For those who have experienced a sudden cardiac arrest, or for the courageous co-survivors who stood by them, the immediate aftermath is often a blur of medical interventions, anxious waits, and the profound relief of survival. But what happens once the acute crisis has passed, and the hospital doors close behind them? The journey to recovery is rarely a straightforward path, often extending far beyond the initial weeks and months. A recent Swiss study sheds important light on this long-term landscape, specifically examining the prevalence of Post-intensive Care Syndrome (PICS) and its impact on the lives of cardiac arrest survivors two years down the line.
Beyond the Brink: What is PICS and Why Does it Matter?
Imagine emerging from a life-altering event only to find that your mind or body isn’t quite the same. This is the reality for many critical illness survivors: a cluster of persistent challenges collectively known as Post-intensive Care Syndrome (PICS). PICS isn’t a single condition but rather a constellation of new or worsening impairments that emerge after a critical illness, affecting physical, cognitive, and mental health. For cardiac arrest survivors, whose brains and bodies have endured immense trauma and oxygen deprivation, understanding PICS is crucial for preparing for the road ahead.
The Swiss study, meticulously following a cohort of cardiac arrest survivors for two years, found that a significant proportion—43% of patients—experienced symptoms of PICS. This isn’t a small number; it represents nearly half of those who survived the initial event. This finding underscores the importance of acknowledging that survival is just the first chapter. The quality of life and the capacity to return to a semblance of normality often hinge on how these longer-term challenges are addressed. For the SCA UK community, this data provides a vital framework for discussion and support. Are we talking enough about the subtle yet profound shifts that can occur in a survivor’s life?
The Body’s Echoes: Physical and Psychological Realities
The study’s findings reveal a clear hierarchy in the types of PICS symptoms experienced. Physical impairments were by far the most prevalent, affecting nearly 39% of survivors. This could manifest as persistent weakness, fatigue, breathlessness, or reduced mobility. It’s a stark reminder that while the heart may have been restarted, the body often carries the scars of its fight for life. Imagine the frustration of wanting to return to activities you once loved, only to find your physical capacity diminished. This isn’t just a physical hurdle; it profoundly impacts independence and self-esteem.
Following closely behind were psychological impairments, affecting just over 15% of survivors. This often includes anxiety, depression, or post-traumatic stress disorder (PTSD) – a natural response to the terrifying experience of cardiac arrest. The memory of the event, the fear of recurrence, or even the feeling of being “different” can weigh heavily. It’s essential to recognise that these psychological wounds are just as real and debilitating as any physical injury. They demand understanding, empathy, and professional support.
Interestingly, neurological impairments, while perhaps what many might expect to be dominant after brain injury, were the least common at 2.8%. This might be because many with severe neurological damage may not survive long-term. However, for those who do experience it, these impairments can range from subtle memory issues to challenges with concentration or executive functions, making everyday tasks surprisingly difficult.
Who is Most at Risk? Unpacking the Predictors
The study not only informed us about what PICS is and its prevalence, but it also began to identify who might be more susceptible to it. Several factors emerged as significant predictors of developing PICS, providing valuable insights for early identification and targeted interventions.
Firstly, female sex was identified as a predictor. This is a crucial finding that warrants further research. Are there biological differences, or perhaps socio-cultural factors that contribute to this disparity? Understanding this could lead to more tailored support for women after cardiac arrest.
Secondly, a longer “no-flow time” during cardiac arrest—the duration before CPR or defibrillation was initiated—was a significant factor. This intuitively makes sense: the longer the brain and organs are deprived of oxygen, the higher the likelihood of subsequent complications. This reinforces the critical importance of immediate bystander CPR and rapid defibrillation. Every second truly counts.
Beyond the initial event, post-discharge job loss also emerged as a predictor. This highlights the profound economic and social impact of cardiac arrest. Losing one’s livelihood can exacerbate stress, erode self-worth, and limit access to resources, creating a vicious cycle that impedes recovery.
Finally, the ongoing need for psychological support or psychopharmacological treatment was a strong indicator of PICS. This points to the persistence of mental health challenges and the importance of continued, accessible care. Seeking help is not a sign of weakness; it’s a sign of strength and a vital step in the recovery process.
The Paradox of Quality of Life: A Glimmer of Hope
Despite the substantial prevalence of PICS symptoms, the study presented a fascinating, and perhaps counterintuitive, finding: long-term survivors of cardiac arrest reported an intact health-related quality of life when compared to the general population. How can this be? If nearly half are experiencing PICS, how can their quality of life remain comparable?
This finding speaks volumes about the remarkable resilience of the human spirit. It suggests that while survivors may face significant challenges, many adapt, find new ways to cope, and recalibrate their perspectives on what constitutes a “good life.” It’s not about being “back to normal” in the way they were before, but about finding a “new normal” that is fulfilling and meaningful. Perhaps the sheer fact of survival, of being given a second chance at life, profoundly impacts their appreciation for it. It’s a powerful message of hope and adaptability.
