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Implants were chosen to guarantee primarily the rotational stability.
Bicon system implants were chosen because of availability and previous experience with this brand.
These implants were chosen because of availability and previous experience with this brand.
Four fixed bearing implants were chosen: PFC (DePuy), PFC Sigma (DePuy), NexGen (Zimmer) and Genesis II (Smith & Nephew).
As already described, 88 women (Groups 1 and 3) enrolled into FDA and NIH protocols investigating the pathogenesis of CTD following silicone implants were chosen for study on the basis of the presence of documented silicone implants and an available serum sample collected for research purposes.
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For this particular study, complete bone-supported design with the two implants was chosen.
Dependent on the malunion, one of the following implants was chosen by the surgeon: A 2.7 mm LCP plate (Synthes, Solothurn, Switzerland), a 2.7 mm LCP ulnar shortening osteotomy plate (Synthes), a 2.4 mm LCP distal radius plate (Synthes), or an Elegantus distal radius plate (Intercus Schweiz GmbH, Aarau, Switzerland).
The dimension of the implants was chosen based on results from previous studies conducted in birds of similar body mass that reported a physiological increase of steroids after implantation (Soma et al. 2000; Tramontin et al. 2003; Hunt and Wingfield 2004).
For our study, the patients were carefully selected, and only young patients with an anatomy believed to be suitable for this special implant were chosen.
Normally the two most central sections from each implant were chosen for analysis, and buccal and lingual surfaces were measured separately.
The appropriate implant was chosen by preoperative templating.
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