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Complete Summary

GUIDELINE TITLE

Low back - lumbar & thoracic (acute & chronic).

BIBLIOGRAPHIC SOURCE(S)

  • Work Loss Data Institute. Low back - lumbar & thoracic (acute & chronic). Corpus Christi (TX): Work Loss Data Institute; 2008. 481 p. [594 references]

GUIDELINE STATUS

This is the current release of the guideline.

This guideline updates a previous version: Work Loss Data Institute. Low back - lumbar & thoracic (acute & chronic). Corpus Christi (TX): Work Loss Data Institute; 2007 Jul 5. 393 p.

The Official Disability Guidelines product line, including ODG Treatment in Workers Comp, is updated annually, as it has been since the first release in 1996.

** REGULATORY ALERT **

FDA WARNING/REGULATORY ALERT

Note from the National Guideline Clearinghouse: This guideline references a drug(s) for which important revised regulatory and/or warning information has been released.

  • July 1, 2009 - Chantix or Champix (Varenicline) and Zyban or Wellbutrin (bupropion or amfebutamone): The U.S. Food and Drug Administration (FDA) notified healthcare professionals and patients that it has required the manufacturers of the smoking cessation aids varenicline (Chantix) and bupropion (Zyban and generics) to add new Boxed Warnings and develop patient Medication Guides highlighting the risk of serious neuropsychiatric symptoms in patients using these products. These symptoms include changes in behavior, hostility, agitation, depressed mood, suicidal thoughts and behavior, and attempted suicide.
  • December 16, 2008 - Antiepileptic drugs: The U.S. Food and Drug Administration (FDA) has completed its analysis of reports of suicidality (suicidal behavior or ideation [thoughts]) from placebo-controlled clinical trials of drugs used to treat epilepsy, psychiatric disorders, and other conditions. Based on the outcome of this review, FDA is requiring that all manufacturers of drugs in this class include a Warning in their labeling and develop a Medication Guide to be provided to patients prescribed these drugs to inform them of the risks of suicidal thoughts or actions. FDA expects that the increased risk of suicidality is shared by all antiepileptic drugs and anticipates that the class labeling change will be applied broadly.

COMPLETE SUMMARY CONTENT

 ** REGULATORY ALERT **
 SCOPE
 METHODOLOGY - including Rating Scheme and Cost Analysis
 RECOMMENDATIONS
 EVIDENCE SUPPORTING THE RECOMMENDATIONS
 BENEFITS/HARMS OF IMPLEMENTING THE GUIDELINE RECOMMENDATIONS
 CONTRAINDICATIONS
 QUALIFYING STATEMENTS
 IMPLEMENTATION OF THE GUIDELINE
 INSTITUTE OF MEDICINE (IOM) NATIONAL HEALTHCARE QUALITY REPORT CATEGORIES
 IDENTIFYING INFORMATION AND AVAILABILITY
 DISCLAIMER

SCOPE

DISEASE/CONDITION(S)

Work-related low back pain

GUIDELINE CATEGORY

Diagnosis
Evaluation
Management
Treatment

CLINICAL SPECIALTY

Chiropractic
Family Practice
Internal Medicine
Orthopedic Surgery
Physical Medicine and Rehabilitation
Surgery

INTENDED USERS

Advanced Practice Nurses
Health Care Providers
Health Plans
Nurses
Physician Assistants
Physicians

GUIDELINE OBJECTIVE(S)

To offer evidence-based step-by-step decision protocols for the assessment and treatment of workers' compensation conditions

TARGET POPULATION

Workers with low back pain

INTERVENTIONS AND PRACTICES CONSIDERED

The following interventions/procedures were considered and recommended as indicated in the original guideline document:

