3D MRI sequences useful for better evaluation of recess stenoses of spine: study

Since the 2010s, the isotropic submillimeter 3D sequences have become steadily more available with different MRI devices – these thin-slice sequences offer superior resolution as compared to the conventional thick-slice (roughly 3–4 mm) MRI sequences. However, the adoption of the 3D sequences to the everyday clinical setup has been rather slow, and conventional thick-slice protocols are still widely in use.

Nevalainen et al conducted a systematic literature review on the diagnostic utility of 3D MRI sequences in the assessment of central canal, recess and foraminal stenosis in the spine.

The databases PubMed, MEDLINE (via OVID) and The Cochrane Central Register of Controlled Trials, were searched for studies that investigated the diagnostic use of 3D MRI to evaluate stenoses in various parts of the spine in humans. Three reviewers examined the literature and conducted systematic review according to PRISMA guidelines.

Key findings of the study were:

• Thirty studies were retrieved from 2595 publications for this systematic review.

• The overall diagnostic performance of 3D MRI outperformed the conventional 2D MRI with reported sensitivities ranging from 79 to 100% and specificities ranging from 86 to 100% regarding the evaluation of central, recess and foraminal stenoses.

• In general, high level of agreement (both intra- and inter rater) regarding visibility and pathology on 3D sequences was reported.

• Studies show that well optimized 3D sequences allow the use of higher spatial resolution, similar scan time and increased SNR and CNR when compared to corresponding 2D sequences. However, the benefit of 3D sequences is in the additional information provided by them and in the possibility to save total protocol scan times.

The authors commented – “Strengths of this review include the rigorous assessment of the literature by three academic medical experts: a neuroradiologist, a musculoskeletal radiologist and a medical physicist. Moreover, we applied the PRISMA recommendations for meticulous reporting of our findings. One limitation is that relevant articles might not have been included due to the limited number of databases used in the search or limitations in the search and screening strategy. The most obvious weakness within this systematic review is vast heterogeneity of the included studies, most importantly the lack of surgical gold standard is worrisome. Accordingly, there was no possibility of meta-analysis. Moreover, the fact that no studies on thoracic spine existed in the literature remains as minor weakness.”

The authors concluded – “In conclusion, the literature of the 3D MRI assessment of spinal stenoses is largely heterogeneous with varying MRI protocols and diagnostic results. Generally, 3D sequences offer similar or superior detection of stenoses with high reliability explained by the better visualization of anatomic structures. Ultimately, the benefit of 3D MRI seems to be the better evaluation of recess stenoses which supports the clinical implementation of these sequences into everyday workflow.” 

Further reading:

Diagnostic utility of 3D MRI sequences in the assessment of central, recess and foraminal stenoses of the spine: a systematic review

Mika T. Nevalainen et al

Skeletal Radiology

https://doi.org/10.1007/s00256-024-04689-1

Powered by WPeMatico

Higher income reduces stroke mortality risk by a third, new study shows

New research, presented at the 10th European Stroke Organisation Conference (ESOC) 2024, has revealed that high-income individuals have a 32% lower risk of post-stroke mortality. Additionally, those with a higher education have a 26% lower risk of death post-stroke, highlighting striking disparities in stroke survival based on key social determinants of health (SDoH).

The register-based study analysed data from 6,901 stroke patients in Gothenburg, Sweden between November 2014 to December 2019 to examine the impact of SDoH factors on post-stroke mortality risk. The study focused on four SDoH factors: living area, country of birth, education and income.

As well as identifying a significant connection between income, education level and post-stroke mortality risk, the study uncovered a concerning trend regarding the cumulative impact of SDoH factors. Patients with one unfavourable SDoH factor faced an 18% higher risk of mortality compared to patients without any unfavourable SDoH factors. This risk escalated to 24% for patients with two to four SDoH factors.

