A progressive fibrotic condition of the palmar fascia in which thickened cords pull the fingers towards the palm, gradually limiting their extension. Most commonly affects the ring and little fingers.
📊 Dupuytren contracture affects around 4% of the UK adult population and up to 20% of people of Northern European descent over the age of 65. It is strongly familial and is sometimes called "Viking disease".
In the palm lies a thin sheet of fibrous tissue called the palmar fascia, which lies just under the skin. In Dupuytren disease, this fascia thickens and shortens, forming nodules and then dense cords that progressively pull the fingers down towards the palm. The condition is painless in itself, but as the cords tighten, the fingers can no longer be fully straightened, making it difficult to put the hand flat on a table, into a pocket, or to shake hands properly.
It is a slow disease, sometimes progressing over decades. Many people have firm nodules in the palm for years before any contracture develops, and some never progress at all. There is a strong genetic component, and it is most common in older men of Northern European descent. It can also affect the soles of the feet (Ledderhose disease) and the penis (Peyronie disease).
Treatment is only offered when the contracture starts to affect hand function. There is no good evidence that any treatment cures the underlying disease, all treatments aim to break or remove the affected cord, knowing that the disease may recur in time. Three main options are available: needle fasciotomy, collagenase injection, and surgical fasciectomy, each with different recovery profiles and recurrence rates.
Who is at risk? A first-degree relative with Dupuytren is the single strongest risk factor. Other risks include male sex, age over 50, Northern European descent, diabetes, smoking, and heavy alcohol use. Onset before age 50, bilateral disease, and involvement of the knuckles (Garrod pads) or feet indicate a more aggressive form ("Dupuytren diathesis").
Symptoms vary depending on the severity and duration of the condition. Common symptoms include:
When to seek help: See your GP or hand specialist if you can no longer place your hand flat on a table, if a finger is significantly bent, or if the condition is starting to affect your daily activities. Painful nodules are uncommon and warrant earlier review.
Your hand surgeon will take a detailed history and examine the hand and wrist. The following investigations may be arranged to confirm the diagnosis:
The threshold for intervention is traditionally a metacarpophalangeal (MCP) joint contracture of 30 degrees or more, or any proximal interphalangeal (PIP) joint contracture. PIP contractures are harder to correct and tend to recur, so are often treated earlier.
Treatment is tailored to the severity of the condition, your age, activity level, and overall health. Most conditions are treated in a stepwise fashion, starting with the least invasive options.
For early disease with palpable nodules or cords but minimal contracture, no treatment is needed. Patients are reassured and advised to seek review if the hand begins to lose function. There is no evidence that splinting, stretching or any topical treatment alters the course of the disease.
A clinic procedure under local anaesthetic in which a needle is used to weaken and divide the cord, which is then snapped manually. Quick recovery (back to normal use within days) and minimal scarring. Best suited to straightforward MCP joint contractures with a clear, well-defined cord. Higher recurrence rate than open surgery.
Collagenase clostridium histolyticum is injected into the cord, which is then manipulated 24-48 hours later to break it. Comparable results to needle fasciotomy. Availability has changed in recent years, this option is not routinely available in the UK at present.
Surgical removal of the diseased cord through a zig-zag incision in the palm and finger. Considered the gold standard, particularly for PIP contractures, recurrent disease, or where the cord is complex. Longer recovery (4-12 weeks) and more involved scarring, but the lowest recurrence rate of the available treatments.
After needle fasciotomy patients are back to most activities within a week. After open surgery the hand is splinted for two weeks, then hand therapy begins, this is a key part of the recovery and not optional. Night splints are often used for several months. Some stiffness, tenderness and scar sensitivity is normal in the first three months.
Most patients achieve excellent correction with any of the available techniques. Recurrence is the major issue: roughly 50-60% by 5 years after needle fasciotomy, lower after open surgery. Patients with strong Dupuytren diathesis tend to recur faster. Younger patients with aggressive disease may need repeated treatment over the course of their lives.
Typical activity timelines for this condition. These are approximate and vary considerably between patients. Always follow the specific guidance given by your surgeon and hand therapist.
| Activity | Typical timeline | Notes |
|---|---|---|
| Drive | 1-2 weeks after fasciectomy | When grip is comfortable and any splint allows safe steering wheel control. Earlier after needle fasciotomy.[3] |
| Shower | When dressing is waterproof | Keep the wound dry until healed. |
| Light hand use | Day 1 | Gentle finger movement starts immediately under hand therapy guidance, this is critical for results.[2] |
| Desk work | 1-2 weeks after fasciectomy | Light desk work usually possible once the dressing is smaller. Earlier after needle fasciotomy.[1] |
| Manual work | 6-12 weeks after fasciectomy | Heavy gripping waits until the wound has healed and strength has returned. Earlier after needle fasciotomy.[1] |
| Wear night splint | Several months | A night extension splint may be advised for 3-6 months after surgery to maintain the correction.[2] |
| Full hand function | 3-6 months | Most patients have settled scar and good function by 3-6 months. Some tenderness may persist longer.[1] |
Common concerns from patients with this condition or recovering from treatment, and whether they are expected or worth mentioning to your team.
References are to UK clinical guidance and patient information from recognised organisations. This page is for general information and does not replace personalised advice from your own clinical team.
If your team has recommended an operation for this condition, our step-by-step prep guide covers what to expect.
Phased exercise programme, key precautions, and what to expect from rehabilitation for this condition.