Thursday, January 17, 2019
Saving Money in Health Care
A good way to redirect the discussion on health care costs and savings is by reading our piece on clinical trials. We need to make sure that each person gets the medicines that we know will work for them. This is how to save lives and save money in our health care system.
Tuesday, August 21, 2018
Redo Recommendations Now: Vitamin D, Fake Data, and Hype
We all need Vitamin D, a hormone, but the challenge is in how to measure levels of Vitamin D, how to determine how much a person needs, and when necessary how to supplement it. Over the years it was difficult for me to reconcile how practically everyone I knew had a Vitamin D deficiency. Since we are not all part of one cohort and we are certainly a group that is diverse in many ways it seemed very odd that we all had the same deficiency.
An answer came in two recent articles. First and most concerning was the August 17, 2018 issue of Science article,"Tide of Lies— The researcher at the center of an epic scientific fraud remains an enigma to the scientists who exposed him."(DOI: 10.1126/science.361.6403.636). This analysis detailed that much of what we know about Vitamin D was based on Dr. Sato's fabricated studies. According to the article his work was "referenced more than 1,000 times, and 23 systematic reviews or meta-analyses have included one or more of the 12 trials." Second, on August 18, 2018 A Kaiser Health News investigation for The New York Times, "Vitamin D, the Sunshine Supplement, Has Shadowy Money Behind It," revealed the effect of one person on an entire field of practice.
Both are disturbing commentary on the state of our knowledge...and our sense of responsibility to one another. How fast will clinical practice change to take this fake data and hype into account? How long will it take to change the Recommendations for Vitamin D Supplementation, the Algorithms in medical decision making and AI, and all the other information that we give and have been giving. Given this evidence how do we answer the question, "Do I stop taking my Vitamin D?"
Labels:
AI,
Algorithms,
Artificial Intelligence,
clinical decision making,
evidence,
Fake Data,
Hormone,
Sato,
Vitamin D
Friday, August 3, 2018
How Can We Do Better...
This has been a year of field research that evidenced that too often efforts to create a better situation ends up compromising a person's health and well-being. Here are three cases to consider.
Heathcare-associated Infections (HAIs)
Frank entered the hospital with pneumonia but upon returning home it seemed that while in the hospital he had contracted an infection of his foot. Several weeks later the infection was much worse and Frank was taken back to the hospital to determine how much of his leg would have to be amputated. There were no plans for rehab.
In 2011 75,000 patients with HAIs died during their hospitalizations.
Best Practice
After Rosa’s stroke she was told that in order to prevent another stroke she needed to have the blockage in her artery cleared, i.e., carotid endarterectomy (CEA). Rosa knew the risks of the procedure but went through with it. Much to her disappointment, a few months later the blockage had reappeared. One year later she still has the blockage but no stroke.
Translational research is a step in the right direction but the continued lag from the bench (research) to the bedside (clinical practice) is unacceptable. At the same time evidence based medicine (EBM) continues to be undermined by the lack of inclusion and analysis by individual characteristics as well as the tendency of clinicians and insurers to apply a rigid set of procedures that are not nuanced to the person in front of you.
Defining Comfort
Agnes was having difficulty breathing and was taken to the hospital. Her initial diagnosis was pneumonia and a UTI; then, suddenly while at the hospital she had two heart attacks. Her family was told that (1) her heart had stopped working and was severely damaged, (2) there were no treatments available, and (3) diagnostic procedures that were invasive were not possible given her age and fragility. Agnes' family was also told that she would die that night in the ICU. Agnes's family decided that given the damage to her heart that "palliative or comfort" care was the best option for her. Somehow Agnes got through the night and after two more nights in the ICU Agnes was moved to a private room. The family was told she could not go home because the levels of oxygen given were higher than allowed in a home setting.
Comfort care what does that mean? How do we know?
Labels:
carotid endarterectomy,
CEA,
EBM,
evidence based medicine,
HAIs,
hospice,
older adults.,
palliative,
stroke
Tuesday, June 27, 2017
Statement on CBO Estimates of Better Care Reconciliation Act
22 million people losing health insurance is unconscionable
“The CBO estimate of 22 million people losing health insurance should be a bill stopper. This bill was supposed to increase the number of people who have health insurance. As it stands the legislation is unconscionable,” said Jane L. Delgado, PhD, MS, President and CEO of the National Alliance for Hispanic Health, the nation’s leading Hispanic health advocacy group.
