New Emirates Medical Journal - Volume 5, Issue 1, 2024
Volume 5, Issue 1, 2024
-
-
Incidentally Discovered Rare Case of Solitary Fibrous Pleural Tumor (SFPT) during Residency Medical Clearance Examination
Background:A wide variety of tumors affect the pleura, both primary and secondary. The most common are metastatic carcinomas, usually of pulmonary origin. They manifest as malignant pleural effusion or multifocal pleural lesions. The extrapulmonary source of metastasis is mentioned but occurs less frequently. Pleural primary tumors other than diffuse malignant mesothelioma are either uncommon or rare and have received less attention. The World Health Organization (WHO) classified primary tumors of the pleura into three broad histogenetic classes of neoplasms, namely mesothelial tumors, mesenchymal tumors, and lymphoproliferative disorders.
Case Report:A 41-year-old male patient was referred to our facility from the prevention medicine department with consolidation in the right lower zone of the chest, diagnosed as a case of encysted pleural effusion to rule out TB. This was discovered during a routine health examination for residency visa renewal. After laps and imaging workup, it was diagnosed as Solitary Fibrous Pleural Tumor (SFPT). The first surgical intervention was hampered by bleeding from the mass itself. Therefore, the patient underwent a second intervention after successful embolization of the arterial supply of the tumor by the interventional radiologist.
Conclusion:Primary pleural neoplasms represent a small but significant group of heterogeneous tumors, many of which may mimic each other. Modern imaging modalities permit diagnosis and play a major role in staging and assessing surgical respectability. Novel molecular and immunohistochemical markers now allow confirmation of diagnosis and potentially form the basis for future targeted therapies. Embolization of tumor perfusion has a lifesaving role when needed.
-
-
-
Medical Uses and Health Benefits of Caffeine - A Study among the Students of Medical University in the United Arab Emirates
Authors: Madjda Khemissa, Ganna Amr Ibrahim Sabri, Boshr Hamdoun and Mohamed Anas PatniBackgroundCaffeine, a stimulant for the central nervous system, is extensively consumed worldwide and can be found in various items such as coffee, tea, chocolate, and energy beverages. In addition to its stimulating properties, caffeine has been shown to provide numerous health advantages, including relief from migraines, treatment for neonatal apnea, and possible protective effects against neurodegenerative diseases and metabolic disorders. Despite its widespread use, the understanding of caffeine's therapeutic uses among healthcare professionals is still quite limited.
ObjectiveThis study was conducted to measure the awareness and knowledge regarding the health impacts of caffeine among medical students and interns at RAKMHSU.
MethodsA cross-sectional study was carried out over six months (September 2023–April 2024) involving 190 participants selected through purposive sampling. Data were gathered using a structured, pretested questionnaire and analyzed with SPSS v29. Both descriptive and inferential statistical methods, including chi-square and independent t-tests, were employed.
ResultsThe majority (70.5%) of the participants were female, with an average age of 20.52 years. Although 67.4% acknowledged caffeine's efficacy in migraine management, awareness of its neuroprotective properties (Parkinson's: 22.6%; Alzheimer's: 28.4%) and metabolic advantages was notably low. Students in clinical years exhibited significantly higher knowledge scores compared to their preclinical peers (p = 0.041). However, no significant differences were found based on gender, college affiliation, or residential status.
ConclusionThere are evident gaps in knowledge regarding caffeine’s health benefits among healthcare students, especially concerning its emerging therapeutic roles. These results highlight the necessity for focused educational initiatives within health sciences programs to improve the understanding and application of evidence-based dietary practices.
-
-
-
Echocardiographic Features of Cardiac Amyloidosis: Insights from a Case Series
Authors: Mohammed Alghamdi, Hatim Kheirallah, Khalid Alkhalifa and Khalid AlanaziIntroductionCardiac amyloidosis, characterized by amyloid fibril deposition in the heart, often leads to heart failure and has a high mortality rate. The early detection of cardiac amyloidosis is critical for improving patient prognosis; however, the subtle and variable presentations of this condition can make early diagnosis challenging. Echocardiography is pivotal for diagnosing this condition. Through this study, we aim to improve the understanding of the echocardiographic features of cardiac amyloidosis.
MethodsThis retrospective case series was based on the data of patients diagnosed with amyloid transthyretin-related cardiac amyloidosis (ATTR cardiac amyloidosis) from 2020 to 2024 at the Prince Sultan Cardiac Center in Riyadh, Saudi Arabia. The collected data included demographic characteristics, medical history, laboratory results, medication use, 12-lead electrocardiography results, and echocardiographic parameters.
ResultsFifteen patients (11 males and four females, aged 41–88 years) were included in the analysis. The most common comorbidities were hypertension (seven patients) and atrial fibrillation (nine patients). The key echocardiographic characteristics were increased left ventricular (LV) wall thickness (mean: 19.9 mm), reduced global longitudinal strain (mean: −10%), and apical sparing. Six patients were positive for the 5-5-5 sign and pericardial effusion.
ConclusionRecognizing echocardiographic features, such as apical sparing and increased LV wall thickness, is essential for the early diagnosis of cardiac amyloidosis. Improved clinical awareness and diagnostic protocols could enhance early detection and patient outcomes.
-
-
-
Connecting the Dots: The Role of Pollution in Lung Cancer Onset
A disproportionately large number of cancer-related deaths are caused by lung cancer, making it a worldwide public health concern. Lung cancer has a complex etiology, although carcinogenic chemicals are key contributors. In this chapter, we delve into the complex web of connections between carcinogenic pollution and the development of lung cancer. An overview of lung cancer, its prevalence, causative factors, and its various subtypes is covered to begin with. A focused discussion of carcinogenic pollutants, their diverse sources encompassing air pollutants, industrial emissions, indoor contaminants, lifestyle-related exposures, and mechanisms of action is also covered. The article delves into factors that have been proven to increase the risk of lung cancer, such as cigarette smoking, air pollutants, occupational risks, and interior pollutants. The chapter delves further into the topic, explaining how environmental influences and genetic predisposition interact in intricate ways. There is extensive citation and reporting of epidemiological, case-control, and cohort research that have confirmed the link between exposure to carcinogenic pollutants and the occurrence of lung cancer. As the chapter progresses, it also explores preventive measures and interventions, including environmental regulations, public health policies, and lifestyle modifications, aimed at reducing pollutant exposure and mitigating lung cancer risk. It provides valuable insights for clinicians, researchers, policymakers, and the general public, facilitating a collective effort to prevent or combat this formidable disease.
-
-
-
Electrocardiographic Predictors of Improvement of Systolic and Diastolic Functions in Ischemic Cardiomyopathy Patients undergoing Percutaneous Coronary Intervention
BackgroundCoronary artery disease (CAD) is a significant contributor to 50%-70% of cardiac failure cases. Successful reperfusion is linked to improved systolic and diastolic functions.
Aim and ObjectivesThis study aimed to detect the correlation between ECG parameters (QRS duration and fragmentation, QTc, Tpe, and Tpe / QTc ratio), which were proved to be correlated with improved reperfusion post-PCI and associated with the improvement in systolic and diastolic function.
MethodsThis prospective research was performed on 54 ischemic cardiomyopathic cases from March 2019 to September 2022. All patients with Ischemic cardiomyopathy (ICM) and an EF less than 40%, along with viable myocardium determined by Dobutamine stress Echocardiography, underwent Complete revascularization of PCI amenable vessels.
ResultsThere was a statistically significant positive correlation between the QTc interval and EF% after 1 month (r=0.29) and between the QTc interval and the percentage of improvement in both systolic and diastolic functions (EF& E/é) with a more positive correlation with improvement in EF (r=0.35 and 0.27 respectively). A stronger positive and significant correlation between the percentage of improvement in EF% with both Tpe interval, Tpe/QTc ratio, and QRS duration (r= 0.57, 0.50, and 0.58, respectively) was found. Also, there was a positive significant correlation between the percentage of improvement in E/é with both Tpe interval, Tpe/QTc ratio, and QRS duration (r= 0.37, 0.26, and 0.32 respectively)
ConclusionECG parameters are capable of predicting improvement of systolic and diastolic functions in ischemic cardiomyopathic patients as observed by improvement in ejection fraction and E/é after PCI compared to before PCI.
-
-
-
Death and COVID-19 Anxiety and its Association with Patients' Experiences and Satisfaction in the COVID-19 Outbreak
IntroductionWith the spread of COVID-19 around the world, this disease became a serious threat to global health and exposed people to coronavirus anxiety and death. Hospitalized patients have faced more anxiety about coronavirus and death, which can affect both the experiences and satisfaction of patients.
AimThe present study investigated the relationship between death anxiety, COVID-19 anxiety, experiences, and satisfaction of patients during the COVID-19 outbreak.
MethodsThis correlational study was performed on 239 patients admitted to Ali-Ibn Abi-Talib Hospital of Rafsanjani, southern Iran, during the COVID-19 outbreak. The socio-demographic characteristics, Templer death anxiety scale (DAS), Corona disease anxiety scale (CDAS), short-form of the Hong Kong inpatient experience questionnaire (SF-HKIEQ), and patient satisfaction instrument (PSI) were used to collect data. The data were then analyzed using SPSS 25.
Results10.9% of participants had high COVID-19 anxiety, and 69.0% had high death anxiety. 77.8% of the participants had problems in the inpatient experience. 69.9% of participants were dissatisfied, and 30.1% had moderate satisfaction. A significant negative correlation between death anxiety and COVID-19 anxiety (r = -0.13; p = 0.04) was observed. Death anxiety hurt experiences, and COVID-19 anxiety had a positive impact on patients' experiences. Also, we found a significant positive correlation between experiences and patients' satisfaction. COVID-19 anxiety, age, death anxiety, and infection with COVID-19 predicted 37% of the variance of patients' experiences. COVID-19 anxiety, inpatient experience, and marital status predicted 14% of the variance in patient satisfaction (p < 0.05).
ConclusionPatients have experienced high levels of death anxiety and moderate levels of COVID-19 anxiety during the outbreak of the COVID-19 pandemic, which has affected their experiences and satisfaction. Professional assistance is needed to improve patient experience and satisfaction during pandemics such as COVID-19 disease. The results of this study may help to prepare suitable future interventions and programs to increase patient satisfaction in hospitals.
-
-
-
Hemolacria in Children with Hematological Disorders: Case Reports
BackgroundHemolacria, the presence of blood in tears, is an uncommon condition with various underlying etiologies. Although it can be alarming, its occurrence is often linked to a range of medical conditions, particularly in pediatric patients.
