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QUINTESSENCE INTERNATIONAL

PERIODONTOLOGY

Juliane Pereira
Butze

Periodontal risk and recall interval evaluation after a


program of comprehensive supragingival plaque control
Juliane Pereira Butze, MScVPatrfcia Daniela M e lch io rs A ngst, MScVRui V ice n te O p p e rm a n n , PhD1
2/
Sabrina C arvalho Gomes, PhD3

Objective: To investigate if a comprehensive supragingival linear models and the Cochran test were used for statistical
control can modify the periodontal risk and suggested recall analysis, considering the dependence of the data. Results: All
interval overtime, using an adaptation of an available model patients were at high risk at baseline. At T,, 20% migrated to
o f periodontal risk assessment (PRA, Perio-Tools® website). medium-risk (P = .002). A tT2, 38% and 8% exhibited medium-
Method and Materials: Single-arm clinical trial data (visible and low-risk, respectively (P < .001). The reduction between
plaque and gingival bleeding indexes, periodontal probing T, and T2 was significant (P = .001). The mean recall interval
depth, bleeding on probing, and clinical attachment level from increased from 3.0 ± 0.0 (T0) to 3.6 + 1.2 (T,), and 4.9 ± 2.6
baseline (day 0, T0), day 30 (T,), and day 180 (T2) from 50 mod- months at T2 (P < .003). The effect that smoking habit exerted
erate-to-severe periodontitis patients (25 never-smokers; 25 on risk was limited to the first 30 days, and no effect on recall
smokers) submitted to a comprehensive supragingival plaque interval was observed. Conclusion: The oral hygiene condi­
control regimen for 180 days were subjected to a secondary tion is an important indicator that influences the risk and the
analysis using an adaptation of the PRA. The periodontal risk recall interval over time, thus deserving attention when evalu­
(high, medium, or low) and suggested recall interval were ating the individual periodontal prognosis. (Quintessence int
calculated per patient and at each experimental time. General 2015;46:765-772; doi: 10.3290/j.qi.a34176)

Key words: biofilm, dental scaling, periodontitis, risk

It is generally recognized th a t risk assessment strategy presents.13 In a d d itio n , th e clinician is also challenged
is an im p o rta n t to o l in th e p re v e n tio n o f d e stru ctive by th e need fo r o b je ctive criteria to establish th e fre ­
form s o f p e rio d o n ta l disease. H owever, in establishing q uency o f th e recall a p p o in tm e n ts . It is clear th a t a
patient's risk th e clinician is o fte n challenged by a large m o d e l o r a c o m p u te r p ro g ra m to m easure th e p e ri­
set o f clinical and laboratoriai data, m aking it d iffic u lt to o d o n ta l risk and to he lp th e clinician to establish a
dra w a clear p ictu re o f th e actual risk th a t th e p a tie n t recall interval w o u ld be very helpful,4 and some propos­
als to m eet th is clinical need are available in th e lite ra ­

1PhD Student, Graduate Program, Dental School, Federal University o f Rio Grande tu re . M ost o f th e m , acco rd in g to Lang e t al,4 are based
do Sul, Porto Alegre, RS, Brazil.
on th e P eriodontal Risk C alculator (PRC) o r th e Peri­
2Fu 11 Professor, Department of Conservative Dentistry, Dental School, Federal
University of Rio Grande do Sul, Porto Alegre, RS, Brazil.
o d o n ta l Risk Assessment (PRA). Page et al5 suggested

Associate Professor, Department of Conservative Dentistry, Dental School, Fed­ th e PRC in 2003. From an analysis o f 523 radiographs
eral University o f Rio Grande do Sul, Porto Alegre, RS, Brazil.
taken over 15 years, th e a uthors calculated th e a m o u n t
C o rre s p o n d e n c e : D r Sabrina C arvalho Gomes, Rua R am iro Barcelos,
o f alveolar b one loss experienced by each p a tie n t, and
2492, Bairro Santana, P orto Alegre, Rio G rande d o Sul, 90035-003 Brazil.
Email: sa brin a go m e s.p erio@ gm ail.com used these data to e stim ate th e in d ivid u a l p e rio d o n ta l

