Pub Date : 2026-03-11eCollection Date: 2026-03-01DOI: 10.7759/cureus.105064
Pedro D Gil de Rubio Cruz, Dorimar Morales Torres, Karolane A Gonzalez Gonzalez
This is the case of a 77-year-old female patient with Alzheimer's disease, complicated by partial complex seizures. Levetiracetam was administered, which provoked hemolytic anemia. An extensive laboratory evaluation was suggestive of a non-immune etiology. Subsequent discontinuation of levetiracetam resulted in improvement of hemoglobin. Pancytopenia has been reported with the use of levetiracetam, but not isolated anemia. With this case report, we want to increase awareness of a potentially serious adverse reaction provoked by levetiracetam, a preferred anticonvulsive drug in the geriatric population.
{"title":"A Rare Case of Levetiracetam-Induced Hemolytic Anemia.","authors":"Pedro D Gil de Rubio Cruz, Dorimar Morales Torres, Karolane A Gonzalez Gonzalez","doi":"10.7759/cureus.105064","DOIUrl":"https://doi.org/10.7759/cureus.105064","url":null,"abstract":"<p><p>This is the case of a 77-year-old female patient with Alzheimer's disease, complicated by partial complex seizures. Levetiracetam was administered, which provoked hemolytic anemia. An extensive laboratory evaluation was suggestive of a non-immune etiology. Subsequent discontinuation of levetiracetam resulted in improvement of hemoglobin. Pancytopenia has been reported with the use of levetiracetam, but not isolated anemia. With this case report, we want to increase awareness of a potentially serious adverse reaction provoked by levetiracetam, a preferred anticonvulsive drug in the geriatric population.</p>","PeriodicalId":93960,"journal":{"name":"Cureus","volume":"18 3","pages":"e105064"},"PeriodicalIF":1.3,"publicationDate":"2026-03-11","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12978846/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"147446492","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2026-03-11eCollection Date: 2026-03-01DOI: 10.7759/cureus.105040
Ngo Cheung
Background: Major depressive disorder (MDD) is increasingly viewed as a disorder of impaired neural plasticity, yet the mechanisms underlying diverse antidepressant classes - glutamatergic (e.g., ketamine), monoaminergic (e.g., selective serotonin reuptake inhibitors (SSRIs)), and GABAergic (e.g., neurosteroids) - remain incompletely integrated. The objective of this study was to extend a pruning-plasticity model of depression and directly compare, from an identical severely pruned baseline state, the efficacy, stress resilience, durability, and relapse vulnerability of three mechanistically distinct interventions: ketamine-like targeted synaptogenesis, SSRI-like gradual refinement of existing connectivity, and neurosteroid-like tonic inhibition. Computational models offer a controlled means to compare these pathways, but prior work has typically examined single mechanisms.
Methods: We extended a pruning-plasticity model of depression by applying 95% magnitude-based synaptic elimination to overparameterized feed-forward networks trained on a four-class Gaussian classification task. From identical pruned states, three interventions were tested: ketamine-like gradient-guided regrowth (50% reinstatement) with consolidation; SSRI-like prolonged low-learning-rate training with gradual internal noise reduction; and neurosteroid-like global tonic inhibition (30% damping plus tanh activations) with brief consolidation. Outcomes included baseline accuracy, resilience to graded internal activation noise (up to σ = 2.5) plus input perturbation, and relapse vulnerability after an additional 40% pruning.
Results: All treatments restored near-ceiling performance on unchallenged inputs. Ketamine-like synaptogenesis uniquely reduced sparsity (to ~47%) and conferred superior stress resilience (extreme noise accuracy 84.5%) with near-zero relapse drop (-0.2%). SSRI-like refinement improved combined stress accuracy to 83.5% but showed limited extreme noise tolerance (44.0%) and substantial relapse vulnerability (10.8% drop). Neurosteroid-like inhibition achieved rapid combined stress recovery (97.5%) while active, but was state-dependent (decline upon removal) with poor extreme noise buffering (42.5%) and moderate relapse drop (4.1%).
Conclusions: These simulations demonstrate that antidepressants operate through mechanistically distinct routes-structural rebuilding (ketamine), gradual optimization of existing connectivity (SSRIs), or reversible dynamic stabilization (neurosteroids)-yielding trade-offs in onset speed, durability, and stress resilience. The findings support a multifaceted plasticity framework for depression and provide computational rationale for mechanism-based treatment selection and combination strategies.
