Medicine chapters
Osteoarthritis
The commonest joint disease of older adults: why cartilage fails, which joints are hit, Heberden and Bouchard nodes, the classic X-ray signs, and a stepwise plan from weight loss to joint replacement.
- Osteoarthritis (OA) is a disease of the whole joint: cartilage loss plus bony reaction (osteophytes, sclerosis, cysts).
- It gives mechanical pain worse with use, short morning stiffness (under 30 minutes), crepitus and bony swelling; ESR, CRP, RF and ANA are normal.
- Treat symptoms, not the X-ray: weight loss, exercise, topical or oral NSAIDs, steroid injection for effusions, and joint replacement for severe disease.
On this page
Overview
Osteoarthritis (OA) is the most common form of arthritis. It is not simple "wear and tear". It is a disease of the whole joint: cartilage, the bone under it, ligaments, menisci, synovium and capsule all change.
Cartilage thins and cracks. The bone underneath reacts by becoming dense and growing bony spurs (osteophytes) at the joint edges. The result is a painful, stiff joint that works less well. In older people, OA of the knee and hip is a leading cause of disability.
Definition and types
- Primary OA: no underlying cause found. Often familial, especially the nodal hand form in women.
- Secondary OA: follows a known joint insult (see table below).
| Group | Causes of secondary OA |
|---|---|
| Earlier joint damage | Rheumatoid arthritis, gout, spondyloarthritis, septic arthritis, trauma, overuse |
| Bone disease | Paget disease, avascular necrosis (e.g. after steroids) |
| Metabolic | Cartilage calcification (pyrophosphate), haemochromatosis, acromegaly |
| Systemic | Haemophilia (repeated bleeds into joints), sickle cell disease, neuropathic joints |
| Developmental | Hip dysplasia, Perthes disease, slipped upper femoral epiphysis |
Risk factors
- Age and female sex (more common in women after about 55 years and around the menopause).
- Obesity: the strongest modifiable risk, mainly for knee and hand OA.
- Heredity: nodal and generalised OA run in families.
- Trauma: fractures into a joint, meniscal and cruciate tears (knee).
- Joint shape problems: hip dysplasia, hypermobility.
- Occupation and sport: farmers (hip), miners (hip, knee), repetitive sport.
- Osteoporosis is linked with a lower risk of OA.
Obesity and old knee injury (meniscus or cruciate tear) are the classic risk factors for knee OA.
Pathology (brief)
- Normal cartilage is mostly water with type II collagen and aggrecan (a proteoglycan).
- In OA, enzymes (matrix metalloproteinases) and cytokines (IL-1, TNF-alpha) break the matrix down faster than it is rebuilt.
- Cartilage surface fibrillates and ulcerates; exposed bone develops microfractures, cysts and sclerosis.
- New bone forms at the margins as osteophytes.
- Mild synovial inflammation is common, so flares can be warm and swollen.
Clinical features
Symptoms
- Pain on movement and weight-bearing, eased by rest (mechanical pain). Late disease may hurt at night.
- Morning stiffness lasting only minutes (usually under 30 minutes), and stiffness after inactivity ("gelling").
- Loss of function: walking, stairs, gripping.
- Usually slow onset and gradual worsening.
Signs
- Crepitus on movement.
- Bony (hard) enlargement of the joint.
- Reduced range of movement; deformity.
- Small effusion and mild warmth in flares.
- Muscle wasting (e.g. quadriceps) and instability.
Clinical patterns
Nodal hand OA
- Typical in women around the menopause, familial.
- Affects the DIP joints more than the PIP joints.
- Early phase: painful, red, swollen finger joints. This settles over months to years.
- Leaves hard bony lumps: Heberden nodes (DIP) and Bouchard nodes (PIP).
- Thumb base (first carpometacarpal) OA often coexists, giving the "squared hand" with an adducted thumb.
- Function is usually fairly well kept.
Heberden is Higher up the finger (distal, DIP); Bouchard is at the Base side (proximal, PIP). Alphabetical too: B before H, proximal before distal.
RA spares the DIP joints and hits MCP, PIP and wrist. OA does the reverse: it loves DIP, PIP and thumb base and spares the MCPs and wrist (except the first carpometacarpal joint).
Knee OA
- Common, often bilateral, strongly linked with obesity.
- The medial compartment is affected most, giving a varus (bow-legged) deformity.
- The patellofemoral joint is often involved (pain on stairs and rising from a chair).
- A Baker (popliteal) cyst may form behind the knee; if it ruptures, calf pain and swelling mimic DVT.
Hip OA
- Pain in the groin, sometimes felt in the thigh or knee.
- Internal rotation is lost first.
- Superior-pole disease is commoner in men and often one-sided; medial disease is commoner in women with hand OA.
Other patterns
- Spine: facet joint OA and disc degeneration (spondylosis); may narrow the canal or root foramina.
- Erosive OA: rare, inflamed DIP and PIP joints with central erosions ("gull-wing" X-ray look).
- Crystal-associated OA: calcium pyrophosphate deposition, typical in the knee and wrist of elderly women.
- Generalised OA: hands plus knees, hips, first MTP and spine.
