Aspartame as Sugar Substitute Supports Better Oral Health: Study Finds

USA: A recent systematic review and meta-analysis published in the Journal of Dentistry has revealed that replacing sugar with aspartame helps maintain a healthier oral pH, reduces the development of dental caries in animals, and decreases oral acid production and dental erosion in lab tests compared to sugar.

The study sheds light on the non-cariogenic properties of aspartame, offering promising insights into its role as a safer alternative to sugar in protecting oral health. Stephen A. Fleming, Traverse Science, Inc., Mundelein, IL, 60060 USA, and colleagues aimed to assess whether aspartame contributes to tooth decay and explore the underlying mechanisms influencing its effects on oral health.

Researchers conducted a comprehensive review of literature across major scientific databases—PubMed, Scopus, Web of Science, and CENTRAL—up to February 16, 2024. The analysis included studies comparing aspartame with sucrose or other controls in human and animal models, as well as, in laboratory-based dental samples. The evaluation focused on parameters such as caries development, acid production in the mouth, changes in oral bacterial composition, and effects on dental mineralization. The strength of evidence was assessed using the GRADE framework.

The findings were from thirteen studies, including two clinical trials, seven preclinical trials in rats, and four studies using bovine tooth samples.

The key findings were as follows:

  • In human studies, aspartame was significantly less acidogenic than sugar and showed effects similar to water, which is considered neutral for oral health.
  • Laboratory-based studies on tooth samples revealed that aspartame exposure led to lower acid production and less dental erosion than sugar.
  • Animal studies demonstrated that rats fed aspartame instead of sugar developed fewer cavities.
  • The reduction in tooth decay was more pronounced when aspartame replaced sugar entirely, but less when used alongside sucrose.
  • There was a modest reduction in sulcal caries with aspartame use.
  • While aspartame did not strongly prevent cavities, it showed clear advantages over sugar in reducing cariogenic effects.

The review also examined how aspartame affects oral bacteria, concluding that its influence on microbial composition was limited. This suggests that its benefits in dental health may not stem from altering bacterial activity but rather from its ability to help reduce overall sugar intake, one of the main contributors to tooth decay.

While aspartame appears non-cariogenic, meaning it does not promote cavities, the study found limited evidence to support any significant anti-cariogenic effects—that is, its ability to prevent dental caries through direct biological mechanisms. The primary advantage of aspartame is its potential to replace free sugars in the diet, thereby reducing one of the main risk factors for tooth decay.

The analysis emphasizes that aspartame, when used as a sugar substitute, may help in maintaining oral pH and reducing caries incidence, especially in comparison to sucrose. However, due to variability across studies and the limited strength of evidence, researchers recommend further long-term clinical trials to better understand aspartame’s role in dental health and its potential in caries prevention strategies.

Reference:

Fleming, S. A., Fleming, R. A., & Peregoy, J. (2025). The non-cariogenic effects of aspartame: A systematic review and meta-analysis. Journal of Dentistry, 157, 105715. https://doi.org/10.1016/j.jdent.2025.105715

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Urine test could reveal prostate cancer, reports research

A newly published study involving researchers from Karolinska Institutet indicates that prostate cancer can be diagnosed at an early stage through a simple urine sample. With the aid of AI and extensive analyses of gene activity in tumours, they have identified new biomarkers of high diagnostic precision.

Prostate cancer is one of the most common causes of male death globally. One of the main diagnostic hurdles is the lack of exact biomarkers able to identify the presence of an early tumour.

In this present study, researchers at Karolinska Institutet (Sweden), Imperial College London (UK) and Xiyuan Hospital, China Academy of Chinese Medical Sciences, Beijing (China), have identified new, precise biomarkers. The results are presented in the journal Cancer Research.

Digital models of prostate cancer

On analysing the mRNA activity of all human genes in thousands of individual cells in prostate tumours, and knowing the position and degree of cancer of each cell, the researchers were able to construct digital models of prostate cancer.

The models were analysed with AI to find proteins that can be used as biomarkers. These biomarkers were then analysed in the blood, prostate tissue and urine of almost 2,000 patients.

