Title: Activity pacing, avoidance, endurance, and associations with patient functioning in chronic pain: a systematic review and meta-analysis.
Author: Andrews NE, Strong J, Meredith PJ.
Affiliation: Division of Occupational Therapy, School of Health and Rehabilitation Sciences, The University of Queensland, St Lucia, Queensland, Australia. [email protected]
Journal: Archives of Physical Medicine and Rehabilitation
Citation: 2012 Nov;93(11):2109-2121.e7. doi: 10.1016/j.apmr.2012.05.029
Publication Year and Month: 2012 11

Abstract: OBJECTIVE:
To systematically review the associations between different approaches to activity (ie, activity pacing, avoidance, or endurance) and indicators of patient functioning in chronic pain samples.

DATA SOURCES:
A key word search was conducted in PsycINFO, MEDLINE via Ovid, EMBASE, and PubMed up to March 2011.

STUDY SELECTION:
To be included, studies had to (1) be written in English, (2) report on an adult chronic pain sample, and (3) report a correlation coefficient between at least 1 measure of 1 of the 3 "approach to activity" variables and an indicator of patient functioning.

DATA EXTRACTION:
Two reviewers independently screened abstracts and full-text articles for eligibility and extracted the data. Results of correlation analyses were grouped on the basis of measure of approach to activity (pacing/avoidance/endurance) and the criterion variable measured (pain/physical functioning/psychological functioning), resulting in 9 categories. Random-effects modeling was then used to pool data across studies in each category.

DATA SYNTHESIS:
Forty-one studies were eligible for inclusion. Results demonstrated that avoidance of activity was consistently associated with more pain, poorer psychological functioning, and more physical disability. While enduring with activity was associated with enhanced physical and psychological functioning, these relationships appeared to be dependent on the measure used, with measures more reflective of persisting with activities to the point of severe pain aggravation (overactivity) linked to poorer outcomes. Pacing was generally linked to better psychological functioning but more pain and disability.

Conclusions: Although causation cannot be determined, results of this study suggest that both avoidance of activity and overactivity are associated with poorer patient outcomes. Unexpected results relating to pacing may reflect either the ineffectiveness of pacing if not used to gradually increase an individual's activity level or the notion that individuals with better psychological functioning but more pain and disability are more inclined to pace activity.

Outcome of Research: More research required

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Title: Fibromyalgia Is Common in a Postpoliomyelitis Clinic
Author: D A Trojan (1), N R Cashman
Affiliation: (1) Department of Neurology, Montreal Neurological Institute and Hospital, McGill University, Quebec.
Journal: Archives of Neurology
Citation: Trojan DA, Cashman NR. Fibromyalgia is common in a postpoliomyelitis clinic. Arch Neurol. 1995 Jun;52(6):620-4. doi: 10.1001/archneur.1995.00540300094019. PMID: 7763212.
Publication Year and Month: 1995 06

Abstract: Objective: To determine prospectively the occurrence and clinical characteristics of fibromyalgia in patients serially presenting to a postpolio clinic. Fibromyalgia may mimic some of the symptoms of postpoliomyelitis syndrome, a disorder characterized by new weakness, fatigue, and pain decades after paralytic poliomyelitis.

Design: Case series.

Setting: A university-affiliated hospital clinic.

Patients: One hundred five patients were evaluated with a standardized history and physical examination during an 18-month period. Ten patients were excluded because of the absence of past paralytic poliomyelitis.

Interventions: Patients with fibromyalgia were treated with low-dose, nighttime amitriptyline hydrochloride or other conservative measures.

Main Outcome Measures: Patients with fibromyalgia had diffuse pain and 11 or more of 18 specific tender points on examination (American College of Rheumatology criteria, 1990). Patients with borderline fibromyalgia had muscle pain and five to 10 tender points on physical examination.

Results: Ten (10.5%) of 95 postpolio patients met the criteria for fibromyalgia, and another 10 patients had borderline fibromyalgia. All patients with fibromyalgia complained of new weakness, fatigue, and pain. Patients with fibromyalgia were more likely than patients without fibromylagia to be female (80% vs 40%, P<.04) and to complain of generalized fatigue (100% vs 71%, P=.057), but were not distinguishable in terms of age at presentation to clinic, age at polio, length of time since polio, physical activity, weakness at polio, motor strength scores on examination, and the presence of new weakness, muscle fatigue, or joint pain. Approximately 50% of patients in both the fibromyalgia and borderline fibromyalgia groups responded to low-dose, nighttime amitriptyline therapy.

Conclusions: Conclusions: (1) Fibromyalgia occurs frequently in a postpolio clinic. (2) Fibromyalgia can mimic some symptoms of postpoliomyelitis syndrome. (3) Fibromyalgia in postpolio patients can respond to specific treatment.

Outcome of Research: Not applicable

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Title: Pain in Post-Polio Syndrome: A separate pain entity?
Author: Evert Christiaan Boshuis, MD (1), Eva Melin, MD, PhD (2) and Kristian Borg, MD, PhD (2)
Affiliation: (1) Department of Psychiatry, Onze Lieve Vrouwe Gasthuis, Amsterdam, The Netherlands

(2) Division of Rehabilitation Medicine, Department of Clinical Sciences, Danderyd Hospital, Karolinska Institutet, Stockholm, Sweden
Journal: Journal of Rehabilitation Medicine (JRM) - formerly Scandanavian Journal of Rehabilitation Medicine
Citation: Clinical Communications, 5, jrmcc00077.
DOI: https://doi.org/10.2340/20030711-1000077
Publication Year and Month: 2022 01

Abstract: Background: Most patients with polio recover from the initial infection, but develop muscle weakness, pain and fatigue after 15–40 years, a condition called post-polio syndrome. Although poliovirus has been almost eliminated, 12–20 million people worldwide still have polio sequelae. The pain is described mainly as nociceptive, but some patients experience neuropathic pain. The aim of this study was to further characterize post-polio pain.

Patients and methods: A total of 20 patients with post-polio syndrome participated in the study. Physical examination was performed, and questionnaires containing pain drawing and visual analogue scales (VAS) for pain intensity during rest and motion and VAS for fatigue were completed. A walk test was performed to evaluate physical performance.

Results: Pain intensity was high (42/100 on the VAS at rest and 62/100 while moving). The pain was localized in both joints and muscles. Pain in the muscles was of “deep aching” character, included “muscle cramps” and was located mainly in polio-weakened limbs.

Conclusion: Muscle pain in patients with post-polio syndrome does not fulfil the criteria for either nociceptive or neuropathic pain; thus, it is suggested that the pain is termed “post-polio muscular pain”. The intensity of post-polio muscular pain is higher while moving, but does not influence physical function, and is separate from fatigue.


LAY ABSTRACT
Most polio patients recover from the initial infection, but develop muscle weakness, pain and fatigue after 15–40 years, a condition called Post-Polio Syndrome. Though the poliovirus has almost been eliminated, 12-20 million people worldwide still have polio-equelae. The pain is mainly described as nociceptive, but some patients experience neuropathic pain. This study was undertaken to further characterize post-polio pain. We examined 20 Post-polio patients and found that the pain was localised in both joints and muscles. The pain in the muscles was of ‘deep aching’ character, included ‘muscle cramps’ and was mainly located in polio-weakened limbs. The intensity of the pain is higher while moving but does not influence the physical function. To know more about the characteristics of the pain perceived gives better possibilities for treatment and rehabilitation

Conclusions: In conclusion, pain in PPS is mostly of deep aching character and muscle cramps, localized in the polio-weakened limb. This type of pain seems to be specific to PPS. It is suggested that this pain is termed post-polio muscular pain (PPMP). Future studies should aim to characterize PPMP and to analyse the influence of motor and sensory dysfunction on the pain.

Outcome of Research: More research required

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Title: Modeling subjective well-being in individuals with chronic pain and a physical disability: the role of pain control and pain catastrophizing.
Author: Furrer, A., Michel, G., Terrill, A.L., Jensen, M.P., Müller, R.
Affiliation: Nil
Journal: Disability and Rehabilitation
Citation: Furrer, A., Michel, G., Terrill, A.L., Jensen, M.P., Müller, R. (2017) Modeling subjective well-being in individuals with chronic pain and a physical disability: the role of pain control and pain catastrophizing. Disability and Rehabilitation 23:1-10 doi: 10.1080/09638288.2017.1390614. [Epub ahead of print]
Publication Year and Month: 2017 10

Abstract: PURPOSE:
To investigate the associations between subjective well-being and pain intensity, pain interference, and depression in individuals with physical disabilities. We hypothesized that (1) pain control and (2) pain catastrophizing mediate the effects of subjective well-being on pain intensity, pain interference, and depression.

METHODS:
Analyses of cross-sectional data from 96 individuals diagnosed with spinal cord injury, multiple sclerosis, neuromuscular disease, or post-polio syndrome, with average pain intensity of ≥4 (0-10) on at least half the days in the past month. Two models tested study hypotheses using structural equation.

RESULTS:
Both models showed acceptable model fit. Pain catastrophizing significantly mediated the effect of subjective well-being on pain intensity and pain interference, but not on depression. Pain control did not significantly mediate the effect of subjective well-being on pain intensity, pain interference, or depression. Path coefficients showed significant direct effects of subjective well-being on pain control (β = 0.39), pain catastrophizing (β = -0.61), pain interference (β = -0.48; -0.42), and depression (β = -0.75; -0.78).

CONCLUSIONS:
This study supports the potential of enhancing subjective well-being and lowering pain catastrophizing for reducing pain intensity, pain interference, and depressive symptoms in individuals with chronic pain and a physical disability. The findings indicate that true experiments to test for causal associations are warranted. Implications for rehabilitation The majority of individuals with physical disabilities report having persistent moderate-to-severe pain that may negatively limit daily activities and quality of life. The present cross-sectional study indicates that individuals who reported greater subjective well-being showed significantly lower pain intensity via the mediating effect of lower pain catastrophizing. Since sample size and respective power are low, these findings should be taken as first indications of potential underlying mechanisms between subjective well-being and pain outcomes that need further confirmation in longitudinal research. However, the findings suggest that treatments which enhance subjective well-being (increasing positive affect and life satisfaction, and decreasing negative affect, e.g., via positive psychology exercises) and reducing pain catastrophizing (via e.g., cognitive-behavioral therapy) may have the highest potential for benefiting individuals with disability-associated chronic pain.

