394 results match your criteria: "Nishtar Medical University.[Affiliation]"

Background and aim The study aimed to address the need for reliable and non-invasive biomarkers (NIBM) for detecting fibrosis among patients with chronic liver disease (CLD). Material and methods This was a diagnostic validation study executed at the Department of Gastroenterology, Jinnah Hospital, Lahore. The study was carried out from July 2023 to June 2024, enrolling a total of 88 patients using non-probability consecutive sampling.

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Familial multiple lipomatosis (FML) is a rare autosomal dominant disorder characterized by the progressive development of encapsulated nodules predominantly on the trunk and extremities. Its genetic basis is linked to HMGA-2 gene over-expression. The condition is diagnosed via clinical history, ultrasound findings, and histological studies, and management mainly comprises surgical excision.

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Background: Childhood obesity is a significant public health issue with far-reaching implications. The World Health Organization reported that in 2020, around 38 million children under five were overweight or obese globally, and in 2016, 340 million children and adolescents aged 5-19 were affected. In Pakistan, the situation is alarming; 66.

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Non-alcoholic fatty liver disease (NAFLD) has emerged as a major global health concern due to its association with increased mortality. While previous studies have indicated a link between NAFLD and mortality, variations in risk factors such as age, sex, and disease severity warrant a comprehensive meta-analysis to clarify these associations. This meta-analysis aimed to evaluate the overall cardiovascular disease (CVD) mortality risk associated with NAFLD, considering various subgroups defined by age, sex, disease severity, presence of cirrhosis or fibrosis, study quality, and follow-up duration.

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This systematic review evaluates the effectiveness of various neuroprotective strategies in enhancing recovery following acute ischemic stroke, focusing on interventions such as normobaric oxygen (NBO), lithium, selective serotonin reuptake inhibitors (SSRIs), and Cerebrolysin. Drawing upon data from six primary studies, including randomized controlled trials (RCTs) and meta-analyses, we assessed these therapies' impact on functional outcomes, motor recovery, and neurological improvement. Normobaric oxygen, across 12 RCTs, demonstrated limited efficacy in improving recovery outcomes or reducing mortality.

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This systematic review evaluates the long-term efficacy and safety of adhesion prevention agents in abdominal and pelvic surgeries, synthesizing data from randomized controlled trials and meta-analyses. Adhesions, common postoperative complications, can lead to significant morbidity, including chronic pain, infertility, and bowel obstruction. Various agents, including hyaluronic acid-carboxymethylcellulose films and icodextrin solutions, have been developed to mitigate these risks.

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Giant cell tumour of the tibia with pulmonary metastasis is very rare and the malignancy usually appears several years after the initial lesion. Imaging at the earliest instance is highly beneficial since surgical resection to remove the metastases raises survival rates; therefore, relentless follow-up in GCT is vital.

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Article Synopsis
  • Scalp arteriovenous malformations (AVMs) are complex vascular issues that can cause severe complications and cosmetic problems, especially in young women; early diagnosis and a team-based treatment approach are critical.
  • A 30-year-old female with a pulsatile scalp mass was diagnosed with a scalp AVM through various imaging techniques and successfully treated with endovascular embolization and surgical resection, resulting in significant symptom relief.
  • The case highlights the importance of interdisciplinary collaboration and advanced imaging in managing scalp AVMs, emphasizing the need for ongoing monitoring to prevent recurrence and ensure long-term success.
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Hereditary spinocerebellar ataxia (SCA) is a group of genetic neurodegenerative disorders caused by a variety of gene variants. At least 44 types of SCAs have been identified to date, and more than 35 genes and hundreds of variants have been reported that are associated with SCAs. We have investigated a Pakistani consanguineous six-generation family with SCA by using whole-exome sequencing analysis.

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  • * In a case study, a pregnant patient faced discomfort due to a large fibroid, prompting a multidisciplinary team to manage her symptoms and ultimately deliver her baby via cesarean section at 35 weeks.
  • * After delivery, she underwent a successful surgery to remove the fibroid, which weighed 7 kg; a cesarean myomectomy wasn't performed during pregnancy due to the fibroid's risky location near major blood vessels.
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This systematic review synthesizes findings from 12 studies to evaluate the effectiveness of dietary interventions in managing irritable bowel syndrome (IBS), with a focus on low-FODMAP (fermentable oligosaccharides, disaccharides, monosaccharides, and polyols) diets, probiotics, and prebiotics. The review rigorously follows the PRISMA (Preferred Reporting Items for Systematic Reviews and Meta-Analyses) guidelines and includes studies selected through comprehensive database searches. In adults diagnosed with IBS, this review assesses how effective dietary interventions, specifically low-FODMAP diets, probiotics, and prebiotics, are compared to standard management or placebo in improving clinical outcomes, modifying gut microbiota composition, and reducing inflammatory markers.