  1. Activity restrictions/work modifications
  2. Aerobic exercise
  3. Age adjustment
  4. Antidepressants in chronic cases
  5. Anti-inflammatory medications (e.g., ibuprofen)
  6. Aquatic therapy (as an optional form of exercise therapy)
  7. Back schools
  8. Behavioral treatment
  9. Chiropractic/manipulation
  10. Cold/heat packs for acute pain
  11. Conservative care (first six months)
  12. Differential diagnosis
  13. Discectomy/laminectomy
  14. Electromyography (needle, not surface)
  15. Epidural steroid injections (ESIs) (treatment and diagnostic)
  16. Evoked potential studies
  17. Exercise
  18. Facet joint diagnostic blocks (injections) prior to facet neurotomy
  19. Facet joint pain, signs and symptoms
  20. Fear-avoidance beliefs questionnaire (FABQ)
  21. Flexibility evaluation as a part of a routine musculoskeletal evaluation
  22. Fluoroscopy (for ESIs)
  23. Functional improvement measures
  24. Fusion (spinal) as an option for spinal fracture, dislocation, spondylolisthesis or frank neurogenic compromise
  25. Gabapentin (Neurontin®)
  26. Hardware injection block for diagnostic evaluation of failed back surgery syndrome
  27. Heat therapy
  28. Herbal medicines
  29. Home health services
  30. H-reflex tests
  31. Hyperbaric oxygen therapy (HBOT) for diabetic skin ulcers
  32. Iliac crest donor-site pain treatment (bupivacaine)
  33. Implantable drug-delivery systems (IDDSs) (as an end-stage treatment alternative)
  34. Kyphoplasty
  35. Laminectomy/laminotomy
  36. Lumbar extension exercise equipment
  37. Magnetic resonance imaging (MRI)
  38. Massage
  39. McKenzie method
  40. Microdiscectomy
  41. Muscle relaxants for acute cases
  42. Myelography
  43. Nonprescription medications (e.g., acetaminophen, aspirin, ibuprofen) for early use only
  44. Occupational/physical therapy
  45. Patient education for treatment
  46. Percutaneous vertebroplasty
  47. Piriformis injections
  48. Psychological screening prior to surgery
  49. Return to work and regular activities
  50. Sacroiliac joint injections (SJI)
  51. Segmental rigidity (diagnosis)
  52. Sequestrectomy
  53. Shoe insoles/shoe lifts
  54. Skilled nursing facility after hospitalization if necessary
  55. Spinal cord stimulation (SCS) for selected patients
  56. Stretching (as part of an exercise program)
  57. Vertebroplasty
  58. Work conditioning/work hardening
  59. Wound dressing
  60. Yoga

The following interventions/procedures were considered optional:

Shoe insoles/shoe lifts

The following interventions/procedures are under study and are not specifically recommended:

  1. Acupressure
  2. Adhesiolysis, spinal endoscopic
  3. Back brace/corsets/lumbar supports for treatment
  4. Bone-growth stimulators
  5. Botulinum toxin (Botox)
  6. Colchicine
  7. Electromagnetic pulsed therapy
  8. Ergonomic interventions for primary prevention
  9. Facet joint intra-articular injections (therapeutic blocks)
  10. Facet rhizotomy/facet joint radiofrequency neurotomy
  11. Feldenkrais
  12. Interspinous decompression device (X-Stop®)
  13. Magnetic resonance (MR) neurography
  14. Mattress selection
  15. Oral corticosteroids
  16. Percutaneous adhesiolysis/epidural neuroplasty
  17. Percutaneous electrical nerve stimulation (PENS)
  18. Topiramate (Topamax®)
  19. Vacuum-assisted closure wound-healing

The following interventions/procedures were considered, but are not recommended:

  1. Acupuncture
  2. Back brace/corsets/lumbar supports for prevention
  3. Bed rest
  4. Biofeedback
  5. Bone scan
  6. Bupropion for low back pain
  7. Chemonucleolysis (chymopapain)
  8. Computed tomography (CT) and CT myelography
  9. Current perception threshold (CPT) testing
  10. Delayed treatment
  11. Device for intervertebral assisted motion (DIAM)
  12. Diathermy
  13. Disc prosthesis/replacement
  14. Discography
  15. Dynamic neutralization system (Dynesys)
  16. Epidural steroid injections, "series of three"
  17. Facet-joint chemical rhizotomy
  18. Facet-joint injections, multiple series and thoracic
  19. Facet joint medial branch blocks for therapy
  20. Flexion/extension imaging studies  as a primary criteria for range of motion
  21. Functional anesthetic discography
  22. F-wave tests
  23. Fusion (spinal, endoscopic)
  24. Gym membership unless monitored and administered by medical professionals
  25. Hospitalization except for major trauma
  26. H-wave stimulation (devices)
  27. Infrared therapy
  28. Interferential therapy
  29. Intradiscal electrothermal annuloplasty (IDET)
  30. Intradiscal steroid injection
  31. Iontophoresis
  32. Ligamentous injections
  33. Low level laser therapy (LLLT)
  34. Lumbar supports for prevention
  35. Magnet therapy
  36. Manipulation under anesthesia (MUA)
  37. Microcurrent electrical stimulation (MENS devices)
  38. NC-stat nerve conduction studies/nerve conduction studies (NCS)
  39. Neuromuscular electrical stimulators (NMES) (except for patients with specific criteria)
  40. Neuroreflexotherapy
  41. Nucleoplasty
  42. Opioids/narcotics (except for short use with severe cases)
  43. Orthotrac vest
  44. Percutaneous discectomy (PCD)
  45. Percutaneous endoscopic laser discectomy (PELD)
  46. Percutaneous intradiscal radiofrequency (thermocoagulation)
  47. Percutaneous neuromodulation therapy (PNT)
  48. (See #62) Prolotherapy, also known as sclerotherapy
  49. Pulsed radiofrequency treatment (PRF)
  50. Radiography in the absence of red flags
  51. Single photon emission computed tomography (SPECT)
  52. Standing MRI
  53. Surface electromyography (SEMG)
  54. Sympathetic therapy
  55. Thermography (infrared stress thermography)
  56. Traction
  57. Transcutaneous electrical neurostimulation (TENS)
  58. Transplantation, intravertebral disc
  59. Trigger point injections in the absence of myofascial pain syndrome
  60. Tumor necrosis factor modifiers
  61. Ultrasound (diagnostic and therapeutic)
  62. Vertebral axial decompression (VAX-D)/powered traction devices
  63. Videofluoroscopy

MAJOR OUTCOMES CONSIDERED

  • Reliability and value of diagnostic assessments
  • Effectiveness of treatment in relieving pain and restoring normal function

METHODOLOGY

METHODS USED TO COLLECT/SELECT EVIDENCE

Hand-searches of Published Literature (Primary Sources)
Searches of Electronic Databases

DESCRIPTION OF METHODS USED TO COLLECT/SELECT THE EVIDENCE

Work Loss Data Institute (WLDI) conducted a comprehensive medical literature review (now ongoing) with preference given to high quality systematic reviews, meta-analyses, and clinical trials published since 1993, plus existing nationally recognized treatment guidelines from the leading specialty societies. WLDI primarily searched MEDLINE and the Cochrane Library. In addition, WLDI also reviewed other relevant treatment guidelines, including those in the National Guideline Clearinghouse, as well as state guidelines and proprietary guidelines maintained in the WLDI guideline library. These guidelines were also used to suggest references or search terms that may otherwise have been missed. In addition, WLDI also searched other databases, including MD Consult, eMedicine, CINAHL, and conference proceedings in occupational health (i.e., American College of Occupational and Environmental medicine [ACOEM]) and disability evaluation (i.e., American Academy of Disability Evaluating Physicians [AADEP], American Board of Independent Medical Examiners [ABIME]). Search terms and questions were diagnosis, treatment, symptom, sign, and/or body-part driven, generated based on new or previously indexed existing evidence, treatment parameters and experience.

In searching the medical literature, answers to the following questions were sought: (1) If the diagnostic criteria for a given condition have changed since 1993, what are the new diagnostic criteria? (2) What occupational exposures or activities are associated causally with the condition? (3) What are the most effective methods and approaches for the early identification and diagnosis of the condition? (4) What historical information, clinical examination findings or ancillary test results (such as laboratory or x-ray studies) are of value in determining whether a condition was caused by the patient's employment? (5) What are the most effective methods and approaches for treating the condition? (6) What are the specific indications, if any, for surgery as a means of treating the condition? (7) What are the relative benefits and harms of the various surgical and non-surgical interventions that may be used to treat the condition? (8) What is the relationship, if any, between a patient's age, gender, socioeconomic status and/or racial or ethnic grouping and specific treatment outcomes for the condition? (9) What instruments or techniques, if any, accurately assess functional limitations in an individual with the condition? (10) What is the natural history of the disorder? (11) Prior to treatment, what are the typical functional limitations for an individual with the condition? (12) Following treatment, what are the typical functional limitations for an individual with the condition? (13) Following treatment, what are the most cost-effective methods for preventing the recurrence of signs or symptoms of the condition, and how does this vary depending upon patient-specific matters such as underlying health problems?

