NEET MDS 2024: AFMS Issues Notice For Sponsored Dental Officers Seeking PG Dental Admissions

New Delhi- Armed Forces Medical Services (AFMS) released a notice for Dental Officers sponsored by Paramilitary Organisations and other Organisations of the Government of India for Postgraduate Courses for MDS through the National Eligibility-Entrance Test-Master of Dental Surgery (NEET-MDS) 2024 exam at AFMS Institute for the year 2024.

AFMS primarily conducts postgraduate training for doctors (Dental Officers) of the Armed Forces Medical Services, to meet the specialist requirements of the Armed Forces Medical Services. On this, additional seats, if any, are offered to sponsored candidates from friendly foreign countries, paramilitary organisations/other organisations of the Government of India, ex-SSC officers of AFMS and civilian doctors.

As per the notice, the ‘Sponsorship Certificate’ of the candidates along with required supporting documents duly endorsed by the competent authority is to be consolidated and forwarded by the concerned Ministry/Headquarters of Paramilitary Organisations/Headquarters of other Government of India Organisations to DGAFMS Office. Only correspondence received through official channels will be accepted and personal correspondence from candidates will not be accepted.

Meanwhile, the Sponsorship Certificate is to be filled as per the guidelines mentioned below-

1 Original ink signed by the Competent Authority (not below the rank of Director or equivalent) in the respective Ministry of Govt of India/ HQ of the Para Military organisation/ Head office of other GoI organisations in which the individual is employed.

2 Duly affixed with the rubber stamp & office seal of the Competent Authority.

3 It is mandatory to specify the subjects for which the candidate (Dental Surgeon) is being sponsored. The candidates are advised to select, during counselling, only the subjects for which they have been sponsored by their respective Ministry/ HQ of Para Military organization/ Head office of other GoI organizations. Under no circumstances will admission be granted in a subject which has not been sponsored by the sponsoring authority.

4 For the upcoming NEET MDS exam, the last date for the sponsorship certificate, from the respective Ministry/ HQ of Para Military organisation/ Head office of other GoI organisations, to reach this office is 05 Jul 2024.

5 Online counselling, consisting of registration, payment, choice filling/ locking and provisional seat allotment for Priority-III, IV & V candidates, for the academic session 2024-27, will be conducted by MCC through their web portal/ website. Seat allotment during counselling by MCC is provisional and subject to fulfilment of all eligibility criteria. The list of candidates eligible for counselling will be forwarded to MCC by this office for counselling and provisional seat allotment.

6 Priority-III candidates will be considered eligible for admission in AFMS Institutions only for those subjects, which are mentioned in their sponsorship certificate as forwarded by the respective sponsoring authority. In case a Priority-III candidate is allotted a seat, during the counselling conducted by the MCC, which is not mentioned in the Sponsorship Certificate forwarded by the sponsoring organization, admission to AFMS PG Teaching Institutes would not be granted and the candidate would be liable to suffer the consequences.

However, the official address to which the sponsorship certificates are to be submitted by the respective Ministry/ HQ of the Para Military organizations/ Head office of other GoI organizations and the email ID for communication and queries are mentioned in the notice.

To view the notice, click the link below

https://medicaldialogues.in/pdf_upload/need-mds-2024-afms-issues-notice-for-sponsored-dental-officers-seeking-pg-dental-admissions-242448.pdf

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Mezagitamab Delivers Strong Platelet Response and Safety Profile in Immune Thrombocytopenia Treatment: Study

USA: Promising findings from the Phase 2b TAK-079-1004 study have been unveiled by Takeda Pharmaceuticals at the 32nd Congress of the International Society on Thrombosis and Haemostasis (ISTH), showcasing the efficacy of mezagitamab (TAK-079) in patients with persistent or chronic primary immune thrombocytopenia (ITP).

