Prophylactic negative pressure wound therapy (NPWT) in laparotomy wounds (PROPEL-2): protocol for a randomized clinical trial

John V. Reynolds, John Calvin Coffey, Michael E. Kelly, D. C. Winter, Ronan A. Cahill, Stephen R. Walsh, Michael J. Kerin, John O. Larkin, Paul Carroll, Patrick Owens, Matthew G. Davey, Noel E. Donlon, Claire L. Donohoe, Deborah A. McNamara, W. B. Robb, Micheal O‘Riordain, Stewart R. Walsh, Peter Neary, Christina Fleming, Dara O. Kavanagh, PROPEL-2 Trial Collaborators, C Peirce, E. T. Condon, S Abd Elwahab, John B. Conneely, Manvydas Varzgalis, Eleanor Faul, Desmond Toomey, E. Andrews, David Kearney, Terence Patrick Murphy, S T Martin, Helen Heneghan, M. Kevin Barry, Fiachra Cooke, S D Johnston, Arnold Hill
2024-07-02

SCID:  54.1/znhpk6ku
BACKGROUND: A proportion of patients undergoing midline laparotomy will develop surgical site infections after surgery. These complications place considerable financial burden on healthcare economies and have negative implications for patient health and quality of life. The prophylactic application of negative pressure wound therapy devices has been mooted as a pragmatic strategy to reduce surgical site infections. Nevertheless, further availability of multicentre randomized clinical trial data evaluating the prophylactic use of negative pressure wound therapy following midline laparotomy is warranted to definitely provide consensus in relation to these closure methods, while also deciphering potential differences among subgroups. The aim of this study is to determine whether prophylactic negative pressure wound therapy reduces postoperative wound complications in patients undergoing midline laparotomy. METHODS: PROPEL-2 is a multicentre prospective randomized clinical trial designed to compare standard surgical dressings (control arm) with negative pressure wound therapy dressings (Prevena™ and PICO™ being the most commonly utilized). Patient recruitment will include adult patients aged 18 years or over, who are indicated to undergo emergency or elective laparotomy. To achieve 90% power at the 5% significance level, 1006 patients will be required in each arm, which when allowing for losses to follow-up, 10% will be added to each arm, leaving the total projected sample size to be 2013 patients, who will be recruited across a 36-month enrolment period. CONCLUSION: The PROPEL-2 trial will be the largest independent multicentre randomized clinical trial designed to assess the role of prophylactic negative pressure wound therapy in patients indicated to undergo midline laparotomy. The comparison of standard treatment to two commercially available negative pressure wound therapy devices will help provide consensus on the routine management of laparotomy wounds. Enrolment to PROPEL-2 began in June 2023. Registration number: NCT05977816 (http://www.clinicaltrials.gov).
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2024-07-02
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Authors
John V. Reynolds
John Calvin Coffey
Michael E. Kelly
D. C. Winter
Ronan A. Cahill
Stephen R. Walsh
Michael J. Kerin
John O. Larkin
Paul Carroll
Patrick Owens
Matthew G. Davey
Noel E. Donlon
Claire L. Donohoe
Deborah A. McNamara
W. B. Robb
Micheal O‘Riordain
Stewart R. Walsh
Peter Neary
Christina Fleming
Dara O. Kavanagh
PROPEL-2 Trial Collaborators
C Peirce
E. T. Condon
S Abd Elwahab
John B. Conneely
Manvydas Varzgalis
Eleanor Faul
Desmond Toomey
E. Andrews
David Kearney
Terence Patrick Murphy
S T Martin
Helen Heneghan
M. Kevin Barry
Fiachra Cooke
S D Johnston
Arnold Hill
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