Quality Measures─ Where’s the Compassion?
Sep 12th
As the field of Hospice and Palliative Medicine grows up and integrates into mainstream medicine, we find ourselves increasingly focused on building the evidence base for our practice and developing quality measures that will drive the best outcomes. That’s a noble endeavor, but as we struggle with the science, we run the risk of losing touch with the heart of our work. What drives us to run toward the medical failures, the suffering, the dying and the bereaved when most of medicine has been running the other way? Many would say it’s a call to compassion.
We remember the patients who taught us something special about how we can make a difference as healthcare professionals. Cicely Saunders never tired of telling the story of David Tasma, the patient who became “the window” in her hospice. I treasure the memory of one of my first hospice patients, a 50 year old male hairdresser who was dying of lymphoma in our inpatient unit. I had admitted him expecting to tune up his pain meds and send him home as good as new, but he started into an accelerating daily decline. I felt it was my duty to break the bad news to him that his time was short. I sat at the head of his bed, leaned in and softly listed all the signs that he was getting worse. His sister sat at the foot of the bed in silence. He nodded his head and listened. Suddenly, he reached up with both hands, grabbed my head and gave my bald spot a big rub. After a moment of shock, his sister and I burst out laughing. He grinned and said “I know─ it’s OK.” He died comfortably at home a few weeks later and I went to the wake. His sister introduced me to the rest of the family as the doctor whose head you rub for good luck. They lined up and took turns rubbing my bald spot and we all laughed. He taught me that sometimes just being myself is worth more than all my medical expertise. How do you develop an evidence base around that practice? How do you capture that positive outcome in a quality measure?
As we parse out the components we hope will define quality palliative care, we have to be careful to preserve the whole experience. When I was an English major, I explicated my share of poems, but analysis of the bits and pieces never came close to capturing the beauty of the whole. As Wordsworth wrote:
Sweet is the lore which Nature brings;
Our meddling intellect
Mis-shapes the beauteous forms of things:–
We murder to dissect.
I was privileged to attend a recent AAHPM summit on quality. We talked about taking the lead in defining quality for our field. We were each asked to offer a personal vision for what the AAHPM Quality and Practice Standards Task Force could be in five years. I put mine in the form of a thank you letter from a future patient:
August 9, 2012
Dear AAHPM Quality Task Force,
When I learned a couple of months ago that I have advanced cancer, I was afraid. Not just of the usual things–having pain, being a burden, dying–even more afraid of how the doctors would treat me. I flashed back to the ordeal we went through when my husband died of cancer 6 years ago. As we moved from hospital to clinic to hospice at home, it seemed everyone treating us had their own agenda. We felt lost and out of control. We were told what to do, not asked. He was in pain for so long before anyone did anything about it. When he finally got pain medication, he got so constipated that the hospice nurse had to remove it manually. We felt like cogs in a machine–a horrible, grisly machine.
I cannot believe how different my experience has been. Every time I go to the clinic, someone asks how I feel and what goals I have and how they can help. They are patient with my questions. They are honest and straight with me and support the choices I make that are right for me. I feel I am driving this bus. And I am always asked about my bowels! I am amazed at the transformation. I hear you all had something to do with it and just want to say thanks.
Sincerely,
Cara Little-Moore
It seems to me that we need to go way beyond the current focus on symptom management and discussing goals of care to develop evidence-based practices and quality measures that actually foster compassion. We must be the standard bearers for patient- and family-centered care. We must promulgate best practices in interdisciplinary collaboration and holistic care. We must advocate for no less than restoring the human touch to health care.
Joe Rotella, MD, MBA, FAAHPM
Senior Vice President, Chief Medical Officer
Hosparus Inc.
Lessons from Palliative Care informed the Creation of Whole Person Care at McGill
Sep 7th
In 2011, our burgeoning palliative care team had the unique experience to spend a week learning from the palliative care teams of McGill University. During that week we learned about the Whole Person Care Program and subsequently invited the Director of Whole Person Care, Dr. Tom Hutchinson to Mayo Clinic to lead a workshop on Whole Person Care. It was my pleasure to interview Dr. Hutchinson about the Whole Person Care (WPC) program at McGill.
Cory: Please share with us, Dr. Hutchinson how the whole person care program at McGill got started.
