Can Probiotics Keep My Gut Healthy?

There’s convincing evidence that probiotics can be helpful in maintaining gastrointestinal health in certain select situations.

But like many natural approaches to maintaining health, there’s been a tendency toward generalizing the benefits, so probiotics are frequently touted as a panacea for all types of health problems. Many advertisements and Internet postings say probiotics are effective for the treatment of asthma, dermatitis, and a wide diversity of other conditions. At best, there is marginal evidence that probiotics are helpful for many of these conditions.

There’s been a lot of work that’s been done on probiotics in the management of irritable bowel, which is important since it’s such a common condition: it’s estimated that upwards of 15% of the U.S. adult population has irritable bowel. I would say that all the studies summarize that certain probiotics seem to help a little bit with irritable bowel, but quite frankly, the magnitude of the benefit tends to be very small. and it’s probably not adequate as the management of irritable bowel by itself.

Where they have been convincingly shown to be beneficial is in the treatment or prevention of certain kinds of diarrhea. Rotavirus is a common cause of infectious diarrhea in infants and children. Once a child has the ‘gastrointestinal flu’, there’s strong evidence to show that probiotics reduce the duration and severity of the illness. There’s less convincing evidence that suggests probiotics can be used to prevent it.

Let’s say your child’s school sends home a note that says 30% of the class is out with gastrointestinal flu. You could give your child the appropriate probiotic with the hope that it might prevent them from developing it. But if they get sick and you administer it to them, it’ll probably shorten the duration of the disease.

The probiotic most consistently shown to be effective in this situation is Lactobacillus GG, which was developed at Tufts University by Sherwood Gorbach and Barry Goldin of the medical school. You can buy it at drugstores under the name Culturelle. A yeast called Saccharomyces boulardii, sold in stores under the name Florastor, also seems to be effective in managing childhood infectious diarrhea.

A second instance where probiotics can be useful is with antibiotic-associated diarrhea. When people go on antibiotics—whatever kind that may be—they frequently develop diarrhea. There have been a number of trials in which people were administered certain probiotics along with the antibiotics used to treat an infection, and that helped prevent diarrhea. Two probiotics have been shown to be effective for this problem: Lactobacillus GG and Saccharomyces boulardii.

For people who often go on antibiotics—say, a woman who gets a lot of bladder infections and then gets diarrhea from the antibiotic—it would make sense to take one of these products along with the antibiotic and extending for a few days after the antibiotic stops. The data suggests that to be effective in the prevention of antibiotic-associated diarrhea, the probiotic should be taken for upwards of a week after you stop taking the antibiotic.

In some cases of antibiotic-associated diarrhea, a very nasty bug called Clostridium difficile takes over because the antibiotics have knocked out the good bacteria in your gut and this bug fills the void. C. diff, as it is known, can cause dysentery, bloody diarrhea and fever, and can even be life-threatening. The only organism that has been shown to convincingly prevent C. difficile is Saccharomyces boulardii.

A major addition to the list of things that probiotics seem to be effective for is traveler’s diarrhea. There are now pretty convincing data that these same two probiotics, Lactobacillus GG and Saccharomyces boulardii, are each effective in reducing the risk of traveler’s diarrhea.

For people who want to avoid developing this kind of traveler’s diarrhea, taking one of these two probiotics seems to sizably reduce the risk. You also can take Pepto Bismol tablets, two tablets four times a day. This has been shown to also be effective. So, there are a couple ways that people can try to protect themselves from developing traveler’s diarrhea aside from being careful about what they eat and drink.

Many people eat yogurt or kefir because it contains probiotic organisms, but studies looking at the potential usefulness of probiotics in a rigorous scientific manner have generally used pure preparations in tablets or capsules, not yogurt. And in many brands, the organisms used to make the yogurt or kefir aren’t necessarily the ones are effective in clinical trials. I can’t say that fermented dairy products aren’t effective. But whether the helpful bacteria you get by eating yogurt are really as effective as pure probiotics is up for debate right now.

People taking probiotics should also be aware that they are not totally innocuous for all individuals. A lot of people say, “This is natural; it might help, and it won’t hurt, so I may as well take it.” Remember that when you’re taking a probiotic, you’re swallowing billions of bacterial spores, and there are rare situations in which those spores can set up a serious infection in your body. Lest I create too much anxiety: this complication seems to occur only in people whose immune systems are suppressed by drugs or other diseases, or who are critically ill.

