RCT on NPWT for Incisions Following Major Lower-limb Amputation to Reduce Surgical Site Infection
Primary Purpose
Amputation Wound, Amputation Stump Complication, Amputation Stump; Infection
Status
Unknown status
Phase
Not Applicable
Locations
Study Type
Interventional
Intervention
Negative pressure wound therapy
Standard dressing
Sponsored by
About this trial
This is an interventional prevention trial for Amputation Wound
Eligibility Criteria
Inclusion Criteria:
- any patient 18 years or older undergoing amputation of the lower limb, either an above knee amputation (AKA) or below knee amputation (BKA)
- ability to read and write English to undergo informed consent
Exclusion Criteria:
- patients in which a complete seal cannot be obtained at the time of vacuum placement
- wounds that are not closed primarily
- existing infection
- patient is anticipated to not follow-up
- inability to read and write English
Sites / Locations
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Other
Arm Label
Negative pressure wound therapy
Standard dressing
Arm Description
A vacuum assisted closure device will be applied in this arm
Standard dressing will be applied to this arm
Outcomes
Primary Outcome Measures
Surgical site infection
Surgical site infection will be defined using the Centre for Disease Control and Prevention Guidelines.
Secondary Outcome Measures
Length of stay
length of hospital stay
Antibiotic use
requirement for antibiotics to treat surgical site infection
Reoperation
requirement for revision of amputation
Death
mortality
Full Information
NCT ID
NCT03144726
First Posted
May 5, 2017
Last Updated
December 6, 2017
Sponsor
London Health Sciences Centre
1. Study Identification
Unique Protocol Identification Number
NCT03144726
Brief Title
RCT on NPWT for Incisions Following Major Lower-limb Amputation to Reduce Surgical Site Infection
Official Title
Single Center Prospective Randomized Control Trial on Negative Pressure Wound Therapy for Incisions Following Major Lower-limb Amputation to Reduce Surgical Site Infection
Study Type
Interventional
2. Study Status
Record Verification Date
December 2017
Overall Recruitment Status
Unknown status
Study Start Date
March 2018 (Anticipated)
Primary Completion Date
July 2019 (Anticipated)
Study Completion Date
July 2020 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
London Health Sciences Centre
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No
5. Study Description
Brief Summary
Surgical site infections following lower extremity amputations have been reported in up to 40% of patients. Surgical site infections have significant morbidity and even mortality in terms of emergency room visits, length of hospital stay, reamputation rates and death. Since its introduction, negative pressure wound therapy has been demonstrated to promote wound healing and possibly decreasing the need for future amputations. The aim of the study is to provide level I evidence for the use of negative pressure wound therapy devices in patients undergoing lower extremity amputation.
Detailed Description
Amputations are common vascular surgery procedures performed on patients with multiple medical comorbidities. Historically, morbidity and mortality following major amputation of the lower extremity in this patient population has been high. Recent studies have cited 30-day mortality rates ranging from 6% to 17%, with greater risk among patients with transfemoral vs transtibial amputation. Postoperative goals after amputation include uncomplicated wound healing and, for appropriate candidates, progression to use of a prosthesis for ambulation or transfer. Perioperative wound complications can be devastating in this already debilitated population and can range from 13% to 40%.
Postoperative wound complications, such as infection, dehiscence, and formation of haematoma or seroma, are common complications of surgical procedures; particularly among patients with risk factors such as obesity and diabetes. Wound complications may delay recovery, increase patient discomfort and reduce overall quality of life. Increased healthcare costs may be incurred due to prolonged inpatient stay, repeat surgery and the need for increased follow-up.
Wounds that are secondary to amputation are reported in 13-40% of cases and are one of the most challenging types of lower extremity wounds to heal. These patients often have compromised healing capacity. Kayssi et al studied Canadian readmission rates, early (<30 days) and late (30-365) readmissions were attributed to stump complications in 13% and 10% of patients respectively.
