* US national suicide hotline: 1-800-273-TALK (8255)
* UK Samaritans hotline: 116 123
You can go to one of these sites for phone numbers in other countries:
* https://www.suicidestop.com/call_a_hotline.html
* https://wikipedia.org/wiki/List_of_suicide_crisis_lines
Whatever happens, whatever you've done, I think your life is worth saving. Even if you don't.
Edit: updated with lists for rest of world.
I have a close, immediate family member who has attempted suicide on numerous occasions. Sometimes she was in a dark place of depression and despair, for sure, but other times she was high on life and full of energy. Those times it would be a sudden urge that came over her, and not an outcome of despair.
If you think, "I want to commit suicide, therefore I must be in a dark place," it's putting the cart before the horse, for sure. Most people are under the illusion that suicidal thoughts stem from feelings of depression / sadness, and the reality is that these are three entirely different things: suicidal thoughts, depression, and sadness are three things which are often very different from each other.
So you think someone must be sad because they have depression, or they must not be depressed because they aren't sad, and these incorrect beliefs can lead to harm.
And you also think that someone who is not acting sad or depressed must not be thinking about suicide, when very often someone who has decided to commit suicide may feel very happy or liberated having made that choice.
It can be really enlightening to talk to different people who have experienced or who experience suicidal ideation, because their experiences are varied, and while suicidal ideation is considered a risk factor, it doesn't mean that you're more likely to commit suicide and the people with suicidal ideation are often reluctant to talk about it because of the stigma. Like, "I experience suicidal thoughts, and I want to talk about them, but if I talk about them, people will wrongly think I want to commit suicide, or wrongly think that I am depressed, or wrongly think I am sad, so I am unlikely to get the sympathy or help I need and it is likely that talking about it will have a negative impact on my relationships."
We get all sorts of desires. The mind is full of inactive, dormant code. But, when we get one of them, then entertain it long enough, and the environment is just right, people most certainly will do horrible things, including killing themselves and others.
I'm not implying that it's all programmable, but more that decisions are the consequence of many variables after the initial temptation.
Is this service confidential?
Yes, except for in certain situations where our safeguarding policy means we may tell someone, for example, by calling an ambulance. Read more about when we do this.
On the phone
When you call Samaritans, your number is not displayed to our volunteer. The phones we use don’t have caller display information on them.
We might ask your name, because it’s a natural question to ask in a conversation, or because of something you have said to us, but you don’t have to tell us if you prefer not to.
Via email
If you've emailed us, your email address will not be shown to the volunteer.
In person
You don’t have to tell us your name if you don’t want to. In the unlikely event that you see the Samaritan volunteer that you spoke to later on the street, the Samaritans volunteer will not acknowledge you, unless you do so first. This is to respect your privacy and the confidentiality of your visit, unless you wish to recognise it.
By Letter
We will need your name and address to reply, but to maintain confidentiality, your letter will be shredded once we have sent you our response.
As further evidence (albeit anecdotal) I have noticed, especially in light of prominent suicides in the last few years, that the information posted seems to be getting more attention, with, as you called it, meme-like inclusion almost everywhere and every time suicide is discussed. This has correlated with an increase in the number of calls they receive.
They have received more than 12,000,000 calls since 2005, with 8,500,000 just between 2014-2018, much faster than the increases in suicide rates.
[0] https://suicidepreventionlifeline.org/wp-content/uploads/201...
People who commit have real problems that a phone call generally doesn’t solve, unless your problem is just about feelings, which is... let’s say it helps those who call for attention a lot, and who would end up with a failed attempt to call for attention, which will attract attention, but it will hide the real x5 numbers behind the scenes of the other gender who actually commits suicide when they try.
It’s time to stop with the « let’s speak about it » attitude, and start with the « let’s give you funds/education/solve your parental problems/throw the book at your boss/mandate your wife to let you see your kids/stop sidestepping you at work/fix the VA together » attitude.
Men are not an option.
I have a certain degree of personal knowledge on this topic, and there are absolutely people who would be dead right know if they made that call... And no one picked up on the other end.
Also, I don't understand why is so much anger around people who are so starving and desperate for attention. You was quite apparently looking for attention too. That you turned frustration at others does not make it less so.