Lead author Professor Katharina Stibrant Sunnerhagen, University of Gothenburg, Clinical Neuroscience, Gothenburg, Sweden, comments, “Our findings underscore a stark reality – an individual’s socioeconomic status can be a matter of life or death in the context of stroke, especially when they are confronted with multiple unfavourable SDoH factors. While our study was conducted in Gothenburg, we believe these insights resonate across Europe, where similar healthcare structures and levels of social vulnerability exist, highlighting a pervasive issue throughout the continent.”

The study also found a link between increased mortality risk and additional risk factors like physical inactivity, diabetes, alcohol abuse and atrial fibrillation.

Notably, insights emerged regarding gender disparities and the potential impact of risk factors when examining patient characteristics within the study cohort. The proportion of female patients increased with the number of unfavourable SDoH factors; 41% of the group with no unfavourable SDoH factors were female, whereas 59% of the group with two to four unfavourable SDoH factors comprised females. Additionally, smoking, whether current or within the past year, was more prevalent in the group with two to four unfavourable SDoH factors compared to those with none (19% versus 12%).

Commenting on the actions required to reduce the future stroke burden, Professor Stibrant Sunnerhagen explains, “As the number of people affected by stroke in Europe is projected to rise by 27% between 2017 and 2047, the need for effective interventions is more pressing than ever.2 In light of our study’s findings, targeted strategies are essential. Policymakers, for instance, must tailor legislation and approaches to account for the specific circumstances and needs of diverse communities, while clinicians should consider identifying patients with unfavourable SDoH factors to prevent post-stroke mortality.”

“By addressing these disparities, we will not only support the principles of health equity, but also have the potential to significantly enhance public health outcomes.”

Reference:

Higher income reduces stroke mortality risk by a third, new study shows, Beyond, Meeting: European Stroke Organisation Conference (ESOC) 2024.

Powered by WPeMatico

Plastic wound protector scores over surgical gauze in surgical site infection reduction: unveils clinical trial

Korea: In the realm of surgical procedures, minimizing postoperative complications remains a top priority for medical practitioners worldwide. Among the myriad of concerns, surgical site infections (SSIs) stand out as a significant threat to patient recovery and well-being. In a groundbreaking development, a randomized clinical trial (RCT) has shed light on a potential game-changer in the fight against SSIs in open gastrointestinal (GI) surgeries: the plastic wound protector. 

The study, published in JAMA Surgery, has shown the effectiveness of plastic wound protectors in reducing surgical site infections in open gastrointestinal surgeries.

“In the RCT of 458 patients, the wound protector reduced SSI risk by 46.8% across bowel surgeries, with a 43.8% decrease for clean-contaminated wounds and 42.5% for superficial SSIs versus surgical gauze,” the researchers reported. “Its effect on contaminated wounds was less certain.”

SSIs are prevalent hospital-acquired infections with significant patient impacts and global healthcare burdens. The World Health Organization (WHO) recommends using wound protector devices in abdominal surgery as a preventive measure to lower SSI risk despite limited evidence. Considering this, Nina Yoo, The Catholic University of Korea, Seoul, Korea, and colleagues aimed to examine the efficacy of a dual-ring, plastic wound protector in reducing the SSI rate in open gastrointestinal (GI) surgery regardless of intra-abdominal contamination levels.

For this purpose, the researchers conducted a multicenter, patient-blinded, parallel-arm randomized clinical trial from 2017 to 2022 at 13 hospitals in an academic setting. Patients undergoing open abdominal bowel surgery (e.g. for bowel perforation) were eligible for inclusion.

Patients were randomized in a 1:1 ratio to a dual-ring, plastic wound protector to protect the incision site of the abdominal wall (experimental group) or a conventional surgical gauze (control group). The primary endpoint was the SSI rate within 30 days of open GI surgery.

A total of 458 patients were randomized; after one was excluded from the control group, 457 were included in the intention-to-treat analysis (mean age, 58.4 years; 56.0% male; 74.6% with a clean-contaminated wound): 228 in the surgical gauze group and 229 in the wound protector group.

