Tuesday, May 24, 2016

Grief, Twice Removed

Good morning.  I'm typing very quickly because I'd like to put up a blog post before the power company de-electrifies me for the day.  This is the 5th attempt to take down our dying old oak tree, and it looks like it may actually happen today. 

And there went the power..... 12 hours later, the power is back and now my house looks naked without it's oak tree.  Not a person-- and it wasn't safe to leave it up any longer-- but I am feeling a bit of grief for both the tree and the shade and the way my house looked when I woke up today.

That said, I wanted to share an article with you that I read in the NYTimes Opinionator.  Grieving my Patient's Friend is a heartwarming piece by Galit Atlas who is a therapist who comes to feel attached to his patient's friend, and then learns she is dying.  I loved this piece because I identified with it so strongly -- I've listened to the stories of other people, imagined what they were like, and gone through their traumas, celebrations and, like the author, even their deaths.  Oddly enough, I sometimes hear about the same people and their stories from several patients, or learn the fate of a friend or family member of one patient years later from another patient.  

So Altas writes:

It isn’t unusual for therapists to feel that they know intimately their patients’ friends, lovers and family. In some ways, we get attached to these people, their stories, their successes and struggles. We accompany them at once closely and from far away, as if they are favorite characters in a beloved book.

She tells the story of her patient, Naomi, and of Naomi's dying friend Isabella.

Naomi had looked at me and then added, “Can you believe it really happened? I lost Isabella. She will never come back.”

Oddly, I felt that I had lost something as well. But mine was an unusual, unrecognized loss. I grieved for a woman I had never really known, and no one could see or acknowledge my pain. I was alone with it.
 It's a poignant piece so I hope you enjoy it.


Wednesday, May 18, 2016

Mental Illness and Violence: Dispelling the Myths and Managing the Risks

I'm passing along this information so that readers can register for this forum if interested:

Mental Illness and Violence: Dispelling the Myths and Managing the Risks
Washington, D.C. – In the aftermath of highly publicized cases of violence, there is a big disconnect about mental illness and its connection to violence. Research shows that people with mental illness are more likely to be victims rather than perpetrators of violence. On Thursday, May 26, the global research institute RTI International will host a policy forum “Mental Illness and Violent Events: Identifying, Managing and Reducing Risks,” where expert researchers working on these issues will clarify the scope of mental illness in relation to violent events, including suicide, gun violence, and victimization.
Often policymakers develop mental health policies as a response – and solution – to incidents of gun violence instead of an investment in needed mental health services, systems, and supports. Panelists will discuss the nuances these policies fail to take into account, and recommend steps for managing and reducing the risk of violence through evidence-based interventions, trainings, and services.
To attend the policy forum, please register here. The forum will also be live streamed. To view the webinar, please register here. Find more information about the event here.
·         Opening address: Tim Gabel, Executive Vice President of Social, Statistical and Environmental Sciences, RTI International
·         Moderator: Richard Van Dorn, PhD, Senior Mental Health Services Researcher, RTI International
·         Duren Banks, PhD, Senior Research Criminologist, RTI International
·         Leslie Citrome, MD, MPH, Clinical Professor of Psychiatry and Behavioral Sciences, New York Medical College
·         Sarah Desmarais, PhD, Associate Professor of Psychology, North Carolina State University
·         Joshua Horwitz, JD, Executive Director, Educational Fund to Stop Gun Violence
·         Jeffrey Swanson, PhD, Professor of Psychiatry and Behavioral Sciences, Duke University              
When: Thursday, May 26, 2016
  Lunch and Registration: 12:00 EDT
  Forum: 12:30 – 2:00 p.m. EDT
Where: Holeman Lounge, National Press Club, 529 14th Street N.W., Washington, D.C.

About RTI International
RTI International is one of the world's leading research institutes, dedicated to improving the human condition by turning knowledge into practice. Our staff of more than 3,700 provides research and technical services to governments and businesses in more than 75 countries in the areas of health and pharmaceuticals, education and training, surveys and statistics, advanced technology, international development, economic and social policy, energy and the environment, and laboratory testing and chemical analysis. For more information, visit www.rti.org.

I just couldn't seem to get the colors right from the copy and paste, but if you're interested, go or listen anyway.

Monday, May 16, 2016

Tweets from APA

APA is in Atlanta this year and I'm not there.  ClinkShrink and Roy are, however, and they are tweeting. With their permission, here's a sampling of what's Twitter-worthy.  I was told not to discuss the zombie game.

