Hybrid · Patient Story & Education

Kato · Patient Lessons for Liver Transplant

How one surgeon’s experience as a critically ill patient can help you prepare, ask better questions, and navigate liver transplant with more confidence.

Dr. Tomoaki Kato, transplant surgeon and patient
Dr. Tomoaki Kato, a pioneer in multiorgan and liver transplantation at NewYork-Presbyterian/Columbia, who later became a critically ill patient with COVID-19 himself. [1][2]
Short biographical video on Dr. Kato’s work in multiorgan and liver transplant, designed for patients and families. [3]

Who Dr. Kato Is — and Why Patients Notice

As a surgeon, Tomoaki Kato, MD, is known for complex multi-organ and liver transplantation, ex vivo tumor surgery, and leadership of abdominal organ transplant programs at NewYork-Presbyterian/Columbia. [1]

For patients, what stands out is something different: he has lived through his own near-fatal illness. That experience changes how he listens, how he explains risk, and how he talks about the slow, messy process of getting better.

This page is not about technical details of ex vivo surgery. It is about what you can borrow from his story to prepare yourself as a liver transplant patient or caregiver.

What He Lived Through — Surgeon Becomes Patient

In 2020, during the early phases of the COVID-19 pandemic, Dr. Kato developed severe infection with multiorgan failure. He required prolonged ICU care, mechanical ventilation, and advanced life support. Columbia and NewYork-Presbyterian later published his story as an “amazing comeback”. [2][4]

After months of rehabilitation, he returned to surgery and completed the New York City Marathon — not as a publicity event, but as a personal marker that life after critical illness can still be meaningful and active. [2]

When he now sits with patients, he brings two perspectives:

  • Technical — decades of experience in some of the most complex abdominal operations performed anywhere.
  • Patient-centered — firsthand knowledge of fear, loss of control, and the long haul of recovery.
His story does not mean everyone will run a marathon after transplant. It does show that recovery is not just about lab values — it is about meaning, goals, and who walks the road with you.

Before Your Visit — How to Prepare Like a Pro

Major centers such as Columbia, NewYork-Presbyterian, and programs described by the NIDDK emphasize the same core steps before transplant: evaluation at a transplant center, review of your liver disease and other conditions, and detailed discussion of the surgery and its long-term demands. [5][6][7]

Drawing from what Dr. Kato often explains to patients, you can prepare by:

1. Know Your Story (Briefly)

  • Write a one-page summary of your liver disease: diagnosis, key tests, hospitalizations, and current symptoms (ascites, encephalopathy, bleeding).
  • Include other major illnesses (heart, lung, kidney, diabetes, cancer).
  • Have a list of your medicines and allergies ready in writing.

2. Understand the Big Picture

  • Why is a liver transplant being considered now?
  • What is your MELD or other priority score and how is it calculated?
  • What alternatives (medical or interventional) are still on the table? [5][8]
One of Dr. Kato’s recurring themes in interviews: patients who come with a clear, written story and questions are easier to help and feel less lost during a complex evaluation visit.

ICU & Early Recovery — What to Expect

After liver transplant surgery, NIDDK and major centers describe a predictable path for most patients: time in the ICU, then time on a step-down unit, and a gradual move toward walking, eating, and self-care. [7][9][10]

From Dr. Kato’s lived experience and transplant guidelines, key realities you and your family should know:

  • Monitors and tubes — expect ventilators (at least early), multiple IVs, arterial lines, drains, and urinary catheters.
  • Delirium and confusion — many patients have patchy memory and strange dreams; this is common after long ICU stays.
  • Pain + exhaustion — effective pain control is important, but no regimen completely removes discomfort after major surgery.
  • Immunosuppression — transplant teams typically start anti-rejection medications immediately; you will likely be on these for life. [9][10]
When he reflects on his own ICU stay, Dr. Kato often emphasizes how much it helped when staff explained things simply and repeatedly — even if he did not remember every conversation. Ask your team to do the same for you.

Long-Term Living — Turning Survival into Life

NIDDK and major transplant centers stress that transplant is not a “cure” but a trade: you move from life-threatening liver failure to a life with a new organ, daily medicines, and ongoing follow-up. [6][9][10]

Lessons patients often draw from Dr. Kato’s marathon-after-COVID story:

  • Set milestones — sitting up, walking to the door, walking the hallway, getting outside, returning to one hobby, etc.
  • Expect setbacks — infections, readmissions, medication side effects, and mood changes are common after major transplant.
  • Stay connected — follow-up visits, blood tests, vaccinations, and communication with your hepatology/transplant team are lifelong tasks. [6][9]
  • Meaning matters — many survivors find that goals like seeing a grandchild, returning to teaching, or simply walking in a park become powerful motivators.
The exact path will be different for every patient. What you can borrow from Kato’s journey is not his marathon time, but his idea that recovery gains power when it is tied to something that matters deeply to you.

Questions to Ask Your Team — Inspired by Kato

If you were sitting with a surgeon who has led multivisceral transplants and also survived life-threatening illness, here are examples of questions you might bring — a blend of technical and human:

Technical & Center Experience

  • How many liver transplants does this center perform each year?
  • How often do you see cases like mine (diagnosis, anatomy, prior surgery)?
  • Who will be in the operating room, and who will lead the operation?
  • What are the biggest risks in my case — bleeding, infection, rejection, clotting, or something else? [7][8][10]

Human, Practical, and Long-Term

  • What will my first week in the ICU probably look like?
  • What are realistic goals for 1 month, 3 months, and 1 year after transplant?
  • What support (social work, psychology, rehab, nutrition) is available?
  • If you were in my position, what would you want to know that patients often forget to ask?
Bring these questions on paper or on your phone. Patients who ask clearly and listen carefully often leave clinic with a better sense of their options, even when the news is difficult.
Educational content — not a substitute for medical advice.
© Dr. Michael Baruch · LiverTransplantGuide.com