The
month of May, I spent assigned to the pediatric surgery service at
Kaiser Permanente Hospital in San Diego. The staff pediatric surgeon,
Dr JD, a former pediatric surgeon at the Naval Hospital,
accepted surgery residents and interns to mentor. This month gave me
the opportunity to get to know Dr CY, the senior resident
also assigned to the service.
As
an unlicensed physician, as most interns are, I had a very limited role
in actual patient care at This hospital for liability reasons. I
primarily observed, not being allowed to write notes and orders in
patient charts, cover inpatient call, not even allowed to “scrub in” on
surgeries. The relaxed pace was sometimes boring but a welcome reprieve
from the frenetic pace of the rest of the year.
Preoccupation
over my upcoming MRI towards the end of the month blurred my memory of
that rotation. One event does, however, stand out. I was informed by
CY of a little boy that had had a percutaneous endoscopic gastrostomy
(PEG) tube for feeding because of a congenital abnormality. He was
having difficulty breathing due to indigestion and bloating. Later that
evening, the father called me with the same complaints. As instructed,
I told him to “burp” the tube and go to the emergency room if his
difficulties continue. I went to bed. Early the next morning, around
three am, the father called me back to inform me his son was dead. I
froze in panic. “My God, what do I say? What do I do?” I thought. I
had never been in a situation like this. Previously I had been a part
of a team in these kind of situations. The more experienced attending
physicians handled this stuff and I stayed in the background with the
rest of the surgical entourage. This time I was alone having to talk
with an acutely grieving parent. I expressed my condolences for his
loss. I hung up the phone with the unsettling feeling that I handled it
all terribly wrong. Eight months later I would learn that there was
nothing I could have said to ease his pain, but to have said nothing
would have been deplorable.
The
morning of Thursday, May 26 I went to the radiology clinic for my MRI.
The machine looked like all the other CT scanners and MRI scanners I
had seen previously. A nut and bolt assembly with the bolt being the
patient lying in a narrow trough-like table, and the nut being the large
square machine that housed the rotating magnets. But this time, I was
the patient lying on the table whose head the unseen magnets would
rotate around. I lay supine on the table. A cage was placed over my
head. I imagined I looked like a hockey goalie or baseball catcher.
The table slid into the scanner, automatically positioning my head in
the narrow opening. “!-!-!” went the scanner, then silence. Suddenly a
loud “gnweuew”, followed by “dupt-dupt-dupt-dupt-dupt-dupt-dupt-dupt,
blop-blop-blop-blop-blop-blop-blop-blop,
doof-doof-doof-doof-doof-doof-doof-doof, rat-tat-tat-tat
tat-tat-tat-tat. The cacophony would have been deafening had it not
been for the headphones placed over my ears. Then silence. A few
seconds later the second cacophonic movement began just like the first.
The
following afternoon I called the radiology department to get the
results. I spoke to the neuroradiology resident who was reluctant to
discuss the preliminary results. Radiologists generally don’t discuss
results with patients, only doctors. Dilemma, I was both. He nervously
stressed the results were only preliminary, not yet reviewed by his
attending radiologist, not yet finalized. With a shaky voice, he then
delivered his preliminary findings which were word for word of the
eventual finalized report, not out of nervousness and insecurity in his
interpretation, but out of concern for what his interpretation meant to
the person on the other end of the phone line, me. I listened, hung up
the phone, and steadily, with heart pounding, throat closing, and eyes
welling, walked to the men’s room. Once the latch clicked behind me, I
collapsed to the floor against the corner, in a heap of wails and sobs.
I wept like I never wept before, and only thrice since.
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