Case Presentation:We present two pediatric cases involving hematological diseases who developed hemolacria as a manifestation of their underlying conditions. Case 1 includes that of an eight-year-old girl with chronic immune thrombocytopenia (ITP) who developed hemolacria during an episode of epistaxis. Case 2 is of a seven-year-old girl with acute lymphoblastic leukemia (ALL) who presented with hemolacria during maintenance chemotherapy. Both cases illustrate the importance of considering hematological disorders in the differential diagnosis of pediatric hemolacria. Both cases were managed using a multidisciplinary strategy tailored to their underlying conditions. Systemic treatments, including intravenous immunoglobulin, thrombopoietin receptor agonists, and chemotherapy, addressed the primary hematological disorders. Localized ocular therapies, such as artificial tears, topical steroids, and antihistamines, were employed to manage symptoms and prevent complications. Supportive care measures, including patient education and infection prevention protocols, were integral to both management plans.
Conclusion:These two cases underscore the importance of recognizing hematological diseases as potential causes of hemolacria in children. Effective management requires a comprehensive, multidisciplinary approach that combines systemic treatment of the underlying disease with targeted local therapies and supportive care. Timely intervention is critical to ensuring favorable outcomes in these rare but significant presentations.
-
-
-
Emotional Intelligence Levels among Nursing Students at RAK Medical and Health Sciences University, United Arab Emirates
Authors: Victoria Funmilayo Hanson, Sneha Pitre and Eman Abdelaziz DabouBackgroundEmotional intelligence (EI) plays a pivotal role in the effectiveness and efficiency of nursing students in their academic and professional pursuits. EI levels differ across academic years and tend to increase with age, often being higher in female students.
AimThis study aimed to assess the EI of RAKMHSU nursing students in the UAE.
MethodsThis descriptive cross-sectional study used the Schutte EI Scale to assess the EI of 214 undergraduate nursing students. The Schutte EI Scale is a five-point Likert scale comprising 33 questions that yields scores between 33 and 165, including reverse scoring for three questions. Data were analysed using IBM SPSS Version 25.
ResultsApproximately 82.7% of the study participants were female and 91.6% were unmarried. The age range of the participants was 18–22 years. Scores of 33–77, 78–121, and >122 on the Schutte EI Scale were considered low, moderate, and high, respectively. No differences were found in the average EI scores of nursing students by academic year. Overall, 68.15% of the students had high EI, 23.83% had moderate EI, and 7% had low EI. The study found no correlation between the EI scores and demographic factors. All EI domain scores except those for emotion perception were consistent between first- and final-year nursing students.
ConclusionThe study showed that many of the nursing students exhibited high EI, which is essential for communication, patient care, and professional development. Further, demographic parameters, including age, gender, and academic year, did not significantly affect the EI scores, suggesting that EI in this cohort of students was stable. Most students demonstrated strong EI, although the perception of the cohort could be improved. These findings highlight the need to integrate EI training in nursing universities to improve students’ emotional abilities, thereby improving patient outcomes and the nursing profession.
-
-
-
Impact of Online Teaching During the COVID-19 Era on Senior Physiotherapy Students’ Clinical Self-efficacy at Fatima College of Health Sciences, UAE
Authors: Salwa B. El-Sobkey and Muhammad Al JarrahIntroductionEntry-level physiotherapists function as autonomous healthcare practitioners within a complex healthcare system, requiring professional competence in the clinical domain. Physiotherapy (PT) educational programs typically emphasize onsite teaching and use summative assessments to evaluate students' achievement of program objectives and learning outcomes. However, possessing knowledge and skills does not guarantee efficacy or confidence in clinical practice. This study aimed to assess the impact of online teaching approaches (TAs) during the COVID-19 era on the physiotherapy self-efficacy (PSE) of senior FCHS physiotherapy students across three clinical areas: musculoskeletal (MSK), neurological (N), and cardiorespiratory (CR), and to explore the influence of academic factors on PSE scores.
MethodsResearchers collected data for this cross-sectional study using a four-section questionnaire. One section specifically addressed the PSE. The study focused on three cohorts of pre-graduation senior PT students at Fatima College of Health Sciences (FCHS) who encountered a combination of onsite, online, and blended TAs due to COVID-19. Nonparametric statistical analysis was employed to analyze the data.
ResultsOf the seventeen participating students (68% participation rate, median age 22), the results indicate a statistically significant decrease in self-efficacy from MSK to N and CR clinical areas. The impact of online TAs on PSE varied by course specialty; TAs related to CR specialty courses significantly correlated with PSE scores, showing a preference for onsite TA to enhance self-efficacy over blended and online TAs. Furthermore, greater exposure to clinical cases and verbal encouragement from clinical educators were associated with higher self-efficacy. Physiological reactions, such as body pain, were also found to be influenced by the specific clinical area.
ConclusionThe impact of online TAs, implemented during the COVID-19 pandemic, on the self-efficacy of senior PT students is dependent on the specialty of the courses. This impact was most significant in CR specialty courses. Moreover, other factors, such as the sufficiency of exposure to clinical cases and clinical educators’ verbal encouragement, significantly contributed to students' self-efficacy.
-
-
-
Can the Fluctuation Observed in the Endotracheal Tube with Compression Applied to the Epigastric Region be Used as a Confirmation Method for Endotracheal Intubation?
Authors: Mustafa Boğan, Tufan Alatlı, Ceren Karakeçili, Kudret Selki, Emre Erdem, Salih Karakoyun and Özkan KömürcüBackgroundThe traditional methods are mostly used to detect tracheal localization and to exclude esophageal localization. Therefore, the aim of this study was to investigate the usefulness of epigastric manual compression in the confirmation of esophageal placement of the tube.
MethodsOut-of-hospital ETE was performed by experienced paramedics working in the emergency ambulance service, while ETE in the emergency department was performed by emergency medicine residents or emergency medicine specialists with at least 2 years of emergency department experience. Epigastric compression was performed by applying pressure to the epigastric region at least three times (in 5 sec) with the volar side of the intubated patient while the patient was ventilated with a balloon-valved mask. Immediately after ETI was performed, Ultrasonography (USG) was performed as the gold standard confirmation method. If a double path sign was observed and the pleural sliding motion was not seen, it was considered unsuccessful.
ResultsA total of 78 patients were included in the study (an equal number of successful and unsuccessful ETE applications). Approximately 59% (n=46) of the patients were female, median age was 73 years (64-80), and 22(28.2%) patients were intubated due to traumatic etiology. The specificity and sensitivity of epigastric fluctuation for esophageal intubations were 83.33% and 60%, respectively. The positive predictive value was 92.31%, and the negative predictive value was 38.46%. Epigastric auscultation airflow sound had a specificity of 86.96% and a sensitivity of 65.45% for esophageal intubation.
ConclusionAlthough the fluctuation that occurs in the tube with epigastric compression is not as sensitive and specific as USG, it is a better method than lung auscultation.
-
-
-
Innovative Gut Microbiome-targeted Strategies: A Promising Frontier for Pediatric Inflammatory Bowel Disease
BackgroundPediatric inflammatory bowel disease [IBD] impacts affected children with many diagnostic, therapeutic, and life challenges. The traditional drugs used for induction and maintenance of remission had many unwanted side effects. Therefore, there was an urgent need for safer, more effective therapeutic strategies. Hence, modifying the gut microbiota [GM] was proposed as an innovative approach based on the theory that restoring the disturbed GM harmony will have a positive impact on IBD activity and remission.
AimThis review aimed to examine each modality used to modify the gut microbiota in children with IBD, addressing their action mode, effectiveness, limitations, and side effects for a more holistic approach to children with IBD.
MethodsFour electronic databases were searched, including WOS, Cochrane Library, PubMed, and Scopus, for articles that investigated modulating GM via exclusive enteral nutrition, prebiotics, dietary fiber, probiotics, fecal microbiota transplantation, and antibiotics.
ResultsThe available evidence was encouraging regarding their effectiveness and safety; however, those studies were hindered by their small sampling size and inconsistency in recruiting cases.
ConclusionFurther work should identify other therapeutic and prognostic avenues for modulating GM for these vulnerable groups.
-
-
-
Association of the ABCB1 C3435T Polymorphism with the Mixed Form of Ankylosing Spondylitis in the Algerian Population: A Case-control Study
IntroductionAnkylosing spondylitis (AS), also known as rheumatic pelvic spondylitis, is considered the primary condition in a group of chronic inflammatory rheumatic diseases collectively referred to as spondyloarthropathies.
ObjectivesThis study aimed to explore the association between ABCB1 C3435T polymorphism and the predisposition to ankylosing spondylitis (AS) in the Algerian population. The frequency of this polymorphism was compared between the group of AS and healthy subjects.
MethodsA case-control study involving 81 AS patients and 98 controls was conducted. DNA genotyping was done using predesigned probe-based allelic discrimination TaqMan® assays. Allele and genotype frequencies were compared between cases and controls, and statistical analyses were executed using SAS software (version 9.1, SAS Institute Inc., Cary, NC).
ResultsNo statistically significant differences were observed in the frequencies of ABCB1 genotypes and alleles between AS cases and the control group. In contrast, the recessive model (CC+CT/TT) (OR = 8.99 [11.97-40.99], p = 0.004) was significantly associated with the mixed form of the disease, while the heterozygous 3435CT genotype provided protection against the axial form. Moreover, a positive association was also found between the ABCB1 C3435T polymorphism and BMI (OR: 5.19 [1.41-19.9], p = 0.01).
ConclusionThis is the first study to explore the association of ABCB1 polymorphisms with susceptibility to ankylosing spondylitis in an Algerian population. It was determined that the ABCB1 C3435T SNP does not influence the risk of AS but rather affects the disease phenotype and body mass index (BMI).
-
-
-
Prevalence and Impact of Selenium in Iron-deficiency Anemia: Insights from a Clinical Trial on Anemia Correction and Symptom Improvement
IntroductionIron-Deficiency Anemia (IDA) is a global burden affecting more than a billion individuals. It is most prevalent due to nutritional deficiencies. Researchers have linked Selenium (Se) to anemia and erythropoiesis.
AimThis interventional-study was designed to investigate the plasma Se concentration and its supplementation impact in IDA patients receiving standard treatment.
MethodologyIn the present study, a total of 215 IDA patients were enrolled from different departments of AIIMS, New Delhi, after getting ethical authorization from the Institutional-Ethical Committee. Iron supplements were administered to patients with only IDA, while a combination of iron and selenium supplements was given to patients with selenium-deficient IDA for 90 days. Parameters such as hemoglobin, hematocrit, RBC count, serum ferritin, transferrin, TIBC, and plasma Se levels were measured on the baseline and the 90th day.
ResultsAll blood parameters were significantly below the normal reference range on the 0th day. Se levels were found to be higher in the study population {57% (122/215) in IDA}. Further, in low plasma Se IDA patients 26% (55/215), treatment with iron and Se supplements for 90 days significantly improved all blood parameters and led to a subjective improvement of the patient’s well-being.
ConclusionSelenium levels are variable in patients with IDA, and no correlation can be drawn for the benefit of selenium in the IDA. Further, the high prevalence of nutrition-related disorders such as IDA highlights the need to avoid blind Se supplementation along with iron. These combination in the form of nutritional supplements having Se are rampantly available and sold over the counter. So, supplements with Se shouldn’t be generalized to IDA patients..
