This study was conducted using a cross-sectional, descriptive-analytical methodology. To reduce the costs of the tests, four sampling points were selected (two pieces of equipment and two surfaces). Based on the obtained results, among the examined types of equipment, suction devices and ventilators were chosen for sampling (noting that suction samples will be taken from the inner part of the tracheal tube). Among the surfaces, the patient's breakfast table and the bar next to the patient's bed were selected based on conditions such as patient mobility and the presence or absence of a companion.
Samples were taken over three months from designated surfaces and equipment in several wards of Kowsar Hospital (male surgical, internal ICU, and post-CCU) following the National Infection Control Care System protocol. This was done without prior notice or sensitization of the staff to avoid any changes in behavior or errors. It should be noted that in addition to the service personnel carrying out the disinfection process, they were also responsible for implementing the plan by selecting comparable surfaces and equipment. This was done once by performing the preparation of disinfectant materials, the disinfection process, and sampling, and another time by performing only the disinfection process.
The steps for sampling were as follows:
(1) Initial coordination with the research vice-chancellor of the university and the hospital management to obtain permits for sampling surfaces and equipment in the special care departments of Kawsar Hospital, Semnan City.
(2) Sampling of surfaces (patient’s breakfast table, security bed rail) and equipment (ventilator, suction, and tracheal tube) in the special care departments of Kawsar Hospital.
(3) Performing the relevant tests in the reference health laboratory of Semnan health center.
The disinfection process was conducted three times per day in the hospital: During the morning shift (5:30 to 6:30 AM), the evening shift (12:30 to 1:30 PM), and at night (5:30 to 6:30 PM). Accordingly, the sampling procedures were conducted during all three shifts.
The first sampling run took place during the Saturday morning shift. Samples were collected before the disinfection process (at 5 AM) and then at one and a half hours (7 AM), two hours (9 AM), and four hours (11 AM) after disinfection.
The second sampling run was performed during the Sunday evening shift, with samples collected before disinfection (12 PM) and then at half an hour (1 PM), two hours (2 PM), and four hours (4 PM) after disinfection.
The third round of sampling occurred during the Monday night shift. Samples were collected one hour before disinfection (5 PM) and at half an hour (6:30 PM), two hours (8 PM), and four hours (11 PM) after disinfection.
Each sample was obtained over a three-month period, with the process conducted regularly across all shifts.
Place a 10 cm-diameter hollow circle on the Talc sheets before swabbing these Talcs sterilely in the environment and taking samples from the surfaces and equipment following the sampling instructions. After swabbing the nutrients from the desired locations, the swab was placed in sterile containers containing 1.5 cc of nutrient media and spun for 20 seconds. After two minutes of vortexing, the samples were incubated for one day at 35°C. Following the samples' incubation in a nutrient broth culture medium, the presence or absence of turbidity in the medium solution was used to determine microbial growth. The grown samples were then transferred to McConkey Agar (MAC) medium and incubated overnight at 35°C (
15). After the necessary investigations, environmental isolates were identified using biochemical tests.
The catalase test was performed by transferring a wooden applicator from the center of a colony to a glass slide, immediately adding a drop of hydrogen peroxide to the colony on the slide, and observing the formation of bubbles. For the examined samples, differential tests for gram-negative and gram-positive organisms were conducted based on the bacteria's gram stain results to confirm the isolated isolates. If the organism was gram-negative, the following protocol was used: Several bacterial colonies were cultured on TSI Agar medium, and the depth was inoculated by piercing the medium. After incubation at 37°C for 24 hours, the results were interpreted. All the study steps are illustrated in
Figure 1.
Study steps: A and B, preparation of culture media; C and D, sampling from the studied surfaces; E and F, cultivation of samples on culture media; G and H, performing the catalase test; I, Gram staining test; J and K, viewing with the microscope and detecting gram-positive cocci bacteria.
It was demonstrated that the production of hydrogen sulfide resulted in the formation of black sediment at the bottom of the tube and the emission of gas with cracks in the environment. A very small amount of the target organism was inoculated onto the surface of the Simon citrate agar gradient. After incubating the bacteria at 37°C, the appearance of a blue color indicated a positive reaction. Escherichia coli reacts negatively in this environment, with no color change observed. To investigate motility in a semi-solid medium, a tube containing SIM medium was used. After deep cultivation in this medium and incubation at 37°C for 24 hours, bacterial motility was indicated by growth not only along the inoculation line but also in the surrounding environment, showing clear growth or turbidity.
For gram-positive bacteria, the following differential tests were used to confirm the isolates: Gram staining was performed first, and if the organism appeared as cluster gram-positive cocci under the microscope, catalase, coagulase, DNase, and mannitol tests were conducted. Based on these test results, Staphylococcus bacteria were isolated (
15).
Data were analyzed using the Statistical Package for Social Sciences (SPSS) software (version 25). Normality was assessed using skewness, the Shapiro-Wilk test, and kurtosis statistics. Repeated measures analysis of variance (RM ANOVA) was conducted to compare baseline and follow-up. An analysis of covariance (ANCOVA) was used to identify between-group changes in the primary and secondary outcomes. A P-value < 0.05 was considered statistically significant.
All of the chemical reagents used in the present study were of analytical grade and did not require further purification.