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Our dedicated Electron Microscopy Department allows the University of Florida Health Pathology Laboratories to be a frontrunner in diagnostics. We actively contribute to advancements in the field of muscle and nerve pathology, and to the education of tomorrow’s pathologists, neurologists, rheumatologists, and allied clinicians. We practice a multidisciplinary approach to the diagnosis and treatment of muscle disorders. In addition to our evaluation of conventional histology and electron microscopy, we routinely utilize a quantitative panel of specialized immunohistochemical, cytogenetic and molecular techniques to provide the highest quality diagnostics in this competitive and everchanging field.

Muscle biopsies allow our neuropathologists to diagnose muscle disorders and actively support the neurology and rheumatology community at large by providing finely tuned comprehensive diagnostics. Our muscle kits are streamlined to provide a minimalistic approach for our submitters, which in turn drop turnaround time and improve patient care. Muscle specimen kits are comprised of 3 biohazard bags, a sterile submission cup, and singleuse saline moistened gauze packet. Also provided are prepaid FedEx return envelopes and labels, which include a Saturday delivery sticker for the occasional Friday sendout. A requisition will be folded and placed on top of the specimen containers.

Inside the kit. Please be sure to follow the included instructions and completely fill out the forms provided. The submission requirements are as follows Once the muscle has been harvested, wrap the specimen in the included saline moistened gauze and seal inside the sterile specimen container. Place the ice in a biohazard bag and double bag it with the largest bag so no leakage occurs. Place the documents in the second biohazard bag and secure the specimen container in third biohazard bag. When the kit is received in the laboratory, the specimen containers.

UF Health Pathology Laboratories Muscle Specimen Collection and Handling Tutorial

And associated documents are crosschecked to ensure that the materials are labeled with two unique patient identifiers such as a name, date of birth, medical record number, and site. This is a requirement that the College of American Pathologists, the most stringent laboratory accreditation agency. If all of the appropriate criteria have been met, the specimen is accessioned and brought to the gross room to begin processing. During the grossing process, a representative longitudinal and transverse section is removed, submitted, and embedded in paraffin for Light Microscopy. An additional representative portion is removed and submitted in glutaraldehyde.

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