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A bidirectional Mendelian randomization study of spleen volume and Crohn disease. 脾脏体积与克罗恩病的双向孟德尔随机研究
IF 1.3 4区 医学 Q2 MEDICINE, GENERAL & INTERNAL Pub Date : 2024-11-15 DOI: 10.1097/MD.0000000000040515
Hang-Hang Song, Hao-Ran Zhang, Xiao-Rong Hu, Xi-Cheng Jiang

In observational studies, there has been an association found between spleen volume and Crohn disease. We conducted a two-way, two-sample Mendelian randomization analysis to determine whether these associations have a causal relationship. Single nucleotide polymorphisms (P < 5 × 10-8) were used as instrumental variables for spleen volume and Crohn disease. Estimates of the genetic associations between spleen volume and Crohn disease were obtained from the Integrative Epidemiology Unit, European Bioinformatics Institute, UK Biobank, and FinnGen databases. Analysis was performed using MR-Egger regression, weighted median estimator, inverse variance weighted, simple model, and weighted model. Genetically predicted spleen volume was found to be associated with Crohn disease. In the IEU database, the odds ratios (ORs) for Crohn disease caused by spleen volume were 1.237 (95% CI, 1.056-1.417, P = .021), and the ORs for spleen volume caused by Crohn disease were 1.015 (95% CI, 0.985-1.044; P = .049). In the EBI database, the ORs for Crohn disease caused by spleen volume were 1.292 (95% CI, 1.120-1.463, P = .003), and the ORs for spleen volume caused by Crohn disease were 1.026 (95% CI, 1.005-1.046; P = .013). Results from the UKB and FinnGen databases showed no causal relationship between the two. The summary results showed that Crohn disease caused an increase in spleen volume, with ORs of 1.009 (95% CI, 1.000-1.018; P = .047). This study provides evidence for a mutual causal relationship between spleen volume and an increased risk of Crohn disease.

观察性研究发现,脾脏体积与克罗恩病之间存在关联。我们进行了双向、双样本孟德尔随机分析,以确定这些关联是否存在因果关系。单核苷酸多态性(P
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引用次数: 0
A child with factor V deficiency with a novel F5 gene mutation misdiagnosed as a left iliac fossa abscess: A case report. 一名因新型 F5 基因突变而被误诊为左髂窝脓肿的 V 因子缺乏症患儿:病例报告。
IF 1.3 4区 医学 Q2 MEDICINE, GENERAL & INTERNAL Pub Date : 2024-11-15 DOI: 10.1097/MD.0000000000040436
Yifan Zhang, Lu Liu, Qin Guo, Yiyuan Li, Shuanghong Luo, Chaomin Wan, Yu Zhu

Rationale: Congenital factor V deficiency is classified as a rare bleeding disorder that is expressed in an autosomal recessive manner and generally occurs in 1 in a million people. This disorder is accompanied by a variety of clinical manifestations, which can easily lead to misdiagnosis. This is the first report to identify the factor V gene variant c.2439delC (p.I814Lfs*23) in exon 13.

Patient concerns: A 13-year-old boy was admitted with a suspected left iliac fossa abscess. He had been previously diagnosed with and underwent management for a left iliac fossa abscess at a local hospital. The patient was treated with antibiotics and underwent surgical excision; however, his left iliac fossa mass reappeared. Platelet count and function, prothrombin time, and activated partial thromboplastin time were all normal.

Diagnoses: The patient was considered to have congenital factor V deficiency following the measurement of coagulation factor activity, and the diagnosis was confirmed by genetic testing.

Interventions: The mass was diagnosed as an abscess and the patient was treated with antibiotics at the local hospital. Surgical resection was performed, after which the mass was identified as a hematoma. The patient was then transferred to our hospital for treatment with fresh frozen plasma (FFP) infusion.

Outcomes: The left iliac fossa mass stopped growing and the coagulation function exhibited a significant improvement. At discharge, the patient was recommended to seek medical help before any surgical intervention or following trauma, and when a deep hemorrhage is identified, the patient should undergo timely infusion with FFP.

Lessons: This case report presents a rare occurrence of congenital factor V deficiency resulting in a left iliac fossa hematoma mistaken for an abscess, which resulted in unnecessary antibiotic therapy and surgery. This case emphasizes that coagulation factor deficiency should be highly suspected for joint mass combined with coagulation dysfunction.

