Featured Article Family Medicine Allergy & Clinical Immunology
2 Min

The efficacy and safety of intratonsillar immunotherapy when used for allergic rhinitis

A recent study demonstrated that the administration of intratonsillar injection containing house dust mite (HDM) extract proved to be both safe and efficacious for individuals suffering from allergic rhinitis (AR). This study's findings were published in the journal, Annals of Allergy, Asthma & Immunology.

In this randomized clinical trial, 80 patients suffering from house dust mite-induced allergic rhinitis were included. The patients were divided into two groups: one group received 6 intratonsillar injections of HDM extract, and the other group received a placebo. Total nasal symptom score (TNSS), visual analogue scale of nasal symptoms, combined symptom and medication score, quality of life questionnaire, and serum allergen-specific IgG4 levels were all evaluated at the baseline and at three months, six months, and twelve months following the completion of the treatment. Both the intent-to-treat and per-protocol sets were analyzed in this study.

At three months following a 3-month 6-injection intratonsillar immunotherapy, patients with AR showed significant improvements in the primary end points TNSS and ΔTNSS compared to those who received placebo treatment in both intent-to-treat and PPS. Additionally, significant enhancements were observed in the combined symptom and medication score, visual analogue scale results, and mini rhinoconjunctivitis quality of life questionnaire outcomes at three months post-treatment in PPS. Additionally, the active group displayed a significantly higher increase in serum Der p IgG4 levels at three, six, and twelve months post-treatment completion compared to the placebo group.

Thus, it can be concluded that the intratonsillar injection with HDM extract is safe and efficacious in AR patients.

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The efficacy and safety of intratonsillar immunotherapy when used for allergic rhinitis

A recent study demonstrated that the administration of intratonsillar injection containing house dust mite (HDM) extract proved to be both safe and efficacious for individuals suffering from allergic rhinitis (AR). This study's findings were published in the journal, Annals of Allergy, Asthma & Immunology.

In this randomized clinical trial, 80 patients suffering from house dust mite-induced allergic rhinitis were included. The patients were divided into two groups: one group received 6 intratonsillar injections of HDM extract, and the other group received a placebo. Total nasal symptom score (TNSS), visual analogue scale of nasal symptoms, combined symptom and medication score, quality of life questionnaire, and serum allergen-specific IgG4 levels were all evaluated at the baseline and at three months, six months, and twelve months following the completion of the treatment. Both the intent-to-treat and per-protocol sets were analyzed in this study.

At three months following a 3-month 6-injection intratonsillar immunotherapy, patients with AR showed significant improvements in the primary end points TNSS and ΔTNSS compared to those who received placebo treatment in both intent-to-treat and PPS. Additionally, significant enhancements were observed in the combined symptom and medication score, visual analogue scale results, and mini rhinoconjunctivitis quality of life questionnaire outcomes at three months post-treatment in PPS. Additionally, the active group displayed a significantly higher increase in serum Der p IgG4 levels at three, six, and twelve months post-treatment completion compared to the placebo group.

Thus, it can be concluded that the intratonsillar injection with HDM extract is safe and efficacious in AR patients.

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Residential Greenness
2 Min Read
Allergic Rhinitis…

Residential Greenness Linked to Reduced Risk of Allergic Rhinitis in Adults

Air pollution, Allergic rhinitis, Greenness, Mediation effect, UK biobank

Residential Greenness Linked to Reduced Risk of Allergic Rhinitis in Adults

A prospective study utilizing UK Biobank data has revealed that increased residential greenness is associated with a reduced incidence of allergic rhinitis in adults. 

The analysis, which tracked 281,699 participants over a median follow-up of 14 years, identified 3,260 new cases of allergic rhinitis.

The results showed that a 10% increase in greenness within a 300-meter buffer around residences was linked to a 2.5% decrease in the risk of developing allergic rhinitis. The relationship exhibited a non-linear, L-shaped dose-response pattern, with a threshold at 54.9% greenness above which no further reduction in risk was observed.

Additionally, the study found that ambient air pollutants, specifically PM10, partially mediated this association, accounting for 26.9% of the relationship between residential greenness and allergic rhinitis risk. This suggests that greenness may help reduce exposure to air pollution, thereby mitigating the risk of allergic rhinitis.

These findings highlight the potential benefits of residential greenness in urban planning and public health initiatives, suggesting that greenness could be an effective strategy for reducing allergic rhinitis, particularly in areas impacted by air pollution.
 

21 Feb 2025
Residential Greenness

Air pollution, Allergic rhinitis, Greenness, Mediation effect, UK biobank

Residential Greenness Linked to Reduced Risk of Allergic Rhinitis in Adults

A prospective study utilizing UK Biobank data has revealed that increased residential greenness is associated with a reduced incidence of allergic rhinitis in adults. 

The analysis, which tracked 281,699 participants over a median follow-up of 14 years, identified 3,260 new cases of allergic rhinitis.

The results showed that a 10% increase in greenness within a 300-meter buffer around residences was linked to a 2.5% decrease in the risk of developing allergic rhinitis. The relationship exhibited a non-linear, L-shaped dose-response pattern, with a threshold at 54.9% greenness above which no further reduction in risk was observed.