The most important message is to pay attention to which probiotics you take. There’s a myth that all probiotics are the same, but because they’re not viewed as drugs, they are not regulated by the Food and Drug Administration, so there can be problems with quality control. When you take a probiotic, you assume you’re ingesting billions of bacterial spores that will hatch and result in live bacteria in your gut.

But there are probiotics you can buy in which 99 percent of the spores are dead—you may as well throw your money away. Moreover, if you’re going to approach this scientifically, you have to pay attention to the particular species of bacteria or yeast that you’re ingesting. When I put patients on probiotics, I’m very specific about what products to take. 

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High glucose and TG levels and low HDL-C levels tied to risk of depression, anxiety, and stress-related disorders: JAMA

Sweden: A recent study published in JAMA Network Open has suggested the involvement of carbohydrate and lipid metabolism in the development of common psychiatric disorders.

The population-based cohort study of more than 200,000 individuals revealed that high levels of triglycerides and glucose and a low level of high-density lipoprotein (HDL) were associated with a higher risk of anxiety, depression, and stress-related disorders. The findings support closer follow-up of people with metabolic dysregulations for the diagnosis and prevention of psychiatric disorders.

Anxiety, depression, and stress-related disorders are common psychiatric disorders that affect approximately one-third of individuals during their life course. Increasing evidence suggests that biomarkers of lipid, apolipoprotein, and carbohydrate metabolism may be associated with the risk for anxiety, depression, and stress-related disorders, but results are inconsistent.

Against the above background, Charilaos Chourpiliadis, Karolinska Institutet, Stockholm, Sweden, and colleagues aimed to investigate whether the biomarkers of lipid, carbohydrate, and apolipoprotein metabolism are associated with the risk of anxiety, depression, and stress-related disorders.

For this purpose, the researchers conducted a population-based cohort study with longitudinal data collection that assessed 211 200 participants from the Apolipoprotein-Related Mortality Risk (AMORIS) cohort who underwent occupational health screening between 1985 and 1996, mainly in the Stockholm region in Sweden.

The main outcomes were the associations between biomarker levels and the risk of developing anxiety, depression, and stress-related disorders through the end of 2020. Nested case-control analyses were conducted within the cohort, including all cases of anxiety, depression, and stress-related disorders, and up to 10 control individuals per case who were individually matched to the case by sex, year of birth, and year of enrollment to the AMORIS cohort, using incidence density sampling.

Population trajectories were used to illustrate the temporal trends in biomarker levels for controls and cases.

The study led to the following findings:

  • 211 200 individuals (mean age at first biomarker measurement, 12.6 years; 58.0% male; 89.4% born in Sweden) participated in the study. During a mean follow-up of 21.0 years, a total of 16,256 individuals were diagnosed with depression, anxiety, or stress-related disorders.
  • High levels of triglycerides (HR, 1.15) and glucose (hazard ratio [HR], 1.30) were associated with an increased subsequent risk of all tested psychiatric disorders, whereas high levels of high-density lipoprotein (HR, 0.88) were associated with a reduced risk. These results were similar for female and male participants and all tested disorders.
  • The nested case-control analyses demonstrated that patients with depression, anxiety, or stress-related disorders had higher levels of glucose, triglycerides, and total cholesterol during the 20 years preceding diagnosis, as well as higher levels of apolipoprotein A-I and apolipoprotein B during the ten years preceding diagnosis, compared with control participants.

In conclusion, the researchers found elevated levels of triglycerides and glucose and reduced levels of HDL-C are linked to a higher risk of subsequent diagnosis of anxiety, depression, and stress-related disorders. The study provides further longitudinal evidence that metabolic syndrome or metabolic dysregulation raises the risk of developing common psychiatric disorders.

“These results add further evidence of the association between cardiometabolic health and psychiatric disorders and potentially advocate for a closer follow-up of individuals with metabolic dysregulations for prevention and early diagnosis of psychiatric disorders,” the researchers wrote.

“There is a need for additional studies to explore whether rigorous or earlier interventions for cardiometabolic diseases could counteract such an association,” they concluded.