The researchers reported the following findings:

  • The overall SSI rate in the intention-to-treat analysis was 15.7%.
  • The SSI rate for the wound protector was 10.9% compared with 20.5% with surgical gauze.
  • The wound protector significantly reduced the risk of SSI, with a relative risk reduction (RRR) of 46.81%.
  • The wound protector significantly decreased the SSI rate for clean-contaminated wounds (RRR, 43.75%), particularly for superficial SSIs (RRR, 42.50%).
  • Length of hospital stay was similar in both groups (mean, 15.2 versus 15.3 days), as were the overall postoperative complication rates (20.1% versus 18.8%).

In conclusion, the randomized clinical trial found a significant reduction in SSI rates when a plastic wound protector was used during open GI surgery versus surgical gaze, supporting the WHO recommendation for wound protector devices in abdominal surgery.

Reference:

Yoo N, Mun JY, Kye B, et al. Plastic Wound Protector vs Surgical Gauze for Surgical Site Infection Reduction in Open GI Surgery: A Randomized Clinical Trial. JAMA Surg. Published online April 24, 2024. doi:10.1001/jamasurg.2024.0765

Powered by WPeMatico

Early diagnosis & treatment of PAD essential to improve outcomes, reduce amputation risk: Study

Timely diagnosis and proper management of peripheral artery disease (PAD), including coordinated care from a multispecialty team, are essential to help prevent amputation and other cardiovascular complications and to allow patients with PAD to live longer lives with better physical function and improved quality of life, according to a new joint guideline published today in the American Heart Association’s flagship, peer-reviewed journal Circulation and simultaneously in the Journal of the American College of Cardiology.

The “2024 AHA/ACC Guideline on the Management of Lower Extremity Peripheral Artery Disease: A Report of the American College of Cardiology/American Heart Association Joint Committee on Clinical Practice Guidelines” provides the latest, evidence-based recommendations to guide clinicians in the diagnosis and treatment of lower extremity PAD across its four clinical presentation subsets: asymptomatic disease, chronic symptomatic PAD, and the more severe subsets of chronic limb-threatening ischemia (CLTI) and acute limb ischemia (ALI).

In addition to being led by the American Heart Association and the American College of Cardiology Joint Committee on Clinical Practice Guidelines, the guideline was developed with and endorsed by the American Association of Cardiovascular and Pulmonary Rehabilitation, the American Podiatric Medical Association, the Association of Black Cardiologists, the Society for Cardiovascular Angiography and Interventions, the Society for Vascular Medicine, the Society for Vascular Nursing, the Society for Vascular Surgery, the Society of Interventional Radiology and the Vascular & Endovascular Surgery Society.

PAD is a serious, progressive cardiovascular disease primarily caused by a buildup of fatty plaque in the blood vessels, or atherosclerosis. This plaque narrows the blood vessels and reduces blood flow to the legs and feet, which may significantly impair physical function, walking performance and quality of life. Approximately 10 million to 12 million adults ages 40 and older in the U.S. have PAD, which increases the risk of amputation, heart attack, stroke and death. Among those ages 65 and older, nearly 50% who underwent limb amputation died within one year after surgery, according to the 2024 Heart Disease and Stroke Statistics: A Report of U.S. and Global Data From the American Heart Association. Risk factors for PAD include smoking; having Type 1 or Type 2 diabetes, high blood pressure, high cholesterol, chronic kidney disease, atherosclerosis in other parts of the body (such as coronary artery disease); and being age 75 years or older.

Effective medical therapies and coordinated care

Once PAD is diagnosed, implementing a plan of care, including guideline-directed medical therapies and management of PAD-related risk amplifiers, is crucial to reduce the risk of progression to more symptomatic and limb-threatening clinical presentations of PAD and to reduce the risk of amputation, heart attack, stroke and death. Although there are highly effective medical, endovascular and surgical therapies for PAD, historically, many people with PAD have been undertreated or do not receive guideline-directed medical therapies at the same rate as peers with other cardiovascular diseases, such as coronary artery disease.

