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Long-term Follow-up of Prophylactic Mesh Reinforcement After Emergency Laparotomy.

Long-term Follow-up of Prophylactic Mesh Reinforcement After Emergency Laparotomy.

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT04578561
Enrollment
187
Registered
2020-10-08
Start date
2010-01-31
Completion date
2020-01-31
Last updated
2020-10-08

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Prevention of Incisional Hernia in Emergency Surgery

Brief summary

Observational Study analyzing the long-term results of prophylactic mesh used for preventing incisional hernia after emergency midline laparotomies.

Detailed description

Background. Prevention of incisional hernias with a prophylactic mesh in emergency surgery is controversial. The present study aimed to analyze the long-term results of prophylactic mesh used for preventing incisional hernia after emergency midline laparotomies. Methods. This study was a retrospective analysis of patients who underwent an emergency midline laparotomy between January 2009 and July 2010 with a follow-up period of longer than 2 years. Long-term outcomes and risk factors for the development of incisional hernias between patients who received a prophylactic reinforcement mesh (Group M) and suture (Group S) were compared.

Interventions

PROCEDUREProphylactic mesh use

After laparotomy sutured clousur the abdominal wall wound is reinforced using a suprafascial synthetic mesh.

Sponsors

José A. Pereira
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
RETROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum

Inclusion criteria

* Patients undergoing emergency midline laparotomy

Exclusion criteria

* Those with need of concomitant hernia repair. * Those who received incisions outside the midline. * Those with delayed abdominal closure. * Those who died in the immediate postoperative period. * Those without a minimum 2 years of follow-up.

Design outcomes

Primary

MeasureTime frameDescription
Incisional hernia2 yearsDetection of clinical or subclinical incisional hernia during postoperative longterm followup

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 22, 2026