Reference:

Chourpiliadis C, Zeng Y, Lovik A, et al. Metabolic Profile and Long-Term Risk of Depression, Anxiety, and Stress-Related Disorders. JAMA Netw Open. 2024;7(4):e244525. doi:10.1001/jamanetworkopen.2024.4525

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Elevated calcitonin gene-related peptide levels linked to rosacea: A Groundbreaking Study

Denmark: A recent study published in the Journal of the European Academy of Dermatology and Venereology has revealed significantly higher calcitonin gene-related peptide (CGRP) levels in rosacea patients even after adjusting for sex and age.

CGRP levels were unaffected by several factors, including sex, age, BMI, rosacea subtypes, migraine, comorbidities, or ongoing treatments. The findings suggest CGRP’s role in the pathogenesis of rosacea. Targeting CGRP signaling might hold therapeutic promise in individuals affected by this disease.

Rosacea, a chronic inflammatory skin condition affecting millions worldwide, has long confounded sufferers and clinicians with its elusive causes and variable symptomatology. Capsaicin, a well-known trigger of rosacea flushing, has been demonstrated to increase dermal skin blood flow in the forearm by activating transient receptor potential vanilloid (TRPV) channels and promoting the release of CGRP.

Traditional treatments for rosacea, such as oral antibiotics and topical agents, primarily address symptoms rather than underlying mechanisms. However, modulating CGRP signaling could represent a more targeted approach, potentially offering improved efficacy and tolerability for patients with refractory or severe disease.

Against the above background, Messoud Ashina, Copenhagen University Hospital – Rigshospitalet, Copenhagen, Denmark, and colleagues aimed to compare plasma levels of CGRP between individuals with rosacea and healthy controls.

For this purpose, the researchers conducted a cross-sectional case-control study in Copenhagen, Denmark. They collected blood samples from the antecubital vein from adults with rosacea and healthy controls. 123 individuals with rosacea and 68 healthy controls were enrolled.

The study revealed the following findings:

  • After adjusting for age and sex, plasma levels of CGRP were significantly higher in individuals with rosacea (mean, 95% confidence interval: 140.21 pmol/L, 128.50–151.92 pmol/L), compared with controls (110.77 pmol/L, 99.91–120.14 pmol/L).
  • Plasma levels of CGRP were not affected by age, sex, BMI, rosacea sub- or phenotype, concomitant migraine, concomitant disease, or current treatment.

The main limitation was that the participants were not age-, sex- and BMI-matched.

In conclusion, the study provides evidence that plasma CGRP levels are elevated in individuals with rosacea versus healthy controls. However, the researchers did not find a correlation between CGRP levels and rosacea severity or subtype, indicating that CGRP might not be a reliable biomarker for diagnosing or assessing rosacea severity.

“Nevertheless, our findings suggest that CGRP might be involved in the pathophysiology of rosacea,” the researchers wrote. “Thus, there is a need for further research to investigate the potential of medications targeting CGRP signaling in managing rosacea.”

Reference:

F. Wienholtz, N. K., Christensen, C. E., Ashina, H., Jørgensen, N. R., Egeberg, A., Thyssen, J. P., & Ashina, M. Elevated plasma levels of calcitonin gene-related peptide in individuals with rosacea: A cross-sectional case–control study. Journal of the European Academy of Dermatology and Venereology. https://doi.org/10.1111/jdv.19954

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Diabetes, anemia and old age may increase Dacron-cuffed catheter related infection risk among hemodialysis patients: Study

Diabetes, anemia and old age may increase risk Dacron-cuffed catheter related infection among hemodialysis patients suggests a study published in the BMC Nephrology.

A study was done to provide theoretical basis for prevention of a Dacron-cuffed catheter related infection (CRI), the risk factors of CRI in hemodialysis patients were systematically evaluated. Eight databases, including PubMed, Cochrane library, EMBASE, Web of Science, China National Knowledge Infrastructure (CNKI), Chinese Biomedical Database (CBM), Wanfang Database and Chinese Scientific Journal Database (VIP), were searched to screen out literatures related to the risk factors of long-term indwelling a Dacron-cuffed CRI in hemodialysis. Meta-analysis of risk factors for a Dacron-cuffed CRI in hemodialysis and publication bias test were performed using RevMan 5.4 software. Results: After screening, 13 literatures involving a Dacron-cuffed CRI were included, with a total of 625 patients, and the infection rate was 11.7%. The combined OR value and 95% confidence interval (CI) of all factors were: Combined with Diabetes (1.94, 1.51 ~ 2.50), Hb (1.82, 1.35 ~ 2.44), age (2.38, 1.06 ~ 5.34), catheter indwelling time (1.79, 1.21 ~ 2.66), serum albumin (2.26, 1.25 ~ 4.08), catheter indwelling site (3.29, 1.74 ~ 6.23) and the number of tube placement (5.40, 2.65 ~ 11.02).The main risk factors for a Dacron-cuffed CRI in hemodialysis were combined with diabetes, hemoglobin level, age, catheter indwelling time, serum albumin level, femoral vein catheter indwelling and catheterization times. In other words, hemodialysis patients are at higher risk of CRI if they have diabetes, or if they have a lower hemoglobin level, or if they are older, or if they have a longer duration of catheterization, or if they have a lower serum albumin level, or if they have a femoral vein catheter, or if they have more catheters.