May 15

Atul Gawande: "Assisted dying is about our failure to give assisted living."
May 15
Atul Gawande: "Your wellbeing is bigger than your health." opening ceremony 

Today Assembly voted to adopt a position against euthanasia of people with mental illness.

I will vote for any presidential candidate who mandates and enforces the Oxford comma.  

Awesome demo of in-home by Jay Shore & “Rachel” (patient actor). Makes it real

Shore: considerations for in-home .
Roywrote and  retweeted:Great book to pick up at . Thank you, Patrick!

I’ll be signing copies of A Common Struggle in the Exhibit Hall at 1 PM—stop by and say hello.
APA President-elect Dr Maria Oquendo discusses the year ahead & some key priorities

Bennett: “In rural Illinois, the price of gas dictates whether patients show up.” The value of .  

In sum, ClinkShrink is thinking about physician assisted suicide (thumbs down for patients with psychiatric disorders) and Roy is thinking about telepsychiatry.
The Zombies are on their own. 

Friday, May 13, 2016

Book News and More

Greetings from Baltimore -- and if you're looking for me at APA in Atlanta this year -- do look for both Roy and ClinkShrink instead--they are both there as APA Assembly members. I decided a while back that a Springtime graduation was all the traveling I wanted to do, and I am pleased to tell you that all went well with my youngest's graduation from #GoBlue.  I enjoyed Michael Bloomberg's commencement speech, the dinners, the celebrating, being with family, seeing my lovely daughter thrive, and knowing that for the foreseeable future, there is no college tuition to be paid.  Young One is off for a couple of weeks in the Middle East traveling and will then work as a camp counselor for the summer before moving across the country to teach biology and conservation in an outdoor school.  She's an adventurer.

As many of you know, from many past posts, ClinkShrink and I have been working on a book since 2013 on forced/involuntary care. Many of you have helped by giving us insights into what it is to have treatments you did and didn't want, some of you (and you know who you are) are  quoted in the book, and many people led me others whom I interviewed and shadowed and learned from.   
I wanted to give you an update. The book, which we originally  called Committed: The Battle Over Forced Psychiatric Care is now called Committed: The Battle Over Involuntary Care.  We preferred the smoothness of a shorter title, and the full impact of the word 'forced,' but authors don't get the final say in book names or covers, and so a committee of marketing folks felt 'forced' conveyed the wrong message.  If you think the title isn't strong enough, don't worry, the cover art is striking and powerful.
The page proofs have been corrected.  Pete Earley wrote the most amazing foreword-- it's not to be missed. I love that Pete's foreword completes the book by adding the perspective of a family member in a way that only Pete can do.  So far, the publisher's reviewers have been very positive (they nix the book if they aren't), and page proofs have been sent out for cover blurbs.  Advance copies for media reviewers will be ordered and sent in June, and the official release date is November 1st, so stand by, I'll have more to say later.  The Johns Hopkins University Press Fall Catalog (see page 21) just came out, and the book has an early Amazon page, waiting for more details.  I just wanted to let you know what's happening, and for those who wonder why we've slowed down on blogging, well, there has been a lot to distract us.

 For the moment, November is tied in my head to this interminable, angst-filled presidential election and it's feeling like it can't come soon enough. 

On another personal note, I am sad to report that the giant oak tree in front of my house needs to come down, and I'm waiting for the power to go off for that to happen today.  I've been slowly mourning the loss of this tree for years.  No, it's not a person, but it's hundreds of years old and it's part of my home.  

Thursday, April 21, 2016

Shrink Rap Turns 10 Years Old Today!

Get out your tuxedos and gowns, the galas are about to begin!
Yes, Shrink Rap is now 10! We are the longest running psychiatry blog and with thousands of posts and years of faithful readers, we couldn't be more excited!

Okay, so no black tie gala.  We had planned a party with chili and beer and a cake with a duck on it, but a family emergency delayed the event -- to be rescheduled soon.

