HEMSTOP bleeding score weakly predicts postpartum hemorrhage risk: BMC

A new study published in the journal of BMC Pregnancy and Childbirth revealed that postpartum hemorrhage (PPH) is not well predicted by the HEMSTOP bleeding score.

In high-income nations, postpartum hemorrhage affects 5% of births and continues to be the primary cause of maternal morbidity and death globally. In order to start active management of delivery and early detection and treatment of PPH, it is imperative to identify women who are at greater risk. Inherited mild-to-moderate bleeding disorders (MBDs) are one of the maternal risk factors for PPH that may be identified and treated.

High percentages of MBDs were identified in 2 recent studies examining hemostasis in women following severe PPH (23% and 56%, respectively). The women in these studies were sent to hemostasis specialists due to an unusual PPH course. The function of MBDs in PPH, particularly in unselected parturients, is therefore little understood. This study was to ascertain the predictive usefulness of the HEMSTOP bleeding score for the incidence of PPH in unselected parturients using prospective data and various adjusted analyses.

Women who completed the HEMSTOP questionnaire before to delivery and had no known bleeding disorders or antithrombotic medications were included in a prospective cohort research that was carried out in a tertiary maternity hospital between 2014 and 2016. Primary PPH > 500 mL after birth was the main result. This research looked at the bleeding score, which ranges from 0 to 7, as an ordinal and continuous variable. They adjusted for PPH risk variables in our multivariable analysis. Also, this study calculated the prognostic accuracy metrics for the bleeding score.

Out of 2,536 women, 116 (4.6%) experienced PPH. When compared to a score of 0, elevated bleeding scores were linked to increased PPH risk, showing a progressive increase in risk along with score escalation (adjusted RR = 1.58; 95% CI, 1.01 to 2.46 for a score of one, adjusted RR = 2.11, 95% CI 0.86 to 5.20 for a score of two, and adjusted RR = 7.20, 95% CI 2.54 to 20.41 for a score of three; P < 0.001).

The accuracy of the bleeding score in predicting PPH had an area under the curve of 0.56. Overall, the evaluation of main PPH risk benefits from the computation of the HEMSTOP bleeding score in pregnant women who are not chosen.

Reference:

Deleu, F., Nebout, S., Peynaud-Debayle, E., Mandelbrot, L., & Keita, H. (2025). A high HEMSTOP bleeding score is a major independent risk factor for postpartum hemorrhage: a prospective cohort study. BMC Pregnancy and Childbirth, 25(1). https://doi.org/10.1186/s12884-025-07281-0

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Chlorhexidine and hydrogen peroxide Effective socket Irrigation Solutions for Mandibular Third Molar Surgery: Study

Researchers have found in a new research that Chlorhexidine and hydrogen peroxide solutions are highly beneficial for socket irrigation after mandibular third molar surgery. These solutions help reduce bacterial load, prevent infections, and promote faster healing. Chlorhexidine is known for its strong antiseptic properties, while hydrogen peroxide aids in debriding the surgical site by breaking down debris and enhancing oxygenation. Regular irrigation with these solutions can improve post-operative outcomes and reduce complications.

The objective of this study was to compare the effects of irrigation solutions containing chlorhexidine, povidone-iodine, or hydrogen peroxide on pain and swelling following mandibular third molar surgery. This prospective randomized controlled trial employed a single-blind design. Overall, 112 patients were randomized to four groups based on the antiseptic assigned for the intervention: control, chlorhexidine (CHX), povidone-iodine (PI), and hydrogen peroxide (HP). The patients were followed up on days 1, 3, 7, and 15 after surgery, and pain and swelling were assessed. Data were analysed using ANOVA and post hoc multiple comparison tests. The CHX and HP groups demonstrated significantly lower mean pain scores compared to the control group on days 3 (P = 0.021, P = 0.033) and 7 (P = 0.002, P = 0.017). Regarding the difference in swelling from baseline (before surgery) on each follow-up day, the CHX and HP groups showed significantly less swelling compared to the control group on days 1 (P = 0.023, P = 0.012), 3 (P = 0.007, P = 0.001), and 7 (P = 0.002, P = 0.018). Moreover, the CHX and HP groups demonstrated significantly lower mean swelling changes from baseline compared to PI: CHX vs PI on day 7 (P = 0.032), HP vs PI on day 1 (P = 0.037). In conclusion, chlorhexidine and hydrogen peroxide solutions are highly beneficial options for socket irrigation following mandibular third molar surgery. This study showed a more prominent reduction in pain and swelling with chlorhexidine and hydrogen peroxide solutions compared to povidone-iodine solution.

