Pub Date : 2025-11-24DOI: 10.3390/clinpract15120220
Dana Nicoleta Mihai, Paul Dan Sîrbu, Liliana Savin, Norin Forna, Claudiu Topoliceanu, Cristina Dascălu, Norina Consuela Forna
The aim of this study was to evaluate the factors associated with the occurrence of oral infection sources in patients scheduled for total hip or knee arthroplasty, with the purpose of establishing standardized preoperative dental triage criteria. Materials and Methods: A retrospective research was conducted on a study group of 89 patients diagnosed with hip osteoarthritis and knee osteoarthritis at the Clinical Rehabilitation Hospital (Iasi, Romania). Patients were divided according to the status of their oral cavity: study group (n = 51)-patients with diagnosed oral infection sites (oral foci of infection); control group (n = 38)-patients without oral foci of infection. The statistical analysis included a univariate stage followed by a multivariate binary logistic regression to identify demographic and clinical factors associated with the presence of oral foci of infection. Results: The strongest predictor of the presence of oral foci of infection was and Oral Hygiene Index (OHI) scorer of 2, which increased the risk 14.583-fold, followed by being aged between 50 and 65 years (OR = 4.038), tooth brushing once a day or less (OR = 3.488), and male sex (OR = 3.433). An OHI score of 2 raises the probability of oral infectious pathology to 30.3%, which increases to 85.1% when combined with being aged between 50 and 65 years. Conclusions: The risk factors for the presence or oral foci of infection in patients scheduled for total knee or hip arthroplasty support the inclusion of the preoperative assessment and management of these factors in order to reduce the risk of the postoperative periprosthetic joint infections.
{"title":"Assessment of Associations Between Sociodemographic and Analysis of Risk Factors for Oral Infectious Pathology in Patients Scheduled for Total Hip and Knee Arthroplasty.","authors":"Dana Nicoleta Mihai, Paul Dan Sîrbu, Liliana Savin, Norin Forna, Claudiu Topoliceanu, Cristina Dascălu, Norina Consuela Forna","doi":"10.3390/clinpract15120220","DOIUrl":"10.3390/clinpract15120220","url":null,"abstract":"<p><p>The aim of this study was to evaluate the factors associated with the occurrence of oral infection sources in patients scheduled for total hip or knee arthroplasty, with the purpose of establishing standardized preoperative dental triage criteria. <b>Materials and Methods:</b> A retrospective research was conducted on a study group of 89 patients diagnosed with hip osteoarthritis and knee osteoarthritis at the Clinical Rehabilitation Hospital (Iasi, Romania). Patients were divided according to the status of their oral cavity: study group (<i>n</i> = 51)-patients with diagnosed oral infection sites (oral foci of infection); control group (<i>n</i> = 38)-patients without oral foci of infection. The statistical analysis included a univariate stage followed by a multivariate binary logistic regression to identify demographic and clinical factors associated with the presence of oral foci of infection. <b>Results:</b> The strongest predictor of the presence of oral foci of infection was and Oral Hygiene Index (OHI) scorer of 2, which increased the risk 14.583-fold, followed by being aged between 50 and 65 years (OR = 4.038), tooth brushing once a day or less (OR = 3.488), and male sex (OR = 3.433). An OHI score of 2 raises the probability of oral infectious pathology to 30.3%, which increases to 85.1% when combined with being aged between 50 and 65 years. <b>Conclusions:</b> The risk factors for the presence or oral foci of infection in patients scheduled for total knee or hip arthroplasty support the inclusion of the preoperative assessment and management of these factors in order to reduce the risk of the postoperative periprosthetic joint infections.</p>","PeriodicalId":45306,"journal":{"name":"Clinics and Practice","volume":"15 12","pages":""},"PeriodicalIF":2.2,"publicationDate":"2025-11-24","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12732232/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145821472","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 : 2025-11-24DOI: 10.3390/clinpract15120218
Mohammed Rafea Kanaan, Meryem Akkoyun, Marcel Lafos, Markus Antonius Kuczyk, Hossein Tezval
Urinary bladder hamartoma is an exceptionally rare benign lesion composed of disorganized yet mature tissue elements native to the bladder, including urothelium, fibrous stroma, smooth muscle, and occasionally adipose tissue. Unlike malignant tumors, it lacks cytological atypia, mitotic activity, or necrosis. Patients most often present with lower urinary tract symptoms (LUTS) or hematuria, though some cases are incidental findings. Associations with syndromic conditions such as Peutz-Jeghers, Beckwith-Wiedemann, Goldenhar, and Loeys-Dietz have been reported. Transurethral resection is the preferred treatment and has generally been curative. We report the first case in Germany-and the 16th worldwide-of urinary bladder hamartoma, occurring in a young adult male with bothersome LUTS. Because of its proximity to both ureteral orifices, only partial transurethral resection was performed, which provided durable symptom relief at 14 months of follow-up. This case highlights partial TUR as a pragmatic, organ-preserving alternative when complete resection is anatomically unsafe, while emphasizing that TURBT remains the standard of care. We provide a detailed discussion of the histopathological features, differential diagnosis, treatment considerations, and an updated narrative review of all reported cases.
