Homage to a Hero: Dr. Brian Reemtsen

I’m usually not at a loss for words (as this blog would indicate), yet I’ve found it very hard to compose a tribute to the key member of Rudy’s team.  There’s a tinge of pathos in saying that my son has the greatest heart surgeon in the world only because it assumes as a given that his condition demands it.  I am sure no one here at UCLA would be offended by my saying that I would much rather Rudy have no need of any surgeon; but as that’s not our reality, it’s difficult to express the deep gratitude we have for Dr. Brian Reemtsen.

 

When we first learned of Rudy’s diagnosis of Hypoplastic Left Heart Syndrome we got several recommendations to seek treatment at Children’s Hospital Los Angeles (CHLA), but we discovered our insurance network was contracted with UCLA.  While we were willing to fight to any extent necessary to get Rudy the right care we also realized the wisdom in reserving our energy for the most important battles, so we decided to do some due diligence and investigate UCLA—at least to have some grounds on which to base an appeal.

 

As I’ve already written, the initial responsiveness of Gary Satou and Dan Levi served as a remarkable introduction to the team at UCLA.  Both spoke no ill of CHLA but also laid out what UCLA could offer—most importantly an expert surgeon, Dr. Brian Reemtsen, to do this very intricate surgery.  Just months before, Dr. Reemtsen had come from CHLA to build a top-notch Pediatric Cardio-Thoracic Surgery program in the new Mattel Children’s Hospital at UCLA.  They had high praise and said that they would speak with Dr. Reemtsen as he would certainly want to consult with us.  This willingness was driven home the next day when Susan, his assistant, called to let me know that Drs. Satou and Levi had already spoken to Dr. Reemsten and he instructed her to call immediately to again affirm that he would make time to see us whenever we could get to LA.

 

Our first meeting with Dr. Reemtsen in September was no let down from the hopes we had built up.  He took the time for a very thorough conversation, entertained any and every question and was straightforward about the challenging diagnosis we were confronting.  He was empathetic, realistic and hopeful; able to put things into understandable terms and patiently allowed us to digest information and repeated himself if we asked.

 

We were forewarned of some the personalities we might encounter when dealing with specialists and surgeons who deal with such complicated diagnoses.  We were warned that the greater the expertise, the more aloofness one might have to contend with.  We were briefed on skilled surgeons who excel in the operating room, but might be less than comforting at bedside (on the rare occasions they make an appearance).  I’m not sure what experiences fed these stereotypes, but meeting with Dr. Reemtsen quickly made it clear they didn’t apply here.

 

I spoke of the very strong recommendations we received for CHLA and Dr. Reemtsen took no offense at this, having nothing bad to say about his former employer and even encouraging us to investigate both options.  In making the case for UCLA, he held forth the promise that he would be hands-on involved in Rudy’s care from delivery to discharge.  His arrangement here is such that this is his only hospital and practice so he’s here every day and can remain very involved with his cases (contrasted to a specialized surgeon who might have patients in multiple hospitals and only pass through on an occasional basis).  He would be by the bed several times a day and constantly interacting with the treatment team in every development and decision.  He would be honest about our circumstances, communicate clearly and not give false hope.

 

It was a very encouraging conversation, at the end of which he pulled out his business card, wrote his e-mail address and cell phone number on the back, and made it clear that we should have no hang-ups about using it for any reason whatsoever.  No answering service.  No automated phone trees.  Straight to him.  I never ended up calling it but remember a few worried evenings in my office, as I tried to take in all the unknowns that lay before us, where simply picking up that card and turning it over to look at that number brought a sense of comfort and reassurance.  We were in good hands.

 

At the outset, I don’t think I would have been able to articulate an itemized list of qualities I would want my son’s cardio-thoracic surgeon to have.  As Rudy’s heart would be very small and would require very steady hands, I remember checking Dr. Reemtsen’s during that first meeting to make sure all the fingers were there and that they didn’t shake excessively.  Overall, I noted no obvious involuntary ticks but did wonder if it would be possible for me to hide in his closet and jump out just to see that he didn’t startle uncontrollably.  Other than that I didn’t have any sophisticated rubrics for evaluation.  Other doctors spoke highly of him and we wouldn’t expect UCLA to hire anyone with blemishes on their record (but I did check), so the main criteria for us to choose our expert had little to do with an educated analysis of his skills, but simply by how we felt about him.