Reference:

Shahraki, M, et al. “Effect of Chlorhexidine, Povidone-iodine, and Hydrogen Peroxide Irrigation On Pain and Swelling After Mandibular Third Molar Surgery: Randomized Controlled Trial.” International Journal of Oral and Maxillofacial Surgery, 2025.

Keywords:

Chlorhexidine, hydrogen peroxide, effective, Socket, Irrigation, Solutions, Mandibular, Third Molar Surgery, study

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Sugemalimab Plus Chemotherapy Improves Survival in Advanced Gastric Cancer, JAMA

A new study published in JAMA determined that the addition of sugemalimab to chemotherapy enhances overall and progression-free survival in patients with previously untreated, unresectable, locally advanced, or metastatic gastric or gastroesophageal junction adenocarcinoma. The GEMSTONE-303 phase 3 trial, which was carried out at 54 centers in China, proved that patients treated with sugemalimab in combination with capecitabine and oxaliplatin (CAPOX) achieved a median overall survival of 15.6 months. This study was conducted by Xiaotian Z. and colleagues.

Gastric cancer, including gastroesophageal junction cancer, is one of the most frequently diagnosed cancers globally, with high mortality. Immune checkpoint inhibitors against PD-1 or PD-L1 have been shown to be beneficial in enhancing survival. Sugemalimab, an anti-PD-L1 fully human monoclonal antibody, had earlier shown promising efficacy and safety in phase 1b when administered together with chemotherapy.

The GEMSTONE-303 was a phase 3, double-blind, randomized, placebo-controlled trial in 54 sites in China.A total of 479 unresectable locally advanced or metastatic gastric or gastroesophageal junction adenocarcinoma patients with PD-L1 CPS ≥5 were enrolled during the period April 9, 2019, to December 29, 2021, with the follow-up performed until July 9, 2023.

Patients received either

  • Sugemalimab (1200 mg intravenously, q3w) and CAPOX (capecitabine and oxaliplatin) for up to 6 cycles, then sugemalimab maintenance for up to 24 months (n=241), or

  • Placebo and CAPOX on the same regimen (n=238).

The overall survival (OS) and investigator-assessed progression-free survival (PFS) were the primary endpoints. The secondary endpoints were objective response rate (ORR), duration of response (DOR), and safety.

Key Findings

  • The overall survival (OS) was significantly better in the group receiving sugemalimab (15.6 months, 95% CI: 13.3-17.8) than the placebo group (12.6 months, 95% CI: 10.6-14.1) with a hazard ratio (HR) of 0.75 (95% CI: 0.61-0.92, p=0.006).

  • The progression-free survival (PFS) at the median was 7.6 months (95% CI: 6.4-7.9) in the sugemalimab arm and 6.1 months (95% CI: 5.1-6.4) in the placebo arm (HR: 0.66, 95% CI: 0.54-0.81, p<0.001).

  • Objective response rate (ORR) was greater in the sugemalimab group (48.1%) than in the placebo group (38.7%).

  • The disease control rate (DCR) was 82.2% with sugemalimab and 74.4% with placebo.

  • Grade 3 or worse treatment-related adverse events (TRAEs) occurred in 53.9% of patients treated with sugemalimab and 50.6% of those treated with placebo.

The safety profile of sugemalimab with CAPOX was in line with previous research on anti-PD-L1 treatments. The most frequent grade 3 or better adverse events were:

  • Neutropenia (15.3% in the sugemalimab arm vs 13.8% in the placebo arm).

  • Anemia (9.8% vs 8.4%).

  • Thrombocytopenia (7.2% vs 6.5%).

  • Elevated alanine aminotransferase (ALT) levels (5.3% vs 4.9%).

  • Severe adverse events were reported in 31.2% of sugemalimab-treated patients and 28.4% of placebo-treated patients.

