Periodontal Risk Assessment Model in a Sample of Regular and Irregular
Transcription
Periodontal Risk Assessment Model in a Sample of Regular and Irregular
Volume 83 • Number 3 Periodontal Risk Assessment Model in a Sample of Regular and Irregular Compliers Under Maintenance Therapy: A 3-Year Prospective Study Fernando Oliveira Costa,* Luı´s Ota´vio Miranda Cota,* Eugeˆnio Jose´ Pereira Lages,* Ana Paula Lima Oliveira,* Sheila Cavalca Cortelli,† Jose´ Roberto Cortelli,† Telma Campos Medeiros Lorentz,* and Jose´ Eusta´quio Costa* Background: The purpose of this study is to investigate the association of the periodontal risk assessment (PRA) model with the recurrence of periodontitis and tooth loss during periodontal maintenance therapy (PMT). Methods: In a prospective PMT program, 75 regular complier (RC) and 89 erratic complier (EC) patients were selected. A periodontal examination and PRA were performed after active periodontal therapy and after 3 years of PMT. Risk profiles (low, moderate, or high) of participants were evaluated, and the recurrence of periodontitis and tooth loss were analyzed using univariate and multivariate analyses. Results: RCs showed less recurrence of periodontitis and tooth loss than ECs (P <0.05). Rates of periodontitis recurrence in RCs and ECs were 2.7% and 3.4%, respectively, for the moderate-risk profile and 6.7% and 11.2%, respectively, for the high-risk profile. During PMT, 49 teeth (0.65 – 1.4 teeth per participant) were lost in the RC group, and 70 teeth (0.78 – 2.1 teeth per participant) were lost in the EC group. High-risk profile participants showed more recurrence of periodontitis and lost significantly more teeth than did participants with moderate- or low-risk profiles in RC and EC groups (P <0.05). Conclusion: The risk profile influenced the recurrence of periodontitis and tooth loss. RCs had less recurrence of periodontitis and less tooth loss. The PRA model can be useful in particularizing the risk of patients and adjusting recall intervals. J Periodontol 2012;83:292-300. KEY WORDS Compliance, patient; maintenance; periodontitis; risk factor; tooth loss. * Department of Periodontology, Dentistry School, Federal University of Minas Gerais, Belo Horizonte, MG, Brazil. † Department of Dentistry, Periodontics Research Division, University of Taubate´, Taubate´, SP, Brazil. T he most usual problem in periodontal maintenance therapy (PMT) is the compliance and return of patients at regular intervals. It was well documented that patients may or may not at all comply with suggested maintenance regimens.1-7 Because treated patients are not equally susceptible to periodontal disease progression,8,9 some patients may attend periodontal maintenance visits at shorter intervals than less-susceptible patients.10 This criterion can be useful to adjust intervals and minimize difficulties in the compliance of patients to PMT.7 The creation of multifactorial riskassessment models that include relevant risk factors for future disease progression was proposed to identify the susceptibility of patients for the recurrence of periodontitis.6,10-13 Lang and Tonetti12 proposed the periodontal risk assessment (PRA), which is a functional diagram composed of six vectors based on six parameters (clinical, systemic, and environmental factors) to evaluate the risk of recurrence of periodontitis at a patient level, classifying patients in a low-risk (LR), moderate-risk (MR), or high-risk (HR) profile. The combined evaluation of these factors provides an individualized total risk profile after active periodontal therapy (APT). doi: 10.1902/jop.2011.110187 292 Costa, Cota, Lages, et al. J Periodontol • March 2012 Only some longitudinal studies6,10,14-16 attempted to validate the effect and reproducibility of this approach. A recent study16 also evaluated the PRA model, and the authors included a limited number of patients (n = 20) treated for severe periodontitis and concluded that the proposed model overestimated the risk for disease recurrence. Leininger et al.6 used the PRA model to evaluate 30 patients who were reexamined after APT and reported that erratic compliers (EC) patients lost more teeth than did regular compliers (RC) patients. At present, a great challenge for periodontitis is to use instruments that can bring benefits to periodontal practice. In this sense, the use of multifunctional risk models can be a powerful tool to monitor the risk of the recurrence of periodontitis, optimize clinical decisions, influence the pattern of compliance and the adherence to PMT, improve oral health, and reduce treatment costs.13 Hence, the aims of this prospective longitudinal study were to: 1) evaluate and classify the patient’s risk through the PRA model proposed by Lang and Tonetti12 in patients enrolled in a PMT program during a 3-year