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Polymorphous adenocarcinoma: a review of the literature and presentation of a case in an uncommon anatomical area. 多形腺癌:文献回顾和一个不常见解剖区域的病例介绍。
Q2 Medicine Pub Date : 2025-07-01 Epub Date: 2025-07-30 DOI: 10.15386/mpr-2882
Bogdan Andrei Bumbu, Mădălina Anca Moldovan, Iuliu George Moldovan, Alexandru Iosif Precup, Raluca Ortensia Iurcov

Background: Polymorphous adenocarcinoma (PAC) is a type of salivary gland tumor that is rare and diverse in morphology. It is typically found in the minor salivary glands, with the palate being the most common location. However, this tumor is often misunderstood, underdiagnosed, and controversial in nomenclature. Its low-grade behavior may be unpredictable, making it challenging to manage.

Case report: In this paper, we detail a case of PAC that developed in the buccal mucosa, which is a less common anatomical location. We discuss the patient's clinical presentation, imaging findings, histological examination results, as well as the surgical treatment and follow-up outcomes. We also examine relevant literature related to the topic to provide a comprehensive understanding of this rare case.

Conclusions: Although complete surgical excision is the primary management for PAC, there is no gold standard treatment for it. It is crucial to follow up on patients with PAC in the long term, as recurrences, lymph nodes, and distant metastasis, even rare, may impair the prognosis in certain patients.

背景:多形态腺癌(PAC)是一种罕见且形态多样的唾液腺肿瘤。它通常在小唾液腺中发现,上颚是最常见的位置。然而,这种肿瘤经常被误解,诊断不足,并在命名上有争议。它的低级行为可能是不可预测的,使其难以管理。病例报告:在本文中,我们详细介绍了一个在口腔黏膜发展的PAC病例,这是一个不太常见的解剖位置。我们讨论患者的临床表现,影像学表现,组织学检查结果,以及手术治疗和随访结果。我们也检视相关的文献,以提供对这个罕见病例的全面了解。结论:虽然完全手术切除是PAC的主要治疗方法,但目前尚无金标准治疗方法。对PAC患者进行长期随访至关重要,因为复发,淋巴结和远处转移,即使罕见,也可能损害某些患者的预后。
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引用次数: 0
Exclusive enteral nutrition in Crohn's disease pediatric patients: from clinical remission to transmural healing. 克罗恩病儿科患者的独家肠内营养:从临床缓解到全壁愈合。
Q2 Medicine Pub Date : 2025-07-01 Epub Date: 2025-07-30 DOI: 10.15386/mpr-2900
Georgia Valentina Tartamus Tita, Daniela Elena Serban, Lacramioara Eliza Chiperi, Cristina Rebeca Fogas, Stefana Arlinda Medan, Vasile Marcel Tantau

Background and aims: Exclusive enteral nutrition (EEN) is a well-established first-line therapy for inducing remission in mild-to-moderate pediatric Crohn's disease (pCD). While clinical remission (CR) and mucosal healing (MH) are widely accepted therapeutic goals, the concept of transmural healing (TH) has gained increasing recognition. This study aimed to evaluate the effectiveness of EEN in pCD patients from Romania, focusing on nutritional status, remission outcomes, and the impact of various factors on treatment efficacy.

Methods: We conducted a retrospective observational study of pCD consecutive patients who received EEN for induction of remission between 2007 and 2017 at a referral center in Cluj-Napoca, Romania. CR was defined as a weighted Pediatric Crohn's Disease Activity Index (wPCDAI) <12.5, MH as a fecal calprotectin level <250 microg/g, and TH as the combination of MH and imagistic remission assessed by intestinal ultrasonography. Statistical analyses included descriptive and comparative approaches, including logistic regression, with p <0.05 considered significant.

Results: Twenty patients with pCD, representing 45% of the cohort, were included. The median age at diagnosis was 14.2 years (9.9-18.4), and 65% were male. EEN was administered with a mean duration of 7.84±1.26 weeks. Body mass index Z-scores significantly improved following EEN (p=0.02). Hypoalbuminemia, detected in 55% of patients at diagnosis, resolved completely after EEN (p=0.00015). CR was achieved in 82% of patients with active clinical disease, MH in 26% of patients with microscopic activity, and TH in 20% of patients with imagistic activity. Age at diagnosis, disease behavior, location, activity, and anti-Saccharomyces cerevisiae antibody status were not significantly associated with CR or MH. Disease activity at initiation, measured by the wPCDAI, was inversely associated with TH (p=0.004).

Conclusions: This is the first study to report on EEN outcomes in pCD patients from Romania. EEN was effective in improving nutritional status and inducing CR, while MH was achieved in about one-quarter of patients. TH was also observed, though less frequently, and was negatively associated with higher baseline clinical disease activity. Regional factors may have influenced these outcomes.