The study authors concluded that the addition of sugemalimab to chemotherapy extended overall survival and progression-free survival significantly in patients with PD-L1 CPS ≥5 gastroesophageal junction or gastric adenocarcinoma. The safety profile of combination therapy was manageable, further substantiating its potential for use as a first-line therapeutic option. Such evidence justifies the inclusion of sugemalimab in guidelines, bringing about a new expectation for advanced gastric cancer patients.

Reference:

Zhang X, Wang J, Wang G, et al. First-Line Sugemalimab Plus Chemotherapy for Advanced Gastric Cancer: The GEMSTONE-303 Randomized Clinical Trial. JAMA. Published online February 24, 2025. doi:10.1001/jama.2024.28463

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Second-Trimester Kidney Function Tied to Adverse Pregnancy Outcomes: Study

USA: Researchers have found in a new study that kidney function during the second trimester plays a crucial role in predicting adverse pregnancy outcomes, particularly in patients with systemic lupus erythematosus (SLE). It was found that both low and high estimated glomerular filtration rate (eGFR) values in this period are associated with complications such as preeclampsia, preterm birth, low birth weight, and fetal loss.

The findings were published online in Kidney360 on February 14, 2025. 

The researchers note that kidney function is not routinely assessed during pregnancy. However, several studies have suggested that renal function, particularly during the second trimester, may serve as a potential predictor of adverse pregnancy outcomes. Patients with systemic lupus erythematosus are already known to be at a higher risk for complications during pregnancy, but the specific relationship between second-trimester kidney function and adverse pregnancy outcomes remains unclear, especially in diverse populations with high obstetrical risk.

Against the above background, Anika Lucas, Department of Medicine, Duke University School of Medicine, Durham, NC, USA, and colleagues aimed to evaluate this association, providing valuable insights into the role of renal function in predicting and managing pregnancy-related complications.

In the observational study of pregnant patients with lupus across North America and Europe from 1995 to 2017, researchers utilized second-trimester creatinine levels and estimated glomerular filtration rate to assess their association with preeclampsia, preterm birth, low birth weight, fetal loss, and a composite of these outcomes. These measures were analyzed using regression models with fractional polynomials, and discrete formulations of eGFR were examined to refine the assessment.

The following were the key findings of the study:

  • The study included 684 pregnancies in patients with lupus.
  • The mean second-trimester creatinine level was 0.63 mg/dL, with a median of 0.60 mg/dL.
  • At least one in three patients experienced an adverse pregnancy outcome.
  • Both U-shaped and linear relationships were observed between kidney function and the log odds of adverse pregnancy outcomes.
  • Stratification based on lupus nephritis status (active, in remission, or absent) revealed differences in the association between kidney function and adverse outcomes.

In conclusion, the investigators observed high rates of adverse pregnancy outcomes among pregnant patients with lupus, regardless of lupus nephritis status. They identified complex relationships between second-trimester kidney function and adverse pregnancy outcomes, which varied based on the specific outcome and the presence or absence of lupus nephritis.

Emphasizing the need for further research, they highlighted the importance of larger cohort studies to assess the link between second-trimester kidney function and outcomes like small-for-gestational-age births and preterm delivery, distinguishing between spontaneous and iatrogenic cases. Additionally, they suggested that tracking eGFR changes from pre-pregnancy through the second trimester could offer deeper insights into obstetrical risk.

Reference:

Lucas, Anika M.1,2,a; Miller, Cameron1; Eudy, Amanda1; Myers, Rachel1; Wyatt, Christina M.1,3; Wheeler, Sarahn4; Petri, Michelle5; Fischer-Betz, Rebecca6; Mokbel, Abir7; Nalli, Cecilia8; Andreoli, Laura8; Tincani, Angela8; Molad, Yair9; Balevic, Stephen3; Gladman, Dafna D.10; Urowitz, Murray10; Clowse, Megan E.B.1. Second (2nd) Trimester Kidney Function and Adverse Pregnancy Outcomes among Patients with Lupus. Kidney360 ():10.34067/KID.0000000738, February 14, 2025. | DOI: 10.34067/KID.0000000738

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Bridging the Gap: Towards Reproductive Justice in Infertility Care – ACOG Recommendations

Diagnostic tests and treatments for infertility must be accessible to all individuals requiring these services. Discrepancies in infertility rates and obstacles to obtaining assisted reproductive technology should be recognized and tackled within the context of reproductive justice. Drawing from the guidelines established in this Committee Statement, the American College of Obstetricians and Gynecologists (ACOG) presents recommendations and insights concerning infertility within historically marginalized and deliberately excluded communities.