Tom: This history is important because WPC grew out of an insight from Palliative Care that subjective quality of life (QOL) could improve at a time when people are objectively becoming more ill. That change to improved QOL during periods of worsening incurable illness is the process of healing.
Cory: Tell me more about the relationship of WPC to Palliative Care (PC).
Tom: What PC did in taking care of incurable people was that they rediscovered the process of healing. Dr. Mount and Dr. Kearney are largely responsible for this rediscovery.
In 1999, they set out to reincorporate the process of healing into the medical mandate. It had been lost track of. We need both the medical science and the healing relationship; whole person care. The approach has been through transforming our approach to training our medical students and faculty and our relationship with the people of Montreal.
We have two main approaches. First with medical students they have a mandatory WPC curriculum that aims at teaching them tactics to provide a space for healing. Our hope is that McGill is producing physicians better able to incorporate a healing approach into their medical practice. Courses in the existential aspects of medical care are taught and mindfulness and meditation are offered as vehicles to facilitate a healing presence.
We also train our faculty so that there is an environment that is receptive to a healing approach where students can grow and develop.
Students are partnered with their faculty mentor for a mentorship process called physician apprenticeship. There are six students for one faculty for the entirety of medical school. Burnout is a significant entity in medicine. We have started to teach mindfulness for self-care and presence with patients.
We have engaged the public as we recognize the yearning of the general public for WPC. They are essential allies in the promotion of WPC. To capture their interest we have developed two forums to explore healing. Firstly, we have developed a film series in which films illustrating the process of healing are viewed and a dialogue is held after the film. The films are well attended.
We also offer a seminar series with a similar purpose. These are invited lectures on topics like empathy, hope, or other topics related to WPC.
Cory: I understand you are going to expand your influence to host the first ever international congress on WPC starting in the fall of 2013.
Tom: That is right. This conference will be held every other year in Montreal. The focus of the conference is to address how we can change the medical mandate to incorporate WPC. This will be a full breadth academic conference to cover topics such as mindfulness, narrative medicine, and methodology to change systems to incorporate WPC in to the standard practice of medicine.
Cory: This last spring you edited the first textbook on WPC. Can you tell us about the book?
Tom: The book attempts to put together the contributors to WPC from McGill and around the globe. It attempts to develop through 18 chapters the concept of WPC from different aspects and approaches. It covers topics from genetics to medical teaching, and concludes on professionalism at McGill. The last chapter lifts the veil and peeks at the future of WPC as a renewed focus on the relationship between the doctor and the patient. That relationship has both an empathic component and includes medical expertise that the patient doesn’t have. Along with that is the mutual respectful relationship and mutual vulnerability to treat them as a whole human being.
I think this is going to happen because this is what doctors really want and why many went into medicine. And it is what patients really want. Medicine is more effective than ever before but somewhat less attractive due to the loss of the approach to healing. A rediscovery of what is important to doctor and patient and gives satisfaction to both parties within the relationship.
Cory: Since WPC grew from lessons learned from PC, how will WPC and PC relate to each other going forward?
Tom: PC remains the best model for WPC that we have. PC is important as an exemplar of WPC. There is a risk that PC may become a more fixing, curing discipline and forget the healing aspect. PC has to remain the model for healing. PC needs to represent WPC for the rest of medicine. PC is a new way of looking at medicine that can change the rest of medicine. It will have a strong relationship with WPC. PC is a beacon for a different type of care.
Cory: How does PC maintain their skill, role and time in the changing health care landscape?
Tom: Not a simple solution. The more we turn medicine into an enterprise that is financially driven and primarily an industrial model of efficiency and cost effectiveness this will be unhelpful for medical practice. What these approaches do is focus on products and forget the reasons for what we do. A model that focuses on efficiency has different effects that particularly may divert away from processes that lead to healing. There is a momentum to the industrial model.
After speaking with Dr. Hutchinson, I can’t help but wish my medical school had had a similar curriculum with attention to WPC. Fortunately, there are ongoing opportunities to learn from the wealth of experience at McGill. I hope to attend the 2013 first international conference on whole person care. I have already read the book and given a copy to each palliative care team at Mayo within the Midwest.
Cory Ingram, M.D.
