Dentinal Hypersensitivity
Dentinal Hypersensitivity is a chronic condition with acute episodes. When dentine is exposed, which usually happens due to gingival recession & enamel damage (erosion, abrasion, attrition, and abfraction), external triggers (such as a cold drink) can stimulate the nerves inside the tooth, causing the characteristic short, sharp sensation of tooth sensitivity.1
The most common trigger for realizing sensitivity is cold.
1. Dababneh RH, Khouri AT, Addy M. Dentine hypersensitivity an enigma? A review of terminology, mechanisms, aetiology and management. Br Dent J.1999;187:606–611
What is Calcium Sodium Phosphosilicate?
CSPS is a particulate, bioactive glass material that degrades in the aqueous oral environment to release calcium and phosphate ions, leading to formation of Hydroxycarbonate Apatite on the dentine surface. This process creates a physical barrier that mitigates the impact of external stimuli on fluid movement within dentinal tubules.1
1. S. Schlafer et al. Journal of Dentistry 91S (2019) 100003.
Why Vantej?
- CSPS as the major ingredient
- Extra foaming & Mint flavor
- Extensively studied molecule
1. Xiong Zheng-hui, et al. Occluding eects of three new calcium desensitizers on dentinal tubules in vitro. Zhongua Kou Qiang Yi Xue Za Zhi. 2011 Apr;46(4):214-7.
Where to Use?
In Dentinal Hypersensitivity
- Dentinal Hypersensitivity is a chronic condition with an acute episodes, usually stimulated by external triggers – mainly a cold beverage.1
- Drinking or eating something cold/freezing is the most common sensation to realize Dentinal Hypersensitivity.2,3
1. Dababneh RH, Khouri AT, Addy M. Dentine hypersensitivity — an enigma? A review of terminology, mechanisms, aetiology and management. Br Dent J.1999;187:606–611.
2. Hydrodynamic Theory Kramer IRH. The relationship between dentine sensitivity and movements in the contents of dentinal tubules. Br Dent J. 1955;98:391–392.
3. Brännström M. The elicitation of pain in human dentine and pulp by chemical stimuli. Arch Oral Biol. 1962;7:59–62
How to Use?
- Squeeze some toothpaste about half the length of the bristle head and brush for 1-2 minutes using a gentle, vertical sweeping motion away from gums.
- Spit out the paste and rinse with water, do not swallow.
- Avoid eating or drinking anything within half an hour of brushing.
- Brush twice daily for best results.
Continued long-term release of Ca and P to build enamel layer
- Vantej, when comes into contact with saliva, water releases particles of calcium and phosphorus ions, protected by the glass particles.
- Saliva gets saturated with the ions needed for remineralization.1
- Demineralized lesions attract Ca & P ions.1
- Building new hydroxy appetite crystals to remineralise the defect from roots to the top.
1. Anora B, et al. NovaMin and Dentin Hypersensitivity – In Vitro Evidence of Ecacy. J Clin Dent 2010
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A recent study has shown that the use of ozone therapy while placing dental implants is effective in minimizing systemic inflammation, pain, and plaque deposition among dental implant recipients. The results of this study were published in the Indian Society for Dental Research.
Forty adult patients scheduled for implant placement were split into two groups: case group of twenty patients received ozone therapy, while the control group of twenty patients received normal saline and gel during the procedure. Inflammation and pain were monitored on the first- and the seventh-day, as well as at three- month intervals, by measuring C-reactive protein (CRP) levels and evaluating visual analogue scale (VAS) scores. At three months, soft tissue outcomes were assessed in terms of gingival index, plaque index, and pocket depth, while crestal bone loss was evaluated using radiographs.
Significantly higher mean CRP levels were observed in the control group in comparison to the case group on first and seventh day follow-ups (P value < 0.05). Additionally, mean VAS scores for pain were lower in the case group at all follow-ups, with statistical significance only on first day (P value = 0.061). The plaque index was significantly lower in the case group compared to the control group at the final follow-up (P value = 0.011). No significant difference was noted between the two groups in terms of crestal bone loss.
The above study demonstrated that the application of ozone therapy has proven to be successful in decreasing systemic inflammation, pain, and plaque deposition in patients who have undergone dental implant procedures.
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Evaluation of normal saline gel and ozone therapy effects on soft and hard tissue health in dental implant surgery
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Forty adult patients scheduled for implant placement were split into two groups: case group of twenty patients received ozone therapy, while the control group of twenty patients received normal saline and gel during the procedure. Inflammation and pain were monitored on the first- and the seventh-day, as well as at three- month intervals, by measuring C-reactive protein (CRP) levels and evaluating visual analogue scale (VAS) scores. At three months, soft tissue outcomes were assessed in terms of gingival index, plaque index, and pocket depth, while crestal bone loss was evaluated using radiographs.
Significantly higher mean CRP levels were observed in the control group in comparison to the case group on first and seventh day follow-ups (P value < 0.05). Additionally, mean VAS scores for pain were lower in the case group at all follow-ups, with statistical significance only on first day (P value = 0.061). The plaque index was significantly lower in the case group compared to the control group at the final follow-up (P value = 0.011). No significant difference was noted between the two groups in terms of crestal bone loss.
