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)