Reference:

Chen, W., Wang, Z., Wang, G. et al. A meta-analysis of risk factors for a Dacron-cuffed catheter related infection in hemodialysis. BMC Nephrol 25, 126 (2024). https://doi.org/10.1186/s12882-024-03568-0

Keywords:

Diabetes, anemia and old age, increase risk, Dacron-cuffed catheter, infection, hemodialysis patients, study, BMC Nephrology, Chen, W., Wang, Z., Wang, G.

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Appendicoscopy with single operator cholangioscope: A novel approach to acute obstructive appendicitis

China: A recent study investigating the efficacy of appendicoscopy utilizing single-operator cholangioscopy (SOC) in managing acute obstructive appendicitis revealed a high success rate of the procedure with a technical success rate of 96.4% & a clinical success rate of 91.8%.

The mean procedure time was 20.9 minutes, and 99.1% of patients experienced rapid relief of abdominal pain within 6 hours post-procedure.

“Appendicoscopy appears to be an effective and feasible alternative therapy for the accurate diagnosis and treatment of acute obstructive appendicitis,” the researchers wrote in Gastrointestinal Endoscopy.

Acute appendicitis, a common surgical emergency, traditionally warrants prompt appendectomy to prevent complications like perforation and peritonitis. However, recent advances in endoscopic technology have paved the way for innovative techniques aimed at minimizing invasiveness while ensuring effective treatment. Among these, appendicoscopy using a single-operator cholangioscope has emerged as a promising alternative in the management of acute obstructive appendicitis.

The procedure begins with conventional colonoscopic insertion, followed by advancement of the SOC into the cecum and identification of the appendiceal orifice. Through meticulous manipulation and visualization, the obstructed appendiceal lumen can be accessed, allowing for decompression, irrigation, and, if necessary, therapeutic interventions such as stone removal or stent placement. Importantly, appendicoscopy with SOC offers the advantage of real-time visualization, enabling precise identification of pathology and confirmation of therapeutic success.

Against the above background, Liying Tao, Digestive Endoscopy Center, Jilin People’s Hospital, Jilin, China, and colleagues aimed to investigate the efficacy and safety of appendicoscopy using SOC for the management of acute obstructive appendicitis.

The researchers described 110 cases of acute obstructive appendicitis managed by appendicoscopy between 2021 and 2023. The success rate (technical + clinical), procedure time, postoperative length of hospital stay, time to relief abdominal pain using the visual analogue scale (VAS), and complication rates were recorded and analyzed.

Following were the study’s key findings:

· The technical success rate of appendicoscopy was 96.4%; the clinical success rate was 91.8%.

· The mean procedure time was 20.9±10 minutes (standard deviation [SD]).

· The abdominal pain score at 6 hours after the procedure was ≤3 (VAS method) in 99.1% of the patients.

· The average length of postoperative hospital stay was 3.5±1.5 days.

· No adverse events occurred.

In conclusion, appendicoscopy with SOC emerges as a promising alternative to conventional appendectomy in the management of acute obstructive appendicitis. By combining the advantages of endoscopic access with the visualization capabilities of the cholangioscope, this innovative approach offers a minimally invasive yet effective means of relieving appendiceal obstruction and facilitating therapeutic interventions.

Reference:

Tao L, Wang H, Guo Q, Guo S, Guo X, Liu S. Appendicoscopy Using Single Operator Cholangioscope in The Management of Acute Obstructive Appendicitis: A Novel Alternative. Gastrointest Endosc. 2024 Apr 7:S0016-5107(24)00227-X. doi: 10.1016/j.gie.2024.04.010. Epub ahead of print. PMID: 38593933.