They won't call the suicide hotline for you. They won't transfer you. They won't share their number. What they'll do is send the police.
I can safely say, in retrospect, that although I survived it, it took nearly a decade to fully heal from that event. But in the mean time, I also learned (thanks to posts like these) about the Samaritans and later in the UK, they helped me get through the tougher moments of this process.
I don't know how significant the effect is, but it's non-zero. :)
I will say -- these phone lines are staffed by human beings. Even with the best of intentions, they're just that, humans. They wont always get it right.
But, when they do, it can be life changing.
I'm always grateful for the kind Samaritans lady who stayed on the phone for over an hour one night.
Personally I am not convinced about that. Or do you mean that from an academic perspective?
Because in the real world, the therapy method I have mostly seen, was and is keeping people calm with pills.
I do a lot of "extracurricular" work, trying to help folks get back on their feet.
So, not academic. Personal.
> Because in the real world, the therapy method I have mostly seen, was and is keeping people calm with pills.
I consider that offensive. It's a fairly classic "strawman" argument that is used to "dehumanize" people that suffer from mental illness, and also dehumanize people trying to help them. I know many people that would be in very dire straits, if not for medication, therapy, and many years of hard work.
I'm pretty upset by this, and by the reactions.
I am not a therapist. Just someone with "skin in the game."
These aren't "data points." These are people, and chances are good that we all have folks in our orbit that have mental health issues.
The poster was simply providing their viewpoint on the state of mental health that differs from yours.
I understand these things can cause strong emotions, but you don't do yourself or your stance any favors by letting it get the best of you here.
Quite frankly, the pills work. A lot of people would unable to lead normal lives without them.
Sometimes they do and sometimes they don't. I had a seizure because of medication I was put on for a mental illness I didn't believe I had. I wasn't 18 and my parents essentially forced me to take them. The pills didn't do anything for me besides give me a seizure that easily could've killed me (I was hospitalized).
There's also actual research suggesting these pills can increase suicide attempts.
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3353604/
There is enormous money to be made suggesting these pills are useful, so I don't just assume it to be true. I also know many other people who feel anti-depressants ruined their lives. I also know many people who feel anti-depressants saved their lives.
It's not black and white. Personally, I feel the efficacy of pills for mental health are greatly exaggerated - but it's easy to see why I might be biased.
I don't know your personal journey, but I think it would be fairly easy to find people with very deep, very real mental health problems who fully believe they do not have a problem.
> The pills didn't do anything for me
Again, I don't know your personal journey, but as a counter anecdote when I started taking medication I couldn't tell if they were having any effect at all, but apparently it had such an effect that some of the people around me could tell me the day I started taking it, along with measurable improvements.
Not to invalidate your experiences, just adding to the anecdotal pool
A board certified doc will never prescribe placebo he will get sued, plenty of ppl are getting them via alternative medicine though
It's not "vague, personal anecdotes." It's real world experience.
But you are right. This is upsetting, and seeing the way that it is being treated by people that I respect, otherwise, is upsetting.
This is the last I'll say anything.
You're taking someone else's valid criticism of the state of the therapy methods available today and taking it personally as well as unwarrantedly attributing it to a lack of sympathy.
You fail to understand that the goal of criticizing the therapy method is precisely so we may find ways to improve it.
I consider that offensive"
You might also consider, that other people might have a "skin in the game", with close, intimate relationship to mental illnes patients, too. Some of them tragic.
And my experience simply is not, that in general psychotherapy evolved a lot. I see rather a trend to favor pills to keep people calm as this is cheaper, than deep psychoanalytical therapy.
So consider that offensive, if you must, downvote, if that makes you feel better, but it does not change my personal experience.
However, support for people with mental health problems is still severly underfunded. The improvements we have seen say as much about the terrible treatment of the past as they do about how well we are doing now.
Almost all studies I have read find that a combination of medication and other therapies provide for the best outcomes. Most people can only get funding for medication, which is often better than nothing, but it really falls short of what society could, relatively easily, provide.
It is really a tragedy, not just to the individuals suffering from mental health problems, but also to society as a whole which misses out from all the untapped productivity and creativity.
https://www.psychologytoday.com/us/blog/out-the-darkness/201...
