JIPMER Invites Application For Research Proposals To IEC Observational Studies November 2024

Puducherry- The Jawaharlal Institute of Postgraduate Medical Education and Research (JIPMER), Puducherry, has issued a circular inviting online applications for the submission of proposals to the Institutional Ethics Committee Observational Studies for the November 2024 session.

The last date for submission of proposals so as to reach the office of the undersigned for consideration of approval by Institutional Ethics Committee for the month of November 2024 is on or before Saturday, 26 October (Saturday). Proposals submitted before the last date will be taken up for discussion in IEC Observational committee meeting scheduled to be held on Thursday, November 07 2024.

Candidates must submit one hard copy of certain documents to the Member-Secretary at the Institute Ethics Committee (IEC) office, Room no. 106, First floor, Administrative block, JIPMER.

DOCUMENTS

• Covering letter

• Signed Declaration form

• Consent forms / Waiver of consent forms

• Research proposal JSAC (ver. July 2020) / UGRMC/PGRMC

• JSAC/ UGRMC/PGRMC certificate

• Data collection proformas

• Curriculum vitae of PI & Co-Investigator (s) / guide & co-guide

The notice states, “Faculty, PhD scholars, P.G., and U.G. Students are invited to submit research proposals approved by JSAC/PGRMC/SCTRC/GJ-STRAUS for approval by Institutional Ethics Committee—Observational studies in the prescribed proforma.”

PIs are instructed to send a soft copy of their signed declaration form, consent forms and scientific proposal along with a cover letter (both as PDF & Word copy) at the email ID, which is mentioned in the notice.

The Jawaharlal Institute of Postgraduate Medical Education & Research (JIPMER) is a medical school in Pondicherry. It is an institute of national importance (INI) and a tertiary care referral hospital. It is under the direct administrative control of the Ministry of Health and Family Welfare and the Indian Government, with autonomy to run its internal administration.

To view the official Notice, Click here :  https://medicaldialogues.in/pdf_upload/iec-os-call-for-proposal-november-2024manager-257305.pdf

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Ayurveda Aahar helps maintaining a balanced body and mind: Union Minister Shri Prataprao Jadhav

New Delhi: On October 16th, 2024, as the world marks World Food Day with the theme ”Right to Food for a Better Life and Future,” the Ministry of Ayush is dedicated to supporting the United Nations’ Sustainable Development Goal 2 (SDG-2), aiming to eradicate hunger and enhance food security.

The Ministry of Ayush is making all efforts in promoting a healthier, disease-free and sustainable world through the power of Ayurveda Aahar.

Marking the significance of World Food Day, the Union Minister of State for Ayush (I/C) Shri Pratap Rao Jhadhav said, “On World Food Day, let’s remember that Ayurveda’s approach to food goes beyond mere sustenance – it aims to nourish the body, bring peace to the mind, and satisfy the soul, reconnecting us to our roots and guiding us to live in harmony with nature. 

Let us acknowledge the significance of Ayurveda Aahar, which sees food as more than just a source of energy, but as a crucial element in maintaining a balanced body and mind. This day serves as a reminder of how a proper diet can impact not only personal health but also global food security and sustainable development, in alignment with Ayurvedic principles.”

Also Read:Union Health Minister launches ‘Ayurveda Aahar’ logo

Ayurveda provides cost-effective, sustainable and nutritious dietary solutions to combat the malnutrition crisis, as well as sustainability of food issue, affecting many regions globally. According to Ayurvedic principles – food is best medicine, thereby advising the consumers to partake right food in right manner, and nutritious enough to have a healthy life.

While underlining the developments around Ayurveda Aahar, Vaidya Rajesh Kotecha, Secretary, Ministry of Ayush informed, “The Food Safety and Standards Authority of India (FSSAI), has notified Ayurveda Aahar regulations through a Gazette notification in 2021. Following this development, we have observed renewed interest from diverse stakeholder groups, including the industry, in the concept of Ayurveda Aahar and this is revolutionizing the sector.”