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Torrent Pharmaceutical Gets CDSCO Panel Nod To Manufacture, Market Antidiabetic FDC

New Delhi: Reviewing the justification presented by the drug major Torrent Pharmaceutical, the Subject Expert Committee (SEC) functional under the Central Drug Standard Control Organisation (CDSCO) has granted approval to manufacture and market the fixed-dose combination (FDC) Alogliptin Benzoate eq. to Alogliptin 25mg/25mg plus Pioglitazone Hydrochloride USP eq. to Pioglitazone 15mg/30mg film-coated tablet.

This came after the drug maker Torrent Pharmaceutical presented their proposal along with justification for clinical trial and bioequivalence (BE) waiver based on the BE study conducted on higher strength i.e. Fixed-Dose Combination of Alogliptin 25 mg and Pioglitazone 45 mg Tablet for export purposes in 2016 before the committee.

In addition to the above, the firm stated that the said FDC is already approved in other countries i.e. USA, Australia, Japan, etc.

Alogliptin is a selective DPP-4 inhibitor. DPP-4 inhibitors lower blood glucose by preventing the breakdown of glucagonlike peptide-1 (GLP-1) and glucose-dependent insulinotropic polypeptide, thus prolonging the activity of these peptides. Alogliptin is used along with diet and exercise to lower blood sugar levels in patients with type 2 diabetes (a condition in which blood sugar is too high because the body does not produce or use insulin normally). Alogliptin is in a class of medications called dipeptidyl peptidase-4 (DPP-4) inhibitors.

Pioglitazone helps to control your blood sugar levels by helping your body make better use of the insulin it produces. Pioglitazone is only available on prescription. Pioglitazone improves glycaemic control in people with Type 2 diabetes by improving insulin sensitivity through its action at PPAR gamma 1 and PPAR gamma 2, and affects lipid metabolism through action at PPAR alpha.

At the recent SEC meeting for Endocrinology and Metabolism held on 21st March 2024, the expert panel reviewed the proposal presented by Torrent Pharmaceutical along with the justification for CT and BE waiver based on the BE study conducted on higher strength i.e. Fixed Dose Combination of Alogliptin 25 mg and Pioglitazone 45 mg Tablet for export purposes in 2016

After detailed deliberation, the committee recommended the grant of permission to manufacture and market the product after submission of data including dissolution data and justification for BE waiver as per the BE Study guideline with the condition that the firm should conduct Phase IV clinical trial.

Accordingly, the expert panel suggested that the firm should submit a Phase IV clinical trial protocol to CDSCO within 03 months of approval for review by the committee.

Also Read:CDSCO Panel Approves J&J’s Protocol Amendment Proposal For Amivantamab, Lazertinib combination

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Dr Reddy’s Swiss to sell entire stake in Dr Reddy’s Venezuela C.A.

Hyderabad: Through a recent BSE filing, Dr Reddy’s Labs has informed that the wholly owned subsidiary
of the Company, namely, Dr Reddy’s Laboratories SA, Switzerland, (referred to hereinafter as “Dr.
Reddy’s Swiss”) has entered into Stock Purchase Agreement for sale/ disposal of its entire stake in Dr
Reddy’s Venezuela C.A., Venezuela, the wholly owned subsidiary of Dr. Reddy’s Swiss. 
Pursuant to the Stock Purchase Agreement, shares will be sold to Kuraduria Holdings Corp (‘KHC’).

Consequently,
Dr. Reddy’s Venezuela C.A. will cease to be a wholly owned subsidiary of Dr. Reddy’s Swiss as well
as step down wholly owned subsidiary of the Company.

The completion of sale/ disposal will be effective by April 17, 2024, as per the Company’s expectation.

Read also: Dr Reddy’s Labs, Bayer collaborate to market, distribute second brand of heart failure drug Vericiguat in India

Established in 1984, Dr Reddy’s Laboratories Ltd. is a global pharmaceutical company headquartered in Hyderabad, India. Dr Reddys offers a portfolio of products and services including APIs, generics, branded generics, biosimilars and OTC. Its major therapeutic areas of focus are gastrointestinal, cardiovascular, diabetology, oncology, pain management and dermatology. Dr Reddys major markets include – USA, India, Russia & CIS countries, China, Brazil and Europe.

