Arthritis Care Res (Hoboken) 2011 (Nov); 63 Suppl 11: S240-252 ~ FULL TEXT
Gillian A. Hawker, Samra Mian, Tetyana Kendzerska, And Melissa French
Women's College Hospital,
University of Toronto,
Toronto, Ontario, Canada.
Learning Outcomes Assessment
From the FULL TEXT Article:
Our purpose is to provide an overview of available generic
and rheumatology population–specific questionnaires
suitable for evaluating pain in adult rheumatology populations.
The content, ease of use, and measurement properties
of the questionnaires are presented and compared
in order to assist both clinicians and researchers select
the questionnaire that is most appropriate for their purpose.
The questionnaires are presented in the following
generic unidimensional pain questionnaires (Visual Analog Scale and Numeric Rating Scale),
generic multidimensional pain questionnaires (Short-form McGill Pain Questionnaire, Chronic Pain Grade Scale, and Short Form-36 Bodily Pain Scale), and finally
an arthritis-specific pain questionnaire (Measure of Intermittent and Constant Osteoarthritis Pain).
Composite measures of arthritis symptoms, including pain and associated disability, specifically the Western Ontario and McMaster Universities Osteoarthritis Index and the Arthritis Impact Measurement Scales, are described in Measures of Knee Function and Measures of Disability, respectively.
Visual Analog Scale (VAS) For Pain
Purpose. The pain VAS is a unidimensional measure of pain intensity , which has been widely used in diverse adult populations, including those with rheumatic diseases. [2-5]
Content. The pain VAS is a continuous scale comprised of a horizontal (HVAS) or vertical (VVAS) line, usually 10 centimeters (100 mm) in length, anchored by 2 verbal descriptors, one for each symptom extreme. [2, 6] Instructions,
time period for reporting, and verbal descriptor anchors
have varied widely in the literature depending on intended use of the scale. 
Number of items. The pain VAS is a single-item scale.
Response options/scale. For pain intensity, the scale is most commonly anchored by “no pain” (score of 0) and “pain as bad as it could be” or “worst imaginable pain” (score of 100 [100-mm scale]). [6-8] To avoid clustering of
scores around a preferred numeric value, numbers or verbal
descriptors at intermediate points are not recommended. [4, 9]
Recall period for items. Varies, but most commonly respondents are asked to report “current” pain intensity or pain intensity “in the last 24 hours.”
How to obtain. The pain VAS is available in the public domain at no cost.  Graphic formats for the VAS may be
obtained from Scott & Huskisson  or online:
Method of administration. The pain VAS is self-completed by the respondent. The respondent is asked to place a line perpendicular to the VAS line at the point that represents their pain intensity. [2, 9, 10]
Scoring. Using a ruler, the score is determined by measuring the distance (mm) on the 10-cm line between the “no pain” anchor and the patient’s mark, providing a range of scores from 0–100. 
Score interpretation. A higher score indicates greater pain intensity. Based on the distribution of pain VAS scores in postsurgical patients (knee replacement, hysterectomy, or laparoscopic myomectomy) who described their postoperative pain intensity as none, mild, moderate, or severe, the following cut points on the pain VAS have been recommended:
no pain (0–4 mm),
mild pain (5–44 mm),
moderate pain (45–74 mm), and
severe pain (75–100 mm). 
Normative values are not available.
Respondent burden. The VAS takes <1 minute to complete. [3, 7]
Administrative burden. The VAS is administered as a paper and pencil measure. As a result, it cannot be administered verbally or by phone. No training is required other than the ability to use a ruler to measure distance to determine a score. [7, 9] Caution is required when photocopying the scale as this may change the length of the
10-cm line.  As slightly lower scores have been reported on the HVAS compared to the VVAS , the same alignment
of scale should be used consistently within the same
Translations/adaptations. Minimal translation difficulties have led to an unknown number of cross-cultural adaptations.
Method of development. The pain VAS originated from continuous visual analog scales developed in the field of psychology to measure well-being. [13, 14] Woodforde and Merskey  first reported use of the VAS pain scale with the descriptor extremes “no pain at all” , and “my pain is as bad as it could possibly be” in patients with a variety of conditions. Subsequently, others reported use of the scale to measure pain in rheumatology patients receiving pharmacologic pain therapy. [2, 6, 9] While variable anchor pain descriptors have been used, there does not appear to be any rationale for selecting one set of descriptors over another.
Acceptability. The pain VAS requires little training to administer and score and has been found to be acceptable to patients. [2, 10] However, older patients with cognitive impairment may have difficulty understanding and therefore completing the scale. [6, 16] Supervision during completion may minimize these errors. 
Reliability. Test–retest reliability has been shown to be good, but higher among literate (r = 0.94, P < 0.001) than illiterate patients
(r = 0.71, P < 0.001) before and after attending a rheumatology outpatient clinic. 
