Rheumatology: Crystal arthritis, osteoarthritis and soft tissue pain
🩺 Crystal arthritis, osteoarthritis and soft tissue pain -page 3 of the Rheumatology chapter. Gout is the commonest inflammatory arthritis (about 1 in 40 UK adults) and is curable with urate-lowering therapy to a target -yet it is often undertreated. Osteoarthritis is the commonest joint disease of all, and exercise and weight loss are its main treatments. Chronic widespread pain (fibromyalgia) is common and needs a positive diagnosis, not endless tests. Septic arthritis is on the Trauma and Orthopaedics page; joint replacement and regional soft tissue problems (shoulder, elbow, foot) are there too.
Your four questions for every patient: Could this hot joint be infected -has it been aspirated? Is this crystal, degenerative or inflammatory disease -or pain without joint disease? What can the patient do themselves (exercise, weight, diet, alcohol)? For gout -is urate-lowering therapy indicated, and is the urate at target?
Gout -Causes and Risk Factors
- Gout -inflammation caused by monosodium urate crystals forming in and around joints when urate levels stay high (hyperuricaemia -above about 360 µmol/L, the saturation point).
- Most hyperuricaemia never causes gout -don't treat high urate without symptoms.
- Causes of high urate:
- Reduced kidney excretion (about 90%) -CKD, diuretics (thiazides and loop), low-dose aspirin, ciclosporin and tacrolimus, pyrazinamide, ethambutol, dehydration, ketoacidosis, lead, hypothyroidism, genetics.
- Increased production -high-purine diet (red meat, offal, seafood), alcohol (especially beer and spirits), sugary drinks (fructose), high cell turnover (myeloproliferative disease, psoriasis, haemolysis), tumour lysis, rare enzyme defects (Lesch–Nyhan).
- Risk factors -men (women after menopause), older age, obesity, metabolic syndrome, hypertension, diabetes, CKD, family history, organ transplant.
- Gout is linked with cardiovascular disease and CKD -assess CV risk in everyone with gout.
- Triggers of a flare -alcohol binges, large meals, dehydration, surgery or acute illness, trauma, new diuretics, starting or changing urate-lowering therapy (urate falls and crystals shift).
Gout -Clinical Features and Diagnosis
- Acute gout flare:
- Sudden severe pain, peaking within 24 hours, often starting at night; can't bear the bedsheet touching the joint.
- Red, hot, swollen, very tender joint; skin may be shiny and peel as it settles.
- First MTP joint (big toe -"podagra") in over half of first attacks; also midfoot, ankle, knee, wrist, fingers, olecranon bursa.
- Usually settles within 1–2 weeks even without treatment.
- May have fever and raised CRP -can look like septic arthritis or cellulitis.
- Chronic gout -recurrent flares, more joints involved (polyarticular), persistent joint pain and damage, tophi (chalky white deposits of urate under the skin -ears, fingers, elbows, Achilles), kidney stones (urate), urate nephropathy.
- Diagnosis:
- Gold standard -joint aspiration showing needle-shaped, negatively birefringent crystals (or aspirate from a tophus) -especially if the diagnosis is uncertain or infection is possible.
- Often clinical in typical first MTP attacks with risk factors (NICE NG219).
- Serum urate -can be normal during a flare (urate falls in acute inflammation) -repeat at least 2 weeks after the flare settles to confirm and to set a baseline.
- Also check U&E, HbA1c, lipids, LFTs, FBC, BP (associated conditions).
- Imaging -X-ray (erosions with overhanging edges -late), ultrasound (double contour sign), dual-energy CT (urate deposits).
Treating a Gout Flare
- Treat early -the sooner treatment starts, the better it works; patients should keep a "pill in the pocket".
- First-line options (NICE NG219) -choose by comorbidities and patient preference:
- NSAID (e.g. naproxen) with a PPI -avoid in CKD, heart failure, peptic ulcer, anticoagulants.
- Colchicine -best started within 24 hours; low dose (500 micrograms 2–4 times a day -see BNF for maximum course dose) is as effective as high dose with fewer side effects; diarrhoea is common; reduce or avoid in CKD; interactions -clarithromycin, erythromycin, ciclosporin, verapamil, diltiazem, some statins (toxicity, myopathy).