interval; and 2) assess and compare the association of the proposed PRA model with the recurrence of periodontitis and tooth loss according to the pattern of compliance (regular or erratic). MATERIALS AND METHODS All participants under PMT from a cohort study that comprised 238 patients (96 males and 142 females; age range: 18 to 62 years) who were monitored in a private dental clinic in Belo Horizonte, Brazil, from November 2006 to November 2009 were determined to be eligible to participate in the present study. Patients with good general health who underwent basic periodontal therapy (comprised of non-surgical and/or surgical procedures) were included in the sample. In addition, these patients also presented the following criteria: 1) diagnosis of chronic moderate–advanced periodontitis before the APT with ‡4 sites with probing depths (PDs) ‡5 mm and clinical attachment loss (AL) ‡3 mm, bleeding on probing (BOP) and/or suppuration (SUP), and radiographic evidence of bone loss;17 2) completion of APT in a period of <4 months before entry into the PMT program; and 3) ‡14 teeth in the oral cavity.18 All participants provided written informed consent. The present study was approved by the Ethics Research Committee, Federal University of Minas Gerais (protocol #060/05). Patient exclusion criteria were: 1) pregnancy (n = 3), 2) debilitating diseases that could impair the immune system (such as human immunodeficiency virus/acquired immune deficiency syndrome, cancer, and autoimmune diseases; n = 4), 3) drug-induced gingival hyperplasia (n = 6), 4) systemic anti- biotics use during APT (n = 14), 5) >2 osseointegrated dental implants (n = 10), 6) <14 teeth present (n = 19), and 7) refusal to participate (n = 18). A sample consisting of 164 volunteer participants was selected and classified according to the criteria proposed by Demirel and Efeodlu.19 Participants were considered: 1) RCs (n = 75) if they presented 100% cooperation with recall visits, or 2) EC (n = 89) if they missed any of the scheduled recall visits but continued to appear irregularly. Data obtained after APT were determined at baseline and compared to data obtained after 3 years of follow-up, which was determined as the final examination (T2). T2 was performed after nine recall visits for RC patients and four recall visits for EC patients. The mean – SD time between recalls in the RC group was 3.3 – 0.5 months and 8.1 – 1.2 months in EC group (no individual had <4 recall visits in the study period). A maximum 4month interval time was proposed for all patients independent of their risk profiles. Data related to the following characteristics were collected from all patients: sex, age, family income, education level, plaque index (PI),5 number of teeth, smoking (non-smokers/ex-smokers and smokers: 10 to 19 or >19 cigarettes per day, respectively),12 and the presence of diabetes (glycemic values >110 mg/dL).20 In all periodontal clinical examinations during monitoring visits, data comprising the PD, clinical AL, furcation involvement, BOP, PI, and SUP were recorded for each patient using the methodology proposed by Lorentz et al.5 Data of interest (clinical parameters, radiographs, and systemic and behavioral variables) collected after APT (baseline) and at T2 were used in this study to construct the PRA model proposed by Lang and Tonetti.12 Radiographs Intraoral periapical and bite-wing radiographs were taken using a long-cone paralleling technique. Alveolar bone loss was measured at both proximal surfaces (mesial and distal) with a negatoscope‡ that magnified nine times the original image size. The distance from the cemento-enamel junction to the alveolar bone crest was measured using a pachymeter.§ The bone loss variable was recorded according to Lang and Tonetti.12 PRA Model On the basis of patient data at APT and T2, the risk for the recurrence of periodontitis was calculated for all 164 patients using the PRA model.12 A summary of definitions of LR, MR, and HR profiles for the recurrence of periodontitis is presented in Table 1. Patients ‡ Ampligraf, Castells, Sa˜o Paulo, SP, Brazil. § Mitutoyo Sul Americana, Suzano, SP, Brazil. 