NobleBlocks

South Hams Hospital

Hospital / health systemKingsbridge, United Kingdom

Research output, citation impact, and the most-cited recent papers from South Hams Hospital (United Kingdom). Aggregated across the NobleBlocks index of 300M+ scholarly works.

Total works
50
Citations
335
h-index
7
i10-index
3
Also known as
South Hams Hospital

Top-cited papers from South Hams Hospital

111Indium autologous leucocytes in inflammatory bowel disease.
S.H. Saverymuttu, A. Michael Peters, J. P. Lavender, H J Hodgson +1 more
1983· Gut88doi:10.1136/gut.24.4.293

A non-invasive method of imaging and assessing inflammatory bowel disease is described. 111Indium labelled leucocyte scans were performed on 33 patients with a wide variety of inflammatory bowel diseases and 25 control patients. All patients with moderate or severe inflammatory bowel disease had positive scans with localisation of abnormal activity corresponding to the sites assessed to be diseased by radiology in either small or large bowel. No false positives were recorded in the control patients. Faecal excretion of 111In labelled leucocytes was increased in patients with inflammatory bowel disease according to disease severity and correlated with disease activity assessed by serum C-reactive protein levels (r = 0.74, p less than 0.001) or in those patients with Crohn's disease by Crohn's Disease Activity Index (r = 0.78, p less than 0.001). These data suggest that 111In labelled leucocytes may be used to provide a safe, non-invasive method of imaging diseased bowel and objectively assessing disease activity.

Identification of high risk labours by labour nomogram.
John Studd, David R. Clegg, R. R. Sanders, A. O. Hughes
1975· BMJ37doi:10.1136/bmj.2.5970.545

The labour stencil representing the expected cervimetric progress of normal labour was used in 741 consecutive spontaneous labours to identify high-risk labours which needed oxytocic stimulation. Uterine contractions were stimulated if progress extended two hours past the nomogram, which resulted in shorter labours, fewer instrumental deliveries and caesarean sections, and babies with higher Apgar scores than in those dysfunctional labours which were not stimulated. According to the protocol used 36% of primigravid and 13% of multigravid labours needed acceleration. The remaining patients did not need any oxytocic interference during the first stage. This selection of patients is important to prevent a major obstetric advance being abused and discredited at a time when the profession and public are questioning the safety of active labour.

Health‐Related Quality of Life of People Living with COPD in a Semiurban Area of Western Nepal: A Community-Based Study
Tara Ballav Adhikari, Anupa Rijal, Pawan Acharya, Marieann Högman +4 more
2021· COPD Journal of Chronic Obstructive Pulmonary Disease9doi:10.1080/15412555.2021.1920903

Chronic Obstructive Pulmonary Disease (COPD) is a major cause of morbidity and mortality in Nepal. It is a progressive lung disease and has a significant impact on the quality of life of patients. Health‐related quality of life (HRQOL) reflects the health‐ and disease‐related facets of quality of life. Limited studies have assessed the impact of COPD on HRQOL and associated factors in Nepal. This study is based on a cross-sectional household survey data from a semiurban area of Western Nepal. A validated Nepali version of St George’s Respiratory Questionnaire (SGRQ) was used to measure the HRQOL. COPD was defined together with post-bronchodilator airflow obstruction and the presence of respiratory symptoms. Post-bronchodilator airflow obstruction was defined as Forced Expiratory Volume in 1st second (FEV1) to Forced Vital Capacity (FVC) ratio < 0.70. COPD was diagnosed in 122 participants, and their median (IQR) total score of HRQOL was 40 (26 − 69); the score of symptoms, activity, and impact area were 53 (37 − 74), 57 (36 − 86), and 26 (13 − 62), respectively. The overall HRQOL was significantly different in terms of age, occupational status, physical activity, and comorbidities. Disease severity and the presence of respiratory symptoms had a significant difference in HRQOL (p = 0.0001). Appropriate measures to improve conditions and addressing the associated factors like respiratory symptoms and enhancing physical activity are necessary and important.