The researchers identified a set of biomarkers in urine that were able to indicate the presence and severity of prostate cancer with a high degree of precision. According to their calculations, they surpass PSA, which is the blood biomarker in current clinical use.

“There are many advantages to measuring biomarkers in urine,” explains principal investigator Mikael Benson, senior researcher at the Department of Clinical Science, Intervention and Technology, Karolinska Institutet. “It’s non-invasive and painless and can potentially be done at home. The sample can then be analysed using routine methods in clinical labs.”

Needs evaluating in clinical studies

Large-scale clinical trials are being planned for the next phase of the research. One such is being discussed with Professor Rakesh Heer of Imperial College London, co-author of the study and head of TRANSFORM, the UK’s national prostate cancer study, which offers a platform for expediting the testing of promising biomarkers.

“New, more precise biomarkers than PSA can lead to earlier diagnosis and better prognoses for men with prostate cancer,” says Dr Benson. “Moreover, it can reduce the number of unnecessary prostate biopsies in healthy men.”

Reference:

Martin Smelik, Combining Spatial Transcriptomics, Pseudotime, and Machine Learning Enables Discovery of Biomarkers for Prostate Cancer, Cancer Research, https://doi.org/10.1158/0008-5472.CAN-25-0269.

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Metabolic Syndrome Increases Risk of Young-Onset Dementia, Reveals Large Korean Study

Korea: A recent nationwide population-based study from Korea has highlighted a significant association between metabolic syndrome (MetS) and an increased risk of young-onset dementia (YOD), which refers to dementia occurring before the age of 65. The findings were published online in the Neurology Journal on April 23, 2025.

The study, involving a large cohort of patients, revealed that both MetS as a whole and its components—such as hypertension, high blood sugar, elevated cholesterol, and abdominal obesity—were linked to a heightened risk of developing dementia at an earlier age. These findings shed light on the potential long-term effects of MetS on cognitive health.

Metabolic syndrome, a cluster of conditions that increase the risk of heart disease, stroke, and type 2 diabetes, has long been a known contributor to various health complications. However, its relationship with cognitive decline, particularly in younger individuals, has not been thoroughly explored until now. Jeong-Yoon Lee, Department of Neurology, Soonchunhyang University Seoul Hospital, Soonchunhyang University College of Medicine, Seoul, Korea, and colleagues aimed to fill that gap by determining whether MetS and its individual components increase the risk of YOD, including all-cause dementia, Alzheimer’s disease (AD), and vascular dementia (VaD).

For this purpose, the researchers conducted a nationwide cohort study using data from the Korean National Insurance Service. The study included individuals aged 40–60 who underwent health check-ups in 2009 and were followed until age 65 or December 31, 2020. Metabolic syndrome (MetS) was defined based on waist circumference, blood pressure, fasting glucose, triglycerides, and HDL cholesterol. The study also considered factors like age, sex, income, smoking, alcohol use, and comorbidities.

The primary outcome was all-cause young-onset dementia, with secondary outcomes of young-onset Alzheimer’s and vascular dementia. Hazard ratios (HRs) with 95% confidence intervals were calculated using multivariable Cox regression.

The study revealed the following findings:

  • A total of 1,979,509 participants were included in the study, with a mean age of 49.0 years; 51.3% were men, and 50.7% had metabolic syndrome (MetS).
  • Over an average follow-up period of 7.75 years, 8,921 individuals (0.45%) developed young-onset dementia.
  • MetS was associated with a 24% higher risk of all-cause YOD (adjusted HR 1.24).
  • MetS was linked to a 12.4% increased risk of Alzheimer’s disease (AD) (HR 1.12).
  • MetS was associated with a 20.9% increased risk of vascular dementia (VaD) (HR 1.21).
  • Significant interactions were observed with younger age (40–49 vs 50–59), female sex, drinking status, obesity, and depression.

In this large Korean cohort study, the authors found that metabolic syndrome and its individual components were significantly associated with an increased risk of young-onset dementia.