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Pain after root canal treatment with various apical finishing sizes
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In this study, fifty teeth belonging to twenty-five individuals were separated into two equal groups, with twenty-five teeth in each group using E3 Azure rotary files. Group A was expanded by two sizes in relation to the Initial Binding File (IBF), extending to 40#/0.04 for the distal canals and 35#/0.04 for the mesial canals. Group B, on the other hand, was expanded by three sizes larger than the IBF: 45#/0.04 for the distal canals and 40#/0.04 for mesial canals. Patients were asked to rate their pain levels on a modified VAS form and describe their pain intensity at twelve, twenty-four, and seventy-two hours, as well as after a week. VAS data were analyzed using Freidman's test, Nemenyi post hoc test for intragroup comparisons and signed-rank test for intergroup comparisons.
The outcomes revealed that irrespective of the timing of the measurement, an enlargement of the apical preparation was significantly linked to increased pain scores (p value < 0.001). In both groups, there was a significant decline in reported pain scores over time, with scores at twelve-and twenty-four hours post-treatment significantly higher than those at other intervals (p value < 0.001). Additionally, pain scores at three days post-treatment were significantly higher than those at one week (p value < 0.001).
Thus, it can be concluded that apical preparation size significantly influenced postoperative pain levels.
Pain after root canal treatment with various apical finishing sizes
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Assessment of postoperative pain following the use of dexamethasone intracanal rinse for irreversible pulpitis
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Sixty patients aged 18 to 50 years, who had been diagnosed with symptomatic irreversible pulpitis were specifically chosen based on set criteria. Root canal therapy (RCT) was initiated under rubber dam after obtaining informed consent. The treatment included a pulpectomy followed by canal preparation. Patients were divided into two groups: Group A (the experimental group) received dexamethasone (4 mg/mL in a 5-mL syringe) as a final rinse, and Group B (the control group) received saline as the final rinse. They were followed up after 1 week to determine the improvement of their pain. Following data collection, teeth were filled, and permanent restoration was placed. The Chi-square test was utilized for the analysis of the data.
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The above study demonstrated that dexamethasone has greater efficacy compared to saline in alleviating postoperative pain when utilized as the final intracanal rinse following root canal instrumentation.
Assessment of postoperative pain following the use of dexamethasone intracanal rinse for irreversible pulpitis
Assessment of postoperative pain following the use of dexamethasone intracanal rinse for irreversible pulpitis
A recent study has shown that dexamethasone is superior to saline in relieving postoperative pain when utilized as the final intracanal rinse after root canal instrumentation. This study's findings were published in the Journal of the College of Physicians and Surgeons Pakistan.
Sixty patients aged 18 to 50 years, who had been diagnosed with symptomatic irreversible pulpitis were specifically chosen based on set criteria. Root canal therapy (RCT) was initiated under rubber dam after obtaining informed consent. The treatment included a pulpectomy followed by canal preparation. Patients were divided into two groups: Group A (the experimental group) received dexamethasone (4 mg/mL in a 5-mL syringe) as a final rinse, and Group B (the control group) received saline as the final rinse. They were followed up after 1 week to determine the improvement of their pain. Following data collection, teeth were filled, and permanent restoration was placed. The Chi-square test was utilized for the analysis of the data.
Dexamethasone showed a significantly higher efficacy compared to saline as a final intracanal rinse, 86.67% and 20.0%, respectively (p value < 0.05), in alleviating postoperative pain in teeth diagnosed with symptomatic irreversible pulpitis.
The above study demonstrated that dexamethasone has greater efficacy compared to saline in alleviating postoperative pain when utilized as the final intracanal rinse following root canal instrumentation.
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Cannabidiol Found Effective as an Analgesic for Acute Dental Pain
This study evaluated the efficacy and safety of cannabidiol (CBD) as an analgesic for acute dental pain, a condition for which nonopioid treatments are limited. In a randomized, placebo-controlled clinical trial, 61 patients with moderate to severe toothache were assigned to one of three groups: CBD10 (10 mg/kg), CBD20 (20 mg/kg), or placebo. Participants received a single oral dose, and pain was assessed over 3 hours.
The primary outcome was pain reduction using a visual analog scale (VAS), while secondary outcomes included pain intensity, time to significant relief, maximum pain relief, bite force changes, psychoactive effects, mood alterations, and other adverse events.
Both CBD groups showed significant reductions in VAS pain scores compared to baseline and placebo, with a maximum median reduction of 73% at 180 minutes (P < 0.05). CBD20 demonstrated a faster onset of pain relief than CBD10 (15 vs. 30 minutes), with both groups achieving maximum relief at 180 minutes. The number needed to treat was 3.1 for CBD10 and 2.4 for CBD20. Bite force significantly increased in both CBD groups (P < 0.05) but not in the placebo group, with CBD20 showing significant changes compared to placebo at 90 and 180 minutes.