Disparities in Accessing Infertility Services

The paper focuses on the disparities in accessing infertility services and the importance of addressing these inequities within a reproductive justice framework. It highlights the need for diagnostic testing and treatment for infertility to be available to all individuals in need. The paper emphasizes that health care professionals should identify specific populations at risk, advocate for insurance coverage for infertility services, policy changes, and evidence-based, affordable treatment options.

Infertility as a Medical Disease

The paper stresses that infertility is a medical disease and not merely a social condition, urging health care professionals to provide medically and ethically sound care tailored to the patient’s diagnosis. Obstetrician-gynecologists are recommended to inquire about reproductive planning and attempts at pregnancy, refer patients to subspecialists when necessary, and understand the specific barriers different populations face in accessing infertility care.

Disparities Highlighted in Infertility Care

Furthermore, the paper highlights disparities in both infertility prevalence and access to services. It mentions that certain racial and ethnic groups, such as Black women and Asian American patients, may have higher rates of infertility. It also discusses lower utilization of infertility services among Hispanic women and American Indian/Alaska Native populations. The paper points out the need for continuing research to improve outcomes, particularly in communities facing obstacles in accessing infertility services.

Reproductive Justice and Fertility Options

Reproductive justice, developed in the 1990s, emphasizes reproductive autonomy and the right to fertility options. Health care professionals are encouraged to address social determinants of health, mitigate biases, collaborate with support agencies, offer patient education on fertility, and advocate for insurance coverage for infertility services. The paper underlines the importance of recognizing and addressing biases in health care delivery, especially related to systemic racism and cultural beliefs affecting access to care.

Economic Barriers in Infertility Treatment Access

Moreover, the paper discusses economic barriers hindering infertility treatment access, particularly for marginalized communities. It calls for comprehensive insurance coverage for fertility treatment and the promotion of evidence-based, cost-effective treatment options. The importance of patient education on fertility, addressing health literacy disparities, and the need for inclusive research reporting to better understand disparities in infertility care are also highlighted.

Promoting Equitable Infertility Care

Overall, the paper emphasizes the significance of promoting access to infertility services, advocating for policy changes, and ensuring equitable care for all individuals, regardless of race, ethnicity, socioeconomic status, or gender identity, to achieve reproductive justice in the realm of infertility care.

Key Points

1.*Disparities in Accessing Infertility Services**: The paper highlights the importance of addressing inequities in accessing infertility services within a reproductive justice framework. It advocates for diagnostic testing and treatment to be available to all in need and stresses the role of health care profess*ionals in identifying at-risk populations and advocating for insurance coverage and policy changes.

2. Infertility as a Medical Disease*: Infertility is depicted as a medical disease rather than solely a social condition. The paper urges healthcare professionals to provide ethically sound care tailored to each patient’s diagnosis. Obstetrician-gynecologists are recommended to inquire about reproductive planning, refer patients to subspecialists as needed, and understand the unique barriers different populations face in accessing infertility care.

3. *Disparities Highlighted in Infertility Care*: Disparities in infertility prevalence and service access are discussed, with certain racial and ethnic groups, such as Black women and Asian American patients, identified as having higher infertility rates. Lower utilization of infertility services is noted among Hispanic women and American Indian/Alaska Native populations, emphasizing the need for further research to improve outcomes, especially in communities facing barriers to infertility services.

4. *Reproductive Justice and Fertility Options*: The concept of reproductive justice, emphasizing reproductive autonomy and the right to fertility options, is introduced. Health care professionals are encouraged to address social determinants of health, mitigate biases, collaborate with support agencies, provide patient education on fertility, and advocate for insurance coverage for infertility services. Recognizing and addressing biases in healthcare delivery, particularly related to systemic racism and cultural beliefs impacting care access, is highlighted.