293 Periodontal Risk Assessment in Maintenance Therapy Volume 83 • Number 3 Table 1. Classification of Risk According to the Parameters of the PRA Model Proposed by Lang and Tonetti12 BOP Sites With PD ‡5 mm Tooth Loss Bone Loss/ Age Ratio (mm)* Smoking Genetic Factor/ Systemic LR 0% to 9% 0 to 4 0 to 4 0 to 0.5 Non-smoker/ex-smoker Negative MR 10% to 25% 5 to 8 5 to 8 >0.5 to 1.0 10- to 19- cigarettes/day – HR >25% >8 >8 >1.0 >19 cigarettes/day Positive Risk Profile – = not applicable. * Bone loss was estimated from the percentage of the root length at the worst site in the posterior region on periapical radiographs or on bitewing radiographs where 1 mm was equivalent to 10% bone loss. determined to be LR yielded all parameters in the LR area or, at the most, one parameter in the MR area. Patients determined to be MR yielded ‡2 parameters in the MR area and, at the most, one parameter in the HR area. Patients determine to be HR yielded ‡2 parameters in the HR area. Recurrence of Periodontitis The progression of periodontitis was defined as an interproximal clinical AL ‡3 mm in ‡2 teeth between two different observation points according to the definition of the fifth European Workshop of Periodontology.21 In the present study, this definition was adapted to define the recurrence of periodontitis between the end of APT and T2.10 Intraexaminer and Interexaminer Reliability Interviews, examinations, and periodontal procedures were conducted by two calibrated and trained periodontists (FOC and EJPL) who were masked to the degree of compliance. Measurements of PD and clinical AL were recorded and repeated within a 1-week interval for 10 patients who were randomly selected from both examinations (APT and T2). Results showed satisfactory intraexaminer and interexaminer k values for PD and clinical AL (k ‡ 0.81). Additionally, intraclass correlation coefficients ‡0.82 were attained in both evaluations. Bone-loss measures and calculations were performed by only one researcher (FOC) who was masked to clinical data. The intraexaminer k test was performed for 20 radiographs within a 15-day interval (k = 0.95). Statistical Analyses Statistical analyses included a characterization of the sample and descriptive analysis of variables of interest. Parametric and non-parametric tests (x2, KruskalWallis, Friedman, Fisher-exact, Student t, and MannWhitney U tests) were used when appropriate. To determine the significance between groups, the correction of Bonferroni was applied. 294 PRA models were constructed twice for each of the 164 patients. Data were compared through the nonparametric Kruskal-Wallis test in relation to the risk profile. A logistic regression analysis was performed to investigate the association among all risk variables and the recurrence of periodontitis and tooth loss. The first model, in which RCs and ECs were separately analyzed in relation to the recurrence of periodontitis, included the following variables: age, sex, number of missing teeth, BOP in >30% of sites, PD >5 mm in 10% of sites, smoking, and diabetes. Subsequently, a second multivariate analysis was separately performed for the recurrence of periodontitis and tooth loss including the continuous variables of the PRA model (as proposed by Matuliene et al.10) percentage of BOP (unit increase of 1% of sites with BOP), number of periodontal pockets with PD ‡5 mm (increase of one pocket), number of missing teeth (increase of one missing tooth), bone loss in relation to age (increase of 1% of bone loss), smoking (yes/no), and diabetes (yes/no). Odds ratio (OR) values and respective 95% confidence intervals (CIs) were reported. All tests were performed using statistical software.i Results were considered significant if a P value <5% was attained (P <0.05). RESULTS The characterization of the sample dichotomized in RC and EC groups is shown in Table 2. Variables such as sex, marital status, smoking, diabetes, age (except for the age group from 31 to 40 years,) and average time of completion of active therapy showed no significant differences between groups, which demonstrated great homogeneity between groups. Table 3 presents the periodontal status of RC and EC groups after active APT and T2. RCs and ECs showed no significant differences regarding the clinical parameters PD, BOP, clinical AL, and SUP after APT i SPSS v.16.0, IBM, Chicago, IL. Costa, Cota, Lages, et al. J Periodontol • March 2012 Table 2. Characterization of RC and EC Patients According to Variables of Interest (N = 164) Characteristic RCs (n = 75) ECs (n = 89) P Sex (n [%]) Females Males 54 (72) 21 (28) 59 (66) 30 (34) Age (range: 18 to 62 years) (years; n [%]) £30 31 to 40 41 to 50 >50 9 19 24 23 7 25 27 30 Marital status (n [%]) With companion Without companion 51 (68.0) 24 (32.0) 57 (64.1) 32 (36.0) NS* NS* Smoking (n [%]) Non-smoker/ex-smoker Smoker 46 (61.3) 29 (38.7) 55 (61.8) 34 (38.2) NS* NS* 8 (10.7) 14 (15.7) NS* Number of recall visits (time between recalls [months; mean – SD]) 9 (3.3 – 0.5) 4 (8.1 – 1.2) 0.002† Time of completion of active therapy (months; average – SD) 39.2 – 1.9 40.3 – 1.7 NS† Diabetes (n [%]) (12.0) (25.3) (32.0) (30.7) (7.9) (28.1) (30.3) (33.7) NS* NS* NS* 0.048* NS* NS* NS = not significant. 