{"title":"Medical Rehabilitation for Life Changing Conditions.","authors":"Edwin C Jesudason","doi":"10.12968/hmed.2025.0667","DOIUrl":"https://doi.org/10.12968/hmed.2025.0667","url":null,"abstract":"","PeriodicalId":9256,"journal":{"name":"British journal of hospital medicine","volume":"86 11","pages":"1-6"},"PeriodicalIF":1.8,"publicationDate":"2025-11-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145585988","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-11-25Epub Date: 2025-11-21DOI: 10.12968/hmed.2025.0291
Sarah Danson, Robert P Jones, Matthew Hallsworth, Gillian Rosenberg, Maria Koufali
{"title":"Advancing Cancer Vaccines: The UK's Strategic Approach to Research and Innovation.","authors":"Sarah Danson, Robert P Jones, Matthew Hallsworth, Gillian Rosenberg, Maria Koufali","doi":"10.12968/hmed.2025.0291","DOIUrl":"https://doi.org/10.12968/hmed.2025.0291","url":null,"abstract":"","PeriodicalId":9256,"journal":{"name":"British journal of hospital medicine","volume":"86 11","pages":"1-6"},"PeriodicalIF":1.8,"publicationDate":"2025-11-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145586072","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-11-25Epub Date: 2025-11-05DOI: 10.12968/hmed.2025.0132
Chengli Lou, Xuanli Tang, Yijing Zhou, Xiuqin Xu, Ke Huang, Xiaoping Fan, Pingxin Hu, Xiangjing Wang, Bo Feng
Aims/Background Membranous nephropathy (MN) is categorized into primary and secondary forms based on its etiology, with autoimmune diseases significantly contributing to the secondary form. The phospholipase A2 receptor (PLA2R) antibody has been widely used as a specific marker for primary MN. However, explaining PLA2R positivity in MN patients who also exhibit typical features of Sjögren's syndrome (SS) is challenging. Case Presentation A 51-year-old male patient presented with acute systemic edema, hypertension, macroalbuminuria, and hypoproteinemia, confirming a diagnosis of nephrotic syndrome. Concurrently, SS, characterized by dry mouth and dry eye symptoms, positive specific antibodies, and positive labial gland biopsy results, was also confirmed. Renal pathology indicated MN (stage I-II) with moderate secondary chronic renal tubulointerstitial lesions. The cluster of differentiation 3 (CD3)+ and CD20+ immunostaining of renal tissue was consistent with renal interstitial damage associated with SS, and the clinical manifestations aligned with the typical presentation of renal tubular acidosis (RTA). PLA2R was negative in the serum but positive in the renal tissue. Conclusion SS is one of the autoimmune diseases associated with secondary membranous nephropathy, which has a low clinical incidence. In this particular case, the diagnosis of SS was confirmed, and the histopathological examination revealed typical tubulointerstitial lesions clinically accompanied by RTA. However, the specific antibody PLA2R, which is typically associated with primary MN, was positive in renal tissue. Additionally, IgG immunodeposition was not observed. Further investigation is warranted to ascertain whether the MN is secondary to SS.
{"title":"The Rare Occurrence of Tissue PLA2R-Positive Membranous Nephropathy in a Patient With Sjögren's Syndrome and Renal Tubular Acidosis.","authors":"Chengli Lou, Xuanli Tang, Yijing Zhou, Xiuqin Xu, Ke Huang, Xiaoping Fan, Pingxin Hu, Xiangjing Wang, Bo Feng","doi":"10.12968/hmed.2025.0132","DOIUrl":"10.12968/hmed.2025.0132","url":null,"abstract":"<p><p><b>Aims/Background</b> Membranous nephropathy (MN) is categorized into primary and secondary forms based on its etiology, with autoimmune diseases significantly contributing to the secondary form. The phospholipase A2 receptor (PLA2R) antibody has been widely used as a specific marker for primary MN. However, explaining PLA2R positivity in MN patients who also exhibit typical features of Sjögren's syndrome (SS) is challenging. <b>Case Presentation</b> A 51-year-old male patient presented with acute systemic edema, hypertension, macroalbuminuria, and hypoproteinemia, confirming a diagnosis of nephrotic syndrome. Concurrently, SS, characterized by dry mouth and dry eye symptoms, positive specific antibodies, and positive labial gland biopsy results, was also confirmed. Renal pathology indicated MN (stage I-II) with moderate secondary chronic renal tubulointerstitial lesions. The cluster of differentiation 3 (CD3)+ and CD20+ immunostaining of renal tissue was consistent with renal interstitial damage associated with SS, and the clinical manifestations aligned with the typical presentation of renal tubular acidosis (RTA). PLA2R was negative in the serum but positive in the renal tissue. <b>Conclusion</b> SS is one of the autoimmune diseases associated with secondary membranous nephropathy, which has a low clinical incidence. In this particular case, the diagnosis of SS was confirmed, and the histopathological examination revealed typical tubulointerstitial lesions clinically accompanied by RTA. However, the specific antibody PLA2R, which is typically associated with primary MN, was positive in renal tissue. Additionally, IgG immunodeposition was not observed. Further investigation is warranted to ascertain whether the MN is secondary to SS.</p>","PeriodicalId":9256,"journal":{"name":"British journal of hospital medicine","volume":"86 11","pages":"1-12"},"PeriodicalIF":1.8,"publicationDate":"2025-11-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145586158","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-11-25Epub Date: 2025-11-07DOI: 10.12968/hmed.2025.0089
