No Incidence of Postoperative Knee Sepsis With Suprapatellar Nailing of Open Tibia Fractures
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Updated: Mar 13, 2026

Combined In vivo Optical and µCT Imaging to Monitor Infection, Inflammation, and Bone Anatomy in an Orthopaedic Implant Infection in Mice
Published on: October 16, 2014
Phillip M Mitchell1, Benjamin M Weisenthal, Cory A Collinge
1Department of Orthopaedics, Vanderbilt University Medical Center, Nashville, TN.
Objective:
To evaluate the incidence of knee sepsis after suprapatellar (SP) nailing of open tibia fractures.
Design:
Retrospective; Setting: ACS level 1 trauma center.
Patients/Participants:
We reviewed 139 open tibia fractures that underwent SP nailing as definitive treatment over a 5-year period (January 1, 2011 to January 1, 2016). Most patients (90%, n = 126) underwent intramedullary nailing at the time of their initial surgery. We defined knee sepsis as intra-articular infection requiring operative debridement, either open or arthroscopically, within 1 month's time.
Intervention:
Open tibia fractures treated with an SP tibial nail.
Main Outcome Measurements:
Demographic data, fracture characteristics, Gustilo and Anderson classification of open fractures, and occurrence of knee sepsis.
Results:
In 139 open tibia fractures, there were no cases of knee sepsis in the 30 days after treatment with an SP intramedullary nail. Eighty-seven percent of our cohort had Gustilo and Anderson type II (41%) or type III (46%) open fractures. Most open fractures (83%) underwent primary wound closure during the index procedures. Twenty-five limbs (18%) had evidence of infection at the open fracture site of their open fracture necessitating operative intervention and/or antibiotics: none, however, developed knee sepsis.
Conclusions:
Although the SP approach carries intra-articular risks, we found a low risk of knee sepsis using this technique in the treatment of open tibia fractures. Our data suggest that there is no greater risk of intra-articular infection using an SP portal as compared with an infrapatellar one.
Level Of Evidence:
Therapeutic Level IV. See Instructions for Authors for a complete description of levels of evidence.
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