Skip to main content
Implementation Science : IS logoLink to Implementation Science : IS
. 2017 Jan 5;12:1. doi: 10.1186/s13012-016-0533-0

Clinical practice guidelines for the management of chronic musculoskeletal pain in primary healthcare: a systematic review

Dawn V Ernstzen 1,✉, Quinette A Louw 1, Susan L Hillier 1,2
PMCID: PMC5217556  PMID: 28057027

Abstract

Background

Up-to-date, high quality, evidence-based clinical practice guidelines (CPGs) that are applicable for primary healthcare are vital to optimize services for the population with chronic musculoskeletal pain (CMSP). The study aimed to systematically identify and appraise the available evidence-based CPGs for the management of CMSP in adults presenting in primary healthcare settings.

Methods

A systematic review was conducted. Twelve guideline clearinghouses and six electronic databases were searched for eligible CPGs published between the years 2000 and May 2015. CPGs meeting the inclusion criteria were appraised by three reviewers using the Appraisal of Guidelines Research and Evaluation (AGREE) II.

Results

Of the 1082 records identified, 34 were eligible, and 12 CPGs were included based on the inclusion and exclusion criteria. The methodological rigor of CPG development was highly variable, and the median domain score was 66%. The median score for stakeholder involvement was 64%. The lowest median score was obtained for the domain applicability (48%). There was inconsistent use of frameworks to aggregate the level of evidence and the strength of the recommendation in the included CPGs. The scope and content of the included CPGs focussed on opioid prescription.

Conclusion

Numerous CPGs that are applicable for the primary healthcare of CMSP exists, varying in their scope and methodological quality. This study highlights specific elements to enhance the development and reporting of CPGs, which may play a role in the uptake of guidelines into clinical practice. These elements include enhanced reporting of methodological aspects, the use of frameworks to enhance decision making processes, the inclusion of patient preferences and values, and the consideration of factors influencing applicability of recommendations.

Trial registration

PROSPERO CRD42015022098.

Electronic supplementary material

The online version of this article (doi:10.1186/s13012-016-0533-0) contains supplementary material, which is available to authorized users.

Keywords: Clinical practice guidelines, Chronic musculoskeletal pain, Primary health, Systematic review

Background

Chronic musculoskeletal pain (CMSP) is a global healthcare concern. The condition is classified as a part of chronic non-malignant pain, which encompasses musculoskeletal, neuropathic and visceral pain, and pain from sickle cell disease [1]. CMSP negatively impacts physical and psychosocial health, daily function, participation in life roles, healthcare utilization, health-related quality of life [2–4]; and its management is associated with high financial, personal and resource costs. This complex condition involves biological, psychological, social and environmental factors. Therefore, a multidisciplinary and holistic approach to the management of CMSP is appropriate [5].

The prevalence of chronic pain is high and increasing [2, 6, 7]. A large proportion of individuals with CMSP present in primary healthcare settings for management [3, 8]. Primary healthcare settings appears to be ideally situated to deliver holistic care for the patient with chronic pain, addressing the health needs within the community [9], while integrating preventative, promotive, curative, and rehabilitation services. The components of primary healthcare are congruent with the proposition that chronic pain management should be multimodal and include rehabilitative options [1, 3, 10]. It is therefore vital that primary healthcare settings are adequately resourced to deal with the service-provision load associated with the holistic management of CMSP [3, 11]. These resources may include human resources, healthcare system, and policy and information resources.

Access to high quality, evidence-based, and up-to-date information resources can assist clinicians in making decisions about the care of patients with CMSP. Clinical practice guidelines (CPG) are one way of providing information on evidence-based and person-centred options for CMSP care. CPGs provide systematically developed clinical recommendations derived from best available evidence to guide clinicians and patients in making decisions about healthcare for specific clinical circumstances [12, 13]. CPGs may support decision-making by managers and policy-makers about the organization and delivery of healthcare [12, 14]. The implementation of CPGs can optimize healthcare by improving the quality, consistency, appropriateness, and cost-effectiveness of care [15–18]. Furthermore, CPGs play a role in enhancing provider and patient satisfaction with care [18]. CPGs are therefore useful means to enhance quality healthcare for the patient with CMSP by implementing evidence-informed management. Ideally, CPGs about CMSP should include a multidisciplinary perspective to facilitate the holistic management of CMSP.

The validity of CPGs depends on how well they were designed and conducted [14]. Clinicians often find it difficult to judge a CPG as trustworthy or of good quality due to the large number of CPGs available and the often contradictory information in them [13, 17]. In a good quality CPG, the clinical recommendations are rigorously developed, based on current, relevant scientific evidence, and it considers the benefits and harms of different healthcare options [13, 17, 19, 20]. Good quality CPGs encourage the use of interventions with proven benefits and discourages the use of ineffective or harmful interventions [21]. The cost-effectiveness of implementation, context-specific factors, and stakeholder involvement are important elements to be considered by a good CPG [20]. Despite the above quality indicators, several authors found the methodological quality of CPGs to be highly variable [16, 18, 20]. Consequently and several criteria have been developed to evaluate the methodological quality of CPGs, for example, the AGREE (Appraisal of Guidelines Research and Evaluation) instrument [13, 20, 22].

High quality, evidence-based, and up-to-date CPGs that are applicable for primary healthcare are crucial to optimize care for CMSP [7]. The multidimensional nature of CMSP, together with its associated burden, heightens the need for multimodal management strategies to prevent and manage the condition. A CPG is an important information resource to facilitate decision-making about care and to translate research findings into clinical practice. When considering the development of a CPG for the management of CMSP in primary healthcare, one needs to consider if such CPGs already exist, if existing CPGs are of high quality and if it represents the holistic and multimodal management for CMSP. The de novo development of CPGs can be expensive and time-consuming. Consequently, it has become a viable option to adopt, adapt, or contextualize existing CPGs in resource-constrained environments [23]. CPG contextualization refers to the consideration of possible differences in contextual factors such as personal and environmental features that may differ from one setting to the other. Knowledge about the existence and quality of CPGs for CMSP in primary healthcare, can inform the choice between adoption, adaptation, contextualization and de novo development of CPGs. The aim of this systematic review was therefore to methodically identify and appraise the available evidence-based CPGs for the management of adults with CMSP in primary healthcare settings.

The primary objectives were to:

  • identify profession-specific or inter-professional CPGs on the management of CMSP in primary healthcare settings;

  • critically appraise the quality of the included CPGs using the AGREE II instrument;

  • determine the currency of the CPGs; and to

  • determine the grading systems used to demarcate the level of evidence and the strength of the recommendation in the CPGs.