Nidhi Rohatgi, Valerie Michele Vaughn, Ebrahim Barkoudah, Blair Pollitt Golden, Farah Acher Kaiksow, Angela Keniston, James David Harrison, Juliessa Marta Pavon, Micah Thomas Prochaska, Ché Matthew Harris
Aims/Background Mentorship is crucial to research success, but a detailed assessment and evaluation of the different types of mentorship models in hospital medicine have not been conducted. We sought to identify and define research mentorship models in hospital medicine. We also assessed the effectiveness of each model for the identified studies that met this narrative review's criteria. Methods Narrative review of peer-reviewed, USA-published literature on hospital medicine research mentorship. Articles from 1996 to 2023 with selected search terms on hospitalists' mentorship in research were searched in PubMed, Scopus and Embase. Finalized articles obtained from the search were approved by the Society of Hospital Medicine's Research Committee. Results Ten articles published between 2008 and 2023 were identified and assessed by the Society of Hospital Medicine's Research Committee members. Three major research mentorship models were identified: (1) traditional mentor-mentee dyad, (2) peer mentorship, and (3) research coaching. Some hospital medicine groups combined mentorship models. All articles reported successful implementation with positive faculty receptivity and/or research output. However, the studies had small sample sizes and short evaluation periods. Conclusion Hospitalist research mentorship is essential to bolstering and enhancing research in hospital medicine. Further studies with larger samples, extended time frames, those conducted outside the USA, and frequent reassessments are urgently needed to determine the sustained effectiveness of any model.
{"title":"Research Mentorship Models in Hospital Medicine: A Narrative Review.","authors":"Nidhi Rohatgi, Valerie Michele Vaughn, Ebrahim Barkoudah, Blair Pollitt Golden, Farah Acher Kaiksow, Angela Keniston, James David Harrison, Juliessa Marta Pavon, Micah Thomas Prochaska, Ché Matthew Harris","doi":"10.12968/hmed.2025.0089","DOIUrl":"10.12968/hmed.2025.0089","url":null,"abstract":"<p><p><b>Aims/Background</b> Mentorship is crucial to research success, but a detailed assessment and evaluation of the different types of mentorship models in hospital medicine have not been conducted. We sought to identify and define research mentorship models in hospital medicine. We also assessed the effectiveness of each model for the identified studies that met this narrative review's criteria. <b>Methods</b> Narrative review of peer-reviewed, USA-published literature on hospital medicine research mentorship. Articles from 1996 to 2023 with selected search terms on hospitalists' mentorship in research were searched in PubMed, Scopus and Embase. Finalized articles obtained from the search were approved by the Society of Hospital Medicine's Research Committee. <b>Results</b> Ten articles published between 2008 and 2023 were identified and assessed by the Society of Hospital Medicine's Research Committee members. Three major research mentorship models were identified: (1) traditional mentor-mentee dyad, (2) peer mentorship, and (3) research coaching. Some hospital medicine groups combined mentorship models. All articles reported successful implementation with positive faculty receptivity and/or research output. However, the studies had small sample sizes and short evaluation periods. <b>Conclusion</b> Hospitalist research mentorship is essential to bolstering and enhancing research in hospital medicine. Further studies with larger samples, extended time frames, those conducted outside the USA, and frequent reassessments are urgently needed to determine the sustained effectiveness of any model.</p>","PeriodicalId":9256,"journal":{"name":"British journal of hospital medicine","volume":"86 11","pages":"1-18"},"PeriodicalIF":1.8,"publicationDate":"2025-11-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145586093","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-11-25Epub Date: 2025-11-07DOI: 10.12968/hmed.2024.0651
Keke Wu, Jie Qin, Feifei Zheng, Juanjuan Lin