背景和目的:独家肠内营养(EEN)是一种成熟的一线治疗方法,可诱导轻度至中度儿童克罗恩病(pCD)缓解。虽然临床缓解(CR)和粘膜愈合(MH)是被广泛接受的治疗目标,但跨壁愈合(TH)的概念也得到了越来越多的认可。本研究旨在评估EEN在罗马尼亚pCD患者中的有效性,重点关注营养状况、缓解结果以及各种因素对治疗效果的影响。方法:我们对2007年至2017年在罗马尼亚克卢日-纳波卡转诊中心连续接受EEN诱导缓解的pCD患者进行了回顾性观察研究。CR被定义为加权儿童克罗恩病活动指数(wPCDAI)。结果:20例pCD患者,占队列的45%。诊断时的中位年龄为14.2岁(9.9-18.4岁),65%为男性。EEN的平均持续时间为7.84±1.26周。EEN后体重指数z得分显著提高(p=0.02)。55%的患者在诊断时发现低白蛋白血症,在EEN后完全消失(p=0.00015)。临床疾病活动性患者中有82%达到CR,显微镜下活动患者中有26%达到MH,影像学活动患者中有20%达到TH。诊断年龄、疾病行为、部位、活性和抗酿酒酵母菌抗体状态与CR或MH无显著相关。wPCDAI测量的发病时的疾病活性与TH呈负相关(p=0.004)。结论:这是首个报道罗马尼亚pCD患者EEN结果的研究。EEN可有效改善营养状况并诱导CR,而约四分之一的患者可达到MH。TH也被观察到,尽管频率较低,并且与较高的基线临床疾病活动性呈负相关。区域因素可能影响了这些结果。
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引用次数: 0
New prospects in oncotherapy: bioactive compounds from Taraxacum officinale. 肿瘤治疗的新前景:蒲公英的生物活性化合物。
Q2 Medicine Pub Date : 2025-07-01 Epub Date: 2025-07-30 DOI: 10.15386/mpr-2875
Daniel Cord, Mirela Claudia Rîmbu, Liliana Popescu

Cancer remains one of the most significant global health challenges, requiring continuous exploration of novel therapeutic agents. Traditional medicine has long used Taraxacum officinale H.Wigg, commonly known as dandelion, for its diverse pharmacological properties. Recent studies have highlighted its potential anticancer effects attributed to a rich phytochemical profile containing flavonoids, terpenoids, phenolic acids, polysaccharides, and sterols. This review systematically examines the available scientific literature regarding Taraxacum officinale, focusing on its ethnomedical application, phytochemical composition, and anticancer mechanism demonstrated in vitro and in vivo models. Key bioactive compounds, such as taraxasterol, chlorogenic acid, chicoric acid, and taraxinic acid, have been identified as promising agents capable of inhibiting tumor cell proliferation and modulating oncogenic pathways. Additionally, the plant's safety profile and toxicological assessments are discussed to evaluate its therapeutic viability. Given its multi-target biological activity and low toxicity, Taraxacum officinale holds significant potential for integration into oncotherapy as an adjuvant treatment. However, further preclinical and clinical investigations remain essential to validate its efficacy and mechanism of action, paving the way for the development of cost-effective, plant-based cancer therapeutics.

癌症仍然是全球最重大的健康挑战之一,需要不断探索新的治疗药物。传统医学长期使用蒲公英(Taraxacum officinale H.Wigg),因为它具有多种药理特性。最近的研究强调了其潜在的抗癌作用,这归功于其丰富的植物化学成分,包括黄酮类、萜类、酚酸、多糖和甾醇。本文系统地回顾了有关蒲公英的现有科学文献,重点介绍了蒲公英的民族医学应用、植物化学成分以及体外和体内模型证明的抗癌机制。关键的生物活性化合物,如taraxasterol,绿原酸,菊酸和taraxinic酸,已经被确定为有希望的药物,能够抑制肿瘤细胞增殖和调节致癌途径。此外,还讨论了该植物的安全性和毒理学评估,以评估其治疗可行性。鉴于其多靶点生物活性和低毒性,蒲公英作为辅助治疗整合到肿瘤治疗中具有巨大的潜力。然而,进一步的临床前和临床研究仍然至关重要,以验证其功效和作用机制,为开发具有成本效益的植物性癌症治疗方法铺平道路。
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引用次数: 0
Effectiveness of steroids and antiviral agents in the treatment of Bell's palsy. 类固醇和抗病毒药物治疗贝尔氏麻痹的有效性。
Q2 Medicine Pub Date : 2025-07-01 Epub Date: 2025-07-30 DOI: 10.15386/mpr-2786
Christos Sialakis, Aikaterini Frantzana, Christos Iliadis, Peter Ouzounakis, Lambrini Kourkouta

Background: This study aims to investigate the effectiveness of steroids plus antivirals versus steroids alone in the treatment of Bell's palsy. Due to conflicting results in the existing literature, we conducted this meta-analysis to synthesize the available evidence and extract a more complete conclusion.

Methods: We searched electronic databases PubMed, CINAHL, ScienceDirect, MEDLINE, OVID, and Scopus. The last search was performed on March 2024. In this study, 7 randomized controlled trials were included. We used random and fixed effects for sensitivity analysis for each outcome, and we further proceeded to perform a Bayesian meta-analysis using priors and calculate the posterior distribution.

Results: Performing frequentist meta-analysis, both the random and fixed effects showed statistical significance, indicating the superiority of the combination treatment. The random log odds ratio was 0.5865 [95% CI: 0.0141 to 1.1589 and the Back-Transform Log Odds Ratio to Odds Ratio was 1.798 [95% CI: 1.014 to 3.186]. The fixed effect log odds ratio was 0.4377 [95%CI: 0.0819 to 0.7934] and the Back-Transform Log Odds Ratio to Odds Ratio was 1.549 [95% CI:1.085 to 2.211]. Neither the rank correlation nor the regression test in both models indicated any funnel plot asymmetry and publication bias.Performing Bayesian meta-analysis, in the posterior distribution the model-averaged log odds ratio was 0.26 [0.00 to 0.90], showing no statistically significant results, as the log odds ratio contains the zero. The inclusion Bayes Factor (BF) for the effect was 1.225 showing anecdotal supporting evidence for the combination treatment. The inclusion BF for the heterogeneity was 0.979, showing no support for its existence in the analysis and the inclusion BF for the publication bias was 0.622, a lower of 1, indicating evidence of its absence in the analysis.

