Acute Low Back Pain
Diagnostically there are three aims in the approach to acute low back pain. The first is to determine whether the presenting complaint is in fact low back pain, and whether it is acute or not. The second aim is to determine whether any referred pain is somatic referred pain or radicular pain. The third aim is to identify any serious conditions. Management is largely aimed at managing symptoms and disability (pain, difficulty moving, inability to work, and fear). An evidence based approach is outlined, however evidence-based management requires extensive time that would usually be well in excess of what is available in routine primary care in New Zealand.
- Main article: Low Back Pain Definitions
Starting with the wrong definition of low back pain can lead to the wrong diagnosis, and so it is important to be clear here. Low back pain is not loin pain, nor is it gluteal pain. The IASP taxonomy categorises low back pain into lumbar spinal pain and sacral spinal pain. There is also an overlapping definition called lumbosacral pain. These three categories constitute the colloquial term "low back pain."
Lumbar spinal pain is pain in a region bounded superiorly by an imaginary transverse line through the tip T12, inferiorly by an imaginary transverse line through the tip of S1, and laterally by vertical lines tangential to the lateral borders of the lumbar erectores spinae.
Sacral Spinal Pain is pain in a region bounded superiorly by an imaginary transverse line through the tip of S1, inferiorly by an imaginary transverse line through the posterior sacrococcygeal joints, and laterally by imaginary lines passing through the posterior superior and posterior inferior iliac spines."
Lumbosacral Pain is pain perceived as arising from a region encompassing or centred over the lower third of the lumbar region as described above and the upper third of the sacral region as described above.
Acute pain is pain that has been present for no longer than 12 weeks. Subacute pain is pain present for longer than 5 or 7 weeks but less than 12 weeks. The management differs depending on the acuity.
- Main article: Low_Back_Pain_Definitions#Referred_Pain
Referred pain is "pain perceived as arising or occurring in a region of the body innervated by nerves or branches of nerves other than those that innervate the actual source of pain"
Visceral referred pain is referred pain where the source lies in an organ or blood vessel of the body. With low back pain, the uterus and abdominal aorta are important considerations. Other viscera with higher segmental supply may cause back pain such as pancreatitis, but this may be due to irritation of the posterior abdominal wall, in which case the pain is not truly referred in nature.
Somatic referred pain is referred pain where the source originates in a tissue or structure of the body wall or limbs. A number of structures in the lumbar spine are capable of nociception including the lumbar zygapophysial joints, intervertebral discs, sacroiliac joints, and more.
Radicular pain is a subset of neuropathic pain, and refers to pain that is evoked with stimulation of the nerve roots or dorsal root ganglion of a spinal nerve. In radicular pain, the pain is felt in the peripheral innervation of the affected nerve.
Somatic referred pain and radicular pain can usually be differentiated based on the quality and spread of the pain, see assessment section below.
Unlike with chronic low back pain there is little research on the aetiology of acute low back pain. No patho-anatomic diagnosis of low back pain can be made clinically without the use of special investigations (e.g. discography, medial branch blocks, sacroiliac joint blocks). Special investigations are not appropriate for acute low back pain, and are reserved for chronic low back pain. Furthermore medical imaging is not able to identify sources of pain other than fractures.
The most important part of the assessment in acute low back pain is evaluating for red flag conditions. Fractures occur between 1-4% of cases, malignancy in 0.2%, and infection in 0.01%. Other conditions that are important to detect are cauda equina, and spondyloarthropathies.
In the acute setting in the absence of red flags, the diagnosis is simply "acute low back pain."
- Main article: Prognosis of Low Back Pain
It is sometimes stated in guidelines that most patients with acute low back pain make an excellent recovery. The evidence is in fact quite conflicting, with markedly different findings across different studies. Overall the treating doctor can relay optimism, but be guarded about prognosis. The data on recurrence rates are also conflicting.
A systematic review of 11 studies performed in the US, Australia and Europe on patients with non-specific back pain found that recovery occurred in 33% of patients at 3 months, and by 1 year 65% still had pain. In studies that used total absence of pain as a criterion, 71% still had pain at 12 months. In studies that had a less stringent criteria, 57% still had pain at 12 months.
Prognostic risk factors are broadly categorised into biological and psychosocial. Predictors of recurrence are often variable across studies, but generally include 
- Sociodemographic: female gender, obesity, poor educational level
- Current History: previous episodes, duration of episode, days to seek care, pain and disability levels, leg pain
- General Health: Smoking, habitual physical activity, perceived health, use of medications
- Psychosocial: Perceived risk of recurrence, depression, anxiety, fear-avoidance behaviour, overprotective family or lack of support.
- Work-related: Involvement in heavy lifting or awkward positions, job satisfaction, compensable case
- Others: MRI findings, qualification of practitioner.
The psychosocial and occupational barriers are termed "yellow flags".
Assessment and Management Algorithm Overview
Because a specific tissue diagnosis cannot be made with any validity in the vast majority of cases of acute low back pain, the management is not based on finding and treating a particular cause, and so a different approach must be used.
Bogduk presented an algorithm for the management of acute low back pain, which was based off a positive RCT by Indahl, and itself found be successful in an Australian case control study published in 2001. The study is considered important at least for the Australian context, but may not be applicable to the New Zealand context (see limitations below). The findings of the study were as follows:
- In both the intervention group (n=431) and usual care group (n=81) there was a dramatic initial improvement
- Consultation number: Average of three in the intervention group (one 50 minute, and two 20 minute), versus one in the usual care group
- Need for continuing care: At three months 77% of the intervention group and 56% of the usual care group required no continuing care. At 12 months they were 77% and 68%, respectively.
- Recovery (zero pain): At three months 67% of the intervention group and 49% of the usual care group had fully recovered, while at 12 months it was 71% and 56%, respectively.
- Recurrences: At three months 16% of the intervention group and 27% of the usual care group had recurrences.
- Cost: Despite more consultations in the intervention group, the overall cost was lower due to less physiotherapy, investigations, medication use, and complimentary care (AUD 276 vs 472)
- Safety and efficiency: The intervention group didn't miss any serious conditions, and didn't use any unnecessary tests.
- Patient satisfaction: 82% of the intervention group and 43% of the usual care group rated their treatment as extremely helpful.
There is one important limitation in the external validity of the study when applied to the New Zealand context. The intervention group had an average of three consultations - one initial 50 minute consultation and two 20 minute consultations. One could argue that the time requirements for evidence based care of acute low back pain are far in excess of what is available in routine general practice in New Zealand. Their study was done in Australia where the doctor can bill external stakeholders for extended consultations. This is not possible in New Zealand, where the external stakeholder funding from ACC or from capitation only covers 15 minutes. The patient has to make up the remaining difference, and so the initial 50 minute "evidence based appointment" would come with a patient co-charge of at least $200 for the initial consultation alone if the GP practice did not donate their time, plus a further $100 for the two follow up appointments, assuming the patient is not a CSC holder or in a VLCA practice. This raises significant equity issues. Whether this added patient cost, or added GP cost if their time is donated, is worthwhile for an NNT of around 5-6 I leave for the reader to decide. Using a usual care consultation time of 15 minutes (usual care time wasn't reported), an NNT of 5.5, the GP would need to consult for an extra 6.25 hours (7.5 hours vs 1.25 hours) to have one patient achieve a better outcome. In areas of GP shortage, this would limit available appointments and potentially have wider negative flow on effects.
