Chronic Low Back Pain β β₯12 WeeksCauda equina = 999 Β· red vs yellow flags Β· NICE NG59 Β· exercise over medication Β· psychosocial barriers
Progress0 / 9
The full reasoning pathway β in persistent back pain, re-screen for missed red flags and inflammatory disease, then manage with a biopsychosocial, exercise-led approach; deprescribe wisely and safety-net.StartDecisionInvestigateActionReferStop / Admit
PresentationChronic back pain (>12 weeks)
Reassess diagnosis, function, mood, and impact. Re-examine for neurology and inflammatory features.
Step 1 Β· Safety β missed red flags / inflammatoryMissed red flags or inflammatory pattern?
New neurology, systemic features, or inflammatory back pain (age <45, insidious, morning stiffness, night pain, good response to NSAIDs).
YES
Stop Β· EscalateInvestigate / refer
Red flags β image/refer. Inflammatory β HLA-B27, CRP, MRI SI joints β rheumatology.
NO
AssessBiopsychosocial
Identify yellow flags (fear-avoidance, low mood, work issues); STarT Back risk stratification.
Step 7 Β· manage
Step 7 Β· ActionExercise-led, self-management
Structured exercise/physiotherapy; address psychosocial factors; consider CBT; limited-role analgesia (avoid long-term opioids). Support return to activity/work.
Step 8 Β· Lifestyle & self-managementThe core treatment, not an add-on
Keep active & keep working β graded exercise/physiotherapy of the patient's choice Β· weight management, stop smoking (disc health) Β· sleep, pacing and ergonomic advice Β· psychological support/CBT for fear-avoidance, low mood and high distress Β· address work and social barriers. Manage expectations: function and flare-control rather than a pain-free spine.
Step 9 Β· review & safety-net
Step 9 Β· Review & safety-netDeprescribe & when to escalate
Review and taper ineffective analgesia β avoid long-term opioids and gabapentinoids (limited benefit, real harms). Same-day / 999 for new bladder/bowel or saddle symptoms or bilateral leg weakness (cauda equina), or systemic red flags (fever, weight loss, night pain) β re-investigate. Re-screen younger patients for inflammatory disease if the pattern evolves.
β οΈ Don't escalate opioids in chronic back pain β the evidence favours exercise, self-management and addressing psychosocial drivers; re-screen for inflammatory disease in younger patients.
1
Safety
Red Flags β Cauda Equina, Cancer & Infection
Check red flags at every consultation β they can develop in a patient with established chronic back pain. Always ask about bladder, bowel, and saddle area.
Cauda equina syndrome Bilateral leg weakness or numbness + saddle anaesthesia (perineum/inner thighs) + new urinary retention or incontinence + new faecal incontinence β 999. Same-day emergency MRI. 48-hour window for surgical decompression β nerve recovery proportional to speed of decompression.
Back pain + weight loss + age >50 Spinal metastases (prostate, breast, lung, kidney, thyroid, myeloma β PBRLKT mnemonic) β urgent MRI spine + cancer screen (PSA, serum protein electrophoresis, Ca125). Myeloma: punched-out lesions, Bence Jones protein, raised ESR, paraprotein. NICE NG12: persistent unexplained back/bone pain 60+ β urgent FBC, calcium & ESR/PV; if consistent with myeloma β urine protein electrophoresis + Bence-Jones protein.
Back pain + fever + IV drug use / recent infection Vertebral osteomyelitis / discitis β CRP + ESR + blood cultures + MRI spine urgently. Staphylococcal vertebral osteomyelitis can cause rapid cord compression. Same-day hospital if systemic compromise.
Severe unrelenting night pain (not positional) Cannot find a comfortable position, worse at night β malignancy, infection, or inflammatory (ankylosing spondylitis in younger patients). X-ray + ESR + CRP + PSA urgently.
Back pain + steroid use / osteoporosis Vertebral compression fracture β plain X-ray urgently. Sudden onset back pain in osteoporotic patient = vertebral fracture until proven otherwise. Risk: postmenopausal women, long-term steroids, hypogonadism.
Progressive neurological deficit Progressive leg weakness, increasing paraesthesia spreading up leg, loss of reflexes β cord or cauda equina compression β urgent MRI. Do not wait for symptoms to stabilise.
Back pain after significant trauma Fall from height, RTA, direct spinal trauma β X-ray / CT spine. Fracture / cord injury risk β do NOT mobilise before imaging in high-energy trauma.
