PHC doctor faces medical negligence allegations after dismissing pregnancy

Erode: A doctor at the Primary Health Centre (PHC) in Siruvalur has come under scrutiny after allegedly telling a pregnant woman that she was not pregnant and attributing her abdominal swelling to bloating.

The woman later underwent a scan at a private hospital, which confirmed that she was four months pregnant. This discrepancy has led to serious allegations of medical negligence

According to the news reports, the 28-year-old woman had been receiving regular prenatal care at the Primary Health Centre (PHC) in Ayalur, which falls under the jurisdiction of the Siruvalur Block PHC in Gobichettipalayam. As part of routine procedures to monitor foetal development, she was referred to the Siruvalur PHC for a follow-up evaluation. 

Also Read: Misdiagnosed for years, Elderly man’s life saved by rare tumour surgery at KGMU

A few days ago, during her visit to the Siruvalur centre, a trainee doctor examined the woman and informed her that she was not pregnant, claiming the abdominal swelling was due to bloating. Shocked and confused, the couple sought a second opinion at a private hospital in Gobichettipalayam, where an ultrasound scan confirmed that she was four months pregnant and the fetus was developing normally.

The couple has since raised allegations of medical negligence against the doctor at the Siruvalur PHC, saying their repeated efforts to meet or speak with the medical officer in question were unsuccessful. They have demanded that appropriate action be taken by the health authorities.

Speaking to the Hindu, Deputy Director of Health Services P. Aruna said that the doctor had cited poor abdominal visibility during the scan as the reason for the confusion. She added that an inquiry was underway.

Also Read: Misdiagnosed Fetal Deformity: Scan Centre slapped Rs 16.5 Lakh compensation

Medical Dialogues had previously reported that the District Consumer Disputes Redressal Commission in Faridkot has ordered a scan and diagnostic centre located in Kotkapura to pay Rs 16.5 lakh compensation for allegedly failing to detect a fetal deformity during multiple ultrasonography scans conducted prior to delivery.

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400 Medical, Health Officers appointed in Assam

Guwahati: Assam Chief Minister Himanta Biswa Sarma on Wednesday distributed appointment letters to 400 health officers, asserting that his government is committed to creating employment opportunities for youths.  

At an official function here, Sarma distributed the appointment letters among ‘Medical and Health Officers’, and said it marked a cumulative total of 1,20,359 recruitments provided to youths in the state.

“Taking a leap towards our goal of over 1.5 lakh government jobs, I am distributing appointment letters to 400 Medical and Health Officers. These officers will add muscle to our efforts of delivering quality healthcare to the last mile at the grassroots,” he said, news agency PTI reported.

Also Read:CM Dhami distributes appointment letters to 1,232 nursing officers

In the last few years, delivering quality healthcare and providing jobs have been the key priorities of the Assam government, Sarma said.

“With these appointments, the aspirations of millions of people of getting better healthcare delivery and services will be fulfilled,” he said.

The CM also said the state government’s robust interventions in the healthcare sector in the last few years have ensured that there has been a rapid reduction in maternal mortality rate and infant mortality rate.

“In recent years, Assam has seen a sharp decline in maternal mortality rate. From 480 when I first took charge as health minister to 167 now, the numbers will plunge more. With continued efforts, Assam is expected to reach the national average in the next 3-4 years. Our efforts in this direction will continue,” he said.

The Assam government’s goal is to have 30 medical colleges by 2029, and it is moving ahead in this direction in a systematic manner, Sarma said.

“From just three in 2006, today we have 13 functional medical colleges, delivering quality healthcare at affordable rates. The results have been gratifying… healthy citizens, finest treatment and also many additional employment opportunities for our youth.

“When I initiated work on Jorhat Medical College as health minister, people questioned my decision and criticised every step taken, but we still succeeded. Today, the inauguration of a medical college has become a routine affair,” he said.

The chief minister also said the private sector should complement public health institutions, not compete with it for patients.

“Only then will our medical landscape evolve into a patient-centric one with clear roles set for public and private health institutions,” he added.