According to late-breaking data announced on June 22, 2024, patients treated with mezagitamab demonstrated significant and sustained increases in platelet counts across all dose levels, accompanied by a favorable safety profile consistent with earlier trials.
Dr. David Kuter, presenting the results, emphasized the pressing need for effective treatments in ITP, stating, “Despite current therapies, there remains a substantial disease burden and demand for well-tolerated disease-modifying treatments.”
ITP, a rare autoimmune disorder characterized by accelerated platelet destruction due to autoantibodies, poses significant health risks including bleeding complications. Regulatory approval benchmarks for new ITP therapies require sustained platelet counts ≥50,000/µL.
Mezagitamab, an IgG1 monoclonal antibody targeting CD83-expressing cells, aims to swiftly restore and maintain functional platelet levels. The US FDA has previously granted Orphan Drug Designation and Fast Track Designation to mezagitamab for treating chronic or persistent ITP.
The Phase 2b trial evaluated subcutaneous mezagitamab across three dose cohorts (100 mg, 300 mg, and 600 mg) versus placebo over an 8-week treatment period, followed by a safety follow-up of at least eight weeks. Primary endpoints included incidences of severe treatment-emergent adverse events (TEAEs), serious adverse events (SAEs), and adverse events leading to drug discontinuation. Secondary endpoints focused on platelet response rates and clinical significance.
Results from the interim analysis revealed that mezagitamab significantly improved platelet response compared to placebo across all dose groups, maintaining responses above therapeutic thresholds through Week 16 post-treatment. The highest response rates were observed in the 600 mg cohort, with 81.8% achieving complete platelet response, 90.9% showing clinically meaningful response, and all patients achieving hemostatic response.
Safety outcomes demonstrated favorable profiles, with no new safety concerns identified and fewer bleeding-related adverse events in the mezagitamab group compared to placebo. Rates of TEAEs leading to discontinuation and severe TEAEs were higher in the mezagitamab cohorts, but consistent with expected profiles from previous studies.
Dr. Kuter expressed optimism about mezagitamab’s potential, affirming, “These Phase 2b findings highlight its efficacy and safety, positioning it as a leading candidate for ITP treatment.”
Takeda plans to advance mezagitamab into a global Phase 3 trial for ITP in late FY2024, signaling a commitment to address unmet patient needs with innovative therapeutic solutions.
“It is a privilege to have these Phase 2b mezagitamab results selected for presentation as a late-breaking abstract at the ISTH Congress,” said Obi Umeh, M.D., M.Sc., Vice President, Franchise Global Program Leader at Takeda. “Based on these results, we plan to initiate a Phase 3 study of mezagitamab in ITP in the second half of FY2024, further underscoring our goal to develop transformative treatments in therapeutic areas with high unmet patient needs.”

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One in Four Patients with Difficult-to-Control Type 2 Diabetes Experience High Levels of Cortisol: ADA

Today, findings from the CATALYST study reveal that hypercortisolism may be a significant factor for why type 2 diabetes (T2D) remains difficult to control for many patients. This study found that 24% of individuals with difficult-to-control type 2 diabetes have hypercortisolism, a condition characterized by high cortisol levels. The results were presented as a late-breaking symposium today at the 84th Scientific Sessions of the American Diabetes Association® (ADA) in Orlando, FL.

Currently, 38.9 to 76.9% of patients with type 2 diabetes have uncontrolled diabetes. Additional research is needed to understand how hypercortisolism may be an underlying contributing cause for difficult-to-control type 2 diabetes. Symptoms of hypercortisolism can include weight gain, high blood pressure, muscle weakness, and mood changes, which can further complicate diabetes management.

The CATALYST study, the largest prospective trial of its kind, screened over 1,000 patients with hemoglobin A1c levels between 7.5% and 11.5% despite multiple diabetes therapies. Researchers used an overnight 1-mg dexamethasone suppression test (DST) to detect hypercortisolism, indicated by a post-DST morning cortisol level above 1.8 μg/dL and a dexamethasone level of 140 ng/dL or higher.