So let me tell you how much I've loved having this blog (a lot) and over the years, there's been a lot of evolution.  I write less than I used to, but I still write.  Clink comes by with updates on conferences and spends more time on Twitter.  Roy is still in it for the food and friendship, but he's moved on to some other endeavors-- perhaps he'll post an update to tell you about them.  We've blogged, we've have 70 episodes of our podcast, My Three Shrinks, there's been our book: Shrink Rap: Three Psychiatrists Explain Their Work, and our columns in Clinical Psychiatry News and Psychology Today, not to mention Twitter and Facebook.  As I've mentioned, our umbrella organization, The Accessible Psychiatry Project, is up for a Scattergood Innovation Award and you are still welcome to add a comment on their website because we'd really like to win!

Now, we're getting for the release of our second book in the fall -- details to follow. Also, Dinah has been working on a website that helps people find psychiatrists quickly in Maryland: http://www.marylandpsychiatrists.net/

So ten years and going strong.  Thank you for being part of our rather unusual psychiatric adventure, and thank you for being part of our lives!

Clink and Roy may have more to add soon.


Tuesday, April 12, 2016

Pushing 70 and Sharing the Wisdom: Guest Blogger Dr. Bruce Hershfield Shares His Experience with Younger Psychiatrists

The article below is being reprinted from this month's edition of The Maryland Psychiatrist.  Dr. Hershfield shares his wisdom on outpatient treatment of patients, and of running a private practice.  Please note the intended audience for this wisdom is younger psychiatrists, in particular, those just starting out.  I'm not a younger psychiatrist just starting out, and in fact, I'd fail on a couple of these measure -- we all have to figure out for ourselves how best to practice in the context of our personality's and in the context of who are patients are and what they need.  Overall, however, I thought Dr. Hershfield makes some excellent points and I wanted to share his wisdom.  With thanks to Bruce Hershfield and to Dr. Nancy Wahls, editor of The Maryland Psychiatrist, for allowing this to be reprinted. The Shaw quote is for Jesse.

By Bruce Hershfield, MD

Now that I’m getting ready to turn 70, I thought I’d summarize what I’ve learned since I finished my residency at the University North Carolina, when I was 28.  Of course, , I didn’t learn all this only by being a psychiatrist, since I would hope that most folks have also learned lots in the last 41 years., But our field  has really changed, and so have I. This is what I tell the Residents, when I get a chance to meet them in a  group:

1      Psychotherapy is important, particularly if the patient is on the right medication.
I won’t do “med checks”, since I would not want them if I was a patient. I figure if it’s simple enough to do in a few minutes, my family doctor can probably handle it or learn how to do it. If it’s complicated, it’s going to take me more than a few minutes. I knew when I was a Resident that psychotherapy was important. I realize now, if you have a severe psychiatric disorder like schizophrenia or bipolar disorder and you are not on the right medicines, you’re in a lot of trouble, no matter how skilled your therapist-- psychiatrist or non—psychiatrist-- is.
2      Splitting the treatment, which was tried at least as far back as the’ 70s, is a serious matter, only to be used when both treaters know and trust each other and are able to  communicate easily. You just don’t know what the other treating professional is actually saying to the patient. Splitting the treatment puts a psychiatrist at great risk of a suit, with little reward.