The approach starts with Triage which refers to undertaking a history and examination in order to confirm the taxonomy, look for neurological disorders, and serious causes of pain, in which case those are pursued in their own right outside of this algorithm.
In the absence of neurological or red flags, the Management phase occurs. Here, a treatment plan is made, checked, and reinforced. Yellow flags are addressed if significant, especially if they are not recovering. Management is targeted at patient complaints rather than anything strictly biomedical: "I hurt," "I can't move," "I can't work," and "I'm scared." Not all of these areas need to be addressed in the first consultation, but can be addressed with longitudinal care.
Following management is Concern which refers to reviewing their progress and seeing if they are responding.
Vigilance occurs with all follow up consultations. It refers to staying vigilant for red flag conditions or lack of recovery. If they are not recovering then an early referral for chronic low back pain is made after two months.
Triage begins with checking that the patient does have back pain and that it is likely to be a benign condition arising from the spine, rather than another serious cause. Red flags have poor predictive value, but this is not their value, they are simply an alerting feature. It lets the doctor know to consider exploring the possibility of serious conditions further.
A pain history should be undertaken. Some authors advocate the traditional systematic approach but this has not been proven to improve diagnostic accuracy and many of the questions have unproven or non-existent validity. This approach may not be viable in primary care, especially when the patient has multiple separate issues to discuss in their 15 minute appointment, and the doctor will need to make a judgement call as to the most pertinent questions to ask while carefully safety netting.
The traditional systematic approach includes questioning around presenting complaint, length of illness, site, location and extent of spread, quality, severity, frequency, duration, time of onset, mode of onset, precipitating factors, aggravating factors, relieving factors, and associated fevers.
The presenting complaint and site are around confirming that they do indeed have back pain as opposed to loin pain or gluteal pain for example. The length of illness is around establishing if it is acute or chronic.
The location and extent of spread and quality are about distinguishing somatic referred from radicular pain. Incorrectly distinguishing radicular pain from somatic referred pain is a common pitfall in diagnosis and with incorrect diagnosis this frequently leads to incorrect treatment.
The patient should be asked where their "main" or "worst" pain is, or where they feel the pain most often and most consistently. Reciprocally they can be asked where they feel the pain only sometimes.
Patients may have a combination of somatic and referred pain from the same process e.g. a herniated disc causing somatic pain from irritation of the dura of the nerve root plus radicular pain from irritation of the nerve root itself.
|Pain quality||Dull, deep ache, or pressure-like, perhaps like an expanding pressure||Shooting, lancinating, or electric-shocks|
|Relation to back pain||Referred pain is always concurrent with back pain. If the back pain ceases then so does the referred pain. If the back pain flares then so does the leg pain intensity and spatial spread.||Not always concurrent with back pain.|
|Distribution||Anywhere in the lower limb, fixed in location, commonly in the buttock or proximal thigh. Spread of pain distal to the knee can occur when severe even to the foot, and it can skip regions such as the thigh. It can feel like an expanding pressure into the lower limb, but remains in location once established without traveling. It can wax and wane, but does so in the same location.||Entire length of lower limb, but below knee > above knee. In mild cases the pain may be restricted proximally.|
|Pattern||Felt in a wide area, with difficult to perceive boundaries, often demonstrated with an open hand rather than pointing finger. The centres in contrast can be confidently indicated.||Travels along a narrow band no more than 5-8 cm wide in a quasi-segmental fashion but not related to dermatomes (dynatomal).|
|Depth||Deep only, lacks any cutaneous quality||Deep as well as superficial|
|Neurological signs||Not characteristic||Favours radicular pain, but not required.|
|Neuroanatomical basis||Discharge of the peripheral nerve endings of Aδ and C fibres from the lower back converge onto second order neurons in the dorsal horn that also receive input from from the lower limb, and so the frontal lobe has no way of knowing where the pain came from.||Heterotopic discharge of Aδ, Aβ, and C fibres through stimulation of a dorsal root or dorsal root ganglion of a spinal nerve, typically in the presence of inflammation, with pain being felt in the peripheral innervation of the affected nerve|
The severity of back pain does not correlate with the severity of the disease process but can be recorded as a baseline VAS. The frequency and duration relates to how it waxes and wanes and how long for, and is usually related to aggravating factors rather than the disease process. They are not of diagnostic value. The time of onset is about whether they have morning stiffness. The sensitivity is moderate but specificity is poor for spondyloarthropathies.
The mode of onset is how it started such as spontaneously or with an injury. Spontaneous pain with an explosive onset is anecdotally concerning. Otherwise the circumstances of onset are not usually helpful in a diagnostic or prognostic sense. Possibly twisting injuries may be a risk for torsion injuries, but a patho-anatomical prediction can't be made. Likewise sudden axial loading may be a risk for a compression injury. Extension injuries in sportspeople may be the exception for relevance as this indicate a pars interarticularis fracture.
Precipitating factors are activities that bring on pain and aren't helpful diagnostically. Aggravating factors are activities that aggravate the pain, and the absence of any mechanical aggravating factors is of concern. Relieving factors are those that improve the pain such as medications, wheat bags, etc. Pain that isn't relieved by rest may raise concern for a serious disorder.
Associated features may be the most helpful category of enquiry in terms of identifying serious causes, and is discussed as part of the red flags section below.
Red flag conditions are rare, and so the pre-test probability is in favour of the pain being benign. Red flag conditions are suspected primarily based on the history and examination. Identifying certain conditions makes no difference to the outcome, while in other cases it does.
A red flag checklist can be used. There are case reports of red flag conditions being missed, and that they may have been identified earlier if the correct questions were asked. Red flags should be checked for at each visit (i.e. vigilance).
- History of: Trauma, sports injury, fever, night sweats, recent surgery, catheterisation, venipuncture, illicit drug use, weight loss, cancer, occupational exposure, hobby exposure, overseas travel, pain severe worsening or unremitting especially at night
- Cardiovascular: Risk factors
- Respiratory: Cough in a smoker or ex-smoker
- Gentio-urinary: Infection, haematuria, retention, stream problems
- Gynaecological: abnormal uterine bleeding, dysmenorrhoea
- Endocrine: Diabetes, corticosteroids, parathyroid
- Musculoskeletal: pain elsewhere
- Neurologic: symptoms/signs including for cauda equina compression
- Skin: Infection, rashes
- Gastrointestinal: Diarrhoea, inflammatory bowel disease
- Demographic: Aged over 50 years with first episode, especially age over 65 years
Cancer:, the pre-test probability is low at less than 0.7%. Most patients who have cancer as a cause are elderly. The single strongest predictor is a past history of cancer. Other indicators of malignancy are lack of relief with bed rest, unexplained weight loss, failure to improve with therapy, and prolonged pain. Cough in a smoker or ex-smoker is a concern for spinal metastases. Myeloma may not be evident on history. Negative predictors are age less than 50, no past history of cancer, no weight loss, and no failure to improve with therapy. With a combination of the above, cancer is extremely unlikely.