{"title":"Divergent Mechanisms of Antidepressant Efficacy: A Unified Computational Comparison of Synaptogenesis, Stabilization, and Tonic Inhibition in a Model of Depression.","authors":"Ngo Cheung","doi":"10.7759/cureus.105040","DOIUrl":"https://doi.org/10.7759/cureus.105040","url":null,"abstract":"<p><strong>Background: </strong>Major depressive disorder (MDD) is increasingly viewed as a disorder of impaired neural plasticity, yet the mechanisms underlying diverse antidepressant classes - glutamatergic (e.g., ketamine), monoaminergic (e.g., selective serotonin reuptake inhibitors (SSRIs)), and GABAergic (e.g., neurosteroids) - remain incompletely integrated. The objective of this study was to extend a pruning-plasticity model of depression and directly compare, from an identical severely pruned baseline state, the efficacy, stress resilience, durability, and relapse vulnerability of three mechanistically distinct interventions: ketamine-like targeted synaptogenesis, SSRI-like gradual refinement of existing connectivity, and neurosteroid-like tonic inhibition. Computational models offer a controlled means to compare these pathways, but prior work has typically examined single mechanisms.</p><p><strong>Methods: </strong>We extended a pruning-plasticity model of depression by applying 95% magnitude-based synaptic elimination to overparameterized feed-forward networks trained on a four-class Gaussian classification task. From identical pruned states, three interventions were tested: ketamine-like gradient-guided regrowth (50% reinstatement) with consolidation; SSRI-like prolonged low-learning-rate training with gradual internal noise reduction; and neurosteroid-like global tonic inhibition (30% damping plus tanh activations) with brief consolidation. Outcomes included baseline accuracy, resilience to graded internal activation noise (up to σ = 2.5) plus input perturbation, and relapse vulnerability after an additional 40% pruning.</p><p><strong>Results: </strong>All treatments restored near-ceiling performance on unchallenged inputs. Ketamine-like synaptogenesis uniquely reduced sparsity (to ~47%) and conferred superior stress resilience (extreme noise accuracy 84.5%) with near-zero relapse drop (-0.2%). SSRI-like refinement improved combined stress accuracy to 83.5% but showed limited extreme noise tolerance (44.0%) and substantial relapse vulnerability (10.8% drop). Neurosteroid-like inhibition achieved rapid combined stress recovery (97.5%) while active, but was state-dependent (decline upon removal) with poor extreme noise buffering (42.5%) and moderate relapse drop (4.1%).</p><p><strong>Conclusions: </strong>These simulations demonstrate that antidepressants operate through mechanistically distinct routes-structural rebuilding (ketamine), gradual optimization of existing connectivity (SSRIs), or reversible dynamic stabilization (neurosteroids)-yielding trade-offs in onset speed, durability, and stress resilience. The findings support a multifaceted plasticity framework for depression and provide computational rationale for mechanism-based treatment selection and combination strategies.</p>","PeriodicalId":93960,"journal":{"name":"Cureus","volume":"18 3","pages":"e105040"},"PeriodicalIF":1.3,"publicationDate":"2026-03-11","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12978026/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"147446533","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2026-03-11eCollection Date: 2026-03-01DOI: 10.7759/cureus.105066
Francisco Oliveira, Virginia Martínez, Carla Moreira, Isabelle Carrilho, Teresa Pipa, Luís Neves, Daniela Azevedo, Ana Teresa Alves, Beatriz Garcia, José Rei
Visceral leishmaniasis is a potentially life-threatening systemic parasitic infection caused by protozoa of the genus Leishmania and transmitted by sandflies. Although uncommon in Portugal, it should be considered in the differential diagnosis of prolonged fever associated with pancytopenia and hepatosplenomegaly, even in immunocompetent individuals. We report a case of a previously healthy young adult who initially presented to an urgent Family Medicine consultation in primary care, where pancytopenia was identified and prompted timely referral to secondary care. Diagnosis was confirmed by the detection of Leishmania amastigotes in bone marrow aspirate during haematological investigation. Treatment with liposomal amphotericin B resulted in complete clinical and laboratory recovery. This case highlights the importance of careful primary care assessment, recognition of red flags, and effective coordination between primary and secondary care in non-endemic settings.
{"title":"From Pancytopenia to Diagnosis: Visceral Leishmaniasis Identified Through Primary Care Assessment.","authors":"Francisco Oliveira, Virginia Martínez, Carla Moreira, Isabelle Carrilho, Teresa Pipa, Luís Neves, Daniela Azevedo, Ana Teresa Alves, Beatriz Garcia, José Rei","doi":"10.7759/cureus.105066","DOIUrl":"https://doi.org/10.7759/cureus.105066","url":null,"abstract":"<p><p>Visceral leishmaniasis is a potentially life-threatening systemic parasitic infection caused by protozoa of the genus Leishmania and transmitted by sandflies. Although uncommon in Portugal, it should be considered in the differential diagnosis of prolonged fever associated with pancytopenia and hepatosplenomegaly, even in immunocompetent individuals. We report a case of a previously healthy young adult who initially presented to an urgent Family Medicine consultation in primary care, where pancytopenia was identified and prompted timely referral to secondary care. Diagnosis was confirmed by the detection of Leishmania amastigotes in bone marrow aspirate during haematological investigation. Treatment with liposomal amphotericin B resulted in complete clinical and laboratory recovery. This case highlights the importance of careful primary care assessment, recognition of red flags, and effective coordination between primary and secondary care in non-endemic settings.</p>","PeriodicalId":93960,"journal":{"name":"Cureus","volume":"18 3","pages":"e105066"},"PeriodicalIF":1.3,"publicationDate":"2026-03-11","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12978848/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"147446517","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2026-03-11eCollection Date: 2026-03-01DOI: 10.7759/cureus.105067
Dima M Almrayati, Mohammad Y Hajeer, Ahmad S Burhan, Wael H Almahdi, Samer T Jaber
Background and objective: This preliminary study aimed to evaluate the effectiveness of a novel, clinically feasible low-intensity pulsed ultrasound (LIPUS) protocol in accelerating functional orthodontic treatment using removable appliances.