3   Try to get along with colleagues, even when they are being provocative. You may need to walk away, and you probably will need to apologize and also to forgive at times. Never fight with secretaries; learn from their observations. I should have read “How to Win Friends & Influence people” long before I turned 60.
4 Try to have as few bosses as possible. If everybody loves the boss, he or she  probably isn’t effective. Never have more than one boss to whom you are reporting. All people – – not just patients – – have transferences, and they usually complicate relationships with bosses.
5 If you’re always agreeing with the general wisdom, particularly if money is involved, you will eventually be dead wrong on something. Atypical antipsychotics helping the negative symptoms of schizophrenia is a good example of conventional wisdom that turned out to be wrong. Beware of fads, don’t trust ads, don’t take professors or studies too seriously.
6 The more we know, the less magic is associated with us and the less respect we receive. It’s part of our attempt to climb out of the Middle Ages.
7 Psychotherapy is more about healing, which usually occurs in – between sessions, than about insight. Patients who are asking for insight are usually unwilling to change their behaviors. Patients who don’t do the homework probably will not learn new ways of handling problems.
8 You can’t tell who is going to be a good patient. Some people with little education and little command of the language can change and get well. People who have addiction problems are the hardest to predict.  You probably should give them a chance if they ask. Even after seven years of chronic depression, for example, some patients recover.
9 People will pay for good medical care, particularly for their children. It is not an accident most psychiatrists are now practicing outside the managed-care system. Don’t allow managed-care companies to tell you how to practice. It doesn’t look good ethically and it doesn’t impress juries. Do what is right, even if it costs you in the short run. You still may get in trouble, for example with administrators, but someone may be impressed and maybe you’ll be rewarded. At least, be kind, if you can’t do any more than that.
10 Stay out of court, if possible. Don’t sue people, don’t dismiss the possibility that anyone can sue you, and be sympathetic when your patients get involved in proceedings. Lincoln was right when he advised a group of lawyers to “eschew litigation”.
11 Join societies and ask for advice from other members. If you’re willing to ask for a consultation, you are almost certainly not negligent. Patients are reluctant to get them. Arrange for consultations with someone whose advice you’ll almost automatically take. Don’t criticize colleagues to others, including to patients.
12 Don’t steal other people’s patients. Ask potential patients if they have ever seen a psychiatrist, when they first call. If it’s in the recent past, ask to have their psychiatrist refer them to you and say you’ll get back to them if that happens. Clarify beforehand if it’s for a one – time consultation or for ongoing treatment. If patients don’t show up for the first visit for any reason, or give you a hard time on the phone, you will eventually regret taking them into your practice.
13 Be available. Return calls. Have a call hour. Answer letters. Encourage patients to call you if they need you. Find someone to substitute for you whom you can trust when you’re away from the office for any significant time. Be very careful about prescribing for the patients of others when you cover for colleagues. Don’t charge for phone time. Most people won’t abuse it. If patients call too much, you probably need to see them more often. Don’t let patients go for more than 90 days without seeing them.
14 Document.  Too much is better than too little. There’s more paperwork each year – – more work in general. Real earnings have been going down since the’ 70s. Follow up on lab tests. Write legibly. Your reputation may depend on the quality of your notes.
15 Be cheerful, even optimistic. It turns out it wasn’t Lincoln, but i someone else who said that he reckoned that people are as happy as they allow themselves to be. You can’t expect depressed patients to be optimistic, and someone has to be, at least to balance their pessimism. If you are a psychiatrist, chances are that most people, and virtually all of your patients, have it worse than you do. Don’t complain.
16 Keep learning. Read books, acquire new skills. I’ve heard that almost everything we know we’ve learned since 1950. Accept that what you know will probably turn out to be wrong or useless. They call that progress. Beware of people who tell you they know the answers. Your training will probably turn out to be a small fraction of your career.
17 Patients are probably right about side effects. Be suspicious about claims made by drug companies, including maximum recommended doses. Ask patients about drinking and about caffeine, not just about illegal drugs. Check with families. Be suspicious if patients forbid you to contact their families or the professionals who used to treat them.
`18 Get to know families. It’s crucial if something like a suicide occurs. Get a family history. I understand the average person carries the genes for 20 disorders, of which four are lethal.
19 Don’t treat members of the same family, or close friends, if you can help it. Don’t write prescriptions for your friends or coworkers. You can’t successfully treat everybody. Somebody else may be a better match. Sometimes, patients return after they drop out.
20 You work for the patient, not the other way around. Dress accordingly, use honorifics like Ms. or Mr., and ask what the patient wants. Set up a valid treatment contract, early on. Be wary of double agentry, like working for the patient and the hospital, or for the patient and the managed-care company.
21 Use “we” interpretations. This is not Europe; people expect to be treated as equals and they aren’t as tied to their traditions and their families as in other places. Sometimes a story or a fairytale can illustrate a point. Be careful about using your own life as the example. Patients can sometimes change if they are laughing, but be careful. If you offend someone, apologize. Patients don’t expect their psychiatrists to be perfect, but they do expect them to display good manners, like holding the door for them or offering them a tissue when they cry. Psychiatric disorders are common and chances are that someone you know, or even you, will get one.
22 If you’re going to work for yourself, you have to stay healthy. Take frequent vacations. Learn how many patients you can safely see in a row and what your personal clock tells you. If you are sleepy, excuse yourself and get some coffee. If you bring it into the session, offer the patient a cup.
23 Make sure you get paid. If you get cheated, learn from it. Don’t pursue it too hard; there are too many ways that disgruntled ex—patients can make you miserable. Be careful to document when patients pay you in cash.
24 When patients miss an appointment the first time, don’t charge. Make sure you call to find out what happened. If they can come later that day, let them. Patients tend to resent paying for missed appointments.
25 Be on time, or at least apologize if you’re not. Try to give extra time of people need it. They rarely abuse it and often appreciate it. Give plenty of warning before you raise your fees.
26 You will like some patients more than others. Some patients will like you more than others. You are neither as good or as bad as your admirers or detractors say you are.
27 Things go wrong. Admit it when you make a mistake. We are always on the verge of disorganizing, as is everything else in the universe according to the second theory of thermodynamics.
28 Diagnoses can be important. Hand the patient the DSM-V if you think that a personality disorder is present. That book has his limitations, but at least it uses a common language we’ve had since 1980. Watch out for indications of learning disorders. You may not want to make a diagnosis of a personality disorder, but it may be present anyhow and completely ignoring it may complicated or destroy the treatment.
29 The public system is in worse shape than the private, since government is not in the business of building reserves and sooner or later finds itself in a financial crisis. Also, there are too many bosses and too many political influences affecting patient care for it to be very good for very long.
I hope I haven’t finished learning. It is upsetting to realize how little we still know about what causes psychiatric problems. Our patients live better lives now than they did 41 years ago and I’m optimistic that we can help them live still better lives in the future. I used to think that I would retire when I turned 70, but I decided not to do that. There’s too much going on for me to quit now.

