. Governments and terrorist organizations which do
not value the individual, inherent worth and equality of “all Men” – to again
reference the Declaration of Independence – are not going to treat their (or
our!) citizens equally. In fact, they may kill them (and us).
If I had to choose one word to describe the ethical
principle I pursue in life and in healthcare, it is love. Not hate, not
selfishness. Not religious dogmatism. And not a “love” of government, cult or
fanaticism that discriminates or (God forbid!) kills others in the name of some
god or political whim. It is the pure Christian commandment to “Love your
neighbor as yourself.”
Is this idealistic? Absolutely. Is it achievable? No, to be
honest. But that doesn’t mean I stop working tirelessly, incessantly toward
that goal. Our country should do the same.
Tuesday, June 7, 2016
The Role of the Hospital Ethics Committee
For
most of my 25 years in medical practice, I have been involved in hospital
ethics committees. You may not know that ethics committees exist, or that there
are ethics consults in hospitals.
An
ethics committee is a group of people ranging from physicians to chaplains,
nurses, social workers, and sometimes community representatives who may meet to
develop policies on topics like end-of-life care or medical decision making. It
is easy to understand that conflict may arise, for example, when a patient is
unable to voice their desires and family members don’t agree; it is much harder
to devise or articulate a process toward a solution. Sometimes state or federal
law dictates a path; more often, a Solomon is needed to split the proverbial
baby. Hence, the Ethics Committee can be consulted to advise on a course of
action.
In
each institution I have been associated with, the Ethics Committee does not
decide which course of action to take. They merely facilitate discussion
between parties, advising on known statutes or regulations, and – more than
anything – making sure each party is hearing what the other is saying. Most
ethics consults end up being non-issues; once communication is clear between
parties, agreement on a course of action is often reached.
On
rare occasions, family members insist on care being provided or continued when,
from a medical standpoint, that care is considered futile (or, in PC-speak,
non-beneficial). This is a perfect example of #firstworldproblems. It was only
in the 1960s that coronary care units came into existence. Prior to that, death
in the home was the norm, with family at the bedside. With the advent of
intensive care, we have come to expect immortality in the Temple of Medicine.
As
reported in 2010 by PBS’s Frontline program Facing Death, nearly half of all
Americans die in a hospital (nearly 70% in a hospital, nursing home or
long-term-care facility), while 7 out of 10 Americans say they would prefer to
die at home. More than 80 percent of patients with chronic diseases say they
want to avoid hospitalization and intensive care when they are dying. Yet only
25% actually die at home. The difference between desire and actual care is
striking.
Why,
if we want a certain type of care, do we not get it? For one, we don’t
effectively make our wishes known. In that same Frontline series, only 20 to 30
percent of Americans report having an advance directive such as a living will.
And, even when patients have an advance directive, physicians are often unaware
of their patients' preferences.
The
default action in hospitals is to provide any and all care possible. Blame our
perverse incentive to do procedures, our desire to avoid litigation, and our misguided
belief that we can save everyone, and you get patients dying in the hospital
not even knowing they are at the end of life. It is this window where a
hospital Ethics Committee is most consulted.
In
my personal experience, the ethical conflicts that arise within a religious
context are the most frustrating. Some patients or families hold on to the
miracle cure lottery ticket, demanding care that is both ineffective and
injurious, afraid to let go of “faith”, as if death itself is under their
control.
That
type of faith – sincere as it may be – is nothing more than magical thinking that
binds God to the believer, making God not even a god, but a puppet. As Billy
Graham reportedly said, “Prayer is the rope that pulls God and man together.
But, it doesn't pull God down to us. It pulls us up to Him.”
In
healthcare, there is no “right” to expect or demand care that is not appropriate.
Physicians have an obligation to “first, do no harm”. This is nowhere more
important than at the end of life, where comfort care and quality of life are
paramount. To bridge this unnecessary divide, open and honest communication
between healthcare professionals, patients and family is key. When
communication breaks down, the Ethics Committee can help.
Tuesday, May 3, 2016
Lung Cancer Screening Saves Lives
For more than 50 years now, we have known the dangers of
smoking. That smoking causes heart disease, emphysema, and lung and other
cancers is not in dispute. For fifty years, we did not have an effective
screening tool for lung cancer.
