Ease and comfort of pre-oxygenation with high-flow nasal oxygen cannulae vs. facemask: a randomised controlled trial.

The Difficult Airway Society recommends that all patients should be pre-oxygenated before the induction of general anaesthesia, but this may not always be easy or comfortable and anaesthesia may often be induced without full pre-oxygenation. We tested the hypothesis that high-flow nasal oxygen cannulae would be easier and more comfortable than facemasks for pre-oxygenation. We randomly allocated 199 patients undergoing elective surgery aged ≥ 10 years to pre-oxygenation using either high-flow nasal oxygen or facemask. Ease and comfort were assessed by anaesthetists and patients on 10-cm visual analogue scale and six-point smiley face scale, respectively. Secondary endpoints included end-tidal oxygen fraction after securing a definitive airway and time to secure an airway. A mean difference (95%CI) between groups in ratings of -0.76 (-1.25 to -0.27) cm for ease of use (p = 0.003) and -0.45 (-0.75 to -0.13) points for comfort (p = 0.006), both favoured high-flow nasal oxygen. A mean difference (95%CI) between groups in end-tidal oxygen fraction of 3.89% (2.41-5.37%) after securing a definitive airway also favoured high-flow nasal oxygen (p < 0.001). There was no significant difference between groups in the number of patients with hypoxaemia (Sp O2 < 90%) or severe hypoxaemia (Sp O2 < 85%) lasting ≥ 1 min or ≥ 2 min; in the proportion of patients with an end-tidal oxygen fraction < 87% in the first 5 min after tracheal intubation (52.2% vs. 58.9% in facemask and high-flow nasal oxygen groups, respectively; p = 0.31); or in time taken to secure an airway (11.6 vs. 12.2 min in facemask and high-flow nasal oxygen groups, respectively; p = 0.65). In conclusion, we found pre-oxygenation with high-flow nasal oxygen to be easier for anaesthetists and more comfortable for patients than pre-oxygenation with a facemask, with no clinically relevant differences in end-tidal oxygen fraction after securing a definitive airway or time to secure an airway. The differences in ease and comfort were modest.

Evaluating the ORSIM® simulator for assessment of anaesthetists' skills in flexible bronchoscopy: aspects of validity and reliability.

BACKGROUND: Developing expertise in flexible bronchoscopy is limited by inadequate opportunities to train on difficult airways. The new ORSIM bronchoscopy simulator aims to address this by creating virtual patients with difficult airways. This study aims to provide evidence on the validity and reliability of the ORSIM for assessment of subjects on both normal and abnormal airway simulations. METHODS: Novice, trainee, and expert subjects performed seven simulations of varying difficulty and scored the perceived difficulty for each. Time to completion was measured. Three blinded raters independently scored videos of each subject's performance. We measured inter-rater agreement and the difference in raters' scores between subject groups. RESULTS: We recruited 28 study subjects, generating 196 videos for analysis. Expert subjects consistently completed the scenarios faster than novices. Overall performance scores showed significant differences between subject groups (P<0.0001). Inter-rater reliability of scores was >0.8. CONCLUSIONS: Our results provide initial evidence on the validity and reliability of the ORSIM bronchoscopy simulator, supporting its potential value in training and assessment.

Functional gracilis flap in thenar reconstruction.

UNLABELLED: Restoration of lost opposition in the context of significant thenar soft tissue defects represents a tremendous reconstructive challenge. Free functioning muscle transfer has been described in this context and has the advantage of providing both a functioning muscle unit as well as soft tissue coverage in a single reconstructive procedure. It adds to the injured limb, and by sparing donor tendons avoids the need for re-education of motor function. We describe the use of a free innervated gracilis muscle flap for functional thenar reconstruction in two unique cases following extensive traumatic loss of thenar skin and musculature. Crucially, in each case, the recurrent motor branch of the median nerve had been destroyed at its point of insertion into the thenar muscle remnants. AIM: To date, the main reported disadvantages of free functioning muscle transfer in thenar reconstruction include difficult flap dissections, donor site morbidity, inadequate strength and excursion of the transplanted muscle and excessively bulky flaps. Our aim was, as far as possible, to address these issues. SURGICAL PROCEDURE: Each thenar defect was measured and a corresponding segment of gracilis muscle, measured in situ, was raised on the proximal neurovascular pedicle. End-side microvascular anastomosis was performed between the medial circumflex femoral artery and the radial artery. The venae comitantes of the pedicle were anastomosed end-end with those of the radial artery and also with the cephalic vein. Epineural anastomosis was performed between the motor branch of the obturator nerve and the recurrent motor branch of the median nerve. Each flap was covered with a split thickness skin graft. RESULTS: Both flaps survived without any complication. Both patients regained excellent voluntary thumb opposition, sufficient to allow return to full-time employment, and had restoration of sufficient thenar bulk. This was achieved with minimal donor site morbidity. CONCLUSIONS: Restoration of lost opposition, in the context of significant thenar soft tissue defects, can be achieved using a free functional gracilis flap. This produces clinically excellent functional results and can be carried out as a single stage reconstructive procedure. This is a novel application of a tremendously versatile donor muscle in functioning free muscle transfer.

Cost benefit analysis of screening spina bifida.

Cost benefit analysis of establishing and running a mass serum alpha-fetoprotein (AFP) screening service for neural tube defects (NTDS) in the Auckland Hospital Board area has been undertaken and a cost benefit index derived. From a population of 14 066 pregnant women per year, assuming present booking patterns continue, 8017 women could be screened for NTDS. Such screening could reduce severe spina bifida in liveborn babies by 38.8 percent.