The findings suggest that targeting MetS through early interventions may help mitigate the risk of developing YOD. However, the authors caution that the study’s observational design limits the ability to draw definitive causal conclusions, and the reliance on claims data may introduce potential misclassification bias. The authors recommend further research using longitudinal designs and comprehensive data collection to validate and expand upon these associations.

Reference:

Lee J-Y et al “Association between metabolic syndrome and young-onset dementia: a nationwide population-based study” Neurology 2025; DOI: 10.1212/WNL.0000000000213599.

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CPAP therapy reduces all-cause and cardiovascular mortality in OSA patients: Lancet

A new study published in The Lancet Respiratory Medicine journal showed positive airway pressure (PAP) treatment to be associated with reduced mortality rates in obstructive sleep apnea (OSA) patients.

There is conflicting information on how positive airway pressure treatment for obstructive sleep apnea affects mortality from all causes. Adam Benjafield and team therefore set out to explore the hypothesis that PAP treatment is linked to lower cardiovascular and all-cause mortality in individuals with OSA in this systematic review and meta-analysis.

Without regard to language or location, this study conducted a search of PubMed, Embase, and the Cochrane Central Register of Controlled Trials for this systematic review and meta-analysis from the beginning of the database until August 22, 2023 (updated September 9, 2024). Abstracts from recent conferences (2022–2023) and reference lists of relevant works were also examined. This research excluded studies that evaluated only PAP adherence and other study types.

Also, outpatient studies (confounder-adjusted, non-randomized controlled studies [NRCSs] or randomised controlled trials [RCTs]) that assessed the incidence of cardiovascular mortality, all-cause mortality, or both in adults (aged ≥18 years) with OSA who were treated versus not treated with PAP were included. To estimate overall HRs and 95% CIs, this study used a linear random-effects model to analyze each log-transformed hazard ratio (HR) and SE. By employing Newcastle–Ottawa Scale for NRCSs and the Cochrane Risk of Bias tool for RCTs, this study assessed the risk of bias.

A total of 30 studies (ten RCTs and twenty NRCSs) were included in the systematic review and meta-analysis after 435 of the 5484 records found by our search were evaluated for eligibility. These studies comprised 11,75,615 individuals, with a mean age of 59·5 (SE 1·4) years and a mean follow-up of 5·1 (0·5) years.

Of these, 9,05,224 (77%) were male and 2,70,391 (23%) were female (SE 1·9). The bias was a low to moderate risk. The clinically meaningful benefit of PAP treatment increased with usage, and the risk of cardiovascular mortality and all-cause mortality was considerably lower in the PAP group than in the no-PAP group. Overall, these findings supported a possible positive impact of PAP treatment on cardiovascular and all-cause mortality in OSA patients. 

Reference:

Benjafield, A. V., Pepin, J.-L., Cistulli, P. A., Wimms, A., Lavergne, F., Sert Kuniyoshi, F. H., Munson, S. H., Schuler, B., Reddy Badikol, S., Wolfe, K. C., Willes, L., Kelly, C., Kendzerska, T., Johnson, D. A., Heinzer, R., Lee, C.-H., Malhotra, A., & medXcloud Group. (2025). Positive airway pressure therapy and all-cause and cardiovascular mortality in people with obstructive sleep apnoea: a systematic review and meta-analysis of randomised controlled trials and confounder-adjusted, non-randomised controlled studies. The Lancet. Respiratory Medicine. https://doi.org/10.1016/S2213-2600(25)00002-5

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Researchers report association between urinary incontinence, cardiovascular disease

A University of Iowa-led research team has found that urinary incontinence may be associated with a greater risk for cardiovascular disease in women.

Urinary incontinence-the loss of bladder control-is a common condition, especially in older adults. Previous studies have stated that it can affect between 38% and 60% of women. The researchers aimed to find out whether urinary incontinence was linked to a decline in physical activity, which can lead to a host of health issues, including greater risk for cardiovascular disease.

In the study, the researchers-led by Lisa VanWiel, assistant professor at the University of Wisconsin-La Crosse who in April earned her doctorate in health and human physiology from Iowa-analyzed medical records over two years from more than 20,000 female patients in the Hartford Healthcare system in Connecticut. Of those patients, 5.4% reported through a questionnaire to have urinary incontinence. All patients were asked to rate their level of physical activity in the questionnaire.