However, this doesn’t diminish the very real struggles that PICS presents. Instead, it highlights that even with these challenges, a good quality of life is achievable. The key is recognising and addressing the PICS symptoms so that survivors can fully embrace their second chance.
Moving Forward: Prevention, Screening, and Support
This study provides compelling evidence that the long-term effects of cardiac arrest extend far beyond the immediate resuscitation. For the SCA UK community, these findings are not just statistics; they are reflections of authentic experiences, real struggles, and real triumphs.
What can we take away from this?
- Awareness is Key: We need to raise awareness of PICS among survivors, their families, and healthcare professionals. Knowing what to look for and understanding that these challenges are common can normalise the experience and encourage seeking help.
- Proactive Screening: Implementing routine screening for PICS symptoms at various follow-up intervals could help identify individuals at risk early. This proactive approach would enable timely interventions.
- Tailored Rehabilitation: Rehabilitation programmes should be holistic, addressing not only physical needs but also psychological and, where necessary, cognitive impairments. This might involve access to physiotherapy, psychological counselling, and occupational therapy.
- Community and Peer Support: The power of shared experience cannot be overstated. Connecting with other survivors and co-survivors through organisations like SCA UK provides invaluable emotional support, practical advice, and a sense of belonging. Knowing you are not alone in your journey can make all the difference.
- Further Research: The study itself calls for additional research into prevention, screening, and treatment strategies for PICS in cardiac arrest survivors. This is an ongoing journey of discovery, and every new piece of research brings us closer to achieving better outcomes.
The journey after a sudden cardiac arrest is a testament to incredible resilience. While the path may present unexpected turns and challenges, such as PICS, understanding these can empower survivors and their loved ones to navigate them with greater awareness and support. As a community, we must continue to champion comprehensive, long-term care that extends beyond mere survival to enable thriving.
What are your thoughts on how we can better support long-term cardiac arrest survivors in their recovery journey?
After our first meet-up in February 2015, I realised I was not alone. It was the first time since my cardiac arrest the previous year that I had spoken face-to-face with someone who had experienced what I had. This was also true for my wife, who also happened to be my lifesaver. From that meet-up, the idea of SCA UK was born. Since then, we have achieved a considerable amount, primarily providing information, resources and support to others in a similar situation but also raising the profile of survivorship and the need for better post-discharge care. We are starting to get traction in this, and with the formation of the charity, I genuinely believe we have a bright future ahead and will make a significant difference in the lives of many who join our ranks.
Great article Paul, I can certainly relate to this.
Karin was asking me last night about how I felt immediately after the event. We’d never discussed it. Made me recall the first days, weeks, months; years even.
This made me realise what a journey we’d both been on.
A great insight to what cardiac arrest survivors experience after the event. I had a completely blocked LAD which caused a heart attack and cardiac arrest. My event caused heart failure so I face the everyday challenges which that throws up and will continue to do so going forward. My short term memory has been greatly affected yet I only saw a “specialist” twice, once in hospital and then again during a visit to my home. Having done the first cognitive test and being unable to recognise basic animals. Being unable to walk when I eventually got out of the hospital bed and then not doing to badly on the second cognitive test I was told I seemed fairly intact and was discharged! I was told if I had any further problems to contact them again… and that was it! I’ve since found my short term memory is appalling and continues to be so nearly 5 years down the track! I can forget things in a “heartbeat” once even saying to my hairdresser.. “I know you’ve washed my hair as I can feel it’s wet but I have literally no recollection of that happening!” It seems worse when I am trying to think of something at the same time or doing things whilst talking! Basically no ability to concentrate on 2 things happening at the same time! No-one has ever followed up with this and I was told things should get better… don’t get me wrong they did initially (I was far worse when I got home from hospital) but it never returned to “normal” This now causes the problem of “you look fine” So along with this and heart failure, yes I do look fine but I’m actually not! More support and understanding needs to be available to cardiac arrest survivors and it’s hard to believe it’s not already out there! Anyway, sorry for the long comment and thanks again for everything you do for SCA survivors and their families x
Hi,
I am so grateful to you for writing this article. Thank you. I’ve wanted to know more about what I’ve been through mentally and physically after my cardiac arrest (July 2023). Although the article didn’t answer all my questions I feel as though the blinds have been lifted and I see more clearly a lot of what I’ve experienced and continue to experience are most likely connected to my cardiac arrest.
I believe what I needed the most after my event was some type of “support” whether in the hospital or a survivors support group after I left the hospital. I wanted to talk to people who had experienced the same thing. To see if what I was or wasn’t experiencing was common for others, as well. I was never offered that support in the hospital and when I reached out to my local hospital I was told they didn’t offer such a group.
I don’t remember ANYTHING about the event or even some weeks before or after it. I have asked my sisters what I had to deal with while I was in the hospital, what they went through, did they think I might die, and so on, so I could get some sort of perspective on what I was going through and how I was feeling. I know I will always feel extremely blessed to have survived and with very few deficits. All glory to God.
I am a different person than I was before the event. I’m still not sure if that’s good or bad. Maybe a little of both!