 

While arrogance is not an attractive trait, when it comes to choosing a heart surgeon neither is too much humility.  You want self-confidence; a person who is well aware of their competencies and does not question them.  While the general population strives for well-roundedness, I prefer my heart surgeon to be somewhat out of balance—a bit too dedicated to work, unable to thwart perfectionist drives, never able to make enough time for hobbies, incapable of leaving work on time or stay away on a weekend.  Someone who will always remember that he’s dealing with MY baby—and that my world has come to a stop.  Someone who realizes that my medical training ended with high school biology, but I’ll be comforted to know relevant information in language I can understand.

 

I trust the number of interactions with Dr. Reemtsen documented in this blog communicates implicitly what is taking me a number of passes to state explicitly.  He is a person that exudes competence; who I suspect doesn’t give much time to things he can’t excel at.  He is purposeful and doesn’t give indication that much time in his day gets wasted, but has time to stop and be friendly.  He wears a mantel of importance, but carries himself without much fanfare.  His attention to his patients knows few bounds as demonstrated by the evening and weekend visits and the late-night phone check-ins I’ve overheard.

 

If the guy who holds my son’s heart in his hands demanded I call him “Spartacus”, I’d have no problem doing it, yet I love the way he introduces himself as “Brian”.  As isolating as life can be here in the CTICU addressing our key source of comfort as “Dr. Reemtsen” would keep him far more distant than we’d like.

 

I make no pretense that I’m motivated largely by my own self-interest in this whole journey.  I want the best outcome.  I want Rudy to have the best.  But this comes at a cost, and I’d be delusional if I thought I was shouldering more than a fraction of this.  In his devotion to our son, Brian has made our burden his (along with so many others here at UCLA) in ways that we never could repay.  We’d like to think we know what’s best for our kids and provide everything for them, but this experience has shown our knowledge and competencies to be shockingly finite.  So thank you, Brian, for having the expertise and skill we could never muster.

 

I also realize that others pay a cost for Brian’s round-the-clock devotion to Rudy.  On several occasions, we’ve heard Brian speak of the Reemtsen ladies.  As their husband’s and father’s commitment to my son undoubtedly makes for absences from them, we are so grateful.  May they realize now and in the future the profound hope he brings to families like ours through what he does each day.

 

Dr. Reemtsen checking on Rudy
Dr. Reemtsen checking on Rudy

Pray for the fluid to stop…

The odd existence we’re living here make times of focused or extended prayer a challenge.  Today, like many days, we uttered a quick “Please, Jesus, let this be a calm day” as we stepped off the elevator on the 5th floor.  Unfortunately we were met with a bump shortly after we got here as we were having a check in with Dr. Reemtsen.  Alarms started to go off and, after a couple nonchalant looks at the screen (the usual first response), the tone got more concerned and then the inexplicable signal went off and six people were suddenly at the bedside dealing with the breathing tube.  Just a few minutes passed and, almost as quickly as they came in, everyone was gone.  No big deal–possibly just an obstruction in the breathing tube.  I’m glad there’s always a couple that check on us before going and we usually lie and go along with the “no big deal” line, but I don’t think we fool them with our ashen complexions and tears welling up.  I don’t think Rudy was ever in significant danger, but I don’t think we’ll ever get used to jolts like this.  Suddenly we’re both in need of comfort foods and are craving Big Macs and lots of french fries (you go to your happy place, we’ll go to ours).

