Trigger finger: etiology, evaluation, and treatment
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- Makkouk, A.H., Oetgen, M.E., Swigart, C.R. et al. Curr Rev Musculoskelet Med (2008) 1: 92. doi:10.1007/s12178-007-9012-1
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Trigger finger is a common finger aliment, thought to be caused by inflammation and subsequent narrowing of the A1 pulley, which causes pain, clicking, catching, and loss of motion of the affected finger. Although it can occur in anyone, it is seen more frequently in the diabetic population and in women, typically in the fifth to sixth decade of life. The diagnosis is usually fairly straightforward, as most patients complain of clicking or locking of the finger, but other pathological processes such as fracture, tumor, or other traumatic soft tissue injuries must be excluded. Treatment modalities, including splinting, corticosteroid injection, or surgical release, are very effective and are tailored to the severity and duration of symptoms.
KeywordsTrigger fingerConservative treatmentPercutaneous releaseSurgical management
The malady trigger finger earns its name from the painful popping or clicking sound elicited by flexion and extension of the involved digit. First described by Notta in 1850 , it is caused by a difference in diameters of a flexor tendon and its retinacular sheath due to thickening and narrowing of the sheath. Though often referred to as stenosing tenosynovitis [2–4], histologic studies have shown that the pathologic inflammatory changes localize specifically to the tendon sheath (tendovagina) and not the tenosynovium . In light of this, the term tendovaginitis has been proposed as a more appropriate description of trigger finger .
Due to its location, the A1 pulley is subjected to the highest forces and pressure gradients during normal as well as power grip . The repeated friction and resulting intratendious swelling caused by movement of the flexor tendon through the A1 pulley has been compared to the fraying at the ends of a string after repeated threading through the eye of a needle . Microscopic examination of trigger A1 pulleys have long shown degeneration and inflammatory cell infiltrate , but recent ultrastructural comparisons of normal and trigger A1 pulleys may have elucidated what may be a key phase in the pathogenesis of trigger finger. Studies using scanning and transmission electron microscopes to examine the gliding surface of the A1 pulleys demonstrated that normal specimens had an amorphous extracellular matrix, including chondrocytes, coating the pulley’s entire innermost layer. Pathologic samples had a similar general appearance, but with varying sized and shaped areas of extracellular matrix loss. These areas were characterized by chondrocyte proliferation and type III collagen production . It has thus been postulated that this fibrocartilagenous metaplasia results from the repeated friction and compression between the flexor tendon and the corresponding inner layer of the A1 pulley .
Several causes of trigger finger have been proposed, though the precise etiology has not been elucidated. Understandably, repetitive finger movements and local trauma are possibilities [13–15], with such stress and degenerative force also accounting for an increased incidence of trigger finger in the dominant hand [8, 16]. There are reports linking trigger finger to occupations requiring extensive gripping and hand flexion, such as use of shears or hand held tools [5, 14, 17]. This relationship is questionable, however, with studies finding no association between trigger finger and the workplace [18, 19]. In reality the causes of trigger finger are multiple and in each individual often multifactorial.
Primary trigger finger occurs most commonly in the middle fifth to sixth decades of life and up to 6 times more frequently in women than men [5, 7, 16, 20], although the reasons for this age and sex predilection are not entirely clear . The lifetime risk of trigger finger development is between 2 and 3%, but increases to up to 10% in diabetics [22, 23]. The incidence in diabetics is associated with actual duration of the disease, not with glycemic control . This also appears to be a higher risk for trigger finger development in patients with carpal tunnel syndrome, de Quervain’s disease, hypothyroidism, rheumatoid arthritis, renal disease, and amyloidosis [24–27]. The ring finger is most commonly affected, followed by the thumb (trigger thumb), long, index, and small fingers in patients with multiple trigger digits [21, 28].
