ABSTRACT
The objective of this prospective study was to assess oral health-related quality of life (OHR-QoL) in patients with periodontitis and nonsurgical periodontal treatment. A prospective, longitudinal case series study was carried out at the University Dental Clinic of the Morales Meseguer Hospital in Murcia. Eighty periodontal patients with periodontitis, aged 22 to 72 years, were included in this study. The Spanish version of the Oral Health Impact Profile 14 (OHIP-14sp) questionnaire was used on two occasions: at the first visit and one month after completing the nonsurgical periodontal treatment. Clinical measurements of probing depth, plaque index and bleeding on probing were performed at baseline and after periodontal therapy. Data were analyzed using Student's t-test and analysis of variance. We found statistically significant differences (p < 0.05) between the pre- and post-treatment in all the dimensions studied except disability. Similarly, statistically significant differences were also found according to the degree or stage of the disease. However, these differences were not observed with respect to the extent of periodontal disease. Periodontal disease has a negative impact on the OHRQoL of periodontal patients, especially in severe stages (III-IV). Basic periodontal treatment can improve the OHRQoL of periodontal patients one month after treatment.
ABSTRACT
Dental implants currently in use are mainly made of titanium or titanium alloys. As these metallic elements are immersed in an electrolytic medium, galvanic currents are produced between them or with other metals present in the mouth. These bimetallic currents have three potentially harmful effects on the patient: micro-discharges, corrosion, and finally, the dispersion of metal ions or their oxides, all of which have been extensively demonstrated in vitro. In this original work, a system for measuring the potentials generated in vivo is developed. Specifically, it is an electrogalvanic measurements system coupled with a periodontal probe that allows measurement of the potentials in the peri-implant sulcus. This device was tested and verified in vitro to guarantee its applicability in vivo. As a conclusion, this system is able to detect galvanic currents in vitro and it can be considered capable of being employed in vivo, so to assess the effects they may cause on dental implants.
ABSTRACT
The purpose of this article was to assess the effectiveness of ozone therapy as an adjunct to mechanical therapy in periodontitis patients. Thirty-two patients diagnosed with generalized periodontitis were selected, with a total of 655 teeth examined. Each patient's mouth was divided into four quadrants (the split-mouth model) to be randomly treated with four sessions of gaseous ozone or air. The following clinical variables were recorded: the gingival index, the periodontal clinical attachment loss, the Miller's mobility index and the clinical improvements, as assessed through the visual analog scale (VAS). In addition, the microorganisms were qualitatively compared. After four weeks of treatment, the teeth of the ozone-treated quadrants showed statistically significant reductions in the gingival index and an improvement in the clinical attachment (p < 0.0001). The same treatment also significantly improved mobility by between 70% and 86% compared to the control group (p < 0.0001). Statistically significant differences were also recorded for the VAS (p < 0.0001). In the qualitative study of the subgingival flora, significant differences were observed (p < 0.0001). The overall results of this trial support the view that ozone treatment is effective and well tolerated in cases of generalized chronic periodontitis.
ABSTRACT
The use of immediate implants in the aesthetic area is a technique widely used in modern implantology. The characteristics of the patient, the implant, and the surgical procedure used may influence the final results. The aim was to assess whether the implant design affects primary (P.S.) and secondary stability (S.S.), bone level (B.L.), and PES/WES evaluation. Twenty implants with two different designs (n = 10) were immediately placed and randomly located in the upper anterior maxilla with no grafting material. Implant-Stability-Quotient (ISQ), B.L., and Pink-Esthetic-Score/White-Esthetic-Score (PES/WES) were evaluated. Shapiro-Wilk normality test was performed to determine the sample normality, as the data did not follow a normal distribution, the Wilcoxon-Mann-Whitney test was applied (p < 0.05). ISQ was determined at placement (PS): control 59.1 (C.I.54.8-63.3); experimental 62.2(C.I.60.1-64.2) and three months after placement (SS): control 62.2.1 (C.I.53.3-71.0); experimental 67.2(C.I.65.8-68.5). The BL was measured at three months after placement: control 0.38 mm (C.I.- 0.06 to + 0.83); experimental 0.76 mm (C.I.0.33-1.19) and at 12 months post-loading: control 0.07 mm (C.I.- 0.50-0.65); experimental 0.90 mm (C.I.0.38-1.42). PES/WES values were evaluated for the control group: 15 (C.I.12.68-17.32), and for the experimental group 15.20 (C.I.11.99-18.41). No significant differences were shown between both implant designs. A good grade of osseointegration and primary/secondary stability was achieved, as well as proper maintenance of crestal bone and adequate PES/WES scores. The criteria for selection for the ideal patient for immediate implant placement is essential.ClinicalTrials Protocol ID: NCT04343833.