Conclusions: The combination of steroids plus an antiviral agent, is more efficacious than steroid monotherapy in treating Bell's palsy. This conclusion is supported by frequentist analysis, but not by the Bayesian approach as the Bayesian meta-analysis was inconclusive, suggesting some uncertainty in the effect size but this could be due to priors influence. Further research with advanced syntheses such as network and Bayesian meta-analysis is needed as well as more double-blinded randomized controlled trials.

背景:本研究旨在探讨类固醇联合抗病毒药物与单独类固醇治疗贝尔氏麻痹的疗效。由于现有文献的结果相互矛盾,我们进行了这项荟萃分析,以综合现有证据并提取更完整的结论。方法:检索PubMed、CINAHL、ScienceDirect、MEDLINE、OVID、Scopus等电子数据库。最后一次搜索是在2024年3月。本研究纳入7项随机对照试验。我们使用随机和固定效应对每个结果进行敏感性分析,并进一步使用先验进行贝叶斯荟萃分析并计算后验分布。结果:经频元分析,随机效应和固定效应均有统计学意义,表明联合治疗的优越性。随机对数比值比为0.5865 [95% CI: 0.0141 ~ 1.1589],反向变换对数比值比为1.798 [95% CI: 1.014 ~ 3.186]。固定效应对数比值比为0.4377 [95%CI: 0.0819 ~ 0.7934],反变换对数比值比为1.549 [95%CI: 1.085 ~ 2.211]。两个模型的秩相关和回归检验均未显示漏斗图不对称和发表偏倚。通过贝叶斯元分析,在后验分布中,模型平均对数优势比为0.26[0.00 ~ 0.90],由于对数优势比中包含零,故结果无统计学意义。该效果的纳入贝叶斯因子(BF)为1.225,显示了联合治疗的轶事支持证据。异质性的纳入BF为0.979,不支持异质性在分析中存在;发表偏倚的纳入BF为0.622,低于1,表明分析中不存在异质性。结论:类固醇联合抗病毒药物治疗贝尔麻痹比类固醇单药治疗更有效。这一结论得到了频率分析的支持,但没有得到贝叶斯方法的支持,因为贝叶斯荟萃分析是不确定的,这表明效应大小存在一些不确定性,但这可能是由于先前的影响。需要进一步的研究,如网络和贝叶斯元分析等先进的综合,以及更多的双盲随机对照试验。
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引用次数: 0
Association between metabolic syndrome and diabetic peripheral neuropathy in patients with type 2 diabetes mellitus: a cross-sectional study. 2型糖尿病患者代谢综合征与糖尿病周围神经病变的相关性:一项横断面研究
Q2 Medicine Pub Date : 2025-07-01 Epub Date: 2025-07-30 DOI: 10.15386/mpr-2779
Abdessamad Malki, Imane Assarrar, Imane Ziani, Fatim Zahra Bentebbaa, Nisrine Bouichrat, Siham Rouf, Hanane Latrech

Background and aims: Diabetic peripheral neuropathy (DPN) is the most prevalent chronic complication of diabetes. Several risk factors have been identified in recent studies, in particular metabolic syndrome (MetS). However, this association remains unclear. We aimed to determine the prevalence of DPN and to study its associated factors, especially the MetS as a potential risk factor of DPN in patients with Type 2 diabetes mellitus (T2DM).

Methods: This was a retrospective and comparative study, with cross-sectional collected data, involving patients with T2DM from North Africa, followed up in the Department of Endocrinology-Diabetology-Nutrition at Mohammed VI University Hospital Center of Oujda, located in the eastern region of Morocco. Patients were grouped according to the presence (T2DM/DPN+, n = 110) or absence of DPN (T2DM/DPN-, n = 290). Data were collected from medical records and analyzed using SPSS software version 21.

Results: DPN was found in 27.5% of the patients. The mean age was similar between the two groups, at 58.96 ± 11.86 years in the T2DM/DPN+ group and 57.10 ± 13.29 years in the T2DM/DPN- group. Males comprised 40.9% of the T2DM/DPN+ group and 31.7% of the T2DM/DPN- group, but this difference was not statistically significant (p = 0.054). Patients with DPN had a significantly longer duration of diabetes (median 10 years vs. 5 years, p < 0.001). Both groups showed glycemic imbalance, with mean HbA1c values of 10.71 ± 2.31% for T2DM/DPN+ and 10.40 ± 2.87% for T2DM/DPN-, without a significant difference. MetS was a significant predictor of neuropathy presence. The prevalence of DPN was greater in individuals with hypertension (p = 0.013), abdominal obesity (p = 0.010), elevated triglyceride levels (p = 0.007), and low HDLc (p = 0.013). Male sex and the duration of diabetes were found to be significant risk factors for the development of DPN.

Conclusion: MetS and its components are strongly associated with the presence of DPN in patients with T2DM. Therefore, screening and optimal control of these risk factors may help prevent DPN in these patients. However, further intervention studies are needed to determine whether comprehensive multifactorial control in patients with T2DM and MetS can effectively prevent DPN.

