_________________________________________________________________________________________________________________
Research
Article
_________________________________________________________________________________________________________________
Effects of
whitening toothpaste and bleaching treatment on resin composite discoloration
caused by cigarette smoke and electronic vapor aerosol
Xiaoyi
Zhao, dds, phd, Filippo Zanetti, phd, Linchuan Wang, DDS,
PhD, Hans Malmstrom, dds, Shoaib
Majeed, ms, Manuel C. Peitsch, phd, Julia Hoeng, phd & Yanfang Ren, dds, phd, mph
Abstract: Purpose: To compare
the effects of whitening toothpaste and bleaching with 6% hydrogen peroxide (H2O2)
on discoloration of dental resin composite caused by cigarette smoke (CS) and
electronic vapor product (EVP) aerosol. Methods: 40 resin composite
discs were divided into three groups: 15 each for CS and EVP aerosol exposure
and 10 for air exposure (control). Exposures were performed for 15 days, with
daily brushing with regular toothpaste. Two whitening sessions, including 21
days of brushing with whitening toothpaste and 3 days of treatments with
take-home bleaching (6% H2O2), were performed after the
exposure. Color and gloss were assessed before exposure, at every 5 days of
exposure, and after each whitening session. Results: After 15 days of
exposure, marked discoloration of resin composite was observed in the CS group
(ΔE = 23.66 ± 2.31), minimal color change in the EVP group (ΔE = 2.77
± 0.75), and no color change in the control group. Resin composites exposed to
CS did not recover their original color after treatment with whitening
toothpaste (ΔE = 20.17 ± 2.68) or takehome bleaching (ΔE = 19.32 ± 2.53), but those exposed to EVP aerosol reverted
to baseline after treatment with whitening toothpaste (ΔE = 0.98 ± 0.37),
and no further change in color was observed following takehome bleaching. The gloss of resin composites exposed to CS, EVP aerosol, and air
decreased equally with exposure time. Brushing with whitening toothpaste
recovered the gloss similarly in all groups, but no further change was observed
following take-home bleaching. (Am J Dent 2021;34:63-69).
Clinical significance: Aerosol
from electronic vapor products induced minimal discoloration of resin
composites that can be completely reverted by brushing with whitening
toothpaste alone. Bleaching with 6% H2O2 did not revert discoloration caused by cigarette smoke. Whitening
toothpaste could help revert the decreased gloss of
resin composites.
Mail: Dr. Yanfang Ren, University
of Rochester Eastman Institute for Oral Health, 625 Elmwood Ave. Rochester, NY
14620, USA. E-mail: yanfang_ren@urmc.rochester.edu
_______________________________________________________________________________________________________________
Research
Article
________________________________________________________________________________________________________________
Effect of two
desensitizing agents applied previous to in-office bleaching on the degree of
whitening and dentin sensitivity: A randomized, controlled, double-blind clinical
trial
Carlos Eduardo Misiak Godoy, dds, msc, Simonides Consani,
dds, msc, phd, Ana Tereza Bittencourt
Guimarães, dds, msc, phd Brenda
Matsunaga Laurindo, dds, msc, Marcio José Mendonça,
dds, msc, phd & Veridiana
Camilotti, dds, msc, phd
Abstract: Purpose: To
evaluate the effect of two desensitizing agents applied before in-office
bleaching, on the degree of whitening and dentin sensitivity. Methods: Participants were randomly assigned to the groups, according to the
desensitizing agent used, with n=10 for each one. The bleaching was performed
with 35% hydrogen peroxide, divided according to the desensitizing agent used
prior to the bleaching procedure: Placebo (PL); Desensibilize KF with potassium nitrate and 0.2% sodium fluoride (PN); and Oxa-Gel with potassium oxalate (PO). The level of color
saturation was assessed at the beginning of treatment and after 1 week of its
completion by means of comparative method with the aid of a color scale. The
degree of sensitivity (DS) was noted by the subjects with the aid of a visual
scale throughout the time that the bleaching agent remained in contact with the
teeth (5, 10, 15, 20, 25 and 30 minutes) as well as 1, 24 and 48 hours after
the end of application. Pain and the degree of color saturation were evaluated
using the Shapiro-Wilk test. The DS was assessed by Kruskal-Wallis and Dunn’s tests. The color was evaluated by
ANOVA and Tukey’s HSD. Results: There was no
significant difference in the degree of bleaching among the groups. DS was
significantly more accentuated in the 48-hour period. The DS was significantly
higher for the PL group and significantly lower for the PO group. The
desensitizing agents reduced the DS without affecting the effectiveness of the
bleaching treatment. (Am J Dent 2021;34:70-74).