Conclusions: Treatments which enhance subjective well-being (increasing positive affect and life satisfaction, and decreasing negative affect, e.g., via positive psychology exercises) and reducing pain catastrophizing (via e.g., cognitive-behavioral therapy) may have the highest potential for benefiting individuals with disability-associated chronic pain.

Outcome of Research: More research required

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Title: Psychosocial factors and adjustment to pain in individuals with postpolio syndrome
Author: Hirsh AT, Kupper AE, Carter GT, Jensen MP
Affiliation: Department of Rehabilitation Medicine, University of Washington School of Medicine, Seattle, Washington 98104, USA
Journal: American Journal of Physical Medicine & Rehabilitation
Citation: Am J Phys Med Rehabil. 2010 Mar;89(3):213-24. doi: 10.1097/PHM.0b013e3181c9f9a1
Publication Year and Month: 2010 03

Abstract: OBJECTIVE: The purpose of the current study was to examine the associations among measures of psychosocial factors, pain, and adjustment in persons with postpoliomyelitis syndrome.

DESIGN: A cross-sectional survey design was used. Sixty-three community-dwelling individuals with postpoliomyelitis syndrome returned completed questionnaires (71% response rate) that included measures of pain intensity and interference, psychological functioning, pain catastrophizing, social support, and pain-related beliefs and coping.

RESULTS: After controlling for demographic variables, the group of psychosocial variables accounted for an additional 23% of the variance in pain intensity. These variables explained an additional 35% and 50% of the variance in pain interference and psychological functioning, respectively, after accounting for demographic variables and pain intensity. Social support was associated with both psychological functioning and pain interference, whereas catastrophizing was most closely related to psychological functioning. Individual pain beliefs and coping strategies were variably related to the three criterion measures.

Conclusions: The overall results of the current study are consistent with a biopsychosocial framework for understanding pain and functioning in individuals with postpoliomyelitis syndrome. Although additional research is needed to clarify the nature of the relationships between individual psychosocial variables and functional indices, the findings suggest the need for a multidisciplinary approach to pain management in individuals with postpoliomyelitis syndrome.

Outcome of Research: More research required.

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Title: Effectiveness of Intravenous Immunoglobulin for Management of Pain in Patients with Postpolio Syndrome
Author: Min Cheol Chang (1), Jin-Sung Park (2), Jong-moon Hwang (3), and Donghwi Park (4)
Affiliation: (1) Department of Rehabilitation Medicine, College of Medicine, Yeungnam University, Daegu, Republic of Korea

(2) Department of Neurology, School of Medicine, Kyungpook National University,
Kyungpook National University Chilgok Hospital, Daegu, Republic of Korea

(3) Department of Rehabilitation Medicine, School of Medicine, Kyungpook National University, Daegu, Republic of Korea

(4) Department of Physical Medicine and Rehabilitation, Ulsan University Hospital, University of Ulsan College of Medicine,
Ulsan, Republic of Korea
Journal: Pain Research and Management
Citation: Volume 2021, Article ID 6637705, 4 pages
https://doi.org/10.1155/2021/6637705
Publication Year and Month: 2021 03

Abstract: Objective.
Many patients with postpolio syndrome (PPS) experience pain. In this study, we aimed to review previous studies to investigate the effectiveness of intravenous immunoglobulin (IVIG) for managing pain in patients with PPS. We performed a narrative review.

Methods.
In PubMed, we searched for the keywords ((Immunoglobulin OR IVIG) AND (poliomyelitis OR poliomyelitis syndrome)). We included articles in which IVIG was infused in patients with PPS and pain severity was measured before and after treatment.

Results.
In the results, five articles (4 randomized controlled trials and 1 prospective observational study) were included in this review. Four of the studies reported that IVIG had a positive pain-reducing effect in patients with PPS. In addition, 4 studies evaluated the outcomes related to muscle strength and function. Of these studies, 3 showed some improvement in measurements for muscle strength and function.

Conclusion.
In conclusion, IVIG might be one of the beneficial options for managing pain in PPS. Pain reduction might be responsible for the improvement of muscle strength or function. To confirm the benefits of IVIG in reducing pain, more high-quality studies are required.

Conclusions: In conclusion, this review shows that IVIG administration might be useful for managing pain in patients with PPS. In the 5 articles reviewed, no major adverse effects were reported. Owing to the small number of studies and inconsistent results between the studies, we cannot make a definite conclusion on the effect of IVIG on pain in PPS. However, we think that the previous studies showed a possibility that IVIG can safely manage pain in patients with PPS. To confirm the benefits of IVIG in reducing pain in patients with PPS, more high-quality studies are required. Moreover, the protocols for IVIG infusion used in each study were heterogeneous; therefore, the most effective protocol for IVIG infusion for controlling pain should be evaluated in the future.

Outcome of Research: More research required

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Title: Activity pacing in chronic pain: concepts, evidence, and future directions
Author: Nielson WR, Jensen MP, Karsdorp PA, Vlaeyen JW.
Affiliation: St Joseph's Health Care London, Lawson Research Institute, London, ON, Canada. [email protected]
Journal: The Clinical Journal of Pain
Citation: 2013 May;29(5):461-8. doi: 10.1097/AJP.0b013e3182608561
Publication Year and Month: 2013 05

Abstract: BACKGROUND:
Activity pacing (AP) is a concept that is central to many chronic pain theories and treatments, yet there remains confusion regarding its definition and effects.

OBJECTIVE:
To review the current knowledge concerning AP and integrate this knowledge in a manner that allows for a clear definition and useful directions for future research.

METHODS:
A narrative review of the major theoretical approaches to AP and of the empirical evidence regarding the effects of AP interventions, followed by an integrative discussion.

RESULTS:
The concept of AP is derived from 2 main traditions: operant and energy conservation. Although there are common elements across these traditions, significant conceptual and practical differences exist, which has led to confusion. Little empirical evidence exists concerning the efficacy of AP as a treatment for chronic pain.

Conclusions: DISCUSSION:
Future research on AP should be based on a clear theoretical foundation, consider the context in which the AP behavior occurs and the type of pacing problem ("underactivity" vs. "overactivity"), and should examine the impact of AP treatment on multiple clinical outcomes. We provide a provisional definition of AP and specific recommendations that we believe will move the field forward.

Outcome of Research: More research required

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Title: The Association of Pain, Fatigue and Functional Capacity with Function in Subjects with Post-Polio Syndrome in Gujarat, India
Author: Sheth Megha S Sheth, MPT (1); Srishti S Sharma, PhD Scholar (2)
Affiliation: (1) SBB College of Physiotherapy

(2) CM Patel College of Physiotherapy
Journal: NEW - PUT DETAILS IN CITATION FIELD
Citation: Journal of Society of Indian Physiotherapists

Volume 1, Issue 2. p. 42-46. Doi No:-10.18231
Publication Year and Month: 2017 08

Abstract: Background:
Almost 80 lakh people are affected by polio in India. Post-polio syndrome (PPS) refers to a clinical disorder affecting polio survivors’ years after the initial polio attack. These patients report new, late onset, neuromuscular symptoms like fatigue, pain, new and unusual muscular deficits, and decreased functional abilities. Although these are common problems in individuals with PPS, less research especially in India, has examined the role that these symptoms might exert on physical or psychological function.

Aims:
To find co-relation of pain, fatigue, functional capacity with function in subjects with Post-Polio Syndrome.

Design:
Co-relational study.

Methods:
A convenience sample of 20 subjects with PPS according to Halstead criteria 1985 was selected. Pain was examined using Brief Pain Inventory (BPI), Fatigue by fatigue severity scale (FSS) and functional capacity by 2 minute walk distance. Physical and psychological functions were examined using PROMIS (Patient Reported Outcomes Measurement Information System) and PHQ-9 (Patient Health Questionnaire-9) questionnaires.

Statistical Analysis:
Spearman’s test for co-relation was applied.

Results:
A positive linear co-relation was found between functional capacity and physiological function (r = 0.873); negative linear co-relation between functional capacity and psychological function (r = -0.743). Fatigue showed a positive linear correlation with psychological function (r = 0.486). A negative correlation was calculated between pain and fatigue with physical function (r = -0.258; r = -0.396 respectively). Correlation of pain and psychological function (r = 0.130) was weak.

Conclusion:
Reduced functional capacity co-relates with the physical and psychological function of subjects with PPS, and fatigue co-relates with psychological function. Physiotherapy for decreasing pain, fatigue and improving functional capacity may improve physical and psychological function.

Keywords: Physical function, Psychological function, Pain, Fatigue, Functional capacity.

Conclusions: Conclusion
There is a strong correlation between functional capacity and physical and psychological function of subjects with PPS, and moderate correlation of fatigue with psychological function. Correlation of pain and fatigue with physical function and of pain and psychological function was weak.

Implications
There is a need for effective and accessible management options in polio survivors. Physiotherapy for decreasing pain, fatigue and improving functional capacity may improve physical and psychological function. The study highlights the need to screen subjects with PPS and suggest interventional strategies to reduce their problems.

Outcome of Research: More research required

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Title: Pain in persons with post-polio syndrome: frequency, intensity, and impact
Author: Stoelb BL, Carter GT, Abresch RT, Purekal S, McDonald CM, Jensen MP
Affiliation: Department of Rehabilitation Medicine, University of Washington School of Medicine, Seattle, WA (Stoelb, Carter, Purekal, Jensen); Department of Physical Medicine and Rehabilitation, University of California/Davis, Sacramento, CA
Journal: Archives of Physical Medicine and Rehabilitation
Citation: Arch Phys Med Rehabil. 2008 Oct; 89(10): 1933–1940. doi: 10.1016/j.apmr.2008.03.018
Publication Year and Month: 2008 10

Abstract: OBJECTIVE: To describe the frequency, intensity, and impact of pain in persons with postpoliomyelitis syndrome (PPS).

