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Cover of Serial X-Ray Radiography for the Diagnosis of Osteomyelitis: A Review of Diagnostic Accuracy, Clinical Utility, Cost-Effectiveness, and Guidelines

Serial X-Ray Radiography for the Diagnosis of Osteomyelitis: A Review of Diagnostic Accuracy, Clinical Utility, Cost-Effectiveness, and Guidelines

CADTH Rapid Response Report: Summary with Critical Appraisal

and .

Abbreviations

CT

Computed tomography

DFI

Diabetic foot infection

EANM

European Association of Nuclear Medicine

EBJIS

European Bone and Joint Infection Society

ESCMID

European Society of Microbiology and Infectious Disease

ESR

European Society of Radiology

IDSA

Infectious Diseases Society of America

MRI

Magnetic resonance imaging

NVO

Native vertebral osteomyelitis

PBI

Peripheral bone infection

PET

Positron emission tomography

PRISMA

Preferred Reporting Items for Systematic Reviews and MetaAnalyses

SPECT

Single-photon emission computed tomography

UMHS

University of Michigan Health System

WBC

White blood cell

Context and Policy Issues

Osteomyelitis is an inflammation of the bone due to infection caused by bacteria, commonly Staphylococcus aureus.1 Bacteria can reach the bone through various means including trauma, surgery, the blood stream, extension from an adjacent soft tissue infection, or diabetic foot infection.1 Osteomyelitis can occur at any age, although the incidence appears to peak at children under the age of five and in adults over 50 years of age.2 It can be classified as acute or chronic, based on histopathological findings.3 Factors associated with osteomyelitis include aging, increased prevalence of trauma, and increased prevalence of diabetic foot infection.4

Early detection of osteomyelitis will likely lead to more favorable outcomes.4 Diagnosis of osteomyelitis requires a multidisciplinary approach including clinical examination, recognition and assessment of clinical symptoms, laboratory investigations and imaging tests.4 There are various imaging modalities that have been used in the characterization and differential diagnosis of osteomyelitis, such as plain X-ray radiography, computed tomography (CT), magnetic resonance imaging (MRI), bone scintigraphy, positron emission tomography (PET), single-photon emission computed tomography (SPECT), and ultrasonography.1,4 The diagnostic accuracies of these imaging tests for diagnosis of osteomyelitis have been systematically reviewed.5 Although plain X-ray radiography has lower sensitivity and specificity compared to other imaging tests, the American College of Radiology Appropriateness Criteria and reviews recommend that X-ray should be used as first line imaging modality to differentiate osteomyelitis from other clinical conditions such as bone fractures or bone malignancies.3,6,7 Plain X-ray radiography, whether or not with positive or negative results, is usually followed by higher sensitivity and specificity imaging modalities for diagnosis of osteomyelitis.8 However, in institutions where the availability of more sophisticated imaging modalities is limited, it is unclear if the use of serial X-ray radiography (i.e., initial assessment with X-rays followed by subsequent X-rays in 1 to 3 weeks), could improve diagnostic accuracy for detection of osteomyelitis.

The aim of this report is to review the diagnostic accuracy, clinical utility, and cost-effectiveness of serial X-ray radiography in adults with suspected osteomyelitis compared to other diagnostic modalities. This report also aims to identify evidence-based guidelines regarding the use of diagnostic modalities in adults with suspected osteomyelitis.

Research Question

  1. What is the diagnostic accuracy of serial X-ray radiography in adults with suspected osteomyelitis?
  2. What is the clinical utility of serial X-ray radiography in adults with suspected osteomyelitis?
  3. What is the cost-effectiveness of serial X-ray radiography in adults with suspected osteomyelitis?
  4. What are the evidence-based guidelines regarding the use of diagnostic modalities in adults with suspected osteomyelitis?

Key Findings

This review included three evidence-based guidelines for diagnosis of peripheral bone infection, diabetic foot infection, and native vertebral osteomyelitis in adults. No studies on the diagnostic accuracy, clinical utility and cost-effectiveness of serial X-ray radiography for diagnosis of osteomyelitis were identified.

