Pain is one of the most common reasons for patients seeking care in EDs, accounting for up to 42% of all emergency room visits. Emergency physicians vary widely in prescribing patterns and often have difficulty assessing patients’ level of pain. There may also be reluctance to provide pain medications due to concerns that patients are trying to obtain prescription drugs for non-therapeutic purposes. “These individuals— who are often labeled as drug-seeking—are a difficult group of patients to manage in the ED,” says Casey A. Grover, MD. “They often present to the ED with conditions that are difficult to evaluate, and may also engage in deceptive behaviors in an effort to fool clinicians into giving them additional medications.”
It is estimated that up to 20% of all ED visits may be due to drug-seeking behavior. “Drug-seeking patients have been known to use large amounts of medical resources,” says Dr. Grover. “They may occupy beds in EDs that would be more appropriately used for people truly in need of emergency care.”
Prescription drug abuse and misuse is a growing epidemic throughout the United States, and more and more emergency physicians are encountering drug-seeking patients in daily practice. “Despite the magnitude of the problem,” Dr. Grover says, “there is still much to learn about these patients, their patterns, and how best to manage them.”
Intriguing New Data on Drug-Seeking Behavior
Studies have been conducted on screening tools to identify drug-seeking behaviors in chronic pain patients, but few have provided quantitative data on such behaviors in the ED. With this in mind, Dr. Grover and colleagues performed a case-control study examining the relative frequency of various drug-seeking behaviors in drug-seeking patients as compared with all ED patients. The study was published in the January 2012 Journal of Emergency Medicine. “Our goal was to provide emergency physicians with information as to which drug-seeking behaviors are most commonly used by drug-seeking patients,” says Dr. Grover. “Identifying behaviors that are most commonly used by drug-seeking patients may help evaluations of patients suspected of drug-seeking behavior.”
A retrospective chart review of 152 drug-seeking patients and of age- and gender-matched controls was conducted, with the authors noting several drug-seeking behaviors that were exhibited over 1 year. Drug-seeking patients accounted for 2,203 visits to the ED, averaging about 14.5 visits per patient per year. For the control group, patients accounted for 315 visits to the ED, which is an average of 2.1 visits per patient per year. Patients in the drug-seeking arm reported their pain level as 10 out of 10 more often than control group patients (Table 1). Additionally, drug-seeking patients occasionally complained of pain levels greater than 10 out of 10, while the control group had no instances of these events. Drug-seeking patients were also significantly more likely to request medications parenterally.
The odds ratios for both requesting parenteral medication and reporting pain levels greater than 10 out of 10 were significantly higher than all others observed in the study (Table 2). These were the most predictive of drug-seeking behavior, while a non-narcotic allergy was less predictive. However, the odds ratio for a non-narcotic allergy was greater than 1, and was still a behavior that was more commonly used by drug-seeking patients than the control group. For other studied behaviors, the confidence intervals were too wide to allow the authors of the study to meaningfully interpret the data.
Challenges Remain in Deciphering Pain
According to Dr. Grover, chronic narcotic use can make patients more sensitive to pain. “These individuals may truly be suffering from the most severe pain possible. On the other hand, patients with narcotic abuse and dependency often exaggerate pain complaints in order to get their desired medication. Chemical dependency can become a major motivating factor for patients to seek emergency care. Unfortunately, it’s nearly impossible to definitively determine if they’re seeking care in an attempt to get medications for non-therapeutic reasons.” The current literature on drug-seeking patients consists largely of small studies, according to Dr. Grover, and larger-scale studies are needed. “These efforts will hopefully help us gain a better overall picture of the frequency of these behaviors and eventually help us establish strategies to optimize how we manage drug-seeking patients.”
References
Grover CA, Close RJH, Wiele ED, et al. Quantifying drug-seeking behavior: a case control study. J Emerg Med. 2012;42:15-21. Available at: http://www.jem-journal.com/article/S0736-4679(11)00632-9/fulltext.
Pletcher MJ, Kertesz SG, Kohn MA, et al. Trends in opioid prescribing by race/ethnicity for patients seeking care in US emergency departments. JAMA. 2008;299:70-78.
Grover CA, Close RJ, Villarreal K, et al. Emergency department frequent user: Pilot study of intensive case management to reduce visits and computed tomography. West J Emerg Med. 2010;11:336-343.
Chou R, Fanciullo GJ, Fine PG, et al. Opioids for chronic noncancer pain: prediction and identification of aberrant drug-related behaviors: a review of the evidence for an American Pain Society and American Academy of Pain Medicine clinical practice guideline. J Pain. 2009;10:131-146.
Chan L, Winegard B. Attributes and behaviors associated with opioid seeking in the emergency department. J Opioid Manag. 2007;3:244-248.
Gianutsos LP, Safranek S, Huber T. Clinical inquiries: is there a well-tested tool to detect drug-seeking behaviors in chronic pain patients? J Fam Pract. 2008;57:609-610.
Tamayo-Sarver JH, Dawson NV, Cydulka RK, et al.Variability in emergency physician decision-making about prescribing opioid analgesics. Ann Emerg Med. 2004;43:483-493.
Hawkins SC, Smeeks F, Hamel J. Emergency management of chronic pain and drug-seeking behavior: an alternative perspective. J Emerg Med. 2008;34:125-129.
Hansen GR. The drug-seeking patient in the emergency room. Emerg Med Clin North Am. 2005;23:349-365.
McCaffery M, Grimm MA, Pasero C, et al. On the meaning of “drug seeking.” Pain Manag Nurs. 2005;6:122-136.
Physicians Weekly
I hate to say it, but as a recovering opioid addict who has seen my way around ERs, almost every single comment here sounds like the intense denial and word salad of people who have become addicted to their pain meds, but still maintain that they need and deserve unquestioned access to whatever amounts of opioids they think they need..
Look—I know that people have chronic pain. But I also know from long experience in the recovery community AND the CP community, that people with long-term opioid prescriptions almost always reach a pretty dangerous point of high tolerance, and emotional reliance upon their pain meds. It gets out of control, and patients get strung out.
They know how to be manipulative about pain and use their medical history to lay on the guilt. It takes a long time to get miserable enough to admit that you have a problem with your meds. Until that point, you end up being righteous and angry at the medical establishment for doing what they MUST do, which is closely monitor the usage of dangerous and highly addictive medications, and limit their use as much as possible.
Learning CBT, and mind/body techniques, as well as physical therapy, are the key solutions that are so often left out of these debates. Everyone here is entirely focused upon opioids—and no other type of CP therapy. It’s either give me more opioids, or my doctor is prejudiced against me because I have chronic pain.
There’s no attempt to take any personal responsibility for becoming an active part of their own pain management, which is what CBT and mind/body techniques give you. They are much more of an active treatment than passively gulping strong pain meds, and it’s a very reliable and powerful group of therapies.
Yeah—to someone who has come through the whole pain meds merry go round and is now on the other side—or to a doctor who is well experienced with how addicts sound, these comments all read as incredibly strung out. I hope these people eventually get to that key point where they realize their lifestyle is unsustainable, and that they need help. Until then, I’m sure it will be a lot more of the righteous anger at not getting all the pain meds they want, and tons of denial. So sad.
I’m 40, full time job as an IT architect working in IT/telecoms since 1999.
What a ridiculous article this is, should start by quantifying bad doctors not being able to listen to their patient just tossing the ‘drug seeking’ conclusion.
Been to the ER several times in 5years, been to all kinds of doctors, they write ‘drug seeking’ or ‘crazy’ in your patient file and you are doomed by prejudice.
Then you get the mass-stupidity effect, any doc’ following visited afterwards will judge you by that ‘drug seeking’ note in your record and not even listen to you.
‘been handled like that for years, now it seems I have serious pancreatic issues, might be the worst getting the verdict from the mri in 3days…. started complaining about chest pressure, weigh loss, diarhea and abdominal pain back in 2015, now 5years later I finally get to a scanner, 2 last years from 84kg to 62kg, malabsorption, hair loss, double vision, nearly lost my job now.
This kind of article and the physisians tapping each other’s backs is straight disgusting!
Just as everywhere, you have a lot of rotten apples making huge mistakes also in the medical area!
