Yesterday was one of those days that I think might be
imprinted in my mind forever. I went
down to the pediatric ward in the morning to round on the kiddos. Rounds were pretty benign (which means I didn’t
stumble upon a kid that was barely breathing and end up spending an hour
literally running (always gets a “heeeeeeeeey….look at the white lady run!) up
and down the hospital trying to save them.
The kids were all stable. I wasn’t
sure what to do about two of the kids so I went and talked to the new doc (he’s
awesome!) about them. He said he’d go
take a look at them and I headed up to the house.
A couple hours later I was doing some homeschooling with
Marie (which no doubt meant that I was inwardly beating my head against the
wall while outwardly calmly pointing out ONCE AGAIN the difference between a
straight and curved line) when the doctors wife came up to ask me something.
She told me that they were bagging a kid (“bagging”= placing a mask over the
kid’s face that’s attached to a bag of air that you squeeze to breath for the
kid when they can’t breathe on their own) and wanted me to teach the family how
to do it so they could all rotate.
Ok. Pause. What? They’re bagging a kid? I didn’t think we did that here? The ICU
nurse inside of me got really excited. When I moved here one of the most difficult
things to get used to medically (don’t
get me started on the food, bugs, larger gross animals, shirtless women, etc)
was that we don’t do any “heroic measures.” That means when a person stops
breathing, we just let them go. (We do
make exceptions for newborns who need a little help to get used to living
outside the womb). This flies in the face of all I’ve been taught as an ICU/ER
nurse. When people are dead, we do our
darndest to reach out there and snatch them back.
I digress. I went down to the Peds ward to see what was
going on. When I walked into the ward I saw that not only were they bagging the
girl, but the doc had intubated her. This means that she had a tube down her
throat into her lungs which allows the air to easily pass through. She was about 12 years old and had been
bitten by a snake approximately 30 minutes before coming to the hospital. When
she came in she was crying and upset but then started vomiting, seizing and
eventually stopped breathing. Hence the intubation.
I showed several family members how to bag and went to find
a suction machine to try and suck some of the junk out of her lungs. I proceeded to accidentally fry our suction
machine when I plugged it into a 220 socket. I’ve been here for 2 ½ years. I
still do that. Darnit. I started heading back to the house to e-mail my dad and
ask for one on the container that’s coming when I noticed a little bit of commotion
in the peds ward. I turned around and went back. (Incidentally, praise the LORD
we had several other suction machines in storage….so I was able to sleep that
night).
When I got there, the doctor and his sister (a nurse that
just got here and is visiting for a couple weeks) were at the bedside of the
little girl. He explained that in the
bagging, we’d essentially collapsed a lung. (Air was on the outside of the lung
and was pushing against the lung, not allowing it to expand). He said that this is inevitable with this
kind of bagging which is why we always put patients on ventilators that
regulate the pressure that’s used to push the air into the lungs. When I’d left
the girls oxygen saturation had been 99% (we want it over 90%). Now it was
50%. He proceeded to stick a needle into
her chest, letting the air out and allowing the lung to inflate again. The dilemma
was what to do next. We needed a one way valve so the air could come out but
not go in. He said, “well, in the books they do this…” and proceeded to take a
rubber glove, cut off the tip of a finger and put a slit in the end. Then he
taped the tip of the glove to the end of the needle. It’s a valiant effort….but not a long term
solution. She needed a chest tube. This
is a tube that’s inserted into the chest to allow the lung to continue to inflate
and deflate. So how do we make a chest tube here?
The next hour was spent trying to find supplies to see if it
would even be possible. And if not, how
can we jimmyrig something so it would work.
We found a contraption called a “pleuraVac” which is what we use in the
ICU for our chest tubes. But as we’re
talking this all out and the doc is making sketches of exactly how we could
make this work, we’re overcome with our limitations. I don’t know how many
times the words, “if we were in America…..” were said.
The fact was, even if we could get this to work, the chance
of this little girl surviving was very slim.
