Long term consumption of dark chocolate beneficial in preventing retinal vascular disease, reveals research

Research published in Scientific Reports reveals that long-term consumption of dark chocolate is beneficial in preventing retinal vascular disease.

There is a lack of knowledge about the effect of flavanols-rich dark chocolate intake on the anatomy and functionality of retinal vessels. The aim of this study prospective, randomized, blind, crossover clinical trial (ClinicalTrials.gov Identifier: NCT05227248, 07/02/2022) was to evaluate the effect of dark-chocolate intake on the functionality and anatomy of the retinal vessels in healthy subjects using dynamic vessel analyzer (DVA) and optical coherence tomography angiography (OCT-A). Twenty eyes of 20 healthy subjects (mean age, 24.4 ± 1.6 years; 12 females) were enrolled. Participants were randomized to consume 20 g of dark chocolate or 7.5 g of milk chocolate. Visual function, DVA and OCT-A parameters were evaluated before chocolate consumption and two hours later. One week later, the same participants were tested before and after consuming the opposite chocolate. Using OCT-A, no differences were disclosed in terms of perfusion density changes after dark-chocolate and milk-chocolate intake analyzing all chorioretinal plexuses (p > 0.09 in all analyses). Using DVA, a significant increase in the arterial dilation percentage after flicker stimulation was disclosed comparing baseline (2.750 ± 2.054%) with values after the dark chocolate intake (4.145 ± 3.055%, p = 0.016). This difference was not disclosed after the milk chocolate intake (p = 0.465). We disclosed that a reasonable amount of flavanols-rich chocolate in healthy subjects has benefic functional short-term effects in retinal vessels measured with DVA. This suggests a potential role of dark chocolate intake on retinal vessels. Further studies with long-term follow-up are warranted to show if the chronic assumption of dark chocolate could play a favorable role in the prevention of retinal diseases.

Reference:

Sacconi, R., Pezzella, M., Ribarich, N. et al. Benefits of dark chocolate intake on retinal vessels functionality: a randomized, blind, crossover clinical trial. Sci Rep 14, 20203 (2024). https://doi.org/10.1038/s41598-024-70289-7

Keywords:

Long term, consumption, dark chocolate, beneficial, preventing, retinal, vascular, disease, reveals, research, Scientific Reports, Sacconi, R., Pezzella, M., Ribarich, N.

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Preoperative Carbohydrate Drinks Improve Safety and Recovery in Elective Cesarean: Study Reveals

India: Recent research highlights the potential benefits of preoperative carbohydrate loading in preventing perioperative ketoacidosis during elective cesarean deliveries. The study suggests that administering an oral carbohydrate drink two hours before surgery can enhance clinical outcomes, providing a safer approach for patients.

“An oral carbohydrate (CHO) drink is safe to administer two hours before uncomplicated elective cesarean deliveries and may positively impact various perioperative clinical outcome markers,” the researchers wrote in the Journal of Anaesthesiology Clinical Pharmacology.

Long periods of fasting during the third trimester of pregnancy can be harmful, as they may cause hypoglycemia, elevated free fatty acid (FFA) levels, and increased ketones in the blood and urine. In these cases, preoperative carbohydrate-rich drinks may help. The Enhanced Recovery After Surgery (ERAS) guidelines suggest offering oral CHO fluid supplementation to nondiabetic pregnant women two hours before a cesarean delivery.

Against the above background, Ankita Sharma, Dayanand Medical College, Ludhiana, Punjab, All India Institute of Medical Sciences Bathinda, Punjab, India, and colleagues aimed to evaluate the effectiveness of preoperative oral CHO loading in preventing perioperative ketoacidosis during elective cesarean deliveries.

For this purpose, the researchers enrolled 120 parturients classified as American Society of Anesthesiologists (ASA) II/III who were undergoing elective cesarean sections with subarachnoid block (SAB). After providing written informed consent, the participants were divided into two groups of 60. Group A received 400 ml of filtered water two hours before surgery, while Group B received 400 ml of a nonparticulate CHO drink.

The primary outcome measured was the incidence of ketonuria, assessed using the dipstick method. Secondary outcomes included hunger and thirst scores, anxiety levels, dominant hand grip strength, and the quality of recovery scores.