Aims/Background Sepsis remains a major cause of mortality in intensive care units (ICUs) worldwide, with conventional treatments showing limited efficacy. Extracorporeal hemopurification (EH) techniques have emerged as promising adjunctive therapies. This study aims to explore the impact of EH techniques, including hemofiltration, hemoperfusion, hemodialysis, and hemosorption, on the clinical prognosis and immune function of patients with sepsis. Methods We searched relevant literature describing patients with a precise clinical diagnosis of sepsis, severe sepsis, or septic shock across various databases, including MEDLINE, AMED, Cochrane Library, Embase, PubMed, China National Knowledge Infrastructure (CNKI), Weipu, and Wanfang, published from January 2010 to October 2023. Both randomized controlled trials and observational studies were included to compare those receiving EH and conventional anti-infective treatment. Meta-analysis was performed using RevMan 5.3 software after two evaluators independently screened the literature, extracted information, and evaluated the methodological quality of the included studies. The primary outcome indicators included in-hospital mortality (IHM) and length of ICU stay (LOS-ICU). Furthermore, the changes in T-helper 1/T-helper 2 (Th1/Th2) levels were analyzed and expressed as relative risk (RR), odds ratio (OR), or mean difference (MD) with corresponding 95% confidence interval (CI) as appropriate for the type of outcome measure. Results This analysis included 30 studies (n = 2262) (1267 in the EH group and 995 in the conventional treatment group). We observed that EH treatment, such as hemopurification, hemofiltration, hemoperfusion, hemodialysis, and hemoadsorption, significantly reduced IHM in sepsis patients (RR = 0.75, 95% CI: 0.68-0.84, p < 0.00001). However, there was no significant impact on LOS-ICU (MD = -0.44, 95% CI: -2.29-1.41, p = 0.64). Subgroup analyses suggested that cytokine adsorption (OR = 0.69, p = 0.17) or polymyxin B blood perfusion (OR = 0.73, p = 0.06) did not reduce IHM in sepsis patients. Similarly, EH did not improve IHM in patients with septic acute renal failure (RR = 0.82, p = 0.27) and IHM in patients with burn-induced sepsis (RR = 0.59, p = 0.07). For sepsis patients with improved Th1/Th2 value of immune factor levels by EH, IHM was not significantly reduced (RR = 0.61, p = 0.08), and LOS-ICU also showed no significant difference (MD = 0.34, 95% CI: -5.92-6.60, p = 0.92). Conclusion For sepsis patients without relevant contraindications, EH holds promise as an adjunctive therapy, but the modulation of immune factor levels during treatment does not consistently influence the LOS-ICU.
目的/背景脓毒症仍然是全球重症监护病房(icu)死亡的主要原因,常规治疗效果有限。体外血液纯化(EH)技术已成为有前途的辅助治疗。本研究旨在探讨EH技术,包括血液滤过、血液灌流、血液透析和血液吸收对脓毒症患者临床预后和免疫功能的影响。方法检索2010年1月至2023年10月发表的MEDLINE、AMED、Cochrane Library、Embase、PubMed、CNKI、Weipu、万方等数据库中描述临床诊断为脓毒症、严重脓毒症或脓毒症休克患者的相关文献。包括随机对照试验和观察性研究,以比较接受EH和常规抗感染治疗的患者。两名评估者独立筛选文献、提取信息并评估纳入研究的方法学质量后,使用RevMan 5.3软件进行meta分析。主要结局指标包括住院死亡率(IHM)和ICU住院时间(LOS-ICU)。此外,分析t -辅助性1/ t -辅助性2 (Th1/Th2)水平的变化,并以相对危险度(RR)、优势比(OR)或平均差异(MD)表示,并根据结果测量的类型使用相应的95%置信区间(CI)。结果共纳入30项研究(n = 2262),其中EH组1267项,常规治疗组995项。我们观察到EH治疗,如血液净化、血液滤过、血液灌流、血液透析和血液吸附,显著降低脓毒症患者的IHM (RR = 0.75, 95% CI: 0.68-0.84, p < 0.00001)。然而,对LOS-ICU无显著影响(MD = -0.44, 95% CI: -2.29-1.41, p = 0.64)。亚组分析显示,细胞因子吸附(OR = 0.69, p = 0.17)或多粘菌素B血灌注(OR = 0.73, p = 0.06)并没有降低脓毒症患者的IHM。同样,EH并没有改善脓毒性急性肾衰竭患者的IHM (RR = 0.82, p = 0.27)和烧伤致脓毒症患者的IHM (RR = 0.59, p = 0.07)。EH改善免疫因子水平Th1/Th2值的脓毒症患者,IHM无显著降低(RR = 0.61, p = 0.08), LOS-ICU也无显著差异(MD = 0.34, 95% CI: -5.92 ~ 6.60, p = 0.92)。结论对于无相关禁忌症的脓毒症患者,EH有希望作为一种辅助治疗,但治疗期间免疫因子水平的调节并不总是影响LOS-ICU。
{"title":"The Effect of Extracorporeal Hemopurification Combined With Conventional Anti-Infection on Clinical Prognosis and Immune Function in Sepsis: A Meta-Analysis.","authors":"Keke Wu, Jie Qin, Feifei Zheng, Juanjuan Lin","doi":"10.12968/hmed.2024.0651","DOIUrl":"10.12968/hmed.2024.0651","url":null,"abstract":"<p><p><b>Aims/Background</b> Sepsis remains a major cause of mortality in intensive care units (ICUs) worldwide, with conventional treatments showing limited efficacy. Extracorporeal hemopurification (EH) techniques have emerged as promising adjunctive therapies. This study aims to explore the impact of EH techniques, including hemofiltration, hemoperfusion, hemodialysis, and hemosorption, on the clinical prognosis and immune function of patients with sepsis. <b>Methods</b> We searched relevant literature describing patients with a precise clinical diagnosis of sepsis, severe sepsis, or septic shock across various databases, including MEDLINE, AMED, Cochrane Library, Embase, PubMed, China National Knowledge Infrastructure (CNKI), Weipu, and Wanfang, published from January 2010 to October 2023. Both randomized controlled trials and observational studies were included to compare those receiving EH and conventional anti-infective treatment. Meta-analysis was