Methods

Study criteria

The study criteria were formulated using the PIPOH format (population, intervention, professions, health outcomes and health setting) for guideline reviews [24]. The types of studies eligible were CPGs available in full text and published between the years 2000 and May 2015. The date cut-off was set to ensure up-to-date CPGs. The target population and disease characteristic of the CPGs included adults with CMSP. It was anticipated that recommendations for CMSP would be included in CPGs for chronic non-malignant pain. CPGs that focused exclusively on chronic pain from non-musculoskeletal origin such as sickle cell disease, neuropathic pain, and malignancy was excluded due to the differences in pathology, pain mechanisms, and possible management strategies.

The types of interventions could include evaluation, diagnosis, and management of CMSP. Examples of such interventions include inter-professional interventions, pharmacological, and non-pharmacological management, rehabilitative options, and self-management. CPGs that targeted any healthcare professionals involved in the management of CMSP were eligible for inclusion. The expected outcomes of CPGs could include patient outcomes, system outcomes, or public health outcomes. For the purpose of this review, only CPGs focused on primary healthcare settings were included. CPGs that focussed solely on secondary, tertiary, or specialist healthcare settings were excluded due to different management options offered.

Search strategy

The primary investigator searched the electronic databases of the following guideline clearinghouses: the US National Guideline Clearinghouse (US NGC); Agency for Healthcare Research and Quality (AHRQ); Guidelines International Network (G-I-N); Scottish Intercollegiate Guidelines (SIGN); United Kingdom’s National Institute for Health and Clinical Excellence (NICE); New Zealand Guidelines Group (NZGG); WHO guidelines; TRIP database; National Institutes of Health (NIH); Monash University Centre for Clinical Effectiveness; Australia’s National Health and Medical Research Council (NHMRC); Canadian Medical Association Clinical Practice Guidelines Infobase, and the Institute for Clinical Systems Improvement (ICSI). In addition, the following online databases were searched to include those guidelines that were peer reviewed and published in journals: CINAHL, PEDro; PubMed, EBSCO host, and Medline. The broad search terms included: clinical practice guidelines; OR clinical guidelines; OR care pathway; OR clinical pathway; OR care protocol; AND chronic pain; OR chronic musculoskeletal pain; OR chronic non-malignant pain; OR chronic non-cancer pain; AND adults; AND primary care; OR primary healthcare.

The initial search was conducted from July to October 2014, and the search was updated during May 2015. The inclusion and exclusion criteria were applied by screening the identified CPG titles and objectives to select the eligible CPGs. The data was extracted in the PIPOH format to enable this analysis. The process was verified by the co-authors on a random audit basis. A record of search yields and decision-making was kept.

Data extraction

The primary investigator extracted the following data into custom built data extraction sheets:

  • The clinical question formulation using the PIPOH format.

  • Guideline currency: the publication date of the CPG and periods covered by the literature search in the guideline, date of revision.

  • General information: the developing organization/authors; country of publication; language of publication.

Critical appraisal

The methodological quality of eligible CPGs was independently assessed by three reviewers using the AGREE II instrument [25]. The AGREE II is an internationally developed, widely accepted, valid, reliable, easy to use, and transparent instrument to assess the methodological rigor of the reported guideline [18, 22]. It contains 23 key quality items categorized in six domains, scored on a 7-point Likert scale. The AGREE II evaluates the process of CPG development and the quality of reporting. However, it does not evaluate the content of the CPG, nor the quality of evidence supporting the recommendations. Each AGREE II domain focuses on a separate aspect of guideline quality, namely, scope and purpose, stakeholder involvement, rigor of development, clarity of presentation, applicability, and editorial independence.

The reviewers’ AGREE scores were entered into a custom built Excel spreadsheet by the primary investigator. Any difference in score higher than two points was discussed amongst the project team to reach consensus. A quality score was calculated for each of the six AGREE II domains using the guiding principles and the following formula provided in the user manual:

Domain score = (obtained score–minimum possible score)/(maximum possible score–minimum possible score) × 100 = %. All item scores in a domain were summed, and the total was standardized as a percentage of the maximum possible score for that domain. The median domain score and interquartile range (IQR) for each domain was then calculated [26].

Results

Search results

The results of the systematic search are summarized in Fig. 1. The search yielded two categories of CPGs, namely, comprehensive CPGs and CPGs that were published in journal article format. Where indicated, contact was made with the authors to obtain full text CPGs. Thirty-four eligible CPG were considered for inclusion. After applying the inclusion/exclusion criteria, 12 CPGs were included. The main reasons for exclusions are summarized in Fig. 1.

Fig. 1.

Fig. 1

Diagram of search results (PRISMA format)

Included clinical practice guidelines

Table 1 summarizes information about the included CPG and their currency. One of the included CPGs originated from a middle-income country (CPG 10). Six out of the 12 included CPGs focused on the prescription of opioids (CPGs 1, 3, 6, 7, 8, and 10), and two focused specifically on the management of musculoskeletal pain (CPG 9 and 12).

Table 1.

Included CPGs (n = 12)

CPG number Title of guideline Organization/authors Country of origin Guideline currency
Date for revision Publication date Search dates covered
CPG 1 Guidelines for responsible opioid prescribing in chronic non-cancer pain: Part 1—evidence; Part 2—guidance American Society of Interventional Pain Physicians (ASIPP) [41] USA June 2015 2012
(update on 2008 version)
Not stated
CPG 2 Assessment and management of chronic pain Institute for Clinical Systems Improvement (ICSI) [31] USA Every 24 months, i.e., December 2015 2013 (update on 2011 version) August 2011–August 2013
CPG 3 Canadian guideline for safe and effective use of opioids for chronic non-cancer pain National Opioid Use Guideline Group (NOUGG) [42] Canada Not stated 2010 2005–July 2009
CPG 4 Assessment and management of pain Registered Nurses’ Association of Ontario (RNAO) [32] Canada Every 5 years, i.e., 2018 2013
(update on 2002, 2007 versions)
2007–2012
CPG 5 Management of chronic pain: a national clinical guideline. Scottish Intercollegiate Guidelines Network (SIGN) [30] UK In 3 years, i.e., 2016 2013 2007–2012
CPG 6 Managing chronic non-terminal pain in adults including prescribing controlled substances University of Michigan Health System (UMHS) [43] USA Not stated (previous was 2009, 2011) 2011 1995–2010;
(search dates 1998 –2002)
CPG 7 Interagency guideline on opioid dosing for chronic non-cancer pain: an educational aid to improve care and safety with opioid treatment Washington State Agency Medical Directors’ Group (WSAMDG) [44] USA Not stated 2010
(update on 2007 version)
Not stated
CGA 8 Clinical guidelines for the use of chronic opioid therapy in chronic non-cancer pain The American pain society (APS)–American academy of pain medicine (AAP) [45] USA 2012 2009 Through to July 2008 (not stated from when)
CGA 9 Managing musculoskeletal complaints with rehabilitation therapy: summary of the Philadelphia panel evidence-based clinical practice guidelines on musculoskeletal The Philadelphia Panel Members and Ottawa Methods Group [46, 47] Canada and USA Not stated 2002 Through to July 2000
CGA 10 South African guideline for the use of chronic opioid therapy for chronic non-cancer pain Raff M, Eppel S, Meyer H, Sarembock B, Webb D [48] SA Not stated 2014 Not stated
four existing CPGs published between 2009–2012 were chosen (CPG 1, 2, 8 in this Table)
CGA 11 Evidence-based clinical practice guidelines for interdisciplinary rehabilitation of chronic non-malignant pain syndrome patients Sanders SH, Harden NR, Vicente PJ [33] USA Every 4 years 2005
(update on 1995, 1999 version)
September 1999 (end date not stated)
CGA 12 Update on guidelines for treatment of chronic musculoskeletal pain Schnitzer TJ [7] USA Not stated 2006 Not stated