Methods: Five patients (mean age: 11.10 ± 0.41 years) diagnosed with Class II Division 1 malocclusion underwent functional orthodontic treatment supplemented with the LIPUS, US PRO 2000™ 2nd Edition device (Current Solutions, Austin, Texas, United States). Ultrasound stimulation was applied twice weekly during the first month, once every two weeks during the second month, and once every three weeks thereafter until completion of active treatment. The primary outcomes assessed were the duration of active treatment and dentoskeletal changes.
Results: The mean duration of active treatment was 170.80 ± 19.76 days. Significant sagittal skeletal improvements were observed, including forward mandibular repositioning, reflected by an increase in the SNB angle "the Sella-Nasion plane to Point B angle" (mean difference (MD) = +1.32°), accompanied by a slight reduction in the SNA angle "the Sella-Nasion plane to Point A angle" (MD = -0.54°), a decrease in the ANB angle "the difference between SNA and SNB angles" (MD = -1.98°), an increase in the SNPog angle "the Sella-Nasion plane to Point Pog angle" (MD = +0.94°) further confirmed anterior mandibular displacement. Vertical skeletal parameters remained largely stable, with no evidence of adverse vertical effects. Dentoalveolar changes included controlled retroclination of the maxillary incisors, proclination of the mandibular incisors, and clinically relevant reductions in overjet (MD = -4.38 mm) and overbite (MD = -1.06 mm).
Conclusions: The modified LIPUS protocol produced favorable skeletal and dentoalveolar effects while maintaining vertical stability, suggesting it may represent a practical alternative to conventional daily ultrasound application during functional orthodontic treatment.
背景和目的:本初步研究旨在评估一种新的、临床可行的低强度脉冲超声(LIPUS)方案在加速使用可移动矫治器的功能正畸治疗中的有效性。方法:5例诊断为II类1分错的患者(平均年龄:11.10±0.41岁)接受了功能正畸治疗,并辅以LIPUS, US PRO 2000™第二版装置(Current Solutions, Austin, Texas, United States)。第一个月每周进行两次超声刺激,第二个月每两周进行一次,此后每三周进行一次,直到积极治疗结束。评估的主要结果是积极治疗的持续时间和牙齿骨骼的变化。结果:积极治疗的平均持续时间为170.80±19.76 d。我们观察到显著的矢状面骨骼改善,包括下颌向前重新定位,反映在SNB角“Sella-Nasion平面到B点角”的增加(平均差值(MD) = +1.32°),伴随着SNA角“Sella-Nasion平面到a点角”的轻微减少(MD = -0.54°),ANB角“SNA和SNB角的差值”的减少(MD = -1.98°)。SNPog角“Sella-Nasion平面到Pog点角”(MD = +0.94°)的增加进一步证实了前下颌移位。垂直骨骼参数基本保持稳定,没有证据表明不利的垂直影响。牙槽牙的变化包括上颌切牙的控制后倾,下颌切牙的前倾,以及临床相关的覆盖(MD = -4.38 mm)和覆盖咬合(MD = -1.06 mm)的减少。结论:改良的LIPUS方案在保持垂直稳定性的同时,对骨骼和牙槽产生了良好的影响,这表明它可能是功能性正畸治疗中常规每日超声应用的实用替代方案。
{"title":"A Novel Protocol to Accelerate Functional Orthopedic Treatment Using Low-Intensity Pulsed Ultrasound in Patients With Skeletal Class II Malocclusion: A Preliminary Clinical Report.","authors":"Dima M Almrayati, Mohammad Y Hajeer, Ahmad S Burhan, Wael H Almahdi, Samer T Jaber","doi":"10.7759/cureus.105067","DOIUrl":"https://doi.org/10.7759/cureus.105067","url":null,"abstract":"<p><strong>Background and objective: </strong>This preliminary study aimed to evaluate the effectiveness of a novel, clinically feasible low-intensity pulsed ultrasound (LIPUS) protocol in accelerating functional orthodontic treatment using removable appliances.</p><p><strong>Methods: </strong>Five patients (mean age: 11.10 ± 0.41 years) diagnosed with Class II Division 1 malocclusion underwent functional orthodontic treatment supplemented with the LIPUS, US PRO 2000™ 2nd Edition device (Current Solutions, Austin, Texas, United States). Ultrasound stimulation was applied twice weekly during the first month, once every two weeks during the second month, and once every three weeks thereafter until completion of active treatment. The primary outcomes assessed were the duration of active treatment and dentoskeletal changes.