Assistant Professor of Family Medicine and Palliative Medicine
Mayo Clinic, College of Medicine
Medical Director – Palliative Medicine
Chair of the Palliative Medicine Specialty Council
Mayo Clinic Health System
Discovering Relief in Our Own Grief
Aug 21st
Formal training in self-care is relatively uncommon in most medical disciplines. Hospice and Palliative Medicine (HPM) specialty may be the exception. Grief if left unnamed can be a source of great pain, and as with any wound, if ignored, runs the risk of festering only to cause even greater discomfort and distress.
Granek et al published a revealing qualitative study earlier this year establishing patterns of grief responses to patient loss among oncologists as negatively impacting both their personal as well as professional lives1. Some of the impacts included worsened emotional irritability and exhaustion as well as the potential for altered patterns of care for future patients in an effort to shield themselves from further pain. Many study participants described their coping mechanisms as one of distancing and denial. Importantly, participants commented on their awareness of these impacts but had no access to altering their behaviors. In fact, several physicians stated this was the first they had ever spoken openly about these emotions due to the taboo of being unprofessional in the medical community.
Perhaps no different from traditional wound care, exploring the depths of grief, risking heightened pain temporarily in favor of providing optimal exposure, may allow for the greatest potential to heal. By actively creating dialogues with colleagues and openly expressing our feelings of connectedness to our patients and families, this acknowledged closeness and care becomes a natural path to grieving in a supportive environment. In fact, it may provide integrated self-care practices offering enhanced resilience and job satisfaction2.
An opportunity for culture change is at our doorstep. With the recent new policy statements issued from the American Society of Clinical Oncology calling for integrated palliative care from the time of advanced cancer diagnosis, and enhanced doctor-patient communication regarding end-of-life care3, an opening for HPM collaboration offering supportive coping and self-care strategies for oncologists is possible. In the past year at UCSF, a portion of our formal curriculum on self-care in the Division of Palliative Medicine has been piloted within the Medical Residency training program with very favorable feedback. We are now in the process of rolling out a program with the UCSF Division of Hematology and Oncology.
Acknowledging loss can take form in countless ways with varying degrees of time commitment. In addition to creating communal condolence cards for those we have served, the UCSF Division of Palliative Medicine has an annual Day of Remembering where families and clinicians come together and openly share stories of grief and love invariably mixed with tears and laughter. What would be possible if clinicians in all specialties were afforded an environment that embraced relationships with our patients with a natural response of grief at the time of loss? What is more human than acknowledging missing someone we have cared deeply for? Perhaps the promise of remembering our patients is the greatest hope we can offer.
References :
1 Granek, L et al. Arch Intern Med 2012,172(12):964-966
2 Mack JW and Smith, TJ. JCO August 1, 2012 vol. 30 no. 22 2715-2717
3 Smith, T.J. et al. JCO Published online before print February 6, 2012, doi: 10.1200/JCO.2011.38.5161
Dawn M. Gross MD, PhD
University of California, San Francisco
Department of Medicine/Division of Hospital Medicine/Palliative Care Service
HPM Workforce Scenarios 2022: Hoping for the Best; Preparing for the Worst
Aug 15th
by Larry Beresford
The most comprehensive assessment of the hospice and palliative medicine (HPM) workforce shortage, conducted by Dale Lupu for AAHPM’s Workforce Task Force in 2010, estimated a gap of between 2,787 and 7,510 FTEs just to satisfy the current need for HPM physicians.[1] And that doesn’t count the coming tsunami of aging Baby Boomers with multiple chronic conditions—or the looming retirements of many of the field’s leaders and pioneers.
The current pipeline of new fellowship-trained HPM physicians adds fewer than 200 new specialists to the workforce each year—with structural constraints on its growth. After this year’s HPM board certification exam in October, the experiential pathway to board certification for mid-career physicians will come to an end. And that is why the Mid-Career Training Task Force convened 43 experts and leaders of the field at the Westin O’Hare Hotel in Chicago August 9 and 10 for a summit designed to grapple with the workforce dilemmas and consider possible future scenarios for this field.
Where is the field of HPM going? Will it continue to experience growth? What will be the impact of an anticipated 4,000 new board-certified HPM doctors following this year’s exam? How does HPM fit into the reforming health care system of medical homes and accountable care organizations? How might the field evolve, revise its focus or even change its name to keep up with those larger changes? Should the focus of AAHPM be narrowed or broadened? If there is a limited resource of HPM specialists, can primary care physicians be taught to play larger roles in providing primary-level palliative care to their patients? What about nurse practitioners and physician assistants? What are best practices in a world where there will never be enough HPM practitioners? What kinds of mid-career alternatives might be envisioned to the full-year, full-time fellowship that will be required for new HPM physicians starting in 2013?