Clinical significance: Both desensitizing agents
provided greater control over pain compared to the placebo group. Potassium oxalate
showed greater pain control than potassium nitrate. Both desensitizing agents
tested did not interfere in the degree of whitening.
Mail: Dr. Veridiana Camilotti,
State University of Western Paraná, School of Dentistry, Universitária Avenue, no 1619 – Universitário, Cascavel,
Paraná, Brazil, 85819-110. E-mail: vericamilotti@hotmail.com
________________________________________________________________________________________________________________
Research
Article
________________________________________________________________________________________________________________
Spectrophotometric evaluation of the efficacy of natural versus commercial
bleaching agents
Shivani Kohli, mds, mfds rcps (glasgow), MFDS RCS (Edinburgh), Afaf
Al-Haddad, phd, Amanda Yan Yin Siew, dds, Woon Lai Nam, dds, Husna
Dayana Binti Hamdan, dds & Qistina
Amani Binti Roslan, dds
Abstract: Purpose: To compare
the bleaching efficacy of in-office (Opalescence), professional home (LumiBrite), over the counter (WhiteLight)
and natural (strawberry extract) bleaching agents. Methods: 80 teeth were selected and divided into two groups which
were stained with black coffee and red wine respectively. The stained specimens
were subdivided into four subgroups to be bleached with Opalescence, LumiBrite, WhiteLight and
strawberry extract. Color measurements were made using spectrophotometer at
baseline level, after staining, after bleaching and 1 week after bleaching. The
∆E00 was calculated post bleaching (∆E001),
after 1-week follow up (∆E002) and color changes between
1-week follow up and baseline (∆E003). Data were analyzed by paired
t-test and ANOVA with a significant difference of P< 0.05. Results: Paired t-test showed
significant differences in ∆E001 and ∆E002
for both stained specimens (P< 0.001). For black coffee stained specimens, Whitelight had significantly higher ∆E002
compared to the other bleaching agents (P< 0.05). For red wine stain, Whitelight also showed the significantly lowest ∆E001
(P< 0.001) and the highest ∆E002 (P< 0.001) compared to
other groups. LumiBrite showed the significantly
lowest ∆E003 for red wine stained specimens (P< 0.05). Whitelight had the poorest bleaching efficacy with
deterioration effect after 1-week follow up. Opalescence, LumiBrite and strawberry extract had clinically perceptible and comparable bleaching
efficacy. Strawberry extract appeared to be a potential natural bleaching agent
with a desirable effect. (Am J Dent 2021;34:75-79).
Clinical
significance: Commercial tooth bleaching agents can cause several undesirable side effects
such as damage to enamel, hypersensitivity and even affecting the pulp. Strawberry
extract is a natural, effective bleaching agent that may have reduced side
effects.