Back pain in patient on anticoagulant + neurological deficit Epidural haematoma β spinal cord compression β 999 emergency. Very rare but reversible if decompressed within hours.
Cauda equina syndrome (CES) is the most catastrophic missed diagnosis in back pain β it is a spinal surgical emergency with a narrow therapeutic window. The cauda equina (horse's tail) is the bundle of nerve roots below L1 that innervates the lower limbs, bladder, bowel, and perineum. Compression (most commonly from a large central disc prolapse at L4/5 or L5/S1) causes rapidly progressive neurological deficit. The surgical window for meaningful recovery is approximately 48 hours β delays beyond this produce permanent paralysis, bladder/bowel dysfunction, and sexual dysfunction. NICE mandates same-day MRI for suspected CES. The GP's clinical rule: ask every back pain patient about bladder (retention = most specific sign β painless inability to pass urine), bowel, and saddle area sensation at every consultation. A positive answer to any of these β 999 immediately. Bilateral leg symptoms, even mild, in a back pain patient must also raise concern.
2
Diagnose
Classification β Non-Specific vs Specific
Non-specific CLBP (90%)
No identifiable anatomical cause. Chronic (>12 weeks). No neurological deficit. No red flags. Influenced by psychosocial factors (yellow flags). NICE NG59: do NOT routinely X-ray or MRI β imaging rarely changes management and may be harmful (catastrophising, over-medicalisation of normal findings). Exercise is the treatment.
Radiculopathy (nerve root)
Radiation of pain below the knee following a dermatomal pattern. L4: medial calf, weakness of knee extension. L5: lateral calf + dorsum of foot, weakness of great toe extension (EHL). S1: posterior calf + sole + small toe, absent ankle jerk, weakness of plantar flexion. Positive straight leg raise (<60Β° = positive for L4/5/S1 disc prolapse).
Spinal stenosis
Neurogenic claudication β bilateral leg pain/heaviness/weakness brought on by walking, relieved by sitting or leaning forward (flexing the spine increases canal space). Age >60. Canal narrowing from OA, facet joint hypertrophy, thickened ligamentum flavum. MRI confirms. Conservative first (exercise, physio) then surgery if severe.
Inflammatory back pain (spondyloarthropathy)
Age <40, insidious onset, morning stiffness >60 min, improves with exercise NOT rest, alternating buttock pain. HLA-B27. CRP/ESR elevated. Sacroiliac joint changes on MRI/X-ray. Ankylosing spondylitis, psoriatic arthritis, reactive, enteropathic. Rheumatology referral.
Chronic CLBP duration
Subacute: 6β12 weeks. Chronic: >12 weeks (this pathway). Of chronic LBP patients, 60% have persistent symptoms at 1 year. 85% of LBP has no specific anatomical cause despite extensive investigation.
NICE NG59 explicitly states: "Do not offer imaging for non-specific low back pain." This is a major departure from historical practice and is frequently misunderstood by patients and clinicians alike. The evidence base is clear: routine MRI in back pain patients without red flags increases catastrophising, disability, and healthcare utilisation without improving outcomes. Degenerative disc changes (disc bulges, facet joint OA, Modic changes) are found in over 80% of pain-free adults over 40 on MRI β they are radiological variants of ageing, not pathological findings requiring treatment. Telling a patient they have a "bulging disc" or "wear and tear changes" significantly increases their pain beliefs, reduces physical activity, and promotes disability behaviour. The GP communication task is to explain that absence of imaging is the evidence-based approach, and that the spine is strong and movement is healing.
3
Diagnose
Yellow Flags β Psychosocial Barriers to Recovery
Yellow flags predict chronicity more reliably than any imaging finding. Screen all CLBP patients using the Γrebro or STarT Back Tool.
Beliefs (catastrophising)
"My back is damaged and fragile" Β· "Pain means harm" Β· "I'll never get better" Β· "Only surgery/injection will fix me." These beliefs are the strongest predictors of disability. Address directly: "Chronic pain does not equal damage β your spine is not crumbling."
Emotions
Depression (PHQ-9) and anxiety (GAD-7) strongly predict back pain chronicity and disability β treat the mental health comorbidity actively. Fear-avoidance behaviour: fear of movement (kinesiophobia) β reduced activity β deconditioning β more pain. Tampa Scale for Kinesiophobia.
