Widespread Dental Pulp Calcification Observed in SLE Patient on Long-Term Steroid Therapy: Case Report

China: A recent case study published in The Open Dentistry Journal sheds light on a dental issue faced by patients with systemic lupus erythematosus (SLE) treated with long-term glucocorticoids (GCs). SLE is an autoimmune disease that causes widespread inflammation, and glucocorticoids are often prescribed to manage its symptoms. However, prolonged use of these medications can lead to complications, including pulp cavity calcification in the teeth.         

The case involved a 30-year-old woman diagnosed with SLE at 17 and treated with methylprednisolone for 13 years. She visited the dental clinic with a fractured tooth (tooth 11) and reported sensitivity to cold. Examination and diagnostic tests, including electric pulp testing and panoramic radiographs, revealed chronic pulpitis and calcification of the pulp cavity in the affected teeth. Cone beam computed tomography (CBCT) confirmed that pulp calcification extended beyond the damaged teeth.

The long-term use of glucocorticoids raised concerns about the role these medications might play in the calcification of her dental pulp. While electric pulp testing indicated normal pulp sensitivity, the radiographs and CBCT scans revealed root canal calcification, complicating the treatment. Initially, a root canal treatment (RCT) was recommended, but the calcification made it difficult to access the root apex.

Given the severity of calcification, the treatment plan was modified. A pulpotomy was performed, and the root canals were temporarily sealed with zinc oxide-eugenol cement. Follow-up imaging confirmed that calcification affected all of the patient’s teeth, making traditional RCT less viable. Further treatment included calcium hydroxide and composite resin to seal the canals, followed by dental crown preparation.

After a year of follow-up, the patient reported no discomfort or inflammation. However, the calcification in the teeth remained a concern. This case highlights the challenges of treating dental issues in patients with SLE on long-term glucocorticoid therapy. The study emphasizes the need for regular dental check-ups for these patients and suggests that a multidisciplinary approach is necessary to address their medical and dental needs.

The case study also emphasizes the importance of early intervention in preventing long-term dental complications in SLE patients. As glucocorticoids can cause significant dental issues, healthcare providers should work together to ensure comprehensive care and minimize the impact of such treatments on oral health.

“Based on the patient’s long-term glucocorticoid use and supporting studies, it appears that extended GC therapy significantly contributes to widespread dental pulp calcification,” Shenjie Xu, Department of Oral Medicine, The Second Affiliated Hospital, School of Medicine, Zhejiang University, Hangzhou, Zhejiang, P.R. China, and colleagues noted. They added, “When multiple teeth are involved, root canal treatment becomes unfeasible.”

They concluded, “Hence, a multidisciplinary approach is essential for managing SLE or other chronic conditions in patients on prolonged GC therapy.”

Reference:

DOI: 10.2174/0118742106321913240820051043

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Febuxostat Linked to Higher Liver Toxicity Than Benzbromarone in Gout Patients: Study

Researchers have found in a recent study that febuxostat carries a significantly greater risk of liver function disturbances compared to benzbromarone in patients with gout. Despite common clinical hesitation to use benzbromarone, the findings suggest it may have lower hepatotoxicity than febuxostat.

The objective of this study was to evaluate and compare the risk of hepatotoxicity associated with the use of febuxostat and benzbromarone in patients with gout. New users of febuxostat or benzbromarone with monitoring of liver function at least three times in a year after initiation of the study drugs were identified from an electronic medical record database. Propensity score matching (PSM) was performed between the two groups 1:1 to match for age, sex, and pre-treatment alanine aminotransferase (ALT) and aspartate aminotransferase (AST). Kaplan-Meier analysis was used to estimate the probability of hepatotoxicity (defined as ALT or AST >3x upper limit of normal). Hazard ratios (HR) and 95% confidence intervals (CI) were calculated using Cox regression. Subgroup analysis was performed based on age, body mass index, and comorbidities. Results: 2,338 patients with gout were eligible. A total of 37% experienced Common Terminology Criteria for Adverse Events (CTCAE) v5 grade 1-3 AST/ALT abnormality. After PSM, 488 febuxostat users were matched with 488 receiving benzbromarone with a mean follow-up of 1.20 years. The incidence of hepatotoxicity was 39.6 and 16.8 per 1,000 person-years for febuxostat users and benzbromarone users, respectively. Febuxostat use was associated with a significantly greater risk of hepatotoxicity than benzbromarone (adjusted HR 2.75, 95% CI 1.28-5.91), especially in patients with elevated transaminases at baseline. Findings did not differ according to pre-specified subgroups. Febuxostat use is associated with a significantly greater risk of mild to moderate perturbation of liver function compared to benzbromarone in patients with gout.