Now we do.
Medical imaging has improved so much that we are now able to
do computerized tomography (CT) scans with significantly lower dose to the
patient and at a low enough cost to warrant widespread use as a screening tool.
Not everyone needs a scan, of course. But smokers who are at high risk of
developing lung cancer now have an option for screening, much like mammography
for early detection of breast cancer.
In 2011, the results of the National Lung Screening Trial (NLST)
were published in the New England Journal of Medicine, arguably the foremost
medical journal in the world. This trial screened current or former heavy
smokers aged 55 to 74 with low-dose CT scanning of the chest and compared it to
standard chest x-ray. The NLST primary trial results show 20 percent fewer lung
cancer deaths among trial participants screened with CT compared to those who
got screened with chest x-rays. This is huge news, because we haven’t cured a
lot of lung cancer over the last 50 years! Based on these results, the Centers
for Medicare & Medicaid Services (CMS) decided in 2015 to start paying for
the procedure on January 1, 2016.
According to the American Cancer Society, in 2016 an
estimated 224,390 people in the U.S. (117,920 men and 106,470 women) will be
diagnosed with, and 158,080 men and women will die of, cancer of the lung and
bronchus, the leading single cancer killer in the U.S. If everyone who was
eligible got screened, more than 30,000 deaths from lung cancer could be
averted every year.
There are more than 94 million current and former smokers in
the U.S. at high risk for lung cancer. In 2014, an estimated 18.1 percent, or 40
million U.S. adults, were current cigarette smokers. Unfortunately, smoking
rates in East Texas are higher than state and national averages. That means a
lot of East Texans are eligible to be screened.
Starting last fall, CHI St. Luke’s Health Memorial began
offering low-dose CT lung cancer screening to eligible patients. Medicare
covers ages 55-77 (commercial insurance 55-80, but Aetna 55-79). Even within
those age ranges, an eligible patient must be a current smoker (or quit no more
than 15 years) with at least a 30 pack-year history of smoking (for example,
smoking 1 pack per day for 30 years, or 2 packs per day for 15 years). And,
eligible patients must have no symptoms of lung cancer (such as coughing up
blood or unexplained weight loss of more than 15 pounds in the last year). If
lung cancer is suspected, a standard CT chest should be done.
Finally, Medicare
requires “shared decision making” on the risks and benefits of lung cancer
screening, which means you must meet face to face with your primary care
provider to get an order for screening.
Since we started screening at CHI St. Luke’s Health
Memorial, more than 70 patients have been screened. Six abnormalities have been
found (including an incidental kidney mass), and two lung cancers have been
diagnosed. Those two cancer patients’ lives may have been saved by screening;
only time will tell.
Of course, the best way to prevent lung cancer is by not
smoking. Ever. Quit if you do smoke. And if you meet the criteria listed above,
talk to your doctor about getting screened for lung cancer. If you have
questions, feel free to contact the Temple Cancer Center at (936) 639-7466 for
more information.
Tuesday, April 5, 2016
Let's Not Get Trumped
I am ashamed. I wrote that phrase recently on a Facebook
post of two Finnish friends who are looking across the ocean with a combination
of disgust and disbelief at the Trump phenomenon. Consider my vow to avoid
public political commentary this year broken.
The first president I ever voted for was Ronald Reagan in
1980. I have voted Republican ever since. But I will not vote for Trump if he
is the Republican nominee. Don’t worry… I’m not voting Bernie Sanders, either.
The socialist movement in the Democratic Party is just as disaffected and
radical as the Trump wing of the Republican Party… and just as dangerous to our
American way of life. We are not Finland. But with Sanders, you know what you
get. With Trump, all bets are off.
Trump's campaign speeches are bullying and belittling, full
of empty rhetoric and supportive of (indeed, encouraging) violence. I don't
care how angry you are at the “establishment”; there is no place in American
politics for Trump’s inflammatory, derogatory speech. Yes, he has a right to
say those things. But shame on each and every American who jumps into the pig
sty with him, eggs him on, and actually votes for him! Regrettably, all of us
on the sidelines have been stained by Trump’s mud.