You might have "skin in the game" but then it is depressing you do not know that almost all mentally ill people would in the long run be healthier without these pills. They mostly only work short-term and absolutely destroy ones health long term. You should be advocating for people to get short-term medically help and long term medicine-free therapeutic help if you really care.
Yes, for some people antipsychotics, antidepressants, etc. are a godsend and the difference between living a mostly normal and productive life vs. jumping off a bridge, dying in a homeless encampment because they cannot feed themselves, or committing violent acts against others. To clarify, none of these are hyperbole or exaggeration -- those are two extremes on outcome with mental health issues and antipsychotics can be the difference between the two.
That being said, many, if not most, physicians I have worked with agree with the parent comment. For many patients these medications are not effective and are used as chemical restraints [0] rather than with the goal of normalizing their mental health. Eventually the logic becomes "we'll never fix them, but we can sedate them so much they won't hurt themselves or others" so dosages progressively increase until the patient becomes more sedated and somewhat zombie like. This isn't hospital specific; I have seen it across 3-4 different hospitals in different states. Neuroscience and psychiatry is a very young field and the truth is that we do not know what causes mental health issues or how to deal with them. The chemical imbalance theory is just that, a theory, and more importantly, one with very little scientific proof and backing [1].
[0] https://www.medicinenet.com/what_is_an_example_of_chemical_r... [1] https://www.healthline.com/health/chemical-imbalance-in-the-...
Serotonin you may say? Okay, how much is the correct amount of serotonin then? Can you just give me a test to see if I have the right amount?
What’s going on here is not quantifiable science. It’s throw something at the wall and see what sticks.
Yes, modern medicine has a large component of throwing stuff at the wall to see if it sticks.
If it sticks, and it passes all the usual clinical trials to prove it does more good than harm, it's approved, even if we don't understand exactly why it works.
For the record, the treatment plan my cardiologist put me on was explained as "all these things seem correlated with not having heart attacks so we'll just do them all and hope it helps you".
Yes basically throw something at the wall and hoping it stick.
These people are fighting for their lives, and are taken advantage of by an industry. It also doesn't help that plenty of antipsychotics are crucial for people to take, but that's because those are drugs that actually make it difficult to think for people whose thoughts get out of control. They don't claim to be eradicating the chemicals or deficiencies of chemicals that cause all psychosis.
The tactic of pharmaceutical companies creating patients' groups to get sufferers together and lobby "on their behalf" has been going on since the 80s. It's bulletproof, and impossible to attack. In the case of antidepressants, they've also guided them into defending these drugs as a class, rather than on an individual basis.
Funded patients' groups also played a huge part in the prescription opiate epidemic; it doesn't matter how much science says that long-term opiates aren't helping chronic pain, you have to be heartless to dismiss someone with a known painful condition or injury when they're pleading for opiates. Even though you know that people who had nothing wrong with them before going on opiates would plead just as intensely.
On another note, there is one thing you are absolutely incorrect about: antipsychotics are not ineffective managing many mental health disorders. Large clinical trials are done before these drugs are even approved for the sole purpose of proving they are better than no treatment.
> Suicide rates ... are skyrocketing.
I'm confused. You seem to be suggesting that having more conversations about mental health is to blame for an increase of people committing suicide.
This is the exact opposite of my lived experience.
Conversations about my mental health and my problems are why I'm alive (and have no intention of taking my own life) today.
If you have a different lived experience, then fair enough.
But I'd respectfully suggest to take care painting with such a wide, sweeping brush next time. Life ain't binary. Especially when it comes to mental health.
I do not see him suggesting that. He was suggesting that "labeling" more and more people as mentally ill might cause more bad, than good.
Allmost everybody has psychological problems. And yes, it is very important to be able to speak about it openly. But it is a different thing to have "mental problems", or to have a "medical mental condition".
It's also probably not possible to convince the government to let doctors prescribe potentially mind altering drugs to people unless they say the people taking drugs are "ill" and the doctors are treating the "illness".
So yes I'd say there is a push to label people as ill.
I feel like back in the day - our grandparents, or their grandparents, perhaps you'd see men who didn't want to go to the doctor.
Now it is completely normal and expected to get a yearly physical. IMHO we all should be getting a yearly "mental", as well (with a psychologist, not a psychiatrist), and it should be both normal and expected.
