Dentinal Hypersensitivity
Dentinal Hypersensitivity (DH) is pain from exposed dentin caused by thermal, tactile or osmotic stimuli. The most accepted cause of DH is Brannstrom's hydrodynamic theory, which states that pain is due to abrupt uid movement within dentinal tubules in response to thermal, osmotic, mechanical, and evaporative stimuli.
Why Vantej Aqua?
- 1.4% Potassium oxalate is the active ingredient
- Rapid action that beats sensitivity
- 100% dental occlusion providing long lasting relief
- 3.6X reduction in pain
What is 1.4% Potassium Oxalate?
1.4% Potassium oxalate is recognised for its efficacy as a desensitising agent and is often described as having an occlusive impact on dentin, however several authors have indicated a neurological effect as well.
It has been described as having two unique e ects on the reduction of dentinal hypersensitivity:
- An immediate effect
- Tubule occlusion by calcium oxalate crystals making it acid resistant
Mode of Action
- Upon rinsing the mouth, soluble potassium oxalate salts react with calcium ions from saliva.
- This reaction forms insoluble calcium oxalate crystals within the dentinal tubules.
- These deep intratubular crystals maintain tubular occlusion due to their low solubility, even under acidic conditions.
- This process helps relieve pain associated with dentin hypersensitivity.
1. Tran V, et al. A comparison of dentin tubule occlusion properties of dipotassium oxalate against potassium nitrate: An in vitro study. J Contemp Dent Pract. 2020;21 (2):119-123.
2. Manohar B, et al. Potassium oxalate-based mouth rinse for rapid relief in dentinal hypersensitivity. J Oral Res Rev. 2024;16(1):72-79.
3. Grover V, et al. ISP Good Clinical Practice Recommendations for the management of dentin hypersensitivity. J Indian Soc Periodontol. 2022;26(4):307-333.
Advantages
- Demonstrates clinical benefit over the other desensitizing products because of significant intratubular subsurface calcium oxalate crystal deposition
- Provides Rapid Relief from DH within 6 rinses
- Safe and efficacious
How to Use?
- Take 10ml of undiluted desensitizing solution and rinse it for 60secs twice daily.
- Spit out the solution after the rinse, do not swallow.
- Use vantej aqua, twice a day, for 5 days and continue with vantej for minimum 2 months for optimal management of DHS1
1. Kakkar A, et al. Knowledge, attitude, and practice of dental practitioners regarding desensitizing agents for the management of dentinal hypersensitivity - A real-world, cross-sectional survey. International Journal Dental and Medical Sciences Research. 2022;4(6): 442-453.
Safety Advice
- A history of sensitivity or allergies to oxalates
Impact of glutamine oral care in decreasing oral mucositis and enhancing oral health following neurosurgery
Impact of glutamine oral care in decreasing oral mucositis and enhancing oral health following neurosurgery
According to a recent study, the utilization of 5% glutamine for oral care has been linked to a decreased occurrence of oral disorders and pneumonia, as well as a notable decrease in oral flora following neurosurgery. This study’s results were published in the journal, Medical science monitor.
In this parallel, double-blind, randomized trial, three hundred patients meeting the inclusion criteria were randomly allocated into three groups. The control group (n=100) received routine oral care with saline, the experimental group (n=100) received oral care with 5% glutamine, and a compound chlorhexidine group (n=100) was used as a positive control. Data on dryness, local debris, halitosis, oral mucositis disorders, oral mucositis, and oral flora types were collected and determined within all groups.
At the end of the study, the glutamine oral care group exhibited a significant decrease in the incidence of local debris, halitosis, oral mucositis, dryness, and other oral mucositis disorders when compared to the control group. Additionally, there was a notable reduction in oral flora types in both the glutamine and chlorhexidine groups.
The above study demonstrated that the use of 5% glutamine in oral care is associated with a lower occurrence of oral disorders and pneumonia, as well as a significant reduction in oral flora after undergoing neurosurgery.
Impact of glutamine oral care in decreasing oral mucositis and enhancing oral health following neurosurgery
Impact of glutamine oral care in decreasing oral mucositis and enhancing oral health following neurosurgery
According to a recent study, the utilization of 5% glutamine for oral care has been linked to a decreased occurrence of oral disorders and pneumonia, as well as a notable decrease in oral flora following neurosurgery. This study’s results were published in the journal, Medical science monitor.
In this parallel, double-blind, randomized trial, three hundred patients meeting the inclusion criteria were randomly allocated into three groups. The control group (n=100) received routine oral care with saline, the experimental group (n=100) received oral care with 5% glutamine, and a compound chlorhexidine group (n=100) was used as a positive control. Data on dryness, local debris, halitosis, oral mucositis disorders, oral mucositis, and oral flora types were collected and determined within all groups.