Findings showed presence of hypercortisolism in 24% of the screened patients. Notably, among those taking three or more hypertension medications, the prevalence of hypercortisolism was approximately one in three. Additionally, CT scans revealed adrenal abnormalities in about one-third of these patients, with a quarter having an adrenal tumor, suggesting that surgical intervention could potentially resolve their hypercortisolism and improve diabetes control.

“These results are significant as they highlight a previously underrecognized factor contributing to the barriers when it comes to managing type 2 diabetes,” said John Buse, MD, PhD, from the University of North Carolina School of Medicine Diabetes Center and Translational and Clinical Sciences Institute and lead author of the study. “By identifying hypercortisolism in these patients, we can target treatments more effectively and potentially improve their outcomes.”

The first part of the CATALYST study underscores the importance of screening for hypercortisolism in patients with difficult-to-control type 2 diabetes The ongoing second part of the study aims to evaluate whether treating hypercortisolism medically can enhance diabetes management and alleviate related health issues.

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India ahead of several countries in ensuring One Health Goals, says Dr VK Paul

New Delhi: “India is ahead of several countries in drafting the legal framework to support and strengthen the implementation of the One Health initiative. This represents India’s advanced thought process and leadership, and showcases our vision in this area. A national consultation with multi partners and stakeholders is not only important but very timely. COVID-19 has forced us to re-focus our attention on the importance of zoonotic diseases and the intricate linkages between the human, animal and plan eco-systems.” This was stated by Dr Vinod Paul, Member (Health), NITI Aayog as he recently inaugurated a two-day National Consultation on Legal Environment Assessment for “One Health” initiative.

Shri Apurva Chandra, Secretary, Ministry of Health & Family Welfare (MoHFW), Ms Leena Nandan, Secretary, Ministry of Environment, Forest and Climate Change (MoEFCC), and Shri Rajiv Mani, Secretary, Ministry of Law & Justice were also present.

Also Read:Health Ministry warns against commercial dealings in organ transplantation of foreigners, emphasizes awareness of transplant laws

Dr Vinod Paul stated that the issues of critical health challenges posed by zoonoses, antimicrobial resistance (AMR), food safety, and climate change are interconnected and require a comprehensive, multi-sectoral approach to breaking down the silos between human health, animal health, and environmental sectors. He added that India has taken the lead in ensuring One Health goals that resonate with the Prime Minister’s vision of “One Earth, One Health” and “we are pushing frontiers for not just our nation but for the world”. Dr Paul said that in lined with the need of alignment of various frameworks, India has taken up framing of National Action Plan (NAP), 2.0 for addressing the issues raised due to Antimicrobial resistance (AMR), had conceptualised the One Health Mission, and working on the broader issues of climate change. He further stressed that to ensure the achievement of One Health goals, state engagement, alignment of Indian laws with international laws, and cross-sectoral response are required.

Highlighting that more than 75% of the diseases that affect humans are zoonotic diseases, Shri Apurva Chandra stated that the Ministry of Health & Family Welfare is committed to preventing and managing risks at the human-animal-plant interface through the One Health approach. “‘One Health’ is a multi-sector and multi-stakeholder initiative; collective and coordinated action needed for its success at the ground level”, he stated. He noted that under PM-ABHIM, states are being strengthened in surveillance, prevention and management of zoonotic and other diseases. He reiterated that India’s current legislative framework, with its separate laws for human health, animal health, and environmental protection, has some gaps and overlaps due to sectoral priorities. He also highlighted the importance of support from the line ministries and the States in implementing One Health goals.

Also Read:Prataprao Ganpatrao Jadhav takes charge as MoS for Health, AYUSH Ministry

In her address, Ms. Leena Nandan, Secretary (MoEFCC), stressed on the need for a commonality of approach among different ministries in ensuring the achievement of One Health goals. She assured that the Environment Ministry is committed to making necessary provisions under the existing Acts of wildlife and environment to ensure the health of human beings and the conservation and preservation of wild animals. She stated that the One Health initiative has been one of the main topics of discussion during the G20 under the One Earth, One Family, One Future umbrella. She emphasised on the need for capacity building of the on-ground functionaries and communities for successful implementation of the One Health initiative.