Criteria for Selecting the Evidence

Preference was given to evidence that met the following criteria: (1) The article was written in the English language, and the article had any of the following attributes: (2) It was a systematic review of the relevant medical literature, or (3) The article reported a controlled trial – randomized or controlled, or (4) The article reports a cohort study, whether prospective or retrospective, or (5) The article reports a case control series involving at least 25 subjects, in which the assessment of outcome was determined by a person or entity independent from the persons or institution that performed the intervention the outcome of which is being assessed.

More information about the selection of evidence is available in "Appendix. ODG Treatment in Workers' Comp. Methodology description using the AGREE instrument" (see "Availability of Companion Documents" field).

NUMBER OF SOURCE DOCUMENTS

Not stated

METHODS USED TO ASSESS THE QUALITY AND STRENGTH OF THE EVIDENCE

Weighting According to a Rating Scheme (Scheme Given)

RATING SCHEME FOR THE STRENGTH OF THE EVIDENCE

Ranking by Type of Evidence

  1. Systematic Review/Meta-Analysis
  2. Controlled Trial-Randomized (RCT) or Controlled
  3. Cohort Study-Prospective or Retrospective
  4. Case Control Series
  5. Unstructured Review
  6. Nationally Recognized Treatment Guideline (from www.guideline.gov)
  7. State Treatment Guideline
  8. Other Treatment Guideline
  9. Textbook
  10. Conference Proceedings/Presentation Slides

Ranking by Quality within Type of Evidence

  1. High Quality
  2. Medium Quality
  3. Low Quality

METHODS USED TO ANALYZE THE EVIDENCE

Review of Published Meta-Analyses
Systematic Review

DESCRIPTION OF THE METHODS USED TO ANALYZE THE EVIDENCE

The Work Loss Data Institute (WLDI) reviewed each article that was relevant to answering the question at issue, with priority given to those that met the following criteria: (1) The article was written in the English language, and the article had any of the following attributes: (2) It was a systematic review of the relevant medical literature, or (3) The article reported a controlled trial – randomized or controlled, or (4) The article reported a cohort study, whether prospective or retrospective, or (5) The article reported a case control series involving at least 25 subjects, in which the assessment of outcome was determined by a person or entity independent from the persons or institution that performed the intervention the outcome of which is being assessed.

Especially when articles on a specific topic that met the above criteria were limited in number and quality, WLDI also reviewed other articles that did not meet the above criteria, but all evidence was ranked alphanumerically (see the Rating Scheme of the Strength of Evidence field) so that the quality of evidence could be clearly determined when making decisions about what to recommend in the Guidelines. Articles with a Ranking by Type of Evidence of Case Reports and Case Series were not used in the evidence base for the Guidelines. These articles were not included because of their low quality (i.e., they tend to be anecdotal descriptions of what happened with no attempt to control for variables that might affect outcome). Not all the evidence provided by WLDI was eventually listed in the bibliography of the published Guidelines. Only the higher quality references were listed. The criteria for inclusion was a final ranking of 1a to 4b (the original inclusion criteria suggested the methodology subgroup), or if the Ranking by Type of Evidence was 5 to 10, the quality ranking should be an "a."

METHODS USED TO FORMULATE THE RECOMMENDATIONS

Not stated

RATING SCHEME FOR THE STRENGTH OF THE RECOMMENDATIONS

Not applicable

COST ANALYSIS

The guideline developers reviewed published cost analyses.

METHOD OF GUIDELINE VALIDATION

External Peer Review

DESCRIPTION OF METHOD OF GUIDELINE VALIDATION

Prior to publication, select organizations and individuals making up a cross-section of medical specialties and typical end-users externally reviewed the guideline.

