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Joan’s Story- Yet Another Example of the Benefits of the ABCDEF Bundle

Joan’s Story: Yet Another Example of the Benefits of the ABCDEF Bundle

Despite all the evidence to the contrary, most ICUs still operate as if the best thing you can do for patients on the ventilator is to ensure they remain sedated and immobile.

But the truth is, there are mountains of evidence to show the harm that these practices can cause for ICU patients, and just as many studies that show the benefits of doing the exact opposite.

Slowly but surely, ICU clinicians around the world are beginning to admit that their previous approach was wrong and starting the process of implementing evidence-based sedation and mobility practices.

Unfortunately, most ventilated patients don’t get to experience this kind of care, but when you analyze the outcomes for the lucky few that do, the benefits couldn’t be more obvious.

I love highlighting these kinds of positive outcomes for patients who do receive the kind of evidence-based care outlined in the ABCDEF Bundle, and the case we’re about to look at offers a great example.

It involves a woman who could very well have died or had her quality of life destroyed had she received conventional care, but she was lucky enough to be admitted to an Awake and Walking ICU.

Her name is Joan, and this is her story.

 

How the ABCDEF Bundle Preserved Joan’s Quality of Life

Joan awake in the ICU

Joan is a 38-year-old woman with a history of tobacco use who was admitted to an outside hospital in September of 2018 for acute respiratory failure secondary to influenza, which then devolved into acute respiratory distress syndrome (ARDS).

She required mechanical ventilation, but fortunately for her, she was transported to the Awake and Walking ICU, which adheres to the evidence-based practices found in the ABCDEF Bundle.

Joan was immediately liberated from sedation and allowed to wake up and mobilize for the rest of her time on the ventilator.

Her mild ARDS persisted, and for many days, her ventilator settings were sitting at a PEEP of 12 and an FIO2 of 60%.

In spite of her illness, Joan was able to text staff and family on her phone, walk, help her kids with their homework, and play an active role in her recovery.

She had an unprecedented gag reflex that is not present in most patients, but still, she stayed calm and tolerant of the tube because she was free of delirium.

“It was horrible. I gagged constantly,” she said when I asked her about what it was like being awake on the ventilator.

When asked how she dealt with this discomfort, she said, “I think it was just the will to survive. I had realized that, you know, I’m not getting out of here unless I do something about it.”

Joan also reports having terrible experiences while under sedation during her transportation to the Awake and Walking ICU and said she would have preferred to endure gagging on the tube rather than having to deal with the terrors she suffered while she was sedated.

Luckily for Joan, she only spent about 12 hours under sedation, as she was airlifted to a different hospital, but she still had to deal with some incredibly disturbing hallucinations, including feeling like one of the nurses was trying to cut off her hand.

“He was just sawing into my wrist. And he kept telling me I’m so sorry. I’m so sorry. And I could have sworn he was sawing my wrist off,” she said.

When I asked her why she preferred to remain awake, rather than be sedated, she said, “If I had to go through that for 17 days, I think I would have been…you would have to put me in a loony bin.”

By the time she was ready to leave the ICU, she was able to walk more than 1000 feet at a time, despite being on the ventilator.

“My nurses and everybody just kept pushing me and said if you want to get better…you’ve got to get up and walk. So, to be able to get up…it’s huge,” she said.

Believe it or not, because she was awake and mobile, Joan was even able to take showers while on the ventilator, which provided her with some much-needed comfort and dignity.

icu patient shower

As you can see from the image above, in order to facilitate this, the nurses who treated Joan had to wheel her ventilator right down to the shower.

“The very first time was very unpleasant,” she said, explaining that at the time, she wasn’t even able to wash herself without help from the nurses.

But with a lot of determination, and the dedication of the ICU staff, Joan was eventually able to take a shower all by herself. “That was probably my favorite part,” she said.

Then, after 17 days of being intubated on mechanical ventilation, Joan was successfully extubated.

And as a result of the evidence-based care she received in the Awake and Walking ICU, she was able to walk out of the ICU doors and go straight home from the hospital.