The following were the key findings of the study:

  • Urine ketone levels were positive (+1) in 8.3% of participants in Group A, compared to only 1.7% in the carbohydrate (CHO) group.
  • The CHO group also reported significantly lower hunger and thirst scores and modified Beck’s anxiety scores.
  • Dominant hand grip strength remained stable in both groups.
  • The quality of recovery score was significantly higher in the CHO group.
  • No serious adverse effects were observed in either group.

The researchers wrote, “From our results, we conclude that allowing clear fluids or a nonparticulate carbohydrate drink up to two hours before surgery is safe for the parturient. This practice may help improve preoperative discomfort related to hunger, thirst, and anxiety.”

They further noted, “the quality of recovery regarding postoperative experiences such as pain, nausea, vomiting, and overall comfort improved with CHO loading. Thus, administering oral CHO drinks before surgery is safe for elective cesarean deliveries and may positively influence perioperative clinical outcomes.”

Reference:

Sharma A, Singh U, Kaur G, Grewal A, Maingi S, Tidyal S. Role of preoperative carbohydrate loading for prevention of perioperative ketoacidosis in elective cesarean delivery. JAnaesthesiol Clin Pharmacol 2024;40:439-44.

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Outcomes of Immediate implant placement in damaged extraction sockets comparable to conventional implant placement finds study

A study published in Quintessence International found outcomes of immediate implant placement in damaged extraction sockets comparable to conventional implant placement.

This study aimed to observe whether immediate implant placement (IIP) into damaged extraction sockets is a successful modality for treating hopeless teeth that require extraction. An electronic search was carried out through four databases (PubMed/MEDLINE, Web of Science, Scopus, and ScienceDirect) to identify randomized controlled trials (2013-2023) to understand whether IIP in damaged sockets is a successful treatment. The focus question was, ‘In a patient with a hopeless tooth that needs extraction with the indication for dental implant treatment, is IIP in damaged extraction sockets, compared to undamaged sockets or healed sites, an effective method for the replacement of hopeless teeth and achieving a favourable clinical result?’ The risk of bias was appraised and a meta-analysis using random effect was applied. Five studies with 135 patients and 138 implants were included. The implant survival rate was 100% for all studies and periods evaluated; the pink esthetic score (PES) scores had no statistically significant result for all articles that evaluated this parameter; two studies reported the soft tissue changes: one found no significant differences and the other showed that the test group experienced reduced soft tissue loss at the 1-year evaluation (measured with digital intraoral scanners); other two studies assessed the marginal bone loss, presenting no differences between groups. The meta-analysis showed homogeneity between the studies. There was an equilibrium among the groups in the various studies included, and age tended to be lower in the test group. The buccal bone tissue and the pink esthetic score showed favouritism for the test group but without statistical significance. This study suggests that IIP in the presence of buccal bone defects can achieve comparable clinical and radiological outcomes to traditional methods in the short term of the limited studies available. The buccal aspect is not possible to be evaluated through radiographs. Bone regeneration was essential to reach optimal results. It is important to emphasize that IIP requires adherence to rigorous criteria to ensure functionally acceptable results.

Reference:

Campi M, Leitão-Almeida B, Pereira M, Shibli JA, Levin L, Fernandes JCH, Fernandes GVO, Borges T. Immediate implant placement in damaged extraction sockets: a systematic review and meta-analysis of randomized controlled trials. Quintessence Int. 2024 Oct 1;0(0):0. doi: 10.3290/j.qi.b5768294. Epub ahead of print. PMID: 39351790.

Keywords:

Outcomes, Immediate, implant, placement, damaged, extraction, sockets, comparable, conventional, implant, placement, finds, study, Campi M, Leitão-Almeida B, Pereira M, Shibli JA, Levin L, Fernandes JCH, Fernandes GVO, Borges T, Buccal bone defect; Compromised extraction sockets; Dental implants; Fresh sockets; Immediate implant placement.