理由先天性 V 因子缺乏症是一种罕见的出血性疾病,表现为常染色体隐性遗传,一般发生率为百万分之一。这种疾病伴有多种临床表现,很容易导致误诊。这是第一份确定第 13 外显子中因子 V 基因变异 c.2439delC (p.I814Lfs*23) 的报告:一名 13 岁男孩因疑似左侧髂窝脓肿入院。他曾在当地一家医院被诊断为左侧髂窝脓肿并接受了治疗。患者接受了抗生素治疗和手术切除,但左侧髂窝肿块再次出现。血小板计数和功能、凝血酶原时间和活化部分凝血活酶时间均正常:诊断:在测量凝血因子活性后,患者被认为患有先天性 V 型因子缺乏症,并通过基因检测确诊:干预措施:肿块被诊断为脓肿,患者在当地医院接受了抗生素治疗。手术切除后,肿块被确认为血肿。随后,患者被转到我院接受新鲜冰冻血浆(FFP)输注治疗:左侧髂窝肿块停止生长,凝血功能明显改善。出院时,医生建议患者在手术治疗前或外伤后及时就医,一旦发现深部出血,应及时输注新鲜冰冻血浆:本病例报告了一起罕见的先天性因子 V 缺乏导致左侧髂窝血肿被误认为脓肿的病例,该病例导致了不必要的抗生素治疗和手术。本病例强调,关节肿块合并凝血功能障碍时应高度怀疑凝血因子缺乏症。
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引用次数: 0
Prevalence and characteristics of positional obstructive sleep apnea in a Saudi population-based cohort. 沙特人群中体位性阻塞性睡眠呼吸暂停的患病率和特征。
IF 1.3 4区 医学 Q2 MEDICINE, GENERAL & INTERNAL Pub Date : 2024-11-15 DOI: 10.1097/MD.0000000000040455
Siraj Wali, Omar Kanbr, Faris Alhejaili, Ranya Alshumrani, Md Dilshad Manzar, Haneen Mansour

Obstructive sleep apnea (OSA), significantly impacts public health, with varying prevalence rates across populations. Positional obstructive sleep apnea (POSA) is a subtype in which OSA predominantly occurs in the supine position. This study investigated the prevalence and characteristics of exclusive positional obstructive sleep apnea (e-POSA) in a representative Saudi population. Data from a previous cohort study on the prevalence of OSA in Saudi Arabia were utilized. A 2-phase approach was used: the first phase involved a screening questionnaire, and the second phase involved confirmatory polysomnography (PSG). E-POSA was defined as an apnea-hypopnea index (AHI) in the supine position at least twice as high as that in the lateral position, with the lateral AHI not exceeding 5. Then, an exploration method was used to estimate the prevalence of e-POSA. There were 235 OSA patients included in this study. The prevalence of e-POSA among the OSA patients was 21.28%, with a higher prevalence in females (26.76%) than in males (18.90%). However, the estimated prevalence of e-POSA in the Saudi population was 1.86%. Patients with e-POSA tended to be younger and to have lower AHI, Epworth Sleepiness Scale (ESS) and arousal index scores (P < .001). Multivariate analysis revealed that the rapid eye movement (REM) related AHI and nonsupine AHI were predictors of e-POSA (P < .01). E-POSA is common in patients with OSA. However, the estimated prevalence of e-POSA across the general population was 1.86%. Patients with e-POSA have milder disease, and the AHI-REM and AHI-nonsupine were identified as predictors.

阻塞性睡眠呼吸暂停(OSA)严重影响公众健康,在不同人群中的发病率各不相同。体位性阻塞性睡眠呼吸暂停(POSA)是 OSA 主要发生在仰卧位的一种亚型。本研究调查了具有代表性的沙特人群中体位性阻塞性睡眠呼吸暂停(e-POSA)的患病率和特征。研究利用了之前一项关于沙特阿拉伯 OSA 患病率的队列研究数据。研究分两个阶段进行:第一阶段为筛查问卷,第二阶段为多导睡眠图(PSG)确诊。E-POSA 的定义是仰卧位的呼吸暂停-低通气指数(AHI)至少是侧卧位的两倍,且侧卧位的 AHI 不超过 5。然后,采用探查法估算出e-POSA的患病率。本研究共纳入 235 名 OSA 患者。在 OSA 患者中,e-POSA 的患病率为 21.28%,其中女性的患病率(26.76%)高于男性(18.90%)。然而,据估计,e-POSA 在沙特人口中的发病率为 1.86%。e-POSA 患者往往更年轻,AHI、埃普沃斯嗜睡量表(ESS)和唤醒指数评分也更低(P<0.05)。
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引用次数: 0
An observational study on efficacy of atrioventricular nodal slow pathway ablation in patients with atrioventricular nodal reentrant tachycardia and its influence on atrioventricular conduction function. 房室结再发性心动过速患者房室结慢通路消融疗效及其对房室传导功能影响的观察性研究。
IF 1.3 4区 医学 Q2 MEDICINE, GENERAL & INTERNAL Pub Date : 2024-11-15 DOI: 10.1097/MD.0000000000040532
Hongwei Wang, Xiumei Li

