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Hi there,
I have managed to find the scoring system for the Arthritis Impact Measurement Scale 2 in the user guide, but was wondering if anyone has the scoring system for the short form of the questionnaire? 
Most of it is probably quite straight forward, but I want to make sure we get the normalization right. 
Thanks,
Rhiannon 
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Can we use pearson's correlation to test correlation for Ranked pain assessment tools like Numerical rating scale and verbal descriptor scales? Can we use Inter class correlation coefficant ICC to assess thier reliability?
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sorry: Scales EVA
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As i know there is no pain receptors in brain. But the quest is if a person bee shoot in the head, would he suffers pain or not?
is the easiest way to be dead by gun is being shoot in the head?
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I disagree to the statement that shooting in the head can be considered as a good method for people who want to have euthanasias, because of two main reason.
First of all, the ball of the gun must pass throw skin so it surly makes pain.
secondly, methods to exam the mentioned hypothesis face a lot of limitation.
Because of the mentioned reasons, I stand behind of my opinion.
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Is VAS for pain (100 mm line) public domain?
If not, do you know how to obtain permission?
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The pain VAS is available in the public domain at no cost. [Burckhardt CS, Jones KD. Adult measures of pain: The McGill Pain Questionnaire (MPQ), Rheumatoid Arthritis Pain Scale (RAPS), Short-Form McGill Pain Questionnaire (SF-MPQ), Verbal Descriptive Scale (VDS), Visual Analog Scale (VAS), and West Haven-Yale Multidisciplinary Pain Inventory (WHYMPI). Arthritis Rheum 2003; 49: S96–104.] [Hawker, G. A., Mian, S., Kendzerska, T. and French, M. Measures of adult pain: Visual Analog Scale for Pain (VAS Pain), Numeric Rating Scale for Pain (NRS Pain), McGill Pain Questionnaire (MPQ), Short-Form McGill Pain Questionnaire (SF-MPQ), Chronic Pain Grade Scale (CPGS), Short Form-36 Bodily Pain Scale (SF-36 BPS), and Measure of Intermittent and Constant Osteoarthritis Pain (ICOAP). Arthritis Care Res, 2011; 63: S240–S252. doi:10.1002/acr.20543]
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Any equivalent to PHQ9 GAD7?
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Tony -You are 100% right. Dennis is a good guy and a careful researcher. However, our group at Johns Hopkins Hospital, which consisted of MDs, including the chairman of neurosurgery, the president of the American Pain Society, the President of the American Academy of Pain Management, and the assistant dean of the medical school, took a more medical approach. We found that 40%-80% of chronic pain patients are misdiagnosed, and have psychological problems as the results of chronic pain and from not being believed, when the doctor couldn't find anything wrong with the patient. The real failure lay with physicians not taking a careful history, and ordering the wrong tests. MRIs miss disc pathology detected by provocative discograms 78% of the time. CT miss pathology detected by 3D-CT 56% of the time. There are more errors which I can share. When properly diagnosed, and correctly tested and treated, we were able to reduce narcotic use 89% of the time, reduce doctor visits 45% of the time, and increase return to work rates, sustained for more than 1 year, to a level 6 X higher than reported by others. So the Pain Validity Test predicted with 95% accuracy who would have abnormal medical testing, and the Diagnostic Paradigm gave correct diagnoses with a 96% correlation with Johns Hopkins doctors diagnosed. We had cost savings of $20,000 to $175,000 for long term case, and an over 54% cost savings on workers' compensation case. All real statistics.-all published. Email me if you would like reprints. DocNelse@aol.com
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Dear Carlo,
I was working on pain assessment in newborns during procedural pain.
Is it possible for me to contribute to the project, and work on the same goal?
regards
Prof d-r Elizabeta Zisovska, pediatrician
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I think yes, you could start using oxytocin in the incision points.The recovery will be fast and better.
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 I have long thought there is a lot of information on "Pain"  which by definition has to have crossed a threshold to become cognitively experienced. 
However, using palpations such as Janet Travel taught, i see children who declare no pain, but leap when cranial and facial trigger points are pressed. 