Fracture:, major trauma is a risk. Minor trauma is only a risk if it is associated with osteoporosis, older age (>50), and/or history of prolonged corticosteroid use. In sports people pars interarticularis fractures should be considered.
Infection:, symptoms are often subtle, but may include malaise and fever. The risk factors are mainly those that make the individual susceptible such as penetrating injuries, or underlying conditions. Exotic infections are more likely with occupational exposure, certain hobbies, or recent travel.
Spondyloarthropathy: The earliest signs are morning stiffness, slow onset at age less than 30, and improvement with exercise. A history of psoriasis and inflammatory bowel disease are also clues. A combination of 4 out of 5 of morning stiffness, improvement with exercise, onset under 40, slow onset, and duration > 3 months has a +LR of 6.3, and -LR of 17. Generally ankylosing spondylitis is impossible to diagnosis early in the evolution and plain films do not generally detect changes in early disease. Note, pain elsewhere is also a clue for a systemic rheumatology conditions.
Other: Hyperparathyroidism and Paget's disease are occult causes of spinal pain. There are usually no clues on history.
Cardiovascular risk factors alert for possible aortic aneurysm.
Neurological features should be assessed along with any spinal pain, along with symptoms of cauda equina compression.
History of a urinary tract infection, haematuria, and urinary retention should lead to assessment of the renal tract.
The aim of the psychological and social history is to identify so called "yellow flags." Psychosocial factors correlate only weakly with pain, but correlate strongly with disability. Psychological factors account for 30% of the variance between patients that become chronic pain sufferers and those who don't. The factors accounting for the remaining variance is undetermined, as biomedical factors don't account for the remaining variance either.
Fear Avoidance Behaviour
One important psychological feature amongst yellow flags is fear-avoidance behaviour. Fearful patients are scared of underlying serious conditions, scared of making it worse, scared of the prognosis, and therefore avoid movement and activity. This is an unhelpful cognitive pattern that leads to worsening disability. A 2011 review found mixed evidence for incorporating fear avoidance belief reducing information into clinical practice, but noted that most trials documented positive outcomes.
Catastrophising is another poor prognostic psychological feature, often linked to fear-avoidance, and is defined as "an exaggerated negative mental set brought to bear during actual or anticipated pain experience." It is associated with greater distress, lower mood, greater disability, and a worse prognosis. Anxiety and depression are other important negative prognostic factors
There are three categories of patients with regards to fear-avoidance beliefs. Most patients are probably misinformed avoiders.
|Element||Misinformed avoiders||Learned pain avoiders||Affective avoiders|
|Emotions||Discouraged||Discouraged||Fearful and highly distressed|
|Beliefs||Pain indicates harm, and the spine is vulnerable||Pain is benign; spine is sound; but pain should be avoided||Distorted significance of pain and concerns about conditions of the spine|
|Basis of beliefs||Past experiences with back pain. Information from multiple sources||Inherent value of pain versus function||Emotionally charged misinterpretation of past experiences and distortion of medical information with magnifying of precautions given.|
|Behaviours||Hypervigilant but usually willing to perform painful activities in a limited way||Choose to stop activities when they are painful||Profound pain inhibition for movements. Will not attempt activities that might induce pain|
|Disability||Mild to moderate||Mild to moderate||Severe and committed to their disabilities.|
|Comorbidities||Uncommon||Uncommon||Catastrophizing, pain hypervigilance, anxiety, depression, concurrent musculoskeletal complaints|
|Treatment||Their beliefs encompass ongoing reasoning and so are amenable to change with new information and experiences (exercise) that challenge beliefs about the importance of pain and restore confidence in the spine.||Unknown. Their disability is based on learned pain avoidance. Exercises that desensitize the pain response to physical stimuli might be considered.||Address dysfunctional cognitions and catastrophic thinking. Disconfirm fears through gradual exposure to feared activities|
It is thought that yellow flags should be identified early in the patients course of low back pain. They are yellow not red because they don't need as urgent recognition. Patients and generally stratified according to their risk of poor outcome in order to provide targeted care. There is no consistent strong evidence that identifying and intervening on psychosocial risk factors early, however it has "conceptual validity," low cost, and so it is recommended to do so.
The STarT Back study (Subgroups for Targeted Treatment) showed that that early detection of psychosocial factors can improve outcomes. It has been validated as a predictive tool, and has also been evaluated in an RCT which showed overall higher adjusted mean changes in Roland Morris Disability Questionnaire scores in the intervention group compared to the control usual care group at 4 months (4.7 vs 3.0, effect size 0.32), and at 12 months (4.3 vs 3.3, effect size 0.19)
STarT Back is a stratified care approach developed in the UK has been shown to improve outcomes including quicker return to work. The findings haven't been reproduced in other health systems like New Zealand. A trial using an adapted STarT Back approach in the United States did not show an improvement in patient outcomes.
STarT have an online training module. The approach includes a nine-item questionnaire that assesses primarily for psychosocial risk factors such as fear avoidance and catastrophising. The original 9-item tool is able to predict persistent disabling and bothersome low back pain at 6 months with a sensitivity of 85%, specificity of 81%, and positive likelihood ratio of 4.5. A modified 6-item tool has a sensitivity of 89%, and specificity of 84%, and positive likelihood ratio of 5.5.
|1||My back pain has spread down my leg(s) at some time in the last 2 weeks|
|2||I have had pain in the shoulder or neck at some time in the last 2 weeks|
|3||I have only walked short distances because of my back pain|
|4||In the last 2 weeks, I have dressed more slowly than usual because of back pain|
|5||It’s not really safe for a person with a condition like mine to be physically active|
|6||Worrying thoughts have been going through my mind a lot of the time|
|7||I feel that my back pain is terrible and it’s never going to get any better|
|8||In general I have not enjoyed all the things I used to enjoy|
|9||Overall, how bothersome has your back pain been in the last 2 weeks?|
|Scoring 9-item questionnaire: Total score 3 or less = Low risk|
Total score 4 or more -> sub score Q5-9 is 3 or less = medium risk; 4 or more = high risk
|Scoring 6-item (Q2, 5, and 6 removed): Total score 2 or less = Low risk|
Total score 3 or more = not at low risk
With the original 9-item questionnaire, the patient is classified as having low, medium, or high risk of poor outcome according to the score in the questionnaire.
