Impact of Forced Air Warming on Perioperative Thermodynamics

NCT ID: NCT03191214

Last Updated: 2017-06-19

Basic Information

• Recruitment Status: UNKNOWN
• Total Enrollment: 24 participants
• Study Classification: OBSERVATIONAL
• Study Start Date: 2017-07-21
• Study Completion Date: 2017-09-15

Brief Summary

The purpose of the study is to assess the temperature changes that take place throughout the body in a real world setting, when a patient is given general anaesthesia. Specifically we will investigate the movement of body heat from the core to the peripheries at the beginning of surgery. This will be measures with a series of temperature sensors and infrared thermography

Detailed Description

Intra-operative hypothermia increases the risk of a wide range of post operative complications; wound infection, damage to heart muscle, and an increased length of hospital stay.

A range of technologies exist for maintaining the temperature of patients undergoing surgical procedures. Yet despite the frequent use of forced air warming devices, a significant reduction in core temperature can occur in the first 60 minutes of some major surgeries.

This is an Observational Cross-Sectional Study, investigating patients undergoing elective surgery in two groups Group 1: Patients undergoing brief surgical procedures of >15 minutes for whom no warming devices are being employed.

Group 2: Patients undergoing surgical procedures in which forced air warming, is being used Potential participants will first be approached by medical staff at their pre-operative assessment clinic. They will be screened for exclusion criteria before being given a participant information sheet, which will be explained to them. They will be invited to contact the researcher if they are interested in participating in the study.

On arrival in hospital the day of their surgery, the patients will be met by their anaesthetist and a researcher who will provide any further information required about the study, and consent will be taken.

Following receipt of informed consent, patients will be involved from 30 minutes before their surgery begins, until the end of their surgery.

The null hypothesis is that there is no difference in the rate of flow of heat from the core to the peripheries between patients who receive warming during surgery, and those who do not. As it would be unethical to randomise a patient to not receive warming, we have designed an observational study to compare patients who are warmed / not warmed as part of their standard care. Patients undergoing surgery <30 minutes long are not routinely warmed during surgery.

Potential participants will be informed of the study at the pre-operative assessment clinic in the weeks preceding surgery. Posters will be located in the clinic rooms and relevant areas, and subjects will be given information by the clinic staff to read prior to their surgery.

Participants will be admitted to hospital the evening prior, or the morning of surgery, whereupon they will undergo standard admission processes, including pre-operative assessment by the anaesthetist assigned to that list. The anaesthetist and researcher will then explain the study again, reiterating the potential risks and benefits of the study to the patient themselves, and to the population as a whole. Written consent will be sought at this point.

Participants will be weighed and four measurements will be taken, comprising : arm length, leg length, trunk length and maximum abdominal width. Participants will stand onto a bioimpedance machine, which will quantify their body fat and body water percentage.

30 minutes before their operation, skin temperature sensors will be placed on the patient's forehead, forearm, finger, hip, calf and toe. An additional SpotOn temperature sensor, placed on the forehead will be used to non invasively measure core temperature.

Measurement of blood pressure, cardiac output and systemic vascular resistance will be obtained by a finger cuff connected to a Nexin Noninvasive cardiac output monitor. These measurements describe the action of the heart and blood vessels. At the end of each surgery the data recorded on this device will be transferred via an encrypted USB key onto a data acquisition laptop.

Temperature measurements from the seven of sensors will taken at 5 second intervals onto a data acquisition laptop.

At 15 minutes intervals Infra red thermography images will be taken from a FLIR a320 device. This equipment will be mounted on a raised boom above the surgeons, in a sterile sleeve. This will not be held over the patient at any point, and will be moved away from the patient between measurements.

Once the surgery has ended, and the patient has been transferred to the recovery area, all temperature sensors will be removed and the patient will exit the trial.

A sample size of 24 patients will be recruited to quantify the effect of warming.

Conditions

Hypothermia Following Anesthesia

Study Design

• Observational Model Type: CASE_CONTROL
• Study Time Perspective: PROSPECTIVE

Study Groups

No Warming

Patients undergoing brief surgical procedures of \>15 minutes for whom no warming devices are being employed.

No interventions assigned to this group

Forced Air Warming

Patients undergoing surgical procedures in which forced air warming, is being used

Intraoperative Forced Air Warming

Intervention Type: DEVICE

As part of their standard care, patients undergoing surgery \>30 min in duration will receive forced air warming in the form of a Bair Hugger. This is a blanket covering their upper torso and arms into which warm air is blown.

Interventions

Intraoperative Forced Air Warming

As part of their standard care, patients undergoing surgery \>30 min in duration will receive forced air warming in the form of a Bair Hugger. This is a blanket covering their upper torso and arms into which warm air is blown.

Intervention Type: DEVICE

Eligibility Criteria

Inclusion Criteria

• Male & Female patients, from 18 - 80 years old, undergoing surgery requiring general anaesthesia, who are deemed to have capacity to give informed consent and have done so in writing prior to commencement of surgery.

The surgeries include :

1. brief surgical procedures of >15 minutes requiring general for whom no warming devices are being employed

2. surgical >30 minutes procedures in which forced air warming, is being used

Exclusion Criteria

Patients who do not adequately understand verbal explanations or written information given in English.

Patients not possessive of capacity to give informed consent. Patients who have not given consent.

Patients with :

• Peripheral vascular disease
• BMI >30
• Aortic aneurysms
• Amputations

Patients with a history of:

• Thyroid disease
• Dysautonomia
• Malignant hyperthermia

• Minimum Eligible Age: 18 Years
• Maximum Eligible Age: 80 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

University College, London

OTHER

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

Fintan Hughes

Role: STUDY_DIRECTOR

Univeristy College London Hospital

Locations

University College London Hospital

London, , United Kingdom

Countries

United Kingdom

Central Contacts

Fintan Hughes

Role: CONTACT

Fintan.hughes@ucl.ac.uk

+44 7731403686

Facility Contacts

Michael Mythen, MB BS

Role: primary

020 3447 2810

Other Identifiers

228666

Identifier Type: -

Identifier Source: org_study_id