</p><p><strong>Results: </strong>The mean duration of active treatment was 170.80 ± 19.76 days. Significant sagittal skeletal improvements were observed, including forward mandibular repositioning, reflected by an increase in the SNB angle \"the Sella-Nasion plane to Point B angle\" (mean difference (MD) = +1.32°), accompanied by a slight reduction in the SNA angle \"the Sella-Nasion plane to Point A angle\" (MD = -0.54°), a decrease in the ANB angle \"the difference between SNA and SNB angles\" (MD = -1.98°), an increase in the SNPog angle \"the Sella-Nasion plane to Point Pog angle\" (MD = +0.94°) further confirmed anterior mandibular displacement. Vertical skeletal parameters remained largely stable, with no evidence of adverse vertical effects. Dentoalveolar changes included controlled retroclination of the maxillary incisors, proclination of the mandibular incisors, and clinically relevant reductions in overjet (MD = -4.38 mm) and overbite (MD = -1.06 mm).</p><p><strong>Conclusions: </strong>The modified LIPUS protocol produced favorable skeletal and dentoalveolar effects while maintaining vertical stability, suggesting it may represent a practical alternative to conventional daily ultrasound application during functional orthodontic treatment.</p>","PeriodicalId":93960,"journal":{"name":"Cureus","volume":"18 3","pages":"e105067"},"PeriodicalIF":1.3,"publicationDate":"2026-03-11","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12978847/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"147446507","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2026-03-11eCollection Date: 2026-03-01DOI: 10.7759/cureus.105024
Adnan Khan, Maheen Shahab, Malik Maqsood Anwar
Introduction Patients with inflammatory bowel disease (IBD), particularly those receiving biologic therapies, are at increased risk of infections due to immunosuppression. Vaccinations play a vital role in reducing this risk, yet adherence to immunisation schedules remains suboptimal. This audit aimed to assess vaccination coverage among IBD patients on biologic therapies at Our Lady's Hospital, Navan, Ireland, and to identify areas for improvement. Aim and objectives The primary aim was to evaluate adherence to recommended immunisation schedules for IBD patients on biologics. Specific objectives were to assess uptake of vaccines including tetanus, diphtheria, and pertussis (Tdap), meningococcal, measles, mumps, and rubella (MMR), severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), influenza, herpes zoster, human papillomavirus (HPV), hepatitis B virus (HBV), hepatitis A virus (HAV), and varicella-zoster virus (VZV), to identify gaps in coverage, and to propose interventions to improve adherence. Methods A retrospective review of 24 patients with IBD receiving regular biologic infusions at the hospital's day ward was conducted. Data collected included demographics, type of IBD, biologic therapy details, and vaccination status. The assessment was based on the European Crohn's and Colitis Organisation (ECCO)-aligned immunisation recommendations. Immunity to VZV was accepted based on documented infection history or serological confirmation. Results Among the 24 patients reviewed, 14 had ulcerative colitis and 10 had Crohn's disease. Sixteen were male and eight female. Twenty patients were on infliximab and four on vedolizumab. Vaccination coverage was generally low: Tdap (5/11, 45.5%), meningococcal (1/4, 25%), MMR (1/2, 50%), SARS-CoV-2 (0/4, 0%), influenza (1/10, 10%), HPV (1/3 eligible females, 33.3%), HBV (2/15, 13.3%), and HAV (0/4, 0%). All six patients with VZV data showed immunity. No documentation was available for herpes zoster vaccination. Conclusion The audit revealed significant gaps in adherence to vaccination guidelines among IBD patients receiving biologics. These findings highlight the need for systematic interventions to improve vaccine uptake, such as routine immunisation status reviews during clinic visits, improved documentation practices, patient education on vaccine safety and necessity, and stronger collaboration between gastroenterologists and primary care providers. Educational materials should be provided during clinic or infusion appointments to address vaccine hesitancy and misinformation. Implementing these changes could reduce the burden of vaccine-preventable diseases in this vulnerable population.