Behaviours
Prolonged rest (NICE: bed rest is harmful and counterproductive β movement is medicine). Passive coping (waiting for someone else to fix the pain). Repetitive healthcare seeking without self-management engagement. Medication over-reliance.
Work and social context
Work dissatisfaction β poor outcomes. Manual or heavy labour with no modified duties available β barrier to return to work. Low socioeconomic status. Social isolation. Medicolegal involvement (compensation claim) β prolongs disability even with treatment.
STarT Back Tool
9-question tool (0β9 score): Low risk (0β3) β reassurance + advice + remain active. Medium risk (4β8 + physical element) β physiotherapy. High risk (4β8 + psychological element) β combined physical + psychological treatment (CBT-informed physiotherapy). Available free at keele.ac.uk/startback.
The STarT Back Tool (Keele University) is the NICE-recommended prognostic tool for stratified care in non-specific LBP. It identifies patients at high risk of chronicity due to psychosocial factors (the high-risk group) who need CBT-informed physiotherapy rather than standard physiotherapy. The large RCT by Hill et al. (2011, Lancet) demonstrated that STarT Back-stratified care produced better outcomes and was more cost-effective than undifferentiated usual care. High-risk patients treated with standard physiotherapy alone show minimal improvement β they need simultaneous psychological intervention (CBT, acceptance and commitment therapy, mindfulness-based interventions) to address catastrophising and fear-avoidance. The tool takes 2 minutes to complete and is available online. GPs should complete it at the first chronic LBP consultation.
4
Diagnose
Examination & Investigations
Neurological examination
Mandatory at every consultation: power (hip flexion L2/3, knee extension L3/4, great toe extension L4/5, plantar flexion S1), sensation (dermatomes L3βS1), reflexes (knee jerk L3/4, ankle jerk S1). Document for deterioration tracking. New deficit β urgent MRI.
Straight leg raise (SLR)
Patient supine, raise straight leg β pain radiating below knee at <60Β° = positive (nerve root tension β L4/L5/S1 disc). Sensitivity 80% for disc prolapse but low specificity. Crossed SLR (pain in symptomatic leg when asymptomatic leg raised) = highly specific for large disc prolapse.
Spinal movement
Schober test (lumbar flexion): mark S1 and 10 cm above β should increase to β₯15 cm with full flexion. <15 cm = restricted β consider inflammatory (ankylosing spondylitis). Extension and lateral flexion also assess. Facet joint loading (pain on extension) = facet arthropathy.
Investigations (NICE NG59)
Do NOT routinely image. Investigate if red flags: X-ray (fracture, metastases, ankylosing spondylitis β bamboo spine). MRI (if surgical candidate: radiculopathy >6 weeks not improving, CES, suspected malignancy/infection). CRP + ESR (infection, inflammatory, malignancy). PSA (prostate cancer). Serum protein electrophoresis (myeloma).
PHQ-9 + GAD-7
Screen at first chronic LBP consultation and annually. Depression and anxiety are found in 35β50% of chronic LBP patients. Treating depression with antidepressant + psychological therapy independently improves pain outcomes. Document and treat actively.
The Schober test for lumbar flexion restriction is the key clinical examination for ankylosing spondylitis in a young patient with back pain and morning stiffness. A lumbar flexion increment of <5 cm (from 0 to β₯5 cm increase in a 10 cm baseline interval) is highly specific for restricted lumbar mobility, consistent with spondyloarthropathy. Combined with elevated CRP and HLA-B27 positivity, this warrants urgent rheumatology referral for MRI sacroiliac joints. Ankylosing spondylitis affects 0.1β0.5% of the population, predominantly young males, and causes irreversible spinal fusion if untreated β but responds dramatically to NSAIDs (near-complete symptomatic response within 48 hours is almost pathognomonic) and biologics (TNF inhibitors). The average diagnostic delay for ankylosing spondylitis is 7β10 years β a significant and preventable failure in primary care.
5
Refer
Referral Pathways
999 / A&E same-day
Cauda equina syndrome (saddle anaesthesia + urinary retention + bilateral leg deficit). Vertebral osteomyelitis with sepsis. Suspected epidural haematoma (anticoagulated + new neurological deficit).