You obviously aren't concerned that the "professional brain jargon talking person" will make things worse. I know from experience they sometimes do.
I don't trust mental health professionals nearly as much as you do.
I'm sure you can think of different social developments that relate to this too if you're a hardline "you are responsible for your own situation" capitalist without much thought given to individual privilege. There's plenty of others. Let's take social media incentivizing only sharing positive things, leading to bias when comparing your situation to others, for instance.
The current system is a band aid on top of structural issues, nothing else. No amount of CBT and SSRIs can fix these.
the labels are a form of victim-blaming.
Bipolar disorder, clinical depression / major depressive issues, etc.
Plus, since each "band aid" in this case is a human life - a person who may then be able to go on to help others and reform the system, I'm definitely a fan of pursuing both avenues at the same time.
But still, my point is I don't believe 100% of mental health issues have the dysfunctions in our society as their root cause.
Which isn't to say that some do and that it's not a big deal - it is.
Not globally. A search suggests suicide rates are down 15% in 10 years. That is, suicides have gone down remarkably.
If we're talking about the UK/US (which I haven't sourced but I can believe), it's more likely that conservative policies are driving people to feel they have no alternative.
I dunno, in most common diseases going around right now the solution is to treat people with pills. How is depression any different?
Secondly: a bacteria infection and the treatment with antibiotic is very well understood - and is actually solving the issue.
The brain is not at all understood. Lifting peoples mood with drugs is not solving, why they were constant unhappy in the first place.
Still, we have only the faintest idea of how the mind truly works.
CBT is great and I personally benefited from it, but it's not a recent phenomenon and its effectiveness is very hard to evaluate. There was a meta-study analysis in 2015 that pointed at a decline in its effectiveness between 1977 and 2014. I wonder whether it's because studying anything to do with a human brain is hard and we can't trust the numbers or if it's because of changes in society that caused people's personality to shift in a direction which makes CBT less effective.
Autism and schizophrenia were differentiated in 1980, so that's not in the last 2 decades.
Homosexuality stopped being a mental illness in 1973 (or 1987 if you include sexual orientation disturbance), so that's not in the last 2 decades. This was a great success, there were studies that pointed at a marked decrease in suicides among people in same-sex relationship over time.
Gender Identity Disorder stopped being a mental illness in 2013 but I think the issue has been politicised and the outcome doesn't necessarily make a lot of sense. I can bring a personal anecdote from a friend of mine who started using a female name for a period and wanted to perform a reaffirmation surgery, who later changed his mind.
- Most kids who experience gender dysphoria before puberty grow out of it.
- Suicide rates are high even after reaffirmation surgery and even in western societies, which are accepting of transgenders. Moreover, if discrimination was the cause of suicide rates, I think we would see a high suicide rate in minorities. There is way more discrimination towards people of color than towards transgender.
- If Gender Identity Disorder is not a mental illness, shouldn't we be consistent and label Body Integrity Dysphoria (aka people who believe they're amputee) as diversity and approve of cutting off of healthy limbs?
I'm skeptical on including this as a win for the field.
And while it's progress for psychology itself, and good for society, it's certainly not an achievement. People were killing themselves and being institutionalized because psychologists were calling them insane, and this stopped happening when psychology chose to stop calling them insane. I can't claim an important discovery in abuse prevention if I choose to stop abusing someone.
Another theory is that methodology doesn’t matter and the result mostly depends on personal qualities of the psychiatrist. And CBT was effective because the best specialists adopted it. When the rest of the profession caught up effectiveness went down.
Depends on your country. The WHO's ICD-9 document, published in 1977, still included homosexuality as a disease. It was removed in ICD-10, but it was only published in 1990. Countries adopted it in the 1990s and early 2000s. Germany belongs to the group which adopted it in the 2000s. So yes, it happened in the last 20 years.
The discussion about 2decades seems to about accepted academic outcome not policy execution, which is always varied.
FGM or homeopathy or chinese medicine is still a problem in many parts of the world. We don't think validaty of science or anatomy depends on your country.
ICD-10 could be one unambiguous way to classify.