Clinical Trial Registration No.CTRI/2023/04/051405
-
-
-
Prevalence of Gestational Diabetes in Metformin-Treated and Non-Treated PCOS Women: A Comparative Analysis
BackgroundPolycystic Ovary Syndrome (PCOS) is one of the most prevalent endocrinal disorders in the reproductive age of women and is, therefore, a risk factor for Gestational Diabetes Mellitus (GDM). One of the medications used in the management of PCOS is metformin and its use has been proposed to decrease the occurrence of GDM. The purpose of this study focuses on the effects of the dose and duration of metformin treatment on the prevalence of GDM among pregnant women affected by PCOS.
MethodsA cross-sectional survey was carried out on 112 pregnant women diagnosed with PCOS in tertiary care hospitals in Karachi. Data were collected through a structured questionnaire, in which 55 patients received metformin and others did not receive metformin. Both groups were compared for the prevalence of GDM. Chi-square test was used in data analysis at a significance level of p < 0. 05.
ResultsGDM was found to be significantly higher in non-metformin group than metformin group (60% vs 40%, P=0.03). The data analysis extended this finding, which concluded that metformin use is inversely related to GDM risk (p = 0.02).
ConclusionThis study shows that metformin therapy reduces the incidence of GDM in pregnant PCOS patients and may be used to prevent GDM in such patients. Such outcomes indicate the possibility of the use of metformin as a means of preventing GDM in this group of patients.
-
-
-
Awareness, Pro-environmental Behaviours, and Strategies for Mitigation of Plastic Pollution among Nursing Students in the United Arab Emirates
Authors: Ramya Kundayi Ravi, Vimala Edwin, Fathima Abdul Rasheed and Aleena Mary JaisonBackgroundThe healthcare sector plays a significant role in the control and mitigation of plastic pollution-associated threats to the environment and human health.
AimThis study aimed to investigate the awareness, pro-environmental behaviors, and strategies for mitigating plastic pollution among nursing students.
MethodsA cross-sectional survey was conducted with 210 undergraduate nursing students using a structured questionnaire. Convenience sampling was used to recruit study participants. Data were analyzed using the Statistical Package for the Social Sciences version 26.
ResultsThe results of the study revealed that the majority of nursing students (71%) had moderately adequate levels of awareness regarding plastic pollution, whereas 70.48% of the students engaged in inadequate levels of pro-environmental behaviors.
ConclusionThe present findings demonstrate the necessity of reinforcing nursing students regarding the reduction of plastic pollution through specific policies and educational involvement. These measures would contribute to further initiatives and encouragement of their student period, future nursing practice, and patient safety at all levels.
-
-
-
A Study on Bacterial Urinary Tract Infections, Antibiogram, and Antimicrobial Practices among Healthcare Providers in a Tertiary Care Facility in India
BackgroundGlobally, urinary tract infections (UTIs) have attracted the attention of clinicians and have become a serious public health threat. Management of UTIs has become a growing concern for clinicians due to increased antimicrobial resistance (AMR). The present study was conducted to identify the most diagnosed uropathogens causing UTIs among Inpatient Department (IPD) and Outpatient Department (OPD) patients visiting a tertiary care health centre and also to analyse the patterns of prescribed antibiotics based on physicians’ empirical and urine culture-based approach. Furthermore, this study sought to evaluate the sensitivity patterns of selected bacteria against antibiotics used to treat UTIs among patients.
MethodsThis study was undertaken for a period of three years at the Department of Medicine in collaboration with the Department of Microbiology. Mid-stream clean catch urine samples were collected from UTI suspects from both IPD and OPD patients and processed for culture and susceptibility testing as per standard guidelines. Univariate and bi-variate descriptive statistical techniques were used to analyse the data.
ResultsA total of 2400 urine samples were processed for culture and sensitivity testing, out of which 200 samples were found positive. Escherichia coli was the most frequently isolated urinary pathogen in both OPD and IPD patients (55.3% and 74.4%, respectively). Empirically, the most commonly prescribed antibiotic was piperacillin/tazobactam (13%), while the culture-based antibiotic was nitrofurantoin (20%). The findings highlight that more than 95% of isolates of the most prevalent uropathogen E. coli were sensitive to amikacin, ciprofloxacin, imipenem, and nitrofurantoin, whereas more than 90% were sensitive to ceftazidime, cefoperazone sulbactam, and piperacillin/tazobactam.
ConclusionIncreasing resistance to common antibiotics necessitates a reevaluation of both empirical and culture-based antibiotic approaches. The findings of this study are of significant importance and highlight the need to develop a targeted antibiogram for UTI, understand the trends in antimicrobial resistance (AMR), and ensure the rational selection and antibiogram both in empirical and culture-based approaches.
-
-
-
Antimicrobial Resistance: Challenges and Innovative Solutions
Authors: Ibtsam Ghulam Nabi, Madiha Khan and Hira MubeenAntimicrobial Resistance (AMR) poses a critical threat to global health, contributing to increased morbidity, mortality, and substantial economic burden. This review highlights the profound clinical and financial consequences of infections caused by multidrug-resistant (MDR) bacteria. Of particular concern is the escalation of bacterial resistance linked to the indiscriminate use of antibiotics during the COVID-19 pandemic, which could lead to increased mortality rates. Additionally, this article emphasizes the significance of Antimicrobial Stewardship (AMS), which is a healthcare strategy aiming to encourage, develop, monitor, and assess the sensible use of antimicrobials in order to protect their long-term success. Consequently, it highlights the value and effects of an Antimicrobial Stewardship Program (ASP) in combating resistance and protecting global health.
Furthermore, the necessity of adopting a holistic “One Health” approach, an integrative, multisectoral strategy, is discussed as essential in addressing the growing AMR crisis. The review advocates for evidence-based policies that support the “One Health” framework, enhance immunization programs, educate healthcare professionals, and raise public awareness about AMR. This article provides a comprehensive overview of the scale, consequences, and potential solutions to AMR, urging collaborative efforts across sectors and stringent measures to combat this global health challenge.
-
-
-
Incidental Gastric Adenomyoma during Bariatric Surgery: Diagnostic and Management Challenges - A Case Report
Authors: Pulimuttil James Zachariah and Rana SalehBackgroundIncidental gastric tumours, including benign gastric adenomyoma (GA) during bariatric surgery, can pose diagnostic and management dilemmas, resulting in misdiagnosis, inappropriate procedures, or even abandoning the procedure.
Case PresentationWe report a rare case of an incidental prepyloric GA discovered during a one-anastomosis gastric bypass performed for diabetes management. Preoperative gastroscopy was unremarkable, but intraoperative laparoscopy revealed a mass near the pylorus resembling a gastrointestinal stromal tumour (GIST). An initial histopathological examination was non-confirmatory. However, subsequently, it was confirmed to be a GA. The patient underwent a staged surgical approach, achieving diabetic control during the primary procedure and tumour excision subsequently. This is the first documented case of GA discovered during bariatric surgery.
ConclusionGastric tumours identified during bariatric procedures necessitate an individualized approach considering the procedure planned, tumour characteristics, and anatomical location, to achieve the best clinical outcomes.
-
-
-
Digital Eye Strain: A Cross-sectional Study Among Undergraduate Medical Students in UAE
Authors: Sohaila Fatima, Raqshan Wajih Siddiqui and Tabish Wajih SiddiquiIntroductionDigital eye strain (DES), also known as computer vision syndrome (CVS), is a common condition affecting individuals who spend prolonged periods focusing on screens, leading to symptoms, such as dry eyes, eye strain, headaches, and blurred vision. University students, including medical students, increasingly spend more time staring at screens for study and research. Therefore, this study assesses the prevalence and impact of DES among medical students, a group increasingly dependent on digital resources for their studies.
MethodsThis cross-sectional study was conducted from November 2023 to February 2024 at RAK Medical and Health Sciences University, UAE. A sample of 209 undergraduate medical students was recruited using non-probability convenience sampling. The sample size was calculated based on a 95% confidence level and a ±5% margin of error, representing 46.4% of the eligible population. Data were collected through a validated electronic questionnaire and analyzed using SPSS version 29, employing descriptive and inferential statistics to explore associations between visual symptoms and factors, such as refractive errors, study duration, and ergonomic practices.
ResultsAmong respondents, 69.9% were female, with a mean age of 19.87 ± 1.58 years. The prevalence of myopia was 49.7%, while hypermetropia and astigmatism were reported at 2.9% and 6.7%, respectively. A striking 92.8% experienced at least one DES symptom, with tired eyes (71.3%) and eye strain (58.9%) being the most common symptoms. Significant correlations were observed, including dry eyes associated with myopia (p = 0.002) and difficulty refocusing linked to hypermetropia (p = 0.029). Ergonomic practices revealed that 80.4% of students used screens closer than recommended, which correlated with increased eye strain (p = 0.001) and tired eyes (p = 0.044). Moreover, adherence to the 20-20-20 rule was low (3.8%), associated with heightened symptoms.
ConclusionThis study highlights a high prevalence of DES symptoms among medical students, related to inadequate ergonomic practices. These findings emphasize the necessity for targeted interventions to enhance eye health and ergonomic awareness in this population. Future research should evaluate the effectiveness of such interventions.
-
-
-
Attention-deficit/hyperactivity Disorder (ADHD) Prevalence among Students aged 7-12 Years Old
Authors: Armon Massoodi, Farzan Kheirkhah, Mojgan Rezvani and Mahdi SepidarkishBackgroundADHD (attention-deficit hyperactivity disorder) is a developmental disorder characterized by inattention and distractibility, as well as hyperactivity.
ObjectiveThis study investigated the prevalence of ADHD in male and female students of primary school in Babol (Iran).
MethodsThis study was a cross-sectional study. The studied population was school-aged children (7-12 years old) in the urban areas of Babol city. A total of 1469 primary school students were included in the study during 2021-2022. In this research, the Revised Conners' Parent Rating Scale (CPRS-R) was used to investigate ADHD disorder.
ResultsThe prevalence of ADHD in the present study was 9.9% (146 people). ADHD subgroups, in the order of prevalence, included mixed type (67 people, 4.6%), hyperactivity-impulsive type (43 people, 2.9%), and then inattentive type (36 people, 2.5%). ADHD prevalence among males and females was 13.4% and 7%, respectively. This was 1.9 times higher in male students than in female students. ADHD subgroups in male students, in order of prevalence, included mixed type (44 people, 50%), impulsive hyperactivity type (32 people, 36.36%), and inattentive type (12 people, 13.63%), and in female students, ADHD subgroups were inattentive type (24 people, 41.37%), mixed type (23 people, 39.65%), and hyperactivity-impulsive type (11 people, 18.96%). ADHD was seen mostly in students with illiterate parents (p≤0.001).
