Monday, September 30, 2019
Size does matter, but it isn't everything: the challenge of modest treatment effects in chronic pain clinical trials
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Thursday, September 26, 2019
[Perspectives] A last cup of tea
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Application of ICD‐11 among individuals with chronic pain: A post hoc analysis of the Stanford Self‐Management Program
Abstract
Background
Chronic primary pain (CPP) is one of seven diagnostic groups within the proposed classification of chronic pain in ICD‐11. Our aims were to apply the proposed ICD‐11 criteria in a large cohort of chronic pain patients participating in the Chronic Pain Self‐Management Program (CPSMP) and further investigate whether participants with CPP differed from participants with chronic secondary pain (CSP) regarding health, health expenditure, and the effect of participating in the CPSMP.
Methods
A secondary analysis of a randomized, controlled trial on the effect of the CPSMP. Four examiners categorized participants’ pain according to ICD‐11 using register‐based medical diagnoses and patients’ self‐reported symptoms. Afterwards, differences between CPP and CSP were examined.
Results
Out of 394 participants, 312 were successfully classified into CPP (n=164) or CSP (n=148) whereas 76 had a mixed pain condition. Participants with CPP were younger, more likely to be women, and had a longer pain duration compared to participants with CSP. Participants with CPP reported worse health‐related quality of life on the SF‐36 Mental Component Summary and subscales of vitality, social functioning, and bodily pain. Participants with CSP had more physical comorbidities and higher total health expenditure. None of the groups benefitted from the CPSMP.
Conclusions
We successfully applied the new classification of chronic pain in ICD‐11 on the basis of ICD‐10 medical diagnoses and symptom self‐report. Participants with CPP differed significantly from participants with CSP on baseline characteristics, self‐reported health measures, and total health expenditure. The CPSMP was not effective in any of the groups.
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Right posterior neck pain and swelling
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Wednesday, September 25, 2019
Effects of smoking on patients with chronic pain: a propensity-weighted analysis on the Collaborative Health Outcomes Information Registry
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Transcriptional profile of spinal dynorphin-lineage interneurons in the developing mouse
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Injustice Appraisal but not Pain Catastrophizing Mediates the Relationship Between Perceived Ethnic Discrimination and Depression and Disability in Low Back Pain
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The decline of endogenous pain modulation with aging: A meta-analysis of temporal summation and conditioned pain modulation
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Nociceptor Interleukin 33 Receptor/ST2 Signaling in Vibration-Induced Muscle Pain in the Rat
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Changes in Trunk and Pelvis Motion among Persons with Unilateral Lower Limb Loss during the First Year of Ambulation
Publication date: Available online 19 September 2019
Source: Archives of Physical Medicine and Rehabilitation
Author(s): Caitlin E. Mahon, Courtney M. Butowicz, Christopher L. Dearth, Brad D. Hendershot
Abstract
Objective
To retrospectively investigate trunk-pelvis kinematic outcomes among persons with unilateral transtibial and transfemoral limb loss with time from initial independent ambulation with a prosthesis, while secondarily describing self-reported presence and intensity of low back pain. Over time, increasing trunk-pelvis range of motion and decreasing trunk-pelvis coordination with increasing presence and/or intensity of low back pain were hypothesized. Additionally, less trunk-pelvis range of motion and more trunk-pelvis coordination for persons with more distal limb loss was hypothesized.
Design
Inception cohort with up to five repeated evaluations, including both biomechanical and subjective outcomes, during a one-year period (0, 2, 4, 6, and 12-months) after initial ambulation with a prosthesis.
Setting
Biomechanics laboratory within Military Treatment Facility.
Participants
Twenty-two males with unilateral transtibial limb loss and ten males with unilateral transfemoral limb loss.
Interventions
Not applicable
Main Outcome Measures
Tri-planar trunk-pelvis range of motion, and intersegmental coordination (continuous relative phase), obtained at self-selected (∼1.30m/s) and controlled (∼1.20m/s) walking velocities. Self-reported presence and intensity of low back pain.
Results
An interaction effect between time and group existed for sagittal (p=.039) and transverse (p=.009) continuous relative phase at self-selected walking velocity, and transverse trunk range of motion (p=.013) and sagittal continuous relative phase (p=.005) at controlled walking velocity. Trunk range of motion generally decreased and trunk-pelvis coordination generally increased with increasing time after initial ambulation. Sagittal trunk and pelvis ROM were always less and frontal trunk-pelvis coordination always greater for persons with more distal limb loss. Low back pain increased for persons with transtibial limb loss and decreased for persons with transfemoral limb loss following the 4-month timepoint.
Conclusions
Temporal changes (or lack thereof) in features of trunk-pelvis motions within the first year of ambulation help elucidate relationships between (biomechanical) risk factors for low back pain after limb loss.
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Acute and chronic pain in children and adolescents with cerebral palsy: prevalence, interference and management
Publication date: Available online 12 September 2019
Source: Archives of Physical Medicine and Rehabilitation
Author(s): Katarina Ostojic, Simon Paget, Maria Kyriagis, Angela Morrow
Abstract
Objective
To determine the prevalence, impact and management of acute and chronic pain amongst youth aged 5-18 years with cerebral palsy, attending outpatient rehabilitation services.
Design
A cross-sectional study using the Faces Pain Scale-Revised, Patient Reporting Outcomes Measurement Information System Pediatric Pain Interference Scale and Cerebral Palsy Quality of Life questionnaire. Where children were unable to self-report, parent/caregiver proxy was obtained.
Setting
Outpatient rehabilitation.
Participants
280 participants with cerebral palsy aged 5-18 years and/or their parent/caregiver. 45.7% (n=128) self-report and 54.3% (n=152) proxy-report.
Interventions
Not applicable.
Main outcome measure
Presence/absence of acute and chronic pain. Secondary measures were pain intensity, pain interference, pain management and quality of life.