背景与目的:糖尿病周围神经病变(DPN)是糖尿病最常见的慢性并发症。在最近的研究中已经确定了几个危险因素,特别是代谢综合征(MetS)。然而,这种联系尚不清楚。我们的目的是确定DPN的患病率,并研究其相关因素,特别是MetS作为2型糖尿病(T2DM)患者DPN的潜在危险因素。方法:这是一项回顾性和比较研究,收集了来自北非的T2DM患者的横断面数据,在位于摩洛哥东部地区Oujda的穆罕默德六世大学医院中心的内分泌-糖尿病-营养科进行了随访。根据是否存在DPN (T2DM/DPN+, n = 110)或是否存在DPN (T2DM/DPN-, n = 290)进行分组。数据从病历中收集,并使用SPSS软件21版进行分析。结果:DPN发生率为27.5%。两组患者的平均年龄相似,T2DM/DPN+组为58.96±11.86岁,T2DM/DPN-组为57.10±13.29岁。男性占T2DM/DPN+组的40.9%,占T2DM/DPN-组的31.7%,但差异无统计学意义(p = 0.054)。DPN患者的糖尿病持续时间明显更长(中位10年vs中位5年,p < 0.001)。两组均出现血糖失衡,T2DM/DPN+组平均HbA1c值为10.71±2.31%,T2DM/DPN-组平均HbA1c值为10.40±2.87%,差异无统计学意义。MetS是神经病变存在的重要预测因子。高血压(p = 0.013)、腹部肥胖(p = 0.010)、甘油三酯水平升高(p = 0.007)和低HDLc (p = 0.013)患者DPN患病率更高。男性性别和糖尿病病程是DPN发生的重要危险因素。结论:T2DM患者中,MetS及其成分与DPN的存在密切相关。因此,筛查和优化控制这些危险因素可能有助于预防这些患者的DPN。然而,T2DM合并MetS患者的综合多因素控制是否能有效预防DPN,还需要进一步的干预研究。
{"title":"Association between metabolic syndrome and diabetic peripheral neuropathy in patients with type 2 diabetes mellitus: a cross-sectional study.","authors":"Abdessamad Malki, Imane Assarrar, Imane Ziani, Fatim Zahra Bentebbaa, Nisrine Bouichrat, Siham Rouf, Hanane Latrech","doi":"10.15386/mpr-2779","DOIUrl":"10.15386/mpr-2779","url":null,"abstract":"<p><strong>Background and aims: </strong>Diabetic peripheral neuropathy (DPN) is the most prevalent chronic complication of diabetes. Several risk factors have been identified in recent studies, in particular metabolic syndrome (MetS). However, this association remains unclear. We aimed to determine the prevalence of DPN and to study its associated factors, especially the MetS as a potential risk factor of DPN in patients with Type 2 diabetes mellitus (T2DM).</p><p><strong>Methods: </strong>This was a retrospective and comparative study, with cross-sectional collected data, involving patients with T2DM from North Africa, followed up in the Department of Endocrinology-Diabetology-Nutrition at Mohammed VI University Hospital Center of Oujda, located in the eastern region of Morocco. Patients were grouped according to the presence (T2DM/DPN+, n = 110) or absence of DPN (T2DM/DPN-, n = 290). Data were collected from medical records and analyzed using SPSS software version 21.</p><p><strong>Results: </strong>DPN was found in 27.5% of the patients. The mean age was similar between the two groups, at 58.96 ± 11.86 years in the T2DM/DPN+ group and 57.10 ± 13.29 years in the T2DM/DPN- group. Males comprised 40.9% of the T2DM/DPN+ group and 31.7% of the T2DM/DPN- group, but this difference was not statistically significant (p = 0.054). Patients with DPN had a significantly longer duration of diabetes (median 10 years vs. 5 years, p < 0.001). Both groups showed glycemic imbalance, with mean HbA1c values of 10.71 ± 2.31% for T2DM/DPN+ and 10.40 ± 2.87% for T2DM/DPN-, without a significant difference. MetS was a significant predictor of neuropathy presence. The prevalence of DPN was greater in individuals with hypertension (p = 0.013), abdominal obesity (p = 0.010), elevated triglyceride levels (p = 0.007), and low HDLc (p = 0.013). Male sex and the duration of diabetes were found to be significant risk factors for the development of DPN.</p><p><strong>Conclusion: </strong>MetS and its components are strongly associated with the presence of DPN in patients with T2DM. Therefore, screening and optimal control of these risk factors may help prevent DPN in these patients. However, further intervention studies are needed to determine whether comprehensive multifactorial control in patients with T2DM and MetS can effectively prevent DPN.</p>","PeriodicalId":18438,"journal":{"name":"Medicine and Pharmacy Reports","volume":"98 3","pages":"342-348"},"PeriodicalIF":0.0,"publicationDate":"2025-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12334214/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144817086","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}
引用次数: 0
Association between proton pump inhibitors and anti-coagulants for a better prevention of gastrointestinal bleeding. 质子泵抑制剂与抗凝血剂之间的关系,以更好地预防胃肠道出血。
Q2 Medicine Pub Date : 2025-07-01 Epub Date: 2025-07-30 DOI: 10.15386/mpr-2767
Fahad Mudhi Alotaibi, Nasser Faihan Alotaibi, Faisal Farraj Alsubaie, Hussain Ali Ekhuraidah, Mohammed Ahmed Koshan, Rayan Hassan Alzahrani, Hamdan Saleh Alghamdi, Abed Houmod Allehibi, Abdulrahman Abdullah Aljumah

Background and aim: Gastrointestinal bleeding (GIB) is one of the most common medical emergencies. Proton pump inhibitors (PPI) are among the most widely used drugs in gastroenterology to treat various types of acid-related disorders. We aim to investigate the safety of proton pump inhibitors (PPIs) when used concurrently with anticoagulants in patients with upper and lower gastrointestinal bleeding (GIB) and assess the risk of hospitalization, GIB, and mortality in patients receiving this combined treatment.