Output characteristics of DeVilbiss No. 40 hand-held jet nebulizers
K N Chan, MM Clay, M Silverman
1990· European Respiratory Journal8doi:10.1183/09031936.93.03101197

DeVilbiss No. 40 hand-held nebulizers are widely used for quantifying airway responsiveness in large populations using pharmacological agents. We examined the aerosol characteristics of five nebulizers. Within each device, the aerosol output and droplet size were reasonably stable over a wide range of bulb pressures, although there were considerable differences in output characteristics between nebulizers. The droplet size was very large compared to conventional aerosol delivery systems, with a mass median diameter greater than 10 microns for three of the five devices. Between 28-50% of the output was in particles sufficiently small for airway deposition (less than 6.2 microns). A more vigorous compression of the bulb caused a small increase output and a reduction in droplet size, resulting in a much bigger variation in the output of the respirable aerosol (less than 6.2 microns) with changes in bulb pressure. The loss due to evaporation was about 3.5%, causing a similar rise in the osmolality of the nebulizer solution. In view of the variable nebulizer output and the marked between-operator variation in bulb pressure, the characteristics of individual DeVilbiss No. 40 nebulizers should be evaluated by individual operators before use in clinical practice or research.

The argon laser in dermatology: safety aspects
J. A. S. Carruth, A L McKenzie
1982· Clinical and Experimental Dermatology8doi:10.1111/j.1365-2230.1982.tb02423.x

The use of the argon laser in the treatment of vascular birthmarks is discussed and the importance of adequate safety standards is stressed. The Southampton Argon Laser Safety Code is given in detail (Appendix 1 and 2).

Management, Outcomes, and Predictors of Mortality of Cryptococcus Infection in Patients Without HIV: A Multicenter Study in 46 Hospitals in Australia and New Zealand
Julien Coussement, Christopher H. Heath, Matthew B. Roberts, Rebekah Lane +4 more
2024· Clinical Infectious Diseases7doi:10.1093/cid/ciae630

BACKGROUND: Limited data exist regarding outcomes of cryptococcosis in patients without human immunodeficiency virus (HIV), and few studies have compared outcomes of Cryptococcus gattii versus Cryptococcus neoformans infection. METHODS: We conducted a retrospective study in 46 Australian and New Zealand hospitals to determine the outcomes of cryptococcosis in patients without HIV diagnosed between 2015 and 2019 and compared outcomes of C. gattii versus C. neoformans infections. Multivariable analysis identified predictors of mortality within 1 year. RESULTS: Of 426 patients, 1-year all-cause mortality was 21%. Cryptococcus gattii infection was associated with lower mortality than C. neoformans (adjusted odds ratio [OR], 0.47; 95% confidence interval [CI], .23-.95), while severe neurological symptoms at presentation were the strongest predictor of death (adjusted OR, 8.46; 95% CI, 2.99-23.98). Almost all (99.5%) patients with central nervous system (CNS) infection received induction antifungal therapy versus 27.7% with isolated pulmonary cryptococcosis. The most common regimen in CNS disease was liposomal amphotericin B with flucytosine (93.8%; mean duration, 31 ± 13 days). Among patients with CNS cryptococcosis, C. gattii infection was associated with higher risk of immune reconstitution inflammatory response (C-IRIS) than C. neoformans (21% versus 3%, P < .001). Nineteen patients received amphotericin B-based re-induction therapy for suspected relapse, but none had microbiological relapse. Serum cryptococcal antigen positivity and lung imaging abnormalities resolved slowly (resolution at 1 year in 25% and 34% of patients, respectively). CONCLUSIONS: Compared with C. neoformans, C. gattii infection demonstrated lower mortality but higher C-IRIS risk in CNS infection. Severe neurological symptoms were the strongest predictor of mortality.