Reference:

Sun, W., Cui, L., Terkeltaub, R., Chen, Y., Li, X., Cheng, X., Liu, T., Dalbeth, N. and Li, C. (2025), Risk of hepatotoxicity in patients with gout treated with febuxostat or benzbromarone: a propensity score-matched cohort study. Arthritis Care Res. Accepted Author Manuscript. https://doi.org/10.1002/acr.25547

Keywords:

Febuxostat, Linked, Higher, Liver, Toxicity, Benzbromarone, Gout Patients:, Study, Sun, W., Cui, L., Terkeltaub, R., Chen, Y., Li, X., Cheng, X., Liu, T., Dalbeth, N. and Li, C

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Common genetic variants linked to drug-resistant epilepsy: Study

Certain common genetic changes might make some people with focal epilepsy less responsive to seizure medications, finds a new global study led by researchers at UCL and UTHealth Houston.

Focal epilepsy is a condition where seizures start in one part of the brain. It is the most common type of epilepsy.

Antiseizure medication is usually prescribed for people with the condition. However, for one in three people with epilepsy (around 20 million individuals worldwide), current antiseizure medications are ineffective. This means that people will continue to have seizures despite taking medication – a condition called ‘drug resistance’.

Drug resistance is associated with additional significant health risks in epilepsy, including a higher risk of sudden unexpected death in epilepsy, alongside substantially higher healthcare costs.

However, until now, there has been little understanding about why antiseizure medications fail to work for some people.

The new international study, published in eBioMedicine, found strong evidence that certain common genetic factors may contribute to drug resistance in epilepsy.

The researchers used data from EpiPGX, an international multicentre research project on epilepsy pharmacogenetics, and Epi25, the largest sequencing study in epilepsy, to examine genetic variation across the entire genome (the complete set of genetic instructions found in an organism’s DNA) in 6,826 people with epilepsy.

The team compared the genomes of those who had drug-resistant epilepsy (4,208 individuals) with those whose seizures were successfully controlled with antiseizure medications (2,618 individuals).

They found that the presence of some specific common genetic variants in two genes-CNIH3, which helps control how certain brain receptors function, and WDR26, which is involved in various cell processes-was associated with a higher risk of having drug resistance in focal epilepsy and may influence a person’s response to antiseizure medications.

Senior author, Professor Sanjay Sisodiya (UCL Queen Square Institute of Neurology) said: “The findings of our study offer new insights about why some people have seizures that are resistant to existing antiseizure medications. Further work may enable doctors to use this information to help predict who may turn out to have drug-resistant epilepsy and may help doctors develop newer treatments for the condition.”

The findings are particularly important as these genetic signatures can be determined at the onset of epilepsy, rather than after several antiseizure medications have been tried without success.

This could eventually help to predict which individuals with epilepsy are likely to develop drug resistance and avoid unnecessary exposure to ineffective medications and their associated side effects.

First author, Assistant Professor Costin Leu (previously UCL Queen Square Institute of Neurology and now UTHealth Houston) said: “Our study provides the first evidence that common genetic variants-usually not addressed in clinical genetic testing-significantly contribute to drug resistance in epilepsy.

“Recognising these genetic variants, which are frequent in the general population yet strongly influence treatment outcomes, underscores the need to expand genetic testing and future therapies to address polygenic epilepsy (a type of epilepsy that is influenced by multiple genes).

“Polygenic epilepsy represents the vast majority of all genetic epilepsy cases, and addressing it through genetics-informed approaches could substantially enhance personalised treatment strategies for many individuals who currently fall outside the scope of targeted genetic medicine.”

