Warming devices

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Chapter 30 Warming devices

Background

Inadvertent perioperative hypothermia (IPH), defined as core body temperature ≤36.0°C, is a common consequence of anaesthesia. It has a number of adverse effects, including greater intraoperative blood loss and consequent blood transfusion,1 an increased rate of wound infection,2 morbid cardiac events3 and pressure sores,4 as well as a longer stay in both recovery and hospital.5 It also causes subjective discomfort.

Maintaining normothermia perioperatively can reduce the incidence of these adverse effects. There are a number of devices that can be used to this end. They may be devices that attempt to conserve the patient’s own heat (passive) or devices that transfer heat from an external source to the patient (active). The latter may warm the patient externally or via warmed intravenous and irrigation fluids.

In 2008, the United Kingdom’s National Institute for Clinical Excellence (NICE) produced the ‘Management of inadvertent perioperative hypothermia in adults’ guideline.6 Its strength is in the fact that it is a clear endorsement of the clinical and cost benefits of perioperative warming, but its weakness is that it does not cover the full range of technology available due to a sparse research base.

The recommendations can be succinctly summarized as:

should receive warming. In addition, all fluid infusions of 500 ml or more should be warmed.7,8 Together, these recommendations, therefore, encompass the majority of operations and most intravenous infusions, and highlight the need for a wide knowledge of the available warming technologies.

Temperature monitoring is covered elsewhere in this book. However, it should not be forgotten that this is an integral part of perioperative thermal management. Unfortunately, there are limitations to all currently available methods of perioperative temperature monitoring and it should be remembered that accuracy in the laboratory does not necessarily imply accuracy in the clinical setting.

Physical principles

These are important in understanding how warming devices work, how heat is lost and gained by the body, how warming devices work and, consequently, the best way to go about maintaining normothermia.

Heat transfer

Heat transfer can only take place down a temperature gradient. Within the body there is a gradient between core and peripheral ‘compartments’. Peripheral tissues are usually 2– 4°C cooler than the core. There is then the much more variable gradient between the peripheral tissues and the environment. This simplistic model is, however, somewhat modified by the body’s control over heat distribution via the circulation. The importance of this is demonstrated by the fact that even during warming, the peripheral compartment remains about 1°C less than the core temperature.

Devices used to prevent perioperative hypothermia

Active devices

Circulating water devices

Initially, prior to the advent of forced-air warming, patients were placed on circulating hot water mattresses in an attempt to counteract heat loss and maintain normothermia. In theory the high specific heat capacity of water in the mattress should be very effective at providing heat. In practice, however, these devices only effectively deliver heat to those areas in direct contact with the mattress, which constitutes a relatively small proportion of the body. Furthermore, those small areas in direct contact are under pressure and so have a compromised blood supply that reduces the amount of heat transfer even further. Additionally, in this situation the relatively high thermal capacity of the water is a disadvantage as it increases the likelihood of thermal damage, which has been described at settings of 39°C.

Newer devices overcome these problems by circulating the water through special garments or pads. They include the Kimberly-Clark Patient Warming System (Figs 30.1A and B), which uses adhesive ‘energy transfer’ pads with micro-channels for circulating water that can be applied to the back, thighs, chest, or any combination of the three, depending on the site of surgery. Another modern system is the Allon circulating-water garment. This conductive heating garment is divided into separate segments for arms and thighs, which allows clinicians to cover different body surfaces depending on the site of surgery. Perhaps unsurprisingly, given the different thermal characteristics of water and air, both the above have both been shown to be more efficient at warming volunteers than forced-air devices (see below).

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