Also Read:GMCH set to become one of India’s largest hospitals, says Assam CM

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Frailty Significantly Increases Mortality and Complications in PCI Patients, NCDR Registry Study Finds

USA: Frailty is common among older patients undergoing percutaneous coronary intervention (PCI) in the United States, with greater frailty linked to significantly higher risks of in-hospital death and procedural complications, according to new findings from the American College of Cardiology’s CathPCI Registry. The study, led by Dr. Benjamin Peterson from the University of Kentucky School of Medicine, was published online in JACC ahead of its June 24, 2025, issue.

The analysis included over 1.3 million patients (mean age 74.6 years; 34% women) aged 65 years or older who underwent PCI between October 2018 and December 2021. Frailty was evaluated using the Canadian Study of Health and Aging Clinical Frailty Scale (CFS), which assesses the ability to perform both basic and instrumental activities of daily living. Patients were classified into four groups: non-frail (CFS 1-2), prefrail (CFS 3-4), frail (CFS 5-6), and severely frail (CFS 7-9).

The key findings were as follows:

  • Frailty was widespread among PCI patients, with 67.8% categorized as prefrail, 21.6% as frail, and 2.2% as severely frail.
  • The overall in-hospital mortality rate was 2.4%.
  • Mortality increased sharply with frailty: 0.5% in nonfrail patients, 1.1% in prefrail, 3.3% in frail, and 20.3% in severely frail patients.
  • More than half of all PCIs were performed in patients over 65 years, who account for nearly 80% of PCI-related mortality.
  • The study demonstrated a clear gradient of increasing risk tied to frailty status, independent of bedside mortality scores and across various clinical subgroups.
  • Among severely frail patients undergoing complex PCI scenarios, mortality rates were 44.2% following cardiac arrest, 51.0% with cardiogenic shock, 46.1% with mechanical circulatory support, 23.9% with chronic total occlusions, 29.6% for left main coronary interventions, and 22.4% with severe calcification.
  • The rates of complications, including bleeding, transfusion need, vascular issues, new dialysis initiation, and stroke, consistently rose with increasing frailty severity.

While the authors caution against using these findings to withhold PCI, especially in acute coronary syndromes, they emphasize the importance of incorporating frailty assessment into routine clinical evaluations. “Frailty status, even at the prefrail level, significantly affects procedural risk and should guide shared decision-making,” the authors noted.

In an accompanying editorial, Dr. John A. Dodson and Dr. Ashok Krishnaswami advocate for incorporating frailty screening into routine patient assessment, similar to vital signs, to enhance outcomes for older adults undergoing PCI.

“To meaningfully improve care for older adults, frailty assessment should become a routine part of clinical practice—integrated into every evaluation just as vital signs are,” they wrote.

Reference:

Peterson, B., Kochar, A., Young, R., Senman, B., Rymer, J., Wojdyla, D., … Bhatt, D. L. (2025). Effect of Frailty on In-Hospital Mortality and Complications of PCI: An NCDR Registry Report (Accepted). Journal of the American College of Cardiology, 85(24), 2416–2420. https://doi.org/10.1016/j.jacc.2025.04.027

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Combination Therapy Halts Progression of COVID-19 Associated sino-maxillary and mandibular mucormycosis, suggests study

Researchers have found in a new research that the combined use of oral posaconazole, adjunctive hyperbaric oxygen (HBO) therapy, and methylene blue effectively prevents further progression of COVID-19 associated sino-maxillary and mandibular mucormycosis.

The study aimed to assess the cumulative role of oral posaconazole, post-debridement Hyperbaric Oxygen (HBO) therapy, along with local application and steam inhalation with methylene blue as an adjunct to surgery to prevent further progression of COVID-19 associated sino-maxillary or mandibular mucormycosis.

A retrospective observational study was conducted on patients diagnosed with sino-maxillary or mandibular mucormycosis associated with COVID-19. A total of 38 patients underwent surgical debridement and received adjunctive treatment with posaconazole, hyperbaric oxygen therapy, and local application and steam inhalation of methylene blue. Medical records were analyzed for COVID-19-related hyperglycemia, prolonged hospitalization, immunosuppressive/steroid therapy, and the use of iron or zinc supplements, which may be linked to increased mucormycosis incidence. Outcomes were evaluated for association with any concurrent infection, complications, need for sequential debridement, and further progression of disease.