These are the kinds of questions that were explored at the Workforce Summit. National leaders like Norman Kahn, MD, executive vice president, Council of Medical Specialty Societies; Clese Erikson, MPAff, director, AAMC Center for Workforce Studies; and William Iobst, MD, vice president of academic affairs, American Board of Internal Medicine, offered insights, hope and useful suggestions and believed that a mid-career solution was at least theoretically possible, working with ABMS and other specialty societies. But first, it is essential for AAHPM to clarify the need — both currently and in anticipation of future need — and craft a proposal.
Clement Bezold, PhD, founder and chairman of the Institute for Alternative Futures, served as a facilitator, helping participants to engage in future scenario planning, which he acknowledged is an uncertain process. “It’s not about prediction but preparation,” he explained. “Success is the degree to which your current thinking changes.” Participants in small groups explored four possible future scenarios for the field, with his charge: “If this is your future, step into it.”
Congratulations to Academy leaders including Workforce Summit co-chairs Amy Abernethy, MD FACP FAAHPM, David Weissman, MD, and Mid-Career Task Force Chair John Mulder, MD FAAHPM for organizing and framing such an important discussion.
[1]Lupu D. Estimate of current hospice and palliative medicine workforce shortage. Journal of Pain and Symptom Management 2010 Dec.; 40(6): 899-911.
Larry Beresford is a freelance medical writer from Oakland, CA, who specializes in hospice and palliative care issues.
Mayo Transform Conference: Calling Out the End of Life Elephant in the Room
Aug 9th
Since 2009, The Center for Innovation at Mayo Clinic has hosted a unique blending of design and medical professionals to hold a 3 day dialogue, at a deeper level, on innovations that shape new ways of providing medical care with over 8 countries and 21 states represented. There are over 125 businesses in attendance. As an iSpot awardee for our transformative approach to Palliative Care known as The Personal Caring Initiative, I sat down with members of the Center of Innovation(CFI) at Mayo Clinic to talk about Transform 2012: The Conversation will Continue, September 9-11, Rochester, Minnesota.
Cory: First of all, thank you for the iSpot award, I am very grateful and humbled with this award. I am new to transform and I understand it is really cool. Perhaps you can share why “Transform” and why is it cool?
CFI: As a very small team over the last few years, the vision is for transforming the experience of healthcare and to disrupt the status quo. Transform brings in people from many disciplines from outside medicine to collaborate about new care deliver models. Transform is an environment for ideas and inspiration. At the core, Transform is reaching beyond medicine to understand health. It is described as a passionate, energetic, excited, and nontypical medical conference. It is in the space between medicine and design.
Cory: I remember my mentor commenting that we can’t change health care by changing health care but rather, we have to mature our culture and transform our communities. I understand that this year Transform is calling out one elephant in the room that has been considered politically radioactive and a major source of misguided rhetoric in the media, namely, end-of-life care.
CFI: Two elephants are being brought out; End of Life Care and Teenage Suicide. We hope the elephants that come storming out will allow us to look differently at other elephants in our institutions and culture. Michael Wolf, journalist, is a panelist on the Elephant in the Room speaking on his experience with his mother’s medical care as illustrated in his New York Magazine article, A Life Worth Ending. Dr. Satow, is speaking on Teenage Suicide and his creation of the Jed Foundation in honor of his son.
Cory: Why end of life care? In fact, Mr. Wolf’s article was very controversial. It seems a bit risky?
CFI: It is a risk. It is a testament to CFI to be a disrupter of the status quo. We pick things you wouldn’t expect. This will resonate with the personal connection of people within Transform. They have been through this. You want this to blend into the everyday fold of their life. Leslie Koch will speak on the Governors Island story as an example of the something unexpected and an extraordinarily novel and relevant approach to transformation.