“It’s time for legislators to go back to the drafting table. The American people deserve bipartisan legislation that will deliver on the promise of insurance for everybody. Congress must (1) ensure access for people with pre-existing conditions instead of enacting barriers to access that may be a death sentence; (2) roll back Medicaid cuts and allow for rates of growth that reflect the reality of an aging population; (3) ensure an orderly transition that does not disrupt care and ensures states can respond to changes in a way that reduces cost growth without compromising quality and access; and, (4) strengthen and expand the network of community health centers that have a proven capacity to deliver quality services,” emphasized Dr. Delgado.
“The one thing that everybody agrees on is that our system is not perfect, so it is time to start working in a bipartisan fashion and serve the interests of the nation. The American people deserve better,” concluded Dr. Delgado.
###
About the National Alliance for Hispanic Health (The Alliance)
The Alliance is the nation's foremost science-based source of information and trusted advocate for the best health outcomes for all. For more information, visit: http://www.healthyamericas.org or call the Alliance's Su Familia National Hispanic Family Health Helpline at 1-866-783-2645.
The Alliance is the nation's foremost science-based source of information and trusted advocate for the best health outcomes for all. For more information, visit: http://www.healthyamericas.org or call the Alliance's Su Familia National Hispanic Family Health Helpline at 1-866-783-2645.
Labels:
access,
CBO,
community health centers,
health care reform,
insurance,
Medicaid,
uninsured
Thursday, June 22, 2017
The New No Gimmick Diet—
The Buena Salud® Guide to Losing Weight and Keeping It Off
The Buena Salud® Guide to Losing Weight and Keeping It Off
I am thrilled by the review and recommendation by Redbook for the latest book in the Buena Salud® Series. You can order the book from Amazon in English or Spanish or through your local bookstore. Let me know what you think. The process of writing and living the book has been quite a journey.
The other books in the Buena Salud series include:
The Buena Salud® Guide for a Healthy Heart
The Buena Salud® Guide to Diabetes and Your Life
The Buena Salud® Guide to Arthritis & Your Life
The Buena Salud® Guide to Overcoming Depression and Enjoying Life
The other books in the Buena Salud series include:
The Buena Salud® Guide for a Healthy Heart
The Buena Salud® Guide to Diabetes and Your Life
The Buena Salud® Guide to Arthritis & Your Life
The Buena Salud® Guide to Overcoming Depression and Enjoying Life
Saturday, May 13, 2017
Considering Arthroscopic Surgery for Your Degenerative Knee Disease?
According to the most recent recommendations published in BMJ it seems that your answer should be,"No." The exceptions are young patients with sports-related injuries, patients with major trauma, and those with a true locked knee. This is a huge concern as according to the article 25% of people 50+ years old have degenerative knee disease.
While a health care provider may be an expert on this procedure and may have been doing it for years...the time has come to rethink when to do it or have it done. The evidence is that in most cases arthroscopic surgery for degenerative knee disease does not produce the desired outcome.
There will be more research to come...in the meantime the challenge is to develop new interventions which are truly helpful.
According to the most recent recommendations published in BMJ it seems that your answer should be,"No." The exceptions are young patients with sports-related injuries, patients with major trauma, and those with a true locked knee. This is a huge concern as according to the article 25% of people 50+ years old have degenerative knee disease.
While a health care provider may be an expert on this procedure and may have been doing it for years...the time has come to rethink when to do it or have it done. The evidence is that in most cases arthroscopic surgery for degenerative knee disease does not produce the desired outcome.
There will be more research to come...in the meantime the challenge is to develop new interventions which are truly helpful.
Friday, February 17, 2017
Back Pain
The data indicate that most people with back pain that lasts less than 12 weeks get better regardless of the treatment. Some people get better even without treatment. Taking all this into consideration as well as all the available evidence, the American College of Physicians recently published new guidelines for the treatment of
back pain. This was the first revision since 2007 and what is recommended is a
departure from past practice.
There are surprises in the new guidelines, e.g., for acute back pain the recommendations include superficial heat, massage, and acupuncture. There are also very specific guidelines as to the medicines a person should take. Take a look at the recommendations and share them with a friend.
The science behind wellness is growing. To make the best decisions for our health and the health of those we care for, we each need to know the
latest science based information.
Monday, August 15, 2016
Another Limit of the Electronic Health Record
Do most
people take the time to review their medical record? Of course not. In my case,
what was supposed to be a tool to improve care missed the mark.
For 35
years I had the same internist. As he changed practices I went with him. Whether
he was a preferred provider or not it was reassuring to know that he had my
whole health history at his fingertips. He could flip through the decades of my
health history and see the changes in my life. It was wonderful to feel the
security inherent in the vision of continuity of care.