The study aimed to evaluate the effectiveness of atrioventricular nodal slow pathway ablation in patients with atrioventricular nodal reentrant tachycardia (AVNRT) and examine its impact on the atrioventricular conduction function. A retrospective analysis was performed on the clinical data of 90 AVNRT patients who underwent radiofrequency ablation at our institution between August 2018 and February 2021. Based on the presence or absence of slow pathway conduction during the procedure, patients were classified into the slow pathway elimination group (SPE group) and the slow pathway improvement group (SPI group). Procedure-related parameters, His bundle electrogram, atrioventricular nodal effective refractory period (AVN-ERP), Wenckebach point of anterograde atrioventricular nodal conduction (AVN-WKB), Wenckebach point of retrograde atrioventricular nodal conduction (VAV-WKB), myocardial function were compared between the 2 groups. Additionally, the recurrence rates 1 and 2 years post-ablation were noted. Both groups reported a 100% success rate for the procedure. Post-ablation, 42 patients exhibited persisting atrioventricular nodal slow pathway, whereas 48 showed its disappearance, signifying the absence of the jump phenomenon and atrial echo. Post-ablation, the SPI group showed an increase in slow pathway AVN-ERP compared to pre-ablation values (P < .05), with no significant change in the fast pathway AVN-ERP (P > .05). The SPE group showed a reduction in both slow pathway and fast pathway AVN-ERP post-ablation (P < .05). Post-ablation, both slow pathway and fast pathway AVN-ERP in the SPI group were higher than in the SPE group (P < .05). AVN-WKB and VAV-WKB values increased in both groups after ablation (P < .05). There were no recurrences 1 or 2 years after ablation in the SPE group and 1 case of recurrence 2 years after ablation in the SPI group (2.38%). Different ablation endpoints during radiofrequency ablation had no apparent impact on atrioventricular conduction time, recurrence rate, and myocardial function in patients with AVNRT, but they advanced AVN-WKB and VAV-WKB. Slow pathway improvement led to an elongation of slow pathway AVN-ERP, while slow pathway elimination resulted in a reduction of both slow pathway and fast pathway AVN-ERP.

该研究旨在评估房室结再发性心动过速(AVNRT)患者房室结慢通路消融术的有效性,并考察其对房室传导功能的影响。我们对2018年8月至2021年2月期间在本院接受射频消融术的90例AVNRT患者的临床数据进行了回顾性分析。根据手术过程中是否出现慢通路传导,将患者分为慢通路消除组(SPE 组)和慢通路改善组(SPI 组)。比较两组患者的手术相关参数、His束电图、房室结有效折返期(AVN-ERP)、房室结前向传导温克巴赫点(AVN-WKB)、房室结逆行传导温克巴赫点(VAV-WKB)和心肌功能。此外,还注意到了消融术后 1 年和 2 年的复发率。两组患者的手术成功率均为 100%。消融术后,42 名患者表现出持续的房室结缓慢通路,而 48 名患者则表现出该通路消失,这表明没有跳跃现象和心房回声。消融术后,SPI 组的慢通路 AVN-ERP 与消融术前的值相比有所增加(P .05)。SPE 组消融后慢通路和快通路 AVN-ERP 均下降(P.05)。
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引用次数: 0
Prognostic value of lncRNA CBR3-AS1 for patients with cancer: A meta-analysis. lncRNA CBR3-AS1 对癌症患者的预后价值:荟萃分析
IF 1.3 4区 医学 Q2 MEDICINE, GENERAL & INTERNAL Pub Date : 2024-11-15 DOI: 10.1097/MD.0000000000040361
Jun Peng, Daidong Wang, Shixue Liu

Background: Several studies have shown that the long noncoding RNA (lncRNA) CBR3-AS1 is overexpressed in various cancers and is playing an oncogene role. This meta-analysis aims to elucidate the relationship between lncRNA CBR3-AS1 expression and the prognosis and clinicopathological features of cancer patients.

