118 results match your criteria: "Dr.B.R.Ambedkar Medical College[Affiliation]"

Article Synopsis
  • - The study investigates the impact of heavy backpacks on musculoskeletal pain among schoolchildren in Bangalore, focusing on posture and weight effects in urban vs. rural settings.
  • - An analysis of 500 students revealed that they carried an average backpack weight of 6.53 kg, leading to pain in over half of the participants, with higher pain rates noted among girls in private schools.
  • - Findings indicate a connection between heavier backpacks and poorer postural angles, highlighting the health risks and the necessity for backpack weight management in schools.
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Background The term "cardiomyopathy" encompasses a wide range of diseases with various underlying causes. Dilated cardiomyopathy (DCM) is characterized by ventricular dilation and impaired cardiac function in the absence of congenital, valvular, hypertensive, or ischemic heart disease (IHD). This study was motivated by the high prevalence of underlying DCM and chronic heart failure, coupled with a lack of comprehensive information on DCM.

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Background Chronic kidney disease (CKD) can lead to serious conditions such as anemia and cardiovascular disease, posing a growing global health challenge. End-stage renal disease (ESRD) requires treatments such as dialysis or kidney transplantation. Despite the widespread impact and rising prevalence of CKD and ESRD, comprehensive data remains limited in India.

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Advances in the field of oncology have led to the advent of doxorubicin (DOX), an anthracycline chemotherapeutic agent, through which cancer survival rates have remarkably improved. There has, however, been a rise in adverse effects from the use of DOX, most notably cardiotoxicity. DOX-induced cardiotoxicity is thought to arise through the generation of reactive oxygen species (ROS), causing mitochondrial dysfunction in the cardiomyocytes.

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  • Castleman disease (CD) is a rare group of disorders involving lymphoid tissue proliferation, which can be categorized into unicentric and multicentric forms, with idiopathic multicentric Castleman disease (iMCD) being particularly difficult to diagnose and treat.
  • A case study describes a 23-year-old woman with a history of iron deficiency anemia who presented with antiphospholipid syndrome and tested positive for human herpesvirus-6, ultimately leading to the diagnosis of the plasma cell variant of CD after finding a gastric mass.
  • The effective treatment with siltuximab and tocilizumab underscores the importance of interleukin-6 in CD's complex etiology and highlights the need for early diagnosis of APS in
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Article Synopsis
  • Evans syndrome (ES) involves autoimmune hemolytic anemia and immune thrombocytopenia due to immune dysregulation that leads to antibodies against blood cells.
  • A case study of a 38-year-old male showed symptoms like shortness of breath and weakness, with findings indicating ES, including hemolysis and thrombocytopenia.
  • Treatment typically starts with corticosteroids and may include additional therapies for resistant cases, emphasizing the need for tailored monitoring and management to achieve remission and reduce relapses.
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Restricted mouth opening is a challenging airway in pediatric patients with temperomandibular joint (TMJ) ankylosis. The fiber-optic bronchoscopic nasotracheal intubation technique continues to be the gold standard for difficult airway, among the techniques available such as submandibular intubation, retrograde intubation, and tracheostomy. However, awake fiber-optic bronchoscopy (FOB) is difficult to achieve in pediatric patients.

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Background: Endotracheal intubation and mechanical ventilation in individuals experiencing acute exacerbations of chronic obstructive pulmonary disease (COPD) are associated with several complications. Therefore, utilizing noninvasive positive pressure ventilation (NIPPV) is the suggested initial management for these individuals. The current study was done to assess and compare the clinical and physiological parameters before and after the application of NIPPV and also to evaluate the outcomes of NIPPV.

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Background Schoolbags or backpacks have been an essential part of the education system for a long time. However, a hefty backpack causes the child to arch the back excessively or bend their head and trunk forward to withstand the weight of the schoolbag. If the student carries the backpack on one shoulder, he/she bends to the opposite side to compensate for the extra weight, which may damage the shoulders and spine.

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Purpose Of Review: Artificial sweeteners have become increasingly popular in today's dietary trends as a healthier and sweeter alternative to sugar. As studies emerge regarding artificial sweeteners, concerns are arising about their side effects, particularly linking them to strokes. This systematic review aims to assess the relationship between artificial sweeteners (AS) and cerebrovascular accidents (CVAs).

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Rosai-Dorfmann Disease: A Rare Disease Presenting as a Unilateral Neck Swelling.

Indian J Otolaryngol Head Neck Surg

February 2024

Department of Otorhinolaryngology, Dr. B R Ambedkar Medical College and Hospital, Kadugondanahalli, Bangalore, Karnataka 560045 India.

Rosai-Dorfman disease (RDD) is a rare histiocytic proliferative disorder of unknown etiology. Usually it presents with massive painless cervical lymph node enlargement. Histologically, it shows proliferation of distinctive histiocytic cells that demonstrate emperipolesis in the background of a mixed inflammatory infiltrates.

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Introduction Anterior shoulder instability results in labral and osseous glenoid injuries. With a large osseous defect, there is a risk of recurrent dislocation of the joint, and therefore the patient has to undergo surgical correction. An MRI evaluation of the patient helps to assess the soft tissue injury.