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risk. Based on the results, the authors concluded that of 1975, as revised in 1983, and was approved by the
the estimated risk scores generally predicted the future Research Ethics Committee of the Sao Paulo State Uni­
periodontal status with good precision and validity. versity at Araraquara (# 32/03).
Also in 2003, Lang and Tonetti6 proposed the PRA, Briefly, in the single-arm clinical trial 50 patients (25
available at the Perio-Tools® website (http://www.peho- smokers, 25 never-smokers) were selected from among
tools.com). According to the authors, the method helps those referred to periodontal treatment at the Dentistry
the clinician to determine the risk for disease progres­ Faculty, between July 2003 and August 2004. The inclu­
sion on the subject level, and also the frequency of the sion criteria were as follows:
periodontal maintenance appointments. The method • absence of any systemic condition that could inter­
estimates susceptibility to periodontal disease progres­ fere with periodontal treatment (eg, diabetes, need
sion by considering not only the periodontal support for antibiotic prophylaxis)
levels (eg, radiographic exams), as seen in the PRC, but • no antibiotic or anti-inflammatory use in the past 3
also the infection level (bleeding on probing [BOP]), months, and no use of chemical agents for supra­
prevalence of residual periodontal probing depth gingival biofilm control
(PPD > 5 mm), number of teeth lost, patient's systemic • no previous periodontal treatment
condition and age, as well as environmental and behav­ • not pregnant or using hormones
ioral factors (eg, smoking habit). • presence of at least 12 teeth
Nevertheless, these models do not include measure­ • clinical diagnosis of gingivitis associated with
ments commonly used in the literature to assess the plaque accumulation and moderate-to-severe gen­
oral hygiene performance such as plaque and gingivitis eralized chronic periodontitis15
indexes. It is well known that one of the most important • four or more teeth having one site with a PPD16 of 3
reasons for treatment failure and relapse of periodontal to 5 mm and another four teeth with at least one
disease in treated patients in spite of professional peri­ site with PPD of 6 to 10 mm, as well as positive
odic debridement is the inadequate daily control of the results for Visible Plaque Index (VPI)17 and Gingival
supragingival biofilm.7'12 Furthermore, Gomes et al13'14 Bleeding Index (GBI),17 BOP,16 and clinical attach­
have shown that clinical and microbiologic conditions ment loss (CAL).16
of the subgingival area are significantly changed by the
performance of adequate oral hygiene alone. For the One single calibrated examiner (weighted ± 1 mm
clinician it is important to establish the impact of oral Kappa values for PPD and CAL up to 0.92, before and
hygiene on assessing patient periodontal risk as well as during the study)13 performed the periodontal exams
to suggest time intervals for the maintenance of peri­ (VPI, GBI, PPD, BOP, and CAL) at days 0, 30, and 180
odontal health in treated patients. The aim of the pres­ (full-mouth; six sites per tooth) (Fig 1). The examiner
ent study was to investigate if a sole supragingival was not involved with the selection of patients and
6-month plaque control regimen on moderate-to- treatment. Nevertheless, due to the nature of the clin­
advanced periodontal patients could alter the results of ical study it was not possible to attest that the examiner
an adaptation of the PRA tools (Perio-Tools® website). was blinded to the experimental period.
The demographic characteristics (age, sex, and
number of cigarettes per day) and periodontal indica­
METHOD AND MATERIALS tors (VPI, GBI, BOP, and CAL) of the patients included in
Study design this secondary analysis, as previously reported,13 are
This descriptive-analytic study constituted a secondary shown in Table 1 (n = 50). In addition, the number of
analysis of a single-arm clinical trial published in 2007,13 sites with PPD > 5 mm per patient, at each examin-
which was in accordance with the Helsinki Declaration

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Day -7 Day 0 Day 30 Day 180
• Patient • Periodontal clinical • Periodontal clinical • Periodontal
screening evaluation evaluation clinical
• Full-mouth supragin­ • Full-mouth supragingival evaluation
gival plaque control plaque control
• Oral hygiene • Oral hygiene
instructions reinforcement

.Day 0_________________________________________ ________________________________________ Day 180,

Every week
• Visible supragingival plaque and marginal bleeding assessments
• Oral hygiene reevaluation and reinforcement

Fig 1 Flowchart of the study.