(CPG clinical practice guideline, CGA clinical guideline in article format, USA United States of America, UK United Kingdom, SA South Africa)

Methodological quality

The AGREE II domain scores (median and range) are provided in Table 2. The domains with the lowest median score were domain 2 (stakeholder involvement), domain 3 (rigor of development), and domain 5 (applicability). Further analysis of each question within a domain is represented in Table 3. Additional file 1 provides more information on the guideline development group and the stated scope for each CPG.

Table 2.

Combined scores of the three reviewers in %

CPG 1 CPG 2 CPG 3 CPG 4 CPG 5 CPG 6 CPG 7 CPG 8 CPG 9 CPG 10 CPG 11 CPG 12 Median IQR
Domain 1: scope and purpose 89 96 98 80 93 48 89 76 67 78 63 48 79 24
Domain 2: stakeholder involvement 65 85 91 70 100 52 63 80 57 35 22 15 64 34
Domain 3: rigor of development 72 85 94 88 94 47 40 84 60 30 51 30 66 41
Domain 4: clarity of presentation 91 89 87 96 98 87 69 90 83 69 57 72 87 19
Domain 5: applicability 60 79 75 92 79 53 32 43 21 14 15 7 48 57
Domain 6: editorial independence 97 100 100 67 67 97 44 100 25 100 0 86 91.5 39
TOTAL 474 534 545 493 531 384 337 473 313 326 208 258
Overall score out of 7 5 5.6 6 5.3 6.5 4 3.6 5 3.6 3 3 3

CPG clinical practice guideline

Table 3.

All domain scores

CPG 1 CPG 2 CPG 3 CPG 4 CPG 5 CPG 6 CPG 7 CPG 8 CPG 9 CPG 10 CPG 11 CPG 12 Total Percentage (%)
Domain 1: scope and purpose
 1. Overall objectives specific 21 20 21 17 18 18 19 17 15 16 13 14 209 83
 2. Health questions specific 18 20 21 19 21 9 18 16 14 15 13 9 193 77
 3. Population is specific 18 21 20 16 20 8 20 17 16 20 17 12 205 81
Domain 2: stakeholder involvement
 4. Guideline development group 19 18 20 15 21 15 18 19 20 7 6 10 188 75
 5. Views and preferences of target population 5 21 18 11 21 6 7 14 2 4 3 3 115 46
 6. Target users clearly defined 20 16 20 21 21 16 18 19 18 17 12 4 202 80
Domain 3: rigor of development
 7. Systematic methods 15 17 21 21 21 19 10 13 12 6 16 4 175 69
 8. Criteria for evidence selection 14 19 21 21 21 17 5 15 19 7 16 4 179 71
 9. Strengths and limitations of evidence 13 19 20 18 18 6 5 20 19 10 9 4 161 64
 10. Methods for formulating recommendations 19 17 21 18 19 8 10 21 17 5 8 11 174 69
 11. Health benefits, side-effects, risks were considered in formulating recommendations 20 19 19 17 19 19 21 21 9 18 12 20 214 85
 12. Explicit link between recommendations and evidence 19 17 21 20 21 12 10 19 17 11 12 12 191 76
 13. Externally reviewed prior to publication 15 18 21 16 21 6 16 18 15 7 10 9 172 68
 14. A procedure for updating guideline 13 20 15 20 19 5 4 18 3 3 14 3 137 54
Domain 4: clarity of presentation
 15. Recommendations specific; unambiguous 20 19 21 20 20 18 17 20 17 15 13 18 218 87
 16. Different options for management 18 19 14 21 21 20 13 18 18 15 15 16 208 83
 17. Key recommendations easily identifiable 20 19 21 20 21 18 16 20 19 14 12 14 214 85
Domain 5: applicability
 18. Barriers and facilitators to application 15 16 19 20 17 11 6 8 11 4 4 5 136 54
 19. Advice/Tools to put recommendations to practice 14 20 21 20 18 8 13 10 9 7 8 6 154 61
 20. Potential resource limitations have been considered 9 13 12 18 15 11 7 12 4 3 3 3 110 44
 21. Monitoring and audit criteria 15 20 14 20 19 20 9 13 3 8 8 3 152 60
Domain 6: editorial independence
 22. Views of funding body vs guideline content 20 21 21 15 10 20 14 21 12 21 3 17 195 77
 23. Competing interests of guideline development group members have been recorded and addressed 21 21 21 15 20 21 8 21 3 21 3 20 195 77

CPG clinical practice guideline

Domain score = (obtained score–minimum possible score)/(maximum possible score–minimum possible score) × 100 = % [25]

CPGs consistently inadequately adhered to topic 5 in domain 2 (views and preferences of target population). Only 3 of the 12 included CPGs reported that they sought patient perspectives as part the CPG development. The methods used in these CPGs included focus groups with patients (CPGs 3 and 2); patients as part of the guideline development group (CPG 5); a literature search of patients’ preferences (CPG 5); an environmental scan through surveys, key informant interviews and focus groups (CPG 2). The strengths and limitations of evidence (topic 9), was also inconsistently adhered to. Within domain 3 (rigor of development), topic 14 had the lowest scores, indicating that few CPGs included a procedure for updating the CPG. All four topics in domain 5 (applicability) were challenging for the CPG developers to report on, as indicated by the low scores.

The analysis of domain 5 (applicability) indicated that algorithms and outcome measure tools for putting recommendations into practice was the most common strategies provided to facilitate implementation of CPG recommendations (see Additional file 2). Although guideline developers mentioned barriers and facilitators for the use of the CPG (CPG 1, 3, 4, 5); this aspect was not covered in-depth. The consideration of resource implications was partially covered. Policies, as well as monitoring and evaluation criteria for opioid therapy was a consideration that was well attended to by the CPGs focusing on opioid prescription (CPG 1, 2, 6, 7, and 8).