Shri Rajiv Mani re-iterated the support from the Ministry of Law and Justice to assist the stakeholders in making required amendments or changes in the existing laws and policy frameworks to align with the One Health principle and mandates of the country for the protection of the health of all species including animals and the climate.

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Daily intake of multivitamins daily not associated with lower risk of death among healthy adults: Study

A large analysis of data from nearly 400,000 healthy U.S. adults followed for more than 20 years has found no association between regular multivitamin use and lower risk of death. The study, led by researchers at the National Institutes of Health’s National Cancer Institute, was published in JAMA Network Open.

Many adults in the United States take multivitamins with the hope of improving their health. However, the benefits and harms of regular multivitamin use remain unclear. Previous studies of multivitamin use and mortality have yielded mixed results and been limited by short follow-up times.

To more deeply explore the relationship between long-term regular multivitamin use and overall mortality and death from cardiovascular disease and cancer, the researchers analyzed data from three large, geographically diverse prospective studies involving a total of 390,124 U.S. adults who were followed for more than 20 years. The participants included in this analysis were generally healthy, with no history of cancer or other chronic diseases.

Because the study population was so large and included lengthy follow-up and extensive information on demographics and lifestyle factors, the researchers were able to mitigate the effects of possible biases that may have influenced the findings of other studies. For example, people who use multivitamins may have healthier lifestyles in general, and sicker patients may be more likely to increase their use of multivitamins.

The analysis showed that people who took daily multivitamins did not have a lower risk of death from any cause than people who took no multivitamins. There were also no differences in mortality from cancer, heart disease, or cerebrovascular diseases. The results were adjusted for factors such as race and ethnicity, education, and diet quality.

The researchers noted that it is important to evaluate multivitamin use and risk of death among different kinds of populations, such as those with documented nutritional deficiencies, as well as the potential impact of regular multivitamin use on other health conditions associated with aging. 

Reference:

Loftfield E, O’Connell CP, Abnet CC, et al. Multivitamin Use and Mortality Risk in 3 Prospective US Cohorts. JAMA Netw Open. 2024;7(6):e2418729. doi:10.1001/jamanetworkopen.2024.18729.

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Real-time MRI may improve the functional diagnosis of SLL insufficiency: study

Clinical-standard MRI is the imaging modality of choice for the wrist, yet limited to static evaluation, thereby potentially missing dynamic instability patterns.

Lena Marie Wilms et al aimed to investigate the clinical benefit of (dynamic) real-time MRI, complemented by automatic analysis, in patients with complete or partial scapholunate ligament (SLL) tears. The study has been published in ‘Skeletal Radiology’ journal.

Both wrists of ten patients (male: 8; female: 2; mean age: 41.2 ± 18.1 years, age range: 24 – 66 years) with unilateral SLL tears (six partial, four complete tears) as diagnosed by clinical-standard MRI were imaged during continuous active radioulnar motion using a 1.5-T MRI scanner (MAGNETOM Avantoft, Siemens Healthineers, Erlangen, Germany) in combination with a custom-made motion device.

Following automatic segmentation of the wrist, the scapholunate and lunotriquetral joint widths were analyzed across the entire range of motion (ROM). Mixed-effects model analysis of variance (ANOVA) followed by Tukey’s posthoc test and two-way ANOVA were used for statistical analysis.

Key findings of the study were:

• In healthy controls, the scapholunate joint width remained stable at around 2 mm over the entire ROM.

• With the increasing extent of SLL tear, the scapholunate joint widths in injured wrists were significantly larger over the entire ROM compared to those of the contralateral healthy wrists (p<0.001).

• Differences between partial and complete tears were most pronounced at 5°–15° ulnar abduction (p <0.001). Motion patterns and trajectories were altered.