Urgent MRI / orthopaedics / neurosurgery
Radiculopathy not improving at 6 weeks despite conservative management (surgical decompression candidate) Β· Progressive neurological deficit Β· Spinal stenosis with severe functional limitation Β· Suspected malignant cord compression (known cancer + new back pain)
Physiotherapy (primary care)
All non-specific CLBP (NICE NG59: offer exercise as first-line). STarT Back Low risk: advice + leaflet + encourage activity. Medium risk: physiotherapy Γ 6β8 sessions. High risk: CBT-informed physiotherapy (combined physical + psychological programme).
Rheumatology
Suspected ankylosing spondylitis / axial spondyloarthropathy (age <45, morning stiffness >60 min, improves with exercise, elevated CRP, HLA-B27 +) Β· RA with spinal involvement Β· Psoriatic arthritis + axial disease
Pain clinic / MSK specialist
Non-specific CLBP not responding to 12 weeks of physiotherapy + pharmacological treatment. Injection procedures (facet joint, epidural steroid). Spinal cord stimulation (NICE approved for failed back surgery syndrome). Multidisciplinary pain programme (NICE NG59).
Occupational health
Work absence >4β6 weeks. Workplace assessment and reasonable adjustments. Phased return to work. Fit note guidance: GP should specify modifications not just "unfit for work" β NICE and RCGP guidance.
Malignant cord compression (MSCC) from vertebral metastases is a spinal emergency that requires urgent MRI of the whole spine β 30% of patients have multiple levels of compression. NICE NG83 (Metastatic Spinal Cord Compression) mandates same-day MRI and corticosteroids (dexamethasone 8 mg IV then 16 mg OD orally) for any patient with known cancer and new back pain or neurological symptoms. GPs should have a low threshold for suspecting MSCC in any back pain patient with a history of cancer β the primary cancer may have been diagnosed years previously. Common primaries: prostate (sclerotic lesions), breast, lung, kidney, thyroid, myeloma. The outcome of MSCC depends critically on the patient's neurological status at the time of decompression β patients who are ambulatory before surgery have a 90% chance of remaining ambulatory; those who are paraplegic at surgery have a 30% chance of recovery.
6
Treat
Pharmacological Treatment Ladder
Step 1Topical NSAIDs first-line (NICE NG59) β diclofenac 1% gel (Voltarol) TDS for localised back pain. Minimal systemic absorption. Evidence: NNT β 6 for β₯50% pain reduction. Paracetamol 1 g QDS: minimal evidence for CLBP but low risk while establishing exercise.
Step 2Oral NSAIDs (short course) β naproxen 500 mg BD or ibuprofen 400 mg TDS with omeprazole 20 mg OD (gastroprotection). Reduce to lowest effective dose. NICE: do not use as long-term monotherapy. Review at 4 weeks. Avoid in CKD, heart failure, peptic ulcer history.
Step 3Amitriptyline 10β30 mg nocte (low-dose) β NICE NG59 first-line for neuropathic component / central sensitisation in CLBP. Start at 10 mg, titrate to 30 mg. Separate from antidepressant dose. Benefits: pain modulation, improved sleep, mild anxiolytic effect. Review at 6 weeks.
Step 4Duloxetine 30β60 mg OD β SNRI, NICE-recommended for CLBP with significant psychological comorbidity (depression + anxiety + chronic pain). Treats pain AND depression simultaneously. Review at 4 weeks for efficacy and tolerability. Maximum 120 mg OD.
Step 5Gabapentin / pregabalin β for radiculopathy only (not non-specific CLBP). Gabapentin 300 mg TDS (titrate). Pregabalin 75 mg BD (titrate). NICE: do not use for non-specific CLBP. Class C controlled drugs (pregabalin Schedule 3). Addiction potential β review regularly and do not prescribe indefinitely without specialist review.
NICE NG59: Do NOT use opioids for non-specific chronic low back pain. Weak opioids (codeine, tramadol) have no evidence of long-term benefit and significant harms (dependence, cognitive impairment, falls, hyperalgesia). If already prescribed, develop a tapering plan. Strong opioids are not appropriate for CLBP.