Evidence grading systems used by the clinical practice guidelines

The CPGs used a variety of grading systems to categorize the levels of evidence and the strength of the recommendation. These grading systems are summarised in Table 4. Three CPGs did not grade the level of evidence or the strength of the recommendation. Four CPGs graded the level of evidence, but not the strength of the recommendation.

Table 4.

Grading systems used to determine the level of evidence and the strength of the recommendation

CPG Name of grading system Level of evidence grading Strength of recommendation
1 ASIPP [41] United States Preventive Services Task Force (USPSTF) criteria Good
Fair
Poor
None
2 ICSI [31] In transition between ISCI system to GRADE. Thus, using an hybrid system High quality evidence
Low quality evidence
None
3 NOUGG [42] – I,
II-1
II-2
II-3
OR III
A,
B,
C
4 RNAO [32] Adapted SIGN Ia
Ib
IIa
IIb
III
IV
None
5 SIGN [30] SIGN 1++, 1+
2++; 2+; 2-
3
4
A,
B,
C,
D,
Good practice point
6 UMHS [43] – A
B
C
D
I
II
III
7 WSAMDG [44] Rating scheme (not provided) Not provided None
8 APS AAP [45] Adapted GRADE methodology. High quality evidence
Medium quality evidence
Low quality evidence
Strong recommendation
Weak recommendation
9 Harris [46, 47] Modified Canadian Task Force Grading System I,
II-1
II-2
II-3
OR III
A,
B,
C
10 Raff [48] – None None
11 Sanders [33] – None None
12 Schnitzer [7] – None None

CPG clinical practice guideline

Guideline content overview

Table 5 provides a content overview of the included CPGs. In CPG 7, 9, 10, 11, and 12, no clear recommendation statements were identifiable, and therefore an overview is presented. The writing style of these CPGs focused on a discussion of relevant information, and was less focused on making clear recommendations. The content of the CPGs focused on assessment of CMSP and on the prescription of opioids. Eight out of the 12 CPGs included at least one position statement about rehabilitation options for CMSP.

Table 5.

Content section areas of the included CPG

Content section CPG
1
CPG
2
CPG
3
CPG
4
CPG
5
CPG
6
CPG
7
CPG
8
CPG
9
CPG
10
CPG
11
CPG
12
Total Percentage (%)
ASIPP ICSI NOUGG RNAO SIGN UMHS WSA MDGa APS-AAP Harrisa Raffa Sandersa Schnitzera
Evaluation/assessment √ √ √ √ √ √ √ √ √ √ 10 83
Diagnosis √ √ √ √ √ √ 6 50
Planning of care √ √ √ √ √ √ √ √ 8 67
Complementary therapy √ √ 2 17
Diet therapy √ √ 2 17
Practitioner education √ 1 8
Occupational therapy √ √ 2 17
Organization and Policy √ 1 8
Pharmacological therapy (non-opioids) √ √ √ √ √ √ √ 7 58
Pharmacological therapy (opioids) √ √ √ √ √ √ √ √ √ √ √ 11 92
Physical therapy √ √ √ √ √ √ √ √ 8 67
Psychologically based therapy √ √ √ √ √ √ 6 50

CPG clinical practice guideline

aNo clear recommendation statements

Discussion

This systematic review, to the knowledge of the authors, is the first to focus on identifying and appraising profession-specific and inter-professional CPGs for the management of CMSP in the primary healthcare settings. One of the main findings was that there are multiple, current CPGs on the topic that had been developed by different organizations and authors. Considerable time, effort, and resources were therefore invested in the development of these CPGs. Two guidelines focus specifically on CMSP management in primary healthcare, and recommendations for the management of CMSP were imbedded in the CPGs for chronic non-malignant pain. CPGs were mainly profession-specific, few took a multidisciplinary perspective, and CPGs varied in their scope, coverage, format, and quality.

The scope of the majority of included CPGs focused on opioid prescription and congruently, the content of the CPGs is also focused on opioid prescription (Tables 1 and 5, Additional file 1). The focus on opioid prescription can be ascribed to the dramatic rise in the prescription of opioids, as a result of the increase in the prevalence of chronic pain and the increase in dosage and frequency of prescription [10, 27–29]. The risks associated with opioid use may have created a growing need for clinical guidance on decision-making for opioid prescription. It is thus likely that high quality, evidence-based CPGs became fundamental to provide guidance for the safe prescription of opioids for CMSP. In contrast, although included CPGs advocated non-pharmacological management options for the management of CMSP in primary healthcare, recommendations about these options were seldom included. SIGN [30], ICSI [31], and RNAO [32] provided multiple recommendations on various rehabilitation options, while Sanders et al. [33] and Schnitzer [7] mentioned multimodal options. The lack of focus of non-pharmacological management options was congruent with the inadequate representation of rehabilitation practitioners in the guideline development teams of included CPGs. Since several high quality CPGs are now available for the prescription of opioids, we recommend the future guidelines should include a holistic and multidisciplinary scope. The prevention and management of CMSP requires a holistic and inter-/multidisciplinary approach to address the complex interaction between biological, psychological, social and environmental factors [5]. We argue that a renewed scope on holistic management, with a congruently aligned multidisciplinary guideline development team, is needed for future CPGs on the primary healthcare of CMSP, to address the burden associated with the condition.

The review revealed three AGREE II domains that require consideration to enhance the quality of future CPGs for CMSP in primary healthcare settings, namely, the domains of rigor of development, stakeholder involvement, and applicability. The findings are congruent with that of Shaneyfelt et al. [16] and Misso et al. [34]. Shaneyfelt et al. [16] reviewed 279 CPGs to determine adherence to quality standards. They identified aspects needing improvement in the reviewed CPG as: the identification of evidence, the formulation of recommendations, guideline expiry date, cost implications, and the role of values and preferences. Misso et al. [34] reviewed CPGs for osteoarthritis of the knee and hip and found stakeholder involvement, rigor of development, applicability. and editorial independence to be poorly addressed.

In our review, the median score for reporting of rigor of development (domain 3) was adequate; however, the range of these scores was wide. The criteria that presented challenges were the aggregation of the strengths and limitations of the body of evidence and updating the CPG. More than half of the included CPGs were current and were published 5 years prior to our systematic search. Guideline developers put little emphasis on providing procedures and dates for updating the CPGs, which was also a key deficiency found in Vernooij’s et al. [35] systematic review of guideline handbooks. Providing details about updating a CPG is important, because they may become outdated as new evidence for interventions become available, emphasizing the need for recommendations to be modified [13, 15]. We recommend that the domain of methodological rigor should receive detailed consideration during future CPG development to improve the credibility of the evidence base on which recommendations are built. Not adhering to the criteria of this domain may threaten the trustworthiness and consequently uptake of CPG recommendations in primary healthcare practice. A thorough, unbiased review and aggregation of the evidence may prevent incorrect or biased recommendations [14].

