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by jkaplowitz
749 days ago
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Valid, yes. But the law could still require that the medical monitoring device have other functions disabled or (depending on what the legislators consider easy enough) not in use while in class except for the t1d monitor + SMS + voice, right? And they could still apply discipline if the student's phone has other functions enabled or (depending on the legislative wording) in use while in class? The law could also use indirect leverage to gradually separate students' medical monitoring from the smartphone over the medium to long term. For example, they could begin a multi-year transition period after which NY-regulated health insurance plans would have to cover a non-smartphone version of these monitoring devices with at least equivalent functionality to any smartphone version they cover, at no greater out-of-pocket cost to the patient, unless no comparable non-smartphone product is on the market from any manufacturer. Then they could eventually require the non-smartphone version in class once it exists, with a fully insurance-paid (no cost-sharing) transition available at that time to children who use the existing smartphone monitoring system. To avoid a gap in insurance coverage, NY could continue to mandate that some version of these devices be covered, so nobody would go without affordable medical monitoring. But as soon as one company decides to make a non-smartphone version, their competitors would have to do the same or else lose market share in NY, so they all would. (Why would that first company take the leap? They'd get a lot of insurance-paid device purchases for the transition for children's existing devices.) And then teachers would have an ADA-compliant way to remove the distractions of smartphones in class even for kids with medical monitoring needs, without causing harm to anyone. |
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I think there are a few issues here.
T1D is already incredibly intrusive in the daily lives of children. Continuous glucose monitors (device 1, on body with bluetooth connection to a smartphone, device 2) track one's blood sugar every 5 minutes or so and gives the child, the parent, and the school nurse the information they need to jointly replace the functionality of the child's pancreas. This might be dosing with insulin through a pump (device 3, sometimes managed via smartphone) to lower blood glucose or cover carbohydrate consumption. Or it might be eating to raise blood glucose.
If the student's blood glucose gets either too high or too low (which can happen in a matter of minutes) the consequences can be fatal or lead to lifelong complications like nerve damage in the extremities or eyes. High stakes stuff.
If I understand correctly, your proposal would introduce a fourth device to separately monitor blood glucose and, I assume, manage the process of uploading this data and sharing it with all parties. This fourth device would mean a few things:
- Yet another piece of expensive, and durable medical equipment you are required to pay for, that insurance rarely fully covers.
- The child would have to tote around now four devices daily to manage a chronic condition.
- Another device to manage and maintain (batteries need to be charged, etc).
- Paying for another 5g plan to ensure that the monitoring device can share information with parents etc.
Despite some of the cons to these systems being integrated into your smartphone, there are considerable advantages to using the networked compute you always have in your pocket. Not to mention that these devices suffer from painfully slow development and approval cycles. Durable medical goods often have to go through federal approval and even small changes to firmware can take years.
Also, just some quick figures. The school age population in NY state as of 2021 was 2,622,879. About 1/400 children ages 0-18 have type 1. So around 6.5k students. This is neither the extreme edge case that others have described (and just one of many chronic diseases that are managed via smartphones) nor is it likely a large enough segment to change product development at these large health tech companies.
I don't think the solution is to try to engineer incentives and overhaul the entire health insurance coverage of durable medical goods. Nor do I think the solution is to require children with T1D to carry around and pay for yet another expensive device.
I think we just need to be careful in the design of legislation like this, as you suggest, especially when it comes to ubiquitous devices that have been integrated into so many facets of people's lives. There is no such thing as a 'trivial exception' to a state law (responding to a commenter further down).