All that
came to an abrupt stop when this past year my internist retired. I was all
prepared to find a new internist when I realized it would be helpful to have a
copy of my medical record. Imagine my surprise when I discovered that 31 years
of my medical history were gone. What
had happened?
It seems that
when my internist changed his practice to being part of MedStar my paper
records did not go with him. MedStar was on an electronic system and the health
record they had was only for the last four years he had been with them. All previous paper records were not with
MedStar. When I asked what happened to 31 years of my health record the MedStar
person referred me to my internist’s former practice.
It seemed
that while Medstar was willing to take the patients that came with the
physician the paper health records of the patient were not welcome.
The
situation became more problematic as I reviewed my electronic record. There
were diagnoses for conditions I never had and prescriptions that were never
given.
My
suggestion to everyone? Carefully review
your medical record and keep a copy of it for yourself. The life you end up
saving may be your own.
Monday, April 18, 2016
Rethinking Clinical Trials
Here is the link to my article that appeared today in El Mundo's (translation below) supplement on innovation and technology (Innovadores). El Mundo is one of the most prestigious newspapers in Spain.
Much has been said about the major discoveries that will change our lives. These range from treatments for cancer to those that change the course of the increasing number of rare and new diseases. Developing cures or treatments aligns with the business goal of developing a product or intervention that will improve lives and generate revenue for the innovator company.
Given all the products that are in the discovery pipeline it is clear that companies want to develop new products that improve or enhance lives. And of course the product must be priced so that it is affordable; without sales there are no revenues. Unfortunately, too often in the discussion of the need to develop new treatments the arguments about price are at best myopic. One way to manage prices is to decrease the cost of drug development that according to industry estimates is about $1.2 to $1.3 billion. Advances in different fields like engineering, information technology, and telecommunications need to be applied to drug development.
Other opportunities lie in building new methodologies for clinical trials so that we know more precisely the characteristics of people who will benefit from the treatments that are in development. What we know is that the bulk of trials are based on models of drug and treatment development that ignore that health is very individualized.
There is much upbeat talk about the promise of precision medicine or personalized medicine but it will remain just talk as long as the clinical trials that underlie the development process continue to be structured in a way that is neither precise nor personalized. The innovator working with regulatory agencies has to rethink these critical aspects of development.
The use of animal studies has long been an essential part of basic research. Yet even in these often seminal efforts there have been huge omissions that effect everything from validity to reliability. Reardon [1]pointed out that, “In 2014, the NIH [United States National Institutes of Health] began requiring researchers to include female animals in studies, and giving out supplementary grants to those who complained about the cost." The omission of female animals was not good science.
Likewise factors that also effect outcomes in animal studies are what the animal has been fed and its living conditions. Research indicates that variations in these conditions change the health and longevity of the animals, which impacts on the outcomes and the ability to replicate the research. Although leading experts indicate that animal studies are becoming less relevant we still often extrapolate from animals to humans.
When it comes to studies of people our failures to develop targeted treatments and interventions are compromised even further. To develop precision or personalized medicine clinical trials must at a minimum include and analyze information using race, ethnicity, and gender. These are characteristics that are essential to understanding the success or failure of treatments. The process will be enhanced as information about the individual’s genetic and microbiome become more available.
The solution is not to spend more money on larger clinical trials but to use the advances in all of the sciences and design trials that are better defined, that are inclusive, and carefully monitored. This will make it possible to develop medicines and treatments that meet the health needs of the individual, the revenue goals of the innovators, and most importantly, continue to support future discoveries to benefit us all.
[1] Reardon, S. "A mouse's house may ruin studies— Environmental factors lie behind many irreproducible rodent experiments." Nature. February 18, 2016 vol. 530 Pg. 254
Thursday, January 7, 2016
Sugar and the 2015-2020 Dietary Guidelines
We are all too
familiar with sugar as a driver for diabetes and excess weight. Yang et al[1]
piled on even more
data to raise our concerns about sugar when their research found that people
who had more sugar in their diet were more likely to die sooner from
cardiovascular disease.
So today when I listened to the Dietary Guidelines Stakeholders Briefing convened
by USDA and DHHS I was very interested in the recommendations on sugar. I knew that
in March 2015 the World Health Organization released a new guideline that recommended
adults and children reduce their daily intake of free sugars to less than 10%
of their total energy intake and that a further reduction to below 5% or
roughly 25 grams (6 teaspoons) per day would provide additional health
benefits. I wanted
to understand the rationale on deciding on the U.S. guideline of 10% instead of 5%.