Table 1 Demographic characteristics (at baseline) and periodontal indicators at baseline (day 0, T0) and at 30
(Tn) and 180 days (T2) for the total sample, and according to the smoking status (never-smokers and
smokers)

Variable Total (n = 50) Never-smokers (n = 25) Smokers (n = 25)


Age (years, m ean ± SD) 46.36 ± 6 .2 5 46.80 ± 7.06 45.92 ± 5.43

Sex (% m en) 48 40 56

C ig a rette s/d a y (mean ± SD) NA NA 19.44 ± 1 1 .6 3

To T T2 To T, T To T T
21.28 21.28 21.28 21.38 21.38 21.38 21.20 21.20 21.20
Teeth (n; m ean ± SD)
± 3 .7 4 ± 3 .7 4 ± 3 .7 4 ± 3 .8 4 ± 3 .8 4 ± 3 .8 4 ± 3 .7 3 ± 3 .7 3 ± 3 .7 3

VPI (positive sites; 89.51 28.48 7.19 91.10 31.99 8.70 88.50 24.96 6.40
m ean ± SD) ± 1 1 .4 2 ± 1 9 .9 3 ± 8 .2 2 ± 8 .1 9 ± 1 9 .9 7 ± 9 .4 2 ± 1 3 .9 6 ± 1 9 .6 5 ± 6 .8 3

GBI (p ositive sites; 79.30 8.38 1.28 83.80 12.34 2.20 76.10 4.42 0.30
m ean ± SD) ± 16.71 ± 9 .3 7 ± 2 .3 9 ± 13.08 ± 10.63 ±3.01 ± 1 8 .6 9 ± 5 .7 9 ± 0 .8 7

BOP (p ositive sites; 120.94 60.00 29.94 121.84 61.32 27.72 120.04 58.68 32.16
m ean ± SD) ± 2 5 .1 6 ± 3 1 .8 5 ± 2 1 .7 7 ± 22.80 ± 30.07 ± 17.26 ± 2 7 .7 6 ±34.11 ± 25.68

PPD > 5 m m (positive sites; 43.32 27.16 19.56 39.60 24.24 17.16 47.00 30.08 21.96
m ean ± SD) ± 2 0 .5 5 ± 18.44 ± 15.66 ± 16.75 ± 16.30 ± 12.37 ± 2 3 .5 3 ± 20.27 ± 18.32

3.82 3.56 3.35 3.43 3.19 3.02 4.20 3.93 3.67


CAL (m m ; m ean ± SD)
± 1 .0 6 ± 1.07 ± 1.10 ± 0 .8 7 ± 0 .8 7 ± 0 .9 2 ± 1 .1 0 ± 1 .1 4 ± 1.18

NA, not applicable.

ation, was recovered from the original study,13 and 1-2,11-12,13-14; Neumar), temporary cavity filling, res­
presented in Table 1. toration adaptations, hopeless-teeth and root extrac­
All subjects were submitted to a protocol of a com­ tions, and endodontic treatments. Participants received
prehensive weekly supragingival plaque control w ith­ oral hygiene instructions according to individual needs,
out subgingival intervention for 180 days. This supra­ identified by means of the supragingival indexes (VPI
gingival control consisted o f an initial full-m outh and GBI). From day 0 onward, plaque control and gingi­
supragingival debridement with hand curettes (Gracey val inflammation were reevaluated weekly and oral

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Figs 2a and 2b Clinical aspect o f a participant from the 180-day comprehensive supragingival plaque control clinical study: (a) at
baseline and (b) after 180 days.