Leslie Koch, President of The Trust for Governors Island, is using a very experimental planning model to re-design something very big. She is overseeing the planning, redevelopment and ongoing operation of the Governors Island transformation in New York Harbor. Under her leadership, the island has been a place for experimentation with the end goal of becoming a vibrant public space for New York. She is approaching this project very openly, transparently and using a very experimental model, essentially co-creating the redesign of this property with visitors and citizens of NYC; people that will use the park. Imagine if we approached transforming health care in such a way, or at a micro–level, transforming the Palliative Care model. Going to the users — the patients and family of receiving Palliative Care — to discover new and transformative approaches we can use to care for people and their families living with serious illness and possibly approaching the end of life. Approaches that we may never even have considered on our own. Ultimately creating a care model that provides greater value and better outcomes to the patient and family — much more than an office visit that we sandwich in between visits that can range from ingrown toenails and annual check-ups. The needs of the patient come first, and a holistic model is the healthiest for touching all palliative patients.
Cory: I am getting the sense that Transform is more than the 3 day dialogue?
CFI: What happens at Transform comes back to the CFI to help us understand things differently. Dr. LaRusso has been pioneering this to bring forth the best solutions. Transform is a continuous conversation and connections with attendees throughout the years. The narrative of attendees is that this is a non-traditional conference.
I think the excitement around new ideas and collaborations is a driving force around people wanting to come. They are not satisfied with the status quo and want to impact the lives of people. We are proud of weaving design into health care.
I am very proud to be allowed to participate in Transform 2012 as an iSpot recipient for our work on The Personal Caring Initiative. I envision The Personal Caring Initiative as a model of care that offers hope for our culture and our society as a paradigm shift towards comprehensive tender loving human to human care to our most frail among us affirming life, all of life, including the part called the end of life. It is my hope that there will be a connection created between the AAHPM and Transform to thoughtfully continue to mature and transform our culture, communities and delivery of the best care possible for seriously ill people and their families.
Cory Ingram, M.D.
Assistant Professor of Family Medicine and Palliative Medicine
Mayo Clinic, College of Medicine
Medical Director – Palliative Medicine
Chair of the Palliative Medicine Specialty Council
Mayo Clinic Health System
McGill to Host World Renowned Palliative Care Experts
Aug 6th
This year McGill will host the 19th International Congress on Palliative Care(ICPC) founded by McGill’s Emeritus Professor and Father of Palliative Medicine in North America, Dr. Balfour Mount. The congress is chaired this year by Dr. Anna Towers. This conference represents the oldest conference in the field, and is led by Dr. Bernard Lapointe, Eric M. Flanders Chair in Palliative Medicine and Director of Palliative Care at McGill, with whom I spoke to better understand what attendees could expect from their pilgrimage to Montreal this October 9th-12th.
Cory: Thank you or taking the time to talk with me about the International Congress on Palliative Care. What makes the ICPC so special?
Bernard: It is a continuation of the vision of Dr. Balfour Mount, who founded the first ICPC in 1976 featuring Elizabeth Kubler-‐Ross, Dame Cecily Saunders and Dr. Mount himself. Secondly, the congress is truly international with over 60 countries and all continents represented all coming together to share their visions on PC. The conference is bilingual with presentations in French and English. Lastly, what sets this conference apart is that we dedicate time for interdisciplinary dialogue, questions, and interaction. We pride ourselves in providing a time rich learning environment that allows for presentation and dialogue. It is truly interdisciplinary, and offers the current status of international PC with 400 posters and 260 presenters from around the world.
This year particularly, we have special sessions on pharmacology, the arts and humanities, volunteers, and architecture. The congress remains the largest venue for pediatric palliative care with two full days dedicated to pediatrics for those interested.
Cory: In celebration of the 45th anniversary of St. Christopher’s Hospice, how are you intending on spotlighting St. Christopher’s?
Bernard: This year as well we will spotlight St. Christopher’s and their 45-‐year anniversary. Most interesting, Dame Barbara Monroe will speak on the history and lessons learned at St. Christopher’s and provide a glimpse of the future of PC at St. Christopher’s. The design is that the spotlight will start with a plenary and then a series of workshops.
Cory: I can only imagine that another highlight from the conference will be the closing plenary from Dr. Balfour Mount, On Healing.
Bernard: This will be a fabulous presentation from Dr. Mount that will serve as an overview of his career and his contribution to Palliative Care. I am looking forward to attending the International Congress and from talking with Dr. Lapointe, I have visions of an experience that will connect with rich history of PC at McGill and St. Christopher’s at the same time showcasing the most recent developments in an international interdisciplinary forum. Not to forget, Montreal is a beautiful and delightful fall destination.