What’s more, only a few months after her discharge, she was back to running her own business.

“I’ve heard other ARDS patients where they say, ‘I’m losing my house and everything,’” she said. “I was so blessed to come back to work soon.”

Joan later joined an ARDS survivor support group on Facebook.

Thankfully, she was unable to relate to most of the conversations this group was having, as she does not suffer from things like post-ICU PTSD, cognitive deficits, tracheal stenosis, or the long-term effects of ICU-acquired weakness.

“You know, most of the ARDS patients I can’t relate to because I wasn’t sedated. I was awake through the whole entire thing,” she said.

“Being awake is so rewarding. I would not change it for anything, as much as the pain. It was the worst pain I’d ever went through. It was the worst nightmare I’d ever went through. But I wouldn’t change it. I’d still want to be awake again.”

At any rate, the choice to allow Joan to wake up and mobilize while she was on the ventilator was likely responsible for saving her life, not to mention sparing her the costly repercussions of sedation and immobility.

In the end, it allowed her to preserve her quality of life and continue to provide for her family in the face of what could have been a grave illness.

If you want to learn more about Joan’s story, from the woman herself, you can hear her talk about her experiences in the Awake and Walking ICU on Episode 17 of my Walking Home From The ICU podcast.

 

Are you ready to do what’s best for your patients, your ICU team, and your bottom line, by implementing the most up-to-date, evidence-based practices? We can walk you through the entire process, so please don’t hesitate to contact us.

 

About the Author, Kali Dayton

Kali Dayton, DNP, AGACNP, is a critical care nurse practitioner, host of the Walking Home From The ICU and Walking You Through The ICU podcasts, and critical care outcomes consultant. She is dedicated to creating Awake and Walking ICUs by ensuring ICU sedation and mobility practices are aligned with current research. She works with ICU teams internationally to transform patient outcomes through early mobility and management of delirium in the ICU.

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Over the last few years I have become aware of the PICS (post-intensive care syndrome) condition and the very serious negative impact that it has on our ICU survivors. I have become much more aware of the potential negative impact of anxiety, depression, PTSD and cognitive dysfunction. Many patients whom we consider saves in the sense they leave the ICU alive have many issues that most people would consider far from a successful experience. Their lives are often dramatically changed in a very negative fashion.

I am a professor of medicine and have been an ICU director for over forty years. What I find very disturbing in my own experience and that of many other intensivists is that this outcome is generally considered acceptable; the patient survived and will get better with time. We have little access to these patients and almost zero information about their condition unless they are unfortunate enough to return to our ICUs. Very few of us have a PICS clinic where we would have a chance to better understand the challenges that some of our patients encounter, and there are very few systems in place to provide feedback to us as ICU clinicians. Therefore, we are blissfully ignorant of the many challenges that a substantial number of our survivors encounter. This is a major problem. The vast majority of ICU survivors and their families will experience cognitive, emotional and physical symptoms which often have devastating impacts on their lives. At this time, with PICS clinics being a rarity, there is no reasonable mechanism for intensivists to have a solid perspective on the frequency and severity of this condition.

How patients and their families are treated in the ICU often has a major impact on how the patient and families survive post discharge. It is generally agreed that most sedation infusions, particularly benzodiazepines, frequently have higher incidences of delirium and post-discharge dysfunction. There are a few hospitals in this country where sedative infusions are rarely used and the incidence of the complications described above are dramatically decreased. I have visited one of these hospitals and was amazed to see how effectively patients on maximum ventilator support can be managed, even walking without sedative infusions. In an effort to explore this treatment option in greater detail I have identified Kali Dayton. She is a nurse practitioner who has practiced in this Awake and Walking ICU for many years and is an amazing source of information on this topic. After extensive discussion with many colleagues, administration and many others, and reviewing the major potential benefits of the program for our patients, we have decided to introduce this program into our hospital.

Peter J. Murphy, MD, FCCP, MRCPI, BSc

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