All three guidelines were considered to be of good methodological quality. Based on moderate to low quality evidence, the guidelines had recommendations for diagnosis of osteomyelitis regarding medical examination, laboratory tests, bone biopsy and bone culture, and imaging tests. Bone biopsy and bone culture are considered as the reference standard to confirm the infection and identify the causative microorganism. Although magnetic resonance imaging, positron emission tomography and single-photon emission computed tomography were found to have higher diagnostic performance than radiography, it is recommended that conventional X-ray radiography should be the first imaging modality for detection of osteomyelitis, particularly for suspected peripheral bone infection or for osteomyelitis in diabetic foot infection. With suspected native vertebral osteomyelitis, spine magnetic resonance imaging, when feasible, is recommended as first imaging of choice. Subsequent imaging tests may be considered depending on the extent of the investigation, the availability of the imaging modalities, the level of diagnostic accuracy required, the complexity of the disease, and any contraindications.

There is a need for studies examining the diagnostic accuracy, clinical utility and cost-effectiveness of serial X-ray radiography for detection of osteomyelitis in adults.

Methods

Literature Search Methods

A limited literature search was conducted by an information specialist on key resources including PubMed, the Cochrane Library, the University of York Centre for Reviews and Dissemination (CRD) databases, the websites of Canadian and major international health technology agencies, as well as a focused Internet search. The search strategy was comprised of both controlled vocabulary, such as the National Library of Medicine’s MeSH (Medical Subject Headings), and keywords. The main search concepts were x-ray radiography and osteomyelitis. No filters were applied to limit the retrieval by study type. Where possible, retrieval was limited to the human population. The search was also limited to English language documents published between January 1, 2015 and February 14, 2020.

Selection Criteria and Methods

One reviewer screened citations and selected studies. In the first level of screening, titles and abstracts were reviewed and potentially relevant articles were retrieved and assessed for inclusion. The final selection of full-text articles was based on the inclusion criteria presented in Table 1.

Table 1. Selection Criteria.

Table 1

Selection Criteria.

Exclusion Criteria

Studies were excluded if they did not meet the selection criteria in Table 1 or if they were published prior to 2015.

Critical Appraisal of Individual Studies

The included evidence-based guidelines were critically appraised using the Appraisal of Guidelines for Research and Development (AGREE) II instrument.9 Summary scores were not calculated for the included guidelines; rather, the strengths and limitations were described narratively.

Summary of Evidence

Quantity of Research Available

A total of 662 citations were identified in the literature search. Following screening of titles and abstracts, 641 citations were excluded and 21 potentially relevant reports from the electronic search were retrieved for full-text review. Two potentially relevant publications were retrieved from the grey literature search. Of the 23 potentially relevant articles, 20 publications were excluded for various reasons; three guidelines met the inclusion criteria and were included in this report. No studies reporting the diagnostic accuracy, clinical utility, or cost-effectiveness of serial X-ray radiography in adults with suspected osteomyelitis were identified. Appendix 1 presents the PRISMA flowchart10 of the study selection.

Summary of Study Characteristics

The detailed characteristics of the included guidelines1113 (Table 2) are presented in Appendix 2.

Study Design

The included guidelines were developed by: four European societies (European Bone and Joint Infection Society [EBJIS], European Society of Clinical Microbiology and Infectious Diseases [ESCMID], European Society of Radiology [ESR], and European Association of Nuclear Medicine [EANM]),11 the University of Michigan Health System (UMHS),12 and the Infectious Diseases Society of America (IDSA).13 All three included guidelines1113 used systematic methods to search for, select, and synthesize evidence. The guidelines were developed by panels of experts in the field of osteomyelitis in general, or diabetic foot infection in particular. The recommendations were developed through discussion and consensus based on evidence level. The joint consensus statements in the EBJIS/ESCMID/ESR/EANM European guideline11 were rated with the associated level evidence, where level 1 represented for evidence from systematic reviews of randomized trials and level 5 from mechanism-based reasoning. In the UMHS guideline,12 the strength of recommendation (e.g., I = generally should be performed, II = may be reasonable to performed, and III = generally should not be performed) and level of evidence (level A = systematic reviews of randomized trials with or without meta-analysis, to level E = expert opinion) were provided for each recommendation statements. In the IDSA guideline,13 the recommendations were graded from strong to weak, while the quality of evidence was assessed as high quality to very low quality. The strength of recommendation and the quality of the evidence were presented together based on the clarity of balance between desirable and undesirable effects, the methodological quality of supporting evidence and implications of recommendations.13 All guidelines were peer-reviewed. Two guidelines were published in 201911,12 and one in 2015.13

Country of Origin

One guideline was developed in Europe,11 and two in the USA.12,13

Patient Population

The target populations for the identified guidelines was adult patients with a suspicion of peripheral bone infection,11 with diabetic foot infection,12 or with native vertebral osteomyelitis.13 The intended users of the guidelines were healthcare professionals.