{"title":"Urinary Bladder Hamartoma: Narrative Literature Review of an Exotic Pathology and Rare Cause of LUTS.","authors":"Mohammed Rafea Kanaan, Meryem Akkoyun, Marcel Lafos, Markus Antonius Kuczyk, Hossein Tezval","doi":"10.3390/clinpract15120218","DOIUrl":"10.3390/clinpract15120218","url":null,"abstract":"<p><p>Urinary bladder hamartoma is an exceptionally rare benign lesion composed of disorganized yet mature tissue elements native to the bladder, including urothelium, fibrous stroma, smooth muscle, and occasionally adipose tissue. Unlike malignant tumors, it lacks cytological atypia, mitotic activity, or necrosis. Patients most often present with lower urinary tract symptoms (LUTS) or hematuria, though some cases are incidental findings. Associations with syndromic conditions such as Peutz-Jeghers, Beckwith-Wiedemann, Goldenhar, and Loeys-Dietz have been reported. Transurethral resection is the preferred treatment and has generally been curative. We report the first case in Germany-and the 16th worldwide-of urinary bladder hamartoma, occurring in a young adult male with bothersome LUTS. Because of its proximity to both ureteral orifices, only partial transurethral resection was performed, which provided durable symptom relief at 14 months of follow-up. This case highlights partial TUR as a pragmatic, organ-preserving alternative when complete resection is anatomically unsafe, while emphasizing that TURBT remains the standard of care. We provide a detailed discussion of the histopathological features, differential diagnosis, treatment considerations, and an updated narrative review of all reported cases.</p>","PeriodicalId":45306,"journal":{"name":"Clinics and Practice","volume":"15 12","pages":""},"PeriodicalIF":2.2,"publicationDate":"2025-11-24","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12731898/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145821647","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 : 2025-11-21DOI: 10.3390/clinpract15120217
Nique Grob, Thomas Rustemeyer, Florentine de Boer
Background: Contact dermatitis (CD) is a prevalent inflammatory skin condition, with diagnostic challenges in distinguishing allergic (ACD) from irritant contact dermatitis (ICD). This study aimed to explore cholesterol-derived biomarkers as potential diagnostic tools. As cholesterol derivatives play key roles in skin barrier integrity and inflammation, they are promising candidates for assessing skin barrier disruption in CD.
Methods: Stratum corneum samples were collected by tape stripping from experimentally induced and chronic lesions, as well as healthy non-lesional skin. Biomarkers Cholesterol Sulfate (Chol-Sulf), Cholesterol Glucosyl (Chol-Glc) and their ratio were quantified. Data were analyzed using ANOVA, Pearson's correlation, logistic regression and ROC curves.
Results: Chol-Glc and the Chol-Glc/Chol-Sulf ratio differed significantly across the diagnostic groups, while Chol-Sulf did not. Logistic regression and ROC analyses revealed a limited standalone diagnostic accuracy for the individual biomarkers (all AUC < 0.6).
Conclusions: Chol-Glc and the ratio exhibit disease-specific patterns relevant for subtype discrimination. Although insufficient as independent diagnostic tools, these markers may contribute to future multivariate diagnostic models for CD diagnosis.
{"title":"Biomarker-Based Diagnosis of Contact Dermatitis: A Step Towards More Accurate and Patient-Friendly Testing.","authors":"Nique Grob, Thomas Rustemeyer, Florentine de Boer","doi":"10.3390/clinpract15120217","DOIUrl":"10.3390/clinpract15120217","url":null,"abstract":"<p><strong>Background: </strong>Contact dermatitis (CD) is a prevalent inflammatory skin condition, with diagnostic challenges in distinguishing allergic (ACD) from irritant contact dermatitis (ICD). This study aimed to explore cholesterol-derived biomarkers as potential diagnostic tools. As cholesterol derivatives play key roles in skin barrier integrity and inflammation, they are promising candidates for assessing skin barrier disruption in CD.</p><p><strong>Methods: </strong>Stratum corneum samples were collected by tape stripping from experimentally induced and chronic lesions, as well as healthy non-lesional skin. Biomarkers Cholesterol Sulfate (Chol-Sulf), Cholesterol Glucosyl (Chol-Glc) and their ratio were quantified. Data were analyzed using ANOVA, Pearson's correlation, logistic regression and ROC curves.</p><p><strong>Results: </strong>Chol-Glc and the Chol-Glc/Chol-Sulf ratio differed significantly across the diagnostic groups, while Chol-Sulf did not. Logistic regression and ROC analyses revealed a limited standalone diagnostic accuracy for the individual biomarkers (all AUC < 0.6).</p><p><strong>Conclusions: </strong>Chol-Glc and the ratio exhibit disease-specific patterns relevant for subtype discrimination. Although insufficient as independent diagnostic tools, these markers may contribute to future multivariate diagnostic models for CD diagnosis.</p>","PeriodicalId":45306,"journal":{"name":"Clinics and Practice","volume":"15 12","pages":""},"PeriodicalIF":2.2,"publicationDate":"2025-11-21","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12731350/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145821410","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}
<p><strong>Background/objective: </strong>Worldwide, ~45% of hypertensives remain undiagnosed, and ~26% are adequately controlled. The active involvement of all healthcare professionals in diagnosing hypertension at primary health care units (PHCUs) is linked to better blood pressure (BP) control. There is currently no research examining the potential role of senior medical students in the diagnosis of hypertension. This study aimed to evaluate the contribution of final-year medical students' active participation in the diagnosis of hypertension. The study also examined the prevalence and control of hypertension among health service users in Greek PHCUs.</p><p><strong>Methods: </strong>This is a cross-sectional convenience sample study. During clinical placement in PHC, sixth-year medical students received systematic training and performed BP measurements, according to the guidelines, in private, well-organized spaces. Adult patients and visitors were enlisted for BP measurements. The BP readings were provided to the participants so they could discuss any concerns about their BP with their physician. Statistical analysis was performed with SPSS. Categorical variables are presented as frequencies. Continuous variables were assessed for normality and, based on their distribution, are expressed as mean ± standard deviation or median (interquartile range). Appropriate tests were performed for the comparisons across groups (chi-square for the categorical variables, and two-sample <i>t</i>-test or Mann-Whitney test for continuous variables). A <i>p</i>-value < 0.05 was considered statistically significant.