I am not having much luck in finding research on the cumulative effects of this.  I suspect there must be many physiological processes involved in this sub-conscious level of  'almost' pain. 
David Zimmerman
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Please let me know if the following references/sites are useful to you:
Central Sensitization: A Generator of Pain Hypersensitivity by Central ...
by A Latremoliere - ‎2009 - ‎Cited by 1508 - ‎Related articles
Recruiting these subthreshold inputs to the output of a neuron markedly alters its .... Interestingly, nociceptor afferents innervating muscles or joints produce a ...
1.  Muscle Pain: Understanding the Mechanisms
Siegfried Mense, ‎Robert D. Gerwin - 2010 - ‎Medical
The strong sensitizing action of NGF-induced subthreshold potentials at the spinal level ... Nociceptive afferent fibers from muscle and other tissues possess ...
2.  Neurosurgery: The Essential Guide to the Oral and Clinical ...
Vivian A. Elwell, ‎Ramez Kirollos, ‎Syed Al-Haddad - 2014 - ‎Medical
Increased responsiveness of nociceptive neurons in the central nervous system to their normal or subthreshold afferent input. Increased responsiveness and ...
3.  Pain Medicine: An Essential Review - Page 433 - Google Books Result
R. Jason Yong, ‎Michael Nguyen, ‎Ehren Nelson - 2017 - ‎Medical
Nociceptive Neuron A central or peripheral neuron of the somatosensory nervous ... in the central nervous system to their normal or subthreshold afferent input.
Dennis
Dennis Mazur
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Almost researchers using thermal plantar analgesia instrument for evaluate thermal hyperalgesia, in limited resources like us, can we use hot plate and magnetic stirrer as alternative instrument?
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I think there is a little misunderstanding about hot plate.
This is the hot plate, which can be used for measuring heat-induced pain:
I suppose you have a hot plate with magnetic stirrer, which is usual lab equipment for heating and mixing solutions:
You cannot use this hot plate for measuring analgesia in rodents!
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Is it necessary to take a lower limit as inclusion criteria for the ODQ? The design from our low back pain study is planned as randomized, sham treatment controlled trial. I am concerned about  getting a to small difference for the stats, if we don´t choose a lower limit.... Especially the between group difference...
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We published a paper in which we show an absolute ODI-value corresponding to patient acceptabel symptomen state (PASS) for the official ODI v.2.1a. An ODI <=22 equals PASS and seems corresponding to 'normal', healthy populations as well. I suggest to use ODI <=22 as a lower limit. Furthermore, it is known that a minimal clinical important difference is at least 10 points or 30% of the baseline value (Ostelo et al. 2008) and literature shows that an ODI >= 41 corresponds to longstanding chronicLBP. Hopefully, this information is of use.
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Hi everyone, 
I'm reading the new Manual of 2011 Knee Scoring System and I have a question about how you manage with missing data and mean score for missing items.
In particular, do you round up or down the value when you need to insert the mean score for missing items? 
I'm waiting for your precious suggestions. 
Thank you so much
Sara
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I'd echo Chris' suggestion.  On reviewing the guidelines for use of the tool, I found the following:
"Q3: Please provide guidance on scoring when there is missing data.
A: It is not possible to provide a truly valid estimate of the score for any domain(e.g.
satisfaction, function, etc) that is missing responses. However, to satisfy the criteria for unidimensionality of each subscale on the instrument, we selected individual items that were themselves strongly correlated which gives robustness to the final estimates of function, satisfaction and expectation In practice, we recommend that clinicians or research investigators: (a) contact the patient and ask them to answer the missing items, or (b) to enter dummy values equal to the average of all of the other items in the same domain. This practice is limited to instances where fewer than 50% of responses are missing, preferably less than 25%." (page 5)
Best wishes,
Rich
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Can someone help me with back pain questionnaire?
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you can use oswestry disability index and nordic musculoskeletel questionnaire 
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Dear colleagues
I am interested in variability of pain threshold or other measure of pain sensitivity among different countries. Inter-ethnic differences is very popular topic in research, but literature on intra-ethnic differences seems to be sparse. I have found this paper:
but its scope does not include pain sensitivity measure in different countries.