The Indian Thali has garnered global attention for its significant impact on nutrition and sustainability, as recognized by the WWF Living Planet Report. This traditional plant-based diet, centered on grains, pulses, lentils, and vegetables, has credited with reducing natural resource usage and greenhouse gas emissions compared to animal-based diets. According to the report, if the world adopts India’s consumption patterns, only 0.84 of an earth will be in need by 2050 to sustain global food production.

Elaborating on the strength and potential of Ayurveda Aahar, Professor National Institute of Ayurveda (NIA) Jaipur, Shri Anupam Srivastava said, “Ministry of Ayush’s innovative approach towards the concept of Ayurveda Aahar, is perfectly aligned with the Sustainable Development Goal-2 (SDG-2) that concerns hunger, food security, nutrition, and sustainability.”

Based on this principle, the Ministry of Ayush has introduced the “Ayush Dietary Advisory for Kuposhan Mukt Bharat” to enhance nutritional outcomes, especially for children, pregnant women, and lactating mothers. In partnership with the Ministry of Women and Child Development, is taking significant strides toward realizing a Nourished India by endorsing an Ayush-based diet and lifestyle.

The Ayush Dietary Advisory seeks to enhance the nutritional well-being of at-risk populations by integrating Ayurvedic dietary principles into daily meals, presenting a distinctive and efficient approach to malnutrition. This aligns with the national mission to eradicate malnutrition and promote the health of future generations.

The Ministry of Ayush highlights how blending traditional wisdom with modern science can provide effective solutions for tackling global hunger and improving health outcomes for everyone through continuous efforts.

As we celebrate World Food Day 2024, the Ministry of Ayush reaffirms its commitment to promoting a disease-free world through the principles of Ayurveda Aahar, emphasizing natural nutrition, prevention, and wellness. By adopting Ayush dietary practices, we can move towards a world where food is a powerful tool for health and longevity. Through collaborative efforts within India and internationally, the Ministry of Ayush continues to advance its mission of improving nutritional outcomes, and creating a brighter, healthier future for all.

This acknowledgement positions India as a leader in sustainable food practices, demonstrating how local traditions can address environmental challenges while promoting overall health.

Also Read:AYUSH Ministry prohibits ‘Miraculous’ claims in advertisements for Ayurveda, Siddha drugs

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MCC NEET MDS 2024 Special Stray vacancy Round Final Results Announced

New Delhi- The Medical Counselling Committee (MCC) has released the final result of the National Eligibility and Entrance Test-Master of Dental Surgery (NEET MDS) Special Stray Vacancy Round Counselling 2024.

As per the result, a total of  63  students have been declared qualified for NEET MDS Special Stray Vacancy Round Counselling 2024.The Final result has been declared on the official website of MCC, candidates can download and view the final result attached below.

Final Allotment Result for Special Stray Vacancy Round MDS 2024 https://medicaldialogues.in/pdf_upload/2024101844-257430.pdf

Also Read: NEET MDS Counselling 2024: DCI Releases Special Stray Vacancy Round Schedule after percentile reduction

Schedule for the Special Stray Vacancy Round is as follows:

Fresh Registration/Payment Choice Filling & Choice Locking Processing of Seat Allotment Publication of the Result Reporting at allotted College
14th October, 2024 to 16th October, 2024 (up to 03:00 P.M of 16.10.2024 as per the server timing) *Payment facility will be available till 06:00 PM of 16th Oct., 2024 (as per the Server timing) 14th October, 2024 to 16th October, 2024 (Choice filling available from 14th Oct. upto 08:00 AM of 17th Oct., 2024) Choice Locking will be available from 08:00 PM of 16th Oct., 2024 up to 08:00 AM of 17th Oct., 2024 (as per the Server timing) 17th October, 2024 18th October, 2024 19th October 2024 to 25th October, 2024 (up to 05:00 PM as per the Server timing)
(3-Days) (3-Days) (1-Day) (1 -Day) (7-Days)

The Medical Counselling Committee (MCC) is an organisation under the Directorate General of Health Services (DGHS) affiliated to the Ministry of Health and Family Welfare, Government of India and responsible for allotting seats for undergraduate, postgraduate and super-speciality medical and dental courses in government-run/aided colleges and deemed-to-be-university colleges.