</p><p><strong>Results: </strong>In the present study, 124 medical students performed BP measurements in 68 PHCUs. BP was measured in 704 individuals, aged 61 (IQR: 48.0-73.0) years old; 58.8% were female, 68.3% of whom were patients. The prevalence of hypertension was 56.7%. The control rate was 44.9% (BP < 140 and 90 mmHg among all hypertensives), and the control rate under treatment was 61.0% (BP < 140 and 90 mmHg among treated hypertensives). The involvement of medical students contributed positively, increasing the diagnosis of hypertension in individuals who might not have their BP measured in routine clinical practice. Ninety-nine newly diagnosed hypertensives were detected. Students identified 220 uncontrolled hypertensives and 112 uncontrolled under-treated patients, who were then referred to the consultant physicians.</p><p><strong>Conclusions: </strong>Students played a critical role in diagnosing hypertension and identifying newly diagnosed hypertensive patients. Embracing interprofessional care in the diagnosis and management of hypertension is essential for achieving better outcomes for our patients. Engaging medical students in BP measurements is a practical and feasible approach to improve hypertension diagnosis and control, taking into consideration the increased workload of PHC physicians. While this action has important medical educ
{"title":"Contribution of Final-Year Medical Students to Hypertension Diagnosis in Primary Care Units.","authors":"Nikolaos Evangelidis, Areti Triantafyllou, Magda Gavana, Vasileios Gkolias, Styliani Ouzouni, Paschalis Evangelidis, Ilias Theodoropoulos, Despoina Symintiridou, Evangelia Naka, Ioannis Staikos, Martha Andreou, Stefanos Tsotoulidis, Stamatina Lamprou, Maria Dragasaki, Eirini Kada, Anna-Bettina Haidich, Michael Doumas, Emmanouil Smyrnakis","doi":"10.3390/clinpract15110216","DOIUrl":"10.3390/clinpract15110216","url":null,"abstract":"<p><strong>Background/objective: </strong>Worldwide, ~45% of hypertensives remain undiagnosed, and ~26% are adequately controlled. The active involvement of all healthcare professionals in diagnosing hypertension at primary health care units (PHCUs) is linked to better blood pressure (BP) control. There is currently no research examining the potential role of senior medical students in the diagnosis of hypertension. This study aimed to evaluate the contribution of final-year medical students' active participation in the diagnosis of hypertension. The study also examined the prevalence and control of hypertension among health service users in Greek PHCUs.</p><p><strong>Methods: </strong>This is a cross-sectional convenience sample study. During clinical placement in PHC, sixth-year medical students received systematic training and performed BP measurements, according to the guidelines, in private, well-organized spaces. Adult patients and visitors were enlisted for BP measurements. The BP readings were provided to the participants so they could discuss any concerns about their BP with their physician. Statistical analysis was performed with SPSS. Categorical variables are presented as frequencies. Continuous variables were assessed for normality and, based on their distribution, are expressed as mean ± standard deviation or median (interquartile range). Appropriate tests were performed for the comparisons across groups (chi-square for the categorical variables, and two-sample <i>t</i>-test or Mann-Whitney test for continuous variables). A <i>p</i>-value < 0.05 was considered statistically significant.</p><p><strong>Results: </strong>In the present study, 124 medical students performed BP measurements in 68 PHCUs. BP was measured in 704 individuals, aged 61 (IQR: 48.0-73.0) years old; 58.8% were female, 68.3% of whom were patients. The prevalence of hypertension was 56.7%. The control rate was 44.9% (BP < 140 and 90 mmHg among all hypertensives), and the control rate under treatment was 61.0% (BP < 140 and 90 mmHg among treated hypertensives). The involvement of medical students contributed positively, increasing the diagnosis of hypertension in individuals who might not have their BP measured in routine clinical practice. Ninety-nine newly diagnosed hypertensives were detected. Students identified 220 uncontrolled hypertensives and 112 uncontrolled under-treated patients, who were then referred to the consultant physicians.</p><p><strong>Conclusions: </strong>Students played a critical role in diagnosing hypertension and identifying newly diagnosed hypertensive patients. Embracing interprofessional care in the diagnosis and management of hypertension is essential for achieving better outcomes for our patients. Engaging medical students in BP measurements is a practical and feasible approach to improve hypertension diagnosis and control, taking into consideration the increased workload of PHC physicians. While this action has important medical educ","PeriodicalId":45306,"journal":{"name":"Clinics and Practice","volume":"15 11","pages":""},"PeriodicalIF":2.2,"publicationDate":"2025-11-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12651626/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145606754","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 : 2025-11-19DOI: 10.3390/clinpract15110215
Hernán Javier Pájaro Huertas, María Viviana Pantoja Echeverri, Gustavo Aroca Martínez, Carlos Guido Musso, Alex Dominguez Vargaz, Henry J González-Torres
Objective: This study aimed to evaluate the sociodemographic, clinical, paraclinical, and microbiological characteristics of kidney transplant recipients with and without urinary tract infection (UTI) and determine their impact on renal function and graft survival in a referral center in Atlántico, Colombia. Methods: We conducted a retrospective, observational, analytical study including 163 kidney transplant recipients between 2015 and 2020. Clinical and microbiological variables were compared according to UTI status. Renal function was assessed using estimated glomerular filtration rate (eGFR). Graft survival was analyzed with Kaplan-Meier curves, and predictors of graft loss were identified using Cox regression models. Results: UTI prevalence was 17.8% (29/163), with a higher proportion of women in the UTI (+) group compared to the UTI (-) group (62% vs. 34%, p = 0.004). Escherichia coli (59%) and Klebsiella spp. (31%) were the predominant pathogens, with MDR in 66% of isolates and carbapenem resistance in 28%. Patients with UTIs had significantly lower baseline and follow-up eGFR (p ≤ 0.002), yet five-year graft survival was comparable (93% vs. 91%, p = 0.54). Baseline eGFR (HR: 0.95, p < 0.001) and institutional referral (HR: 9.7, p = 0.010) were independent predictors of graft loss, whereas UTIs were not associated with increased risk. Conclusions: Post-transplant UTIs in Atlántico were characterized by high antimicrobial resistance and reduced renal function, but did not affect graft survival. Antimicrobial stewardship and institutional optimization strategies are essential to improve outcomes in this vulnerable population.