Results: A total of 38 patients (range: 23–68) were included, comprising 24 males and 14 females. Isolated sino-maxillary involvement was observed in 32 cases (84.21%), and mandibular involvement in 5 cases (13.15%). No further disease progression was noted during the 2-year follow-up, based on clinical evaluation and postoperative computed tomography (CT) scans. Actinomycosis co-infection was identified in 21.05% of cases.

Complications included wound dehiscence (39.47%), pus discharge (5.26%), reversible hearing impairment during HBO therapy (5.26%), and flap necrosis (2.63%). Four patients (10.52%) required sequential surgical debridement for sequestrum removal. It was concluded that concurrent use of oral posaconazole, adjunct HBO therapy and methylene blue prevents further progression of COVID-19 associated sino-maxillary and mandibular mucormycosis.

Reference:

Mohanty, S., Bansal, N., Verma, A. et al. Adjunctive use of posaconazole, hyperbaric oxygen therapy, and methylene blue for COVID-19-associated mucormycosis. Oral Maxillofac Surg 29, 126 (2025). https://doi.org/10.1007/s10006-025-01419-2

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Enlicitide Decanoate Promising as Oral PCSK9 Inhibitor in Hyperlipidemia in Phase 3 trials

Phase 3 trials have demonstrated that enlicitide decanoate significantly reduces LDL cholesterol, showing strong potential as an oral PCSK9 inhibitor for patients with hyperlipidemia and heterozygous familial hypercholesterolemia (HeFH).

The CORALreef HeFH and CORALreef AddOn trials successfully met their primary and all key secondary endpoints, demonstrating statistically significant and clinically meaningful greater reductions in low-density lipoprotein cholesterol (LDL-C) for enlicitide compared to placebo (CORALreef HeFH) and compared to other oral non-statin therapies (CORALreef AddOn). There were no clinically meaningful differences in incidences of adverse events (AE) and serious adverse events (SAE) in either trial.

Results from the three Phase 3 trials in the CORALreef clinical development program will be presented at a future scientific congress.

Key takeaways from CORALreef HeFH and CORALreef AddOn studies:

• CORALreef HeFH: statistically significant and clinically meaningful reductions in LDL-C for enlicitide versus placebo in adults with heterozygous familial hypercholesterolemia (HeFH) who have a history of or are at risk for atherosclerotic cardiovascular disease (ASCVD) and are treated with a statin.

• CORALreef AddOn: statistically significant and clinically meaningful reductions in LDL-C for enlicitide versus ezetimibe, versus bempedoic acid and versus ezetimibe and bempedoic acid in adults with hyperlipidemia who have a history of or are at risk for ASCVD and are treated with a statin.

“We are thrilled to bring forward the first Phase 3 results from our clinical development program evaluating enlicitide, which, if approved, would be the first marketed oral PCSK9 inhibitor in the U.S.,” said Dr. Dean Y. Li, president, Merck Research Laboratories. “Enlicitide is a novel macrocyclic peptide that has the potential to deliver antibody-like efficacy and specificity for the validated PCSK9 mechanism in the form of a daily oral pill. We are working with urgency to make this oral therapy available to patients worldwide.”

“Atherosclerotic cardiovascular disease accounts for 85 percent of cardiovascular deaths. Despite available treatment options, cardiovascular-related deaths remain the leading cause of death worldwide and continue to rise,” said Dr. Christie M. Ballantyne, principal investigator of the CORALreef HeFH study and Professor of Medicine at Baylor College of Medicine. “LDL-C is a major modifiable risk driver for atherosclerosis and prioritization of LDL-C management should be a cornerstone of cardiovascular risk prevention. Early intervention and intensification of lipid treatment would allow more patients to achieve LDL-C goals.”