performed using RevMan 5.3 software after two evaluators independently screened the literature, extracted information, and evaluated the methodological quality of the included studies. The primary outcome indicators included in-hospital mortality (IHM) and length of ICU stay (LOS-ICU). Furthermore, the changes in T-helper 1/T-helper 2 (Th1/Th2) levels were analyzed and expressed as relative risk (RR), odds ratio (OR), or mean difference (MD) with corresponding 95% confidence interval (CI) as appropriate for the type of outcome measure. <b>Results</b> This analysis included 30 studies (<i>n</i> = 2262) (1267 in the EH group and 995 in the conventional treatment group). We observed that EH treatment, such as hemopurification, hemofiltration, hemoperfusion, hemodialysis, and hemoadsorption, significantly reduced IHM in sepsis patients (RR = 0.75, 95% CI: 0.68-0.84, <i>p</i> < 0.00001). However, there was no significant impact on LOS-ICU (MD = -0.44, 95% CI: -2.29-1.41, <i>p</i> = 0.64). Subgroup analyses suggested that cytokine adsorption (OR = 0.69, <i>p</i> = 0.17) or polymyxin B blood perfusion (OR = 0.73, <i>p</i> = 0.06) did not reduce IHM in sepsis patients. Similarly, EH did not improve IHM in patients with septic acute renal failure (RR = 0.82, <i>p</i> = 0.27) and IHM in patients with burn-induced sepsis (RR = 0.59, <i>p</i> = 0.07). For sepsis patients with improved Th1/Th2 value of immune factor levels by EH, IHM was not significantly reduced (RR = 0.61, <i>p</i> = 0.08), and LOS-ICU also showed no significant difference (MD = 0.34, 95% CI: -5.92-6.60, <i>p</i> = 0.92). <b>Conclusion</b> For sepsis patients without relevant contraindications, EH holds promise as an adjunctive therapy, but the modulation of immune factor levels during treatment does not consistently influence the LOS-ICU.</p>","PeriodicalId":9256,"journal":{"name":"British journal of hospital medicine","volume":"86 11","pages":"1-16"},"PeriodicalIF":1.8,"publicationDate":"2025-11-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145586150","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-11-25Epub Date: 2025-11-07DOI: 10.12968/hmed.2024.0776
Hui Sun, Yuyu Li
<p><p><b>Aims/Background</b> The efficacy of antiplatelet therapy exhibits interindividual variability, highlighting the need to identify underlying factors contributing to this heterogeneity in clinical settings. Increasing clinical attention has been directed toward genetic polymorphisms, aiming to optimise antiplatelet therapy based on patient genotype to enhance treatment efficacy and improve prognosis. This study aimed to analyse the relationship between cytochrome P450 2C19 (<i>CYP2C19</i>) and glycoprotein 1b alpha subunit gene (<i>GP1BA</i>) polymorphism and the efficacy of antiplatelet therapy and prognosis in patients with acute cerebral infarction (ACI). <b>Methods</b> A total of 200 ACI patients treated at First Affiliated Hospital of Bengbu Medical University between January 2021 and May 2024 were enrolled. The distributions of <i>CYP2C19</i> and <i>GP1BA</i> gene polymorphisms were determined. Differences in platelet inhibition rates among patients with various <i>CYP2C19</i> and <i>GP1BA</i> genotypes were compared. Clinical characteristics and genotype distributions were analysed between patients with varying prognoses. A nomogram model was constructed to predict prognosis. <b>Results</b> Among the <i>CYP2C19</i> genotypes, 84 patients were classified as fast metabolizers, 82 as intermediate metabolizers, and 34 as slow metabolizers. For <i>GP1BA</i>, 94 patients had the <i>CC</i> genotype, 78 had <i>CT</i>, and 28 had <i>TT</i>. The platelet inhibition rate in slow metabolizers was (50.12 ± 13.32) %, markedly lower than in fast and intermediate metabolizers (<i>p</i> < 0.05). Among <i>GP1BA</i> genotypes, the platelet inhibition rate in <i>CC</i> type patients was (55.30 ± 9.92) %, significantly lower than in <i>CT</i> and <i>TT</i> types (<i>p</i> < 0.05). Patients with poor prognosis had a mean age of (65.59 ± 9.92) years and a baseline National Institutes of Health Stroke Scale (NIHSS) score of (14.50 ± 2.02), both significantly higher than those in the good prognosis group (<i>p</i> < 0.05). The proportion of patients with diabetes in the poor prognosis group was 43.75%, significantly higher than in the good prognosis group (<i>p</i> < 0.05). Significant differences in <i>CYP2C19</i> and <i>GP1BA</i> genotype distributions were observed between patients with poor and good prognoses (<i>p</i> < 0.05). Logistic regression analysis identified age, NIHSS score at admission, diabetes, and both <i>CYP2C19</i> and <i>GP1BA</i> genotypes as independent factors influencing poor prognosis (<i>p</i> < 0.05). The nomogram model constructed for prognosis prediction showed good performance, with the area under the curve (AUC) of 0.815 (95% confidence interval [CI]: 0.737-0.894, <i>p</i> < 0.05). The model demonstrated a sensitivity of 87.5% and a specificity of 65.90%. <b>Conclusion</b> <i>CYP2C19</i> and <i>GP1BA</i> polymorphisms are related to the efficacy of antiplatelet therapy and are influencing factors for prognosis in ACI patients