Is someone familiar with and can recommend other studies on intra-ethnic differences in pain?
Thank you
Wacław
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Because pain sensitivity is dependent on both genetics and experience, individuals who have more frequent painful procedure pain will have a higher sensitivity.  So if an ethnic group generally finds itself on the lower economic rungs of the societal ladder, that ethnic group may have more pain sensitivity due  to the lower quality techniques and procedure pain control it experiences during inoculations, blood draws and emergency room visits.   In the United States, the Center for Disease Control recommends 25 different inoculations by age 3.  Kids that come from families under financial stress, transportation issues with parents working two jobs and cannot always make medical appointments reliably are likely to see their children receive 4 or 5 vaccinations at one appointment.  After the first injection, the child's attention is turned to the procedure and this increases their pain perception for the next 3 or 4 injections.  These kids experience long term sensitization and classical fear conditioning.  They are highly sensitized.  40 years ago clinicians would come back to the US after donating services in developing countries and they would report how stoic and compliant the children were.  They would say "American kids are such crybabies".   Now, these "developing" countries have developed western style medicine in the form of abundant inoculations and the clinicians returning from them have no idea what I am talking about when I tell that story.  They would say, "No.  Those kids had a lot of anxiety."  Moral of the story here is that an ethnic group will have high or low sensitivity to pain depending on if it has access to western style medicine.  When it does have access, the quality of that access will matter too.  So an ethnic group in one country may have high sensitivity while in another it may be low.  my hunch is that this effect will be a confounding factor that will limit your ability to make broad conclusions about any ethnic group's sensitivity to pain unless you are a brilliant epidemiologist who can control for these factors.  No matter what, you have asked a good question and I would be interested in any new light that you could shed on the matter.  Good luck! 
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I'm trying to determine pain levels in mice (not allodynia or hyperalgesia, but regular pain). 
As pain is rather subjective, it is hard to quantify, especially in rodents. What are the most common and most well supported methods for quantifying pain?
I've seen the "grimace scale", which may work, but I thought about asking on RG first.
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It depend on the pain. In case of the arthritic pain use computerized analysis of audible and ultrasonic vocalizations (J Neurosci Methods 2005, 141(2):261-9). Otherwise refer to M.Barrot’s review (Neuroscience 2012, 211: 39-50).
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I will be investigating the effect on pain ( NRS, GBOs,CPM and TS) of attentional modalities 
Thank-you
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Antiinflammatory or morphine ?
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I have now an patient with an toral feotal attitude . The only respons is the push away othese that gives an decrease on tone in the whole body, She is lying on an firm matras with het best side to the wall.
When she lioes in this orthese she looks angry and push with there feet the orthesis away but when this movement occur the re face is ligthing and the tone decrease and here cognition is increase. No medication was given 
In this case there was the feeling of instabvility and that is no poain but fear !! 
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Hi, planning some experiments and wondering where we might be able to get some cold pressor apparatus for testing pain threshold/tolerance in the UK? Really grateful for any advice! Thanks... 
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I use a mobicool C40 'frost-box' and a simple submersion pump (Reich, 10 L/min, 0.5 bar) running of a 12v battery. All of which are relatively inexpensive (less than £200 in total) and can be purchased online or in shops which sell camping equipment.
...you will need to keep the water in circulation during CPTesting ... this is important!
The mobicool box is thermostate controlled and with a bit of fiddling, you can get it just right where it keeps the water at 0-2 Celsius. You will need a regular thermometer to confirm the temperature. Also, until you get the thermostat setting right -- do not leave the thermometer in the water overnight as you are likely to find a block of ice in there on the first few attempts, and you don't want a cracked thermometer.
For easy cleaning, I keep the water in a plastic contained inside the mobicool box.
I place a neodynium magnet on the outside of the plastic contained to hold the submersible pump in place near the bottom (on the inside) of the plastic container ... otherwise it will start moving about once it is turned on and it will eventually get close to the surface and spray water all over the place.