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Glucagon-like peptide-1 receptor agonists may be new treatment for opioid and alcohol use disorder, finds study

Ozempic is one of several medications, called glucagon-like peptide-1 receptor agonists or GLP-1 RAs, that are prescribed to treat diabetes, obesity, and other weight-related medical conditions. 

A new study published in the scientific journal Addiction has found that people with opioid or alcohol use disorder (OUD, AUD) who take Ozempic or similar medications to treat diabetic/weight-related conditions appear to have a 40% lower rate of opioid overdose and a 50% lower rate of alcohol intoxication than people with OUD and AUD who do not take Ozempic or similar medications.

Glucagon-like peptide-1 receptor agonists interact with a region of the brain – the mesolimbic system – to reduce appetite and trigger satisfaction after eating. The mesolimbic system overlaps with the brain processes that govern addictive behaviors. This overlap suggests that GLP-1 RAs and similar medications might also alter the reward-response pathways associated with substance use. ‘Similar medications’ include glucose-dependent insulinotropic polypeptide (GIP) agonists like the weight-loss medication Mounjaro.

Until now, most of the existing research into using GLP-1 RAs and GIPs to treat substance use disorders consists of animal studies and small-scale clinical trials.

This new large-scale human study looked at 503,747 people with a history of opioid use disorder (OUD), of which 8,103 had a prescription for a GLP-1 RA or GIP. The study found that people with OUD who had a GLP-1 RA or GIP prescription had a 40% lower rate of opioid overdose compared with those who did not have a prescription.

The study also looked at 817,309 people with a history of alcohol use disorder (AUD), of which 5,621 had a prescription for a GLP-1 RA or GIP. The study found that people with AUD who had a GLP-1 RA or GIP prescription had a 50% lower rate of alcohol intoxication compared with those who did not have a prescription.

This study may introduce a promising new treatment for substance use disorders.

Reference:

Fares Qeadan, Ashlie McCunn, Benjamin Tingey, The association between glucose-dependent insulinotropic polypeptide and/or glucagon-like peptide-1 receptor agonist prescriptions and substance-related outcomes in patients with opioid and alcohol use disorders: A real-world data analysis, Addiction, https://doi.org/10.1111/add.16679.

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Blue Index: A Comprehensive Tool for Enhancing Patient-Centered Diabetes Care, Study Reveals

India: A new tool known as the Blue Index (BI) is gaining attention for its potential to enhance diabetes management by providing a comprehensive, patient-centered care assessment.

A recent study published in the Journal of the Association of Physicians of India showed that the index includes a range of parameters that address various facets of diabetes care, including complications. The researchers suggest that it can be utilized by not only endocrinologists but also all physicians as a resource for monitoring and enhancing diabetic care.

Diabetes is a complex condition that requires meticulous management to prevent complications such as cardiovascular disease, neuropathy, and kidney failure. Traditional assessment methods often focus on isolated metrics, which can overlook the multifaceted nature of the disease. Assessing diabetes health encompasses a range of factors, including metabolic and nonmetabolic measures, as well as self-care practices such as diet, exercise, and follow-up habits. In contrast, the complications index focuses on macro and microvascular issues related to diabetes and foot complications.

The Blue Index (BI) is a comprehensive tool that integrates these health-related parameters and the systemic complications arising from diabetes into a unified assessment. In the study, Rupak Chatterjee, Senior Resident, Department of Medicine, College of Medicine and Sagore Dutta Hospital, Kolkata, West Bengal, India, and colleagues sought to assess the diabetes control status of patients using a single index.

For this purpose, the researchers conducted a prospective, observational study involving 100 adult diabetic patients, assessing their diabetic health status (DHS) and Komplications Score (KS) related to cardiovascular/macrovascular, microvascular, and foot complications. The Blue Index (BI) was calculated as a composite ratio, with measurements taken at baseline, after three months, and again at six months. The collected data was then statistically analyzed.