Surgical treatment of Candida albicans spondylodiscitis
Prashant Adhıkarı, Nishma Pokharel, Sulochana Khadka, Ishwar Lohani +4 more
2023· Annals of Medicine and Surgery6doi:10.1097/ms9.0000000000001114

Introduction: Spinal infection poses a demanding diagnostic and treatment problem for which a multidisciplinary approach with spine surgeons, radiologists, and infectious disease specialists is required. Infections are usually caused by bacterial microorganisms, although fungal infections can also occur. Most patients with spinal infections diagnosed in the early stages can be successfully managed conservatively with antibiotics, bed rest, and spinal braces. In cases of gross or pending instability, progressive neurological deficits, failure of conservative treatment, spinal abscess formation, severe symptoms indicating sepsis, and failure of previous conservative treatment, surgical treatment is required. Case presentation: A 64-year-old male presented to the Outpatient Department with a complaint of pain in bilateral upper extremities for 4 months. The pain was shooting in type, radiating to bilateral arms, forearms, and hands with no aggravating and relieving factors. He is a known case of carcinoma pyriform sinus for which he underwent various cycles of chemotherapy. Ten years later, a tracheostomy was performed for laryngeal edema, and again, an endoscopic gastrostomy was performed due to feeding difficulties. He then developed fever and cervical pain along with pain in the bilateral upper extremities. An infectious etiology was suspected for which multiple antibiotics were started with no positive response. An MRI was performed, which was suggestive of spondylodiscitis probably of tubercular origin. A biopsy was done to confirm the diagnosis, following which antitubercular (HRZE) therapy was started. He was also treated with Duloxetine and gabapentin, which resulted in minor improvements. Subsequent MRIs showed diffuse involvement of the multiple cervical vertebrae along with cord compression. Two stages of anterior corpectomy followed by posterior instrumentation were done. Following the procedure, the patient developed an infection, which was managed with antibiotics. The titanium implant was not removed. A muscle graft was planned with the pectoralis muscle and flap closure was done. The tissue was also sent for Gram stain, AFB stain, and GeneXpert, which showed normal findings. Finally, in tissue culture, Candida albicans was isolated. On performing the enzyme immunoassay test, it was found to be Aspergillus (Galactomannan antigen) positive as well. Antitubercular treatment was stopped. Then, he was managed with an antifungal, oral voriconazole, for the duration of 1 and a half years. Clinical discussion: Patients diagnosed with Candida spondylodiscitis tend to have favorable outcomes, likely linked to timely identification, thorough surgical debridement, and proper azole medication. Our case achieved success by promptly identifying and confirming it through tissue culture, detecting spinal cord compression, decompressing it, and initiating specific antifungal treatment. A delay in commencing antifungal therapy has been associated with poorer outcomes, especially in neurological health. Our patient received voriconazole for a full year, suggesting that favorable outcomes are achievable for fungal spondylodiscitis with swift and appropriate surgery and antifungal medication. Conclusion: In summary, evaluation for fungal infection is essential in all cases of unexplained spinal infection in immunocompromised patients, regardless of presentation. If the antifungal treatment proves ineffective, a surgical approach is typically employed for the management of fungal spondylodiscitis. Our report details a successful case of fungal spondylodiscitis treated with a surgical approach and highlights the potential for a fungal infection to be a causative factor in noncompressive myelopathy, which may be sometimes mistaken for radiation myelitis.

Open Versus Robotic Radical Cystectomy With Intracorporeal Neobladder: A Decade‐Long Single‐Surgeon Experience
Neeraja Tillu, Zachary Dovey, Manish C. Choudhary, Arjun K. Venkatesh +4 more
2025· International Journal of Urology4doi:10.1111/iju.70139

