Table 1.
Reference | Country | No. of incisions | Type of surgery | Treatment* | Inclusion and exclusion criteria | Outcome measures† | Follow‐up |
---|---|---|---|---|---|---|---|
Howell et al.33 | USA | 60 | Total knee arthroplasty | VAC® versus sterile gauze (dressing not described) (all wounds were assessed after 48 h) | Inclusion: BMI ≥ 30 kg/m2 and enoxaparin sodium for DVT | Primary: days to a dry wound (no drainage on gauze for 24 h) | 12 months |
Exclusion: revision total knee replacement, previous knee surgery and documented diabetes | Secondary: total wound drainage, no. of gauze dressings applied to the wound, duration of hospital stay, incidence of infection, readmission | ||||||
Pachowsky et al.34 | Germany | 19 | Total hip arthroplasty | Prevena™ versus ‘a dry wound coverage’ (dressing not described) (5 days versus n.s.) | n.s. | Primary: seroma (ultrasound imaging of the wound was used to show a seroma) | 10 days |
Grauhan et al.35 | Germany | 150 | Median sternotomy | Prevena™ versus conventional wound dressings (dressing not described) (6–7 days versus 1–2 days) | Inclusion: BMI ≥ 30 kg/m2, and absence of preoperative signs of inflammation Exclusion: immunological disease, immunosuppressive therapy, skin disease | Primary: wound infection (defined according to US Centers for Disease Control and Prevention criteria) | 90 days |
Secondary: dehiscence of skin or sternum | |||||||
Masden et al.36 | USA | 81 | Primary or delayed primary closure of lower extremity or abdominal wounds | VAC® versus standard dry sterile dressing (Mepitel®) and a bacteriostatic single silver layer (Acticoat™) (all wounds assessed on day 3) | Inclusion: scheduled to undergo primary or delayed primary closure | Primary: wound infection, wound dehiscence (evaluated by a member of the research team, blinded to randomization groups) | Average of 113 days |
Exclusion: patients allergic to tape or who could not tolerate NPWT; patients with lower‐extremity amputations distal to forefoot | |||||||
Secondary: reoperation, duration of hospital stay | |||||||
Stannard et al.37 | USA | 263 | High‐risk lower extremity fractures (tibial plateau, pilon, calcaneus) | VAC® versus standard postoperative dressing (dressing not described) (all wounds assessed on day 2) | Inclusion: presence of a high‐energy tibial plateau, pilon or calcaneus fractures | Primary: wound infection (defined with a combination of clinical signs and symptoms and laboratory data), wound dehiscence (defined as any separation of the incision that required wound care or reoperation) | n.s. |
Exclusion: non‐operative or open fractures, receiving definitive surgery more than 16 days after injury, pregnant women and patients with low‐energy fractures | |||||||
Pauser et al.38 | Germany | 21 | Hemiathroplasty | Prevena™ versus ‘a dry wound coverage’ (dressing not described) (5 days versus n.s.) | n.s. | Primary: seroma (ultrasound imaging of the wound was used to show a seroma) | 10 days |
Nordmeyer et al.39 | Germany | 20 | Spinal fracture | PICO™ versus ‘a dry wound coverage’ (dressing not described) (5 days versus n.s.) | n.s. | Primary: seroma (ultrasound imaging of the wound was used to show a seroma) | 10 days |
B. D. Crist et al. (personal communication) | USA | 90 | Pelvic, acetabular and hip fractures | VAC® versus a standard gauze (dressing not described) (all wounds assessed on day 2) | Inclusion: age 18 years or older, scheduled for surgical repair of pelvic and/or acetabular fracture, and subject/guardian able to provide informed consent | Primary: deep wound infection (‘Deep infection was one that went to the OR’) Secondary: wound drainage, duration of hospital stay, dressing supply costs, nursing time cost for dressing changes | 12 months |
Exclusion: pregnancy, injury treated percutaneously without open surgery | |||||||
S. Karlakki et al. (personal communication) | UK | 209 | Hip and knee replacement | PICO™ versus Mepore® or Tegaderm™ + Pad (3 M) (7 days versus 2 days) | Exclusion: known allergies to dressings, and those on warfarin | Primary: exudate from the surgical wound (predefined grading of wound exudate) | 6 weeks |
Secondary: wound complications, readmissions, no. of dressing changes, overall cost‐effectiveness | |||||||
R. Galiano et al. (personal communication) | USA, South Africa, France and the Netherlands | 398 | Bilateral breast reduction | PICO™ versus Steri‐Strip™ (7 days versus 7 days) | n.s. | Primary: delayed healing, dehiscence, wound infection (predefined description of primary outcome not stated) | 21 days |
Secondary: scar quality | 90 days |
Text in parentheses indicates
duration of treatment before first dressing change and
predefined description of primary outcome. Mepitel™ (Mölnlycke Health Care, Gothenburg, Sweden); Acticoat™ (Smith & Nephew, Hull, UK); Mepore® (Mölnlycke Health Care); Tegaderm™ (3 M, St Paul, Minnesota, USA); Steri‐Strip™ (3 M). BMI, body mass index; DVT, deep vein thrombosis; n.s., not stated; NPWT, negative‐pressure wound therapy; OR, operating room.