{"title":"Adherence to Recommended Immunisation Schedules for Patients With Inflammatory Bowel Disease (IBD) on Biologics: A Retrospective Study at Our Lady's Hospital, Navan, Ireland.","authors":"Adnan Khan, Maheen Shahab, Malik Maqsood Anwar","doi":"10.7759/cureus.105024","DOIUrl":"10.7759/cureus.105024","url":null,"abstract":"<p><p>Introduction Patients with inflammatory bowel disease (IBD), particularly those receiving biologic therapies, are at increased risk of infections due to immunosuppression. Vaccinations play a vital role in reducing this risk, yet adherence to immunisation schedules remains suboptimal. This audit aimed to assess vaccination coverage among IBD patients on biologic therapies at Our Lady's Hospital, Navan, Ireland, and to identify areas for improvement. Aim and objectives The primary aim was to evaluate adherence to recommended immunisation schedules for IBD patients on biologics. Specific objectives were to assess uptake of vaccines including tetanus, diphtheria, and pertussis (Tdap), meningococcal, measles, mumps, and rubella (MMR), severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), influenza, herpes zoster, human papillomavirus (HPV), hepatitis B virus (HBV), hepatitis A virus (HAV), and varicella-zoster virus (VZV), to identify gaps in coverage, and to propose interventions to improve adherence. Methods A retrospective review of 24 patients with IBD receiving regular biologic infusions at the hospital's day ward was conducted. Data collected included demographics, type of IBD, biologic therapy details, and vaccination status. The assessment was based on the European Crohn's and Colitis Organisation (ECCO)-aligned immunisation recommendations. Immunity to VZV was accepted based on documented infection history or serological confirmation. Results Among the 24 patients reviewed, 14 had ulcerative colitis and 10 had Crohn's disease. Sixteen were male and eight female. Twenty patients were on infliximab and four on vedolizumab. Vaccination coverage was generally low: Tdap (5/11, 45.5%), meningococcal (1/4, 25%), MMR (1/2, 50%), SARS-CoV-2 (0/4, 0%), influenza (1/10, 10%), HPV (1/3 eligible females, 33.3%), HBV (2/15, 13.3%), and HAV (0/4, 0%). All six patients with VZV data showed immunity. No documentation was available for herpes zoster vaccination. Conclusion The audit revealed significant gaps in adherence to vaccination guidelines among IBD patients receiving biologics. These findings highlight the need for systematic interventions to improve vaccine uptake, such as routine immunisation status reviews during clinic visits, improved documentation practices, patient education on vaccine safety and necessity, and stronger collaboration between gastroenterologists and primary care providers. Educational materials should be provided during clinic or infusion appointments to address vaccine hesitancy and misinformation. Implementing these changes could reduce the burden of vaccine-preventable diseases in this vulnerable population.</p>","PeriodicalId":93960,"journal":{"name":"Cureus","volume":"18 3","pages":"e105024"},"PeriodicalIF":1.3,"publicationDate":"2026-03-11","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12981608/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"147464503","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2026-03-10eCollection Date: 2026-03-01DOI: 10.7759/cureus.105004
Raghad O Alsaedi, Mohammed K Al-Hanawi
Background Chronic diseases are emerging as a growing concern in Saudi Arabia, contributing to increased morbidity, mortality, healthcare costs, and reduced health-related quality of life (HRQoL). HRQoL is influenced by disease and treatment and is commonly assessed using the EuroQol five-dimensions five-levels (EQ-5D-5L) instrument. Assessing HRQoL helps in identifying areas that can be improved, ultimately leading to enhanced patient care and outcomes. Objective The study aims to evaluate the HRQoL among patients with chronic diseases and to assess the association of sociodemographic, clinical, lifestyle, and disease-related factors with HRQoL in Jeddah, Saudi Arabia. Methods A cross-sectional, multicenter study was conducted. Data were obtained using either interview-administered or self-administered questionnaires. The first section included patients' specific variables, while the second section consisted of the EQ-5D instrument. Results The study included 503 participants. The mean age of the participants was 44.3±13.8 years. The mean EQ-5D index score was 0.84±0.23, and the mean EQ-visual analogue scale (EQ-VAS) score was 77.22±20.60, indicating a generally good level of HRQoL at the population level. A strong relationship was observed between increasing chronic disease burden (multimorbidity) and poorer HRQoL across the overall sample, whereas the mean disease duration was not significantly related to HRQoL. Conclusion Patients with chronic diseases in Jeddah reported moderate to good HRQoL, the overall mean EQ-5D index score was 0.84±0.23, and the mean EQ-VAS score was 77.22±20.60. More than half of the participants experienced impaired health, especially in pain and psychological well-being. Multimorbidity was the most significant cause of impaired HRQoL, whereas the disease duration was not significantly related to HRQoL.
