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Updated: May 10, 2026

Development of a Benchtop Model for Evaluating the Compatibility of Wound Dressing Materials with Negative Pressure Wound Therapy Systems
Published on: May 2, 2025
Efficacy and Safety of Negative Pressure Wound Therapy in Managing Lower Limb Amputation; An Updated Systematic
Abdullah Elrefae1, Mohamed Elghouneimy2,3, Mirna Morad Mashhour4
1Northwick Park Hospital, Harrow, UK.
Abstract:
Major lower-limb amputation often leads to wound complications that delay recovery and prosthetic use. Negative Pressure Wound Therapy (NPWT) has been suggested to improve outcomes, but evidence is inconsistent. The objective of this study is to compare NPWT with standard wound therapy in fresh amputation stumps. A systematic review and meta-analysis following PRISMA and Cochrane guidelines included randomised and controlled observational trials. Primary outcomes were wound complications, including surgical-site infections (SSI) and wound dehiscence. Secondary outcomes included re-amputation, healing, and resource use. Seventeen papers including over 6745 patients were analysed. NPWT significantly reduced total wound complications (RR 0.49, 95% CI 0.37-0.66) and SSIs (RR 0.50, 95% CI 0.27-0.90), including both superficial (RR 0.30, 95% CI 0.12-0.73) and deep infections (RR 0.26, 95% CI 0.11-0.63). The secondary amputation risk was lowered by one-third (RR 0.67, 95% CI 0.50-0.89). Wound dehiscence risk decreased (RR 0.53, 95% CI 0.30-0.94). Mortality, readmission, and hospital stay showed no significant differences between groups. Healing outcomes strongly favoured NPWT: mean time to ≥ 76% granulation was shortened by 25 days, while complete closure occurred nearly two weeks earlier. Kaplan-Meier reconstruction confirmed that NPWT accelerated wound maturation by 77% (HR 0.23, 95% CI 0.12-0.44). Economic evaluations, though limited, indicated fewer dressing changes, reduced outpatient visits, and overall cost savings. NPWT after major lower-limb amputation halves wound complications and infections, lowers re-amputation, and accelerates healing. Despite unchanged systemic outcomes, the local benefits are clinically significant, supporting its use in standard post-amputation care. Trial Registration: CRD420251088214.
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