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Compound from mushroom new colorectal cancer therapy, reveals surgery

Novel chemical compounds from a fungus could provide new perspectives for treating colorectal cancer, one of the most common and deadliest cancers worldwide. In the journal Angewandte Chemie, researchers have reported on the isolation and characterization of a previously unknown class of metabolites (terpene-nonadride heterodimers). One of these compounds effectively kills colorectal cancer cells by attacking the enzyme DCTPP1, which thus may serve as a potential biomarker for colorectal cancer and a therapeutic target.

Rather than using conventional cytostatic drugs, which have many side effects, modern cancer treatment frequently involves targeted tumor therapies directed at specific target molecules in the tumor cells. However, the prognosis for colorectal cancer patients remains grim-there is a need for new targets and novel drugs.

Targeted tumor therapies are mostly based on small molecules from plants, fungi, bacteria, and marine organisms. About half of current cancer medications were developed from natural substances. A team led by Ninghua Tan, Yi Ma, and Zhe Wang at the China Pharmaceutical University (Nanjing, China) chose to use Bipolaris victoriae S27, a fungus that lives on plants, as the starting point in their search for new drugs.

The team first analyzed metabolic products by cultivating the fungus under many different conditions (OSMAC method, one strain, many compounds). They discovered twelve unusual chemical structures belonging to a previously unknown class of compounds: terpene-nonadride heterodimers, molecules made from one terpene and one nonadride unit. Widely found in nature, terpenes are a large group of compounds with very varied carbon frameworks based on isoprene units. Nonadrides are nine-membered carbon rings with maleic anhydride groups. The monomers making up this class of dimers termed “bipoterprides” were also identified and were found to contain additional structural novelties (bicyclic 5/6-nonadrides with carbon rearrangements).

Nine of the bipoterprides were effective against colorectal cancer cells. The most effective was bipoterpride No. 2, which killed tumor cells as effectively as the classic cytostatic drug Cisplatin. In mouse models, it caused tumors to shrink with no toxic side effects.

The team used a variety of methods to analyze the drug’s mechanism: bipoterpride 2 inhibits dCTP-pyrophosphatase 1 (DCTPP1), an enzyme that regulates the cellular nucleotide pool. The heterodimer binds significantly more tightly than each of its individual monomers. The activity of DCTPP1 is elevated in certain types of tumors, promoting the invasion, migration, and proliferation of the cancer cells while also inhibiting programmed cell death. It can also help cancer cells to resist treatment. Bipoterpride 2 inhibits this enzymatic activity and disrupts the-pathologically altered-amino acid metabolism in the tumor cells.

The team was thus able to identify DCTPP1 as a new target for the treatment of colorectal cancer and bipoterprides as new potential drug candidates.

Reference:

Dr. Li Feng, Xinjia Wang, Xinrui Guo, Liyuan Shi, Shihuang Su, Xinjing Li, Dr. Jia Wang, Prof. Ninghua Tan, Prof. Yi Ma, Prof. Zhe Wang, Identification of Novel Target DCTPP1 for Colorectal Cancer Therapy with the Natural Small-Molecule Inhibitors Regulating Metabolic Reprogramming, Angewandte Chemie International Edition, https://doi.org/10.1002/anie.202402543.

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Mini-PCNL Safe and Effective for Treating Kidney Stones in Children: Study Reveals

Iraq: A recent study published in Urolithiasis Journal has highlighted the safety and efficacy of miniaturized percutaneous nephrolithotomy (mini-PCNL) as a treatment for kidney stones in pediatric patients. This innovative surgical technique offers a minimally invasive option for addressing renal stones, which can cause significant discomfort and complications if left untreated.

The study found that mini-PCNL is safe and achieves a high stone-free rate, making it an appealing choice for patients and healthcare providers.

“In patients with stones larger than 15 mm, the stone-free rate was 87.01%, comparable to the 88.57% observed in adults. Although adults experienced a slightly greater drop in hemoglobin levels, there were no significant differences in complications, including blood transfusions, postoperative fever, or the need for additional interventions,” the researchers wrote.

Mini-PCNL is a refined version of traditional percutaneous nephrolithotomy (PCNL), designed specifically for children. It employs smaller instruments and accesses the kidney through a tiny incision, reducing tissue damage and recovery time. Waleed N. Jaffal, College of Medicine, University of Anbar, Ramadi, Al Anbar, Iraq, and colleagues aimed to evaluate the safety and efficacy of mini-PCNL for treating renal stones in children.