2) Transgender people do not have the legal protections that people of color do. There have only recently been laws to protect transgender people to be employed, have healthcare, etc. on the federal level- and what protections exist can be easily stripped away due to "moral disagreement" of the employer. You cannot refuse as an employer to give a black woman healthcare because you have a "moral disagreement" with her being black.
Is it though?
Its only a conundrum because of the way we have organised data, with NO regard for the people the data comes from. We could have had data collected WITH consent only.
The privacy boat left the port long ago - personal privacy was intentionally eroded, and this is just one example.
Personally, on ethical grounds, I could never have designed a system like that, with so little regard for others, externalising private information so that a permanent record is kept. Once private data is exteralised, who knows where it ends up, even if it is in the name of some good cause (eg an improvement in therapy). Plenty of people warned of these sorts of outcomes.
At this point, if you care about your privacy, you really only have the option of not engaging with the system. Or engaging as little as possible.
My bread'n'butter is patient systems. I cannot think of a way to say this that is not patronising or condescending on some level. Your suggestion will not work. At all. On any level. If we implemented a system like this people would die. Hospitals and Doctors would be sued to oblivion, and rightfully so, but only if they don't succumb to bankruptcy due to malfeasance and incompetence first.
Ethically building a patient administration system requires that you collect relevant information, that is patient-centric, and that identifies fully the patient, their needs, their location and their past episodes of care.
> At this point, if you care about your privacy, you really only have the option of not engaging with the system. Or engaging as little as possible.
The spectrum between privacy and effectiveness with patient and clinical systems is simple and stark. If you want absolute privacy you will receive care that will be truncated, untailored, unfit and unlinked.
I don't think the system can work in the ideal way I would like - the system's priority is the system itself, regardless of the wishes of the individual. As you say, doctors would be sued. I would say that suing, etc relates to the culture that has grown up around the system. And perhaps the medical system was always this way - ie system-centric, rather than patient-centric. With the onset of the 'IT age', we get to see that system-centric fruit fully 'ripen' such that everyone's data can be seen by anyone.
You might say - as I do - that it is for the person who is being treated to be the collector of their information. A different culture would have grown had we had the patient at the center of our considerations.
I'm sure people have been warning all the way down the line, about the issues over privacy. It is frustrating that at every turn the expediency over the system overrides all other concerns. After, what 100 years(?) we find ourselves where we are no, with the patient having no control (and often no knowledge) of the issues that relate to them, while the system has it all. I would go further and say that this outcome is by design, as those running the system - those who govern us - would prefer that we were ignorant while they are informed. Its pretty dystopian anyway.
I'd argue this, but I recognise I am in a privileged position of knowing how the systems work. HIPAA (in the US) and similar legislation in other countries actually puts a lot of power in the hands of patients - if they know how to use it.
You are never going to be in the situation where the patient controls their data completely (what happens if they are non-responsive, drunk or psychotic and unable to legally consent to an intervention they desperately want). I think we shall move towards access to data, and possibly interpretation of that data, but not ownership. Control of the data will always come with caveats, as the body paying for the treatment will always assert their right to how the data is transmitted to minimise costs.
Are you sure your expertise in this area is up to date?
Even with "unlinked": Signal can do discovery without the server storing a social graph. There's nothing stored on a server for a hacker to ransom.
Rank speculation, but I'd imagine there are current designs even at Apple that protect user's health data, and those designs contradict your claim of a shrug-while-we-work dichotomy between "privacy and effectiveness."
Edit: clarification, added a barb :)
It's a constantly changing field, but Health data systems are not the fastest changing field. Change is bound to lower pace layers (governance, usually) and so the capabilities of these systems are ground slowly but incredibly fine.
> Rank speculation, but I'd imagine there are current designs even at Apple that protect user's health data, and those designs contradict your claim of a shrug-while-we-work dichotomy between "privacy and effectiveness."
Cool. I always enjoy new ideas for how to do things. If you can solve these issues, you would upend a HUUUUUGE industry overnight and would be richer than Bezos.
Ppl will likely die because of this leak, I don't think there was any informed decision weighing the risks of both approaches before making the choice.
Every year I see leak after leak in medical data, I am only an developer not in the industry, but the nature of the leak has always indicated massive incompetentence and poor design or ops, rather than than real need for patience care.
