Postoperative Surgical Site Infection afterENT Bone Flap Surgery

NCT04492826 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 39

Last updated 2020-07-30

No results posted yet for this study

Summary

In 2017, the French Society in anesthesia and reanimation published new recommendations on intraoperative antibiotic prophylaxis. Now, no more than 48 hours of antibiotic prophylaxis applies to any otolaryngology surgery, regardless of patient's medical history or type of flap used to rebuild. This has resulted in an alignment of our local protocol in Croix-Rousse hospital.

However, after few years, our local impressions are that bone flap surgeries are very likely to provide surgical site infections (osteo-articular or non-osteo-articular infections).

The prejudice of these postoperative site infections is significant, with serious consequences,. of both functional and aesthetic sides.

We wanted to objectify this impression by retrospectively analyzing the data relating to patients operated on for bone flapsurgeries.

Knowing the operation site infection rate after surgery for otolaryngology bone flap surgery will allow us to objectively understand the infectious risk of these surgeries, in particular the risk of osteoarticular infection. Identifying operation site infection factors will allow us to better target and prevent them.

The goal is to find out if the antibiotic prophylaxis currently recommended is sufficient and effective for this type of surgery.

Conditions

  • Rate of Infections
  • Operating Site
  • Post-operative Surgery
  • Bone Flap Surgery
  • Otolaryngology

Interventions

PROCEDURE

Postoperative infections rate

Assess the postoperative infection rate after otolaryngology bone flap surgery.

Sponsors & Collaborators

  • Hospices Civils de Lyon

    lead OTHER

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2012-09-30
Primary Completion
2012-09-30
Completion
2019-02-28

Countries

  • France

Study Locations

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Read the full study record

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View NCT04492826 on ClinicalTrials.gov