Absolute focus on creating a gold standard in Total Intravenous Anaesthesia (TIVA)

Total intravenous anaesthesia (TIVA) is a technique of general anaesthesia which uses a combination of agents given exclusively by the intravenous route without the use of inhalation agents (Gas Anaesthesia)[1].

There is a solid rationale for the use of TIVA in some patient cases where the delivery of inhaled anaesthetics is impossible or disadvantageous, or in scenarios where traditional anaesthetic delivery systems may be unavailable or impractical. In other cases, the use of TIVA could make the process more efficient and advantageous for the patient.

Compared generally to traditional volatile anaesthetic techniques, TIVA offers several potential advantages. These include reduced incidence of post-operative nausea and vomiting, reduced atmospheric pollution, more predictable and rapid recovery, greater haemodynamic stability, preservation of hypoxic pulmonary vasoconstriction, reduction in intracerebral pressure and reduced risk of organ toxicity.

In comparison to traditional inhalation anaesthesia, the inherent benefits of TIVA via a Target Controlled Infusion (TCI) make it a more straightforward and user-friendly technique for the caregiver, while at the same time offering a faster and more comfortable patient recovery[2]. 

Guidelines for the safe practice of total intravenous anaesthesia (TIVA)

Surveys of anaesthetists working in the UK and Ireland have concluded that training in TIVA is currently inconsistent. The 5th National Audit Project (NAP5) on accidental awareness during general anaesthesia found that self-reported cases of awareness were more common when TIVA was used, but that most of the cases were preventable and that the commonest contributory factor was inadequate education and training [3]. The report recommended that ‘the relevant anaesthetic organisations should establish a set of standards and recommendations for best practice in the use of TIVA’. These guidelines have been produced by the Society for Intravenous Anaesthesia (SIVA) and the Association of Anaesthetists in response to that recommendation.

 The guidelines recommend that: The infusion set through which TIVA is delivered should have a Luer-lock connector at each end, an antisyphon valve on the drug delivery line(s) and an anti-reflux valve on any fluid administration line. Drug and fluid lines should join as close to the patient as possible to minimise dead space. All Tivatek sets include a high flow, one-way Codan valve on the wide bore gravity line. All valves are tested for failures and leaks and have a clinical dead space of 0.68ml.

Guaranteeing drug delivery in Total Intravenous Anaesthesia (TIVA)

Based on a report produced by The Safe Anaesthesia Liaison Group (SALG) [4], Tivatek follows recommendations for guaranteeing the safe delivery of intravenous anaesthesia:

1. Using a one-way valve on the intravenous line
   It is suggested a one-way valve is used on the I.V. fluid port when multi-lumen I.V. connectors are used. All Tivatek sets include a high flow, one-way Codan valve on the wide bore gravity line. All valves are tested for failures and leaks.
2. The site of the cannula must be monitored throughout the procedure
   Disconnection of the Infusion or displacement of the cannula can go unnoticed, cannula sites should be visually checked at regular intervals as a practical and simple risk reduction. Tivalok™, provides an additional visual aid and added safety from disconnection. It ensures your cannula remains securely in place during a procedure and is highly visible and easily accessible. 
3. Using Medical Equipment
   When using medical equipment, it is essential clinical staff know all uses and limitations. 
A comprehensive IFU (instructions for use) is dispatched with all Tivatek equipment.
4. Organisations should ensure all one-way valves purchased are clearly labelled
   Clear and informative packaging will aid correct selection of the appropriate system required for TIVA administration. Tivatek sets are delivered as a complete, sterile kit so there is no need to purchase an additional one-way valve or multi-lumen/y connector. This ensures all appropriate and necessary equipment is set up, ready for use. All products are labelled clearly for intended use.

References:

1. ‘Total Intravenous Anesthesia using a target controlled infusion – A pocket reference’, College of Anesthesiologists, Academy of Medicine Malaysia (retrieved 07.10.15).
2. Ozkose, Z., Ercan, B., Ünal, Y., Yardim, S., Kaymaz, M., Dogulu, F., & Pasaoglu, A. (2001). Inhalation versus total intravenous anesthesia for lumbar disc herniation: comparison of hemodynamic effects, recovery characteristics, and cost. Journal of neurosurgical anesthesiology, 13(4), 296-302.
3. Pandit JJ, Andrade J, Bogod DG, et al. The 5th National Audit Project (NAP5) on accidental awareness during general anaesthesia: summary of main findings and risk factors. Anaesthesia 2014; 69: 1089–101.
4. ‘Guaranteeing Drug Delivery in Total Intravenous Anaesthesia’, Safe Anaesthesia Liaison Group, 2009

Product features to support/optimise safe TIVA practice

 The NHS released recommendations for product features to support/optimise safe TIVA practice, the chart below shows how Europlaz’s TIVA sets meet all recommendations.