Investigations
| Test | Finding in OA |
|---|---|
| ESR and CRP | Normal (CRP may be very slightly raised) |
| Rheumatoid factor and ANA | Negative |
| Plain X-ray | Loss of joint space, Osteophytes, Subchondral sclerosis, Subchondral cysts |
| Standing knee X-ray | Shows true cartilage loss under load |
| MRI | Meniscal tears, early cartilage loss, bone marrow lesions |
| Joint aspirate | Viscous, clear fluid with few white cells |
OA X-ray = LOSS: Loss of joint space, Osteophytes, Subchondral sclerosis, Subchondral cysts.
Blood tests are normal in OA. A raised ESR or positive RF should make you think of another diagnosis (or coincidental age-related RF positivity).
X-ray severity and pain do not match well. Some people with bad X-rays have little pain, and quadriceps weakness and low mood predict knee pain better than the X-ray.
Differential diagnosis
| Feature | Osteoarthritis | Rheumatoid arthritis |
|---|---|---|
| Age | Older | Often 30–50 years |
| Morning stiffness | Minutes | Hours (over 30 minutes) |
| Joints | DIP, PIP, thumb base, knee, hip | MCP, PIP, wrist, MTP; DIP spared |
| Swelling | Hard, bony | Soft, boggy (synovitis) |
| ESR/CRP | Normal | Raised |
| RF / anti-CCP | Negative | Usually positive |
| X-ray | Osteophytes, sclerosis, narrowing | Juxta-articular osteopenia, marginal erosions |
Also consider gout or pseudogout (acute hot joint), psoriatic arthritis (DIP joints with nail changes) and referred pain (hip pain felt in the knee).
Management
The aim is to relieve pain and keep function. Treat the patient's symptoms, not the X-ray.
1. Education and lifestyle (for everyone)
- Explain the condition; reassure that it is not always progressive.
- Weight loss if overweight: even a small loss reduces knee load and pain.
- Exercise: quadriceps and hip strengthening, land-based programmes, hydrotherapy.
- Walking stick held in the hand opposite the painful hip or knee; good footwear and insoles.
2. Drugs
- Topical NSAIDs (good for knee and hand) or oral NSAIDs/coxibs, used intermittently at the lowest effective dose.
- With an oral NSAID in older patients or those with dyspepsia, add a proton pump inhibitor.
- Paracetamol has only a small effect but is still used as a simple add-on.
- Topical capsaicin as an extra.
- Intra-articular corticosteroid for a painful flare with effusion; short-term benefit; avoid frequent repeats in one joint.
- Opioids: last resort, with care in the elderly.
- Glucosamine and chondroitin: no meaningful benefit. Hyaluronic acid injections: limited benefit.
No drug has been shown to stop or reverse OA. Long-term high-dose aspirin or NSAIDs in OA patients can cause gastric ulcers and bleeding.
3. Surgery
- Total hip or knee replacement (arthroplasty) for severe pain or disability despite other measures. It greatly improves pain and function.
- Main serious risks: venous thromboembolism and infection.
- Others: unicompartmental knee replacement, realignment osteotomy, joint fusion (e.g. first MTP), excision arthroplasty of the thumb base.
- Arthroscopic washout of an OA knee rarely helps.
Complications and prognosis
- Progressive pain, deformity and loss of independence.
- Falls and reduced mobility; depression.
- Drug side effects (NSAID gastric and renal damage).
- Many patients stay stable for years; X-ray changes do not always worsen.
Expect: Heberden versus Bouchard nodes, the X-ray signs (joint space narrowing, osteophytes, subchondral sclerosis and cysts), normal ESR and negative RF, short morning stiffness compared with RA, medial knee compartment and varus deformity, causes of secondary OA (haemochromatosis, acromegaly, haemophilia, Paget), obesity as the key modifiable risk, NSAID gastric ulcers, and the place of weight loss, exercise, steroid injection and joint replacement.
Quick revision
- OA = whole-joint disease; cartilage loss plus bony overgrowth.
- Pain worse with use; stiffness lasts minutes.
- DIP = Heberden; PIP = Bouchard; thumb base gives the squared hand.
- X-ray: LOSS (narrowing, osteophytes, sclerosis, cysts).
- ESR, CRP, RF, ANA normal; aspirate viscous with few cells.
- Knee: medial compartment, varus deformity, Baker cyst.
- Weight loss and exercise first; topical/oral NSAIDs; steroid injection for effusion.
- Severe disease: joint replacement.
Written by The House Job from standard references (Kumar and Clark's Clinical Medicine; Apley's System of Orthopaedics and Fractures).
FAQ
What is the difference between Heberden and Bouchard nodes?
Both are bony swellings from osteophytes in hand OA: Heberden nodes are at the distal interphalangeal joints and Bouchard nodes at the proximal interphalangeal joints.
Are blood tests useful in osteoarthritis?
Mainly to exclude other diseases. ESR and CRP are normal or only slightly raised, and rheumatoid factor and ANA are negative.
Which knee compartment is usually affected in OA?
The medial compartment, which produces a varus (bow-legged) deformity.
Do glucosamine supplements help osteoarthritis?
No. Studies show no clinically useful effect on pain or on joint space narrowing.
When is joint replacement offered?
When pain and loss of function remain severe despite weight loss, exercise and drug treatment.