The carpal tunnel is a fibro-osseous structure formed by the carpal bones interconnected by numerous ligaments. The eight irregularly shaped carpal bones are intricately arranged with the intercarpal ligaments to establish the medial, lateral, and dorsal boundaries of the tunnel. The proximal row of the carpal bones consists of the pisiform, triquetrum, lunate, and scaphoid, while the distal row comprises the hamate, capitate, trapezoid, and trapezium. The volar aspect of the carpal tunnel is spanned by the transverse carpal ligament (TCL). This band of fibrous tissue inserts radially into the scaphoid tuberosity and trapezial ridge, and ulnarly into the pisiform and the hook of the hamate. The thenar and hypothenar muscles are an integral part of the carpal tunnel structure, because the TCL serves as attachment sites for these hand muscles, 1,2 and contraction of these muscles causes biomechanical interactions with the carpal tunnel via the TCL. 3
AbstractThe transverse carpal ligament (TCL) is a significant constituent of the wrist structure and forms the volar boundary of the carpal tunnel. It serves biomechanical and physiological functions, acting as a pulley for the flexor tendons, anchoring the thenar and hypothenar muscles, stabilizing the bony structure, and providing wrist proprioception. This article mainly describes and reviews our recent studies regarding the biomechanical role of the TCL in the compliant characteristics of the carpal tunnel. First, force applied to the TCL from within the carpal tunnel increased arch height and area due to arch width narrowing from the migration of the bony insertion sites of the TCL. The experimental findings were accounted for by a geometric model that elucidated the relationships among arch width, height, and area. Second, carpal arch deformation showed that the carpal tunnel was more flexible at the proximal level than at the distal level and was more compliant in the inward direction than in the outward direction. The hamate-capitate joint had larger angular rotations than the capitate-trapezoid and trapezoid-trapezium joints for their contributions to changes of the carpal arch width. Lastly, pressure application inside the intact and released carpal tunnels led to increased carpal tunnel cross-sectional areas, which were mainly attributable to the expansion of the carpal arch formed by the TCL. Transection of the TCL led to an increase of carpal arch compliance that was nine times greater than that of the intact carpal tunnel. The carpal tunnel, while regarded as a stabile structure, demonstrates compliant properties that help to accommodate biomechanical and physiological variants such as changes in carpal tunnel pressure.