Interventions and Comparators

The interventions considered in the guidelines were interventions for the diagnosis and management of adult patients with peripheral bone infection,11 diabetic foot infection,12 and native vertebral osteomyelitis.13 Imaging modalities mentioned in the guidelines included plain X-ray radiography, CT, MRI, PET, SPECT and scintigraphy. Serial X-ray radiography was not mentioned in any of the included guidelines.

Outcomes

All included guidelines had recommendations regarding the diagnosis of osteomyelitis, specifically peripheral bone infection,11 diabetic foot infections,12 or native vertebral osteomyelitis13 in adults. The guidelines considered all outcomes related to diagnosis and management of osteomyelitis, including clinical assessment, symptoms, signs, laboratory parameters, bone biopsy, and imaging tests. In addition to diagnostic outcomes, the availability of diagnostic procedures, patient acceptance, tolerability, complications, and costs were considered in developing the recommendations.

Summary of Critical Appraisal

The detailed quality assessments of the included guidelines1113 (Table 3) are presented in Appendix 3.

All three included guidelines1113 were explicit in terms of scope and purpose (i.e., objectives, health questions and populations), and had clear presentation (i.e., specific and unambiguous recommendations, different options for management of the condition or health issue, and easy to find key recommendations). In terms of stakeholder involvement, the guidelines clearly defined target users and the development groups included individuals from all relevant professional groups, and sought the views and preferences of the target populations. For rigour of development, the guidelines explicitly reported details of systematic searches for evidence, criteria for selecting evidence, strengths and limitations of the body of evidence, methods of formulating the recommendations, health benefits, side effects, and risks in formulating the recommendations, and all were peer-reviewed prior to publication. Two guidelines11,12 provided a procedure for updating. For applicability, all guidelines were explicit in terms of facilitators and barriers to application, advice and/or tools on how the recommendations can be put into practice, resource (cost) implications, and monitoring and or auditing criteria. For editorial independence, it was unclear if the funding bodies influenced the content of the guidelines. The EBJIS/ESCMID/ESR/EANM European guideline11 did not mention its funding source, the UMHS guideline12 declared no financial support, and the IDSA guideline13 was funded its own organization. The competing interests of guideline development group members were reported in all three guidelines. Overall, all three included guidelines had good methodological quality.

Summary of Findings

Diagnostic Accuracy of Serial X-Ray Radiography

No studies regarding the diagnostic accuracy of serial X-ray radiography in adults with suspected osteomyelitis were identified; therefore, no summary can be provided.

Clinical Utility of Serial X-Ray Radiography

No studies regarding the clinical utility of serial X-ray radiography in adults with suspected osteomyelitis were identified; therefore, no summary can be provided.

Cost-Effectiveness of Serial X-Ray Radiography

No studies regarding the cost-effectiveness of serial X-ray radiography in adults with suspected osteomyelitis were identified; therefore, no summary can be provided.

Guidelines Regarding the Use of Diagnostic Modalities in Detecting Osteomyelitis in Adults

The key recommendations of the guidelines1113 (Table 4) are presented in Appendix 4.

The joint EBJIS/ESCMID/ESR/EANM guideline provided recommendations specific to patients with suspected peripheral bone infection.11 The guideline11 recommends laboratory tests of C-reactive protein, erythrocyte sedimentation rate, and white blood cell count be performed in patients with suspected peripheral bone infection for diagnosis purposes (Level of evidence: 4). The guideline recommends conventional X-ray radiography to be used as first imaging modality for diagnosis and follow-up of suspected peripheral bone infection (Level of evidence: 3). Once peripheral bone infection is diagnosed by clinical and radiological means, bone biopsy is the reference standard to confirm the infection and should be conducted to identify the microorganism causing the infection (Level of evidence: 4). In complex anatomic areas, CT is recommended as an adjunct imaging modality to the conventional radiographs to detect bone sequestra (Level of evidence: 4). The guideline acknowledges that non-contrast MRI has high diagnostic performance (Level of evidence: 2), three-phase bone scintigraphy is sensitive, but not highly specific (Level of evidence: 2), and white blood cell scintigraphy and antigranulocyte antibody scintigraphy have similar diagnostic accuracy (Level of evidence: 2) in diagnosis of peripheral bone infection. The guideline also acknowledges that PET has high diagnostic accuracy in diagnosis of peripheral bone infection without fracture and osteosynthesis (Level of evidence: 2). No specific recommendations were provided for these diagnostic modalities. The guideline suggests that the use of hybrid SPECT-CT imaging can improve the detection of exact localization of infection (Level of evidence: 2). When hematogenous spread of the infection is suspected, the guideline recommends PET/CT to be used as the first imaging modality (Level of evidence: 5).