I can’t wait until the primary care or ER doctor’ gets automated!!!! Screw the prejudice!!!
I’m 32 but I have had to go to the ER twice in my early 20s as I suffer severe and I mean SEVERE cluster migraines. I have legitimate weird as heck allergies (lol and random) to things like artificial grape flavorings, ants, and other oddball things lol! But, here’s the main issue I’m also allergic to ibuprofen, dyclofenac, triptans, and naproxen; I.e. all of the medications they typically use to treat migraines. I have tried designer drugs and many other but my body is just weird I suppose! The issue with my allergies is its on the list of drug seeking behaviours to say you are allergic to them leaving only strong I.v. narcotics as the only option…. I am legitimately telling them the truth and im cowering in a ball rocking from pain because I avoid going to the hospital at all costs as I am the strong one in the family who worries about everyone but myself. So it isn’t until I’ve lost vision and the pain is a full 10 that I will finally give in and to, but, I still will downplay it to an 8 because I feel guilty for saying 10 as someone could be in the next room with a flaming chainsaw in their chest and I never feel like I have the right to use the almighty 10. So I’m there rocking back and forth in excruciating pain with tears steadily falling from my eyes and all I get is accusatory looks and a whole LOT of benadryl being given to me saying its “morphine” for 2 hours trying to get the reaction of “ty amazing it worked” trick then after they realize oh no its not working then they finally give me pain meds just hardly any not enough to even take the edge off and kick me out!! I’m handed a brochure about addiction and off I go having wasted my time and extended my suffering with them flashing those bright lights on my eyes and the loud roar of the er because I don’t warrant anything but a plastic chair in the hallway as I’m not a “real” patient. Any advice for dealing with douchbag docs anyone?? Because raven though I’m currently suffering right now and typing while blind in one eye I’m afraid of the same experience happening again…..
No info to help. But here’s my horror story. First I have MS which is painful, legally blind, achaladia which is a painful, rare esophagus disease. It’s another autoimmune and dysphagia which means I have problem swallowing, even liquid, ataxia *shake like a parkinson patient* heartattack at 47 due to small vessel disease. It means the vessels around heart are smaller than normal. They did one cath. on me and said don’t try again. So I end up in hospital on a Saturday looking nine months pregnant and awful pain. They do nothing but give a stomach medicine and Tylenol 3. On Monday worse, go back to ER. Doc doesn’t even see me but give 42 mg of ketamine and adds to medical records that will be seen from now on and cannot be changed DRUG SERKING BEHAVIOR SUSPECTED. Everytime I go to any hospital in the USA that info will come up. Due to heart disease PTSD and neurological disorders a i should have NEVER been given Ketamine. I went into a K-HOLE life death experience and been fighting with hospital. If someone is suspected drug seekers you don’t give them Ketamine. If you do give ketamine the highest dosage for acute pain is 0.35mg and go as high as 1mg. I’m getting a lawyer Monday. This happen Sept. 28th, 2020. Just received stupid form letter Nov. 23rd. I sit here typing because I can’t sleep and will fall asleep 9nce Suncoast up. I’ve been having terrible nightmares screaming in the night. So I understand how you feel. Doctors screw up a lot and hospitals cover for them. Everyone at one hospital knew a nurse was killing patients, they did nothing about it and were glad when she transfered and started killing somewhere else.
As a recovering opioid addict, it can be extremely frustrating to seek any kind of pain relief from an official setting. Unfortunately, I’ve found that the quality of my healthcare has always declined after being honest about my history with substance abuse. This, despite the fact that I would always preface my statements with, “I am not looking for any kind of narcotic. I am a recovering opioid addict.”
Even with that qualifying statement, my quality of care almost always declines. It’s made me hate going to the doctor, hospital, or even the dentist. Unfortunately, it’s just part of the path I must walk now.
I understand Jacob. I live with a constant pain level of 8. My quality of life declines steadily but physicians DON’T CARE ABOUT WHAT TAKING YOUR MEDS AWAY DOES TO US! To them everyone is a drug seeker. Every test, x-ray, mri they say nothing is wrong. BUT I have seen some of them and it’s just not accurate, but their opinion is drug seeker. They keep insinuating and actually been told that ” your just getting high”. Walk a mile in my shoes. They tell you parables to convince you they are right. I could go on and on. I have and always will be truthful unlike most care providers. I’ve caught them saying one thing then doing another. Bottom line, THEY HAVE AN AGENDA WHERE THE END JUSTIFES THE MEANS… What happened to the Golden Rule, Code of DO NO HARM????
I guess you all didn’t like my comment at all either because you sure didn’t post the truth typical just like everybody else. You posted every other person’s opinion and issues up there but down here in Kentucky were all junkies evidently
Best this! I was in Chronic pain management for 17yrs after a severe sawmill accident amputated my left hand, they reattached it, at Jewish hospital in Louisville KY back in 2001. Broke and fractured several bones in my arm and fractured my neck. So for years(off and on) by choice I went to pain management when the pain was overwhelming the older I became. IVE NEVER failed a urine test for ANYTHING in my life. Only smoked pot way back in my early 20s I’m now 48. I was in a pain management center in Paducah KY for the last 8 years, never failed anything. One day outta the blue they say I’m + for Meth! At first they cut me straight off! After knowing me all those years, gave me another chance after 2 months, failed again!! Then they cut me completely off and told me I had to pass 3 drug screens in order to receive just tramadol I was on oxycodone 10 mg 4 times a day for the past 10 years. I was mad as hell because I have never in my entire life use that drug or seen that drug. Later I find out during my visits with my 12 year old daughter in Indiana my ex-wife without my knowledge had been smoking that crap in her apartment it got in my daughter’s system they took removed her from my wife’s care and put her with not her grandmother . So I tell my doctor that had to be the way it was getting in my system without my knowledge he acted like that was impossible but if a 12 year old girl can’t get it secondhand why couldn’t I? Especially a man who has never failed a drug screen for anything just be tossed out like trash called a junkie all because my wife was smoking that garbage in the apartment I didn’t smell it all I knew was my daughter was hiker a lot. Now I’m an outcast no doctor will see me because it’s on my record my wife later went to prison for endangering the welfare of a minor over that charge even a judge was going to tell my doctor what had happened my doctor wouldn’t even consider listening to me they all acted like I was crazy and a liar why in the world I told them what a man wait till he’s 48 years old to decide to but starts using methamphetamine out of the blue now I’m left in severe pain no doctor will treat me and I have nowhere left to turn that’s what I think about your doctors in your medical establishment they have no doctor patient relationship anymore it’s all comes permit test they don’t want to dig any deeper because they got plenty of patience and money to take your place now I hurt every day of my life. Thanks a lot to dr. Mala at the pain management centers of Paducah for having my back.
I have chronic pain the reality is i live a 8 out of 10 for pain. Ive got scoliosis, deteriorating disk desease. Spinal stenosis, bulging disk in my neck also now, and arthritis in my neck and spine, last time i was at the hospital they told me it was all in advanced stsges, now ive had plenty of xrays and scans and images to verify what i say is true about my problems, but they wont give me anything for pain at all, nothing, and i just saw and read the drug seeking patient stuff, yes ive done meth and occasionally still do, but that has no bearing on my wanting pain meds, shit there is no meth in the meth anyway, and yes ill do almost any drug i can get my hands on to try to get rid of or mask the pain, ill get addicted to other drugs because i cant get any pain meds from a doctor, so my coming drug problems will be because doctors wont do there jobs, the doctors that i see are not good doctors anymore and i use the VA for my medical care, used to be excellent care now it sucks has steadily gotten worse, i am on medicare also and i think im going to start going to doctor after doctor until i can find one that will give me pain meds
Hang in there, Chris,
I am sure that somewhere out there, someone is going to help. I wish I could tell you who and where to go, but I am praying for you! This stuff has to end and end soon! The pendulum has swung too far, and I hope it centers for you soon. You have to be your best advocate!~ Fight and don’t stop fighting that’s the only way. Your fight will help others!