Additionally, the study found that ambient air pollutants, specifically PM10, partially mediated this association, accounting for 26.9% of the relationship between residential greenness and allergic rhinitis risk. This suggests that greenness may help reduce exposure to air pollution, thereby mitigating the risk of allergic rhinitis.

These findings highlight the potential benefits of residential greenness in urban planning and public health initiatives, suggesting that greenness could be an effective strategy for reducing allergic rhinitis, particularly in areas impacted by air pollution.
 

Residential Greenness
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Residential Greenness
Allergic Rhinitis…

Residential Greenness Linked to Reduced Risk of Allergic Rhinitis in Adults

Air pollution, Allergic rhinitis, Greenness, Mediation effect, UK biobank

Residential Greenness Linked to Reduced Risk of Allergic Rhinitis in Adults

A prospective study utilizing UK Biobank data has revealed that increased residential greenness is associated with a reduced incidence of allergic rhinitis in adults. 

The analysis, which tracked 281,699 participants over a median follow-up of 14 years, identified 3,260 new cases of allergic rhinitis.

The results showed that a 10% increase in greenness within a 300-meter buffer around residences was linked to a 2.5% decrease in the risk of developing allergic rhinitis. The relationship exhibited a non-linear, L-shaped dose-response pattern, with a threshold at 54.9% greenness above which no further reduction in risk was observed.

Additionally, the study found that ambient air pollutants, specifically PM10, partially mediated this association, accounting for 26.9% of the relationship between residential greenness and allergic rhinitis risk. This suggests that greenness may help reduce exposure to air pollution, thereby mitigating the risk of allergic rhinitis.

These findings highlight the potential benefits of residential greenness in urban planning and public health initiatives, suggesting that greenness could be an effective strategy for reducing allergic rhinitis, particularly in areas impacted by air pollution.
 

21 Feb 2025
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Anemia Treatment
2 Min Read
Renal anemia

Early Anemia Treatment Linked to Better Cardiovascular Outcomes in Nondialysis-Dependent CKD

Anemia in chronic kidney disease, Cardiovascular outcomes, Erythropoiesis-stimulating agent, Nationwide databases, Nondialysis-dependent chronic kidney disease

Early Anemia Treatment Linked to Better Cardiovascular Outcomes in Nondialysis-Dependent CKD

A recent retrospective cohort study explored the impact of early versus delayed anemia treatment on renal and cardiovascular outcomes in patients with nondialysis-dependent (NDD) chronic kidney disease (CKD). 
 

Using data from two Japanese databases (Medical Data Vision Co. Ltd. and Real World Data Co. Ltd), the study analyzed patients who were initiated on long-acting erythropoiesis-stimulating agents (ESAs). 
 

Patients were classified into early (hemoglobin levels ≥9.0 g/dl) and delayed (<9.0 g/dl) treatment groups.
 

The primary outcome measured was a renal composite, including renal replacement therapy, significant reductions in estimated glomerular filtration rate (eGFR), and all-cause mortality, while secondary outcomes focused on cardiovascular events such as ischemic heart disease, stroke, heart failure, and cardiovascular death. 
 

After propensity score matching, 2,736 patients (1,472 from MDV and 1,264 from RWD) were included in the analysis.
 

The study found that delayed treatment was not associated with an increased risk of renal events. However, delayed treatment significantly increased the risk of cardiovascular outcomes, including heart failure and all-cause mortality. 
 

Specifically, delayed anemia treatment was linked to a higher risk of cardiovascular events (HR: 1.47, 95% CI: 1.16-1.84) and all-cause mortality (HR: 1.83, 95% CI: 1.32-2.54).
 

These findings highlight the importance of initiating anemia treatment early in NDD-CKD patients, before hemoglobin levels drop below 9.0 g/dl, to mitigate the risks of cardiovascular events and mortality.

21 Feb 2025
Anemia Treatment

Anemia in chronic kidney disease, Cardiovascular outcomes, Erythropoiesis-stimulating agent, Nationwide databases, Nondialysis-dependent chronic kidney disease

Early Anemia Treatment Linked to Better Cardiovascular Outcomes in Nondialysis-Dependent CKD

A recent retrospective cohort study explored the impact of early versus delayed anemia treatment on renal and cardiovascular outcomes in patients with nondialysis-dependent (NDD) chronic kidney disease (CKD). 
 

Using data from two Japanese databases (Medical Data Vision Co. Ltd. and Real World Data Co. Ltd), the study analyzed patients who were initiated on long-acting erythropoiesis-stimulating agents (ESAs). 
 

Patients were classified into early (hemoglobin levels ≥9.0 g/dl) and delayed (<9.0 g/dl) treatment groups.
 

The primary outcome measured was a renal composite, including renal replacement therapy, significant reductions in estimated glomerular filtration rate (eGFR), and all-cause mortality, while secondary outcomes focused on cardiovascular events such as ischemic heart disease, stroke, heart failure, and cardiovascular death. 
 

After propensity score matching, 2,736 patients (1,472 from MDV and 1,264 from RWD) were included in the analysis.
 

The study found that delayed treatment was not associated with an increased risk of renal events. However, delayed treatment significantly increased the risk of cardiovascular outcomes, including heart failure and all-cause mortality. 
 