Methods: A retrospective multicenter study was conducted at two tertiary care hospitals. Patients were selected according to inclusion and exclusion criteria. Demographic data, vital signs, medical history, physical examinations, comorbid conditions, medications, laboratory investigations, endoscopy findings, management, and complications were retrieved from the medical records of all participants.Data obtained from all patients' medical records were reviewed. Endoscopic findings and management of the bleeding site were collected according to the presenting symptoms. Statistical analyses were performed using IBM SPSS version 25.0 software.

Results: Our results revealed a significant increase in acute GIB risk with the number of concurrent anticoagulants used, particularly in patients not using PPIs. Those using four anticoagulants along with PPIs had a lower likelihood of acute GIB at 6.3% (P = 0.0001). Patients taking two or three anticoagulants also experienced reduced GIB risk when PPIs were added (P ≤ 0.05). Age played a role, with a statistically significant difference between PPI users and non-users, especially in the 31-40 age group, where PPI users had a higher incidence of GIB (69.80%) compared to non-users (30.20%) (P < 0.05). Comparing patients on anticoagulants with or without PPIs, the study found a lower risk of hospitalization (adjusted hazard ratio, AHR: 1.02; 95% CI: 0.92-1.57) and mortality (AHR: 1.00; 95% CI: 0.84-1.11) in those using Rivaroxaban and PPIs concurrently. By contrast, patients using Rivaroxaban alone without PPIs faced an increased risk of hospitalization (AHR: 1.15; 95% CI: 0.98-2.35) and mortality (AHR: 1.12; 95% CI: 0.90-1.37).

Conclusions: Combining PPIs with anticoagulant drugs reduced the risk of GIB, hospitalization, and mortality, particularly in older adults, thereby mitigating potential complications.

背景与目的:胃肠道出血是最常见的急症之一。质子泵抑制剂(PPI)是胃肠病学中应用最广泛的药物之一,用于治疗各种类型的酸相关疾病。我们的目的是研究质子泵抑制剂(PPIs)与抗凝剂同时应用于上消化道和下消化道出血(GIB)患者的安全性,并评估接受这种联合治疗的患者住院、GIB和死亡率的风险。方法:在两所三级医院进行回顾性多中心研究。根据纳入和排除标准选择患者。从所有参与者的医疗记录中检索人口统计数据、生命体征、病史、体格检查、合并症、药物、实验室调查、内窥镜检查结果、管理和并发症。审查了从所有患者医疗记录中获得的数据。根据出现的症状收集内窥镜检查结果和出血部位的处理。采用IBM SPSS 25.0软件进行统计分析。结果:我们的研究结果显示,急性GIB风险与同时使用抗凝剂的数量显著增加,特别是在不使用PPIs的患者中。使用四种抗凝剂和PPIs的患者发生急性GIB的可能性较低,为6.3% (P = 0.0001)。服用两种或三种抗凝药物的患者在添加PPIs后,GIB风险也降低(P≤0.05)。年龄也有影响,PPI使用者与非PPI使用者之间的差异有统计学意义,特别是在31-40岁年龄组,PPI使用者的GIB发生率(69.80%)高于非PPI使用者(30.20%)(P < 0.05)。比较使用抗凝剂和不使用PPIs的患者,研究发现住院风险较低(校正风险比,AHR: 1.02;95% CI: 0.92-1.57)和死亡率(AHR: 1.00;95% CI: 0.84-1.11),同时使用利伐沙班和PPIs的患者。相比之下,单独使用利伐沙班而不使用PPIs的患者面临更高的住院风险(AHR: 1.15;95% CI: 0.98-2.35)和死亡率(AHR: 1.12;95% ci: 0.90-1.37)。结论:PPIs联合抗凝药物降低了GIB的风险、住院和死亡率,特别是在老年人中,从而减轻了潜在的并发症。
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引用次数: 0
Addressing immunization gaps in children with congenital heart disease - a narrative review. 解决先天性心脏病儿童免疫缺口——叙述性综述
Q2 Medicine Pub Date : 2025-07-01 Epub Date: 2025-07-30 DOI: 10.15386/mpr-2814
Diana Jecan-Toader, Cristina Filip, Simona Sorana Căinap

Vaccination programs have had a pivotal part in the successful reduction of global morbidity and mortality of infectious diseases. Despite their undeniable success, vaccination rates among children with congenital heart disease (CHD) remain suboptimal. This article aims to address the challenges surrounding immunization in CHD patients and provide guidance for immunization practices within this population. Most experts advocate for adherence to standard immunization practices in CHD patients who are immunocompetent and in good health. Supplemental vaccinations against rotavirus, varicella, meningococcus, hepatitis A and influenza are recommended. RSV prophylaxis with palivizumab is advisable in patients with hemodynamically significant CHD during winter season. However, special considerations are warranted in specific situations, such as around cardiac surgery or in patients who are immunocompromised. Furthermore, adjustments to the vaccination schedule might be necessary for patients who require antithrombotic prophylaxis or blood transfusions. Lastly, special attention should be given to individuals at a high risk of decompensation after immunization, who might require close parental or medical monitoring for up to 72 hours post-vaccination.