- Short course of oral steroid (e.g. prednisolone 30–35 mg daily for 3–5 days) -useful when NSAIDs and colchicine are unsuitable (CKD, heart failure).
- Second-line -intra-articular steroid injection (once infection excluded) or IM steroid; IL-1 inhibitors (anakinra, canakinumab -specialist) if others are unsuitable.
- Supportive -rest, raise the limb, ice packs, fluids; avoid alcohol.
- Don't stop urate-lowering therapy during a flare if already taking it.
- Review diuretics -switch from a thiazide or loop diuretic if possible (e.g. for hypertension -consider losartan or amlodipine, which lower urate slightly). Don't stop diuretics needed for heart failure.
⚠️ Safety Pearl -a hot joint in a patient with "known gout" can still be septic. If the patient is unwell, febrile, immunosuppressed, has a prosthetic joint, or the attack is atypical -aspirate.
Urate-lowering Therapy
- Offer urate-lowering therapy (ULT) to everyone with gout after discussing it, especially if (NICE NG219):
- Recurrent flares (2 or more a year).
- Tophi.
- Chronic gouty arthritis or joint damage.
- CKD stage 3–5.
- Diuretic therapy that can't be stopped.
- Kidney stones, or young age at onset (under 40).
- When to start -usually 2–4 weeks after a flare settles (or during a flare if flares are frequent).
- Treat to target -serum urate below 360 µmol/L; below 300 µmol/L if tophi, chronic gouty arthritis or ongoing frequent flares (dissolves crystals faster). Once at target for some years and tophi have gone, a target under 360 is enough.
- Drugs:
- Allopurinol (xanthine oxidase inhibitor) -first-line; start low (100 mg daily, or lower in CKD) and increase monthly (by 100 mg) according to urate until at target (often 300–600 mg or more; up to 900 mg); check urate monthly while titrating.
- Febuxostat -if allopurinol is not tolerated or not effective; caution in major cardiovascular disease (MHRA) -allopurinol is preferred in those patients.
- Uricosurics (benzbromarone, sulfinpyrazone -specialist; probenecid), pegloticase (severe tophaceous gout -rarely used).
- Flare prophylaxis when starting ULT -colchicine 500 micrograms once or twice daily (or low-dose NSAID or steroid if unsuitable) for up to 6 months; warn that flares may increase at first.
- Allopurinol hypersensitivity syndrome -rare but life-threatening (fever, rash -SJS/TEN or DRESS, hepatitis, kidney injury); higher risk in CKD, high starting doses, and people of Han Chinese, Thai or Korean descent with HLA-B*58:01 (test before starting in these groups). Stop at the first sign of rash.
- Interaction -azathioprine and mercaptopurine with allopurinol or febuxostat → severe marrow toxicity -avoid or greatly reduce the dose (specialist).
- Lifestyle -weight loss, regular exercise, reduce alcohol (especially beer and spirits), avoid sugary drinks, keep hydrated, stop smoking; diet alone rarely lowers urate enough.
- Long-term -ULT is usually lifelong; check urate annually once at target; adherence is the main problem (education helps).
Gout in Special Situations
- CKD -gout is common; colchicine and NSAIDs are limited -use steroids for flares; allopurinol is still used (start low, increase slowly to target -not limited by eGFR-based maximums if monitored); febuxostat needs no dose change in mild to moderate CKD.
- Heart failure -avoid NSAIDs; diuretics often unavoidable; colchicine or steroids for flares.
- Transplant recipients -ciclosporin and tacrolimus raise urate; colchicine interacts with ciclosporin; allopurinol interacts with azathioprine -specialist advice.
- Tumour lysis syndrome -chemotherapy for bulky leukaemias and lymphomas; high urate, potassium and phosphate, low calcium, AKI -prevent with IV fluids, allopurinol or rasburicase (high risk; avoid in G6PD deficiency) (see the Oncological Emergencies chapter).
- Women -gout before menopause is unusual -look for CKD, diuretics or a genetic cause.
- Gout in young people (under 25) or with kidney stones -consider enzyme defects or familial juvenile hyperuricaemic nephropathy.
- Hospital inpatients -flares are common after surgery, dehydration or diuretic changes; continue ULT during admission.
