Oral Hygiene Tools for Biofilm Removal Around Implants

The present investigation was designed as a randomized clinical trial and approved by the Ethics Committee of the Universitat Internacional de Catalunya (Barcelona, Spain) (Protocol reference PER-ECL-2019-01). The study was performed in accordance with the Declaration of Helsinki for research involving humans. After being informed about the study procedures, all patients read and signed an appropriate informed consent document prior to being included. The CONSORT guidelines for randomized clinical trials were followed.

Participants:

Periodontally healthy patients with at least one single screw-retained implant-supported crown (loaded for more than one year) on a molar or premolar site with neighboring teeth were recruited. The implants had to present ≤ 4 mm of probing pocket depth and have an appropriate prosthetic design allowing proper oral hygiene. Subjects were excluded under the following conditions: (1) drug consumption that could cause gingival enlargement, such as phenytoin, cyclosporin, and/or calcium channel blockers; (2) presence of uncontrolled diabetes mellitus; (3) smokers; (4) presence or signs of peri-implant diseases or uncontrolled periodontal disease; and (5) prosthetic design that did not allow for proper interproximal hygiene (determined by using the smallest size of interproximal brush).

One calibrated investigator (C.T.) consecutively evaluated patients for screening and was responsible for enrollment. The clinician conducted an anamnesis of the patient's medical history and recorded the clinical information.

Subsequently, patients were randomly assigned to one of the following treatment groups:

Dental Floss (Vitis®, Dentaid, Barcelona, Spain) Superfloss (Oral B®, Procter \& Gamble, USA) Oral Irrigator (Waterpick®, Water Pik, Inc., CO., USA) Interproximal Brushes (Interprox®, Vitis, Dentaid, Spain) Randomization was performed using a computer-generated randomization list with permuted blocks of four, and the allocation was concealed using opaque envelopes labeled with the patient study number, which were opened just before the commencement of the intervention.

During the visit, the full mouth plaque index (FMPI) and modified plaque index at the implant site (mPI) were recorded (Mombelli et al., 1987). The mPI was assessed as follows:

Score 0: No detection of plaque. Score 1: Plaque only recognized by running a probe across the smooth marginal surface of the implant.

Score 2: Plaque visible to the naked eye. Score 3: Abundance of soft matter.

A line was drawn on the implant-supported crown with a permanent marker following the outline of the gingival margin to delimit the supragingival from the subgingival part of the crown. The screw-retained implant-supported prosthesis was subsequently removed with caution to avoid touching the interproximal areas and the cervical third of the crown, and an individualized silicone key for fixing and positioning the crown was made. Erythrosine was applied to the cervical third of the prosthesis, washed with a water syringe, and replaced in the silicone key. A standardized picture (Canon EOS 750D with annular flash Yongnuo YN14EX and macro Canon lens EF 100mm 1:28 at a distance of 44 cm and macro at 3 1.60 0.49) of the apical/subgingival third of the prosthesis was taken (Pre-area). This picture was acquired so that the plane containing the prosthetic margin was parallel to the ground and to the focal plane of the camera. The prosthesis was then replaced and screwed. At this point, the prosthesis was cleaned by the instructed operator (CT) using one of the four devices as follows:

Dental Floss: A piece of about 40-50 cm of dental floss was taken and placed between the index and middle fingers of each hand, leaving about 2-3 cm free in the middle. The dental floss was inserted, embracing the mesial and distal surfaces, and flossing up and down three times on each side.

Superfloss: The stiffened end was used to introduce the thread and the spongy-floss between the interproximal areas in both the mesial and distal parts, and a soft back-and-forth motion was applied to remove bacterial plaque. The spongy-floss was then pulled through to the regular floss section, slid gently under the gumline, and followed by an up-and-down motion. These movements were repeated three times on each side.

Oral Irrigator: The finest tip was selected and placed in the mesiobuccal, distobuccal, mesiolingual, and distolingual interproximal spaces. The irrigator was activated at medium power (2/3), and the process was repeated three times on each side for five seconds.

Interproximal Brush: According to the interproximal space, the appropriate size was selected for each case. The brush was placed horizontally in the interproximal space mesially and distally, and a back-and-forth movement was performed three times on each side.

After the interproximal cleaning was completed, the crown was unscrewed again, and a second standardized photograph was taken after removal of the crown and replaced using the silicone key with the same parameters as before (Post-area).

Image Analysis The examination was conducted based on two standardized photographs. The first photograph refers to the erythrosine-stained area of biofilm on the prosthesis at the time of removal before performing the interproximal cleaning. The second photograph refers to the residual erythrosine-stained area of the biofilm on the prosthesis at the time of removal after interproximal hygiene. Image analysis was performed using Image J® software (image processing analysis). In the first photograph, the total area delimited by the drawn margin was calculated. Subsequently, the erythrosine-colored area was delimited, determining the biofilm percentage (Pre-area). In the second picture, the residual stained area (Post-area) was calculated in the same way. The percentage reduction of plaque between the two images was then calculated.

An experienced professional (C.T.) performed the image analysis. A calibration exercise was conducted by repeating the area assessment with 40 samples, resulting in high inter-examiner reproducibility (Cronbach's α = 0.98).

Statistical Analysis Qualitative variables were described with absolute frequencies and percentages. The description of quantitative variables was performed using the mean and standard deviation (SD). The Kolmogorov-Smirnov test was used to assess the normality of distributions. Patient characteristics and clinical variables were compared according to the study groups. For the qualitative variables, the chi-squared test (Fisher exact test correction in the event of expected frequencies < 5) was used. The ANOVA test was performed to compare quantitative variables (Kruskal-Wallis test for variables with a non-normal distribution). The Bonferroni test for multiple comparisons was also performed. The intragroup biofilm reduction was analyzed using the Wilcoxon test and was also compared according to the variables of interest using the T-Student test (or U-Mann Whitney test).

The analyses were performed using R Studio software (V2.5.1). For all tests, a statistically significant difference was set at P < .05.