To my fellow Christians in particular, Trump – in his
campaign rhetoric, at least – displays no evidence of being a Christian, which
he claims to be. There, I said it. Forgive me if you think I am being
judgmental, but I simply don’t see the fruit. This is not about waffling on
various social issues on which well-meaning Christians can and do disagree. Consistently,
his public demeanor is far from “Love God”, much less “Love thy neighbor as
thyself.” If Trump loved anything as much as himself, we’d all be better off.
I don’t get how so many people – Christians in particular –
are following like lemmings in the wake of a reality show Pied Piper – one who
plays an enticing (but fundamentally deadly) tune. It is ironic that Jerry
Springer, who long ago helped set the nasty reality TV tone that is emblematic
of Trump’s campaign, can’t believe we would elect Trump as president.
I get that Trump is tapping into popular themes like
immigration and "making America great again" – whatever that means –
but the reality TV emperor has no policy clothes. In effect, Trump supporters
are saying they want an angry president who doesn't know what he is doing. That
is both startling and dangerous. Anger does not lead to sound foreign policy.
Trump's narcissism, lack of a verbal editor and foul speech suggest
a personality disorder at a minimum. More worrisome, they expose a disturbing lack
of compassion and respect for the innate value of other human beings. Add in a
questionable moral compass and I truly fear the international fallout with his impulsive
finger on the nuclear trigger. He’s just plain scary.
Ultimately, this column is not really about Trump. It is
about me. By what ethic do I live my life and cast my vote? Do I believe that
might makes right? Does the end justify the means? God forbid!
What about you?
If the Republican Party implodes (or if the Democrat Party
nominates a Socialist), I do not blame the "establishment". I blame
voters on both sides of the aisle who can't tell the difference between a slot
machine and a voting booth. They just blindly pull the red or blue lever hoping
for a jackpot. If only they could see, with that approach we are all going to
lose.
Tuesday, March 1, 2016
Cancer Brings Out a Range of Emotions
I hate cancer.
Hate is a bad word, I know. My mother always got on to me
when I said I hated something or someone. We raise our children not to hate,
because hate is one of those harmful emotions and temperaments that threaten to
make us less than human. Of course, kids are prone to tantrum-throwing exaggeration
when it comes to hating. Lima beans, anyone?
But I am a cancer physician and I truly hate cancer. It is
insidious… evil… scary. I respect cancer
- like I respect a wild animal - but I still want to kill it.
I hate some things that cause cancer. Like smoking. I don't
hate the smoker, and – though some may disagree – I am not in your face about
smoking. I also discourage other lifestyle decisions or factors that increase
our risk of cancer (tanning, obesity, etc.). But I don't hate people. We are,
after all, human. And, I know all too well that I could be next to get cancer,
whether it is from something I did or did not do.
As a matter of fact, I fully expect to get diagnosed with
cancer. Perhaps you should, too. I'm not being morbid, just realistic. As a
man, all things being equal, my chance of developing invasive cancer at some
point in my lifetime is 42%. Women have a lifetime probability of 38%. Notice,
I did not say I fully expect to die from cancer. Today, the odds of surviving
cancer are well in my favor. The American Cancer Society reports that over the
past 3 decades, the 5-year relative survival rate for all cancers combined has
increased 20% among whites and 23% among blacks. Today, roughly 7 out of 10
cancer patients are cured.
Contrary to popular belief, the overall incidence of cancer
is declining. It may seem that more people we know are getting cancer, because
as we age our risk goes up. The principal reason for lower rates of cancer is
fewer people smoking. And the biggest factor of persistently elevated cancer
risk, especially in deep East Texas, is also smoking. East Texans still smoke
more than the rest of the state. I applaud Stephen F. Austin University for
their recent decision to join other college campuses in going smoke- and vape-free.
The current trend of vaping is a dangerous prelude to smoking for young people
and needs to be stopped dead in its tracks.