Hi
Long story short. In an RN who contracted cdiff because they put em all on the oncology floors.no one wanted to take care of then so I did. Per diem at the time and so sick so fast I had no clue but I spent every hr in bed. Cried when I had to go to work. Couldnt eat or drink due to it just running outta me. I ended up with 6 years bfore I realized a dr whom didnt like my attitude black flagged me. 2 more years nearly dead my boyfriend took me to a new system and with held my records. I was diagnosed cdiff, ulcerative cholitis, reactive arthritis, ankylosing spondylitis, and scoriatic arthritis. I worked hard my entire life. Still no one wants to help my pain even though I never asked for pain meds..rather diagnosis and treatment. I had to try to work againwith all my joints hot swollen stiff, unable to eat or drink. Dr took me out after I woke up behind the wheel with a blood pressure of 68/28! The disability judge was rude and fixated on drugs. The only problem I had with drugs is needing them and not getting em. Went to jail twice for suspicion of DUI first time due to stroke I had from dehydration. Nothing in my system. I cry every day trying to get down my stairs and I still cannot eat much. All the chemo drugs cause bad reactions so I’m totally alone. My boyfriend died in jan. I have no one on my side. I tried to kill myself and it didnt work. These drs and nurses sabotage any help pt might get by their unethical behaviors and writing their opinions in our charts. Something has to change. Only people getting pain pills are the ones that dont need them and they sell them. Its ridiculous. One last thing. I was taught your biased opinion has no place on a pts permanent record. Its profiling, unethical and harmful. I want to change this but have no idea how to go about it.
Rebecca Crowningshield RN
I have Chronic Regional Pain Syndrome, f/k/a RSD. Most painful neurologic pain disease in the world, very rare. Rates higher than natural child birth on McGill Pain Chart. Can I get any respect in ED when I flare, opioids are now off limits to CRPS patients, or decent medical help? No. No cure, it’s also known as the “suicide disease”. You sign off on it in the fine print every surgery. This is so wrong. Fail AMA.
After being on hydrocodone 1 pill 3 times a day which helps with my chronic pain (I am 52) I will be 4th generation to have or get osteoporosis and arthritis and that could be why or part of why I’m in pain. My doctor doesn’t believe in fibromyalgia. Anyway now that he is on medical leave the other doctors are refusing me my medicines and want me to go to pain management. I’ve never been addicted to anything or ever been into taking drugs, I only take the pain medicines because I hurt. So now I have to wait to see primary physician with no medicines.
Wow. I can tell you that as somebody who’s been addicted to drugs on and off throughout the years, there ain’t no high worth the hell that these patients go through. If they even get a high anymore, which is unlikely. Not only are you in extreme pain from whatever your pain stems from but then you also get physically sick. That would be absolutely unbearable and I could see why suicide has become an option for so many. This is terrifying. I don’t get it, pain management specialist should know exactly what these patients are going through? If you don’t refill the prescription or black list a patient, they’re going to get really sick and in so much pain that death may be even be an option. So when they come into the ER and they’re begging, now they’re going to be labeled a drug seeker? And now they have to buy pain medication off the street and be labeled an addict. These doctors should be charged. This is a sick joke. This is the devil making its way through the hands those who are supposed to be healers. Disgusting.
Some people malinger for drugs and when they successfully con a doctor they usually tell others. A common topic of discussion among prescription drug abusers is which doctors are easy to get drugs from. They tell what they said when they complained to the medical staff that they believe resulted in them successfully obtaining drugs. There are healthcare workers, mental health practitioners, students, and workers in the field knowing DSM criteria to develop factititous disorder for drugs and disability payments. Faking medical issues gets deep.
After reading all of these stories it must be a nightmare to be a pain patient in the US I’m in Canada and its much more relaxed here. I do have spondylitis in my lower spine which causes the bones to fuse and it is painful so i went to my family doctor and asked for percocet because nothing else was working and I walked out with a script no problems at all.
I’ve never heard of anyone being kicked out of the ER or out of a family physician’s practice because they were a drug seeker. It just doesn’t happen here. Every doctor or surgeon or nurse always treats patients with respect and dignity. And to top it off our heathcare is free.
I really feel bad for you folks south of the border it must be very frustrating.
I’m curious – pain meds in general have rarely ever had any effect on me for as long as I can remember…. And i broke bones and got hurt as a child and as an adult. NSAIDS help with inflammation etc and aspirin etc is good for headaches but I have even been given hydrocodone and dilauded(?) via IV in the ER due to shooting pain in my arm. I could taste that crap roll across the back of my tongue for each push they did, and it did NOTHING. I told them that after the hydro and again after the other stuff – and since I knew what they were thinking I informed them not to bother giving me anymore bc it wasnt working for the pain. Muscle relaxers worked great though to help me sleep a little though. Has anyone ever heard of this kind of thing before?
We have a broken medical system, at least when it comes to managing chronic pain. I’ve lived w/neuropathic pain for 24yrs following an auto accident. Shortly after the accident, I felt I was so lucky to come out of that accident alive. Today, after all the yrs of suffering, losing abilities, and being harmed by the very ppl I’m supposed to turn to for help, I’d say the lucky person would have died in the accident. I’ve been on opioids for 22yrs. While opioids aren’t certainly have their issues, it’s better than nothing. I’m on the same dose I started on. I have never abused or misused any substance but I’ve been treated as if I have even though there isn’t a shred of evidence to support that. I see a medical community who seem to be getting some kind of reward or pleasure out of making innocent patients out to be drug seekers. An epidemic of med prof who they themselves could use either further training or psychological counseling. I had a spinal fusion some yrs back. The surgeon put me on a different opioid but errored on the conversion putting me on 1/3 the dose I should’ve been on. I felt like I wanted to die and complained of pain but was blown off/ignored. So, I started investigating myself. The nurse told me the unformilar opioid I was put on was the same medicine just different name. I informed the nurse it was the wrong dose. By that evening, there was no change to my medicine, I was in tears and trying to figure out if there was a way I could kill myself w/the IV machine bc the pain was intolerable and the ppl who I was paying to help me weren’t. 2 mos later, I had to switch the opioid I’m on due to an insurance change. This physiatrist was in the same office as my surgeon. She put me on the same med the surgeon had me on for 2wks post-op and made the same conversion error. It caused my trigeminal neuralgia to become severe. I informed the doc’s office something was wrong but again I was blown off. I began doing what I could to prepare for suicide bc the pain was intolerable, quality of life was zero, I didn’t think I was going to be able to hold on much longer, and bc I didn’t think I’d find a new dr to help me knowing no Dr wants a patient on opioids. However, before I turned to death to manage chronic pain, I turned to the ER 3x over the 6wk period to see if they could figure out what was causing the flare up. When I was on the med following surgery, the pain eventually went down but this time it wasn’t and I didn’t know why. The 1st 2 ER docs gave me a pain cocktail and treated me well. However, the 3rd ER doc and his male nurse treated me as if I was a drug seeker.Prior to this med change, I had not been to an ER for 10 or 11yrs. I went by myself bc when my TN gets that bad, any movement of the eyes or facial muscles can cause shocks. I get sensitive to light, noise, and my jaw hurts so bad that I limit the movement of my right jaw as much as I can but that makes it somewhat difficult to understand what I’m saying. When I’ve had someone w/me, especially my mother, I get irritated easily and for some, it’s hurts them to see me in so much pain. Unfortunately, that means I have no witness or bodyguard to protect me from some who have no business being a dr or nurse. I was physically assaulted by the male nurse. I was again contemplating suicide bc of the pain and bc of how I was treated but didn’t bc my dr finally agreed, when talking to the ER doc, to fit me in her schedule. I switched my insurance back to what I had been on and my doc put me back on the opioid I had been on previously. Ironically, about 1yr prior to my fusion surgery, my doc’s office doubled my opioid dosage by mistake. I informed the doc @an office visit and for about 6mos, her office kept writing my rx for the doubled dosage but I identified the error while still at the office and asked them to correct it. I missed 2wks of work just as I was scheduled to return after surgery. After I got the pain under control, I found a new doc. Since then I’ve been kicked out of 1 drs office 2x several yrs apart. The 1st time, I called the nurse and asked if the contract allows a patient to just get info, no treatment, from a dr about the pain stimulation. The dr I