Reference:

Genome-wide association meta-analyses of drug resistant epilepsy, eBioMedicine (2025).

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Diabetes mellitus remission observed in first year following bariatric surgery, reports research

A new study published in the journal of Diabetes Research and Clinical Practice showed that following bariatric surgery, patients with long-standing type 2 diabetes mellitus experienced remission. Also, results were closely correlated with β-cell activity and the percentage of total weight lost.

The β-cell function appears to have reached a point of no return in patients with type 2 diabetes that has been present for more than 10 years. Observing the first-phase insulin secretion in long-term T2DM patients with diabetes remission and investigating the major determinants of diabetes remission in patients with a period of T2DM ≥ 10 years who went through bariatric surgery, which includes the outcomes of insulin-treated patients (I-T2DM) and non-insulin-treated patients (NI-T2DM), were the goals of this study.

The patients who had bariatric surgery and have had type 2 diabetes for at least 10 years were included retrospectively and monitored. An HbA1c < 6.5% (48 mmol/mol) at least three months after stopping hypoglycemic medications was considered remission of diabetes. The patients who were in remission from diabetes had an intravenous glucose tolerance test (IVGTT).

Nearly, 59.6% of the 203 individuals with T2DM who had been treated with insulin prior to bariatric surgery had been with the disease for at least 10 years. Remission rates at one, two, and three years after surgery were 65.6%, 53.8%, and 41.9%, respectively.

According to Cox regression analysis, the percentage of total weight loss (%TWL) and β-cell function had the strongest correlations with the probabilities of remission one year after bariatric surgery. In 50 individuals with diabetic remission, the first-phase insulin production peak was around 5–8 times the fasting insulin level.

Overall, this study found that one year following bariatric surgery, the diabetes remission rate for T2DM patients who have had the disease for at least ten years can still exceed two-thirds. But between years 1 and 3, the remission rate dropped by around 10% a year, underscoring the significance of long-term monitoring for these individuals.

Source:

Zhang, N., Zhou, B., Wang, H., Xue, X., Huang, Y., Wang, S., Wang, Z., Niu, W., Liu, B., Nie, Y., Li, Z., Zhang, L., Wang, P., Chou, S., Yao, L., Ran, S., Lv, J., Liu, G., Li, G., … ODHM(Obesity and Diabetes Health Management) Study Group. (2025). Predictors of diabetes remission after bariatric surgery in patients with type 2 diabetes mellitus duration ≥ 10 years: A retrospective cohort study. Diabetes Research and Clinical Practice, 112164, 112164. https://doi.org/10.1016/j.diabres.2025.112164

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New drug delivery system effective against rare eye cancer, finds study

 A multi-institutional study led by Moffitt Cancer Center found that percutaneous hepatic perfusion using a melphalan hepatic delivery system may help patients with a rare eye cancer that has spread to their liver. This disease, known as metastatic uveal melanoma, is traditionally very hard to treat and usually has poor outcomes.

The phase 3 FOCUS trial, published in the Annals of Surgical Oncology, compared two treatments for metastatic uveal melanoma. One group of patients received the melphalan hepatic delivery system treatment, while the other group received standard of care treatment. Patients treated with the melphalan hepatic delivery system experienced significantly improved outcomes than those receiving alternative care. The median progression-free survival for these patients was 9.1 months, compared with 3.3 months for those on standard treatments.

The objective response rate was 27.5%, nearly three times the 9.4% observed in the comparison group. The disease control rate also substantially increased from 46.9% to 80.0%. Patients treated with the melphalan hepatic delivery system lived a median of 18.5 months, compared with 14.5 months for those receiving other forms of care. Although there were some side effects, mostly related to blood cell counts, these were treated with standard care as an outpatient and mostly resolved with observation alone.

“This new treatment gives hope to patients with this historically tough-to-treat cancer,” said Jonathan Zager, M.D., surgical oncologist in the Cutaneous Oncology Department at Moffitt and lead author of the study. “This is the second publication in Annals of Surgical Oncology on the results of the FOCUS trial and definitely shows that treatment with the melphalan hepatic delivery system can help control the cancer in the liver. The treatment provides an option that does not interfere with their quality of life and gives patients a chance at longer survival.”

