I like Dr. Spencer’s advice. I would point out that not every healthcare organization has a palliative care program. Perhaps this is where patients and families should expand their search for locally available palliative services. Does the local hospital provide palliative care? How can I access this service? Healthcare organizations should strive to ensure they have palliative care services available to their patients. Perhaps CMS should consider revising its HCAHPS survey. Instead of asking about food services, they should ask if hospitals have a palliative care service. Better yet, why not add this to the survey instead of substituting? We also need to normalize conversations about transitioning care when we arrive at end-of-life, emphasizing that we are not stopping care, just changing the goals. We cannot stop the biological clock, but we can ensure patients receive high-quality symptom management. How fortunate that we have a federal entitlement to provide end-of-life care. It's a shame we still struggle with having explicit conversations about hospice care. It's time to change that! 👇 #hospice #hospicecare #palliative #palliativemedicine #palliativecare
Absolutely agree!Andy Arwari MD MS FACP SFHM FAAHPM HMDC Expanding the search for palliative care services is crucial, especially when not every healthcare organization offers them. Your point about revising the HCAHPS survey is spot on—highlighting the availability of palliative care could drive more hospitals to prioritize these essential services. Normalizing end-of-life care conversations is also key to ensuring patients receive the compassionate care they deserve. Let's keep pushing for these important changes!
Excellent! I find this so true. Sometimes patients, but often families, are looking to us to tell them it’s okay to change focus. They often know this but don’t want to be the ones to bring it up….and they shouldn’t have to be.
Point well made. We are not giving up. We are adjusting our goals for care.
Fully informed care. Listening to what people desire for their life and planning for the transition to end of life. So valuable and much needed. Thank you for the post.
excellent article. We have to advocate for ourselves and educate our loved ones to advocate for themselves.
I’m in violent agreement. Normalizing the conversation increases the “N” to push for change. It’s time to invite death into the room.
People asking people. Different to physicians telling patients. Inequality when we are our most vulnerable... thanks Andy Arwari MD MS FACP SFHM FAAHPM HMDC
very good guidance/advice on public health education on benefits of EOL care
Exactly! Communication and access are crucial to caring for our loved ones and for self care. Ask your hospital and your Attorney what is available. 🙏
I once saw the analogy of being tied to railroad track and being given binoculars to see the train coming sooner,! this was in the context of restaging or rescanning for metastatic disease and cancer patients but do we really want people focusing on what is wrong with them or what symptom burden they have rather than helping to solve those symptoms. I work in community palliative care and I have found that I can be in the home and see exactly what is going on and what the needs are and many times some of the issues are the multi prescribing and no one really knowing all the different meds that someone is on. We can start symptomsChasing with medication’s which leads to needing other medication’s for the symptoms that we caused from the medication’s and maybe not even from the disease process. We need to de-prescribe