Purpose: To evaluate pulse type technology used to remove lens fragments during phacoemulsification.
Setting: John A. Moran Eye Center Laboratories, University of Utah, Salt Lake City, Utah, USA.
Design: Experimental study.
Methods: Lens nuclei soaked in 10 mL of 10% neutral buffered formalin for 2 hours were placed in 10 mL of balanced salt solution. Lenses were cut into 2 mm × 2 mm cubes; no more than 36 hours later, cubes were randomly selected for testing. Two aspiration and 2 vacuum settings were assessed at moderate- and high-flow and vacuum (30 mL/min and 300 mm/Hg, low-flow vacuum; 50 mL/min and 500 mm/Hg, high-flow vacuum), with continuous 50 milliseconds on and off (long pulse) and 6 milliseconds on and off (micropulse) ultrasound.
Results: There was a significant difference in efficiency favoring micropulse compared with combined long pulse and continuous pulse in high-flow vacuum at 80% power (P = .018) and between combined long pulse and continuous pulse versus micropulse in high-flow vacuum at 20% power (P = .019). Low-flow vacuum micropulse was more efficient than continuous (19.7%) (P < .0001) and long pulse (22.7%) (P < .0001). Continuous and long pulses were not significantly different from one other. There was a significant difference in chatter rates between high-flow vacuum and low-flow vacuum when all results were compared (P < .0001), with no additional significant differences found.
Conclusion: Micropulse technology was better than continuous and long pulse at moderate but not high-flow and vacuum settings. At the higher setting, chatter was observed less often, with all modalities more efficient than the lower setting.
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http://dx.doi.org/10.1016/j.jcrs.2015.06.030 | DOI Listing |
Ann Biomed Eng
October 2024
Department of Bioengineering, University of California, Riverside, CA, USA.
Many biomedical devices are powered and controlled by electrical components. These electronics add to the cost of a device (possibly making the device too expensive for use in resource-limited or point-of-care settings) and can also render the device unsuitable for use in some environments (for example, high-humidity areas such as incubators where condensation could cause electrical short circuits, ovens where electronic components may overheat, or explosive or flammable environments where electric sparks could cause serious accidents). In this work, we show that pneumatic logic can be used to power and control biomedical devices without the need for electricity or electric components.
View Article and Find Full Text PDFRespir Care
March 2024
Mr Vieira and Drs Rodrigues, Sklar, and Brochard are affiliated with Keenan Research Centre, Li Ka Shing Knowledge Institute, St. Michael's Hospital, Unity Health Toronto, Ontario, Canada; and Interdepartmental Division of Critical Care Medicine, University of Toronto, Toronto, Ontario, Canada. Dr Masy is affiliated with Keenan Research Centre, Li Ka Shing Knowledge Institute, St. Michael's Hospital, Unity Health Toronto, Ontario, Canada; Interdepartmental Division of Critical Care Medicine, University of Toronto, Toronto, Ontario, Canada; and Division of Pediatric Critical Care, Hospital for Sick Children, University of Toronto, Toronto, Ontario, Canada. Messrs LaRue and Laengert and Dr de Lannoy are affiliated with McMaster University, Center of Excellence in Protective Equipment and Materials, Hamilton, Ontario, Canada; and McMaster University, Department of Chemical Engineering, Hamilton, Ontario, Canada. Dr Lo is affiliated with Department of Anesthesiology and Pain Service, St. Michael's Hospital, Toronto, Ontario, Canada. Dr Petrosoniak is affiliated with Emergency Physician and Trauma Team, St. Michael's and Department of Medicine, University of Toronto, Ontario, Canada. Dr Rezende-Neto is affiliated with Trauma and Acute Care General Surgery, Department of Surgery, St. Michael's Hospital, Toronto, Ontario, Canada.
Background: Aerosol barrier enclosure systems have been designed to prevent airborne contamination, but their safety has been questioned. A vacuum tent was designed with active continuous suctioning to minimize risks of aerosol dispersion. We tested its efficacy, risk of rebreathing, and usability on a bench, in healthy volunteers, and in an ergonomic clinical assessment study.
View Article and Find Full Text PDFActas Urol Esp (Engl Ed)
December 2023
Servicio de Urología, Hospital Universitario de Getafe, Getafe, Madrid, Spain; Facultad de Medicina, Universidad Francisco de Vitoria, Madrid, Spain.
Introduction: The vacuum-assisted access sheath is a new device for the treatment of kidney stones with percutaneous nephrolithotomy (PCNL).
Objective: Our aim was to compare the stone-free rate (SFR) and complications between standard mini percutaneous nephrolithotomy (Mini-PCNL) and vacuum-assisted PCNL (Va-PCNL).
Methods: Retrospective study of patients undergoing Mini-PCNL and Va-PCNL from January 2018 to June 2022.
Membranes (Basel)
February 2023
Department of Biology, Biotechnical Faculty, University of Ljubljana, Jamnikarjeva 101, 1000 Ljubljana, Slovenia.
Low-cost, readily available, or even disposable membranes in water purification or downstream biopharma processes are becoming attractive alternatives to expensive polymeric columns or filters. In this article, the potential of microfiltration membranes prepared from differently orientated viscose fibre slivers, infused with ultrafine quaternised (qCNF) and amino-hydrophobised (aCNF) cellulose nanofibrils, were investigated for capturing and deactivating the bacteria from water during vacuum filtration. The morphology and capturing mechanism of the single- and multi-layer structured membranes were evaluated using microscopic imaging and colloidal particles.
View Article and Find Full Text PDFEur J Mech B Fluids
September 2022
Mechanical Engineering, College of Engineering and Informatics, National University of Ireland, Galway, Ireland.
The Covid-19 global pandemic has reshaped the requirements of healthcare sectors worldwide. Following the exposure risks associated with Covid-19, this paper aims to design, optimise, and validate a wearable medical device that reduces the risk of transmission of contagious droplets from infected patients in a hospital setting. This study specifically focuses on those receiving high-flow nasal oxygen therapy.
View Article and Find Full Text PDFEnter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!