The researchers found that the respondents with urinary incontinence did not report engaging in less physical activity than those who did not have the condition. But the team did find an association between patients with urinary incontinence and cardiovascular disease risk factors or events, such as dyslipidemia, type 2 diabetes, and stroke.

“There is an association between incontinence and cardiovascular disease (CVD) risk,” the study authors write. “Women should be screened for incontinence regularly as it may contribute to CVD risk, and women with CVD risk factors should be screened for undiagnosed incontinence.” 

Reference:

Lisa L. VanWiel, Lucas J. Carr, Dale S. Bond, Yin Wu, Elena Tunitsky-Bitton, Paul Tulikangas, Adam C. Steinberg, Kara M. Whitaker, Associations of urinary incontinence, physical activity and cardiovascular disease risk among women in the United States, Preventive Medicine, https://doi.org/10.1016/j.ypmed.2025.108277.

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Phase 3 Trial Backs Ivarmacitinib as Effective Oral Option for Moderate to Severe Atopic Dermatitis

China: A recent phase 3 randomized clinical trial has shown that ivarmacitinib significantly improves symptoms in adolescents and adults with moderate to severe atopic dermatitis (AD).

“In the phase 3 randomized clinical trial, once-daily oral ivarmacitinib (4 or 8 mg) led to significant improvements in the signs and symptoms of moderate to severe atopic dermatitis in both adolescents and adults, showing a favorable balance between efficacy and safety compared to placebo,” the researchers wrote in JAMA Dermatology.

Ivarmacitinib, a selective oral Janus kinase 1 inhibitor, has previously shown promise in managing moderate to severe atopic dermatitis in adults during phase 2 trials. Building on this evidence, Yan Zhao, Department of Dermatology, Peking University People’s Hospital, Beijing, China, and colleagues aimed to assess its efficacy and safety profile in a broader population, including both adolescents and adults affected by moderate to severe AD.

For this purpose, the researchers conducted a multicenter, double-blind, placebo-controlled phase 3 trial across 53 sites in Canada and China, enrolling patients aged 12 to 75 years with moderate to severe atopic dermatitis. Participants were randomly assigned to receive either 4 mg or 8 mg of oral ivarmacitinib or a placebo once daily for 16 weeks.

The main outcomes assessed were the proportion of patients achieving clear or almost clear skin (IGA score of 0 or 1 with at least a 2-grade improvement) and a 75% improvement in Eczema Area and Severity Index (EASI-75) by week 16.

The study led to the following findings:

  • A total of 336 patients were randomized, with an average age of 31.1 years; 63.4% were male and 85.1% were Asian. Of these, 113 received 4 mg ivarmacitinib, 112 received 8 mg ivarmacitinib, and 111 received a placebo.
  • At week 16, 36.3% of patients on 4 mg and 42.0% on 8 mg ivarmacitinib achieved clear or almost clear skin with at least a 2-grade improvement in IGA score, compared to just 9.0% in the placebo group.
  • EASI-75 responses were also better with treatment: 54.0% in the 4 mg group and 66.1% in the 8 mg group, compared to 21.6% in the placebo group.
  • Treatment-emergent adverse events were reported in 69.0% of the 4 mg group, 66.1% of the 8 mg group, and 64.9% of the placebo group.
  • Serious adverse events were low across all groups, occurring in 2.7% of the 4 mg group, 1.8% of the 8 mg group, and 2.7% of the placebo group.

“These findings highlight ivarmacitinib as a promising and effective oral treatment with a favorable risk-benefit profile for moderate to severe atopic dermatitis, especially in patients who do not respond well to topical therapies,” the authors concluded.

Reference:

Zhao Y, Gooderham M, Yang B, et al. Ivarmacitinib for Moderate to Severe Atopic Dermatitis in Adults and Adolescents: A Phase 3 Randomized Clinical Trial. JAMA Dermatol. Published online April 30, 2025. doi:10.1001/jamadermatol.2025.0982

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Mom’s hypertension can affect preterm infant brain and neurodevelopment: Study

Many women already know that preeclampsia-a dangerous form of high blood pressure during pregnancy-can lead to serious complications including kidney failure, stroke, and even death. Preeclampsia also is a well-known cause of preterm birth, which can pose a number of health risks for the baby.

