Rise in Kayakalp facilities from 97 in FY 2015-16 to 13915 in FY 2021-22, MoS Health informs Lok Sabha

New Delhi: In a notable development of the Kayakalp facilities, the count of Public Health Facilities up to District Hospitals, has witnessed a substantial rise, soaring from 97 in the fiscal year 2015-16 to an impressive 13,915 in the fiscal year 2021-22.

The evolving landscape introduced a new thematic dimension in the criteria for these facilities in 2021-22, emphasizing the adoption of eco-friendly practices. 

Adding to the transformative measures, the Kayakalp scheme has undergone a noteworthy transition, now being classified as an “incentive scheme.” This initiative operates on dual fronts, encompassing Public Health Facilities up to District Hospitals and Central Government Hospitals. The expansion in the number of facilities underscores the government’s commitment to enhancing public healthcare infrastructure, ensuring wider accessibility and improved services. The incorporation of an eco-friendly aspect reflects a growing emphasis on sustainable and environmentally conscious practices within the healthcare domain.

Also Read: Kayakalp Team pays visit to AIIMS Bhubaneswar

The Kayakalp scheme’s reclassification as an incentive scheme underscores the intention to motivate and reward excellence in maintaining high standards of cleanliness, hygiene, and overall quality in public health facilities. This multifaceted approach aims to create a healthier, more sustainable healthcare environment at both district and central government levels.

Dr Bharati Pravin Pawar, Minister of State for Health and Family Welfare, in a written reply in Lok Sabha, stated, “The Kayakalp scheme was launched to complement the efforts of Swachh Bharat Abhiyan to promote cleanliness in public spaces. It is a national initiative to recognize and incentivize such public health facilities that demonstrate high levels of cleanliness, hygiene, and infection control.” 
Further, responding to a question raised by Shri Parbatbhai Savabhai Patel, Dr Pawar clarified the objectives of the scheme. The Kayakalp scheme aims to foster cleanliness, hygiene, and infection control practices in public health care facilities, setting forth specific objectives. It seeks to provide incentives and recognition to those facilities that exhibit exemplary performance in adhering to standardized cleanliness and infection control protocols.
Additionally, the scheme endeavours to instill a culture of continuous assessment and peer review, emphasizing hygiene, cleanliness, and sanitation practices. Another key objective is to facilitate the creation and dissemination of sustainable practices linked to improved cleanliness, with a positive impact on health outcomes in public health facilities.
The Kayakalp assessment is a comprehensive three-tier process involving internal, peer, and external evaluations, ensuring a rigorous evaluation mechanism. At the commencement of each financial year, health facilities undergo assessment, scoring, and documentation using a predefined assessment tool.

For Public Health facilities upto district Hospitals, the assessment tool has a checklist arranged around eight thematic areas including Hospital/Facility Upkeep, Sanitation and Hygiene, Waste Management, Infection Control, Support Services, Hygiene Promotion, Cleanliness beyond hospital boundary wall and Eco-friendly facility. For Central Government Hospitals, the assessment tool has the following thematic areas including Hospital Upkeep, Sanitation and hygiene, Support Services, Waste Management, infection Control, Hygiene Promotion and Feedback Mechanism from Public on Cleanliness.

Also Read: Phagwara’s Rajan Eye Care Hospital gets recognition under cleanliness survey

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Wockhardt loss narrows to Rs 86 crore in Q3

New Delhi: Pharmaceuticals firm Wockhardt Ltd has reported narrowing of consolidated net loss to Rs 86 crore for the third quarter ended December 31, 2023.

The company had incurred a loss of Rs 102 crore in the third quarter last fiscal, Wockhardt Ltd said in a regulatory filing.

Revenue from operations during the quarter under review stood at Rs 701 crore as compared to Rs 699 crore in the year-ago period, the company said.

Total expenses were lower at Rs 796 crore as against Rs 803 crore in the same period last fiscal.

Read also: Wockhardt Gets CDSCO Panel Nod To study combination of cefepime and zidebactam

Headquartered in Mumbai, Wockhardt is an Indian pharmaceutical and biotechnology company. The Company produces biopharmaceuticals, nutrition products, formulations, vaccines and active pharmaceutical ingredients (APIs). Its manufacturing plants are located in India, UK, Ireland, France and US, and subsidiaries in US, UK, Ireland and France.