This systematic review highlights the inconsistent use of frameworks to aggregate the level or body of evidence and the strength of the recommendation by the included CPGs. The criterion of using a framework to rate the strengths and limitations of the body of evidence is evaluated in the AGREE II domain of methodological rigor (topic 9). The AGREE II considers formal or informal methods for this domain. A framework that guides the decision-making process for recommendations ensures transparency and objectivity [14] and provides logical methods for considering the entire body of evidence relevant to a particular clinical question. Determining the body of evidence that underpins a CPG recommendation is critical in the guideline development process. Without transparency of the framework used to aggregate the body of evidence, guideline users cannot determine whether recommendations are built on strong evidence or weak evidence [14]. Furthermore, few included CPGs used the body of evidence together with the strength of the recommendation to frame recommendations. Determining the strength of the recommendation guides the applicability and implementability of the recommendations. The strength of the recommendation is dependent on the quality of the evidence, the balance between desirable and undesirable effects, values and preferences of the stakeholders and cost of implementation [36]. During the development of FORM (Australian method for formulating and grading recommendations), several efficient frameworks for developing recommendations were identified [37]. These frameworks included GRADE (Grading of Recommendations Assessment, Development and Evaluation), SIGN (Scottish Intercollegiate Guidelines) and SORT (Strength-of-Recommendation Taxonomy) [37]. The frameworks consider the evidence base (study quality, size, precision of results, bias); the consistency of different study findings; the clinical impact based on the body of evidence; generalizability of the results; and the applicability to the context that it is intended for [37]. The process of guideline development is evolving, and recently, more emphasis has been placed on the decision-making process of moving from evidence to recommendations. The use of evidence to decision frameworks is advocated as a systematic and transparent process to formulate recommendations [38]. In the review, guideline developers reported to use formal or informal consensus processes to make decisions. However, the use of evidence to decision frameworks was not explicitly stated in the included CPGs (also not a criterion for AGREE II). CPGs using GRADE (see Table 4), may have used a framework to consider factors that influence the strength and direction of the recommendation. The use of frameworks or a writing guide to frame recommendations, to grade the body of evidence and to determine the strength of the recommendation is advocated as a way to ensure consistency and transparency when making decisions and writing recommendations. Guideline developers are encouraged to use frameworks such as FORM, GRADE, SIGN, and SORT to enhance systematic decision-making processes in CPG construction.

The inclusion of stakeholders in the development process of CPGs is assessed as part of AGREE II (domain 2), and adherence to this quality criterion is thought to enhance a sense of ownership, thereby facilitating the uptake of the guideline [19]. While most included CPGs representation from professional groups, guideline developers did not commonly include the views and preferences of the target populations (patients and public). Shaneyfelt et al. [16] and Misso et al. [34] likewise found that patient values and preferences were not effectively addressed during CPG development. Patient perspectives and preferences influences healthcare utilization, therefore, patient perspectives about CMSP and its treatment are important in CPG development [20]. Patient preferences and concerns are shaped by context factors, which in turn impact the formulation and applicability of guideline recommendations. Consequently, some recommendations in a CPG may be preference sensitive. The inclusion of patient perspectives in the guideline development process is an important step towards facilitating relevant, person-centred care, and autonomy [39].

The AGREE domain of applicability (relevance) considers context factors that may impact CPG implementation, namely, the facilitators, barriers, and resource implications for implementation; tools for putting recommendations into practice, as well as monitoring and auditing criteria that influence the uptake and implementation of a CPG. These criteria therefore represent the features of the healthcare system, resources, cultural, and organizational factors that should be considered in framing guideline recommendations [15, 17, 19, 36]. Gagliardi et al. [12] contends that information on implementability within a CPG may assist the end-users to adopt the recommendations. In this review, the domain of applicability received the lowest median score. It is plausible that context features were not included in the CPG document, but were a part of the implementation plan for the CPG in a particular setting. The RNAO [32] and SIGN [30] contend that each setting/institution may benefit from a tailor-made implementation plan. Participation of local stakeholders can ensure that the CPG and its recommendations are compatible with the local context. It is possible that explicit statements on implementation parameters were not included as they may differ from one setting to the other. Additionally, the use of evidence to decision frameworks considers population or patient-specific outcomes, including cost-effectiveness, applicability, feasibility, subgroups, and generalizability when framing recommendations [37, 38]. The use of these frameworks may provide useful information about the context and application of recommendations, which may enhance CPG quality and uptake, and inform processes such as CPG adoption, adaptation, and contextualization [23, 24]. Regardless of the use of frameworks, it is advisable that future CPG on CMSP include more information on potential resource implications and barriers and facilitators to implementation.

Transparency and specificity regarding context factors that may impact recommendations is becoming increasingly important due to the option of adopting, adapting, or contextualizing CPGs for different settings, when de novo development of CPGs is not a feasible option. Knowledge about the context sensitive recommendations, may inform the above processes of CPG development. It is therefore an option that future CPGs on CMSP highlights preference or context sensitive recommendations [39]; and link these recommendations to context applicable implementation strategies, since context factors may play a vital role in applicability. An example of signposting context sensitive recommendations, is illustrated in the novel concept of CPG contextualization, whereby context and practice points are produced and linked to relevant context sensitive recommendations [23, 40]. The inclusion of context and practice points is thought to enhance CPG the application of recommendations in practice.

CPGs can be an important information resource for the evidence-based and holistic management of CMSP and has the potential to influence policy and practice about CMSP care. Given the multidimensional nature of CMSP, it is important that the scope of future CPGs include a multidisciplinary approach, which implies that healthcare systems in which CMSP is managed should ideally allow for a multidisciplinary management approach. While some included CPGs elaborated on the cost and cost-effectiveness of interventions, the findings of this review indicate that there is great opportunity for CPGs to elaborate on cost and policy implications that guideline recommendations may have. The RNAO [32] included the potential impact of CPG recommendations on policy, legislation, healthcare systems, and health professions education for CMSP. One policy aspect that was well addressed in the CPGs was the need for policy on the prescription and monitoring of opioids for CMSP. The inclusion of information on policy and practice implications is useful and may play a role in the organizational acceptance and implementation of the CPG.

We identified several strengths in the CPGs, which included that guideline developers clearly communicated the overall objectives, scope, and focus of the CPG. The domain on clarity of presentation obtained a high score, indicating that CPGs presented their recommendations in a clear, easily identifiable, and specific format. Editorial independence had also been adhered to in most included CPGs.

