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Skin temperature of the knee was effectively reduced when using a new continuous cold-flow cryocompression device: a randomised controlled crossover trial

Skin temperature of the knee was effectively reduced when using a new continuous cold-flow cryocompression device: a randomised controlled crossover trial
Skin temperature of the knee was effectively reduced when using a new continuous cold-flow cryocompression device: a randomised controlled crossover trial
Objective: to determine which temperature settings on a new continuous cold-flow cryocompression device effectively reduce knee skin temperature to 10–15 °C, where pain and swelling are expected to be attenuated.

Design: randomised controlled crossover trial.

Setting: university laboratory.

Participants: 32 healthy adult participants recruited (1 dropout) with no contraindications to cryocompressive therapy.

Intervention: a k-type thermocouple was used to record skin temperature at baseline and every five minutes during a 30-minute cryocompression treatment in a control condition and when using four different device temperature settings (6 °C, 8 °C, 10 °C, and 12 °C) on a continuous cold-flow cryocompression device. Conditions were labelled Control, Con-6, Con-8, Con-10, and Con-12, respectively.

Main outcome measures: skin temperature change (°C) throughout cryocompression; time taken (mins) to achieve skin temperature < 15 °C; and the difference between final skin temperature and device temperature setting (°C).

Results: median (IQR) skin temperature after cryocompression was 32.1 °C (29.3–33.4), 12.8 °C (12.1–14.6), 14.3 °C (13.8–15.7), 16.1 °C (15.2–17.3), and 17.7 °C (16.9–18.9) for the Control condition and Con-6, Con-8, Con-10 and Con-12, respectively. It took 20 min (Con-6) and 25 min (Con-8) for skin temperature to reach < 15 °C. A median (IQR) difference of 6.8 °C (6.1–8.6), 6.3 °C (5.8–7.7), 6.1 °C (5.2–7.3), and 5.7 °C (4.9–6.9) for Con-6, Con-8, Con-10, and Con-12, respectively was observed between device temperature setting and final skin temperature.

Conclusions: the device is recommended as it reduced skin temperature to the therapeutic range of 10–15 °C during a 30-minute treatment when using the 6 °C or 8 °C device temperature settings. Future research should determine optimal treatment lengths for cryocompression.
Arthroplasty, Arthroscopy, Cryotherapy, Rehabilitation, Skin temperature
0031-9406
11-18
Belsey, James
e80f02d4-839c-4aef-ad92-f6ab1f861e76
Gregory, Ryan
7cbdc7e8-154b-4acc-bcad-f2710e4aeb1f
Paine, Eloise
0eaebc3a-0c08-42f3-8cef-ad1a250dd8a3
Faulkner, James
b2bd38c9-667c-42e8-ad1e-6df58d1e3f7a
Belsey, James
e80f02d4-839c-4aef-ad92-f6ab1f861e76
Gregory, Ryan
7cbdc7e8-154b-4acc-bcad-f2710e4aeb1f
Paine, Eloise
0eaebc3a-0c08-42f3-8cef-ad1a250dd8a3
Faulkner, James
b2bd38c9-667c-42e8-ad1e-6df58d1e3f7a

Belsey, James, Gregory, Ryan, Paine, Eloise and Faulkner, James (2024) Skin temperature of the knee was effectively reduced when using a new continuous cold-flow cryocompression device: a randomised controlled crossover trial. Physiotherapy, 123, 11-18. (doi:10.1016/j.physio.2023.12.001).

Record type: Article

Abstract

Objective: to determine which temperature settings on a new continuous cold-flow cryocompression device effectively reduce knee skin temperature to 10–15 °C, where pain and swelling are expected to be attenuated.

Design: randomised controlled crossover trial.

Setting: university laboratory.

Participants: 32 healthy adult participants recruited (1 dropout) with no contraindications to cryocompressive therapy.

Intervention: a k-type thermocouple was used to record skin temperature at baseline and every five minutes during a 30-minute cryocompression treatment in a control condition and when using four different device temperature settings (6 °C, 8 °C, 10 °C, and 12 °C) on a continuous cold-flow cryocompression device. Conditions were labelled Control, Con-6, Con-8, Con-10, and Con-12, respectively.

Main outcome measures: skin temperature change (°C) throughout cryocompression; time taken (mins) to achieve skin temperature < 15 °C; and the difference between final skin temperature and device temperature setting (°C).

Results: median (IQR) skin temperature after cryocompression was 32.1 °C (29.3–33.4), 12.8 °C (12.1–14.6), 14.3 °C (13.8–15.7), 16.1 °C (15.2–17.3), and 17.7 °C (16.9–18.9) for the Control condition and Con-6, Con-8, Con-10 and Con-12, respectively. It took 20 min (Con-6) and 25 min (Con-8) for skin temperature to reach < 15 °C. A median (IQR) difference of 6.8 °C (6.1–8.6), 6.3 °C (5.8–7.7), 6.1 °C (5.2–7.3), and 5.7 °C (4.9–6.9) for Con-6, Con-8, Con-10, and Con-12, respectively was observed between device temperature setting and final skin temperature.

Conclusions: the device is recommended as it reduced skin temperature to the therapeutic range of 10–15 °C during a 30-minute treatment when using the 6 °C or 8 °C device temperature settings. Future research should determine optimal treatment lengths for cryocompression.

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e-pub ahead of print date: 14 December 2023
Published date: 19 January 2024
Additional Information: Copyright © 2023 The Author(s). Published by Elsevier Ltd.. All rights reserved.
Keywords: Arthroplasty, Arthroscopy, Cryotherapy, Rehabilitation, Skin temperature

Identifiers

Local EPrints ID: 497705
URI: http://eprints.soton.ac.uk/id/eprint/497705
ISSN: 0031-9406
PURE UUID: 948d2fba-1fe1-4118-8007-3d2f880c880a
ORCID for James Faulkner: ORCID iD orcid.org/0000-0002-3704-6737

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Date deposited: 29 Jan 2025 18:34
Last modified: 30 Jan 2025 03:31

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Contributors

Author: James Belsey
Author: Ryan Gregory
Author: Eloise Paine
Author: James Faulkner ORCID iD

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