I was glad to be part of this briefing and
liked the transparency of of being encouraged to type in our questions. As I typed
in my question I could see the questions that others had asked and was looking
forward to the answers about soy, caffeine, etc. When the moment for Q & A’s
came up I was shocked that none of the questions that were posted were asked. I
typed my question in again just in case someone had missed it…and still no
response. I sent an email to ASHMedia@hhs.gov
and am still waiting for a response. A simple answer would be informative. But I guess it is all related to why the 2015-2020 Dietary
Guidelines were not released until 2016.
[1] Yang, Q.,
Zhang, Z., Gregg, E.W., Flanders, W., Merritt, R., Hu, F.B. “Added Sugar Intake
and Cardiovascular Diseases Mortality Among US Adults,” JAMA Internal
Medicine. 2014;174(4) Pgs. 516-524.
doi:10.1001/jamainternmed.2013.13563.
Tuesday, December 29, 2015
Myths We Love
Megan Scudellari’s, “Myths that will not die,” (Nature, Dec.
17, 2015 Vol. 528 pages 322-325) http://www.nature.com/news/the-science-myths-that-will-not-die-1.19022 focused on five myths: (1) screening saves lives for all types of cancer; (2) antioxidants are good and free radicals are bad; (3) humans have exceptionally large brains; (4) individuals learn best when taught in their preferred
learning style; and, (5) the human population is growing exponentially.
Each statement had some initial evidence to support it but
over time more research challenged the initial outcomes. What was compelling as
I read the article was realizing that there were factors that seem to
perpetuate if not strengthen a myth. These factors include a vocal community of
supporters; the development of products, industries, and research lines to address or remedy the
situation; and, attempts to discredit new research. As a result, myths
like lies that are repeated, become accepted as truth. In the end the damage is
done to all of us because rather than moving forward with science we are in a
chokehold because of what others want us to believe.
As I look forward to 2016 and beyond, my hope is that as our knowledge grows we
will use information wisely and change what we know and espouse. "Trust, but verify," should apply to much of what we do in
health so that we can achieve the healthier
and longer lives we all want.
Labels:
"trust,
antioxidants,
but verify",
cancer,
free radicals,
myths,
Nature,
prevention
Wednesday, August 26, 2015
Me and Burgers
I love hamburgers but lately I only eat them at home. I do not want to seem like a wuss but it seemed to me that when I ate burgers outside my home my microbiome let me know that they were displeased with my selection. Some of the people I know thought that I was just being picky when I said that I preferred meat that did not have added antibiotics or hormones. Today's Washington Post made clear that my microbiome led me to a healthier choice.
Sunday, August 9, 2015
Coca-Cola Funds Global Energy Balance Network
WHO is recommending limits in sugar intake because of the worldwide increase in people who have excess weight. Drinking one typical can of sugar sweetened beverage exceeds the limit. Nevertheless, it seems that Coca-Cola is interested in research that documents that excess weight is not due to bad diets but to not enough exercise http://nyti.ms/1KZUZ4e They just funded the Global Energy Balance Network to lead this work.
Labels:
Coca-Cola,
excess weight,
obesity,
sugar sweetened beverage
Thursday, May 7, 2015
How to Reach the Hispanic Community...
Here is the link to my article that appeared on May 6, 2015 in El Mundo, Section on Business and Innovation, Madrid, Spain. http://www.elmundo.es/economia/2015/05/06/5549dfc8e2704ee34b8b4574.html . The translation is below.
Reaching Everybody
I was
having a conversation with the CEO of a major company about how to reach 57
million peple in the United States. When I mentioned that I was talking about reaching
the Hispanic consumer there was a pause and a palpable change in the
conversation. The enthusiastic CEO went into automatic mode accentuated by polite
comments that indicated interest and understanding. Then the entire project was
handed off to the person responsible for Diversity — a death knell for
meaningful work.
The Chief
Diversity Officer is a C suite position without budget responsibilities that
lacks the clout that is necessary to execute. These positions are meant to
deflect challenges to the status quo rather than define the possibilities and
the opportunities in a growing market. With neither a place in the chain of
command nor the portfolio that could make the necessary investments it is a place
where ideas go to die. The Diversity person is there to make the company appear
like they are doing something to serve their diverse consumer base.