RECOMMENDATIONS

MAJOR RECOMMENDATIONS

Identify Radicular Signs

  • First visit: may be with Primary Care Physician MD/DO (50%), Orthopedist (33%), or Chiropractor (17%)
  • Determine presence or absence of radiculopathy:
    • Medical history
    • Sensation: Feeling pain radiating below the knee (calf or lower), not just referred pain (pain radiating to buttocks or thighs), and dermatological sensory loss
    • Straight leg raising test (sitting and supine), productive of leg pain
    • Motor strength and deep tendon reflexes
    • Document flexibility/range of motion (ROM) (fingertip test), muscle atrophy (calf measurement), local areas of tenderness, visual pain analog, sensation alternation
    • Note: Radiculopathy is often over-diagnosed. For unequivocal evidence of radiculopathy, refer to the American Medical Association (AMA) Guides to the Evaluation of Permanent Impairment, 5th Edition, pg. 382-83.
  • Rule out "red flag" diagnoses, including diagnostic studies, for specialist referral:
    • Cauda Equina Syndrome (Schedule emergency procedure) (Refer to the original guideline document for International Classification of Diseases, Ninth Revision [ICD-9] codes for this and other diagnoses)
    • Fracture, Compression fracture, Dislocation, Wound
    • Cancer, Infection
    • Dissecting/Ruptured Aortic Aneurysm
    • Others (prostate problems, endometriosis/gynecological disorders, urinary tract infections, and renal pathology)
    • Note: This guideline should not be used to suggest appropriate procedures for other conditions or comorbidities. When the treating doctor suspects any other diagnosis, they may decide what necessary testing should be performed, which may include laboratory tests such as erythrocyte sedimentation rate (ESR), complete blood count (CBC), and urinalysis (UA) to screen for nonspecific medical diseases (especially infection and tumor) of the low back.

Without Radiculopathy (90% of cases)

  • Also first visit (day 1):
    • Prescribe activity modification, if necessary, based on severity and difficulty of job, while encouraging return to activity as much as possible; limited passive therapy with heat/ice (3 to 4 times/day); stretching/exercise (training by physical therapist OK); appropriate analgesia (i.e., acetaminophen) and/or anti-inflammatory (i.e., ibuprofen) [Benchmark cost: $14]; back to work except for severe cases in 72 hours, possibly modified duty. Avoid bed rest.
    • REASSURE PATIENT: Patient education - common problem (90% of patients recover spontaneously in 4 weeks)
    • No x-rays unless significant trauma (e.g., a fall)
    • If muscle spasms, then consider muscle relaxant with limited sedative side effects [Benchmark cost: $44]

      Note: The purpose of muscle relaxants is to facilitate return to activity, but muscle relaxants have not been shown to be more effective than non-steroidal anti-inflammatory drugs [NSAIDs].

Official Disability Guidelines (ODG) Return-To-Work Pathways (lumbar sprain and lumbago)

Modified Duty --

Mild, (Grade I)1, clerical/modified work: 0 days

Severe, (Grade II-III)1, clerical/modified work: 3 days

(See ODG Capabilities & Activity Modifications for Restricted Work under "Work" in the Procedure Summary for Ergonomic accommodations of the original guideline document)

1Definition of Sprain/Strain Severity Grade: In general, a Grade I or mild sprain/strain is caused by overstretching or slight tearing of the ligament/muscle/tendon with no instability, and a person with a mild sprain usually experiences minimal pain, swelling, and little or no loss of functional ability. Although the injured muscle is tender and painful, it has normal strength. A Grade II sprain/strain is caused by incomplete tearing of the ligament/muscle/tendon and is characterized by bruising, moderate pain, and swelling, and a Grade III sprain/strain means complete tear or rupture of a ligament/muscle/tendon. A sprain is a stretch and/or tear of a ligament (a band of fibrous tissue that connects two or more bones at a joint). A strain is an injury to either a muscle or a tendon (fibrous cords of tissue that connect muscle to bone).