Implications for practice

This systematic review highlights the strengths and limitations of current CPGs on the management of CMSP in primary healthcare settings. Guideline developers who are considering adopting, adapting, contextualizing, updating existing CPGs, or developing new CPGs for CMSP should consider the findings of this systematic review to optimize the methodological quality and uptake of CPGs. Based on the findings of this review, the authors recommend that future CPGs should:

  • Include decision-making frameworks for the level of evidence, strength of recommendation, and framing recommendations in the CPG development process.

  • Include the relevant stakeholders and end-users in the process of CPG development.

  • Consider and document barriers and facilitators that may influence the uptake of clinical guideline recommendations in the intended setting.

  • Develop and document strategies to facilitate the successful uptake and implementation of CPGs into practice.

  • Provide dates and procedures for updating the CPG.

We further recommend that, due to the many CPGs on the topic, existing high quality CPGs be contextualized to local circumstances, particularly in resource-constrained environments. In this way, resources may be used to further the uptake of CPG recommendations with a rigorous implementation and sustainability strategy, instead of resources being spent on de novo CPG development [23]. Where de novo development of CPGs are feasible and the focus should be on a multidisciplinary scope. We found that CPGs written in the article format had several limitations that can be attributed to the restrictions of the journal. We recommend that in the case of a journal format, supplementary material be made available about methodological development.

The similarities between the findings of this systematic review and that of Shaneyfelt et al. [16] and Misso et al. [34] indicate after more than a decade guideline developers are still finding it challenging to adhere to certain quality standards of developing CPGs. The reasons for this phenomenon warrant further investigation.

Limitations

Our review had some limitations of its own. We applied the AGREE II instrument, which evaluates the reported rigor of development and not the content of the CPG. The next step in our process is the content analysis of high quality CPGs for CMSP in primary healthcare settings. Our focus was specific to primary healthcare settings, and this may have excluded some guidelines that are applicable in this setting, but not stated overtly to be so. The CPGs we identified were predominantly from developed countries, so the appropriateness of these guidelines in other countries is uncertain. Furthermore, we acknowledge that although we did an extensive literature search, we may have missed eligible CPGs.

Conclusion

The systematic review found several CPGs that are applicable for the primary healthcare of CMSP. The included CPGs vary in their scope and methodological rigor. There was little emphasis on non-pharmacological strategies in the composition of the guideline development team, the stated scope, and the content of the CPGs.This study highlights specific elements for enhancement in the development and reporting of future CPGs, which may play a role in the uptake of CPGs into clinical practice. These elements include enhanced reporting of rigor of development, the inclusion of stakeholder preferences and values and the consideration of context specific factors (e.g., culture, healthcare setting). Further research on methods to include patient preferences and how this impacts CPG content and implementation is needed.

Acknowledgements

The authors would like to thank Dr S-M Van Niekerk and Ms D Leibbrandt for their assistance with the screening and assessment of the clinical practice guidelines. DE obtained funding for the project. QL is a member of the South African Guidelines Excellence (SAGE) Project.

Funding

This work is based on the research supported in part by the Stellenbosch University Rural Medical Education Partnership Initiative, the National Research Foundation of South Africa for grant 85086. Any opinion, finding, and conclusion or recommendation expressed in this material are that of the author, and the National Research Foundation does not accept any liability in this regard. The PhD from which this study emanated was funded by the Medical Research Council of South Africa under SAMRC Clinician Researcher Programme. Any opinions, findings, conclusions, or recommendations expressed in this publication are those of the author(s) and do not necessarily reflect the view of the South African Medical Research Council. The funding bodies did not take part in the design, data collection, data interpretation, or writing the manuscript.

Availability of data and materials

The dataset supporting the conclusions of the article is included within the article.

Authors’ contributions

DE conceptualised and designed this study as part of her PhD project, under the supervision and guidance of QL and SH. All authors contributed to analysis and interpretation of data. DE drafted the manuscript. All authors provided critical revision and approval of the manuscript.

Competing interests

The authors declare that they have no competing interests.

Consent for publication

Not applicable as the manuscript does not contain any individual person’s data.

Ethics approval and consent to participate

The study protocol was approved by the Health Research Ethics Committee of Stellenbosch University, SA (S14/01/018), as part of a broader study on clinical practice guidelines for chronic pain.

Abbreviations

AAP

American academy of pain medicine

AGREE II

Appraisal of guidelines research and evaluation, version II

APS

The American pain society

ASIPP

American society of interventional pain physicians

CMSP

Chronic musculoskeletal pain

CGA

Clinical guideline in article format

CPG

Clinical practice guideline

FORM

An Australian method for formulating and grading recommendations in evidence-based clinical guidelines

GRADE

Grading of recommendations assessment, development and evaluation

ICSI

Institute for clinical systems improvement

IOM

Institute of medicine

IQR

Interquartile range

NICE

United Kingdom’s National Institute for Health and Clinical Excellence

NOUGG

National opioid use guideline group

PIPOH

Population, intervention, professions, health outcomes, and health setting

RNAO

Registered nurses’ association of Ontario

SIGN

Scottish intercollegiate guidelines

SORT

Strength-of-recommendation taxonomy

UK

United Kingdom

UMHS

University of Michigan health system

USA

United States of America

USPSTF

United States preventive services task force

WHO

World Health Organization

WSAMDG

Washington state agency medical directors' group

Additional files

Additional file 1: (21KB, docx)

Scope and development group members of CPGs. (DOCX 20 kb)

Additional file 2: (17.9KB, docx)

More on DOMAIN 5: applicability. (DOCX 17 kb)