Methods: A comprehensive and systematic search was conducted in PubMed, Web of Science, Cochrane Library, and EMBASE database. Pooled odds ratios (ORs) and hazard ratios (HRs) with 95% confidence intervals (CIs) were employed to evaluate the association between lncRNA CBR3-AS1 expression and clinical outcomes and clinicopathological features in cancer patients.

Results: This meta-analysis finally enrolled 9 studies comprising 800 cancer patients. The combined results indicated that lncRNA CBR3-AS1 overexpression was significantly associated with shorter overall survival (pooled hazard ratios = 1.69, 95% CI 1.28-2.21, P < .001). Furthermore, elevated lncRNA CBR3-AS1 expression was closely correlated with larger tumor size (large vs small OR = 2.17, 95% CI: 1.50-3.14, P < .0001), lymph node metastasis (yes vs no OR = 2.75, 95% CI: 1.67-4.51, P < .0001), distant metastasis (yes vs no OR = 3.08, 95% CI: 1.82-5.23, P < .0001), and advanced tumour, node, metastasis stage (III/IV vs I/II OR = 2.82, 95% CI: 1.68-4.75, P < .0001).

Conclusion: Upregulated expression of lncRNA CBR3-AS1 showed significant association with unfavorable survival and indicated worse clinicopathological outcomes in multiple kinds of human cancer, and therefore might serve as a promising prognosis biomarker and therapeutic target for cancers.

背景:多项研究表明,长非编码RNA(lncRNA)CBR3-AS1在多种癌症中过度表达,并发挥着癌基因的作用。本荟萃分析旨在阐明 lncRNA CBR3-AS1 表达与癌症患者预后和临床病理特征之间的关系:方法:在PubMed、Web of Science、Cochrane Library和EMBASE数据库中进行了全面系统的检索。方法:在PubMed、Web Science、Cochrane Library和EMBASE数据库中进行了全面、系统的检索,采用汇总的几率比(ORs)和危险比(HRs)及95%置信区间(CIs)来评估lncRNA CBR3-AS1表达与癌症患者临床预后和临床病理特征之间的关系:这项荟萃分析最终纳入了9项研究,包括800名癌症患者。综合结果表明,lncRNA CBR3-AS1 的过表达与较短的总生存期显著相关(汇总危险比 = 1.69,95% CI 1.28-2.21,P 结论:lncRNA CBR3-AS1 的过表达与较短的总生存期显著相关:在多种人类癌症中,lncRNA CBR3-AS1的上调表达与不利的生存期明显相关,表明临床病理结果更差,因此可作为一种有前景的癌症预后生物标志物和治疗靶点。
{"title":"Prognostic value of lncRNA CBR3-AS1 for patients with cancer: A meta-analysis.","authors":"Jun Peng, Daidong Wang, Shixue Liu","doi":"10.1097/MD.0000000000040361","DOIUrl":"10.1097/MD.0000000000040361","url":null,"abstract":"<p><strong>Background: </strong>Several studies have shown that the long noncoding RNA (lncRNA) CBR3-AS1 is overexpressed in various cancers and is playing an oncogene role. This meta-analysis aims to elucidate the relationship between lncRNA CBR3-AS1 expression and the prognosis and clinicopathological features of cancer patients.</p><p><strong>Methods: </strong>A comprehensive and systematic search was conducted in PubMed, Web of Science, Cochrane Library, and EMBASE database. Pooled odds ratios (ORs) and hazard ratios (HRs) with 95% confidence intervals (CIs) were employed to evaluate the association between lncRNA CBR3-AS1 expression and clinical outcomes and clinicopathological features in cancer patients.</p><p><strong>Results: </strong>This meta-analysis finally enrolled 9 studies comprising 800 cancer patients. The combined results indicated that lncRNA CBR3-AS1 overexpression was significantly associated with shorter overall survival (pooled hazard ratios = 1.69, 95% CI 1.28-2.21, P < .001). Furthermore, elevated lncRNA CBR3-AS1 expression was closely correlated with larger tumor size (large vs small OR = 2.17, 95% CI: 1.50-3.14, P < .0001), lymph node metastasis (yes vs no OR = 2.75, 95% CI: 1.67-4.51, P < .0001), distant metastasis (yes vs no OR = 3.08, 95% CI: 1.82-5.23, P < .0001), and advanced tumour, node, metastasis stage (III/IV vs I/II OR = 2.82, 95% CI: 1.68-4.75, P < .0001).</p><p><strong>Conclusion: </strong>Upregulated expression of lncRNA CBR3-AS1 showed significant association with unfavorable survival and indicated worse clinicopathological outcomes in multiple kinds of human cancer, and therefore might serve as a promising prognosis biomarker and therapeutic target for cancers.</p>","PeriodicalId":18549,"journal":{"name":"Medicine","volume":"103 46","pages":"e40361"},"PeriodicalIF":1.3,"publicationDate":"2024-11-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11576033/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142668186","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Reoperation after short-segment lumbar spinal fusion surgery in dialysis patients: A retrospective cohort study. 透析患者短节段腰椎融合手术后的再手术:一项回顾性队列研究。
IF 1.3 4区 医学 Q2 MEDICINE, GENERAL & INTERNAL Pub Date : 2024-11-15 DOI: 10.1097/MD.0000000000040581
Tomohisa Inoue, Keiji Wada, Jun Sugaya, Ken Okazaki, Toru Doi