2 * x test. † Student t test for independent samples. (baseline) (P >0.05). However, great differences regarding these parameters at T2 revealed a worse periodontal condition among EC patients. The classification of periodontal risk for RC and EC patients according to the PRA model after APT and at T2 as well as changes in risk classification in the PRA model from after APT to T2 are shown in Table 4. It was observed that RC and EC patients showed no significant differences in risk classifications after APT. However, the EC group presented a higher incidence of HR patients at T2 (an increase of 6.7%) and a lower incidence of MR patients (a reduction of 12.4%) compared to the changes in the RC group (an increase of 4% in HR and a reduction of 17.4% in MR). In both groups, there was an increase of LR patients (RCs: an increase of 13.3%; ECs: an increase of 5.6%). It was observed at T2 that the EC group had a significantly greater number of patients presenting a recurrence of periodontitis (n = 15 [16.8%]) and tooth loss (n = 27 [30.3%]) compared to the RC group (n = 8 [10.6%] and n = 17 [22.6%], respectively) (P = 0.027). In addition, when analyzing HR patients, it was observed that the recurrence of periodontitis and tooth loss among ECs (11.2% and 21.3%, respectively) was significantly higher than among RCs (6.7% and 18.6%, respectively) (P <0.02). The reasons for tooth loss were considered dichotomously (i.e., tooth loss from periodontal disease and other reasons altogether [cariogenic, prosthetic, and endodontic reasons and root fracture). In the RC and EC groups, respectively, 35 and 55 teeth (71.4% and 78.6%) were lost due to periodontal disease, and 14 and 15 teeth (28.6% and 21.4%) were lost because of other reasons. In both groups, the loss due to periodontitis was significantly higher than for reasons other than periodontal disease (P <0.001). Thus, at the end of the 3-year period, 119 teeth were lost (0.72 – 1.9 teeth per patient). The RC group had 49 lost teeth (0.65 – 1.4 teeth per patient), and the EC group had 70 lost teeth (0.78 – 2.1 teeth per patient). The following results were reported for the occurrence of tooth loss among RC and EC patients at T2 according to the PRA profile: In the RC group, three individuals (4%) at MR lost 10 teeth, and 14 individuals (18.6%) at HR lost 39 teeth; no tooth loss was observed in LR individuals. In the EC group, one individual (1.1%) at LR lost four teeth, seven individuals (7.9%) at MR lost 21 teeth, and 19 individuals at HR (21.3%) lost 45 teeth. The multivariate model for the recurrence of periodontitis among RC patients at T2 included smoking, BOP in >30% of the sites, and number of missing teeth. 295 Periodontal Risk Assessment in Maintenance Therapy Volume 83 • Number 3 Table 3. Periodontal Status of RC and EC Patients After APT and at T2 T2† APT (baseline)* RC Periodontal Parameters EC RC EC Mean SD Mean SD Mean SD Mean SD 2.3 0.9 – 1.2 – 0.2 2.7 1.1 – 1.5 – 0.6 2.5A 1.2A – 3.3 – 0.5 4.7B 1.8B – 3.7 – 0.9 Clinical AL (% affected sites) 4 to 5 mm 11.6 ‡ 6 mm 7.1 – 1.3 – 0.9 12.3 7.3 – 1.8 – 1.3 12.3A 7.8A – 1.7 – 1.2 13.6B 9.7B – 2.3 – 1.8 BOP (% affected sites) – 3.3 25.7 – 4.4 27.1A – 4.1 32.9B – 5.8 PD (% affected sites) 4 to 5 mm ‡ 6 mm Suppuration (% affected sites) 24.1 0.05A – 0.07 0.07 – 0.13 0.11A – 0.04 0.19B – 0.25 PI 30.5 – 9.2 33.6 – 10.1 32.9A – 4.8 37.8B – 7.7 Mean number of teeth per patient 24.6 – 23.4 – 22.7A – 20.05B – – = not applicable. Total sample = 164 patients (75 RC and 89 EC patients). APT = After active periodontal therapy. * Comparisons between RC and EC patients after APT (baseline) and at T2 (P >0.05). † Comparisons between RC and EC patients at T2: values followed by different capital letters in rows were significantly different (P <0.05). Student t test was used for independent samples; Bonferroni correction was used for multiple comparisons (P <0.005). Among EC patients, the multivariate final model included BOP in >30% of sites, smoking, PD >5 mm in 10% of sites, diabetes, and the number of missing teeth (Table 5). A second multivariate logistic regression analysis was performed separately for tooth loss and the recurrence of periodontitis that occurred between APT and T2 considering sample characteristics and parameters of the PRA model. Odds ratio values and respective 95% confidence intervals are shown in Table 6. The multivariate model, considering the parameters of the PRA model as continuous variables, included BOP, the number of missing teeth, bone loss/age ratio, diabetes, and smoking for tooth loss and BOP, diabetes, and smoking for the recurrence of periodontitis. DISCUSSION The present prospective study presents two distinct objectives: 1) to evaluate and classify patient risk using the PRA model proposed by Lang and Tonetti,12 and 2) to determine the association of this risk classification with the recurrence of periodontitis and tooth loss according to the pattern of the compliance level of the 164 patients during 3 years of PMT. EC and RC groups had a significantly greater number of individuals classified as