Contributor Information

Dawn V. Ernstzen, Phone: +27 219389300, Email: dd2@sun.ac.za

Quinette A. Louw, Phone: +27 219389300, Email: qalouw@sun.ac.za

Susan L. Hillier, Phone: +61 (0)8 83022544, Email: susan.hillier@unisa.edu.au

References

  • 1.World Health Organization (WHO). Normative guidelines on pain management: Report of a Delphi Study to determine the need for guidelines and to identify the number and topics of guidelines that should be developed by WHO. Geneva: WHO; 2007. http://www.readbag.com/who-medicines-areas-quality-safety-delphi-study-pain-guidelines. Accessed 13 Apr 2016.
  • 2.Foster NE, Pincus T, Underwood MR, Vogel S, Breen A, Harding G. Understanding the care for musculoskeletal conditions – why a biomedical process is inadequate. Rheumatology. 2003;42:401–3. [PubMed] [Google Scholar]
  • 3.Smith BH, Hopton JL, Chambers WA. Chronic pain in primary care. Fam Pract. 1999;16(5):475–82. doi: 10.1093/fampra/16.5.475. [DOI] [PubMed] [Google Scholar]
  • 4.Rauf WN, Meyer HP, Marcus TS, Becker PJ. The impact of chronic pain on the quality of life of patients attending primary healthcare clinics. S Afr J Anaesth Analg. 2014;20(2):122–6. [Google Scholar]
  • 5.Scascighini L, Toma V, Dober-Spielmann S, Sprott H. Multidisciplinary treatment for chronic pain: a systematic review of interventions and outcomes. Rheumatology. 2008;47(5):670–8. doi: 10.1093/rheumatology/ken021. [DOI] [PubMed] [Google Scholar]
  • 6.Harstall C, Ospina M. How prevalent is chronic pain? Pain Clin Update. 2003;11:1–4. doi: 10.1016/S1070-7212(03)00004-6. [DOI] [Google Scholar]
  • 7.Schnitzer TJ. Update on guidelines for the treatment of chronic musculoskeletal pain. Clin Rheumatol. 2006;25(Suppl 1):S22–S29. doi: 10.1007/s10067-006-0203-8. [DOI] [PubMed] [Google Scholar]
  • 8.Gureje O, Von Korff M, Simon GE, Gater R. Persistent pain and well-being. A World Health Organization study in primary care. JAMA. 1998;280(2):147–151. doi: 10.1001/jama.280.2.147. [DOI] [PubMed] [Google Scholar]
  • 9.World Health Organisation. Primary health care – Now more than ever. 2008. http://www.who.int/whr/2008/en/. Accessed Sept 2012.
  • 10.Stein C, Reinecke H, Sorgatz H. Opioid use in chronic non-cancer pain: guidelines revisited. Curr Opin Anaesthesiol. 2010;23:598–601. doi: 10.1097/ACO.0b013e32833c57a8. [DOI] [PubMed] [Google Scholar]
  • 11.Rauf WN, Meyer HP, Marcus TS, Becker PJ. Prevalence of chronic pain in patients attending primary healthcare facilities in South-West Tshwane. S Afr Fam Pract. 2013;55(1):85–89. doi: 10.1080/20786204.2013.10874308. [DOI] [Google Scholar]
  • 12.Gagliardi AR, Brouwers MC, Palda VA, Lemieux-Charles L, Grimshaw JM. How can we improve guideline use? A conceptual framework of implementability. Implement Sci. 2011;6:26. doi: 10.1186/1748-5908-6-26. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 13.Institute of Medicine (IOM) Clinical practice guidelines we can trust. National Academy of Sciences. 2011. https://www.nationalacademies.org/hmd/Reports/2011/Clinical-Practice-Guidelines-We-Can-Trust.aspx. Accessed 21 May 2015.
  • 14.Chou R. Using evidence in pain practice: part II using evidence in pain practice. Pain Med. 2008;14(9):531–41. doi: 10.1111/j.1526-4637.2008.00422_2.x. [DOI] [PubMed] [Google Scholar]
  • 15.Shekelle P, Woolf S, Grimshaw JM, Schünemann HJ, Eccles MP. Developing clinical practice guidelines: reviewing, reporting, and publishing guidelines; updating guidelines; and the emerging issues of enhancing guideline implementability and accounting for comorbid conditions in guideline development. Implement Sci. 2012;7:62. doi: 10.1186/1748-5908-7-62. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 16.Shaneyfelt TM, Mayo-Smith MF, Rothwangl J. Are guidelines following guidelines? The methodological quality of clinical practice guidelines in the peer-reviewed medical literature. JAMA. 1999;281(20):1900–1905. doi: 10.1001/jama.281.20.1900. [DOI] [PubMed] [Google Scholar]
  • 17.Graham ID, Harrison M, Brouwers M, Davies BL, Dunn S. Facilitating the use of evidence in practice: evaluating and adapting clinical practice guidelines for local use by health care organisations. J Obstet Gynecol Neonatal Nurs. 2002;31:599–611. doi: 10.1111/j.1552-6909.2002.tb00086.x. [DOI] [PubMed] [Google Scholar]
  • 18.Vlayen J, Aertgeerts B, Hannes K, Sermeus W, Ramaekers D. A systematic review of appraisal tools for clinical practice guidelines: multiple similarities and one common deficit. Int J Qual Health Care. 2005;17(3):235–42. doi: 10.1093/intqhc/mzi027. [DOI] [PubMed] [Google Scholar]
  • 19.Harrison MB, Legare F, Graham ID, Fervers B. Adapting clinical practice guidelines to local context and assessing barriers to their use. CMAJ. 2010;182(2):e78–e84. doi: 10.1503/cmaj.081232. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 20.Qaseem A, Forland F, Macbeth F, Ollenschlager G, Philips S, Van der Wees P. On behalf of the Board of trustees of the Guidelines International Network. Guidelines International Network: toward international standards for clinical practice guidelines. Ann Intern Med. 2012;156(7):525–32. doi: 10.7326/0003-4819-156-7-201204030-00009. [DOI] [PubMed] [Google Scholar]
  • 21.Woolf SH, Grol R, Hutchinson A, Eccles M, Grimshaw J. Potential benefits, limitations, and harms of clinical guidelines. BMJ. 1999;318:20. doi: 10.1136/bmj.318.7182.527. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 22.Brouwers M, Kho ME, Browman GP, Burgers JS, Cluzeau F, Feder G, Fervers B, Graham ID, Grimshaw J, Hanna S, Littlejohns P, Makarski J. Zitzelsberger L for the AGREE Next Steps Consortium. AGREE II: advancing guideline development, reporting and evaluation in healthcare. CMAJ. 2010;182:E839–842. doi: 10.1503/cmaj.090449. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 23.Gonzalez-Suarez C, Grimmer-Somers K, Dizon J, King E, Lorenzo S, Valdecanas C, Gambito E, Fidel B. Contextualizing Western guidelines for stroke and low back pain to a developing country (Philippines): an innovative approach to putting evidence into practice efficiently. J Healthc Leadersh. 2012;4:141–56. doi: 10.2147/JHL.S35370. [DOI] [Google Scholar]
  • 24.ADAPTE II Collaboration. 2009. http://www.g-i-n.net/document-store/working-groups-documents/adaptation/adapte-resource-toolkit-guideline-adaptation-2-0.pdf. Accessed 15 Aug 2014.
  • 25.Next Steps Consortium AGREE. The AGREE II Instrument. 2013. [Google Scholar]
