The Global Spinal Osteosynthesis Units Market is driven by rising spinal disorders
Spinal osteosynthesis units are medical devices used for treating spinal fractures and stabilizing the spinal column. They are made of metallic implants like plates, screws, rods or cages that provide internal fixation and support to the injured vertebrae. Spinal osteosynthesis involves surgically placing these implants across the spinal segment with injuries to immobilize and join the bones as they heal. It allows early mobilization of patients and alleviates pain caused by unstable spinal fractures. The devices find application in treating traumatic fractures due to accidents or falls, compression fractures from osteoporosis, and correcting deformities. The procedure is a minimally invasive alternative to spinal fusion and helps patients regain mobility faster.
The Spinal Osteosynthesis Units Market is estimated to be valued at USD 10.25 billion in 2024 and is expected to reach USD 19.50 billion by 2031, growing at a compound annual growth rate (CAGR) of 8.2% from 2024 to 2031.
Market Drivers
Rising incidence of spine injuries and spinal deformities associated with lifestyle diseases and aging population is a key driver for the Spinal Osteosynthesis Units Market. Spinal fractures account for over 30% of all injury-related hospitalizations globally. Moreover, the growing obese and geriatric population prone to osteoporosis and spinal issues will augment the need for corrective spinal surgeries using osteosynthesis implants during the forecast period.
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Acellular dermal matrix, commonly referred to as ADM, is a soft tissue reinforcement material used in plastic and reconstructive surgery procedures. ADM is created by processing donated human dermal tissue to remove cellular components while preserving the natural collagen structure and biochemical constituents within the dermis. This processing allows the ADM graft to integrate with the recipient's tissues without eliciting an immune reaction or being rejected.
How ADM is Produced
To produce Acellular Dermal Matrices grafts, donated human dermal tissue is subjected to a multi-step process that removes cellular material through chemical or enzymatic means. The precise processing methods vary depending on the specific ADM product, but they all utilize controlled methods such detergents, acids, or enzymatic treatments to eliminate cellular debris while retaining the innate extracellular matrix structure. This decellularization process leaves behind the acellular collagen matrix, growth factors, and biochemical cues that facilitate host tissue ingrowth and integration. The processed acellular dermal grafts can then be prepared in sheet or particulate forms suitable for a variety of reconstructive uses.
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