Calcium Pyrophosphate Deposition (Pseudogout)
- Calcium pyrophosphate (CPP) crystals deposit in cartilage; commonest in older people (most over 65).
- Forms:
- Chondrocalcinosis -calcium in cartilage on X-ray (knee menisci, wrist triangular fibrocartilage, symphysis pubis) -often without symptoms.
- Acute CPP crystal arthritis ("pseudogout") -sudden hot swollen joint, usually the knee or wrist; often during acute illness, after surgery or trauma; fever and confusion in older people.
- Chronic CPP arthritis -OA-like disease in unusual joints (wrists, MCPs, shoulders, elbows) with flares.
- Crowned dens syndrome -acute severe neck pain and stiffness with fever and high CRP in older people (CPPD around C2) -mimics meningitis or PMR; CT neck.
- Diagnosis -joint aspiration: rhomboid, weakly positively birefringent crystals; exclude infection (can coexist).
- Treatment of acute attacks -aspiration (relieves pain) and intra-articular steroid; NSAIDs or colchicine (with caution in older people); oral steroids. No treatment removes CPP crystals.
- Recurrent attacks -low-dose colchicine prophylaxis; methotrexate or hydroxychloroquine (limited evidence).
- Look for metabolic causes -especially if under 55 or with widespread chondrocalcinosis:
- Haemochromatosis (ferritin, transferrin saturation).
- Hyperparathyroidism (calcium, PTH).
- Hypomagnesaemia (including Gitelman syndrome; PPIs).
- Hypophosphatasia (low ALP).
- Wilson's disease (rare).
Basic Calcium Phosphate Disease
- Basic calcium phosphate (hydroxyapatite) crystals -not visible on standard polarised microscopy.
- Calcific tendinopathy -calcium deposits in tendons, especially the supraspinatus (shoulder); acute calcific periarthritis causes sudden, severe pain, redness and swelling (mimics gout or infection); NSAIDs, steroid injection, ultrasound-guided barbotage.
- Milwaukee shoulder -older women; rapidly destructive shoulder arthritis with large, often blood-stained effusions and rotator cuff loss.
- Calcinosis -calcium deposits in the skin in systemic sclerosis (limited -CREST) and dermatomyositis (especially in children); may ulcerate and discharge chalky material.
- Metastatic calcification -high calcium–phosphate product (advanced CKD -calciphylaxis risk).
Osteoarthritis -Features and Diagnosis
- Osteoarthritis (OA) -the commonest joint disease; a process of joint damage and repair affecting cartilage, bone, synovium and ligaments -not simply "wear and tear".
- Risk factors -age, obesity (knees and hands), female sex, previous joint injury or surgery (meniscectomy, ACL tear), joint malalignment, occupation (kneeling, heavy lifting), genetics, muscle weakness.
- Joints affected -knees, hips, hands (DIP, PIP, thumb base), cervical and lumbar spine, first MTP; uncommon in the wrist, elbow, shoulder and ankle (think trauma, CPPD, or another cause).
- Symptoms -pain on use, eased by rest; short morning stiffness (under 30 minutes); "gelling" after inactivity; reduced function; night pain in advanced disease.
- Signs -bony swelling, crepitus, reduced and painful movement, effusion (cool), deformity (varus knee), quadriceps wasting, joint line tenderness.
- Diagnose clinically without imaging (NICE NG226) if:
- Age 45 or over, AND
- Activity-related joint pain, AND
- No morning stiffness, or stiffness lasting no longer than 30 minutes.
- Consider other diagnoses if atypical -history of trauma, prolonged morning stiffness, rapid deterioration, a hot swollen joint (gout, CPPD, infection), night pain or weight loss (cancer), younger age.
- X-ray (if needed) -LOSS: Loss of joint space (asymmetric), Osteophytes, Subchondral sclerosis, Subchondral cysts. X-ray changes correlate poorly with symptoms.
- Blood tests are normal in OA.
Managing Osteoarthritis
- Core treatments for everyone (NICE NG226):
- Exercise -tailored strengthening and general aerobic fitness (physiotherapy, group classes such as ESCAPE-pain); combine with education.
- Weight loss if overweight -even 5–10% weight loss helps knee pain.
- Information and self-management -OA is not inevitably progressive; activity does not "wear out" joints.