5. *Economic Barriers in Infertility Treatment Access*: Economic barriers that hinder access to infertility treatment, particularly for marginalized communities, are discussed. Comprehensive insurance coverage for fertility treatment, promotion of evidence-based and cost-effective treatment options, patient education on fertility, addressing health literacy disparities, and inclusive research reporting to better understand disparities in infertility care are emphasized.

6. *Promoting Equitable Infertility Care*: The paper underscores the importance of promoting access to infertility services, advocating for policy changes, and ensuring equitable care for all individuals regardless of race, ethnicity, socioeconomic status, or gender identity. This inclusive approach aims to achieve reproductive justice in infertility care, emphasizing the need for fairness and equality in accessing and receiving infertility services.

Reference –

Infertility: Disparities and Access to Services: ACOG Committee Statement No. 14. Obstet Gynecol. 2025 Jan 1;145(1):e51-e57. doi: 10.1097/AOG.0000000000005769. PMID: 39666991.

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Do seizures in newborns increase children’s risk of developing epilepsy?

Seizures in newborns are one of the most frequent acute neurological conditions among infants admitted to neonatal care units. A study published in Developmental Medicine & Child Neurology indicates that newborns experiencing such neonatal seizures face an elevated risk of developing epilepsy.

For the study, investigators analyzed data on all children born in Denmark between 1997 and 2018, with the goal of comparing the risk of epilepsy in children with and without neonatal seizures.

Among 1,294,377 children, the researchers identified 1,998 who experienced neonatal seizures. The cumulative risk of epilepsy was 20.4% among children with neonatal seizures compared with 1.15% among children without. This indicates that 1 in 5 newborns with neonatal seizures will develop epilepsy.

Epilepsy was diagnosed before 1 year of age in 11.4% of children with neonatal seizures, in an additional 4.5% between 1 and 5 years, 3.1% between 5 and 10 years, and 1.4% between 10 and 22 years. Stroke, hemorrhage, or structural brain malformations in newborns, as well as low Apgar scores, were associated with the highest risks of developing epilepsy.

“Our study highlights that there are risk factors that may be used to identify infants for tailored follow-up and preventive measures,” said corresponding author Jeanette Tinggaard, MD, PhD, of Copenhagen University Hospital – Rigshospitalet. “Importantly, four out of five neonatal survivors with a history of neonatal seizures did not develop epilepsy, and we suggest future studies to explore a potential genetic predisposition.”

Reference:

Jeanette Tinggaard, Signe V. Pedersen, Mads L. Larsen, Andreas K. Jensen, Gorm Greisen, Bo M. Hansen, Christina E. Hoei-Hansen, The risk of epilepsy after neonatal seizures, Developmental Medicine & Child Neurology, https://doi.org/10.1111/dmcn.16255

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Prenatal vitamins may reduce risk of infant death, reveals research

Dongqing Wang, an assistant professor of Global and Community Health at George Mason’s College of Public Health, is pioneering research in prenatal nutritional interventions. His latest report identifies prenatal supplements that reduce health risks to small and vulnerable babies. This research was published in the prestigious The Lancet Global Health journal and funded by the Bill and Melinda Gates Foundation.

Wang found that compared to folic acid and iron alone, a multiple micronutrient supplement led to a 27% lower risk of giving birth to “small vulnerable newborn types,” or babies who suffered from preterm birth, low birthweight, and small-for-gestational-age birth-the three groups most likely to result in infant death.

In the past, these birth outcomes were all treated as separate conditions. Wang, however, delves into emerging science to look at different combinations across the three outcomes. Low birthweight, for example, can occur because of a short pregnancy, and growth restrictions can lead to babies born too small for their developmental age.

“Small vulnerable newborn types may have distinct mechanisms, health impacts, and intervention strategies,” says Wang. “This work is the first to examine the effects of prenatal multiple micronutrient supplements and small-quantity lipid-based nutrient supplements on the emerging outcomes of small vulnerable newborns.”

Folic acid and iron have been used to support prenatal health since the 1970s. Wang explored the effects of two additional types of prenatal supplements on women in low- and middle-income countries: prenatal multiple micronutrient supplements (MMS), similar to a common multivitamin, and small-quantity lipid-based nutrient supplements (SQ-LNS), which provide caloric nutrition and fatty acids in addition to vitamins.