The conversation with Dr. Reemtsen did set forth a plan for the week.  Rudy’s cardiac function continues to be very strong, so much that Dr. Harrison recommended that his next echocardiogram be at his discharge.  Everything they are addressing now has little to do with heart function, the biggest issue being the chylothorax (lymphatic fluid in the chest cavity).  The hope has been that the drainage into the chest drain would taper off, but that hasn’t been the case.  The medicine they’ve been giving him (Octreotide) should have worked by now, but they’re going to give it a few more days.  If there’s no change, the plan is to do another surgery on Thursday to ligate the thoracic duct.  Not a major surgery, but surely one we’d rather not see Rudy have to endure, so please pray that this would heal itself and the flow of fluid to the drains would stop.  So far we’ve seen fluids be very responsive to prayer so let’s channel the same effort that went into producing urine into the ceasing of lymphatic fluid.

Dr. Reemtsen feels that Rudy won’t make much progress until this can be corrected as all of his nutrition is likely just flowing out of his body into the drains.  They are also looking closely at his endocrine system as they are wondering if there’s some steriod deficiency or ongoing thyroid issues that are hindering his ability to move forward.  There’s also been consultation with the infectious diseases team as, though no significant cultures have grown, some of his symptoms (low blood pressure, occasional fevers) are making it tough to rule out).  In any case of extended hospitalization, the threat of infection emerges, so we’re praying against this.

That’s this morning’s update.  In the midst of it all, Rudy is lying very calmly and loves looking up at his aquarium.  I do wonder often what kind of thoughts are going on in his little mind through all of this.

Tougher Than the Rest

If your rough enough for love, baby I’m tougher than the rest.  —Bruce Springsteen

This lyric seems relevant tonight as we had another one of those afternoons that are all too commonplace in this process; one that stretches us and makes us realize that this process with Rudy takes toughness.  Just when you think you’ve been pushed as far as you can go, there’s another shove.

The chest drain went in smoothly and gave off lots of fluid, but Rudy’s low blood pressure was of concern all afternoon.  We went out to get some fresh air with the kids and shortly after we returned to the room the activity in the room suddenly picked up.  I still wonder how these ICU people communicate–first just a doctor and a nurse…then a second doctor…then more nurses and care partners.  The room stayed quiet, but focused and intense to where we could pick up that it would be best to pull out the kids and Oma and Opa out to make room for 8 people that were now at Rudy’s bedside.  The phones started ringing as other members of the team answered their pages and I could pick up the concern as I stood watching from the doorway.  I don’t think Rudy was in as much distress as some of the previous episodes and, probably in shorter time than it felt, they were able to find the right cocktail of medications to get his BP where it needed, but it was disheartening for me to watch.  He’s so fragile and delicate and the going is so slow that it really doesn’t feel like we’ve made much progress over where we were a week ago.  My kids were in the next room–they need us just as much as Rudy does.  Yet it’s so hard for me to focus my attention anywhere else.

That Springsteen lyric first came to me yesterday as we were watching the pediatric patients trick or treat down the hallway outside.  The staff had taken time to set up at different doorways so they could have as realistic an experience as possible.  The kids were cute, but I couldn’t take my eyes off the parents even though few of us were able to make more than a few seconds eye contact.  This wasn’t the Halloween they hoped for, yet they show up for their kids and enthusiastically wheel them down the hallway, making sure that IV lines don’t snag and that costumes can somehow be tied on around the medical equipment that needs to stay attached to their kids.  Some of them do it very tentatively and hesitantly and I hope that means that this holiday in the hospital is an anomaly.  But other parents move instinctively and maneuver the equipment with a second nature that makes it clear that this isn’t the first time they’ve had to do this.  These are the tough ones–tougher than the rest.  Who knew what our love for our kids would demand of us.

 

Another morning mystery…

Rudy had a very peaceful night and we were hopeful that today would be a day of gaining strength for him, but unfortunately he’s run into difficulty breathing over the last couple of hours and the team is trying to figure things out.  They ran a full battery of exams at about 7am which all came back clear (blood tests, chest Xray, etc) but they’ve just ordered a repeat of them all (it’s 11:45).  They’ve backed the ventilator way up and are trying to figure out the low blood pressure.  Another one of those mornings where there’s lots of activity in the room and several hushed conversations at bedside between doctors, nurses and respiratory techs.  I hear the distinctive sound of the Xray machine rolling down the hallway toward our room right now, so we’ll have to clear out.