“Because of the complexities of PAD, to improve outcomes and reduce the risk of limb loss for these patients, a multispecialty care team approach that is focused on comprehensively addressing risk factor management, foot care and revascularization is needed to promote collaboration, avoid duplication of care and optimize patient outcomes,” said Chair of the guideline writing committee Heather Gornik, M.D., FAHA, co-director of the Vascular Center at the University Hospitals Harrington Heart & Vascular Institute and a professor of medicine at Case Western Reserve University School of Medicine, both in Cleveland, Ohio.

Effective medical therapies for patients with PAD, including medications to prevent blood clotting, manage blood sugar and reduce high blood pressure and high cholesterol, should be prescribed to prevent major adverse cardiovascular events and reduce the risk of amputation. All patients with PAD should be treated with high-intensity statin therapy. For people with PAD who are not at an increased risk of bleeding, new evidence supports the use of low-dose rivaroxaban (2.5 mg twice daily) combined with low-dose aspirin (81 mg daily).

For patients with PAD and Type 1 or Type 2 diabetes, clinicians should coordinate care to address diet, exercise, weight management, medications to control blood sugar, management of other cardiovascular risk factors and routinely check the feet of their patients for foot ulcer prevention. Foot care is important for patients across the four clinical presentation subsets of PAD. Comprehensive treatment includes patient education, preventive foot care, more intensive wound care and pressure off-loading to minimize amputation in patients with more severe forms of PAD.

Health care professionals should also encourage patients to quit smoking or using other forms of tobacco to reduce the risk of developing PAD, to slow the progression of established PAD and to reduce the risk of limb-related conditions or death. Pharmacological and behavioral-based strategies often increase the smoking cessation rate in people with PAD, however, these strategies are underused.

A core component of care for patients with symptomatic PAD is structured exercise therapy programs, including both community- and home-based programs, as well as supervised exercise therapy delivered in a clinic or hospital setting. Multiple studies have shown that these programs improve functional status, walking performance and quality of life compared to usual care.

“Supervised exercise therapy, the gold standard exercise therapy for patients with PAD, is woefully underutilized despite its known health benefits and the fact that it is covered by Medicare and most health insurance plans,” said Gornik. “Rates of referral for supervised exercise therapy among PAD patients are incredibly low. It has been estimated that less than 5% of patients with PAD in the U.S. are prescribed to participate in a supervised exercise program.”

If left untreated, PAD may progress to severe forms known as chronic limb-threatening ischemia (CLTI) and acute limb ischemia (ALI). Both are the result of severe blockage in the arteries of the legs that significantly reduces blood flow, causes pain in the legs at rest or with minimal activity, impairs physical function and significantly increases the risk of amputation and death. For these patients, timely diagnosis and treatments, including revascularization procedures to reconstruct diseased arteries, are essential to prevent tissue loss and preserve the limb. Endovascular (a catheter procedure), surgical or hybrid revascularization techniques may be performed to improve blood flow to the limb, with the goals of healing wounds, relieving PAD-associated pain, maintaining walking ability and preventing amputation.

Disparities in risk factors for PAD and health outcomes

The disparities in PAD care and outcomes are significant among people from under-resourced communities in the U.S. Black adults have a nearly 30% lifetime risk of developing PAD compared to 19% for white adults. Black adults with PAD in the U.S. are often identified at a more advanced stage and have a four-fold higher rate of major limb amputation, 30% higher heart disease mortality rate and 45% higher rate of stroke compared to white adults.

Social determinants of health, and other factors such as race and ethnicity, disparities in housing, health care access, education and socioeconomic status, may also affect the prevalence of PAD and patient outcomes.

“Racial and ethnic disparities in the detection, management and health outcomes of PAD have long been present in the U.S. and are an important public health issue to be addressed,” said Gornik. “These disparities highlight opportunities for initiatives focused on early disease detection and improving access to effective PAD treatments for people in under-resourced, at-risk communities.”