The UMHS guideline12 provided recommendations specific to patients with diabetic foot infection. It recommends bone biopsy and bone culture for suspected osteomyelitis in diabetic foot infections (Strength of recommendation: I; Level of evidence: C). For imaging tests, the guideline recommends that X-ray radiography is used firstly to evaluate suspected non-superficial soft tissue infection or osteomyelitis (Strength of recommendation: I; Level of evidence: C). With suspected soft tissue abscess, MRI is recommended as the next imaging test (Strength of recommendation: II; Level of evidence: E). In case if negative or equivocal radiograph of suspected osteomyelitis, or if there is a need to evaluate the extent of osteomyelitis on positive radiograph, the guideline recommends MRI as the next imaging test (Strength of recommendation: I; Level of evidence: C). If MRI is not available, the guideline recommends the use of triple-phase bone scan in combination with tagged white blood cell scan (Strength of recommendation: I; Level of evidence: C).

The IDSA guideline13 provided recommendations specific to patients with suspected native vertebral osteomyelitis. It recommends a medical and neurological examination, as well as laboratory tests including bacterial (aerobic and anaerobic) blood cultures, baseline erythrocyte sedimentation rate and C-reactive protein in patients with suspected native vertebral osteomyelitis (Strong recommendation; Low-quality evidence). The guideline recommends spine MRI in patients with suspected native vertebral osteomyelitis (Strong recommendation; Low-quality evidence). When MRI is not available or cannot be obtained in patients having implantable cardiac devices, cochlear implants, or claustrophobia, the guideline suggests the use of a combination of spine gallium/Tc99 bone scan, or a CT scan, or a PET scan (Weak recommendation; Low-quality evidence). In patients with subacute native vertebral osteomyelitis who are living in endemic area for brucellosis, the guideline recommends performing blood cultures and serologic tests for Brucella species (Strong recommendation; Low-quality evidence). Performing fungal blood cultures is suggested in patients with suspected native vertebral osteomyelitis and at risk of fungal infection (Weak recommendation; Low-quality evidence). In patients with subacute native vertebral osteomyelitis and at risk of Mycobacterium tuberculosis, the guideline suggests conducting a purified protein derivative test or obtaining an interferon-ɣ release assay (Weak recommendation; Low-quality evidence).

Limitations

There was a lack of evidence regarding the diagnostic accuracy of serial X-rays (i.e., initial assessment with X-rays followed by subsequent X-rays in 1 to 3 weeks) in adults with suspected osteomyelitis. Similarly, there was a lack of evidence regarding the clinical utility and cost-effectiveness of serial X-ray radiography for the detection of osteomyelitis in adults.

Conclusions and Implications for Decision or Policy Making

This review included three evidence-based guidelines for diagnosis of peripheral bone infection,11 diabetic foot infection12 and native vertebral osteomyelitis13 in adults.

The included guidelines had recommendations for diagnosis of osteomyelitis at different body parts (i.e., peripheral bone infection,11 diabetic foot infection12 and native vertebral osteomyelitis13), regarding medical examinations, laboratory tests, bone biopsies and bone cultures, and imaging tests. Two guidelines11,12 recommend X-ray radiography to be used as first-line imaging modality for the diagnosis of osteomyelitis in peripheral bone infection or in diabetic foot infection. One guideline13 recommends spine MRI in patients with suspected native vertebral osteomyelitis, without mentioning anything about radiography. Bone biopsy and bone culture are considered as the reference standard to confirm the infection and identify the causative microorganism.1113 All three guidelines1113 had recommendations for the use other imaging modalities including MRI, CT, PET, SPECT, scintigraphy depending on the extent of the investigation, the availability of the imaging modalities, the level of diagnostic accuracy required, the complexity of the disease, and patients’ contraindication.