Now, a new study led by experts at Cincinnati Children’s reports that preterm infants born to women who battled preeclampsia also show signs of brain injury soon after birth and worse neurodevelopment two years later. And to a lesser extent, so do the preterm-born toddlers of women who had gestational hypertension and chronic hypertension (a growing global health concern).

Specifically, a group of more than 340 preterm infants cared for at five Ohio neonatal intensive care units showed decreased cognitive and language scores at age 2 if they were born to mothers affected by high blood pressure.

These findings were published April 29, 2025, in JAMA Network Open by investigators with the Cincinnati Infant Neurodevelopment Early Prediction Study (CINEPS). Shipra Jain, MD, Division of Neonatology and Pulmonary Biology, was lead author and Nehal Parikh, DO, MS, a neonatologist with Cincinnati Children’s Perinatal Institute was the senior author.

“These reduced scores can be clinically meaningful because even slight differences can signal increased risk for later cognitive, language, or motor impairments,” Parikh says. “Since development is dynamic, even a small early disadvantage can compound over time, especially if the child lacks supportive interventions, potentially affecting school readiness and/or later academic achievement.”

The risks of hypertension

Preeclampsia affects 2% to 5% of all pregnancies, while a broader category that also includes gestational hypertension and chronic hypertension impacts up to 15% of all pregnancies. The brain development deficits among infants are believed to be caused by reduced blood flow to the placenta, reduced oxygen levels in the blood, tissue inflammation, and tissue damage caused by oxidative stress.

While some of these problems have been previously documented in full-term infants born to mothers with high blood pressure, previous studies focused on preterm infants had shown mixed results. Some studies have reported worse cognitive and motor outcomes, others have found no association, while a few even suggested a protective role.

This study accounted for several confounding variables that impacted other studies, and by doing so, the research team confirmed adverse brain impacts among preterm infants born at 32 weeks or less. Maternal high blood pressure was significantly associated with adverse cognitive and language outcomes, with the greatest effects among preeclampsia-exposed infants, independent of other risk factors. Additionally, the study found these adverse effects may be partially caused by early abnormalities in brain development.

What do these children need?

The study co-authors say these findings suggest that even mild effects occurring at birth – if left undetected or unaddressed – can magnify into larger deficits as children approach school age.

“Our findings thus support an association between maternal high blood pressure and early brain abnormalities and potentially harmful direct effects on cognitive and language development,” Jain says. “We believe early identification of brain abnormalities can allow for targeted interventions, such as early speech therapy, occupational therapy, or enriched learning environments, which can improve long-term educational, behavioral, and health outcomes, especially when preeclampsia occurs.”

One way to detect the risk may be to conduct MRI brain scans to detect brain abnormalities, especially in the white matter, for all preterm infants affected by preeclampsia. The researchers recommend incorporating such brain scans into future clinical trials evaluating therapies to manage or prevent maternal hypertension or preeclampsia.

Reference:

Jain S, Fu TT, Barnes-Davis ME, et al. Maternal Hypertension and Adverse Neurodevelopment in a Cohort of Preterm Infants. JAMA Netw Open. 2025;8(4):e257788. doi:10.1001/jamanetworkopen.2025.7788.

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Smoking cessation drug varenicline helps young adults quit vaping: Study

A new study by investigators from Mass General Brigham showed that teens and young adults who took varenicline-an FDA-approved, twice-daily smoking cessation pill for adults-are more than three times as likely to successfully quit vaping compared to those who received only behavioral counseling. Results are published in JAMA.

“Vaping is extremely popular among kids, and we know that this early nicotine exposure can make drugs like cocaine more addictive down the line, yet ours is the first treatment study to look at this vulnerable population,” said lead author A. Eden Evins, MD, MPH, director of the Center for Addiction Medicine at Massachusetts General Hospital (MGH), a founding member of the Mass General Brigham healthcare system. “We wanted to help teens and young adults quit, and we found that prescribing varenicline is the best way to do that.”