- Low risk patients are given advice, reassurance, education, pain medication if required, their concerns are addressed, and they are booked for a review if necessary.
- Medium risk patients receive the same key messages and a short course of routine physiotherapy (or osteopathy or chiropractic) with clear functionally based treatment goals. Deterioration results in referral back to the GP, and if they don't respond after four weeks or don't meet their goals after three months then they are referred for specialist opinion or pain services.
- High risk patients receive the same key messages, conventional physiotherapy if indicated, plus psychologically informed physiotherapy. Psychologically informed physiotherapy includes CBT, addressing unhelpful beliefs, promoting self-management, building confidence and self-efficacy, grading and pacing, physical activity, and facilitating return to usual activities.
The FREE study was a pragmatic cluster-randomised controlled trial in General Practices in New Zealand. Eight general practices were randomly assigned to intervention practices (34 GPs in 4 practices), and control practices (29 GPs) in 3 practices. The Intervention GPs were trained in the FREE approach which prioritises early identification and management of barriers to recovery. 88% of patients had pain of less than 6 weeks duration. At 6 months there was no difference in the primary outcome of adjusted mean RMDQ.
The full list of typical yellow flags is shown below.
|Belief that all pain must be abolished before attempting to return to work or normal activity||Passive attitude to rehabilitation|
|Expecting increased pain with activity or work||Use of extended rest|
|Belief that work is harmful||Reduced activity with significant withdrawal from activities of daily living|
|Poor work history||Avoidance of normal activity|
|Unsupportive work environment||Increased alcohol consumption or other unhelpful substances since pain onset|
|Belief that pain is harmful, resulting in fear-avoidance behaviour||Depression|
|Catastrophising||Feeling useless and not needed|
|Misinterpreting bodily symptoms||Irritability|
|Belief that pain is uncontrollable||Anxiety about heightened bodily sensations|
|Poor compliance with exercise||Reduced interest in socialising|
|Expectation of a passive "heroic" medical intervention that will completely cure their pain||Over-protective or conversely socially punitive partner|
|Low educational background||Lack of social support|
- Main article: Lumbar Spine Examination
The physical examination of the lumbar spine in general lacks reliability and validity. In short, it does not provide a diagnosis of acute low back pain. However, there are three main reason for doing a physical examination.
- The first reason is that patients expect it, and doing it shows interest and caring.
- The second reason is that if no signs of somatic dysfunction are found in the spine, then this could indicate a serious underlying visceral or vascular condition. However, due to visceral referred pain, patients with visceral pathology can still have somatic segmental dysfunction. Therefore an abdominal and vascular examination is still warranted in those at increased risk.
- The third reason is that the doctor can provide positive reinforcement (e.g. celebrating normal findings) with the view of reducing patient fear.
The lumbar spine exam involves inspection, palpation, and movement testing.
- Inspection: posture standing and sitting (scoliosis, kyphosis, loss of lordosis), dynamic posture (antalgic gait), deformities, scars, puncture marks, swelling. The reliability reported in studies has varied. The validity is unknown.
- Palpation: altered sensitivity (hypoesthesia, hyperesthesia), tenderness and its relationship to bony landmarks, and whether localised or diffuse. The reliability is excellent for tenderness somewhere in the lumbar spine (kappa 1.0), but when the location is specified the agreement is variable. Tenderness over the iliac crest superomedial to the PSIS is good (kappa 0.66), but the validity is unknown.
- Movement testing: active, passive, and accessory movement testing. Active and passive ranges are tested in flexion and extension, side bending, and rotation. Quadrant tested can also be done (e.g. extension with rotation). The reliability is fair to moderate, but the validity is unknown.
There are a variety of other tests. For the McKenzie assessment, the reliability is variable depending on the study, and the validity in acute low back pain is unknown, and only modest predictive value in chronic low back pain. Tests of the sacroiliac joint are reliable but their validity in acute low back pain is unknown. In chronic low back pain they have moderate validity.
A neurological examination is not required in the absence of neurological symptoms. If a patient has weakness, numbness, or radicular pain then certainly it is warranted, however the indication is the neurological symptoms, not the back pain. Neurological signs don't present with back pain as the only symptom.
A neurological examination can however be done with the goal of "appearing thorough." In that case a screening examination is sufficient. The L5 and S1 myotomes can be assessed quickly by having the patient walk on their heels and toes. Sensation can be assessed quickly with light touch. The reliability is good (kappa > 0.6). Reflex testing isn't needed in the absence of neurological symptoms but can be useful for positive reinforcement to the patient.
An abdominal examination and vascular examination are important for assessing for visceral (e.g. masses) and vascular (abdominal aortic aneurysm) disorders.
The demeanor of the patient can be helpful in identifying serious causes. Some patients with conditions like discitis or cancer can just "look unwell," with a serious and quietly guarded presentation. The aphorism is beware the quiet patient with severe pain.
It is important to explain what you are doing during the examination, i.e. what is being done and what is found. Give the patient positive feedback when positive findings are found. For example when testing the reflexes explain that a good reflex means that there is no blockage of signal. If they move well tell them. If their back muscles seem strong again tell them that their back seems strong and that their muscles are in good shape.
If a red flag condition is suspected then appropriate investigations should be done. Such investigations are not recommended as part of the routine assessment of low back pain, as they are not designed to investigate the cause of back pain. They also aren't screening tests in the absence of concern.
|Category||Clinical Features||Specific conditions||Investigations|
|Simple low back pain||No risk factors||N/A||Nil. Reassess after 4 to 6 weeks if no improvement|
|Primary tumours (rare, 0.04% of all tumours)||myeloma||Myeloma screen|
|bone and cartilage tumours||Imaging|
|Secondary tumours (0.7%)||History of cancer, age greater than 50, failure to improve, weight loss, pain not relieved by rest||Prostate||Calcium, ALP, PSA, ESR and/or CRP, imaging|
|Breast, lung, thyroid, kidney, gastrointestinal, melanoma||Plain radiography, ESR and/or CRP. If radiograph normal but elevated markers then MRI.|
|Infection||fever, sweating, immunosupression, dialysis, IVDU, invasive procedure, trauma to skin or mucous membrane, diabetes, alcoholism||Osteomyelitis, epidural abscess||MRI if moderate to high risk. ESR and/or CRP if low risk, with MRI if elevated.|
|Fracture||Significant trauma||Vertebral compression fracture||Plain radiograph|
|Mild trauma in the elderly or history or risk factors for osteoporosis, elderly||Vertebral compression fracture||Plain radiograph|
|Sporting activity involving extension, rotation, or both.||Stress fracture||Bone scan or MRI|
|Spondyloarthropathy (0.3 - 0.9%)||Ankylosing spondylitis||ESR and/or CRP|
|Metabolic bone disease||Paget's disease, Hyperparathyroidism||Calcium|
|Visceral disease||Smoking, hypertension, palpable mass||Aortic aneurysm||Abdominal exam, ultrasound (e.g. bedside)|
|Retroperitoneal disease||Abdominal exam, ultrasound (e.g. bedside)|
|Pelvic disease||Pelvic examination, rectal examination|
|Modified from Bogduk et al. Management of Acute and Chronic Low Back Pain. Elsevier 2002.|
- Main article: Lumbar Spine Radiographs
Deyo and Diehl validated criteria for lumbar spine radiographs when screening for red flag conditions. However using these criteria can lead to an increased rate of radiograph utilisation. Some of their criteria like over 50 and seeking compensation criteria can generally be relaxed. It may be better to use one's own intuitive protocol. Bogduk, using findings from other studies like from Reinus et al, re-cast their criteria as follows:
- History of cancer
- Significant trauma
- Weight loss
- Temperature > 37.8
- Risk factors for infection
- Neurological deficit
- Minor trauma in patients
- Over the age of 50 years, or
- Known to have osteoporosis, or
- Taking corticosteroids
- No improvement over one month
In other cases plain radiographs are not indicated as a routine investigation for acute low back pain. Patients often have misconceptions about the diagnostic validity and need for lumbar spine radiographs. They may incorrectly think that radiographs will show the problem, that a normal radiograph excludes serious problems, and that they are completely safe. Careful communication is required around these misconceptions.