Detection of PAD in most patients is accomplished through a thorough medical history, physical examination and resting ankle-brachial index (ABI), which measures the ratio of the systolic blood pressure at the ankle to the upper arm. The guideline recommends patient-centered efforts to address health disparities, such as intensified efforts to identify patients in at-risk populations for symptoms and signs of PAD, and equitable access to regular physical examinations including thorough assessment of the legs and feet.

Get with The Guidelines: The PAD National Action Plan

In 2021, the American Heart Association published the PAD National Action Plan, which is endorsed by the American College of Cardiology, that outlines six strategic goals to improve awareness, detection and treatment of PAD nationwide. In the plan, the Association proposed a goal of reducing nontraumatic limb amputation in the U.S. by 20% by 2030.

The guideline writing committee notes that interventions are needed to address the disparity gap in amputation and revascularization procedures among people in diverse racial and ethnic populations and to improve limb and cardiovascular outcomes for all patients with PAD.

“It’s important to recognize the signs and symptoms of PAD and move quickly to initiate treatment to improve outcomes and reduce risks,” said Gornik. “With these updated guidelines, we have the tools necessary to make a positive impact on outcomes in our patients with PAD. Now, we need to work together to implement them as broadly as possible.”

This joint guideline was prepared by a volunteer writing group on behalf of the American Heart Association/American College of Cardiology Joint Committee on Clinical Practice Guidelines, and developed with and endorsed by the American Association of Cardiovascular and Pulmonary Rehabilitation, the American Podiatric Medical Association, the Association of Black Cardiologists, the Society for Cardiovascular Angiography and Interventions, the Society for Vascular Medicine, the Society for Vascular Nursing, the Society for Vascular Surgery, the Society of Interventional Radiology, and the Vascular & Endovascular Surgery Society. This joint guideline provides the official clinical practice recommendations for the diagnosis and treatment of peripheral artery disease, or PAD.

Reference:

Heather L. Gornik, Herbert D. Aronow, Philip P. Goodney, Shipra Arya, Luke Packard Brewster, Lori Byrd, Venita Chandra, Douglas E. Drachman, Jennifer M. Eaves, Jonathan K. Ehrman, 2024 ACC/AHA/AACVPR/APMA/ABC/SCAI/SVM/SVN/SVS/SIR/VESS Guideline for the Management of Lower Extremity Peripheral Artery Disease: A Report of the American College of Cardiology/American Heart Association Joint Committee on Clinical Practice Guidelines, Circulation, https://doi.org/10.1161/CIR.0000000000001251.

Powered by WPeMatico

Limited tourniquet application in primary unilateral TKA may not increase incidence of perioperative complications: study

Limited tourniquet application in primary unilateral TKA does not increase the incidence of perioperative complications: study

Tourniquet application in total knee arthroplasty (TKA) has many benefits and may have a role in the incidence of perioperative complications. Doried Diri et al conducted a study to examine the safety of applying a tourniquet for a limited amount of time during primary unilateral TKA (specifically, during cementation and final component fixation only) and to compare perioperative complications between the limited-application group and the full-application group. The study was conducted at Damascus University, Damascus, Syria. It has been published in ‘JBJS Open Access’.

The authors conducted a randomized controlled study of 62 patients undergoing primary unilateral TKA. Patients were randomly allocated to either the limited or full tourniquet application. The follow-up period was 6 months. They evaluated intraoperative, postoperative, total, and hidden blood loss as the primary outcome measures and clearance of the surgical field, operative duration, and perioperative complications as the secondary outcome measures.

Key findings of the study were:

• No patients were lost to follow-up and all patients attended their follow-up visits.

• No significant differences in patient demographics and characteristics were found between treatment groups

• Surgical field clearance, as evaluated by the surgeon, was significantly different between the groups.

• There was no significant difference in total, hidden, or postoperative blood loss between the groups.