ConclusionIt seems that the prevalence of ADHD in children of elementary schools in Babol was not significantly different from the prevalence reported in other cities of Iran and globally.
-
-
-
Facilitating Implementation of Addictive Learning across Medical Institutions
More LessAddictive learning in the field of medical education refers to the process wherein medical students are highly engaged in the learning process. The aim of the current article is to evaluate the effectiveness of addictive learning strategies, identify barriers, and propose solutions to effectively implement addictive learning in medical education. Addictive learning ensures an increase in the level of student engagement, which in turn determines a better understanding of complex concepts, knowledge retention for longer periods of time, and development of critical thinking and problem-solving skills. Even though addictive learning has been linked with multiple benefits for students, it has its share of challenges, such as a mismatch between engagement and learning objectives, superficial learning, lack of accessibility and inclusivity, questionable long-term effectiveness, concerns about data privacy and security, rising costs, etc., in the educational settings. In conclusion, addictive learning in medical education plays an important role in facilitating learning among medical students. However, this process of planning and implementation of addictive learning in medical education delivery has been linked with multiple concerns. The need of the hour is to adopt a comprehensive package of interventions, such as faculty training or curriculum design, to enable its successful implementation in medical colleges.
-
-
-
Understanding the Bariatric Surgery: Conceptions and Misconceptions in Future Health Care Professionals
IntroductionMedically-complicated obesity, a major public health issue due to the ineffectiveness of traditional treatments, is increasingly managed through bariatric surgery. This study investigates the knowledge of clinical year students about bariatric surgery at RAKMHSU. It aims to assess their awareness and understanding of this crucial intervention for severe obesity and its related health risks.
Materials and MethodsThis cross-sectional study was conducted over three months at RAK Medical and Health Sciences University (RAKMHSU) and utilized a survey to assess perception regarding bariatric surgery among clinical year students from RAK College of Medical Sciences (RAKCOMS) and RAK College of Nursing (RAKCONS). A pre-validated questionnaire was employed, and participants were randomly selected. Data analysis focused on the reliability of the tool and the student’s perception.
ResultsThe study included 197 participants, comprising 162 medical and 35 nursing students. Significant differences emerged in three areas: nursing students preferred daily exercise more (Q6), believed in the greater likelihood of weight regain post-surgery (Q9), and were more aware of disease susceptibility (Q13) compared to medical students. Correlation analysis revealed that students who felt body shape affected self-confidence had better bariatric surgery knowledge and BMI calculation experience. Notable correlations were found between specific questions, with significant positive correlations observed among nursing students but not medical students.
DiscussionObesity is a global epidemic with rising prevalence, including in the UAE, where 43% of expatriates are overweight and 32.3% obese. Environmental factors, such as low physical activity due to climate and cultural norms, exacerbate the issue. Our study revealed good knowledge of BMI among participants, reflecting awareness of obesity's risks. However, concerns about bariatric surgery safety persist, with 32% of participants wary of complications. Despite this, the most recognized bariatric surgery is a viable option for medical conditions like PCOS. Educational interventions are essential to address misconceptions, promote informed decisions, and bridge gaps in exercise habits and referral practices.
ConclusionIn conclusion, while many medical and nursing students demonstrate a solid understanding of bariatric surgery, hesitations and misconceptions persist. Continuous education is essential to address these concerns, enhance knowledge, and align perceptions with clinical advancements. By doing so, future healthcare professionals can make informed decisions and provide better care for patients with severe obesity, ultimately improving outcomes and fostering greater acceptance of evidence-based surgical interventions.
-
-
-
Understanding Primary Endometrial Squamous Cell Carcinoma: A Narrative Analysis
By Naina KumarPrimary Endometrial Squamous Cell Carcinoma (PESCC) is a rare variant of endometrial carcinoma accounting for <1% of all endometrial malignancies. It is a highly aggressive tumor and carries a very poor prognosis with a 5-year survival reaching up to zero. The exact pathogenesis of PESCC is unclear, and different theories have been proposed for its origin. The most widely accepted theory proposes the endometrial squamous metaplasia, progressing to dysplasia and frank squamous cell carcinoma. The role of human papillomavirus infection in its pathogenesis is controversial. The present review aims to brief the clinical features, pathogenesis, diagnosis, and management of PESCC. The literature was searched from March 2003 till April 2024 using different databases like PubMed, SCOPUS, and EMBASE and many English peer-reviewed journals. The following search terms were used: “Primary endometrial squamous cell carcinoma,” “Pathogenesis of PESCC,” “Ichthyosis uteri and PESCC,” and “Management of PESCC.” PESCC is a rare endometrial malignancy, and very few cases have been reported in the literature. The overall prognosis of the disease is poor, and management includes total hysterectomy with lymph node resection followed by chemoradiotherapy, depending on the stage of the malignancy.
-
-
-
Prevalence of Prediabetes and its Associated Factors among Patients in the Northern Part of Afghanistan
IntroductionPrediabetes is associated with an increased risk of diabetes. However, there is currently no cohesive picture of the prevalence of prediabetes and its risk factors in Afghanistan. Therefore, we conducted a study to examine the prevalence of prediabetes and its risk factors among adult outpatients in Afghanistan.
MethodsWe conducted a cross-sectional study on outpatients aged 18 years or over (n=1766) from April 2023 to October 2023. The sociodemographic characteristics and clinical variables of the patients were collected through an interview-based survey. Regression analysis was used to examine the association between prediabetes and its risk factors.
ResultsThe study included 54.6% females and 45.4% males, with a mean age of 48.9 (±10.8). The prevalence of prediabetes was 27.9%. Males were more likely to have prediabetes with increased odds (OR = 1.48; 95% CI: 1.17–1.89; p < 0.001) compared with females. There were higher odds of having prediabetes for overweight or obese (OR = 2.10; 95% CI 1.15-3.84; P = 0.016), smoking (OR = 7.26; 95% CI 3.00-11.05; p < 0.001), hypertension (OR = 2.76; 95% CI 2.00-3.81; p < 0.001), and high cholesterol levels (OR = 1.48; 95% CI 1.16-1.90; P = 0.002), compared to participants without prediabetes.
ConclusionThe prevalence of prediabetes in our study was high. Risk factors that were related to prediabetes included male gender, obesity or overweight, smoking, hypertension, and high cholesterol levels. Focusing control and prevention efforts on these risk factors linked to prediabetes can significantly reduce its prevalence and mitigate future consequences.
-
-
-
Dietary Risk Factors of Nasopharyngeal Carcinoma: A Case-Control Study in Western Algeria
ObjectiveNasopharyngeal carcinoma (NPC) is a prevalent cancer in Algeria, where it ranks as the most common cancer of the aerodigestive tract in men, with an incidence rate of 5.1 cases per 100,000 persons per year. The etiology of NPC is multifactorial. Thus, this research aims to identify specific dietary risk factors prevalent in the western Algerian region.
MethodsWe conducted a case-control study comprising 120 incident cases of histologically confirmed nasopharyngeal carcinoma, carefully matched with 120 controls.
ResultsNasopharyngeal cancer, more common in males (average age 45.2 ± 2.5 years), is linked to consuming traditionally preserved foods (khlii, salted fats, boiled milk, processed meats), elevating NPC risk. Significant associations include hot chili peppers, citrus fruits, and dried vegetables, while increased fruit and coffee intake reduces risk. High-temperature cooking and fried food show a strong link. Multivariate analysis identifies hot chilli, citrus fruits, fresh fruits, and coffee as the key factors significantly associated with NPC.
ConclusionThis research provides essential insights for implementing primary prevention measures to combat nasopharyngeal carcinoma effectively. By identifying specific dietary risk factors prevalent in the western Algerian region, healthcare authorities can focus on targeted interventions to reduce the burden of NPC in this population.
-
-
-
Diagnosis and Management of PAH in Special Populations in the UAE
Authors: Hani Sabbour, Yasser El Hennawi, Ahmed Reda Taha, Mohammed B Al Saiari, Ashraf Alzaabi, Bassam Mahboub, Khaled Saleh, Mohamed Farghaly, Asim A. Elnour, Abdullah Shehab, Hazem El Badaoui, Arun Kumar, Rizwan Ahmed, Mohammad Daud Khan, Mohamed El Harari, Magdi Tofeig, Amrish Agrawal, Hosam Zaky, Noha Yaseen, Govinda Bodi, Ramzi Khashkousha, Usman Ahmed, Sharina Aldhaheri, Wael Al Mahmeed, Bashir Salih, Vivek Kakar, Said Isse, Fady Hamed, Yogeeswari Vellore Satyanarayanan, Aref Al Hakami, Jihad Mallat, Walid Ahmed and Hussein HeshmatDiagnosis and management of pulmonary hypertension (PH) in special populations, including pregnant women, patients requiring intensive care unit admission, and patients who develop complications such as ascites, pericardial effusion or develop COVID-19 infection, are very challenging.
PH is associated with poor outcomes in pregnant women as the haemodynamic changes during pregnancy greatly increase maternal mortality. If PH is suspected in pregnant women, further investigation using transthoracic echocardiography is essential, and confirmation with right heart catheterisation is required. All global guidelines recommend avoidance of pregnancy in patients diagnosed with PAH. However, if the patient becomes pregnant, the risks involved with the continuation of the pregnancy and termination of the pregnancy should be discussed.
Intensive care may be required in patients with PH for the management of comorbid conditions and following major surgeries and irrespective of the underlying cause of PH, haemodynamic compromise in these patients leads to right heart failure. The PH expert centre plays an important role in the critical care management of patients with PH. Patients with PH may also develop complications such as ascites and pericardial effusion; if not rapidly recognised and treated, these complications can lead to poor prognosis in affected patients.
This chapter aims to provide guidance to healthcare professionals in the clinical decision-making process for the diagnosis and management of PH in special populations.
-
-
-
Group 5 PH: Diagnosis and Management of Pulmonary Hypertension in Patients with a Focus on Chronic Haemolytic Diseases in the UAE
Group 5 pulmonary hypertension (PH) encompasses PH associated with chronic haemolytic diseases, which is the major cause of morbidity and mortality in patients. The prevalence of PH is notably high in sickle cell disease (SCD), thalassemia, hereditary spherocytosis, and paroxysmal nocturnal haemoglobinuria.
Pulmonary symptoms are common with haematological diseases; therefore, systematic evaluation of patients who are at increased risk of developing PH is vital. Evaluation by NT-pro BNP and echocardiography (ECHO) is essential for early referral to PH centres. Right heart catheterisation in patients with haemoglobinopathies is recommended in making a diagnosis of precapillary PH. A V/Q scan should be considered in the evaluation of dyspnoea for detecting thrombotic events in SCD.