Validity. In the absence of a gold standard for pain, criterion validity cannot be evaluated. For construct validity, in patients with a variety of rheumatic diseases, the pain VAS has been shown to be highly correlated with a 5-point verbal descriptive scale (“nil,” “mild,” “moderate,” “severe,” and “very severe”) and a numeric rating scale (with response options from “no pain” to “unbearable pain”), with correlations ranging from 0.71–0.78 and
0.62–0.91, respectively).  The correlation between vertical and horizontal orientations of the VAS is 0.99. 
Ability to detect change. In patients with chronic inflammatory
or degenerative joint pain, the pain VAS has
demonstrated sensitivity to changes in pain assessed
hourly for a maximum of 4 hours and weekly for up to 4
weeks following analgesic therapy (P < 0.001).  In
patients with rheumatoid arthritis, the minimal clinically
significant change has been estimated as 1.1 points on an
11-point scale (or 11 points on a 100-point scale).  A
minimum clinically important difference of 1.37 cm has
been determined for a 10-cm pain VAS in patients with
rotator cuff disease evaluated after 6 weeks of nonoperative
Critical Appraisal of Overall Value to the Rheumatology Community
Strengths/caveats and cautions/clinical and research usability. The VAS is widely used due to its simplicity and adaptability to a broad range of populations and settings. Its acceptability as a generic pain measure was demonstrated in the early 1970s. Limitations to the use of the pain VAS include the following: older patients may have difficulty completing the pain VAS due to cognitive impairments or motor skill issues, scoring is more complicated
than that for the Numeric Rating Scale for pain (described below), and it cannot be administered by telephone,
limiting its usefulness in research.
Numeric Rating Scale (NRS) For Pain
Purpose. The NRS for pain is a unidimensional measure of pain intensity in adults [19-21], including those with chronic pain due to rheumatic diseases. [3, 8] Although various iterations exist, the most commonly used is the 11-item NRS , which is described here.
Content. The NRS is a segmented numeric version of the visual analog scale (VAS) in which a respondent selects a whole number (0–10 integers) that best reflects the intensity of their pain.  The common format is a horizontal
bar or line.  Similar to the pain VAS, the NRS is anchored by terms describing pain severity extremes. [3,20,21]
Number of items. The pain NRS is a single 11-point numeric scale. 
Response options/scale. An 11-point numeric scale (NRS 11) with 0 representing one pain extreme (e.g., “no pain”) and 10 representing the other pain extreme (e.g., “pain as bad as you can imagine” and “worst pain imaginable”). [20, 21]
Recall period for items. Varies, but most commonly respondents are asked to report pain intensity “in the last 24 hours” or average pain intensity. 
How to obtain. Available from the web site:
Method of administration. The NRS can be administered verbally (therefore also by telephone) or graphically for self-completion.  The respondent is asked to indicate the numeric value on the segmented scale that best describes their pain intensity.
Scoring. The number that the respondent indicates on the scale to rate their pain intensity is recorded. Scores range from 0–10.
Score interpretation. Higher scores indicate greater pain intensity.
Respondent burden. The pain NRS takes <1 minute to complete.
Administrative burden. The pain NRS is easy to administer and score. [6, 25]
Translations/adaptations. Like the pain VAS, minimal language translation difficulties support the use of the NRS across cultures and languages. 
Method of development. To improve discrimination for detecting relatively small changes, an NRS comprised of numbers along a scale was used in a population of 100 patients with a variety of rheumatic diseases.  Variations in pain descriptors used as anchors for end points on the pain NRS have been reported in the literature. [3, 6, 24] However, the methodology used to develop these various anchor terms is unknown.
Acceptability. Chronic pain patients prefer the NRS over other measures of pain intensity, including the pain VAS, due to comprehensibility and ease of completion.  However, focus groups of patients with chronic back pain and symptomatic hip and knee osteoarthritis (OA) have found that the pain NRS is inadequate in capturing the complexity and idiosyncratic nature of the pain experience or improvements due to symptom fluctuations. [28, 29]
Reliability. High test–retest reliability has been observed in both literate and illiterate patients with rheumatoid arthritis (r = 0.96 and 0.95, respectively) before and after medical consultation. 
Validity. For construct validity, the NRS was shown to be highly correlated to the VAS in patients with rheumatic and other chronic pain conditions (pain >6 months): correlations range from 0.86 to 0.95. [3, 8]
Ability to detect change. In clinical trials of pregabalin for diabetic neuropathy, postherpetic neuralgia, chronic low back pain, fibromyalgia, and OA, analyses of the relationships
between changes in pain NRS scores and patient reports of overall improvement, measured using a standard 7-point patient global impression of change, demonstrated a reduction of 2 points, or 30%, on the pain NRS scores to be clinically important.  Similar results were found in low back pain patients when changes in pain NRS scores were compared to patient improvements in
pain after physical therapy, using a 15-point Global Rating
of Change scale. 
Critical Appraisal of Overall Value to the Rheumatology Community
Strengths/caveats and cautions/clinical and research usability. The pain NRS is a valid and reliable scale to measure pain intensity. Strengths of this measure over the pain VAS are the ability to be administered both verbally (therefore by telephone) and in writing, as well as its simplicity of scoring. However, similar to the pain VAS, the pain NRS evaluates only 1 component of the pain experience, pain intensity, and therefore does not capture
the complexity and idiosyncratic nature of the pain experience
or improvements due to symptom fluctuations.