INTRODUCTION: This single-surgeon, long-term study aims to evaluate open radical cystectomy (ORC) and robot-assisted radical cystectomy (RARC) with Studer urinary diversion in bladder cancer patients in terms of perioperative, oncological, and functional outcomes. METHODS: This was a single-center, single-surgeon study analyzing patients who underwent open versus robotic intracorporeal neobladder (RIN) from January 2009 to January 2020. We recorded baseline characteristics, perioperative variables, outcomes, including cancer-specific survival (CSS) and overall survival (OS), and functional outcomes. RESULTS: The study included 454 patients (242 open, 212 robotic) with an overall follow-up of 120 months. The RIN group had significantly lower blood loss (p < 0.001), more unilateral nerve sparing (p = 0.008), and higher lymph node yield (p = 0.042). The number of 30-day readmissions favored RIN significantly (p = 0.041). Complication rates (major and minor) were similar between groups (p = 0.56 and 0.61, respectively). The RIN group had improved severe daytime continence (p = 0.03), though no significant difference was found in erectile function (p = 0.56). The robotic cohort showed improved 10-year CSS in T3 disease (68.3% vs. 50.5%, p = 0.04). The OS for the entire cohort was 66.5% for the robotic cohort and 61.6% for open at 10 years (p = 0.08). CONCLUSIONS: In this series, RIN had decreased blood loss, an increased lymph node yield, decreased rate of hospital readmissions, lesser hospital stay, and improved severe daytime continence compared to the open approach.

HEPARIN-BINDING PROTEIN AS A DIAGNOSTIC AND PROGNOSTIC MARKER OF INFECTIONS: A SYSTEMATIC REVIEW AND META-ANALYSIS
Wenshan Yang, Wei Dong
2025· Mediterranean Journal of Hematology and Infectious Diseases4doi:10.4084/mjhid.2025.029

Heparin-binding protein (HBP) is a granule protein derived from neutrophils, located in secretory vesicles and neutrophilic granules, also known as cationic antimicrobial protein of 37 kDa (CAP37) or azurocidin. This study evaluates the diagnostic and prognostic value of HBP levels in relation to infection, organ dysfunction, and mortality in adult patients. A systematic review and meta-analysis were conducted by searching PubMed, Web of Science, EMBASE, and the Cochrane Database from their inception through June 2024. Original studies assessing HBP levels' diagnostic and prognostic utility in predicting infection and disease severity in critically ill adult patients were included. The primary outcome was the diagnostic and predictive role of HBP in infection and severity. The Quality Assessment of Diagnostic Accuracy Studies 2 (QUADAS-2) tool was used to evaluate bias risk. A total of 56 studies involving 11,486 patients were included. Pooled analysis showed HBP had a sensitivity of 0.87 (95% CI, 0.82-0.91), specificity of 0.87 (95% CI, 0.79-0.92), and an AUC of 0.93 (95% CI, 0.91-0.95) for infection diagnosis. For prognostic assessment, sensitivity was 0.77 (95% CI, 0.74-0.80), specificity was 0.72 (95% CI, 0.68-0.76), and AUC was 0.81 (95% CI, 0.78-0.85). HBP outperformed procalcitonin (PCT), C-reactive protein (CRP), and white blood cell count (WBC) in diagnosing and predicting critical illness. No publication bias was detected. HBP demonstrates high sensitivity and specificity for diagnosing infections in critically ill adult patients. Additionally, it effectively predicts disease progression, including organ dysfunction and mortality, surpassing traditional biomarkers such as PCT, CRP, and WBC. All that cannot be true for subjects with severe neutropenia.

Bone tumors in the maxilla and the tibia leading to the diagnosis of asymptomatic primary hyperparathyroidism in a 17-year-old male: A case report
Saja Karaja, William Borghol, Ahed Assaf, Nabeha Haytham Alibrahim +2 more
2025· International Journal of Surgery Case Reports3doi:10.1016/j.ijscr.2025.111182