• Mean intraoperative blood loss was significantly lower in the full-application group than in the limited-application group (171.742 ± 19.710 versus 226.258 ± 50.290 mL; p = 0.001).

• The mean (and standard deviation) operative duration was 56.177 ± 6.075 minutes. Operative duration did not differ significantly between the groups

• Perioperative complications, including allogeneic blood transfusion rates, did not significantly differ between the groups.

The authors concluded – “The use of limited tourniquet application is safe for low-risk patients undergoing primary unilateral TKA performed by an expert surgeon. When compared with the full application regimen, the limited application regimen showed no increased rates of perioperative complications or total blood loss”

Level of Evidence: Therapeutic Level I.

Further reading:

Blood Loss in Primary Unilateral Total Knee Arthroplasty with Limited Tourniquet Application A Randomized Controlled Trial

Doried Diri et al

JBJS Open Access 2023:e23.00020.

http://dx.doi.org/10.2106/JBJS.OA.23.00020

Powered by WPeMatico

Amidst NEET Paper Leak Scandal, Aspirants Demand Re-Exam

New Delhi: Amidst the paper leak scandal involving the National Eligibility-cum-Entrance Undergraduate (NEET-UG) Exam, the centralised common entrance test for admission to the MBBS course, the aspirants have started demanding re-conduction of the examination.

Referring to instances where the government swiftly cancels the examinations for confirmed leaks, the candidates are urging the authorities to ensure justice by conducting a re-examination.

This comes after around 13 people, including four examinees and their family members were arrested in Bihar for their alleged involvement in the paper leak of NEET-UG exam. Patna police sources had earlier claimed that the NEET-UG question papers along with their answers were provided to around 20 aspirants a day before the date of the exam i.e. May 5, 2024.

Recently, the Economic Offences Unit (EOU) of Bihar Police, which took over the investigation, revealed that the brokers involved in the NEET paper leak scam took between Rs 30 lakh to Rs 50 lakh from each of the medical aspirants in exchange of giving them the question paper of the NEET UG 2024 question paper ahead of the examination.

Also Read: NEET Paper Leak Scandal Rocks Bihar: Questions-Answers allegedly given to 20 Aspirants Day Before Exam

EOU had earlier mentioned in a release that as per the investigation, the question papers of NEET-UG and their answers were provided to around 35 aspirants before the May 5 exam.

Aspirants Demand Re-Examination: 

Amid the reports of NEET paper leak, the aspirants have started expressing their frustration at the social media platforms like X (formerly Twitter) and demanding a fair re-examination of NEET 2024. Photos of aspirants holding placards saying “We Demand a Fair Examination” have been circulating on social media platforms.

Questioning “where’s the justice”, an X user wrote, “Government of India is sleeping or busy with elections? Come out of your election otherwise the youth will crash you down. @NTA_Exams conduct re neet asap otherwise wait till the case goes to SC.” The post also tagged the Prime Minister of India and the Union Education Minister.

Also Read: NEET Candidates paid up to Rs 50 lakhs for getting Question Papers in Advance: Bihar EOU

Demanding re-neet, the user wrote in another post, “WE DEMAND RE NEET large number of aspirants got the paper a night before. Teachers solved aspirant’s question paper at the hall itself And many more…. Is this a joke??”

Meanwhile, an user slammed the whole education system and wrote, “Nowadays this is the actual reality of whole education system…… Or i can say this is the reality of every system. Corruption on its peak.”

An X page called NEET UG Leak also opined that the entire examination should be cancelled and it should be conducted fairly again. The X post stated, “It is requested to the government that the examination should be cancelled and it should be conducted fairly again. Unqualified students have been benefited by paper leak and its roots are very deep.”

Raising the matter, socio political activist Mukesh Choudhary wrote, “The government should take a decision in the interest of the youth as soon as possible regarding the NEET UG paper leak.” He questioned when the aspirants would get justice.