{"title":"Association of <i>CYP2C19</i> and <i>GP1BA</i> Genetic Variants With Antiplatelet Efficacy, and Prognosis in Patients With Acute Cerebral Infarction, and the Development of a Prognostic Risk Nomogram Model.","authors":"Hui Sun, Yuyu Li","doi":"10.12968/hmed.2024.0776","DOIUrl":"10.12968/hmed.2024.0776","url":null,"abstract":"<p><p><b>Aims/Background</b> The efficacy of antiplatelet therapy exhibits interindividual variability, highlighting the need to identify underlying factors contributing to this heterogeneity in clinical settings. Increasing clinical attention has been directed toward genetic polymorphisms, aiming to optimise antiplatelet therapy based on patient genotype to enhance treatment efficacy and improve prognosis. This study aimed to analyse the relationship between cytochrome P450 2C19 (<i>CYP2C19</i>) and glycoprotein 1b alpha subunit gene (<i>GP1BA</i>) polymorphism and the efficacy of antiplatelet therapy and prognosis in patients with acute cerebral infarction (ACI). <b>Methods</b> A total of 200 ACI patients treated at First Affiliated Hospital of Bengbu Medical University between January 2021 and May 2024 were enrolled. The distributions of <i>CYP2C19</i> and <i>GP1BA</i> gene polymorphisms were determined. Differences in platelet inhibition rates among patients with various <i>CYP2C19</i> and <i>GP1BA</i> genotypes were compared. Clinical characteristics and genotype distributions were analysed between patients with varying prognoses. A nomogram model was constructed to predict prognosis. <b>Results</b> Among the <i>CYP2C19</i> genotypes, 84 patients were classified as fast metabolizers, 82 as intermediate metabolizers, and 34 as slow metabolizers. For <i>GP1BA</i>, 94 patients had the <i>CC</i> genotype, 78 had <i>CT</i>, and 28 had <i>TT</i>. The platelet inhibition rate in slow metabolizers was (50.12 ± 13.32) %, markedly lower than in fast and intermediate metabolizers (<i>p</i> < 0.05). Among <i>GP1BA</i> genotypes, the platelet inhibition rate in <i>CC</i> type patients was (55.30 ± 9.92) %, significantly lower than in <i>CT</i> and <i>TT</i> types (<i>p</i> < 0.05). Patients with poor prognosis had a mean age of (65.59 ± 9.92) years and a baseline National Institutes of Health Stroke Scale (NIHSS) score of (14.50 ± 2.02), both significantly higher than those in the good prognosis group (<i>p</i> < 0.05). The proportion of patients with diabetes in the poor prognosis group was 43.75%, significantly higher than in the good prognosis group (<i>p</i> < 0.05). Significant differences in <i>CYP2C19</i> and <i>GP1BA</i> genotype distributions were observed between patients with poor and good prognoses (<i>p</i> < 0.05). Logistic regression analysis identified age, NIHSS score at admission, diabetes, and both <i>CYP2C19</i> and <i>GP1BA</i> genotypes as independent factors influencing poor prognosis (<i>p</i> < 0.05). The nomogram model constructed for prognosis prediction showed good performance, with the area under the curve (AUC) of 0.815 (95% confidence interval [CI]: 0.737-0.894, <i>p</i> < 0.05). The model demonstrated a sensitivity of 87.5% and a specificity of 65.90%. <b>Conclusion</b> <i>CYP2C19</i> and <i>GP1BA</i> polymorphisms are related to the efficacy of antiplatelet therapy and are influencing factors for prognosis in ACI patients","PeriodicalId":9256,"journal":{"name":"British journal of hospital medicine","volume":"86 11","pages":"1-15"},"PeriodicalIF":1.8,"publicationDate":"2025-11-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145586054","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Varinder Kaur, Hannah Deacon, Michael Philip Barnes, David John Nutt
Epilepsy is a serious neurological condition that can affect individuals of all ages. Treatment is far from perfect, and roughly 30% of patients can experience seizures that are resistant to antiseizure medications. Interestingly, the cannabis plant, specifically the phytocannabinoids, cannabidiol and delta-9-tetrahydrocannabinol, has been shown to possess anticonvulsant properties and are effective in the treatment of seizures. The clinical evidence base for cannabis for epileptic conditions has been growing in the last few decades with studies aiming to establish the clinical efficacy and safety profile of the plant. Despite the advancements that are being made, clinicians and medical regulatory bodies are still reluctant for epilepsy patients to use cannabis. Thus, it is essential that individuals are educated about the therapeutic properties of cannabis and the clinical evidence base to help patients gain access to cannabis medicines.