Results
Acute pain and chronic pain were reported by 67.1% and 31.4% of participants respectively. Of those reporting acute pain, 42% also experienced chronic pain. Factors that increased the odds of chronic pain were: predominately dyskinesia (OR= 3.52; 95% CI: 1.64-7.55); mixed spasticity-dyskinesia (OR= 1.93; 95% CI: 1.07-3.47); bilateral involvement (OR= 3.22; 95% CI: 1.844-5.61) and GMFCS level IV (OR= 2.32; 95% CI: 1.02 – 5.25) and V (OR= 3.73; 95% CI: 1.70 – 8.20). Pain frequently interferes with sleep, attention, ability to have fun and quality of life. Short-acting pharmacological analgesics, thermotherapy, hydrotherapy and massage were commonly used for pain management.
Conclusions
Routine screening for pain is critical for early identification and intervention. Multimodal interventions are needed to address the biopsychosocial model of pain, and should be tailored for all abilities across the CP spectrum.
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Frequency of primary neck pain in mild traumatic brain injury/concussion patients
Publication date: Available online 4 September 2019
Source: Archives of Physical Medicine and Rehabilitation
Author(s): Jeffrey A. King, Michael A. McCrea, Lindsay D. Nelson
Abstract
Objectives
To determine (1) the frequency of neck pain overall and relative to other symptoms in patients presenting to a level I trauma center emergency department (ED) with mild traumatic brain injury (mTBI) and (2) the predictors of primary neck pain in this population.
Design
Cohort study.
Setting
Level I trauma center ED.
Participants
95 patients presenting to the ED with symptoms of mTBI having been exposed to an event that could have caused a mTBI.
Interventions
Not applicable.
Main outcome measures
Frequency of self-reported neck pain as measured by Sport Concussion Assessment Tool—3 (SCAT3) symptom questionnaire at <3, 8, 15, and 45 days post-injury. Primary neck pain defined in two ways (1) neck pain rated as equal or greater in severity than all other SCAT3 symptoms and (2) neck pain worse than all other symptoms.
Results
The frequency of any reported neck pain was 68.4%, 50.6%, 49%, and 41.9% within 72 hours and at 8, 15, and 45 days, respectively. Frequency of primary neck pain (equal or worse/worse definitions) was 35.8%/17.9%, 34.9%/14.5%, 37%/14.8% and 39.2%/10.8% across the four follow-up assessments. Participants who sustained their injuries in motor vehicle crashes had a higher rate of primary neck pain than those injured due to falls.
Conclusions
A sizable percentage of patients who present to level I trauma center EDs with mTBI report neck pain, which is commonly rated as similar to or worse than other mTBI-related symptoms. Primary neck pain is more common after motor vehicle crashes than falls. These findings support consensus statements identifying cervical injury as an important potential concurrent diagnosis in patients with mTBI.
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The Effectiveness of Instrument-Assisted Soft Tissue Mobilization in Athletes, Participants Without Extremity or Spinal Conditions, and Individuals with Upper Extremity, Lower Extremity, and Spinal Conditions: A Systematic Review
Publication date: September 2019
Source: Archives of Physical Medicine and Rehabilitation, Volume 100, Issue 9
Author(s): Goris Nazari, Pavlos Bobos, Joy C. MacDermid, Trevor Birmingham
Abstract
Objective
To assess the effectiveness of instrument-assisted soft tissue mobilization (IASTM) to other treatments or placebo in athletes or participants without extremity or spinal conditions and individuals with upper extremity, lower extremity, and spinal conditions.
Data Sources
The MEDLINE, EMBASE, CINAHL, and PEDro electronic databases were searched from January 1998 to March 2018.
Study Selection
Randomized controlled trials of participants without extremity or spinal conditions or athletes and people with upper extremity, lower extremity, or spinal conditions, who revived IASTM vs other active treatment, placebo, or control (no treatment), to improve outcome (function, pain, range of motion).
Data Extraction
Two independent review authors extracted data, assessed the trials for risk of bias using the Cochrane Risk of Bias tool in included studies, and performed the rating of quality of individual trials per outcome across trials was also performed using the Grading of Recommendations, Assessment, Development, and Evaluations guidelines.
Data Synthesis
Nine trials with 43 reported outcomes (function, pain, range of motion, grip strength), compared the addition of IASTM over other treatments vs other treatments. Six trials with 36 outcomes reported no clinically important differences in outcomes between the 2 groups. Two trials with 2 outcomes displayed clinically important differences favoring the other treatment (without IASTM) group. Six trials with 15 reported outcomes (pressure sensitivity, pain, range of motion, muscle performance), compared IASTM vs control (no treatment). Three trials with 5 outcomes reported no clinically important differences in outcomes between the 2 groups. Furthermore, in 1 trial with 5 outcomes, IASTM demonstrated small effects (standard mean difference range 0.03-0.24) in terms of improvement muscle performance in physically active individuals when compared to a no treatment group.
Conclusion
The current evidence does not support the use of IASTM to improve pain, function, or range of motion in individuals without extremity or spinal conditions or those with varied pathologies.
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Effectiveness of Botulinum Toxin Treatment for Upper Limb Spasticity Poststroke Over Different ICF Domains: A Systematic Review and Meta-Analysis
Publication date: September 2019
Source: Archives of Physical Medicine and Rehabilitation, Volume 100, Issue 9
Author(s): Aukje Andringa, Ingrid van de Port, Erwin van Wegen, Johannes Ket, Carel Meskers, Gert Kwakkel
Abstract
Objective
To provide a comprehensive overview of reported effects and scientific robustness of botulinum toxin (BoNT) treatment regarding the main clinical goals related to poststroke upper limb spasticity, using the International Classification of Functioning, Disability and Health.
Data Sources
Embase, PubMed, Wiley/Cochrane Library, and Ebsco/CINAHL were searched from inception up to May 16, 2018.
Study Selection
We included randomized controlled trials comparing upper limb BoNT injections with a control intervention in patients with a history of stroke. A total of 1212 unique records were screened by 2 independent reviewers. Forty trials were identified, including 2718 patients with history of stroke.