Assistant Professor of Family and Palliative Medicine
Mayo Clinic, College of Medicine
Chair of the Palliative Medicine Specialty Council
Mayo Clinic Health System
Preparing for the Board Exam- Test Taking Skills
Aug 2nd
Well, the board review course is complete and many of you are now beginning your studies in earnest. For many of you, it may be the first test you have taken in a number of years. While there is never a substitute for knowing the material, brushing up on your test-taking skills can give you that extra edge.
Bruce Chamberlain, MD has completed an excellent slide presentation on Test Taking Skills and Strategies for the HPM Board Exam. Some pointers include:
- Never get “hung up” on one tough question. Skip it and come back to the question later. Sometimes later questions can provide hints to the answer.
- Answer all of the questions. There is no penalty for guessing.
- Always determine what the question is really asking. Don’t try to insert your “real world” experience.
- With long questions, skip down to the actual question. This can help you focus your approach to the information.
The majority of questions are based on patient presentations occurring in settings that reflect current medical practice.
Remember. Take your time! What do they call the last person to leave the test with a passing score? Board Certified!
Good luck!
Vincent Vanston, MD FAAHPM
It is time for you to act! Help expand the palliative care workforce.
Jul 20th
Yesterday, July 19, AAHPM’s efforts in crafting legislation aimed at expanding opportunities for interdisciplinary education and training in palliative care came to fruition when the Palliative Care and Hospice Education and Training Act (PCHETA) was introduced in the United States Congress. The bill was introduced as S.3407 by Sen. Ron Wyden (D-OR) and as H.R.6155 by Representative Eliot Engel (D-NY17). (Read a summary of the bill.)
Here I am meeting with Missouri Sen. Roy Blunt on July 17. I was one of 21 Academy physicians to take part in AAHPM’s Capitol Hill Days on July 16-18. We met with our representatives in Congress and their staff to help them learn more about palliative care and hospice and to encourage their support of the PCHETA bill.What do you need to do?
Contact your representatives in Congress and ask them to support the bill. Better yet, ask them to sign on as a cosponsor of the legislation. You can help ensure this legislation has the positive momentum that is so critical to moving it forward.
Contacting your elected officials is easy using AAHPM’s Legislative Action Center.
Got Concerns?
Here are the TOP 5 Myths about policy advocacy debunked-
- Myth: I’m Too Busy: This is important. Imagine how busy you will be in a few years with more patients needing palliative care but no increase in the workforce. Take the time.
- Myth: It will take too long: The Academy has set up a quick and easy-to-use interface to reach your legislators. Have plenty of time? Great, personalize your response. But even if no time, you can do this in just a couple of minutes. Do it now.
- Myth: My voice doesn’t matter: It does. You are a constituent. Hearing your voice is key. Take the time
- Myth: I’m from the wrong political party: This is not a partisan issue. The needs of our patients transcend party. Tell the story of helping patients. This can be done.
- Myth: The timing of the bill is wrong: In truth, moving from a bill to law is going to take time. It will not happen overnight. But it has to start. And you taking the time to develop a relationship with your elected officials and their staff will help speed the process along.
Got More Concerns?
Then getting involved with advocacy may be right up you alley. Contact Patrick Hermes, AAHPM Manager of Health Policy & Advocacy.And the next time you see the AAHPM staff, thank them for their hard work on this.
Paul Tatum, MD FAAHPM
The Best Care Possible: A Conversation with Dr. Byock
Jul 9th
In his new book, Dr. Byock shares his refined, crisp, socially and politically attractive call to action for people of our country to join in a thoughtful dialogue about how we all care for each through the end of life. The Best Care Possible follows The Four Things That Matter Most and Dying Well as a foundational contribution to Palliative Care and the American culture. Ira reframes the principles of palliative care in four simple words, The Best Care Possible. I spoke with my mentor about his new book.
Cory: I know you have been touring with your book, doing radio, television and press interviews. What is the dialogue you are hoping to incite?
Ira: The book is not the thing. I wrote the book to provoke discussion in the professional and general public about how we care for each other through the end of life. It is not from ill intention that people are dying badly, but rather because our culture doesn’t have a good sense of what good care is. Culturally we have to grow the rest of the way up. I want to feed the cultural imagination about what is possible through the end of life.