INTRODUCTION: Primary hyperparathyroidism is a common endocrine disorder, especially among postmenopausal women, characterized by elevated calcium levels and excessive secretion of parathyroid hormone due to hyperactive parathyroid glands. PRESENTATION OF CASE: A 17-year-old male presented with a painless mass in the maxilla, which developed six months after a cystic lesion was diagnosed in his right knee. Subsequent examinations identified a parathyroid tumor, leading to surgical excision of the right lower parathyroid gland, and the patient developed hypocalcemia postoperatively, indicative of Hungry Bone Syndrome. DISCUSSION: Primary hyperparathyroidism occurs mostly in females aged 50 to 60 and presents with many clinical symptoms and signs, but our patient was a 17-year-old male and had one of the complications of this disease, which is a brown tumor, without the appearance of the common typical symptoms of the disease, which led to excluding the diagnosis of a brown tumor and suspecting a giant cell tumor due to the histological similarity. CONCLUSION: This case report emphasizes the critical need to consider primary hyperparathyroidism in atypical demographics, such as young males. Notably, the formation of a brown tumor prior to overt hyperparathyroidism symptoms suggests potential early complications. This case reinforces the importance of surgical expertise in successful parathyroidectomy in countries without advanced imaging.

Early diagnosis and delayed treatment of anorectal melanoma in a 19-year-old female: A case report
Yousef Saffaf, Hazem Arab, Ahmed Aldolly, Rafif Terkaoui +1 more
2025· International Journal of Surgery Case Reports2doi:10.1016/j.ijscr.2025.111518

INTRODUCTION AND IMPORTANCE: decades of life. The diagnosis is often delayed due to non-specific symptoms, resulting in many patients presenting with metastases. Treatment options include radical or palliative surgery, radiotherapy, chemotherapy, and immunotherapy. CASE PRESENTATION: We are presenting a case of a 19-year-old female who was diagnosed with anorectal melanoma at an early stage. However, due to the rejection of abdominoperineal resection several times, she developed advanced-stage melanoma with metastasis in the lung, so the patient will undergo colostomy for treatment when complete obstruction is present, following her consent and that of her parents. CLINICAL DISCUSSION: This case demonstrates the importance of early intervention in young patients with anorectal melanoma. The decision to undergo abdominoperineal resection in young patients is challenging and carries long-term lifestyle implications. CONCLUSION: Anorectal melanoma can occur at any age but is extremely rare in young individuals according to medical literature. It may present as a polyp, so this diagnosis should be considered when such a presentation is observed. Early diagnosis and treatment are necessary to improve the overall survival rate and prevent the disease from progressing to a more advanced stage.

Study on the relationship between genetic polymorphism of reductive folic acid carrier and the risk of neural tube defects
Xusen Yang, Guofeng Fan, Zengliang Wang, Shaoshan Li +4 more
2022· Child s Nervous System2doi:10.1007/s00381-022-05805-z

BACKGROUND: To investigate the association of folate metabolism gene polymorphism with neural tube defects (NTDs) in Chinese population. METHODS: The subjects were divided into two groups, 495 children with NTDs (NTD group) and 255 healthy children (control group). RESULTS: The levels of folic acid, s-adenosine methionine (SAM), and Sam/s-adenosine homocysteine (SAH) in NTD group were lower than those in control group. There were significant differences in hey, SAH, and Sam levels between two groups, but there was no significant difference in folic acid content. High fever in early pregnancy, taking antiepileptic drugs, father's exposure to organic solvents, folic acid deficiency, and mother's diabetes were the important risk factors in NTDs. MTHFR 677C > T gene was a risk factor for NTD in children, while 1298A > C gene was a protective factor. CONCLUSION: Folic acid metabolism markers were different in NTD children and their mothers, and the overall trend showed that folate, SAM, and SAM/SAH levels were decreased, while Hcy and SAH levels were increased; MTHFR 677C > T gene of SNPs was a risk factor for the occurrence of NTDs, and MTHFR 1298A > C gene was a protective factor, and the environmental risk factor had a synergistic effect on occurrence of NTDs.