Specifically, delayed anemia treatment was linked to a higher risk of cardiovascular events (HR: 1.47, 95% CI: 1.16-1.84) and all-cause mortality (HR: 1.83, 95% CI: 1.32-2.54).
 

These findings highlight the importance of initiating anemia treatment early in NDD-CKD patients, before hemoglobin levels drop below 9.0 g/dl, to mitigate the risks of cardiovascular events and mortality.

Anemia Treatment
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Anemia Treatment
Renal anemia

Early Anemia Treatment Linked to Better Cardiovascular Outcomes in Nondialysis-Dependent CKD

Anemia in chronic kidney disease, Cardiovascular outcomes, Erythropoiesis-stimulating agent, Nationwide databases, Nondialysis-dependent chronic kidney disease

Early Anemia Treatment Linked to Better Cardiovascular Outcomes in Nondialysis-Dependent CKD

A recent retrospective cohort study explored the impact of early versus delayed anemia treatment on renal and cardiovascular outcomes in patients with nondialysis-dependent (NDD) chronic kidney disease (CKD). 
 

Using data from two Japanese databases (Medical Data Vision Co. Ltd. and Real World Data Co. Ltd), the study analyzed patients who were initiated on long-acting erythropoiesis-stimulating agents (ESAs). 
 

Patients were classified into early (hemoglobin levels ≥9.0 g/dl) and delayed (<9.0 g/dl) treatment groups.
 

The primary outcome measured was a renal composite, including renal replacement therapy, significant reductions in estimated glomerular filtration rate (eGFR), and all-cause mortality, while secondary outcomes focused on cardiovascular events such as ischemic heart disease, stroke, heart failure, and cardiovascular death. 
 

After propensity score matching, 2,736 patients (1,472 from MDV and 1,264 from RWD) were included in the analysis.
 

The study found that delayed treatment was not associated with an increased risk of renal events. However, delayed treatment significantly increased the risk of cardiovascular outcomes, including heart failure and all-cause mortality. 
 

Specifically, delayed anemia treatment was linked to a higher risk of cardiovascular events (HR: 1.47, 95% CI: 1.16-1.84) and all-cause mortality (HR: 1.83, 95% CI: 1.32-2.54).
 

These findings highlight the importance of initiating anemia treatment early in NDD-CKD patients, before hemoglobin levels drop below 9.0 g/dl, to mitigate the risks of cardiovascular events and mortality.

21 Feb 2025
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Improve cough strength
2 Min Read
Cough

Inspiratory Muscle Training Improves Cough Strength in Frail Older Adults

Cough peak flow, Cough strength, Frail older people, Inspiratory muscle training, Rehabilitation.

Inspiratory Muscle Training Improves Cough Strength in Frail Older Adults

A recent randomized controlled trial has shown that inspiratory muscle training (IMT) significantly enhances cough strength in older adults with frailty, suggesting its potential as a targeted intervention for this vulnerable population.

The study involved 60 frail older adults, with 52 completing the trial. Participants were randomly assigned to either an IMT group, which performed inspiratory muscle exercises alongside general exercise training, or a control group that engaged in general exercise training alone. 

IMT participants used a threshold device set at 30% of their maximum inspiratory pressure, performing 30 breaths twice daily over eight weeks.

The primary outcome, cough peak flow (CPF), demonstrated notable improvement in the IMT group, with an average increase of 28.7 ± 44.4 L/min compared to a decrease of -7.4 ± 26.6 L/min in the control group. The mean difference between groups was 36.3 L/min (95% CI: 16.7–55.9), with a large effect size of 0.99.

These findings indicate that IMT is a practical and effective approach to strengthening respiratory muscles, leading to improved cough function in frail older adults. Enhanced cough strength can play a critical role in reducing the risk of complications such as aspiration and respiratory infections, offering a valuable addition to care strategies for this demographic.
 

20 Feb 2025
Improve cough strength

Cough peak flow, Cough strength, Frail older people, Inspiratory muscle training, Rehabilitation.

Inspiratory Muscle Training Improves Cough Strength in Frail Older Adults

A recent randomized controlled trial has shown that inspiratory muscle training (IMT) significantly enhances cough strength in older adults with frailty, suggesting its potential as a targeted intervention for this vulnerable population.

The study involved 60 frail older adults, with 52 completing the trial. Participants were randomly assigned to either an IMT group, which performed inspiratory muscle exercises alongside general exercise training, or a control group that engaged in general exercise training alone. 

IMT participants used a threshold device set at 30% of their maximum inspiratory pressure, performing 30 breaths twice daily over eight weeks.

The primary outcome, cough peak flow (CPF), demonstrated notable improvement in the IMT group, with an average increase of 28.7 ± 44.4 L/min compared to a decrease of -7.4 ± 26.6 L/min in the control group. The mean difference between groups was 36.3 L/min (95% CI: 16.7–55.9), with a large effect size of 0.99.

These findings indicate that IMT is a practical and effective approach to strengthening respiratory muscles, leading to improved cough function in frail older adults. Enhanced cough strength can play a critical role in reducing the risk of complications such as aspiration and respiratory infections, offering a valuable addition to care strategies for this demographic.
 