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High cumulative oxytocin doses during labor tied to adverse postpartum outcomes

High cumulative oxytocin doses during labour tied to adverse postpartum outcomes suggests a new study published in the European Journal of Obstetrics and Gynecology and Reproductive Biology.

The reproductive hormone oxytocin facilitates labour, birth and postpartum adaptations for women and newborns. Synthetic oxytocin is commonly given to induce or augment labour and to decrease postpartum bleeding. A study was done to systematically review studies measuring plasma oxytocin levels in women and newborns following maternal administration of synthetic oxytocin during labour, birth and/or postpartum and to consider possible impacts on endogenous oxytocin and related systems.

Systematic searches of PubMed, CINAHL, PsycINFO and Scopus databases followed PRISMA guidelines, including all peer-reviewed studies in languages understood by the authors. Thirty-five publications met the inclusion criteria, including 1373 women and 148 newborns. Studies varied substantially in design and methodology, so classical meta-analysis was not possible. Therefore, results were categorized, analysed and summarised in text and tables. Results: Infusions of synthetic oxytocin increased maternal plasma oxytocin levels dose-dependently; doubling the infusion rate approximately doubled oxytocin levels. Infusions below 10 milliunits per minute (mU/min) did not raise maternal oxytocin above the range observed in physiological labour. At high intrapartum infusion rates (up to 32 mU/min) maternal plasma oxytocin reached 2–3 times physiological levels. Postpartum synthetic oxytocin regimens used comparatively higher doses with shorter duration compared to labour, giving greater but transient maternal oxytocin elevations. Total postpartum dose was comparable to the total intrapartum dose following vaginal birth, but post-caesarean dosages were higher. Newborn oxytocin levels were higher in the umbilical artery vs. umbilical vein, and both were higher than maternal plasma levels, implying substantial fetal oxytocin production in labour. Newborn oxytocin levels were not further elevated following maternal intrapartum synthetic oxytocin, suggesting that synthetic oxytocin at clinical doses does not cross from mother to fetus. Synthetic oxytocin infusion during labour increased maternal plasma oxytocin levels 2–3-fold at the highest doses and was not associated with neonatal plasma oxytocin elevations. Therefore, direct effects from synthetic oxytocin transfer to the maternal brain or fetus are unlikely. However, infusions of synthetic oxytocin in labour change uterine contraction patterns. This may influence uterine blood flow and maternal autonomic nervous system activity, potentially harming the fetus and increasing maternal pain and stress.

Reference:

Buckley S, Uvnäs-Moberg K, Pajalic Z, Luegmair K, Ekström-Bergström A, Dencker A, Massarotti C, Kotlowska A, Callaway L, Morano S, Olza I, Magistretti CM. Maternal and newborn plasma oxytocin levels in response to maternal synthetic oxytocin administration during labour, birth and postpartum – a systematic review with implications for the function of the oxytocinergic system. BMC Pregnancy Childbirth. 2023 Mar 2;23(1):137. doi: 10.1186/s12884-022-05221-w. PMID: 36864410; PMCID: PMC9979579.

Keywords:

High cumulative oxytocin doses, labour, adverse postpartum outcomes, European Journal of Obstetrics and Gynecology and Reproductive Biology, Buckley S, Uvnäs-Moberg K, Pajalic Z, Luegmair K, Ekström-Bergström A, Dencker A, Massarotti C, Kotlowska A, Callaway L, Morano S, Olza I, Magistretti CM, Oxytocin, Maternal oxytocin, Newborn oxytocin, Synthetic oxytocin, Pitocin, Syntocinon, Postpartum oxytocin, Induction of labour, Augmentation of labour

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Age not a contraindication for microvascular reconstruction of advanced oral cancer

Age is not a contraindication for microvascular reconstruction of advanced oral cancer suggests a new study published in the Oral Surgery, Oral Medicine, Oral Pathology and Oral Radiology.