was seeing didn’t do the pain stem and she was and out of my visits so fast that it was difficult to get info from her. I was kicked out for that. Where is the common sense? I think u can be pretty sure if a patient asks for permission, they likely have no plans to pull a fast one. If they did, I’m pretty sure they wouldn’t be stupid enough to call their doc. The 2nd time, I had to change 1 of my meds. The new med wasn’t as effective and I had finals soon. I asked my doc if there were any other treatment options that might be helpful. She put me on the med I had been on previously and quickly walked out. So, I didn’t get a chance to ask why or inform her fda doesn’t want me taking that med w/another med I’m on nor ask about Botox which was what I thought might help. Shortly after, I received a letter kicking me out and stating I needed to see a psychologist. I had 2wks left of 1 of my meds. I was in such distress, fearing I wasn’t going to find a dr w/in 2wks, and trying to prepare for death in the event I couldn’t find a dr while trying to focus on my studies. I did horrible on my finals and that may prevent me from getting into a very competitive grad program. I have gone off the opioid I’m on and have no problem doing that. The issue I have is that the pain gets too severe and when it gets severe, I start turning to death. Patients need some process they can turn to when a dr misdiagnosis them as a drug seeker. Drs should have to pass along whatever evidence they have and allow an independent judge to decide if that dr needs to correct the medical records. Making false statements in their med records and leaving them at a serious disadvantage in finding a new dr who will care for them is just wrong. I know of no other condition that’s handled in the manor chronic pain is. I think the government should take over and provide true multidisciplinary approach. At least the government has an incentive to not cause patients to lose their jobs, negatively impact the patients schooling and future, come up with more effective treatments to prevent disability or help disabled patients to heal enough that they can return to the workforce as well as not overprescrib pain meds. Just 2 months prior to the incident, I asked her husband, also a pain doc, if I could decrease or eliminate 2 meds; 1 opioid and 1 anticonvulsant and which 1 I should decrease 1st. He recommended the anticonvulsant which I planned to do once I found a job. For any med professionals, there aren’t nearly as many drug seekers as u believe there are. It’s tragic that so many ppl r abusing these opioids and losing their lives but please find a better way to treat chronic pain. What I see is a group of medical professionals who’ve been infected w/a mind virus. A virus that makes u believe “all/most patients w/moderate to severe pain r drug seekers” and if given a opportunity to get multiple rx’s from multiple docs, they will. That’s just not the case. Like alcohol, most ppl can take opioids as prescribed and never develop an addiction problem. Stop trying to judge a person’s intent and instead judge when there’s clear evidence that the patient is abusing or misusing meds. When u accuse an innocent person, ur causing unnecessary harm, causing patient’s to distrust med prof,, causing ptsd, depression, anxiety, and for some, enough harm that it pushes them into suicide. Making them believe they have a condition that steals their quality of life and which can’t be treated or which docs don’t want to treat leaving death as the only option they have access to. I see a death notice about every 3mos in the TN support groups. Keep things in perspective. I understand that it may be frustrating to see a patient and feel they’re drug seeking. But, imagine what it’s like to be the patient. To show up for ur appt and see a doc essentially making a joke out of a condition that’s really painful for u and having a significant negative impact on ur life. And then imagine ur doctor treating u w/disrespect, giving u “what u deserve”, and then billing u for it. Think that’s frustrating? In my opinion, medical professionals act a lot like drug seekers. For many in the medical community, the opioid epidemic and knowing the patient can’t just find a new Dr has become a license to be physically and/or psychologically abusive. To use patients suffering in pain as ur punching bags while u all get whatever the reward is for finding another drug seekers. Never mind it’s just a figment of ur imagination. At least often, it’s a problem manufactured by those in the medical community. I really disliked those who abuse and misuse these meds bc of how their actions have impacted my life and nearly taken it on several occasions but after that ER trip where I was assaulted, I now feel sorry for those w/ any kind of addiction problem who end up in the ER only to be abused by ppl who have veered off track and lost their way to be the healers they used to be. Whether I was a drug seeker or not, the behavior of that dr and male nurse were inappropriate for either condition. The medical community needs to decide if they want to be healers and live up to the Hippocratic Oath or if they want to be equivalent to serial rapist/murderers, causing a similar magnitude of harm to many patients. I hope those in the medical community find themselves trying to live the best life they can w/a painful medical condition someday and r met w/med prof just like themselves. I don’t say that to be mean but bc I think it would make them a better person and better med prof.
Hi Kim, I was warned that the pain doc I had is planning to try to accuse me of being a drug seeker. I missed my appointment in Feb. because of a blizzard. Could not get another appointment until Mar.,Was to see the doc on Mar. 12th. but my Rx for Oxycodone ran out on Mar.4th. I had not had a nerve block in four months and the doc would not write me a RX as he was going out of town from Mar. 5th. to Mar. 12th. I was told to go to the ER or take over the counter products. The ER is not an option because they will not help me and over the counter does nothing for me. I called numerous times to try to get doc to help me , was told to do as he said.And even asked if I could see somebody else till he returned, they did not call me back. I started to take aspirin and on the 7th. was so desperate I called the after hour service and told them to tell docs office that i took 26 aspirin. He said he would send them the message in the morning. They still did not call me. I had not taken all these aspirin at once but told them I did out of desperation. I called again on the 8th. to docs office and his staff told me that I had to do as he said and wait till he came back. I saw him on the 12th. and he took my Oxycodone that he was to give to me when he returned. I filed a greivance and my identity was revealed. Hospital says they give him free rein as to what he does. They all lie for each other. i am told he is dismissing me and trying to ban me from the clinics. He states in my records that I am not an abuser or addict and is now trying to supposedly call me a drug seeker. He abused me and neglected me. He put me in situation that happened and I will not be quiet about it. Will be filing with the State Medical Board. Had surgery on abdoman on Apr. 10th. to try to remove the nerve and help my pain but am on post -op day 4 and do not notice any relief. really fed up.
If you go to er for anything, if you pain med not working, if you have a tattoo or on pain med not helping the er I go to automatically accesses you of being drug addict or drug seeking behavior. I’ve had several surgeries and almost all them was screwed up by Dr. Keep complaining about system, but keep saying nothing’s wrong so on my hand surgery thanks to the Dr that done it cut the never completely into. And had still continued saying nothing wrong. I found great Dr. He found out what other Dr did but still never admitted to wrong doing.licking the Dr that prepared was hand specialist. He done best he could to fix other Dr’s. Mistake. But even tho he fixed it problems are reoccurring he said he didint want to go back into my hand didn’t know if he could do any more fore me. NOW my hand is f****\,med up for rest my life and am opposing use of my hand. Previous Dr that screwed it up still didn’t admit, doesn’t even know I know the truth, but he still doing his thing but made sure I could not legally do anything to make him pay for what he done. So keep b’sing me so I had no chance making he at least admit his mistake. And usually you cannot find a Dr to fix another Dr’s mistake. But I did and I’m grateful for what he done for me. But he still can’t guarantee me he can fix my hand where I don’t loose total use of it. I had other blotches up surgeries. I’m not seeking drugs. I get them thru pain management. I want them fix what’s wrong get me out of this outrageously severe pain so I can life at least have normal life. Without having to depend on ppl for help all the time. They have meds that will control most my problems but will not let me get them. Then I would have go to Dr two to three times a Month. Why make someone SUFFER when you can help that person almost be pain free.
I’ve been labeled drug seeking behavior all I want is be out pain much as possible and have mostly normal life.
I know drug addicts , and I don’t ever want be like them. But I also being in so much pain at time a person don’t want live because of it.. I’d rather die than become like the addicts I seen in the past and those that of are why that ppl that really need the meds and the help that Dr’s don’t care enough anymore to listen and find out what going on and fix it. I hate taking pills or shots. But I don’t want to be in so much pain, I’d be thinking not be alive. I got a lot to live for but pain really unbearable. The pain I have now is nothing like I’ve ever had before. But they won’t put me in hospital run whatever or all test they can to get rid of problems. So I’m between rock and hard place.