DESIGN: Retrospective, cross-sectional survey.

SETTING: Community-based survey.

PARTICIPANTS: Convenience sample of people with PPS.

INTERVENTIONS: Not applicable.

MAIN OUTCOME MEASURES: Overall intensity and duration of pain, pain sites, pain interference, pain treatments, and relief provided by pain treatments.

RESULTS: A total of 91% (n=57) of the study participants (N=63) reported pain. The most frequently reported pain sites were the shoulders, lower back, legs, and hips. Participants reported pain intensity to be the greatest in the knees, legs, wrists, lower back, and head. Pain interfered most with sleep and with activities requiring a high level of musculoskeletal involvement. Respondents also reported pain problems that were more severe than those of the general population and than those of a sample of people with multiple sclerosis. Many treatments had been tried previously for pain, but continued use of treatments was reported by relatively few participants at the time of the survey.

Conclusions: The findings indicate that pain is a persistent and common problem in persons with PPS, highlighting the need for effective and accessible pain treatments for this population.

Outcome of Research: Not applicable.

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Title: Predictive factors and correlates for pain in postpoliomyelitis syndrome patients
Author: Vasiliadis HM, Collet JP, Shapiro S, Venturini A, Trojan DA
Affiliation: Department of Epidemiology and Biostatistics, Jewish General Hospital, McGill University, Montreal, Que, Canada
Journal: Archives of Physical Medicine and Rehabilitation
Citation: Arch Phys Med Rehabil. 2002 Aug;83(8):1109-15
Publication Year and Month: 2002 08

Abstract: OBJECTIVE: To identify predictive and associated factors for muscle and joint pain in postpoliomyelitis syndrome (PPS).

DESIGN: Cross-sectional study design.

SETTING: Postpolio clinics.

PARTICIPANTS: Baseline data on 126 PPS patients entered into a multicentered clinical trial.

INTERVENTIONS: Not applicable.

MAIN OUTCOME MEASURES: Adjusted odds ratios were computed by using logistic regression modeling. Patients with or without muscle or joint pain were compared with regard to predictors and associated factors.

RESULTS: In multivariate analyses for muscle pain, significant predictive and associated factors were female gender (P=.0006), longer duration of general fatigue (P=.019), and a lower score on the general health scale (P=.009) of the Medical Outcomes Study 36-Item Short-From Health Survey (SF-36). In multivariate analyses for joint pain, significant predictive and associated factors were female gender (P<.003), longer latency (duration of stability after polio; P=.008), younger age at interview (P<.002), greater weakness at acute polio (P<.07), weaker lower-extremity muscle strength (P<.04), and a lower SF-36 general health scale score (P<.02).

Conclusions: Women are more likely to report muscle and joint pain in PPS. Greater initial motor unit involvement and lower-extremity weakness may be additional important factors for determining joint pain. Both muscle and joint pain are associated with reductions in quality of life.

Outcome of Research: More research required

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Title: Impact of pain on quality of life in patients with post-polio syndrome
Author: Werhagen L, Borg K
Affiliation: Division of Rehabilitation Medicine, Department of Clinical Sciences, Karolinska Institutet Danderyd Hospital, Stockholm, Sweden
Journal: Journal of Rehabilitation Medicine
Citation: J Rehabil Med. 2013; 45: 161–163. doi: 10.2340/16501977-1096
Publication Year and Month: 2013 00

Abstract: OBJECTIVE: Post-polio syndrome is a neurological disorder occurring several years after an acute polio infection. The main symptoms are increased muscular weakness and atrophy, fatigue and pain. Pain is present more often in younger individuals and in females and, according to the visual analogue scale (VAS), the intensity of pain is relatively high. The aim of the present study was to analyse the impact of pain on quality of life in patients with post-polio syndrome.

DESIGN: Transversal study.

PATIENTS AND METHODS: Patients with post-polio syndrome underwent a thorough neurological and general examination. They were interviewed about the presence and intensity of pain during the previous 3 months, then completed the quality of life inventory Short-Form 36 (SF-36), which included questions about pain during the previous 4 weeks, and rated their pain intensity during the previous 24 h according to the VAS.

RESULTS: Seventy-seven of the patients (68%) experienced pain at the examination. Pain was found to have a significant impact on the SF-36 subdomains Vitality and General health. A correlation was found between pain during the previous 3 months, the previous 4 weeks, and the previous 24 h.

DISCUSSION: Pain is common in patients with post-polio syndrome. Although patients have a high mean VAS score the pain only affects quality of life for Vitality and General Health, but not for other physical and mental domains.

Conclusions:

Outcome of Research: Not applicable.

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Title: Analysis of long-standing nociceptive and neuropathic pain in patients with post-polio syndrome
Author: Werhagen L, Borg K
Affiliation: Division of Rehabilitation Medicine, Department of Clinical Sciences, Karolinska Institutet Danderyds Hospital, Stockholm, Sweden. [email protected]
Journal: Journal of Neurology
Citation: J Neurol. 2010 Jun;257(6):1027-31. doi: 10.1007/s00415-010-5456-0
Publication Year and Month: 2010 06

Abstract: The purpose of this study was to analyze pain, both nociceptive and neuropathic, in patients with post-polio syndrome (PPS) and relate the pain to age at the initial polio infection, age at examination, to gender and disability. The study was conducted in a university hospital department. Patients with PPS were interviewed at their regular visits about pain, its character, intensity and localization. A clinical examination, including a thorough neurological examination, was performed. Data included age at time of polio infection, age at time of examination and gender. Pain intensity was measured with the VAS-scale and walking capability by the WISCI-scale. One hundred sixty-three (88 women, 75 men) patients were included in the study. Pain was present in 109 (67%). Pain was more frequently reported by women (82%) than by men (49%). 96 patients experienced nociceptive pain, 10 patients both neuropathic and nociceptive pain and three experienced pure neuropathic pain. Half of the patients with pain experienced pain in more than one body region. When neuropathic pain was present, another additional neurological disorder was diagnosed. Pain was more often found in younger patients (around 70%) than in older patients (around 50%). In summary pain is common in patients with PPS and most patients experienced nociceptive pain. Women have pain more often than men. Older patients experience pain more seldom than younger patients. Age at time of primary polio infection is important for the development of pain. When neuropathic pain is present, it is important to proceed with neurological examination to find an adequate diagnosis.

Conclusions:

Outcome of Research: Not applicable.

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There are currently 12 papers in this category.

Title: Psychosocial factors and adjustment to pain in individuals with postpolio syndrome
Author: Hirsh AT, Kupper AE, Carter GT, Jensen MP
Affiliation: Department of Rehabilitation Medicine, University of Washington School of Medicine, Seattle, Washington 98104, USA
Journal: American Journal of Physical Medicine & Rehabilitation
Citation: Am J Phys Med Rehabil. 2010 Mar;89(3):213-24. doi: 10.1097/PHM.0b013e3181c9f9a1
Publication Year and Month: 2010 03

Abstract: OBJECTIVE: The purpose of the current study was to examine the associations among measures of psychosocial factors, pain, and adjustment in persons with postpoliomyelitis syndrome.

DESIGN: A cross-sectional survey design was used. Sixty-three community-dwelling individuals with postpoliomyelitis syndrome returned completed questionnaires (71% response rate) that included measures of pain intensity and interference, psychological functioning, pain catastrophizing, social support, and pain-related beliefs and coping.

RESULTS: After controlling for demographic variables, the group of psychosocial variables accounted for an additional 23% of the variance in pain intensity. These variables explained an additional 35% and 50% of the variance in pain interference and psychological functioning, respectively, after accounting for demographic variables and pain intensity. Social support was associated with both psychological functioning and pain interference, whereas catastrophizing was most closely related to psychological functioning. Individual pain beliefs and coping strategies were variably related to the three criterion measures.

Conclusions: The overall results of the current study are consistent with a biopsychosocial framework for understanding pain and functioning in individuals with postpoliomyelitis syndrome. Although additional research is needed to clarify the nature of the relationships between individual psychosocial variables and functional indices, the findings suggest the need for a multidisciplinary approach to pain management in individuals with postpoliomyelitis syndrome.

Outcome of Research: More research required.

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Title: Fibromyalgia Is Common in a Postpoliomyelitis Clinic
Author: D A Trojan (1), N R Cashman
Affiliation: (1) Department of Neurology, Montreal Neurological Institute and Hospital, McGill University, Quebec.
Journal: Archives of Neurology
Citation: Trojan DA, Cashman NR. Fibromyalgia is common in a postpoliomyelitis clinic. Arch Neurol. 1995 Jun;52(6):620-4. doi: 10.1001/archneur.1995.00540300094019. PMID: 7763212.
Publication Year and Month: 1995 06

Abstract: Objective: To determine prospectively the occurrence and clinical characteristics of fibromyalgia in patients serially presenting to a postpolio clinic. Fibromyalgia may mimic some of the symptoms of postpoliomyelitis syndrome, a disorder characterized by new weakness, fatigue, and pain decades after paralytic poliomyelitis.

Design: Case series.

Setting: A university-affiliated hospital clinic.

Patients: One hundred five patients were evaluated with a standardized history and physical examination during an 18-month period. Ten patients were excluded because of the absence of past paralytic poliomyelitis.

Interventions: Patients with fibromyalgia were treated with low-dose, nighttime amitriptyline hydrochloride or other conservative measures.

Main Outcome Measures: Patients with fibromyalgia had diffuse pain and 11 or more of 18 specific tender points on examination (American College of Rheumatology criteria, 1990). Patients with borderline fibromyalgia had muscle pain and five to 10 tender points on physical examination.