Sunday, April 10, 2016

Will Changing Privacy Laws Help Patients?

Over on Twitter, one of my pals, @namipolicywonk wrote: I'm a big proponent of civil rights, but whose rights are we protecting in a situation like this?

Please do read the article, but in a few sentences, here's the synopsis.  A mom is writing an oped piece about her daughter who lives in a group home in New York and has a chronic mental illness.  The daughter went missing from her group home, off her medications, and reportedly because of HIPAA laws, the group home did not tell the parents the daughter was missing. In fact, they repeatedly said she was "not home," which in my book is dishonest.  The story gets worse, the police initially wouldn't take a report, and eventually the daughter was located 28 days later in a shelter in a terribly deteriorated state.  If that's not bad enough: the daughter was on Assisted Outpatient Treatment (the mom call's it Kendra's Law ) and known to be dangerous off her medications, so she was court-ordered to treatment, and the group home still didn't report this to the parent or the police for some prolonged period of time.  The point of the article is a plug for Rep. Tim Murphy's Helping Families in Mental Health Crisis Act, now stalled in Congress, because the mom contends that if this law passed then the group home would have had to release information to her and they could have helped their daughter if they'd known she was  missing.

If you've been paying attention here, you know that I'm not a fan of this segment of the proposed legislation that essentially says that a person with a psychiatric diagnosis can not refuse to allow his mental health professionals to communicate certain information (diagnosis, medications, follow-up appointments) to his caretakers.  I've written before about my concerns, but I'll restate them: such a law singles out those with mental illnesses as the only people who can't decide not to share their medical information: it's stigmatizing, and it may lead people to avoid getting care because it will be translated as "psych patients don't have HIPAA rights."  It's not that I'm any great fan of HIPAA, but HIPAA is misunderstood.  It doesn't say who a doctor can't talk to without permission, it says who medical folks can talk to without permission (and there are plenty of entities that can get your medical information without your permission).  Before HIPAA ~and yes, I'm old enough to remember this~ we didn't release information to family members without permission and patients had the right to confidentiality, this is not new.  Furthermore, I think most of these catastrophes are about a misinterpretation of the bill or even laziness.  'I can't tell you if your family member is hospitalized on our unit because of HIPAA. ' But, dear unit clerk, you can go see if the chart has a release to talk to family, or you could go tell the patient his family is looking for him and ask if you can call them back.  Finally, The no-HIPAA for psych patients legislation assumes that the sick person is sick and the family is well.  What if a person with mental illness doesn't want their family involved because they hound him, because they've been abusive, or because a psychotic relative believes he's in danger from the KGB and is intrusive with his own delusional beliefs?  What if family has previously discouraged treatment or medications and is critical of a person's decisions to get care?  The bill assumes the caretaker will facilitate treatment and that may not be correct.  That's why I don't like the HIPAA exclusion.  