Patients with dialysis are at high risk of reoperation after lumbar spinal fusion surgery. However, the risk of reoperation after short-segment (≤2 fusion levels) lumbar spinal fusion surgery in this patient group has not been completely investigated. This study aimed to compare the risk of reoperation after short-segment lumbar spinal fusion surgery between patients with dialysis and matched controls without dialysis. We retrospectively evaluated 85 patients who underwent short-segment lumbar spinal fusion surgery at a single institution. Based on the current dialysis treatment, patients were divided into the non-dialysis and dialysis groups. We compared the patients' characteristics, surgical data, pre- and postoperative radiographic measurements, locomotive functional levels in activities of daily living (ADL), rate of whole reoperation, and cause-specific incidence of reoperation such as adjacent segmental disease (ASD) and implant failure between the non-dialysis and dialysis groups. Then, these variables were compared after adjusting for age, sex, and body mass index (BMI) via a propensity-score-matched analysis. In total, 68 patients in the non-dialysis group and 17 patients in the dialysis group were included in this study. The dialysis group was significantly younger and had a lower postoperative ADL status than the non-dialysis group. Moreover, the dialysis group had a significantly higher rate of whole reoperation (8.8% vs 41.2%, P = .003), reoperation due to ASD (4.4% vs 23.5%, P = .027), and reoperation due to implant failure (0.8% vs 11.8%, P = .038) than in the non-dialysis group. Based on a propensity-score-matched analysis, the dialysis group had a significantly higher rate reoperation rate after short-segment lumbar spinal fusion surgery than the non-dialysis group (0.0% vs 58.3%, P = .005). The current study firstly clarified that patients with dialysis are at significantly high risk of reoperation even after short-segment lumbar spinal fusion surgery.

透析患者在腰椎融合手术后再次手术的风险很高。然而,对这一患者群体进行短节段(≤2个融合水平)腰椎融合手术后再次手术的风险尚未进行全面调查。本研究旨在比较透析患者与未透析的匹配对照组在短节段腰椎融合手术后再次手术的风险。我们回顾性评估了在一家医疗机构接受短节段腰椎融合手术的 85 名患者。根据目前的透析治疗情况,患者被分为非透析组和透析组。我们比较了非透析组和透析组患者的特征、手术数据、术前和术后影像学测量结果、日常生活活动(ADL)中的运动功能水平、整个再手术率以及再手术的特定原因发生率,如邻近节段疾病(ASD)和植入失败。然后,通过倾向分数匹配分析,在调整年龄、性别和体重指数(BMI)后对这些变量进行比较。本研究共纳入了 68 名非透析组患者和 17 名透析组患者。与非透析组相比,透析组患者明显更年轻,术后ADL状况也更差。此外,透析组患者的整个再手术率(8.8% vs 41.2%,P = .003)、因 ASD 导致的再手术率(4.4% vs 23.5%,P = .027)和因植入失败导致的再手术率(0.8% vs 11.8%,P = .038)均明显高于非透析组。根据倾向分数匹配分析,透析组在短节段腰椎融合手术后的再手术率(0.0% vs 58.3%,P = .005)明显高于非透析组。本研究首次明确了透析患者即使在短节段腰椎融合手术后再次手术的风险也明显较高。
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引用次数: 0
Research frontiers and hotspots of coronary chronic total occlusion: A bibliometric analysis. 冠状动脉慢性全闭塞的研究前沿和热点:文献计量分析。
IF 1.3 4区 医学 Q2 MEDICINE, GENERAL & INTERNAL Pub Date : 2024-11-15 DOI: 10.1097/MD.0000000000040537
Shudi Li, Menghe Zhang, Wenwen Li, Zhenhai Sun, Yunxiao Zhang, Yaoyao Zuo, Shouqiang Chen