Improve cough strength
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Improve cough strength
Cough

Inspiratory Muscle Training Improves Cough Strength in Frail Older Adults

Cough peak flow, Cough strength, Frail older people, Inspiratory muscle training, Rehabilitation.

Inspiratory Muscle Training Improves Cough Strength in Frail Older Adults

A recent randomized controlled trial has shown that inspiratory muscle training (IMT) significantly enhances cough strength in older adults with frailty, suggesting its potential as a targeted intervention for this vulnerable population.

The study involved 60 frail older adults, with 52 completing the trial. Participants were randomly assigned to either an IMT group, which performed inspiratory muscle exercises alongside general exercise training, or a control group that engaged in general exercise training alone. 

IMT participants used a threshold device set at 30% of their maximum inspiratory pressure, performing 30 breaths twice daily over eight weeks.

The primary outcome, cough peak flow (CPF), demonstrated notable improvement in the IMT group, with an average increase of 28.7 ± 44.4 L/min compared to a decrease of -7.4 ± 26.6 L/min in the control group. The mean difference between groups was 36.3 L/min (95% CI: 16.7–55.9), with a large effect size of 0.99.

These findings indicate that IMT is a practical and effective approach to strengthening respiratory muscles, leading to improved cough function in frail older adults. Enhanced cough strength can play a critical role in reducing the risk of complications such as aspiration and respiratory infections, offering a valuable addition to care strategies for this demographic.
 

20 Feb 2025
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LUTS due to BPH
2 Min Read
LUTS due to BPH…

Combination Therapy with Tadalafil and Tamsulosin Enhances LUTS Outcomes but Increases Side Effects

Medical news, Docvidya, Tadalafil, Tamsulosin, Monotherapy, Lower urinary tract symptoms, Benign prostatic hyperplasia, Erectile dysfunction

Combination Therapy with Tadalafil and Tamsulosin Enhances LUTS Outcomes but Increases Side Effects

A meta-analysis of 12 randomized controlled trials involving 1,531 patients has demonstrated that combination therapy with tadalafil and tamsulosin is more effective than monotherapy for managing lower urinary tract symptoms (LUTS) caused by benign prostatic hyperplasia (BPH), with or without erectile dysfunction (ED). However, this combined approach also leads to higher rates of adverse effects.

The analysis revealed significant improvements in the total International Prostate Symptom Score (IPSS), maximum urinary flow rate (Qmax), and quality of life (QoL) for patients receiving combination therapy compared to monotherapy. 

Specifically, the combined treatment enhanced IPSS voiding scores and reduced postvoid residual urine (PVR) more effectively than tamsulosin alone, although PVR outcomes were similar to tadalafil monotherapy.

In terms of erectile function, measured by the International Index of Erectile Function (IIEF), the combined therapy outperformed tamsulosin but did not show additional benefits over tadalafil alone. Importantly, while no serious adverse events were reported, the incidence of minor side effects was higher in the combination therapy group than in the monotherapy groups.

These findings suggest that tadalafil and tamsulosin combination therapy provides superior outcomes for LUTS/BPH management, though its benefits for ED are less clear. Clinicians should weigh these advantages against the increased likelihood of mild adverse effects when considering combination treatment for their patients.
 

19 Feb 2025
LUTS due to BPH

Medical news, Docvidya, Tadalafil, Tamsulosin, Monotherapy, Lower urinary tract symptoms, Benign prostatic hyperplasia, Erectile dysfunction

Combination Therapy with Tadalafil and Tamsulosin Enhances LUTS Outcomes but Increases Side Effects

A meta-analysis of 12 randomized controlled trials involving 1,531 patients has demonstrated that combination therapy with tadalafil and tamsulosin is more effective than monotherapy for managing lower urinary tract symptoms (LUTS) caused by benign prostatic hyperplasia (BPH), with or without erectile dysfunction (ED). However, this combined approach also leads to higher rates of adverse effects.

The analysis revealed significant improvements in the total International Prostate Symptom Score (IPSS), maximum urinary flow rate (Qmax), and quality of life (QoL) for patients receiving combination therapy compared to monotherapy. 

Specifically, the combined treatment enhanced IPSS voiding scores and reduced postvoid residual urine (PVR) more effectively than tamsulosin alone, although PVR outcomes were similar to tadalafil monotherapy.

In terms of erectile function, measured by the International Index of Erectile Function (IIEF), the combined therapy outperformed tamsulosin but did not show additional benefits over tadalafil alone. Importantly, while no serious adverse events were reported, the incidence of minor side effects was higher in the combination therapy group than in the monotherapy groups.

These findings suggest that tadalafil and tamsulosin combination therapy provides superior outcomes for LUTS/BPH management, though its benefits for ED are less clear. Clinicians should weigh these advantages against the increased likelihood of mild adverse effects when considering combination treatment for their patients.
 

LUTS due to BPH
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LUTS due to BPH
LUTS due to BPH…

Combination Therapy with Tadalafil and Tamsulosin Enhances LUTS Outcomes but Increases Side Effects

Medical news, Docvidya, Tadalafil, Tamsulosin, Monotherapy, Lower urinary tract symptoms, Benign prostatic hyperplasia, Erectile dysfunction

Combination Therapy with Tadalafil and Tamsulosin Enhances LUTS Outcomes but Increases Side Effects

A meta-analysis of 12 randomized controlled trials involving 1,531 patients has demonstrated that combination therapy with tadalafil and tamsulosin is more effective than monotherapy for managing lower urinary tract symptoms (LUTS) caused by benign prostatic hyperplasia (BPH), with or without erectile dysfunction (ED). However, this combined approach also leads to higher rates of adverse effects.

