New non-invasive device to promote primary closure of the fascia and prevent loss of domain in the open abdomen: a pilot study

Background Primary closure of the fascia at the conclusion of a stage laparotomy can be a challenging task. Current techniques to medialize the fascial edges in open abdomens entail several trips to the operating room and could result in fascial damage. We conducted a pilot study to investigate a no...

Full description

Bibliographic Details
Main Authors: Joao Baptista Rezende-Neto, Bruna Gewehr Camilotti
Format: Article
Language:English
Published: BMJ Publishing Group 2020-12-01
Series:Trauma Surgery & Acute Care Open
Online Access:https://tsaco.bmj.com/content/5/1/e000523.full
id doaj-cf62b8f06cfd4123950625ddc45d5190
record_format Article
spelling doaj-cf62b8f06cfd4123950625ddc45d51902021-02-01T17:00:48ZengBMJ Publishing GroupTrauma Surgery & Acute Care Open2397-57762020-12-015110.1136/tsaco-2020-000523New non-invasive device to promote primary closure of the fascia and prevent loss of domain in the open abdomen: a pilot studyJoao Baptista Rezende-Neto0Bruna Gewehr Camilotti1Surgery, University of Toronto Faculty of Medicine, Toronto, Ontario, CanadaGeneral Surgery, St Michael's Hospital, Toronto, Ontario, CanadaBackground Primary closure of the fascia at the conclusion of a stage laparotomy can be a challenging task. Current techniques to medialize the fascial edges in open abdomens entail several trips to the operating room and could result in fascial damage. We conducted a pilot study to investigate a novel non-invasive device for gradual reapproximation of the abdominal wall fascia in the open abdomen.Methods Mechanically ventilated patients ≥16 years of age with the abdominal fascia deliberately left open after a midline laparotomy for trauma and acute care surgery were randomized into two groups. Control group patients underwent standard care with negative pressure therapy only. Device group patients were treated with negative pressure therapy in conjunction with the new device for fascial reapproximation. Exclusion criteria: pregnancy, traumatic hernias, pre-existing ventral hernias, burns, and body mass index ≥40 kg/m2. The primary outcome was successful fascial closure by direct suture of the fascia without mesh or component separation. Secondary outcomes were abdominal wall complications.Results Thirty-eight patients were investigated, 20 in the device group and 18 in the control group. Primary closure of the fascia by direct suture without mesh or component separation was achieved in 17 patients (85%) in the device group and only 10 patients (55.6%) in the control group (p=0.0457). Device group patients were 53% more likely to experience primary fascial closure by direct suture than control group patients. Device group showed gradual reduction (p<0.005) in the size of the fascial defects; not seen in control group. There were no complications related to the device.Conclusions The new device applied externally on the abdominal wall promoted reapproximation of the fascia in the midline, preserved the integrity of the fascia, and improved primary fascial closure rate compared with negative pressure therapy system only.Level of evidence I, randomized controlled trial.https://tsaco.bmj.com/content/5/1/e000523.full
collection DOAJ
language English
format Article
sources DOAJ
author Joao Baptista Rezende-Neto
Bruna Gewehr Camilotti
spellingShingle Joao Baptista Rezende-Neto
Bruna Gewehr Camilotti
New non-invasive device to promote primary closure of the fascia and prevent loss of domain in the open abdomen: a pilot study
Trauma Surgery & Acute Care Open
author_facet Joao Baptista Rezende-Neto
Bruna Gewehr Camilotti
author_sort Joao Baptista Rezende-Neto
title New non-invasive device to promote primary closure of the fascia and prevent loss of domain in the open abdomen: a pilot study
title_short New non-invasive device to promote primary closure of the fascia and prevent loss of domain in the open abdomen: a pilot study
title_full New non-invasive device to promote primary closure of the fascia and prevent loss of domain in the open abdomen: a pilot study
title_fullStr New non-invasive device to promote primary closure of the fascia and prevent loss of domain in the open abdomen: a pilot study
title_full_unstemmed New non-invasive device to promote primary closure of the fascia and prevent loss of domain in the open abdomen: a pilot study
title_sort new non-invasive device to promote primary closure of the fascia and prevent loss of domain in the open abdomen: a pilot study
publisher BMJ Publishing Group
series Trauma Surgery & Acute Care Open
issn 2397-5776
publishDate 2020-12-01
description Background Primary closure of the fascia at the conclusion of a stage laparotomy can be a challenging task. Current techniques to medialize the fascial edges in open abdomens entail several trips to the operating room and could result in fascial damage. We conducted a pilot study to investigate a novel non-invasive device for gradual reapproximation of the abdominal wall fascia in the open abdomen.Methods Mechanically ventilated patients ≥16 years of age with the abdominal fascia deliberately left open after a midline laparotomy for trauma and acute care surgery were randomized into two groups. Control group patients underwent standard care with negative pressure therapy only. Device group patients were treated with negative pressure therapy in conjunction with the new device for fascial reapproximation. Exclusion criteria: pregnancy, traumatic hernias, pre-existing ventral hernias, burns, and body mass index ≥40 kg/m2. The primary outcome was successful fascial closure by direct suture of the fascia without mesh or component separation. Secondary outcomes were abdominal wall complications.Results Thirty-eight patients were investigated, 20 in the device group and 18 in the control group. Primary closure of the fascia by direct suture without mesh or component separation was achieved in 17 patients (85%) in the device group and only 10 patients (55.6%) in the control group (p=0.0457). Device group patients were 53% more likely to experience primary fascial closure by direct suture than control group patients. Device group showed gradual reduction (p<0.005) in the size of the fascial defects; not seen in control group. There were no complications related to the device.Conclusions The new device applied externally on the abdominal wall promoted reapproximation of the fascia in the midline, preserved the integrity of the fascia, and improved primary fascial closure rate compared with negative pressure therapy system only.Level of evidence I, randomized controlled trial.
url https://tsaco.bmj.com/content/5/1/e000523.full
work_keys_str_mv AT joaobaptistarezendeneto newnoninvasivedevicetopromoteprimaryclosureofthefasciaandpreventlossofdomainintheopenabdomenapilotstudy
AT brunagewehrcamilotti newnoninvasivedevicetopromoteprimaryclosureofthefasciaandpreventlossofdomainintheopenabdomenapilotstudy
_version_ 1724315117412155392