A controlled study found that five minutes of careful communication moderately reduced misconceptions around radiographs but there were no differences in patient satisfaction. Also one study has shown no difference to outcome with early radiography, while another found worse outcomes at 3 months.
- See also: Lumbar Spine MRI
CT imaging is not indicated as a screening tool in low back pain. Likewise MRI is not justified in the investigation of acute low back pain, even as a screen for red flag conditions. This is in contrast to chronic low back pain where it does have some validity as a screening test and can provide an imperfect aid in identifying the source of pain.
A randomised study comparing early MRI or CT versus delayed imaging until clinical need found no different in outcome. However a study done in Auckland, New Zealand found evidence that the public criteria for MRI is too strict, and should possibly be loosened. They found that 1 in every 6.5 patients had serious pathology on MRI, which is exceptionally high for international standards.
See Lemmers et al for a systematic review on the costs, healthcare utilisation, and absence from work associated with spinal imaging.
Bone scanning is not commonly done in acute low back pain in New Zealand. It has typically been studied as a modality for detecting acute pars fractures, but they are an imperfect tool with a high false negative rate, and a very low yield of positive scans. If a scan is positive a radiograph should be performed to detect a fracture, if there is no fracture then rest should be advised to avoid progression to fracture. If the bone scan and radiograph are both positive then the fracture may be recent but it isn't guaranteed to be the source of pain, however it may still be possible for bony healing to occur.
- See also: Good Back Consultation
Cardinal to management is good communication. A narrative should be spun that provides reassurance, and explanation for their pain, and encouragement to continue physical activity. They should be supported to take responsibility for their own rehabilitation. Good management does not necessitate routine referral to allied health practitioners; this is rather reserved for those with risk factors for chronicity in which case a psychologically informed allied health practitioner is preferred.
The Bogdukian algorithm for the assessment and management of acute low back pain was found to be successful in improving long term outcomes in a case control study by McGuirk et al. In this algorithm, management refers to targeting specific domains amongst patient complaints: "I hurt," "I can't move," "I can't work," and "I'm scared." Not all of these domains need to be addressed in the first consultation, but can be addressed with longitudinal care. However at the initial consultation it is best to flag all relevant domains, and try to improve at least one.
Explanation and Information
Effective patient education involves an explanation for their pain (what they have and what they don't have), information about their prognosis, as well as reassurance.
The explanation should be biologically based but not necessarily "valid" from an academic standpoint. For example they can be told they have a small disc injury that is inflamed and sore but that the odds are in their favour and that they have every chance of recovering even regardless of treatment. There should also be an explanation about how the chances of a serious cause are extremely low, and even lower because of the lack of red flags.
There are 8 Cs of what a good explanation should involve that maximises outcomes and avoids the nocebo effect.
- Calm: it should be unpanicked less their fears are reinforced
- Clear: it should be understandable
- Credible: it should fit their circumstances
- Confident: it should be delivered with conviction, as uncertainty can lead to worsening fear
- Convincing: the response of the patient to the explanation should be monitored, and any uncertainties should be addressed
- Concerted: the doctor should make an effort
- Cares: the doctor should care about the problem
- Concern: the doctor should take the patient seriously
If the patient asks about imaging an explanation is given about why it isn't indicated. This explanation should cover how it doesn't show up pain, it can create a false sense of security if negative, it can show up a completely irrelevant but disconcerting finding, and radiographs expose them to radiation. The patient can be asked why they want an x-ray, what they think it will show, and what they know about x-rays. Be conciliatory if required advising that if investigations can be considered if they don't recover.
Information goes hand in hand with explanation. It refers to informing the patient that they have every chance of making a good recovery, and that some 80% can be expected to fully recover if they are managed well, but that it may take time. During recovery there are certain things that can be done to ease the recovery (e.g. analgesia, stretches, manual therapy etc).
There is no medication with proven efficacy over placebo for acute low back pain. There are also no agents that are completely safe. The various side effects are discussed in the articles of the relevant pharmaceuticals.
Simple analgesics: Paracetamol is no more effective than placebo. NSAIDs are statistically more effective than placebo in reducing pain and disability but the magnitude of the effect is clinically insignificant, and six patients need to be treated for one to achieve a short term clinically significant benefit. Furthermore, the combination of ibuprofen plus paracetamol is not superior to ibuprofen alone.
Muscle relaxants: Diazepam is no better than placebo when added to naproxen. There is very low quality evidence that the use of non-benzodiazepine muscle relaxants results in a small reduction in pain but not disability with their use. Most of these are not available in New Zealand, including none of the ones that are possibly more effective (cyclobenzaprine, methocarbamol, carisoprodol, and tizanidine). Only orphenadrine is available: this was compared to naproxen, and there was no difference. There is another old study of poor methodology comparing orphenadrine vs placebo that found 9/20 had reduced pain with orphenadrine versus 4/20 with placebo.
Other oral agents: Most studies on opioids focus on chronic pain where there is no benefit over simple analgesics. One study in acute low back pain found no difference between naproxen versus naproxen plus oxycodone/paracetamol. There are no studies evaluating tramadol for acute low back pain, but it has unclear effects in chronic low back pain. Oral corticosteroids as well have not been shown to be effective.
Heat: Heat wrap therapy has been evaluated by several trials and there is moderate quality evidence that they provide a small short term reduction in pain and disability compared to placebo. One interesting trial found that they were more effective than ibuprofen and paracetamol.