I am also a recovering opiate addict and it kills me to see my mom and other loved ones in so much pain because doctors are afraid to prescribe pain meds at all, even to people who really do need the. I take alot of the blame because I used to go to the E.R too when I was withdrawing. I was in extreme pain just not the kind I told them I was in. I would always say my pain was 8,9 or 10 because all three of those seemed to get me what I needed to not be completly miserable and sick. They do catch on though so if you end up having real pain they might not believe you and that scary. Good job on almost two years clean. I know how hard it is to get off pills. To the doctors that might read this, please dont punish all pain patients for our addictions.
I have several chronic pain medical issues. Several issues my my lower back and spine. Also have complex regional pain syndrome. And now ive also been diagnosed with colitis. I end up in the er cause my pain and vomiting and such has become unbearable. Cause im in pain management for my back and crps, the docs stop right there and usually dont even get to see a doctor, just a nurse practitioner. I often leave feeling worse than when i went. 3 weeks ago i went to the er im supposed to go to, the one that keeps pushing me out. And 4 hours later i ended up at another er getting a folley catheter, 3 days later i was back to find out i have colitis. Ive lost 16 lbs in just 3 weeks. I was again in the er lastnight cause of vomiting and diarrhea. Before i even ask for anything, they said no narcotics. I never argue or ask why or anything, just do and go along with the docs orders. Im here now doubled over in pain, but the treatment ive been getting pushes me away. I knoe im retaining urine but will wait until ny belly is about to burst before i go in. Its become very depressing and stressful and give me extreme anxiety. I bet if the docs experienced pain and sickness like i do every single day maybe they might have some compassion and not come up with their own speculation. I
It is interesting to learn about the large amounts of people that need help with treatment. This is a big deal that should not be overlooked. My uncle may like this insight as he looks into help with pain pills for his son.
What made you decide to get clean? How did you get through the withdrawal process? Congrats on getting/being clean and helping others to understand some of the inner workings and thoughts of ER drug seekers. Here’s to 21 more months of sobriety and beyond!
Wow! Thank you for sharing your story and congratulations on your road to recovery! You’ve provided valuable information to the medical profession about your experience.
Can someone please explain something to me? OK I lived in Delaware and suffer from ulcerative colitis I was prescribed opiates from the gate at a very young age. At 15 I was put on tylenol3 by 23 I was on oxycontin 40s. Now after I me a seeker, the ERs never turned me away…they even went as far to tell me we aren’t giving you any narcotics but we will check you out to make sure your not seriously injured or whatever. So how do your ERs turn you away? I always thought this was illegal? Also why aren’t Doctors allowed to come out and say I think your a drug addict? I had a Dr tell me-after I finally went to my fave ER for help that they had been waiting for this day…why not just say it? I mean I understand they can get in trouble for accusing someone of something and its false but if its not the addict isn’t going g to complain?
I want to take a moment to point out how political and media-fueled fear of all opiates is affecting people with chronic pain. I am an RN. I am 32 years old. About 16 months ago, I started having terrible mid/upper back pain. I took tylenol and ibuprofen with no help. I tried physical therapy and a chiropractor – still no luck. My primary doctor reluctantly prescribes tramadol – this gets the pain down to a 5 or 6 only – which is not tolerable. They’ve started nortryptiline a few days ago. It is not helping. By MRI and x-ray, I have “mild disc degeneration and scoliosis to the right.” I should not be in this pain — but I am. I am suffering. I’m terrified of this pain with “no cause” and no hope – and doctors who are afraid/reluctant to relieve pain because of drug seekers. I don’t know what to do. I can’t go to the ER even when I’m 7-8/10 because I know I’ll be labelled as a drug seeker. This isn’t fair to millions of people like me who just want their suffering reduced to a tolerable level.
Your a nurse? There should be automatic trust in my opinion. As a nurse you probably have access to all the pain meds you could ever want. Even tho I dont know you I would assume you dont touch those pain meds . There is no reason why you shouldnt be allowed to get a narcotic medication that works, and I am sorry your so under medicated. The DEA needs to get off the docs backs so the docs can appropriately treat peoples pain!!!
Agreed and patient profiling, bullying and shamings tactics from ER physicians. Patients who have chronic pains and diseases should be treated in conservative treatment to controls symptoms. This needs legislature in federal to changes law. No patients needed to suffers.
I am a chronic pain patient started w a slipped disk too much hydrocodoen then a fractured cervical vertbrae too much oxy then the worstI got a lumbar spine Iinfection so painful I was kickd out of er 3 times crying bc security was gonna be called bc I was a seeker. Finally on my 3 visit over 6 months the infection had gotten so big I lost two vertebrae and a disk and spent 2 weeks in hosp- I was released w morphine to taper off the dilaudid hi dosed pump in hosp I didnt have insurance no primary I went to er on week 3 of iv antibiotics and was kicked out AGAIN as a seeker even tho ky mris zhow no bone diak and spinL compression- last time I had a seizure on tramadol tbey toook me to er handcuffed me to bed told me id tried to commit suicide by narcotic overdose and could not leave. They accused me of heroin abuse! I smoke pot yes to SLLEP bc lying down in unbearable… but now? I have no pcp she dropped me the er wont trear me and im considered a heroin user even tho I never tested positive for it orhad track marks…. sentara virginia beach will see me Iin their er AGAIN only next time w my lawyer so I get fair TREATMENT
I do not know how many times I have been to an ER because of pain. I get the same questions all the time, are seeing your specialist, when is your appointment, is this chronic. I get varied answers such as we do not treat chronic pain, this is not an emergency, I do not believe in giving pain medications. When I go it is because the pain is unbearable. I cannot take any NSAID’s like aspirin, tylenol, etc due to bleeding ulcers that are grade B because my stomach ends up bleeding and then I get admitted to the ER and scoped again. But they always think I am there seeking the drugs so they may give me some pain medication but they will give me low dosages and tell me to follow up with my doctor or pain management. Pain management only wants to do injections but I cannot have them due to my platelet levels being so low I could bleed to death. My GP does not want to prescribe pain medications so I am in a catch 22. It took me almost 4 years to find someone who would treat my condition and them I had to move because my health got worse. Oh yeah, if you go on pain meds you are expected to take them and maintain levels in your blood stream to ensure you are not selling them or giving them away or you get discharged from the practice. My chronic pain is not so unbearable I need them all the time but the way they have to protect their license is to make sure I am doped up appropriately. You cannot be honest because there is no winning. I decided when I get certain types of behaviors from staff I start filing medical board complaints on the state and federal levels. Because if I have to be in pain, they can take the hours of answering for their conduct and lack of treatment. I also advise the doctor now I would be doing so and its their choice. Treat me as a reasonable mature adult who makes health decisions with me not for me or spend the time writing more paperwork. I also let them know I realize it may not go anywhere but if they are going to waste my time I will take the time to make sure I waste theirs as well since in the long run time is equal to money in their field. I hate to have to use the system in this manner however my complaint of pain is legitimate and if you are going to treat me as a “seeker” I am going to take offense and I am going to report you. After a while when they get so many complaints, then the board will start taking them seriously due to the pattern of abuse or indifference on behalf of the provider you have seen
I too have chronic pain due to many different causes from musculoskeletal pain to Crohn’s disease so I feel your pain with this stuff. (No pun intended) A couple things I wanted to point out. First, Tylenol(acetaminophen) is a pain reliever/fever reducer and does not fall into the NSAID category. It is very well documented that over use of Tylenol can cause liver problems but since it is not an NSAID it shouldn’t cause stomach ulcer or stomach bleeding problems like ibuprofen or aspirin. Also, the most prescribed narcotic in the world is hydrocodone. Hydrocodone is almost always combined with acetaminophen. 500 mg acetaminophen = Vicodin while 325mg of acetaminophen= norco and 300 mg of acetiminophen= xodol. All of which are combined with either 5,7.5 or 10 mg of hydrocodone. So the notion of not being able to take Tylenol for the reasons stated are not as valid and if you tell the dr that and then are ok with taking Vicodin or norco or lortab or even Percocet (oxycodone/acetaminophen) then the dr might think you are just lying then to get narcotics. I’m not saying you are not in the pain you are in but being as consistent and accurate with the info you give plays a big role in how they view you from the start. Next, I will say that I like the approach of reporting them as a means to waste their time. They certainly have no problems playing games and wasting ours and we are still forced to pay in the end for a service that wasn’t acceptable for us and we all know how precious their time is to them just by how much of a hurry they seem to be in and interrupting patients and having a rushing type of attitude constantly so I do like that method of retaliation. For the record, I was not trying to attack you in the first half of my response, just trying to inform you and maybe help find a reason why they may be so hard pressed to give you something stronger. I’ve ran into problems also and even with them telling me I have a bowel obstruction, admitting me into the hospital then as soon as I’m up in the room, nurses and Drs start playing games with the pain meds only coincidentally. It infuriates me cuz I came for pain relief and I could sit at home in pain for free without dealing with childish games that I have to combat and fight about which makes my pain and blood pressure skyrocket! So hopefully this helps you in the future
You are the reason people don’t prescribe
You don’t bully people. By law they d not have to prescribe anything for pain. It won’t kill you. If they don’t treat diabetes htn…sure….fine….but pain….every complaint you make.will be “looked into”to make you feel better but even the medical.board can’t make anyone prescribe narcotics. If anyone hears that bs from you I hope they flag you and DC you immediately until no one sees you. You are digging your own hole.