As I said, I do not hate people who have cancer. On the
contrary, I have a great deal of compassion for those diagnosed with cancer. Their
fighting spirit motivates me. I applaud the new American Cancer Society “Advantage
Humans” ad campaign highlighting traits that emerge with a diagnosis of cancer,
such as courage, defiance, and anger. The ads are positive but edgy, acknowledging
that raw emotions are real and battling cancer is tough.
Of course, preventing cancer – where we can – is still the
best option. How? Don’t smoke; vaccinate against human papillomavirus (HPV); don’t
tan; screen for colorectal and cervical cancer. Catch cancer early with
mammograms and low-dose CT for lung cancer. And treat cancer appropriately per
national guidelines such as those developed by the National Comprehensive
Cancer Network (NCCN). Go to www.cancer.org for tremendous resources, and stay
local for treatment where you have excellent facilities and the support of
family and friends.
It is ok to hate cancer. In a strange way, our humanity is
enhanced by hating what is evil (while also clinging to what is good, Romans
12:9). But use that hate constructively to motivate yourself to prevent, to fight,
to come together, and ultimately to win.
Tuesday, February 2, 2016
Doctors Must Reinstill Sense of Duty
This article was originally published at Houston Chronicle http://www.houstonchronicle.com/opinion/outlook/article/Doctors-must-reinstill-sense-of-duty-6733668.php?t=d4a64f80cb&cmpid=email-premium and is reprinted here with permission from the author (me).
I am a physician. Being a doctor defines me. Whether I am seeing patients in my Cancer Center or dining at a restaurant, I am Dr. Roberts. I have expectations of myself in my role of physician, certainly. But the broader community has expectations of me, as well - expectations of competence, compassion and especially availability. Surveys and patient satisfaction scores, however, show that physicians are not meeting those expectations.
I see two broad reasons for this disconnect. One is related to how we practice medicine in the 21st century (in front of a computer rather than in front of our patients). The other has to do with what we see our role to be as physicians.
As a member of my hospital's Performance Improvement Committee, patient safety is our primary concern. Too often, though, we get bogged down in an ever-increasing slough of statistics. Some data we need to track (mortality rates, infection rates, etc.) but other data (such as whether patients think the bathroom is clean enough) are, to put it mildly, distracting.
Chasing data has become the focus of American medicine, and the individual patient has been lost in the process. On top of this is the stress and frustration of working with a bloated and perversely incentivized health-care bureaucracy that views every failure to dot an "i" or cross a "t" as fraud and abuse. Not surprisingly, not only has patient satisfaction declined, but physician satisfaction with the practice of medicine has tanked as well.
It isn't simply about computers and bureaucracy. Since I started practice in 1991, the percentage of physicians in private practice has dropped dramatically. "The New England Journal of Medicine's" CareerCenter website posted that physicians coming out of residency are increasingly gravitating toward contracted rather than private practice positions. Anecdotal reports put the desire to be employed as high as 80 percent. Various reasons are given, including the uncertain direction of health-care reform, declining reimbursement and rising overhead costs. Increasingly, physicians just want to show up at work, practice medicine (without having to deal with administrative and insurance issues), and then go home. They believe that employed positions offer a more predictable work schedule than private practice.
This growing employment model, not just among millennials, coincides with a major shift in attitude among physicians about their role - dare I say duty? - when it comes to patient care. "Becker's Hospital Review," an industry magazine, noted that physicians increasingly expect their affiliated hospitals to provide compensation for on-call coverage, which used to be an expectation of all physicians who had hospital privileges. By 2001, nearly two-thirds of health care organizations provided call pay to at least some physicians.
In our hospital committee meetings, we - the self-selected 10-percenters who are involved in medical staff leadership - bemoan the loss of a sense of citizenship among physicians. We opine on the privilege of being on a medical staff, and that there are responsibilities that come with those staff privileges. Ultimately, we just want our fellow physicians to "do what is right." That simple ethical imperative is the heart and soul of the practice of medicine. Not just doing what is expedient. Certainly not just doing what you hope (or demand) to get paid for.
I fear this is where we are in medicine today. Being a physician is no longer a profession - a calling, a responsibility - it is simply a job. The art and practice of medicine has been reduced to a series of individual transactions, each separately identified in an ever-complex system of billing codes, rather than an ongoing relationship not just between doctor and patient, but between doctor and community.
