Chronic Pain Syndromes
Pain persisting beyond the expected healing time (typically >3 months) that becomes a condition in its own right rather than a symptom of tissue damage. Classified by ICD-11 as chronic primary pain and chronic secondary pain. Management is multimodal, combining physical, psychological, and pharmacological approaches.
Key Facts
Chronic pain affects approximately 28 million adults in the UK (~43% of the population report chronic pain); severe/disabling in ~10% ICD-11 classifies chronic pain as chronic primary pain (fibromyalgia, CRPS, chronic widespread pain) and chronic secondary pain (musculoskeletal, neuropathic, post-surgical, cancer) NICE NG193 (2021): landmark guideline; recommends supervised group exercise, psychological therapy (CBT, ACT), and acupuncture for chronic primary pain NICE NG193 advises AGAINST paracetamol, NSAIDs, benzodiazepines, opioids, gabapentinoids, antidepressants (except for comorbid depression) for chronic primary pain For chronic secondary pain: pharmacological options include amitriptyline, duloxetine, gabapentin/pregabalin (neuropathic), topical treatments Opioid prescribing for chronic non-cancer pain: associated with significant harm (dependence, hyperalgesia, no long-term benefit); deprescribing is a priority Biopsychosocial model: pain experience is influenced by biological, psychological (catastrophising, fear-avoidance), and social (employment, relationships) factors Pain management programmes: multidisciplinary approach combining exercise, psychology, education; most effective model for chronic primary pain
Overview
Key Facts
Chronic pain is a major public health problem and a leading cause of disability worldwide. The paradigm has shifted from a biomedical model (find and fix the damage) to a biopsychosocial model (address the whole person).
Epidemiology
- ~28 million adults in the UK affected
- Prevalence increases with age, deprivation, female sex
- Accounts for significant NHS costs and work absence
- 7.8 million prescriptions for gabapentinoids in 2019 (a 150% increase over 5 years)
Pathophysiology
- Peripheral sensitisation: increased excitability of peripheral nociceptors
- Central sensitisation: enhanced CNS processing of nociceptive and non-nociceptive inputs
- Neuroplasticity: structural and functional brain changes maintain chronic pain
- Descending inhibitory pathway dysfunction: reduced serotonin/noradrenaline-mediated pain inhibition
- Psychological amplifiers: catastrophising, fear-avoidance beliefs, hypervigilance
- Social context: employment, relationships, benefits, litigation
Clinical Presentation
Chronic Primary Pain
- Pain not explained by tissue damage or disease process
- Examples: fibromyalgia, chronic widespread pain, chronic primary headache, CRPS, chronic visceral pain
- Often associated with fatigue, sleep disturbance, mood changes
- Normal investigations
Chronic Secondary Pain
- Pain attributable to an underlying condition
- Musculoskeletal: OA, chronic back pain, RA
- Neuropathic: diabetic neuropathy, post-herpetic neuralgia, trigeminal neuralgia
- Post-surgical: persistent post-operative pain
- Cancer pain: tumour-related, treatment-related
- Visceral: chronic pancreatitis, endometriosis
Assessment
- Pain history: location, character, duration, aggravating/relieving factors
- Impact: sleep, mood, function, work, relationships
- Psychological assessment: PHQ-9 (depression), GAD-7 (anxiety), pain catastrophising scale
- Medication review: current analgesics, previous trials, opioid use
- Red flags: weight loss, night pain, neurological deficit (exclude serious pathology)
Red Flags
- New neurological deficit → structural cause
- Weight loss, night sweats → malignancy
- Fever → infection
- Worsening pain despite treatment → reassess diagnosis
Differential Diagnosis
| Diagnosis | Key Features | Investigation |
|---|---|---|
| Fibromyalgia | Widespread pain, fatigue, sleep disturbance | Clinical diagnosis |
| Depression/anxiety | Low mood, anhedonia; pain may improve with mental health treatment | PHQ-9, GAD-7 |
| Neuropathic pain | Burning, shooting, allodynia, dermatomal distribution | Clinical, NCS |
| Inflammatory arthritis | Joint swelling, morning stiffness, raised ESR/CRP | RF, CCP, ESR |
| Malignancy | Weight loss, progressive, night pain | Imaging, blood tests |
| Hypothyroidism | Fatigue, myalgia, cold intolerance | TFTs |
Diagnosis / Investigation
For Chronic Primary Pain
- Limited investigations: avoid over-investigation (reinforces illness behaviour)
- Baseline bloods: FBC, ESR/CRP, TFTs, calcium, vitamin D, HbA1c – to exclude secondary causes
- Imaging ONLY if red flags or specific indication
For Chronic Secondary Pain
- Guided by underlying condition: X-ray, MRI, nerve conduction studies, etc.