- Drug treatment (alongside core treatment):
- Topical NSAIDs -first choice for knee OA (and hand OA).
- Oral NSAIDs -lowest dose, shortest time, with a PPI, considering GI, renal and CV risks.
- Don't routinely offer paracetamol (alone), weak opioids (unless short-term and other options unsuitable), strong opioids, glucosamine, chondroitin, or hyaluronic acid injections.
- Intra-articular steroid -short-term relief (weeks) for flares when other treatments aren't enough.
- Aids -walking aids (stick in the opposite hand to the painful hip or knee), supportive footwear, assistive devices; acupuncture is not recommended; arthroscopic washout is not recommended (unless locking).
- Refer for joint replacement when symptoms substantially affect quality of life despite non-surgical treatment -don't exclude people based on age, weight, smoking or comorbidities alone (see the Trauma and Orthopaedics page).
- Also manage -sleep, low mood, other conditions; review regularly.
Hand Osteoarthritis
- Nodal OA -Heberden's nodes (DIP joints) and Bouchard's nodes (PIP joints); middle-aged women, family history; often painful early then less painful as nodes form.
- Thumb base OA (first carpometacarpal joint) -pain on pinching and gripping (opening jars), "squaring" of the thumb base; splints, injections, surgery (trapeziectomy).
- Erosive hand OA -painful, inflammatory attacks of the interphalangeal joints; "gull-wing" central erosions on X-ray; can look like inflammatory arthritis (bloods normal).
- Treatment -hand exercises, OT (joint protection, aids), splints, topical NSAIDs, oral NSAIDs for short periods, steroid injection (thumb base); hydroxychloroquine does not help.
- Mucous cysts -small cysts over DIP joints (linked with OA) -may cause nail grooves.
- DIP involvement differential -OA, psoriatic arthritis (nail changes, dactylitis), gout.
Fibromyalgia and Chronic Widespread Pain
- Fibromyalgia -chronic widespread pain (over 3 months) with fatigue, unrefreshing sleep and cognitive difficulties ("fibro fog"), often with headaches, IBS, bladder symptoms, anxiety and low mood; a disorder of pain processing (central sensitisation). It is a type of chronic primary pain.
- Who -more common in women, middle age; often follows stress, illness or injury; common alongside RA, SLE and other diseases.
- Diagnosis -clinical (ACR 2016 criteria -widespread pain index and symptom severity score); examination is normal apart from widespread tenderness; no swelling.
- Tests to exclude mimics (keep limited) -FBC, CRP/ESR, U&E, LFTs, bone profile, TFTs, CK, vitamin D, HbA1c, coeliac serology if relevant. Don't test ANA or RF without other features (false positives cause harm).
- Management (NICE NG193 -chronic primary pain):
- Give a clear diagnosis and explanation -the pain is real; the body is not being damaged.
- Exercise -graded, regular activity (supervised programmes).
- Psychological therapies -CBT or acceptance and commitment therapy (ACT); acupuncture (NICE allows a course).
- Antidepressants can be considered (e.g. amitriptyline, duloxetine, SSRIs) -for pain, sleep and mood.
- Avoid starting -opioids, gabapentinoids, NSAIDs, paracetamol, benzodiazepines, local anaesthetics (NICE) -they lack benefit and cause harm.
- Sleep hygiene, pacing, return-to-work support.
- Chronic fatigue syndrome / ME overlaps -see NICE NG206.
Joint Hypermobility
- Joint hypermobility -joints that move beyond the normal range; common and often harmless (dancers, gymnasts).
- Beighton score (out of 9) -little finger extension beyond 90° (1 each side), thumb to forearm (1 each side), elbow hyperextension over 10° (1 each side), knee hyperextension over 10° (1 each side), palms flat on the floor with knees straight (1). Hypermobility is usually 5 or more in adults (4 or more over 50).
- Hypermobility spectrum disorder and hypermobile Ehlers–Danlos syndrome (hEDS) -hypermobility with symptoms: joint pain, recurrent sprains, subluxations and dislocations, fatigue; associated POTS (postural tachycardia), gut symptoms, anxiety.
- Management -physiotherapy (strengthening, proprioception), pacing, pain management; avoid unnecessary surgery.