I Agree! Great reply! You nailed it!
I don’t know who he thinks he is! Doctors owe him Nothing!
Little twerp!
Going to guess you aren’t a pain patient. Imagine being in so much pain you can’t function, can’t sleep..eat..
Now imagine all doctors, hospitals, clinics, etc refusing to help you because they think you >might< be a drug seeker. You have nowhere to turn, and the pain ever lingers. You try to be civil, and they treat you as sub-human.
Imagine being so desperate you eventually lose control and kill yourself to end the pain.
I hope you can imagine it, because that situation is the source of a very large portion of suicides in the states.
Millions of people suffering with no relief, because a minority of drug seekers led to the feds passing insane regulations on ALL effective pain medications.
I sincerely hope one day you develop some extremely painful disease, and get the exact same treatment.
You’re f****** idiot…. Pain has biological marker changes in the body, raises cortisol, prevents healing ,lowers the immune system …. You clearly know nothing about medicine much less about the chronically ill and suffering… Pain does kill ! Also it is also against medical ethics to not treat pain it’s one of the five vital in medicine and in the Hippocratic Oath…. So how about you educate yourself a little bit more before you run your mouth .
Just a little advice. I can’t take any NSAIDS either because of severe stomach disease. It also causes bleeding in my stomach. You can however, take toradol IV or IM it doesn’t go in your stomach
“Tylenol “ is a brand name for acetaminophen…it is NOT an NSAID so you should be safe to take it as long as you follow the proper dosage. I am a Nurse Practitioner as well as an anticoagulation patient. I suffer from two genetic clotting disorders and I’ve suffered from five pulmonary embolisms. I am on a high dose of Coumadin along with Enoxaprin injections in the abdomen twice daily and will be for the rest of my life. I wanted to offer a bit of advice to help you if I could. I have to tell my hematology pharmacist about any otc medicine I take bc Pharmacy doses my Coumadin according to my INR levels…and being a chronic pain sufferer I told the pharmacist I DO take a lot of ibuprofen even though it’s FORBIDDEN bc of the pain… and you know what they said??? They’re Not too worried about it! They said just to make sure and take an antacid along with my dose so I don’t get a bleed in my stomach lining! So in between docs, ERs, pain specialists…if you need some type of relief you should be safe to take acetaminophen AND ibuprofen for your pain! Another bit of info is you can actually take them both together when you’re in extreme pain. I hope that helps and bless your heart. I DO PRAY YOU FIND A GOOD DOC WHO WILL TREAT YOUR PAIN AND TREAT YOU WITH RESPECT! Take care now.
I have been a chronic pain patient since 97.. I have been on and off of opioids . I had had multiple surgeries for my knees due to a auto accident.
My ED is great . I have gone in at the advice of a couple of my pain management Dr’s . I have 2 herniated disks and there have been times that the pain gets so horrible that I just couldn’t take it anymore. I called my pain dr and they advised me to go in. So I did. I am always up front with the ED. I tell the dr that what my condition is and that even though yes I am being treated for pain at that moment the pain is just too much for me to handle and that my medication isn’t helping as much as it should. They’ve always been great well with exception of one dr but everyone else has been great. They always give me pain treatment and usually do an x- ray to make sure I didn’t hurt myself in some way and may not know it. I find if I am just straight up and honest they are much more willing to help me. Also though I have had awful experience ‘ s at other ER’S . I had an ovarian cyst and I was driving while I was driving I had such sharp pains that I had to pull over so I was close to the ED and I went in and told them what was up . They acted like I had purposely made it up just to try for opioids. I told them they were hideous and I would not even send my dog to them. So I came to my hometown ED and they were awesome, I had been awaiting surgery for this issue however they got me on IV pain meds . They did a ultrasound and what the other ER failed to treat and could have been dangerous was that my ovary had been tortioned and it was in a dangerous position. So they got me admitted and I had surgery on a Saturday. My point is I get that the ED has to be careful however I don’t think there should be a set guide line for determining pain especially for chronic pain patient’s. We have chronic pain yes. However we get other injuries as well and if we are on something well if we came to you our medication is not doing its job as effectively as it should and we need just a tad more help. When this happens we are upset and scared and did not want to leave to come sit in a waiting room with “people with MORE emergent issues”. As the woman whose a nurse wrote… I was kind of offended by that statement because who are you to say that pain isn’t emergent? Unless you suffer from it then I’d wisely refrain from comments as such. We aren’t addicts .
Pain patients never rest; if we are not fighting pain that overwhelms our senses, we are fighting a nasty minded system that judges pain when they have none themselves!
Dad took 1 pain pill in college, felt heavenly & decided never to do it again; it could take him over if he did! And he didn’t because once upon a time, citizens felt responsible for their ethics & now, they want a big bad problem to be at fault; but the pill didn’t jump into anyone’s mouth; they had to take it off protocol which is illegal! How is that our fault who suffer such pain? That’s our crutches we depend on them we treat them as a valuable aid and are grateful for such relief so we can be more productive! I have never been without pain; never in my life!
Hi,
I have been doing some reading on this subject, as I had a recent applicable experience.
Please bear with me.
I arrived at a local, affluent neighborhood, ER, and was dropped off at the door by a friend I had asked to take me to the hospital.
I knew that he had other commitments, so I assured him that I could grad a cab home, once I’d been seen. It was only a few miles… I should note that most would consider the van I arrived in to be somewhat “beat up”.
I had been working in my garage all day, making room for new equipment. After unloading the last piece, I managed to hurt myself badly. I was sure I had broken my arm or wrist.
I entered the ER on my own, quite dirty, unshaven, and advised them right away that I was currently un-insured, un-employed, had no PCP, and was effectively broke.
They put me on an IV, which did little or nothing to relieve my pain. I was very self-conscious because I was moaning/wailing out loud. I was truly in an enormous amount of pain.
X-rays were taken, and I was moved back to the ER. Eventually, the Dr. returned and assured me that I would live, and nothing was broken. I had simply hyper-extended my wrist (sprained it).
I repeatedly expressed my concern regarding the level of pain I was in; expressing that I was worried that I had hurt myself badly, and did not know how I was going to pay for it. The Dr., as well as some other ER staff, assured me that severe sprains are very often much more painful than breaks, and can sometimes take months to heal.
I related to the Dr. that my back was itching terribly, and basically begged him, and anyone else nearby, for some implement I could use in my good hand, to scratch my back.
No one ever gave me anything. The Dr. said that he had added Benadryl, I believe, to my IV, to combat the itching. He asked if I had any allergies to drugs, and I told him that I did not, as far as I know. I mentioned that, many years prior, after having 4 impacted wisdom teeth removed, and dry-sockets developed, I was given demerol, which had no impact. I was given dilaudid, still no impact, I was then given, percodan, which seemed to help some. He wrote me a prescription for some pain-killer, splinted my wrist, and advised me that if I wasn’t comfortable with his diagnosis, I should follow up with a local specialist, or my PCP, A.S.A.P. I asked again if he was sure about my injury, and he walked me over to a PC where he showed me an x-ray. He basically said “See?… Nothing broken…”, then he walked me to the exit door. After waiting for some 30 minutes for a promised cab, I asked a patient in the parking lot if I could pay them for a ride home.