McGill Pain Questionnaire (MPQ)
Purpose. A multidimensional pain questionnaire designed to measure the sensory, affective and evaluative aspects of pain and pain intensity in adults with chronic pain, including pain due to rheumatic diseases. [30, 31]
Content. The scale contains 4 subscales evaluating the sensory, affective and evaluative, and miscellaneous aspects of pain, responses to which comprise the Pain Rating Index, and a 5-point pain intensity scale (Present Pain Intensity).
Number of items. The Pain Rating Index contains 78 pain descriptor items categorized into 20 subclasses, each containing 2–6 words that fall into 4 major subscales:
sensory (subclasses 1–10),
affective (subclasses 11–15),
evaluative (subclass 16), and
miscellaneous (subclasses 17–20).
There is also a 1-item pain intensity scale. 
Response options/scale. The value (score) associated with each descriptor is based on its position or rank order within the word set. The Present Pain Intensity scale, a measure of the magnitude of pain experienced by an individual, is a numeric-verbal combination that indicates
overall pain intensity  and includes 6 levels:
horrible (4), and
excruciating (5) (32).
Recall period for items. Present pain. 
Examples of use. The MPQ can be used to evaluate the efficacy and effectiveness of pain interventions and to identify qualities of pain associated with distinct nocioceptive disorders and neuropathic pain disorders, including arthritis. 
How to obtain. The MPQ is available at no cost from the developer, Ronald Melzack, PhD, Department of Psychology, McGill University, 1205 Dr. Penfield Avenue, Montreal, Quebec H3A 1B1, Canada, and online (http://www.qolid.org) by paying a membership fee.
Method of administration. The MPQ is interviewer-administrated
using paper and pencil. The interviewer must read instructions to the respondent and define any words that the respondent does not understand. For each subclass of words, the respondent is instructed to select 1 word that fits their present pain. If none of the words describe their pain, then no word is selected. [30, 33]
Scoring. The MPQ is scored by hand by first counting the number of words selected to obtain a Number of Words Chosen score (0–20 words). Pain Rating Index scores range from 0–78 based on the rank values of the chosen words. The value (score) associated with each descriptor is based on its position or rank order in the word set, such that the first word is given a value of 1, the next a value of 2 and so on. Rank values are summed within each subclass as well
as overall. Scores on the Present Pain Intensity scale range
from 0–5. 
Score interpretation. A higher score on the MPQ indicates worse pain. The Pain Rating Index is interpreted both in terms of quantity of pain, as evidenced by the number of words used and the rank values of the words, as well as the quality of pain, as evidenced by the particular words that are chosen. The normative mean scores across painful conditions ranged from 24–50% of the maximum score. 
Respondent burden. Completion of the MPQ can take up to 20 minutes. 
Administrative burden. No training is required to score and interpret the MPQ, other than the ability of the interviewer to define each word. [30, 33] Time to score is 2–5
Translations/adaptations. There are a total of 44 different versions of the MPQ, representing 26 different languages/cultures.  The MPQ has been translated into English, French , German [36-38], Norwegian , Danish , Italian , Japanese , Finnish , Spanish , Chinese , Dutch , Amharic , Slovak , Turkish , and Portuguese. [50-52]
Method of development. Pain descriptors were derived from recording the words used by chronic pain patients to describe their pain; these descriptors were then categorized into subclasses and rank ordered by intensity using a numerical scale by groups of physicians, patients, and students. [31, 53]
Acceptability. Some respondents have difficulty with the complexity of the vocabulary used, resulting in failure to read the instructions carefully and to see essential features. 
Reliability. In a study of general rheumatology clinic patients, test–retest reliability for the 3 MPQ pain items (“nagging,” “aching,” and “stabbing”) ranged from a high of 0.81 for 1-day recall to a low of 0.59 for 7-day recall.  These findings are consistent with those of other studies
evaluating test–retest reliability in populations with a variety
of other conditions including arthritis and other musculoskeletal conditions (r = >0.70). [31, 56, 57]
Validity. Content validity. Arthritis patients, regardless of their disease severity, used similar words to describe the sensory aspects of their pain. MPQ words have been shown to differentiate between 4 different circumstances of rheumatoid arthritis (RA) pain (i.e., overall pain at rest, overall pain on movement, joint pain at rest, and joint pain on
movement).  The MPQ has the ability to detect mild pain due to the multidimensional nature of the scale and the large number of pain descriptor options. 
Construct validity. In RA, the number of sensory and affective MPQ words selected has been positively correlated with visual analog scale (VAS) scores of severity of
pain at rest and on movement (r = 0.27, P < 0.01 and r =
0.17, P < 0.05, respectively).  Higher Pain Rating Index
scores are associated with negative affect (e.g., Minnesota
Multiphasic Personality Inventory, Pain Catastrophizing
Scale).  In knee pain or knee osteoarthritis patients, higher MPQ scores were associated with greater anxiety and depression (r = 0.30, P < 0.05 and r = 0.31, P < 0.05, respectively) , and greater symptoms and disability using the Western Ontario and McMaster Universities pain scale (r = 0.34–0.38). 