hygiene reinstructions were given, individually, over ing habit and the level of exposure). Based on the poly­
time. Dental floss and interdental brushes were also gon surface information, the tool defined the patient's
prescribed accordingly. Toothbrushes and fluoride periodontal risk (high, medium, or low) and their sug­
toothpastes (CloseUp, Unilever) were provided to the gested recall interval (Reclnt).
participants during the experimental period.
Figure 2 shows the clinical aspect of a participant at Statistical analysis
baseline and at the end of the 180-day comprehensive Initially, descriptive analysis of the data generated the
supragingival plaque control regimen.13 means and standard deviations (SDs) for Reclnt and the
absolute frequencies for the categorical variable (peri­
Instruments and measurements odontal risk) at an individual level. These variables were
The primary outcome of this secondary analysis was then calculated considering the total sample (n = 50), at
the periodontal risk of patients who had undergone each experimental moment (T0 = day 0; T ^ d a y 30;
supragingival control. Periodontal risk was evaluated T2= day 180). Confidence intervals (95% Cl) were esti­
using the Periodontal Risk Assesment6tool (version 3.1) mated for Reclnt. The analysis also included compari­
available at the Perio-Tools® website. However, the PRA sons between smokers (n = 25) and never-smokers
was adapted, as the original version uses alveolar bone (n = 25).
loss (ABL) based on radiographs and, in the current In sequence, the Kolmogorov-Smirnov test was
investigation, the mean CAL was used. used to verify the normal distribution of the data. Intra­
Once the patient's data (Table 1) were entered, the group comparisons were performed by means of Gen­
tool generated a m ultifunctional diagram called a eral Linear Models for repeated measures, with Bonfer-
"polygon". The polygon surface was constructed on the roni post-hoc test (if applicable), for quantitative
basis of demographic factors (eg, patient's age, number variable, and by means of Cochran test, with McNemar
of teeth), existence of systemic conditions (eg, type I or post-hoc tests (if applicable), for categorical variable.
II diabetes mellitus, polymorphisms, stress), number of The SPSS v.18.0 program (SPSS) was used to analyze
missing teeth, periodontal indicators (eg, number of the data, considering the individual as the unit of analy­
sites with PPD>5mm, the mean CAL replacing the sis. Differences were considered statistically significant
ABL, number of sites with positive BOP), information for P < .05.
about the periodontal examination (eg, number of sites
examined per tooth), and behavioral factors (eg, smok­

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Table 2 Periodontal risk score and suggested recall interval (Reclnt; in months) for patients in the total sam­
ple, and according to the smoking status (never-smokers and smokers), at baseline (T0) and after 30
days (T,) and 180 days (T2) of a comprehensive supragingival plaque control based on the results of an
adaptation in the Periodontal Risk Assessment (PerioTools®)

Total (n = 50) Never-smokers (n = 25) Smokers (n = 25)

To T, t2 T0 T, t2 T„ T, t2
High [n (%)] 50(100) 40 (80) 27 (54) 25 (100) 18(72) 12(48) 25 (100) 22 (88) 15(60)
Medium [n (%)] 0 10(20) 19(38) 0 7(28) 9(36) 0 3(12) 10(40)
Low [n (%)] 0 0 4(8) 0 0 4(16) 0 0 0
Risk
P value T,,-!, .002 .016 .250
P value T,-T2 .001 .031 .039
Pvalue T0-T2 < 0.001 < 0.001 0.002
3.0 ± 0.0 3.6 ± 1.2 4.9 ± 2.6 3.0 ± 0.0 3.8 ± 1.4 5.5 ± 3.2 3.0 ±0.0 3.4 ± 0.9 4.2 ± 1.5
Mean ± SD (95% Cl) (3.000 - (3.259- (4.149 - (3.000 - (3.357 - (4.514- (3.000 - (2.877- (3.194-
3.000) 3.941) 5.571) 3.000) 4.323) 6.526) 3.000) 3.843) 5.206)
Reclnt p value T0-T, .003

Rvalue T,-T2 <.001


Pvalue T0-T2 <•001

RESULTS DISCUSSION

All individuals showed a high periodontal risk at base­ The present study showed that the supragingival
line (Table 2). At day 30, 20% of patients exhibited plaque control significantly modified the assessment of
medium risk (P = .002). After 180 days, about half ofthe the periodontal risk and the recall interval suggested
patients presented medium (38%) or low (8%) risk by an adaptation ofthe PRA. These results suggest that
[P < .001). The comparison between 30 and 180 days determination of periodontal individual risk and main­
was also significant (P = .001). tenance recall can be improved when simple and avail­
Reductions in the periodontal risk for smokers were able oral hygiene methods are incorporated in the daily
not significant after 30 days of supragingival plaque clinical routine, even when a well-known risk factor, like
control (P = .250). At the final examination, 40% of the tobacco exposure, is present.
smokers had changed to medium risk (P = .002) Clinical data from a study where the supragingival
(Table 2). The decrease of periodontal risk observed for control was the sole treatment to test the hypothesis
never-smokers was significant from day 30 onwards. that the supragingival environment could modify the
Between days 0 and 30, 28% of never-smokers subgingival one were used in the present investiga­
migrated to medium risk (P= .016). At the final examin­ tion.13 Herein, at baseline, the PRA results classified as
ation, 52% of never-smokers had changed risk category high risk the entire group of patients. However, by day
(36% medium, 16% low) (P< .001). 30 of supragingival plaque control a significant reduc­
The results related to the Reclnt also are shown in tion of 20% in the high-risk PRA score was observed.
Table 2. The mean Reclnt increased from 3.0 months at Interestingly, as long as the supragingival control was
baseline to 3.6 months at day 30, and 4.9 months at day performed, additional and significant reductions in
180 (all comparisons with P < .003). Smoking status did scores of an adaptation of PRA were observed. At T2,
not influence this outcome (P = .094). the proportion of high-risk patients was reduced to