The following were the key findings of the study:

  • Diabetic health status showed a significant increase in both the third and sixth months compared to baseline.
  • The Komplications Score decreased significantly at these time points relative to baseline measures.
  • The composite BI scores exhibited a steady rise, with increases of 9.62 at three months and 13.14 at six months compared to baseline.
  • When analyzing based on the duration of diabetes diagnosis, DHS, KS, and BI scores demonstrated consistent changes.
  • In terms of gender differences, DHS was notably higher in females at baseline compared to males, with both groups showing gradual improvements over time.
  • Males had significantly lower KS scores than females, with a gradual decrease over the study period, indicating an improvement in complications.
  • DHS was significantly correlated with both the duration of diabetes detection and age.

The findings suggest that the Blue Index (BI) is a straightforward tool that integrates multiple parameters addressing various facets of diabetes care, including complications. It can be utilized not only by endocrinologists but by all physicians to monitor and enhance diabetic management.

However, the authors noted some limitations, including a small sample size and its single-center design. Additionally, there were challenges in establishing clear distinctions based on the grading of retinopathy in the complications score, resulting in some overlaps.

Reference:

Chatterjee R, Naskar A, Samajdar SS, et al. Blue Index as a Comprehensive, Patient-centered Assessment of Care in Diabetic Patients. J Assoc Physicians India 2024;72(10):e1–e5.

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Long-Term Study Reveals Comparable Outcomes for iFR and FFR in Coronary Revascularization: DEFINE FLAIR Trial

Spain: A recent 5-year follow-up of the DEFINE FLAIR randomized clinical trial has provided new insights into the effectiveness of coronary revascularization strategies guided by either fractional flow reserve (FFR) or instantaneous wave-free ratio (iFR).

The DEFINE FLAIR trial initially compared the two approaches in a cohort of patients undergoing revascularization. At the 5-year mark, the study, published in JAMA Cardiology, revealed that an iFR-based strategy was not statistically different from an FFR-based approach in guiding revascularization regarding major adverse cardiovascular events (MACE), nonfatal myocardial infarction, and unplanned revascularization.

Javier Escaned, Hospital Clinico San Carlos IDISSC, Complutense University of Madrid and CIBERCV, Madrid, Spain, and colleagues aimed to compare the long-term outcomes of iFR- and FFR-based strategies for guiding revascularization, noting that the long-term differences between these two approaches remain unclear.

The DEFINE-FLAIR multicenter study randomized patients with coronary artery disease to utilize either iFR or FFR as a pressure index to guide revascularization. Participants were drawn from five continents and had angiographically intermediate severity stenoses, undergoing hemodynamic interrogation with pressure wires. Data for this analysis were collected from March 13, 2014, to April 27, 2021.

The primary outcome measures included five-year major adverse cardiac events (MACE), which is a composite of all-cause death, nonfatal myocardial infarction, and unplanned revascularization, along with the individual components of this combined endpoint.

The following were the key findings of the study:

  • At the 5-year follow-up, no significant differences were observed between the iFR group (mean age 65.5 years, 77.5% male) and the FFR group (mean age 65.2 years, 74.3% male) regarding major adverse cardiac events (MACE), with rates of 21.1% for iFR and 18.4% for FFR (hazard ratio [HR], 1.18).
  • Although all-cause mortality was slightly higher in the iFR group, this increase was not attributed to myocardial infarction (6.3% in iFR versus 6.2% in FFR; HR, 1.01) or unplanned revascularization (11.9% in iFR versus 12.2% in FFR; HR, 0.98).
  • Patients for whom revascularization was deferred based on either iFR or FFR exhibited similar MACE rates (17.9% for iFR versus 17.5% for FFR; HR, 1.03), with comparable rates of individual MACE components, including all-cause death.
  • Among those who underwent revascularization following physiological assessment, the incidence of MACE was higher in the iFR group at 24.6%, compared to 19.2% in the FFR group (HR, 1.36).