The melphalan hepatic delivery system treatment was approved by the U.S. Food and Drug Administration in August 2023 based on the phase 3 trial results. Unlike regular chemotherapy, this treatment delivers a high dose of the drug directly into the liver, which is isolated with a series of catheters and balloons via percutaneous insertions. The chemotherapy is filtered out before it gets introduced to the rest of the body. This targeted approach helps reduce harmful side effects in the rest of the body. More research is planned to test the benefits of the melphalan hepatic delivery system. Studies will also look at combining this treatment with other new therapies.

Reference:

Zager, J.S., Orloff, M., Ferrucci, P.F. et al. An Open-label, Randomized Study of Melphalan/Hepatic Delivery System Versus Best Alternative Care in Patients with Unresectable Metastatic Uveal Melanoma. Ann Surg Oncol (2025). https://doi.org/10.1245/s10434-025-17231-x

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New guidance for managing obesity in children and adolescents released

A new guideline to help health care providers manage obesity in children and adolescents takes a patient-centred approach, emphasizing behavioural and psychological supports that focus on outcomes valued by patients and their families.

The guideline based on the latest evidence, is published in CMAJ (Canadian Medical Association Journal).

It was developed by Obesity Canada through an extensive, 4-year-long collaboration involving adolescents and caregivers with lived obesity experience, methodologists, health care providers, and more than 50 multidisciplinary experts.

“The guideline is designed to support shared and informed clinical decision-making rooted in systematic, interpretable summaries of scientific evidence,” said Dr. Bradley Johnston, associate professor of nutrition and health research methods and co-chair of the guideline development committee. “To achieve that, we devised a transparent process to assess the totality of scientific evidence for relevant interventions to manage pediatric obesity, while prioritizing outcomes that matter the most to children, adolescents, and their families.”

These outcomes include quality of life, mental health, related cardiovascular risk factors, avoiding harms, and more.

Pediatric obesity is a complex, chronic, progressive, and stigmatized condition that increases risk for more than 200 health conditions. In Canada, about 1 in 4 children aged 11 years or younger and 1 in 3 adolescents aged 12–17 years have an elevated body mass index, suggesting overweight or obesity. International data indicate that severe obesity appears to be on the rise globally.

“The health consequences and persistence of pediatric obesity into adulthood highlight the need for available, accessible, family-oriented interventions for effective obesity management,” says Dr. Sanjeev Sockalingam, scientific director, Obesity Canada. “Success in managing pediatric obesity is most likely when children and their families can access support and practical strategies to make and sustain positive behavioural changes, complemented by pharmacologic and surgical interventions, if necessary and available.”

The guideline contains 10 recommendations, including guidance on nutritional, physical activity, psychological, and technology interventions, and medications and surgical options, as well as 9 good practice statements. The authors recommend combining at least 2 options to help manage obesity.

“We know the time to act on pediatric obesity is now. Waiting until children and adolescents become adults before providing meaningful, informed, evidence-based care and support only heightens the risk for developing complications and prolongs the experience of living with a stigmatized chronic disease, which can worsen further physical and mental health outcomes,” said Lisa Schaffer, executive director, Obesity Canada.

Reference:

Geoff D.C. Ball, Roah Merdad, Catherine S. Birken, Tamara R. Cohen, Brenndon Goodman, Stasia Hadjiyannakis, Jill Hamilton, Mélanie Henderson, John Lammey, Katherine M. Morrison, Sarah A. Moore, Aislin R. Mushquash, Ian Patton, Nicole Pearce, Managing obesity in children: a clinical practice guideline, Canadian Medical Association Journal, DOI: https://doi.org/10.1503/cmaj.241456.

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Semaglutide promising alternative treatment for chronic myopathy of hyperkalemic periodic paralysis: a case report

Semaglutide promising alternative treatment for chronic myopathy of hyperkalemic periodic paralysis suggests a case report published in the BMC Nephrology.