How can we recover the profession? How do we reinstill a sense of duty? Of moral obligation?
Medical schools have the initial obligation to provide a strong ethical foundation for the practice of medicine. But organizations that provide ongoing training and continuing medical education are responsible as well. The Texas Medical Board requires two ethics and/or professional responsibility CME credits every 24 months as part of a total of 48 credits required.
The Texas Medical Association, which has more than 48,000 physician and medical student members, offers 62 ethics-related CME courses ranging from communication skills and dealing with difficult patients to stress and burnout and HIPAA compliance. However, there is not a single course on basic ethical principles, which have guided the practice of medicine in Western civilization for centuries. Maybe that is because an ethical imperative to "do what is right" presupposes we know (and are willing to agree on) what "right" is.
The United States Conference of Catholic Bishops produced a document - Ethical and Religious Directives for Catholic Health Care Services - which guides all Catholic healthcare institutions, including CHI St. Luke's Health hospitals. Physicians of all faiths would be well served to read and abide by these directives, which first and foremost stem from a sacred view of human dignity. If nothing else, physicians should re-read the Hippocratic Oath, which for centuries has united physicians in a common, patient-centered cause.
Finally, we should look to physician role models around us. The Lufkin/Angelina County Chamber of Commerce hosts an annual Salute to Healthcare banquet where they honor a Healthcare Professional of the Year, Nurse of the Year, Individual of Merit, and a Lifetime Achievement Award winner. In November, I had the honor again of emceeing the event. As I announced the Lifetime Achievement award recipient, I emphasized the award is not just about showing up at work for 40 years and then retiring. That's just doing your job. What we honor each year is the extra - the above and beyond - that exemplifies a career marked by service not just to patients but to society. I hope that by honoring those who set a great example of leadership, compassion, and generosity over and above medical skill, younger physicians will be inspired to follow these examples of care beyond the dollar.
I challenge my physician colleagues, young and old alike, to "do what is right" by all patients. This is your profession, if you will still claim it.
I am a physician. Being a doctor defines me. Whether I am seeing patients in my Cancer Center or dining at a restaurant, I am Dr. Roberts. I have expectations of myself in my role of physician, certainly. But the broader community has expectations of me, as well - expectations of competence, compassion and especially availability. Surveys and patient satisfaction scores, however, show that physicians are not meeting those expectations.
I see two broad reasons for this disconnect. One is related to how we practice medicine in the 21st century (in front of a computer rather than in front of our patients). The other has to do with what we see our role to be as physicians.
As a member of my hospital's Performance Improvement Committee, patient safety is our primary concern. Too often, though, we get bogged down in an ever-increasing slough of statistics. Some data we need to track (mortality rates, infection rates, etc.) but other data (such as whether patients think the bathroom is clean enough) are, to put it mildly, distracting.
Chasing data has become the focus of American medicine, and the individual patient has been lost in the process. On top of this is the stress and frustration of working with a bloated and perversely incentivized health-care bureaucracy that views every failure to dot an "i" or cross a "t" as fraud and abuse. Not surprisingly, not only has patient satisfaction declined, but physician satisfaction with the practice of medicine has tanked as well.
It isn't simply about computers and bureaucracy. Since I started practice in 1991, the percentage of physicians in private practice has dropped dramatically. "The New England Journal of Medicine's" CareerCenter website posted that physicians coming out of residency are increasingly gravitating toward contracted rather than private practice positions. Anecdotal reports put the desire to be employed as high as 80 percent. Various reasons are given, including the uncertain direction of health-care reform, declining reimbursement and rising overhead costs. Increasingly, physicians just want to show up at work, practice medicine (without having to deal with administrative and insurance issues), and then go home. They believe that employed positions offer a more predictable work schedule than private practice.
This growing employment model, not just among millennials, coincides with a major shift in attitude among physicians about their role - dare I say duty? - when it comes to patient care. "Becker's Hospital Review," an industry magazine, noted that physicians increasingly expect their affiliated hospitals to provide compensation for on-call coverage, which used to be an expectation of all physicians who had hospital privileges. By 2001, nearly two-thirds of health care organizations provided call pay to at least some physicians.