• Complete SLL deficiency resulted in complex alterations of the lunotriquetral joint widths.

The authors concluded – “Real-time MRI may improve the functional diagnosis of SLL insufficiency and aid therapeutic decision-making by revealing dynamic forms of dissociative instability within the proximal carpus. Static MRI best differentiates SLL-injured wrists at 5°–15° of ulnar abduction.

Further reading:

Dynamic assessment of scapholunate ligament status by real time magnetic resonance imaging: an exploratory clinical study Lena Marie Wilms et al Skeletal Radiology (2024) 53:791–800 https://doi.org/10.1007/s00256-023-04466-6

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Can Weight loss plus remission of prediabetes prevent against diabetes?

People with prediabetes are advised to reduce their weight in order to prevent manifest diabetes. Researchers from the Institute for Diabetes Research and Metabolic Diseases of Helmholtz Munich at the University of Tübingen, a partner in the German Center for Diabetes Research (DZD), together with US colleagues in the renowned ”Diabetes Prevention Program (DPP),” have now been able to show for the first time that people achieve the best diabetes protection when they reduce their weight and at the same time normalize blood sugar regulation.

In the specialist journal Diabetologia, the authors argue that the normalization of blood sugar levels in prediabetes should be included as a therapeutic goal in the guidelines in order to improve the prevention of type 2 diabetes.

Diabetes is widespread and is associated with an increased risk of a number of life-threatening complications such as stroke, heart attack and kidney failure. “In order to prevent the development of the disease, early therapies are already important in the prediabetes stage, a preliminary stage of type 2 diabetes. Our results can be used to change the goals of these early lifestyle interventions in order to reduce the overall development rates of diabetes,” explains first author Reiner Jumpertz-von Schwartzenberg.

Prediabetes drastically increases the risk of diabetes

Prediabetes is diagnosed when there is no manifest type 2 diabetes yet, but the fasting blood sugar is already elevated and glucose tolerance is impaired. To prevent prediabetes from becoming diabetes, affected patients are advised to reduce their weight. US guidelines from the American Diabetes Association (ADA), for example, recommend reducing body weight by at least 7 percent. This recommendation is based on the DPP study.

The research team from the Department of Internal Medicine IV, Diabetology, Endocrinology and Nephrology at the Medical University Hospital of Tübingen, the Institute for Diabetes Research and Metabolic Diseases of Helmholtz Munich in Tübingen and the Phoenix Epidemiology and Clinical Research Branch at the National Institute of Diabetes and Digestive and Kidney Diseases in Phoenix, USA, investigated whether this weight loss is sufficient, or whether it is not better to prevent diabetes by also reducing blood sugar levels such that prediabetes goes into remission.

Prevention through one-year lifestyle intervention

They analyzed data from 480 people with prediabetes who participated in the US Diabetes Prevention Program (DPP) and had lost at least 7 percent of their body weight through a one-year lifestyle intervention. In 114 of them, prediabetes also went into remission during the intervention, meaning that their fasting blood sugar, glucose tolerance and HbA1c had normalized. However, the majority of the 366 study participants had not managed to significantly improve their blood sugar regulation despite successfully losing weight. Their prediabetes was not in remission at the end of the intervention.

The researchers found that significantly fewer people in the group that had lost weight and achieved prediabetes remission developed manifest diabetes thereafter. The additional remission of prediabetes resulted in a relative risk reduction for the development of diabetes of 76 percent compared to those who had not achieved normalization of their blood sugar levels. The absolute risk reduction was higher than 10%.

“In the group with additional remission of prediabetes, there was even no type 2 diabetes at all in the first 4 years after the lifestyle intervention,” reports last author Andreas Birkenfeld. “In the group that had ‘only’ lost weight, however, some study participants did develop manifest diabetes during that period.”

Jumpertz-von Schwartzenberg and Birkenfeld draw a clear conclusion: “Our results show that remission of prediabetes brings a further significant benefit in addition to weight reduction. We therefore advocate that the goal of prediabetes remission should be included in the objectives of the practice guidelines in order to significantly improve the prevention of type 2 diabetes.”