Subject(s)
Dental Implantation/methods , Dental Implants , Esthetics, Dental , Aged , Aged, 80 and over , Double-Blind Method , Female , Follow-Up Studies , Humans , Male , Middle Aged , Osseointegration , Risk Factors , Tooth Socket/surgery , Treatment OutcomeABSTRACT
Microsurgical scalp reconstruction is indicated in patients with large scalp defects. The aim of this study was to compare the outcomes of scalp reconstruction in oncologic patients reconstructed with latissimus dorsi (LD), anterolateral thigh (ALT), and omental (OM) free flaps. Thirty oncologic patients underwent scalp reconstruction with LD (10), ALT (11), and OM (9) flaps. The length of the vascular pedicle, the operation time, the possibility of a two-team approach, the length of hospital stays, the complications, and the aesthetic results were evaluated. The OM flap was the flap with the shortest vascular pedicle length with a mean of 6.26 ± 0.16 cm, compared to the LD flap, which was 12.34 ± 0.55 cm and the ALT flap with 13.20 ± 0.26 cm (p < 0.05). The average time of surgery was 6.6 ± 0.14 h in patients reconstructed with OM, compared to the LD flap, which was 8.91 ± 0.32 h and the ALT flap with 7.53 ± 0.22 h (p < 0.05). A two-team approach was performed in all patients for OM flaps and ALT flaps, but only in two patients reconstructed with the LD flap (p < 0.001). In patients reconstructed with the OM flap, a very satisfactory or satisfactory result was reported in seven patients (77.8%). Eight patients reported a very unsatisfactory or unsatisfactory result with LD flap (80%) and 10 patients with ALT flap (90.9%) (p = 0.002). The mean hospital stay after surgery was not statistically significant (p > 0.05). As for complications, two patients reconstructed with OM flap, five LT flaps, and two ALT flaps developed complications, not statistically significant (p = 0.235). Omental flap, latissimus dorsi flap, and anterolateral thigh flap fulfill most of the characteristics for complex scalp reconstruction. The decision on which flap to use should be based on clinical aspects of the patients taking into account that the three flaps show similar rates of complications and length of hospital stay. Regarding the aesthetic outcome, OM flap or LD flap should be considered for reconstruction of extensive scalp defects.
ABSTRACT
Two-phase implants must be exposed to the external environment after the period of osteointegration has elapsed. For this purpose, a healing abutment is placed passing through the mucosa while forming the emergence profile. The continuous connection and disconnection can lead to an alteration in the tissue maturation, both because of the contact of bacterial plaque and because of the mechanical trauma that involves its manipulation, manifesting with different degrees of erythema or bleeding. To assess whether this epithelium disruption can be counteracted, a blinded study design was developed on 150 unitary implant patients divided into three groups (n = 50), applying chlorhexidine (group 1), ultraviolet C (UV-C) at a wavelength of 254 nm (group 2)and no treatment as a control group (group 3), during each of the disconnections and connections during the prosthodontic treatment (1 time per week for four weeks). All groups showed a better epithelium aspect at the end of the evaluation. Although there were no statistically significant differences in the degree of inflammation, the UV-C treated group had the lowest plaque accumulation, and the highest was for the chlorhexidine-treated group.