{"title":"Evaluation of Factors Associated With Health-Related Quality of Life in Patients With Chronic Diseases in Jeddah, Saudi Arabia: A Cross-Sectional Study.","authors":"Raghad O Alsaedi, Mohammed K Al-Hanawi","doi":"10.7759/cureus.105004","DOIUrl":"https://doi.org/10.7759/cureus.105004","url":null,"abstract":"<p><p>Background Chronic diseases are emerging as a growing concern in Saudi Arabia, contributing to increased morbidity, mortality, healthcare costs, and reduced health-related quality of life (HRQoL). HRQoL is influenced by disease and treatment and is commonly assessed using the EuroQol five-dimensions five-levels (EQ-5D-5L) instrument. Assessing HRQoL helps in identifying areas that can be improved, ultimately leading to enhanced patient care and outcomes. Objective The study aims to evaluate the HRQoL among patients with chronic diseases and to assess the association of sociodemographic, clinical, lifestyle, and disease-related factors with HRQoL in Jeddah, Saudi Arabia. Methods A cross-sectional, multicenter study was conducted. Data were obtained using either interview-administered or self-administered questionnaires. The first section included patients' specific variables, while the second section consisted of the EQ-5D instrument. Results The study included 503 participants. The mean age of the participants was 44.3±13.8 years. The mean EQ-5D index score was 0.84±0.23, and the mean EQ-visual analogue scale (EQ-VAS) score was 77.22±20.60, indicating a generally good level of HRQoL at the population level. A strong relationship was observed between increasing chronic disease burden (multimorbidity) and poorer HRQoL across the overall sample, whereas the mean disease duration was not significantly related to HRQoL. Conclusion Patients with chronic diseases in Jeddah reported moderate to good HRQoL, the overall mean EQ-5D index score was 0.84±0.23, and the mean EQ-VAS score was 77.22±20.60. More than half of the participants experienced impaired health, especially in pain and psychological well-being. Multimorbidity was the most significant cause of impaired HRQoL, whereas the disease duration was not significantly related to HRQoL.</p>","PeriodicalId":93960,"journal":{"name":"Cureus","volume":"18 3","pages":"e105004"},"PeriodicalIF":1.3,"publicationDate":"2026-03-10","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12975146/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"147438455","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2026-03-10eCollection Date: 2026-03-01DOI: 10.7759/cureus.105016
Bruno Bordoni, Enricomaria Mattia, Bruno Morabito
Chronic obstructive pulmonary disease (COPD) is a condition that inevitably leads to airflow limitation. COPD is among the leading causes of increased mortality and morbidity worldwide. A non-invasive and non-pharmacological approach is rehabilitation training, where the patient follows an active program to stimulate the limb and respiratory muscles. Training involves a constant increase in workloads throughout the rehabilitation process. A fundamental concept absent from the literature is that of including training sessions with reduced loads and periods of "unloading" intensity within the rehabilitation program. Without adequate recovery and rest between sessions, the patient may lack the resources necessary to tackle a subsequent demanding rehabilitation session. This situation could lead to the onset of overtraining syndrome (OTS), where the patient experiences an unexplained decline in performance. The article reviews the muscular adaptation of COPD patients and the planned rehabilitation and emphasizes the concept that clinicians should structure the rehabilitation training program not in a linear fashion (constantly increasing loads), but in a wave-like fashion (scheduling some sessions with decreased loads). This organization could benefit the patient's performance, reducing the risk of OTS.
{"title":"Chronic Obstructive Pulmonary Disease and Overtraining Syndrome: A Narrative Review.","authors":"Bruno Bordoni, Enricomaria Mattia, Bruno Morabito","doi":"10.7759/cureus.105016","DOIUrl":"https://doi.org/10.7759/cureus.105016","url":null,"abstract":"<p><p>Chronic obstructive pulmonary disease (COPD) is a condition that inevitably leads to airflow limitation. COPD is among the leading causes of increased mortality and morbidity worldwide. A non-invasive and non-pharmacological approach is rehabilitation training, where the patient follows an active program to stimulate the limb and respiratory muscles. Training involves a constant increase in workloads throughout the rehabilitation process. A fundamental concept absent from the literature is that of including training sessions with reduced loads and periods of \"unloading\" intensity within the rehabilitation program. Without adequate recovery and rest between sessions, the patient may lack the resources necessary to tackle a subsequent demanding rehabilitation session. This situation could lead to the onset of overtraining syndrome (OTS), where the patient experiences an unexplained decline in performance. The article reviews the muscular adaptation of COPD patients and the planned rehabilitation and emphasizes the concept that clinicians should structure the rehabilitation training program not in a linear fashion (constantly increasing loads), but in a wave-like fashion (scheduling some sessions with decreased loads). This organization could benefit the patient's performance, reducing the risk of OTS.</p>","PeriodicalId":93960,"journal":{"name":"Cureus","volume":"18 3","pages":"e105016"},"PeriodicalIF":1.3,"publicationDate":"2026-03-10","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12976572/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"147446474","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2026-03-10eCollection Date: 2026-03-01DOI: 10.7759/cureus.104994
Mohamed A Areed, Mohamed Elawdy, Ali Albalushi, Shahad S Almamari
Foreign body (FB) ingestion is common in children below six years of age. Most FBs are passed spontaneously through the gastrointestinal tract. However, multiple magnetic ingestion increases the risk of intestinal obstruction and perforation via magnetic attraction through bowel walls. We report a case of a four-year-old boy who came with a delayed presentation of multiple magnet ingestion over a year before presentation to the emergency department. The diagnosis was overlooked in the first presentation by the primary health care doctor, and the FBs in the X-ray were interpreted as being an artifact. This case underscores the need for increased clinician awareness of having a high index of suspicion of FB ingestion in pediatric cases presenting with prolonged vague abdominal pain and to be vigilant upon reviewing radiological images.