By analyzing the relevant literature, we can accurately grasp the current status of diagnosis and treatment of chronic total occlusion of coronary artery, and clarify the development trend, research frontiers and hotspots of this disease. A literature search with "chronic total occlusion" as the title was performed in the Web of Science database. The title, author, abstract, keywords, institution, publication, country, reference, and other endnotes of the selected literature were exported in the form of text. The author, country, institution, and keywords of the literature were analyzed through Citespace and VOSviewer. The United States has the highest proportion of articles. The institution with the largest number of publications in this field is the Minneapolis Heart Institute Foundation. Brilakis Emmanouil S is the author with the most published articles. The journal system with the largest number of articles in this field is Cardiac Cardiovascular Systems. The keywords with the highest frequency are "chronic total occlusion," "percutaneous coronary intervention," "recanalization," and "revascularization." The burst detection analysis of hot keywords shows that "algorithm," "management," and "mortality" are the research hotspots in this field in recent years. At present, the research on this disease mainly focuses on the opening of occluded coronary arteries through various treatment methods. In the near future and the next few years, the research hotspots may be the scoring system algorithms for the treatment of chronic total occlusion of coronary artery and the management strategies for patients.

通过对相关文献的分析,我们可以准确把握慢性冠状动脉全闭塞的诊治现状,明确该病的发展趋势、研究前沿和热点。在 Web of Science 数据库中以 "慢性冠状动脉完全闭塞 "为标题进行文献检索。将所选文献的标题、作者、摘要、关键词、机构、刊物、国家、参考文献和其他尾注以文本形式导出。通过 Citespace 和 VOSviewer 对文献的作者、国家、机构和关键词进行了分析。美国的文章比例最高。在该领域发表论文最多的机构是明尼阿波利斯心脏研究所基金会。发表文章最多的作者是 Brilakis Emmanouil S。该领域发表文章最多的期刊系统是《Cardiac Cardiovascular Systems》。出现频率最高的关键词是 "慢性全闭塞"、"经皮冠状动脉介入"、"再通畅 "和 "血管再通"。对热点关键词的突发性检测分析表明,"算法"、"管理 "和 "死亡率 "是近年来该领域的研究热点。目前,对该疾病的研究主要集中在通过各种治疗方法打通闭塞的冠状动脉。近期和未来几年的研究热点可能是慢性冠状动脉完全闭塞治疗的评分系统算法和患者的管理策略。
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引用次数: 0
Characteristics of the current situation of drug use in elderly patients with chronic diseases in Chongqing: A cross-sectional survey. 重庆市老年慢性病患者的用药现状特征:横断面调查
IF 1.3 4区 医学 Q2 MEDICINE, GENERAL & INTERNAL Pub Date : 2024-11-15 DOI: 10.1097/MD.0000000000040470
Xiaolei Hu, Min Tang, Jie Feng, Weiqiong Chen, Guangcan Li, Ling Ding, Mo Cheng, Mengying Liu, Jun Zhou, Xiaofei Liu, Jia Liu