The efficacy and safety of enlicitide are being evaluated through the comprehensive CORALreef Phase 3 clinical development program, which aims to enroll approximately 17,000 patients across several trials, including two large ongoing trials, CORALreef Lipids and CORALreef Outcomes.

About CORALreef HeFH

CORALreef HeFH (NCT05952869) is a Phase 3, randomized, double-blind, placebo-controlled, multicenter study designed to evaluate the safety and efficacy of enlicitide compared to placebo in adults with HeFH who have a history of or were at risk for a major ASCVD event and are treated with a moderate or high intensity statin with or without other lipid-lowering therapies. The primary endpoints were mean percent change from baseline in LDL-C at week 24, number of participants with one or more adverse events (AEs), and number of participants who discontinued study drug due to an AE. Secondary endpoints included mean percent change from baseline in LDL-C at week 52, mean percent change from baseline in non-HDL-C, ApoB and percent change in Lp(a) at week 24.

About CORALreef AddOn

CORALreef AddOn (NCT06450366) is a Phase 3, randomized, double-blind, multicenter study designed to evaluate the efficacy and safety of enlicitide compared to ezetimibe, to bempedoic acid, and to ezetimibe and bempedoic acid, in patients with hypercholesterolemia who had a history of a major ASCVD event or were at risk for a major ASCVD event and are treated with a statin. The primary endpoint was the mean percent change from baseline in LDL-C at week 8. Secondary endpoints included mean percent change from baseline in non-HDL-C and ApoB.

About enlicitide and PCSK9

Enlicitide is an investigational, potentially first oral PCSK9 inhibitor designed to lower LDL-C via the same biological mechanism as currently approved monoclonal antibody injectable PCSK9 inhibitors but in a daily pill form. Enlicitide is a novel oral macrocyclic peptide that binds to PCSK9 and inhibits the interaction of PCSK9 with LDL receptors.

PCSK9 plays a key role in cholesterol homeostasis by regulating levels of the LDL receptor, which is responsible for the uptake of cholesterol into cells. Inhibition of PCSK9 with enlicitide prevents the interaction of PCSK9 with LDL receptors. This results in greater numbers of LDL receptors available on the cell surface to remove LDL cholesterol from the blood.

About hyperlipidemia

Hyperlipidemia is a disorder characterized by an excess of lipids or fats in the blood, affecting approximately 86 million adults (aged 20 and older) in the U.S. Despite adjusting diet or other lifestyle factors, some individuals may not reach recommended lipid levels and will require medication to treat and manage hyperlipidemia. Hyperlipidemia is a major risk driver for the development of ASCVD events, such as heart attacks and strokes, which account for 85 percent of cardiovascular deaths.

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Zydus Gets CDSCO Panel Nod to Conduct Phase IV Trial for Indacaterol-Budesonide FDC Inhalation

New Delhi: In response to the proposal presented by Zydus Healthcare, the Subject Expert Committee (SEC) functional under the Central Drug Standard Control Organisation (CDSCO) has recommended the drug maker to conduct the Phase IV clinical trial of the fixed dose combination (FDC) Indacaterol maleate plus Budesonide Powder for inhalation (capsules).

In addition, the committee recommended the firm to submit the Phase IV clinical trial report of the FDC Indacaterol maleate plus Budesonide Powder for inhalation.

This came after the firm presented the Phase IV clinical trial protocol before the committee.

Indacaterol is a long-acting β2-adrenoceptor agonist and bronchodilator with a rapid onset of action. It was developed by Novartis. It is used to relax bronchial smooth muscle and improve symptoms and airflow obstruction caused by Chronic Obstructive Pulmonary Disease (COPD) and moderate to severe asthma.

Budesonide is a glucocorticoid that acts as an anti-inflammatory and immunomodulator. Budesonide inhalation is a treatment for asthma and chronic obstructive pulmonary disease (COPD).

At the recent SEC meeting, the expert panel reviewed the Phase IV clinical trial protocol before the committee.

After detailed deliberation, the committee recommended for grant of permission to conduct of the Phase IV clinical trial. “Accordingly, the firm should submit the Phase IV clinical trial report to CDSCO for further review by the committee,” the Panel noted.