So back to the story, and let me start by saying I don't know the mom, the patient, the group home, or anyone else.  So my first thought is: a potentially dangerous patient disappears from a group home and no one is notified?  Is a group home even a health care facility?  If you don't answer your phone and your parents call your building superintendent, they'll look in your apartment.  Isn't there an emergency number listed with the group home--if so, disappearing off medications seems like an emergency and it would be okay to notify the emergency contact?   The patient is court-ordered to treatment and off medications, can't the police be informed and told to bring the patient to an Emergency Room for evaluation as Kendra's Law allows for?  And the police can certainly inform parents--they have no HIPAA issues. It seems that if the parents have been involved all along then someone at the group home would know them to communicate-- and it seems mom knew that the patient was off her medications and psychotic before she left, so she was likely in communication with her daughter.  Is there more to this story --we only heard one side-- because it seems like there must be.  Or is the group home misinterpreting the law to say they can't release information when really they could?  Perhaps they've been negligent and are hoping the patient will return so their negligence won't be noticed and questioned?  I don't know the case, but nothing I've read of HIPAA says that a living facility can't report a missing person to the police, notify an emergency contact when they go missing, or even just tell an involved family member that someone has left their facility.  Is the facility afraid that a vulnerable, psychotic, person who is court-ordered to care is going to sue them for releasing information? Shouldn't they be more afraid that they'll be sued or sanctioned for a bad outcome?  What about doing the right thing?  Would it ever be the right thing to say a very sick person has gone missing and no one will be notified?

Lastly, let me say that I don't think the provisions of the Murphy Bill would have changed this.  The changes in the bill allow for a mental health professional to release specific information to the caretaker.  In this case, the patient is living in the facility-- they are the caretaker.  I don't believe it covers an interested parent who is not the one responsible for getting the patient to appointments or helping the patient obtain medications.

We don't need to revise HIPAA just for mental health patients; though it would be nice if we got rid of it for everyone for many other reasons.  We do need to talk with patients.  When they are well, we need to ask them who we can share information with during an emergency.  The issue isn't the legislation, it's how it is interpreted, and new legislation will be misinterpreted.  We need to use common sense.  Really, as health care providers, we need to do the right thing.   

Wednesday, April 06, 2016

No Escape From Aetna....

On March 13th, I wrote a post: "To Aetna: I am NOT in Your Network about how I was trying to reach Aetna to clarify that I am not a psychiatrist in their network.  I wanted this clarified because I was getting so many calls from people asking to see me because I am listed on Aetna's website.  I called and called again, but the voicemail prompts left me with no where to go.  When I reached a live person, I was told that Network Services would contact me within 48 hours.  That never happened.  I wrote in through their website.  Nothing.  And finally, I contacted the Maryland Insurance Commission, who contacted Aetna, and  a real live, very helpful person at Aetna did in fact call me.  

So I spoke to the real live person at Aetna who had a name and an direct line phone number.  Why did they think I was in their network?  People have to apply for this, and I had no memory of filling out paperwork.  The real live person, whom I fist spoke with on March 23rd, clarified that I had been an Aetna provider through two clinics where I had once worked.  These are different from my private practice, and participation is based on the billing address.   So I was registered as a provider at an outpatient clinic that I left in 1998, and at another clinic that I left in 2013.  Hmmm, so why did they have me registered at my private office?  Well, apparently last May they received a claim form for out-of-network services and a clerk 'updated' my file, added my address, phone number, tax information, and Voila! I was an involuntary Aetna provider.  No worries, the real live person would fix this and call me.  Only that has not yet happened.  

So the Aetna referrals continue to come, and this continues to take up my time as I call prospective patients back only to explain that I'm not actually in their network.  So I called back the real live person --it's been weeks, and still I'm listed as a participating provider on their website.  How long can it take to remove someone from a website?  Ah, they'll work on it and call me. The days go by, and then the weeks, and Aetna,  I'm waiting......
Update on 4/9: phone call from Aetna saying they had taken me out of their system.  

Tuesday, April 05, 2016

Utah : Just Say "NO!"

This is not a post on abortion.  Let's not even go there.  This is a post on who gets to practice medicine.

So Utah passed a law -- signed by their governor after how many years of medical school? -- that mandates doctors to give general anesthesia to women having abortions after 20 weeks of gestation.  Legislators sometimes unwittingly attempt to practice medicine and pass laws that interfere with the doctor patient relationship, but this is the first time I've heard of legislation that demands a procedure that endangers a patient's life.  The theory is that the fetus might feel pain and that general anesthesia given to the mother might alleviate any pain felt by the fetus.  I'm not sure there is any basis for that-- at one time mothers were routinely given general anesthesia and I believe the babies still cried upon arrival into the world (~alas, I was one of those babies born during the era of giving anesthesia to the moms, but I can't say I remember much).  Babies are no longer born with the routine use of general anesthesia for the mother in childbirth because it's dangerous.  You can read about the Utah law here.

