I had the opportunity this week
to tour the hospital’s point-of-care and central diagnostic laboratories. The point-of-care lab contains a variety of
portable diagnostic instrumentation to provide timely support for critical care
and ER patients. Some examples include devices
for measuring blood gases and biomarkers such as glucose and troponin, which is
a highly specific marker for cardiac disorders. These devices are able to wirelessly upload
patient diagnostic data, which are subsequently processed in middleware
including RALS and LIS and are then transferred to the Epic electronic health
record system all clinicians use. Unlike
the point-of-care lab, the central lab is a much larger facility that takes an
assembly line approach to support the majority of the hospital’s diagnostic
demands. The facility is full of
automated sample processing instrumentation and additionally has a cool pneumatic
tube system in place for receiving patient samples from various locations
within the hospital.
In the clinic, the cases I
shadowed with Dr. Vielemeyer were generally not as exotic as some of the cases
we saw in the previous weeks. The most
interesting case this week was a patient with stage 4 metastatic cancer who was
put on hiatus from chemotherapy due to a bone infection incurred after a tooth
extraction procedure.
For my research in Dr. Kirkman’s
lab, I was able to successfully amplify the beta subunit 2 gene from p. falciparum. I redesigned the primers for beta subunit
3 as the ones previous designed did
not work and I also designed primers for the remaining subunits 4, 6, and 7. For beta subunits 1, 2, and 5, which have all
been successfully isolated, the DNA fragments were inserted into plasmids and
amplified in E. coli with the TOPO
blunt PCR cloning technique.
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