LR at T2 (RCs: 17.3%; 296 ECs: 10.3%). This finding showed a beneficial effect of PMT in both groups. Thus, the pattern of compliance and regular recall visits during PMT strongly influenced the risk profiles of patients. This finding was in accordance with previous studies reporting that compliance and adherence to PMT strongly reduced the risk of disease recurrence and tooth loss over time.10,22-25 A great problem during PMT is the adherence to follow-up visits. Many studies reported low rates of compliance.1,2,4,9,24,26-28 In relation to the average time between recalls, the present study showed an important difference between the RC group (3.3 months) and EC group (8.1 months). This difference was strongly related to the worse periodontal condition observed among EC patients. Thus, in the present study, the range of 4 months is ideally recommended. However, this time is very difficult to establish in clinical practice. The results of the present and other studies10,24,26-28 suggested that RCs, who complied with suggested maintenance schedules, substantially reduced the risk for a recurrence of periodontitis and tooth loss compared to ECs. In this sense, the use of the PRA model as a way to individualize risk and customize recall visits can be useful to optimize periodontal care, reduce treatment costs, avoid treatment overestimation, and minimize the recurrence of periodontitis and tooth loss. The Costa, Cota, Lages, et al. J Periodontol • March 2012 Table 4. Risk Classification and Risk Profile Changes for RC and EC Patients (n [%]) After APT (baseline examination) and at T2 Individuals With Changes in PRA Model From APT to T2 No Risk Change Risk Increase† RC EC RC 4 (4.5) 0 (0) 19 (25.4) 30 (33.7) 27 (36) 33 (37) Risk Decrease* Risk Profile RC EC LR 10 (13.3) 5 (5.6) MR 13 (17.4) 11 (12.4) HR 0 (0) 3 (4) 0 (0) APT T2 RC (n = 75) EC (n = 89) RC (n = 75) EC (n = 89) 0 (0) 3 (4) 4 (4.5) 13 (17.3) 9 (10.1) 0 (0) 0 (0) 45 (60) 52 (58.3) 32 (42.8) 41 (46,1) 3 (4) 6 (6.7) 27 (36) 33 (37.2) 30 (40) 39 (43.7) EC * Lower PRA profile at T2 in relation to after APT. † Higher PRA profile at T2 in relation to after APT. Table 5. Multivariate Logistic Regression Model for the Recurrence of Periodontitis for RC and EC Patients at T2 Recurrence of Periodontitis RC patients (n = 75) Smoking BOP >30% of sites Number of missing teeth Constant (coefficient: 0.027) ECs patients (n = 89) Smoking BOP >30% of sites PD >5 mm in 10% of sites Diabetes Number of missing teeth Constant (coefficient: 0.08) OR (95% CI) P 4.5 (1.36 to 9.71) 2.9 (1.02 to 10.1) 1.82 (1.04 to 6.45) – 0.001 0.032 0.041 0.000 6.3 3.4 3.6 1.82 3.46 <0.001 0.038 0.025 0.031 0.002 0.000 (1.23 (1.27 (1.02 (1.02 (1.19 – to to to to to 11.3) 10.9) 5.21) 2.72) 5.89) – = not applicable. PRA model showed that EC patients classified as HR had a significantly greater recurrence of periodontitis and tooth loss (ECs: 11.2% and 21.3%, respectively; RCs: 6.7% and 18.6%, respectively). Previous studies10,16 using the PRA model in PMT programs reported significantly higher rates of disease recurrence and tooth loss than those reported in our study. In a retrospective cohort, Matuliene et al.,10 performed PRAs of 160 patients after periodontal therapy and after 9.5 years of PMT. The authors reported rates of periodontitis recurrence of 18.2% in LR, 42.2% in MR, and 49.2% in HR patients. During PMT, 1.61 teeth per patient were lost. Despite using the same criteria proposed in our study, a longer period of study and a greater interval time between recalls may have contributed to this difference. Jansson and Norderyd,16 using a PRA model in 20 patients treated for severe periodontitis, concluded that the proposed model overestimated the risk for disease recurrence. However, additional comparisons with this study16 are discouraged because the sample included a very small number of patients (n = 20). Various retrospective6,23,29-32 and prospective studies5,10,15,32 of PMT reported a higher prevalence of tooth loss among EC compared to RC patients. The present study reported a high rate of tooth loss of a total of 119 teeth; 49 teeth were lost among RC patients, and 70 teeth were lost among EC patients, which corresponded to an annual average of 0.216 teeth per patient and 0.260 teeth per patient, respectively. The higher rates of tooth loss were observed among HR patients (79% in the RC group and 64.3% in the EC group). A greater number of missing teeth was concentrated in a small number of individuals. Previous studies10,15 using the PRA model showed different annual rates of tooth loss: Eickholz et al.15 reported 0.049 for regular and 0.257 for irregular compliers; Matuliene et al.10 reported 1.08 for regular and 3.12 for irregular compliers in 9.5 years, which corresponded to 0.13 and 0.30 annually, respectively. Therefore, ECs