Data Extraction
Outcome data were pooled according to assessment timing (ie, 4-8wk and 12wk after injection), and categorized into 6 main clinical goals (ie, spasticity-related pain, involuntary movements, passive joint motion, care ability, arm and hand use, and standing and walking performance). Sensitivity analyses were performed for the influence of study and intervention characteristics, involvement of pharmaceutical industry, and publication bias.
Data Synthesis
Robust evidence is shown for the effectiveness of BoNT in reducing resistance to passive movement, as measured with the (Modified) Ashworth Score, and improving self-care ability for the affected hand and arm after intervention (P<.005) and at follow-up (P<.005). In addition, robust evidence is shown for the absence of effect on arm-hand capacity at follow-up. BoNT was found to significantly reduce involuntary movements, spasticity-related pain, and caregiver burden, and improve passive range of motion, while no evidence was found for arm and hand use after intervention.
Conclusions
In view of the robustness of current evidence, no further trials are needed to investigate BoNT for its favorable effects on resistance to passive movement of the spastic wrist and fingers, and on self-care. No trials are needed to further confirm the lack of effects of BoNT on arm-hand capacity, whereas additional trials are needed to establish the suggested favorable effects of BoNT on other body functions, which may result in clinically meaningful outcomes at activity and participation levels.
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A Randomized Controlled Trial on the Effects of Low-Dose Extracorporeal Shockwave Therapy in Patients With Knee Osteoarthritis
Publication date: September 2019
Source: Archives of Physical Medicine and Rehabilitation, Volume 100, Issue 9
Author(s): Zongye Zhong, Bangzhong Liu, Guanghua Liu, Jun Chen, Yun Li, Jianxin Chen, Xinxin Liu, Yiwen Hu
Abstract
Objective
To test the efficacy of low-dose extracorporeal shockwave therapy (ESWT) on osteoarthritis knee pain, lower limb function, and cartilage alteration for patients with knee osteoarthritis.
Design
Randomized controlled trial with placebo control.
Setting
Outpatient physical therapy clinics within a hospital network.
Participants
Eligible volunteers (N=63) with knee osteoarthritis (Kellgren-Lawrence grade II or III) were randomly assigned to 2 groups.
Interventions
Patients in the experimental group received low-dose ESWT for 4 weeks while those in the placebo group got sham shockwave therapy. Both groups maintained a usual level of home exercise.
Main Outcome Measures
Knee pain and physical function were measured using a visual analog scale (VAS), the Western Ontario and McMaster Universities Osteoarthritis Index (WOMAC), and the Lequesne index at baseline, 5 weeks, and 12 weeks. Cartilage alteration was measured analyzing the transverse relaxation time (T2) mapping.
Results
The VAS score, WOMAC, and Lequesne index of the ESWT group were significantly better than those of the placebo group at 5 and 12 weeks (P<.05). Both groups showed improvement in pain and disability scores over the 12-week follow-up period (P<.05). In terms of imaging results, there was no significant difference in T2 values between groups during the trial, although T2 values of the ESWT group at 12 weeks significantly increased compared to those at baseline (P=.004). The number and prevalence of adverse effects were similar between the 2 groups, and no serious side effects were found.
Conclusions
A 4-week treatment of low-dose ESWT was superior to placebo for pain easement and functional improvement in patients with mild to moderate knee osteoarthritis but had some negative effects on articular cartilage.
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Efficacy of Topical Vibratory Stimulation for Reducing Pain During Trigger Point Injection to the Gastrocnemius: A Randomized Controlled Trial
Publication date: September 2019
Source: Archives of Physical Medicine and Rehabilitation, Volume 100, Issue 9
Author(s): Young-Eun Moon, Sang-Hyun Kim, Hyun Seok, Seung Yeol Lee
Abstract
Objective
To evaluate the efficacy of topical vibratory stimulation for reducing pain during trigger point injection (TPI).
Design
Double-blind randomized placebo-controlled clinical trial.
Setting
Tertiary care university hospital.
Participants
A total of 136 participants were randomly recruited from among patients with myofascial pain syndrome who were scheduled for TPI. Of these, 65 were excluded because they met the exclusion criteria, and 11 because they refused to participate. Finally, 60 participants were enrolled. No participants dropped out of the study.
Intervention
Participants were randomly assigned to the vibration group or control group. TPI was performed with 0.5% lidocaine using a 25-gauge needle. A vibrator was applied to the popliteal fossa for 3 to 5 seconds prior to and during TPI to the gastrocnemius; 100-Hz vibration was turned on for the vibration group and turned off for the control group.
Main Outcome Measures
Pain intensity during TPI was assessed using a 100-mm visual analog scale (VAS) as a primary outcome, and participant satisfaction and preference for repeated use were measured using 5-point Likert scales as a secondary outcome. These parameters were evaluated immediately after TPI. The primary outcome was evaluated using analysis of covariance and secondary outcome using the Mann-Whitney U test.
Results
VAS scores for pain during TPI were significantly lower in the vibration group (30.30; 95% confidence interval [CI], 22.65-39.26) compared with the control group (47.58; 95% CI, 38.80-56.52; F=7.74; P< .01). The mean difference in VAS scores between the 2 groups was 17.27 (95% CI, 5.24-29.30). Participant satisfaction and preference for repeated use were significantly higher in the vibration group than in the control group (P<.05). No participant showed any side effects.
Conclusion
Topical vibratory stimulation significantly decreased pain during TPI of the gastrocnemius.
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Tuesday, September 24, 2019
High frequency medical cannabis use is associated with worse pain among individuals with chronic pain
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A Systematic Review on the Effects of Group Singing on Persistent Pain in People with Long‐term Health Conditions
Abstract
Background and Objectives
Singing can have a range of health benefits; this paper reviews evidence of the effects of group singing for chronic pain in people with long‐term health conditions.
Database and Data Treatment
We searched for published peer‐reviewed singing studies reporting pain measures (intensity, interference and depression) using major electronic databases (last search date 31/07/2018). After screening 123 full texts, 13 studies met the inclusion criteria: five RCTs, seven non‐RCTs and one qualitative study. Included studies were appraised using Downs and Black and CASP quality assessments.