{"title":"Multiple Magnet Ingestion in a Child With an Overlooked Diagnosis Leading to Intestinal Perforation.","authors":"Mohamed A Areed, Mohamed Elawdy, Ali Albalushi, Shahad S Almamari","doi":"10.7759/cureus.104994","DOIUrl":"https://doi.org/10.7759/cureus.104994","url":null,"abstract":"<p><p>Foreign body (FB) ingestion is common in children below six years of age. Most FBs are passed spontaneously through the gastrointestinal tract. However, multiple magnetic ingestion increases the risk of intestinal obstruction and perforation via magnetic attraction through bowel walls. We report a case of a four-year-old boy who came with a delayed presentation of multiple magnet ingestion over a year before presentation to the emergency department. The diagnosis was overlooked in the first presentation by the primary health care doctor, and the FBs in the X-ray were interpreted as being an artifact. This case underscores the need for increased clinician awareness of having a high index of suspicion of FB ingestion in pediatric cases presenting with prolonged vague abdominal pain and to be vigilant upon reviewing radiological images.</p>","PeriodicalId":93960,"journal":{"name":"Cureus","volume":"18 3","pages":"e104994"},"PeriodicalIF":1.3,"publicationDate":"2026-03-10","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12977819/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"147446485","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2026-03-10eCollection Date: 2026-03-01DOI: 10.7759/cureus.105009
Roberto R Gonzalez Alvarez
Drug reaction with eosinophilia and systemic symptoms (DRESS), also known as drug-induced hypersensitivity syndrome (DIHS), is a severe, multiorgan, delayed hypersensitivity reaction with significant morbidity. Diagnosis is often delayed due to its mimicry of other conditions. We present the case of a 69-year-old Hispanic male with hypertension and stage two chronic kidney disease who developed trigeminal neuralgia and was started on carbamazepine. Approximately seven weeks later, he presented with a generalized rash, angioedema, and mucosal swelling, initially attributed to his concurrent lisinopril therapy. Despite discontinuation of lisinopril and treatment with corticosteroids and antihistamines, his condition progressed with new systemic symptoms, including paresthesia, dysgeusia, polydipsia, polyuria, and weight loss. The progression of symptoms despite this intervention was the pivotal diagnostic clue. Hospital admission revealed marked eosinophilia (8.9 percent), mild transaminitis, and a diffuse erythrodermic rash involving more than 90 percent of his body surface area. A diagnosis of probable DRESS syndrome (RegiSCAR score six) secondary to carbamazepine was made. Immediate discontinuation of carbamazepine and initiation of intravenous corticosteroids led to rapid clinical and laboratory improvement. He was discharged on a prolonged oral steroid taper with complete resolution at follow-up. This case underscores the critical importance of considering DRESS in any patient with a rash and systemic symptoms occurring two to eight weeks after initiation of a high-risk drug, even in the presence of other potential culprits. It highlights that clinical progression despite withdrawal of one suspected agent should prompt urgent re-evaluation for an alternative etiology, such as DRESS.
{"title":"A Diagnostic Pitfall: Carbamazepine-Induced Drug Reaction With Eosinophilia and Systemic Symptoms (DRESS) Syndrome Masquerading As Angiotensin-Converting Enzyme Inhibitor Angioedema.","authors":"Roberto R Gonzalez Alvarez","doi":"10.7759/cureus.105009","DOIUrl":"https://doi.org/10.7759/cureus.105009","url":null,"abstract":"<p><p>Drug reaction with eosinophilia and systemic symptoms (DRESS), also known as drug-induced hypersensitivity syndrome (DIHS), is a severe, multiorgan, delayed hypersensitivity reaction with significant morbidity. Diagnosis is often delayed due to its mimicry of other conditions. We present the case of a 69-year-old Hispanic male with hypertension and stage two chronic kidney disease who developed trigeminal neuralgia and was started on carbamazepine. Approximately seven weeks later, he presented with a generalized rash, angioedema, and mucosal swelling, initially attributed to his concurrent lisinopril therapy. Despite discontinuation of lisinopril and treatment with corticosteroids and antihistamines, his condition progressed with new systemic symptoms, including paresthesia, dysgeusia, polydipsia, polyuria, and weight loss. The progression of symptoms despite this intervention was the pivotal diagnostic clue. Hospital admission revealed marked eosinophilia (8.9 percent), mild transaminitis, and a diffuse erythrodermic rash involving more than 90 percent of his body surface area. A diagnosis of probable DRESS syndrome (RegiSCAR score six) secondary to carbamazepine was made. Immediate discontinuation of carbamazepine and initiation of intravenous corticosteroids led to rapid clinical and laboratory improvement. He was discharged on a prolonged oral steroid taper with complete resolution at follow-up. This case underscores the critical importance of considering DRESS in any patient with a rash and systemic symptoms occurring two to eight weeks after initiation of a high-risk drug, even in the presence of other potential culprits. It highlights that clinical progression despite withdrawal of one suspected agent should prompt urgent re-evaluation for an alternative etiology, such as DRESS.</p>","PeriodicalId":93960,"journal":{"name":"Cureus","volume":"18 3","pages":"e105009"},"PeriodicalIF":1.3,"publicationDate":"2026-03-10","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12978419/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"147446476","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2026-03-10eCollection Date: 2026-03-01DOI: 10.7759/cureus.104983
Mustafa Kraidi, Iain Wilkinson, Somaditya Bandyopadhyay