lost a higher number of teeth compared to RCs in both groups when considering HR patients. Differences observed between these groups may be related to lower rates of a recurrence of periodontitis, lower values of PDs and clinical ALs, a greater compliance and adherence with the PMT program, and, especially, a higher professional vigilance for patients classified as HR patients. The number of lost teeth was extensively reported as a reliable indicator of the risk for the recurrence of periodontitis.6,10,23,29-31 Individuals with >2 dental implants were excluded from the present study because the peri-implant clinical data were not suited for inclusion in the PRA model. Thus, there is a need for risk-assessment 297 Periodontal Risk Assessment in Maintenance Therapy Volume 83 • Number 3 Table 6. Multivariate Logistic Regression Models for Tooth Loss and Recurrence of Periodontitis During PMT in Relation to Patient Characteristics and Parameters Determining Risk Profiles at APT Recurrence of Periodontitis OR (95% CI) Variable Tooth Loss OR (95% CI) (P) Sample characteristic RCs versus ECs 2.35 (1.02 to 5.23) (0.015) 1.64 (1.08 to 3.62) (0.001) Parameters of PRA model BOP Sites with PD ‡5 mm Number of missing teeth Bone loss/age ratio Diabetes (yes versus no) Smoking (yes versus no) 2.23 1.81 2.21 2.73 1.92 3.41 1.88 1.04 1.69 1.21 1.66 3.78 (1.02 (0.96 (1.13 (1.04 (1.01 (1.26 to to to to to to 5.68) (0.021) 1.94) (0.361) 5.31) (0.022) 4.92) (<0.001) 7.28) (0.026) 11.41) (<0.001) (1.01 (0.64 (0.79 (0.42 (1.21 (1.32 to to to to to to 5.46) 1.89) 2.72) 3.46) 4.62) 7.28) (0.03) (0.483) (0.582) (0.662) (0.004) (<0.003) Significant P values are shown in bold. models that include the evaluation of implants, especially in patients partially rehabilitated with implants. The multivariate logistic model for the recurrence of periodontitis included classic risk factors such as smoking, BOP in >30% of the sites, and the number of lost teeth for RC and EC groups. In addition, PDs >5 mm in 10% of the sites and diabetes were also retained in the EC model. The inclusion of behavioral and biologic variables together with clinical parameters was similar to a previous study.10 In a multivariate logistic regression analysis, Matuliene et al.10 reported that an HR profile according to the PRA model was associated with the recurrence of periodontitis. Another significant factor for the recurrence of periodontitis was a PMT duration >9.5 years. The second multivariate logistic model analyzing characteristics of the sample showed that ECs had a 2.3-times higher odds of tooth loss and a 1.6-times higher odds of a recurrence of periodontitis compared to RCs. In the analysis for tooth loss, when including the continuous variables of the PRA model, a higher number of PRA parameters were retained as significant variables (BOP, tooth loss, bone loss/age ratio, and smoking). In the analysis for the recurrence of periodontitis, the model included BOP as an indicator of inflammation and risk for further clinical AL,33,34 and PRA parameters determining an HR profile such as smoking and diabetes.12 A number of studies7,10,18,35,36 related smoking to a higher risk for clinical AL and tooth loss. According to Matuliene et al.,37 among the six parameters used to determine periodontal risk in the PRA model, only smoking was considered a good predictor for the recurrence of periodontitis. The high frequency of BOP among patients under PMT in the present study can lead to some questions 298 regarding the adherence of patients to treatment and their plaque-control abilities. Percentages of BOP from 20% to 30% determined an HR for the recurrence of periodontitis in studies from Badersten et al.38 and Claffey et al.33 In addition, bleeding gums can be a self-perceived sign and alert subjects of the need for a PMT visit.7,34 Similar results were reported by Jansson and Norderyd16 using a PRA model in 20 patients treated for severe periodontitis. When they16 compared all patients by only using the BOP mean prevalence of 20% as a cutoff, 15 patients were categorized as having a low–moderate risk (75%) for periodontitis progression, and five patients (25%) were categorized as having a HR for disease progression. Studies have indicated that diabetes mellitus affects the susceptibility, severity, and recurrence of periodontitis.7,28,35,39,40 Our results showed that diabetes was associated with the recurrence of periodontitis in the EC group. Patients with diabetes had a 1.66-times higher chance of a recurrence of periodontitis and a 1.92-times higher chance of tooth loss. These findings reaffirmed that factors related to the host susceptibility should be carefully monitored during PMT. However, in the RC group, this association was not observed. This finding could have reflected the beneficial