Results
Included studies reported differences in the type of singing intervention, long‐term condition and pain measures. Due to the high heterogeneity, we conducted a narrative review. There is a positive trend of singing interventions reducing pain intensity, but more equivocal support for reductions in pain interference and depression. Additionally, qualitative data synthesis identified three key linked and complementary themes: physical, psychological and social benefits.
Conclusion
Group singing appears to have potential to reduce pain intensity, pain interference and depression; however, we conclude there is only partial support for singing on some pain outcomes based on the limited available evidence of varied quality. Given the positive findings of qualitative studies, this review recommends that practitioners are encouraged to continue this work. More studies of better quality are needed. Future studies should adopt more robust methodology and report their singing intervention in details. Group singing may be an effective and safe approach for reducing persistent pain and depression in people with long‐term health conditions.
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Friday, September 20, 2019
Changes in Trunk and Pelvis Motion among Persons with Unilateral Lower Limb Loss during the First Year of Ambulation
Publication date: Available online 19 September 2019
Source: Archives of Physical Medicine and Rehabilitation
Author(s): Caitlin E. Mahon, Courtney M. Butowicz, Christopher L. Dearth, Brad D. Hendershot
Abstract
Objective
To retrospectively investigate trunk-pelvis kinematic outcomes among persons with unilateral transtibial and transfemoral limb loss with time from initial independent ambulation with a prosthesis, while secondarily describing self-reported presence and intensity of low back pain. Over time, increasing trunk-pelvis range of motion and decreasing trunk-pelvis coordination with increasing presence and/or intensity of low back pain were hypothesized. Additionally, less trunk-pelvis range of motion and more trunk-pelvis coordination for persons with more distal limb loss was hypothesized.
Design
Inception cohort with up to five repeated evaluations, including both biomechanical and subjective outcomes, during a one-year period (0, 2, 4, 6, and 12-months) after initial ambulation with a prosthesis.
Setting
Biomechanics laboratory within Military Treatment Facility.
Participants
Twenty-two males with unilateral transtibial limb loss and ten males with unilateral transfemoral limb loss.
Interventions
Not applicable
Main Outcome Measures
Tri-planar trunk-pelvis range of motion, and intersegmental coordination (continuous relative phase), obtained at self-selected (∼1.30m/s) and controlled (∼1.20m/s) walking velocities. Self-reported presence and intensity of low back pain.
Results
An interaction effect between time and group existed for sagittal (p=.039) and transverse (p=.009) continuous relative phase at self-selected walking velocity, and transverse trunk range of motion (p=.013) and sagittal continuous relative phase (p=.005) at controlled walking velocity. Trunk range of motion generally decreased and trunk-pelvis coordination generally increased with increasing time after initial ambulation. Sagittal trunk and pelvis ROM were always less and frontal trunk-pelvis coordination always greater for persons with more distal limb loss. Low back pain increased for persons with transtibial limb loss and decreased for persons with transfemoral limb loss following the 4-month timepoint.
Conclusions
Temporal changes (or lack thereof) in features of trunk-pelvis motions within the first year of ambulation help elucidate relationships between (biomechanical) risk factors for low back pain after limb loss.
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Wednesday, September 18, 2019
Psychometric evaluation of the Optimal Screening for Prediction of Referral and Outcome Yellow Flag (OSPRO-YF) tool: factor structure, reliability, and validity
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Changes in pain-related fear and pain when avoidance behaviour is no longer effective
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Saturday, September 14, 2019
Linking non-restorative sleep and activity interference through pain catastrophizing and pain severity: An intra-day process model among individuals with fibromyalgia
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Observational pain assessment in older persons with dementia in four countries: observer agreement of items and factor structure of the Pain Assessment in Impaired Cognition
Abstract
Background
Recognition of pain in people with dementia is challenging. Observational scales have been developed, but there is a need to harmonise and improve the assessment process. In EU initiative COST‐Action TD1005, 36 promising items were selected from existing scales to be tested further. We aimed to study the observer agreement of each item, and to analyse the factor structure of the complete set.
Methods
190 older persons with dementia were recruited in four different countries (Italy, Serbia, Spain and The Netherlands) from different types of healthcare facilities. Patients represented a convenience sample, with no pre‐selection on presence of (suspected) pain. The Pain Assessment in Impaired Cognition (PAIC, research version) item pool includes facial expressions of pain (15 items), body movements (10 items), and vocalisations (11 items). Participants were observed by health professionals in two situations, at rest and during movement. Intrarater and interrater reliability was analysed by percentage agreement. The factor structure was examined with principal component analysis with orthogonal rotation.
Results
Health professionals performed observations in 40 to 57 patients in each country. Intrarater and interrater agreement was generally high (≥70%). However, for some facial expression items, agreement was sometimes below 70%. Factor analyses showed a 6‐component solution, which were named as follows: Vocal pain expression, Face anatomical descriptors, Protective body movements, Vocal defence, Tension, and Lack of affect.
Conclusions
Observation of PAIC items can be done reliably in healthcare settings. Observer agreement is quite promising already without extensive training.
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Friday, September 13, 2019
Incidence of shoulder pain in 40‐year‐olds and over and associated factors: a systematic review
Abstract
Background
Shoulder pain is one of the most frequent musculoskeletal complaints, and its prevalence and consequences increase with age. However, little is known about the incidence of shoulder pain among aging adults. We conducted this review to estimate the incidence of shoulder pain in ageing adults and its associated factors.
Databases And Data Treatment
We conducted a systematic review of cohort studies in which the incidence of shoulder pain and associated factors were explored in adults aged 40 years and over. PubMed, Embase, and Web of Science databases were consulted.
Results
We retrieved 3332 studies and included six, of which five were prospective cohort studies and one was retrospective. For adults aged 45–64 years, the annual cumulative incidence was 2.4%. The incidence density was estimated at 17.3 per 1,000 person‐years for adults in the 45–64 years age group, at 12.8 per 1000 person‐years for those in the 65–74 years group and at 6.7 per 1000 person‐years among those aged 75 years and over. Occupational factors, notably physical demands of work, were associated with the incidence of shoulder pain. Non‐occupational factors were also linked to the occurrence of shoulder pain.