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Angiosarcoma (AS) is a rare malignant tumor of vascular or lymphatic epithelium, typically presenting as a bruise-like patch over the face or scalp in the seventh-ninth decades. Here, we report a case of cutaneous AS (cAS) in a 51-year-old male patient who presented with a cauliflower-like growth in the groin with skin-colored shiny flat-topped satellite papules in the surrounding areas, some of which were umbilicated. Based on examination, the patient was considered retro positive and the following differentials were considered: Buschke-Lowenstein tumor with giant molluscum, Kaposi sarcoma, and squamous cell carcinoma.

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Extramammary Paget's disease is an intraepithelial neoplasm, usually found in areas rich in apocrine gland concentration. The clinical features, histopathology, immunohistochemistry and management details of five patients (F = 3, M = 2) have been described here. While a well-defined persistent plaque with crusting and erosion was the most common presentation, hyperpigmentation, hypopigmentation and depigmentation were also observed in two patients.

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Article Synopsis
  • * The review focuses on the latest evidence regarding preventive strategies and treatments to reduce cardiovascular risks in diabetic patients, emphasizing the role of hyperglycemia in worsening vascular damage.
  • * Understanding the link between diabetes and CVD is essential for healthcare providers to improve patient outcomes and reduce the associated health risks through informed management strategies.
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Immunotherapy has emerged as a pioneering therapeutic approach that harnesses the immune system's abilities to combat diseases, particularly in the field of oncology where it has led to significant advancements. However, despite its significant impact in the field of oncology, the potential of immunotherapy in the context of cardiovascular disease (CVD) has not been thoroughly investigated. The purpose of this narrative review is to address the existing knowledge and potential uses of immunotherapy in the field of cardiovascular disease (CVD), with the intention of filling the existing gap in understanding.

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Background: Dystrophic epidermolysis bullosa (DEB) is due to variation in the COL7A1 gene. The clinical phenotype and severity depends on the type of variation and domain of the affected protein.

Objectives: To characterize the spectrum of COL7A1 variations in a cohort of DEB patients from India, to correlate these findings with clinical phenotypes and to establish a genotype-phenotype correlation.

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A comprehensive, bed-side scoring system to predict difficult lumbar puncture.

J Anaesthesiol Clin Pharmacol

January 2022

Department of Anesthesiology, Dr. B. R. Ambedkar Medical College and Hospital, Gandhi Nagar, Kadugondanahalli, Bengaluru, Karnataka, India.

Background And Aims: Spinal anesthesia (SA) is the most widely practiced neuraxial anesthesia. Lumbar puncture (LP) at multiple levels and multiple attempts due to any reason may cause discomfort and even serious complications. Hence the study was conducted to evaluate the patient variables that can predict difficult LP thus allowing for the use of alternate techniques.

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Levosimendan (LS) has been progressively used for the treatment of patients developing acute as well as chronic or advanced cardiac dysfunction. It has proven to be a better inotropic agent than its counterparts in terms of its ability to increase the cardiac output in an acutely or chronically decompensated heart without an increase in the myocardial oxygen demand. The purpose of this systematic review, which was carried out in accordance with Preferred Reporting Items for Systematic Reviews and Meta-analyses (PRISMA) 2020, was to determine the efficacy and advantages of utilizing LS in patients with both acute and chronic heart failure.

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DiGeorge syndrome (DGS) is a rare genetic disorder caused by a deletion or abnormality of a small piece of chromosome 22. This condition can affect multiple organs in the body, including the heart, thymus, and parathyroid glands. While speech and language difficulties are common in individuals with DGS, the complete absence of speech is a rare presentation.

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Goldenhar syndrome is a rare congenital disorder that affects the development of the craniofacial region, spine, and ears. It is characterized by a wide range of symptoms that can vary in severity and may include facial asymmetry, microtia or anotia, cleft lip or palate, vertebral anomalies, and eye abnormalities. Although the cause of Goldenhar syndrome is not fully understood, it is thought to be related to disruptions in the early embryonic development of the affected tissues.

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Article Synopsis
  • - Sjögren-Larsson syndrome (SLS) is a rare disorder that families can pass down, and it causes problems like tight muscles, dry skin, and learning difficulties.
  • - It happens because a certain enzyme that helps break down fats isn't working properly, which leads to a build-up of fatty substances in the body.
  • - To help people with SLS, it's important to teach them how to take care of their dry skin and offer advice about their family's health history.
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The current meta-analysis aims to explore the effect of metformin use on vitamin B12 deficiency in patients with type 2 diabetes mellitus (T2DM) and the factors associated with it. This meta-analysis followed the Meta-analysis Of Observational Studies in Epidemiology (MOOSE) guidelines and the Preferred Reporting Items for Systematic reviews and Meta-Analysis (PRISMA) guidelines. We searched PubMed and EMBASE from January 1, 2010, to October 31, 2022, to collect the studies that reported the effect of metformin on the deficiency of vitamin B12 in patients with T2DM and the factors associated with it.

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