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adit_ya1

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Almost every point follows the same structure:

"Here is a real concern about implementation" → "Therefore you should refuse entirely"

This skips the middle step of "therefore we should implement it well."

I'm not convinced that we should be allowing doctors to record patient visits at this stage yet, but I'm really not convinced by these points, which largely don't hold up under closer examination.

A few that stuck out:

"Privacy" - Labs are routinely sent to third-party companies, and we don't do informed consent for that. The third-party argument isn't unique to recording.

"False promise of efficiency" - This doesn't really have anything to do with patients at all. It's a criticism of medical office management, not of physician-patient interactions. Telling patients to refuse a tool because management might exploit the productivity gains is asking patients to fight a labor battle on the provider's behalf.

"Consent can't be revoked mid-visit" - Consent typically can't be revoked in the middle of an appendectomy, or halfway through administering a vaccine either. Practical irrevocability is a normal feature of informed consent, not a special problem unique to recording. Proper consent processes in medical offices are a broader issue than consent about voice recordings specifically. Had the authors made the point that providers are being asked to obtain consent for tools whose technical implementation and privacy risks fall outside the provider's own domain knowledge — that would be a stronger argument. But that isn't quite the point they made, and their current framing doesn't wholly convince.

Out of curiosity, what's the prioritization of evidence (RTC Metanalysis > RTC > observational ) etc, and what's the end user benefit over a tool like OpenEvidence? You mention that other tools are expensive, slow, or increasingly heavy with pharma ads, but OpenEvidence for now seems to be pretty similiar with offerings, speed, and responses. What's your pitch as to why one should prefer this?