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almost 50%. The m edium -risk patients increased from im portant and known risk factor, smoking.3'1924 When
10 to 19 patients between T, and T2, w hile the low-risk smoking status was considered, only the never-smok-
also increase from 0 to 4 patients. Possibly, the results ers showed significant risk m odification during the first
observed here were determ ined by the effect o f the 30 days o f plaque control. At day 30, 88% o f smokers
supragingival control in reducing PPD and BOP, since and 72% o f never-smokers were at high-risk. Both
the other variables (number o f teeth, smoking habit, reductions represented a m igration to the medium-risk
systemic co nd itio n) were n ot m odified during the category. From day 30 onward, the periodontal risk of
study. It is im portant to emphasize th a t the proposed both smokers and never-smokers were similar and sig­
model o f supragingival regimen consisting o f 6 months nificantly m odified. The PRA to o l also indicates the
o f weekly appointm ents is tim e-consum ing and ques­ "ideal" recall frequency. In fact, no "ideal frequency"
tionable as a clinical protocol. In fact, th e greatest between appointm ents for periodontal maintenance
reductions in the clinical variables were observed in the has been suggested in the literature.3'4 Traditionally, an
first 30 days. If a clinical recom m endation could be empirical approach has been used to justify the interval
drawn from this observation it is th a t short-term effec­ between appointm ents, w ith clinical indicators (eg,
tive oral hygiene w ill determ ine significant reductions PPD, BOP, and CAL) and physical or subjective condi­
in the inflam m atory parameters associated w ith peri­ tions being used.19'2a25‘27The suggestion for recall inter­
odontal disease. The experim ental design o f the pres­ val varied over tim e in the present study. According to
ent study cannot rule out the possible influence o f the the patient status at baseline, the recall appointm ents
Hawthorne effect on the results. This effect is known to should occur every 3 months. After being subm itted to
be present in studies o f similar nature. The response of supragingival control, however, the suggested recall
the individual is a result o f participation in the study interval increased to 3.6 months at T, and to 4.9 months
but also a result o f the knowledge acquisition associ­ at T2. Smoking status did not determ ine differences in
ated w ith behavioral orientations provided throughout the frequency o f recall interval.
the study.18While the Hawthorne effect seems to be o f Periodontal disease is known to relapse in noncom-
short duration, knowledge acquisition requires a larger pliant patients.19'20'2526 Am ong other reasons this may
exposure tim e but results in more permanent changes happen because the patient is not adequately m oti­
in habits. In this sense, a reduction o f almost 50% in the vated or because the professional has not been able to
high-risk category, based solely on oral hygiene orien­ draw a precise picture o f the patient needs.320Thus, risk
tation, underscores one im p orta nt perspective to the assessment models may represent an im p orta nt tool
clinician in the management o f the periodontal patient th a t the clinician may use to directly determ ine prog­
over tim e. Also, these results favor discussions on the nosis as well as offer protocols o f maintenance for the
lim itations o f models th a t aim to investigate risk or treated patient.4 In this sense, initiatives such as PRA
determ ine recall intervals w ith o u t evaluating the oral are very im p orta nt as an auxiliary tool for the profes­
hygiene scores. sional. In particular, PRA is composed o f clinical, labora­
The individuals involved on the single-arm trial,13 tory, and dem ographic data known to influence the
besides th eir periodontal condition, were systemically establishment and progression o f periodontal disease.6
healthy. The addition o f the analysis o f systemic condi­ Based on the evaluation o f each patient this tool allows
tions to evaluate risk and consultation interval would the professional to assess risk on an individual basis.
be very interesting and helpful to the clinician, and Herein, an adaptation o f the PRA model was used.
would meet more criteria considered by the PRA (Perio- According to the PRA, the CAL calculation depends on
Tools®). However, it is believed th a t the hom ogeniza­ the extension of ABL that should be taken at a posterior
tion o f sample regarding the systemic condition pro­ to o th w ith the greatest CAL value. This calculation,
vided the o p p o rtu n ity to discuss at least one very however, may represent a relevant concern when con-