Allied health interventions: Physical therapies have been shown to have no effect or only a small clinically insignificant effect over sham treatments. The evidence for exercise therapy is unclear. Manipulative therapy is not more effective than other treatments. Acupuncture results have been inconsistent but positive results when reported have been clinically insignificant for pain, while there appears to be no effect on function. Massage therapy may have small short term benefits.
Miscellaneous ineffective interventions: There are many other interventions that either lack evidence of efficacy or have been shown to be effective should not be recommended as part of evidence based management. They include: cold, traction, therapeutic ultrasound, low-level laser, bed rest, lumbar supports, TENS, and back school.
Movement and Activation
Patients may have impaired movement due to it causing pain aggravation, or it may be due to an underlying attitude. Firstly an explanation for the impaired movement is provided. The patient can be told that the muscles have tightened in response to pain, which then adds to the pain.
Linking in to treatment, the patient is then informed that the aim is therefore to reduce tightness. Again whether this is biologically valid is besides the point, it provides a narrative for for encouraging activity. The patient is encouraged to:
Engage in simple stretches: The patient is empowered to treat themselves and achieve mobility and use them as needed for first-aid, as a warmup before activities, and during planned times in the day. Stretching isn't aimed at improving pain but at encouraging movement. The stretches should ideally be able to be done at any location such as simple erector spinae stretches. An example are the exercises used by Indahl (login required to access)
Resume normal activities: this can be using graded exposure principles if required. The baseline and reasonable goals are established, and achievement is celebrated. The goals are set by the patient, and may include walking or other activities. Explain that returning to activity sooner is proven to aid in recovery, and that rest is not recommended.
Ask the patient what they mean by "I can't work". They may be fearful of being injured, have an unsupportive employer, or dislike work. Explore whether work actually does aggravate the pain or is it simply their expectation that it will. Discuss whether their fears are rational and realistic. Provide the facts: that those who stay away from work have a greater chance of never returning, and that those who return have every chance of remaining at work.
Assess whether there are any impediments to returning to work. If there are none other than fear, then provide encouragement. Follow up with them, monitor their progress, and reinforce the message as needed rather than dismissing them after telling them to get back to work.
Overall, postponing return to work doesn't tend make it any easier to return. One cohort study found that keeping patients at work, with modified duties if needed, resulted in better outcomes than usual care. Sometimes there may be some changes that need to be recommended to the employer to allow return to work. Modified duties are preferred over "light duties" the difference being that light duties may be different and usually more menial in nature. Any restrictions should be progressively reduced over time with improvement in their condition, and the patient should have close monitoring.
At other times a workplace assessment is needed. Workplace intervention either on its own or when added to clinical intervention has been shown to improve outcomes in an RCT. The specific ergonomic interventions are not what is most important, what is important is that the patient has an advocate that works to solve problems, and the patient feels that "something is being done" which can reduce fear and dissatisfaction with their workplace. GPs do not have the time to do such an assessment but if the patient has an ACC claim then they can ask for ACC to instigate this, or they can refer to an occupational physician.
Patient beliefs, fears, and catastrophising are what is associated with disability rather than pain. Therefore beliefs and fears should be addressed. Ask the patient what their ideas are about their problem, their concerns, expectations, and plan. Any unhelpful beliefs should be corrected. The patient should be reassured cognitively rather than emotionally, as emotional reassurance wears off more quickly. Provide solutions to simple ergonomic problems, and suggest more productive ways of coping.
If they have had imaging for some reason and they are worried about "degenerative changes" explain that this is a normal part of aging and has no correlation with pain. Reassure that spondylosis is simply the body doing a good job at compensation by increasing the surface area to distribute load.
Give the patients a "first-aid" plan to pain exacerbations such as analgesia, stretches, and heat or ice packs. Advise them to warm up before engaging in potentially painful activities. Encourage them to be the master of their own destiny.
A routine follow up visit should be scheduled. In the study by McGuirk the superior intervention group averaged one initial and three subsequent consultations, lasting 50 minutes, and 20 minutes each, respectively. The usual care group averaged one consultation without any follow ups.
In what Bogduk calls the "Concern" part of the management algorithm their progress is assessed. If left up to the patient to decide, many do not return, continue to languish, or go somewhere else. They may feel that there is no point of returning if the initial treatment was unsuccessful.
As GP care is not fully subsidised the follow up visit may be a financial barrier, notwithstanding the time off work. Therefore if they have recovered they can be advised to call to cancel their appointment. If the appointment is cancelled it is best to call to confirm that they have recovered.
At follow up visits the patient their recovery progress is assessed. If they haven't recovered them their understanding of the previous recommendations is checked. Compliance is checked, and recommendations are reinforced.
Pain diaries are not recommended as they encourage patients to focus on the pain potentially hindering recovery.
Also at each follow up visit, what Bogduk calls "Vigilance" is displayed. Vigilance towards red flag conditions is needed as some patients may present early in their serious condition without displaying any concerning symptoms at the initial visit.
Yellow flags become increasingly important at each follow up visit. In the presence of significant yellow flags, consider referring them to a psychologically informed physiotherapy program or similar. Such intervention is only warranted at the subacute phase of their low back pain.
For those patients where it appears likely that they will convert to chronic low back pain (as they are statistically destined to do in spite of best medical care), it is often wise to plan early for referral under the category of chronic low back pain. This is due to the wait lists involved with more specialist care, investigations, or interventions. Bogduk suggests considering this after two months.
- ↑ 1.0 1.1 1.2 1.3 Wade King and Nikolai Bogduk. Acute Low Back Pain. Bonica's Management of Pain. 2018
- ↑ Bogduk et al. Medical Management of Acute and Chronic Low Back Pain. Chapter 3. Elsevier 2002.
- ↑ Itz CJ, Geurts JW, van Kleef M, Nelemans P. Clinical Course of Non-Specific Low Back Pain: A Systematic Review of Prospective Cohort Studies Set in Primary Care. Eur J Pain. 2013;17(1):5-15. doi: 10.1002/j.1532-2149.2012.00170.x.
- ↑ Machado GC, et al. Can Recurrence After an Acute Episode of Low Back Pain Be Predicted? Phys Ther. 2017 Sep 1;97(9):889-895. doi: 10.1093/ptj/pzx067. PMID: 28969347
- ↑ National Health Committee. Low Back Pain: A Pathway to Prioritisation. 2015. Full Text
- ↑ 6.0 6.1 6.2 Bogduk. Algorithm for acute low back pain In: Medical Management of Acute and Chronic Low Back Pain. Elsevier 2002.
- ↑ 7.0 7.1 Indahl A, Velund L, Reikeraas O. Good prognosis for low back pain when left untampered. A randomized clinical trial. Spine (Phila Pa 1976). 1995 Feb 15;20(4):473-7. doi: 10.1097/00007632-199502001-00011. PMID: 7747232.