I have cut a small groove in the upper edge of the mobicool box to pass the flex/wire for the pump into the box and still allow it to close and seal completely. This helps keep the temperature just right.
For VAS scale: below is a link to an online VAScale I have made, which is simple to use -- it samples the VAS score every second and can be controlled with a regular computer mouse, albeit I use a trackball mouse instead. After use it reports the time, max-score, time-to-max-score and raw data. I'd like som feedback if you find it useful: http://smerteforskning.dk/tools/freeVAS/scale.php
I have found that participants who will not tolerate CPT normally quite within 60 seconds. Most who can tolerate it for 1+ minute will tolerate it for as long as you care to keep testing.
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Need information about Zoletil's doses (tiletamine/zolazepam) for mice. Perhaps someone worked with this or have data? Appreciate any help.
PS I know, Zoletil isn't recomended for mice. Unfortunately, we have no choice now.
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Hi Roman,
We always use Zoletil mix with Rompun (4:1) to anesthetize mice. The concentration are 20-40 mg/kg and 5-10 mg/kg, respectively. If you concerned the overdose you give to mice. I suggest that you could mix Z & R with the same volume of PBS (1:1) before injection and give about 20-40 ul to mice (IM). It's very workable for us, hope you too.
Good Luck~
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Hi all
How the Margolis pain drawing system (which each participant asked to shade according to whether they were currently experiencing pain) scored? and how one calculate the mean and standard deviations for the whole sample?
Many thanks for any help 
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we have developed a software, which can average and overlay pain drawings, which then present as contour lines of different intensity of color (I attached a paper showing). If you are only interested in mean and SD I suggest a "primitive" solution: Copy the drawing on standard paper, cut out the marked area and weigh the paper on a fine balance, and then compare to a standard area (e.g. the complete body representation of your scheme). The ration gives you the precentage of full body area). Than calculate your numbers as usual. By the way, our software does something very similar, it scans at 600 dpi resolution and identifies the marked area in numbers of pixels. Xaver's [Hi, and kind regards across the river ;-))] comment points to a similar technique. A paper attached to demonstrate
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What are the barriers to pain assessment in older adults in nursing homes? Please research articles will be of great help to me thanks 
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I wish to add the older adults would not like to be regarded as people who are always complaining by the younger adults. They do not want to be disturbing their families and other health care team such as the nurses.
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Clinical pain is an important public health problem world wide. It is vital to understand the pain mechanism contributing to acute and chronic levels. It is noted that the inter-individual variability as the most crucial factor of pain prediction. 
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Wasana, not clear exactly what you are asking here.  Pain is extremely complex, and a physiological process strongly influenced by perceptual processes, particularly so in chronic pain. The meaning of acute pain is injury avoidance or damage notification; that of chronic pain is much more ambiguous. Pain comprises several components, not only nociception (physical sensation). Cognitive, motivational, emotional and communicative elements make up the "pie" of pain.  Numerous studies show that expectations and anxiety, mood and other psychological dimensions all modify both degree of reported pain and amount of self-medicaltion with different analgesics. People who are anxious and depressed report more pain, irrespective of the level of nociception. Phantom limb pain illustrates that pain is a central process as much as it is due to peripheral release of inflammatory agents at the injury site.  Changes to the local biochemical environment occur but cognitive and emotional changes interact to confer different meanings on the nociception.  So chronic pain from disc herniation can be as severe as that from cancer, sometimes worse, but the meaning of the two are completely different and this affects the resultant experience of suffering.  All of this needs disentangling.  Good pain control requires good psychological skill as well as pharmacological knowledge.
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Hello,
I am a student at Ghent university. I am doing research on chronic wounds and the use of sugar as a wound dressing. 
I am looking for a validated wound healing assesment tool that can be used to measure al the aspects of healing wounds. I have found several tools in English but I can't find any dutch translations. can anyone help me with this?
best regards, laura
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Dear Laura, 
if you contact the authors -they are here on RG-  you could get an answer: 
Deleted research item The research item mentioned here has been deleted
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Hello, 
I am looking at the impact of an early life stress on pain sensitivity. Interleukins have been shown to act on pain sensitivity and early life stress to lead altered IL serum levels.