About a quarter of 18-to-25-year-olds vaped in 2023, and roughly 8% of high schoolers vaped in 2024. Vapes have become a popular alternative to cigarettes with the added challenge of being easy to conceal and easy to use in public places. Yet they contain many of the same familiar health threats, like nicotine addiction, carcinogen and heavy metal exposure, and pulmonary inflammation. Exploring treatment plans is crucial to provide teens and young adults with safe, effective avenues to quit.

To identify such a treatment avenue, the Mass General Brigham team recruited 261 participants aged 16-to-25 into a randomized clinical trial. Participants were sorted into three treatment groups. The first was varenicline, weekly behavioral counseling, and access to a free text support service called “This is Quitting.” The second was placebo pills, weekly behavioral counseling, and the text service. The third was the text service alone. Each group was treated for 12 weeks, then checked on monthly for another 12 weeks post-treatment.

Each week, participants reported whether they had successfully quit vaping, and their responses were verified with cotinine saliva tests. At the end of 12 weeks of treatment and at three-month follow-up, the varenicline group had the highest quitting success rate. At 12 weeks, 51% of varenicline users had stopped vaping, compared to 14% of placebo users and 6% of text-only users. At 24 weeks, 28% of varenicline users had stopped vaping, compared to 7% of placebo users and 4% of text-only users.

These findings demonstrate the importance of medication to help young people who are addicted to nicotine quit vaping, since the varenicline group had three times more success quitting vaping than their placebo counterparts-despite both engaging in behavioral therapy. Further research is needed to explore the potential impact of other therapeutic approaches, as well as to look at even younger people who use nicotine vapes.

Because varenicline is already approved for smoking cessation in adults, it can be prescribed for anyone aged 16 to 25 wanting to quit nicotine vaping.

“Not only was varenicline effective in this age group-it was safe. Crucially, we didn’t see any participants that quit vaping turn to cigarettes,” said Randi Schuster, PhD, founding director of the Center for School Behavioral Health at MGH. “Our findings illustrate the effectiveness and safety of this therapy to address the urgent public health concern of adolescents addicted to nicotine because of vapes.”

Reference:

Evins AE, Cather C, Reeder HT, et al. Varenicline for Youth Nicotine Vaping Cessation: A Randomized Clinical Trial. JAMA. Published online April 23, 2025. doi:10.1001/jama.2025.3810.

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Study Warns of Increased Risk of Postpartum Urinary Retention Following Cesarean Section

China: A recent retrospective analysis based on a nationwide inpatient sample has found that postpartum urinary retention (PUR) affects around 0.20% of women undergoing cesarean section (CS) in the United States. Although relatively rare, PUR is clinically significant due to its association with various risk factors and adverse outcomes.

The study showed that women aged 25 and older, especially those above 35 and those with pre-existing comorbidities (OR 1.51–1.79) were more likely to develop PUR. Conditions such as fluid and electrolyte imbalances (OR 2.46), paralysis (OR 3.24), and recent weight loss (OR 2.34) further elevated the risk.

“Key contributing complications included catheter placement (OR 22.57), bladder and renal injuries (OR 6.12), renal failure (OR 4.74), and puerperal infections (OR 3.31). On the other hand, a history of prior CS and undergoing low cervical cesarean deliveries appeared to reduce the risk, indicating a potential protective effect,” the researchers reported in BMC Women’s Health.

Jian Wang from Southern Medical University, Guangzhou, China, and colleagues conducted the study. Their goal was to assess risk factors for PUR after cesarean delivery and evaluate associated morbidity using a population-based retrospective case-control design.

For this purpose, the team analyzed data from the National Inpatient Sample (2010–2019), categorizing women based on whether they experienced PUR post-CS. Multivariate logistic regression was used to identify predictors, adjusting for maternal demographics and clinical variables.