Ability to detect change. In clinical trials designed to evaluate the efficacy of different pain therapies on postoperative pain after general surgical and orthopedic procedures, the relative effect sizes for the MPQ-Pain Rating Index compared with a 4-point categorical verbal rating scale and a pain VAS were 1.08 (moderate) and 1.12 (good), respectively. 
Critical Appraisal of Overall Value to the Rheumatology Community
Strengths/caveats and cautions/clinical and research usability. The MPQ is a valid and reliable tool that evaluates both the quality and quantity of pain through use of unique pain descriptors. This may be useful in epidemiologic studies and clinical trials of older patients with multimorbidity, in whom pain may arise from multiple causes. Specifically, use of the MPQ may help to identify neuropathic type pain from nocioceptive type pain. A
limitation of the MPQ is the rich vocabulary required of
respondents for completion. Further, sex and ethnic differences
may affect selection of pain descriptors. However,
the interviewer can facilitate MPQ completion by providing
Short-Form McGill Pain Questionnaire (SF-MPQ)
Purpose. The SF-MPQ, a shorter version of the MPQ, is a multidimensional measure of perceived pain in adults with chronic pain, including pain due to rheumatic diseases. [30, 33]
Content. The SF-MPQ is comprised of 15 words (11 sensory and 4 affective) from the original MPQ. 
Number of items. The Pain Rating Index is comprised of 2 subscales: 1) sensory subscale with 11 words or items and 2) affective subscale with 4 words or items, which are rated on an intensity scale as 0 = none, 1 = mild, 2 = moderate, or 3 = severe. The SF-MPQ also includes 1 item for present pain intensity and 1 item for a 10-cm visual analog scale (VAS) for average pain (33).
Recall period for items. Present time.
Examples of use. To discriminate among different pain syndromes [33, 63, 64] and evaluate the responsiveness of different symptoms to treatment. [65, 66]
How to obtain. See this section for the MPQ above.
Method of administration. See this section for the MPQ
Scoring. For the Pain Rating Index, each selected word is scored from 0 (none) to 3 (severe). The total Pain Rating Index score is obtained by summing the item scores (range 0–45). Scores on the Present Pain Intensity range from 0–5 and on the VAS from 0–10.
Score interpretation. There are no established critical cut points. As for the MPQ, a higher score indicates worse pain.
Respondent burden. The SF-MPQ takes ~ 2–5 minutes to complete. 
Administrative burden. No training is required to score and interpret the SF-MPQ other than the ability of the interviewer to define each word.  Time to score is ~ 1 minute.
Translations/adaptations. The SF-MPQ has been translated
into the following languages: English, French, Amharic , Chinese , Czech , Danish , Farsi , Greek [71, 72], Hebrew , Hindi , Korean [75, 76], Norwegian , Swedish , Thai , and Turkish. [49, 80]
Method of development. In addition to indices of overall pain intensity (the Present Pain Intensity  and VAS ), a selection of pain descriptors representing sensory and affective categories were retained from the original version of the MPQ.  Other than for one descriptor
(“splitting”), those selected for inclusion in the SF-MPQ
were those chosen by greater than one-third of patients
with various types of pain). [31, 82–84]
Acceptability. Standardized instructions for patient completion have not been published. Some difficulties with completion have been reported and attributed to unfamiliar descriptors and unclear written instructions. However, experience in completing the SF-MPQ and verbal instructions improved completion among osteoarthritis
(OA) patients. 
Reliability. For internal consistency, using the SF-MPQ in rheumatoid arthritis (RA) and fibromyalgia patients, Cronbach’s alphas were estimated at α 0.73–0.89. 
In the same study , test–retest reliability ranged from 0.45–0.73 for 1-month and 3-month intervals. Among rheumatology patients, test–retest reliability was 0.79–0.93 at intervals of 1 to 3 days.  In an OA population, high intraclass correlations were demonstrated for the total, sensory, affective, and average pain scores (5-day period): 0.96, 0.95, 0.88, and 0.89, respectively. 
Validity. The SF-MPQ was found to have more content validity among patients with fibromyalgia than for those with RA. Percentage of use of 15 pain descriptors by 2 groups was significantly different for all words except “throbbing” and “punishing-cruel.” The mean intensity score for each word ranged from 1.69 for “sickening” to 2.60 for “tender” in the fibromyalgia group and 1.57 for
“fearful” to 2.18 for “aching” in the RA group.  For construct validity, the SF-MPQ was found to be moderately correlated with both the Western and Ontario and McMaster Universities Osteoarthritis Index and the Short Form 36 Health Survey bodily pain scales (r = 0.36 and –0.36, respectively; P < 0.01) in 200 patients with hip and
knee OA. 