Conclusion
Few studies have estimated the incidence of shoulder pain and associated factors among ageing adults. From this systematic review, we conclude that studies on the incidence of shoulder pain are scarce, and that both occupational and non‐occupational factors could be associated with the onset of shoulder pain among adults 40 years and over. This very limited evidence calls for more studies on this topic.
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Acute and chronic pain in children and adolescents with cerebral palsy: prevalence, interference and management
Publication date: Available online 12 September 2019
Source: Archives of Physical Medicine and Rehabilitation
Author(s): Katarina Ostojic, Simon Paget, Maria Kyriagis, Angela Morrow
Abstract
Objective
To determine the prevalence, impact and management of acute and chronic pain amongst youth aged 5-18 years with cerebral palsy, attending outpatient rehabilitation services.
Design
A cross-sectional study using the Faces Pain Scale-Revised, Patient Reporting Outcomes Measurement Information System Pediatric Pain Interference Scale and Cerebral Palsy Quality of Life questionnaire. Where children were unable to self-report, parent/caregiver proxy was obtained.
Setting
Outpatient rehabilitation.
Participants
280 participants with cerebral palsy aged 5-18 years and/or their parent/caregiver. 45.7% (n=128) self-report and 54.3% (n=152) proxy-report.
Interventions
Not applicable.
Main outcome measure
Presence/absence of acute and chronic pain. Secondary measures were pain intensity, pain interference, pain management and quality of life.
Results
Acute pain and chronic pain were reported by 67.1% and 31.4% of participants respectively. Of those reporting acute pain, 42% also experienced chronic pain. Factors that increased the odds of chronic pain were: predominately dyskinesia (OR= 3.52; 95% CI: 1.64-7.55); mixed spasticity-dyskinesia (OR= 1.93; 95% CI: 1.07-3.47); bilateral involvement (OR= 3.22; 95% CI: 1.844-5.61) and GMFCS level IV (OR= 2.32; 95% CI: 1.02 – 5.25) and V (OR= 3.73; 95% CI: 1.70 – 8.20). Pain frequently interferes with sleep, attention, ability to have fun and quality of life. Short-acting pharmacological analgesics, thermotherapy, hydrotherapy and massage were commonly used for pain management.
Conclusions
Routine screening for pain is critical for early identification and intervention. Multimodal interventions are needed to address the biopsychosocial model of pain, and should be tailored for all abilities across the CP spectrum.
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Acute and chronic pain in children and adolescents with cerebral palsy: prevalence, interference and management
Publication date: Available online 12 September 2019
Source: Archives of Physical Medicine and Rehabilitation
Author(s): Katarina Ostojic, Simon Paget, Maria Kyriagis, Angela Morrow
Abstract
Objective
To determine the prevalence, impact and management of acute and chronic pain amongst youth aged 5-18 years with cerebral palsy, attending outpatient rehabilitation services.
Design
A cross-sectional study using the Faces Pain Scale-Revised, Patient Reporting Outcomes Measurement Information System Pediatric Pain Interference Scale and Cerebral Palsy Quality of Life questionnaire. Where children were unable to self-report, parent/caregiver proxy was obtained.
Setting
Outpatient rehabilitation.
Participants
280 participants with cerebral palsy aged 5-18 years and/or their parent/caregiver. 45.7% (n=128) self-report and 54.3% (n=152) proxy-report.
Interventions
Not applicable.
Main outcome measure
Presence/absence of acute and chronic pain. Secondary measures were pain intensity, pain interference, pain management and quality of life.
Results
Acute pain and chronic pain were reported by 67.1% and 31.4% of participants respectively. Of those reporting acute pain, 42% also experienced chronic pain. Factors that increased the odds of chronic pain were: predominately dyskinesia (OR= 3.52; 95% CI: 1.64-7.55); mixed spasticity-dyskinesia (OR= 1.93; 95% CI: 1.07-3.47); bilateral involvement (OR= 3.22; 95% CI: 1.844-5.61) and GMFCS level IV (OR= 2.32; 95% CI: 1.02 – 5.25) and V (OR= 3.73; 95% CI: 1.70 – 8.20). Pain frequently interferes with sleep, attention, ability to have fun and quality of life. Short-acting pharmacological analgesics, thermotherapy, hydrotherapy and massage were commonly used for pain management.
Conclusions
Routine screening for pain is critical for early identification and intervention. Multimodal interventions are needed to address the biopsychosocial model of pain, and should be tailored for all abilities across the CP spectrum.
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Acute and chronic pain in children and adolescents with cerebral palsy: prevalence, interference and management
Publication date: Available online 12 September 2019
Source: Archives of Physical Medicine and Rehabilitation
Author(s): Katarina Ostojic, Simon Paget, Maria Kyriagis, Angela Morrow
Abstract
Objective
To determine the prevalence, impact and management of acute and chronic pain amongst youth aged 5-18 years with cerebral palsy, attending outpatient rehabilitation services.
Design
A cross-sectional study using the Faces Pain Scale-Revised, Patient Reporting Outcomes Measurement Information System Pediatric Pain Interference Scale and Cerebral Palsy Quality of Life questionnaire. Where children were unable to self-report, parent/caregiver proxy was obtained.
Setting
Outpatient rehabilitation.
Participants
280 participants with cerebral palsy aged 5-18 years and/or their parent/caregiver. 45.7% (n=128) self-report and 54.3% (n=152) proxy-report.
Interventions
Not applicable.
Main outcome measure
Presence/absence of acute and chronic pain. Secondary measures were pain intensity, pain interference, pain management and quality of life.
Results
Acute pain and chronic pain were reported by 67.1% and 31.4% of participants respectively. Of those reporting acute pain, 42% also experienced chronic pain. Factors that increased the odds of chronic pain were: predominately dyskinesia (OR= 3.52; 95% CI: 1.64-7.55); mixed spasticity-dyskinesia (OR= 1.93; 95% CI: 1.07-3.47); bilateral involvement (OR= 3.22; 95% CI: 1.844-5.61) and GMFCS level IV (OR= 2.32; 95% CI: 1.02 – 5.25) and V (OR= 3.73; 95% CI: 1.70 – 8.20). Pain frequently interferes with sleep, attention, ability to have fun and quality of life. Short-acting pharmacological analgesics, thermotherapy, hydrotherapy and massage were commonly used for pain management.