Wound complications in major limb amputation frequently result in the need for further major surgery in a group of patients with significant co-morbidity and enhanced operative risk. 1, 3, and 5 year reamputation rates for diabetics who have had major amputations are 4.7%, 11.8%, and 13.3% respectively. Henry et al suggested that undergoing multiple amputation revisions may indicate aggressive measures to treat critical limb ischemia or chronic infection that precede conversion to a more proximal amputation. Kono et al studied the incidence and risk factors for reamputation after forefoot amputation. They found that 16/116 (14%) patients developed postoperative infection, and 10 of these required reamputation (62.5%). Five of the ten reamputations occurred within 30 days after the patients developed postoperative infections.
In addition to the morbidity from infection there is also an increased rate of phantom pain as well as a delay to mobilisation with prosthesis. Minimizing postoperative infections would likely have improvements in clinical outcomes, quality of life, and utilization of resources. Currently, all patients are given prophylactic broad spectrum antibiotics to reduce the incidence of wound infection. Sadat et al investigated whether a prolonged 5 day course of antibiotics wound reduce stump infections, their results were positive however this treatment is associated with the increased risk of antimicrobial resistance and c. difficile infection.
Negative-pressure wound therapy (NPWT) has traditionally been used for the treatment of open wounds. In recent years, the indication for NPWT has been extended to include treatment of closed surgical incisions. Armstrong et al conducted a randomized controlled trial to determine whether NPWT delivered by the VAC system was clinically efficacious in treating amputation wounds of the diabetic foot to improve the proportion of wounds with complete closure. Treatment with NPWT resulted in a higher proportion of wounds that healed, faster healing rates, and fewer re-amputations than with standard treatment. No randomized controlled trials have been performed to assess NPWT and infection rates after major lower limb amputation.
There is a paucity of scientific literature reporting outcomes following major amputation in patients with critical limb ischemia, particularly with regards to wound problems and infection. The purpose of this study is to provide Level I evidence on whether negative pressure wound therapy is an effective strategy to significantly reduce postoperative infections after major lower extremity amputation, thereby reducing patient morbidity and mortality from this procedure.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Amputation Wound, Amputation Stump Complication, Amputation Stump; Infection, Infection
7. Study Design
Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Outcomes Assessor
Allocation
Randomized
Enrollment
290 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
Negative pressure wound therapy
Arm Type
Experimental
Arm Description
A vacuum assisted closure device will be applied in this arm
Arm Title
Standard dressing
Arm Type
Other
Arm Description
Standard dressing will be applied to this arm
Intervention Type
Device
Intervention Name(s)
Negative pressure wound therapy
Intervention Description
Negative pressure wound therapy is a commonly utilized tool in the hospital setting and will be applied to amputations in our study to determine the effect on surgical site infections
Intervention Type
Other
Intervention Name(s)
Standard dressing
Intervention Description
A standard dressing will be applied to the amputations in this arm of the study
Primary Outcome Measure Information:
Title
Surgical site infection
Description
Surgical site infection will be defined using the Centre for Disease Control and Prevention Guidelines.
Time Frame
30 days
Secondary Outcome Measure Information:
Title
Length of stay
Description
length of hospital stay
Time Frame
30 days
Title
Antibiotic use
Description
requirement for antibiotics to treat surgical site infection
Time Frame
30 days
Title
Reoperation
Description
requirement for revision of amputation
Time Frame
30 days
Title
Death
Description
mortality
Time Frame
30 days
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
any patient 18 years or older undergoing amputation of the lower limb, either an above knee amputation (AKA) or below knee amputation (BKA)
ability to read and write English to undergo informed consent
Exclusion Criteria:
patients in which a complete seal cannot be obtained at the time of vacuum placement
wounds that are not closed primarily
existing infection
patient is anticipated to not follow-up
inability to read and write English
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Oonagh Scallan, MD
Phone
6478761954
Email
oonagh.scallan@lhsc.on.ca
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Adam Power, MD
Organizational Affiliation
London Health Sciences Centre
Official's Role
Principal Investigator
12. IPD Sharing Statement
Plan to Share IPD
Undecided
Learn more about this trial
RCT on NPWT for Incisions Following Major Lower-limb Amputation to Reduce Surgical Site Infection
We'll reach out to this number within 24 hrs