- ↑ 8.0 8.1 McGuirk B, King W, Govind J, Lowry J, Bogduk N. Safety, efficacy, and cost effectiveness of evidence-based guidelines for the management of acute low back pain in primary care. Spine (Phila Pa 1976). 2001 Dec 1;26(23):2615-22. doi: 10.1097/00007632-200112010-00017. PMID: 11725244.
- ↑ Bogduk et al. Management of Acute and Chronic Low Back Pain. Chapter 5. Elsevier 2002
- ↑ Bogduk et al. Medical Management of Acute and Chronic Low Back Pain: An Evidence Based Approach. Elsevier Science. 2002
- ↑ 11.0 11.1 Bogduk et al. Chapter 10 Psychosocial Assessment In: Medical Management of Acute and Chronic Low Back Pain. Elsevier 2002
- ↑ 12.0 12.1 12.2 Rainville J, Smeets RJ, Bendix T, Tveito TH, Poiraudeau S, Indahl AJ. Fear-avoidance beliefs and pain avoidance in low back pain--translating research into clinical practice. Spine J. 2011 Sep;11(9):895-903. doi: 10.1016/j.spinee.2011.08.006. Epub 2011 Sep 9. PMID: 21907633.
- ↑ Sowden G, Hill JC, Konstantinou K, Khanna M, Main CJ, Salmon P, Somerville S, Wathall S, Foster NE; IMPaCT Back study team. Targeted treatment in primary care for low back pain: the treatment system and clinical training programmes used in the IMPaCT Back study (ISRCTN 55174281). Fam Pract. 2012 Feb;29(1):50-62. doi: 10.1093/fampra/cmr037. Epub 2011 Jun 27. PMID: 21708984; PMCID: PMC3261797.
- ↑ Hill JC, Whitehurst DG, Lewis M, Bryan S, Dunn KM, Foster NE, Konstantinou K, Main CJ, Mason E, Somerville S, Sowden G, Vohora K, Hay EM. Comparison of stratified primary care management for low back pain with current best practice (STarT Back): a randomised controlled trial. Lancet. 2011 Oct 29;378(9802):1560-71. doi: 10.1016/S0140-6736(11)60937-9. Epub 2011 Sep 28. PMID: 21963002; PMCID: PMC3208163.
- ↑ Cherkin D, Balderson B, Wellman R, Hsu C, Sherman KJ, Evers SC, Hawkes R, Cook A, Levine MD, Piekara D, Rock P, Estlin KT, Brewer G, Jensen M, LaPorte AM, Yeoman J, Sowden G, Hill JC, Foster NE. Effect of Low Back Pain Risk-Stratification Strategy on Patient Outcomes and Care Processes: the MATCH Randomized Trial in Primary Care. J Gen Intern Med. 2018 Aug;33(8):1324-1336. doi: 10.1007/s11606-018-4468-9. Epub 2018 May 22. PMID: 29790073; PMCID: PMC6082187.
- ↑ Darlow B, Stanley J, Dean S, Abbott JH, Garrett S, Wilson R, Mathieson F, Dowell A. The Fear Reduction Exercised Early (FREE) approach to management of low back pain in general practice: A pragmatic cluster-randomised controlled trial. PLoS Med. 2019 Sep 9;16(9):e1002897. doi: 10.1371/journal.pmed.1002897. PMID: 31498799; PMCID: PMC6733445.
- ↑ Bogduk et al. Management of Acute and Chronic Low Back Pain. Chapter 7. Elsevier 2002.
- ↑ 18.0 18.1 Waddell G, Main CJ, Morris EW, Venner RM, Rae PS, Sharmy SH, Galloway H. Normality and reliability in the clinical assessment of backache. Br Med J (Clin Res Ed). 1982 May 22;284(6328):1519-23. doi: 10.1136/bmj.284.6328.1519. PMID: 6211214; PMCID: PMC1498438.
- ↑ Njoo KH, van der Does E, Stam HJ. Interobserver agreement on iliac crest pain syndrome in general practice. J Rheumatol. 1995 Aug;22(8):1532-5. PMID: 7473479.
- ↑ McCombe PF, Fairbank JC, Cockersole BC, Pynsent PB. 1989 Volvo Award in clinical sciences. Reproducibility of physical signs in low-back pain. Spine (Phila Pa 1976). 1989 Sep;14(9):908-18. doi: 10.1097/00007632-198909000-00002. PMID: 2528822.
- ↑ Deyo RA, Diehl AK. Lumbar spine films in primary care: current use and effects of selective ordering criteria. J Gen Intern Med. 1986 Jan-Feb;1(1):20-5. doi: 10.1007/BF02596320. PMID: 2945915.
- ↑ Reinus WR, Strome G, Zwemer FL Jr. Use of lumbosacral spine radiographs in a level II emergency department. AJR Am J Roentgenol. 1998 Feb;170(2):443-7. doi: 10.2214/ajr.170.2.9456961. PMID: 9456961.
- ↑ 23.0 23.1 23.2 Bogduk et al. Management of Acute and Chronic Low Back Pain. Chapter 8 Imaging. Elsevier 2002
- ↑ Deyo RA, Diehl AK, Rosenthal M. Reducing roentgenography use. Can patient expectations be altered? Arch Intern Med. 1987 Jan;147(1):141-5. doi: 10.1001/archinte.147.1.141. PMID: 2948466.
- ↑ Kendrick D, Fielding K, Bentley E, Kerslake R, Miller P, Pringle M. Radiography of the lumbar spine in primary care patients with low back pain: randomised controlled trial. BMJ. 2001 Feb 17;322(7283):400-5. doi: 10.1136/bmj.322.7283.400. PMID: 11179160; PMCID: PMC26570.
- ↑ Ferriman A. Early x ray for low back pain confers little benefit. BMJ. 2000 Dec 16;321(7275):1489. PMID: 11118171; PMCID: PMC1119214.
- ↑ Gilbert FJ, Grant AM, Gillan MG, Vale LD, Campbell MK, Scott NW, Knight DJ, Wardlaw D; Scottish Back Trial Group. Low back pain: influence of early MR imaging or CT on treatment and outcome--multicenter randomized trial. Radiology. 2004 May;231(2):343-51. doi: 10.1148/radiol.2312030886. Epub 2004 Mar 18. PMID: 15031430.
- ↑ Street KJ, White SG, Vandal AC. Clinical prevalence and population incidence of serious pathologies among patients undergoing magnetic resonance imaging for low back pain. Spine J. 2020 Jan;20(1):101-111. doi: 10.1016/j.spinee.2019.09.002. Epub 2019 Sep 10. PMID: 31518682.
- ↑ Lemmers GPG, van Lankveld W, Westert GP, van der Wees PJ, Staal JB. Imaging versus no imaging for low back pain: a systematic review, measuring costs, healthcare utilization and absence from work. Eur Spine J. 2019 May;28(5):937-950. doi: 10.1007/s00586-019-05918-1. Epub 2019 Feb 22. PMID: 30796513.
