A novel method for electronic measurement and recording of surgical drain output.

Surgical drains are used to collect and measure fluids (e.g. serous fluid, lymph, blood, etc.). The volume of fluid in the container is measured using graded markings on the container and then recorded manually on a "drain chart" allowing for manual rate calculations. This method is dependant on regularly checking the volume of the drain and recording the value accurately; unfortunately, this is often not feasible due to staffing levels and time constraints. This results in inaccurate "drain charts" making clinical decisions based on these figures unreliable. Often the lack of confidence in these measurements leads to delayed drain removal with consequent increased infection risks and potential delayed discharge. Accurate digital measurement of drain content would have a significant impact on clinical care. This paper describes a digital technology to measure volume, making use of a positive terminal at the lowest point of the vessel and negative (sensor) terminals placed at accurate intervals along an axis of the vessel. A proof-of-concept prototype was developed using commercially available electronic components to test the feasibility of a technology for electronic measurement and recording of surgical drain content. In a simulated environment, the proposed technology was shown to be effective and accurate. The proposed electronic drain has a number of advantages over currently used devices in saving time and easing pressure on nursing staff, reduce disturbance of patients, and allows for preset alarms.

A novel safety mechanism to reduce the risk of inadvertent electrosurgical injury.

Thousands of laparoscopic procedures requiring the use of electrosurgical devices are performed worldwide on a daily basis. The use of electrosurgery carries with it inherent risks related to the use of an energy source within the abdomen. Inadvertent tissue injury due to the use of electrosurgical devices is rare, but is associated with a high morbidity and mortality if undetected. This paper describes a novel, yet simple method using instrument markers and image processing algorithms to reduce the risk of unsafe activation of electrosurgical instruments during laparoscopy. The method was tested in a simulated environment and measured against the decision of an experienced laparoscopic surgeon. Results showed that the position of an instrument in a visual field could be accurately determined using an image processing algorithm to ascertain whether it was safe for activation in agreement with the decisions made by manual inspection.

Constraints in posterior-stabilised TKA kinematics: a comparison of two generations of an implant.

PURPOSE: This study tests the hypothesis that the design changes incorporated in the newer generation Triathlon posterior-stabilised TKA design result in kinematics that more closely reproduce the kinematics observed in healthy knees than those achieved by the older generation Scorpio posterior-stabilised TKA design. METHODS: Eleven patients with Triathlon posterior-stabilised TKA, twelve patients with Scorpio posterior-stabilised TKA, and 22 subjects with normal asymptomatic knees underwent fluoroscopic assessment of the knee during a step-up exercise and a weight-bearing deep knee bend. Two-dimensional and three-dimensional knee kinematics were assessed including the maximum flexion, the patella tendon angle (PTA), the patella flexion angle (PFA), the minimum distance between cam and post, and the tibio-femoral contact positions. RESULTS: The average maximum flexion achieved was 114° (SD 3°), 91° (SD 10°), and 143° (SD 14°) for the Triathlon, Scorpio, and Normal groups. The average cam/post mechanism engagement was at 63° (SD 24°) and 82° (SD 16°) for the Triathlon and Scorpio groups. The condylar contact points showed a paradoxical anterior slide for the Scorpio group which was not present in the Triathlon group. The PTA and PFA values of both implants showed significant differences from normal. CONCLUSION: Overall, the Triathlon implant design, as compared to Scorpio TKA, produced kinematics closer to that of normal knees as proposed by the hypothesis. However, despite being closer to normal, the kinematics exhibited by the Triathlon group were still different from normal. A comparison of kinematic performance, taking into account altered design parameters, will contribute to improved understanding and future design considerations.