I spent the next couple of weeks in a fog of pain and sleep. I’d wake up in agony, take the meds, and fall asleep again.
To shorten the story a bit, I’ll skip some detail…
After almost a full year of thinking I was slowly recovering, I managed to secure insurance via a new employer. I immediately went in search of a second opinion. It was quickly discovered that I had a volarly dislocated distal radio-ulnar joint.
After hearing the same diagnosis from three different sources, I decided that I would have to let the specialist perform surgery. An open reduction, hopefully saving the distal radio-ulnar head.
I obtained the x-rays from my ER visit a year earlier, and asked the Dr. if the injury was visible in them. He documented that he could, indeed, see the injury in the original x-rays.
When picking up the x-rays from the ER, I also asked for the doctor’s notes.
Within the Dr’s notes, I find that he documented my extreme distress, wailing, and my concern over the injury, and how I was going to pay. I also find that he included the following…
“The patient seemed to have a very high tolerance for narcotic pain medication”
His notes relating to the x-rays stated “…no bone or joint abnormalities present”
Almost two years have elapsed now, since that night in the ER, and I know that the malpractice statute of limitations is approaching within weeks. I have had the surgery, ironically at the same hospital, where the distal end of my left ulna had to be cut off, and replaced with a $13,000.00 metal replacement. I am receiving bills in excess of $30,000.00, still suffering with a great deal of pain, and enduring permanent limited use of my left hand/wrist. The Dr. who performed the surgery stated that as a result of the injury/surgery, I now have osteo-arthritis in that wrist.
I questioned the Dr. regarding what should have been done immediately after the injury, and he stated that, if it had been diagnosed initially, a “closed reduction” could very likely have been performed within 6-8 hours of the injury. … It could/should have been “popped back in place”…
It is enormously clear to me, after doing some research, what happened that night.
The Dr. and ER staff had identified me as an ER drug seeker, and clearly treated me accordingly.
I fit the “profile”, if you will, like a glove.
I was dropped off alone by a beat-up van, at the most affluent ER in town…
I was dirty, disheveled, and unshaven…
I was un-employed, un-insured, broke, and had no primary care physician…
I was moaning/wailing out loud, with no regard for who might hear me…
I repeatedly related my pain level as 10/10, and may have even stated higher than 10.
I was able to articulate to the Dr. specific pain meds that had been ineffective in my past…
Clearly, as evidenced by his comment regarding my very high tolerance, the Dr. was sure of his diagnosis, and had decided that my extreme distress was un-warranted, or ignorable.
I recall that when the Dr. tried to check my supination/pronation by manually rotating my wrist, I screamed in pain, and he stopped. There is no mention in his notes regarding supination/pronation tests/results. In fact, my wrist was trapped in full pronation by the dislocation. The Dr. had a splint applied, locking my wrist in the least painful orientation, and checked it. He approved.
In my layman’s mind, I’m confident that a thorough test for supination/pronation would be a standard part of any examination relating to wrist pain/injury. This did not happen in my case, or the Dr. would have seen clearly that I was completely locked in full pronation.
I’m sure that closer examination would have quiclky revealed my serious injury.
If the injury had been discovered, I would not have been allowed to leave the ER.
I was in need of emergency surgery, closed reduction of the DRUJ in this case.
A DRUJ (Dislocated Radio-Ulnar Joint) is an incredibly painful injury. My wailing was justified.
When I continued to report enormous pain, the Dr. had to decide if I was really hurt, or dramatizing. Obviously, he concluded that additional diagnosis wasn’t warranted at that time. I should “… see this specialist, or your PCP… A.S.A.P…”
A DRUJ is not hard to identify… If you are looking for something…
I could really use some professional insight.
Have my Patient Rights been violated?
Have my Civil Rights been violated?
I have spoken with several malpractice attorneys, who have all declined the case, as “I didn’t die…” and “He instructed you to follow up…”
A.S.A.P.
Who gets to define that?
In MY mind, I DID follow up “A.S.A.P”. I went as soon as I could pay…
The Dr. knew that I was broke and un-insured.
He knew that I had no PCP, and that the specialist he noted does not see indigent cases.
I did actually call them at one point, and was advised that they would bill me, but that I would have to pay $100.00 before even being seen. I did not have $100.00 at that time.
Additionally, a medical professional, an actual Doctor, had assured me that I had simply sprained my wrist. From my perspective, he might as well have said “You’re fine…”.
What sort of “follow up” is normally required for a sprained wrist?
I recall having sprained my ankle once, but can’t recall any follow-up being required.
I am clearly a victim of ER profiling, for lack of a more descriptive term.
Please, if anyone can offer me any advice, I’d be very grateful.
I have approached the hospital’s patient relations staff, who promptly advised me that I am mistaken, and turned my complaint over to their Risk Management department, who has stated that their specialists do not see the injury in the original x-rays, so they will not accept my claim.
In other words… Sue us…
Help? Anybody? Am I simply out of luck?
I’ll watch my e-mail for any responses.
Thanks for taking the time to hear my story.
T.OliverBridges@gmail.com
Drug Seeker!
TO PETER M. BROWN:
Chronic pain is awful. Suffering is bad. No one is denying this. But opiates are dangerous and tolerance builds over time; that is why chronic pain that requires opiate treatment should ONLY be handled by a pain management specialist or at the very least by ONE physician. This is chronic pain only relieved by opiates; failing to MANAGE the opiate treatment is a diservice to the patient. Without management the tolerance for the opiates increases too rapidly and a person has to escalaute their dosages so rapidly that they reach and then exceed the safe dosage within months or years when they have a condition that last a life time. Pain management is not just about avoiding abuse; It’s primary goal is to treat a chronic condition as safely, effectively, and FOR AS LONG AS CAN BE DONE. I’m not saying chronic pain patients can’t come to the ER; only that they can not be treated with opiates.
Now if you have chronic pain not being managed by a specialist then you should. As an ER nurse, I can promise you that your 2-3 hour wait in triage is more likely because all of our beds are filled people whose pain, whether legitimate or not, can only be treated with an opiate. And if you have ever been in an ER then I can promise you that if you had any delay in your care it is because the ER is being drowned in overly demanding, rude, and most often threatening patients, again only treated by opiates.
TO CAROL:
If you have cancer, you would be better of treating it with medical marijuana along with your paych. I’m not just saying this, I’m not some up tight self rightious idiot that thinks drugs are just wrong. I just think they should be used in the best interest of the user.
I see both sides. I feel for people who suffer from Chronic Pain. I had cancer and took over 40 plus doses of radiation tonmy pelvis
Then came surgeries I lost count of those ! I am on a Pain Patch now and fear for the day I must go to ED
All I ask is give me a chance
My Pain is REAL
Put yourself inmy shoes
I think that Dr. Grover’s comment about the need of further research in the field of pain is very germane. This seems to be an aspect of the solipsistic nature of human beings. I would say that if you have not felt the pain of another person, you have absolutely no right to make judgements about that person’s physical or mental state. That includes everyone, including doctors and nurses. I know that Peter is serious about his condition and am appalled at his doctor’s lack of understanding and compassion
I would like to add an additional comment to the ones I’ve posted above. My major concern is that ED doctors might be operating under the delusion that it’s somehow possible to determine whether a patient is truly in severe pain or whether they are faking it in order to get high. ED doctors must come to the realization that a considerable amount of harm can come to those patients who are really in pain but the doctor walks into the situation with the belief that he will be able to apply a well set rule which he either believes is foolproof and is confident that he can tell the fakers from those truly in pain from the substance abusers trying to get high. If a patient with severe chronic pain walks into an ER its because they have wrestled with making the decision to seek help knowing that he might be branded with the title “narcotics seeking behavior” which will do considerable harm to the patients state of mind all for the sole reason of worrying about letting a substance abuser fool the doctor into giving them narcotics for recreational use. The damage to the psyche can be so severe as to cause the person to commit suicide or at least make an attempt. Nothing on the face of this planet is worth risking that from happening merely so that the doctors ego doesn’t get bruised by allowing himself to be fooled. How do I know about this? It’s because I’m one of those people to whom this has happened. In my last attempt I took a razor and started slashing my throat open. It was a nightmarish image that will remain in my mind for the rest of my life because some ignorant doctor claimed that my pain is
“all in your mind.” You need to understand what damage you are causing a person who is asking you for help and you tell him to get lost and don’t seek narcotics at your ED. I’ve had Acute Myloid Leukemia before and fighting that was a cake walk compared to fighting chronic pain from degenerative disk disease. Almost all doctors seem incapable of understanding what chronic untreated pain can do to a person’s mind. Being dismissed as being “weak minded and not able to suck up the pain” is an absolutely horrible thing to put on a person who has suffered as much as I have. Before you go to bed tonight praise God that you don’t suffer from chronic pain folks.