Therefore I am wondering if there is a more or less direct correlation between serum levels and tissular levels of interleukins
Thank you
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Hi Mateus ! Thanks for this very interesting review 
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There may be altered joint arthrokinematics and other mechanical issue of an adjacent structure, which may contribute to lateral knee pain. So, what will be the best physiotherapy management?
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Hi Peter,
Very informative..... Thanks a lot.
Warm regards,
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As the patients do exercises,Can they use drugs less than other patients that they do not exercise???
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Physical exercises are necessary for the Rheumatoid patients as the joints remain flexible and soft tissues mobile. Despite this it will be better to do them when the inflammation is better (so better not during acute inflammatory phases where the patient will be benefitted by rest). Medication has to be monitored and controlled by having regular follow up reviews and the regime has to be changed accordingly.
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There are many suggestions to use hypnosis for pain management.  What are the best pain assessment/decision making steps to decide if hypnosis is the most appropriate for certain patients?
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Hi Gloria,
I enjoy using West Haven Yale Multidimensional Pain Inventory (WHYMPI) for measuring pain with my patients.  It classifies the pain intensity in a number of ways as well as pain affect and pain coping.  It is very commonly used in research and is also very useful clinically.  Its very useful for screening functional vs dysfunctional coping styles for referrals to psychological consults.  
I am very happy to answer your question about hypnotic assessment as well.  Many people assume that whatever method that they like to practice with patients is the best method to use with every patient.  This is a terrible assumption as we know from research that people vary wildly in terms of their experience of their mind body relationship.  About a good 15% of the population has a fairly impoverished experience of their mind/body relationship (classified as low hypnotizables) and it would be best to use biofeedback with them to begin clinical work.  These patients would also do poorly with medium level techniques like mindfulness meditation which requires a certain level of absorption potential.  
I recommend that you use the phenomenology of consciousness inventory to get a good picture of your patients' hypnotic (mind/body) abilities.  For example, that instrument can reveal that a patient is good with imagery although their sense of an altered state of consciousness is fairly impoverished.  Here is a paper that I wrote outlining my strategy to assessment in mind body medicine with hypnosis, biofeedback, meditation, and other methods such as yoga.  No one method is really good for every patient.  Assessment is necessary to figure out the right plan for each patient at their stage of development of their mind/body relationship.
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Cardiff university adult nursing student
interested if there is any welsh studies or policies regarding this topic.
In need of direction of the best way to direct my literature review.
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Excellent question!!  An article from one of the journals from AACN (Critical Care Nurse. 2013;33[3]:68-79), Stites, M, revealed that CPOT had a higher and more consistent inter rater reliability than the BPS, however dementia or chronic illness may effect the scoring.  The assessment of pain needs to be an effective culmination of the observational behavior of the patient, the self-report of the pain, the physical findings of the patient, as well as the situational background causing the patient's pain.  My suggestion is to start w/ this study and take note of all of the studies that are sited in this article--you will find that it is comprehensive.
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We have been using 45°C on our Columbus Instruments Hot/Cold Plate Analgesiometer with 3-6 month old Sprague-Dawley rats. Previously, this gave us a reliable baseline latency of 100-200 seconds before paw-licking. Recently, all the animals have started to respond below 100s, some of them dramatically below. Has anyone experienced this effect? Any ideas as to the cause?
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I assume you have made sure the hot plate is actually at 45 degrees and that there isnt an issue with the kit. 
There an numerous factors what can affect pain behaviour:
Firstly, have you changed supplier or have the supplier started sending you rats from a different colony? Are you certian they are sending SD rats? Has the constituents of the diet changed? (Seltzer et al saw a significant reduction in neuropathic pain behaviour when soy protein was added to their rat chow without them knowing). Have you changed experimenters, if not have you changed after shave or shampoo? Have there been any changed in animal care staff? Are there any works in the facility or in the surrounding buildings? Stress induced hyperalgesia is as real a problem as stress induced analgesia. The list could go on!