- Other heritable connective tissue disorders to recognise:
- Vascular EDS (COL3A1) -thin translucent skin, easy bruising, arterial, bowel and uterine rupture -serious.
- Marfan syndrome (FBN1) -tall, long limbs, lens dislocation (upwards), aortic root dilatation and dissection -echo and monitoring.
- Osteogenesis imperfecta -fractures, blue sclerae, hearing loss.
Metabolic and Endocrine Arthropathies
| Condition | Musculoskeletal features |
|---|---|
| Haemochromatosis | Arthropathy of the 2nd and 3rd MCP joints ("hook-like" osteophytes), CPPD, fatigue; check ferritin and transferrin saturation; venesection doesn't usually help the joints |
| Hypothyroidism | Myalgia, stiffness, raised CK, carpal tunnel syndrome, effusions, CPPD |
| Hyperthyroidism | Proximal myopathy, osteoporosis, thyroid acropachy (Graves') |
| Hyperparathyroidism | Bone pain, CPPD, osteoporosis, (osteitis fibrosa cystica rarely) |
| Acromegaly | Large joint OA-like arthropathy, back pain, carpal tunnel syndrome |
| Diabetes | Cheiroarthropathy (stiff hands -"prayer sign"), frozen shoulder, Dupuytren's, trigger finger, carpal tunnel, Charcot foot, DISH, diabetic muscle infarction |
| Sickle cell disease | Bone pain crises, avascular necrosis (femoral head), dactylitis in children, osteomyelitis (Salmonella), septic arthritis |
| Haemophilia | Recurrent haemarthroses → destructive arthropathy |
| Steroid use and alcohol | Avascular necrosis (hip, shoulder, knee), osteoporosis, myopathy (steroids) |
| Osteomalacia | Bone pain, proximal weakness, waddling gait, low vitamin D and phosphate, raised ALP (see Bone Medicine) |
Other Joint Conditions to Know
- Diffuse idiopathic skeletal hyperostosis (DISH) -older men, obesity, diabetes; "flowing" ossification along the front of at least 4 vertebrae (right side of the thoracic spine), stiffness; sacroiliac joints are normal (unlike ankylosing spondylitis); dysphagia from cervical osteophytes.
- Avascular necrosis (osteonecrosis) -loss of blood supply to bone -steroids, alcohol, sickle cell disease, SLE, antiphospholipid syndrome, radiotherapy, decompression sickness, bisphosphonates (jaw); hip pain with normal early X-rays -MRI; protected weight bearing, core decompression or joint replacement.
- Charcot (neuropathic) joint -painless joint destruction with lost sensation (diabetes -foot; syringomyelia -shoulder; tabes dorsalis -knee); the acute hot swollen foot needs urgent offloading (see the Vascular Surgery page).
- Pigmented villonodular synovitis (tenosynovial giant cell tumour) -young adults; recurrent blood-stained effusions in one joint (knee); MRI; synovectomy.
- Lyme arthritis -tick bite (UK -New Forest, Scottish Highlands, Lake District); erythema migrans, then large-joint arthritis (knee) weeks to months later; serology; doxycycline (see the Infectious Diseases chapter).
- Rheumatic fever -2–4 weeks after streptococcal throat infection; flitting large-joint polyarthritis (Jones criteria -carditis, chorea, erythema marginatum, nodules) -rare in the UK now.
- Hypertrophic pulmonary osteoarthropathy -clubbing with painful wrists and ankles (periosteal new bone) -lung cancer (especially adenocarcinoma), bronchiectasis, mesothelioma.
- Paget's disease of bone -older people, bone pain, deformity, raised ALP with normal calcium (see the Bone Medicine chapter).
