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Delta III Reverse-Ball-and-Socket Total Shoulder Prosthesis

1. Nyfeller, RW, et al. "Biomechanical Relevance of Glenoid Component Positioning in the Reverse Delta III Prosthesis." Journal Shoulder Elbow Surgery 2005 Sept-Oct; 14(5): 524-528. 2. Middernacht, BO, et al. "Anatomy of the Glenoid: Consequences For Implantation of the Reverse Prosthesis."

Analysis of a retrieved Delta III total shoulder prosthesis.

The authors report on their experience in revision total shoulder arthroplasty using the Delta III® shoulder prosthesis, a reversed constrained prosthe-sis which is known to give good functional results in the rotator cuff-deficient shoulder. It was implanted in patients with a failed total or hemishoulder pros-thesis. The Constant-Murley score was used to assess the functional outcome. The preliminary results achieved in four patients (one bilaterally) are dis-cussed and compared with the results of other treat-ments. After two years follow-up, the Constant-Murley score has improved from 14/100 preopera-tively to 62/100 postoperatively. Although these ini-tially good functional results may be temporary and loosening may occur over the longer term, the authors recommend the Delta III ® shoulder prosthe-sis as an alternative solution for revision shoulder arthroplasty.

the Delta III reverse prosthesis ..

The reverse shoulder prosthesis (Delta III) in acute shoulder fractures: technical considerations with respect to stability.

New clinical trial results from the Argus II Study Group, an international consortium of eye and vision researchers, confirm that the Argus II, also called the "bionic eye," is a safe, reliable, and effective device that "significantly improves visual function and quality of life for people blinded by retinitis pigmentosa." The latest research, entitled Long-Term Results from an Epiretinal [i.e, "on," "upon," "near," or "against" the retina] Prosthesis

Second Sight Medical Products, Inc., of Sylmar, California, has announced that its Argus® II Retinal Prosthesis System, also called the "artificial retina" or "bionic eye," will be offered in 12 implantation centers across the United States to treat patients with severe to profound retinitis pigmentosa (RP). The mission of Second Sight is to "develop, manufacture, and market implantable visual prosthetics to enable blind individuals to achieve greater independence."

with the Delta III reverse shoulder prosthesis.

“The Reverse Shoulder Prosthesis (Delta III) in Acute Shoulder Fractures: Technical Considerations with Respect to Stability.”  72 (2006): 474–477.

On February 14, 2013, Second Sight Medical Products, Inc. received approval from the U.S. Food and Drug Administration (FDA) for the Argus II Retinal Prosthesis System, also called the "artificial retina" or "bionic eye." The mission of Sylmar, California-based Second Sight is to "develop, manufacture, and market implantable visual prosthetics to enable blind individuals to achieve greater independence." The Argus II has been approved to treat adults with severe to profound

During the past several years, there has been much "buzz" in the popular press about the capabilities of the so-called "bionic" eye, described variously as "miraculous," "restoring sight," and "letting me see again." At VisionAware, we have followed the development of "bionic" or "prosthetic" vision closely, avoiding hyperbole and striving to report factual, research-based information about the limitations of restored vision. Now, in this month's edition of the Journal of Vision Impairment & Blindness, two researchers who are pioneers in the study of prosthetic vision analyze the current state of the art in

in the reverse Delta III total shoulder prosthesis J ..
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