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DFSP is a cutaneous soft tissue sarcoma. A 35 year old male patient presented with DFSP in the inguinal region which is a rare soft tissue sarcoma which usually presents in the torso, occurring very rarely in the inguinal region. Hence in case of any swelling in the inguinal region, DFSP should be in differential diagnosis.

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Article Synopsis
  • - The study analyzed 117 adults with pancytopenia, focusing on demographic, clinical, and diagnostic characteristics, and included bone marrow examinations for accurate assessment.
  • - Common symptoms of pancytopenia included weakness (72.65%), fever (64.1%), dyspnea (54.70%), bleeding (34.2%), and weight loss (25.6%), with liver and spleen abnormalities observed in many participants.
  • - Key diagnostic findings revealed conditions like aplastic anemia (17.1%) and myelodysplastic syndromes (12.8%), highlighting the importance of thorough evaluation for appropriate patient management.
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This systematic review evaluates the impact and implementation strategies of the World Health Organization's Surgical Safety Checklist (WHO SSC) across diverse healthcare settings since its introduction in 2008. Our comprehensive analysis synthesizes findings from various study designs, including randomized controlled trials, qualitative studies, and meta-analyses, focusing on the checklist's effectiveness in reducing surgical complications and enhancing safety cultures within surgical teams. Despite its widespread endorsement and documented benefits, the review highlights significant variability in implementation quality and adherence, influenced by cultural, institutional, and procedural factors.

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This report describes the rare co-occurrence of acute myeloid leukemia (AML) French-American-British type M2 in a 4.5-year-old boy with previously diagnosed thalassemia major, an inherited hemoglobinopathy, typically presenting with severe, transfusion-dependent anemia. Chronic transfusions, though lifesaving, can lead to iron overload, which may generate free radicals and potentially contribute to malignancy.

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Background & Objective: One third of the neonatal deaths worldwide are attributed to perinatal asphyxia. We aimed to determine the prevalence and determinants of cardiac dysfunction, through echocardiographic evaluation, in term neonates with perinatal asphyxia.

Methods: This cross-sectional study was conducted at a tertiary care setting over a period of six months from 1 January 2021 to 30 June 2021.

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Background: Hypertension affects 26.7% of Pakistan's population, with only 6% achieving control. This study investigates antihypertensive medication adherence in Multan, focusing on socioeconomic and patient-related factors influencing non-adherence to study the lack of adherence to antihypertensive medications in hypertensive patients and its associated factors at Nishtar Hospital in Multan, Pakistan.

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  • A meta-analysis of clinical trials evaluated the FDA-approved antifungal drug rezafungin for treating serious fungal infections like candidemia, showing no significant advantages over the existing treatment, caspofungin, in cure rates or mortality.
  • Rezafungin offers unique benefits, such as a new mechanism of action and once-weekly dosing, which might improve patient adherence, but its clinical significance remains questionable given the costs involved.
  • The study highlights the importance of continued research and monitoring of rezafungin post-approval to fully assess its effectiveness and safety in real-world scenarios.
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  • The study aimed to understand the genetic factors of prostate cancer by analyzing 14 genes linked to cancer susceptibility using Next Generation Sequencing (NGS).
  • Key findings revealed pathogenic mutations in genes like BRCA1, BRCA2, and TP53, along with benign variations, highlighting their differing roles in cancer progression.
  • Functional tests showed that mutations in BRCA1 and BRCA2 were linked to lower expression levels and increased sensitivity to certain chemotherapy drugs, while mutations in TP53 did not notably affect drug response.
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Teratomas are rare tumors that originate from all three primary germinal layers and can develop anywhere along the body's midline, most commonly in the sacrococcygeal area. Within the head-and-neck region, they are infrequent, especially in the oropharyngeal area, and predominantly occur in infants. This case report presents an unusual instance of a teratoma in the left palatine tonsil, also known as giant epignathus, of a 25-year-old female.

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