At the end of the study, the glutamine oral care group exhibited a significant decrease in the incidence of local debris, halitosis, oral mucositis, dryness, and other oral mucositis disorders when compared to the control group. Additionally, there was a notable reduction in oral flora types in both the glutamine and chlorhexidine groups.
The above study demonstrated that the use of 5% glutamine in oral care is associated with a lower occurrence of oral disorders and pneumonia, as well as a significant reduction in oral flora after undergoing neurosurgery.
Analgesic onset of FA-acetaminophen in a postoperative dental impaction pain model
Analgesic onset of FA-acetaminophen in a postoperative dental impaction pain model
A recent study has shown that fast-acting acetaminophen (FA-acetaminophen) had a quicker onset of action than both commercial acetaminophen caplets (ES-acetaminophen) and commercial ibuprofen liquid-filled gelatin capsules (LG-Ibuprofen). This study findings were published in the journal, Current Medical Research and Opinion.
Two single-center, randomized, inpatient, placebo-controlled, double-blind design clinical trials were carried out utilizing the postoperative dental impaction pain model. Study 1 included 240 subjects, whereas study 2 had 420 subjects. The individuals involved in this study were between the ages of 17 and 50 and were suffering from moderate to severe pain after undergoing the surgical extraction of a minimum of three impacted third molars. The two studies evaluated four different treatment groups: 1,000 mg of FA-acetaminophen, 400 mg of LG-ibuprofen, 1,000 mg of ES-acetaminophen, and a placebo. The double-stopwatch method was used to determine the times to confirm perceptible pain relief (TCPR) and meaningful pain relief (TMPR). Pain intensity and relief were assessed using a 0-10 numerical rating scale for a duration of 6 hours after administering the drug.
The efficacy results demonstrated that all active treatments were statistically superior to the placebo. Within study 1, TCPR was significantly shorter for FA-acetaminophen in comparison to ES-acetaminophen and LG-ibuprofen. Additionally, FA-acetaminophen 1,000 mg showed a significantly shorter TMPR compared to LG-ibuprofen. In both studies 1 and 2, at the 15-minute mark post-administration of the study drug, PID and PAR scores were higher for FA-acetaminophen than LG-ibuprofen.
It can be concluded that FA-acetaminophen demonstrated a faster onset of action in comparison to both ES-acetaminophen and LG-Ibuprofen.
Analgesic onset of FA-acetaminophen in a postoperative dental impaction pain model
Analgesic onset of FA-acetaminophen in a postoperative dental impaction pain model
A recent study has shown that fast-acting acetaminophen (FA-acetaminophen) had a quicker onset of action than both commercial acetaminophen caplets (ES-acetaminophen) and commercial ibuprofen liquid-filled gelatin capsules (LG-Ibuprofen). This study findings were published in the journal, Current Medical Research and Opinion.
Two single-center, randomized, inpatient, placebo-controlled, double-blind design clinical trials were carried out utilizing the postoperative dental impaction pain model. Study 1 included 240 subjects, whereas study 2 had 420 subjects. The individuals involved in this study were between the ages of 17 and 50 and were suffering from moderate to severe pain after undergoing the surgical extraction of a minimum of three impacted third molars. The two studies evaluated four different treatment groups: 1,000 mg of FA-acetaminophen, 400 mg of LG-ibuprofen, 1,000 mg of ES-acetaminophen, and a placebo. The double-stopwatch method was used to determine the times to confirm perceptible pain relief (TCPR) and meaningful pain relief (TMPR). Pain intensity and relief were assessed using a 0-10 numerical rating scale for a duration of 6 hours after administering the drug.
The efficacy results demonstrated that all active treatments were statistically superior to the placebo. Within study 1, TCPR was significantly shorter for FA-acetaminophen in comparison to ES-acetaminophen and LG-ibuprofen. Additionally, FA-acetaminophen 1,000 mg showed a significantly shorter TMPR compared to LG-ibuprofen. In both studies 1 and 2, at the 15-minute mark post-administration of the study drug, PID and PAR scores were higher for FA-acetaminophen than LG-ibuprofen.
It can be concluded that FA-acetaminophen demonstrated a faster onset of action in comparison to both ES-acetaminophen and LG-Ibuprofen.
B-Gn-F plane proves as the most accurate best mandibular midsagittal plane to segment and identify mandible anatomical landmarks
B-Gn-F plane proves as the most accurate best mandibular midsagittal plane to segment and identify mandible anatomical landmarks
According to a recent study, deep learning can segment and identify mandibular midline landmarks with the help of the best mandibular midsagittal plane (MMSP), which is B-Gn-F. This study was published in the European Journal of Medical Research.