目的:本研究旨在评估有和没有尿路感染(UTI)的肾移植受者的社会人口学、临床、临床旁和微生物学特征,并确定其对哥伦比亚Atlántico转诊中心肾功能和移植物存活的影响。方法:我们在2015年至2020年期间对163名肾移植受者进行了回顾性、观察性和分析性研究。根据尿路感染情况比较临床和微生物指标。采用肾小球滤过率(eGFR)评估肾功能。用Kaplan-Meier曲线分析移植物存活,用Cox回归模型确定移植物损失的预测因素。结果:UTI患病率为17.8%(29/163),其中UTI(+)组女性比例高于UTI(-)组(62% vs. 34%, p = 0.004)。大肠埃希菌(59%)和克雷伯氏菌(31%)是主要病原菌,66%的分离株耐多药,28%的分离株耐碳青霉烯类药物。uti患者的基线和随访eGFR显著降低(p≤0.002),但5年移植物生存率相当(93% vs 91%, p = 0.54)。基线eGFR (HR: 0.95, p < 0.001)和机构转诊(HR: 9.7, p = 0.010)是移植物损失的独立预测因素,而uti与风险增加无关。结论:Atlántico患者移植后尿路感染表现为高耐药性和肾功能下降,但不影响移植物存活。抗菌药物管理和机构优化战略对于改善这一弱势群体的结果至关重要。
{"title":"Urinary Tract Infections and Bacterial Multidrug Resistance in Kidney Transplant Impact on Function and Graft Survival.","authors":"Hernán Javier Pájaro Huertas, María Viviana Pantoja Echeverri, Gustavo Aroca Martínez, Carlos Guido Musso, Alex Dominguez Vargaz, Henry J González-Torres","doi":"10.3390/clinpract15110215","DOIUrl":"10.3390/clinpract15110215","url":null,"abstract":"<p><p><b>Objective</b>: This study aimed to evaluate the sociodemographic, clinical, paraclinical, and microbiological characteristics of kidney transplant recipients with and without urinary tract infection (UTI) and determine their impact on renal function and graft survival in a referral center in Atlántico, Colombia. <b>Methods</b>: We conducted a retrospective, observational, analytical study including 163 kidney transplant recipients between 2015 and 2020. Clinical and microbiological variables were compared according to UTI status. Renal function was assessed using estimated glomerular filtration rate (eGFR). Graft survival was analyzed with Kaplan-Meier curves, and predictors of graft loss were identified using Cox regression models. <b>Results</b>: UTI prevalence was 17.8% (29/163), with a higher proportion of women in the UTI (+) group compared to the UTI (-) group (62% vs. 34%, <i>p</i> = 0.004). <i>Escherichia coli</i> (59%) and <i>Klebsiella</i> spp. (31%) were the predominant pathogens, with MDR in 66% of isolates and carbapenem resistance in 28%. Patients with UTIs had significantly lower baseline and follow-up eGFR (<i>p</i> ≤ 0.002), yet five-year graft survival was comparable (93% vs. 91%, <i>p</i> = 0.54). Baseline eGFR (HR: 0.95, <i>p</i> < 0.001) and institutional referral (HR: 9.7, <i>p</i> = 0.010) were independent predictors of graft loss, whereas UTIs were not associated with increased risk. <b>Conclusions</b>: Post-transplant UTIs in Atlántico were characterized by high antimicrobial resistance and reduced renal function, but did not affect graft survival. Antimicrobial stewardship and institutional optimization strategies are essential to improve outcomes in this vulnerable population.</p>","PeriodicalId":45306,"journal":{"name":"Clinics and Practice","volume":"15 11","pages":""},"PeriodicalIF":2.2,"publicationDate":"2025-11-19","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12651641/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145606347","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}
Background: Emergency contraception (EC), also known as postcoital contraception, is a method used to prevent an unintended pregnancy following unprotected or inadequately protected sexual intercourse. The available options include emergency contraceptive pills or the insertion of an intrauterine device (IUD). Emergency contraception pills contain either levonorgestrel (a single 1.5 mg dose, effective within 72 h) or ulipristal acetate (a single 30 mg dose, effective within 120 h), both of which are most effective when taken as soon as possible after unprotected intercourse. Another highly effective option is the insertion of a copper or levonorgestrel-releasing intrauterine device, although IUDs are not registered for EC use in all countries. The aims of this cross-sectional, comparative, observational study were to collect data on the emergency contraception methods used by adolescent girls and young women to examine their association with various factors, such as religious beliefs, and to evaluate the effectiveness of different emergency contraception methods, including hormonal options and intrauterine devices. Methods: Data were collected from 240 women who attended our Family Planning Clinic using a structured questionnaire that included items on their demographic characteristics, religious beliefs, medical history, lifestyle factors, contraceptive use and side effects, prior use of emergency contraception, method selected, and reasons for seeking emergency contraception. Descriptive statistics were used to summarize the data, comparisons between religious groups were conducted using chi-square tests, and factors related to the timing of emergency contraceptive use were investigated using multinomial logistic regression analysis. Results: Most of the reasons for emergency contraception use did not differ significantly between Christian and Muslim participants. However, Christians were significantly more likely to use emergency contraception due to missed contraceptive doses (20.9% vs. 6.7%, p = 0.004) or the failure to take a progesterone-only pill (19.1% vs. 3.3%, p = 0.001). Levonorgestrel was the most frequently used method in both groups (48.9% of Christians vs. 60% of Muslims, p = 0.132), followed by ulipristal acetate (30.9% vs. 40%, p = 0.180). Notably, 18.5% of Christian participants used an intrauterine device (IUD) for emergency contraception, while no Muslim participants reported IUD use (p < 0.001), indicating a significant difference potentially influenced by cultural or religious factors. Conclusions: Both religious and individual sociodemographic factors affect not only the choice of emergency contraception but also the urgency with which the emergency contraception is used. Interventions aimed at improving contraception education, addressing partner-related challenges, and promoting timely access could improve reproductive health outcomes.