The initial complaint associated with trigger finger may be of a painless clicking with digital manipulation. Further development of the condition can cause the catching or popping to become painful with both flexion and extension, and be related as occurring at either the metacarpophalangeal (MCP) or PIP joints. Other patients may notice a feeling of stiffness and then progressive loss of full flexion and/or extension of the affected digit without ever developing the catching and locking of a “typical” trigger finger. A painful nodule, a result of intratendinous swelling, may be palpated in the palmar MCP area. The patient may report MCP stiffness or swelling in the morning, or that they awaken with the digit locked and that it loosens throughout the day. A history of recent trauma to the area may also be reported. With continued deterioration the finger may present locked in flexion, requiring passive manipulation to achieve full extension. This occurs because the flexor mechanisms of the digit are generally strong enough to overcome the restrictive and narrowed retinacular sheath, while the extensors are not. Over time, the patient’s desire to avoid the painful triggering caused by manipulation or use of the involved digit may lead to the development of secondary PIP contractures and digital stiffness.
The classic presentation of popping and locking of a trigger finger is typically all that is needed for diagnosis; however, with acute onset of symptoms patients may present with pain and swelling over the involved flexor sheath with avoidance of finger motion. In these cases, the classic popping and triggering are not seen and the diagnosis of trigger finger must be differentiated from infection or some other traumatic injury. If desired, the diagnosis may be confirmed with an injection of lidocaine into the flexor sheath, which should relieve the pain associated with the triggering and allow the digit to become actively or passively extended. There is no role for imaging in diagnosis, with x-rays considered unnecessary in patients without history of inflammatory disease or trauma .
The finding of a locking digit is not unique to trigger finger, and can be associated with dislocation, Dupuytren’s contracture, focal dystonia, flexor tendon/sheath tumor, sesamoid bone anomalies, post-traumatic tendon entrapment on the metacarpal head, and even hysteria. The differential diagnosis of pain at the MCP joint includes de Quervain’s tenosynovitis (for trigger thumb only), ulnar collateral ligament injury of the thumb (gamekeeper’s thumb), MCP joint sprain, extensor apparatus injury, and MCP osteoarthritis [30–34]. Imaging with ultrasound or MRI may help with these diagnoses in atypical presentations of trigger finger.
Initial management of trigger finger is conservative and involves activity modification , non-steroidal anti-inflammatory drugs for pain control, MCP joint immobilization, and corticosteroid injection.
The goal of splinting is to prevent the friction caused by flexor tendon movement through the affected A1 pulley until the inflammation there resolves . It is generally considered that splinting is an appropriate treatment option in patients who refuse or wish to avoid corticosteroid injection. A study of manual workers with distal interphalangeal (DIP) joint splints in full extension for 6 weeks demonstrated abatement of symptoms in over 50% of the patients . In another study, splints of the MCP joint at 15 degrees of flexion (leaving the PIP and DIP joints free) were shown to provide resolution of symptoms in 65% of patients at 1-year follow-up . For patients who are most bothered by symptoms of locking in the morning, splinting the PIP joint at night can be effective. Splinting yields lower success rates in patients with severe triggering or longstanding duration of symptoms.
Operative treatment, whether by percutaneous or open release, is highly successful and widely regarded as the ultimate treatment for trigger finger. Indication for surgical treatment is generally failure of conservative treatment to resolve pain and symptoms. The timing of surgery is somewhat controversial with data suggesting surgical consideration after failure of both a single as well as multiple corticosteroid injections [44, 45].
The percutaneous trigger finger release has been described and was first introduced by Lorthioir in 1958 . In this procedure, the MCP joint is hyperextended with the palm up, thus stretching out the A1 pulley and shifting the neurovascular structures dorsally. After ethyl chloride is sprayed and lidocaine injected for pain management, a needle is inserted through the skin and onto the A1 pulley. It is then swept to slice the pulley proximal and distal to the injection site. Success rates have been reported as over 90% with this procedure ; however, use of this technique is tempered by the risk of digital nerve or artery injury. Other complications, including tendon bowstringing, infection, and pain are less common [47–49].
Trigger finger is a long recognized condition characterized by a sometimes painful locking of the digit on flexion and extension. It is caused by the inflammation and subsequent narrowing of the A1 pulley through which the flexor tendon passes at the metacarpal head, leading to restricted movement of the tendon through the pulley. It is much more common in women than men, may be related to occupations involving constant gripping or repetitive local trauma and appears to be associated with systemic inflammatory diseases. The diagnosis is typically made by the characteristic presentation and findings on exam, and first-line treatment includes splinting and corticosteroid injections. Surgical management of this condition is indicated with recurrence after or failure of conservative management or initially in cases of >6 months duration and is highly effective with low complication and recurrence rates.