For this purpose, the researchers enrolled 77 patients under the age of 15 with renal stones larger than 15 mm in a prospective case-controlled study conducted at Al-Ramadi Teaching Hospital, Ar Razi Private Hospital, and Ghazi Al-Hariri Hospital for Surgical Specialties in Anbar and Baghdad, Iraq, from January 2020 to January 2024. This group, referred to as group A, was compared to a control group (group B) comprising 70 adult patients aged 18 to 60. Both groups underwent mini-PCNL procedures.

The study compared various factors, including gender, stone size, and location, operation time, stone-free rate, hemoglobin drop, need for blood transfusion, incidence of postoperative fever, any associated visceral injuries, and the requirement for further interventions such as extracorporeal shock wave lithotripsy or flexible ureteroscopy (ESWL or FURS).

The following were the key findings of the study:

  • The ages of patients in group A ranged from 8 months to 15 years, with a mean of 4.30 ± 3.16 years, while group B included adults aged 18 to 60 years, with a mean age of 36.3 ± 12.0 years.
  • There were no significant differences in gender distribution, stone size, or location.
  • The stone-free rate was 87.01% for group A and 88.57% for group B, showing no statistical difference.
  • The average hemoglobin drop was 1.096 ± 0.412 in group A and 1.195 ± 0.110 in group B.
  • Blood transfusions were required in one case from each group, with no significant difference.
  • There were three cases in group A and two in group B needing ESWL, with no statistical difference between the groups.
  • FURS was required in four cases in group A and three in group B.
  • The operative time ranged from 30 to 125 minutes for group A and from 34 to 129 minutes for group B.
  • Postoperative fever occurred in 23 cases in group A and 21 cases in group B (p-value 0.986).
  • Minor liver injuries were reported in one case from each group.

“The findings indicate that mini-PCNL is a safe and effective method for treating renal stones in children, with a low rate of significant complications and a high stone-free rate,” the researchers concluded.

Reference:

Jaffal, W.N., Al-Timimi, H.F.H., Hassan, O.A. et al. The safety and efficacy of miniaturized percutaneous nephrolithotomy in children. Urolithiasis 52, 142 (2024). https://doi.org/10.1007/s00240-024-01643-7

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Medication and cognitive behavioral therapy can reduce fatigue among MS patients, finds study

In a study of commonly used treatments for people with multiple sclerosis, both medical and behavioral interventions, and a combination of the two, resulted in meaningful improvements in fatigue, a University of Michigan-led study finds.

The randomized clinical trial compared the effectiveness of modafinil, a wake-promoting medication used to treat sleepiness in people with sleep disorders, and cognitive behavioral therapy, or CBT, on reducing fatigue for over 300 adults with multiple sclerosis whose symptoms interfered with their daily activities.

Overall, investigators found that treatment with either modafinil or CBT alone, which was delivered over the phone, was associated with significant reductions of fatigue over 12 weeks.

A combination of both treatments also worked as well as each individual treatment but did not result in better fatigue scores than the independent interventions.

The findings are published in The Lancet Neurology.

“Fatigue is one of the most common and debilitating symptoms of multiple sclerosis, yet there is still uncertainty about how available treatments should be used or how medication-based treatments compare to behavioral treatments in the real world” said first author Tiffany J. Braley, M.D., M.S., director of the Multiple Sclerosis/Neuroimmunology Division and co-founder of the Multidisciplinary MS Fatigue and Sleep Clinic at University of Michigan Health.

“This research offers new evidence to show that both CBT and modafinil are comparably effective for MS fatigue, which could shape treatment approaches to one of the most challenging symptoms experienced by people with multiple sclerosis.”

Of nearly 3 million people with multiple sclerosis worldwide, up to 90% experience fatigue. Nearly half describe it as their most disabling and impactful symptom.

The research used a real world approach that more closely resembled clinical practice than traditional clinical trials and included stakeholders with MS who helped design the study.

More than 60% of participants in each group of the study reported clinically meaningful improvement in fatigue, which was measured with a survey called the Modified Fatigue Impact Scale.

