Wound Surgical, Diabetes, Obesity, Chronic Kidney Diseases, Smoking
Conditions
Keywords
Total Knee Arthroplasty, Total Knee Replacement
Brief summary
This study is a single-center, prospective, randomized, open-label clinical trial evaluating three commercially available closed-incision negative pressure wound therapy (ciNPWT) devices: NPseal, PICO, and Prevena, in adult patients undergoing primary total knee arthroplasty (TKA) who meet predefined high-risk criteria for wound complications. A total of approximately 300 participants will be enrolled and randomized in a 1:1:1 fashion to receive one of the three study dressings applied over the closed surgical incision at the end of the procedure. All participants will otherwise receive standard perioperative and postoperative care. The primary follow-up period will extend through 90 days after surgery. The primary objective is to compare the incidence of 90-day surgical site complications, including superficial infection, wound dehiscence, seroma, and hematoma, across the three dressing groups. Secondary objectives include evaluation of device usability, patient experience, and device-related issues (such as loss of seal, alarms, tubing or pump problems, fluid saturation, and premature dressing changes), as well as assessment of the interaction between skin closure method and device performance. Research-specific activities are limited to eligibility confirmation, informed consent, randomization, administration of a brief postoperative patient survey at approximately postoperative day 7 and/or dressing removal, provider assessment of the dressing at removal, and collection of clinical outcomes from the medical record. No additional blood draws, imaging, or invasive procedures are required for participation. This study is designed to address a gap in the literature by providing head-to-head comparative data on commonly used ciNPWT systems in a high-risk primary TKA population, with the goal of informing postoperative wound management strategies in clinical practice.
Interventions
Designed to maintain negative pressure without an external battery-powered pump or canister.
Designed to deliver negative pressure for up to 7 days and has visual alerts for issues such as air leaks, low battery, or dressing change
Designed to deliver continuous negative pressure over the closed incision and collect fluid in a separate canister.
Sponsors
Study design
Eligibility
Inclusion criteria
* Age 18 years or older * Undergoing primary total knee arthroplasty * Able to understand the study, provide informed consent, and participate in study procedures Meet at least one of the following co-morbidities: * BMI ≥35 * Diabetes * Prior surgical incision(s) in the operative area * Chronic kidney disease
Exclusion criteria
* Prisoners * Pregnant women * Patients who indicate they may not comply with post-operative instructions * Patients with active bleeding
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Surgical complications | From day of surgery to 90days post-op | Incidence of 90-day surgical site complications among patients receiving NPseal, PICO, or Prevena dressings. |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Patient Post-Operative Dressing Survey | From day of surgery to 90days post-op | Patient-reported experience to evaluate device usability, satisfaction, and device-related issues (including adequacy of instructions, maintenance of seal/suction, device alarms or warnings, tubing or pump disconnections, fluid saturation, need for early dressing replacement, ease of use, provider communication regarding device benefits, and willingness to use the dressing again). |
| Provider Assessment Survey | From day of surgery to 90days post-op | Clinical evaluation of the skin closure technique and the compatibility of device performance on wound healing |