Ability to detect change. Although designed for descriptive purposes, the SF-MPQ has been found to be sensitive to the effects of pain therapies in a variety of population settings. [86 88] In patients with a range of musculoskeletal conditions reporting improvements in pain after rehabilitation and surgical interventions, the Norwegian SF
(NSF)-MPQ scores were found to be responsive to change
(standardized response mean values >0.80): a mean improvement
in NSF-MPQ total scores >5 on the 0–45 scale demonstrated a clinically important change.  In an OA population, the minimum detectable change for total, sensory, affective, average, and current pain components have been estimated as 5.2, 4.5, 2.8, 1.4, and 1.4 cm, respectively. 
Critical Appraisal of Overall Value to the Rheumatology Community.
Strengths/caveats and cautions/clinical and research usability. The SF-MPQ is easier to use and takes less time to administer and complete than the longer form. The word choices are not as complex, and the intensity ranking of mild, moderate, and severe is better understood by patients.  However, sufficient experience is required to adequately complete the SF-MPQ; therefore, new users require supervision during completion.  In 2009, the short form was further revised for use in neuropathic
and nonneuropathic pain conditions (SF-MPQ-2). The
SF-MPQ-2 includes 7 additional symptoms relevant to
neuropathic pain, for a total of 22 items with 0–10 numerical
response options.  We await further psychometric testing of this revised measure, which may play a useful role in the future with respect to identifying rheumatic disease patients with neuropathic versus nociceptive pain patterns.
Chronic Pain Grade Scale (CPGS)
Purpose. The CPGS is a multidimensional measure that assesses 2 dimensions of overall chronic pain severity: pain intensity and pain-related disability. It is suitable for use in all chronic pain conditions, including chronic musculoskeletal
(MSK) and low back pain. 
Content. Subscale scores for pain intensity and disability are combined to calculate a chronic pain grade that enables classification of chronic pain patients into 5 hierarchical categories: grades 0 (no pain) to IV (high disability-severely limiting). 
Number of items. The CPGS is comprised of 7 items.
Response options/scale. All items are scored on an 11-point Likert scale, with responses ranging from 0–10.
Recall period for items. Pain in the past 3–6 months.
Examples of use. The CPGS has been used in epidemiologic studies and clinical trials to evaluate and compare pain severity across groups and in response to treatment effects, and in clinical practice to improve the prognostic judgments of physicians. [91-93]
How to obtain. Please note that the scale is available in the original reference , as well as directly from the author.
Method of administration. The CPGS is an interview-administered
questionnaire that can also be self-completed by respondents.
Scoring. Scores are calculated for 3 subscales: the characteristic pain intensity score, which ranges from 0–100,
is calculated as the mean intensity ratings for reported
current, worst, and average pain; the disability score,
which ranges from 0–100, is calculated as the mean rating
for difficulty performing daily, social, and work activities;
and the disability points score, which ranges from 0–3, is
derived from a combination of ranked categories of number
of disability days and disability score.
The 3 subscale scores (characteristic pain intensity, disability score, and the disability points score) are used to classify subjects into 1 of the 5 pain severity grades: grade 0 for no pain, grade I for low disability-low intensity, grade II for low disability-high intensity, grade III for high disability-moderately limiting, and grade IV for high disability-severely limiting.
Respondent burden. Time to complete the CPGS does not exceed 10 minutes.
Administrative burden. The CPGS is easy to administer. Scoring is complex.
Translations/adaptations. The CPGS has been adapted into UK English.  An Italian version has been developed to evaluate severity in chronic pain patients. 
Method of development. Interviews were conducted with primary care patients with back pain, headache, and temporomandibular disorder.  The development of the graded classification drew on concepts by Turk and Rudy of chronic pain severity. [97, 98] Two of the items used in the disability score were adapted from their Multidimensional Pain Inventory.  The Guttman scaling method was used to develop the graded classification of chronic pain. 
Acceptability. The CPGS is easy to understand and complete based on a high response rate (76.3%) to a postal survey sent to general practice patients in the UK. 
Among MSK chronic pain patients, missing values were only noted in < 3% of each of the questions in an Italian version of the CPGS. 
Reliability. For internal consistency, Cronbach’s alpha was shown to be α = 0.74 among patients with chronic back pain.  In an Italian version of CPGS, Cronbach’s alpha ranged from 0.81–0.89 for subscales and global
scores in patients with chronic MSK pain.  In UK general practice patients with low back pain, test–retest reliability was high after a 2-week interval (weighted 0.81 [95% confidence interval 0.65–0.98]). 
Validity. For construct validity, cross-sectional and longitudinal
studies of general practice patients have shown that higher scores on the CPGS, indicating greater chronic pain, are significantly associated with higher rates of unemployment,
greater pain impact scale scores, greater use of opioid analgesics and physician visits, depressed mood, and lower self-rated health status. [90, 94, 102] Comparisons of CPGS scores with the Short Form 36 Health Survey (SF-36) indicate that a higher chronic pain grade using the CPGS is associated with poorer physical, psychological, social, and general health as measured by the SF-36 (P = 0.001)  and worse scores on the SF-36 bodily pain scale (ρ = –0.545,
P < 0.0001).  Spearman’s correlation coefficients for the CPGS scores and the various dimensions of SF-36 were highest for the pain dimension
(r = –0.71 to –0.84) and lowest for the mental health
dimension (r = –0.28 to –0.38). 