Mail: Dr. Shivani Kohli, Division
of Clinical Dentistry, School of Dentistry, International Medical University,
Kuala Lumpur, Malaysia. E-mail: ShivaniKohli@imu.edu.my
________________________________________________________________________________________________________________
Research
Article
________________________________________________________________________________________________________________
Effect of double layer application on
bond durability of universal adhesives to proximal dentin-cementum gingival margins
Ashraf
I. Ali, bds, msd, phd, Hoda S. Ismail, bds, msd & Franklin
Garcia-Godoy, dds, ms, phd, phd
Abstract: Purposes: To evaluate
and compare the effect on micro-tensile bond strength (μTBS)
of a double layer application of three universal adhesives applied in self-etch
mode to proximal dentin/cementum gingival margins of
class II direct composite restorations, immediately and after 12 months water
storage. Methods: 66 molars with compound class II cavities, with
gingival margin 1 mm below CEJ, were divided into three groups according to the
universal adhesive used. The adhesives evaluated included All-Bond Universal
(AB), Single Bond Universal (SB), and Prime&Bond Elect (PB). The groups were further subdivided according to adhesive
application technique, either single layer or double layer application. All
teeth were restored with the same nanofilled resin
composite. μTBS were
examined at a crosshead speed of 0.5 mm/minute after 24 hours or 12 months
water storage. Fracture mode was assessed under stereomicroscope. Data were
analyzed by two-way analysis of variance (ANOVA) followed by Tukey’s post hoc test (P< 0.05). Results: The
double layer application μTBS values were
significantly higher than single layer application in all groups. Regardless of
the type of adhesive or application technique, all subgroups showed
significantly decreased bond strength after aging. There were significant lower μTBS values for AB adhesive compared with the
other two adhesives that demonstrated no significant differences between them.
The double layer application technique was effective in enhancing μTBS values of all tested adhesives bonded to proximal
dentin/cementum gingival margins compared to single
layer application. Regardless of application technique, all tested adhesives
were incapable of defying long-term water aging. (Am J Dent 2021;34:80-86)
Clinical significance: The double layer application
technique may be recommended to enhance the bonding durability of universal
adhesives to face challenges in bonding to dentin-cementum cervical margins.
Mail: Dr. Hoda Saleh Ismail, Department of Operative Dentistry,
Faculty of Dentistry, Mansoura University, Algomhoria Street, PO Box 35516, Mansoura,
Egypt. E-mail: hoda_saleh@mans.edu.eg
________________________________________________________________________________________________________________
Research
Article
_________________________________________________________________________________________________________________
A clinical study
to assess the gingivitis reduction efficacy of a novel stannous-containing
fluoride dentifrice
Zhipeng
Xu, mds, Tao He, dds, phd, Yanyan
He, ms, Phil Fei, ms, Lily Sun, ms, Yamei Chen, bs & Jiahui
Li, bs
Abstract: Purpose: To
assess the gingivitis reduction efficacy of a novel stannous-containing
fluoride dentifrice relative to a negative control. Methods: 100
generally healthy adults with 10 or more gingival bleeding sites based on the Mazza Modification of the Papillary Bleeding Index (Mazza GI) were enrolled into a 2-week randomized,
controlled, double-blind, single-center, two-treatment, parallel group clinical
study. The subjects were randomly assigned to the stannous-containing
dentifrice group (experimental group) or the sodium fluoride dentifrice group
(negative control group). An oral examination and Mazza GI examination were conducted at Baseline, Day 3 and Week 2 post-baseline by a
qualified dental examiner. Results: 98 subjects completed the study. The
experimental group provided a significant reduction in Mazza GI scores and number of bleeding sites relative to baseline at Day 3 and Week 2
(P< 0.0001). The negative control did not provide significant reductions
versus baseline for either measure at either timepoint (P> 0.3). At Day 3, the experimental group provided a statistically
significant reduction of Mazza GI scores and number
of bleeding sites compared with the negative control group (P< 0.0001). At Week
2, the experimental group showed 24.11% lower Mazza GI scores and 54.81% fewer bleeding sites than the negative control group (P<
0.0001). (Am J Dent 2021;34:87-90).
Clinical significance: The results demonstrated that
the novel stannous-containing fluoride dentifrice had a superior
anti-gingivitis effect compared to the sodium fluoride negative control
dentifrice, which was evident as quickly as 3 days after use and further
improved after 2 weeks of usage.