The analysis revealed significant improvements in the total International Prostate Symptom Score (IPSS), maximum urinary flow rate (Qmax), and quality of life (QoL) for patients receiving combination therapy compared to monotherapy. 

Specifically, the combined treatment enhanced IPSS voiding scores and reduced postvoid residual urine (PVR) more effectively than tamsulosin alone, although PVR outcomes were similar to tadalafil monotherapy.

In terms of erectile function, measured by the International Index of Erectile Function (IIEF), the combined therapy outperformed tamsulosin but did not show additional benefits over tadalafil alone. Importantly, while no serious adverse events were reported, the incidence of minor side effects was higher in the combination therapy group than in the monotherapy groups.

These findings suggest that tadalafil and tamsulosin combination therapy provides superior outcomes for LUTS/BPH management, though its benefits for ED are less clear. Clinicians should weigh these advantages against the increased likelihood of mild adverse effects when considering combination treatment for their patients.
 

19 Feb 2025
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Preemptive ibuprofen
2 Min Read
Dentinal Hypersensit…

Preemptive Ibuprofen and Potassium Fluoride Combination Reduces Tooth Sensitivity After Whitening

Dental bleaching, Ibuprofen, Tooth sensitivity, Preemptive, Visual analog scale

Preemptive Ibuprofen and Potassium Fluoride Combination Reduces Tooth Sensitivity After Whitening

A triple-blind, randomized clinical trial has shown that the preemptive use of ibuprofen (IBU) combined with potassium fluoride 2% (KF2) significantly reduces tooth sensitivity immediately after in-office bleaching procedures.

The study involved 15 participants using a crossover and split-mouth design to evaluate the analgesic effects of the combined treatment compared to ibuprofen or potassium fluoride alone and placebo. Participants reported tooth sensitivity levels on a visual analog scale at four intervals: immediately post-bleaching and at 6, 30, and 54 hours.

The combination of 400 mg of ibuprofen and 2% potassium fluoride outperformed the placebo group in reducing immediate tooth sensitivity (P < 0.05). Notably, the risk of experiencing moderate or severe sensitivity was four times higher in the placebo group compared to the combined treatment group (relative risk 4.00, 95% CI: 1.01–15.81, P = 0.025).

These findings suggest that the synergistic use of ibuprofen and potassium fluoride provides superior pain management during bleaching, making it a practical preemptive strategy for patients undergoing tooth whitening procedures. This approach can enhance patient comfort and satisfaction by minimizing post-bleaching sensitivity.
 

19 Feb 2025
Preemptive ibuprofen

Dental bleaching, Ibuprofen, Tooth sensitivity, Preemptive, Visual analog scale

Preemptive Ibuprofen and Potassium Fluoride Combination Reduces Tooth Sensitivity After Whitening

A triple-blind, randomized clinical trial has shown that the preemptive use of ibuprofen (IBU) combined with potassium fluoride 2% (KF2) significantly reduces tooth sensitivity immediately after in-office bleaching procedures.

The study involved 15 participants using a crossover and split-mouth design to evaluate the analgesic effects of the combined treatment compared to ibuprofen or potassium fluoride alone and placebo. Participants reported tooth sensitivity levels on a visual analog scale at four intervals: immediately post-bleaching and at 6, 30, and 54 hours.

The combination of 400 mg of ibuprofen and 2% potassium fluoride outperformed the placebo group in reducing immediate tooth sensitivity (P < 0.05). Notably, the risk of experiencing moderate or severe sensitivity was four times higher in the placebo group compared to the combined treatment group (relative risk 4.00, 95% CI: 1.01–15.81, P = 0.025).

These findings suggest that the synergistic use of ibuprofen and potassium fluoride provides superior pain management during bleaching, making it a practical preemptive strategy for patients undergoing tooth whitening procedures. This approach can enhance patient comfort and satisfaction by minimizing post-bleaching sensitivity.
 

Preemptive ibuprofen
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Preemptive ibuprofen
Dentinal Hypersensit…

Preemptive Ibuprofen and Potassium Fluoride Combination Reduces Tooth Sensitivity After Whitening

Dental bleaching, Ibuprofen, Tooth sensitivity, Preemptive, Visual analog scale

Preemptive Ibuprofen and Potassium Fluoride Combination Reduces Tooth Sensitivity After Whitening

A triple-blind, randomized clinical trial has shown that the preemptive use of ibuprofen (IBU) combined with potassium fluoride 2% (KF2) significantly reduces tooth sensitivity immediately after in-office bleaching procedures.

The study involved 15 participants using a crossover and split-mouth design to evaluate the analgesic effects of the combined treatment compared to ibuprofen or potassium fluoride alone and placebo. Participants reported tooth sensitivity levels on a visual analog scale at four intervals: immediately post-bleaching and at 6, 30, and 54 hours.