Ability to detect change.
Among patients with moderate to severe chronic MSK pain, the CPGS has been shown to be modestly responsive to changes after 12 months of treatment with an efficacious pain intervention, with standardized effect sizes for the intensity and disability subscales of 0.41 and 0.43, respectively. Among participants with chronic knee or hip pain, the standardized effect size for the CPGS intensity was 0.32. 
Critical Appraisal of Overall Value to the Rheumatology Community
Strengths/caveats and cautions/clinical and research usability. The CPGS is a valid and reliable tool that is useful for the evaluation of chronic MSK pain; it allows for grading of the global severity of chronic pain and therefore analysis of the qualitative changes in chronic pain over time. Further, the CPGS assesses not only aspects of the pain itself, but also the impact of the pain on daily, social, and work activities, which is a significant advantage over many other pain questionnaires. A limitation of the CPGS relative to the other scales reported here is the complexity of scoring, which renders it less useful for assessment of pain at point of care. Additionally, further
research is needed to be able to compare scoring methods
and cut points.
Short Form 36 Bodily Pain Scale (SF-36 BPS)
Purpose. The SF-36 BPS is 1 of 8 subscales of the Medical Outcomes Study SF-36 questionnaire [103, 104], a
generic measure of health status designed for use in population
surveys.  In 1996, version 2.0 of the SF-36 (SF-36v2) was introduced to correct deficiencies identified in the original version, SF-36v1.  The 2-item SF-36
BPS subscale assesses bodily pain as a dimension of health
status. [104, 105]
Content. The SF-36 BPS assesses bodily pain intensity and interference of pain with normal activities.
Number of items. The SF-36 BPS is a 2-item scale.
Response options/scale. Intensity of bodily pain is evaluated using a 6-point rating scale of “none” to “very severe.” The extent to which pain has interfered with work is evaluated on a 5-point rating scale from “not at all” to “extremely.”
Recall period for items. The SF-36 BPS is available in both standard (4 week) and acute (1 week) recall versions. [105, 106]
Examples of use. The SF-36 and its subscales, including the BPS, have been used in epidemiologic studies to compare health status across populations and within population subgroups, such as in estimating the relative burden of different diseases, including rheumatic diseases , and differentiating the health benefits of different treatments. 
How to obtain. The SF-36 and its various versions have been developed by the Rand Corporation and John E. Ware (SF-36 Health Survey, The Health Institute, New England Medical Center Hospitals, Box 345, 750 Washington Street, Boston, MA, 02111). The Medical Outcomes Trust, Health Assessment Lab, and Quality Metric Incorporated are cocopyright holders of all SF-36 and SF-12 surveys. All
SF-36 survey instruments, scoring manuals, and licenses for use are available from QualityMetric at www.quality metric.com. Different charges are levied for academic and commercial use.
Method of administration. The SF-36 BPS is suitable for self-administration, computerized administration, or administration by a trained interviewer in person or by telephone. Telephone voice recognition interactive systems and online administrations are currently being evaluated.
Scoring. Responses for each of the 2 SF-36 BPS items are recoded into final item values.  The raw scale score is computed as a simple algebraic sum of the recoded item values. The raw scale score is then transformed to a 0–100 scale. Norm-based scores may be calculated for SF-36v2 by including population normative data in the scoring algorithms. The BPS score is only calculated if both items are completed.
Score interpretation. SF-36v1 BPS scores range from 0–100. A higher score indicates lack of bodily pain. SF-36v2 uses norm-based scoring, where 50 is the “average” for the population. Therefore, scores above or below 50 can be considered above or below, respectively,
the population average health status for bodily pain, and
scores can be interpreted based on deviance from the mean
(10 points = 1 SD). Population normative data are available
for the US and UK.
Respondent burden. The BPS takes <2 minutes to complete.
Administrative burden. Training to administer, score, and interpret is minimal. Administration guidelines are specific and clearly outlined.
Translations/adaptations. SF-36 has been translated and adapted for use in more than 50 countries as part of the International Quality of Life Assessment (IQOLA) Project. Currently, published forms include the German , Spanish , Swedish , and Italian  translations and English-language adaptations for use in Australia/New Zealand, Canada, and the UK. Information about translations is available from the IQOLA Program of the Health Assessment Lab in Boston, Massachusetts (http://www.iqola.org).
Method of development. The Medical Outcomes Study researchers selected and adapted questionnaire items from instruments in use since the 1970s and 1980s [114-117] to
develop a new 149-item Functioning and Well-Being Profile.
Items were subsequently reduced and improvements were made in item wording, format, and scoring to produce the SF-36. One item on pain intensity was retained from an earlier version of the SF-20 question regarding bodily pain or discomfort. In order to improve prediction of best total scores for the Behavioural Effects of Pain Scale in the Medical Outcomes Study , a second item was added to measure the extent to which pain interferes in activities. 