“The 5-year follow-up results indicated that an iFR-based strategy was not statistically different from an FFR strategy in guiding revascularization concerning major adverse cardiovascular events,” the researchers concluded.

Reference:

Escaned J, Travieso A, Dehbi H, et al. Coronary Revascularization Guided With Fractional Flow Reserve or Instantaneous Wave-Free Ratio: A 5-Year Follow-Up of the DEFINE FLAIR Randomized Clinical Trial. JAMA Cardiol. Published online October 16, 2024. doi:10.1001/jamacardio.2024.3314

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GLP-1 RAs Superior to Metformin for Blood Sugar Control, Yet Metformin Shows Higher Adherence in Prediabetes: Study

Denmark: A recent nationwide cohort study has shed light on the effectiveness of glucagon-like peptide-1 receptor agonists (GLP-1 RAs) compared to metformin in drug-naive patients with type 2 diabetes.

The research, published in the Journal of Diabetes, revealed that GLP-1 receptor agonists were linked to a lower likelihood of requiring additional glucose-lowering medications and demonstrated superior control of glycated hemoglobin levels overall. However, in patients with prediabetes, metformin was associated with higher rates of treatment adherence.

GLP-1 RAs are increasingly being prescribed in drug-naive patients. Kathrine Kold Sørensen, Department of Cardiology, Nordsjælland Hospital, Hillerød, Denmark, and colleagues aimed to compare add-on therapy, adherence, and changes in biomarkers one year after starting treatment with either GLP-1 receptor agonists or metformin.

For this purpose, the researchers utilized Danish nationwide registers to include new users of GLP-1 receptor agonists or metformin from 2018 to 2021, specifically those with glycated hemoglobin (HbA1c) levels of ≥42 mmol/mol. GLP-1 RA initiators were matched to metformin initiators in a 1:1 ratio to evaluate outcomes in both prediabetes and diabetes.

The main outcomes analyzed included the one-year risk of requiring additional glucose-lowering medications and the one-year risk of non-adherence. One-year risks were estimated using multiple logistic regression and standardized methods, while multiple linear regression was applied to assess average differences in changes to biomarkers.

Based on the study, the researchers reported the following findings:

  • The study included 1,778 individuals initiating treatment with GLP-1 receptor agonists or metformin.
  • After adjusting for various factors, GLP-1 RA was linked to a lower one-year risk of requiring additional glucose-lowering treatment in patients with prediabetes (one-year risk ratio [RR]: 0.27) and diabetes (RR: 0.67).
  • Among patients with prediabetes, GLP-1 RA was associated with a higher one-year risk of nonadherence (RR: 1.60), while there was no significant difference in patients with diabetes (RR: 0.88).
  • Compared to metformin, GLP-1 RA was associated with greater reductions in HbA1c levels, with a decrease of −2.59 mmol/mol for prediabetes and −3.79 mmol/mol for diabetes.

The findings indicated that in patients with prediabetes, starting treatment with GLP-1 receptor agonists was linked to a reduced risk of needing additional glucose-lowering therapy compared to metformin. However, those initiating metformin demonstrated significantly higher levels of adherence.

“In patients with diabetes, GLP-1 RA initiation similarly resulted in a lower risk of requiring extra glucose-lowering therapy, but there was no difference in nonadherence rates when compared to metformin initiation,” the researchers wrote.

Reference:

Sørensen, K. K., Gerds, T. A., Køber, L., Fosbøl, E. L., Poulsen, H. E., Møller, A. L., Andersen, M. P., Pedersen-Bjergaard, U., Torp-Pedersen, C., & Zareini, B. (2024). Comparing Glucagon-like peptide-1 receptor agonists versus metformin in drug-naive patients: A nationwide cohort study. Journal of Diabetes, 16(10), e70000. https://doi.org/10.1111/1753-0407.70000

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Mindfulness meditation in patients effectively reduces anxiety symptoms: JAMA

A new study published in the Journal of American Medical Association found that mindfulness meditation seems to reduce anxiety symptoms after 8 weeks similarly to escitalopram. Anxiety disorders have demonstrated the effectiveness of mindfulness-based therapies, such as mindfulness-based stress reduction (MBSR). The previously published randomized clinical trial with a predefined margin, showed that 8 weeks of MBSR was non-inferior to escitalopram for the treatment of anxiety disorders. Therefore, Hiroe Hu and colleagues provided the secondary outcomes of trial, such as depression, anxiety, and quality of life (QOL) as stated by the patients.