Just like EEO
Offices of decades past or the more recent renaming of similar offices as Minority,
Disparities, Equity, or some other politically palatable name of the moment these
offices do little more than develop plans and do training. Most companies take
a 20th century approach and establish an employee group that is made
up of the targeted community to advise them; hire outside expertise on the
targeted group; create an advisory group of stakeholders; create a diversity,
health equity, multicultural, or alliance development office; translate
existing documents, webpages, etc. to the target language; add pictures of the
target group; add food selections at corporate cafeterias that cover a variety
of countries; and, sponsor “Month of…” events.
While these
may be well-intentioned the totality of activities make it obvious that what
has been accomplished is mostly veneer. Even worse they can be seen as a
defensive response devoid of the tools to create the type of meaningful inclusion
that produces financial results. This is bad for business and for our economy.
Reaching
Hispanics or any target group means reaching individuals with an image, work,
and product that resonates with who they are and what they want. It takes more
than a diversity office to do that…it takes leadership and the commitment by
every person in a company. That
leadership is hard to come by when Hispanics are one in six persons in the U.S.
but at Fortune 500 companies are less than 2% of the CEOs and less than 4% of
the Boards of Directors.
Trust and brand loyalty go
hand-on-hand and today each individual wants to know that a company knows who
they are and what they want. Too often I hear that Hispanics are too diverse
and because of that it is hard/incorrect/disrespectful to get a single message
that resonates with everyone. That type of strategy reveals a lack of
understanding of the American marketplace.
With the rare exception of being in a
building that is on fire and yelling ”Fire,” it is unlikely that a single word can
reach everyone. The era of the single message went the way of having only a
handful of major networks. Each person wants and expects to be reached with a
message that is tailored to them; that is why Google has been so successful.
Google knows each of their users and craft messages for them.
So when I am asked how do you reach
Hispanics? It’s the same strategy that you use for everybody—use language and
images that are meaningful to the individual, make clear that you understand
what they want and desire, and as a result earn trust and respect. You do
different things at different times. Reaching everybody is no longer a one shot
deal.
Labels:
C-Suite,
Chief Diversity Officer,
diversity,
Fortune 500,
Google,
Hispanic,
leadership
Thursday, March 5, 2015
Big Data and You
El Mundo, one of the most prestigious newspapers in Spain, created a daily supplement on innovation and entrepreneurship (title Innovadores) and as an advisor to Bankinter's Future Forum I wrote this article on "Big Data and You."
Here is the translation:
Big Data and You
We
all accept that there is an abundance of data that are used to define everything
about us. The data that are collected are then harvested by all types of
entities and put together in ways that communicate more to others than we may
want to share. But with the promise that the data cannot be traced back to the
individual we release much of what is private about our lives. Nowhere is this
more evident than in the health care setting where data are being merged from
different sources to produce predictive models for deciding upon the type of
treatment an individual should receive.
The
use of big health data has been heralded as a giant leap forward in that
information from different people can be used to give a fuller picture of what
are the risk factors that we need to pay attention to. With these aggregated
data and the risk profiles they provide health care providers at every level are
equipped with an array of protocols about how to treat a patient. These data
can also provide new and compelling alternatives to what would be considered
the usual standard of care.
But
we must proceed with great caution. Recent
research[1] funded
by the National Heart Blood Lung Institute in the U.S. documented that commonly
used risk assessments of atherosclerotic
cardiovascular disease (ASCVD) overestimated the risk by 37 to 154% in men
and from 8 to 67% in women. That translates into a huge amount of people
getting treatment they did not need.
Big
data are the results of combining lots of smaller bits of information. How big
data are gathered and how they are merged can become a problem. This is made
worse if at the point of care risk scores replace talking to the patient or the
ever elusive listening to what the patient says. The promise of health care
providers to “Do no harm” can be compromised by the overreliance on tools that
are meant to add to the clinical conversation and not dominate them.
Jane
L Delgado, PhD, MS,
President
and CEO
National
Alliance for Hispanic Health
Washington,
DC
janeonhealth@gmail.com
[1] Andrew P. DeFilippis, MD, MSc*; Rebekah Young, PhD*; Christopher J. Carrubba, MD; John W. McEvoy, MB, BCh, BAO;
Matthew J. Budoff, MD; Roger S. Blumenthal, MD; Richard A. Kronmal, PhD; Robyn
L. McClelland, PhD; Khurram Nasir, MD, MPH; and Michael J. Blaha, MD, MPH. An
Analysis of Calibration and Discrimination Among Multiple Cardiovascular Risk
Scores in a Modern Multiethnic Cohort. Ann Intern Med. 2015;162(4):266-275.
doi:10.7326/M14-1281
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