Key findings included:

  • Analysis of 2,397,168 cesarean deliveries from the NIS database.
  • PUR incidence stood at 0.20%.
  • Affected patients had longer hospital stays, higher medical costs, and more complications.
  • The risk was elevated in women aged ≥25, particularly ≥35.
  • Asian and Pacific Islander women had a higher PUR risk.
  • One or more comorbidities significantly increased the likelihood.
  • Deliveries at large, teaching or Eastern hospitals were more prone to PUR.
  • Coagulation disorders, electrolyte disturbances, neurological issues, paralysis, and recent weight loss were notable risk factors.
  • PUR was linked to complications such as bladder or ureteral injury, acute renal failure, respiratory failure, endometritis, hemorrhage, uterine rupture, hysterectomy, peritonitis, puerperal infections, and chorioamnionitis.
  • Obstetric factors like cephalopelvic disproportion, fetal malposition, placenta previa, multiple gestation, and abnormal bladder anatomy raised the risk.
  • Bladder catheter placement and IV infusion were strongly associated with PUR, with catheter use showing the highest odds.
  • Conversely, previous CS, low cervical CS, and cord prolapse were associated with reduced PUR risk.

The authors concluded that PUR is relatively uncommon, however, it carries significant clinical implications. They stressed the need for antenatal screening to identify high-risk patients and advocated for an elective over emergency CS when feasible.

“Early intervention during the antenatal and postnatal periods could help mitigate the risk and improve patient outcomes,” they wrote.

Reference:

Zhang, F., Huang, J., Huang, X. et al. Incidence and risk factors of postpartum urinary retention following cesarean section: a retrospective nationwide inpatient sample database study. BMC Women’s Health 25, 180 (2025). https://doi.org/10.1186/s12905-025-03728-w

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Topical Tranexamic Acid during Surgical Exposure enhances isolation, makes Bracket Bonding more effective: Study

Researchers have found in a new study that Topical application of tranexamic acid during therapeutic surgical exposure enhances isolation, making bracket bonding more effective. The technique is cost-efficient, simple to use, and has no reported adverse effects. When combined with a hemostatic agent, it leads to shorter procedure times, reduced bond failure, smooth healing, and greater satisfaction for both patients and surgeons.

Therapeutic surgical exposure and placing a bracket on the impacted tooth is an approach which involves both maxillofacial surgeon and an orthodontist. The prime requirement is complete hemostasis and isolation which sometimes is difficult to achieve. This study was conducted to evaluate the efficacy of topical application of Tranexamic acid (TA) intra-operatively to facilitate this Procedure. Time, duration from exposure of the crown of the impacted tooth to bonding of brackets, allergic reactions, intra-operative blood loss, surgeon’s perception and patient’s comfort were the criteria’s which were evaluated. This prospective observational study had two groups, for which 10 patients selected with impacted teeth. In first group topical application of TA soaked gauze pieces were used, and in second group normal saline soaked gauze pieces were used as control. Results: Statistically significant results were achieved for experimental group in terms of Intra operative time duration and intra operative blood loss which inferenced that better isolation was achieved with the local use of Tranexamic acid, Surgeon’s perception was good which inferenced that Surgeon was more comfortable in experimental group, Also Patients were more comfortable and postoperative wound healing was better in experimental group and no adverse reactions were reported in any group. Topical use of tranexamic acid achieved better results for therapeutic surgical exposure showing good isolation for bonding the brackets. This technique is very cost effective, easy to apply with no adverse effects. With additional use of hemostatic agent topically; reduction in time duration, less bond failure, uneventful healing and improved patient’s and surgeon’s satisfaction is achieved.

Reference:

Mahajan A, Patel A, Shukla N, Shah N. Novel Use of Tranexamic Acid to Reduce Time Taken During Bracket Placement for Orthodontic Traction of Impacted Teeth: An Observational Study. J Maxillofac Oral Surg. 2025 Apr;24(2):536-541. doi: 10.1007/s12663-022-01813-3. Epub 2022 Nov 4. PMID: 40182449; PMCID: PMC11961823.

Keywords:

Topical, Tranexamic Acid, Surgical, Exposure, enhances, isolation, Bracket, Bonding, effective, study, Bonding; Bracket placement; Impacted teeth; Topical application; Tranexamic acid, Mahajan A, Patel A, Shukla N, Shah N. Novel

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