疫苗接种计划在成功降低全球传染病发病率和死亡率方面发挥了关键作用。尽管取得了不可否认的成功,但先天性心脏病(CHD)儿童的疫苗接种率仍然不理想。本文旨在解决冠心病患者免疫接种面临的挑战,并为该人群的免疫接种实践提供指导。大多数专家提倡对具有免疫能力和健康状况良好的冠心病患者坚持标准免疫做法。建议补充接种轮状病毒、水痘、脑膜炎球菌、甲型肝炎和流感疫苗。在冬季有血流动力学显著的冠心病患者,建议使用帕利珠单抗预防RSV。然而,在特殊情况下,如心脏手术或免疫功能低下的患者,需要特别考虑。此外,对于需要抗血栓预防或输血的患者,可能需要调整疫苗接种计划。最后,应特别注意免疫接种后代偿失代偿风险高的个人,他们可能需要在接种疫苗后72小时内进行密切的父母或医疗监测。
{"title":"Addressing immunization gaps in children with congenital heart disease - a narrative review.","authors":"Diana Jecan-Toader, Cristina Filip, Simona Sorana Căinap","doi":"10.15386/mpr-2814","DOIUrl":"10.15386/mpr-2814","url":null,"abstract":"<p><p>Vaccination programs have had a pivotal part in the successful reduction of global morbidity and mortality of infectious diseases. Despite their undeniable success, vaccination rates among children with congenital heart disease (CHD) remain suboptimal. This article aims to address the challenges surrounding immunization in CHD patients and provide guidance for immunization practices within this population. Most experts advocate for adherence to standard immunization practices in CHD patients who are immunocompetent and in good health. Supplemental vaccinations against rotavirus, varicella, meningococcus, hepatitis A and influenza are recommended. RSV prophylaxis with palivizumab is advisable in patients with hemodynamically significant CHD during winter season. However, special considerations are warranted in specific situations, such as around cardiac surgery or in patients who are immunocompromised. Furthermore, adjustments to the vaccination schedule might be necessary for patients who require antithrombotic prophylaxis or blood transfusions. Lastly, special attention should be given to individuals at a high risk of decompensation after immunization, who might require close parental or medical monitoring for up to 72 hours post-vaccination.</p>","PeriodicalId":18438,"journal":{"name":"Medicine and Pharmacy Reports","volume":"98 3","pages":"283-289"},"PeriodicalIF":0.0,"publicationDate":"2025-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12334210/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144817084","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}
引用次数: 0
A case of multi-plug flow control technique treating high flow cirsoid renal arteriovenous malformations. 多塞血流控制技术治疗高流量硬体肾动静脉畸形一例。
Q2 Medicine Pub Date : 2025-07-01 Epub Date: 2025-07-30 DOI: 10.15386/mpr-2769
Emre Can Çelebioğlu, Aysegul Coruh Gursoy, Matheus Dabus, Sadık Bilgiç

Introduction: Renal arteriovenous malformations (AVMs) are rare vascular lesions mostly diagnosed when they become symptomatic. These lesions can be treated using a variety of endovascular techniques and devices.

Case report: We present a 51-year-old male who presented with acute onset right flank pain, hematuria and refractory hypertension. The patient was treated using a multi-plug flow control technique using multiple balloon catheters and microcatheters. Two operators worked synchronously during the procedure using two different dilutions of glue. The patient's symptoms resolved immediately after the embolization and at 1 month follow up the CT demonstrated complete obliteration of the AVM with little renal parenchymal loss. The patient remained clinically asymptomatic at the 6-months follow-up.

Conclusion: This case illustrates the feasibility and safety use of synchronous embolization in the treatment of complex renal AVMs.

肾动静脉畸形(AVMs)是一种罕见的血管病变,大多在出现症状时才被诊断出来。这些病变可以使用多种血管内技术和设备进行治疗。病例报告:我们提出了一个51岁的男性谁提出急性发作的右侧疼痛,血尿和顽固性高血压。患者采用多塞流控制技术,使用多个球囊导管和微导管。两名操作人员在使用两种不同稀释度的胶水的过程中同步工作。患者的症状在栓塞后立即消失,随访1个月时,CT显示AVM完全闭塞,肾实质很少损失。在6个月的随访中,患者仍无临床症状。结论:本病例说明同步栓塞治疗复杂肾动静脉畸形的可行性和安全性。
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引用次数: 0
Emotional distress and quality of life in high and moderate penetrance germline mutations carriers diagnosed with breast cancer: a preliminary study. 乳腺癌高外显率和中等外显率生殖系突变携带者的情绪困扰和生活质量:一项初步研究
Q2 Medicine Pub Date : 2025-07-01 Epub Date: 2025-07-30 DOI: 10.15386/mpr-2898
Claudiu Ioan Filip, Lorin-Manuel Pîrlog, Andrada-Adelaida Pătrăşcanu, Mariela Sanda Militaru, Irina Iordănescu, George Călin Dindelegan

Background/objectives: Genetic testing plays a critical role in breast cancer management by identifying individuals with high or moderate penetrance gene mutations. While clinical implications are well established, less is known about the psychological and quality-of-life impact of different genetic risk levels. This preliminary study aimed to explore whether breast cancer patients with high penetrance mutations experience different levels of distress compared to those with moderate penetrance mutations.