Overall, despite MRI, PET and SPECT having been found to have higher diagnostic performance than radiography, it is recommended that conventional X-ray radiography should be the first imaging modality for detection of osteomyelitis, particularly in peripheral bone infection or in diabetic foot infection. With suspected native vertebral osteomyelitis, spine MRI, when feasible, is recommended as first imaging choice for diagnosis.

There is a need for studies examining the diagnostic accuracy, clinical utility and cost-effectiveness of serial X-ray radiography for detection of osteomyelitis in adults.

References

1.
Bires AM, Kerr B, George L. Osteomyelitis: an overview of imaging modalities. Crit Care Nurs Q. 2015;38(2):154–164. [PubMed: 25741956]
2.
Jaramillo D. Infection: musculoskeletal. Pediatr Radiol. 2011;41: Suppl 1:S127–134. [PubMed: 21523583]
3.
Hatzenbuehler J, Pulling TJ. Diagnosis and management of osteomyelitis. Am Fam Physician. 2011;84(9):1027–1033. [PubMed: 22046943]
4.
Panteli M, Giannoudis PV. Chronic osteomyelitis: what the surgeon needs to know. EFORT Open Rev. 2016;1(5):128–135. [PMC free article: PMC5367612] [PubMed: 28461939]
5.
Llewellyn A, Jones-Diette J, Kraft J, et al. Imaging tests for the detection of osteomyelitis: a systematic review. Health Technol Assess. 2019;23(61):1–128. [PMC free article: PMC6843114] [PubMed: 31670644]
6.
Beaman FD, von Herrmann PF, Kransdorf MJ, et al. ACR appropriateness criteria((R)) suspected osteomyelitis, septic arthritis, or soft tissue infection (excluding spine and diabetic foot). J Am Coll Radiol. 2017;14(5s):S326–S337. [PubMed: 28473089]
7.
Simpfendorfer CS. Radiologic approach to musculoskeletal infections. Infect Dis Clin North Am. 2017;31(2):299–324. [PubMed: 28366223]
8.
Mandell JC, Khurana B, Smith JT, et al. Osteomyelitis of the lower extremity: pathophysiology, imaging, and classification, with an emphasis on diabetic foot infection. Emerg Radiol. 2018;25(2):175–188. [PubMed: 29058098]
9.
Agree Next Steps Consortium. AGREE II instrument. Hamilton (ON): AGREE Enterprise; 2017: https://www​.agreetrust​.org/wp-content/uploads​/2017/12/AGREE-II-Users-Manual-and-23-item-Instrument-2009-Update-2017.pdf. Accessed 2020 Mar 12.
10.
Liberati A, Altman DG, Tetzlaff J, et al. The PRISMA statement for reporting systematic reviews and meta-analyses of studies that evaluate health care interventions: explanation and elaboration. J Clin Epidemiol. 2009;62(10):e1–e34. [PubMed: 19631507]
11.
Glaudemans A, Jutte PC, Cataldo MA, et al. Consensus document for the diagnosis of peripheral bone infection in adults: a joint paper by the EANM, EBJIS, and ESR (with ESCMID endorsement). Eur J Nucl Med Mol Imaging. 2019;46(4):957–970. [PMC free article: PMC6450853] [PubMed: 30675635]
12.
Mills JP, Patel P, Broekhuizen E, et al. Michigan Medicine Clinical Care Guidelines. Diabetic foot infections. Ann Arbor (MI): Michigan Medicine University of Michigan; 2019. [PubMed: 31967768]
13.
Berbari EF, Kanj SS, Kowalski TJ, et al. 2015 Infectious Diseases Society of America (IDSA) clinical practice guidelines for the diagnosis and treatment of native vertebral osteomyelitis in adults. Clin Infect Dis. 2015;61(6):e26–46. [PubMed: 26229122]
14.
OCEBM Levels of Evidence Working Group. The Oxford levels of evidence. Oxford (GB): Oxford Centre for Evidence-Based Medicine; 2011: https://www​.cebm.net​/wp-content/uploads/2014​/06/CEBM-Levels-of-Evidence-2.1.pdf. Accessed 2020 Mar 12.