Flap complications continue to be a challenge in microsurgical reconstruction for older adults.They aimed to evaluate the impact of age on surgical outcomes after microvascular reconstruction. They retrospectively investigated 103 patients with oral squamous cell carcinoma who had undergone microvascular reconstruction surgery to compare microsurgical reconstruction, common postoperative complications, and flap success rates in geriatric (>75 years) and non-geriatric (<75 years) patients. We also evaluated differences based on the American Society of Anesthesiologists Physical Status score. They found no significant differences between the geriatric and non-geriatric groups in peri-operative, postoperative, or general complications. Conversely, they found that delirium and aspiration pneumonia were significantly more likely to occur in geriatric patients and that multiple medical complications were significantly more likely to occur in geriatric patients with a high American Society of Anesthesiologists score. Microvascular reconstruction can be performed effectively and without excessive complications in geriatric patients, and age should not be considered a contraindication for this procedure. Comorbidities play a stronger role in the prediction of adverse events. As microvascular reconstruction for advanced oral cancer can be performed effectively and without excessive complications in geriatric patients, age should not be considered a contraindication for this procedure. A patient’s ASA PS score, considering the presence of comorbidities, plays a stronger role in predicting the incidence of adverse events.

Reference:

Kouketsu A, Kaneuji T, Yamaguma Y, Yamauchi K, Sugiura T, Takahashi T, Ito H, Yamashita Y. Microvascular reconstruction for oral cancer in older adult patients: the impact of age on surgical outcomes. Oral Surg Oral Med Oral Pathol Oral Radiol. 2024 Jan;137(1):6-11. doi: 10.1016/j.oooo.2023.06.010. Epub 2023 Jun 29. PMID: 37612162.

Keywords:

Age, contraindication, microvascular reconstruction, advanced oral cancer, Kouketsu A, Kaneuji T, Yamaguma Y, Yamauchi K, Sugiura T, Takahashi T, Ito H, Yamashita Y, Oral Surgery, Oral Medicine, Oral Pathology and Oral Radiology

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Can Higher HDL levels lead to reversion to normoglycemia from prediabetes?

China: An analysis based on data from a retrospective cohort study revealed an independent connection between high-density lipoprotein cholesterol (HDL-C) and regression to normoglycemia in Chinese adults with prediabetes, revealing a specific non-linear relationship and threshold effect.

In their study, published in Scientific Reports, the researchers observed a significant positive connection between HDL-C levels and the regression from Pre-DM to normoglycemia to normoglycemia, specifically when HDL-C levels were below the inflection point. Consequently, keeping HDL-C levels near the inflection point in prediabetes patients may greatly raise the likelihood of reversion from pre-DM to normoglycemia.

Higher HDL-C levels show a positive association with prediabetes reversal to normoglycemia in Chinese adults, but only up to a certain threshold, the researchers stated.

Prediabetes is characterized by a blood glucose level above the “normal” range but below the diagnostic threshold for type 2 diabetes (T2D). Previous studies have shown that even a temporary return to normal blood glucose levels in pre-DM patients is related to a significantly reduced chance of developing T2D. Therefore, it is important to highlight the significant clinical advantages of transitioning from Pre-DM to normoglycemia. The primary objective of screening and treating prediabetes should be to restore normoglycemia.

The available evidence on the connection between HDL-C levels and the reversion from prediabetes to normoglycemia is currently limited. Therefore, Yong Han, The First Affiliated Hospital of Shenzhen University, Shenzhen, Guangdong Province, China, and colleagues sought to investigate the connection between HDL-C levels and the regression from Pre-DM to normoglycemia in a population of Chinese adults.

The study included 15,420 prediabetes patients in China who underwent health screening between 2010 and 2016. The researchers investigated the connection between HDL-C levels and reversion from Pre-DM to normoglycemia using the Cox proportional hazards regression model.

The Cox proportional hazards regression model with cubic spline functions and smooth curve fitting was employed to ascertain the nonlinear association between HDL-C and reversion from prediabetes to normoglycemia. A set of sensitivity analyses and subgroup analyses were also employed.