Storing data in public S3 bucket has nothing to do with patient care, unwilling to invest to upgrade from windows XP has nothing to do with abiltiy to give care. Ransomware attacks because of aging stack has nought to do with privacy or care.
There is very very little need to aggregate data given the risk of leaks, and very little value to any single patient when his data gets aggregatated. A system not influenced by pharma or software industry would make it incredibly expensive or hard to collect aggregate data, while keeping individual records usuable
The harsh reality is hospital administration and regulation tends to be skewed with doctors, it is the same with legislators who tend to be lawyers, or professional management tend to be sales than tech. None of these groups understand the nuances of tech always to manage or regulate them better, sometimes they are smart or trust their advisors and get it right, but it hit and miss.
Data is money today , so industry is not interested in better safety of medical data either, preventing aggregate collection will loose a lot of value for med tech companies.
I'm reading this as a header declaration.
You are arguing a range of items without actually touching on my point - that health data patterns require a link from encounter and observations back to a patient record. I think that you are arguing a number of these points with incomplete information (i.e. that you have little understanding of the pressures which result in the continued existence of Windows XP within the health ecosystem), and on other points you are completely missing the point (storing patient data on the cloud is a whole different argument).
> Data is money today , so industry is not interested in better safety of medical data either, preventing aggregate collection will loose a lot of value for med tech companies.
The data has relatively minimal value for the makers of patient record systems. The value of these systems are in the licensing and ancillary/secondary services.
I don't need to have an understanding, I am just a regular Joe who's data security your industry does not give a thought about and his data leaked constantly[1].
After so many leaks, I do not see an acknowledgement of systemic issues. I see no discourse on how the industry can step up and improve their security practices. I see no significant update to regulation in response to any of this.
If your industry cannot move fast enough with the consumer tech industry then you should not be basing your tech stack on a OS like XP in the first place , XP always was going to have limited window of mainline support.
Core banking is perfectly happy using COBOL and zOS for the last 50 years. [2]
If you don't believe the architectural choices the industry makes and attitude towards tech has anything to do with the data security problems there is nothing I can say to convince you.
[1] I am focusing on one thing only security not privacy or anything else, i.e. unintentionally sharing data.
[2] it is not that fin tech is without its problems either, however in general fin tech has responded to security concerns.
Effective care requires knowledge of patient history, co-ordination between providers, etc. Your general practitioner needs to identify you to a downstream specialist using a strong-identifiable source. Your hospital requires knowledge of your allergies, of your heritage, of your past medical history, etc, in order to ensure you receive the best therapies and medicines. This does not even touch of things such as funding models or holistic healthcare plans.
The best any care provider would be able to do, in lieu of a trustworthy patient data source, is to offer general medicines and stabilisation.
At least in this mental health practice, you charted on paper / locally to the providers systems. We had a billing team (in old model) that only uploaded key patient info (MRN / DOB / Service date / time / billing code) to a billing system. This was done using billing slips that went to someone trained on it (who could handle all the weird hassles around eligibility etc etc).
Provider would actually talk to patients etc etc. The notes were pretty focused afterwards. And yes - pretty secure - it was actually hard to just browse around - providers locked up their notes in their office, and their office was locked (we had a three lock rule -> front door with alarm (metal gate), office locked, file drawer locked.
What people don't tell you is with the electronic health record, they also required that all these required elements be "charted" - on EVERY visit. So in new system pretty soon charts become a pages of boilerplate per visit - copy and paste stuff. It was not useful anymore to do a case history from this chart.
So we made the admin folks happy, but what a trash experience - the EHR folks are selling bills of goods and the admin folks implementing and the compliance folks mandating endless boilerplate and macro entries to get anything approved are wasting all our time and money.
I got out, never felt better - the people were great, the ordered from on high decade old java app through a double VPN that worked 50% of the time with no user experience thinking - a nightmare.
And in this new system, every sysadmin could basically snoop on anyone (all in the name of patient coordination) as could lots of others who just ended up with the extra permissions because the system was so locked down we all basically had to be superusers. To run billing reports you needed access to every record - so they had to give you these ridiculous permission levels. And to avoid QC issues billing staff are reading all the chart notes to make sure all the required boilerplate is in them. Such BS. This system was integrated with a lot of providers, so you could also see everything related to that person everywhere (all the office / admin / billing staff at literally every provider included). While a bit helpful if you had a billing issue (same unit type billed at an unapproved frequency) all the benefits focused on that type stuff (admin ease) and privacy was zero across that backend system.