So doctors in Utah, how does this work?  Do you unnecessarily endanger the life of a mother for no valid medical reason, not to mention jacking up the cost of procedure, because a legislative body says you must?  Or do you refuse and risk sanctions?  Or do abortions for woman who are more than 20 weeks pregnant just stop?

So if law makers can mandate risky procedures and the unnecessary administration of powerful medications, regardless of patient need, then where does it stop?  Can they mandate that all patients brought to psychiatry ERs  by the police must be injected with anti-psychotics, regardless of whether they are indicated?  Can they mandate that everyone who has had a suicide attempt must take Prozac for life?  Where does it stop?  

Utah, what are your doctors thinking?  Why aren't they screaming their heads off?  Congratulations, your governor is now your doctor.

Sunday, April 03, 2016

The Accessible Psychiatry Project, Updated & Please Do Comment on the Scattergood Site

Later this month, Shrink Rap will be celebrating it's 10th anniversary!  More later, but we are the longest running psychiatry blog, and we're looking forward to the cake.

As you may know, Shrink Rap is part of a larger group of projects that the three of us, in various combinations, work on.  The list has morphed over the years, and the Accessible Psychiatry Project is now up for a Scattergood Innovation Award.  The nominations closed last week, and public comment is not being requested.  We'd love to have our Shrink Rap readers visit the Scattergood site and leave an encouraging comment.  The Scattergood site is here and comments can be added at the end of The Accessible Psychiatry Project's description: 
If you do add a comment, please accept our thanks.  

For a recap of our projects over time:

The Accessible Psychiatry Project

The Accessible Psychiatry Project
Encouraging dialogue about psychiatry across media.
--Steven R. Daviss, M.D.­­
--Annette Hanson, M.D.
--Dinah Miller, M.D.

Mission Statement:
The Accessible Psychiatry Project strives to encourage dialogue about psychiatric disorders and their treatment in order to explore issues of controversy and misunderstanding in our field. Through open dialogue, in both new media and print, we hope to foster discussion about the work psychiatrists do, and to decrease stigma associated with the treatment of mental disorders.

Components of The Accessible Psychiatry Project include:

Shrink Rap: The longest running psychiatry blog 

on the Internet, since April, 2006

Shrink Rap News: A blog and print column for 

Clinical Psychiatry News

Shrink Rap Today: A collateral blog on the 

Psychology Today Website. 

My Three Shrinks podcast;

November, 2006- 2012,  70 episodes aired

Featured on the iTunes Medical Podcasts Webpage

ShrinkRapRoy tweets about psychiatry and health care.
  • HITshrink tweets about health information technology and health care reform (HITshrink's blog is here).

ClinkShrink tweets about issues pertaining to psychiatry & the law; sometimes about birds

ShrinkRapDinah tweets mostly on mental health issues.

Access to Care: MarylandPsychiatrists.Net  is a website designed to facilitate quick entry to outpatient care.

Find us on Facebook at ShrinkRapBook : http://www.facebook.com/shrinkrapbook.

Committed: The Battle Over Involuntary Psychiatric Care, by Dinah Miller and Annette Hanson, In Press, Johns Hopkins University Press for Fall, 2016.

Shrink Rap: Three Psychiatrists Explain Their Work, by Dinah Miller, Annette Hanson, and Steven Roy Daviss,  Johns Hopkins University Press, Baltimore, 2011. 

The Shrink Rappers give talks on: 
~ The Public Face of Psychiatry Across Media
~Access to Care
~Psychiatry and Technology (Dr. Daviss)
~Forensic Psychiatry (Dr. Hanson)
~soon: Involuntary/Forced Psychiatric Care
~soon: Mental Illness, Violence, and Violence Prevention

Sunday, March 27, 2016

The Final Report on the Germanwings Tragedy

Over on Clinical Psychiatry News, I have an article up on the final report about the Germanwings pilot who crashed the plane into the French Alps.  A sad topic, but do read it.