- ↑ McGuirk B, King W, Govind J, Lowry J, Bogduk N. Safety, efficacy, and cost effectiveness of evidence-based guidelines for the management of acute low back pain in primary care. Spine (Phila Pa 1976). 2001 Dec 1;26(23):2615-22. doi: 10.1097/00007632-200112010-00017. PMID: 11725244.
- ↑ Saragiotto BT, Machado GC, Ferreira ML, Pinheiro MB, Abdel Shaheed C, Maher CG. Paracetamol for low back pain. Cochrane Database Syst Rev. 2016 Jun 7;2016(6):CD012230. doi: 10.1002/14651858.CD012230. PMID: 27271789; PMCID: PMC6353046.
- ↑ Machado GC, Maher CG, Ferreira PH, Day RO, Pinheiro MB, Ferreira ML. Non-steroidal anti-inflammatory drugs for spinal pain: a systematic review and meta-analysis. Ann Rheum Dis. 2017 Jul;76(7):1269-1278. doi: 10.1136/annrheumdis-2016-210597. Epub 2017 Feb 2. PMID: 28153830.
- ↑ Friedman BW, Irizarry E, Chertoff A, Feliciano C, Solorzano C, Zias E, Gallagher EJ. Ibuprofen Plus Acetaminophen Versus Ibuprofen Alone for Acute Low Back Pain: An Emergency Department-based Randomized Study. Acad Emerg Med. 2020 Mar;27(3):229-235. doi: 10.1111/acem.13898. Epub 2020 Jan 7. PMID: 31811673.
- ↑ Friedman BW, Irizarry E, Solorzano C, Khankel N, Zapata J, Zias E, Gallagher EJ. Diazepam Is No Better Than Placebo When Added to Naproxen for Acute Low Back Pain. Ann Emerg Med. 2017 Aug;70(2):169-176.e1. doi: 10.1016/j.annemergmed.2016.10.002. Epub 2017 Feb 7. PMID: 28187918; PMCID: PMC5517351.
- ↑ Cashin AG, Folly T, Bagg MK, Wewege MA, Jones MD, Ferraro MC, Leake HB, Rizzo RRN, Schabrun SM, Gustin SM, Day R, Williams CM, McAuley JH. Efficacy, acceptability, and safety of muscle relaxants for adults with non-specific low back pain: systematic review and meta-analysis. BMJ. 2021 Jul 7;374:n1446. doi: 10.1136/bmj.n1446. PMID: 34233900; PMCID: PMC8262447.
- ↑ Friedman BW, Cisewski D, Irizarry E, Davitt M, Solorzano C, Nassery A, Pearlman S, White D, Gallagher EJ. A Randomized, Double-Blind, Placebo-Controlled Trial of Naproxen With or Without Orphenadrine or Methocarbamol for Acute Low Back Pain. Ann Emerg Med. 2018 Mar;71(3):348-356.e5. doi: 10.1016/j.annemergmed.2017.09.031. Epub 2017 Oct 28. PMID: 29089169; PMCID: PMC5820149.
- ↑ Gold RH. Orphenadrine citrate: sedative or muscle relaxant? Clin Ther 1978;1:451-3.
- ↑ Krebs EE, Gravely A, Nugent S, Jensen AC, DeRonne B, Goldsmith ES, Kroenke K, Bair MJ, Noorbaloochi S. Effect of Opioid vs Nonopioid Medications on Pain-Related Function in Patients With Chronic Back Pain or Hip or Knee Osteoarthritis Pain: The SPACE Randomized Clinical Trial. JAMA. 2018 Mar 6;319(9):872-882. doi: 10.1001/jama.2018.0899. PMID: 29509867; PMCID: PMC5885909.
- ↑ Friedman BW, Dym AA, Davitt M, Holden L, Solorzano C, Esses D, Bijur PE, Gallagher EJ. Naproxen With Cyclobenzaprine, Oxycodone/Acetaminophen, or Placebo for Treating Acute Low Back Pain: A Randomized Clinical Trial. JAMA. 2015 Oct 20;314(15):1572-80. doi: 10.1001/jama.2015.13043. PMID: 26501533
- ↑ Chen S, Argáez C. Tramadol for the Management of Pain in Adult Patients: A Review of Clinical Effectiveness — An Update [Internet]. Ottawa (ON): Canadian Agency for Drugs and Technologies in Health; 2018 Nov 16. Available from: https://www.ncbi.nlm.nih.gov/books/NBK538277/
- ↑ Chou R, Deyo R, Friedly J, Skelly A, Weimer M, Fu R, Dana T, Kraegel P, Griffin J, Grusing S. Systemic Pharmacologic Therapies for Low Back Pain: A Systematic Review for an American College of Physicians Clinical Practice Guideline. Ann Intern Med. 2017 Apr 4;166(7):480-492. doi: 10.7326/M16-2458. Epub 2017 Feb 14. PMID: 28192790.
- ↑ French SD, Cameron M, Walker BF, Reggars JW, Esterman AJ. A Cochrane review of superficial heat or cold for low back pain. Spine (Phila Pa 1976). 2006 Apr 20;31(9):998-1006. doi: 10.1097/01.brs.0000214881.10814.64. PMID: 16641776.
- ↑ Nadler SF, Steiner DJ, Erasala GN, Hengehold DA, Hinkle RT, Beth Goodale M, Abeln SB, Weingand KW. Continuous low-level heat wrap therapy provides more efficacy than Ibuprofen and acetaminophen for acute low back pain. Spine (Phila Pa 1976). 2002 May 15;27(10):1012-7. doi: 10.1097/00007632-200205150-00003. PMID: 12004166.
- ↑ Chou R, Deyo R, Friedly J, Skelly A, Hashimoto R, Weimer M, Fu R, Dana T, Kraegel P, Griffin J, Grusing S, Brodt ED. Nonpharmacologic Therapies for Low Back Pain: A Systematic Review for an American College of Physicians Clinical Practice Guideline. Ann Intern Med. 2017 Apr 4;166(7):493-505. doi: 10.7326/M16-2459. Epub 2017 Feb 14. PMID: 28192793.
- ↑ McGuirk B, Bogduk N. Evidence-based care for low back pain in workers eligible for compensation. Occup Med (Lond). 2007 Jan;57(1):36-42. doi: 10.1093/occmed/kql102. Epub 2006 Oct 17. PMID: 17046988
- ↑ Loisel P, Abenhaim L, Durand P, Esdaile JM, Suissa S, Gosselin L, Simard R, Turcotte J, Lemaire J. A population-based, randomized clinical trial on back pain management. Spine (Phila Pa 1976). 1997 Dec 15;22(24):2911-8. doi: 10.1097/00007632-199712150-00014. PMID: 9431627.
- ↑ Ferrari, Robert. “Effect of a pain diary use on recovery from acute low back (lumbar) sprain.” Rheumatology international vol. 35,1 (2015): 55-9. doi:10.1007/s00296-014-3082-3
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