Educational Problems — The Performance of AirAngel® Videolaryngoscope
Citation(s)
Coles-Black J, Chao I, Chuen J Three-dimensional printing in medicine. Med J Aust. 2017 Aug 7;207(3):102-103. doi: 10.5694/mja16.01073. No abstract available.
Cook TM, Kelly FE A national survey of videolaryngoscopy in the United Kingdom. Br J Anaesth. 2017 Apr 1;118(4):593-600. doi: 10.1093/bja/aex052.
Lambert CT, John SC, John AV Development and performance testing of the low-cost, 3D-printed, smartphone-compatible 'Tansen Videolaryngoscope' vs. Pentax-AWS videolaryngoscope vs. direct Macintosh laryngoscope: A manikin study. Eur J Anaesthesiol. 2020 Nov;37(11):992-998. doi: 10.1097/EJA.0000000000001264.
Maruyama K, Yamada T, Kawakami R, Hara K Randomized cross-over comparison of cervical-spine motion with the AirWay Scope or Macintosh laryngoscope with in-line stabilization: a video-fluoroscopic study. Br J Anaesth. 2008 Oct;101(4):563-7. doi: 10.1093/bja/aen207. Epub 2008 Jul 25.
Pieters BMA, Maas EHA, Knape JTA, van Zundert AAJ Videolaryngoscopy vs. direct laryngoscopy use by experienced anaesthetists in patients with known difficult airways: a systematic review and meta-analysis. Anaesthesia. 2017 Dec;72(12):1532-1541. doi: 10.1111/anae.14057. Epub 2017 Sep 22.
Zaouter C, Calderon J, Hemmerling TM Videolaryngoscopy as a new standard of care. Br J Anaesth. 2015 Feb;114(2):181-3. doi: 10.1093/bja/aeu266. Epub 2014 Aug 23. No abstract available.
Comparison of AirAngel® vs Storz® Videolaryngoscope and Macintosh® Laryngoscope for Endotracheal Intubation Training: Prospective Randomized Crossover Study
Interventional studies are often prospective and are specifically tailored to evaluate direct impacts of treatment or preventive measures on disease.
Observational studies are often retrospective and are used to assess potential causation in exposure-outcome relationships and therefore influence preventive methods.
Expanded access is a means by which manufacturers make investigational new drugs available, under certain circumstances, to treat a patient(s) with a serious disease or condition who cannot participate in a controlled clinical trial.
Clinical trials are conducted in a series of steps, called phases - each phase is designed to answer a separate research question.
Phase 1: Researchers test a new drug or treatment in a small group of people for the first time to evaluate its safety, determine a safe dosage range, and identify side effects.
Phase 2: The drug or treatment is given to a larger group of people to see if it is effective and to further evaluate its safety.
Phase 3: The drug or treatment is given to large groups of people to confirm its effectiveness, monitor side effects, compare it to commonly used treatments, and collect information that will allow the drug or treatment to be used safely.
Phase 4: Studies are done after the drug or treatment has been marketed to gather information on the drug's effect in various populations and any side effects associated with long-term use.