Showing posts with label medications. Show all posts
Showing posts with label medications. Show all posts

04 May 2012

Post Op Day 3

So Eddie is resting very quietly right now and continues to improve since his surgery on Tuesday. Each child responds very differently to a new heart based on how their previous condition affected their various systems. In Eddie's case, where his body was accustomed to relatively weak blood flow, it will take a bit of time to readjust to a strong and healthy heart.

At the moment, Eddie is on a variety of support meds and gases to help him through the transition. Nitric oxide to help open the pulmonary arteries and allow the pressures between his right and left side to equilibrate, milrinone to increase contractility in his right ventricle as well as vasodilating his blood vessels, isoproterenol to increase heart rate, dexmedetomidine to keep Eddie sedated, and a rash of other meds for pain relief.

Admittedly, we are chasing our tail a bit since each of these meds cause downstream effects . . . which then have to be mitigated by other treatments. Over the past 24 hours, however, Eddie has stabilized and seems to be in a relatively happy place. Heart rate and pressures are steady, kidney function is good, and when he's awake, Eddie is asking for water, bubbles, and Thomas (the train, of course) showing he is neurologically "appropriate" :-) Can you tell we've been in the hospital a wee bit too long?

So overall, we are very happy with Eddie's progress. We are still in shock that his heart is here and functioning.

Sarah and I are tired, but managed to get relatively good sleep the past two nights. Adrenaline can get you a long way, but taking advantage of a quiet room and a few hours of uninterrupted rest has been super important for us.

I am excited to head home this afternoon to manage the chaos that is our eight year-old's birthday party!

Our biggest hope today is that we can extubate and put some real food into Eddie's mouth. Will know more during rounds. And after that, we hope to share some more photos as Eddie improves.

Have said it many times before, but we are so thankful for the many nurses that have cared for Eddie over the past two months. The doctors often get the credit for saving lives, but Sarah and I will tell you that it is the nurses that have kept our boy strong in his worst moments. They have been by his bedside every hour of every day and, in their own special way, have contributed to his endurance, healing, and recovery. To all you nurses, you are amazing and we love you!

More soon . . .

02 May 2012

Looking Ahead

Spent the past few hours with Eddie. He is still quite sedated and we're trying to keep him relaxed since he is very delicate after such a major surgery, but overall, he is doing great.

Medically, Eddie is strong on all counts. His new heart is being paced by an external pacemaker (common in transplant patients), since it will take some time before he can run completely unsupported. He is receiving a variety of meds to help control heart function, pain, and sedation and he will begin receiving diuretics, steroids, and immunosuppressant meds in the next day or two.

At this moment, I am thinking of a line from Jose Saramago, one of my favorite writers who passed away last year. He said: "All the scheming and plotting in the world won't result in something lasting, transcendent. Anything that's authentic, that's real, comes in the form of a gift." So appropriate on a beautiful new day for Eddie . . .