- Neuropathic pain assessment: LANSS score, DN4 questionnaire
Psychological Assessment
- PHQ-9: depression screening
- GAD-7: anxiety screening
- Pain Catastrophising Scale
- Brief Pain Inventory: pain severity and interference
Management
Chronic Primary Pain (NICE NG193)
Recommended:
- Supervised group exercise programmes: most effective intervention; aerobic and strength
- Psychological therapies: CBT, acceptance and commitment therapy (ACT)
- Acupuncture: single course may be offered
- Antidepressants (amitriptyline, duloxetine, SSRI/SNRI): ONLY if comorbid depression/anxiety; NOT for pain alone
NOT recommended for chronic primary pain:
- Paracetamol, NSAIDs, opioids, gabapentinoids, benzodiazepines, corticosteroid injections, ketamine, antiepileptics
Chronic Secondary Pain
Neuropathic pain (NICE CG173):
- Amitriptyline 10-75mg or duloxetine 60-120mg or gabapentin 300-3600mg or pregabalin 150-600mg: first-line options
- Topical capsaicin or lidocaine patches: localised neuropathic pain
- Tramadol: short-term, cautious use
Musculoskeletal pain:
- Exercise, physiotherapy
- Topical NSAIDs, oral NSAIDs (short-term)
- Intra-articular injections where appropriate
Opioid Deprescribing
- Gradual dose reduction: typically 10% per week/fortnight
- Patient education: explain rationale (no long-term benefit, harm reduction)
- Support: psychology, pain management programme
- NICE: do not initiate opioids for chronic primary pain
Pain Management Programmes
- Multidisciplinary: physiotherapy, psychology, occupational therapy, pharmacy, nursing
- Group-based: peer support, shared experience
- Goals: improve function and quality of life (not eliminate pain)
- Evidence base: strongest for chronic primary pain/fibromyalgia
Referral Criteria
- Chronic pain significantly impacting function → pain management team
- Diagnostic uncertainty → rheumatology (one-off assessment)
- Significant psychological comorbidity → psychology/psychiatry
- Opioid dependence → addiction services
Prognosis
- Chronic primary pain: chronic condition; complete resolution uncommon
- Self-management: patients who engage with exercise and psychological strategies have the best outcomes
- Pain management programmes: 50-60% report meaningful improvement in function and quality of life
- Opioids: long-term use associated with worsening outcomes, not improvement
- Return to work: a key prognostic indicator; prolonged absence worsens outcomes
- Neuropathic pain: ~50% achieve ≥50% pain reduction with appropriate pharmacotherapy
Other Relevant Information
NICE NG193 Key Recommendations Summary
| Intervention | Chronic Primary Pain | Chronic Secondary Pain |
|---|---|---|
| Exercise | Recommended (group) | Recommended |
| CBT/ACT | Recommended | Recommended |
| Amitriptyline | Only for comorbid depression | First-line (neuropathic) |
| Duloxetine | Only for comorbid depression | First-line (neuropathic) |
| Gabapentin/pregabalin | NOT recommended | First-line (neuropathic) |
| Opioids | NOT recommended | Short-term only, cautious |
| NSAIDs | NOT recommended | Short-term (musculoskeletal) |
| Paracetamol | NOT recommended | Limited role |
WHO Pain Ladder (Modified for Non-Cancer Pain)
- Step 1: Paracetamol, NSAIDs
- Step 2: Weak opioids (codeine, tramadol) – increasingly questioned
- Step 3: Strong opioids – NOT recommended for chronic non-cancer pain
- Modern approach: multimodal (physical + psychological + pharmacological)