The NICE NG59 recommendation against opioids for non-specific chronic low back pain is based on robust evidence that opioids produce minimal pain reduction (<10 mm on 100 mm VAS at 1 year) while causing significant harms: dependence (30% of long-term users develop opioid use disorder), opioid-induced hyperalgesia (opioids paradoxically increase pain sensitivity with chronic use), constipation, cognitive impairment, falls (especially in elderly), sexual dysfunction (opioid-induced androgen deficiency), and overdose risk. The average GP practice in the UK has 5β10% of chronic pain patients on long-term opioids β many of these patients would benefit from a structured opioid tapering programme combined with psychologically-informed physiotherapy. Opioid tapering for CLBP is an active RCGP GP guidance priority and is specifically tested in SCA examination scenarios. A key phrase for the SCA: "I can help you come off these medications β they may actually be making your pain worse in the long run."
7
Treat
Non-Pharmacological Interventions
Exercise (NICE NG59 β FIRST LINE)
Any form of exercise is beneficial β there is no evidence that one type is superior. Aerobic exercise (walking, swimming, cycling), strengthening (core stabilisation, resistance training), yoga, Pilates, tai chi. Prescribe 30 min moderate intensity 5 days/week. Referral to physiotherapy for tailored programme. Physical activity is more effective than any medication for CLBP.
Physiotherapy
Manual therapy (manipulation and mobilisation) β short-term benefit in acute/subacute CLBP as adjunct to exercise, not as standalone long-term treatment. Transcutaneous electrical nerve stimulation (TENS) β not routinely recommended by NICE but used widely; patient preference. Heat therapy β temporary relief, adjunct only.
NICE NG59 (2016): acupuncture is NOT recommended for CLBP β evidence shows it is no better than sham acupuncture. This is frequently misunderstood by patients (many request it). Explain that NICE evidence does not support it for back pain specifically, though it may help other pain conditions.
Spinal injections
Epidural steroid injection (ESI): NICE does not recommend for non-specific CLBP. Evidence: short-term benefit for radiculopathy only (not non-specific pain). Facet joint injection: no long-term benefit in RCTs. Medial branch block + radiofrequency denervation (RFA): better evidence for facet joint pain β pain clinic decision.
Exercise is the single most evidence-based treatment for chronic low back pain β Cochrane systematic reviews of >200 RCTs demonstrate that exercise produces moderate-to-large improvements in pain and function in CLBP. The type of exercise is less important than adherence and consistency β patients should be encouraged to choose an activity they enjoy (swimming, walking, yoga, tai chi) rather than a specific "back exercise" programme, because enjoyment predicts adherence and adherence predicts outcome. The neurobiological mechanisms by which exercise reduces chronic pain include: endogenous opioid release, central pain inhibition (reduced central sensitisation), anti-inflammatory cytokine production, improved sleep, and mood enhancement via serotonin/dopamine. The GP's most important CLBP communication task is to explain that movement does not damage the back β the spine is a strong structure designed for movement, and pain does not equal damage in CLBP.
8
Lifestyle
Active Self-Management β The Core Message
Movement is medicine The most powerful message in CLBP management: "Your back is not damaged. Movement will not harm you β it will help you." Prolonged rest worsens CLBP (disc nutrition depends on movement, muscle deconditioning accelerates within days). Start with 10-min walks and build up. Every step is therapeutic.
Posture and ergonomics No single "correct" posture prevents CLBP β varying position is more important than maintaining any specific posture. Standing desks: use alternating sitting/standing every 30β45 min. Lifting: bend knees, keep load close to body, avoid twisting. Driving: lumbar support, regular breaks. Regular micro-movements every 20β30 min.
Sleep quality Poor sleep worsens pain perception (increases central sensitisation) β addressing sleep hygiene independently improves CLBP outcomes. Mattress: medium-firm evidence-based. Sleep position: pillow between knees for side sleepers. Treat insomnia actively (CBT-I, sleep restriction therapy via IAPT).
Weight management Obesity is an independent risk factor for CLBP β each additional 10 kg increases lumbar disc compressive load by 100 kg. BMI reduction reduces pain, improves function, and reduces disability. Evidence: each 5-unit BMI reduction produces measurable CLBP improvement. Exercise + dietary support. Tier 3 if BMI >35.
Smoking cessation Smoking is an independent risk factor for CLBP β impairs disc nutrition (reduced blood flow to avascular discs), promotes inflammation, impairs bone healing. Stopping smoking reduces chronic pain severity over 12β24 months. Stop Smoking Service + pharmacotherapy (varenicline most effective).