In our hospital committee meetings, we - the self-selected 10-percenters who are involved in medical staff leadership - bemoan the loss of a sense of citizenship among physicians. We opine on the privilege of being on a medical staff, and that there are responsibilities that come with those staff privileges. Ultimately, we just want our fellow physicians to "do what is right." That simple ethical imperative is the heart and soul of the practice of medicine. Not just doing what is expedient. Certainly not just doing what you hope (or demand) to get paid for.
I fear this is where we are in medicine today. Being a physician is no longer a profession - a calling, a responsibility - it is simply a job. The art and practice of medicine has been reduced to a series of individual transactions, each separately identified in an ever-complex system of billing codes, rather than an ongoing relationship not just between doctor and patient, but between doctor and community.
How can we recover the profession? How do we reinstill a sense of duty? Of moral obligation?
Medical schools have the initial obligation to provide a strong ethical foundation for the practice of medicine. But organizations that provide ongoing training and continuing medical education are responsible as well. The Texas Medical Board requires two ethics and/or professional responsibility CME credits every 24 months as part of a total of 48 credits required.
The Texas Medical Association, which has more than 48,000 physician and medical student members, offers 62 ethics-related CME courses ranging from communication skills and dealing with difficult patients to stress and burnout and HIPAA compliance. However, there is not a single course on basic ethical principles, which have guided the practice of medicine in Western civilization for centuries. Maybe that is because an ethical imperative to "do what is right" presupposes we know (and are willing to agree on) what "right" is.
The United States Conference of Catholic Bishops produced a document - Ethical and Religious Directives for Catholic Health Care Services - which guides all Catholic healthcare institutions, including CHI St. Luke's Health hospitals. Physicians of all faiths would be well served to read and abide by these directives, which first and foremost stem from a sacred view of human dignity. If nothing else, physicians should re-read the Hippocratic Oath, which for centuries has united physicians in a common, patient-centered cause.
Finally, we should look to physician role models around us. The Lufkin/Angelina County Chamber of Commerce hosts an annual Salute to Healthcare banquet where they honor a Healthcare Professional of the Year, Nurse of the Year, Individual of Merit, and a Lifetime Achievement Award winner. In November, I had the honor again of emceeing the event. As I announced the Lifetime Achievement award recipient, I emphasized the award is not just about showing up at work for 40 years and then retiring. That's just doing your job. What we honor each year is the extra - the above and beyond - that exemplifies a career marked by service not just to patients but to society. I hope that by honoring those who set a great example of leadership, compassion, and generosity over and above medical skill, younger physicians will be inspired to follow these examples of care beyond the dollar.
I challenge my physician colleagues, young and old alike, to "do what is right" by all patients. This is your profession, if you will still claim it.
Tuesday, January 5, 2016
Social Media Diet for the New Year
I have resolved to start a new diet this year. Not the typical food diet, mind you – there is certainly nothing wrong with that. I am going on a social media diet.
When Facebook first came out, I signed up in order to keep up with my kids. They have long since moved on from Facebook. Instagram and especially Snap Chat are more the rage now. Meanwhile, I still troll Facebook’s News Feed several times a day looking for the occasional gem in the garbage can of posts and reposts. I guess I feel compelled to know what is going on in the lives of people I care about. Unfortunately, what most people share is not in the least what I care about.
You know exactly what I mean. I am happy to “like” a post about a significant event in someone’s life, be it a birthday, anniversary, or other meaningful milestone. But please don’t tell me about your bodily complaints, the thing your pet did that was only cute to you, or – hear me now, football fans – play by play about UT, A&M, Dallas Cowboys, or any other team. Think before you post: Is this post worthy of being eternally stored and linked to your name in the Cloud?
For every meaningful, personal post, I have to scroll through a dozen or more platitudes or opinions that only make me feel sorry for the person who wasted their time sharing such meaningless drivel. Even religious posts that may be important to you in the moment rarely have an impact on others. And I fear 2016 – with a presidential election around the corner – is going to be filled with poisonous arrows back and forth between staunch conservatives and bleeding liberals, whose posts are designed to demean and belittle their opponents (and by extension, their supporters). I want no part of that.