My organisation has done many EHR/EMR, PAS and EMPI implementations using systems from third party vendors (i.e. I don't have any dog in the which-system-is-best fight). With modern systems (i.e. applications developed during and after the HIPAA act) we have seen significant reductions in error rates relating to drug interactions and dosing.
> What people don't tell you is with the electronic health record, they also required that all these required elements be "charted" - on EVERY visit. So in new system pretty soon charts become a pages of boilerplate per visit - copy and paste stuff. It was not useful anymore to do a case history from this chart.
I did not know we were meant to keep this a secret. Yes, it is important that you record every encounter with "boilerplate" code. There are funding impacts (as case complexity rises with these lifestyle and prior history codes). If a patient presents with a cough and blood in the sputum, it is important to know that they were once a smoker. If a patient presents with a broken leg and they have a history of diabetes, their treatment will be considerably more difficult and expensive.
> And in this new system, every sysadmin could basically snoop on anyone (all in the name of patient coordination) as could lots of others who just ended up with the extra permissions because the system was so locked down we all basically had to be superusers.
I have worked on these systems as well. I find more recent systems to be far better better at accountability with regards to patient record access tracking. It has been a long evolutionary path, however.
The patient wants time with their clinician. So in a 20-30 minute visit either the clinician has to be busy charting away (we called them progress notes) or you get actual patient time and more summarized to the point notes. Why can't charts include decision useful info.
For example, if a patient has 5 objectives in their plan, why make EVERY 20 minute encounter go over all these objectives yadda yadda - is it unfair to expect the clincian will be working on these issues during their visit. Now every progress note has to have. We discussed patients success and potential tools to help them improve in their ability to control X, including various strategies and evidence tested techniques shown to demonstrate good results in this area. We discussed patients success and potential tools to help them improve in their ability to control Y, including various strategies and evidence tested techniques shown to demonstrate good results in this area.
This was govt delivered / managed care BTW - so in reality, the EHR made clear that they gave to craps about patients or outcomes and just wanted to check boxes, so everything was both insanely detailed and offered no decision usefulness.
The tell is that most of these systems have been total top down forced (from national level). That's a good good sign there is not much natural desire for them.
In other fields you get bottom up adoption of tools - a proof in the pudding point of evidence that folks find value in them (beyond the admins).
Yeah, MH is an odd beast. I think the slowness of health data change is exacerbated by the complete lack of funding to this area (at least in countries with public MH services).
I'm sure that it makes a difference to some people, but so does the vulnerability of privacy. How many people will simply not see a doctor because they're worried about this?
Also your healthcare providers kept their fully-identified records.
And, yes, it was signficantly less effective with higher error rates, etc.
> How many people will simply not see a doctor because they're worried about this?
Very few, I suspect. None that I have ever heard of outside of people with significant anxiety disorders (this is literally true, and not my implying anything).
I.E. software engineers can become ... real engineers!
At what point should we refrain from releasing a tool that may powerfully help people but also powerfully hurt people?
I deliberately avoided reading this thread for quite a while, because I could see where it was going. It's pretty depressing how willing (and even enthusiastic) we can be, in dehumanizing other people.
I have been deliberately vague, in specifics, because even a bit more specific could lead to people figuring out some of the identities of the folks I have known. I have enough respect for these people, and for the extreme damage that can be done, if it leaks, that I'm willing to take shots from the "Give us concrete examples, or you're a liar!" crowd.
Here's an example of how tools could be misused. One of the things that I've done, over the years, is design a Web-driven, decentralized system for aggregating 12-Step fellowship (drug recovery) meetings. It's pretty much becoming the de facto world standard.
In some nations (I'm looking at you, Philippines), people can be killed, just for being drug addicts. In other nations (I'm looking at you, Mexico), drug rehabs and recovery gatherings can be targeted by mass-murderers, in efforts to kill just one member.
It's entirely possible that the tool I wrote could become a "murder menu" for these places, and that is not a thought that I take lightly.