Prior to 1:1 randomization, the trial comprised community-dwelling people with a main anxiety condition (agoraphobia, generalized anxiety, panic, or social anxiety disorder) identified by a doctor. The MBSR intervention includes weekly courses that covered the philosophy and practice of several kinds of mindfulness meditation. Escitalopram participants were given a flexible dosage (10-20 mg/d) and visited with a prescriber at baseline, weeks 1, 2, 4, 6, 8, and 12. The trial protocol was approved by local institutional review boards, and the patients gave their informed permission. Blinded assessors evaluated anxiety results reported by both patients and clinicians.

Depression symptoms were measured using the PROMIS Depression scale, while QOL and role functioning were measured using the PROMIS Satisfaction. Bivariate statistics and multivariable regression analysis were employed to compare the groups. The intent-to-treat principle was applied to adjusted analyses, which employed linear mixed models that included every participant at baseline regardless of missing data at later time points.

This study involved a total of 276 individuals. The participants were indicated as Asian, Hispanic, or a different race or ethnicity. Except for BAI scores, there were no significant differences between the groups in demographic variables or baseline outcome measures. The participants in both groups reported reduced anxiety symptoms, with between-group variations matching to minor effect sizes.

No substantial variations were found at week 8 (the major end point). At week 4 (mid-treatment), substantial variations in PROMIS Anxiety and PROMIS Depression scores developed, with escitalopram providing more improvement, despite these differences were no longer significant by week 8. However, 110 escitalopram users (78.6%) reported at least one study-related adverse event when compared to 21 MBSR patients. Overall, this results are in line with other research showing that mindfulness may effectively treat panic and social anxiety disorders.

Reference:

Hu, H., Mete, M., Rustgi, N. K., Washington, C. I., Sanghavi, K., Dutton, M. A., Simon, N. M., Baker, A. W., Bui, E., & Hoge, E. A. (2024). Mindfulness Meditation vs Escitalopram for Treatment of Anxiety Disorders. In JAMA Network Open (Vol. 7, Issue 10, p. e2438453). American Medical Association (AMA). https://doi.org/10.1001/jamanetworkopen.2024.38453

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Study Finds Baseline Forced Oscillation Technique Effective in Predicting Exacerbation Risk in Adults with Asthma

Japan: A recent study published in Annals of Allergy, Asthma & Immunology has highlighted the potential of the baseline forced oscillation technique (FOT) as a valuable tool for predicting exacerbations in adults with asthma.

The prospective research, conducted over 12 months, showed that R20 may be an effective predictor of future exacerbations in asthma patients. The findings could enhance the evaluation of adults with asthma who have normal FEV1 levels.

“Our findings established the baseline FOT as an important tool for predicting clinical remission in adults with asthma over 12 months,” the researchers wrote. “Notably, FOT parameters, especially resistance at 20 Hz (R20), effectively differentiated between those who achieved clinical remission and those who did not. Lower R20 values were significantly linked to clinical remission, with an adjusted odds ratio of 0.32.”

Asthma exacerbations can significantly impact patients’ quality of life, leading to increased healthcare costs and reduced lung function. Traditional methods of monitoring asthma rely on FEV1 measurements, which can sometimes fail to capture the complexity of the disease in certain patients.

The forced oscillation technique (FOT) is a minimally invasive method for assessing asthma during resting ventilation. However, its effectiveness in long-term evaluations, such as monitoring clinical remission, is still not well understood. Therefore, Yoshito Miyata, Showa University School of Medicine, Tokyo, Japan, and colleagues aimed to evaluate asthma clinical remission over time and identify parameters from baseline FOT that predict remission at the 12-month mark.