Once haemolytic disease is confirmed as the cause of PH, the underlying cause of haemolytic disease is managed with an emphasis on the reversal of hypoxaemia. Evidence suggests that hydroxyurea can treat patients with haemolytic disease and PH, but exchange blood transfusions are used as an alternative when patients are unresponsive to hydroxyurea. Riociguat, a soluble guanylate cyclase stimulator, has been found to be safe and effective in sickle-cell-related pulmonary arterial hypertension. Novel drugs like voxelotor (FDA approved) and crizanlizumab have shown their efficacy in patients with SCD and vaso-occlusive crisis.
Hence, this study emphasises the systematic evaluation of patients for early diagnosis and early positioning of novel agents to prevent PH associated with chronic haemolytic diseases, particularly SCD.
-
-
-
Diagnosis and Management of Group 4 PH (Chronic Thromboembolic Pulmonary Hypertension (CTEPH)) in the UAE
Authors: Hani Sabbour, Khaled Saleh, Mohammed B Al Saiari, Ashraf Alzaabi, Bassam Mahboub, Noha Yaseen, Govinda Bodi, Ramzi Khashkousha, Usman Ahmed, Wisam Ahmed, Sharina Aldhaheri, Ahmed Reda Taha, Vivek Kakar, Yasser El Hennawi, Said Isse, Fady Hamed, Yogeeswari Vellore Satyanarayanan, Jihad Mallat, Asim A. Elnour and Abdullah ShehabChronic thromboembolic pulmonary hypertension (CTEPH) is a distinct and treatable form of pulmonary hypertension (PH). It occurs due to persistent thromboembolic obstruction of pulmonary arteries, leading to an increase in pulmonary vascular resistance (PVR) and right ventricular failure. The prognosis of CTEPH patients is poor if left untreated.
The diagnosis of CTEPH is challenging and usually delayed due to non-specific CTEPH symptoms, asymptomatic patients or patient negligence in highlighting specific symptoms, and lack of screening tools. A ventilation/perfusion (V/Q) scan can help detect the early stage of CTEPH, i.e., chronic thromboembolic disease (CTED). Computed tomography (CT) pulmonary angiography is used for determining vascular abnormalities and assessing operability in CTEPH. In the absence of a perfusion defect, haemodynamic measurement while exercising during right heart catheterisation (RHC) serves as an important diagnostic tool in patients with normal haemodynamic at rest.
Once CTEPH is diagnosed, pulmonary endarterectomy (PEA) becomes the treatment of choice in operable cases. If residual pulmonary artery hypertension (PAH) post-PEA occurs, medical therapy with or without percutaneous balloon pulmonary angioplasty (BPA) is given. Anticoagulants (vitamin K antagonists), diuretics, and riociguat (guanylate cyclase–stimulator) are recommended medical therapies for inoperable patients.
It can be concluded that, with the correct diagnostic approach, prevention of misdiagnosis and early detection of CTEPH is possible. Proper diagnosis offers the possibility of a cure for non-operable patients with PEA. The treatment algorithm emphasises the need for a multidisciplinary team with an individualised approach to ensure an optimal treatment response.
-
-
-
Diagnosis and Management of Group 3 Pulmonary Hypertension in the UAE: Pulmonary Hypertension Associated with Chronic Lung Disease (PH-CLD)
Chronic Lung Diseases (CLDs) constitute one of the most frequent causes of pulmonary hypertension (PH) and rank second after PH due to left heart disease. In PH-CLD, destruction of lung parenchyma is associated with decreased functional capacity, diminished quality of life, increased oxygen requirements, and a heightened risk of death.
As both pulmonary arterial hypertension (PAH) and PH due to lung disease are categorized as precapillary PH, it is essential to distinguish between the two conditions, particularly when the lung disease is present with the severe form of PH. If the diagnosis confirms a severe form of PH-CLD, then individualised care is essential in patients with severe lung disease and evidence of right-sided heart failure, particularly those with lower-limb oedema. Moreover, echocardiography (ECHO) and N-terminal-pro hormone B-type natriuretic peptide (NT-proBNP) evaluation are of high importance and must be ordered by the pulmonologist. Right Heart Catheterisation (RHC) is also essential for the determination of the extent and severity of pulmonary vascular involvement. The use of inhaled vasodilators, along with a referral for right heart catheterisation, should be considered at an earlier phase of interstitial lung disease. In addition to therapy, cardiopulmonary rehabilitation programmes have been found to improve six-minute walking tests (6MWT), oxygenation, and functional capacity.
This article discusses the screening of PH-CLD along with the treatment algorithm and suggests the promising role of vasodilators in PH-CLD.
-
-
-
Diagnosis and Management of Group 2 Pulmonary Hypertension Due to Left Heart Disease in the UAE
Authors: Hani Sabbour, Mohammed B Al Saiari, Ashraf Alzaabi, Hazem El Badaoui, Rizwan Ahmed, Hadi Skouri, Mohammad Daud Khan, Mohamed El Harari, Magdi Tofeig, Amrish Agrawal, Hosam Zaky, Noha Yaseen, Wael Al Mahmeed, Ahmed Reda Taha, Vivek Kakar, Yasser El Hennawi, Yogeeswari Vellore Satyanarayanan, Aref Al Hakami, Anwar Al Zaabi, Hussein Heshmat, Asim A. Alnour, Abdullah Shehab and Adbha Saleh Al MubarakPulmonary hypertension (PH) due to left heart disease (PH-LHD) is the most common type of PH and is observed in patients with underlying left heart disease conditions, including valvular heart disease, heart failure (HF) with preserved ejection fraction (HFpEF), HF with reduced ejection fraction (HFrEF), cardiomyopathies, and arrhythmic diseases. Group 2 PH is postcapillary PH categorised into 2 components as isolated postcapillary PH (IpcPH) and combined precapillary and postcapillary PH (CpcPH), based on the value of pulmonary vascular resistance (PVR).
PH-LHD diagnosis is a three-step process and includes identification of clinical phenotype, determination of pre-test probability for invasive evaluation, and haemodynamic assessments. Management of PH-LHD primarily encompasses optimisation of treatment of underlying conditions, such as hypertension, obesity and diabetes mellitus, and treatment of PH-LHD with targeted PAH-specific drugs, like phosphodiesterase type 5 inhibitors (PDE5i) and sildenafil. In patients with PH-LHD, the use of PAH-specific drugs can lead to pulmonary oedema and clinical deterioration.
The article aimed to provide updated information on diagnosis and emerging treatment options for PH-LHD. Although the emerging alternative treatment options are not approved, the randomised studies discussed provide insight into the management and thus demand future clinical trials to establish the safety and efficacy of novel molecules and combination therapies.
-
-
-
Diagnosis and Management of the Connective Tissue Disease-associated PAH in the UAE
Pulmonary arterial hypertension (PAH) is a frequent complication of connective tissue diseases (CTDs), such as systemic sclerosis (SSc), mixed connective tissue disease, systemic lupus erythematosus (SLE), and, to a lesser extent, dermatomyositis, rheumatoid arthritis, and Sjögren syndrome. Connective tissue disease-associated PAH (CTD-PAH) is the second most common cause of PAH, following the idiopathic form of PAH. Nearly 15%–30% of patients with SSc develop PAH and have a very poor prognosis and survival rates compared to idiopathic PAH. Also, the majority of these patients present with substantial functional impairment and severe hemodynamics at diagnosis. Therefore, an early diagnosis of CTD-PAH through annual systematic screening and appropriate treatment is crucial in order to achieve optimal clinical outcomes and has been strongly recommended with the highest level of evidence in rheumatology, cardiology, and pulmonary guidelines since 2014. Unfortunately, annual screening in at-risk CTD-PAH patients is not being performed in the majority of patients, leading to substantial delays in therapy.
-
-
-
Diagnosis and Management of Group 1 Pulmonary Arterial Hypertension in the UAE
Group 1 pulmonary artery hypertension (PAH) is a debilitating disease characterized by progressively increased pulmonary vascular resistance (PVR) and mean pulmonary arterial pressure (mPAP) due to obstructions in the pulmonary vasculature. Group 1 PAH is further subdivided into idiopathic PAH, PAH associated with congenital heart disease (PAH-CHD), PAH associated with connective tissue disease (CTD-PAH), portopulmonary hypertension (PoPH), and paediatric PAH, out of which the first 3 contribute to substantial disease burden. Evidence from registries suggests that survival rates are better in PAH-CHD, followed by idiopathic PAH and PAH-CTD. The cause of idiopathic PAH is not evident, but one-third of the patients belong to this group. CTD-PAH is the second most common cause of PAH, following idiopathic PAH. In all cases, lung transplantation is generally considered the last option when medical therapies are not working.
The current article discusses the various unmet needs in the UAE, including less effective monotherapy (exception considered in specific subsets of PAH), late referral to the PH expert center, no systemic follow-up (in patients with PAH-CHD), no routine assessment, and underutilization of screening and treatment algorithms.
This article highlights the current approach to classification, screening, diagnosis, and management of each type of Group 1 PAH. This also emphasizes the need for tailored therapy for each patient. Screening and treatment algorithms can help healthcare professionals in the early detection and effective management of PAH, respectively.
-
-
-
Risk Stratification in Pulmonary Hypertension in the UAE
Risk stratification in pulmonary arterial hypertension is critical in determining therapeutic strategies for patients. Patients are stratified into low-, intermediate-, and high-risk groups based on determinants of prognosis like clinical assessment, exercise tests, biochemical markers, echocardiography, and haemodynamic tests. The primary objective of treatment is to shift each of the component tests into a low-risk zone either by treatment escalation alone, as in the case of intermediate-risk patients, or by a combination of treatment escalation and repeat evaluation by right heart catheterisation in high-risk patients. Low-risk patients should be clinically assessed at least every 3 months, but follow-up is more frequent for intermediate- and high-risk patients. Apart from improving survival rates, health-related quality of life is also assessed at baseline and follow-up visits, which may predict the prognosis. Additionally, therapeutic drug monitoring is also essential during visits due to the risk of major side effects during treatment initiation or dose escalation. Initial and follow-up risk stratification can prevent delays in the intensification of therapy, but insurance denials act as a barrier to this approach. Therefore, a dedicated insurance team is required for approval of testing and therapies and a fast-track process to communicate with the pulmonary hypertension expert centre. It can be concluded that risk stratification improves the treatment approach and helps make individualised treatment decisions. It also helps healthcare professionals better allocate treatment resources in cases of scarcity.
-
-
-
Diagnosis of Pulmonary Hypertension
Authors: Hani Sabbour, Mohammed B Al Seiari, Ashraf Alzaabi, Jamal Al-Saleh, Suad Hannawi, Khalid A. Alnaqbi, Bassam Mahboub, Khaled Saleh, Hazem El Badaoui, Shiva Kumar, Arun Kumar, Rizwan Ahmed, Mohammad Daud Khan, Mohamed El Harari, Noha Yaseen, Ramzi Khashkousha, Yogeeswari Vellore Satyanarayanan, Aref Al Hakami, Anwar Al Zaabi, Rajaie Namas, Hussein Heshmat, Asim A. Elnour and Abdullah ShehabDiagnosis of pulmonary arterial hypertension (PAH) is generally challenging due to nonspecific symptom presentation and several potential contributing conditions. Timely diagnosis of PAH is very important as the disease is progressive in nature and associated with increased morbidity and mortality. Therefore, the implementation of appropriate strategies that can reduce the delay in diagnosis of PAH, increase awareness among primary healthcare practitioners, and expedite referral to PAH specialists, are very crucial.