{"title":"Medical Cannabis and Epilepsy: The Evidence.","authors":"Varinder Kaur, Hannah Deacon, Michael Philip Barnes, David John Nutt","doi":"10.12968/hmed.2024.0903","DOIUrl":"10.12968/hmed.2024.0903","url":null,"abstract":"<p><p>Epilepsy is a serious neurological condition that can affect individuals of all ages. Treatment is far from perfect, and roughly 30% of patients can experience seizures that are resistant to antiseizure medications. Interestingly, the cannabis plant, specifically the phytocannabinoids, cannabidiol and delta-9-tetrahydrocannabinol, has been shown to possess anticonvulsant properties and are effective in the treatment of seizures. The clinical evidence base for cannabis for epileptic conditions has been growing in the last few decades with studies aiming to establish the clinical efficacy and safety profile of the plant. Despite the advancements that are being made, clinicians and medical regulatory bodies are still reluctant for epilepsy patients to use cannabis. Thus, it is essential that individuals are educated about the therapeutic properties of cannabis and the clinical evidence base to help patients gain access to cannabis medicines.</p>","PeriodicalId":9256,"journal":{"name":"British journal of hospital medicine","volume":"86 11","pages":"1-20"},"PeriodicalIF":1.8,"publicationDate":"2025-11-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145586069","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-11-25Epub Date: 2025-11-21DOI: 10.12968/hmed.2025.0795
Jiwei Huang, Yuniang Xie
Aims/Background Peripheral neuropathy (PN) is a common and debilitating complication in patients with multiple myeloma (MM), which results from both disease-related mechanisms and treatment-induced neurotoxicity. Despite its clinical significance, comprehensive investigations assessing PN risk in MM, along with examining demographic, clinical, nutritional, and inflammatory factors, remain limited. Therefore, this study aimed to investigate independent risk predictors associated with PN in MM patients using univariate and multivariate logistic regression analysis, thereby enhancing clinical risk management and improving treatment outcomes. Methods This retrospective observational study included 161 MM patients who were treated at Ganzhou People's Hospital between February 2020 and February 2024. Study participants were divided into the PN (n = 45) and non-PN (n = 116) groups. PN diagnosis was conducted based on new neurological signs and symptoms post-treatment, confirmed through abnormal sensory, motor, autonomic, or nerve conduction assessments. Baseline characteristics, including demographic information, clinical features, and laboratory parameters, were compared between the two groups using Mann-Whitney U and Chi-square tests. Univariate logistic regression analysis evaluated potential parameters associated with PN. Furthermore, a multivariate logistic model was used to assess independent risk predictors. Finally, model performance was evaluated via receiver operating characteristic (ROC) curve analysis. Results This study analyzed 161 patients, of whom 45 (27.95%) developed PN. Patients in the PN group were significantly older, and had higher body mass index (BMI), increased immunoglobulin G (IgG) and interleukin-6 (IL-6) levels, and increased diabetes prevalence than the non-PN group. However, they exhibited lower hemoglobin (Hb) and serum 25-hydroxyvitamin D [25(OH)D] levels (p < 0.05). Multivariate logistic regression analysis identified older age (odds ratio [OR] = 1.49, 95% confidence interval [CI]: 1.07-2.08), higher BMI (OR = 2.05, 95% CI: 1.01-4.17), reduced 25(OH)D levels (OR = 0.54, 95% CI: 0.29-0.97), elevated IgG (OR = 1.64, 95% CI: 1.12-2.41), and increased IL-6 (OR = 2.07, 95% CI: 1.10-3.88) as independent PN predictor. The model showed excellent discrimination capability (area under the curve [AUC] = 0.998, 95% CI: 0.996-1.000, p < 0.001). Conclusion This study identified older age, higher BMI, vitamin D deficiency, elevated IgG, and increased IL-6 levels as independent risk predictors for PN. Assessing these parameters in the early stages facilitates the identification of high-risk patients, allowing for targeted preventive strategies and personalized nursing interventions in MM patients which can reduce PN incidence and enhance overall clinical outcomes.