The study led to the following findings:

  • Following the adjustment of covariates, the findings revealed a positive connection between HDL-C levels and the likelihood of reversion from Pre-DM to normoglycemia (HR 1.898).
  • There was a non-linear relationship between HDL-C and the reversion from Pre-DM to normoglycemia in both genders, and the inflection point of HDL-C was 1.540 mmol/L in males and 1.620 mmol/L in females.
  • There was a strong positive correlation between HDL-C and the reversion from Pre-DM to normoglycemia on the left of the inflection point (Male: HR 2.783; Female: HR 2.217). The sensitivity analysis confirmed the robustness of these findings.
  • Subgroup analyses indicated that patients with SBP < 140 mmHg and ever smoker exhibited a more pronounced correlation between HDL-C levels and the reversion from Pre-DM to normoglycemia.
  • There was a less robust correlation among patients with SBP ≥ 140 mmHg, current and never smokers.

The study provides evidence of a positive and nonlinear association between HDL-C levels and the reversion from prediabetes to normoglycemia in Chinese patients.

“Implementing intensified intervention measures to control the HDL-C levels of prediabetes patients around the inflection point may substantially enhance the likelihood of regression to normoglycemia,” the researchers concluded.

Reference:

Mo, Z., Hu, H., Han, Y., Cao, C., & Zheng, X. (2024). Association between high-density lipoprotein cholesterol and reversion to normoglycemia from prediabetes: An analysis based on data from a retrospective cohort study. Scientific Reports, 14(1), 1-14. https://doi.org/10.1038/s41598-023-50539-w

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Biologic drug abatacept used for treatment of RA could prevent disease as well, clinical trial shows

Biologic drug abatacept which used to treat rheumatoid arthritis could also prevent the disease in individuals deemed to be at risk, reveals new clinical trial.

Results from a Phase 2b clinical trial, published today in The Lancet by researchers led by King’s College London, provides hope for arthritis sufferers after it was shown that the biologic drug abatacept reduces progression to this agonising chronic inflammatory disease.

Rheumatoid arthritis affects half a million people in the UK and develops when the body’s immune system attacks itself, causing joint pain, swelling and significant disability. The disease most commonly begins in middle age, but much younger age groups can be afflicted, and until now there is no cure or prevention.

Abatacept is currently used as an effective second or third line treatment for people living with established rheumatoid arthritis and is given by weekly injections at home or in hospital via a drip.

Researchers from King’s College London recruited 213 patients at high risk of the disease to understand whether a year-long treatment of the biologic drug could be used to prevent progression to rheumatoid arthritis.

They recruited men and women over the age of 18 with early symptoms such as joint pain but no joint swelling, and treated half with the drug and half with a placebo every week for a year. The study drug was then stopped, and study participants monitored for a further 12 months.

After twelve months of treatment, 6% of patients treated with abatacept had developed arthritis compared to 29% in the placebo arm. By 24 months, the differences were still significant, with a total of 25% progressing to rheumatoid arthritis in the abatacept arm compared to 37% in the placebo arm.

Professor Andrew Cope, from King’s College London, said: “This is the largest rheumatoid arthritis prevention trial to date and the first to show that a therapy licensed for use in treating established rheumatoid arthritis is also effective in preventing the onset of disease in people at risk. These initial results could be good news for people at risk of arthritis as we show that the drug not only prevents disease onset during the treatment phase but can also ease symptoms such as pain and fatigue. This is also promising news for the NHS as the disease affects people as they age and will become more expensive to treat with a growing aging population.”

Secondary outcomes for the trial showed that abatacept was associated with improvements in pain scores, function and quality of life measurements, as well as lower scores of inflammation of the lining of joints detectable by ultrasound scan.

Philip Day, a 35-year-old software engineer and founder of FootballMatcher from Eltham, was at high-risk for rheumatoid arthritis. A keen football player, Philip’s joint pain deterred him from playing and affected his day-to-day life. He was enrolled in the trial in 2018, at the age of the 30, and was prescribed abatacept.

He said: “The pain got so terrible I stopped going to football, and I got lazier and felt progressively worse physically and mentally. The pain was unpredictable, it would show up in my knees one day, my elbows the next, and then my wrists or even my neck. At the time, my wife and I wanted to have children and I realised my future was pretty bleak if the disease progressed. I’d always wanted to be the kind of dad that played football with his son and I knew the pain would stop me from realising that dream.

“Enrolling in the trial was a no-brainer; it was a ray of hope at a dark time. Within a few months I had no more aches or pains and five years on I’d say I’ve been cured. Now, I can play football with my three-year-old son and have a normal life.”