Also Read: CDSCO Panel Accepts Mylan’s Post-Marketing Surveillance Report for Liposomal Amphotericin B Injection

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Digital Inhalers Improve Asthma Control, May Lower Risk of Severe Exacerbations: Study Shows

Canada: A comprehensive meta-analysis has found that patient-facing digital inhalers may significantly improve asthma management, particularly among individuals who struggle with medication adherence or inhalation techniques. The findings, published in The Journal of Allergy and Clinical Immunology: In Practice, indicate that these devices likely enhance asthma control and could lower the risk of severe asthma exacerbations with minimal associated harm.

Digital inhalers have sensors that provide real-time feedback to patients regarding their medication usage and inhalation technique. These tools aim to address the long-standing issue of poor adherence, estimated to affect around 43% of asthma patients globally.

To better understand their clinical utility, Leonardo Ologundudu, from McMaster University in Ontario, Canada, and colleagues conducted a systematic review of 12 randomized controlled trials involving 2,483 children (ages 4–17) and adults. This work was undertaken in the context of developing new clinical guidelines for severe and difficult-to-control asthma by the American Academy of Allergy, Asthma & Immunology and the American College of Allergy, Asthma, and Immunology Joint Task Force.

Based on the study, the researchers reported the following findings:

  • Digital inhalers likely improve asthma symptom control, with 44.3% of users achieving at least a three-point increase in Asthma Control Test scores, compared to 39.8% in the control group.
  • The study suggests that digital inhalers may reduce the incidence of severe asthma exacerbations, particularly in patients at high risk, with an 11% relative reduction, though the certainty of this finding is low.
  • On average, digital inhalers may result in 45 fewer severe exacerbations per 1,000 patients.
  • The review found minimal harm associated with digital inhalers, with a median device failure rate of about 12%.
  • Technical issues, such as sensor synchronization with smartphones, were the primary cause of failure.
  • One trial reported a case of protected health information exposure, but overall, adverse outcomes were rare.

The authors emphasize considering the benefits of digital inhalers within a broader clinical context. Patients already demonstrating consistent adherence and proper technique may derive limited additional benefit, whereas those requiring ongoing support might find digital inhalers especially helpful.

However, limitations exist. Many studies lacked blinded outcome assessors, and few enrolled older adults above 60. Moreover, the combined effect of digital inhalers and remote clinician monitoring was commonly studied, making it difficult to isolate its standalone impact.

Still, the findings are expected to influence future clinical practice. “These results support the incorporation of digital inhalers into asthma management, particularly for select patient subgroups. Updated guidelines should reflect this evolving landscape,” the researchers concluded.

Reference:

Ologundudu L, Rayner DG, Oppenheimer J, Sumino K, Hoyte F, RiveraSpoljaric K, Perry TT, Nyenhuis SM, Chipps B, Israel E, Shade LE, Press VG, Rangel S, Guyatt GH, McCabe E, O’Byrne PM, Hall L, Orr H, Sue-Wah-Sing D, Melendez A, Winders T, Przywara K, Gardner DD, Rank MA, Bacharier LB, Mosnaim G, Chu DK, Patient-facing digital inhalers for asthma: a systematic review and meta-analysis, The Journal of Allergy and Clinical Immunology: In Practice (2025), doi: https://doi.org/10.1016/j.jaip.2025.04.039.

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Gepotidacin Offers Safe and Effective Oral Alternative for Urogenital Gonorrhoea: Lancet

A new study published in The Lancet journal showed that Gepotidacin was non-inferior to the standard treatment of ceftriaxone plus azithromycin for urogenital Neisseria gonorrhoeae, with no new safety concerns reported. This highlights gepotidacin as a promising novel oral treatment option for uncomplicated urogenital gonorrhoea.

It has been demonstrated that gepotidacin, a first-in-class, bactericidal, triazaacenaphthylene antibiotic that prevents bacterial DNA replication, is both effective and well-tolerated when used to treat simple UTIs. Thus, to assess the safety and effectiveness of gepotidacin for the treatment of uncomplicated urogenital gonorrhea, Jonathan Ross and colleagues carried out this investigation.