He found that nearly all of these vitamins conferred some type of benefit-and some of them were hugely beneficial.

“This study underscores the important promise of nutritional supplements in prenatal care in low- and middle-income countries,” says Wang. “In particular, the protective effects of prenatal multiple micronutrients on most small vulnerable newborn types, particularly those with the greatest mortality risk, strongly supports switching from iron and folic acid supplements to MMS as the standard care.”

Combining 16 different studies, Wang analyzed how prenatal nutrition correlates to the occurrence of small vulnerable newborns. He believes that the right prenatal supplements can help mitigate them. Since more than 90% of pregnancies resulting in low birthweight occur in low- and middle-income countries, including those in sub-Saharan Africa and South Asia, Wang focused this work on those regions.

Reference:

Wang, Dongqing, Adu-Afarwuah, Seth et al. The effects of prenatal multiple micronutrient supplementation and small-quantity lipid-based nutrient supplementation on small vulnerable newborn types in low-income and middle-income countries: a meta-analysis of individual participant data, The Lancet Global Health.

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Is Immediate Surgery Necessary? Research Supports Delayed Approach for Type C Esophageal Atresia

China: A recent study published in BMC Surgery explored whether thoracoscopic repair of type C esophageal atresia requires emergency intervention, providing valuable insights into surgical timing and outcomes. The findings suggest that advancements in neonatal surveillance enable appropriately delayed surgery without increasing respiratory infection risk, allowing surgeons to refine treatment plans.

The researchers note that thoracoscopic repair of esophageal atresia (EA) with tracheoesophageal fistula (TEF) is performed more frequently. While many children undergo surgery within the first three days of life, the ideal timing for the procedure remains uncertain. Therefore, Shao-tao Tang, Huazhong University of Science and Technology, Wuhan, China, and colleagues aimed to evaluate the appropriate timing for thoracoscopic repair of type C EA and assess its mid-term clinical outcomes.

For this purpose, the researchers retrospectively analyzed 142 patients with esophageal atresia (EA) treated between 2009 and 2023. Among them, 109 patients with type C EA who underwent thoracoscopic one-stage repair were included. Based on surgical timing, patients were categorized into two groups: the early repair group (< 5 days) and the delayed repair group (≥ 5 days). Propensity score matching (PSM) was applied to minimize imbalances caused by severe cardiac complications, gestational age, and birth weight, ensuring a more accurate comparison between the two groups.

The study led to the following findings:

  • The median age at surgery was 5 days, ranging from 1 to 16 days.
  • After matching, 43 out of 59 patients in the early repair group (Group A) and 43 out of 50 patients in the delayed repair group (Group B) were included in the validation cohort.
  • All 86 cases successfully underwent thoracoscopic one-stage repair surgery.
  • Delayed surgery did not increase the incidence of preoperative or postoperative respiratory tract infections.
  • Intraoperative and postoperative complications were similar between the two groups.
  • Patients in Group B required fewer balloon dilations for anastomotic stricture during follow-up (1.8 ± 0.8 versus 3.1 ± 1.1).

The study showed that in patients with type C esophageal atresia, delayed thoracoscopic repair is a safe and viable option, with postoperative outcomes comparable to early repair. Performing the surgery at or after five days in a well-equipped NICU does not increase the risk of preoperative respiratory infections compared to earlier interventions.

“These findings support a more flexible surgical approach, allowing better allocation of operating room resources by postponing emergency repairs to scheduled surgical days without compromising patient outcomes,” the researchers concluded.

Reference:

Wang, C., Cao, G., Li, K. et al. Does thoracoscopic repair of type C esophageal atresia require emergency treatment? BMC Surg 25, 66 (2025). https://doi.org/10.1186/s12893-025-02798-9

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Dental Radiographs effective in Detecting Pulp Stones, suggests study

Researchers have found in a new study that radiographs are effective in detecting pulp stones. However, further research is needed to evaluate their potential as a screening tool for early detection of systemic diseases.