{"title":"Diagnostic Potential of the Risk Factors Associated With Peripheral Neuropathy in Multiple Myeloma: Evidence From Logistic Regression Analysis.","authors":"Jiwei Huang, Yuniang Xie","doi":"10.12968/hmed.2025.0795","DOIUrl":"10.12968/hmed.2025.0795","url":null,"abstract":"<p><p><b>Aims/Background</b> Peripheral neuropathy (PN) is a common and debilitating complication in patients with multiple myeloma (MM), which results from both disease-related mechanisms and treatment-induced neurotoxicity. Despite its clinical significance, comprehensive investigations assessing PN risk in MM, along with examining demographic, clinical, nutritional, and inflammatory factors, remain limited. Therefore, this study aimed to investigate independent risk predictors associated with PN in MM patients using univariate and multivariate logistic regression analysis, thereby enhancing clinical risk management and improving treatment outcomes. <b>Methods</b> This retrospective observational study included 161 MM patients who were treated at Ganzhou People's Hospital between February 2020 and February 2024. Study participants were divided into the PN (n = 45) and non-PN (n = 116) groups. PN diagnosis was conducted based on new neurological signs and symptoms post-treatment, confirmed through abnormal sensory, motor, autonomic, or nerve conduction assessments. Baseline characteristics, including demographic information, clinical features, and laboratory parameters, were compared between the two groups using Mann-Whitney U and Chi-square tests. Univariate logistic regression analysis evaluated potential parameters associated with PN. Furthermore, a multivariate logistic model was used to assess independent risk predictors. Finally, model performance was evaluated via receiver operating characteristic (ROC) curve analysis. <b>Results</b> This study analyzed 161 patients, of whom 45 (27.95%) developed PN. Patients in the PN group were significantly older, and had higher body mass index (BMI), increased immunoglobulin G (IgG) and interleukin-6 (IL-6) levels, and increased diabetes prevalence than the non-PN group. However, they exhibited lower hemoglobin (Hb) and serum 25-hydroxyvitamin D [25(OH)D] levels (<i>p</i> < 0.05). Multivariate logistic regression analysis identified older age (odds ratio [OR] = 1.49, 95% confidence interval [CI]: 1.07-2.08), higher BMI (OR = 2.05, 95% CI: 1.01-4.17), reduced 25(OH)D levels (OR = 0.54, 95% CI: 0.29-0.97), elevated IgG (OR = 1.64, 95% CI: 1.12-2.41), and increased IL-6 (OR = 2.07, 95% CI: 1.10-3.88) as independent PN predictor. The model showed excellent discrimination capability (area under the curve [AUC] = 0.998, 95% CI: 0.996-1.000, <i>p</i> < 0.001). <b>Conclusion</b> This study identified older age, higher BMI, vitamin D deficiency, elevated IgG, and increased IL-6 levels as independent risk predictors for PN. Assessing these parameters in the early stages facilitates the identification of high-risk patients, allowing for targeted preventive strategies and personalized nursing interventions in MM patients which can reduce PN incidence and enhance overall clinical outcomes.</p>","PeriodicalId":9256,"journal":{"name":"British journal of hospital medicine","volume":"86 11","pages":"1-14"},"PeriodicalIF":1.8,"publicationDate":"2025-11-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145585982","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-11-25Epub Date: 2025-11-05DOI: 10.12968/hmed.2024.1053
Owen J Lawrence, Shafi Ahmed, George J M Hourston, Phillip Johnston
Metacarpal fractures are one of the most common types of upper extremity fractures. During fracture, the balanced force couple of the hand flexors and extensors is disrupted, allowing shortening, angulation and rotation of the metacarpal shaft. Malunion is the most common complication, though it can largely be treated conservatively. When malunion leads to significant functional deficit surgical approaches must be explored to restore the biomechanics of the hand to allow functional return. This review article aims to explore the current concepts in surgical management of malunited metacarpal shaft fractures to ensure the latest advances are available to the hand surgeons of today.
{"title":"Management of Malunited Metacarpal Shaft Fractures-A Narrative Review.","authors":"Owen J Lawrence, Shafi Ahmed, George J M Hourston, Phillip Johnston","doi":"10.12968/hmed.2024.1053","DOIUrl":"10.12968/hmed.2024.1053","url":null,"abstract":"<p><p>Metacarpal fractures are one of the most common types of upper extremity fractures. During fracture, the balanced force couple of the hand flexors and extensors is disrupted, allowing shortening, angulation and rotation of the metacarpal shaft. Malunion is the most common complication, though it can largely be treated conservatively. When malunion leads to significant functional deficit surgical approaches must be explored to restore the biomechanics of the hand to allow functional return. This review article aims to explore the current concepts in surgical management of malunited metacarpal shaft fractures to ensure the latest advances are available to the hand surgeons of today.</p>","PeriodicalId":9256,"journal":{"name":"British journal of hospital medicine","volume":"86 11","pages":"1-10"},"PeriodicalIF":1.8,"publicationDate":"2025-11-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145586009","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Aims/Background In rheumatoid arthritis (RA) patients, malnutrition and sarcopenia are commonly associated with poor prognosis. The prognostic nutritional index (PNI), which includes serum albumin levels and lymphocyte counts, reflects the nutritional and inflammatory status of the patient. Therefore, this study aims to assess the relationship between PNI and sarcopenia in RA and examine its role as a diagnostic tool. Methods This retrospective study analysed data from 178 RA patients hospitalised at Affiliated Jinhua Hospital, Zhejiang University School of Medicine, between June 2023 and June 2025. Sarcopenia was diagnosed following the 2019 Asian Working Group for Sarcopenia (AWGS) criteria. Demographic, clinical, and laboratory data were collected, and PNI was calculated. Univariate and multivariate logistic regression analyses were performed to examine the association between PNI and sarcopenia, and receiver operating characteristic (ROC) curves were used to evaluate its diagnostic performance. Results Out of the total 178, 56 (31.5%) patients were diagnosed with sarcopenia. Multivariate regression analysis indicated lower PNI as an independent risk factor for sarcopenia (odds ratio [OR] = 0.88, 95% confidence interval [CI]: 0.80-0.97, p = 0.007), indicating that each 1-point increase in PNI was associated with a 12% decrease in risk. Older age (OR = 1.07), longer RA disease duration (OR = 1.50), and higher C-reactive protein (CRP) (OR = 1.06) were also independent risk factors. A prediction model combining age, PNI, disease duration, and CRP showed excellent discriminatory ability for sarcopenia, with an area under the curve (AUC) of 0.92 (95% CI: 0.87-0.97, p < 0.001), a sensitivity of 95.1%, and a specificity of 80.4%. Conclusion PNI is a simple, cost-effective measure that integrates nutritional (albumin) and inflammatory (lymphocyte) markers, facilitating early identification of RA patients at higher risk for sarcopenia and providing a basis for timely intervention.
