Surgical Hand Scrubbing Methods and the Duration of Scrubbing Time

October 5, 2020 updated by: Emine Arici Parlak, Saglik Bilimleri Universitesi Gulhane Tip Fakultesi

The Effect of Different Surgical Hand Scrubbing Methods and the Duration of Scrubbing Time on the Bacterial Flora

Surgical hand scrubbing is the removal of transient flora and reduction of permanent flora as much as possible before any sterile gloves are worn before any surgical intervention. It is a cheap and easy method to prevent infections. Effective use of surgical hand scrubbing has an important role in preventing and reducing the transfer of health-related infections. Although many studies have been performed on surgical hand scrubbing, no standard practice has been found in the method of scrubbing and optimal duration of scrubbing time. The aim of this study is to compare evidence-based surgical hand scrubbing methods in order to prevent surgical site infections.

Methods H0: There is no difference between the effectiveness of different surgical hand scrubbing methods on the bacterial flora in the hand H1: There is a difference between the effectiveness of different surgical hand scrubbing methods on the bacterial flora in the hand.

Time H0: There is no difference between the effectiveness of different the duration of scrubbing time on the bacterial flora in the hand.

H1: There is a difference between the effectiveness of different the duration of scrubbing time on the bacterial flora in the hand.

Study Overview

Status

Completed

Conditions

Intervention / Treatment

Detailed Description

Original Value: Surgical site infections (SSI) are a serious problem due to increased morbidity and mortality, prolonged hospitalization, hospitalization and consumption of health resources. It is reported from guides that the several factors like hair removal, skin antisepsis, prevention of hypothermia, antimicrobial prophylaxis, providing adequate oxygenation applied in intraoperative period reduce SSI. In addition to these factors, it is known that hand antisepsis of the surgical team is one of the most important factors in preventing SSI. Surgical hand scrubbing is the removal of transient flora and reduction of permanent flora as much as possible before any sterile gloves are worn before any surgical intervention. It is a cheap and easy method to prevent infections. Effective use of surgical hand scrubbing has an important role in preventing and reducing the transfer of health-related infections. Therefore, the research topic is directly related to patient safety and is considered to be one of the important areas of health services at national and international level in terms of establishing institutional culture in the prevention of surgical site infections. Although many studies have been performed on surgical hand scrubbing, no standard practice has been found in the method of scrubbing and optimal duration of scrubbing time. The aim of this study is to compare evidence-based surgical hand scrubbing methods in order to prevent surgical site infections.

Method: The research is a randomized controlled prospective study. The universe of the research was surgeon and operating room nurses in Gulhane Training and Research Hospital. The sample size is at least 180 people for one-way analysis of variance with G * Power version 3.1.19 software to determine a medium level (0.25) effect size between 4 groups at 0.80 power and 0.05 type I error level calculated (Tsai, 2016). Participants was divided into 4 groups by randomization method.

The participants in the first group performed the surgical hand scrubbing for 1 minute and with using a nail brush.

The participants in the second group performed the surgical hand scrubbing for 1 minute and without using a nail brush.

The participants in the third group performed the surgical hand scrubbing for 2 minute and with using a nail brush.

The participants in the fourth group performed the surgical hand scrubbing for 2 minute and without using a nail brush.

Standard Practices in All Groups

  • The application will take place during the first surgeries entered in the morning.
  • All groups will be used hand antiseptic (4% Chlorhexidine gluconate) which is used in the operating room.
  • It will be examined whether the nails are smaller than 2 mm. If the nails are long, individuals will be asked to cut their nails with the help of disposable nail scissors before surgical hand scrubbing.
  • There will be no nail polish on the nails and there will be no jewelry on the hand and the ring.
  • 3 ml of antiseptic solution will be used at each washing stage.

Volunteers' Exclusion Criteria (Different from Exclusion Criteria):

  • Participants want to leave the research
  • Expected surgery time is less than 1,5 hours.
  • A tear / puncture in the glove during the operation.
  • During the operation, data collection will be terminated in cases where the sterility of the glove is impaired.

This research will take place in three stages. At all stages (before surgical hand scrubbing, immediately after and at the end of the surgery), culture will be taken from the active hands of the participants with the Glove Juice Method. At all stages, culture will be taken from the participants via Glove Juice Method.