Mail: Zhipeng Xu, Shaanxi Provincial People’s Hospital No. 256 Youyi West Road 710068 Xi’an, Shannxi, China. E-mail:
sxkq88@163.com
________________________________________________________________________________________________________________
Research
Article
________________________________________________________________________________________________________________
Biaxial flexural
strength of various CAD-CAM glass-ceramic materials
Layali Alakkad, bds, msc, Aikaterini Kostagianni, dmd, dds, msc, Matthew
Finkelman, phd, Ahmed Maawadh,
bds, msc dscd, Ala Ali,
bds, msc, dsc,
dmd & Aikaterini Papathanasiou, dmd, dds
Abstract: Purpose: To
evaluate and compare the flexural strength of three CAD-CAM glass-ceramic
materials and to investigate the effect of various surface treatments on their
flexural strength. Methods: 120 rectangular specimens were fabricated
from three different types of CAD-CAM ceramic blocks and were divided into
three groups: zirconia-reinforced lithium silicate (Celtra Duo, Group 1), leucite-reinforced
glass-ceramic (IPS Empress CAD, Group 2), and lithium disilicate ceramic (IPS e.max CAD, Group 3). Dimensions of the specimens were standardized
to 14.5×12.5 mm and 1.5 mm thickness. Specimens in each group were randomized
into four subgroups. The first subgroup (NS) did not undergo any surface
treatment; the second subgroup (P) underwent polishing only; the third subgroup
(G) underwent glazing only; and the fourth subgroup (PG) underwent both
polishing and glazing surface treatments. Biaxial flexural strength (FS)
testing was performed until fracture occurred; FS was calculated in MPa. All analyses were performed using SPSS version 24. Results: Group NS2 showed the lowest FS (89.34 ± 25.30 MPa).
Group PG3 showed a significantly higher FS (365.38 ± 52.52 MPa)
than Group P3 (268.15 ± 48.34). There was a statistically significant
difference among the material groups for each surface treatment: IPS e.max CAD
showed the highest FS, which was significantly greater than that of both Celtra Duo and IPS Empress CAD. The combination of
polishing and glazing surface treatment resulted in significantly higher
flexural strength than polishing alone for all three materials tested. For each
material, no significant difference was found between the following surface
treatments: control and polishing-only surface treatments; glazing-alone and
the combination of polishing and glazing surface treatments. For each surface
treatment, Celtra Duo showed significantly lower
flexural strength than IPS e.max CAD. However, it displayed higher flexural
strength than IPS Empress CAD, although the difference was only significant for
glazing and the combination of polishing and glazing. (Am J Dent 2021;34:91-96).
Clinical significance: This study provides the
clinician with an estimate of the flexural strength of glass-ceramic materials
and shows how various surface treatments affect their strength.
Mail: Dr. Aikaterini
Papathanasiou, Department of Prosthodontics, Tufts
University School of Dental Medicine, 1 Kneeland Street,
Suite 221, Boston, MA 02111, USA. E-mail: Aikaterini.Papathanasiou@tufts.edu
__________________________________________________________________________________________________________________
Research
Article
__________________________________________________________________________________________________________________
Periodontal
disease in acute coronary syndrome patients
Ying Gu, dds, phd, Lorne M.
Golub, dmd, msc, dsc, mdsc(h), FNAI, Hsi-Ming Lee, phd, Wei Hou,
phd & Maria
E. Ryan, dds, phd
Abstract: Purpose: This
pilot study assessed the periodontal status and biomarkers of systemic
inflammation in acute coronary syndrome (ACS) patients. Methods: 15 ACS
patients on statin (anti-cholesterol) therapy, were recruited into the study an average of 9
months after discharge from university hospital. Blood and mouthrinse samples were collected for analysis of inflammatory biomarkers including high
sensitivity C-reactive protein (hsCRP), IL-6,
IL-1β, TNF-α, and MMP-9. Full-mouth
periodontal examination, including pocket depth (PD), clinical attachment
levels (CAL), bleeding on probing (BOP), and tooth mobility, was performed. Results: When their periodontal status was assessed by CAL, 100% of these statin-treated ACS patients exhibited moderate (66.7%) to
severe (33.3%) periodontal disease, which appears to be higher than the rate
described for the general adult population (i.e., 47% for periodontitis). In
addition, (1) their blood hsCRP levels ranged from
0.94 to 12.6 mg/L with a mean of 3.41 mg/L, which is considered high risk for cardiovascular
disease (CVD) in spite of their statin therapy, and
(2) the data demonstrated a positive correlation between severe periodontitis
and elevated blood hsCRP levels (P< 0.05),
consistent with systemic inflammation. (Am J Dent 2021;34:97-100).