  • 26.Kredo T, Gerritsen A, Van Heerden J, Conway S, Siegfried N. Clinical practice guidelines within the Southern African development community: a descriptive study of the quality of guideline development and concordance with best evidence for five priority diseases. Health Res Pol Syst. 2012;10(1). [DOI] [PMC free article] [PubMed]
  • 27.Furlan AD, Reardon R, Weppler C. Opioids for chronic noncancer pain: a new Canadian practice guideline. Can Med Assoc J. 2010;182:923–930. doi: 10.1503/cmaj.100187. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 28.Kahan M, Mailis-Gagnon A, Wilson L, Srivastava A. Canadian guideline for safe and effective use of opioids for chronic noncancer pain cinical summary for family physicians. Part 1: general population. Can Fam Physician. 2011;57:1257–66. [PMC free article] [PubMed] [Google Scholar]
  • 29.Cheung CW, Qiu Q, Choi S, Moore B, Goucke R, Irwin M. Chronic opioid therapy for chronic non-cancer pain: a review and comparison of treatment guidelines. Pain Physician. 2014;17:402–414. [PubMed] [Google Scholar]
  • 30.Scottish Intercollegiate Guidelines Network (SIGN). Management of chronic pain. Edinburgh: SIGN publication no. 136; 2013. http://sign.ac.uk/guidelines/fulltext/136/index.html. Accessed 13 Apr 2016.
  • 31.Hooten WM, Timming R, Belgrade M, Gaul J, Goertz M, et al. Assessment and Management of Chronic Pain. 2013. for the Institute for Clinical Systems Improvement. [Google Scholar]
  • 32.Registered Nurses’ Association of Ontario (RNAO). Assessment and Management of Pain. 3rd ed. Toronto: Registered Nurses’ Association of Ontario; 2013. http://rnao.ca/bpg/guidelines/assessment-and-management-pain. Accessed 13 Apr 2016.
  • 33.Sanders SH, Harden NR, Vicente PJ. Evidence-based clinical practice guidelines for interdisciplinary rehabilitation of chronic non-malignant pain syndrome patients. Pain Prac. 2005;4(5):303–15. doi: 10.1111/j.1533-2500.2005.00033.x. [DOI] [PubMed] [Google Scholar]
  • 34.Misso ML, Pitt VJ, Jones KM, Barnes HN, Piterman L, Green SE. Quality and consistency of CPG for diagnosis and management of osteoarthritis of the hip and knee: a descriptive overview of published guidelines. MJA. 2008;189(7):394–9. doi: 10.5694/j.1326-5377.2008.tb02086.x. [DOI] [PubMed] [Google Scholar]
  • 35.Vernooij RWM, Sanabria AJ, Solà I, Alonso-Coello P, Martínez GL. Guidance for updating clinical practice guidelines: a systematic review of methodological handbooks. Implement Sci. 2014;9:3. doi: 10.1186/1748-5908-9-3. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 36.Woolf SH, Schünemann HJ, Eccles MP, Grimshaw JM, Shekelle P. Developing clinical practice guidelines: types of evidence and outcomes; values and economics, synthesis, grading, and presentation and deriving recommendations. Implement Sci. 2012;7:61. doi: 10.1186/1748-5908-7-61. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 37.Hillier S, Grimmer-Somers K, Merlin T, Middleton P, Salisbury J, Tooher R, Weston A. FORM: an Australian method for grading recommendations in evidence-based clinical guidelines. BMC Med Res Methodol. 2011;11:23. doi: 10.1186/1471-2288-11-23. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 38.Alonso-Coello P, Oxman AD, Moberg J, Brignardello-Petersen R, Akl EA, Davoli M, Treweek S, Mustafa RA, Vandvik PO, Meerpohl J, Guyatt GH, Schünemann HJ. the GRADE Working Group. GRADE Evidence to Decision (EtD) frameworks: a systematic and transparent approach to making well informed healthcare choices. 2: Clinical practice guidelines. BMJ. 2016;353:i2089. doi: 10.1136/bmj.i2089. [DOI] [PubMed] [Google Scholar]
  • 39.Krahn M, Naglie G. The next step in guideline development: incorporating patient preferences. JAMA. 2008;300(4):436–8. doi: 10.1001/jama.300.4.436. [DOI] [PubMed] [Google Scholar]
  • 40.Dizon JM, Machingaidze S, Grimmer K. To adopt, to adapt, or to contextualise? The big question in clinical practice guideline development. BMC Res Notes. 2016;9:442. doi: 10.1186/s13104-016-2244-7. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 41.Manchikanti L, Abdi S, Atluri S, Balog CC, et al. American Society of Interventional Pain Physicians (ASIPP) Guidelines for responsible opioid prescribing in chronic non-cancer pain: Part I – evidence assessment Part 2 – Guidance. Pain Physician. 2012;15(Suppl S1-S66):S67–S116. [PubMed] [Google Scholar]
  • 42.National Opioid Use Guideline Group (NOUGG). Canadian guideline for safe and effective use of opioids for chronic non-cancer pain Part A: executive summary and background Part B: Recommendations for practice. 2010. http://nationalpaincentre.mcmaster.ca/opioid/. Accessed 13 Apr 2016.
  • 43.University of Michigan Health System. Managing chronic non-terminal pain in adults including prescribing controlled substances. 2011. http://www.med.umich.edu/1info/FHP/practiceguides/pain/pain.pdf. Accessed 13 Apr 2015.
  • 44.Washington State Agency Medical Directors’ Group. Interagency guideline on opioid dosing for chronic non-cancer pain: an educational aid to improve care and safety with opioid treatment. Olympia (WA): Washington State Department of Labor and Industries. 2010. http://www.agencymeddirectors.wa.gov/files/opioidgdline.pdf. Accessed 13 Apr 2016.
  • 45.Chou R, Fanciullo GJ, Fine PG, Adler JA, et al. For the American pain society–American academy of pain medicine opioids guidelines panel. Opioid treatment guidelines: clinical guidelines for the use of chronic opioid therapy in chronic noncancer pain. J Pain. 2009;10(2):113–30. doi: 10.1016/j.jpain.2008.10.008. [DOI] [PubMed] [Google Scholar]
  • 46.Harris GR, Susman JL. Managing musculoskeletal complaints with rehabilitation therapy: summary of the Philadelphia panel evidence-based clinical practice guidelines on musculoskeletal rehabilitation interventions. J Fam Pract. 2002;51(12):1042–46. [PubMed] [Google Scholar]
  • 47.The Philadelphia Panel Members and Ottawa Methods Group Philadelphia panel evidence-based clinical practice guidelines on selected rehabilitation interventions: Overview and Methodology. Phys Ther. 2001;81(10):1629 – 40. [PubMed]
  • 48.Raff M, Eppel S, Meyer H, Sarembock B, Webb D. South African guideline for the use of chronic opioid therapy for chronic non-cancer pain. S Afr Med J. 2014;104(1 Suppl 1):78–89. doi: 10.7196/samj.7316. [DOI] [PubMed] [Google Scholar]

Associated Data

This section collects any data citations, data availability statements, or supplementary materials included in this article.

Data Availability Statement

The dataset supporting the conclusions of the article is included within the article.


Articles from Implementation Science : IS are provided here courtesy of BMC

RESOURCES