Appendix 1. Selection of Included Studies

Image app1f1

Appendix 2. Characteristics of Included Studies

Table 2Characteristics of Included Guidelines

First Author, Society/Group Name, Publication Year, Country, FundingIntended Users and Target PopulationIntervention and Practice ConsideredMajor Outcomes ConsideredEvidence Collection, Selection and SynthesisRecommendations Development and EvaluationGuideline Validation

EANM, EBJIS, ESR, and ESCMID, Glaudemans et al., 201911

Europe

Funding: Unclear

Intended users: Healthcare professionals

Target population: Adult patients with a suspicion of peripheral bone infection (PBI)

Diagnostic management of adult patients with PBI. Diagnostic imaging modalities considered included radiography, CT, MRI, PET, SPECT and scintigraphyAll outcomes related to diagnosis of PBI (clinical assessment, symptoms, sings, laboratory parameters, bone biopsy, radiological and nuclear medicine imaging methods)Systematic methods were used to search for evidence, selection and synthesisThe guideline was developed by members from four European societies, who defined clinical questions to be addressed, reviewed the literature and evaluated the diagnostic accuracy of each diagnostic technique. Each consensus statement was followed by a level of evidencea created by the Oxford Centre for Evidence-Based Medicine 201114The guideline was peer-reviewed

UMHS, Mills et al., 201912

USA

Funding: No financial support

Intended users: All healthcare professionals involving in the care of patients with diabetic foot infection (DFI)

Target population: Adult patients with DFI

Diagnostic management of adult patients with DFI. Diagnostic imaging modalities considered included radiography, MRI, and scintigraphyAll outcomes related to diagnosis, imaging and treatment of DFISystematic methods were used to search for evidence, selection and synthesis

The guideline was developed by team members who are experts in the field of DFI.

The strength of recommendationsb were graded based on the level of evidencec

The guideline was peer-reviewed

IDSA, Berbari et al., 201513

USA

Funding: IDSA

Intended users: Infectious disease specialists, orthopedic surgeons, neurosurgeons, radiologists, and other healthcare professionals who care for patients with native vertebral osteomyelitis (NVO)

Target population: Adult patients with NVO

Diagnosis and treatment of NVO in adults. Diagnostic imaging modalities considered included MRI, gallium/Tc99 bone scan, CT, and PETAll outcomes related to diagnosis, and management of NVOSystematic methods were used to search for evidence, selection and synthesis

The guideline was developed by an expert panel.

The strength of recommendation and quality of evidence were systematically weighted using GRADE (Grading of Recommendations Assessment, Development and Evaluation) system.d

The guideline was peer-reviewed

CT = computed tomography; DFI = diabetic foot infection; EANM = European Association of Nuclear Medicine; EBJIS = European Bone and Joint Infection Society; ESCMID = European Society of Microbiology and Infectious Disease; ESR = European Society of Radiology; IDSA = Infectious Diseases Society of America; MRI = magnetic resonance imaging; NVO = native vertebral osteomyelitis; PBI = peripheral bone infection; PET = positron emission tomography; SPECT = single-photon emission computed tomography; UMHS = University of Michigan Health System.

a

Level of evidence

  • Level 1: Systematic review of randomized trials
  • Level 2: Randomized trial
  • Level 3: Non-randomized controlled cohort/follow-up study
  • Level 4: Case-series, case-control, or historical controlled studies
  • Level 5: Mechanism-based reasoning

b

Strength of recommendation:

  • I = Generally should be performed
  • II = May be reasonable to perform
  • III = Generally should not be performed

c

Level of evidence:

  • A = systematic review of randomized controlled trials with or without meta-analysis
  • B = randomized controlled trials
  • C = systematic review of non-randomized controlled trials or observational studies, non-randomized controlled trials, group observational studies (cohort, cross-sectional, case-control)
  • D = individual observational studies (case study/case series)
  • E = expert opinion regarding benefits and harm

d

Details of the strength of recommendations, quality of evidence, clarity of balance between desirable and undesirable effects, and implications are presented in the published guideline.13 The recommendations were graded from strong to weak, while the quality of evidence was assessed as high quality to very low quality. The strength of recommendation and the quality of the evidence were presented together based on the clarity of balance between desirable and undesirable effects, the methodological quality of supporting evidence and implications of recommendations.