References: Jumpertz von Schwartzenberg, R., Vazquez Arreola, E., Sandforth, A. et al. Role of weight loss-induced prediabetes remission in the prevention of type 2 diabetes: time to improve diabetes prevention. Diabetologia (2024). https://doi.org/10.1007/s00125-024-06178-5

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Advancing Quality of Life and Nutritional Outcomes: Stomach-Preserving Surgery for Early Gastric Cancer

South Korea: In a groundbreaking development in oncology, a secondary analysis of the SENORITA randomized clinical trial (RCT) has shed light on the promising outcomes of stomach-preserving surgery for early gastric cancer. The study underscores the significance of preserving gastric function while effectively treating cancer.

The secondary analysis of 451 participants from the Sentinel Node Oriented Tailored Approach (SENORITA) randomized clinical trial revealed that stomach-preserving surgery could be a favorable treatment option for early-stage gastric cancer.

“The stomach-preserving group showed little changes in quality-of-life (QoL) scores and nutritional indicators, which returned to their preoperative values,” the researchers reported. “The stomach-preserving group had significantly better QoL and nutritional outcomes than the standard group.”

The SENORITA RCT evaluated nutritional outcomes and quality of life between the laparoscopic standard gastrectomy (LSG) and laparoscopic sentinel node navigation surgery (LSNNS). However, no study has reported QoL and nutritional outcomes of patients who underwent stomach-preserving surgery among the LSNNS group.

To fill this knowledge gap, Bang Wool Eom, Center of Gastric Cancer, National Cancer Center, Goyang, Republic of Korea, and colleagues aimed to compare long-term nutritional outcomes and QoL between patients who underwent stomach-preserving surgery and those who underwent standard gastrectomy and to identify factors associated with poor QoL outcomes in patients who underwent stomach-preserving surgery.

For this purpose, the research team conducted a secondary analysis of the SENORITA trial, a randomized clinical trial comparing LSNNS with LSG. It enrolled patients from 7 tertiary or general hospitals across the Republic of Korea from 2013 to 2016, with follow-up through 5 years. Among trial participants, the analysis included patients who underwent actual laparoscopic standard gastrectomy in the LSG group and those who underwent stomach-preserving surgery in the LSNNS group. It excluded patients who did not complete the baseline or any follow-up questionnaire.

The main outcomes were overall European Organization for Research and Treatment of Cancer QoL Questionnaire Core 30 (EORTC QLQ-C30) and stomach module (STO22) scores, hemoglobin, body mass index, protein, and albumin levels.

The study included 194 and 257 patients who underwent stomach-preserving surgery and standard gastrectomy, respectively (mean age, 55.6 years; 55.2% were males).

The study led to the following findings:

  • The stomach-preserving group had better QoL scores at three months postoperatively in terms of physical function (87.2 versus 83.9), appetite loss (13.1 versus 19.4), dyspnea (5.9 versus 11.2), dysphagia (8.0 versus 12.7), anxiety (29.0 versus 35.2), eating restriction (10.9 versus 18.2), taste change (7.4 versus 13.0), and body image (19.5 versus 27.2).
  • At one year postoperatively, the stomach-preserving group had significantly higher body mass index (23.9 versus 22.1, calculated as weight in kilograms divided by height in meters squared) and hemoglobin (14.3 versus 13.3 g/dL), albumin (4.3 versus 4.25 g/dL), and protein (7.3 versus 7.1 g/dL) levels compared to the standard group.
  • Multivariable analyses showed that tumor location (greater curvature, lower third) was favorably associated with global health status (β, 10.5), reflux (β, −8.4), and eating restriction (β, −5.7) at three months postoperatively in the stomach-preserving group.
  • Segmental resection was associated with a risk of eating restriction (β, 15.1) and diarrhea (β, 40.6) at 3 years postoperatively.

