Comparison of Surgical Site Infection After Skin Closure by Prolene or Staples in Bilateral Knee Arthroplasty Patients

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

UNKNOWN

Clinical Phase

NA

Total Enrollment

82 participants

Study Classification

INTERVENTIONAL

Study Start Date

2020-11-30

Study Completion Date

2021-12-31

Brief Summary

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Knee arthroplasty also known as the total knee replacement is an orthopedic surgical procedure done to resurface the knee that has been severely damaged by arthritis. The optimal goal of skin closure after the procedure is to promote rapid healing and an acceptable cosmetic result while minimizing the risk of infection. Skin closure after knee arthroplasty is done by using either of the two widely used sutures i.e. polypropylene (Prolene) sutures or the skin staple sutures. The literature is very scarce on knee arthroplasty patients and the results of the studies conducted have been inconclusive of the studies conducted on the patients of knee arthroplasty. Moreover, there are no standard guidelines as to which type of suture should be used. The type of sutures is being selected on the orders and wishes of the surgeon at the time of skin closure. Prolene sutures are made up of a synthetic steroisomer known as polypropylene. It is a monofilament non-absorbable, sterile surgical suture. They are indicated for use in general soft tissue. It Provides permanent tensile strength retention in tissue, even in the presence of infection. These sutures are exceptionally smooth for an easy passage through the tissue. Prolene sutures are widely used in cardiovascular, orthopedics, ophthalmic, and neurological surgical procedures. Another type of sutures that are used to close the surgical wound are the staple sutures. They are used as an alternative to the traditional Prolene sutures. They are non-absorbable and usually used on surgical wounds that are big, complex or hard to close by using Prolene. These are specialized staples made up of titanium, stainless steel or plastic.

Interventions:

The study will have 2 intervention arms. The patients will be randomized to receive either Prolene sutures for wound closure or staple sutures for wound closure. After the application of the intervention, routine care would be given to the patients postoperatively.

Hypothesis:

The investigators hypothesize that there is no difference in the incidence of surgical site infection in bilateral TKR patients with wound closure by Prolene vs staple.

Study Design:

This study will be conducted as an open blinded, parallel design, equivalence randomized controlled trial. The patients would be randomized to receive either of the two interventions i.e. Prolene or Staple sutures.

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Detailed Description

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Study Enrollment Procedures:

Enrollment will be a continuous process with screening and enrolling eligible patients admitted through the clinic electively for primary TKR. Informed consent will be taken from the patient as per routine protocol before the arthroplasty procedures in the hospital. Research objectives, methodology, risks, and benefits will be explained in detail. Consent for the participation in the study will only be taken by the primary investigator at his clinic or the surgical resident on call preoperatively along with the consent for the surgical procedure.

Pre-Randomization Evaluations Screening:

The screening will involve the routine history taking and physical examination by the doctor and nursing staff in the clinic. Screening won't involve performing procedures that are not part of routine management.

On-study/on-intervention evaluations:

After screening and assessing the eligibility, patients will be randomly allocated by a 1:1 ratio to the two intervention groups i.e. prolene or staple using a computer-generated randomization sequence by the clinical trials unit (CTU), which they will provide to the PI, after patients' admission in the hospital. Patients will be followed from the time they reach the ward after surgery until their hospital discharge, which is usually around 7 days.

Data Collection:

The data collection will be done by the surgical site infection (SSI) nurses from the infection control department of AKUH. These nurses are well-trained to assess the surgical site infections in all the surgery patients admitted to the hospital. Training of data collectors will be done by the PI to ensure the reliability and validity of the study. The data collectors will be strictly instructed to respect the autonomy of participants. Data collection will be done by the data collectors under the supervision of the PI and CTU. Questionnaires will be checked for consistency and logical data entries. Data entry will be done, and counter checked by the PI at regular intervals.

Data Storage:

Data collected will be coded and kept confidential without the identifiable information of patients. The confidentiality of the study participants will be maintained throughout the study period. Data collected will be kept confidential without identifiable information of patients who are identified by a number assigned. The hard copy forms will be retained in a secured location with the PI after data entry into computer software and will be kept as per hospital protocol. The password-protected drives will be used to store data with only the PI having access to it. The data will be available for AKUH ethical review committee on request and might be published in a journal without disclosing any identifiable information of patients. Filled questionnaires will be stored for 5 years after the study is completed as per the policy of the institute.

Sample Size:

The sample size was calculated via open epi software version 3.01. The level of significance was kept at 5% with a power of 80%. The percentage of exposed (staple sutures) with outcome (surgical site infection) was 66%. The percentage of non-exposed (Prolene sutures) with outcome (surgical site infection) was 33%. The estimated risk ratio taken from a study was 2. After adding the non-response rate of 10% the final sample size came out to be 82 patients with 41 patients in each arm.

Plan of Analysis:

Statistical analysis will be done by using STATA software version 15. The normality assumption for the quantitative variables would be assessed using the shapiro wilk test. Mean ± SD will be computed for all the normally distributed quantitative variables. The median and interquartile range would be reported for the non-normally distributed quantitative variables. The categorical variables would be expressed in frequencies and percentages. The Cox Proportional Hazard regression will be used for the univariate and multivariable analysis. Univariate analysis will be conducted, and crude risk ratios and their 95% confidence intervals will be obtained. All significant independent variables at the univariate stage will be regressed in a multivariable cox proportional hazard regression using the stepwise method in the multivariable model and the adjusted risk ratios will be obtained.

Conditions

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Total Knee Replacement

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

PREVENTION

Blinding Strategy

NONE

Study Groups

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Interventional Arm 1

After total knee replacement, the skin closure of the patients in this group will be done using polypropylene (PROLENE) sutures.

Group Type EXPERIMENTAL

Polypropylene (PROLENE) sutures

Intervention Type PROCEDURE

After total knee replacement, the skin closure of the patients in this group will be done using polypropylene (PROLENE) sutures.

Interventional Arm 2

After total knee replacement, the skin closure of the patients in this group will be done using staple sutures.

Group Type ACTIVE_COMPARATOR

Staple Sutures

Intervention Type PROCEDURE

After total knee replacement, the skin closure of the patients in this group will be done using staple sutures.

Interventions

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Polypropylene (PROLENE) sutures

After total knee replacement, the skin closure of the patients in this group will be done using polypropylene (PROLENE) sutures.

Intervention Type PROCEDURE

Staple Sutures

After total knee replacement, the skin closure of the patients in this group will be done using staple sutures.

Intervention Type PROCEDURE

Eligibility Criteria

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Inclusion Criteria

* Adult patients of age 40-70 years
* Undergoing bilateral knee arthroplasty at AKUH Karachi.
* Both the genders would be included.
* Patients having American Society of Anesthesiologists (ASA) level of I, II and III
* Patients having functional class of I, II and III pre-operatively
* Patients opting to undergo Bilateral knee arthroplasty under care of the selected surgeon (A) for the study.
* Patients undergoing bilateral TKR electively

Exclusion Criteria

* Patients unwilling to consent.
* Patients unable to comprehend due to the language barrier
* Patients who have a Glasgow Coma Scale i.e. GCS\<15 (cognitive impairment)
* Patients undergoing a knee revision surgery
* Patients having a previous incision/scar in the operative field will be excluded
* Patients having documented allergy to Prolene or stainless steel
* Patients having a documented underlying malignancy
* Patients undergoing unilateral TKR or staged bilateral TKR
* Patients undergoing emergency TKR.
* Patients having undergoing surgery due to trauma or fracture

Minimum Eligible Age

40 Years

Maximum Eligible Age

70 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No