The combination of 400 mg of ibuprofen and 2% potassium fluoride outperformed the placebo group in reducing immediate tooth sensitivity (P < 0.05). Notably, the risk of experiencing moderate or severe sensitivity was four times higher in the placebo group compared to the combined treatment group (relative risk 4.00, 95% CI: 1.01–15.81, P = 0.025).

These findings suggest that the synergistic use of ibuprofen and potassium fluoride provides superior pain management during bleaching, making it a practical preemptive strategy for patients undergoing tooth whitening procedures. This approach can enhance patient comfort and satisfaction by minimizing post-bleaching sensitivity.
 

19 Feb 2025
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Serum periostin 97
2 Min Read
Allergic Rhinitis…

Serum Periostin, A Promising Biomarker for Diagnosing and Assessing Allergic Rhinitis Severity

Allergic rhinitis, Biomarkers, Fractional exhaled nitric oxide, Inflammation; Periostin

Serum Periostin, A Promising Biomarker for Diagnosing and Assessing Allergic Rhinitis Severity

A pilot study has identified serum periostin as a potential biomarker for diagnosing allergic rhinitis (AR) and evaluating disease severity, suggesting its role in assessing airway inflammation.

The study involved 40 AR patients and 22 healthy controls, all over 18 years of age. Participants' serum levels of periostin, total IgE, specific IgE, and remodeling-related factors were measured, alongside assessments of fractional exhaled nitric oxide (FeNO) and nasal nitric oxide (FnNO).

Key findings include:

Serum periostin levels were significantly higher in AR patients compared to controls (p < 0.001).

A positive correlation was found between serum periostin and FeNO (r = 0.398, p = 0.012), FnNO (r = 0.379, p = 0.017), and ocular tearing (r = 0.351, p = 0.026).

Periostin levels were higher in moderate-to-severe AR patients compared to those with mild AR (p = 0.045).

The study found that serum periostin could moderately predict AR diagnosis, with an AUC of 0.773 (p < 0.001).

These results suggest that serum periostin may serve as a reliable biomarker for AR detection and a surrogate marker for evaluating airway inflammation, offering a potential tool for better management of AR patients.

18 Feb 2025
Serum periostin 97

Allergic rhinitis, Biomarkers, Fractional exhaled nitric oxide, Inflammation; Periostin

Serum Periostin, A Promising Biomarker for Diagnosing and Assessing Allergic Rhinitis Severity

A pilot study has identified serum periostin as a potential biomarker for diagnosing allergic rhinitis (AR) and evaluating disease severity, suggesting its role in assessing airway inflammation.

The study involved 40 AR patients and 22 healthy controls, all over 18 years of age. Participants' serum levels of periostin, total IgE, specific IgE, and remodeling-related factors were measured, alongside assessments of fractional exhaled nitric oxide (FeNO) and nasal nitric oxide (FnNO).

Key findings include:

Serum periostin levels were significantly higher in AR patients compared to controls (p < 0.001).

A positive correlation was found between serum periostin and FeNO (r = 0.398, p = 0.012), FnNO (r = 0.379, p = 0.017), and ocular tearing (r = 0.351, p = 0.026).

Periostin levels were higher in moderate-to-severe AR patients compared to those with mild AR (p = 0.045).

The study found that serum periostin could moderately predict AR diagnosis, with an AUC of 0.773 (p < 0.001).

These results suggest that serum periostin may serve as a reliable biomarker for AR detection and a surrogate marker for evaluating airway inflammation, offering a potential tool for better management of AR patients.

Serum periostin 97
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Serum periostin 97
Allergic Rhinitis…

Serum Periostin, A Promising Biomarker for Diagnosing and Assessing Allergic Rhinitis Severity

Allergic rhinitis, Biomarkers, Fractional exhaled nitric oxide, Inflammation; Periostin

Serum Periostin, A Promising Biomarker for Diagnosing and Assessing Allergic Rhinitis Severity

A pilot study has identified serum periostin as a potential biomarker for diagnosing allergic rhinitis (AR) and evaluating disease severity, suggesting its role in assessing airway inflammation.

The study involved 40 AR patients and 22 healthy controls, all over 18 years of age. Participants' serum levels of periostin, total IgE, specific IgE, and remodeling-related factors were measured, alongside assessments of fractional exhaled nitric oxide (FeNO) and nasal nitric oxide (FnNO).

Key findings include:

Serum periostin levels were significantly higher in AR patients compared to controls (p < 0.001).

A positive correlation was found between serum periostin and FeNO (r = 0.398, p = 0.012), FnNO (r = 0.379, p = 0.017), and ocular tearing (r = 0.351, p = 0.026).

Periostin levels were higher in moderate-to-severe AR patients compared to those with mild AR (p = 0.045).

The study found that serum periostin could moderately predict AR diagnosis, with an AUC of 0.773 (p < 0.001).

These results suggest that serum periostin may serve as a reliable biomarker for AR detection and a surrogate marker for evaluating airway inflammation, offering a potential tool for better management of AR patients.