背景:紧急避孕(EC),也称为性交后避孕,是一种用于防止无保护或保护不充分的性交后意外怀孕的方法。可用的选择包括紧急避孕药或插入宫内节育器(IUD)。紧急避孕药含有左炔诺孕酮(单次1.5毫克剂量,72小时内有效)或醋酸乌普利司妥(单次30毫克剂量,120小时内有效),这两种药物在无保护性交后尽快服用最有效。另一个非常有效的选择是插入铜或左炔诺孕酮释放宫内节育器,尽管宫内节育器并没有在所有国家注册用于EC。这项横断面、比较、观察性研究的目的是收集青春期女孩和年轻妇女使用的紧急避孕方法的数据,以检查其与各种因素(如宗教信仰)的关系,并评估不同紧急避孕方法的有效性,包括激素选择和宫内节育器。方法:采用结构化问卷收集240名在计划生育诊所就诊的妇女的数据,问卷内容包括人口统计学特征、宗教信仰、病史、生活方式因素、避孕药具使用情况和副作用、既往使用紧急避孕药具、选择的方法和寻求紧急避孕药具的原因。采用描述性统计对数据进行汇总,采用卡方检验对不同宗教群体进行比较,采用多项logistic回归分析对与紧急避孕药使用时间相关的因素进行调查。结果:大多数紧急避孕使用的原因在基督徒和穆斯林参与者之间没有显著差异。然而,由于错过避孕剂量(20.9% vs. 6.7%, p = 0.004)或未能服用黄体酮类药物(19.1% vs. 3.3%, p = 0.001),基督徒更有可能使用紧急避孕措施。左炔诺孕酮是两组中最常用的方法(48.9%的基督徒对60%的穆斯林,p = 0.132),其次是醋酸乌普利司特(30.9%对40%,p = 0.180)。值得注意的是,18.5%的基督徒参与者使用宫内节育器(IUD)进行紧急避孕,而没有穆斯林参与者报告使用宫内节育器(p < 0.001),这表明可能受到文化或宗教因素影响的显著差异。结论:宗教和个体社会人口因素不仅影响紧急避孕药的选择,而且影响紧急避孕药的使用紧迫性。旨在改进避孕教育、解决与伴侣有关的挑战和促进及时获得避孕服务的干预措施可以改善生殖健康结果。
{"title":"The Use and Effectiveness of Different Emergency Contraception Methods Among Adolescent Girls and Young Women in a Greek Clinic: A Cross-Sectional, Comparative, Observational Study.","authors":"Athanasia Chatzilazarou, Christina Pagkaki, Anastasia Bothou, Vasiliki Kourti, Dimitrios Lamprinos, Nektaria Kritsotaki, Efthymios Oikonomou, Nikolaos Machairiotis, Angeliki Gerede, Nikoletta Koutlaki, Panagiotis Tsikouras","doi":"10.3390/clinpract15110212","DOIUrl":"10.3390/clinpract15110212","url":null,"abstract":"<p><p><b>Background:</b> Emergency contraception (EC), also known as postcoital contraception, is a method used to prevent an unintended pregnancy following unprotected or inadequately protected sexual intercourse. The available options include emergency contraceptive pills or the insertion of an intrauterine device (IUD). Emergency contraception pills contain either levonorgestrel (a single 1.5 mg dose, effective within 72 h) or ulipristal acetate (a single 30 mg dose, effective within 120 h), both of which are most effective when taken as soon as possible after unprotected intercourse. Another highly effective option is the insertion of a copper or levonorgestrel-releasing intrauterine device, although IUDs are not registered for EC use in all countries. The aims of this cross-sectional, comparative, observational study were to collect data on the emergency contraception methods used by adolescent girls and young women to examine their association with various factors, such as religious beliefs, and to evaluate the effectiveness of different emergency contraception methods, including hormonal options and intrauterine devices. <b>Methods</b>: Data were collected from 240 women who attended our Family Planning Clinic using a structured questionnaire that included items on their demographic characteristics, religious beliefs, medical history, lifestyle factors, contraceptive use and side effects, prior use of emergency contraception, method selected, and reasons for seeking emergency contraception. Descriptive statistics were used to summarize the data, comparisons between religious groups were conducted using chi-square tests, and factors related to the timing of emergency contraceptive use were investigated using multinomial logistic regression analysis. <b>Results:</b> Most of the reasons for emergency contraception use did not differ significantly between Christian and Muslim participants. However, Christians were significantly more likely to use emergency contraception due to missed contraceptive doses (20.9% vs. 6.7%, <i>p</i> = 0.004) or the failure to take a progesterone-only pill (19.1% vs. 3.3%, <i>p</i> = 0.001). Levonorgestrel was the most frequently used method in both groups (48.9% of Christians vs. 60% of Muslims, <i>p</i> = 0.132), followed by ulipristal acetate (30.9% vs. 40%, <i>p</i> = 0.180). Notably, 18.5% of Christian participants used an intrauterine device (IUD) for emergency contraception, while no Muslim participants reported IUD use (<i>p</i> < 0.001), indicating a significant difference potentially influenced by cultural or religious factors. <b>Conclusions:</b> Both religious and individual sociodemographic factors affect not only the choice of emergency contraception but also the urgency with which the emergency contraception is used. Interventions aimed at improving contraception education, addressing partner-related challenges, and promoting timely access could improve reproductive health outcomes.</p>","PeriodicalId":45306,"journal":{"name":"Clinics and Practice","volume":"15 11","pages":""},"PeriodicalIF":2.2,"publicationDate":"2025-11-18","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12650810/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145606342","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 : 2025-11-18DOI: 10.3390/clinpract15110214
Alenka Kravos, Ksenija Gersak, Simona Gaberscek, Irena Hocevar-Boltezar
Background/objectives: Previous studies have shown that hypothyroidism with myxedema may significantly affect the vocal folds. The aim of this study was to investigate thyroid dysfunction and other possible risk factors, including smoking, for the development of Reinke's edema (RE) in a group of men.