ABSTRACT
This study investigated whether a 6-Watt ultraviolet C-lamp was capable of producing photofunctionalization on commercial implants during a medium observation term of 8 weeks. A total of 20 implants were inserted in 5 New Zealand rabbits, with each animal receiving 2 implants per tibia (one photofunctionalized and one untreated), according to a previously established randomization sequence. All implants were inserted by a single surgeon following the manufacturer's instructions. Histological analysis was performed by an evaluator who was blinded to the treatment condition. After 8 weeks of healing, the 2 groups showed no statistically significant differences in terms of bone-to-implant contact. Compared to control implants, the photofunctionalized implants showed improved wettability and more homogenous results. Within the limits of the present study, the use of this 6-W ultraviolet C-lamp, for an irradiation time of 15 minutes at a distance of 15 cm, did not improve the percentages of bone-to-implant contact in rabbits at an osseointegration time of 8 weeks.
Subject(s)
Dental Implants , Osseointegration , Animals , Rabbits , Surface Properties , Tibia , Titanium , WettabilityABSTRACT
Double-barrel flap, vertical distraction and iliac crest graft are used to reconstruct the vertical height of the fibula. Twenty-four patients with fibula flap were reconstructed comparing these techniques (eight patients in each group) in terms of height of bone, bone resorption, implant success rate and the effects of radiotherapy. The increase in vertical bone with vertical distraction, double-barrel flap and iliac crest was 12.5 ± 0.78 mm, 18.5 ± 0.5 mm, and 17.75 ± 0.6 mm, (p < 0.001). The perimplant bone resorption was 2.31 ± 0.12 mm, 1.23 ± 0.09 mm and 1.43 ± 0.042 mm (p < 0.001), respectively. There were significant differences in vertical bone reconstruction and bone resorption between double-barrel flap and vertical distraction and between iliac crest and vertical distraction (p < 0.001). The study did not show significant differences in implant failure (p = 0.346). Radiotherapy did not affect vertical bone reconstruction (p = 0.125) or bone resorption (p = 0.237) but it showed higher implant failure in radiated patients (p = 0.015). The double-barrel flap and iliac crest graft showed better stability in the height of bone and less bone resorption and higher implant success rates compared with vertical distraction. Radiation therapy did not affect the vertical bone reconstruction but resulted in a higher implant failure.
ABSTRACT
The mechanisms of early failures in dental implant osseointegration are unclear. A possible cause of low levels of bone formation is lubricant contamination on implants during insertion. To explore the impact of lubricant contamination on dental implants, we used 5 New Zealand rabbits and inserted 2 implants per tibia in each animal for a total of 4 implants per animal (20 implants in total). In general, bicorticalization was achieved. The first implant was placed as suggested by the manufacturer with no lubricant used (control). The second implant was placed using a freshly lubricated contra-angle handpiece, which was used only for the test implants. Implant allocation was randomized, and the examining histologist was blinded to the results. All implants were placed by the same surgeon. The animals were maintained in accordance with animal experimentation guidelines. None of the implants failed to osseointegrate. Moreover, no significant difference was observed between the test and control groups. Based on the results of this study, the use of rotary instrument mineral oil lubricant did not jeopardize the osseointegration of dental implants in New Zealand rabbits.
Subject(s)
Dental Implants , Mineral Oil , Osseointegration , Animals , Dental Implantation, Endosseous , Implants, Experimental , Lubricants , Mineral Oil/pharmacology , Rabbits , Random Allocation , Tibia , TitaniumABSTRACT
The fear of postoperative pain is often mentioned by patients as one of the factors that is most frequently associated with dental implants. To reduce this factor, a single oral dose of 25 mg dexketoprofen trometamol (DKT) or placebo was administered 15 minutes before implant surgery. One hundred patients who required single-implant treatments were randomly assigned to 1 of 2 blinded groups. The patients in the test group were given 25 mg DKT (DKT group), and those in the control group were given 500 mg vitamin C as a placebo (PLACEBO group). A subjective visual analogue scale of 100 mm in length was used to evaluate pain. Inflammation and complications were assessed using a 5-point Likert scale. An analysis of variance, t-tests, and a Mann-Whitney U test were performed. Among the 100 patients, 83 completed the study (there were 8 dropouts in the PLACEBO group and 9 in the DKT group). The patients who received DKT reported a lower pain intensity during the immediate postoperative period. The inflammatory response was weaker in the DKT group than the control group at 48 hours, but bleeding was greater. There were no other complications in either of the groups. In conclusion, the preemptive use of 25 mg soluble DKT administered orally 15 minutes before implant surgery can reduce the severity of immediate postoperative pain.