Unusual case of staphylococcus epidermidis-induced spinal epidural abscess in an adolescent: Clinical insights and diagnostic considerations
Saja Karaja, Ayham Qatza, Mulham Alkassem, Ahmed Aldolly +4 more
2025· Radiology Case Reports1doi:10.1016/j.radcr.2025.02.051

Spinal epidural abscess (SEA) is an uncommon infection typically caused by Staphylococcus aureus, predominantly affecting older adults with risk factors such as advanced age, comorbidities, and prior surgical interventions. This report details a case involving a 14-year-old male presenting with acute lumbar pain, lower limb weakness, urinary retention, and skin pustules. The patient had no history of immunologic diseases, diabetes, or drug use. Contrast-enhanced magnetic resonance imaging (MRI) with gadolinium demonstrated a peripheral fluid signal surrounding the thoracic spinal cord, consistent with an epidural abscess from T9-T12 to L1, causing spinal cord compression. Cultures from the abscess and skin pustules identified Staphylococcus epidermidis (S. epidermidis). The patient underwent surgical drainage and remained stable postoperatively. This case highlights an unusual SEA presentation in an adolescent without typical risk factors, emphasizing the importance of considering atypical pathogens and further investigation into infection sources.

Successful management of Leydig Cell Tumor in a 65-year-Old patient: A rare case report
Hasan Haydar, Ayham Qatza, Saja Karaja, Anagheem Alkhleef +2 more
2025· Urology Case Reports1doi:10.1016/j.eucr.2024.102927

Leydig cell tumors (LCTs) are rare testicular neoplasms, representing 1-3% of all testicular tumors. A 65-year-old male presented with a painless left scrotal mass. Ultrasound revealed a 61 × 53 × 35 mm tumor with heterogeneous echogenicity and abundant blood supply. Radical orchidectomy was performed, and immunohistochemistry confirmed LCT with positivity for Inhibin A and calretinin, and negativity for CK, chromogranin, LCA, and low Ki67. Postoperative follow-up at 6 months showed improved condition, no scrotal masses, and normal tumor markers. Finally, LCTs in older males require differential diagnosis; hormonal activity impacts presentation. Conservative management and monitoring are crucial.

The challenges of an unusual case of miliary tuberculosis control: A case report from Syria
Ayham Qatza, Ahmad Almohamed, Saja Karaja, Moumina Baroudi +3 more
2024· Radiology Case Reports1doi:10.1016/j.radcr.2024.09.093

Tuberculosis (TB) remains a significant global health challenge, with the Eastern Mediterranean accounting for 8.1% of cases. Miliary tuberculosis (MTB) is a rare form, representing 1%-2% of TB cases and 8% of extrapulmonary cases. This report discusses a 39-year-old woman's case who experienced a generalized tonic-clonic seizure, with a normal chest X-ray delaying her diagnosis of MTB and leading to severe outcomes. It highlights the limitations of chest radiography in detecting MTB and emphasizes the need for chest CT or MRI to identify typical miliary patterns. Prompt treatment is crucial in developing countries facing medical resource shortages due to war and poverty to prevent severe complications from MTB.

Antithrombotic Adherence to guideline-directed therapy and risk profile among Non-Valvular Atrial fibrillation patients
Kunjang Sherpa, Chandra Mani Adhikari, Dipanker Prajapati, Reeju Manandhar +4 more
2023· Nepalese Heart Journal1doi:10.3126/nhj.v20i2.59445