Methods: Serum levels of thyroid-stimulating hormone (TSH), free thyroxine (fT4), and free triiodothyronine (fT3) were measured in a group of men with first occurrence or recurrent RE and in age- and gender-matched control subjects without laryngeal pathology. All participants completed a questionnaire on other possible etiologic factors for the development of RE, especially smoking. Risk factors were compared between the two groups. Levels of TSH and thyroid hormones were also compared between patients with recurrent disease and those with a first occurrence of RE.
Results: A total of 53 men with RE (mean age 53.82 years) and 45 controls (mean age 57.71 years) completed the study protocol. TSH and thyroid hormone levels were within the normal limits in all participants. Serum fT3 levels were significantly higher in patients with RE compared to controls (p = 0.034). After univariate analysis, all risk factors were included in a multivariate regression model. Only smoking remained a significant variable. Thyroid hormone levels did not differ between patients with first-onset RE and those with recurrent RE.
Conclusions: An association between hypothyroidism and the development of RE was not confirmed. The significantly higher fT3 levels in patients compared to controls were still within the normal range and may reflect normal variation. Regression analysis of possible risk factors for RE showed the primacy of smoking.
{"title":"Does Thyroid Dysfunction Have a Role in the Etiology of Vocal Fold Edema?","authors":"Alenka Kravos, Ksenija Gersak, Simona Gaberscek, Irena Hocevar-Boltezar","doi":"10.3390/clinpract15110214","DOIUrl":"10.3390/clinpract15110214","url":null,"abstract":"<p><strong>Background/objectives: </strong>Previous studies have shown that hypothyroidism with myxedema may significantly affect the vocal folds. The aim of this study was to investigate thyroid dysfunction and other possible risk factors, including smoking, for the development of Reinke's edema (RE) in a group of men.</p><p><strong>Methods: </strong>Serum levels of thyroid-stimulating hormone (TSH), free thyroxine (fT4), and free triiodothyronine (fT3) were measured in a group of men with first occurrence or recurrent RE and in age- and gender-matched control subjects without laryngeal pathology. All participants completed a questionnaire on other possible etiologic factors for the development of RE, especially smoking. Risk factors were compared between the two groups. Levels of TSH and thyroid hormones were also compared between patients with recurrent disease and those with a first occurrence of RE.</p><p><strong>Results: </strong>A total of 53 men with RE (mean age 53.82 years) and 45 controls (mean age 57.71 years) completed the study protocol. TSH and thyroid hormone levels were within the normal limits in all participants. Serum fT3 levels were significantly higher in patients with RE compared to controls (<i>p</i> = 0.034). After univariate analysis, all risk factors were included in a multivariate regression model. Only smoking remained a significant variable. Thyroid hormone levels did not differ between patients with first-onset RE and those with recurrent RE.</p><p><strong>Conclusions: </strong>An association between hypothyroidism and the development of RE was not confirmed. The significantly higher fT3 levels in patients compared to controls were still within the normal range and may reflect normal variation. Regression analysis of possible risk factors for RE showed the primacy of smoking.</p>","PeriodicalId":45306,"journal":{"name":"Clinics and Practice","volume":"15 11","pages":""},"PeriodicalIF":2.2,"publicationDate":"2025-11-18","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12650799/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145606705","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 : 2025-11-18DOI: 10.3390/clinpract15110213
Matthanja Bieze, Karen Foley, W Scott Beattie, Jo Carroll, Humara Poonawala, Lian-Kah Ti, George Djaiani
Background/Objectives: An increasing number of older individuals require general anaesthesia for major non-cardiac surgery, with 20% displaying postoperative complications. Regional cerebral oxygen saturation (rSO2) correlates with the gold standard of mixed venous oxygen saturation, indicating global perfusion. We hypothesised that rSO2-based anaesthesia reduces organ dysfunction and morbidity after major non-cardiac surgery. Methods: In Singapore and Toronto, we conducted a prospective, double-blind, randomised controlled trial in elderly patients undergoing major non-cardiac surgery, after obtaining research ethics board permission and informed consent. This RCT followed the CONSORT guidelines. Patients received bilateral cerebral oximetry sensors, and the control group received standard care. In the intervention group, an algorithm restored rSO2 if it dropped 10% below baseline for >15 s by adjusting cerebral perfusion pressure, inspired oxygen concentration, end-tidal carbon dioxide, depth of anaesthesia, haemoglobin, and cardiac index. Postoperative complications and outcomes were noted. Categorical data were analysed using Chi-square or Fisher's exact tests and continuous data using a t-test or a Mann-Whitney U test. The study was powered for 394 patients, but due to the COVID-19 pandemic and funding constraints, this study was terminated at 101 patients. Results: Of 101 patients, 49 were randomised to the control and 52 to the intervention group. A total of 31 (63%) patients in the control group and 30 (58%) in the interventional exhibited bilateral cerebral desaturation. Time of cumulative cerebral desaturation was longer in the control group (23 ± 48 min vs. 9 ± 15 min, respectively, p = 0.01). A total of 142 algorithm-based treatments were employed, restoring rSO2 in 29 (86%) patients. Both groups displayed equal postoperative outcomes. Conclusions: In major non-cardiac surgery, cerebral desaturation is prevalent in over 85% of patients. Although algorithm-guided therapy restored rSO2 in the majority of patients, it did not result in reduced postoperative morbidity.