Results: Ten (10.5%) of 95 postpolio patients met the criteria for fibromyalgia, and another 10 patients had borderline fibromyalgia. All patients with fibromyalgia complained of new weakness, fatigue, and pain. Patients with fibromyalgia were more likely than patients without fibromylagia to be female (80% vs 40%, P<.04) and to complain of generalized fatigue (100% vs 71%, P=.057), but were not distinguishable in terms of age at presentation to clinic, age at polio, length of time since polio, physical activity, weakness at polio, motor strength scores on examination, and the presence of new weakness, muscle fatigue, or joint pain. Approximately 50% of patients in both the fibromyalgia and borderline fibromyalgia groups responded to low-dose, nighttime amitriptyline therapy.

Conclusions: Conclusions: (1) Fibromyalgia occurs frequently in a postpolio clinic. (2) Fibromyalgia can mimic some symptoms of postpoliomyelitis syndrome. (3) Fibromyalgia in postpolio patients can respond to specific treatment.

Outcome of Research: Not applicable

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Title: Pain in persons with post-polio syndrome: frequency, intensity, and impact
Author: Stoelb BL, Carter GT, Abresch RT, Purekal S, McDonald CM, Jensen MP
Affiliation: Department of Rehabilitation Medicine, University of Washington School of Medicine, Seattle, WA (Stoelb, Carter, Purekal, Jensen); Department of Physical Medicine and Rehabilitation, University of California/Davis, Sacramento, CA
Journal: Archives of Physical Medicine and Rehabilitation
Citation: Arch Phys Med Rehabil. 2008 Oct; 89(10): 1933–1940. doi: 10.1016/j.apmr.2008.03.018
Publication Year and Month: 2008 10

Abstract: OBJECTIVE: To describe the frequency, intensity, and impact of pain in persons with postpoliomyelitis syndrome (PPS).

DESIGN: Retrospective, cross-sectional survey.

SETTING: Community-based survey.

PARTICIPANTS: Convenience sample of people with PPS.

INTERVENTIONS: Not applicable.

MAIN OUTCOME MEASURES: Overall intensity and duration of pain, pain sites, pain interference, pain treatments, and relief provided by pain treatments.

RESULTS: A total of 91% (n=57) of the study participants (N=63) reported pain. The most frequently reported pain sites were the shoulders, lower back, legs, and hips. Participants reported pain intensity to be the greatest in the knees, legs, wrists, lower back, and head. Pain interfered most with sleep and with activities requiring a high level of musculoskeletal involvement. Respondents also reported pain problems that were more severe than those of the general population and than those of a sample of people with multiple sclerosis. Many treatments had been tried previously for pain, but continued use of treatments was reported by relatively few participants at the time of the survey.

Conclusions: The findings indicate that pain is a persistent and common problem in persons with PPS, highlighting the need for effective and accessible pain treatments for this population.

Outcome of Research: Not applicable.

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Title: Predictive factors and correlates for pain in postpoliomyelitis syndrome patients
Author: Vasiliadis HM, Collet JP, Shapiro S, Venturini A, Trojan DA
Affiliation: Department of Epidemiology and Biostatistics, Jewish General Hospital, McGill University, Montreal, Que, Canada
Journal: Archives of Physical Medicine and Rehabilitation
Citation: Arch Phys Med Rehabil. 2002 Aug;83(8):1109-15
Publication Year and Month: 2002 08

Abstract: OBJECTIVE: To identify predictive and associated factors for muscle and joint pain in postpoliomyelitis syndrome (PPS).

DESIGN: Cross-sectional study design.

SETTING: Postpolio clinics.

PARTICIPANTS: Baseline data on 126 PPS patients entered into a multicentered clinical trial.

INTERVENTIONS: Not applicable.

MAIN OUTCOME MEASURES: Adjusted odds ratios were computed by using logistic regression modeling. Patients with or without muscle or joint pain were compared with regard to predictors and associated factors.

RESULTS: In multivariate analyses for muscle pain, significant predictive and associated factors were female gender (P=.0006), longer duration of general fatigue (P=.019), and a lower score on the general health scale (P=.009) of the Medical Outcomes Study 36-Item Short-From Health Survey (SF-36). In multivariate analyses for joint pain, significant predictive and associated factors were female gender (P<.003), longer latency (duration of stability after polio; P=.008), younger age at interview (P<.002), greater weakness at acute polio (P<.07), weaker lower-extremity muscle strength (P<.04), and a lower SF-36 general health scale score (P<.02).

Conclusions: Women are more likely to report muscle and joint pain in PPS. Greater initial motor unit involvement and lower-extremity weakness may be additional important factors for determining joint pain. Both muscle and joint pain are associated with reductions in quality of life.

Outcome of Research: More research required

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Title: Activity pacing, avoidance, endurance, and associations with patient functioning in chronic pain: a systematic review and meta-analysis.
Author: Andrews NE, Strong J, Meredith PJ.
Affiliation: Division of Occupational Therapy, School of Health and Rehabilitation Sciences, The University of Queensland, St Lucia, Queensland, Australia. [email protected]
Journal: Archives of Physical Medicine and Rehabilitation
Citation: 2012 Nov;93(11):2109-2121.e7. doi: 10.1016/j.apmr.2012.05.029
Publication Year and Month: 2012 11

Abstract: OBJECTIVE:
To systematically review the associations between different approaches to activity (ie, activity pacing, avoidance, or endurance) and indicators of patient functioning in chronic pain samples.

DATA SOURCES:
A key word search was conducted in PsycINFO, MEDLINE via Ovid, EMBASE, and PubMed up to March 2011.

STUDY SELECTION:
To be included, studies had to (1) be written in English, (2) report on an adult chronic pain sample, and (3) report a correlation coefficient between at least 1 measure of 1 of the 3 "approach to activity" variables and an indicator of patient functioning.

DATA EXTRACTION:
Two reviewers independently screened abstracts and full-text articles for eligibility and extracted the data. Results of correlation analyses were grouped on the basis of measure of approach to activity (pacing/avoidance/endurance) and the criterion variable measured (pain/physical functioning/psychological functioning), resulting in 9 categories. Random-effects modeling was then used to pool data across studies in each category.

DATA SYNTHESIS:
Forty-one studies were eligible for inclusion. Results demonstrated that avoidance of activity was consistently associated with more pain, poorer psychological functioning, and more physical disability. While enduring with activity was associated with enhanced physical and psychological functioning, these relationships appeared to be dependent on the measure used, with measures more reflective of persisting with activities to the point of severe pain aggravation (overactivity) linked to poorer outcomes. Pacing was generally linked to better psychological functioning but more pain and disability.

Conclusions: Although causation cannot be determined, results of this study suggest that both avoidance of activity and overactivity are associated with poorer patient outcomes. Unexpected results relating to pacing may reflect either the ineffectiveness of pacing if not used to gradually increase an individual's activity level or the notion that individuals with better psychological functioning but more pain and disability are more inclined to pace activity.

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Title: Modeling subjective well-being in individuals with chronic pain and a physical disability: the role of pain control and pain catastrophizing.
Author: Furrer, A., Michel, G., Terrill, A.L., Jensen, M.P., Müller, R.
Affiliation: Nil
Journal: Disability and Rehabilitation
Citation: Furrer, A., Michel, G., Terrill, A.L., Jensen, M.P., Müller, R. (2017) Modeling subjective well-being in individuals with chronic pain and a physical disability: the role of pain control and pain catastrophizing. Disability and Rehabilitation 23:1-10 doi: 10.1080/09638288.2017.1390614. [Epub ahead of print]
Publication Year and Month: 2017 10

Abstract: PURPOSE:
To investigate the associations between subjective well-being and pain intensity, pain interference, and depression in individuals with physical disabilities. We hypothesized that (1) pain control and (2) pain catastrophizing mediate the effects of subjective well-being on pain intensity, pain interference, and depression.

METHODS:
Analyses of cross-sectional data from 96 individuals diagnosed with spinal cord injury, multiple sclerosis, neuromuscular disease, or post-polio syndrome, with average pain intensity of ≥4 (0-10) on at least half the days in the past month. Two models tested study hypotheses using structural equation.

RESULTS:
Both models showed acceptable model fit. Pain catastrophizing significantly mediated the effect of subjective well-being on pain intensity and pain interference, but not on depression. Pain control did not significantly mediate the effect of subjective well-being on pain intensity, pain interference, or depression. Path coefficients showed significant direct effects of subjective well-being on pain control (β = 0.39), pain catastrophizing (β = -0.61), pain interference (β = -0.48; -0.42), and depression (β = -0.75; -0.78).

CONCLUSIONS:
This study supports the potential of enhancing subjective well-being and lowering pain catastrophizing for reducing pain intensity, pain interference, and depressive symptoms in individuals with chronic pain and a physical disability. The findings indicate that true experiments to test for causal associations are warranted. Implications for rehabilitation The majority of individuals with physical disabilities report having persistent moderate-to-severe pain that may negatively limit daily activities and quality of life. The present cross-sectional study indicates that individuals who reported greater subjective well-being showed significantly lower pain intensity via the mediating effect of lower pain catastrophizing. Since sample size and respective power are low, these findings should be taken as first indications of potential underlying mechanisms between subjective well-being and pain outcomes that need further confirmation in longitudinal research. However, the findings suggest that treatments which enhance subjective well-being (increasing positive affect and life satisfaction, and decreasing negative affect, e.g., via positive psychology exercises) and reducing pain catastrophizing (via e.g., cognitive-behavioral therapy) may have the highest potential for benefiting individuals with disability-associated chronic pain.

Conclusions: Treatments which enhance subjective well-being (increasing positive affect and life satisfaction, and decreasing negative affect, e.g., via positive psychology exercises) and reducing pain catastrophizing (via e.g., cognitive-behavioral therapy) may have the highest potential for benefiting individuals with disability-associated chronic pain.

