Takeaways
My goal going into this externship was to explore ways in which I can incorporate public health endeavors into my practice as a physician, and I am glad to say that that goal was achieved. The past month and a half has had its challenges, but it provided me with excellent insight into the research realm of the public health world. In particular, I was able to learn about cancer epidemiology, specifically, prostate cancer epidemiology.
The importance of tying together epidemiological research and clinical practice, for me, is so that neither the individual nor the population’s health is overlooked. This particular study that I was working on, entitled Treatment Options for Prostate Cancer Study, was looking at the broader population of men with prostate cancer and how they decided on a treatment. Although this question may have arose in clinic during an individual office visit, the findings from the study can be applied on a much larger scale and may help many men achieve a better quality of life.
Additionally, an individual’s decision to go ahead with surgery or chemo may be influenced by socioeconomic status or race. These are important considerations to take into account when making recommendations regarding prostate cancer treatment for the general male population and when speaking with a patient one-on-one in the office. I was fortunate enough to have had the opportunity to witness firsthand how physicians are able to individualize recommendations for prostate cancer treatment. In addition, I was able to see how patients can influence the approval of research proposals, and just how crucial it is for them to be able to do so.
Aside from learning the broad scope of how physicians can combine public health research and clinical practice, I also learned about the nitty gritty details of the cancer registry and how to carry out large-scale studies. For example, eligible patients are identified through the Surveillance, Epidemiology, and End Results Program which contains lab results and diagnostic information. The physicians of these patients are then contacted and if they agree that the patient can participate in the study then we contact the patient. All of this information, and the survey data if the patient chooses to participant, is tracked in a large database. Although this sounds simple, the amount of detail and manpower that goes into keeping track of thousands of surveys is astounding.
Overall, I have a better idea of how I want to integrate medicine with public health. Working on the TOPCS study helped me understand how much detail goes into this kind of project, and how to incorporate the information gained from this study into clinical practice.