Dental pulp stones are distinct calcified bodies that can be found in teeth that are healthy, diseased, or even unerupted. Pulp stones are suggested to be a manifestation of various systemic and genetic diseases affecting different organs of the body. Therefore, this study aimed to correlate the prevalence of pulp stones with gender, nationality, age, dental status, and systemic diseases. The medical records and radiographs of patients who visited the screening clinics and the Department of Oral Diagnosis at the College of Dentistry, Imam Abdulrahman Bin Faisal University, Dammam, Saudi Arabia, between January 2017 and June 2018 were analyzed in this study. Two examiners evaluated the digital orthopantomographs (OPGs) to identify the prevalence of pulp stones concerning the patient’s age, gender, nationality, arch position, and medical condition. RESULTS: A total of 153 patient records were examined, and pulp stones were detected in 43.1% of the patients. Among the nationalities, Saudi patients were the most affected at 57.6%, while 42.4% were non-Saudi. The maximum occurrence of pulp stones was observed in age group 4 (9.2%), while the minimum occurrence was in age group 8 (0.7%). The maximum occurrence of pulp stones (21.2%) was observed in age group 4 (36-45 years), while the minimum occurrence was 7.6% in age group 2 (16-25 years). Out of all examined patients, 46 (30.1%) patients were medically compromised. Among these medically compromised patients, radiographic examination showed that 56.5% (n=26) had pulp stones. This study supports the idea that dental radiographs are useful in detecting pulp stones. Further research is required to explore the potential of using dental radiographs as a screening tool for the early detection of systemic diseases.

Reference:

Fairozekhan, Arishiya T., et al. “Prevalence of Pulp Stones in Patients Visiting the Dental Hospital of Imam Abdulrahman Bin Faisal University: a Correlative Retrospective Study.” Cureus, vol. 17, no. 1, 2025, pp. E77765.

Keywords:

Dental, Radiographs, effective, Detecting, Pulp, Stones, suggests, study, Fairozekhan, Arishiya T

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Biocon launches Liraglutide for diabetes, obesity in UK

Bengaluru: Biocon Limited, an innovation-led global biopharmaceutical company, has announced the launch of its GLP-1 peptide, Liraglutide, for diabetes and obesity, in the United Kingdom (U.K.).

The drug-device combination will be marketed in the U.K. under the brand names Liraglutide Biocon for
diabetes (gVictoza) and Biolide for chronic weight management (gSaxenda).

The launch follows the approval from the Medicines and Healthcare Products Regulatory Agency (MHRA), U.K.,
earlier this year, making Biocon Limited the first generics company to obtain approval for gLiraglutide in a
major regulated market.


Siddharth Mittal, Chief Executive Officer and Managing Director, Biocon Limited, said, “The launch of our
gLiraglutide for diabetes and obesity in the U.K. marks a significant milestone for Biocon. Making this GLP-1
peptide more accessible and affordable to patients dealing with these conditions is testament to our
unwavering commitment to enhancing healthcare outcomes across the globe. The timely launch will offer
healthcare providers and patients affordable access to this drug and help fulfil an unmet need. The launch also
underpins Biocon’s scientific and manufacturing capabilities in developing and bringing to market complex,
vertically integrated, GLP-1 formulations. We will continue to focus our efforts towards expanding the reach of
gLiraglutide into other European markets, the U.S. and select MoW geographies, as well as enhancing our
pipeline of GLP-1 peptide products.”

Glucagon-like peptide-1 (GLP-1) are medications that help lower
blood sugar levels and promote weight loss. They are physiological hormones that have multiple actions on
glucose, mediated by the GLP-1 receptors released from gut enteroendocrine cells and control meal-related
glycemic excursions through augmentation of insulin and inhibition of glucagon secretion. GLP-1 also inhibits
gastric emptying and food intake actions, maximizing nutrient absorption while limiting weight gain.

Liraglutide is a synthetic analog of GLP-1 peptide and is administered as a once-daily
injection. It was approved for medical use in the European Union in 2009, and in the United States in 2010.
Liraglutide was approved by the US FDA in 2014, and by the EMA a year later, for adults who are either obese
or overweight with atleast one weight-related condition. In 2019, it was approved by the US FDA for the
treatment of children who are ten years or older with type 2 diabetes, making it the first non-insulin drug
approved to treat type 2 diabetes in children since metformin was approved in 2000.

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