Subject(s)
Dental Implants/adverse effects , Ketoprofen/analogs & derivatives , Pain, Postoperative/drug therapy , Tromethamine/pharmacology , Administration, Oral , Analysis of Variance , Anti-Inflammatory Agents, Non-Steroidal/administration & dosage , Anti-Inflammatory Agents, Non-Steroidal/pharmacology , Ascorbic Acid , Double-Blind Method , Humans , Ketoprofen/administration & dosage , Ketoprofen/pharmacology , Pain Measurement , Statistics, Nonparametric , Time Factors , Treatment Outcome , Tromethamine/administration & dosageABSTRACT
OBJECTIVES: To determine the position of the mandibular medial lingual foramen with cone-beam CT (CBCT) 3D imaging modalities when implants are to be placed in the anterior symphysis of the mandible. MATERIALS AND METHODS: A total of 111 CBCTs were considered acceptable and analyzed. The variables measured were as follows: (1) length of the outlet duct; (2) distance from the canal to the buccal cortex; (3) distance from the canal to the inferior cortex; (4) distance from the canal to the lingual cortex; (5) distance from the canal to the alveoli of the nearest tooth in dentate patients and distance from the canal to the marginal crest in edentulous patients; (6) angle of the duct to the horizontal Frankfurt plane; (7) diameter of the exit orifice; and (8) output level of the socket in relation to the teeth and the presence of bifurcations. RESULTS: A single canal was observed in 64% of patients; 2 canals were observed in 33% of patients; and a triple foramen was observed in 3% of patients. Women showed slightly lower values than men for each of the analyzed variables, with statistically significant differences in the length of the canal in edentulous (P = 0.029) and dentate patients (P = 0.027). CONCLUSION: The medial lingual foramen should be considered while performing presurgical planning. Careful attention is needed while setting the placement position of the dental implant to decrease the risk of complications.
Subject(s)
Chin/diagnostic imaging , Cone-Beam Computed Tomography , Dental Implantation, Endosseous/methods , Adolescent , Adult , Aged , Chin/anatomy & histology , Cone-Beam Computed Tomography/methods , Dental Implants , Female , Humans , Male , Middle Aged , Retrospective Studies , Sex Factors , Young AdultABSTRACT
Objetivos. Evaluar el valor pronóstico de la movilidad primaria (momento de inserción del implante) y secundaria (fase protésica), así como el de la densidad ósea en el resultado de éxito o fracaso del implante durante un seguimiento continuado al año, a los 5 años y a los 10 años. Material y métodos. Se realizó un estudio longitudinal prospectivo con un seguimiento a 10 años en el que se incluyeron 151 implantes colocados en 71 pacientes, no fumadores, durante los años 2005 y 2006. A cada uno de los implantes se les midió las estabilidades primaria y secundaria a través de un valor Periotest® (VPT) y se anotó la densidad ósea presente en el momento de la implantación. De los 151 implantes colocados inicialmente, completaron el estudio 109. Resultados. No se observaron diferencias estadísticamente significativas respecto a la movilidad del implante en el momento de inserción o en la fase protésica y el éxito o fracaso del mismo al año, a los 5 años, o transcurridos 10 años desde su inserción. Sí encontramos diferencias estadísticamente significativas con relación al tipo de densidad ósea donde se colocó el implante a los 5 y 10 años (p<0,05). Conclusiones. La movilidad primaria o secundaria del implante carece de valor pronóstico significativo sobre el éxito del mismo transcurridos 10 años desde su inserción. Por el contrario, la densidad de hueso inicial tiene una clara influencia en el éxito del implante a los 10 años, siendo más proclives al fracaso los huesos de alta densidad ósea (AU)
Purposes. To prospectively analyze the prognosis value of the primary mobility (at the moment of implant insertion) and secondary (prosthetic phase), as well as bone density, in the implant success or failure after one year, five years and ten years. Materials and methods. Between 2005 and 2006, 151 implants were placed in 71 non-smoking patients. Primary (at the moment of surgery) and secondary (once osseointegrated) stabilities were measured in each implant through a Periotest® value (PTV) and the bone density was scored at the moment of implantation. One hundred nine of 151 implants placed initially completed the study. Results. There were no statistically significant differences regarding implant mobility at the moment of its insertion or once osseointegrated and the implant success or failure after 10 years. However, statistically significant differences were found respect to the bone density where the implant was placed after 5 and 10 years (P<.05). Conclusions. Primary or secondary mobility of the implant has no significant prognosis value on the implant success after 10 years. On the other hand, bone density has a clear influence on long time implant success. High density bones are more predictable to fail than low density bones after a long time (AU)
