In vitro evaluation of a hybrid negative pressure system for wound therapy

Fuente: Wiley Open Access
Gespeichert in:
Bibliographische Detailangaben
Hauptverfasser: Jack S. Davey, Wye Li Chong, Jake Fountain, Jane Heller, Rui Sul, Kieri Jermyn, Jacob Michelsen, Louisa Ho Eckart
Format: Artículo Open Access
Veröffentlicht: Wiley 2024
Schlagworte:
Online-Zugang:
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
_version_ 1867008174333100033
author Jack S. Davey
Wye Li Chong
Jake Fountain
Jane Heller
Rui Sul
Kieri Jermyn
Jacob Michelsen
Louisa Ho Eckart
author_facet Jack S. Davey
Wye Li Chong
Jake Fountain
Jane Heller
Rui Sul
Kieri Jermyn
Jacob Michelsen
Louisa Ho Eckart
Jack S. Davey
Wye Li Chong
Jake Fountain
Jane Heller
Rui Sul
Kieri Jermyn
Jacob Michelsen
Louisa Ho Eckart
collection Wiley Open Access
contents In vitro evaluation of a hybrid negative pressure system for wound therapy Jack S. Davey Wye Li Chong Jake Fountain Jane Heller Rui Sul Kieri Jermyn Jacob Michelsen Louisa Ho Eckart Veterinary Surgery AbstractObjectiveThe objective of this study was to assess whether negative pressure could be maintained accurately and repeatably with a wall‐suction‐based hybrid negative pressure wound therapy (h‐NPWT) system by comparing it with a commercial negative pressure wound therapy (NPWT) device.Study designIn vitro experimental study.MethodsA commercial NPWT device (control) and three h‐NPWT devices, with 0, 3, and 6 meters of additional tubing using the hospital‐wall suction (groups 1, 2, and 3 respectively), were applied sequentially to a commercial NPWT dressing on a silicone skin substrate and set to run at a continuous pressure of −125 mmHg. The pressure within the wound space was monitored at 10 second intervals for 24 h. The process was repeated five times for each group.ResultsThe commercial NPWT device produced an average pressure variance of 3.02 mmHg, and the h‐NPWT produced average variances of 4.38, 4.24 and 4.20 mmHg for groups 1, 2 and 3, respectively. All groups produced an average pressure within 0.15 mmHg of −125 mmHg over the 24‐hour period, and the h‐NPWT systems produced the smallest range with all values remaining within a ±5% variation from −125 mmHg.ConclusionThe h‐NPWT system achieved negative pressures that were comparable to those of a commercial control NPWT device. The addition of tubing between the skin substrate and the canister did not affect the pressure applied at the wound site.Clinical significanceThe h‐NPWT device tested in this study can be considered as an alternative for negative wound therapy when a commercial device cannot be used. 10.1111/vsu.14101 http://creativecommons.org/licenses/by-nc/4.0/
doi_str_mv 10.1111/vsu.14101
format Artículo Open Access
id wiley_oa_10_1111_vsu_14101
institution Wiley Open Access
license_str_mv http://creativecommons.org/licenses/by-nc/4.0/
publishDate 2024
publisher Wiley
record_format wiley_oa
spellingShingle In vitro evaluation of a hybrid negative pressure system for wound therapy
Jack S. Davey
Wye Li Chong
Jake Fountain
Jane Heller
Rui Sul
Kieri Jermyn
Jacob Michelsen
Louisa Ho Eckart
Veterinary Surgery
In vitro evaluation of a hybrid negative pressure system for wound therapy Jack S. Davey Wye Li Chong Jake Fountain Jane Heller Rui Sul Kieri Jermyn Jacob Michelsen Louisa Ho Eckart Veterinary Surgery AbstractObjectiveThe objective of this study was to assess whether negative pressure could be maintained accurately and repeatably with a wall‐suction‐based hybrid negative pressure wound therapy (h‐NPWT) system by comparing it with a commercial negative pressure wound therapy (NPWT) device.Study designIn vitro experimental study.MethodsA commercial NPWT device (control) and three h‐NPWT devices, with 0, 3, and 6 meters of additional tubing using the hospital‐wall suction (groups 1, 2, and 3 respectively), were applied sequentially to a commercial NPWT dressing on a silicone skin substrate and set to run at a continuous pressure of −125 mmHg. The pressure within the wound space was monitored at 10 second intervals for 24 h. The process was repeated five times for each group.ResultsThe commercial NPWT device produced an average pressure variance of 3.02 mmHg, and the h‐NPWT produced average variances of 4.38, 4.24 and 4.20 mmHg for groups 1, 2 and 3, respectively. All groups produced an average pressure within 0.15 mmHg of −125 mmHg over the 24‐hour period, and the h‐NPWT systems produced the smallest range with all values remaining within a ±5% variation from −125 mmHg.ConclusionThe h‐NPWT system achieved negative pressures that were comparable to those of a commercial control NPWT device. The addition of tubing between the skin substrate and the canister did not affect the pressure applied at the wound site.Clinical significanceThe h‐NPWT device tested in this study can be considered as an alternative for negative wound therapy when a commercial device cannot be used. 10.1111/vsu.14101 http://creativecommons.org/licenses/by-nc/4.0/
title In vitro evaluation of a hybrid negative pressure system for wound therapy
topic Veterinary Surgery
url https://onlinelibrary.wiley.com/doi/10.1111/vsu.14101