Hyperkalemic Periodic Paralysis (HyperPP) is a rare autosomal dominant channelopathy characterized by episodic muscle weakness or paralysis, often triggered by elevated extracellular potassium levels. This condition is frequently linked to mutations in the SCN4A gene, encoding a skeletal muscle sodium channel. Traditional management strategies, such as potassium avoidance, low-potassium diets, and carbonic anhydrase inhibitors like acetazolamide and diclofenamide, have provided limited long-term relief, particularly in addressing the progressive myopathy associated with the disease.

Case Report
A 48-year-old male with a confirmed SCN4A mutation (Threonine to Methionine at position 704) presented with longstanding muscle weakness. Symptom onset occurred in childhood, with progressive deterioration into permanent weakness by his thirties. Conventional therapies were ineffective. In 2023, the patient began weekly semaglutide injections for weight loss. Remarkable improvement in muscle strength and mobility was noted within a year, with the patient regaining the ability to rise unaided from a chair and walk at a normal pace. Semaglutide, a glucagon-like peptide-1 receptor agonist (GLP-1 RA), is primarily indicated for type 2 diabetes and obesity. However, this case suggests its potential in neuromuscular disorders. GLP-1 RAs may exert anabolic effects on skeletal muscle through insulin-dependent and insulin-independent pathways, improving mitochondrial function, glucose uptake, and reducing inflammation—factors potentially beneficial in muscle channelopathies This case provides preliminary evidence that semaglutide may reverse chronic myopathy in HyperPP patients. Larger studies are needed to evaluate its therapeutic potential, safety, and mechanisms in muscular channelopathies.

References:

Brand, K., Landry, D., Mulhern, J. et al. Semaglutide reverses the chronic myopathy of hyperkalemic periodic paralysis: a case report. BMC Nephrol 26, 179 (2025). https://doi.org/10.1186/s12882-025-04068-5

Keywords:
Hyperkalemic periodic paralysis, SCN4A mutation, Semaglutide, Myopathy, GLP-1 receptor agonist, Skeletal muscle, Channelopathy, Case report

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Pediatric investigation review explains future of artificial intelligence in diagnosis and control of myopia: Study

Myopia, or nearsightedness, affects two billion people worldwide. Uncorrected myopia can impair vision, disrupting education, career prospects, and quality of life. By 2050, nearly half of the global population is estimated to become myopic. High myopia is often associated with complications that can lead to visual impairment, affecting patients’ quality of life and increasing the global medical and economic burden. Therefore, early diagnosis of myopia is important for the prevention of vision damage in patients with myopia.

Artificial intelligence (AI) has opened up new frontiers in the medical field and may be a solution to this global health concern. The subsets of AI, such as machine learning (ML) and deep learning (DL) can help analyze data to diagnose diseases and predict risk factors, biomarkers, and outcomes.

In a new literature review, Dr. Li Li, Dr. Jifeng Yu, and Dr. Nan Liu, all from the Department of Ophthalmology, Capital Medical University, China, have summarized the applications and challenges of AI in myopia, including detection, risk factor assessment, and prediction models. This study was published in the journal of Pediatric Investigation on 18 March 2025.

Interestingly, AI models can be trained using ML/DL to detect myopia from fundus photos and optical coherence tomography images. By feeding a model with a large quantity of fundus images from myopic patients, the AI can be taught to discern minute changes in color and pattern in the retina that are associated with myopia. This allows the model to diagnose future patients from their fundus photos.

In addition, self-monitoring equipment such as SVOne, a handheld device that uses a wavefront sensor to measure eye defects, can use AI algorithms to detect refractive errors in the eyes. The device could access an online database of images, which the AI can use as a reference to diagnose myopia. Moreover, AI can be trained to detect behavioral changes associated with the onset of myopia. Such detection is especially useful for the early detection of myopia in children, which is often ignored otherwise. For example, the Vivior monitor uses ML algorithms to note changes in visual behaviors, such as time spent on near vision activities, in children aged 6–16 years.