One year’s treatment with abatacept costs the NHS about £10,000 per patient and is not without risk. Side effects include upper respiratory tract infections, dizziness, nausea and diarrhoea, but these are generally mild.

Professor Cope added: “There are currently no drugs available that prevent this potentially crippling disease. Our next steps are to understand people at risk in more detail so that we can be absolutely sure that those at highest risk of developing rheumatoid arthritis receive the drug.”

Rheumatologist Professor Sir Ravinder N Maini FRS FMedSci FRCP, who was not involved in the research, said: “Professor Cope and colleagues from King’s College, London, in collaboration with researchers in the UK and Netherlands, have published the results of an exciting clinical trial in The Lancet, which demonstrates that it is now possible to prevent the onset of RA, a disease that remains incurable despite great advances in its treatment in the recent past.

“The results clearly show that during the treatment period almost all individuals receiving the biologic drug showed no symptoms or signs of RA compared with the control population amongst many more developed RA. In the follow up period of 1 year off treatment, it is interesting to note that some appeared to go into remission.

“Prevention of disease is of course a highly desirable goal in preventing the ravages of disabling RA, which is associated with a significant social and financial burden. Many further questions arise from this important study. For example, will this preventive approach be safe and cost effective if continued long term or can the selection of suitable populations be refined so that only those likely to benefit most are treated with a short course of treatment?”

Reference:

Prof Andrew P Cope, Marianna Jasenecova, Prof Andrew Filer, Abatacept in individuals at high risk of rheumatoid arthritis (APIPPRA): a randomised, double-blind, multicentre, parallel, placebo-controlled, phase 2b clinical trial, The Lancet, https://doi.org/10.1016/S0140-6736(23)02649-1.

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Herpes virus infection may double likelihood of developing dementia: Uppala University Study

People who have had the herpes virus at some point in their lives are twice as likely to develop dementia compared to those who have never been infected. A new study from Uppsala University confirms previous research on whether herpes can be a possible risk factor for dementia.

The researchers studied 1,000 70-year-olds from Uppsala over a period of 15 years. The study, now published in the Journal of Alzheimer’s Disease, found that people who had been infected with the herpes simplex virus at some point in their lives were twice as likely to develop dementia, compared to those who had never been infected. The herpes simplex virus is very common and up to 80 percent of Swedish adults may be infected. The infection is lifelong, but the symptoms can come and go over different periods of life. Many people never get any symptoms linked to their infection.

“What’s special about this particular study is that the participants are roughly the same age, which makes the results even more reliable since age differences, which are otherwise linked to the development of dementia, cannot confuse the results,” explains Erika Vestin, a medical student at Uppsala University.

55 million people worldwide are affected by dementia. Advanced age and carrying the apolipoprotein ε4 risk gene are already known risk factors. Research has previously been conducted to investigate whether the herpes simplex virus could also be a possible risk factor for dementia; something now confirmed in this study.

“It is exciting that the results confirm previous studies. More and more evidence is emerging from studies that, like our findings, point to the herpes simplex virus as a risk factor for dementia,” continues Vestin.

Important conclusions from the study include the need to further investigate whether already known drugs against the herpes simplex virus can reduce the risk of dementia and the possibility of developing new vaccines.

“The results may drive dementia research further towards treating the illness at an early stage using common anti-herpes virus drugs, or preventing the disease before it occurs,” adds Vestin.

Reference:

Vestin, Erikaa, Boström, Gustafa; Olsson, Janc, Elgh, Fredrikc, Lind, Larsd, Kilander, Lenaa, Lövheim, Hugoe, Herpes Simplex Viral Infection Doubles the Risk of Dementia in a Contemporary Cohort of Older Adults: A Prospective Study, Journal of Alzheimer’s Disease, DOI: 10.3233/JAD-230718.

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Plasma proteomic profiles may predict onset of dementia

A recent study published in the Nature Aging journal unveiled the promising use of proteomics in predicting the onset of dementia which offers hope for early detection and intervention.