Outcome of Research: More research required

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Title: Analysis of long-standing nociceptive and neuropathic pain in patients with post-polio syndrome
Author: Werhagen L, Borg K
Affiliation: Division of Rehabilitation Medicine, Department of Clinical Sciences, Karolinska Institutet Danderyds Hospital, Stockholm, Sweden. [email protected]
Journal: Journal of Neurology
Citation: J Neurol. 2010 Jun;257(6):1027-31. doi: 10.1007/s00415-010-5456-0
Publication Year and Month: 2010 06

Abstract: The purpose of this study was to analyze pain, both nociceptive and neuropathic, in patients with post-polio syndrome (PPS) and relate the pain to age at the initial polio infection, age at examination, to gender and disability. The study was conducted in a university hospital department. Patients with PPS were interviewed at their regular visits about pain, its character, intensity and localization. A clinical examination, including a thorough neurological examination, was performed. Data included age at time of polio infection, age at time of examination and gender. Pain intensity was measured with the VAS-scale and walking capability by the WISCI-scale. One hundred sixty-three (88 women, 75 men) patients were included in the study. Pain was present in 109 (67%). Pain was more frequently reported by women (82%) than by men (49%). 96 patients experienced nociceptive pain, 10 patients both neuropathic and nociceptive pain and three experienced pure neuropathic pain. Half of the patients with pain experienced pain in more than one body region. When neuropathic pain was present, another additional neurological disorder was diagnosed. Pain was more often found in younger patients (around 70%) than in older patients (around 50%). In summary pain is common in patients with PPS and most patients experienced nociceptive pain. Women have pain more often than men. Older patients experience pain more seldom than younger patients. Age at time of primary polio infection is important for the development of pain. When neuropathic pain is present, it is important to proceed with neurological examination to find an adequate diagnosis.

Conclusions:

Outcome of Research: Not applicable.

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Title: Impact of pain on quality of life in patients with post-polio syndrome
Author: Werhagen L, Borg K
Affiliation: Division of Rehabilitation Medicine, Department of Clinical Sciences, Karolinska Institutet Danderyd Hospital, Stockholm, Sweden
Journal: Journal of Rehabilitation Medicine
Citation: J Rehabil Med. 2013; 45: 161–163. doi: 10.2340/16501977-1096
Publication Year and Month: 2013 00

Abstract: OBJECTIVE: Post-polio syndrome is a neurological disorder occurring several years after an acute polio infection. The main symptoms are increased muscular weakness and atrophy, fatigue and pain. Pain is present more often in younger individuals and in females and, according to the visual analogue scale (VAS), the intensity of pain is relatively high. The aim of the present study was to analyse the impact of pain on quality of life in patients with post-polio syndrome.

DESIGN: Transversal study.

PATIENTS AND METHODS: Patients with post-polio syndrome underwent a thorough neurological and general examination. They were interviewed about the presence and intensity of pain during the previous 3 months, then completed the quality of life inventory Short-Form 36 (SF-36), which included questions about pain during the previous 4 weeks, and rated their pain intensity during the previous 24 h according to the VAS.

RESULTS: Seventy-seven of the patients (68%) experienced pain at the examination. Pain was found to have a significant impact on the SF-36 subdomains Vitality and General health. A correlation was found between pain during the previous 3 months, the previous 4 weeks, and the previous 24 h.

DISCUSSION: Pain is common in patients with post-polio syndrome. Although patients have a high mean VAS score the pain only affects quality of life for Vitality and General Health, but not for other physical and mental domains.

Conclusions:

Outcome of Research: Not applicable.

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Title: Pain in Post-Polio Syndrome: A separate pain entity?
Author: Evert Christiaan Boshuis, MD (1), Eva Melin, MD, PhD (2) and Kristian Borg, MD, PhD (2)
Affiliation: (1) Department of Psychiatry, Onze Lieve Vrouwe Gasthuis, Amsterdam, The Netherlands

(2) Division of Rehabilitation Medicine, Department of Clinical Sciences, Danderyd Hospital, Karolinska Institutet, Stockholm, Sweden
Journal: Journal of Rehabilitation Medicine (JRM) - formerly Scandanavian Journal of Rehabilitation Medicine
Citation: Clinical Communications, 5, jrmcc00077.
DOI: https://doi.org/10.2340/20030711-1000077
Publication Year and Month: 2022 01

Abstract: Background: Most patients with polio recover from the initial infection, but develop muscle weakness, pain and fatigue after 15–40 years, a condition called post-polio syndrome. Although poliovirus has been almost eliminated, 12–20 million people worldwide still have polio sequelae. The pain is described mainly as nociceptive, but some patients experience neuropathic pain. The aim of this study was to further characterize post-polio pain.

Patients and methods: A total of 20 patients with post-polio syndrome participated in the study. Physical examination was performed, and questionnaires containing pain drawing and visual analogue scales (VAS) for pain intensity during rest and motion and VAS for fatigue were completed. A walk test was performed to evaluate physical performance.

Results: Pain intensity was high (42/100 on the VAS at rest and 62/100 while moving). The pain was localized in both joints and muscles. Pain in the muscles was of “deep aching” character, included “muscle cramps” and was located mainly in polio-weakened limbs.

Conclusion: Muscle pain in patients with post-polio syndrome does not fulfil the criteria for either nociceptive or neuropathic pain; thus, it is suggested that the pain is termed “post-polio muscular pain”. The intensity of post-polio muscular pain is higher while moving, but does not influence physical function, and is separate from fatigue.


LAY ABSTRACT
Most polio patients recover from the initial infection, but develop muscle weakness, pain and fatigue after 15–40 years, a condition called Post-Polio Syndrome. Though the poliovirus has almost been eliminated, 12-20 million people worldwide still have polio-equelae. The pain is mainly described as nociceptive, but some patients experience neuropathic pain. This study was undertaken to further characterize post-polio pain. We examined 20 Post-polio patients and found that the pain was localised in both joints and muscles. The pain in the muscles was of ‘deep aching’ character, included ‘muscle cramps’ and was mainly located in polio-weakened limbs. The intensity of the pain is higher while moving but does not influence the physical function. To know more about the characteristics of the pain perceived gives better possibilities for treatment and rehabilitation

Conclusions: In conclusion, pain in PPS is mostly of deep aching character and muscle cramps, localized in the polio-weakened limb. This type of pain seems to be specific to PPS. It is suggested that this pain is termed post-polio muscular pain (PPMP). Future studies should aim to characterize PPMP and to analyse the influence of motor and sensory dysfunction on the pain.

Outcome of Research: More research required

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Title: The Association of Pain, Fatigue and Functional Capacity with Function in Subjects with Post-Polio Syndrome in Gujarat, India
Author: Sheth Megha S Sheth, MPT (1); Srishti S Sharma, PhD Scholar (2)
Affiliation: (1) SBB College of Physiotherapy

(2) CM Patel College of Physiotherapy
Journal: NEW - PUT DETAILS IN CITATION FIELD
Citation: Journal of Society of Indian Physiotherapists

Volume 1, Issue 2. p. 42-46. Doi No:-10.18231
Publication Year and Month: 2017 08

Abstract: Background:
Almost 80 lakh people are affected by polio in India. Post-polio syndrome (PPS) refers to a clinical disorder affecting polio survivors’ years after the initial polio attack. These patients report new, late onset, neuromuscular symptoms like fatigue, pain, new and unusual muscular deficits, and decreased functional abilities. Although these are common problems in individuals with PPS, less research especially in India, has examined the role that these symptoms might exert on physical or psychological function.

Aims:
To find co-relation of pain, fatigue, functional capacity with function in subjects with Post-Polio Syndrome.

Design:
Co-relational study.

Methods:
A convenience sample of 20 subjects with PPS according to Halstead criteria 1985 was selected. Pain was examined using Brief Pain Inventory (BPI), Fatigue by fatigue severity scale (FSS) and functional capacity by 2 minute walk distance. Physical and psychological functions were examined using PROMIS (Patient Reported Outcomes Measurement Information System) and PHQ-9 (Patient Health Questionnaire-9) questionnaires.

Statistical Analysis:
Spearman’s test for co-relation was applied.

Results:
A positive linear co-relation was found between functional capacity and physiological function (r = 0.873); negative linear co-relation between functional capacity and psychological function (r = -0.743). Fatigue showed a positive linear correlation with psychological function (r = 0.486). A negative correlation was calculated between pain and fatigue with physical function (r = -0.258; r = -0.396 respectively). Correlation of pain and psychological function (r = 0.130) was weak.

Conclusion:
Reduced functional capacity co-relates with the physical and psychological function of subjects with PPS, and fatigue co-relates with psychological function. Physiotherapy for decreasing pain, fatigue and improving functional capacity may improve physical and psychological function.

Keywords: Physical function, Psychological function, Pain, Fatigue, Functional capacity.

Conclusions: Conclusion
There is a strong correlation between functional capacity and physical and psychological function of subjects with PPS, and moderate correlation of fatigue with psychological function. Correlation of pain and fatigue with physical function and of pain and psychological function was weak.

Implications
There is a need for effective and accessible management options in polio survivors. Physiotherapy for decreasing pain, fatigue and improving functional capacity may improve physical and psychological function. The study highlights the need to screen subjects with PPS and suggest interventional strategies to reduce their problems.

Outcome of Research: More research required

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Title: Effectiveness of Intravenous Immunoglobulin for Management of Pain in Patients with Postpolio Syndrome
Author: Min Cheol Chang (1), Jin-Sung Park (2), Jong-moon Hwang (3), and Donghwi Park (4)
Affiliation: (1) Department of Rehabilitation Medicine, College of Medicine, Yeungnam University, Daegu, Republic of Korea

(2) Department of Neurology, School of Medicine, Kyungpook National University,
Kyungpook National University Chilgok Hospital, Daegu, Republic of Korea

(3) Department of Rehabilitation Medicine, School of Medicine, Kyungpook National University, Daegu, Republic of Korea

(4) Department of Physical Medicine and Rehabilitation, Ulsan University Hospital, University of Ulsan College of Medicine,
Ulsan, Republic of Korea
Journal: Pain Research and Management
Citation: Volume 2021, Article ID 6637705, 4 pages
https://doi.org/10.1155/2021/6637705
Publication Year and Month: 2021 03

Abstract: Objective.
Many patients with postpolio syndrome (PPS) experience pain. In this study, we aimed to review previous studies to investigate the effectiveness of intravenous immunoglobulin (IVIG) for managing pain in patients with PPS. We performed a narrative review.