Subject(s)
Humans , Bone Density , Tooth Mobility/diagnosis , Tooth Mobility/surgery , Dental Implantation/methods , Dental Implantation/trends , Dental Implantation, Endosseous/trends , Prospective Studies , Longitudinal Studies , Treatment Failure , Data AnalysisABSTRACT
BACKGROUND: One of the disadvantages of the zirconia implants is the lack of elasticity, which is increased with the use of ceramic or zirconia crowns. The consequences that could result from this lack of elasticity have led to the search for new materials with improved mechanical properties. CASE PRESENTATION: A patient who is a 45-year-old woman, non-smoker and has no medical record of interest with a longitudinal fracture in the palatal root of molar tooth 1.7 and absence of tooth 1.6 was selected in order to receive a zirconia implant with a PEEK-based restoration and a composite coating. The following case report describes and analyses treatment with zirconia implants in molars following a flapless surgical technique. Zirconia implants are an alternative to titanium implants in patients with allergies or who are sensitive to metal alloys. However, one of the disadvantages that they have is their lack of elasticity, which increases with the use of ceramic or zirconia crowns. The consequences that can arise from this lack of elasticity have led to the search for new materials with better mechanical properties to cushion occlusal loads. PEEK-based restoration in implant prosthetics can compensate these occlusal forces, facilitating cushioning while chewing. CONCLUSION: This procedure provides excellent elasticity and resembles natural tooth structure. This clinical case suggests that PEEK restorations can be used in zirconia implants in dentistry.
ABSTRACT
PURPOSE: To analyze the anatomical findings and alterations of the maxillary sinus in asymptomatic patients observed by cone beam computed tomography. MATERIALS AND METHODS: A cross-sectional retrospective study of the anatomical variations and alterations of the maxillary sinus was made in 160 patients-71 males (44.3%) and 89 females (55.6%), with an age range of 18 to 74 years-measuring the thickness of the Schneiderian membrane and the cortical thickness of the lower margin of the maxillary sinus (in its most caudal portion), and correlations among the different study variables were assessed. RESULTS: Sinus pneumatization was the most frequent anatomical finding (81.3%). A negative correlation was observed between the thickness of the Schneiderian membrane and the presence of Underwood septa (P < 0.005). Mucosal thickening of more than 2 mm was directly correlated with the presence of maxillary sinus lesions (opacification, discontinuity of the floor of the sinus, polypoid lesions, or air-liquid levels). CONCLUSION: The presence or absence of septa seems to be related to the thickness of the Schneiderian membrane.
Subject(s)
Cone-Beam Computed Tomography/methods , Maxillary Sinus/diagnostic imaging , Adolescent , Adult , Aged , Cross-Sectional Studies , Female , Humans , Male , Maxillary Sinus/anatomy & histology , Middle Aged , Nasal Mucosa/anatomy & histology , Nasal Mucosa/diagnostic imaging , Radiography, Panoramic , Retrospective Studies , Young AdultABSTRACT
PURPOSE: To date, no ideal strategy has been established for treating or preventing medication-related osteonecrosis of the jaw (MRONJ). The aim of the present work was to perform a systematic literature review to determine the efficacy of autologous platelet concentrate (APC) application, for prevention or treatment of MRONJ, together with surgical debridement. MATERIAL AND METHODS: An electronic search was performed using MEDLINE (PubMed), EMBASE, and Cochrane databases until January 2015 using the following search terms: osteonecrosis, bisphosphonates, antiresorptive, antiangiogenic therapy, BRONJ, platelet concentrate, PRP, PRF, and PRGF. Two reviewers assessed the eligibility of articles independently and extracted key data. The methodology used met PRISMA criteria. The Newcastle-Ottawa scale was used to assess the quality of the articles. RESULTS: Preventive applications of platelet-rich plasma (PLP) were reported in 697 dental extractions in patients taking bisphosphonates intravenously, of whom seven patients developed osteonecrosis (five mandibular and two maxillary). In cases of established osteonecrosis, eight studies reported treatment by surgery combined with APC (seven with PRP and one with leukocyte-rich and platelet-rich fibrin) in 123 patients (34 men and 89 women) with ONJ, who received 157 treatments, of which 135 achieved complete resolution (85.98%). CONCLUSION: There are no published scientific data to sufficiently support any specific treatment protocol, including the use of APC together with surgical debridement, for the management of MRONJ. Randomized controlled clinical trials of the use of APC are needed.