The study analyzed data from the UK Biobank which included a total of 52,645 adults without dementia and tracked 1,417 incident cases over a span of 14.1 years. The focus of the research was on examining plasma proteins; out of 1,463 proteins studied, GFAP, NEFL, GDF15 and LTBP2 was found to be associated with incident all-cause dementia (ACD), Alzheimer’s disease (AD) and vascular dementia (VaD).

These proteins significantly ranked high in importance ordering and expressed promise in predicting dementia onset when combined with demographic factors. For instance, combining GFAP (or GDF15) with demographics produced highly accurate predictions for ACD (AUC = 0.891) and AD (AUC = 0.872) (or VaD (AUC = 0.912)), even over a 10-year period.

The participants with elevated levels of GFAP were found to be 2.32 times more risk to develop dementia by underlining its potential as a major biomarker for early detection. Also, GFAP and LTBP2 demonstrated high specificity for dementia prediction. Changes in GFAP and NEFL were observed at least a decade before dementia diagnosis which highlights the possibility of identifying high-risk individuals well in advance.

The findings of this study highlight the intricate mechanisms underlying dementia but also offer a hope for proactive screening and intervention strategies. Leveraging proteomics and understanding the predictive power of specific proteins could enable the healthcare professionals to identify individuals at risk of dementia long before symptoms manifest by improving the targeted interventions and outcomes.

Reference:

Guo, Y., You, J., Zhang, Y., Liu, W.-S., Huang, Y.-Y., Zhang, Y.-R., Zhang, W., Dong, Q., Feng, J.-F., Cheng, W., & Yu, J.-T. (2024). Plasma proteomic profiles predict future dementia in healthy adults. In Nature Aging. Springer Science and Business Media LLC. https://doi.org/10.1038/s43587-023-00565-0

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Subcutaneous Nivolumab as Effective as IV injection for Renal Cell Carcinoma-With Much Faster Treatment Time

Subcutaneous injection of the immunotherapy nivolumab (brand name Opdivo) is noninferior to intravenous delivery and dramatically reduces treatment time in patients with renal cell carcinoma, as seen in the results of a large phase 3 clinical trial reported today at the 2024 American Society of Clinical Oncology (ASCO) Genitourinary Cancers Symposium in San Francisco, California. Saby George, MD, FACP, Professor of Oncology and Medicine and Director of Network Clinical Trials at Roswell Park Comprehensive Cancer Center, will deliver an oral abstract summarizing the findings of “A Study of Subcutaneous Nivolumab Versus Intravenous Nivolumab in Participants with Previously Treated Clear Cell Renal Carcinoma That Is Advanced or Has Spread (CheckMate-67T)” (NCT04810078).

“The burden of treatment felt by cancer patients is tremendous. If nivolumab can be given as a subcutaneous injection instead of an intravenous infusion, their treatment experience will be significantly improved,” says Dr. George, who is the presenting author, a member of the clinical trial steering committee and site principal investigator at Roswell Park. “Instead of one hour in an infusion chair, they will get the injection done in five minutes.”

He points to the high demand for infusion chair appointments at most cancer centers, which can result in treatment delays of a week or more.

“If nivolumab becomes available subcutaneously, we can administer it in the clinic instead of sending patients to infusion centers,” he says. That outcome could simultaneously speed treatment time for patients receiving nivolumab and shorten wait times for patients who still need to receive treatment in an infusion center.

The availability of injectable nivolumab could also reduce health disparities. “One of the major problems is access to treatment,” says Dr. George, noting that some patients live a long distance from an infusion center and do not have a way to get there. “Patients who don’t live near an infusion center could get treatment closer to home, at a clinic, and that could improve access and help reduce disparities.”

Sponsored by Bristol Myers Squibb, the drug’s manufacturer, the clinical trial began in May 2021, randomizing 495 patients at 73 centers in 17 countries. Roswell Park was one of only three participating sites in the U.S. and the only one in New York State.

Patients in the study had advanced or metastatic renal cell carcinoma, had received no more than two prior treatments with systemic therapies and no prior immunotherapy. They were randomized 1:1 to receive nivolumab either subcutaneously or intravenously. Nivolumab is FDA-approved and the standard-of-care treatment for those patients.