Clinical significance: This pilot study provides
preliminary data for future large-scale studies to define the relationship
between ACS and chronic periodontitis, the underlying mechanisms, and the
potential therapeutic efficacy of appropriate periodontal management to reduce
the risk for cardiovascular disease.
Mail: Dr. Ying Gu,
Department of General Dentistry, School of Dental Medicine, Stony Brook University,
Stony Brook, NY 11794-8706, USA. E-mail:ying.gu@stonybrook.edu
________________________________________________________________________________________________________________
Research
Article
________________________________________________________________________________________________________________
Reliability of
magnetic resonance imaging on detecting degenerative bone changes of the temporomandibular joint
Juliane
Piragine Araujo, dds, phd, Marcelo
Eduardo Pereira Dutra, dds, phd, Alan
Motta Canto, dds, msc & Jefferson
Xavier Oliveira, dds, phd
Abstract: Purpose: To evaluate
and describe the most frequent TMJ degenerative bone alterations on MRI and CT
and to determine the accuracy, sensitivity, and specificity of MRI. Methods: Images of 80 subjects were selected and evaluated from a database and 57 were
selected. The subjects were submitted to CT and MRI exams (each subject on the
same day). The joints were evaluated in the sagittal and coronal planes under closed mouth position. Each individual parameter was
scored as absent or present. Absolute and relative frequencies were obtained
and the Kappa concordance index test and equality of two proportions were used.
To correlate the presence of bone alterations, the Chi-Square test was
performed. A significance level of 0.05 (5%) was defined, with 95% of
statistical confidence interval. Results: Of the 57 subjects, (47
female, 10 male), the ages ranged from 18-83 years (mean 43 years). The intra
and inter-rater agreement tests demonstrated reliability among the examiners
for all variables analyzed on MRI and CT. (Am J Dent 2021;34:101-104).
Clinical significance: MRI is a reliable and valid method
for observing bone changes in the TMJ, with the advantage of non-exposure to
radiation and cost-effectiveness due to the use of only one exam.
Mail: Dr.
Juliane Piragine Araujo,
Discipline of Oral Radiology, Department of Stomatology,
School of Dentistry, University of Sao Paulo, Av. Professor Lineu Prestes 2227, Butanta, São
Paulo, SP, 05508-000, Brazil. E-mail: ju_piragine@hotmail.com
_______________________________________________________________________________________________________________
Research
Article
_______________________________________________________________________________________________________________
Effect of phosphorylated chitosan and carbodiimide biomodification on
the chemical composition of eroded dentin
Mirian
Saavedra Lopes Ururahy, msd, phd, Fabiana Almeida Curylofo-Zotti, dds,
msd, phd, Gustavo Teodoro Costa Lizarelli, Arlete Barbosa dos Reis, phd, Ana
Paula Ramos, phd & Silmara
Aparecida Milori Corona, msd, phd
Abstract: Purpose: To evaluate
the chemical composition and morphological properties of eroded dentin after biomodification with phosphorylated chitosan (P-Chi) and carbodiimide (EDC). Methods: 42 bovine dentin specimens were used; 21 of these
specimens were subjected to erosive challenge with 0.3% citric acid (pH = 3.2)
for 2 hours. The specimens were randomly divided into six groups according to
dentin substrate (sound or eroded) and biomodification [with 2.5% P-Chi, with 0.5 mol/L EDC, or no biomodification (control)]. The specimens were analyzed by Fourier-transform infrared
spectroscopy (FTIR, n= 5, in triplicate) and atomic force microscopy (AFM, n=
2) to verify the phosphate, carbonate, and organic matrix absorption peaks and
to investigate surface morphology, respectively. The data were analyzed with
Origin 6.0. Results: Dentin erosion reduced the intensity of the
phosphate (1,100 cm-1) and carbonate (872
cm-1) related bands, which evidenced demineralization. Eroded dentin
consisted of a more irregular surface containing slightly more open tubules.