Acceptability. Generally easy to administer and complete. [103, 118]
Reliability. For internal consistency, Cronbach’s α for the SF-36 BPS administered in hip  and knee  osteoarthritis (OA) patients was 0.72 and 0.77, respectively;
using a Chinese version of the SF-36 BPS in rheumatoid
arthritis (RA) patients, Cronbach’s α was 0.91.  In adults with persistent back, hip, or knee pain recruited from primary care, Cronbach’s α was 0.59.  Among patients from 2 general practices in the UK, the test–retest reliability over a 2-week period was 0.78.  Over a 14-day interval, test–retest reliability of a Chinese SF-36 version used in Chinese-speaking RA patients was 0.82. 
Validity. Regarding face and content validity, items were derived from pre-existing questionnaires used in large population studies. However, both floor and ceiling effects have been reported.  Regarding construct validity,
the proportions reporting no pain on the Western Ontario and McMaster Universities Osteoarthritis Index (WOMAC) and the SF-36 BPS were 32.2% and 13.6%, respectively, and pain scores were modestly correlated (–0.55)  among patients who had undergone joint replacement surgery. In the same study, the WOMAC better discriminated subjects with varying severity of knee problems, whereas the SF-36 BPS better discriminated subjects with varying levels of self-reported health status and comorbidity. In patients with hip and knee OA, correlations between the WOMAC pain scale and the SF-36 BPS are in the range of 0.6–0.7. [61, 121, 123] In Chinese-speaking
patients with RA, moderate correlations were reported between the Chinese SF-36 BPS and physician global assessment of disease activity (r = –0.34), physician’s assessment of global disease activity (r = –0.35), and patient pain assessment based on a pain visual analog scale (r = –0.48). 
Ability to detect change. Although the SF-BPS is designed to measure the health status of populations, it has been shown to be responsive to improvements in pain. Among patients undergoing knee replacement surgery, the estimated minimum clinically important difference
(MCID) ranged from 16.86/100 (SD 31.83) at 6 months to 6.69/100 (SD 29.20) at 2 years.  In a similar study on hip replacement, the estimated MCID ranged from 14.67/100 (SD 26.46) to 18.34/100 (SD 27.06) at 6 months and 2 years, respectively.  The minimal detectable change for the SF-36 BPS ranged from 37.91/100 (knee OA) to 38.09/100 (hip OA) at 6 months. [118, 119]
Critical Appraisal of Overall Value to the Rheumatology Community
Strengths/caveats and cautions/clinical and research usability. The SF-36 BPS is a valid and reliable generic questionnaire designed to evaluate bodily pain as a dimension of overall health status and has been widely used internationally and in diverse populations. Its advantages include simplicity of administration and usefulness in making comparisons across populations for research purposes.
At point of patient care, a disease-specific pain measure may be more useful to discriminate levels of pain severity, and therefore response to treatment.
Measure Of Intermittent And Constant Osteoarthritis Pain (ICOAP)
The ICOAP measure is a multidimensional osteoarthritis (OA)-specific measure designed to comprehensively evaluate the pain experience in people with hip or knee OA, including pain intensity, frequency, and impact on mood, sleep, and quality of life, independent of the effect of pain on physical function.  It is intended
for use alongside a measure of physical disability. Content. The ICOAP is an 11-item scale evaluating 2 pain domains: a 5-item scale evaluates constant pain and a 6-item scale evaluates intermittent pain or “pain that comes and goes”.  Two supplementary questions can
be used to assess predictability of intermittent pain when
present.  Both a hip and knee joint version of the ICOAP are available. 
Number of items:
11 items in 2 domains with 2 supplementary items on intermittent pain predictability.
All items are constructed as rating scales with 5 levels of response. For items asking about intensity, response options are “not at all,” “mildly,” “moderately,” “severely,” and “extremely.” For items about frequency, response options are “never,” “rarely,” “sometimes,” “often,” and “very often”.  For the supplementary items asking about predictability of pain, the response options are “never,” “rarely,” “sometimes,” “often,” and “very often”. 
Recall period for items.
Osteoarthritis Research Society International (OARSI)/Outcome Measures in Rheumatology (OMERACT) Initiative.
How to obtain.
The ICOAP and ICOAP Users Guide can be obtained free of charge from the OARSI web site, www.oarsi.org.
Method of administration.
The measure can be interviewer-
administered in person or by telephone.  Respondents should complete both subscales. 
Scoring. Each ICOAP item is scored from 0–4. A score
is separately produced for each subscale by summing the
items’ subscale scores and then normalizing each score
from 0 (no pain) to 100 (extreme pain). A total ICOAP score
can be calculated by summing the 2 subscale scores, and
normalizing from 0 (no pain) to 100 (extreme pain). Rules
have been created to deal with missing data.  No scoring guidelines are available for the 2 supplementary items.
Higher scores indicate a worse pain experience.
The ICOAP takes < 10 minutes to
Easy to administer and score.