Patients with systemic sclerosis, human immunodeficiency virus, heritable disease, portal hypertension, and congenital heart disease are at high-risk of developing PAH. A definitive screening test is recommended for patients with these high-risk conditions to reduce the time to diagnosis. The diagnosis of pulmonary hypertension begins with a clinical suspicion generally based on symptoms, which is followed by physical examination of the patient and evaluation of haemodynamic criteria.
Integration of a high index of clinical suspicion with any expected abnormalities in basic diagnostic tests, substantially increases the likelihood of early diagnosis of PAH. The diagnostic tests required in the clinical assessment of suspected cases of PAH can be broadly categorised as essential diagnostic tests and additional diagnostic tests. The essential tests required in the diagnosis of PAH include electrocardiography, haematological testing, pulmonary function tests, echocardiography, ventilation-perfusion scan of the lungs, computed tomography scan, right heart catheterisation, genetic testing, and advanced imaging testing.
This article is an attempt to provide guidance to healthcare professionals in the clinical decision-making process for the diagnosis of PAH, which would benefit patients as PAH is progressive in nature.
-
-
-
Introduction, Clinical Classification, and Genetics of Pulmonary Hypertension in the UAE
Pulmonary hypertension (PH) is a progressive disease characterized by elevation of pulmonary arterial pressure over 25mmHg. PH has become a global issue associated with substantial morbidity and mortality despite the emergence of several treatment options in the last two decades.
The Emirates Thoracic Society, Emirates Rheumatology Society, and Emirates Cardiac Society took up the task of coming up with regional practical recommendations. The recommendations were formulated based on a careful consideration of scientific and medical knowledge and the evidence available at the time of publication. All endeavors were directed towards making the updated guideline handy for practicing clinicians in the region involved in the management of patients with PH.
This article highlights the updated guidelines in a reader-friendly format and highlights the recent updates made by the 6th World Symposium on Pulmonary Hypertension and the updated ESC ERS 2022 guidelines on PH with regards to classification. Group 1 sub-group has been further classified into “definitive” and “possible” with the inclusion of sub-group “pulmonary arterial hypertension (PAH) long-term responders to calcium channel blockers” and “PAH with overt features of venous/capillaries (pulmonary veno-occlusive disease/ pulmonary capillary haemangiomatosis) involvement”. Group 2.1 was re-named “PH due to heart failure with preserved left ventricular ejection fraction” and Group 2.2 was re-named “PH due to heart failure with reduced left ventricular ejection fraction”. Group 5 has two major updates: (i) removing splenectomy and thyroid disorders, and (ii) the classification of LAM-associated PH together with other parenchymal lung diseases in group 3.
This article highlights the clinical classification updates and the gaps and challenges associated with genetic testing in the region.
-
-
-
Empagliflozin Pharmacotherapy: An Updated Overview
More LessIt has been estimated that by 2030, the number of patients with diabetes is expected to rise to 552 million. Moreover, an estimated 20 million new cancer cases were reported in 2022, and 64 million people worldwide are currently suffering from heart failure. Recently, there has been an increasing interest regarding the prescription of a drug that was approved for use in May, 2014, which is called empagliflozin. Up to now, limited data is available on the efficacy, safety, and side effects of empagliflozin against a variety of diseases, including diabetes, heart failure, and cancer. Therefore, this study aimed to gather relevant data on empagliflozin by searching electronic databases, such as Web of Science, Scopus, Pubmed, and Cochrane Library, through October 9th, 2024. One hundred thirty-eight relevant studies, including review articles, clinical trials, and case reports, were assessed. It was found that orally, once daily use of empagliflozin, in addition to the glucose-lowering effect, suppresses inflammation and improves diastolic function. Empagliflozin inhibits breast cancer stemness by inactivating transcription factors and enzyme pyruvate kinase M2 via enhanced miR-128-3p expression. By inhibiting the sodium-glucose cotransporter, the drug has a well-known safety and efficacy in patients with breast cancer, type 1 or 2 diabetes, acute septic renal injury, renal disease, and heart failure. Regarding efficacy, empagliflozin acts as an angiotensin-converting enzyme inhibitor, angiotensin receptor blocker, sodium-glucose cotransporter type 2 inhibitor, vascular resistance prevention, and albuminuria-lowering agent. A recently published observational study confirmed the efficacy and safety of empagliflozin in improving kidney function and glycemic profile and reducing cardiovascular events in diabetic patients with advanced chronic kidney disease. In addition, empagliflozin is efficient as a blood pressure-lowering agent in patients with hypertension and those at higher risk of cardiovascular disease. Furthermore, for patients with diabetes and obesity, empagliflozin reduces the progression of kidney disease and improves clinical conditions in those with high blood pressure. It has a beneficial effect on hemoglobin A1c (HbA1c), body weight, glucose variability, and total daily insulin use in people with type 1 diabetes. Itching or redness of the genital area, genital infection, hematuria, difficulty in urination, bladder pain, painful sexual intercourse, peripheral amputations, and Fournier’s gangrene (rarely informed adverse effects) are the most commonly reported side effects. Additionally, pancreatitis, bad odor, and suicide attempts were recorded in some published case reports. Further evidence-based polypharmacological benefits studies' of empagliflozin associated with its nephroprotective, cardioprotective, and glucose-lowering effects and in cancer were reported to be advantageous.
-
-
-
Awareness and Attitudes Toward Transcranial Magnetic Stimulation Among Psychiatrists in Oman
BackgroundRepetitive Transcranial Magnetic Stimulation (rTMS) is a non-invasive treatment modality that is gaining prominence due to the limitations of existing pharmacotherapy approaches. To date, there is a paucity of research examining the awareness of rTMS among psychiatrists in the Arabian Gulf region. In this region, treatment resistance is prevalent due to the cultural attribution of psychological distress to somatic factors and the stigma associated with pharmacotherapy.
AimsThis study aims to assess the comprehension and attitudes of psychiatrists towards rTMS and determine the factors that contribute to their knowledge of rTMS in Oman.
MethodsA quantitative, observational, cross-sectional study was conducted utilizing an online survey. The survey collected demographic information, and a validated measure was used to assess variations in knowledge and attitudes towards rTMS. Univariate analysis and multiple linear regression were performed to identify risk factors associated with knowledge levels.
ResultsFifty psychiatrists participated in this study, resulting in a response rate of 53%. The mean age of the participants was 32.7±4.3 years (range: 26.0–41.0), with more than half being female (n=28, 56.0%) and classified as residents (junior/senior) (n=25, 50.0%). Most of the sample was Omani (n=45, 90.0%) and were employed in tertiary hospitals (n=38, 76.0%). The mean scores for knowledge and attitudes towards rTMS in this sample were 14.5±3.8 and 22.5±6.3, respectively. The linear model indicated that senior residents and older participants had a higher level of knowledge than junior residents (β=4.65, p<.001). Furthermore, participants who had access to an rTMS device at work demonstrated a higher level of knowledge than those who did not (β=1.88, p=0.027).
ConclusionThree factors significantly influence the knowledge of psychiatrists about rTMS: their educational level, access to an rTMS device at work, and the availability of standardized training in rTMS.
-
-
-
Knowledge, Attitude, and Practices of Caregivers in the Management of Asthmatic and Non-asthmatic Children: A Community-based Study
BackgroundBronchial asthma, a chronic inflammatory condition, poses significant health challenges for children. Proper management of childhood asthma requires the knowledge, attitudes, and practices (KAP) of the caregivers. This study assesses the KAP of caregivers in the management of asthmatic and non-asthmatic children in the UAE.
MethodsA cross-sectional study was conducted in Ras Al Khaimah over four months, involving 182 children aged 6-16 years. Data were collected through a pre-validated KAP questionnaire distributed to caregivers of asthmatic and non-asthmatic children across schools, parks, and private clinics. Descriptive statistics were used to analyze the responses.
ResultsAmong caregivers of asthmatic children, 77.1% demonstrated adequate knowledge, while 45.83% held a positive attitude towards asthma. In contrast, caregivers of non-asthmatic children had lower knowledge (37%) and attitudes (26.88%). Lack of adequate knowledge led to poor asthma management practices, with only 75% of caregivers conducting regular follow-ups. Better caregiver knowledge was associated with improved asthma control, while misconceptions and negative attitudes led to suboptimal care.
ConclusionSignificant gaps in caregiver KAP were identified, with a need for targeted educational programs to enhance asthma management. Improving caregiver understanding and attitudes through regular physician visits and educational initiatives is crucial for optimizing asthma outcomes in children.
-
-
-
Prevalence and Demographic Correlates of Social Anxiety Disorder among Medical Students at Sultan Qaboos University: A Cross-sectional Study
Authors: Rania A. Kadhim, Mohammed Al Azri, Abdullah Al Lawati and Hamed Al SinawiIntroduction and Objective:Social anxiety disorder (SAD) is an excessive and irrational fear of social situations, leading to an avoidance of those situations. Individuals with SAD may fear acting in a certain way or exhibiting anxiety symptoms in front of others, which can significantly impact their daily functioning and quality of life. Among medical students, SAD can negatively influence academic performance, particularly in exams, and lead to employment difficulties. The COVID-19 pandemic introduced unique stressors, including social isolation and the transition to online learning, which may have exacerbated anxiety-related conditions. Understanding the prevalence and associated factors of SAD during this period is essential to develop targeted interventions for students. Thus, this work aimed to assess the prevalence and demographic correlates of SAD among medical students at the College of Medicine and Health Sciences at Sultan Qaboos University (SQU) in Oman during the pandemic.
Methods:A questionnaire-based cross-sectional study was conducted from September to October 2020 in SQU, College of Medicine and Health Sciences. Medical students from all academic years were invited to complete demographic data and the Liebowitz social anxiety scale (LSAS). The LSAS is a 24-item self-rating scale to assess SAD. An analysis using a Chi-square test was performed to obtain the factors associated with SAD.
Results:A total of 558 students completed the questionnaire, of which 348 were female (62%). The total prevalence of SAD was 64%, whereas moderate grade SAD accounted for 27% of the participants, marked grade 19%, severe grade 11%, and very severe grade 7%. Among the students who had the disorder, 71% suffered a generalized subtype of SAD. A significant association between SAD and phase of study (p<0.001), age group (p<0.001), and gender (p<0.001) was found. Phase 1 (69%) exhibited the highest prevalence, followed by phase 2 (66%) and phase 3 (48%). Among the age groups, 17-19 years group (67%) demonstrated the highest prevalence, followed by age groups 20-22 (64%) and 23-25 (46%). In terms of gender, females (70%) were more likely to display SAD symptoms than males (52%).