Cory:I want to ask a question that you likely haven’t been asked. As you taught me to state the obvious with patients and families, such as, “I want to make sure you receive the best care possible.” I can see your new book as a reframing of the principles of palliative care in four simple words, The Best Care Possible. I am interested to know how you would call the Academy to action to influence the national dialogue?
Ira: To the Academy’s members, I have to say that time is up. We have been talking for years about what needs to happen. We have been worried about what happens when the baby boomers approach the end of life. Now they have started to show up in the obituaries; 78 million of us. In medicine we have also created chronic illness with many people living with multiple serious illnesses.
I want the field to at least struggle with what is unfolding. Despite all the progress in hospice and palliative care, we are not ready. Look at all the technological advances in medicine, including the creation of the chronically critically ill patients….we are not ready. We have to rise to an unprecedented challenge to preserve western civilizations’ values of caring for each other and preserving the inherent dignity of each and every person as they approach the end of life.
The Academy has a leadership role in helping the culture grow the rest of the way up. There has to be a social and cultural transformation. We have to reframe illness and dying and the care throughout the end of life and reclaim caregiving through the end of life as a profoundly personal and only partially medical experience.
The Academy has to affirm the founding principles of the specialty. Physician-assisted suicide is one case in point. We can’t be neutral about the discipline’s stance. Physician assisted suicide and euthanasia are not the role of palliative care specialists. If you just think about it; we palliative care specialists are all pro-life. Preserving life is at the foundation of western civilization. That is why we have fire departments and police, to serve and protect. We have sanitation and clean water; these are pro-life parts of our society. To somehow allow a political movement to take that language from us and give it to those activists is far more power than they deserve. The Academy needs to start with affirming the principles of the discipline, the inherent dignity of people, the fact that we are pro-life, and that physician-assisted suicide is not part of medical practice.
The cultural transformation has to include being honest about preserving life and being honest about medical possibilities towards the end of life. As a culture we must recognize that we are mortal.
Branding what we do as providing “the best care possible” is consistent with enhancing quality of life, but has “social marketing” advantages. The boomers have always wanted the best. It is a simple message that works really well.
Cory: How is the Academy adopting this?
Ira: It is good language and messaging. In meeting new patients, I often say, “I want to give you the best care possible” as a way of framing the clinical relationship. The term is a vessel in which to pour individualized meaning. But the term is also effective in a social marketing. Giving and receiving “the best care” is meaningful individually and to the macro society. At all levels, palliative care is a way of delivering that goal.
After my conversation with Ira, I am doubly convinced that the best care possible isn’t a slogan or a sound bite. It is authentic. It cuts to the core of palliative care as we match medical possibilities to patient’s preferences and goals while managing symptoms, coordinating care with other medical providers, improving quality of life, providing a space for healing fractured relationships, fostering human development, honoring spiritual traditions and values, and baring witness to the bare and tender emotions of serious illness. Palliative care is the specialty that overflows the vessel of The Best Care Possible through the end of life. I thank Ira for his wisdom, vision and mentorship.
Cory Ingram, M.D.
Assistant Professor of Family and Palliative Medicine
Mayo Clinic, College of Medicine
Medical Director of Palliative Care
Chair of the Palliative Medicine Specialty Council
Mayo Clinic Health System
Medical Marijuana: What Should Palliative Care Specialists Know?
Jul 5th
by Chad D. Kollas, MD FACP FCLM FAAHPM
Read the full article from the summer issue of AAHPM Quarterly.
No matter where you live, if you’ve practiced palliative care long enough, one of your patients has asked you about medical marijuana. “Does it help pain? Does it help nausea or poor appetite? And, perhaps the scariest question for some of us, “Will you prescribe it for me?”
In a surprising move in November 2009, the American Medical Association changed its position on medical marijuana, calling for changes to encourage research about its potential benefits. Other influential medical specialty societies subsequently published similar position statements.
Intrigued by that trend, I co-presented a session about medical marijuana at the Academy’s 2011 Annual Assembly in Vancouver. Several attendees expressed interest in the topic and agreed that AAHPM should consider a position statement about medical marijuana. This article represents a written update of that presentation, and it revisits a controversial question: Should AAHPM consider creating a policy statement about medical marijuana?

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