Nevertheless, those are "might," scenarios, and there's no question at all, that the tool has saved many, many lives.
I don't think that it's being used in the Philippines, but they are considering using it in Mexico.
I did my due diligence in the design of the tool. A number of compromises needed to be made, in order to ensure that it would be adopted by its intended user base, but it's pretty hard to abuse. Also, the team that took over after I turned it over, includes a number of security experts, so I leave it in good hands.
I can't tell you what to do, but, if you feel that you have done all you can, legitimately, to secure it, then you can probably confidently release it, maybe with some published guidance, outlining risks.
I feel grateful that you've not only built the tool and put it out there, but that you took the time to share with me a little of your story and that it sounds like you have also felt the weight of such a decision. I'm sure other people feel it as well, I just rarely, if ever, have heard someone articulate the saving a life vs taking a life aspects of such technology.
Thank you.
You sound like a decent chap. I like “martial art for an open heart.”
We can use as much of that as possible, in today’s world.
I know I still need it and imagine there is always at least one other person who may as well :-D
You sound like decent chap as well. I have a lot of friends who have benefited strongly from the 12-step process. I also imagine I might have other friends in some of those nations you mentioned who benefit from the care you put into protecting their privacy.
Good luck to you as well!
We can always say "might" but is there any evidence of this at all? On what theory would you even think it would?
But do we need new therapies? CBT, mindfulness, etc - there are a lot of therapies that work VERY WELL. Especially (and this is anecdotal, from friends), combined with things like replacing alcohol with marijuana, reducing or eliminating caffeine, eating well (avoiding sugar / white bread and other carbs), and getting regular exercise.
But we live in a sick society, where the above are often untenable.
Therapy? That's 1:1, time intensive, and insurance abhors it if a pill can do the job.
Marijuana? Illegal, or expensive and over regulated when legal.
Exercise? Hard to do if you have long hours and a long commute.
Healthy food? Expensive, sometimes hard to cook. (I looked at an Indian recipe book for vegetarian ideas and many of the things I love, like palak paneer, are very labor intensive).
But put someone on antidepressants or other pills that are covered by insurance or purchased in generic? That's a simple solution, so it's what's used, even as patients suffer HORRIFIC symptoms going off these meds when they do not work.
Imagine mustering the courage to ask for help, being given a pill that does not, and makes you have trouble doing the work that gets you insurance.
And then not to mention the therapists themselves - having to find the right one, and that's if you just don't mesh and don't have a very bad experience.
I'd argue a lot of what we call "depression" or "anxiety" are actually quite normal responses to a sick system in desperate need of change and people are often "nudged" by the system to do the "wrong" thing then punished for following the path laid out for them.
This 100% is not true.
We can't properly even see rates of STI increases in communities quickly, so worrying about an AI that would have IQ's at human level, which is decades away, is not relevant.
This 100% could be done with written notes.
Cost is the only factor.
Making a therapist cheaper will save lives.
I suspect electronic notes saves pennies in the dollar, compared to the other expenses of therapy.
Growth of data based technologies and information surely create risks to privacy, which is another story. However, treating people data as just data is neither new nor dehumanising. Science does that with everything and that is called abstraction. Just make sure that personal data protection measures are there.
In the 50 some odd years I've been on this planet, it has been my observation has been most every time someone says something isn't applicable to their argument at the same time they are making the argument, it is.
The ability to digitize and aggregate the data, and maybe even subject it to some kinds of AI, might result in massive improvement in therapy.
Mental health treatment has come an incredibly long way, just in the last couple of decades. It's even more amazing, when you look at how it went a hundred years ago. Some of the reasons are because of the ability to study treatment methodologies and outcomes.
But having the data in a place that can happen, is very, very risky.
People with mental health problems tend to be treated as "disposable people" by a lot of folks. I guarantee that the first thing the hackers did, was find a way to "dehumanize" the people in their data. Having the people as "data" went a long way towards that.
But people will die as a direct result of this breach. That's not hyperbole. It will happen. Some people will commit suicide, some will avoid treatment, causing all kinds of collateral damage, and some may actually kill other people, because of this.
I have a lot of close, personal experience with people suffering from mental health issues, and this is about as bad a nightmare as you can imagine.
It will reverberate around the world.