<p><strong>Background: </strong>The procollagen type 1 N-terminal propeptide (P1NP), a byproduct of type I collagen synthesis, is useful in clinically monitoring anti-resorption medications. The role of P1NP in anti-resorption therapy in older bisphosphonate-taking individuals who have suffered another fracture is unclear.</p><p><strong>Objectives: </strong> This study aims to describe serum P1NP levels in patients aged ≥60 years who sustained a fragility neck of femur fracture while receiving osteoporosis therapy and to describe how P1NP results were associated with subsequent bone health management decisions, defined as documented decisions to continue, stop, or change osteoporosis therapy (including switch/escalation) and/or request additional investigations.</p><p><strong>Methods: </strong>This retrospective descriptive cohort study, conducted between March 2017 and September 2021, involved patients aged 60 years or older who experienced intra- or extracapsular femoral neck fractures while receiving osteoporosis therapy and had serum P1NP assessed before surgery. Routinely collected data were extracted from departmental databases and systems accessible through the NHS computers at East Surrey Hospital as part of an ongoing quality improvement project.</p><p><strong>Results: </strong> Out of the 2,303 total fractures during the study period, 58 patients (2.5%) had serum P1NP levels tested. The mean age was 84.6 ± 8.08 years, with a female-to-male ratio of 8.7:1; 34 (58.6%) had intracapsular and 24 (41.6%) had extracapsular types of fractures. Eighteen patients (31%) had P1NP levels of 40 ug/l or higher; six (10.3%) had P1NP levels between 36 and 39 ug/l, and 34 patients (58.6%) exhibited suppressed P1NP levels (below 35 ug/l). For those who had suppressed P1NP, five (55.6%) of the nine patients (who had been receiving treatment for over five years) had their treatment discontinued, two (22.2%) had their treatment plans modified because of DXA scan results, and two remained on the same treatment plan. Three patients on therapy for up to five years had P1NP levels above 40 ug/l owing to memory loss or inexperience with oral alendronate; therefore, adherence was low. Change to IV zoledronate or patient education was offered.</p><p><strong>Conclusion: </strong> In this selected cohort, measuring pre-operative P1NP levels supported patient-centred multidisciplinary (MDT) bone health planning. Clinicians considered P1NP alongside DXA findings and the broader clinical context when documenting MDT post-fracture bone health plans, with management changes commonly recorded among patients receiving long-term therapy (>5 years). Notably, in this long-term treated group, suppressed P1NP commonly coincided with documented decisions to stop or adjust therapy. Given the retrospective design, small sample size, lack of a comparator group, and absence of outcome data, these findings provide real-world insight into current practice and may support development of
{"title":"Can P1NP Levels Influence Management Planning for Patients With a Fragility Hip Fracture Receiving Anti-resorptive Medications?","authors":"Mustafa Kraidi, Iain Wilkinson, Somaditya Bandyopadhyay","doi":"10.7759/cureus.104983","DOIUrl":"https://doi.org/10.7759/cureus.104983","url":null,"abstract":"<p><strong>Background: </strong>The procollagen type 1 N-terminal propeptide (P1NP), a byproduct of type I collagen synthesis, is useful in clinically monitoring anti-resorption medications. The role of P1NP in anti-resorption therapy in older bisphosphonate-taking individuals who have suffered another fracture is unclear.</p><p><strong>Objectives: </strong> This study aims to describe serum P1NP levels in patients aged ≥60 years who sustained a fragility neck of femur fracture while receiving osteoporosis therapy and to describe how P1NP results were associated with subsequent bone health management decisions, defined as documented decisions to continue, stop, or change osteoporosis therapy (including switch/escalation) and/or request additional investigations.</p><p><strong>Methods: </strong>This retrospective descriptive cohort study, conducted between March 2017 and September 2021, involved patients aged 60 years or older who experienced intra- or extracapsular femoral neck fractures while receiving osteoporosis therapy and had serum P1NP assessed before surgery. Routinely collected data were extracted from departmental databases and systems accessible through the NHS computers at East Surrey Hospital as part of an ongoing quality improvement project.</p><p><strong>Results: </strong> Out of the 2,303 total fractures during the study period, 58 patients (2.5%) had serum P1NP levels tested. The mean age was 84.6 ± 8.08 years, with a female-to-male ratio of 8.7:1; 34 (58.6%) had intracapsular and 24 (41.6%) had extracapsular types of fractures. Eighteen patients (31%) had P1NP levels of 40 ug/l or higher; six (10.3%) had P1NP levels between 36 and 39 ug/l, and 34 patients (58.6%) exhibited suppressed P1NP levels (below 35 ug/l). For those who had suppressed P1NP, five (55.6%) of the nine patients (who had been receiving treatment for over five years) had their treatment discontinued, two (22.2%) had their treatment plans modified because of DXA scan results, and two remained on the same treatment plan. Three patients on therapy for up to five years had P1NP levels above 40 ug/l owing to memory loss or inexperience with oral alendronate; therefore, adherence was low. Change to IV zoledronate or patient education was offered.</p><p><strong>Conclusion: </strong> In this selected cohort, measuring pre-operative P1NP levels supported patient-centred multidisciplinary (MDT) bone health planning. Clinicians considered P1NP alongside DXA findings and the broader clinical context when documenting MDT post-fracture bone health plans, with management changes commonly recorded among patients receiving long-term therapy (>5 years). Notably, in this long-term treated group, suppressed P1NP commonly coincided with documented decisions to stop or adjust therapy. Given the retrospective design, small sample size, lack of a comparator group, and absence of outcome data, these findings provide real-world insight into current practice and may support development of","PeriodicalId":93960,"journal":{"name":"Cureus","volume":"18 3","pages":"e104983"},"PeriodicalIF":1.3,"publicationDate":"2026-03-10","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12977867/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"147446503","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}