The Aspen® Lumbosacral Bracing System™ provides superior motion restriction, increased comfort, and better patient outcomes. A complete set consists of four LSO sizes and three TLSO upgrade kits.
Code L0462 Approved
Modular Design
The modular design of the Aspen® Lumbosacral Bracing System™ lets you progressively tailor the amount of motion restriction to the changing needs of each patient. By removing the shoulder straps, torso control straps, or the padded chest panel, the system can be “stepped down” to parallel the overall progress of the patient.
Rigid Layered Support
Forms a structurally rigd polyethylene cylinder that restricts motion, yet is easy to trim or shape while on the patient.
VectorPoint™ Chest Panel
Adjusts to the height and profile of each patient. This padded chest panel anchors the front and back of the brace to an anterior vector point in teh upper thoracic region.
Torso Control Straps
Further limit flexion and rotation by linking the padded chest panel to a second location on the back brace.
Easy LeverLatch™ Closure
Gives the patient a strong mechanical advantage to easily and effectively tighten the orthosis for better immobilization and pain relief.
CushionFlex Tabs™
Soften the edges of the orthosis. Can be cut to further splay outward or trimmed back for better comfort.
Product Info Sheets contain specific product dimensions, product accessories, and catalog numbers.
READ INSTRUCTIONS BEFORE USE. Proper training in the use of this device should take place before it is applied. These directions are guidelines only and are not offered as medical recommendations.
THIS PRODUCT IS INTENDED FOR APPLICATION BY LICENSED HEALTH CARE PRACTITIONERS AS DIRECTED BY A PHYSICIAN OR OTHER QUALIFIED MEDICAL AUTHORITY. PERMANENT INJURY MAY RESULT FROM USE OTHER THAN AS DIRECTED BY A PHYSICIAN OR OTHER MEDICAL AUTHORITY. ASPEN MEDICAL PRODUCTS SPECIFICALLY DISCLAIMS ANY OBLIGATION OR LIABILITY FOR INJURY OR DAMAGE BY REASON OF ANY APPLICATION OF THIS PRODUCT. PLEASE SEE THE ACCOMPANYING LIMITED WARRANTY FOR FURTHER INFORMATION IN THIS REGARD.
Comparison of Motion Restriction and Trunk Stiffness Provided by Three Thoracolumbosacral Orthoses (TLSOs)Krag, MH; Fox, MS, J; Haugh, LD AbstractSTUDY DESIGN: Four conditions (three orthoses, one no orthosis), full cross-over, randomized order, 12 subjects tested 3 months after a lumbar surgical arthrodesis. OBJECTIVES: To assess whole torso and lumbar motions and comfort for each orthoses condition during performance of activities of daily living. SUMMARY OF BACKGROUND DATA: Previous noninvasive studies measured whole torso (not just lumbar) movement. Recent development of a low profile, flexible, strain-gauged device ("Lordosimeter") facilitated this study. MATERIALS AND METHODS: The Lordosimeter was taped to the skin along the midline of the lumbosacral region. Orthoses studied were Boston anterior opening, Aspen lumbosacral, and Cybertech. Specified activities of daily living were performed for each orthosis condition. Subject effort during the flexion/extension task was assessed by surface electromyography (EMG). Comfort was assessed by visual analog scale. RESULTS: There were no significant differences in EMG between orthoses. For lumbar flexion, trunk flexion, total lumbar motion, and total trunk motion, the mean values for Aspen and Boston (but not Cybertech) were significantly smaller than for no orthosis for most of the tasks and there were no significant differences between Aspen and Boston. The total lumbar motion allowed by each orthosis (averaged across tasks and relative to the no orthosis condition) was 81% for Aspen, 79% for Boston, and 97% for Cybertech. The comfort rating averaged across tasks was 2.24 for Aspen, 4.12 for Boston, and 3.92 for Cybertech (0 = very comfortable, 10 = very uncomfortable). Aspen was significantly more comfortable than Boston or Cybertech. Boston and Cybertech did not differ significantly. CONCLUSIONS: The Lordosimeter is useful for measuring lumbar motion during orthosis wear. The Aspen and the Boston orthoses provided significant flexion-extension motion restriction compared with no orthosis, but for almost all of the motion measures did not differ from each other. The Cybertech did not differ significantly from the no orthosis condition. The Aspen orthosis was rated significantly more comfortable than the Boston or the Cybertech. Selected Quotations
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The Incidence of Skin Breakdown Associated with Use of Cervical CollarsPowers, J; Daniels, D; McGuire, C; Hilbish, C AbstractThe most common adverse complication associated with cervical immobilization is skin breakdown. The purpose of this prospective, descriptive study was to assess the incidence of tissue breakdown associated with cervical immobilization. In this convenience sample of 484 patients, skin breakdown was noted in 33 (6.8%) patients. All cases of documented skin breakdown were stage I or II, with only 2% (0.4%) patients having stage III breakdown. Days in cervical collar is a significant predictor of skin breakdown, along with presence of edema. Results from this study demonstrate that there is a very low incidence of complications of skin breakdown associated with the use of Aspen cervical collars. The collars are safe and effective to use in patients with actual or suspected head or spine injuries. Selected Quotations
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| Short/Small Pads | 991035 |
| Short/Large Pads | 991036 |
| Tall/Small Pads | 991075 |
| Tall/Large Pads | 991076 |
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