I’m a new nurse, and have been reading up on determining the difference between pain seeking patients and patients truly in pain. It seems that the characteristic of patients requesting the drug to be pushed fast – faster than recommended practice – is the biggest red flag for me, along with patients who request a combination of IV drugs (e.g. Benadryl delivered with Dilaudid), but doesn’t seem to be covered in what I’ve read. More often than not, the patients who I think may be pain seeking tend to know that other nurses push a drug fast (despite this practice being against protocol), will get raging mad if you insist on pushing the drug slow and/or dilute it, and request a drug cocktail.
Dear Jane – I would like to recommend rethinking your position on this point. I don’t know if you’re aware of it but with some people opiates make them itch really bad. Benadryl stops the itching. Also, when a person goes to the ER it’s because their pain has become too much for them to handle on their own. You then need to take into account the fact that anybody who is in pain wants not to be in pain and the faster the better. Please don’t judge us too harshly because people like myself who live with chronic pain want our pain to go away as soon as humanly possible. Chronic pain is a hideous disease. It never gives you a moment’s peace. When we with chronic pain go to an ER then you can be certain that we’re at a level of desperation for the pain to stop that we are willing to endure the terrible irritation of waiting in an ER. Waiting in an ER when they are in pain makes people anxious. It’s a well-established fact that anxiety magnifies the perception of the pain that someone is experiencing.
By the way, I’m confused over the use of your terminology. Why do you refer to this as “pain seeking”? People aren’t seeking pain. They’re people who are in pain seeking a reprieve from the pain.
Pete
I’m a nurse, and I also have chronic pain, at 36. I received a dose of dilaudid before, for gall stone pain. It wiped every drop of pain in my body right away…felt so relieving. I felt the pain coming back a little while later, well, I was anticipating it in fear because it was so bad and I was now feeling so pain free. I told the nurse, and I was quickly discharged with a prescription for vicodin and referral to GI surgeon. I got the prescription filled , used it a day or so, along with some home remedy lemon water I found online, and I was good as new, back to my old chronic neck and back pain. I was used to my chronic pain, and only needed a little ibuprofen once in a whole if it got unbearable. I didn’t over due the ibuprofen because I also have ulcers and hemorrhoids…..yes, I’m in bad shape.
So,my take in this situation….pain med seeking……is that It sickens me. Do you know how it feels to be late medicating a 75 y/o hip fracture, or 18 y/o appe, chole, kidney stone, bone fracture….All c/o 3/10 pain?All the while I’m coddling some 36y/o with 10/10 mystery pain not backed up by any diagnostic pathology with IV diluadid plus cocktail every 2 hours. The emergency room and hospital are for people with life threatening, acute conditions. I’m am so thankful they didn’t give me anymore dilaudid. I swear I was scared passing gas would hurt, …..but I didn’t get it, and guess what, I didn’t die. I still have my gallbladder, stones and all. I know it will go bad soon, but I have a host of comorbidities, and everything is manageable. I can wait until an acute intervention is unavoidalbe. I’m not suffering, and I’m not crazy, I just do what health professionals have to constantly do…consider the risk of excessive treatments……prolonged hospitalization, infections, scar tissue and lesion pain, med interractions…..and ADDICTION….to meds AND ATTENTION! The amount of money WASTED in America’s health care system is astronomical. The government thinks hcapps have an impact on decreasing health care costs….
Yeah right! The government is forcing hospitals to turn nurses and doctors in to drug dealers, hooking both naive and manipulative patients left and right. But guess who gets the best, most accurate care, the 75 y/o hip replacements and youngsters with appes, choles, stones and fractures. Their pain meds are apprpiately reduced, and mobilization encouraged. Before long, they are good as gold. Prolonged use of IV pain meds and and po narcs have direct negative effect on recovery. Obviously…..chronic pain and pain med addiction are not being adequately addressed or treated in the acute care setting. Addicts and middle aged people who just want to numb their bodies and emotions for a while should seek treatment elsewhere, from doctors and nurses that specialize in coddling and baby sitting egos.
Im not trying to be insensitive or judgmental, I just see a disfuctional system that is draining our nation. Like EMS workers and police officers, nurses and doctors suffer ptsd from the mental anguish caused by drug seekers, especially like some of the ones on here threatening to complain and cause extra paperwork. WOW.
So, as to cause myself less anguish and dread….I’m giving up on discouraging pain med addicts…intentional, or not. You can have whatever they prescibe, as soon as I can get it to you, and I will ask for whatever you request…as long as it’s not unsafe at that moment. I no longer care about your risks for pneumonia and peristalsis. If you want a chopped up stomach and intubation…..be my guest…..then you can get even more pain meds….yay for u. So….just keep on coming, keep on asking for more, until you finally aquire something to instantly qualify you for the max dose iv pain, nausea, itching, anxiety, depression, psych cocktale. Hopefully, u won’t overdose, or have an MI or CVA from severe bradycardia aND hypotension…..maybe. But then, you can always just get more pain meds for that too. Maybe you won’t fall,…and not get up…..be found down with renal failure from rhabdo..that really sucks, but they have pain meds for that too. And the gi fistula and resection you need after peristalsis and sbo can also be treated with some good old high dose dilaudid.
So, have no fear….I’m here to respect your pain, and keep u comfy. I’ll tell granny next door to put a sock in it if she waits 8 whole hours for her 25 mg of po tramadol, right when your q 2 hour cocktail is due…..boy she’s got nerve.
Despite what how it seems, I’m not insensitive, just frustrated with an ineffective treatment plan. There are so many other ways to treat pain besides narcotics. GOOD OUTPATIENT specialists should embrace their specialty, even for the indigent, so that acute care facilities and adequately treat their own specialty population.
You are an extremely judge mental person who I pray never to have you come near me, let alone treatment! You are full of hateful attitudes and really should not work with fragile people! I have chronic pain since youth and I always knew nurses were making these nasty judgements but you clearly can’t see how entrenched your abusive thinking is; please leave nursing to the truly compassionate among us!
Nikki Will I just read your long ass comment and I’m sitting here with my jaw in the floor reading this coming from a nurse I’m just gona say this…. you are part of the problem due to not being informed about addiction and your ignorance. I pray you’re never my nurse or someone I loves nurse. You really need to get educated. Addiction is not easy and god bless those who are struggling.
Jane, it is actually very common for normal pain management to include narcs with Benadryl or Phenergan to relieve the possible side effects of the narc. Now one thing I want to point out is someone who is physically addicted to narcs are going to be in pain, so they are not in essence lying about their pain. Who is at fault for this addiction/are we helping the problem by treating the physical addiction, that is up for debate.
I would also like to point out that many cases I think it is very similar to our super bugs now. Are we going to not treat patients that have a resistant bug because they more than likely took ABs inappropriately. What about someone who comes in with a bleeding ulcer because of their alcohol addiction. Cancer r/t tobacco addiction. Can we say we will not treat you because you are to blame?
I would never say go against guidelines on any medication or give drugs against MD orders but to say that the patient is drug seeking because they are always saying it is a 10 is not justified. What likely happens is these patients are on 1 of dilauded q4 for weeks or months. We send them home of Percocets q6. Of course they will hurt because they are detoxing from the drugs we gave them and we did not order a consult for pain management or someone who can work through this secondary issue.
This patient may find drugs on the street that relieve the detoxing pain. this eventually turns into herion because of the cost associated with the increasing tolerance that is developing. and when this person can not get what they need to not detox they come to the ED because they do have a pain of 10 r/t detoxing off of narcs.