Subject(s)
Bisphosphonate-Associated Osteonecrosis of the Jaw/therapy , Platelet-Rich Plasma , Bisphosphonate-Associated Osteonecrosis of the Jaw/prevention & control , Bisphosphonate-Associated Osteonecrosis of the Jaw/surgery , Combined Modality Therapy , Debridement , Female , Humans , Leukocytes , MaleABSTRACT
BACKGROUND: Surgery of the anterior maxillary zone has a strong impact upon dental and facial aesthetics and function. PURPOSE: To determine the anatomical characteristics and dimensions of the nasopalatine canal and alveolar bone using cone beam computed tomography (CBCT). MATERIALS AND METHODS: A retrospective, cross-sectional study was made of the nasopalatine canal in 122 randomly selected CBCT scans corresponding to 66 males (44.3%) and 56 females (55.6%). The following measurements were made: maximum length and diameters of the nasal and oral openings of the nasopalatine canal; distance from the crestal margin to the buccal wall (at apical, middle, and coronal level); and angulation of the nasopalatine canal. The anatomical variants were morphologically classified as follows: A (single canal), B (double canal), or C (Y-shaped canal). RESULTS: The anatomy of the nasopalatine canal showed important variability in terms of morphology and dimensions. Type A was observed in 48 patients (39.34%), type B in 10 (8.19%), and type C in 64 (52.45%). The mean diameter of the nasal opening or orifice was 3.02 ± 1.0 mm versus 3.29 ± 1.0 mm in the case of the oral opening. The mean length of the canal was 11.02 ± 2.4 mm. Significant differences were found between males and females, with greater canal dimensions and alveolar bone thickness values anterior to the nasal canal zone among males (p < .05). CONCLUSIONS: Our study shows gender to exert a significant influence upon the anatomical dimensions of the anterior maxilla and incisor canal. Given the anatomical variability characterizing the nasopalatine canal, we recommend CBCT evaluation prior to any type of surgery of the anterior maxillary zone.
Subject(s)
Palate/anatomy & histology , Adult , Alveolar Process/anatomy & histology , Alveolar Process/diagnostic imaging , Cone-Beam Computed Tomography , Cross-Sectional Studies , Female , Humans , Male , Maxilla/anatomy & histology , Maxilla/diagnostic imaging , Palate/diagnostic imaging , Retrospective StudiesABSTRACT
PURPOSE: To evaluate postoperative pain after successful implant surgery and compare pain experienced using conventional flap and flapless techniques. MATERIALS AND METHODS: Between January 2007 and September 2012, consecutive patients with bilateral partially edentulous maxillae or mandibles were included in the study. Patients were randomly allocated to receive implants with an atraumatic flapless procedure or with a conventional flap procedure in a split-mouth design in a two-stage surgery. This randomized blinded prospective clinical study considered each patient as one unit. The data were analyzed using the Mann-Whitney and chi-square tests. RESULTS: One hundred eight implants were placed in 19 patients. Radiographic and clinical examination showed that all implants were successful. Postoperative pain was significantly more intense after surgery with the conventional flap technique than after surgery with the atraumatic flapless technique. Likewise, the inflammatory response was more intense with the flap technique. CONCLUSIONS: Postoperative pain depends on the surgical technique used and is less intense with a flapless technique.
