Situational Awareness for Novel Epidemic Response - Local Development build (v0.1.0). See the Directory of published versions
Definitions are critical during times of crisis. Knowing and understanding these definitions enables the implementors of this specification to operate from a common understanding of meaning, and those using the data produced from those implementations to respond accordingly.
There are a number of different counts for tracking hospital beds that are relevant in bed availability:
Under normal circumstances the relationship between this is that occupied <= staffed <= licensed. In crises situations, those relationships need not hold. Governments have the authority to waive licensing and staffing restrictions in order to provide adequate care.
The State of Louisiana describes these different categories in their []Definition of Bed Poll Terms](https://esf8.dhh.la.gov/documentportal/Download/Public/Definitions%20of%20Bed%20Poll%20Terms.pdf) documentation, which is informed by the Standardized Hospital Bed Definitions from the AHRQ HAvBED project.
To these definitions this specification adds:
Overflow Beds :Beds that are vacant and and to which patients can be transported immediately, but for which there may NOT be adequate supporting space, equipment, medical material, ancillary or support services to operate under normal circumstances. These beds ARE NOT necessarily licensed, though they ARE physically available, and have staff on hand to attend to the patient under emergency circumstances.
Temporary space is already being planned for in Philadelphia, using an event space at Temple University according to an Action News report. Information about these facilities will likely need to be manually reported until systems can be configured to track and manage them.
Similarly, ventilators can be shared, so the important number for ventilators may not be the number of devices, but rather the number of patients that can be accomodated (ventilator outputs). New York-Presbyterian Hospital began ventilator sharing in late March as reported in a March 26 New York Times article.
There are also numerous efforts to increase the supply of ventilator devices, and various organizations are created plans to construct and actually build mechanical ventilators from readily available hardware.
Others have noted that respiratory assistance can be provided by non-invasive ventilation (e.g, a CPAP or BiPAP(r) machine or similar device).
Test kits are consumable medical devices that support the completion of a diagnostic test for a given disease. There are many medical devices that operate on a variety of different principles that can support COVID testing. Viral testing ranges from decoding the RNA of viral samples, to looking for specific antibodies in the blood that react to specialized reagents (manufactured chemicals or biologics that react in a certain way in the present of specific molecules in a specimen) and others.
To be clear, this section is talking about diagnostic quality tests, which can confirm or deny the presence of disease, rather than screening tests which might readily rule out disease, but will cannot adequately confirm it.
Reagents can be packaged in quantity to support more than a single use, thus a definition of a test kit is needed in order to enable counting of test kits, since they may not be individually packaged.
Presently, most COVID-19 testing is performed using specimens collected using a nasal (nasopharyngeal to use the precise language) swab and collection technique. However, there are already existing blood tests and manufacturers are working quickly to deliver point of care blood testing systems.