Methods.
In PubMed, we searched for the keywords ((Immunoglobulin OR IVIG) AND (poliomyelitis OR poliomyelitis syndrome)). We included articles in which IVIG was infused in patients with PPS and pain severity was measured before and after treatment.

Results.
In the results, five articles (4 randomized controlled trials and 1 prospective observational study) were included in this review. Four of the studies reported that IVIG had a positive pain-reducing effect in patients with PPS. In addition, 4 studies evaluated the outcomes related to muscle strength and function. Of these studies, 3 showed some improvement in measurements for muscle strength and function.

Conclusion.
In conclusion, IVIG might be one of the beneficial options for managing pain in PPS. Pain reduction might be responsible for the improvement of muscle strength or function. To confirm the benefits of IVIG in reducing pain, more high-quality studies are required.

Conclusions: In conclusion, this review shows that IVIG administration might be useful for managing pain in patients with PPS. In the 5 articles reviewed, no major adverse effects were reported. Owing to the small number of studies and inconsistent results between the studies, we cannot make a definite conclusion on the effect of IVIG on pain in PPS. However, we think that the previous studies showed a possibility that IVIG can safely manage pain in patients with PPS. To confirm the benefits of IVIG in reducing pain in patients with PPS, more high-quality studies are required. Moreover, the protocols for IVIG infusion used in each study were heterogeneous; therefore, the most effective protocol for IVIG infusion for controlling pain should be evaluated in the future.

Outcome of Research: More research required

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Title: Activity pacing in chronic pain: concepts, evidence, and future directions
Author: Nielson WR, Jensen MP, Karsdorp PA, Vlaeyen JW.
Affiliation: St Joseph's Health Care London, Lawson Research Institute, London, ON, Canada. [email protected]
Journal: The Clinical Journal of Pain
Citation: 2013 May;29(5):461-8. doi: 10.1097/AJP.0b013e3182608561
Publication Year and Month: 2013 05

Abstract: BACKGROUND:
Activity pacing (AP) is a concept that is central to many chronic pain theories and treatments, yet there remains confusion regarding its definition and effects.

OBJECTIVE:
To review the current knowledge concerning AP and integrate this knowledge in a manner that allows for a clear definition and useful directions for future research.

METHODS:
A narrative review of the major theoretical approaches to AP and of the empirical evidence regarding the effects of AP interventions, followed by an integrative discussion.

RESULTS:
The concept of AP is derived from 2 main traditions: operant and energy conservation. Although there are common elements across these traditions, significant conceptual and practical differences exist, which has led to confusion. Little empirical evidence exists concerning the efficacy of AP as a treatment for chronic pain.

Conclusions: DISCUSSION:
Future research on AP should be based on a clear theoretical foundation, consider the context in which the AP behavior occurs and the type of pacing problem ("underactivity" vs. "overactivity"), and should examine the impact of AP treatment on multiple clinical outcomes. We provide a provisional definition of AP and specific recommendations that we believe will move the field forward.

Outcome of Research: More research required

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There are currently 12 papers in this category.

Title: Pain in Post-Polio Syndrome: A separate pain entity?
Author: Evert Christiaan Boshuis, MD (1), Eva Melin, MD, PhD (2) and Kristian Borg, MD, PhD (2)
Affiliation: (1) Department of Psychiatry, Onze Lieve Vrouwe Gasthuis, Amsterdam, The Netherlands

(2) Division of Rehabilitation Medicine, Department of Clinical Sciences, Danderyd Hospital, Karolinska Institutet, Stockholm, Sweden
Journal: Journal of Rehabilitation Medicine (JRM) - formerly Scandanavian Journal of Rehabilitation Medicine
Citation: Clinical Communications, 5, jrmcc00077.
DOI: https://doi.org/10.2340/20030711-1000077
Publication Year and Month: 2022 01

Abstract: Background: Most patients with polio recover from the initial infection, but develop muscle weakness, pain and fatigue after 15–40 years, a condition called post-polio syndrome. Although poliovirus has been almost eliminated, 12–20 million people worldwide still have polio sequelae. The pain is described mainly as nociceptive, but some patients experience neuropathic pain. The aim of this study was to further characterize post-polio pain.

Patients and methods: A total of 20 patients with post-polio syndrome participated in the study. Physical examination was performed, and questionnaires containing pain drawing and visual analogue scales (VAS) for pain intensity during rest and motion and VAS for fatigue were completed. A walk test was performed to evaluate physical performance.

Results: Pain intensity was high (42/100 on the VAS at rest and 62/100 while moving). The pain was localized in both joints and muscles. Pain in the muscles was of “deep aching” character, included “muscle cramps” and was located mainly in polio-weakened limbs.

Conclusion: Muscle pain in patients with post-polio syndrome does not fulfil the criteria for either nociceptive or neuropathic pain; thus, it is suggested that the pain is termed “post-polio muscular pain”. The intensity of post-polio muscular pain is higher while moving, but does not influence physical function, and is separate from fatigue.


LAY ABSTRACT
Most polio patients recover from the initial infection, but develop muscle weakness, pain and fatigue after 15–40 years, a condition called Post-Polio Syndrome. Though the poliovirus has almost been eliminated, 12-20 million people worldwide still have polio-equelae. The pain is mainly described as nociceptive, but some patients experience neuropathic pain. This study was undertaken to further characterize post-polio pain. We examined 20 Post-polio patients and found that the pain was localised in both joints and muscles. The pain in the muscles was of ‘deep aching’ character, included ‘muscle cramps’ and was mainly located in polio-weakened limbs. The intensity of the pain is higher while moving but does not influence the physical function. To know more about the characteristics of the pain perceived gives better possibilities for treatment and rehabilitation

Conclusions: In conclusion, pain in PPS is mostly of deep aching character and muscle cramps, localized in the polio-weakened limb. This type of pain seems to be specific to PPS. It is suggested that this pain is termed post-polio muscular pain (PPMP). Future studies should aim to characterize PPMP and to analyse the influence of motor and sensory dysfunction on the pain.

Outcome of Research: More research required

Availability of Paper: The full text of this paper has been generously made available by the publisher.

Comments (if any):

Link to Paper (if available): Click here to view full text or to download

Title: Effectiveness of Intravenous Immunoglobulin for Management of Pain in Patients with Postpolio Syndrome
Author: Min Cheol Chang (1), Jin-Sung Park (2), Jong-moon Hwang (3), and Donghwi Park (4)
Affiliation: (1) Department of Rehabilitation Medicine, College of Medicine, Yeungnam University, Daegu, Republic of Korea

(2) Department of Neurology, School of Medicine, Kyungpook National University,
Kyungpook National University Chilgok Hospital, Daegu, Republic of Korea

(3) Department of Rehabilitation Medicine, School of Medicine, Kyungpook National University, Daegu, Republic of Korea

(4) Department of Physical Medicine and Rehabilitation, Ulsan University Hospital, University of Ulsan College of Medicine,
Ulsan, Republic of Korea
Journal: Pain Research and Management
Citation: Volume 2021, Article ID 6637705, 4 pages
https://doi.org/10.1155/2021/6637705
Publication Year and Month: 2021 03

Abstract: Objective.
Many patients with postpolio syndrome (PPS) experience pain. In this study, we aimed to review previous studies to investigate the effectiveness of intravenous immunoglobulin (IVIG) for managing pain in patients with PPS. We performed a narrative review.

Methods.
In PubMed, we searched for the keywords ((Immunoglobulin OR IVIG) AND (poliomyelitis OR poliomyelitis syndrome)). We included articles in which IVIG was infused in patients with PPS and pain severity was measured before and after treatment.

Results.
In the results, five articles (4 randomized controlled trials and 1 prospective observational study) were included in this review. Four of the studies reported that IVIG had a positive pain-reducing effect in patients with PPS. In addition, 4 studies evaluated the outcomes related to muscle strength and function. Of these studies, 3 showed some improvement in measurements for muscle strength and function.

Conclusion.
In conclusion, IVIG might be one of the beneficial options for managing pain in PPS. Pain reduction might be responsible for the improvement of muscle strength or function. To confirm the benefits of IVIG in reducing pain, more high-quality studies are required.

Conclusions: In conclusion, this review shows that IVIG administration might be useful for managing pain in patients with PPS. In the 5 articles reviewed, no major adverse effects were reported. Owing to the small number of studies and inconsistent results between the studies, we cannot make a definite conclusion on the effect of IVIG on pain in PPS. However, we think that the previous studies showed a possibility that IVIG can safely manage pain in patients with PPS. To confirm the benefits of IVIG in reducing pain in patients with PPS, more high-quality studies are required. Moreover, the protocols for IVIG infusion used in each study were heterogeneous; therefore, the most effective protocol for IVIG infusion for controlling pain should be evaluated in the future.

Outcome of Research: More research required

Availability of Paper: The full text of this paper has been generously made available by the publisher.

Comments (if any):

Link to Paper (if available): Click here to view full text or to download

Title: Modeling subjective well-being in individuals with chronic pain and a physical disability: the role of pain control and pain catastrophizing.
Author: Furrer, A., Michel, G., Terrill, A.L., Jensen, M.P., Müller, R.
Affiliation: Nil
Journal: Disability and Rehabilitation
Citation: Furrer, A., Michel, G., Terrill, A.L., Jensen, M.P., Müller, R. (2017) Modeling subjective well-being in individuals with chronic pain and a physical disability: the role of pain control and pain catastrophizing. Disability and Rehabilitation 23:1-10 doi: 10.1080/09638288.2017.1390614. [Epub ahead of print]
Publication Year and Month: 2017 10

Abstract: PURPOSE:
To investigate the associations between subjective well-being and pain intensity, pain interference, and depression in individuals with physical disabilities. We hypothesized that (1) pain control and (2) pain catastrophizing mediate the effects of subjective well-being on pain intensity, pain interference, and depression.