Introduction: Patients with Atrial fbrillation (AF) are at fivefold higher risk for Ischemic stroke than in the general population. Although the current therapeutic guidelines recommend the use of anticoagulants for thromboembolic prophylaxis in patients with nonvalvular AF (NVAF) with additional risk factor(s) for stroke, the global registry data show non-adherence to guidelines for the management of stroke in diferent regions of the world. The current study conducted at the tertiary referral cardiac center of Nepal for addressing the risk profle of stroke based on the current risk scores and the use of antithrombotic agents NVAF patients. Methodology: This was a descriptive observational cross sectional study conducted at Shahid Gangalal National Heart Centre (SGNHC), Kathmandu, Nepal from December 2020 to June 2020 which included patients with Nonvalvular AF. The main objective of the study was to study the clinical characteristics, stroke risk profle based on CHA ₂DS₂-VaSc score and risk of bleeding based on HAS-BLED score and the patterns of use of antithrombotic agents in NVAF patients. Results: A total of 79 cases of NVAF were included with 48(60.8%) males and 31(39.2%) females. The mean CHA₂DS₂-VaSc and HAS-BLED score were 2.44±1.2 and 1.51±1.4 respectively. The majority patients 38% had permanent AF followed by 25.5% had paroxysmal AF. Majority of patients were symptomatic with 67.1% presented with palpitation while 32.9% presented with shortness of breath (SOB). Based on the European Heart Rhythm Association (EHRA) AF related symptoms score, 41.8% had EHRA 2a and 2b while 1.3% had EHRA 4 score. The use of anticoagulants in patients with Nonvalvular AF was 41.6%, with NOACS in 33 % and warfarin used in 8.9% cases. The majority of patients 51.8% of study population were using anti-platelet agents with aspirin in 49.3 % and clopidogrel in 2.5 % cases while no medication in 6.3% of cases. Although 70.8% patients had CHA₂DS₂-VaSc score of 2 or more but the use of anticoagulants was only 58.9% with 46.4% NOACS and 12.5% using warfarin among this group of patients. Conclusion: Although the use of anticoagulant with NOACS in patients with higher risk of stroke is increasing, it is still underused in the majority of cases .There is a need of nationwide AF registry and the need of adoption of the current recommended guidelines to increase use of Anticoagulants in patients with Nonvalvular AF patients for the prevention of stroke .

Rare circle of Willis variants associated with multiple intracranial aneurysms and subarachnoid hemorrhage
Mohamad H. Mosi, Hisham Alfarra, Nawwar Soliman, Moaaz Khalouf Alshaar +2 more
2026· Medicinedoi:10.1097/md.0000000000050402

RATIONALE: Subarachnoid hemorrhage from a ruptured intracranial aneurysm is a type of stroke with high rates of mortality and disability, and the prevalence of aneurysm formation increases in the presence of Circle of Willis variants. PATIENT CONCERNS: A 64-year-old man with a history of hypertension and psoriatic arthritis presented with a sudden severe headache and walking difficulties without any loss of consciousness. DIAGNOSES: Non-contrast computed tomography showed a diffuse subarachnoid hemorrhage. Computed tomography angiography demonstrated multiple intracranial aneurysms together with variants of the posterior communicating artery and posterior cerebral artery, which may have contributed to aneurysm formation. INTERVENTIONS: The patient was started on oral Nimodipine to prevent cerebral vasospasm and underwent stent-assisted coil embolization of the ruptured aneurysm. OUTCOMES: His symptoms and clinical condition improved a few days after the embolization, and he was discharged after 18 days. LESSONS: This is the first documented case report from Syria, and possibly the first ever, detailing such Circle of Willis variants associated with cerebral aneurysms. It underscores the need for further studies exploring the relationship between the type of variants and the number and size of cerebral aneurysms, which is important for a better understanding of the epidemiology of cerebral aneurysms.

EP433 - ECE_1386 - Emotional and psychological dimensions of living with type 1 diabetes: a qualitative study of adolescents, parents, and healthcare providers in Nepal
Binaya Bhattarai
2026· European Journal of Endocrinologydoi:10.1093/ejendo/lvag096.942

Abstract Background Type 1 diabetes mellitus (T1DM) presents not only a chronic physical burden but also a significant psychological challenge, particularly among adolescents and young adults. Despite increasing recognition of the emotional toll of diabetes, mental health care remains inadequately integrated into routine diabetes management. Objective This qualitative study explores the lived psychological experiences of adolescents and young adults living with diabetes (AYALD), their parents, and healthcare professionals to identify key emotional stressors, coping mechanisms, and systemic gaps in psychosocial support. Methods A phenomenological design was employed using five focus group discussions (FGDs): two with AYALD, two with their parents (n = 20 per group), and one with healthcare professionals (n = 15). Discussions were audio-recorded, transcribed verbatim, and thematically analyzed using NVivo software following a six-step framework that included data familiarization, coding, theme development, and synthesis. Results Three major themes emerged: (1) Emotional Burden, characterized by fear, isolation, and stigma at diagnosis and during daily management; (2) Diabetes and School, highlighting inadequate institutional preparedness and experiences of stigmatization; and (3) Diabetes and Depression, revealing prevalent depressive symptoms and gaps in mental health referral and integration. Subthemes included emotional masking, parental overprotection, and the pivotal role of peer support and diabetes camps. A key finding was the disconnect between increased mental health referrals by medical professionals and low patient uptake, suggesting structural barriers within pediatric mental health care pathways. Conclusions Living with T1DM extends beyond metabolic regulation; it is a deeply emotional experience shaped by social, familial, and institutional factors. Effective diabetes care requires systemic reforms to integrate psychological support into routine management, strengthen peer-support networks, enhance school-level awareness, and improve interdisciplinary communication. Further research is warranted to validate emotional masking as a potential clinical indicator and to examine long-term psychosocial outcomes among youth living with diabetes.