effect of PMT during regular recall visits. One limitation of the present study is the inclusion of numerous variables in the multivariate models. Thus, in small samples, the statistical power can be reduced. However, these analysis strategies were often reported in general literature, and longitudinal studies in larger samples are difficult to obtain and require great cost and logistics.5 In addition, all variables included in the final logistic models were recognized indicators or risk factors for the progression of periodontitis and tooth loss. Costa, Cota, Lages, et al. J Periodontol • March 2012 CONCLUSIONS It was concluded that the risk profile predicated the recurrence of periodontitis and tooth loss, and RCs had a lower recurrence of periodontitis and tooth loss. These findings reflect the need for an individual risk classification in an attempt to optimize adherence and customize recall intervals in PMT programs. The use of a PRA model can be an important tool in monitoring individual risk variables in relation to the recurrence of periodontitis and tooth loss. ACKNOWLEDGMENTS This study was supported by grants from the Research Support Foundation of Minas Gerais, Belo Horizonte, Brazil (project #10137) and the National Research Council, Brası´lia, Brazil (project #471616/2007-9). The authors thank Dr. Leonardo Costa Lima and dental hygienists Milene Aparecida Mendes Rocha, and Wilciane Alessandra Machado, private practice, Belo Horizonte, Brazil, for their assistance during the monitoring period of the study. The authors report no conflicts of interest related to this study. 11. 12. 13. 14. 15. 16. 17. REFERENCES 1. Mendoza AR, Newcomb GM, Nixon KC. Compliance with supportive periodontal therapy. J Periodontol 1991;62:731-736. 2. Wilson TG Jr., Hale S, Temple R. The results of efforts to improve compliance with supportive periodontal treatment in a private practice. J Periodontol 1993;64: 311-314. 3. Demetriou N, Tsami-Pandi A, Parashis A. Compliance with supportive periodontal treatment in private periodontal practice. A 14-year retrospective study. J Periodontol 1995;66:145-149. 4. Soolari A, Rokn AR. Adherence to periodontal maintenance in Tehran, Iran. A 7-year retrospective study. Quintessence Int 2003;34:215-219. 5. Lorentz TC, Cota LO, Cortelli JR, Vargas AM, Costa FO. Prospective study of complier individuals under periodontal maintenance therapy: Analysis of clinical periodontal parameters, risk predictors and the progression of periodontitis. J Clin Periodontol 2009;36:58-67. 6. Leininger M, Tenenbaum H, Davideau JL. Modified periodontal risk assessment score: Long-term predictive value of treatment outcomes. A retrospective study. J Clin Periodontol 2010;37:427-435. 7. Costa FO, Cota LO, Lages EJ, et al. Progression of periodontitis in a sample of regular and irregular compliers under maintenance therapy: A 3-year follow-up study. J Periodontol 2011; 82:1279-1287. ¨ m MK, Socransky SS, 8. Rosling B, Serino G, Hellstro Lindhe J. Longitudinal periodontal tissue alterations during supportive therapy. Findings from subjects with normal and high susceptibility to periodontal disease. J Clin Periodontol 2001;28:241-249. 9. Famili P, Short E. Compliance with periodontal maintenance at the University of Pittsburgh: Retrospective analysis of 315 cases. Gen Dent 2010;58:e42-e47. 10. Matuliene G, Studer R, Lang NP, et al. Significance of Periodontal Risk Assessment in the recurrence of peri- 18. 19. 20. 21. 22. 23. 24. 25. 26. 27. odontitis and tooth loss. J Clin Periodontol 2010;37: 191-199. Tonetti MS, Muller-Campanile V, Lang NP. Changes in the prevalence of residual pockets and tooth loss in treated periodontal patients during a supportive maintenance care program. J Clin Periodontol 1998;25: 1008-1016. Lang NP, Tonetti MS. Periodontal risk assessment (PRA) for patients in supportive periodontal therapy (SPT). Oral Health Prev Dent 2003;1:7-16. Trombelli L, Farina R, Ferrari S, Pasetti P, Calura G. Comparison between two methods for periodontal risk assessment. Minerva Stomatol 2009;58:277-287. Persson GR, Matuliene´ G, Ramseier CA, Persson RE, Tonetti MS, Lang NP. Influence of interleukin-1 gene polymorphism on the outcome of supportive periodontal therapy explored by a multi-factorial periodontal risk assessment model (PRA). Oral Health Prev Dent 2003;1:17-27. Eickholz P, Kaltschmitt J, Berbig J, Reitmeir P, Pretzl B. Tooth loss after active periodontal therapy. 