Lemmy, I really would like to hear your opinions on this. I am bipolar. after almost a decade of being misdiagnosed and on medication that made my manic symptoms worse, I found stable employment with good insurance and have been able to find a good psychiatrist. I’ve been consistently medicated for the past 3 years, and this is the most stable I have been in my entire life.

The office has rolled out the use of an app called MYIO app. My knee jerk reaction was to not be happy about the app, but I managed my emotions, took a breath and vowed to give it a chance. After being sent the link to validate my account, the app would force restart my phone at the last step of activation. (I have my phone locked down pretty tight, and lots of google shit, and data sharing is disabled, so I’m thinking that might be the cause. My phone is also like 4-5 years old, so that could also be the cause.)

Luckily I was able to complete the steps on PC and activate that way. Once I was in the account there were standard forms to sign, like the HIPAA release. There was also a form there requesting I consent to the use of AI. Hell to the NO. That’s a no for me dawg.jpg.

I’m really emotional and not thinking rationally. I am hoping for the opinions of cooler heads.

If my doctor refuses to let me be a patient if I don’t consent to AI, what should I do? What would you do? Agree even though this is a major line in the sand for me, or consent to keep a provider I have a rapport with, who knows me well enough to know when my meds need adjusting?

EDIT: This is the text of the AI agreement. As part of their ongoing commitment to provide the best possible service, your provider has opted to use an artificial intelligence note-taking tool that assists in generating clinical documentation based on your sessions. This allows for more time and focus to be spent on our interactions instead of taking time to jot down notes or trying to remember all the important details. A temporary recording and transcript or summary of the conversation may be created and used to generate the clinical note for that session. Your provider then reviews the content of that note to ensure its accuracy and completeness. After the note has been created, the recording and transcript are automatically deleted.

This artificial intelligence tool prioritizes the privacy and confidentiality of your personal health information. Your session information is strictly used for the purpose of your ongoing medical care. Your information is subject to strict data privacy regulations and is always secured and encrypted. Stringent business associate agreements ensure data privacy and HIPAA compliance.

  • Cellari@lemmy.world
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    22 hours ago

    AI is really good at concepts, not logic. But even then the performance is going to be dependant of the data it was modelled with.

    You can ask for a specific symptom of pneumonia and it can answer. You can also ask for a summary of pneumonia, as someone has most likely wrote one already and AI understand to use it because of the concept relevance. But if you ask it to summarize a patient information, it will split the patient information into blocks it can summarise based on what summarisation information it has in the model data. I can assure you it cannot ever have all the possibilities pretrained already.

    • leadore@lemmy.world
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      12 hours ago

      My fear is that the models merge all kind of patient record info together as the statistical model so the ‘summaries’ will write the most likely word to come next in the phrase, so wrong information and incorrect diagnoses will be recorded into a person’s record, or that important information will be omitted.

      I predict that people will be harmed or die because of missing or false information patient records. But it will be difficult for the public to find out about it because of privacy issues and the unwillingness of institutions to acknowledge it.

      Drugs have to go through multiple stages of testing and trials before they’re allowed to be used on patients. But no one is doing any kind of testing on the effects of this at all, let alone controlled trial rollouts with review, before allowing general use.