4 resultados para Philips LPC2292

em Aston University Research Archive


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Reports on the issues addressed at the Bar Council-Aimhigher widening participation conference, "How to get to the Bar" held at St Philips Chambers, Birmingham on July 12, 2010 and attended by 80 sixth form students.

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Unrepeatered 115.6 Gbit/s per channel WDM DP-QPSK transmission with novel URFL based amplification is demonstrated. Transmission of 1.4 Tb/s was possible in 350 km link and 2.2 Tb/s was achieved in 325 km without employing ROPA or speciality fibres.

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Unrepeatered 100 Gbit/s per channel wave-divisionmultiplexed dual-polarization-QPSK transmission with random distributed feedback fiber laser-based Raman amplification using fiber Bragg grating is demonstrated. Transmission of 1.4 Tb/s (14 × 100 Gbit/s) was possible in 352.8 km link and 2.2 Tb/s (22 × 100 Gbit/s) was achieved in 327.6 km without employing remote optically pumped amplifier or speciality fibers.

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troduct I on . An observational longitudinal study. P ur P ose . Assess the relationship between obstructive sleep apnoea (OSA) and DR cross-sectionally and longitudinally. M ethods . Adults with Type 2 diabetes mellitus (T2DM), who were re - cruited from a hospital-based diabetes clinic in the UK. Patients with pre-existing OSA, end-stage renal disease and non-diabetic retinopa - thy were excluded. OSA (apnoea hypopnea index ≥ 5 events/hour) was assessed by a single overnight home-based cardio-respiratory study (Alice PDX, Philips Respironics, USA). DR was assessed us - ing retinal images between 2007 and 2012. Sight threatening diabetic retinopathy (STDR) was defined as presence of pre-proliferative or proliferative DR, maculopathy or photocoagulation. Advanced DR was defined as pre-proliferative or proliferative DR. r esults . 199 patients were included (57.3% (n=114) men, 47.7% (n=95) White Europeans). STDR and OSA prevalence were 38.7% (n=77) and 62.8% respectively. A t b A sel I ne . STR prevalence was higher in patients with OSA (OSA+) compared to those without OSA (OSA-) [48.8% n=61 vs. 21.6% n=16, p<0.001]. After adjustment for confounders, OSA remained independently associated with STR (OR 3.7, 95% CI 1.6-8.9, p=0.006), maculopathy (OR 4.5, 95% CI 1.8-11.4, p=0.002) and advanced DR (OR 3.9, 95% CI 1.02-15.3, p=0.047). Mild and moderate to severe OSA were independently associated with STR and maculopathy and only moderate to severe OSA was associated with advanced DR following adjustment for con - founders. l ong I tud I n A lly . Over the follow-up period of (4.4±1 years), more OSA+ patients progressed from no or background DR to advanced DR (15.3% (n=17) vs. 3% (n=2), p=0.01). OSA was an independent pre - dictor of advanced DR development after adjustment for confounders (OR 6.6, 95% CI 1.2-35.1, p=0.03). OSA did not predict the develop - ment of maculopathy. c onclus I ons . OSA is independently associated with STR and predicts the development of preproliferative and proliferative DR. Intervention - al studies are needed to assess the impact of OSA treatment on DR.