A 52-year-old male with C5–C6 cage migration, developed to dysphagia: a rare case report
Alhammam Hammoud, Emad Rouh, Ahmed Aboud Al-Aboud, Ayat Al-Abood +4 more
2025· International Journal of Surgery Opendoi:10.1097/io9.0000000000000331

Introduction and importance: The anterior approach to the cervical spine is a recognized surgical technique for various spinal disorders. While generally effective, it poses risks of serious complications, such as cervical plate and cage displacement. Case presentation: A 52-year-old male with a history of cervical myelopathy and cardiac catheterization presented with left arm numbness and pain. Following surgery for spinal stenosis and a displaced cervical plate, he developed persistent dysphagia, initially alleviated by Hasytriptyline but recurred after a work-related neck injury. A cervical CT on 15 May 2024, revealed C5–C6 cage migration, with magnetic resonance imaging (MRI) showing midline displacement, complicating surgical retrieval. Clinical discussion: Various diagnostic methods, including endoscopy and imaging, showed normal results for dysphagia, with significant improvement after Hasytriptyline treatment. MRI later revealed calcified herniated discs at C3–C6, prompting surgery. Two years after cervical trauma, imaging showed cage migration, complicating surgery. Post-expulsion, no severe complications were found, suggesting a potential esophageal-tracheal fistula. Conclusion: Cervical cage migration is a rare but significant complication that can potentially cause compression of nearby structures, such as the larynx. Further research is essential for understanding its etiology.

Beyond the murmur: unmasking a rare sinus venosus ASD in an adolescent with chronic respiratory infections: A case report
Ahmad Alhamid, Hadi Alabdullah, Mais Alreem Basel Mohaisen, Mohammad Atia +4 more
2025· Medicinedoi:10.1097/md.0000000000045437

RATIONALE: Overall, 5% to 10% of all atrial septal defects (ASDs) are of the sinus venosus type, a rare congenital disease. This defect must be identified and treated immediately since it might cause significant left atrial dilatation and dyspnea. PATIENT CONCERNS: A 15-year-old male presented with previously undetected sinus venosus type ASD. The patient arrived with a high-grade heart murmur and a history of recurring respiratory illnesses. DIAGNOSES: A clinical examination identified a 3/6 systolic ejection murmur in the second left intercostal gap and a fixed split second heart sound. Electrocardiography revealed sinus rhythm with partial right bundle branch block, while echocardiography indicated considerable enlargement of the right atrium and right ventricle, accompanied by a D-shaped left ventricle. A sinus venosus type ASD with an inferior vena cava-right atrial shunt was verified. INTERVENTIONS: The patient had surgical closure of the defect via midline sternotomy, thereafter gaining access to the right atrium and performing pericardial patch repair. OUTCOMES: Two months postoperatively, the patient's right ventricular diameters and pulmonary artery pressures were significantly diminished (25-30 mm Hg), and his overall status was excellent. LESSONS: Sinus venosus type ASD is an infrequent etiology of persistent respiratory problems in adolescents. Early detection by thorough clinical and echocardiographic assessment, followed by timely surgical intervention, may lead to superior functional recovery and improved long-term quality of life.