The study showed that stomach-preserving surgery after sentinel node evaluation was tied to better long-term QoL and nutritional outcomes than standard gastrectomy.

“These findings may help facilitate decision-making regarding treatment for patients with early-stage gastric cancer,” the researchers concluded.

Reference:

Eom BW, Yoon HM, Kim Y, et al. Quality of Life and Nutritional Outcomes of Stomach-Preserving Surgery for Early Gastric Cancer: A Secondary Analysis of the SENORITA Randomized Clinical Trial. JAMA Surg. Published online May 29, 2024. doi:10.1001/jamasurg.2024.1210

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Study Compares Ultra-sonographic neuraxial target window of spine in Different Sitting Positions

Patient positioning is crucial for the successful administration of neuraxial blocks. Recently published study aimed to compare the ultrasonographic dimensions of the spine’s acoustic target window in four different sitting positions, namely cross leg sitting (CLP), hamstring stretch (HSP), classical sitting (CSP), and rider’s sitting position (RSP). The primary objective was to measure the neuraxial acoustic target window, specifically the interlaminar distance between L3-L4 lamina, while the secondary objective was to compare the depth of the ligamentum flavum from the skin, the diameter of the intrathecal space, and the comfort score in the different sitting positions.

The findings of the study revealed that there was no statistically significant difference in the interlaminar distance among the four sitting positions, with a mean interlaminar distance ranging from 1.40 cm to 1.44 cm. This suggests that all four positions are equally effective for spinal/epidural intervention. However, the classical sitting position (CSP) was identified as the most comfortable among the four positions, with a significantly better comfort score compared to the others. As a result, the study emphasized giving more importance to patient comfort during the procedure, as it can increase the success rate of the intervention.

The study also provided insights into the significance of patient positioning in the success of neuraxial blocks and highlighted the importance of ultrasonographic measurements for identifying various dimensions of the acoustic target window of the spine. Additionally, the study compared its findings with previous research and discussed the implications of the results in the context of the Indian population. The study acknowledged its limitations and recommended further research, particularly randomized control trials on the patient population, to provide additional evidence.

Summary and Implications –

In conclusion, the study found that all four sitting positions (CLP, HSP, CSP, RSP) are comparable in terms of the acoustic target window. However, the CSP was identified as the most comfortable position for the participants, indicating that patient comfort should be a crucial consideration in choosing a sitting position for neuraxial block procedures. The study’s comprehensive analysis and comparison of the different positions provide valuable insights for practitioners and researchers in the field of neuraxial anesthesia.

Key Points –

– The study compared the ultrasonographic dimensions of the spine’s acoustic target window in four different sitting positions: cross leg sitting (CLP), hamstring stretch (HSP), classical sitting (CSP), and rider’s sitting position (RSP). The primary objective was to measure the neuraxial acoustic target window, specifically the interlaminar distance between L3-L4 lamina, while the secondary objective was to compare the depth of the ligamentum flavum from the skin, the diameter of the intrathecal space, and the comfort score in the different sitting positions.

– The findings revealed that there was no statistically significant difference in the interlaminar distance among the four sitting positions, suggesting that all four positions are equally effective for spinal/epidural intervention. However, the classical sitting position (CSP) was identified as the most comfortable among the four positions, with a significantly better comfort score compared to the others. The study emphasized the importance of patient comfort during the procedure, as it can increase the success rate of the intervention. Additionally, the study highlighted the significance of patient positioning in the success of neuraxial blocks and the importance of ultrasonographic measurements for identifying various dimensions of the acoustic target window of the spine.

– In conclusion, the study found that all four sitting positions (CLP, HSP, CSP, RSP) are comparable in terms of the acoustic target window. However, the CSP was identified as the most comfortable position for the participants, indicating that patient comfort should be a crucial consideration in choosing a sitting position for neuraxial block procedures. The study’s comprehensive analysis and comparison of the different positions provide valuable insights for practitioners and researchers in the field of neuraxial anesthesia.