Crystal, Degenerative and Pain Conditions at a Glance
| Condition | Key clues | Management |
|---|---|---|
| Acute gout | Sudden red hot big toe, peaks within 24 hours | NSAID, colchicine or steroid; ice; review diuretics |
| Chronic tophaceous gout | Tophi, recurrent flares, erosions | Allopurinol to urate under 300; colchicine cover |
| Pseudogout | Older person, hot knee, illness or surgery | Aspirate, intra-articular steroid; check metabolic causes if young |
| Crowned dens | Severe neck pain and fever in an older person | CT neck; NSAIDs or steroids |
| Calcific periarthritis | Sudden severe shoulder pain, calcium in tendon | NSAIDs, injection, barbotage |
| Knee or hip OA | Over 45, pain on use, stiffness under 30 min | Exercise, weight loss, topical NSAIDs; replacement if severe |
| Nodal hand OA | Heberden's and Bouchard's nodes | Hand exercises, splints, topical NSAIDs |
| Fibromyalgia | Widespread pain, fatigue, poor sleep, normal tests | Explanation, exercise, CBT, antidepressant; no opioids |
| Hypermobility spectrum disorder | Beighton 5+, pain, subluxations | Physiotherapy, pacing |
| Haemochromatosis arthropathy | 2nd/3rd MCP OA, CPPD | Ferritin and transferrin saturation |
| Avascular necrosis | Hip pain on steroids or alcohol, normal X-ray | MRI; offload, decompression or replacement |
| DISH | Flowing anterior ossification, normal SI joints | Analgesia, physio |
Spot the Diagnosis
| Clue | Diagnosis |
|---|---|
| Excruciating red big toe overnight after a wedding, on bendroflumethiazide | Acute gout |
| Normal urate during an attack of probable gout | Urate falls in flares -recheck in 2 weeks |
| Chalky white lumps on the ear helix | Gouty tophi |
| Rash and fever 4 weeks after starting allopurinol in CKD | Allopurinol hypersensitivity -stop |
| Severe diarrhoea and myalgia after clarithromycin in a man on colchicine | Colchicine toxicity |
| Flare of gout 2 weeks after starting allopurinol | Mobilisation flare -continue ULT, add colchicine cover |
| Hyperuricaemia, AKI and high potassium after chemotherapy for lymphoma | Tumour lysis syndrome |
| Hot knee 3 days after a hip operation in an 80-year-old | Pseudogout (exclude infection) |
| Chondrocalcinosis in a 45-year-old with diabetes and a bronze tan | Haemochromatosis |
| Neck pain, fever and high CRP in an 82-year-old with no meningism | Crowned dens syndrome |
| Sudden severe shoulder pain with calcium in the supraspinatus tendon | Acute calcific periarthritis |
| Knee pain on walking in a 62-year-old, 10 minutes' morning stiffness | Knee osteoarthritis -clinical diagnosis |
| Pain at the thumb base on opening jars | First CMC joint OA |
| Painful inflamed DIPs with central erosions and normal bloods | Erosive hand OA |
| Widespread pain, poor sleep and fatigue with normal examination and bloods | Fibromyalgia |
| Recurrent shoulder dislocations, Beighton 7/9 and dizziness on standing | Hypermobility spectrum disorder with POTS |
| Easy bruising, thin skin and a ruptured colon at 30 | Vascular Ehlers–Danlos syndrome |
| Stiff hands with a positive prayer sign in type 1 diabetes | Diabetic cheiroarthropathy |
| Hip pain with normal X-ray in a man on long-term prednisolone | Avascular necrosis -MRI |
| Flowing ossification on the right of the thoracic spine with normal SI joints | DISH |
| Recurrent blood-stained knee effusions in a 30-year-old | PVNS (tenosynovial giant cell tumour) |
| Clubbing with painful swollen wrists in a smoker | Hypertrophic pulmonary osteoarthropathy |
Exam-style Scenarios
1. A 56-year-old man on bendroflumethiazide has his third attack of gout this year. His urate (2 weeks after the flare) is 520 µmol/L; eGFR 70. He has no tophi.
Answer: Recurrent gout -start urate-lowering therapy.
- Start allopurinol 100 mg daily, increasing by 100 mg every month according to urate (checked monthly) to a target below 360 µmol/L.
- Give colchicine 500 micrograms once or twice daily as flare prophylaxis for up to 6 months; provide a rescue plan for flares.
- Switch the thiazide (e.g. to losartan or amlodipine); assess CV risk, HbA1c and lipids; advise on alcohol, sugary drinks and weight.
2. An 81-year-old woman is admitted with pneumonia. On day 3 she develops a hot, swollen right knee and fever. The knee X-ray shows chondrocalcinosis.
Answer: Probable acute CPP crystal arthritis -but infection must be excluded.