Another point is that over the years I've seen dramatic alteration of pain behaviour over the course of a year with a marked reduction over winter months. I've never had the resource to look into this effect methodically but I'm certain its not an artifact. 
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This is a preterm pain assessment scale.
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Hello,
I tried to look for, but I found only a manual about COMFORT Pain Scale
Ages Birth - Adult
I hope will be usefull.
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Hi All,
I observed this 55 yrs old male fell from a two level double decker bus over ten steps spiralling face foward.
His head and operated shoulder hit the steps and the handle bar and he was sent to ED in neck brace.
He had 2 weeks earlier underwent a Subacromial Decompression (SAD) with intra-operation of supraspinatus (SSP) tear repair.
The ED found during the right shoulder X-Ray, that there is subtle inferior subluxation of the right humeral head which may "suggest a small right shoulder joint effusion".
Except for head and body bumps, bruises and degenerative spine, hips, neck and age-old head involition, his right shoulder is more pronounced with pain.
Nothing was done to the body except given pain-killers and for the shoulder, the orthopedic surgeon sent his MO not to assess the pain but to STO only with no further instruction but to return in 6 months time for "pain assessment".
Question -
1) What is the likeable treatment given such scenario?
2) Is another shoulder repair required to normalise the ailing shoulder?
3) Else, what is the "gold standard" for the "small" right shoulder joint effusion treatment.
Appreciate any feedback - Thanks - Mariam
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Thanks Paritosh,
Now that the 6 weeks is up. The pain of falling from the double decker bus has taken its toll. The patient is given morphine every 2 hrs because the ssp pain is excruciating. Is it safe now to do another arthroscopy for SAD and remove the oedema as the MRI indicated the latter has spread to the deltoid region even with new ssp tendonis is found?
FYI passive ROM indicated the oedema is present and precluding the patient from performing active ROM. Tq.
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A 22 year old patient complains of left leg pain. It is on the medial aspect of her leg, mainly at the junction of the upper third and the lower two thirds of her leg. It has first occurred 2 years ago. This pain is recurrent. It occurs after walking long distances or running. It doesn't occur immediately, but several hours later (when she wakes up the next day). A stress fracture was suspected and an X-Ray was done. There were no findings. Pain is still present, its intensity varies. What could possibly cause this pain. 
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I Think that the pain could have origin by a compartimental sindrome or periostytis inserzionale of the tibial muscles 
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If there are any references you can provide, that would be appreciated.
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Hourly and again if there is a status change. I can look around for a source. Hth!
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I need to perform von Frey test on mice. I am going to use Chaplan's up-and-down method. But how long do I need to wait until I would be able to perform another trial, for example 24 hours later? Or the necessary interval between trials?
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I reckon that would depend on how long your experiment would be. If you need to measure only three time points after a treatment it would be ok to test them twice (morning and evening) on the first day and then 24 hrs later. However, if you are planning a longer experiment I would not recommend a daily testing schedule. Repeated testing (considering the long acclimatization time and testing time in mice) will cause stress and thus weight loss over time, which of course would be an animal welfare concern.
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Patients have several pain scores before and after medication treatment. Would like to apply a longitudinal or time series model to compare slopes before and after and evaluate the medication effect on pain reduction.  
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Hello David! I have another suggestion: the pain trajectory. This simple approach describes the pain of your patients with a regression line. 
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Do you use a standardized way to analyse and communicate the results? How?
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Thank you! Anyone use any kind of objective analysis method?
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I am in the state of Texas at an acute care hospital. Use or withholding pain medication occurs frequently. In extreme pain situations, pain medication is given and a next of kin is used for consent. If a tool like the HCAT were available, the patient could maintain control.  The use of HCAT would be allow us to treatment patients pain in a timely manner.
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Competency is only a consideration as it relates to the Informed Consent. Patient competency does not have any relationship to treatment regimen. Perhaps the wording of my question did not give you a clear picture.