背景/目的:越来越多的老年人需要全身麻醉进行重大非心脏手术,其中20%出现术后并发症。局部脑氧饱和度(rSO2)与混合静脉血氧饱和度的金标准相关,提示全脑灌注。我们假设基于二氧化硫的麻醉可以减少重大非心脏手术后的器官功能障碍和发病率。方法:在获得研究伦理委员会许可和知情同意后,我们在新加坡和多伦多对接受重大非心脏手术的老年患者进行了一项前瞻性、双盲、随机对照试验。该随机对照试验遵循CONSORT指南。患者接受双侧脑血氧仪测量,对照组接受标准治疗。在干预组,通过调整脑灌注压、吸入氧浓度、潮末二氧化碳、麻醉深度、血红蛋白和心脏指数,如果rSO2低于基线10%并持续bbb15s,则算法恢复rSO2。观察术后并发症及预后。分类数据使用卡方检验或Fisher精确检验进行分析,连续数据使用t检验或Mann-Whitney U检验。该研究为394名患者提供了支持,但由于COVID-19大流行和资金限制,该研究在101名患者中终止。结果:101例患者中,49例随机分为对照组,52例随机分为干预组。对照组共有31例(63%)患者,介入组有30例(58%)患者表现为双侧脑去饱和。对照组累积脑去饱和时间更长(分别为23±48 min和9±15 min, p = 0.01)。总共采用了142种基于算法的治疗方法,29例(86%)患者的rSO2恢复。两组术后结果相同。结论:在大型非心脏手术中,85%以上的患者普遍存在脑不饱和。虽然算法引导的治疗在大多数患者中恢复了rSO2,但它并没有降低术后发病率。
{"title":"Role of Cerebral Oximetry in Reducing Postoperative End-Organ Dysfunction After Major Non-Cardiac Surgery: A Randomised Controlled Trial.","authors":"Matthanja Bieze, Karen Foley, W Scott Beattie, Jo Carroll, Humara Poonawala, Lian-Kah Ti, George Djaiani","doi":"10.3390/clinpract15110213","DOIUrl":"10.3390/clinpract15110213","url":null,"abstract":"<p><p><b>Background/Objectives</b>: An increasing number of older individuals require general anaesthesia for major non-cardiac surgery, with 20% displaying postoperative complications. Regional cerebral oxygen saturation (rSO<sub>2</sub>) correlates with the gold standard of mixed venous oxygen saturation, indicating global perfusion. We hypothesised that rSO<sub>2</sub>-based anaesthesia reduces organ dysfunction and morbidity after major non-cardiac surgery. <b>Methods</b>: In Singapore and Toronto, we conducted a prospective, double-blind, randomised controlled trial in elderly patients undergoing major non-cardiac surgery, after obtaining research ethics board permission and informed consent. This RCT followed the CONSORT guidelines. Patients received bilateral cerebral oximetry sensors, and the control group received standard care. In the intervention group, an algorithm restored rSO<sub>2</sub> if it dropped 10% below baseline for >15 s by adjusting cerebral perfusion pressure, inspired oxygen concentration, end-tidal carbon dioxide, depth of anaesthesia, haemoglobin, and cardiac index. Postoperative complications and outcomes were noted. Categorical data were analysed using Chi-square or Fisher's exact tests and continuous data using a <i>t</i>-test or a Mann-Whitney U test. The study was powered for 394 patients, but due to the COVID-19 pandemic and funding constraints, this study was terminated at 101 patients. <b>Results</b>: Of 101 patients, 49 were randomised to the control and 52 to the intervention group. A total of 31 (63%) patients in the control group and 30 (58%) in the interventional exhibited bilateral cerebral desaturation. Time of cumulative cerebral desaturation was longer in the control group (23 ± 48 min vs. 9 ± 15 min, respectively, <i>p</i> = 0.01). A total of 142 algorithm-based treatments were employed, restoring rSO<sub>2</sub> in 29 (86%) patients. Both groups displayed equal postoperative outcomes. <b>Conclusions</b>: In major non-cardiac surgery, cerebral desaturation is prevalent in over 85% of patients. Although algorithm-guided therapy restored rSO<sub>2</sub> in the majority of patients, it did not result in reduced postoperative morbidity.</p>","PeriodicalId":45306,"journal":{"name":"Clinics and Practice","volume":"15 11","pages":""},"PeriodicalIF":2.2,"publicationDate":"2025-11-18","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12651021/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145606802","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 : 2025-11-17DOI: 10.3390/clinpract15110210
Sara Vodopivec, Gorazd Kavšek, Polona Pečlin, Mirjam Druškovič
Objectives: The aim of our study was to assess the efficacy and safety of two different labor induction methods in patients after fetal demise beyond 28 weeks, with an unfavorable cervix: misoprostol-prostaglandin E1 analog (PGE1) and dinoprostone-prostaglandin E2 analog (PGE2). Methods: This retrospective single-center cohort study included all labor cases after fetal demise (intrauterine fetal death or termination of pregnancy with feticide) from 28 to 40 weeks of gestation, where labor was induced by either PGE1 or PGE2. The primary outcome was the induction-to-delivery time interval. Secondary outcomes included the proportion of patients who delivered within 24 h, the failed induction rate, the length of labor, pain during induction, the adverse outcome rate, and the post-labor hospital stay. Results: The induction-to-delivery time interval was shorter in the PGE1 group (p = 0.048). There was no statistically significant difference in the proportion of patients who delivered within 24 h (p = 0.651) and failed inductions (p = 0.18) between groups. The duration of labor was longer in the PGE2 group (p = 0.01). Oxytocin augmentation was more common in the PGE2 group (p < 0.001). Pain during induction was greater in women in the PGE1 group (p < 0.001). There were no statistically significant differences in adverse effects between groups. There was no significant difference in induction to delivery interval between the two methods when comparing lower and higher gestational ages (28 to 34 weeks, p = 0.18; 35 to 40 weeks, p = 0.343). Conclusions: Our findings support the use of a PGE1 regimen for third-trimester labor induction after fetal demise, when no contraindications exist. This approach appears to improve the efficiency of induction and may enhance overall patient care by reducing intervention needs.