- Aspirate the knee -Gram stain, culture and crystals; blood cultures.
- If CPP crystals with no infection -aspiration plus intra-articular steroid; or a short oral steroid course (NSAIDs and colchicine are riskier at her age).
- Calcium and magnesium check; mobilise when settled.
3. A 67-year-old woman with a BMI of 33 has 2 years of right knee pain on walking and stairs, with 15 minutes of morning stiffness. The knee is bony and creaky with no effusion. She asks for an X-ray and "something strong for pain".
Answer: Knee osteoarthritis -clinical diagnosis.
- No X-ray needed for diagnosis (age over 45, activity-related pain, short stiffness).
- Exercise (strengthening -physio-led programme) and support for weight loss; topical NSAID; avoid strong opioids.
- Consider intra-articular steroid for a flare; refer for replacement if symptoms severely affect quality of life despite these.
4. A 42-year-old woman has 2 years of widespread aching, exhaustion, poor sleep and poor concentration. Examination shows tenderness everywhere but no joint swelling. FBC, CRP, TFTs, CK, calcium and vitamin D are normal. She has been prescribed codeine and pregabalin.
Answer: Fibromyalgia (chronic primary pain).
- Make a positive diagnosis and explain it; avoid further investigations (ANA, RF) without new features.
- Graded exercise, CBT or ACT, sleep hygiene, pacing; consider amitriptyline or duloxetine.
- Plan to taper and stop codeine and pregabalin (not recommended for chronic primary pain); screen for depression.
5. A 48-year-old man with chronic tophaceous gout has had flares despite allopurinol 300 mg for a year. His urate is 450 µmol/L. He has a kidney transplant and takes azathioprine.
Answer: Uncontrolled gout with a dangerous drug interaction.
- Allopurinol plus azathioprine risks severe marrow suppression -check FBC urgently and contact the transplant team.
- Options -switch azathioprine to mycophenolate (transplant team) and then titrate allopurinol to a target below 300 µmol/L (tophi); or specialist alternatives.
- Flares -steroids preferred (colchicine interacts with ciclosporin; NSAIDs harm the graft).
Key Points
- Gout -sudden red hot joint (often the big toe) peaking within 24 hours; crystals are needle-shaped and negatively birefringent.
- Urate may be normal during a flare -recheck at least 2 weeks later.
- Flares -NSAID (+ PPI), colchicine or short oral steroid; don't stop ULT during a flare.
- Offer ULT to all with gout -especially recurrent flares, tophi, CKD, diuretics, young onset.
- Allopurinol first -start low, increase monthly to urate under 360 (under 300 with tophi).
- Colchicine cover for up to 6 months when starting ULT.
- Allopurinol plus azathioprine -dangerous; colchicine plus clarithromycin -toxic.
- Febuxostat -caution in major cardiovascular disease.
- Pseudogout -older people, knee or wrist, during illness; rhomboid positive crystals; look for metabolic causes if young.
- Always exclude infection in a hot joint, even with known crystal disease.
- OA -clinical diagnosis over 45 with activity pain and stiffness under 30 minutes; no X-ray needed.
- OA treatment -exercise and weight loss first; topical NSAIDs; avoid paracetamol alone and strong opioids.
- Heberden's nodes at the DIPs, Bouchard's at the PIPs; thumb base OA is common.
- Fibromyalgia -positive diagnosis, exercise, CBT, antidepressants; avoid opioids and gabapentinoids.
- Hypermobility -Beighton score; watch for vascular EDS and Marfan syndrome.
- Avascular necrosis -steroids, alcohol, sickle cell; MRI if X-ray normal.
Guidelines and Further Reading
- NICE NG219: Gout -diagnosis and management
- BSR: Guideline for the management of gout
- EULAR: Recommendations for calcium pyrophosphate deposition
- MHRA Drug Safety Update: Febuxostat -increased risk of cardiovascular death
- NICE NG226: Osteoarthritis in over 16s -diagnosis and management
- ESCAPE-pain programme (exercise for knee and hip pain)
- NICE NG193: Chronic pain (primary and secondary) in over 16s
- ACR 2016: Revised fibromyalgia diagnostic criteria
- Ehlers–Danlos Society: 2017 International classification of EDS and hypermobility spectrum disorders
- BNF -for current doses