There was a very important article written in the NY Times today. It highlighted a common medical scenario in my world—the defibrillator (ICD) world.
I am going to talk about ICDs here, but the big picture inherent in this story illustrates the important issue of how best to apply invasive therapy to elderly and sicker patients.
The Times piece delved into medical decision-making when patients present with battery depletion of their defibrillator. The battery longevity of these devices ranges about 5 years. The default amongst many heart doctors is to assume that patients still need or want their ICD. I can say from personal experience that this is an incorrect assumption. There are other options. The device can be deactivated and left in place, or it can be exchanged for a non-shocking pacemaker.
Times author, Paula Span, smartly featured an interview with Harvard doctor, Daniel Kramer, who has been a strong and sensible voice in the electrophysiology world. He was a great person to interview for the story because he dares question the status quo. I loved the piece, but was surprised by the vitriol of some of the commenters.
Harvard doctors generally do not need mere medical bloggers to come to their support. But after reading the comments, which I am afraid, may be representative of many, I feel compelled to stand up for Dr. Kramer. Though we have never met, I am a huge fan of his work.
As an ICD implanter, I have seen both the good and bad of these potentially lifesaving devices. Like most invasive treatments in Medicine, the good can be very good and the bad, really horrific. One particular ICD patient comes to my mind: A man brave and strong enough to storm the beaches of Normandy in WWII was transformed to a scared and depressed old man in the years after his defibrillator misfired 72 times. It was awful. These stories stick with you.
Readers need to know that this NY Times piece recapped an important article that Dr. Kramer recently published in the NEJM. In it, he and co-workers spoke frankly to the medical community about ICD generator changes. The excellent article garnered little fanfare with heart doctors.
Going against strong headwinds in his own community of heart specialists, Dr. Kramer emphasizes three important issues that come about when older patients with ICDs face battery depletion: First, he asks heart doctors to re-evaluate whether the patient still benefits from the ICD. Perhaps, the original heart problem has improved? Secondly, he points out that a patient’s experience living with the device may have changed their mind about keeping it active. Perhaps, a patient with inappropriate shocks no longer wants the device? Thirdly, since the original implant, a patient may have changed their goals of care. Many patients no longer desire life-sustaining shocks—for whatever reason. It’s their choice; but they aren’t often asked.
You may wonder why such obviousness isn’t the norm?
It’s because our healthcare system imparts significant barriers. Dr. Kramer nicely explains two important hurdles: One is that healthcare in the US is fragmented, especially for the infirmed and elderly. Patients may have many doctors, and care is often not well-coordinated. This means, an installer, a proceduralist like me, is left discussing end-of-life care with patients immediately before ICD surgery. That’s not good. I am married to a hospice doctor, so I sort of know how to manage these conversations. This is not the norm for procedure-oriented heart doctors. The other barrier to getting the elderly the best care is our system’s misguided incentives. In our current fee-for-service system, I am rewarded for doing, not discussing not doing. In fact, not doing stuff is very risky—both legally and professionally (ie, loss of referrals.)
Finally, Dr. Kramer and his colleagues call for heart doctors to take the lead in starting “the conversation” with ICD patients. He wants us to share the decision of using invasive, potentially dangerous or ineffective care with the patient. He also asks the scientific community to study the outcomes of patients who undergo elective ICD generator changes. These should not be controversial recommendations.
It’s a huge mistake to equate this kind of smart thinking to rationing. Aligning evidence-based care, especially potentially burdensome surgery in elderly patients, with the goals of the patient is not rationing; it’s moral, ethical and obvious.
JMM
Rosemary says
Why is it that personal preferences are so disturbing and distasteful for end of life decisions?
It has been argued that those who are depressed or lonely do not have the rational mindset to make these life-altering decisions. Understandably, the pressure is put on younger patients to weigh all things considered whereas older patients may not have the same “liabilities” of choice.
However, as our population ages and our society adapts to this increasing geriatric population, many of these quality of life discussions should naturally progress. But what do we do in the meanwhile?
“Ensure that there are no physical or mental stressors that play into the decision making strata” has been our response. But what if physical and/or mental stressors are inherent to the decision itself? How comfortable is it for an octogenarian to deal with atrial fibrillations comparatively to a person half their age? What recourses do each of these patients have?
When viewed in a comparative manner and then assessed, the differences become obvious. But why then don’t the treatment options change accordingly?
Jackie Fox says
Sadly, vitriolic comments don’t surprise me. As a former and future patient (not heart-related–yet) I will do what I can to help spread the word by retweeting this fine post.