Furthermore, ML methods like support vector machine, logistic regression, and XGBoost can be employed to identify risk factors of myopia. “An XGBoost-based model can be fed large quantities of longitudinal data, allowing it to learn the outcomes and associated risk factors of myopia in numerous patients. This, in turn, allows the model to assess the risk factors of new patients based on their genetics, family history, environment, and physiological parameters,” explains Dr. Li Li.

Predicting the progression and outcome of myopia can help doctors adjust their clinical approach. Taken on a large scale, it can shape clinical practice and policymaking that help in myopia control. By feeding an AI model large quantities of biometric data, refractive data, treatment responses, and ocular images from numerous myopia patients, the AI can be taught to predict outcomes of myopia in new patients.

Despite the great potential of AI in myopia, several challenges need to be overcome. Firstly, it is important to ensure that the dataset used to train an AI model is correct and of high quality. Bias, false negatives/positives, and poor data quality can negatively impact the diagnostic and prediction accuracy of the model. Secondly, most AI models are trained using data from large hospitals, which may not be representative of patients going to smaller clinics. This creates a discrepancy between real-world and training populations. Thirdly, an AI model is not a trained doctor and may not be able to provide a clinical basis for its diagnosis, which can cause the diagnosis to be rejected by medical professionals. Finally, with such vast quantities of patient data used to train AI models, it is important to ensure the privacy of patients’ medical records.

“While our study highlights the remarkable progress made in the clinical application of AI in myopia, further studies are needed to overcome the technological challenges. By building high-quality datasets, improving the model’s capacity to process multimodal image data, and improving human-computer interaction capability, the AI models can be further improved for widespread clinical application,” concludes Dr. Jifeng Yu.

Reference:

Nan Liu, Li Li, Jifeng Yu, Application of artificial intelligence in myopia prevention and control, Pediatric Investigation, https://doi.org/10.1002/ped4.70001

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Early Crohn’s disease detection with capsule endoscopy improve long-term prognosis, finds study

A recent study by Yuya Ogino and colleagues created a scoring model for early Crohn’s disease (CD) diagnosis based on results from small bowel capsule endoscopy (SBCE), which may help improve CD’s long-term prognosis. The findings of this study were published in the Journal of Gastroenterology.

A minimally invasive technique called small bowel capsule endoscopy is utilized to see inflammatory alterations in the Crohn’s disease small intestinal mucosa. The therapeutic utility of SBCE in CD has been highlighted in a number of professional guidelines. Currently, 2 grading methods are used to evaluate small bowel CD lesions found by SBCE: the Capsule Endoscopy Crohn’s Disease Activity Index (CECDAI) and the Lewis Score (LS).

Although a number of studies have looked at the relationship between these 2 scoring systems, CD can present with a broad range of diseases, such as inflammation and stenosis, therefore it is hard to adequately identify the pathology using these scores alone. Using the results of the SBCE, this study created a scoring model for CD early diagnosis.

A total of 110 individuals with small intestinal mucosal lesions had their clinical and SBCE data gathered which was then randomly assigned them to derivation and validation groups. The accepted model was identified after variables were chosen for scoring models using univariate analysis. Each variable’s score was determined by the odds ratio derived from multivariate analysis, and receiver operating characteristic analysis was used to look at the cut-off value for the CD diagnosis. 

The model with the best fit (odds ratios of 4.97, 7.56, and 5.34, respectively) included age (≤ 30 vs. ≥ 31), linear degradation, and circumferential alignment. 4 points were assigned to the linear erosion score, four to the circumferential alignment, and three to the age of less than 30 years.

The scoring model’s sensitivity, specificity, positive predictive value, and negative predictive value for diagnosing CD were 85.4%, 80.0%, 83.7%, and 82.1%, respectively, when the cut-off value was set at 7. Like the derivation cohort, the validation cohort showed an area under the curve of 0.93.

Overall, the advantages of optimizing therapy for Crohn’s disease in remission using video capsule endoscopy (VCE) were confirmed by this investigation. The flare incidence was 25% for high-risk patients with a Lewis inflammatory score of ≥350 in the treat-to-target group and 70% for those receiving conventional therapy.