Work and activity Staying at work (or returning quickly) is one of the most important outcomes in CLBP β work absence beyond 6 weeks is a major chronicity predictor. Fit note: specify modifications ("can do light duties / avoid heavy lifting / standing breaks") rather than total incapacity where possible. Occupational health referral early.
Pacing and flare management Teach activity pacing: do activities in small chunks with scheduled rest β avoids boom-and-bust cycle (overdoing β crash β bed rest β deconditioning). During flares: short course NSAIDs + continue gentle movement + avoid prolonged bed rest. Written flare management plan.
Back pain resources NHS Pain Toolkit (paintoolkit.org): free self-management guide. Versus Arthritis (versusarthritis.org): back pain information. MIND back pain and mental health resources. Prescription for an online pain management programme (PMP): Pathway Through Pain (NHS digital). Refer to social prescriber for community activity.
The "boom-and-bust" cycle is one of the most important concepts in chronic pain self-management β patients with CLBP frequently overdo activities on "good days" (boom), experience a pain flare from overexertion (bust), then rest for days (which deconditions them further). This cycle gradually escalates disability. Pacing (doing a set quota of activity regardless of pain level β not stopping when pain increases, not overdoing when pain is low) breaks this cycle. The concept comes from operant pain management theory (Fordyce, 1976) and is the foundation of all evidence-based pain management programmes. Teaching pacing explicitly in a GP consultation takes 3β5 minutes and is one of the highest-impact behavioural interventions available in primary care for CLBP. The pain toolkit (paintoolkit.org) is a free resource developed by Pete Moore (a chronic pain patient) that encapsulates all these principles in patient-friendly language.
9
Safety
Follow-Up & Safety-Netting
6 weeks
STarT Back stratification completed? Physiotherapy commenced and engaged? Medication reviewed β escalate or rationalise. Depression/anxiety treated? If opioids prescribed β review tapering plan. Repeat neurological examination β any new deficit?
3 months
Exercise programme sustained? Functional improvement (patient-reported outcome measure β e.g. Roland Morris Disability Questionnaire or Oswestry Disability Index at baseline and 3 months). Refer pain clinic if no meaningful improvement after 12 weeks optimised treatment. Opioid tapering progress?
Annual review
All chronic LBP patients: annual review of function, medications (rationalise opioids), mental health screen (PHQ-9/GAD-7), occupational status, red flag screen. Document functional status (Oswestry). Consider stepping down medications if pain stable.
Fit note review
Review fit note at every issuing β avoid open-ended fit notes for CLBP. Specify modifications where possible. Goal: phased return to work within 6 weeks. >3 months absence β referral to occupational health / Fit for Work service.
Opioid review
Patients on long-term opioids for CLBP: review quarterly. Assess efficacy (functional improvement β not just pain relief), side effects, dependence signs. Offer structured tapering (10% dose reduction every 2 weeks). Buprenorphine patch as bridge during taper (specialist initiation).
999 safety-net
Any new bladder/bowel change or saddle area numbness β 999 (CES). Sudden severe back pain in known osteoporosis/cancer (vertebral fracture/cord compression). New rapidly progressive leg weakness.
Same-day GP
New or worsening neurological signs (leg weakness, new foot drop, spreading paraesthesia), new fever + back pain (vertebral osteomyelitis), sudden intractable pain in patient with known cancer
The Oswestry Disability Index (ODI) is the gold standard patient-reported outcome measure (PROM) for low back pain β it is a 10-item questionnaire covering personal care, lifting, walking, sitting, standing, sleeping, social life, travelling, and pain intensity. Scores: 0β20% = minimal disability; 21β40% = moderate; 41β60% = severe; 61β80% = crippled; 81β100% = bedbound. Documenting ODI at baseline and at 3-month intervals provides an objective functional measure to guide escalation decisions, evidence treatment response, and support referral justification. Significant improvement is defined as β₯10-point reduction. For the SCA examination, being able to name a validated functional outcome measure for back pain and explain its clinical application demonstrates clinical knowledge at examiner-quality level. The Roland Morris Disability Questionnaire (24-item) is an alternative PROM that is simpler to complete.
Educational use only. Based on NICE NG59 (Low Back Pain and Sciatica, 2016 β updated 2022), NICE NG83 (Metastatic Spinal Cord Compression), STarT Back Tool (Keele University), RCGP opioid prescribing guidance, BSR ankylosing spondylitis guidelines, Cochrane systematic reviews of exercise for CLBP. Always adapt to individual patient context.