Conclusions
Routine screening for pain is critical for early identification and intervention. Multimodal interventions are needed to address the biopsychosocial model of pain, and should be tailored for all abilities across the CP spectrum.
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Thursday, September 12, 2019
[Perspectives] The pain and glory of ageing
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Spinal DN-9, a peptidic multifunctional opioid/neuropeptide FF agonist produced potent nontolerance forming analgesia with limited side effects
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Profiling Modifiable Psychosocial Factors among Children with Chronic Pain: A Person-Centered Methodology
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Evaluating the effects of acupuncture using a dental pain model in healthy subjects – a randomized, cross-over trial
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Wednesday, September 11, 2019
Pain acceptance in people with chronic pain and spinal cord injury: Daily fluctuation and impacts on physical and psychosocial functioning
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Predictors of Functional Outcome in Musculoskeletal Healthcare: An Umbrella Review
Abstract
Background
Multiple cohort and systematic review studies exist, reporting independent predictive factors associated with outcome in musculoskeletal populations. These studies have found evidence for a number of ‘generic' factors that have been shown to predict outcome across musculoskeletal patient cohorts. This review provides a higher level review of the evidence with a focus on generic patient factors associated with functional musculoskeletal outcome with a view to informing predictive modelling.
Objectives
a) Identify patient factors found to have evidence to support their association with functional outcome, and b) review these findings across body areas/conditions to identify generic predictive factors.
Databases and Data Treatment: Electronic databases of MEDLINE, AMED, EMBASE, CINAHL and Cochrane were searched for eligible studies. Two reviewers independently extracted data and assessed quality using an established checklist for umbrella reviews.
Results
Twenty one systematic reviews met inclusion criteria, all were of moderate/high quality. Six independent predictors were found to have strong evidence of association with worse musculoskeletal functional outcome across anatomical body sites (worse baseline function, higher symptom/pain severity, worse mental wellbeing, more comorbidities, older age and higher body mass index). Longer duration of symptoms, worse pain coping, presence of workers compensation, lower vitality and lower education were also found to have moderate evidence of association with worse functional outcome across body sites.
Conclusions
This study identifies a number of factors associated with musculoskeletal functional outcome. The generic predictive factors identified should be considered for inclusion into musculoskeletal prognostic models, including models used for case‐mix‐adjustment of patient reported outcome measure data.
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Treading the tightrope of opioid restrictions
Nature, Published online: 11 September 2019; doi:10.1038/d41586-019-02687-1
US efforts to control opioid prescriptions are having unintended effects on people with chronic pain.from Nature - Issue - nature.com science feeds https://ift.tt/34CkDca
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Operating without opioids
Nature, Published online: 11 September 2019; doi:10.1038/d41586-019-02685-3
The opioid crisis is driving a rethink of pain relief in surgery.from Nature - Issue - nature.com science feeds https://ift.tt/34DetbA
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The painful truth about pain
Nature, Published online: 11 September 2019; doi:10.1038/d41586-019-02688-0
A harrowing medical experience gave Travis N. Rieder more insight than he would have wished for into how people end up hooked on opioids.from Nature - Issue - nature.com science feeds https://ift.tt/304CsNr
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Analgesia without opioids
Nature, Published online: 11 September 2019; doi:10.1038/d41586-019-02683-5
Fresh strategies and targets for chronic pain could deliver much needed replacements for opioid-based painkillers.from Nature - Issue - nature.com science feeds https://ift.tt/34DepZo
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Tuesday, September 10, 2019
Sex Differences in Rat Intervertebral Disc Structure and Function Following Annular Puncture Injury
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Preoperative Chronic Opioid Therapy Negatively Impacts Long-term Outcomes Following Cervical Fusion Surgery
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Non-mobile Adjacent Level Cervical Spondylolisthesis Does Not Always Require Fusion in Patients Undergoing ACDF
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Geography of Lumbar Paravertebral Muscle Fatty Infiltration: The Influence of Demographics, Low Back Pain, and Disability
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Cross-cultural Adaptation and Validation of the Hausa Version of the Oswestry Disability Index 2.1a for Patients With Low Back Pain
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The Association Between Patient Reported Outcomes of Spinal Surgery and Societal Costs: A Register Based Study
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Intrusive imagery associated with pain
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Monday, September 9, 2019
Technical and clinical performance of the thermo‐test device “Q‐Sense” to assess small fibre function: A head‐to‐head comparison with the “Thermal Sensory Analyzer” TSA in diabetic patients and healthy volunteers
Abstract
Background
Thermo‐test devices are rarely used outside specialized pain centres because of high acquisition costs. Recently, a new, portable device (“Q‐Sense”) was introduced, which is less expensive but has reduced cooling capacity (20°C). We assessed the reliability/validity of the “Q‐Sense” by comparing it with the Thermal Sensory Analyzer (TSA).
Methods
Using a phantom‐skin model, the physical characteristics of both devices were compared. The clinical performance was assessed in a multicentre study by performing Quantitative Sensory Testing (QST) in 121 healthy volunteers and 83 diabetic patients (Eudra‐Med‐No. CIV‐12‐05‐006501).
Results
Both device types showed ~40% slower temperature ramps for heating/cooling than nominal data. Cold/warm detection thresholds (CDT, WDT) and heat pain thresholds (HPT) of healthy subjects did not differ between device types. Cold pain thresholds (CPT) were biased for Q‐Sense by a floor effect (p < .001). According to intraclass correlation coefficients (ICC), agreement between TSA and Q‐Sense was good/excellent for CDT (ICC = 0.894) and WDT (ICC = 0.898), moderate for HPT (ICC = 0.525) and poor for CPT (ICC = 0.305). In diabetic patients, the sensitivity of Q‐Sense to detect cold hypoesthesia was reduced in males >60 years. Moderate correlations between thermal detection thresholds and morphological data from skin biopsies (n = 51) were similar for both devices.