This study included 400 participants who were randomly assigned into a training group (n=360) and a validation group (n=40), along with a test group (n=50) comprising normal individuals. PoseNet identified 27 anatomic landmarks from the mandible images from cone-beam computed tomography (CBCT) using the PointRend deep learning mechanism. For the test group, three-dimensional (3D) coordinates were obtained for five central landmarks and two pairs of side landmarks. Using the template mapping technique, every 35 combinations of 3 midline landmarks were screened. For each of the 35 mirror planes, the asymmetry index (AI) was calculated. The top 4 planes having the smallest AIs were compared through volume difference, similarity index, and distance in order to find the plane with the least errors.
At the end of the study, it was found that in 10 ± 1.5 seconds, the mandible was automatically segmented with a 0.98 Dice similarity coefficient. Among the 27 landmarks, the average localization error was 1.04 ± 0.28 mm. The plane created by B (supramentale), Gn (gnathion), and F (mandibular foramen) should be used by MMSP. The average AI grade observed was 1.6. No significant difference was seen in volume or distance, although the similarity index was significantly different.
From the above results, it can be concluded that deep learning may segment and identify mandibular midline landmarks with the help of the best mandibular midsagittal plane (MMSP), which is B-Gn-F.
B-Gn-F plane proves as the most accurate best mandibular midsagittal plane to segment and identify mandible anatomical landmarks
B-Gn-F plane proves as the most accurate best mandibular midsagittal plane to segment and identify mandible anatomical landmarks
According to a recent study, deep learning can segment and identify mandibular midline landmarks with the help of the best mandibular midsagittal plane (MMSP), which is B-Gn-F. This study was published in the European Journal of Medical Research.
This study included 400 participants who were randomly assigned into a training group (n=360) and a validation group (n=40), along with a test group (n=50) comprising normal individuals. PoseNet identified 27 anatomic landmarks from the mandible images from cone-beam computed tomography (CBCT) using the PointRend deep learning mechanism. For the test group, three-dimensional (3D) coordinates were obtained for five central landmarks and two pairs of side landmarks. Using the template mapping technique, every 35 combinations of 3 midline landmarks were screened. For each of the 35 mirror planes, the asymmetry index (AI) was calculated. The top 4 planes having the smallest AIs were compared through volume difference, similarity index, and distance in order to find the plane with the least errors.
At the end of the study, it was found that in 10 ± 1.5 seconds, the mandible was automatically segmented with a 0.98 Dice similarity coefficient. Among the 27 landmarks, the average localization error was 1.04 ± 0.28 mm. The plane created by B (supramentale), Gn (gnathion), and F (mandibular foramen) should be used by MMSP. The average AI grade observed was 1.6. No significant difference was seen in volume or distance, although the similarity index was significantly different.
From the above results, it can be concluded that deep learning may segment and identify mandibular midline landmarks with the help of the best mandibular midsagittal plane (MMSP), which is B-Gn-F.
Evaluation and comparison of the effectiveness of low-level laser therapy and low-intensity pulsed ultrasound in reducing orthodontic pain
Evaluation and comparison of the effectiveness of low-level laser therapy and low-intensity pulsed ultrasound in reducing orthodontic pain
According to a recent study, low-level laser therapy (LLLT) and low-intensity pulsed ultrasound (LIPUS) effectively reduced separation pain when applied in multiple doses during orthodontic treatment. The results of this study were published in the journal, BMC Oral Health.
150 patients were randomly assigned to three groups in this single-blind, randomized controlled trial: the LLLT group, the LIPUS group, and the control group. The first dose of the laser or ultrasound was applied 5 min from the separators' placement, second dose was given after 24 h, and the last dose was administered on both maxillary and mandibular first molars after 48 h. The patients were exposed to the laser for 20 s, using an 810-nm aluminum-gallium-arsenide (AlGaAs) diode laser on continuous mode. For 20 minutes, 1.6 MHz ultrasonic toothbrush treatment was applied (5 minutes for each first molar). The control group was administered the separator without any other intervention. Pain intensity was assessed at several time intervals during the first four days post the separator’s placement, using a Visual Analog Scale (VAS 100 mm).
It was found after assessing 145 patients that a significant difference in pain perception was observed among the three groups after 5 min. Pain level reached its maximum intensity after 24 h. All the assessment time points showed a statistically significant decrease in pain scores for both the laser and the ultrasound groups when compared to the control group. Moreover, the laser and ultrasound group showed no difference between them in terms of reducing the pain scores.
Hence, it can be concluded that LLLT and the LIPUS may effectively reduce the separation pain experienced during orthodontic treatment after the application of multiple doses, without any difference between them.