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It is concerning this article: The Effects of a Co-Application of Menthol and Capsaicin on Nociceptive Behaviors of the Rat on the Operant Orofacial Pain Assessment Device (Anderson et al., 2014)
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Thank you both so much! This was hugely helpful.
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I am looking for Baby FACS coders to assist with a research project
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Thank you
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Hello!
What format video files are associated with the software you use?
I use Ethovision, but am looking to make a set of raw data files available for analysis by others and would like to make sure they are in a format which works for other analysis software such as JWatcher. 
If anyone could share their video file parameters, I would be very grateful e.g. minimum resolution, frame rate, file format, other file formats successfully used, and let me know what type of software they routinely use to analyse open field behaviour, I would very much appreciate it!
Thanks
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ethovision is very good software but we use panlab harvard apparatuse and it's very simple to use. don't worry about the video formats because you can converte all formats to each other by converter softwares without loosing quality. 
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The VAS was used to assess pain among a group of patients but a panelist strongly feels that the job was very poor, JUST BECAUSE the visual analogue scale (VAS) was used. Every other thing was okayed, from conception through methodology to presentation...BUT use of VAS for assessing pain was not acceptable to the panel, NO scientific backing was proffered anyway. There is need therefore to seek opinion of the science world on the VAS as an instrument for pain assessment.
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Pain is subjective and there is no fail safe method of assessing pain in patients. But additional parameters might be helpful. VAS alone does have it's limitations. The use of pain diagram, healthy related quality of life, and emotional aspects of the pain need to be assessed for better results I believe.
My thesis was on TMJ disorders. I used the pain scale (Numerical Rating Scale - NRS) which was part of the then RDC/TMD (it has now been revised into the new CDC/TMD) which includes screeners and pain diagrams.I also used Jaw function Limitation Scale along with Mandibular Function assessment.
You can consider a similar multiple assessment approach for more relevant answers.
http://www.ncbi.nlm.nih.gov/pubmed/21621130 This article might be helpful as well
And if you haven't read the discussion on similar topic already in researchgate. please do so here at: https://www.researchgate.net/post/Are_VAS_scales_appropriate_for_pain_measurement
Regards,
Dr. Akilesh R
India
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I want to know when, based on HIT-6 scores, a patient is clinically improving, e.g. pre- or post-treatment. I'm looking for specific data for tension-type (episodic) and cervicogenic headaches.
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We want to know if there is some kind of cut-off score that correlates with a minimal clinical improvement/deterioration. For instance a patient scores 74/78 on intake, during the intervention he scored a 62/78. How can this be interpreted? Can one say that he actually has a 'better' quality of life? 
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In a study of extra-intestinal symptoms in IBS patients we found that thigh pain, muscle and joint pain, and back pain are more frequent in IBS-C than IBS-D and IBS-M. What could be the underlying mechanism for such association?
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Well I have a very simple answer. They sit for hours on persian toilet, As you know this is very difficult and may impose lots of physical stress on thigh and back.
Best.
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An indirect evaluation of infants' acute pain can be given by using complicated pain scales, that use simultaneously several parameters. These scales have been criticised for their complexity but also for the scarce need of scoring pain during acute pain. In fact, pain scoring is useful during cronical pain, but in the case of acute pain such as during injections, tracheal aspirations, heel-pricks and so on, it has scarce utility. I argue that all these scales decontextualize pain, i.e. they  assess pain without any reference to the type of painful stimulation. I believe that it is sufficient to be aware of the risk of provoking pain with reference to the type of stymulus and to the part of the body (and its state) where it is apllied to, of course, avoid it. Do you want to be sure you are provoking pain? First, consider if you are touching an area with nociceptors; second, see if this provokes a sudden reaction: this is the clear signal of pain with no need of scales: there's no need for scoring pain after provoking it, because any pain provoked to a baby is always a failure. 
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I'm sure that chronic-pain scales are useful to score pain in order to modulate analgesics. While acute-pain scales have scarce utility. Thus, I suggest not to score acute pain but just to detect it (pain we provoke - at any score level - is always a failure). Detecting pain is easy: you just have to know if you are activating parts of the body with nociceptors and then to assess if a sudden reaction (crying or increase in heart rate) appears.