We needed 24 hour electricity in order for the chest tube to even
work. Our solar usually goes off around
11pm at night. There’s no way the patients family could afford to pay to run
the generator all night and the hospital doesn’t even have enough money to run
it for 2 hours a night to give the staff homes a little electricity in the
evenings. Things are VERY tight right
now. He said that she would need the
chest tube for at least 3 days. Then there was the issue of the ventilator. We
don’t have one. Someone would need to bag for 24 hours. And the same thing
would happen again. The air would start going into the wrong places and she’d
blow up like a balloon….and then die.
There just wasn’t anything we could do.
Which as health care providers is VERY frustrating!!! As we hashed it out between ourselves we realized
there was just no way this was going to work.
So I prepared to do something that I haven’t done in years. Withdraw life support. Only this time it wasn’t
on an 87 year old man who’d coded in the nursing home, it was on a 12 year old
girl who was helping her family on the farm and was in the wrong place at the
wrong time and got bit by a stupid snake.
We went back to the ward and asked to see the girls mom and
dad. When we were told that the mother
had left, the doc asked them to go get her. In that moment I realized that I’ve
been here for awhile. I put myself in
this doc’s place (newly arrived) and of COURSE you have the parents come. They’ll
sit with their child and say goodbye while she goes. That’s what we do. In America. Not here. Here, the parents
usually leave when it looks like the child is going to die. They can’t bear to
watch. (Incidentally I was talking about
this with my friend Peter (Sierra Leonean) and he was equally horrified by our
culture’s need to be present as I was at the parent’s absence here. “How could
you sit there and just watch your child die?!?!!)
So I knew that asking for the parents and waiting until they
got back was not going to work. We had
asked for the parents, but the family brought us the grandfather. They said he
was the “strongest one.” The doctor
proceeded to explain everything. He explained what we’d done, what our goal had
been in intubating her to begin with (see if we could breathe for her long
enough for the paralyzing poison to wear off) but that we’d reached a point
where we just couldn’t do anything else. And we were suggesting removing the
tube….which meant that the child would die.
The grandfather agreed.
We removed the tube. She had
absolutely no respiratory effort of her own. And we sat there and held her
hand, touched her foot and cried with her mother….wherever she was, as her
child slipped away.
Later that night I went down to the doctor’s house to see
how he was doing. Both he and his sister had taken off (totally know that
feeling when you just have to get away).
I started talking with his wife about what happened that day and she
asked me how I do it. How do I stay here and keep working with no supplies, so
much death, etc. She’d asked me that before so I’d been dwelling on it for a
little while. I think the answer is probably different for everyone, but mine
is pretty simple. Number one, I STILL
get frustrated with the death, the lack of supplies, etc. It’s a DAILY struggle. Number two, I think some of it is just time.
It’s a BIG jump to go from working in a country with some of the best medical
care in the world to working in a place that has one doctor for how many tens
of thousands of patients. A BIG
jump. But this is my reality. And at
some point you have to start accepting your reality or go crazy. I’ve been here
for almost three years. They just got here. They didn’t see me when I first
arrived!! J
But I think the biggest thing the enables me to stay here is
that medicine is not my end goal. If it was, I absolutely would go crazy. When I saw that little girl intubated
yesterday, the ICU nurse in me got really excited. We were going to get to radically try to save
a life. But in the end, we failed. As we were sitting there holding her hand
while she passed away, her grandfather had tears in his eyes but looked
repeatedly at the doctor and said, “You tried. You really tried.” And we did. We did everything in our power to
save the little girl but in the end it wasn’t enough. And while I get SO
frustrated and tired of death, I know that while we couldn’t save her,
yesterday we showed her family that their child was important. We loved them by
loving their child. I can’t save
everyone. I believe that ultimately, God is the giver of life. So I’ll work as
hard as I can for them but whether or not I can save them, I will love them.
And someday when I stand before God, I think He’ll say it was enough. “His
grace is sufficient for me.”