Conclusion:The results of this study indicated a high prevalence of SAD among medical students and showed a significant association between SAD and the phase of study, age group, and gender. These results could help justify the establishment of targeted mental health interventions to support medical students in managing their anxiety, which can ultimately result in an improvement in their academic performance and overall quality of life. University administrators and psychologists should aim to develop supportive programs for students.
-
-
-
Effects of COVID-19 on Oral Health Status: A Review
Authors: Pragi ., Varun Kumar and Monika .The SARS-CoV-2 virus is the cause of the COVID-19 illness, which has been discovered to have a number of side effects. The purpose of this study is to present the most recent scientific data about oral symptoms of SARS-CoV-2 and the difficulties the dental system faced throughout the pandemic. When COVID-19 is suspected or confirmed, it is advised that patients undergo a routine intraoral examination because oral symptoms occasionally signal a serious illness or even a life-threatening condition. We think it is crucial to have a thorough understanding of all COVID-19 symptoms, including oral lesions, given the current state of the spread of the disease and the unknown future effects of newly developing viral variations. The internet databases of PubMed, Scopus, Embase, Cochrane Central, Web of Science, and Science Direct were investigated to find out how COVID-19 influences oral health. Our suggestions were based on the most recent recommendations from the American Dental Association, WHO, and the Centers for Disease Control and Prevention's Infection Control Practices for Dentistry. The objectives of this review were to analyze current infection control recommendations and shed light on the oral effects of COVID-19 using the evidence that is currently available. With the present understanding of the pathophysiology and biological behavior of COVID-19, the main question addressed in this review was whether it is reasonable to believe that oral symptoms are a direct result of SARS-CoV-2 infection. In this review, we will look at the possible oral and dental consequences of COVID-19 based on the information that is currently available.
-
-
-
Epidemiology, Pathogenesis, and Induction of Peptic Ulcer: A Comprehensive Review
Authors: Saswat Swarup Badapanda, Amanjot Kaur, Divya Jain and Deepika BhatiaPeptic ulcers have a significant impact on global mortality and morbidity rates. The primary causative factors explored in this review include H. pylori infection, unhealthy lifestyle choices, and the use of nonsteroidal anti-inflammatory drugs (NSAIDs). Addressing this pressing health issue requires raising awareness and developing novel medications and therapies, which necessitates further research. This article encompasses a wide range of information on peptic ulcers, covering their epidemiology, etiological factors, pathogenesis, antiulcer agents, synthetic compounds, and experimental animal models. It serves as a valuable resource for researchers, healthcare professionals, and policymakers by providing a comprehensive overview of peptic ulcer disease. The review emphasizes the critical role of experimental animal models in advancing our understanding of the disease and facilitating the development of novel treatments. By utilizing these models, researchers can gain deeper insights into the pathogenesis of peptic ulcers and evaluate potential therapeutic interventions. Furthermore, this review highlights the need for continued research efforts to address the challenges posed by peptic ulcer disease. By fostering awareness, promoting research, and encouraging the implementation of effective therapies, we can collectively strive towards reducing the burden of peptic ulcer disease and improving the health and well-being of individuals worldwide.
-
-
-
Early Exposure to Research: Its Impact on Medical Students’ Educational Experience and Interest in Future Research
Authors: Zahra Shahriyari Afshar, Sara Esmaeli, Farah Azhar and Ramya RathanIntroductionIntegration of research into medical education is crucial for cultivating physician-scientists capable of advancing medical breakthroughs. It is imperative to take these measures for early medical students to establish a strong research foundation for future healthcare professionals.
MethodsThis study investigated the impact of early research exposure on pre-clinical medical students at Gulf Medical University (GMU). A sample size of 85 MD students participated in the study, which spanned six months. In GMU, early exposure to research begins with sessions integrated into the Medical Education and Lifelong Learning (MEL) course during the first year, covering the structure and function of different sections of a research paper and practical application through Journal Article Discussions (JADs) in journal clubs in the 2nd year.
ResultsThe intervention involved the evaluation of these measures through pre-validated MCQs and a self-administered questionnaire. MCQ results revealed that over 70% of students scored above 40% on research knowledge assessments. Additionally, a questionnaire comprising open and close-ended questions revealed that most of the students reported a positive agreement in understanding research structures.
ConclusionThe findings underscored the necessity of incorporating research into medical curricula to enhance students' research competencies and foster a positive attitude toward research. This study highlighted the importance of early research exposure in developing future physician-scientists.
-
-
-
Evaluation of Factors Associated with Mortality in Patients with Crush Syndrome Acquired from the February 6 Kahramanmaras Earthquake
Authors: Ali Akin and Talat Soner YilmazBackgroundCrush syndrome is the second most common cause of death in earthquakes, following direct trauma. Crush syndrome develops when toxic substances released after tissue injury or crushing reach the bloodstream. The aim of this study was to investigate factors associated with morbidity and mortality in patients rescued from the rubble after the February 6 earthquake and admitted to our hospital who had crush syndrome by retrospectively analyzing their data.
MethodsHemodialysis, fasciotomy, and other parameters during hospitalization and time to transfer to a ward or death of 36 adult patients with crush syndrome who were rescued from the rubble and hospitalized after the February 6 earthquake were retrospectively analyzed.
ResultsThirty-six patients were included in the study. There was no significant correlation between the mortality of patients according to their time of rescue or need for fasciotomy, dialysis, or inotropes (p=0.767, p=0.294, p=0.625, p=0.865, respectively). There was a high inverse correlation between the time of rescue and time to death. There was a weak inverse correlation between the time of rescue and hospitalization duration (r=-0.767 and r=-0.341, respectively). There was a significant correlation between the need for inotropes and mortality (p<0.001). No one who didn't need dialysis passed away. Dialysis was necessary for all six of the deceased individuals. We can conclude that one significant factor in predicting death in CS patients is the requirement for dialysis.
ConclusionCrush syndrome, which develops in patients rescued from the rubble alive, is a life-threatening condition. It is an important syndrome and an important cause of mortality for earthquake victims. Further large-scale studies are needed to elucidate the association of time of rescue, the need for fasciotomy and hemodialysis, and other factors with mortality.
-
-
-
UAE Consensus on Patient Profiles for Pre-exposure Prophylaxis with Monoclonal Antibodies against COVID-19 in Hematological Malignancies and Immunocompromised States
IntroductionDespite significant advancements in COVID-19 treatment and prevention, immunocompromised individuals, particularly those with hematological malignancies, remain at high risk for severe infection and suboptimal vaccine response. Pre-exposure prophylaxis strategies for these vulnerable populations have been limited. Monoclonal antibodies, proteins designed to target specific antigens, offer a promising preventive solution for individuals unable to mount a sufficient immune response to vaccination. However, there is a critical unmet need to establish clear patient selection criteria for pre-exposure prophylaxis with monoclonal antibodies in these groups. This consensus statement explores recent research to address this gap, outlining profiles of patients most likely to benefit from monoclonal antibody-based prophylaxis.
MethodologyThe consensus statement was developed through a rigorous process, utilizing a pre-Delphi search method and a modified Delphi technique to gather expert opinions. This approach ensured a comprehensive and informed consensus among experts in the field. Initially, nine distinct patient categories requiring pre-exposure prophylaxis with monoclonal antibodies were identified. Through iterative rounds of expert feedback, discussion, and refinement, these nine categories were expanded and subdivided into twelve more specific groups of hematological malignancies and immunocompromised disorders. This refinement aimed to better capture the diverse patient profiles requiring prophylaxis, providing a more detailed framework for the targeted administration of monoclonal antibodies.
ResultsThe study resulted in the panel members agreeing on nine categories for the use of monoclonal antibodies in COVID-19 prevention for high-risk patients. Achieving consensus among experts is crucial as it reflects the collective validation of evidence-based recommendations that can be reliably applied in clinical practice. A 100% agreement was reached for HIV and AIDS, underscoring the unanimous recognition of the vulnerability of this group to severe COVID-19 outcomes. Similarly, 96% agreement was reached for patients on immunomodulatory drugs (IMiDs), and 90.5% for those with hematological diseases, highlighting strong expert support for prophylaxis in these categories. Immunodeficiencies and renal conditions garnered 86% agreement, indicating broad, although slightly more varied, expert consensus on these groups. Lastly, 80% of the panel supported patients with solid organ cancer, liver conditions, rare neurological disorders, and severe life-limiting neuro-disabilities, reflecting recognition of their elevated risk despite more diverse opinions for these categories.
ConclusionThis consensus statement offers healthcare professionals in the UAE a clear, evidence-based framework for the use of monoclonal antibodies in preventing COVID-19 among patients with hematological malignancies and immunocompromised conditions. By outlining specific patient categories, the statement provides a practical guide that enables clinicians to make informed decisions about pre-exposure prophylaxis, ensuring that high-risk individuals receive timely and appropriate protection. The consensus not only enhances the ability of healthcare providers to identify and prioritize at-risk populations, but also optimizes patient outcomes by streamlining preventive measures in clinical practice. In addition, these findings lay the groundwork for future research and the development of standardized protocols, ultimately improving the management of vulnerable populations in the ongoing fight against COVID-19.
-
-
-
Montelukast-associated Serious Mental Health Adverse Effects: An Overview
Authors: Naina Mohamed Pakkir Maideen, Sulthan Al Rashid and Asiya NabiMontelukast, a leukotriene receptor antagonist, is frequently used to treat asthma and allergic rhinitis. Despite its effectiveness, there are rising concerns about potential neuropsychiatric side effects, such as agitation, anxiety, depression, hallucinations, sleep disturbances, and suicidal ideation. It is crucial to examine clinical evidence to better understand these adverse reactions and ensure patient safety.
This review aims to assess the clinical evidence regarding neuropsychiatric side effects associated with montelukast use. By analyzing studies from various databases, the goal is to equip healthcare professionals with a thorough understanding of these side effects, encouraging cautious use of montelukast in clinical settings.
The literature was searched in databases, such as Medline/Pubmed/PMC, Scopus, Web of Science, Google Scholar, ScienceDirect, Ebsco, Embase, and reference lists, to identify publications relevant to neuropsychiatric side effects associated with the use of montelukast.
Various studies consistently reported a range of neuropsychiatric adverse reactions, including agitation, anxiety, depression, hallucinations, sleep disturbances, and suicidal ideation. The findings indicated a notable association between montelukast and these neuropsychiatric symptoms across various patient populations and age groups.
Clinicians should be aware of the serious mental health side effects of montelukast.