18 Feb 2025
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Dental pain
2 Min Read
Dental Pain

Evaluation of post-operative pain in non-surgical root canal therapy: Comparison of sealer-based obturation with warm vertical compaction

post-operative, non-surgical, root canal, Docvidya, Medshorts, Acute Dental Pain, Dentist, Dental &amp; Oral Health, Acute dental pain, Maximum pain relief, Bite force changes

Evaluation of post-operative pain in non-surgical root canal therapy: Comparison of sealer-based obturation with warm vertical compaction

Recent study results indicated that the sealer-based obturation (SBO) technique utilizing calcium silicate sealer (CSS) is correlated with similar post-operative pain levels and analgesic consumption as warm-vertical compaction (WVC) with resin-based sealer (RBS). Therefore, SBO with CSS may be a practical clinical alternative in the context of post-operative pain. The International Endodontic Journal has highlighted the results of this study.

This study included 195 patients who were referred for non-surgical root canal treatment (NSRCT) and fulfilled the essential inclusion criteria. Before the treatment, periapical radiographs and CBCT scans were conducted, and pain was assessed using a numerical rating scale (NRS). After completing the canal instrumentation, participants were randomly assigned to either Group SBO, which received SBO with CSS, or Group WVC, which utilized warm-vertical compaction with RBS. Post-operative pain levels and analgesic use were recorded at one, three, and seven days following the endodontic procedure. The differences in pain scores among the groups were assessed using the Mann-Whitney U and Friedman tests, while a generalized estimating equation was applied to evaluate correlations at different time points within each treatment group.

In the final analysis, 194 participants and 211 teeth were included, producing a response rate of 99.5%. There were no significant differences in post-operative pain or the use of analgesics between the two groups at any time point (p value > .05). On the other hand, pre-operative pain, age, apical diagnosis, and post-operative analgesic intake were significantly linked to post-operative pain (p value < .05).

The above findings indicated that the sealer-based obturation technique utilizing CSS is linked to post-operative pain and analgesic use that are comparable to warm-vertical compaction WVC with RBS. Therefore, SBO with CSS could be a practical alternative for managing pain after surgery.

17 Feb 2025
Dental pain

post-operative, non-surgical, root canal, Docvidya, Medshorts, Acute Dental Pain, Dentist, Dental &amp; Oral Health, Acute dental pain, Maximum pain relief, Bite force changes

Evaluation of post-operative pain in non-surgical root canal therapy: Comparison of sealer-based obturation with warm vertical compaction

Recent study results indicated that the sealer-based obturation (SBO) technique utilizing calcium silicate sealer (CSS) is correlated with similar post-operative pain levels and analgesic consumption as warm-vertical compaction (WVC) with resin-based sealer (RBS). Therefore, SBO with CSS may be a practical clinical alternative in the context of post-operative pain. The International Endodontic Journal has highlighted the results of this study.

This study included 195 patients who were referred for non-surgical root canal treatment (NSRCT) and fulfilled the essential inclusion criteria. Before the treatment, periapical radiographs and CBCT scans were conducted, and pain was assessed using a numerical rating scale (NRS). After completing the canal instrumentation, participants were randomly assigned to either Group SBO, which received SBO with CSS, or Group WVC, which utilized warm-vertical compaction with RBS. Post-operative pain levels and analgesic use were recorded at one, three, and seven days following the endodontic procedure. The differences in pain scores among the groups were assessed using the Mann-Whitney U and Friedman tests, while a generalized estimating equation was applied to evaluate correlations at different time points within each treatment group.

In the final analysis, 194 participants and 211 teeth were included, producing a response rate of 99.5%. There were no significant differences in post-operative pain or the use of analgesics between the two groups at any time point (p value > .05). On the other hand, pre-operative pain, age, apical diagnosis, and post-operative analgesic intake were significantly linked to post-operative pain (p value < .05).

The above findings indicated that the sealer-based obturation technique utilizing CSS is linked to post-operative pain and analgesic use that are comparable to warm-vertical compaction WVC with RBS. Therefore, SBO with CSS could be a practical alternative for managing pain after surgery.

Dental pain
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Dental pain
Dental Pain

Evaluation of post-operative pain in non-surgical root canal therapy: Comparison of sealer-based obturation with warm vertical compaction

post-operative, non-surgical, root canal, Docvidya, Medshorts, Acute Dental Pain, Dentist, Dental &amp; Oral Health, Acute dental pain, Maximum pain relief, Bite force changes

Evaluation of post-operative pain in non-surgical root canal therapy: Comparison of sealer-based obturation with warm vertical compaction

Recent study results indicated that the sealer-based obturation (SBO) technique utilizing calcium silicate sealer (CSS) is correlated with similar post-operative pain levels and analgesic consumption as warm-vertical compaction (WVC) with resin-based sealer (RBS). Therefore, SBO with CSS may be a practical clinical alternative in the context of post-operative pain. The International Endodontic Journal has highlighted the results of this study.

This study included 195 patients who were referred for non-surgical root canal treatment (NSRCT) and fulfilled the essential inclusion criteria. Before the treatment, periapical radiographs and CBCT scans were conducted, and pain was assessed using a numerical rating scale (NRS). After completing the canal instrumentation, participants were randomly assigned to either Group SBO, which received SBO with CSS, or Group WVC, which utilized warm-vertical compaction with RBS. Post-operative pain levels and analgesic use were recorded at one, three, and seven days following the endodontic procedure. The differences in pain scores among the groups were assessed using the Mann-Whitney U and Friedman tests, while a generalized estimating equation was applied to evaluate correlations at different time points within each treatment group.