Modification with P-Chi removed intertubular dentin,
which was compatible with surface demineralization; however, this modification
obliterated dentin tubules. EDC did not promote demineralization. Biomodified dentin had a more irregular surface,
irrespective of substrate type. (Am J Dent 2021;34:105-109).
Clinical significance: Eroded dentin demineralization
promoted by biomodification with 2.5% phosphorylated chitosan (P-Chi)
is a promising indicator for further studies and highlights the dentin
intrinsic characteristics. From the point of view of dentin surface chemical
analysis, more studies with P-Chi should be conducted to achieve greater
interactions with surfaces and to improve the adhesive interface.
Mail: Prof. Silmara Aparecida Milori Corona, Department
of Restorative Dentistry, School of Dentistry of Ribeirão Preto, University of São Paulo, Av.
do Café, Ribeirão Preto -
SP, 14040-904, Brazil. E-mail: silmaracorona@forp.usp.br
_________________________________________________________________________________________________________________
Research
Article
_________________________________________________________________________________________________________________
Randomized
clinical trial assessing anti-gingivitis efficacy of two stannous fluoride
dentifrices and zinc/arginine dentifrice
Tao He, dds, phd, Sigal Mazor, mph, dmd, Yuanshu Zou,
phd, Julie
Grender, phd, Svetlana
Farrell, dds, phd, Paul Sagel, bsche, Aaron R.
Biesbrock, dmd, phd, ms, Hans
Timm, phd & Avi Zini, dmd, mph, phd
Abstract: Purpose: To evaluate
the anti-gingivitis efficacy of two bioavailable stannous fluoride (SnF2) dentifrices versus a zinc/arginine dentifrice and a negative control dentifrice, and
to compare the plaque control benefits. Methods: This was a
single-center, randomized, controlled, four-treatment, parallel-group,
double-blind, 3-month clinical trial. Healthy adult
subjects with gingivitis were randomly assigned to one of four different
dentifrice treatment groups: SnF2 dentifrice A, SnF2 (1,100 ppm F) + sodium fluoride (350 ppm F) + sodium hexametaphosphate (Procter & Gamble); SnF2 dentifrice B, SnF2 (1,100 ppm F) + sodium fluoride (350 ppm F) + citrate (Procter & Gamble); Zn/Arg dentifrice, zinc/arginine + sodium fluoride (1,450 ppm F) (Colgate-Palmolive); negative control dentifrice,
sodium monofluoro-phosphate (1,000 ppm F) + sodium fluoride (450 ppm F) (Colgate-Palmolive). Subjects brushed with their assigned treatment
dentifrice and an assigned manual toothbrush (Oral-B Indicator) for 1 minute,
twice daily, for the duration of the study. Gingivitis was assessed at Baseline
and at Weeks 2, 4 and 12 by calculating the total number of gingival bleeding
sites using the Gingival Bleeding Index, and plaque was assessed at Baseline
and at Week 12 using the Turesky Modified
Quigley-Hein Index. A repeated measures model was carried out across Weeks 2,
4, and 12 to determine bleeding efficacy (total number of bleeding sites). An
ANCOVA with baseline plaque as the covariate was used to evaluate plaque
efficacy at Week 12. Results: 161 subjects were randomized (mean age=
38.8 years). 154 subjects completed the study and 153 had evaluable data at
Week 12. The mean (SD) number of Baseline bleeding sites overall was 78.74
(31.16) with no significant difference between groups (P= 0.537). SnF2 dentifrice A significantly reduced the number of bleeding sites relative to the
negative control dentifrice at Weeks 2, 4 and 12 by 15.4%, 13.7% and 17.2%,
respectively. SnF2 dentifrice B significantly reduced the number of
bleeding sites relative to the negative control dentifrice at Week 4 by 13.9%
(P= 0.041). Relative to the Zn/Arg dentifrice,
SnF2 dentifrice A produced significantly greater reductions in
gingival bleeding sites at Weeks 2, 4 and 12 by 23.4%, 17.2% and 20.9%,
respectively (P≤ 0.007). SnF2 dentifrice B produced
significantly greater bleeding reductions versus the Zn/Arg dentifrice at Weeks 4 and 12 by 17.4% and 14.4%, respectively (P≤ 0.035).