“These treatments, both individually and as a combination, should be considered as potential options for people with multiple sclerosis with chronic, problematic fatigue,” said senior author Anna L. Kratz, Ph.D., professor of physical medicine and rehabilitation at U-M Medical School.

Braley and Kratz co-led the study, which was funded by the Patient-Centered Outcomes Research Institute.

Collaborators at a secondary study site, the University of Washington, contributed to this pragmatic trial.

“This study focused intently on patient-centered outcomes, and our findings highlight the importance of shared decision making about treatment selection, with consideration of patient characteristics and broader treatment goals,” Braley said.

Trial participants who received only CBT maintained lower fatigue scores at an additional follow-up appointment 12 weeks after the study treatments ended.

CBT has shown robust and durable effects on fatigue in previous research.

“While many people with multiple sclerosis have limited access to behavioral health care like CBT, offering the treatment through telehealth can help reach more patients,” Kratz said.

“Our study shows that CBT is a feasible treatment that teaches fatigue management skills that can be employed indefinitely, with enduring benefits that last well beyond the treatment period.”

Although the three treatment assignments worked similarly well overall, participants’ sleep habits, or “sleep hygiene”, affected how well the treatment worked for fatigue.

Those with poor sleep hygiene tended to have better fatigue outcomes with CBT, and participants with very good sleep hygiene showed better fatigue outcomes with modafinil.

“Using wake promoting medications such as modafinil could worsen sleep quality in patients whose sleep problems are behavioral in nature,” Braley said.

“As sleep disturbances also contribute to fatigue in people with MS, it is important to avoid selecting fatigue treatments that could make sleep worse. Behavioral treatments such as CBT that include sleep education may be preferable for people with MS who have poor sleep habits.”

Reference:

Braley, Tiffany J et al., Comparative effectiveness of cognitive behavioural therapy, modafinil, and their combination for treating fatigue in multiple sclerosis (COMBO-MS): a randomised, statistician-blinded, parallel-arm trial, The Lancet Neurology, DOI:10.1016/S1474-4422(24)00354-5 

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Benzodiazepine Use in Ischemic Stroke Patients: Decline in Initiation, Yet Excess Supply Persists, Study Reveals

USA: A recent study examining benzodiazepine utilization among ischemic stroke survivors highlights concerning trends in prescription practices. Despite a gradual decline in the initiation of benzodiazepine therapy from 2013 to 2021, researchers found a continued over-prescription of these medications following discharge from acute ischemic stroke care. This situation raises significant questions about the appropriateness of benzodiazepine use in this vulnerable population.

The researchers noted, “Although there was a gradual decrease in the initiation of benzodiazepine prescriptions from 2013 to 2021, the findings revealed an excessive supply of these medications following discharge after an acute ischemic stroke. This situation highlights the urgent need for better prescribing policies.”

The findings were published online on October 17, 2024, in Stroke, the official journal of the American Heart Association (AHA).

Benzodiazepines are commonly prescribed for anxiety, insomnia, and other conditions, but they come with risks, particularly for older adults and those recovering from significant medical events like a stroke. The potential for dependency, increased risk of falls, and cognitive impairment are particularly concerning in stroke survivors, who may already face challenges related to mobility and mental health. While guidelines recommend against prescribing to individuals aged 65 and older, there is limited knowledge about national prescription patterns in this demographic.

To fill this knowledge gap, Julianne D. Brooks, Department of Neurology, Massachusetts General Hospital, Harvard Medical School, Boston, and colleagues aimed to analyze the patterns of benzodiazepine prescriptions among ischemic stroke survivors, particularly focusing on the prevalence of excessive supply following discharge and examining longitudinal trends in usage, especially in patients aged 65 and older, where guidelines recommend against such prescriptions.

For this purpose, the researchers analyzed a 20% sample of Medicare claims from April 1, 2013, to September 30, 2021. They focused on beneficiaries aged 65 and older who were discharged alive after an acute ischemic stroke and had traditional Medicare coverage, along with six months of prior enrollment in Parts A (hospital insurance), B (medical insurance), and D (drug coverage).