Adverse effects, including sedation, diarrhea, and abdominal pain, were more common in CBD groups (P < 0.05). This trial provides initial evidence that oral CBD is an effective and safe alternative analgesic for acute dental pain.
Cannabidiol Found Effective as an Analgesic for Acute Dental Pain
Cannabidiol Found Effective as an Analgesic for Acute Dental Pain
This study evaluated the efficacy and safety of cannabidiol (CBD) as an analgesic for acute dental pain, a condition for which nonopioid treatments are limited. In a randomized, placebo-controlled clinical trial, 61 patients with moderate to severe toothache were assigned to one of three groups: CBD10 (10 mg/kg), CBD20 (20 mg/kg), or placebo. Participants received a single oral dose, and pain was assessed over 3 hours.
The primary outcome was pain reduction using a visual analog scale (VAS), while secondary outcomes included pain intensity, time to significant relief, maximum pain relief, bite force changes, psychoactive effects, mood alterations, and other adverse events.
Both CBD groups showed significant reductions in VAS pain scores compared to baseline and placebo, with a maximum median reduction of 73% at 180 minutes (P < 0.05). CBD20 demonstrated a faster onset of pain relief than CBD10 (15 vs. 30 minutes), with both groups achieving maximum relief at 180 minutes. The number needed to treat was 3.1 for CBD10 and 2.4 for CBD20. Bite force significantly increased in both CBD groups (P < 0.05) but not in the placebo group, with CBD20 showing significant changes compared to placebo at 90 and 180 minutes.
Adverse effects, including sedation, diarrhea, and abdominal pain, were more common in CBD groups (P < 0.05). This trial provides initial evidence that oral CBD is an effective and safe alternative analgesic for acute dental pain.
The effect of various desensitizers on pulpal blood flow after full crown preparation using laser Doppler flowmetry
The effect of various desensitizers on pulpal blood flow after full crown preparation using laser Doppler flowmetry
In a recent study, similar levels of effectiveness were observed in treating dentine hypersensitivity and pulpal blood flow with Bifluoride 12, Teethmate, and Copal Varnish. This study’s findings were published in the journal Odontology.
18 patients with a total of 42 teeth suffering from dentine hypersensitivity after full crown preparations were randomly divided to receive treatment with Bifluoride 12, Teethmate, or Copal Varnish. The severity of dentine hypersensitivity was assessed using a Schiff air index (SAI) and visual analog scale (VAS). The assessment of pulpal blood flow involved the use of laser Doppler flowmetry (LDF), with the findings recorded in perfusion units (PU). Evaluations were conducted at the initial stage, after five minutes, after seven days, and after one month subsequent to the administration of desensitizing agents. Statistical analysis was carried out using Wilcoxon and two-way ANOVA tests (p value < 0.05).
The tested desensitizers did not show any significant difference in terms of VAS and PU values. VAS values significantly decreased at seven days and one month after the desensitizers were applied, compared to the baseline in all groups. Only the Copal Varnish group exhibited a notable difference in PU values at the five-minute and seven-day intervals post-desensitizer application (p value < 0.05). A statistically significant difference was found between different time points in relation to SAI scores in all groups (p value < 0.05).
Thus, it can be concluded that Bifluoride 12, Teethmate, and Copal Varnish demonstrated similar effectiveness in managing dentine hypersensitivity and pulpal blood flow. To fully evaluate their impact on pulpal status, it is important to conduct long-term clinical trials with larger sample sizes and histological studies.
The effect of various desensitizers on pulpal blood flow after full crown preparation using laser Doppler flowmetry
The effect of various desensitizers on pulpal blood flow after full crown preparation using laser Doppler flowmetry
In a recent study, similar levels of effectiveness were observed in treating dentine hypersensitivity and pulpal blood flow with Bifluoride 12, Teethmate, and Copal Varnish. This study’s findings were published in the journal Odontology.
18 patients with a total of 42 teeth suffering from dentine hypersensitivity after full crown preparations were randomly divided to receive treatment with Bifluoride 12, Teethmate, or Copal Varnish. The severity of dentine hypersensitivity was assessed using a Schiff air index (SAI) and visual analog scale (VAS). The assessment of pulpal blood flow involved the use of laser Doppler flowmetry (LDF), with the findings recorded in perfusion units (PU). Evaluations were conducted at the initial stage, after five minutes, after seven days, and after one month subsequent to the administration of desensitizing agents. Statistical analysis was carried out using Wilcoxon and two-way ANOVA tests (p value < 0.05).
The tested desensitizers did not show any significant difference in terms of VAS and PU values. VAS values significantly decreased at seven days and one month after the desensitizers were applied, compared to the baseline in all groups. Only the Copal Varnish group exhibited a notable difference in PU values at the five-minute and seven-day intervals post-desensitizer application (p value < 0.05). A statistically significant difference was found between different time points in relation to SAI scores in all groups (p value < 0.05).
Thus, it can be concluded that Bifluoride 12, Teethmate, and Copal Varnish demonstrated similar effectiveness in managing dentine hypersensitivity and pulpal blood flow. To fully evaluate their impact on pulpal status, it is important to conduct long-term clinical trials with larger sample sizes and histological studies.
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