-
-
-
Exploring the Intricacies of Polycystic Ovarian Syndrome (PCOS): A Comprehensive Review-from Prevalence to Natural Solutions
Authors: Priyanka Soni, Divya Jain, Manisha Bhatti, Deepika Bhatia and Chandan SharmaIntroduction:Among women of reproductive age, Polycystic Ovarian Syndrome (PCOS) is a common endocrine condition marked by insulin resistance, metabolic abnormalities, and hormonal imbalances. Infertility, irregular menstrual periods, acne, hirsutism, and obesity are among the symptoms that this illness frequently causes. Traditional PCOS therapies usually include drugs like insulin sensitizers and oral contraceptives, which can have negative side effects and might not deal with the underlying causes of the condition. This study aims to examine the etiology of PCOS and the effectiveness of natural management techniques in reducing symptoms and enhancing general health outcomes.
Aims and Objective:The objective of this study is to comprehend the pathophysiology and underlying mechanisms of PCOS, including hormonal and metabolic factors, assess the effectiveness of natural management strategies, such as dietary changes, herbal supplements, physical activity, and lifestyle interventions, in managing symptoms, investigate the effects of particular diets and lifestyle changes on insulin sensitivity, inflammation, and hormonal balance in PCOS patients, compare natural strategies with conventional treatments to determine the advantages and disadvantages of each treatment, identify research gaps, and suggest areas for future study.
Methodology:A thorough examination of pertinent literature, including clinical studies, randomized controlled trials, and meta-analyses published in peer-reviewed journals, was a part of the search approach. Studies on the pathophysiology of PCOS, traditional therapies, and natural management strategies were found using databases like PubMed, Scopus, and Web of Science.
Results:The review concentrated on studies conducted within the last 15 years to guarantee that the most recent findings were included. This study intends to shed light on the possible advantages of incorporating natural methods into PCOS care by combining the available data and comprehensive treatment choices.
Conclusion:In summary, PCOS is a common and complex disorder that affects women's health worldwide. Effective management requires knowledge of its symptoms, risk factors, and underlying mechanisms. Women can be empowered to manage PCOS better and enhance their general well-being by emphasizing a holistic approach that incorporates lifestyle changes and natural therapies.
-
-
-
Effects of Daily Low-calorie Fruit Consumption on Vitamin C Levels, Oxidative Stress, and Cardiovascular Risk Factors in Prediabetic Individuals
BackgroundThe study investigated the impact of incorporating fruits or fruit juices into the diets of prediabetic individuals to mitigate oxidative stress. Previous research presented divergent approaches, making replication of findings challenging. This study aimed to evaluate whether advising the consumption of two low-calorie fruits daily could improve oxidative stress, glycemic control, and anthropometric measurements in prediabetic individuals.
MethodsAn open-label, parallel, randomized controlled trial was conducted at a medical college hospital in Mangalore, Karnataka, India. Thirty participants, aged 40-70 years, with impaired fasting glucose or impaired glucose tolerance, were recruited through screening of first-degree relatives of patients with type 2 diabetes. Participants were randomly allocated in a 1:1 ratio to either the intervention group, which consumed two low-calorie fruits daily or a wait-list control group. The inclusion criteria were adults aged 40-70 years with prediabetes. Exclusion criteria included a history of diabetes, chronic diseases, normal glucose tolerance, smoking, alcohol use, recent antioxidant/vitamin use, and participation in dietary trials within the past year. Outcomes included plasma vitamin C levels and blood pressure, oxidative stress markers, glycemic parameters, and anthropometric measures. Over three months, measurements were taken at the beginning and end of the study. Statistical analysis was performed using the Wilcoxon signed-rank test and Mann-Whitney U test, with a significance level set at p < 0.05.
ResultsThe mean age of participants was 43.1 ± 10.1 years in the intervention group and 44.7 ± 9.6 years in the control group. The intervention group demonstrated a significant 15% increase in plasma vitamin C levels (mean change: 4.0 µmol/L; p = 0.021; 95% CI: 1.2–6.8), whereas the control group experienced a 9% decrease. Systolic blood pressure decreased significantly in the intervention group (mean change: -3.0 mmHg; p = 0.04; 95% CI: -4.5 to -1.5), while the control group showed an increase. No significant differences were observed between groups in terms of oxidative stress markers, glycemic parameters, or anthropometric measures.
ConclusionOverall, our study provided insights into the effects of incorporating low-calorie fruits into the diet of individuals with prediabetes. While improvements in vitamin C levels and systolic blood pressure were observed, there were no significant changes in oxidative stress, glycemic status, anthropometry, and other antioxidant measures. These findings contribute to the existing literature on the potential benefits of fruit consumption in individuals with prediabetes, highlighting the importance of vitamin C as a biomarker and its potential role in blood pressure regulation and cardiovascular benefits. This study also highlights plasma vitamin C as a promising biomarker for assessing the effects of fruit supplementation. Additionally, this study suggests that broader dietary and lifestyle modifications may be necessary to achieve comprehensive metabolic improvements, particularly in prediabetic individuals.
Clinical Trial Registration Number(CTRI/2011/05/001739).
-
-
-
Tracking of SARS-CoV-2 Variants of Concern by RT-PCR Assay in the Post-Pandemic Era
BackgroundThe global impact of COVID-19 resulted in widespread illness and death. The rapid evolution of SARS-CoV-2, accompanied by increased transmission caused by Variants of Concern (VOC), became a significant concern in the post-pandemic.
ObjectivesThis study has been conducted to evaluate the performance of multiplexed real-time reverse transcription-PCR (RT-PCR) assays for COVID-19 detection and the use of specific mutation RT-PCR-based approach to identify VOC in SARS-CoV-2 positive samples in the northern part of the UAE.
MethodsWe selected 200 respiratory specimens tested between October 2022 to January 2023, at the Pure Lab, COVID Screening Lab, Al Qassimi Women's and Children's Hospital, Sharjah, UAE. We evaluated the performance of four commercially available RT-PCR kits for COVID-19 detection. Further, the positive samples were used to identify variants by variant detection kit as required for mutations in Spike protein (HV 69-70 DEL, N501Y, E484K, K417N) to identify Omicron, British and SARS-CoV-2 wild type (WT) E Gene variants, respectively.
ResultsIn the post-pandemic period, 153/200 (76.5%) positivity was observed. There was a higher prevalence of COVID-19 among males, accounting for 52% of the cases, in comparison to females 48% aged between 20-40 years. Variant analysis showed that 50 samples were detected for the SARS-CoV-2 OMICRON variant (B.1.1.529), 4 samples were detected for the SARS-CoV-2 British variant (B.1.1.7), however, 99 samples were detected for SARS-CoV-2 wild type (WT) E gene with no mutation.
ConclusionThis study demonstrates the efficacy of a rapid and cost-effective RT-PCR assay designed to detect spike mutations to effectively contribute to public health response efforts. Additionally, by performance evaluation of PCR kits for COVID-19 detection with the Cycle Threshold (CT) values obtained from diagnostic PCR, we can gather valuable insights into the viral load of samples. This information helps us gauge the extent of transmission and assess the severity of the disease within the population.
-
-
-
Phosphodiesterase Inhibitors for Diabetes: From Mechanistic Insights to Therapeutic Innovations
Authors: Aman Chaudhary, Sonal Bansal, Sunam Saha, Swamita Arora, Wasim Akram and Shivendra KumarPhosphodiesterase inhibitors (PDEIs) have emerged as potential agents in managing diabetes, offering novel avenues for therapeutic intervention. This comprehensive review explores the diverse mechanisms, clinical applications, and the evolving landscape of phosphodiesterase inhibitors in the context of diabetes mellitus. The molecular mechanisms underlying the impact of PDEIs on diabetes form a cornerstone of this review. PDEs, a family of enzymes that regulate cyclic nucleotide levels, play a crucial role in intracellular signaling cascades. Understanding these intricate mechanisms is essential for unraveling the therapeutic potential of PDEIs in diabetes. Clinical applications of PDEIs in diabetes management are explored, highlighting their multifaceted roles. The review discusses pivotal preclinical and clinical studies that showcase the efficacy of PDEIs in lowering hyperglycemia, enhancing lipid profiles, and averting diabetic sequelae such as neuropathy and nephropathy. Moreover, synergistic effects have been shown in combination therapy, including PDEIs and already available antidiabetic drugs, improving overall therapeutic effectiveness. Recent studies have unveiled new PDE targets and refined inhibitor designs, contributing to the continuous evolution of this therapeutic approach. Despite these advancements, issues with patient-specific responses, dose optimization, and long-term safety still exist. The necessity of further study into PDEIs, particularly their role in customized medicine for the treatment of diabetes, is emphasized in the review's conclusion. The creation of next-generation PDE inhibitors with higher metabolic benefits, fewer side effects, and better selectivity is one of the future goals.
Furthermore, the review delves into the prospects of PDEIs in diabetes management. It explores emerging technologies, such as targeted drug delivery systems and precision medicine, that aim to enhance the therapeutic efficacy of PDEIs while minimizing adverse effects. The potential role of PDEIs in addressing specific diabetes subtypes and complications, including diabetic neuropathy and cardiovascular complications, is also contemplated.
-
-
-
Exploring the Lived Experiences of Clinical Educators: Challenges, Motivations, and Future Perspectives
Authors: Farah Azhar, Nooreen Adnan, Lubna Ahmed and Syeda Rubaba AzimIntroductionThis study examines the factors contributing to the shortage of medical doctors teaching medical students despite their crucial role in training the future medical workforce.
MethodsTo analyze the factors behind the lack of medical doctors in the training of medical students, we used ‘phenomenology’ to understand clinical educators' lived experiences and their constructed meanings. Within the domain of phenomenology, we applied hermeneutic (interpretive) phenomenology. The experiences of eight clinical educators at the Gulf Medical University were explored through interviews and analyzed using Interpretative Phenomenological Analysis (IPA) and Socio-Cognitive Career Theory (SCCT).
ResultsThe findings revealed that entry into medical education often occurred serendipitously due to inadequate career counseling and the undervaluation of the field. Acquiring a postgraduate qualification in medical education contributed to professional growth of the participants by enhancing expertise and fostering a stronger professional identity. Key motivators included a passion for the field, student interaction, support from colleagues, and an encouraging working environment. Clinical educators faced challenges, particularly when they compared their careers to those of practicing clinicians. These challenges included perceived undervaluing of their field, an unclear professional identity, slower career progression (notably in the UAE) and low income. Furthermore, clinicians who serve as educators as well, often struggle with insufficient time dedicated to teaching responsibilities. Coping strategies involved cultivating a positive work environment and maintaining optimism. Growing awareness and a positive outlook for medical education were noted.
ConclusionThis study uncovered the underlying issues faced by clinical educators through their lived experiences. To change the status quo, we propose facilitating medical students and young doctors in joining the field of Medical Education early in their careers. This can be achieved by providing strong career counseling and establishing clear entry and progression pathways in the field of Medical Education, through medical universities and health centers. Medical educators should be facilitated by providing an encouraging environment, acknowledging their medical education-related qualifications, and improving remuneration.
-
Volumes & issues
Most Read This Month