In the final analysis, 194 participants and 211 teeth were included, producing a response rate of 99.5%. There were no significant differences in post-operative pain or the use of analgesics between the two groups at any time point (p value > .05). On the other hand, pre-operative pain, age, apical diagnosis, and post-operative analgesic intake were significantly linked to post-operative pain (p value < .05).

The above findings indicated that the sealer-based obturation technique utilizing CSS is linked to post-operative pain and analgesic use that are comparable to warm-vertical compaction WVC with RBS. Therefore, SBO with CSS could be a practical alternative for managing pain after surgery.

17 Feb 2025
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Treats Renal Anemia in Patients
2 Min Read
Renal anemia

Roxadustat Effectively Treats Renal Anemia in Patients with Systemic Macroinflammation

Iron metabolism, Macroinflammation, Renal anemia, Roxadustat,Anemia

Roxadustat Effectively Treats Renal Anemia in Patients with Systemic Macroinflammation

A retrospective cohort study has demonstrated the efficacy of roxadustat, a first-in-class treatment for renal anemia, in patients with systemic macroinflammation. 

The study enrolled 107 patients with chronic kidney disease (CKD), dividing them into three groups based on high-sensitivity C-reactive protein (hsCRP) levels: 

•    non-inflammation (NI)

•    microinflammation (MI)

•    macroinflammation (MA)

Patients were treated with roxadustat three times a week for 52 weeks.

The study found that roxadustat significantly increased hemoglobin levels across all groups, with no significant differences in hemoglobin responses between the groups, even for those with macroinflammation (MA). At both 12 and 52 weeks, the hemoglobin response rate in the MA group was comparable to the NI group, indicating that roxadustat's effect was independent of baseline hsCRP levels.

Additionally, roxadustat was shown to significantly reduce ferritin and serum iron levels, while increasing total iron-binding capacity in all groups, with no significant differences between them. This suggests that roxadustat is effective in improving anemia regardless of the level of systemic inflammation.

In conclusion, roxadustat is an effective treatment for anemia in CKD patients, including those with systemic macroinflammation, offering a promising therapeutic option for this challenging patient population.
 

14 Feb 2025
Treats Renal Anemia in Patients

Iron metabolism, Macroinflammation, Renal anemia, Roxadustat,Anemia

Roxadustat Effectively Treats Renal Anemia in Patients with Systemic Macroinflammation

A retrospective cohort study has demonstrated the efficacy of roxadustat, a first-in-class treatment for renal anemia, in patients with systemic macroinflammation. 

The study enrolled 107 patients with chronic kidney disease (CKD), dividing them into three groups based on high-sensitivity C-reactive protein (hsCRP) levels: 

•    non-inflammation (NI)

•    microinflammation (MI)

•    macroinflammation (MA)

Patients were treated with roxadustat three times a week for 52 weeks.

The study found that roxadustat significantly increased hemoglobin levels across all groups, with no significant differences in hemoglobin responses between the groups, even for those with macroinflammation (MA). At both 12 and 52 weeks, the hemoglobin response rate in the MA group was comparable to the NI group, indicating that roxadustat's effect was independent of baseline hsCRP levels.

Additionally, roxadustat was shown to significantly reduce ferritin and serum iron levels, while increasing total iron-binding capacity in all groups, with no significant differences between them. This suggests that roxadustat is effective in improving anemia regardless of the level of systemic inflammation.

In conclusion, roxadustat is an effective treatment for anemia in CKD patients, including those with systemic macroinflammation, offering a promising therapeutic option for this challenging patient population.
 

Treats Renal Anemia in Patients
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Treats Renal Anemia in Patients
Renal anemia

Roxadustat Effectively Treats Renal Anemia in Patients with Systemic Macroinflammation

Iron metabolism, Macroinflammation, Renal anemia, Roxadustat,Anemia

Roxadustat Effectively Treats Renal Anemia in Patients with Systemic Macroinflammation

A retrospective cohort study has demonstrated the efficacy of roxadustat, a first-in-class treatment for renal anemia, in patients with systemic macroinflammation. 

The study enrolled 107 patients with chronic kidney disease (CKD), dividing them into three groups based on high-sensitivity C-reactive protein (hsCRP) levels: 

•    non-inflammation (NI)

•    microinflammation (MI)

•    macroinflammation (MA)

Patients were treated with roxadustat three times a week for 52 weeks.

The study found that roxadustat significantly increased hemoglobin levels across all groups, with no significant differences in hemoglobin responses between the groups, even for those with macroinflammation (MA). At both 12 and 52 weeks, the hemoglobin response rate in the MA group was comparable to the NI group, indicating that roxadustat's effect was independent of baseline hsCRP levels.

Additionally, roxadustat was shown to significantly reduce ferritin and serum iron levels, while increasing total iron-binding capacity in all groups, with no significant differences between them. This suggests that roxadustat is effective in improving anemia regardless of the level of systemic inflammation.

In conclusion, roxadustat is an effective treatment for anemia in CKD patients, including those with systemic macroinflammation, offering a promising therapeutic option for this challenging patient population.
 

14 Feb 2025
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