Source:

Ogino, Y., Sadashima, K., Yoshida, Y., Takedomi, H., Tsuruoka, N., Sakata, Y., Takamori, A., Hisamatsu, T., Matsumoto, T., & Esaki, M. (2025). Development of a capsule endoscopy scoring system for the early diagnosis of small bowel Crohn’s disease. Journal of Gastroenterology. https://doi.org/10.1007/s00535-025-02235-x

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Betamethasone Retreatment Restores Benefits for Severe Intraventricular Hemorrhage Among Preterm Infants: Study

USA: Researchers have found in a new study that betamethasone retreatment restores benefits for severe intraventricular hemorrhage among infants less than 28 weeks gestation.

The study, published in the American Journal of Obstetrics and Gynecology, found that betamethasone’s benefits on severe intraventricular hemorrhage decline after the first dose, and a second course of treatment appears to reinstate its protective effects. Therefore, retreatment may be beneficial for sustained neuroprotection in vulnerable patients.

Antenatal corticosteroids play a crucial role in reducing the risk of severe intraventricular hemorrhage (IVH) in preterm infants. However, it remains uncertain whether their protective effects diminish over time, as seen in neonatal respiratory distress, and whether a second course of betamethasone can restore these benefits.

Previous randomized trials on betamethasone retreatment did not show a significant reduction in severe IVH rates. However, these studies may not have included a sufficient number of extremely preterm infants, who are at the highest risk. Severe IVH predominantly affects infants born before 28 weeks of gestation, yet only a small proportion (7% on average) of participants in these trials fell into this category.

Ronald I. Clyman, Department of Pediatrics, University of California San Francisco, San Francisco, CA, and colleagues aimed to address these gaps by evaluating whether the risk of severe IVH increases when the interval between betamethasone administration and delivery exceeds nine days. Additionally, they examined whether retreatment before delivery could lower the incidence of severe IVH in infants born before 28 weeks.

For this purpose, the researchers conducted an observational study to assess the incidence of intraventricular hemorrhage (IVH) before and after a practice change that encouraged obstetricians to retreat high-risk pregnancies if more than nine days had passed since the first betamethasone dose. They analyzed data from 410 infants born before 28 weeks of gestation, comparing IVH rates between those delivered within 1 to 9 days of the initial betamethasone course (n=290) and those delivered after 10 or more days, who were eligible for retreatment (n=120). Multivariable analyses using logistic regression helped evaluate the impact of this approach on IVH rates.

The key findings of the study were as follows:

  • Infants delivered 10 or more days after a single betamethasone course had a higher risk of severe intraventricular hemorrhage (IVH) or IVH-related death within four days compared to those delivered within 1 to 9 days (odds ratio: 2.8).
  • Among the 120 infants delivered after 10 or more days, 53% (n=64) received a second course of betamethasone.
  • The rate of severe IVH in infants whose mothers received a second course was similar to those delivered within 1 to 9 days and significantly lower than in those delivered after 10 or more days without retreatment (odds ratio: 0.10).
  • After the guideline change, the rate of betamethasone retreatment in infants delivered 10 or more days after the first dose (but before 28 weeks) increased from 25% to 87%.
  • Following the increased retreatment, the severe IVH rate in this group dropped from 22% to 0%.
  • In contrast, severe IVH rates remained unchanged (12% to 11%) in infants delivered within 1 to 9 days who were not eligible for retreatment.

The study revealed that betamethasone’s protective effect against severe intraventricular hemorrhage diminishes overtime after the first dose. However, retreatment with a second course appears to restore this benefit.

“Encouraging timely retreatment in high-risk pregnancies before 28 weeks of gestation was linked to a significant reduction in severe IVH rates, highlighting the importance of optimizing antenatal corticosteroid strategies for better neonatal outcomes,” the authors concluded.

Reference:

Clyman, R. I., Rosenstein, M. G., Liebowitz, M. C., Rogers, E. E., Kramer, K. P., & Hills, N. K. (2025). Betamethasone treatment-to-delivery interval, retreatment, and severe intraventricular hemorrhage in infants <28 weeks gestation. American Journal of Obstetrics and Gynecology, 232(4), 400.e1-400.e10. https://doi.org/10.1016/j.ajog.2024.06.048

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