METHODS:
Analyses of cross-sectional data from 96 individuals diagnosed with spinal cord injury, multiple sclerosis, neuromuscular disease, or post-polio syndrome, with average pain intensity of ≥4 (0-10) on at least half the days in the past month. Two models tested study hypotheses using structural equation.

RESULTS:
Both models showed acceptable model fit. Pain catastrophizing significantly mediated the effect of subjective well-being on pain intensity and pain interference, but not on depression. Pain control did not significantly mediate the effect of subjective well-being on pain intensity, pain interference, or depression. Path coefficients showed significant direct effects of subjective well-being on pain control (β = 0.39), pain catastrophizing (β = -0.61), pain interference (β = -0.48; -0.42), and depression (β = -0.75; -0.78).

CONCLUSIONS:
This study supports the potential of enhancing subjective well-being and lowering pain catastrophizing for reducing pain intensity, pain interference, and depressive symptoms in individuals with chronic pain and a physical disability. The findings indicate that true experiments to test for causal associations are warranted. Implications for rehabilitation The majority of individuals with physical disabilities report having persistent moderate-to-severe pain that may negatively limit daily activities and quality of life. The present cross-sectional study indicates that individuals who reported greater subjective well-being showed significantly lower pain intensity via the mediating effect of lower pain catastrophizing. Since sample size and respective power are low, these findings should be taken as first indications of potential underlying mechanisms between subjective well-being and pain outcomes that need further confirmation in longitudinal research. However, the findings suggest that treatments which enhance subjective well-being (increasing positive affect and life satisfaction, and decreasing negative affect, e.g., via positive psychology exercises) and reducing pain catastrophizing (via e.g., cognitive-behavioral therapy) may have the highest potential for benefiting individuals with disability-associated chronic pain.

Conclusions: Treatments which enhance subjective well-being (increasing positive affect and life satisfaction, and decreasing negative affect, e.g., via positive psychology exercises) and reducing pain catastrophizing (via e.g., cognitive-behavioral therapy) may have the highest potential for benefiting individuals with disability-associated chronic pain.

Outcome of Research: More research required

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Title: The Association of Pain, Fatigue and Functional Capacity with Function in Subjects with Post-Polio Syndrome in Gujarat, India
Author: Sheth Megha S Sheth, MPT (1); Srishti S Sharma, PhD Scholar (2)
Affiliation: (1) SBB College of Physiotherapy

(2) CM Patel College of Physiotherapy
Journal: NEW - PUT DETAILS IN CITATION FIELD
Citation: Journal of Society of Indian Physiotherapists

Volume 1, Issue 2. p. 42-46. Doi No:-10.18231
Publication Year and Month: 2017 08

Abstract: Background:
Almost 80 lakh people are affected by polio in India. Post-polio syndrome (PPS) refers to a clinical disorder affecting polio survivors’ years after the initial polio attack. These patients report new, late onset, neuromuscular symptoms like fatigue, pain, new and unusual muscular deficits, and decreased functional abilities. Although these are common problems in individuals with PPS, less research especially in India, has examined the role that these symptoms might exert on physical or psychological function.

Aims:
To find co-relation of pain, fatigue, functional capacity with function in subjects with Post-Polio Syndrome.

Design:
Co-relational study.

Methods:
A convenience sample of 20 subjects with PPS according to Halstead criteria 1985 was selected. Pain was examined using Brief Pain Inventory (BPI), Fatigue by fatigue severity scale (FSS) and functional capacity by 2 minute walk distance. Physical and psychological functions were examined using PROMIS (Patient Reported Outcomes Measurement Information System) and PHQ-9 (Patient Health Questionnaire-9) questionnaires.

Statistical Analysis:
Spearman’s test for co-relation was applied.

Results:
A positive linear co-relation was found between functional capacity and physiological function (r = 0.873); negative linear co-relation between functional capacity and psychological function (r = -0.743). Fatigue showed a positive linear correlation with psychological function (r = 0.486). A negative correlation was calculated between pain and fatigue with physical function (r = -0.258; r = -0.396 respectively). Correlation of pain and psychological function (r = 0.130) was weak.

Conclusion:
Reduced functional capacity co-relates with the physical and psychological function of subjects with PPS, and fatigue co-relates with psychological function. Physiotherapy for decreasing pain, fatigue and improving functional capacity may improve physical and psychological function.

Keywords: Physical function, Psychological function, Pain, Fatigue, Functional capacity.

Conclusions: Conclusion
There is a strong correlation between functional capacity and physical and psychological function of subjects with PPS, and moderate correlation of fatigue with psychological function. Correlation of pain and fatigue with physical function and of pain and psychological function was weak.

Implications
There is a need for effective and accessible management options in polio survivors. Physiotherapy for decreasing pain, fatigue and improving functional capacity may improve physical and psychological function. The study highlights the need to screen subjects with PPS and suggest interventional strategies to reduce their problems.

Outcome of Research: More research required

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Title: Activity pacing in chronic pain: concepts, evidence, and future directions
Author: Nielson WR, Jensen MP, Karsdorp PA, Vlaeyen JW.
Affiliation: St Joseph's Health Care London, Lawson Research Institute, London, ON, Canada. [email protected]
Journal: The Clinical Journal of Pain
Citation: 2013 May;29(5):461-8. doi: 10.1097/AJP.0b013e3182608561
Publication Year and Month: 2013 05

Abstract: BACKGROUND:
Activity pacing (AP) is a concept that is central to many chronic pain theories and treatments, yet there remains confusion regarding its definition and effects.

OBJECTIVE:
To review the current knowledge concerning AP and integrate this knowledge in a manner that allows for a clear definition and useful directions for future research.

METHODS:
A narrative review of the major theoretical approaches to AP and of the empirical evidence regarding the effects of AP interventions, followed by an integrative discussion.

RESULTS:
The concept of AP is derived from 2 main traditions: operant and energy conservation. Although there are common elements across these traditions, significant conceptual and practical differences exist, which has led to confusion. Little empirical evidence exists concerning the efficacy of AP as a treatment for chronic pain.

Conclusions: DISCUSSION:
Future research on AP should be based on a clear theoretical foundation, consider the context in which the AP behavior occurs and the type of pacing problem ("underactivity" vs. "overactivity"), and should examine the impact of AP treatment on multiple clinical outcomes. We provide a provisional definition of AP and specific recommendations that we believe will move the field forward.

Outcome of Research: More research required

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Title: Impact of pain on quality of life in patients with post-polio syndrome
Author: Werhagen L, Borg K
Affiliation: Division of Rehabilitation Medicine, Department of Clinical Sciences, Karolinska Institutet Danderyd Hospital, Stockholm, Sweden
Journal: Journal of Rehabilitation Medicine
Citation: J Rehabil Med. 2013; 45: 161–163. doi: 10.2340/16501977-1096
Publication Year and Month: 2013 00

Abstract: OBJECTIVE: Post-polio syndrome is a neurological disorder occurring several years after an acute polio infection. The main symptoms are increased muscular weakness and atrophy, fatigue and pain. Pain is present more often in younger individuals and in females and, according to the visual analogue scale (VAS), the intensity of pain is relatively high. The aim of the present study was to analyse the impact of pain on quality of life in patients with post-polio syndrome.

DESIGN: Transversal study.

PATIENTS AND METHODS: Patients with post-polio syndrome underwent a thorough neurological and general examination. They were interviewed about the presence and intensity of pain during the previous 3 months, then completed the quality of life inventory Short-Form 36 (SF-36), which included questions about pain during the previous 4 weeks, and rated their pain intensity during the previous 24 h according to the VAS.

RESULTS: Seventy-seven of the patients (68%) experienced pain at the examination. Pain was found to have a significant impact on the SF-36 subdomains Vitality and General health. A correlation was found between pain during the previous 3 months, the previous 4 weeks, and the previous 24 h.

DISCUSSION: Pain is common in patients with post-polio syndrome. Although patients have a high mean VAS score the pain only affects quality of life for Vitality and General Health, but not for other physical and mental domains.

Conclusions:

Outcome of Research: Not applicable.

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Title: Activity pacing, avoidance, endurance, and associations with patient functioning in chronic pain: a systematic review and meta-analysis.
Author: Andrews NE, Strong J, Meredith PJ.
Affiliation: Division of Occupational Therapy, School of Health and Rehabilitation Sciences, The University of Queensland, St Lucia, Queensland, Australia. [email protected]
Journal: Archives of Physical Medicine and Rehabilitation
Citation: 2012 Nov;93(11):2109-2121.e7. doi: 10.1016/j.apmr.2012.05.029
Publication Year and Month: 2012 11

Abstract: OBJECTIVE:
To systematically review the associations between different approaches to activity (ie, activity pacing, avoidance, or endurance) and indicators of patient functioning in chronic pain samples.

DATA SOURCES:
A key word search was conducted in PsycINFO, MEDLINE via Ovid, EMBASE, and PubMed up to March 2011.

STUDY SELECTION:
To be included, studies had to (1) be written in English, (2) report on an adult chronic pain sample, and (3) report a correlation coefficient between at least 1 measure of 1 of the 3 "approach to activity" variables and an indicator of patient functioning.

DATA EXTRACTION:
Two reviewers independently screened abstracts and full-text articles for eligibility and extracted the data. Results of correlation analyses were grouped on the basis of measure of approach to activity (pacing/avoidance/endurance) and the criterion variable measured (pain/physical functioning/psychological functioning), resulting in 9 categories. Random-effects modeling was then used to pool data across studies in each category.

DATA SYNTHESIS:
Forty-one studies were eligible for inclusion. Results demonstrated that avoidance of activity was consistently associated with more pain, poorer psychological functioning, and more physical disability. While enduring with activity was associated with enhanced physical and psychological functioning, these relationships appeared to be dependent on the measure used, with measures more reflective of persisting with activities to the point of severe pain aggravation (overactivity) linked to poorer outcomes. Pacing was generally linked to better psychological functioning but more pain and disability.