Conclusions
Physical characteristics of both thermo‐test devices are similarly limited by the poor temperature conduction of the skin. The Q‐Sense is useful for thermal detection thresholds but of limited use for pain thresholds. For full clinical use, the lower cut‐off temperature should be set to ≤18°C.
Significance
High purchase costs prevent a widespread use of thermo‐test devices for diagnosing small fibre neuropathy. The air‐cooled “Q‐Sense” could be a lower cost alternative, but its technical/clinical performance needs to be assessed because of its restricted cut‐off for cooling (20°C). This study provides critical information on the physical characteristics and the clinical validity/reliability of the Q‐Sense compared to the “Thermal Sensory Analyzer” (TSA). We recommend lowering the cut‐off value of the Q‐Sense to ≤18°C for its full clinical use.
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Botulinum toxin type A for painful temporomandibular disorders: systematic review and meta-analysis
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A neuronal circuit for activating descending modulation of neuropathic pain
Nature Neuroscience, Published online: 09 September 2019; doi:10.1038/s41593-019-0481-5
Huang and colleagues functionally map a brain circuit connecting the amygdala and the spinal cord that is altered after nerve injury and contributes to chronic pain.from Nature Neuroscience - Issue - nature.com science feeds https://ift.tt/2N56heL
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Sunday, September 8, 2019
The COX‐2 inhibitor etoricoxib reduces experimental osteoarthritis and nociception in rats: The roles of TGF‐β1 and NGF expressions in chondrocytes
Abstract
Background
Osteoarthritis (OA) is the most common joint disease, especially affecting the knee joint. Etoricoxib, a highly selective cyclooxygenase (COX)‐2 inhibitor which can reduce postoperative pain after orthopedic surgery. The aim of this study was to investigate the effects of oral etoricoxib on the development of OA and to examine concomitant changes in the nociceptive behavior of rats.
Method
OA was induced in wistar rats by anterior cruciate ligament transection (ACLT) of the right knee. The ACLT + etoricoxib groups received 6.7 or 33.3 mg/kg of oral etoricoxib three times a week for 12 consecutive weeks, starting at week 8 after ACLT. Nociceptive behaviors and changes in knee joint width during OA development were analyzed. Histopathological studies were then performed on the cartilage. Immunohistochemical analysis was performed to examine the effect of etoricoxib on the expression of transforming growth factor‐beta (TGF‐β) and nerve growth factor (NGF) in articular cartilage chondrocytes.
Results
OA rats receiving etoricoxib showed a significantly lower degree of cartilage degeneration than the rats receiving placebo. Nociceptive behavior studies showed significant improvement in the ACLT + etoricoxib groups compared to that in the ACLT group. Moreover, etoricoxib attenuated NGF expression, but increased TGF‐β expression, in OA‐affected cartilage.
Conclusions
Oral etoricoxib in a rat OA model (1) attenuates the development of OA, (2) concomitantly reduces nociception, and (3) modulates chondrocyte metabolism, possibly by inhibiting NGF expression and increasing TGF‐β expression.
This article is protected by copyright. All rights reserved.
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Metacognition, perseverative thinking, and pain catastrophizing: a moderated‐mediation analysis
Abstract
Background
Pain catastrophizing is linked to a range of negative health and treatment outcomes, although debate continues about how best to define and treat it, since most interventions produce only modest benefit. This study aimed to contribute to theory‐driven development of these treatments by exploring the role of perseverative thinking in pain catastrophizing, along with the higher order beliefs, called metacognitions, that might shape it.
Methods
An internet sample of 510 people with chronic pain (≥3 months), who mostly (54.9%) had clinical levels of catastrophizing, completed self‐report measures of pain intensity, disability, perseverative thinking, pain catastrophizing, depression, anxiety, and pain metacognition. Regression‐based moderated mediation analysis tested the conditional indirect effect of pain intensity on pain catastrophizing via perseverative thinking at varying levels of unhelpful pain metacognition.
Results
Perseverative thinking partially mediated the effect of pain intensity on pain catastrophizing, accounting for 20% of the total effect. This indirect effect was conditional on both positive and negative metacognition. Higher levels of both forms of unhelpful metacognition strengthened the indirect effect, which was not significant below the 50th percentile for positive metacognitions or below the 60th percentile for negative metacognitions.
Conclusions
Strongly believing that thinking about pain helps you solve problems or cope with pain (positive metacognition), or that it is harmful and uncontrollable (negative metacognition), can increase the amount you worry or ruminate as pain increases. This is associated with increased pain catastrophizing. Identifying and modifying these unhelpful pain metacognitions may improve treatments for pain catastrophizing and thereby chronic pain generally.
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Friday, September 6, 2019
“Some exercise is good, more is better,” say medical chiefs in new guidance
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Thursday, September 5, 2019
The Pain Assessment in Impaired Cognition scale (PAIC15): a multidisciplinary and international approach to develop and test a meta‐tool for pain assessment in impaired cognition, especially dementia
Abstract
Background
Over the last decades, a considerable number of observational scales have been developed to assess pain in persons with dementia. The time seems ripe now to build on the knowledge and expertise implemented in these scales to form an improved, “best‐of” meta‐tool. The EU‐COST initiative “Pain in impaired cognition, especially dementia” aimed to do this by selecting items out of existing observational scales and critically re‐assessing their suitability to detect pain in dementia. This paper reports on the final phase of this collaborative task.
Methods
Items from existing observational pain scales were tested for “frequency of occurrence (item difficulty)”, “reliability”, and “validity”. This psychometric testing was carried out in eight countries, in different healthcare settings, and included clinical as well as experimental pain conditions.
Results
Across all studies, 587 persons with dementia, 27 individuals with intellectual disability, 12 Huntington's disease patients, and 59 cognitively healthy controls were observed during rest and movement situations or while receiving experimental pressure pain, respectively. The psychometric outcomes for each item across the different studies were evaluated within an international and multidisciplinary team of experts and led a final selection of 15 items (5x facial expressions, 5x body movements, 5x vocalizations).
