Austin Daniel C, Donegan Derek, Mehta Samir
*Department of Orthopaedics, Dartmouth Hitchcock Medical Center, Lebanon, NH; and †Orthopaedic Trauma and Fracture Service, Department of Orthopaedic Surgery, Hospital of the University of Pennsylvania, Philadelphia, PA.
J Orthop Trauma. 2015 Aug;29(8):e259-65. doi: 10.1097/BOT.0000000000000329.
To quantify the infection risks of temporary lower extremity traction pins and compare these rates to nationwide and institution-specific surgical site infection rates. Additionally, to qualitatively describe pin site infections and to analyze the impact of traction pins on infection risks at associated open reduction internal fixation (ORIF) surgical sites.
A retrospective case-control study.
Level I Urban University Trauma Center.
One hundred sixty-nine cases of traction pin application occurring in 157 unique patients extracted from a trauma patient database.
Bedside application of a traction pin in the femur or tibia.
Rates of 90-day and 1-year minor and major infections at pin insertion locations and at ORIF wounds associated with traction pins.
A single infection, a septic knee, was reported. There were no superficial infections or osteomyelitis cases observed. The 90-day and 1-year rates of infection were identical with a per pin infection rate of 0.6% [95% confidence interval (CI), 0.1%-3.4%], a minor infection rate of 0.0% (95% CI, 0.0%-2.3%), and a major infection rate of 0.6% (95% CI, 0.1%-3.4%). Observed rates were lower than, but statistically similar to, nationwide infection rates for open reduction procedures and similar to institution-specific infection rates for arthroplasty procedures. Infection rates at associated ORIF wounds were not increased in comparison with nationwide controls. Pin placement played a definitive role in the infection observed.
Temporary lower extremity traction pins have low infection rates and can be safely placed at the bedside. Careful pin placement and review of postinsertion radiographs is necessary to avoid iatrogenic infection.
Prognostic Level IV. See Instructions for Authors for a complete description of levels of evidence.
量化临时下肢牵引针的感染风险,并将这些发生率与全国范围及特定机构的手术部位感染率进行比较。此外,定性描述针道感染情况,并分析牵引针对于相关切开复位内固定(ORIF)手术部位感染风险的影响。
一项回顾性病例对照研究。
一级城市大学创伤中心。
从创伤患者数据库中提取的157例独特患者发生的169例牵引针应用病例。
在股骨或胫骨处床边应用牵引针。
牵引针插入部位以及与牵引针相关的ORIF伤口处90天和1年的轻度及重度感染发生率。
报告了1例感染,即化脓性膝关节炎。未观察到浅表感染或骨髓炎病例。90天和1年的感染率相同,每根针的感染率为0.6%[95%置信区间(CI),0.1%-3.4%],轻度感染率为0.0%(95%CI,0.0%-2.3%),重度感染率为0.6%(95%CI,0.1%-3.4%)。观察到的发生率低于全国范围切开复位手术的感染率,但在统计学上相似,且与特定机构关节成形术的感染率相似。与全国范围的对照相比,相关ORIF伤口处的感染率并未增加。针的放置在观察到的感染中起决定性作用。
临时下肢牵引针感染率低,可在床边安全放置。为避免医源性感染,仔细放置牵引针并复查插入后X线片很有必要。
预后IV级。有关证据水平的完整描述,请参阅作者须知。