Individuals with prior benzodiazepine prescriptions, those who self-discharged, or those discharged to skilled nursing facilities were excluded from the study. The researchers analyzed demographics, comorbidities, the duration of initial prescription supplies, and the cumulative incidence of benzodiazepine fills within 90 days after discharge. They also analyzed geographic and yearly trends.

The study led to the following findings:

  • The study included 126,050 beneficiaries with a mean age of 78 years (SD, 8), of whom 54% were female and 82% were White.
  • Within 90 days post-discharge, 6,127 individuals (4.9%) started a benzodiazepine.
  • Among the new prescriptions, lorazepam (40%) and alprazolam (33%) were the most commonly prescribed.
  • Most initial fills (76%) were supplied of more than 7 days, with 55% offering between 15 and 30 days.
  • The initiation rates were higher for females (5.5%) than males (3.8%).
  • Geographically, initiation rates were highest in the Southeast (5.1%) and lowest in the Midwest (4.0%), with a modest decline in nationwide initiation rates from 2013 to 2021 (cumulative incidence difference of 1.6%).

“While the number of new prescriptions decreased over the study period, the total supply of benzodiazepines remained disproportionately high. This discrepancy suggests that many patients continue to receive these medications even when they may not be clinically justified,” the researchers concluded.

Reference:

Lomachinsky Torres V, et al “Benzodiazepine utilization in ischemic stroke survivors: analyzing initial excess supply and longitudinal trends” Stroke 2024; DOI: 10.1161/STROKEAHA.124.047257.

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Delta neutrophil index promising biomarker for detecting fetal growth restriction processes and its complications, finds study

A study published in the BMC Pregnancy and Childbirth found that the delta neutrophil index is a promising biomarker for detecting fetal growth restriction processes and their complications.

This study investigates the role of Delta Neutrophil Index (DNI), an inflammation marker, in late-onset fetal growth restriction (LO-FGR) and its prediction of composite adverse neonatal outcomes. A retrospective study was conducted on 684 pregnant women (456 with normal fetal development and 228 with LO-FGR) who delivered at Health Sciences University Etlik Zubeyde Hanim Women’s Health Training and Research Hospital between January 1, 2015, and June 30, 2018. Composite adverse neonatal outcomes were defined as at least one of the following: 5th minute APGAR score < 7, respiratory distress syndrome (RDS), or neonatal intensive care unit (NICU) admission. Results: The FGR group had significantly higher levels of neutrophil to lymphocyte ratio (NLR), platelet to lymphocyte ratio (PLR), monocyte to lymphocyte ratio (MLR), and DNI compared to controls (p < 0.05, for all). For FGR diagnosis, the DNI demonstrated the highest area under the curve (AUC = 0.677, 95% CI: 0.642–0.711) with a cut-off value of > -2.9, yielding a sensitivity of 78.41%, a specificity of 52.97%, a positive likelihood ratio (+ LR) of 1.68, and a negative likelihood ratio (-LR) of 0.37 (p < 0.001). For predicting composite adverse neonatal outcomes in the FGR group, DNI again demonstrated superior performance with an AUC of 0.635 (95% CI: 0.598–0.670), a cut-off value of > -2.2, a sensitivity of 69.90%, a specificity of 55.36%, a + LR of 1.56, and a -LR of 0.51 (p < 0.001). NLR, PLR, and MLR had AUCs below 0.55, indicating poor discriminative ability, with none reaching statistical significance. This study highlights the potential role of DNI as a promising biomarker for detecting inflammatory processes associated with LO-FGR and its complications.

Reference:

Tonyali, N.V., Sarsmaz, K., Bayraktar, B. et al. Delta neutrophil index (DNI) as a potential biomarker for fetal growth restriction: insights from maternal hematological changes and neonatal outcomes. BMC Pregnancy Childbirth 24, 655 (2024). https://doi.org/10.1186/s12884-024-06853-w

Keywords:

Delta, neutrophil, index, promising, biomarker, detecting, fetal, growth, restriction, processes, its complications, finds, study, BMC Pregnancy and Childbirth, Tonyali, N.V., Sarsmaz, K., Bayraktar, B, Fetal growth restriction, Delta neutrophil index, Neutrophil to lymphocyte ratio, Platelet to lymphocyte ratio, Monocyte to lymphocyte ratio, Perinatal outcomes

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AIIMS Releases Date Sheet Of DM, MCh Professional Exams December 2024, Details

New Delhi : Through a recent notice, the AIIMS has released the Schedule of Post Graduate/Post Doctoral – DM/MCh Professional Examinations planned to be held in December 2024.