Glove Juice Method It is a method used to determine the number of bacteria on hand. In this method, individuals will be provided to wear gloves on their dominant hand. Powder-free sterile gloves were used for all sampling. Then, 50 ml of 'Tryptic Soy Broth' medium was placed inside the glove and all surfaces of the gloved hand were massaged for 60 seconds by the researcher. A sample was taken from the liquid in the glove using aseptic techniques and analyzed.

Applications in Medical Microbiology Laboratory Before surgical hand scrubbing, samples taken with glove liquid technique were diluted 1:10 in Müller Hinton Broth broth in the laboratory (500 μl sample, 4.5 ml. Müeller Hinton Broth). And 300 μl of it was placed on 5% sheep blood agar plates with sterile micropipettes. 1 ml each of the other samples (after surgical hand scrubbing and at the end of the surgery) was spread diluted into three 5 % sheep blood agar plates with sterile micropipettes. All samples were incubated at 35° C for 48 hours under atmospheric conditions. Total bacterial load was determined by counting the total colony forming units (CFU) on the plates.

Statistical Method SPSS (Statistical Package for the Social Sciences) Windows Version 22.00 package program will be used in the statistical analysis of the data obtained at the end of the study. Number,%, mean ± standard deviation, median (25% -75%) values will be used in defining the data. Kolmogorov-Smirnov test will be used to evaluate the suitability for normal distribution. In comparative statistics, appropriate tests will be used according to the normal distribution of the sample. In statistical decisions, p ≤ 0.05 level will be accepted as an indicator of significant difference.

Study Type

Interventional

Enrollment (Actual)

212

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

      • Ankara, Turkey
        • UNIVERSITY OF HEALTH SCIENCES GULHANE FACULTY OF NURSING

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

  • Child
  • Adult
  • Older Adult

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Description

Inclusion Criteria:

  • Being a surgeon or operating room nurse
  • Having six months and more surgical experience
  • Agree to participate in the research

Exclusion Criteria:

  • Not wanting to participate in the research
  • Being allergic to the skin due to surgical antiseptic use
  • Being latex allergy
  • Wounds and abrasions on the hand and nail edges
  • To have used a systematic antibiotic at the data collection stage and within two weeks

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Prevention
  • Allocation: Randomized
  • Interventional Model: Sequential Assignment
  • Masking: Single

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Group I (Brushed-1 minute)
Surgical hand scrubbing will be performed in 1 minute using a brush.
Surgical hand scrubbing will be performed in 1 minute and 2 minutes using a disposable nail brush.
No Intervention: Group II (Brushless-1 minute)
Surgical hand scrubbing will be performed in 1 minute without using a brush.
Experimental: Group III (Brushed-2 minutes)
Surgical hand scrubbing will be performed in 2 minute using a brush.
Surgical hand scrubbing will be performed in 1 minute and 2 minutes using a disposable nail brush.
No Intervention: Group IV (Brushless-2 minutes)
Surgical hand scrubbing will be performed in 2 minute without using a brush.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
The number of bacteria on hand
Time Frame: ''just before surgical hand scrubbing''
The effect of brush usage and time on bacterial flora in hand during surgical hand. Bacterial analysis was carried out in three consecutive measurement.
''just before surgical hand scrubbing''
The number of bacteria on hand
Time Frame: 'immediately after surgical hand scrubbing''
The effect of brush usage and time on bacterial flora in hand during surgical hand scrubbing
'immediately after surgical hand scrubbing''
The number of bacteria on hand
Time Frame: ''after surgery (between 90-120 minutes after surgical hand scrubbing)''
The effect of brush usage and time on bacterial flora in hand during surgical hand scrubbing
''after surgery (between 90-120 minutes after surgical hand scrubbing)''

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Sponsor

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

November 5, 2019

Primary Completion (Actual)

March 9, 2020

Study Completion (Actual)

April 30, 2020

Study Registration Dates

First Submitted

September 21, 2020

First Submitted That Met QC Criteria

October 5, 2020

First Posted (Actual)

October 8, 2020

Study Record Updates

Last Update Posted (Actual)

October 8, 2020

Last Update Submitted That Met QC Criteria

October 5, 2020

Last Verified

October 1, 2020

More Information

Terms related to this study

Other Study ID Numbers

  • 13131313

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

No

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

Clinical Trials on Surgical Site Infection

Clinical Trials on Using a brush

Search Similar Trials