Thursday, March 24, 2016

Guest Blogger Dr. Thomas Franklin Writes About His Own Experiences With Major Depression and Why He's Doing A Triathlon

Becoming an Ironman for Myself and My Patients

The sliver of light coming under the door of the windowless office seemed unbearably bright and offensive. I turned away from it and closed my eyes. There is a flat spot on the back of my head that, if angled just right, would lie on the textbook I was using as a pillow. In a few moments, I would be asleep again. I was supposed to be out seeing patients, but it was all I could do to show up at work and hide in my office. My supervisor was a gentle woman who would come check on me a couple of times a day. She would crack the door and ask, “Dr. Franklin, why don’t you come out and see one of the new patients?” 
“I can’t. I just can’t... I’m no good to anyone.”
Drifting in and out of consciousness in that dark room seemed far superior to being up and about, feeling the pain that seemed to emanate from my chest and flow throughout my body. It was as if my blood had been replaced by some impossibly dense material that could barely flow, making every step I took an effort. If I didn’t lie on that floor and feel my body supported all the way from that flat part of my skull to the small of my back, to the backs of my ankles, it felt like I might fall through to the center of the earth, through the dirt, rock, and then to the molten core where I would be incinerated. I wondered if that might be better than living like this.

Fearing Stigma but Seeking Help

I was a psychiatric intern at the time, and I was depressed. But I couldn’t bring myself to seek treatment. I suffered like that for months until I saw a colleague in consultation, where I described suffering the symptoms of attention deficit disorder, but suggested that a third-line medication for that diagnosis, also used for depression, might help me. I needed so much more than that medication, but my depression, my own inhibitions, and stigma kept me from getting the help I needed. Difficulty concentrating seemed a safer problem to admit to than depression. I was worried that I wouldn’t be taken seriously as a psychiatrist if it became known that I, too, was a patient. 
I continued to suffer off and on for years, finally getting into real treatment for the first time after my training was over. A combination of psychotherapy and medications led to the relief of stabilization. Ultimately, psychoanalysis, a more intensive therapy experience, helped me to fundamentally change how I thought about myself and the world, which led to not just relief, but a transformation of how my mind worked. Eventually, I was able to stop taking medicines. The way I had felt only years before seemed so far away. I felt a part of the human race. 
Until now, I have kept quiet about my experience. A continued fear of stigma has kept me quiet. I felt that if I was known as a psychiatric patient, even a so-called “cured” one, I would be labeled or disgraced or stereotyped. I thought it might hold back my career.
But the only way to combat stigma is to speak out. This is not easy, but I am inspired by those that have travelled before me on this road and by my current patients. I can’t go on urging them to be courageous, to face down the stigma they were feeling, without doing all I can to fight stigma myself. Only by shining the light of truth on people’s lived experience of mental illness will stigma finally become a thing of the past. 

Why a Triathlon?

After my psychoanalysis was over, I took up triathlons. Exercise has not only helped my mood, but I found that endurance sports are a powerful metaphor for what living with a mental illness can be like. In some ways, training for and finishing races makes me feel that I have mastery over that part of me that suffered so much.
In triathlons, like in depression, you have to go on putting one foot in front of another for as long as it takes. It will be painful. Your best-laid plans will go awry. Small mistakes early in the race can turn into big problems before the end of the day. The finish line will seem an impossibly long way away. There are moments of despair, but also moments of triumph. There is beauty around the next corner that can give you hope, if you only look up long enough to take it in. But preparing for and finishing the race is much more about your mind than your body. 
On July 24th, I will be racing the 140.6 miles of the Ironman Lake Placid triathlon to fight stigma, to show people that are suffering that treatment works, and to raise money for the Sheppard Pratt Patient Care Fund so that no one has to go without the treatment they need. 100 percent of the monies donated to this fund are spent on patient care. Maybe someone we help get treated will become the next courageous voice in the fight against stigma. Please give generously, whatever that means for you in your life. Thank you for your support.

Dr. Thomas Franklin is the medical director of The Retreat at Sheppard Pratt. He is a clinical assistant professor of psychiatry at the University of Maryland School of Medicine and a candidate at the Washington Center for Psychoanalysis. He is Board Certified in Addiction Medicine and Psychiatry, and has extensive experience in psychotherapy, psychopharmacology, and addictions and co-occurring disorders. Dr. Franklin previously served as medical director of Ruxton House, The Retreat’s transitional living program, before assuming the role of medical director of The Retreat in 2014.