This trial compared conventional therapy for uncomplicated urogenital gonorrhea (500 mg IM ceftriaxone + 1 g oral azithromycin) with oral gepotidacin (two 3000 mg doses, 10–12 hours apart). The participants were randomized 1:1, stratified by age, sex, and sexual orientation, and had to be at least 12 years old, weigh more than 45 kg, and have a proven or suspected infection. Microbiological success, or the culture-confirmed eradication of Neisseria gonorrhoeae at days 4–8, was the main endpoint, with a non-inferiority margin of −10%.

All participants randomly assigned to a study treatment who acquired at least one dose of their study treatment and were found to have ceftriaxone-susceptible N. gonorrhoeae isolated from the baseline culture of their urogenital specimen were evaluated for the primary outcome in the microbiological intention-to-treat (micro-ITT) population.

A total of 628 participants were randomized evenly to either ceftriaxone plus azithromycin or gepotidacin from October 2019 to October 2023 and 39% of them were lost to follow-up. There were 406 individuals in the micro-ITT population (204 receiving conventional treatment and 202 receiving gepotidacin).

The majority (92%) were men, and MSM made up a larger percentage (71%) than MSW (20%). 74% were White, 15% were Black/African American, and 17% were Hispanic or Latino. Non-inferiority was demonstrated by the microbiological success rates at test-of-cure, which were 92.6% in the gepotidacin group and 91.2% in the ceftriaxone + azithromycin group.

In neither group did urogenital N. gonorrhoeae persist. Mild to moderate gastrointestinal problems were the most common drug-related side events in the gepotidacin group. Neither group experienced any severe or major adverse effects. Overall, with no new safety issues, gepotidacin showed no inferiority to ceftriaxone with azithromycin for urogenital N. gonorrhoeae, providing a new oral treatment option for simple urogenital gonorrhea.

Source:

Ross, J. D. C., Wilson, J., Workowski, K. A., Taylor, S. N., Lewis, D. A., Gatsi, S., Flight, W., Scangarella-Oman, N. E., Jakielaszek, C., Lythgoe, D., Powell, M., Janmohamed, S., Absalon, J., & Perry, C. (2025). Oral gepotidacin for the treatment of uncomplicated urogenital gonorrhoea (EAGLE-1): a phase 3 randomised, open-label, non-inferiority, multicentre study. Lancet, 405(10489), 1608–1620. https://doi.org/10.1016/S0140-6736(25)00628-2

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Vitiligo Linked to Increased Risk of Heart, Autoimmune, and Mental Health Conditions: Study Shows

USA: In a recent case-control study utilizing data from the All of Us research program, researchers have uncovered a broad spectrum of comorbidities linked to vitiligo, extending well beyond its traditionally recognized autoimmune associations. The study, published in Clinical and Experimental Dermatology, was led by Austin J Piontkowski and colleagues from the Department of Dermatology at the Icahn School of Medicine at Mount Sinai, New York.

“The All of Us study revealed that vitiligo patients face significantly higher risks of cardiovascular and autoimmune comorbidities. Notably, they showed increased odds of hyperlipidemia (OR 2.32), atherosclerotic disease (OR 1.78), and hypertension (OR 1.75),” the researchers reported The condition was also linked to bone and joint, endocrine, and psychiatric disorders, highlighting the importance of a comprehensive, multidisciplinary approach to patient care.

Vitiligo, a condition characterized by the loss of skin pigmentation, has long been associated with other autoimmune disorders. However, this new analysis suggests that individuals with vitiligo may also face heightened risks for several systemic health issues.

The researchers examined health data from 1,074 individuals with vitiligo and compared them with 4,296 matched controls. Using conditional logistic regression models, they assessed the odds of developing 29 pre-selected comorbid conditions. P-values were adjusted using the Benjamini-Hochberg method to account for multiple comparisons.

