I can’t speak to what happens in hospitals. However, as an outpatient rheumatologist, I have noticed that community neurologists seem to have become progressively less “useful” over the last several years. My last example of this: I was seeing a patient with SLE who had just moved here from far away. He’d also had seizures before, and he was in several anticonvulsants which nobody was monitoring currently. So, I sent him to neurology to get established. It takes him months to see the neurologist…and after he goes there, the note contains some lengthy babble about neuropathy, and literally no discussion of his seizures whatsoever. I send a message to the neurologist and get back some confused response like “oh I was seeing him for seizures?” No ****, dude, why do you think he’s on a laundry list of seizure meds? Did you see my consult order which listed “seizures” as the reason for referral? Did you read my note? (On second thought, I know you didn’t, because nobody ever seems to read other doctors’ notes anymore). You think I’m the one monitoring those seizure meds?
I wish I could say this was a one-time occurrence, but I have seen goofy nonsense like this over and over and over again from neurologists across four different states in which I have worked. I’m not sure if the whole specialty has just gone off the rails or something, but it seems to be very difficult to get a “useful” neurology consultation at this point. The visits/notes seem to be all sound and fury, signifying nothing.
yeah this is my biggest annoyance in the community
yes it's easier when its a hospital system and it's all in one EMR...
it's harder in the community as not everyone sends notes
i also seldom get a referral note sent in...
I tried to institute a "please have your PCP efax us a referral and prior workup" and that led to a ****storm of whining *****ing and moaning by patients to my front desk to the point of harassment. ****ing new yorkers. seriously.
in fact my template for my new consults autopopulates as:
"Pulmonary Consultation
Reason for referral: No referral sheet or prior workup sent in by referring physician
Chief Complaint:
PMD: based on the medication list, radiology portal reports, and insurance portal eligibility profile page it seems to be Dr (blank) "
I make ****ing make sure that my consult notes are sent and delivered. I personally send out consultation notes (every single one I write) to the PCP and relevant specialists involved. After I check out I just hit "new consult note" and send a few clicks and efax. Then i have my staff check the efax log and make sure it says SUCCESS on the next day. Whenver another physicians office complains to my front desk saying "they never got anything," I make sure my front desk sends them ANOTEHR COPY with the snapshot of the EFAX SUCCESS on the initial day of consultation.
While a courteous "hey I can't find the copy. please send it again" is fine and all, these other community doctosr front desk just gas light the patients with a "that doctor didn't send me anything." then the gaslit patient *****es and moans to my front desk and to me. I just whip out the proof of efax success and say "did you come here to fight tough guy/gal patient or something? what did you hope to accomplish? it's obviously your PCP's front desk is grossly incompetent and felt going to Page 2 on the inbox was too much work"
Although my notes are very very and somewhat hard to read quickly, I do put in BOLD on top of each problem list box what the recommendations/management items are to make the primary's lives easier. If they want to read the impression i write then more power to them.
I will admit when I see another consultant's notes in my inbox (RARE), I just check it in without a second glance. but when the patient VISITS me later, you can be sure I am reviewing it and transcribing the general idea into my note
but I digress...
yes I would agree that the Community neurologists aroud my neck of the woods seem more interested in doing (unnecessary) carotid dopplers and TCDs, pseudomotor autonomic testing, saline trigger point injections, EMGs, EEGs, portable sleep studies than tackling the harder cases.
I mean I get it.. more procedures more money. the "physical exam only and talking it out cases" just take more time and billing a higher 99215 has diminishing returns versus 99213 + procedures, but they seem to dislike treating movement disorders and dysphagia/dementia as much as a community GI hates irritable bowel syndrome...
heck I'm the one that is getting outpatient SLP, MBS, barium esophagrams etc.. done AFTER the patient has aspirated and had pneumonia already despite a glaring long term chronic dysphagia history... even after the same patient has seen GI and neurology in the community already. I mean SLP is a hospital based only service and there are myriad scheduling barriers (especially for low motivation patients) so its a lot of hard work.... but is important at the end of the day.