1: Patient-related factors for risk, prognosis, and quality of outcome. J Clin Periodontol 2008;35:165-174. Jansson H, Norderyd O. Evaluation of a periodontal risk assessment model in subjects with severe periodontitis. A 5-year retrospective study. Swed Dent J 2008;32:1-7. American Academy of Periodontology. Parameters on comprehensive periodontal examination. J Periodontol 2000;71:847-883. Papantonopoulos GH. Effect of periodontal therapy in smokers and non-smokers with advanced periodontal disease: Results after maintenance therapy for a minimum of 5 years. J Periodontol 2004;75:839-843. Demirel K, Efeodlu A. Retrospective evaluation of patient compliance with supportive periodontal treatment. J Nihon Univ Sch Dent 1995;37:131-137. American Diabetes Association. Diagnosis and classification of diabetes mellitus. Position statement. Diabetes Care 2005;28(Suppl.1):S37-S42. Tonetti MS, Claffey N; European Workshop in Periodontology group C. Advances in the progression of periodontitis and proposal of definitions of a periodontitis case and disease progression for use in risk factor research. Group C consensus report of the 5th European Workshop in Periodontology. J Clin Periodontol 2005;32(Suppl. 6):210-213. ¨ nig J, Dzierzon U, Sawaf H, Plagmann Kocher T, Ko H-C. Disease progression in periodontally treated and untreated patients – A retrospective study. J Clin Periodontol 2000;27:866-872. ¨ nig J, Plagmann HC, Langenfeld N, Kocher T. Ko Retrospective comparison of clinical variables between compliant and non-compliant patients. J Clin Periodontol 2001;28:227-232. Fardal O, Johannessen AC, Linden GJ. Compliance in a Norwegian periodontal practice. Oral Health Prev Dent 2003;1:93-98. Fardal O. Interviews and assessments of returning non-compliant periodontal maintenance patients. J Clin Periodontol 2006;33:216-220. Novaes AB Jr., Novaes AB, Bustamanti A, Villavicencio JJ, Muller E, Pulido J. Supportive periodontal therapy in South America. A retrospective multi-practice study on compliance. J Periodontol 1999;70:301-306. Cohen RE; Research, Science and Therapy Committee, American Academy of Periodontology. Position 299 Periodontal Risk Assessment in Maintenance Therapy 28. 29. 30. 31. 32. 33. 34. 300 paper: Periodontal maintenance. J Periodontol 2003; 74:1395-1401. Costa FO, Cota LO, Lages EJ, et al. Oral impact on daily performance, personality traits and compliance in periodontal maintenance therapy. J Periodontol 2011 Feb 2. [Epub ahead of print]. Checchi L, Montevecchi M, Gatto MR, Trombelli L. Retrospective study of tooth loss in 92 treated periodontal patients. J Clin Periodontol 2002;29: 651-656. Chambrone LA, Chambrone L. Tooth loss in wellmaintained patients with chronic periodontitis during long-term supportive therapy in Brazil. J Clin Periodontol 2006;33:759-764. Miyamoto T, Kumagai T, Jones JA, Van Dyke TE, Nunn ME. Compliance as a prognostic indicator: Retrospective study of 505 patients treated and maintained for 15 years. J Periodontol 2006;77:223232. Chambrone L, Chambrone D, Lima LA, Chambrone LA. Predictors of tooth loss during long-term periodontal maintenance: A systematic review of observational studies. J Clin Periodontol 2010;37:675-684. Claffey N, Nylund K, Kiger R, Garrett S, Egelberg J. Diagnostic predictability of scores of plaque, bleeding, suppuration and probing depth for probing attachment loss. 3 1/2 years of observation following initial periodontal therapy. J Clin Periodontol 1990;17:108114. Oliveira Costa F, Cota LO, Costa JE, Pordeus IA. Periodontal disease progression among young subjects with no preventive dental care: A 52-month follow-up study. J Periodontol 2007;78:198-203. Volume 83 • Number 3 35. Heitz-Mayfield LJA. Disease progression: Identification of high-risk groups and individuals for periodontitis. J Clin Periodontol 2005;32(Suppl. 6):196-209. 36. Fisher S, Kells L, Picard J-P, et al. Progression of periodontal disease in a maintenance population of smokers and non-smokers: A 3-year longitudinal study. J Periodontol 2008;79:461-468. 37. Matuliene G, Pjetursson BE, Salvi GE, et al. Influence of residual pockets on progression of periodontitis and tooth loss: Results after 11 years of maintenance. J Clin Periodontol 2008;35:685-695. 38. Badersten A, Nilve´us R, Egelberg J. Scores of plaque, bleeding, suppuration and probing depth to predict probing attachment loss. 5 years of observation following nonsurgical periodontal therapy. J Clin Periodontol 1990;17:102-107. ¨ stalo PV, Knuuttila ML. Confounding and effect 39. Ylo modification: Possible explanation for variation in the results on the association between oral and systemic diseases. J Clin Periodontol 2006;33:104-108. 40. Bandyopadhyay D, Marlow NM, Fernandes JK, Leite RS. Periodontal disease progression and glycaemic control among Gullah African Americans with type2 diabetes. J Clin Periodontol 2010;37:501-509. Correspondence: Dr. Fernando Oliveira Costa, Department of Periodontology, Federal University of Minas ˆ nio Carlos Avenue, 6627, Pampulha, P.O. Gerais, Anto Box 359, Belo Horizonte, MG 31270-901, Brazil. Fax: 5531-3282-6787; e-mail: focperio@uol.com.br. Submitted March 23, 2011; accepted for publication June 1, 2011.