The kids are showing up in the next hour and I sure wish they would get to see Rudy at his best, but for some reason he’s having a battle during most of their visits.  Right now, he clearly doesn’t like what their doing and is letting us know with one of his silent tantrums.  He’s not making any noise, but as he’s lifting his heart rate above 200 bpm and dropping his O2 saturation below 50%, it’s by no means quiet in here–plenty of racket from all of the alarms.

We’ve had a lot of discharges on the unit.  Hopefully it means a lot fewer kids had to spend Halloween here.  For staffing purposes, they moved just about everyone they could to another wing so it’s a bit of a ghost town on our end with lots of empty rooms.  The upside is I can go into the vacated rooms and exchange our chairs for better ones (kind of funny all the swapping that goes on here as patients leave).

The Xray just came back and it showed a significant accumulation of fluid, so they’re going to have to replace the chest tube.  Up until now, they’ve watched it closely and been a bit surprised that the fluid hasn’t come back, but things have changed quickly since today’s early morning Xray.  So, unfortunately the kids will have about 15 minutes to say hello and then we have to clear out for the procedure.

Happy Halloween 2008

It has been a challenging day getting Rudy’s blood pressure stable after the morning attempt at re-inserting the left chest tube.  He is calm and alert this afternoon and the team has decided not to make another attempt at the chest tube today.  They’ll take another chest x-ray in the morning and see.  The good news is that Rudy’s breathing has remained strong throughout the day.  There hasn’t been a need to up the bpm’s on the ventilator and he is holding steady at 14 bpm.  So we continue to wait, wait, wait.  To break up the monotony, we had a little Halloween fun as you can see.  The pediatric patients on the floor had a costume parade earlier today which Rolf and I attended since Rudy was asleep anyway…it was very sweet and they all had a fun time but it was also heart-wrenching to see the kids parade around with their rolling IV towers, etc…  I couldn’t help but think about Wilson (aka Davy Crockett), Max (aka Jack Sparrow) and Olivia (aka a cowgirl) who are, most likely at this moment, getting dressed for their night of candy collecting!!  Have fun little ones!  We’re looking forward to a family visit tomorrow!!

'Not quite sure he likes being a pumpkin...

Waiting…waiting…waiting…

Having learned the lesson Charlie Brown never could (that Lucy was never going to let him kick the football), we try not to get our hopes up every morning that this will be the one where the breathing tube is pulled.  Probably wise, because this morning they decided to sedate Rudy so they could re-install the drain line that came out last night.  Unfortunately they weren’t able to get it in, so they’ll probably have another go at it this afternoon.  So it’ll be another day of seeing if Rudy can hold the line.  His numbers have been good and they didn’t need to scale back the ventilator this time and it’s holding at 16 bpm.  While it’s a bit disappointing to have the progress slowed for another day, it’s certainly better than holding off only to have him go into distress over the weekend and lose several.

Quick Update–another tube fell out

Just this evening as we were sitting here, nurse Cheryl discovered the drain tube on the other side fell out.  My first response was to get disheartened as it could mean that tomorrow would be a repeat of today where we needed to knock Rudy out for another procedure so that they could re-install it, but the docs have some reason to believe that may not be the case.

When they originally put the drains in, Rudy was swollen up like the Michelin Man, but as fluid drained, the skin around them became looser to where they often lose hold and fall out.  Right when it came out, Dr. Abel called for an Xray so he could look for an air pocket as this could lead to his lung collapsing.  Fortunately, they didn’t any sign of this.  As it was, the doctors were discussing whether to pull that drain today or tomorrow (to prevent infection I think), so please pray that no further fluid amasses and that the medicine they started tonight to stop the fluid from secreting would act quickly.

He’ll be off the ventilator by Kindergarten…

I heard from a few subscribers today about no update going out last night.  Sorry about that–we didn’t get the post up before the automated send deadline.  Thanks for your dedicated reading.  I noticed today on our stats site that Rudy’s Beat crossed over 25,000 hits today.  Wow, that’s amazing!  The support and interest in our little warrior is overwhelming.