Extending support to the aspirants demanding re-conduction of the examination, another user questioned, “When it is accepted , even by almost all media that #NEET_PAPER_LEAK did happen then Why the Demand of #RENEET is being ignored ? The Students who studied hard and gave #NEETexam with honesty actually deserve #ReNeet2024.”

Also Read: NEET 2024 Cheating Scandal: More than 24 culprits including 14 impersonators arrested by Bihar Police

Social activist Dr. Vivek Pandey also raised the matter and he questioned the stand of the National Testing Agency (NTA) denying claims of NEET paper leak. He wrote, “As per @NTA_Exams they don’t have any strong evidence of paper leak. Patna police already said in their press release that paper was leaked, even they told the same to court. Then why NTA denying facts ?”

Opining that the charge of conducting NEET should be transferred to AIIMS, Dr. Pandey mentioned in another post, “Facing issues with NTA exams isn’t new. From admit card glitches to paper leaks, students have endured. It’s time to reconsider, perhaps shift Neet UG’s authority from NTA to AIIMS.”

Medical Dialogues had earlier reported that the Bihar Police had arrested more than two dozen individuals, including 14 impersonators and candidates for cheating in the NEET UG 2024 exam. Among those arrested, an FIR was registered against 14 people, who were accused of impersonating registered candidates during the examination. During the interrogation, the accused known as “solvers” had revealed that Rs 5-10 lakh each was given to several centres by the gang members.

Earlier the National Testing Agency (NTA) had issued a clarification ensuring fair conduct of the NEET 2024 examination and it allowed 120 candidates to reappear for the exam after the question papers were distributed incorrectly at an exam centre. While several social media posts claimed that NEET 2-24 question paper was leaked, NTA had denied such claims.

In the notice, NTA stated that “it assures the public that apart from this isolated incident, the NEET (UG) 2024 examination commenced smoothly and is being conducted peacefully at all other examination centres across the country. The NTA emphasizes that this incident has not compromised the integrity of the examination process at other centres.”

Also Read: Incorrect distribution of NEET 2024 question paper, NTA allows 120 aspirants to reappear in exam, denies ‘paper-leak’ claims

Powered by WPeMatico

PCI issues Guidelines for Inspections of Pharmacy Institutions for academic year 2024- 2025

New Delhi: The Pharmacy Council of India (PCI) has issued comprehensive guidelines for the inspection process of pharmacy institutions for the academic year 2024-2025.

These guidelines are applicable to existing and new institutions applying for approval for the first time.

Referencing PCI circulars numbered 1.14-56/2022-PCI (Approval Process for 2024-25 a.s.) dated December 14, 2023, and subsequent updates, the guidelines aim to streamline the inspection and verification process for all stakeholders involved, including pharmacy institutions, examining authorities (universities/boards), and state governments.

The notice declared that all the institutions are requested to follow the guidelines during the inspection and verification process.

In this connection, the notice stated that the PCI will start the inspection process of the Pharmacy institutions for the 2024-2025 academic sessions at the earliest.

“All inspections will be done through the mobile inspection application only as provided in the Google Play Store (https://play.google.com/store/apps/details?id=cdg.com.pci inspection&hl=en&gl=U S&pli=l).” the notice added.

In accordance with the notice, all institutions are requested to follow the below guidelines during the inspection and verification process:

Regarding Students:

  • Mandatory attendance for all the students enrolled in the institutions.
  • Mandatory registration for all the students on the PCI Portal.
  • All students are to have the Smart Card with them at the time of the inspection process.

Regarding Faculties:

  • Mandatory attendance for all the faculties enrolled in the institutions.
  • Mandatory presence for all the faculties enrolled in the institutions, during the time of inspection process.
  • If any faculty is on leave, the leave letter is to be submitted to the inspectors and the same is to be documented on the app along with the reason for absence.
  • Mandatory registration for all the faculties on the PCI Portal.
  • All faculty members must have their Smart Card with them at the time of the inspection process.
  • All faculties must carry their relevant documents with them at the time of the inspection and verification process.