  • Second visit (day 3 to 10 - about 1 week after first visit or sooner because delayed treatment is not recommended)
    • Document progress (flexibility, areas of tenderness, motor strength, straight leg raise--sitting and supine)
    • If still 50% disabled (i.e., cannot return to work) then consider referral for exercise/instruction/manual therapy [Benchmark cost: $250]: Options are physical therapist, chiropractor, massage therapist, or occupational therapist (3 visits in first week), or by treating DO/MD (Choose providers supporting active therapy and not just passive modalities. The focus of treatment should not be symptom reduction, but improving function with a goal to return to work.) Consider screening for psychosocial symptoms in cases with expectations of delayed recovery
    • Discontinue muscle relaxant
ODG Return-To-Work Pathways (lumbar sprain and lumbago)

Manual Work --

Mild, manual work: 7 to 10 days

Severe, manual work: 14 to 17 days

  • Third visit (day 10 to 17 - about 1 week after second visit)
    • Document progress
    • Prescribe muscle-conditioning exercises
    • At this point 66% to 75% should be back to regular work
    • While not indicated in the absence of red flags, if still disabled, then consider imaging study (anterior-posterior [AP]/lateral 2-view x-ray of lumbar) [Benchmark cost: $150] to rule out tumor, fracture, osteoporosis, myelopathy
    • Maintain therapy, continue focus on active therapy and not passive modalities, 2 visits in next week, teach home exercises
    • End manual therapy at 4 weeks (1 visit in last week)
ODG Return-To-Work Pathways (lumbar sprain and lumbago)

Manual & Heavy Manual Work --

Severe, manual work: 14 to 17 days

Severe, heavy manual work: 35 days

With Radiculopathy (10% of cases)

  • Also first visit (day 1)
    • Same as non-radicular
ODG Return-To-Work Pathways (intervertebral disc disorders)

Disc bulge --

Mild cases with back pain, avoid strenuous activity: 0 days

Herniated disc --

Initial conservative medical treatment, clerical/modified work: 3 days

  • Second visit (day 3-10 - about 1 week after first visit)
    • Same as non-radicular
    • Reassure, but if increased numbness or weakness of either leg, get back to provider in one day
    • Consider referral to nonsurgical musculoskeletal physician (Orthopedist/Physical Medicine/Sports Medicine)
  • Third visit (day 10 to 17 - about 1 week after second visit)
    • Same as non-radicular
    • About 50% can be back at modified duty
    • If improvement, then add strengthening exercises, increased activity
  • Fourth visit (day 21 to 28 - about 1 to 2 weeks after third visit)
    • Document objective findings, if no improvement then:
    • First magnetic resonance imaging (MRI) (about 3% of total cases, or 30% of radicular cases) to confirm extruded disk with nerve root displacement (>1 month conservative therapy) [Benchmark cost: $1,600]
    • MRI or computed tomography (CT) not indicated without obvious clinical level of nerve root dysfunction, clear radicular findings, or before 3 to 4 weeks
    • EMGs (electromyography) may be useful to obtain unequivocal evidence of radiculopathy, after 4 to 8 weeks conservative therapy, but EMGs are not necessary if radiculopathy is already clinically obvious
    • Consider an epidural steroid injection (ESI) for severe cases hoping to avoid surgery [Benchmark cost: $676] (Note: The purpose of ESI is to reduce pain and inflammation, restoring range of motion and thereby facilitating progress in more active treatment programs, but this treatment alone offers no significant long-term functional benefit)
    • If psychological factors retarding recovery are suspected, possibly refer to psychologist for testing [Benchmark cost: $540]
    • Education: Consider back school as an option, if available
    • If no improvement 7 to 14 days after the first ESI, consider prescribing 2nd ESI [Benchmark cost: $615]; there should be a maximum of two ESIs, and the second ESI can be 7 to 14 days after the first, depending upon the patient's response and functional gain
ODG Return-To-Work Pathways (intervertebral disc disorders)

Initial conservative medical treatment, manual work: 28 days

Initial conservative medical treatment, regular work if cause of disability: 84 days

