It's shocking that we've already completed two full weeks of our Immersion Term! During this week, I was still held up with a few administrative and
logistic issues that prevented me from engaging hands-on in lab. Luckily,
though, I was able to attend a few different conferences and shadow some of the
researchers in the Bostrom lab.
On
Thursday, I listened to some presentations from the fellows at the Hospital for
Special Surgery. The subjects that they discussed covered a wide array of different
orthopedic and rheumatological disorders. Out of all of the different topics
that were covered, one that discussed the benefits of minimally-invasive and
open techniques in lumbar surgery. From what I’ve read about in recent times,
it seems that patients undergoing surgery generally prefer minimally-invasive techniques,
because of the lessened scarring and shorter lengths of stay in the hospital. I
found it pretty interesting to hear a clinical perspective on this matter and
further understand some of the benefits and drawbacks that are associated with both
of these different surgical styles. Some of the other topics that the fellows
discussed during this presentation included spinopelvic alignment following hip
replacement surgeries, MRI analysis used to detect and measure osteoporosis, lymphatic
responses in mouse models, hemoglobin and hematocrit monitoring in total joint
arthroplasty patients, and solutions for hallux rigidus.
Generally
speaking, I found it interesting to see the juxtaposition between a
clinically-based presentation as compared to the research-based presentations
that I’ve been able to frequent more often thus far during my time as a PhD
student. One point that I noted is the amount of variability in clinical data
compared to the data collected in controlled laboratory environments. Being
that clinical research uses human samples, there is a wide range of stochasticity
that cannot be controlled throughout the experimental procedures. In laboratory
settings, we often attempt to control the experiment in such a way that it
prevents major sources of variability (such as using animals of the same species
strain and age); however, in clinical settings, it’s nearly impossible to control
these factors. When presenting, most of the fellows discussed ways in which they
attempt to account for this variability in their data analysis processes.
Seeing the comparison between the laboratory-based and clinical-based experimental
and analysis procedures was eye-opening—I never expected there to be so many
differences between the two!
In lab, I
was able to talk with some of the different members of the Bostrom group to
understand more of the work that they regularly work on. One of the lab members
(who worked in the van der Meulen lab during undergrad!), talked to me about
some of the work that she does performing RNA-sequencing in the Bostrom group.
I found it pretty interesting to hear her perspective, discussing some of the
challenges that she faced as she transitioned from working in the van der
Meulen lab to the Bostrom lab. One thing that she mentioned that surprised me
was the discrepancies in results based on the different equipment in the two
labs. It was interesting to get a first-hand
perspective on some of the difficulties that can arise in lab because of
external factors, such as equipment variability.
Outside of
lab, I had a lot of fun exploring different areas of New York City! Emily,
Garrett, Mariela and I got a chance to explore Chelsea Market and try some of
the different food offerings. Daniela, Emily, Mariela and I checked out some of
the small shops scattered throughout SoHo last weekend as well. Hopefully, we’ll
get a chance to explore more of the NYC boroughs throughout our time during
Immersion!
What was the clinical perspective on minimally invasive vs. highly invasive? Did they also prefer the minimally invasive procedures, or is it just highly situationally dependent?
ReplyDeleteThe high variability in clinical data also means you generally need larger data sets to be able to tell if something is significant. Just like you normally need larger sets of mice than you do cells. It is crazy to see how different. Did you notice any major differences in presentations style, or mostly the data itself?
It seemed as if the preference among the clinicians was highly situationally dependent, based on the discussions. A lot of the presentations were based on meta-analysis studies, though, so it could be that this generalized preference was swayed by the bias of the individual study authors (and it was not specified if these study authors were clinicians, researchers, etc).
ReplyDeleteIn terms of presentation style, I noticed that a lot of more time was focused on detailing the results - as opposed to the methodology - in clinical presentations compared to research presentations. However, these were very short presentations (I think with a time limit of 5 minutes), so this could have just been due to time constraints.