To date, the ICOAP has been translated into the following languages: English (North America and UK), Czech, Dutch, French (France), German , Italian, Norwegian, Spanish (Castillan), North and Central American Spanish, Swedish, Portuguese , Greek, Romanian, and Russian.  Translated versions
are available at www.oarsi.org.
Method of development.
Focus groups were conducted in individuals with painful hip or knee OA in 4 countries (US, UK, Canada, and Australia) to generate items pertaining to the OA pain experience. [28, 127] Content analysis of
resulting transcripts was used to identify themes, which
were verified with participants. Subsequent psychometric
testing was conducted in subjects age ≥ 40 years with hip
or knee OA drawn from rheumatologists’ practices, joint
replacement wait lists, and from among the members of an
existing OA cohort. 
The ICOAP has been shown to be easy to understand and complete; subjects felt positive about the inclusion of the 2 distinct pain domains (constant pain and pain that comes and goes). 
Regarding content validity, Cronbach’s α was 0.93  for 100 individuals with hip and knee OA. Test–retest reliability in 76 individuals with hip and knee OA, age ≥ 40 years, demonstrated an intraclass correlation coefficient of 0.85 (95% confidence interval 0.76–0.91). 
Content and face validity were determined through focus groups used to develop the ICOAP. For construct validity, descriptive analyses of items demonstrated good distribution of response options across all items.  Total and subscale ICOAP scores are significantly correlated with scores on the Western Ontario and McMaster Universities Osteoarthritis Index (WOMAC) pain scale, the Knee Injury and OA Outcome Score (KOOS) symptoms scale, and self-rated effect of hip/knee problems on quality of life, with Spearman’s correlation coefficients ranging in magnitude from 0.60 (KOOS symptoms) to 0.81 (WOMAC pain scale). 
Ability to detect change.
The ICOAP has been found to be responsive to changes in OA pain in response to pharmacologic interventions  and joint replacement surgery.  For the knee, standard response means (SRMs) ranged from 0.49–0.57 for the ICOAP intermittent, constant, and total scores comparable to that for the WOMAC pain (SRM 0.54). For the hip, SRMs ranged from 0.11–
0.19, again comparable to that for the WOMAC (SRM 0.15).  The ICOAP detected large improvements in pain resulting from joint replacement surgery with SRMs (0.84–1.02 for knee replacement and 1.50–2.29 for hip replacement). 
Critical Appraisal of Overall Value to the Rheumatology Community
Strengths/caveats and cautions/clinical and research usability.
The ICOAP is a valid and reliable measure that is unique in that it is intended to evaluate the multidimensional
pain experience in OA, distinct from the impact of pain on physical functioning. Prior experience with the WOMAC, the most commonly used OA measure, has shown high correlations between the pain and physical function subscales. As a result, evaluation of OA pain using the WOMAC is confounded by physical disability. The ICOAP is intended for use together with a measure of OA disability. Although the ICOAP has been translated
from English into a number of languages, only a few have been evaluated for validity, reliability, and responsiveness.
There are multiple measures available to assess pain in
adult rheumatology populations. Each measure has its
own strengths and weaknesses. Both the Visual Analog
Scale for Pain and the Numeric Rating Scale (NRS) for Pain
are unidimensional single-item scales that provide an estimate
of patients’ pain intensity. They are easy to administer,
complete, and score. Of the 2, the pain NRS may be
preferred at point of patient care due to simpler scoring.
In research, the pain NRS may similarly be preferred due to
its ability to be administered both verbally and in writing.
However, neither measure provides a comprehensive evaluation
of pain in patients with rheumatic disease. To evaluate
the multiple dimensions of acute and chronic pain, a
number of valid and reliable questionnaires are available.
The McGill Pain Questionnaire (MPQ) is a generic pain
measure useful largely for research purposes to describe
not only the quantity (intensity), but also the quality of the
The Chronic Pain Grade Scale (CPGS) is similarly a generic pain measure useful for research purposes to describe, evaluate and compare chronic pain severity (its intensity and impact) across groups and in response to treatment effects.
The third generic multidimensional pain measure, the Short Form-36 Bodily Pain Scale (SF-36 BPS), is useful in evaluating pain in the context of overall health status, and therefore most suitable for use in making comparisons across populations
and between subgroups within populations. Unlike the
MPQ and CPGS, the SF-36 BPS is simple enough for use at
point of care.
Finally, the Measure of Intermittent and Constant Osteoarthritis Pain is an osteoarthritis-specific pain measure that is recommended for descriptive and evaluative purposes in both clinical practice and research to provide a comprehensive evaluation of the pain experience in osteoarthritis, including the impact of pain on mood, sleep and quality of life, separate and distinct from the impact of pain on functioning.
Due to the variability in purpose, content, method of administration, respondent and administrative burden, and evidence to support the psychometric properties of each measure, no one pain measure can be recommended for use in all situations. We encourage clinicians and researchers to use this information presented in this chapter to help guide the selection of the questionnaire that is most appropriate for their specific purpose.
All authors were involved in drafting the article or revising it critically for important intellectual content, and all authors approved the final version to be published.
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