  • Surgery (three months or more -- after appropriate work-up and consultation, concordance between radicular findings on radiologic evaluation and physical exam findings) (about 2% of total cases, or 20% of radicular cases) (See also ODG Indications for Surgery™ -- Discectomy in the Procedure Summary of the original guideline document). Unequivocal objective findings are required based on neurological examination and testing.
    • Refer to fellowship trained Spine Surgeon: Neurosurgeon (50%), Orthopedist (50%)
    • Before surgery, screen for psychological symptoms that could affect surgical outcome (e.g., substance abuse, child abuse, work conflicts, somatization, verbalizations, attorney involvement, smoking)
    • Review options/outcomes with patient, let patient be part of decision making
    • Simple discectomy/laminectomy, minimally invasive [Benchmark cost: $17,400]
    • Post-operative pain, walking exercises, physical therapy
ODG Return-To-Work Pathways (intervertebral disc disorders)

Discectomy, clerical/modified work: 28 days

Discectomy, manual work: 56 days

Discectomy, heavy manual work: 126 days to indefinite

Laminectomy, clerical/modified work: 28 days

Laminectomy, manual work: 70 days

Laminectomy, heavy manual work: 105 days to indefinite

  • Failure to recover: See the Procedure Summary (in the original guideline document) for options that may be available, along with links to the medical evidence. Also see the Chronic Pain Chapter.

CLINICAL ALGORITHM(S)

None provided

EVIDENCE SUPPORTING THE RECOMMENDATIONS

TYPE OF EVIDENCE SUPPORTING THE RECOMMENDATIONS

During the comprehensive medical literature review, preference was given to high quality systematic reviews, meta-analyses, and clinical trials over the past ten years, plus existing nationally recognized treatment guidelines from the leading specialty societies.

The heart of each Work Loss Data Institute guideline is the Procedure Summary (see the original guideline document), which provides a concise synopsis of effectiveness, if any, of each treatment method based on existing medical evidence. Each summary and subsequent recommendation is hyper-linked into the studies on which they are based, in abstract form, which have been ranked, highlighted and indexed.

BENEFITS/HARMS OF IMPLEMENTING THE GUIDELINE RECOMMENDATIONS

POTENTIAL BENEFITS

These guidelines unite evidence-based protocols for medical treatment with normative expectations for disability duration. They also bridge the interests of the many professional groups involved in diagnosing and treating work-related low back pain.

POTENTIAL HARMS

  • Muscle relaxants have potential side effects, including drowsiness in up to 30 percent of patients.
  • Gabapentin is associated with increased sedation and dizziness.
  • There should be caution about daily doses of acetaminophen and liver disease if over 4,000 mg per day or in combination with other non-steroidal anti-inflammatory drugs (NSAIDs).

CONTRAINDICATIONS

CONTRAINDICATIONS

Potential cautions or contraindications to manipulations include coagulopathy, fracture, and progressive neurologic deficit.

QUALIFYING STATEMENTS

QUALIFYING STATEMENTS

The Treatment Planning sections outline the most common pathways to recovery, but there is no single approach that is right for every patient and these protocols do not mention every treatment that may be recommended. See the Procedure Summaries (in the original guideline document) for complete lists of the various options that may be available, along with links to the medical evidence.

IMPLEMENTATION OF THE GUIDELINE

DESCRIPTION OF IMPLEMENTATION STRATEGY

An implementation strategy was not provided.

IMPLEMENTATION TOOLS

Patient Resources

For information about availability, see the "Availability of Companion Documents" and "Patient Resources" fields below.

INSTITUTE OF MEDICINE (IOM) NATIONAL HEALTHCARE QUALITY REPORT CATEGORIES

IOM CARE NEED

Getting Better
Living with Illness

IOM DOMAIN

Effectiveness
Patient-centeredness

IDENTIFYING INFORMATION AND AVAILABILITY

BIBLIOGRAPHIC SOURCE(S)

  • Work Loss Data Institute. Low back - lumbar & thoracic (acute & chronic). Corpus Christi (TX): Work Loss Data Institute; 2008. 481 p. [594 references]

ADAPTATION

Not applicable: The guideline was not adapted from another source.