Conclusions: Although causation cannot be determined, results of this study suggest that both avoidance of activity and overactivity are associated with poorer patient outcomes. Unexpected results relating to pacing may reflect either the ineffectiveness of pacing if not used to gradually increase an individual's activity level or the notion that individuals with better psychological functioning but more pain and disability are more inclined to pace activity.

Outcome of Research: More research required

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Title: Analysis of long-standing nociceptive and neuropathic pain in patients with post-polio syndrome
Author: Werhagen L, Borg K
Affiliation: Division of Rehabilitation Medicine, Department of Clinical Sciences, Karolinska Institutet Danderyds Hospital, Stockholm, Sweden. [email protected]
Journal: Journal of Neurology
Citation: J Neurol. 2010 Jun;257(6):1027-31. doi: 10.1007/s00415-010-5456-0
Publication Year and Month: 2010 06

Abstract: The purpose of this study was to analyze pain, both nociceptive and neuropathic, in patients with post-polio syndrome (PPS) and relate the pain to age at the initial polio infection, age at examination, to gender and disability. The study was conducted in a university hospital department. Patients with PPS were interviewed at their regular visits about pain, its character, intensity and localization. A clinical examination, including a thorough neurological examination, was performed. Data included age at time of polio infection, age at time of examination and gender. Pain intensity was measured with the VAS-scale and walking capability by the WISCI-scale. One hundred sixty-three (88 women, 75 men) patients were included in the study. Pain was present in 109 (67%). Pain was more frequently reported by women (82%) than by men (49%). 96 patients experienced nociceptive pain, 10 patients both neuropathic and nociceptive pain and three experienced pure neuropathic pain. Half of the patients with pain experienced pain in more than one body region. When neuropathic pain was present, another additional neurological disorder was diagnosed. Pain was more often found in younger patients (around 70%) than in older patients (around 50%). In summary pain is common in patients with PPS and most patients experienced nociceptive pain. Women have pain more often than men. Older patients experience pain more seldom than younger patients. Age at time of primary polio infection is important for the development of pain. When neuropathic pain is present, it is important to proceed with neurological examination to find an adequate diagnosis.

Conclusions:

Outcome of Research: Not applicable.

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Title: Psychosocial factors and adjustment to pain in individuals with postpolio syndrome
Author: Hirsh AT, Kupper AE, Carter GT, Jensen MP
Affiliation: Department of Rehabilitation Medicine, University of Washington School of Medicine, Seattle, Washington 98104, USA
Journal: American Journal of Physical Medicine & Rehabilitation
Citation: Am J Phys Med Rehabil. 2010 Mar;89(3):213-24. doi: 10.1097/PHM.0b013e3181c9f9a1
Publication Year and Month: 2010 03

Abstract: OBJECTIVE: The purpose of the current study was to examine the associations among measures of psychosocial factors, pain, and adjustment in persons with postpoliomyelitis syndrome.

DESIGN: A cross-sectional survey design was used. Sixty-three community-dwelling individuals with postpoliomyelitis syndrome returned completed questionnaires (71% response rate) that included measures of pain intensity and interference, psychological functioning, pain catastrophizing, social support, and pain-related beliefs and coping.

RESULTS: After controlling for demographic variables, the group of psychosocial variables accounted for an additional 23% of the variance in pain intensity. These variables explained an additional 35% and 50% of the variance in pain interference and psychological functioning, respectively, after accounting for demographic variables and pain intensity. Social support was associated with both psychological functioning and pain interference, whereas catastrophizing was most closely related to psychological functioning. Individual pain beliefs and coping strategies were variably related to the three criterion measures.

Conclusions: The overall results of the current study are consistent with a biopsychosocial framework for understanding pain and functioning in individuals with postpoliomyelitis syndrome. Although additional research is needed to clarify the nature of the relationships between individual psychosocial variables and functional indices, the findings suggest the need for a multidisciplinary approach to pain management in individuals with postpoliomyelitis syndrome.

Outcome of Research: More research required.

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Title: Pain in persons with post-polio syndrome: frequency, intensity, and impact
Author: Stoelb BL, Carter GT, Abresch RT, Purekal S, McDonald CM, Jensen MP
Affiliation: Department of Rehabilitation Medicine, University of Washington School of Medicine, Seattle, WA (Stoelb, Carter, Purekal, Jensen); Department of Physical Medicine and Rehabilitation, University of California/Davis, Sacramento, CA
Journal: Archives of Physical Medicine and Rehabilitation
Citation: Arch Phys Med Rehabil. 2008 Oct; 89(10): 1933–1940. doi: 10.1016/j.apmr.2008.03.018
Publication Year and Month: 2008 10

Abstract: OBJECTIVE: To describe the frequency, intensity, and impact of pain in persons with postpoliomyelitis syndrome (PPS).

DESIGN: Retrospective, cross-sectional survey.

SETTING: Community-based survey.

PARTICIPANTS: Convenience sample of people with PPS.

INTERVENTIONS: Not applicable.

MAIN OUTCOME MEASURES: Overall intensity and duration of pain, pain sites, pain interference, pain treatments, and relief provided by pain treatments.

RESULTS: A total of 91% (n=57) of the study participants (N=63) reported pain. The most frequently reported pain sites were the shoulders, lower back, legs, and hips. Participants reported pain intensity to be the greatest in the knees, legs, wrists, lower back, and head. Pain interfered most with sleep and with activities requiring a high level of musculoskeletal involvement. Respondents also reported pain problems that were more severe than those of the general population and than those of a sample of people with multiple sclerosis. Many treatments had been tried previously for pain, but continued use of treatments was reported by relatively few participants at the time of the survey.

Conclusions: The findings indicate that pain is a persistent and common problem in persons with PPS, highlighting the need for effective and accessible pain treatments for this population.

Outcome of Research: Not applicable.

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Title: Predictive factors and correlates for pain in postpoliomyelitis syndrome patients
Author: Vasiliadis HM, Collet JP, Shapiro S, Venturini A, Trojan DA
Affiliation: Department of Epidemiology and Biostatistics, Jewish General Hospital, McGill University, Montreal, Que, Canada
Journal: Archives of Physical Medicine and Rehabilitation
Citation: Arch Phys Med Rehabil. 2002 Aug;83(8):1109-15
Publication Year and Month: 2002 08

Abstract: OBJECTIVE: To identify predictive and associated factors for muscle and joint pain in postpoliomyelitis syndrome (PPS).

DESIGN: Cross-sectional study design.

SETTING: Postpolio clinics.

PARTICIPANTS: Baseline data on 126 PPS patients entered into a multicentered clinical trial.

INTERVENTIONS: Not applicable.

MAIN OUTCOME MEASURES: Adjusted odds ratios were computed by using logistic regression modeling. Patients with or without muscle or joint pain were compared with regard to predictors and associated factors.

RESULTS: In multivariate analyses for muscle pain, significant predictive and associated factors were female gender (P=.0006), longer duration of general fatigue (P=.019), and a lower score on the general health scale (P=.009) of the Medical Outcomes Study 36-Item Short-From Health Survey (SF-36). In multivariate analyses for joint pain, significant predictive and associated factors were female gender (P<.003), longer latency (duration of stability after polio; P=.008), younger age at interview (P<.002), greater weakness at acute polio (P<.07), weaker lower-extremity muscle strength (P<.04), and a lower SF-36 general health scale score (P<.02).

Conclusions: Women are more likely to report muscle and joint pain in PPS. Greater initial motor unit involvement and lower-extremity weakness may be additional important factors for determining joint pain. Both muscle and joint pain are associated with reductions in quality of life.

Outcome of Research: More research required

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Title: Fibromyalgia Is Common in a Postpoliomyelitis Clinic
Author: D A Trojan (1), N R Cashman
Affiliation: (1) Department of Neurology, Montreal Neurological Institute and Hospital, McGill University, Quebec.
Journal: Archives of Neurology
Citation: Trojan DA, Cashman NR. Fibromyalgia is common in a postpoliomyelitis clinic. Arch Neurol. 1995 Jun;52(6):620-4. doi: 10.1001/archneur.1995.00540300094019. PMID: 7763212.
Publication Year and Month: 1995 06

Abstract: Objective: To determine prospectively the occurrence and clinical characteristics of fibromyalgia in patients serially presenting to a postpolio clinic. Fibromyalgia may mimic some of the symptoms of postpoliomyelitis syndrome, a disorder characterized by new weakness, fatigue, and pain decades after paralytic poliomyelitis.

Design: Case series.

Setting: A university-affiliated hospital clinic.

Patients: One hundred five patients were evaluated with a standardized history and physical examination during an 18-month period. Ten patients were excluded because of the absence of past paralytic poliomyelitis.

Interventions: Patients with fibromyalgia were treated with low-dose, nighttime amitriptyline hydrochloride or other conservative measures.

Main Outcome Measures: Patients with fibromyalgia had diffuse pain and 11 or more of 18 specific tender points on examination (American College of Rheumatology criteria, 1990). Patients with borderline fibromyalgia had muscle pain and five to 10 tender points on physical examination.

Results: Ten (10.5%) of 95 postpolio patients met the criteria for fibromyalgia, and another 10 patients had borderline fibromyalgia. All patients with fibromyalgia complained of new weakness, fatigue, and pain. Patients with fibromyalgia were more likely than patients without fibromylagia to be female (80% vs 40%, P<.04) and to complain of generalized fatigue (100% vs 71%, P=.057), but were not distinguishable in terms of age at presentation to clinic, age at polio, length of time since polio, physical activity, weakness at polio, motor strength scores on examination, and the presence of new weakness, muscle fatigue, or joint pain. Approximately 50% of patients in both the fibromyalgia and borderline fibromyalgia groups responded to low-dose, nighttime amitriptyline therapy.

Conclusions: Conclusions: (1) Fibromyalgia occurs frequently in a postpolio clinic. (2) Fibromyalgia can mimic some symptoms of postpoliomyelitis syndrome. (3) Fibromyalgia in postpolio patients can respond to specific treatment.

Outcome of Research: Not applicable

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