Reference –

Singh G, Sethi P, Kaur M, Bhatia P, Garg PK, Kumari K, et al. Comparison of neuraxial acoustic target window of the spine among rider sitting, cross leg, hamstring stretch, and classical sitting position:An observational study. J Anaesthesiol Clin Pharmacol 2024;40:318‑23.

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Case Report of Management of TAFRO Syndrome after Vaccination with Cyclosporine Treatment

Japan: In a rare medical occurrence shedding light on potential post-vaccination complications, a case of TAFRO syndrome has been reported, marking a significant milestone in understanding and treating this elusive condition. The patient’s successful treatment with cyclosporine highlights a promising therapeutic approach in managing TAFRO syndrome, a condition characterized by thrombocytopenia, anasarca (generalized swelling), fever, reticulin fibrosis, and organomegaly.

While previous reports have documented instances of TAFRO syndrome following COVID-19 vaccination, this case is notable for the patient achieving remission and being discharged. Additionally, a renal biopsy was conducted, aligning with findings from prior cases. The positive treatment outcome offers significant insights into managing TAFRO syndrome effectively.
The case, published in BMC Nephrology, concerns an 82-year-old woman who received two doses of the BNT162b2 mRNA vaccine three weeks apart. After two weeks, she was admitted to the hospital with edema accompanied by thrombocytopenia and renal failure.
Following a thorough examination, she received a diagnosis of TAFRO syndrome. She was treated with cyclosporine, steroids, and thrombopoietin receptor agonists. The patient was released from the hospital following a period of remission lasting several months.
TAFRO syndrome is an uncommon condition characterized by generalized edema, thrombocytopenia, organ enlargement, fever, and renal dysfunction.
There have been limited reports linking TAFRO syndrome to vaccines, with few cases undergoing renal biopsy. TAFRO syndrome is frequently severe and can be fatal, and its underlying cause remains unidentified. Here, Yasuyuki Mimura, Hyogo Medical University, 1-1 Mukogawa-Cho, Nishinomiya, Hyogo, Japan, and colleagues presented a case of TAFRO syndrome following vaccination with the COVID-19 vaccine.
“Despite developing TAFRO syndrome post COVID-19 vaccination, a condition known for its severity, the patient responded well to treatment with steroids and cyclosporine, achieving recovery to the extent of being discharged to outpatient care. Any similar post-vaccination condition should prompt consideration of TAFRO syndrome in differential diagnosis,” the researchers wrote.
Various conditions, such as adult multisystemic inflammatory syndrome (MIS-A), systemic capillary leak syndrome (SCLS), and idiopathic thrombocytopenic purpura (ITP) have been linked to COVID-19 vaccines. MIS-A is characterized by cytokine-induced organ inflammation leading to multiorgan damage, while SCLS results in systemic edema due to vascular endothelial cell damage, and ITP causes decreased platelet counts due to the production of antiplatelet antibodies.
In TAFRO syndrome, elevated levels of IL-6, VEGF, and platelet-associated IgG are often observed, similar to this case, suggesting a potential overlap with MIS-A, SCLS, and ITP. When encountering unexplained edema and thrombocytopenia following vaccination, clinicians should consider TAFRO syndrome as part of the differential diagnosis. The case report aims to contribute to understanding the TAFRO syndrome’s pathogenesis.
In conclusion, a case of TAFRO syndrome is reported that progressed rapidly after vaccination with Pfizer’s COVID-19 vaccine but improved to the point that the patient was discharged from the hospital and returned to the hospital as an outpatient after treatment. After reporting this case of TAFRO syndrome and its relation to vaccination, the researchers also reviewed the relevant literature.
Reference:
Mimura, Y., Kojima, K., Fujikawa, A. et al. A case of TAFRO syndrome after vaccination, successfully treated with cyclosporine. BMC Nephrol 25, 196 (2024). https://doi.org/10.1186/s12882-024-03630-x

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