Subject(s)
Dental Implantation, Endosseous/methods , Jaw, Edentulous, Partially/surgery , Pain, Postoperative , Surgical Flaps , Adult , Chi-Square Distribution , Cross-Over Studies , Dental Implantation, Endosseous/adverse effects , Female , Humans , Jaw, Edentulous, Partially/rehabilitation , Male , Middle Aged , Pilot Projects , Prospective Studies , Statistics, NonparametricABSTRACT
The aim of this study was to assess the presence of aspartate aminotransferase (AST) in peri-implant crevicular fluid, with or without clinical signs of mucositis, to determine its predictive diagnostic value, sensitivity, and specificity. The AST levels were determined (at a threshold of 1200 µIU/mL) for 60 clinically successful implants in 25 patients with or without peri-implant mucositis. Samples were taken prior (AST1) to peri-implant probing with a manual constant-pressure probe (0.2 N) and 15 minutes after probing (AST2). Clinical assessments included radiographic determination of preexisting bone loss, probing, and the evaluation of mucositis, plaque, and bleeding upon probing. Analysis was performed at both the level of the implant and the patient as a unit. We detected a significant difference between AST1 and AST2 at both levels. A significant difference was observed at AST1 between implants that bled upon probing and those that did not. However, when we considered the patient as a unit, there were no significant differences. The plaque index was not significant at either level. AST1 had high specificity and positive predictive diagnostic value (80%) for bleeding upon probing. Probing induces a greater release of AST from inflamed tissues compared with healthy tissues in situ but not at the systemic level. At the implant level, the implant position could be responsible for this difference. Aspartate aminotransferase was a reliable predictor of patients with mucositis.
Subject(s)
Aspartate Aminotransferases/analysis , Dental Implants , Gingival Crevicular Fluid/enzymology , Stomatitis/enzymology , Adolescent , Adult , Aged , Alveolar Bone Loss/enzymology , Dental Plaque Index , Female , Gingival Hemorrhage/enzymology , Humans , Male , Middle Aged , Osseointegration/physiology , Periodontal Index , Periodontal Pocket/enzymology , Predictive Value of Tests , Radiography, Bitewing , Sensitivity and Specificity , Young AdultABSTRACT
OBJECTIVE: The aim of this study was to evaluate periimplant tissue temperature in a successful implant. It has been shown that periimplant disease and mucositis are inflammatory diseases. As such, one of the main clinical signs is the change in temperature. We try to establish normal values of temperature with an easy to use appliance. DESIGN: Fifty-one individuals were enrolled in this study. Only 1 implant per patient was included. The implants were clinically and radiographically examined and diagnosed as clinical successful implants. An infrared ear thermometer was used to measure periimplant temperature (PIT) and the difference with the sublingual temperature (ΔT). These data were analyzed using the Student t test, analysis of variance, and cluster analysis. RESULTS: Statistically significant differences in PIT were observed between the second sextant and the fourth and fifth sextants. These differences were not significant on considering ΔT. In addition, for the clinically and radiographically successful implants, ΔT for all sextants showed a mean of 0.81 (CI, 0.57-1.04). CONCLUSIONS: We have found a difference in outcome between periimplant temperature and the temperature differential. PIT depends on the anatomical location, though ΔT is an independent measurement with a value of 0.81°C.
Subject(s)
Body Temperature , Dental Implants , Gingiva/physiology , Mouth Mucosa/physiology , Analysis of Variance , Cluster Analysis , Dental Prosthesis, Implant-Supported , Female , Humans , Male , Middle Aged , Mouth Floor/physiology , Observation , Reference ValuesABSTRACT
Implant fracture is an infrequent and late biomechanical complication with a serious clinical outcome. In effect,such fractures pose important problems for both the patient and the dental surgeon. According to most literaturesources, the prevalence of dental implant fractures is very low (approximately 2 fractures per 1000 implants inthe mouth). Considering that implant placement is becoming increasingly popular, an increase in the number offailures due to late fractures is to be expected. Clearly, careful treatment can contribute to reduce the incidenceof fracture. An early diagnosis of the signs alerting to implant fatigue, such as loosening, torsion or fracture ofthe post screws and prosthetic ceramic fracture, can help prevent an undesirable outcome. The present literaturereview describes the management options and discusses the possible causal mechanisms underlying such failures,as well as the factors believed to contribute to implant fracture (AU)
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