Conclusions
The final list of 15 observational items have demonstrated psychometric quality and clinical usefulness both in their former scales and in the present international evaluation; accordingly, they qualified twice to form a new internationally agreed‐on meta‐tool for Pain Assessment in Impaired Cognition, the PAIC‐15 scale.
This article is protected by copyright. All rights reserved.
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How and for whom does a positive affect intervention work in fibromyalgia: An analysis of mediators and moderators
Abstract
Objectives
Psychological interventions designed to enhance positive affect are promising ways to promote adaptive functioning in people with chronic pain. However, few studies have addressed the efficacy of positive affect interventions in chronic pain populations and examined which patients can benefit more from them. The aim of the present study was to identify mediators and moderators of the best possible self intervention (BPS) in fibromyalgia patients.
Methods
We used data from a previous randomized controlled trial that examined changes in pain interference, depression, self‐efficacy, and quality of life after the BPS intervention.
Results
Mediation analyses showed that depression mediated changes in pain interference. Positive and negative affect were significant mediators of the change in depression and quality of life. No significant mediators of the change in self‐efficacy were found. Baseline levels of quality of life, emotion regulation strategies of negative and positive affect, and rumination moderated the effects of the intervention on depressive symptomatology.
Discussion
In fibromyalgia patients, the effects of the BPS on the outcomes seem to be more related to changes in affect than to changes in future expectations.
Significance
This is the first study to present evidence about who can benefit from an intervention designed to augment positive affect and promote positive functioning in FMS patients and how these changes occur. It extends previous findings on patient characteristics associated with the response to pain management interventions.
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Change in Fatigue in Acceptance and Commitment Therapy‐Based Treatment for Chronic Pain and Its Association with Enhanced Psychological Flexibility
Abstract
Fatigue is commonly reported by people with chronic pain. The purpose of the current study was to examine Acceptance and Commitment Therapy (ACT), based on the Psychological Flexibility (PF) model, for fatigue in chronic pain. This study included 354 adults attending an interdisciplinary ACT‐oriented treatment for chronic pain. T‐tests and analyses of clinically meaningful change were used to investigate participant improvements in fatigue interference after the treatment. Pearson's correlations and hierarchical regressions were conducted to investigate associations between improvement in fatigue interference and improvements in PF processes. Finally, mixed effects models were used to explore associations between baseline fatigue interference and changes in treatment outcome measures. Participants improved in fatigue interference (d=.37), pain, some PF processes, and daily functioning (d=.18‐1.08). 39.7% of participants demonstrated clinically meaningfully improvements in fatigue interference. Changes in fatigue interference was associated with changes in pain, PF processes and daily functioning, |r|= .20‐.46. Change in fatigue interference was associated with change in pain acceptance independent of change in pain, β=‐.36, p<.001. However, baseline fatigue interference did not predict any treatment outcome. Overall, people with fatigue appeared to benefit from the ACT‐oriented interdisciplinary treatment for chronic pain, and relatively higher levels of fatigue did not appear to impede this benefit. ACT‐based treatments may benefit people with chronic pain and fatigue. Future studies including experimental designs, and studies investigating other PF processes, are needed to better understand the utility of ACT for co‐morbid fatigue and pain.
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Calcium channel α2δ1 subunit mediates secondary orofacial hyperalgesia through PKC-TRPA1/gap junction signaling
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Effects of oxytocin on placebo and nocebo effects in a pain conditioning paradigm: a randomized controlled trial.
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Pain, physical and psychosocial functioning in adolescents at-risk for developing chronic pain: A longitudinal case-control study
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Therapy Habituation at 12 Months: Spinal Cord Stimulation Versus Dorsal Root Ganglion Stimulation for Complex Regional Pain Syndrome Type I and II
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Frequency of primary neck pain in mild traumatic brain injury/concussion patients
Publication date: Available online 4 September 2019
Source: Archives of Physical Medicine and Rehabilitation
Author(s): Jeffrey A. King, Michael A. McCrea, Lindsay D. Nelson
Abstract
Objectives
To determine (1) the frequency of neck pain overall and relative to other symptoms in patients presenting to a level I trauma center emergency department (ED) with mild traumatic brain injury (mTBI) and (2) the predictors of primary neck pain in this population.
Design
Cohort study.
Setting
Level I trauma center ED.
Participants
95 patients presenting to the ED with symptoms of mTBI having been exposed to an event that could have caused a mTBI.
Interventions
Not applicable.
Main outcome measures
Frequency of self-reported neck pain as measured by Sport Concussion Assessment Tool—3 (SCAT3) symptom questionnaire at <3, 8, 15, and 45 days post-injury. Primary neck pain defined in two ways (1) neck pain rated as equal or greater in severity than all other SCAT3 symptoms and (2) neck pain worse than all other symptoms.
Results
The frequency of any reported neck pain was 68.4%, 50.6%, 49%, and 41.9% within 72 hours and at 8, 15, and 45 days, respectively. Frequency of primary neck pain (equal or worse/worse definitions) was 35.8%/17.9%, 34.9%/14.5%, 37%/14.8% and 39.2%/10.8% across the four follow-up assessments. Participants who sustained their injuries in motor vehicle crashes had a higher rate of primary neck pain than those injured due to falls.
Conclusions
A sizable percentage of patients who present to level I trauma center EDs with mTBI report neck pain, which is commonly rated as similar to or worse than other mTBI-related symptoms. Primary neck pain is more common after motor vehicle crashes than falls. These findings support consensus statements identifying cervical injury as an important potential concurrent diagnosis in patients with mTBI.
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Wednesday, September 4, 2019
AAAPT Diagnostic Criteria for Acute Pain Following Breast Surgery
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Mechanisms of below-level pain following spinal cord injury (SCI)
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Monday, September 2, 2019
Preferred self-administered questionnaires to assess depression, anxiety and somatization in people with musculoskeletal pain – A modified Delphi study
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