The Zn/Arg dentifrice did not differ significantly in
the number of bleeding sites (P≥ 0.127) or plaque (P= 0.175) relative to
the negative control dentifrice. Both SnF2 dentifrices significantly
reduced plaque levels (P≤ 0.029) relative to both negative control
dentifrice and Zn/Arg dentifrice at Week 12. All
dentifrices were well tolerated. (Am J Dent 2021;34:110-115).
Clinical significance: Two different SnF2 dentifrices showed significantly reduced gingival bleeding and plaque levels
relative to a Zn/arginine dentifrice.
Mail: Dr. Tao He, The Procter & Gamble Company, 8700 Mason-Montgomery
Road, Mason, OH, 45040, USA. E-mail: he.t@pg.com
________________________________________________________________________________________________________________
Research
Article
________________________________________________________________________________________________________________
Radiant-exposure
attenuation through Class-2 proximal slots
Dave D.
Kojic, dmd, md, phd, Omar
El-Mowafy, bds, phd, Olesya
Falenchuk, phd, Christopher
J. Felix, bsc, Rafael Francisco Lia Mondelli, dds,
ms, phd & Juliana Fraga Soares Bombonatti, dds,
ms, phd
Abstract: Purpose: To
determine the extent of radiant exposure (RE) attenuation of three LED light-polymerization
units (LPUs), and their beam-profile, at the bottom of the Class-2 slot, using
MARC-PS. Methods: 10 seconds RE was delivered to MARC-PS’ anterior
sensor by Bluephase-Style, Demi-Plus,
and Deep-Cure-S. Two ivorine lower first-molars
received Class-2 proximal box preparations: (3´2´4 mm
and 4´4´4 mm) and were sectioned horizontally above the cementoenamel junction. Tofflemire matrix-retainer was placed around each tooth and secured with a low-fusing
compound. Each LPU tested delivered 10 seconds RE to MARC-PS through proximal
slots. Mean RE of three readings per group was obtained. Data were analyzed
using Pearson correlation, mixed ANOVAs with a pre-set alpha of 0.05. Results: RE attenuation ratio calculated from the baseline to 4´4´4/3´2´4
Class-2 boxes were: 58.25/80.03 Bluephase-Style;
49.36/80.25 Demi-Plus; 32.8/77.43 Deep-Cure-S. A
significant and strong correlation (r= 0.86, P< 0.001) between the reduction
in aperture size and RE was found. The beam profile of LED-LPUs tested decreased
RE values at the bottom of a proximal box. More than 80% RE value reduction
from the baseline to the smallest Class-2 cavity 3´2´4 aperture was observed. (Am J Dent 2021;34:116-119).
Clinical significance: Polymerization of
resin-composites at the bottom of the Class-2 box is challenging due to the
small aperture size, depth, and hard-to-reach location. Inadequate
polymerization at the bottom of the Class-2 proximal box is a causative factor
for secondary caries and, ultimately, restoration failure.
Mail: Dr. Dave D. Kojic, Department
of Restorative Dentistry, Faculty of Dentistry, University of Toronto, 124
Edward Street, Rm 350B, Toronto, Ontario M5G 1G6,
Canada. E-mail: dave.kojic@utoronto.ca