All Candidates are advised to submit their Examination Fees before the last date of Registration (to be announced later) and take a print out of Admit Card form the website, the AIIMS stated in the notice.

No Candidate will be permitted to enter the examination hall without Admit Card and Identity Card. No candidate will be allowed to enter the Examination Hall after the entry time mentioned in the Admit Card, the notice added.

The students must note that the List of Speciality will be published separately.  

I.
THEORY EXAMINATIONS
Date Day Paper
No.
Courses Venue
& Time
03.12.2024 Tuesday I DM/M.Ch Examination
Section Convergence Block, 1st Floor, AIIMS, New Delhi 9:30 AM to 12:30 PM
05.12.2024 Thursday II -do-
07.12.2024 Saturday III -do-
II.
PRACTICAL/ CLINICAL/ VIVA VOCE EXAM
DM/M.Ch Concerned
Department will fix the date, time and venue likely from 10 th December,2024
(Tuesday)to 17 th December,2024 (Tuesday)

Also Read:AIIMS INI SS January 2025: DM, MCh Seats added to AIIMS Bhubaneswar, check details

An Act of Parliament in 1956 established the All India Institute of Medical Sciences (AIIMS) as an autonomous institution of national importance and defined its objectives and functions. By virtue of this Act, the Institute awards its own medical degrees and other academic distinctions. The degrees awarded by the Institute under the All India Institute of Medical Sciences Act are recognized medical qualifications for the purpose of the Indian Medical Council Act and notwithstanding anything contained therein, are deemed to be included in the first schedule of that Act, entitling the holders to the same privileges as those attached to the equivalent awards from the recognized Universities of India.

To view the official Notice, Click here :  https://medicaldialogues.in/pdf_upload/dm-mch-date-sheet-dec-2024-for-net-256193.pdf

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AstraZeneca gets CDSCO Panel nod to study Budesonide, Glycopyrronium and Formoterol Fumarate

New Delhi: The drug major AstraZeneca has got approval from the Subject Expert Committee (SEC) functional under the Central Drug Standard Control Organisation (CDSCO) to conduct the phase III clinical study of Budesonide, Glycopyrronium, and Formoterol Fumarate.

This came after the firm presented Phase III clinical study protocol No. : D5989C00001: CSP Version 2.0 dated 28 Jan 2024. Addendum IND-1, Version 1.0, 10 Jan 2024.

This is a randomized, double-blind, parallel-group, multi-center, Phase III study to assess the efficacy of Budesonide, Glycopyrronium, and Formoterol Fumarate metered dose inhalers relative to Glycopyrronium and Formoterol Fumarate MDI on cardiopulmonary outcomes in Chronic Obstructive Pulmonary Disease.

Budesonide, glycopyrrolate, and formoterol combination is used as long-term maintenance treatment of chronic obstructive pulmonary disease (COPD), including chronic bronchitis and emphysema. This medicine helps improve and reduce the number of flare-ups of the symptoms of COPD.

Inhaled budesonide belongs to the family of medicines known as corticosteroids (cortisone-like medicines). It works by preventing inflammation (swelling) in the lungs that causes an asthma attack.

Glycopyrrolate and formoterol are long-acting bronchodilators. Bronchodilators are medicines that are breathed in through the mouth to open up the bronchial tubes (air passages) in the lungs. They relieve coughing, wheezing, and trouble breathing by increasing the flow of air through the bronchial tubes.

At the recent SEC meeting for pulmonary held on 3rd October 2024, the expert panel reviewed the Phase III clinical study protocol No. : D5989C00001: CSP Version 2.0 dated 28 Jan 2024. Addendum IND-1, Version 1.0, 10 Jan 2024.

After detailed deliberation, the committee recommended a grant of permission to conduct the trial as presented by the firm.

Also Read:Soon, harsher penalties for submitting false data for drug approval

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