Appendix 3. Quality Assessment of Included Studies

Table 3Quality Assessment of Guidelines

AGREE II checklist9EANM, EBJIS, ESR, and ESCMID, Glaudema ns et al., 201911UMHS, Mills et al., 201912IDSA, Berbari et al., 201513
Scope and purpose
1. Objectives and target patient population were explicitYesYesYes
2. The health question covered by the guidelines is specifically describedYesYesYes
3. The population to whom the guidelines is meant to apply is specifically describedYesYesYes
Stakeholder involvement
4. The guideline development group includes individuals from all relevant professional groupsYesYesYes
5. The views and preferences of the target population have been soughtYesYesYes
6. The target users of the guideline are clearly definedYesYesYes
Rigour of development
7. Systematic methods were used to search for evidenceYesYesYes
8. The criteria for selecting the evidence are clearly describedYesYesYes
9. The strengths and limitations of the body of evidence are clearly describedYesYesYes
10. The methods of formulating the recommendations are clearly describedYesYesYes
11. The health benefits, side effects, and risks have been considered in formulating the recommendationsYesYesYes
12. There is an explicit link between the recommendations and the supporting evidenceYesYesYes
13. The guideline has been externally reviewed by experts prior to its publicationYesYesYes
14. A procedure for updating the guideline is providedYesYesUnclear
Clarity of presentation
15. The recommendations are specific and unambiguousYesYesYes
16. The different options for management of the condition or health issue are clearly presentedYesYesYes
17. Key recommendations are easily identifiedYesYesYes
Applicability
18. The guideline describes facilitators and barriers to its applicationYesYesYes
19. The guidelines provides advice and/or tools on how the recommendations can be put into practiceYesYesYes
20. The potential resource (cost) implications of applying the recommendations have been consideredYesYesYes
21. The guideline presents monitoring and/or auditing criteriaYesYesYes
Editorial independence
22. The views of the funding body have not influenced the content of the guidelineUnclearUnclearUnclear
23. Competing interests of guideline development group members have been recorded and addressedYesYesYes

EANM = European Association of Nuclear Medicine; EBJIS = European Bone and Joint Infection Society; ESR = European Society of Radiology; ESCMID = European Society of Microbiology and Infectious Disease; IDSA = Infectious Diseases Society of America; UMHS = University of Michigan Health System.

Appendix 4. Recommendations in Included Guidelines

Table 4. Summary of Recommendations in Included Guidelines (PDF, 239K)

Appendix 5. Additional References of Potential Interest

About the Series

CADTH Rapid Response Report: Summary with Critical Appraisal
ISSN: 1922-8147

Version: 1.0

Funding: CADTH receives funding from Canada’s federal, provincial, and territorial governments, with the exception of Quebec.

Suggested citation:

Serial X-Ray Radiography for the Diagnosis of Osteomyelitis: A Review of Diagnostic Accuracy, Clinical Utility, Cost Effectiveness, and Guidelines. Ottawa: CADTH; 2020 Mar. (CADTH rapid response report: summary with critical appraisal).

Disclaimer: The information in this document is intended to help Canadian health care decision-makers, health care professionals, health systems leaders, and policy-makers make well-informed decisions and thereby improve the quality of health care services. While patients and others may access this document, the document is made available for informational purposes only and no representations or warranties are made with respect to its fitness for any particular purpose. The information in this document should not be used as a substitute for professional medical advice or as a substitute for the application of clinical judgment in respect of the care of a particular patient or other professional judgment in any decision-making process. The Canadian Agency for Drugs and Technologies in Health (CADTH) does not endorse any information, drugs, therapies, treatments, products, processes, or services.

While care has been taken to ensure that the information prepared by CADTH in this document is accurate, complete, and up-to-date as at the applicable date the material was first published by CADTH, CADTH does not make any guarantees to that effect. CADTH does not guarantee and is not responsible for the quality, currency, propriety, accuracy, or reasonableness of any statements, information, or conclusions contained in any third-party materials used in preparing this document. The views and opinions of third parties published in this document do not necessarily state or reflect those of CADTH.

CADTH is not responsible for any errors, omissions, injury, loss, or damage arising from or relating to the use (or misuse) of any information, statements, or conclusions contained in or implied by the contents of this document or any of the source materials.

This document may contain links to third-party websites. CADTH does not have control over the content of such sites. Use of third-party sites is governed by the third-party website owners’ own terms and conditions set out for such sites. CADTH does not make any guarantee with respect to any information contained on such third-party sites and CADTH is not responsible for any injury, loss, or damage suffered as a result of using such third-party sites. CADTH has no responsibility for the collection, use, and disclosure of personal information by third-party sites.

Subject to the aforementioned limitations, the views expressed herein are those of CADTH and do not necessarily represent the views of Canada’s federal, provincial, or territorial governments or any third party supplier of information.

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