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I need Shneidman's psychological pain assessment scale. Where can I find it?
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Thank you very much.
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Can anybody help me with this question?
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Quizás puedas dividir la muestra y homogeneizar una parte en algún medio sin rojo fenol para la medición de NO?
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Least invasive pain route is well established in palliative medicine but IM injections are still common in acute managment. Specifically, I need to make a valid case to change practice of IM injections for immediate post-operative patients.
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As Mr. Enrique has suggested, severety of post operative pain can vary with the type of surgery (caesarean to open chest surgery, amputation or tumour removal. The mechanism of pain varies, the mode should vary and as Mr Borja suggested, multimodal and rotatory schedule with multiple agents suits peri and immediate post op. pain management (to manage inflammation, release of endotheins by tumour cells leading to pain, neuropathic pain etc.). As you suggested, the least invasive mode is intramuscular or oral, which works well with caesarean patients, and good old practice of acupuncture. This case needs a meta analysis on the use of oral or intramuscular route.
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In addition to the potential use of HRV from remote measurements, the inclusion of cessation of a behavior, such as tail wagging upon palpation of a surgical site, would likely provide increased sensitivity for our pain evaluations. After using the FDA accepted modified Glasgow scale for a post-op pain study, the need for pain scale refinement was noted.
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Sorry if this question was misleading. Pain scales were developed to determine if we have adequate analgesia on-board; i.e. are we sufficiently preventing pain. Since dogs can't talk, like infants, pain scales based on their behavior have been developed. The Glasgow pain scale, or a modification of that scale, is the most extensively used. It does not however, include that the cessation of a normal behavior may occur with pain. For example, if a dog is wagging its tail and it stops, this may indicate discomfort. This question was intended for veterinarians working in the field of analgesia and pain management in animals. We are working towards more comprehensive and objective ways to ensure that animals DON'T suffer.
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Nociception is known to cause pain in a wide range of situations. However, nociception itself is not sufficient nor necessary for a person to feel pain according to several researchers.
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@Bronnie
We are not in disagreement at all I think. I have never disputed, nor am I reluctant to integrate the psychosocial with the biological aspects of pain when discussing the theoretical aspects of pain. It is just that you and I probably see, in the main, the opposite ends of the spectrum While most of my patients have a "bio" component that predominates in terms of treatment needs and the psychosocial is along for the ride, I suspect you see the other end where the "bio" is so buried in the psychosocial dimension that the bio seems incapable of being teased out from the complexity of the florid chronic pain patient. I do see these patients too but less frequently. Even the most obvious 'bio' case - like a fracture or a wound carries with it the learned experiences and responses to past instances of pain woven into a behaviour pattern. This is why one patient with bones sticking out of the leg will grit his teeth and make humorous comments to the ambulance officers about how he will have to put off the Tongariro traverse until next month, while another will scream and cry, wail and moan as if he will be crippled and in pain forever. The injury is the same but the responses are different. The treatment - at least initially is not that different though - provide relief from nociceptive input, reduce the fracture, stabilize it and let nature do the physical healing. However, the different responses are cues to how pain relief and rehab should proceed. They are cues only however. I have seen the former patient become disabled and chronically painful because of poor management and interaction with the health care system despite the initial rather positive response type. Conversely I have seen the latter case calm down rapidly once pain is under control and proceed through rehab without a hitch despite the initial 'yellow flag' type of behavour initially.
My point here is that the clinician must be responsive to what is needed when it is needed, and not doctrinaire in either direction about what approach or mixtures of approach are needed, for it can and does change from patient to patient, and for any given patient throughout the process of acute presentation to rehabilitation.
Again, I reiterate, I have no quibble with your statement "..that psychological and social factors are present in all experiences of pain." Absolutely correct - we are not insects but perceptual / cognitive / emotional entities, enormously complex and individually unique. Nociception is a primitive sensory level data input and pain is the experience of, and the behaviour in response to, that sensory input. I think pain arising completely de novo is rather rare is it not?