{"title":"Induction of Labor After Fetal Demise in Third Trimester-A Retrospective Cohort Study.","authors":"Sara Vodopivec, Gorazd Kavšek, Polona Pečlin, Mirjam Druškovič","doi":"10.3390/clinpract15110210","DOIUrl":"10.3390/clinpract15110210","url":null,"abstract":"<p><p><b>Objectives</b>: The aim of our study was to assess the efficacy and safety of two different labor induction methods in patients after fetal demise beyond 28 weeks, with an unfavorable cervix: misoprostol-prostaglandin E1 analog (PGE1) and dinoprostone-prostaglandin E2 analog (PGE2). <b>Methods</b>: This retrospective single-center cohort study included all labor cases after fetal demise (intrauterine fetal death or termination of pregnancy with feticide) from 28 to 40 weeks of gestation, where labor was induced by either PGE1 or PGE2. The primary outcome was the induction-to-delivery time interval. Secondary outcomes included the proportion of patients who delivered within 24 h, the failed induction rate, the length of labor, pain during induction, the adverse outcome rate, and the post-labor hospital stay. <b>Results</b>: The induction-to-delivery time interval was shorter in the PGE1 group (<i>p</i> = 0.048). There was no statistically significant difference in the proportion of patients who delivered within 24 h (<i>p</i> = 0.651) and failed inductions (<i>p</i> = 0.18) between groups. The duration of labor was longer in the PGE2 group (<i>p</i> = 0.01). Oxytocin augmentation was more common in the PGE2 group (<i>p</i> < 0.001). Pain during induction was greater in women in the PGE1 group (<i>p</i> < 0.001). There were no statistically significant differences in adverse effects between groups. There was no significant difference in induction to delivery interval between the two methods when comparing lower and higher gestational ages (28 to 34 weeks, <i>p</i> = 0.18; 35 to 40 weeks, <i>p</i> = 0.343). <b>Conclusions</b>: Our findings support the use of a PGE1 regimen for third-trimester labor induction after fetal demise, when no contraindications exist. This approach appears to improve the efficiency of induction and may enhance overall patient care by reducing intervention needs.</p>","PeriodicalId":45306,"journal":{"name":"Clinics and Practice","volume":"15 11","pages":""},"PeriodicalIF":2.2,"publicationDate":"2025-11-17","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12651065/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145606728","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 : 2025-11-17DOI: 10.3390/clinpract15110211
Javier Varela Gonzalez-Aller, Pablo Nadal, Salome Cañizares, Carmen Muñoz, Anna Valer, Eva Gonzalez-Barca, Eva Domingo, Ana Sureda, Silvana Novelli
Background/Objectives: Asparaginase (ASP)-based chemotherapy has substantially improved clinical outcomes in Epstein-Barr virus (EBV)-positive NK/T-cell lymphomas (NKTCL). However, as a bacterial-derived enzyme, ASP is frequently associated with immune-mediated adverse events, particularly hypersensitivity reactions (HSRs), which may compromise both treatment efficacy and patient safety. This report presents a case of an ASP-related HSR and reviews the incidence within our institutional cohort. Detailed Case Description: A 60-year-old female presented an immediate Grade 2 HSR during her second PEG-asparaginase infusion, with pruritus, vomiting, and presyncope. The infusion was discontinued, and she was subsequently transitioned to crisantaspase-an alternative formulation-which was well tolerated without further adverse events. She remains disease-free to date. A retrospective review of institutional records (2015-2025) identified six patients with NKTCL treated with ASP-containing chemotherapy. The incidence of HSRs in this cohort was 1 of 6 (16.7%). Conclusions: As in acute lymphoblastic leukemia, HSRs to asparaginase remains a major challenge in the management of NKTCL with potential implications for treatment safety and efficacy. The establishment of standardized, consensus-based criteria for the diagnosis, classification, and management of ASP-related HSRs is urgently needed to optimize patient outcomes.
{"title":"Asparaginase Hypersensitivity Reactions in NK/T-Cell Lymphomas.","authors":"Javier Varela Gonzalez-Aller, Pablo Nadal, Salome Cañizares, Carmen Muñoz, Anna Valer, Eva Gonzalez-Barca, Eva Domingo, Ana Sureda, Silvana Novelli","doi":"10.3390/clinpract15110211","DOIUrl":"10.3390/clinpract15110211","url":null,"abstract":"<p><p><b>Background/Objectives</b>: Asparaginase (ASP)-based chemotherapy has substantially improved clinical outcomes in Epstein-Barr virus (EBV)-positive NK/T-cell lymphomas (NKTCL). However, as a bacterial-derived enzyme, ASP is frequently associated with immune-mediated adverse events, particularly hypersensitivity reactions (HSRs), which may compromise both treatment efficacy and patient safety. This report presents a case of an ASP-related HSR and reviews the incidence within our institutional cohort. <b>Detailed Case Description</b>: A 60-year-old female presented an immediate Grade 2 HSR during her second PEG-asparaginase infusion, with pruritus, vomiting, and presyncope. The infusion was discontinued, and she was subsequently transitioned to crisantaspase-an alternative formulation-which was well tolerated without further adverse events. She remains disease-free to date. A retrospective review of institutional records (2015-2025) identified six patients with NKTCL treated with ASP-containing chemotherapy. The incidence of HSRs in this cohort was 1 of 6 (16.7%). <b>Conclusions</b>: As in acute lymphoblastic leukemia, HSRs to asparaginase remains a major challenge in the management of NKTCL with potential implications for treatment safety and efficacy. The establishment of standardized, consensus-based criteria for the diagnosis, classification, and management of ASP-related HSRs is urgently needed to optimize patient outcomes.</p>","PeriodicalId":45306,"journal":{"name":"Clinics and Practice","volume":"15 11","pages":""},"PeriodicalIF":2.2,"publicationDate":"2025-11-17","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12651928/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145606647","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}