Week 3 - Shenghao Tan

I spent the Sunday at NYP lower Manhattan since my clinician was on call there. Compared to the main hospital it is not as busy and, according to the clinician, allows better communication between the doctors and nursing staff. Lower Manhattan has integrated dialysis boxes in the rooms, which is apparently not common. For the weekdays I spend most of the mornings in the microbiology lab observing the benches, mostly urine and respiratory samples. I was able to observe the different methods of processing and pathogen IDing. One aspect I didn't expect was  the difference in diagnostic methods between benches: stool  samples are exclusively processed with nucleic acid amplification in BioFire GI panel; urine samples are processed by  colony morphology, staining and biochemical tests to identify the pathogens, and not much NAA; blood bench starts with incubation in  both aerobic an anaerobic bottles, with pathogen presence  identified from CO2 production, proceeded with identification via  NAA, biochemical tests, and MALDI-TOF. Matrix assisted laser desorption / ionization (MALDI) is a really cool mass spectroscopy technique to quantify different bacterial proteins to identify the pathogen. Each ID only takes around 20 seconds and reports the bacteria / yeast / fungi species, which is much faster than conventional PCR or biochemical methods. Another surprise was the mycology bench: unlike all other benches, the identification of  fungi is almost always through morphology under a microscope.

On Wednesday night I watched couple folks getting their MRI done for reasearch purposes. Got to see some brains and spines :D. The postdoc was really nice and knowledgable.

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