Infrastructure:

  • Mandatory active QR code on the institutions’ infrastructure comprising-

• Institutions Classrooms,

• Institutions Laboratories,

• Institutions Common Facility,

• Institutions Computer Labs and other facilities,

• Institutions Amenities,

• Master’s Degree Equipment,

• Bachelor’s Degree Equipments,

• Others;

  • Mandatory active QR code on all the equipment present in the institutions during the inspection process.
  • If any infrastructure or equipment is found without the QR code or the QR code not working at the time of inspection, the institutions are to be counted in the deficiency list.

Documents:

  • All faculties are to possess the relevant documents with them at the time of the inspection and verification process.
  • Institutions must possess all the relevant documents with them as information filled in Standard Inspection Format (SIF) at the time of inspection and verification process

In addition, the notice added that the above points shall be applicable to all other information in the SIF filled by institutions.

To view the notice, click the below link:

Also Read:Madras Medical College’s pharmacy institute likely to lose approval, face punitive action for violating PCI norms: Report

Powered by WPeMatico

India new dietary guidelines limit sugar intake to 5 percent of daily calories

The new dietary guidelines issued by the Indian Council of Medical Research-National Institute of Nutrition (ICMR-NIN) recommends no sugar for children under two years old and limiting sugar intake to 5% of daily calories for individuals over two. Another study by ICMR, in collaboration with Madras Diabetes Research Foundation, revealed that one in four Indians is diabetic, pre-diabetic, or obese, largely due to dietary habits and sedentary lifestyles.
Feeding infants and young children with food products containing added sugar has been shown to increase their risk of early childhood obesity and non-communicable diseases later in life, the guidelines stated.

Powered by WPeMatico

SC pulls up IMA chief in Patanjali ads case

The Supreme Court on Tuesday i.e. May 14, 2024, reserved its verdict on the pending contempt proceedings against Patanjali Ltd., its managing Director Acharya Balkrishna, and co-founder Baba Ramdev, who were accused of publishing misleading medical advertisements in breach of a court undertaking.
However, the top court bench dismissed the apology tendered by the president of the Indian Medical Association (IMA) Dr. RV Asokan, for his remarks on the court’s ruling in the misleading ads case against Patanjali.

Powered by WPeMatico

Rajasthan Govt to utilize ODK app for real time monitoring of sesonal diseases

Jaipur: The Medical Department of Rajasthan have announced their plan to utilize a mobile application for monitoring seasonal diseases, aiming for real-time surveillance.   

Additional Chief Secretary of the Medical and Health Department Shubhra Singh said that the online monitoring of seasonal diseases will now be done by the department through the app, reported news agency PTI.  

She said that this innovation will enable real-time monitoring of seasonal diseases across the state and effective steps can be taken quickly for prevention and control.  

“The main objective of the app is to reduce the cases of malaria, dengue and chikungunya,” she said.  

“The intensity of mosquito-borne diseases like malaria, dengue, and chikungunya usually remains from the beginning of the rainy season in July-August to October-November. In recent years, due to lifestyle and weather changes, the spread of seasonal diseases has started increasing,” she said.

According to a PTI report, she said, “Through the app, photographs of mosquito breeding sites and places where larvae are found will be taken and sent to the local self-government department or the Panchayati Raj Department… The concerned departments will carry out anti-larva and anti-mosquito activities at those places”.

Medical Dialogues team had earlier reported that the Uttarakhand health department has taken proactive measures to address the rising cases of dengue and chikungunya patients in the state by issuing comprehensive guidelines to all districts. Twenty key points have been communicated to District Magistrates and Chief Medical Officers (CMOs) to ensure effective prevention and treatment. Dr R Rajesh Kumar, Secretary of Health, has been conducting regular review meetings to strategize the prevention of dengue and chikungunya. In consultation with health experts, the department has formulated guidelines aimed at the treatment and prevention of these diseases.

Powered by WPeMatico