We had decided not to mention the possibility of extubating Rudy this morning as I’m not sure how many nights we’ve left with that being the plan only to have a change in course overnight.  Unfortunately, that was the case again.  Rudy had a great day yesterday–alert with consistent numbers where they all should be–so they were going to steadily dial down the vent overnight to see if they could get to 8 bpm by 6am.  A routine chest Xray at 4am (if there is anything routine about an Xray at 4am) showed a plural effusion on his right side–fluid on his lungs.  The drain on that side had fallen out yesterday and the team decided not to replace it, but took the course of monitoring things closely.

The good news is that the accumlating fluid was detected quickly before other signs of distress kicked in.  The ventilator was bumped back up and he underwent a procedure this morning to install a new drain (more generic bears again).  All of the numbers have held fairly well during the day, so the main issues we had to overcome were the sedation that knocked him out most of the day and the always closely-monitored flow of urine.  We’re still waiting for the latter to come back where it needs to be to let us know his kidneys are OK, but we’re glad that Rudy woke up and joined us again about an hour ago–the good kind of awake, where he can focus and looks at me with quiet, patient but questioning eyes.  We can drive ourselves crazy if we focus too much on getting that horrible tube out of his mouth.   Tomorrow!?  Tomorrow!?  Tomorrow!?  Dr. Harrison came on today and like everyone else, he’s optimistic but wisely non-committal as to a timeline.  I was able to extract a promise from him that it’ll certainly be out by Rudy’s first day of kindergarten.

We’ve noticed a respectful debate emerging between the Cardiology and the ICU docs regarding Rudy and the ventilator.  The former would want a quicker wean while the latter argue for a more gradual process (Note–if Reemtsen ever teaches swimming lessons, verify that his pool has a shallow end before you sign up your kids).  I am grateful that multiple minds, each holding their own perspectives, are involved in this key discussion.

UPDATE–THIS JUST IN!!!  As I’ve been typing Dr. Mary (pronounced as the French–“Marie”) came in and discovered 10ml in the pee tube.  Yahoo!  She also reported that Dr. Harrison feels that Rudy is far enough out of the woods on any intestinal issues that they can start some powerful medication for his chylothorax (the liquid that keeps collecting on his chest).  This will hopefully stop the fluid from collecting over the next few days so we can get rid of the drains and reduce the risk of infection from them.

We said goodbye to Robin and “Papa”, her baby boy, today.  They arrived just a few days after us from Lompoc and were part of our temporary community that formed here over the last month in the ICU.  We feel a bit like year-round residents in a resort community of some kind.  The neighbors come and go every few days, but we’re still here.  We wave to them from the front porch as they drive away.  Blessings, peace and health to you, Robin and Papa!

All’s Calm on the Night Watch

As Trish posted earlier today, Rudy settled down nicely today and has spent most of the day sleeping peacefully.  After the commotion yesterday with alarms going off every ten minutes for breathing, blood pressure, O2 and CO2 levels, today has been very calm and quiet.  While he is being treated for infection, there are fewer indicators that this is a major issue.  There are so many factors playing into his condition that isolating one cause is usually unrealistic, but one of the key items might have been decreasing a steroid medication too quickly.  Now that it’s been restarted along with some other adjustments to his medication, he’s got all the numbers in the right ranges–in a deep sleep no less which means he doesn’t have to work at it.

Again, conversations with the doctors–Andy, Abel, Brian, and Ryan–have been very assuring and we were especlally encouraged by Gary Satou stopping by for a sit-down check in just to see how we were doing.  One of our nurses from last week, Denise, stopped by for a comforting chat on her break and ended up cleaning Rudy’s mouth since she couldn’t stand all the gunk from the tape on his lips.  He immediately gnawed on the sponge she was using so I think he’s hankering for some chow–enough with these intravenous feeds.  Right now peaceful sleep is a good thing (and we hope to get some of our own tonight) as it’s helping him summon strength.  There are some decisions to be made about how to proceed with the ventilator, but we’ll see what tomorrow brings.