Methods: A total of 110 breast cancer patients treated at the Regina Maria Private Health Network in Cluj-Napoca, Romania, were included based on specific eligibility criteria. Participants completed a shortened version of the BREAST-Q questionnaire, focused on core dimensions such as emotional distress, self-concept, appearance, relationships, and financial burden. Descriptive statistics were calculated, and independent t-tests were performed to compare responses between the two genetic risk groups.

Results: Patients with high penetrance mutations reported significantly higher distress levels in several domains, including overall emotional distress (p = 0.039), concern for daughters or relatives (p = 0.043), changes in appearance (p = 0.038), and self-concept (p = 0.043). Other factors, such as fear of diagnosis, financial burden, and impact on sexuality, did not show statistically significant differences between groups.

Conclusions: This preliminary study suggests that genetic risk classification may influence the psychosocial experience of breast cancer patients, with high penetrance mutation carriers experiencing greater distress in specific areas. These findings highlight the need for personalized psychosocial support based on genetic profiles and warrant further investigation in larger, longitudinal cohorts.

背景/目的:基因检测通过识别具有高外显率或中等外显率基因突变的个体,在乳腺癌管理中起着关键作用。虽然临床意义已经确立,但人们对不同遗传风险水平对心理和生活质量的影响知之甚少。这项初步研究旨在探讨高外显率突变的乳腺癌患者与中等外显率突变的乳腺癌患者是否会经历不同程度的痛苦。方法:根据特定的资格标准,在罗马尼亚克卢日-纳波卡的里贾纳玛丽亚私人健康网络接受治疗的110名乳腺癌患者被纳入研究。参与者完成了一份精简版的BREAST-Q问卷,主要关注诸如情绪困扰、自我概念、外表、人际关系和经济负担等核心维度。计算描述性统计,并进行独立t检验来比较两个遗传风险组之间的反应。结果:高外显率突变的患者在几个领域表现出明显更高的痛苦水平,包括总体情绪困扰(p = 0.039)、对女儿或亲属的关注(p = 0.043)、外貌变化(p = 0.038)和自我概念(p = 0.043)。其他因素,如对诊断的恐惧、经济负担和对性行为的影响,在组间没有统计学上的显著差异。结论:这项初步研究表明,遗传风险分类可能会影响乳腺癌患者的心理社会体验,高外显率突变携带者在特定区域经历更大的痛苦。这些发现强调了基于遗传谱的个性化社会心理支持的必要性,并证明了在更大的纵向队列中进一步调查的必要性。
{"title":"Emotional distress and quality of life in high and moderate penetrance germline mutations carriers diagnosed with breast cancer: a preliminary study.","authors":"Claudiu Ioan Filip, Lorin-Manuel Pîrlog, Andrada-Adelaida Pătrăşcanu, Mariela Sanda Militaru, Irina Iordănescu, George Călin Dindelegan","doi":"10.15386/mpr-2898","DOIUrl":"10.15386/mpr-2898","url":null,"abstract":"<p><strong>Background/objectives: </strong>Genetic testing plays a critical role in breast cancer management by identifying individuals with high or moderate penetrance gene mutations. While clinical implications are well established, less is known about the psychological and quality-of-life impact of different genetic risk levels. This preliminary study aimed to explore whether breast cancer patients with high penetrance mutations experience different levels of distress compared to those with moderate penetrance mutations.</p><p><strong>Methods: </strong>A total of 110 breast cancer patients treated at the Regina Maria Private Health Network in Cluj-Napoca, Romania, were included based on specific eligibility criteria. Participants completed a shortened version of the BREAST-Q questionnaire, focused on core dimensions such as emotional distress, self-concept, appearance, relationships, and financial burden. Descriptive statistics were calculated, and independent t-tests were performed to compare responses between the two genetic risk groups.</p><p><strong>Results: </strong>Patients with high penetrance mutations reported significantly higher distress levels in several domains, including overall emotional distress (p = 0.039), concern for daughters or relatives (p = 0.043), changes in appearance (p = 0.038), and self-concept (p = 0.043). Other factors, such as fear of diagnosis, financial burden, and impact on sexuality, did not show statistically significant differences between groups.</p><p><strong>Conclusions: </strong>This preliminary study suggests that genetic risk classification may influence the psychosocial experience of breast cancer patients, with high penetrance mutation carriers experiencing greater distress in specific areas. These findings highlight the need for personalized psychosocial support based on genetic profiles and warrant further investigation in larger, longitudinal cohorts.</p>","PeriodicalId":18438,"journal":{"name":"Medicine and Pharmacy Reports","volume":"98 3","pages":"349-357"},"PeriodicalIF":0.0,"publicationDate":"2025-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12334241/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144817091","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}
引用次数: 0
Pancreatic cancer: a persistently challenging prognosis - a single center three-year retrospective study. 胰腺癌:持续具有挑战性的预后-一项单中心三年回顾性研究。
Q2 Medicine Pub Date : 2025-07-01 Epub Date: 2025-07-30 DOI: 10.15386/mpr-2848
Paul-Cristian Borz, Mihnea-Bogdan Borz, Oliviu-Cristian Borz, Toader Zaharie, Claudia Hagiu, Lidia Munteanu, Ana Maria Fit, Simona Gurzu

Background: Pancreatic adenocarcinoma (PDAC) is a leading cause of cancer-related mortality due to its aggressive progression and late diagnosis. Despite advances in diagnosis and treatment, survival outcomes remain poor, with a median survival of 5.8 months.