Read also: Dr Reddy’s Labs arm introduces AI, machine learning assisted drug discovery platform Aurigene.AI

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Medical Council denies registration over non-recognition of PG medical courses, Kerala doctors to protest

Thiruvananthapuram: Around 200 doctors from Kerala, who completed their postgraduate studies this year, are upset with the decision of the Travancore-Cochin Medical Council (TCMC) to deny their registration. The medical council decided not to register these doctors noting their courses were not recognised by the erstwhile Medical Council of India (MCI), now the National Medical Commission (NMC).

Therefore, despite completing their PG medical courses, these doctors will continue to be treated as MBBS-qualified doctors.

According to a recent report by TNIE, upset over the medical council’s denial, now the doctors are planning an agitation under the aegis of the Kerala Medical Post Graduates Association (KMPGA). They are also considering to seek the Government’s intervention in this regard.

Registration from the Medical Council is mandatory for doctors wishing to pursue further studies by joining super speciality courses or to be able to seek jobs.

However, as per the State President of KMPGA, Dr Jathin, there are hundreds of other doctors who are affected by the decision of the medical council.

Also Read:Kerala: Medical Council calls for compulsory registration of PG Medical students, faces objection

Commenting on the matter, Dr Jathin informed The New Indian Express, “An estimated 600 doctors, who completed PG in the last three years, are still waiting for a TCMC registration. This cannot be justified.”

Further mentioning that they were planning to approach the Government to seek a solution, Dr. Jathin added, “The issue is not new and has been around for quite some time. If the government does not take any step, then the KMPGA would be forced to agitate.”

He also highlighted that the erstwhile MCI, surprisingly, recognised some seats in the same departments of a medical college. However, the Apex Medical Council refused to recognise others.

Blaming the State for the situation, Dr. Jathin further said, “For instance, 10 out of 14 seats in the Medicine Department of Kottayam Medical College are recognised, while four are not. So, all PG doctors in the department have been denied the TCMC registration.”

“The MCI allowed the government to admit students in PG courses on the assurance that it would address the issues needed for recognition. But, the government did not uphold its end of the bargain, which resulted in some seats losing MCI’s recognition. The doctor is not at fault for completing PG course from such seats. The government should have taken steps to get recognition,” he mentioned.

Extending their support to the affected doctors, the State President of Kerala Government PG Medical Teachers’ Association Dr Ajith Prasad J S and IMA State President Dr. A V Jayakrishnan have also opined that the doctors should be allowed to register as otherwise their future would be affected.

Meanwhile, commenting on the issue, a member of the Travancore-Cochin Medical Council and former State President of the Indian Medical Association (IMA) Dr Sreejith N Kumar informed the Daily that the council had written to the State Government and the NMC asking about which steps to take for registration. 

While agreeing that the doctors should get registration, he added, “But, the TCMC cannot override the rules. If it allows registration to the PG qualified doctors, it would be in clear violation of the existing rules. It is now for the Centre to take a decision in the matter.”

Also Read: Fee Hike but not Stipend Hike: Kerala PG doctors to go on 24 hour strike on 8th November

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Study shows use of fairness cream driving hike in kidney problems in India

A recent study published in Kidney International highlights the concerning correlation between the widespread use of skin fairness creams and an increase in kidney problems in India. The obsession with fair skin in society has fueled a lucrative market for these creams, but their high mercury content poses serious health risks, particularly to the kidneys.

The study, conducted by researchers including Dr. Sajeesh Sivadas from the Department of Nephrology at Aster MIMS Hospital in Kottakkal, Kerala, found a direct link between the use of fairness creams and Membranous Nephropathy (MN), a condition that damages kidney filters and leads to protein leakage.

Reference: NELL-1 associated membranous nephropathy linked to skin fairness cream use- insights from an Indian case series, Ranjit Narayanan, Sajeesh Sivadas, Anila Abraham Kurien, DOI:https://doi.org/10.1016/j.kint.2024.03.025

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Mid-Surgery tissue sample transported via drone for Pathological Testing

The Indian Council of Medical Research (ICMR) on Wednesday announced the successful transportation of a tissue sample via drone from a peripheral hospital to a tertiary setting for advanced pathological testing.

This innovative approach aims to expedite the determination of whether the resected tissue is cancerous, potentially revolutionizing surgical decision-making.

For more details, check out the full story on the link below: 

37 Km In 16 Minutes: Mid-Surgery Tissue Sample Transported Via Drone For Pathological Testing

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