The key findings of the study were as follows:

  • Vitiligo patients showed significantly higher odds of hyperlipidemia (OR 2.32).
  • They had an increased risk of atherosclerotic disease (OR 1.78).
  • The likelihood of developing hypertension was also elevated (OR 1.75).
  • Vitiligo was linked to a higher burden of musculoskeletal conditions.
  • Endocrine disorders were more prevalent among individuals with vitiligo.
  • There was a notable association between vitiligo and autoimmune diseases.
  • Psychiatric conditions were also more common in vitiligo patients.
  • These findings suggest that vitiligo may involve broader systemic health impacts beyond skin depigmentation.

“These results point to the complex and multifaceted nature of vitiligo,” the authors noted, suggesting that systemic inflammation may be a common underlying factor contributing to these associations.

The findings carry important clinical implications. The authors emphasize the need for integrated care strategies with vitiligo patients facing elevated risks for a broad range of comorbidities. Instead of treating vitiligo in isolation, healthcare providers should consider comprehensive management approaches that address co-existing cardiovascular, autoimmune, endocrine, and mental health issues.

The study contributes to a growing body of evidence highlighting the systemic burden of vitiligo and calls for future research into therapeutic options that target both skin symptoms and underlying inflammatory processes.

The large-scale analysis from the All of Us database sheds new light on the health risks individuals face with vitiligo. The findings advocate for a more holistic treatment approach, emphasizing early identification and management of associated conditions to improve overall patient outcomes.

Reference:

Piontkowski, A. J., Dubin, C., Thakker, S., Orloff, J., Powers, C., Silver, C., Ungar, B., & Gulati, N. Vitiligo and associated comorbidities: A case-control study in the All of Us database. Clinical and Experimental Dermatology. https://doi.org/10.1093/ced/llaf228

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Tamsulosin Fails to prevent urinary retention After Inguinal Hernioplasty under spinal anesthesia, suggests study

Researchers have found in a new study that Prophylactic use of tamsulosin did not significantly lower the incidence of postoperative urinary retention (POUR) in patients undergoing inguinal hernioplasty under spinal anesthesia.

Inguinal hernioplasty is a common surgical procedure, often associated with complications such as post-operative urinary retention (POUR). Post-operative urinary retention, characterized by an inability to urinate despite a full bladder following a surgery that may need foley catheterization that on its own can lead to urinary tract infection, stricture, prolonged hospitalization, and increases cost of hospital care. Tamsulosin is a selective alpha-1 adrenergic blocker that can increase urine flow by relaxing the smooth muscle of urethra and prostate, thereby as a less invasive method may be effective in prevention of post-operative urinary retention. This randomized clinical trial involved 179 male participants over 50 undergoing unilateral hernioplasty under spinal anesthesia. Group A (87 subjects) received 0.4 mg Tamsulosin 8 hours before surgery, then 6 to 12 hours post-operatively. Group B (92 subjects) received a placebo on the same schedule. Both were monitored for post-operative urinary retention incidence within 24 hours post-surgery. Data were analyzed using SPSS software version 18 and the P < 0.05 was considered statistically significant. Results: The mean age of participants was 63.37±10.62 years. Post-operative urinary retention requiring catheterization occurred in 10.3% of Group A and 16.3% of Group B. However, the difference was not statistically significant (p=0.242). Logistic regression showed no significant prophylactic effect of Tamsulosin (p=0.171), hypertension (p=0.166), diabetes mellitus (p=0.196), or benign prostatic hyperplasia (p=0.273) on post-operative urinary retention incidence. Prophylactic Tamsulosin did not significantly reduce the incidence of post-operative urinary retention following inguinal hernioplasty under spinal anesthesia.

Reference:

prophylactic effect of Tamsulosin on postoperative urinary retention in Inguinal hernia repair under spinal anesthesia. Seyedinnavadeh, Seyedehatefe et al. The American Journal of Surgery, Volume 0, Issue 0, 116455

Keywords:

Tamsulosin, Fails, prevent, urinary, retention, After, Inguinal, Hernioplasty, under, spinal, anesthesia, suggests, study , Tamsulosin, urinary retention, inguinal hernia, post-operative, The American Journal of Surgery

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