After my kids moved on from Facebook, Instagram became the draw. It still bothers me that every time I want to enlarge an Instagram post, my double tapping the photo (a la iPhone) I end up “liking” the photo instead. Then there is Twitter. @justinbieber has 72.4M followers, and is following 247.5K. I, on the other hand, have a measly 110 followers, most of whom I don’t know (and therefore I wonder why they follow me). To be honest, there is nothing (or no one) I follow that provides information I can’t get elsewhere, and there is nothing so urgent that a tweet would change anything I do.
Finally, there are the KTRE and Lufkin News app notifications that pop up on my phone. I tweeted KTRE at one point, saying (in 140 characters or less), “@KTREnews you send out too many alerts. I’ll give you one a day; make it a meaningful one! #wasteoftime” KTRE actually “liked” that tweet, but they still send out too many alerts.
I must admit, I made a conscious decision with both Instagram and Twitter to limit the number of people I follow. Even so, contemplating a social media diet is giving me angst. What will I miss? Who will notice if I don’t wish them Happy Birthday or “Like” their post? But that insecurity is simply pride. I know who I am and who my friends are, and I don’t need Facebook to confirm that for me.
Will I delete these apps entirely? I don’t think so. Will I restrict my viewing and posting? Absolutely. Just don’t judge me when you read this column after it is tweeted and posted on Facebook. It is a diet, after all, not total starvation.
When Facebook first came out, I signed up in order to keep up with my kids. They have long since moved on from Facebook. Instagram and especially Snap Chat are more the rage now. Meanwhile, I still troll Facebook’s News Feed several times a day looking for the occasional gem in the garbage can of posts and reposts. I guess I feel compelled to know what is going on in the lives of people I care about. Unfortunately, what most people share is not in the least what I care about.
You know exactly what I mean. I am happy to “like” a post about a significant event in someone’s life, be it a birthday, anniversary, or other meaningful milestone. But please don’t tell me about your bodily complaints, the thing your pet did that was only cute to you, or – hear me now, football fans – play by play about UT, A&M, Dallas Cowboys, or any other team. Think before you post: Is this post worthy of being eternally stored and linked to your name in the Cloud?
For every meaningful, personal post, I have to scroll through a dozen or more platitudes or opinions that only make me feel sorry for the person who wasted their time sharing such meaningless drivel. Even religious posts that may be important to you in the moment rarely have an impact on others. And I fear 2016 – with a presidential election around the corner – is going to be filled with poisonous arrows back and forth between staunch conservatives and bleeding liberals, whose posts are designed to demean and belittle their opponents (and by extension, their supporters). I want no part of that.
After my kids moved on from Facebook, Instagram became the draw. It still bothers me that every time I want to enlarge an Instagram post, my double tapping the photo (a la iPhone) I end up “liking” the photo instead. Then there is Twitter. @justinbieber has 72.4M followers, and is following 247.5K. I, on the other hand, have a measly 110 followers, most of whom I don’t know (and therefore I wonder why they follow me). To be honest, there is nothing (or no one) I follow that provides information I can’t get elsewhere, and there is nothing so urgent that a tweet would change anything I do.
Finally, there are the KTRE and Lufkin News app notifications that pop up on my phone. I tweeted KTRE at one point, saying (in 140 characters or less), “@KTREnews you send out too many alerts. I’ll give you one a day; make it a meaningful one! #wasteoftime” KTRE actually “liked” that tweet, but they still send out too many alerts.
I must admit, I made a conscious decision with both Instagram and Twitter to limit the number of people I follow. Even so, contemplating a social media diet is giving me angst. What will I miss? Who will notice if I don’t wish them Happy Birthday or “Like” their post? But that insecurity is simply pride. I know who I am and who my friends are, and I don’t need Facebook to confirm that for me.
Will I delete these apps entirely? I don’t think so. Will I restrict my viewing and posting? Absolutely. Just don’t judge me when you read this column after it is tweeted and posted on Facebook. It is a diet, after all, not total starvation.
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