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sidering the assessment of risk, first because it is not The PRA has received some criticism. According to
possible to guarantee radiographic standardization for Jansson and Norderyd, 33 the PRA tool seems to overes­
all patients; second, because if the site with the great­ timate the periodontal risk due to the difficulties in
est CAL is a buccal or lingual/palatal one, it is not pos­ establishing appropriate and/or representative thresh­
sible to measure the ABL;28'29 and third, because it is not olds and adequate correlations between the variables
possible to assume that all patients present posterior evaluated in the model. Lang et al4 observed that even
teeth. Nevertheless, the gold-standard method for eval­ if available tools may predict periodontitis progression,
uating periodontal damage is the assessment of CAL.30 no data are available on the impact that such risk
Bearing all these observations in mind, the present assessment may have on patient management. Fur­
study used the full-mouth periodontal examination31 of thermore, although the idea of using the risk assess­
the CAL instead of radiographic measures to feed the ment tools to determine the frequency of recall
tool. The other variables, however, were used as pro­ appointments is rational and may help in treatment
posed by the PRA tool. planning, such suggestions remain unsubstantiated.
It is also important to highlight that the PRA was Accordingly, the results of the present study indicate
developed to assess risk in treated patients, ie patients that both the risk assessment and patient management
that have completed the periodontal therapy, not only may be better implemented if systems such as PRA
the supragingival control phase.6 On the other hand, incorporate in their set of data information on the oral
the results of the present study showed that PRA hygiene status of the patients and its effect on gingival
responds to clinical changes in the status of patients and periodontal health.
also when only part of the periodontal treatment was
performed. To the best of our knowledge, models pro­
posed to assess periodontal risk do not include direct
CONCLUSION
assessment of oral hygiene such as plaque and gingival Within the limits of the present study, the results illus­
indexes. Within the limits of the present proposal, the trate that supragingival plaque control was able to
impact of the supragingival control on the PRA results significantly modify the risk of the periodontal patients,
were assessed in order to promote a discussion on the as well as the suggested recall interval derived from a
need to incorporate oral hygiene evaluation on a regu­ risk assessment tool. These results emphasize the role
lar basis in daily clinical practice. Failures in periodontal of the clinician in health education, prom oting
treatm ent as well as recurrence of the disease in improvement in the prognosis of a periodontal patient
treated patients are commonly associated with poor irrespective of remaining difficulties related to risk and
oral hygiene, subgingival therapy deficiency, and/or recall interval determinants. Future studies might try to
systemic conditions that may influence the imbalance explore the impact of the supragingival indicators
between bacteria and host.3'2123 The present results when included in models that aim to assess the indi­
suggest that a comprehensive supragingival control vidual risk of the development of CAL, in order to add
that altered subgingival parameters was able to alter to the clinical management of a periodontal patient.
the periodontal risk indications of PRA. Several studies
have shown that this control is an important interven­
tion to reduce subgingival treatment failure, prevent­
ACKNOWLEDGMENTS
ing or minimizing loss of attachment in the long term.7' Funding fo r th e original study (Gomes e t al13) was provided by the
National Counsel ofT echnological and S cientific D evelopm ent (CNPq)
12 Recent inform ation also suggests that the
and C om m ittee for P ostgraduate Courses in H igher Education (CAPES)
supragingival environment is determinant to the sub­
Foundation (n. 0550/04-3), Brasilia, Federal District (DF), Brazil. The to o th ­
gingival stability, from both clinical and microbiologic brushes and toothpastes were a donation from the Unilever, Valinhos, SP,
standpoints . 13' 14'32 Brazil. The present investigation was entirely supported by the authors.

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19. Lorentz TC, Cota LO, Cortelli JR, Vargas AM, Costa FO. Prospective study of
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772 VOLUME 46 ■ NUMBER 9 • OCTOBER 2015


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