DATE RELEASED

2003 (revised 2008 Jun 10)

GUIDELINE DEVELOPER(S)

Work Loss Data Institute - Public For Profit Organization

SOURCE(S) OF FUNDING

Not stated

GUIDELINE COMMITTEE

Not stated

COMPOSITION OF GROUP THAT AUTHORED THE GUIDELINE

FINANCIAL DISCLOSURES/CONFLICTS OF INTEREST

There are no conflicts of interest among the guideline development members.

GUIDELINE STATUS

This is the current release of the guideline.

This guideline updates a previous version: Work Loss Data Institute. Low back - lumbar & thoracic (acute & chronic). Corpus Christi (TX): Work Loss Data Institute; 2007 Jul 5. 393 p.

The Official Disability Guidelines product line, including ODG Treatment in Workers Comp, is updated annually, as it has been since the first release in 1996.

GUIDELINE AVAILABILITY

Electronic copies: Available to subscribers from the Work Loss Data Institute Web site.

Print copies: Available from the Work Loss Data Institute, 169 Saxony Road, Suite 210, Encinitas, CA 92024; Phone: 800-488-5548, 760-753-9992, Fax: 760-753-9995; www.worklossdata.com.

AVAILABILITY OF COMPANION DOCUMENTS

PATIENT RESOURCES

The following is available:

  • Appendix C. ODG Treatment in Workers' Comp. Patient information resources. 2008.

Electronic copies: Available to subscribers from the Work Loss Data Institute Web site.

Print copies: Available from the Work Loss Data Institute, 169 Saxony Road, Suite 210, Encinitas, CA 92024; Phone: 800-488-5548, 760-753-9992, Fax: 760-753-9995; www.worklossdata.com.

Please note: This patient information is intended to provide health professionals with information to share with their patients to help them better understand their health and their diagnosed disorders. By providing access to this patient information, it is not the intention of NGC to provide specific medical advice for particular patients. Rather we urge patients and their representatives to review this material and then to consult with a licensed health professional for evaluation of treatment options suitable for them as well as for diagnosis and answers to their personal medical questions. This patient information has been derived and prepared from a guideline for health care professionals included on NGC by the authors or publishers of that original guideline. The patient information is not reviewed by NGC to establish whether or not it accurately reflects the original guideline's content.

NGC STATUS

This summary was completed by ECRI on February 2, 2004. The information was verified by the guideline developer on February 13, 2004. This NGC summary was updated by ECRI on March 28, 2005, January 3, 2006, April 11, 2006, November 10, 2006, and March 30, 2007. This summary was updated by ECRI Institute on May 17, 2007 following the U.S. Food and Drug advisory on Colchicine. This NGC summary was updated by ECRI Institute on August 28, 2007. This summary was updated by ECRI Institute on October 31, 2007, following the U.S. Food and Drug Administration advisory on Antidepressant drugs. This NGC summary was updated by ECRI Institute on January 22, 2009. This summary was updated by ECRI Institute on May 1, 2009 following the U.S. Food and Drug Administration advisory on antiepileptic drugs. This summary was updated by ECRI Institute on July 20, 2009 following the U.S. Food and Drug Administration advisory on Varenicline and Bupropion.

COPYRIGHT STATEMENT

This NGC summary is based on the original guideline, which is subject to the guideline developer's copyright restrictions.

DISCLAIMER

NGC DISCLAIMER

The National Guideline Clearinghouse™ (NGC) does not develop, produce, approve, or endorse the guidelines represented on this site.

All guidelines summarized by NGC and hosted on our site are produced under the auspices of medical specialty societies, relevant professional associations, public or private organizations, other government agencies, health care organizations or plans, and similar entities.

Guidelines represented on the NGC Web site are submitted by guideline developers, and are screened solely to determine that they meet the NGC Inclusion Criteria which may be found at http://www.guideline.gov/about/inclusion.aspx .

NGC, AHRQ, and its contractor ECRI Institute make no warranties concerning the content or clinical efficacy or effectiveness of the clinical practice guidelines and related materials represented on this site. Moreover, the views and opinions of developers or authors of guidelines represented on this site do not necessarily state or reflect those of NGC, AHRQ, or its contractor ECRI Institute, and inclusion or hosting of guidelines in NGC may not be used for advertising or commercial endorsement purposes.

Readers with questions regarding guideline content are directed to contact the guideline developer.


 

 

   
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