Objective: The aim of the study is to evaluate the impact of diagnostic and therapeutic approaches on survival outcomes in patients with pancreatic adenocarcinoma, while also assessing the risk factors for PDAC.

Methods: This study is a retrospective analysis of 68 patients with suspected pancreatic tumors who underwent endoscopic ultrasound-guided fine needle aspiration biopsy (EUS-FNAB) between 2019 and 2022 at the Cluj-Napoca County Emergency Clinical Hospital. Patient demographics, risk factors, histopathological results, and treatment outcomes were analyzed using statistical methods.

Results: Of 68 patients, 35 were diagnosed with PDAC. Modifiable risk factors, such as alcohol and smoking, alongside non-modifiable factors like age and hereditary predisposition, were prominent. Among PDAC patients, 42.8% received palliative chemotherapy, while only 8.6% underwent curative surgical intervention due to advanced disease stages. Median survival varied significantly based on treatment: 2.4 months for untreated patients versus 8.1 months for those receiving oncological or surgical management (p=0.0082).

Conclusion: Modifiable and non-modifiable risk factors significantly raise the incidence of pancreatic cancer. Therefore, employing a multidisciplinary approach to detect the disease in its early stages and optimize personalized treatment plans can enhance patient outcomes. At the same time, traditional oncological treatments improve survival and quality of life, but newer approaches, such as immunotherapy combined with conventional radiotherapy, chemotherapy, molecular targeted therapy, and other diverse treatment modalities, have the potential to further extend survival.

背景:胰腺腺癌(PDAC)由于其侵袭性进展和晚期诊断,是癌症相关死亡的主要原因。尽管在诊断和治疗方面取得了进展,但生存结果仍然很差,中位生存期为5.8个月。目的:本研究的目的是评估诊断和治疗方法对胰腺腺癌患者生存结局的影响,同时评估PDAC的危险因素。方法:回顾性分析2019年至2022年在克卢日-纳波卡县急诊临床医院行内镜超声引导下细针穿刺活检(EUS-FNAB)的68例疑似胰腺肿瘤患者。采用统计学方法分析患者人口统计学、危险因素、组织病理学结果和治疗结果。结果:68例患者中,35例确诊为PDAC。可改变的风险因素,如酒精和吸烟,以及不可改变的因素,如年龄和遗传易感性,是突出的。在PDAC患者中,42.8%的患者接受了姑息性化疗,而只有8.6%的患者因疾病晚期接受了根治性手术干预。中位生存期因治疗而有显著差异:未经治疗的患者为2.4个月,接受肿瘤或手术治疗的患者为8.1个月(p=0.0082)。结论:可改变和不可改变的危险因素可显著提高胰腺癌的发病率。因此,采用多学科方法在早期发现疾病并优化个性化治疗方案可以提高患者的预后。与此同时,传统的肿瘤治疗方法提高了生存率和生活质量,但新的方法,如免疫治疗联合常规放疗、化疗、分子靶向治疗等多种治疗方式,有可能进一步延长生存期。
{"title":"Pancreatic cancer: a persistently challenging prognosis - a single center three-year retrospective study.","authors":"Paul-Cristian Borz, Mihnea-Bogdan Borz, Oliviu-Cristian Borz, Toader Zaharie, Claudia Hagiu, Lidia Munteanu, Ana Maria Fit, Simona Gurzu","doi":"10.15386/mpr-2848","DOIUrl":"10.15386/mpr-2848","url":null,"abstract":"<p><strong>Background: </strong>Pancreatic adenocarcinoma (PDAC) is a leading cause of cancer-related mortality due to its aggressive progression and late diagnosis. Despite advances in diagnosis and treatment, survival outcomes remain poor, with a median survival of 5.8 months.</p><p><strong>Objective: </strong>The aim of the study is to evaluate the impact of diagnostic and therapeutic approaches on survival outcomes in patients with pancreatic adenocarcinoma, while also assessing the risk factors for PDAC.</p><p><strong>Methods: </strong>This study is a retrospective analysis of 68 patients with suspected pancreatic tumors who underwent endoscopic ultrasound-guided fine needle aspiration biopsy (EUS-FNAB) between 2019 and 2022 at the Cluj-Napoca County Emergency Clinical Hospital. Patient demographics, risk factors, histopathological results, and treatment outcomes were analyzed using statistical methods.</p><p><strong>Results: </strong>Of 68 patients, 35 were diagnosed with PDAC. Modifiable risk factors, such as alcohol and smoking, alongside non-modifiable factors like age and hereditary predisposition, were prominent. Among PDAC patients, 42.8% received palliative chemotherapy, while only 8.6% underwent curative surgical intervention due to advanced disease stages. Median survival varied significantly based on treatment: 2.4 months for untreated patients versus 8.1 months for those receiving oncological or surgical management (p=0.0082).</p><p><strong>Conclusion: </strong>Modifiable and non-modifiable risk factors significantly raise the incidence of pancreatic cancer. Therefore, employing a multidisciplinary approach to detect the disease in its early stages and optimize personalized treatment plans can enhance patient outcomes. At the same time, traditional oncological treatments improve survival and quality of life, but newer approaches, such as immunotherapy combined with conventional radiotherapy, chemotherapy, molecular targeted therapy, and other diverse treatment modalities, have the potential to further extend survival.</p>","PeriodicalId":18438,"journal":{"name":"Medicine and Pharmacy Reports","volume":"98 3","pages":"325-332"},"PeriodicalIF":0.0,"publicationDate":"2025-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12334243/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144817096","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}
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