Evaluation and comparison of the effectiveness of low-level laser therapy and low-intensity pulsed ultrasound in reducing orthodontic pain
Evaluation and comparison of the effectiveness of low-level laser therapy and low-intensity pulsed ultrasound in reducing orthodontic pain
According to a recent study, low-level laser therapy (LLLT) and low-intensity pulsed ultrasound (LIPUS) effectively reduced separation pain when applied in multiple doses during orthodontic treatment. The results of this study were published in the journal, BMC Oral Health.
150 patients were randomly assigned to three groups in this single-blind, randomized controlled trial: the LLLT group, the LIPUS group, and the control group. The first dose of the laser or ultrasound was applied 5 min from the separators' placement, second dose was given after 24 h, and the last dose was administered on both maxillary and mandibular first molars after 48 h. The patients were exposed to the laser for 20 s, using an 810-nm aluminum-gallium-arsenide (AlGaAs) diode laser on continuous mode. For 20 minutes, 1.6 MHz ultrasonic toothbrush treatment was applied (5 minutes for each first molar). The control group was administered the separator without any other intervention. Pain intensity was assessed at several time intervals during the first four days post the separator’s placement, using a Visual Analog Scale (VAS 100 mm).
It was found after assessing 145 patients that a significant difference in pain perception was observed among the three groups after 5 min. Pain level reached its maximum intensity after 24 h. All the assessment time points showed a statistically significant decrease in pain scores for both the laser and the ultrasound groups when compared to the control group. Moreover, the laser and ultrasound group showed no difference between them in terms of reducing the pain scores.
Hence, it can be concluded that LLLT and the LIPUS may effectively reduce the separation pain experienced during orthodontic treatment after the application of multiple doses, without any difference between them.
Impact of silver diamine fluoride and nano silver fluoride on the oral health-related quality of life of children
Impact of silver diamine fluoride and nano silver fluoride on the oral health-related quality of life of children
According to a recent study, Silver diamine fluoride (SDF) and Nano Silver Fluoride (NSF) after 6 months exhibited significant enhancements in children's Oral Health-Related Quality of Life (OHRQoL). It was observed that NSF had a significantly superior impact on OHRQoL compared to SDF. This study’s results were published in the Journal of dentistry.
This study involved 360 children under the age of 4, each having at least one active lesion with an International Caries Detection and Assessment System (ICDAS) score of ≥3. They were randomly divided into two groups: one receiving NSF at the beginning, and the other receiving SDF at the start and after 6 months. The Oral Health-Related Quality of Life (OHRQoL) was assessed using the Arabic version of the Early Childhood Oral Health Impact Scale (A-ECOHIS). Additionally, group comparisons were made using the chi-square test, and the impact of the intervention on OHRQoL was analyzed through multiple linear regression.
In the bivariate analysis and regression analysis (B= -5.02) with confounder adjustments, it was observed that NSF exhibited significantly lower A-ECOHIS scores compared to SDF after a period of 6 months. Both groups showed significant decreases in the A-ECOHIS domain and total scores, except for the social interaction domain in the SDF group.
The above study demonstrated that after a 6-month period, both NSF and SDF led to a significant improvement in children's OHRQoL. However, NSF had a notably greater impact on OHRQoL compared to SDF.
Impact of silver diamine fluoride and nano silver fluoride on the oral health-related quality of life of children
Impact of silver diamine fluoride and nano silver fluoride on the oral health-related quality of life of children
According to a recent study, Silver diamine fluoride (SDF) and Nano Silver Fluoride (NSF) after 6 months exhibited significant enhancements in children's Oral Health-Related Quality of Life (OHRQoL). It was observed that NSF had a significantly superior impact on OHRQoL compared to SDF. This study’s results were published in the Journal of dentistry.
This study involved 360 children under the age of 4, each having at least one active lesion with an International Caries Detection and Assessment System (ICDAS) score of ≥3. They were randomly divided into two groups: one receiving NSF at the beginning, and the other receiving SDF at the start and after 6 months. The Oral Health-Related Quality of Life (OHRQoL) was assessed using the Arabic version of the Early Childhood Oral Health Impact Scale (A-ECOHIS). Additionally, group comparisons were made using the chi-square test, and the impact of the intervention on OHRQoL was analyzed through multiple linear regression.
In the bivariate analysis and regression analysis (B= -5.02) with confounder adjustments, it was observed that NSF exhibited significantly lower A-ECOHIS scores compared to SDF after a period of 6 months. Both groups showed significant decreases in the A-ECOHIS domain and total scores, except for the social interaction domain in the SDF group.
The above study demonstrated that after a 6-month period, both NSF and SDF led to a significant improvement in children's OHRQoL. However, NSF had a notably greater impact on OHRQoL compared to SDF.
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