For this purpose, the researchers enrolled adult patients with asthma at their university hospital from April 2022 to May 2023 in a prospective observational study. Participants were evaluated over 12 months to determine if they met the clinical remission criteria: an asthma control test score of ≥20 at both enrollment and 12 months, no exacerbations during that period, and no regular oral corticosteroid use. The FOT parameters collected at enrollment were then analyzed for their association with clinical remission.

The following were the key findings of the study:

  • Ninety-four asthma patients completed the study and were divided into clinical and non-clinical remission groups.
  • Comparing pulmonary function tests, including FOT, revealed significant differences in resistance at 5 Hz and 20 Hz (R20), while there were no differences in FEV1.
  • Multivariate logistic regression analysis indicated that R20 was linked to clinical remission, with adjusted odds ratios of 0.32 for R20.

The study emphasizes the value of baseline forced oscillation technique measurements, particularly R20, in predicting future exacerbations in adults with asthma. These insights could transform clinical practices, allowing for more effective monitoring and management of asthma, especially in patients with normal lung function.

“As the medical community continues to seek innovative ways to enhance asthma care, FOT may play a pivotal role in shaping future treatment strategies,” the researchers concluded.

Reference:

Miyata Y, Tanaka A, Ebato T, Kashima A, Nojo M, Matsunaga T, Kaneko K, Okazaki T, Ohta S, Homma T, Watanabe Y, Kusumoto S, Suzuki S, Sagara H. Baseline forced oscillation technique predicting lack of exacerbations in adult with asthma: A 12-month prospective. Ann Allergy Asthma Immunol. 2024 Oct 4:S1081-1206(24)01553-9. doi: 10.1016/j.anai.2024.09.018. Epub ahead of print. PMID: 39370038.

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Use of higher concentrations of NaOCl as irrigant during RCT linked to postendodontic pain, suggests study

Use of higher concentrations of NaOCl as irrigant during RCT linked to postendodontic pain, suggests a study published in the Journal of Endodontics.

This study systematically reviewed literature regarding the effect of different concentrations of sodium hypochlorite (NaOCl) used during root canal treatment (RCT) on postendodontic pain (PEP) and rescue analgesia. Following registration with PROSPERO (CRD42023388916), a search was conducted using PubMed, Scopus, Web of Science, and Embase databases. Randomized controlled trials of patients receiving RCT which assessed PEP at different time intervals were included. Following data extraction and Cochrane risk of bias assessment 2, meta-analyses were performed to evaluate PEP during the first 48 hours along with rescue analgesic intake. The certainty of the evidence was evaluated using the Grading of Recommendations, Assessment, Development, and Evaluation approach.

Results: Five randomized controlled trials with 674 patients were included. One study exhibited a low risk of bias, while 4 raised some concerns. Patients treated with low concentrations of NaOCl (≤3%) were significantly less likely to report PEP at 24 hours (OR = 2.32; [95% CI, 1.63–3.31]; P < .05) and 48 hours (OR = 2.49; [95% CI, 1.73–3.59]; P < .05) as compared with high concentrations of NaOCl (≥5%). Furthermore, with low concentrations of NaOCl, significantly lesser moderate-severe PEP was reported at 24 hours (OR = 2.32; [95% CI, 1.47–3.62]; P < .05) and 48 hours (OR = 2.35; [95% CI, 1.32–4.16]; P < .05) and lesser analgesia was needed (OR = 2.43; [95% CI, 1.48–4.00]; P < .05).

While PEP can be influenced by several factors, low certainty evidence suggests that when NaOCl is used as an irrigant during RCT, PEP may be less likely with lower concentrations of NaOCl. Moderate certainty evidence indicates that lesser analgesia may be required with lower concentrations of NaOCl. These results should be cautiously interprete

Reference:

Sodium Hypochlorite Concentration and Postendodontic Pain – Unveiling the Optimal Balance: A Systematic Review and Meta-Analysis. Prasad, Niharika et al.. Journal of Endodontics, Volume 50, Issue 9, 1233 – 1244

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