目的/背景在类风湿关节炎(RA)患者中,营养不良和肌肉减少症通常与不良预后相关。预后营养指数(PNI),包括血清白蛋白水平和淋巴细胞计数,反映了患者的营养和炎症状况。因此,本研究旨在评估PNI与RA中肌肉减少症的关系,并研究其作为诊断工具的作用。方法回顾性分析2023年6月至2025年6月在浙江大学医学院附属金华医院住院的178例RA患者的资料。肌少症是根据2019年亚洲肌少症工作组(AWGS)标准诊断的。收集人口统计学、临床和实验室数据,并计算PNI。采用单因素和多因素logistic回归分析来检验PNI与肌肉减少症之间的关系,并使用受试者工作特征(ROC)曲线来评估其诊断性能。结果178例患者中56例(31.5%)诊断为肌肉减少症。多因素回归分析表明,较低的PNI是肌少症的独立危险因素(优势比[OR] = 0.88, 95%可信区间[CI]: 0.80-0.97, p = 0.007),表明PNI每增加1点,风险降低12%。年龄较大(OR = 1.07)、RA病程较长(OR = 1.50)、c反应蛋白(CRP)升高(OR = 1.06)也是独立危险因素。结合年龄、PNI、病程、CRP的预测模型对肌少症的鉴别能力较好,曲线下面积(AUC)为0.92 (95% CI: 0.87-0.97, p < 0.001),敏感性为95.1%,特异性为80.4%。结论PNI是一种简单、经济的综合营养(白蛋白)和炎症(淋巴细胞)标志物的检测方法,有助于早期发现RA患者肌少症的高危人群,为及时干预提供依据。
{"title":"A Correlation Between Prognostic Nutritional Index and Sarcopenia in Patients With Rheumatoid Arthritis.","authors":"Xiaowei Shi, Yingfang Wang, Li Hua","doi":"10.12968/hmed.2025.0703","DOIUrl":"10.12968/hmed.2025.0703","url":null,"abstract":"<p><p><b>Aims/Background</b> In rheumatoid arthritis (RA) patients, malnutrition and sarcopenia are commonly associated with poor prognosis. The prognostic nutritional index (PNI), which includes serum albumin levels and lymphocyte counts, reflects the nutritional and inflammatory status of the patient. Therefore, this study aims to assess the relationship between PNI and sarcopenia in RA and examine its role as a diagnostic tool. <b>Methods</b> This retrospective study analysed data from 178 RA patients hospitalised at Affiliated Jinhua Hospital, Zhejiang University School of Medicine, between June 2023 and June 2025. Sarcopenia was diagnosed following the 2019 Asian Working Group for Sarcopenia (AWGS) criteria. Demographic, clinical, and laboratory data were collected, and PNI was calculated. Univariate and multivariate logistic regression analyses were performed to examine the association between PNI and sarcopenia, and receiver operating characteristic (ROC) curves were used to evaluate its diagnostic performance. <b>Results</b> Out of the total 178, 56 (31.5%) patients were diagnosed with sarcopenia. Multivariate regression analysis indicated lower PNI as an independent risk factor for sarcopenia (odds ratio [OR] = 0.88, 95% confidence interval [CI]: 0.80-0.97, <i>p</i> = 0.007), indicating that each 1-point increase in PNI was associated with a 12% decrease in risk. Older age (OR = 1.07), longer RA disease duration (OR = 1.50), and higher C-reactive protein (CRP) (OR = 1.06) were also independent risk factors. A prediction model combining age, PNI, disease duration, and CRP showed excellent discriminatory ability for sarcopenia, with an area under the curve (AUC) of 0.92 (95% CI: 0.87-0.97, <i>p</i> < 0.001), a sensitivity of 95.1%, and a specificity of 80.4%. <b>Conclusion</b> PNI is a simple, cost-effective measure that integrates nutritional (albumin) and inflammatory (lymphocyte) markers, facilitating early identification of RA patients at higher risk for sarcopenia and providing a basis for timely intervention.</p>","PeriodicalId":9256,"journal":{"name":"British journal of hospital medicine","volume":"86 11","pages":"1-15"},"PeriodicalIF":1.8,"publicationDate":"2025-11-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145586022","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}