The study’s primary objective was to evaluate the pharmacokinetics of subcutaneous vs. intravenous delivery-how the body interacted with the nivolumab, including whether blood levels of the drug were comparable in the two groups over time. Those measures included the daily average concentration of the drug in the blood over 28 days (Cavgd28) and the concentration of the drug at the end of the dosing cycle (Cminss). Both measures were noninferior to intravenous nivolumab, as evidenced in pharmacokinetic measures and overall response rate.

The objective response rate for the subcutaneous group-the percentage of patients who achieved a complete or partial response, measured by blinded independent central review-proved noninferior to the intravenous group, at 24.2% vs. 18.2%, respectively. Median progression-free survival stood at 7.23 months for the subcutaneous group vs. 5.65 months for the IV group. The safety profile was similar for both groups.

More than 80,000 new cases of renal cell carcinoma are diagnosed in the U.S. each year.

Because nivolumab is already FDA-approved for more than 20 indications across multiple malignancies, CheckMate-67T will likely serve as a gateway to additional studies evaluating the effectiveness of the subcutaneous formula in other patient populations.

“This is a groundbreaking achievement for patients and physicians, and will definitely make treatment easier for patients,” says Dr. George.

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COVID-19 vaccination and booster dose during pregnancy protects infants finds study

Women who receive an mRNA-based COVID-19 vaccination or booster during pregnancy can provide their infants with strong protection against symptomatic COVID-19 infection for at least six months after birth, according to a study from the National Institute of Allergy and Infectious Diseases (NIAID), part of the National Institutes of Health. These findings, published in Pediatrics, reinforce the importance of receiving both a COVID-19 vaccine and booster during pregnancy to ensure that infants are born with robust protection that lasts until they are old enough to be vaccinated.

COVID-19 is especially dangerous for newborns and young infants, and even healthy infants are vulnerable to COVID-19 and are at risk for severe disease. No COVID-19 vaccines currently are available for infants under six months old. Earlier results from the Multisite Observational Maternal and Infant COVID-19 Vaccine (MOMI-Vax) study revealed that when pregnant volunteers received both doses of an mRNA COVID-19 vaccine, antibodies induced by the vaccine could be found in their newborns’ cord blood. This suggested that the infants likely had some protection against COVID-19 when they were still too young to receive a vaccine. However, researchers at the NIAID-funded Infectious Diseases Clinical Research Consortium (IDCRC), which conducted the study, did not know how long these antibody levels would last or how well the infants would actually be protected. The research team hoped to gather this information by following the infants through their first six months of life.

In this portion of the study, researchers analyzed data from 475 infants born while their pregnant mothers were enrolled in the MOMI-Vax study. The study took place at nine sites across the United States. It included 271 infants whose mothers had received two doses of an mRNA COVID-19 vaccine during pregnancy. The remaining 204 infants in the study were born to mothers who had received both doses of an mRNA COVID-19 vaccine as well as a COVID-19 booster. To supplement data gathered during pregnancy and at birth, the infants were evaluated during at least one follow-up visit during their first six months after birth. Parents also reported whether their infants had become infected or had demonstrated COVID-19 symptoms.

Based on blood samples from the infants, the researchers found that newborns with high antibody levels at birth also had greater protection from COVID-19 infection during their first six months. While infants of mothers who received two COVID-19 vaccine doses had a robust antibody response at birth, infants whose mothers had received an additional booster dose during pregnancy had both higher levels of antibodies at birth and greater protection from COVID-19 infection at their follow-up visits.

While older children and adults should continue to follow guidance from the Centers for Disease Control and Prevention (CDC) to stay up-to-date on their COVID-19 vaccines and boosters, this study highlights how much maternal vaccination can benefit newborns too young to take advantage of the vaccine: During the course of this study, none of the infants examined required hospitalization for COVID-19. Researchers will continue to evaluate the data from the MOMI-Vax study for further insights concerning COVID-19 protection in infants.

Reference:

Cristina V. Cardemil, Yi Cao, Christine M. Posavad, Martina L. Badell, Katherine Bunge, Mark J. Mulligan, Lalitha Parameswaran, Courtney Olson-Chen,  Richard M. Novak, Rebecca C. Brady, Emily DeFranco, Maternal COVID-19 Vaccination and Prevention of Symptomatic Infection in Infants,https://doi.org/10.1542/peds.2023-064252.

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