Following improved accessibility to medical services, the phenomenon of polypharmacy in elderly patients with comorbidity has been increasing globally. Polypharmacy patients are prone to drug interactions, adverse drug reactions, and even the risk of death etc. Therefore, there is an urgent need to fully understand the current status and characteristics of drug use in elderly patients with chronic diseases, focusing on polypharmacy factors to ensure that medications for elderly patients are effective and safe. To collect and analyze the characteristics of the current drug use situation in elderly patients with chronic diseases in Chongqing and further explore the influencing factors for polypharmacy, providing references for formulating more effective and safe medication regimens for elderly patients. Most elderly patients affected with chronic diseases in Chongqing were willing to go to hospitals or pharmacies to buy medicines. However, they were not familiar with their disease conditions and drug-related adverse reactions and could not be regularly followed up or monitored. The number of diseases, medications, and adverse drug reactions increased with the increasing age of elderly patients. The problem of irrational use of drugs in elderly patients with chronic diseases was relatively prominent, especially the use of traditional Chinese medicines. The medication situation in elderly patients with chronic diseases was not optimistic, and the problem of polypharmacy was relatively prominent. Further large-scale studies are needed to provide a certain reference for improving the current status of drug use in elderly patients.

随着医疗服务可及性的提高,全球合并症老年患者的多重用药现象日益增多。使用多种药物的患者容易发生药物相互作用、药物不良反应,甚至死亡风险等。因此,迫切需要全面了解老年慢性病患者的用药现状和特点,重点关注多药因素,确保老年患者用药的有效性和安全性。收集和分析重庆市老年慢性病患者的用药现状特点,进一步探讨多重用药的影响因素,为老年患者制定更有效、更安全的用药方案提供参考。重庆市大部分老年慢性病患者都愿意去医院或药店买药。然而,他们对自己的病情和药物相关不良反应并不熟悉,无法定期随访或监测。随着老年患者年龄的增长,疾病、药物和药物不良反应的数量也在增加。老年慢性病患者不合理用药问题较为突出,尤其是中药的使用。老年慢性病患者的用药情况不容乐观,多药合用问题较为突出。需要进一步开展大规模研究,为改善老年患者用药现状提供一定参考。
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引用次数: 0
The role of integrin-related genes in atherosclerosis complicated by abdominal aortic aneurysm. 整合素相关基因在腹主动脉瘤并发动脉粥样硬化中的作用
IF 1.3 4区 医学 Q2 MEDICINE, GENERAL & INTERNAL Pub Date : 2024-11-15 DOI: 10.1097/MD.0000000000040293
Degao Hong, Likang Ma, Lei Jin, Lele Tang, Liangwan Chen, Zhihuang Qiu

Increasingly, the shared risk factors and pathological processes of atherosclerosis and abdominal aortic aneurysm (AAA) are being recognized. The aim of our study was to identify the hub genes involved in the pathogenesis of atherosclerosis and AAA. The analysis was based on 2 gene expression profiles for atherosclerosis (GSE28829) and AAA (GSE7084), downloaded from the Gene Expression Omnibus database. Common differential genes were identified and an enrichment analysis of differential genes was conducted, with construction of protein-protein interaction networks, and identification of common hub genes, and predicted transcription factors. The analysis identified 133 differentially expressed genes (116 upregulated and 17 downregulated), with the enrichment analysis identifying a potential important role of integrins and chemokines in the common immune and inflammatory responses of atherosclerosis and AAA. Regulation of the complement and coagulation cascades and regulation of the actin cytoskeleton were associated with both diseases, with 10 important hub genes identified: TYROBP, PTPRC, integrin subunit beta 2, ITGAM, PLEK, cathepsin S, lymphocyte antigen 86, ITGAX, CCL4, and FCER1G. Findings identified a common pathogenetic pathway between atherosclerosis and AAA, with integrin-related genes playing a significant role. The common pathways and hub genes identified provide new insights into the shared mechanisms of these 2 diseases and can contribute to identifying new therapeutic targets and predicting the therapeutic effect of biological agents.

越来越多的人认识到动脉粥样硬化和腹主动脉瘤(AAA)具有共同的危险因素和病理过程。我们的研究旨在确定参与动脉粥样硬化和腹主动脉瘤发病机制的枢纽基因。分析基于从基因表达总库数据库下载的动脉粥样硬化(GSE28829)和腹主动脉瘤(AAA)的两个基因表达谱(GSE7084)。通过构建蛋白质-蛋白质相互作用网络、识别常见的中枢基因和预测的转录因子,确定了常见的差异基因,并对差异基因进行了富集分析。分析确定了 133 个差异表达基因(116 个上调,17 个下调),富集分析确定了整合素和趋化因子在动脉粥样硬化和 AAA 的常见免疫和炎症反应中的潜在重要作用。补体和凝血级联的调控以及肌动蛋白细胞骨架的调控与这两种疾病都有关联,其中发现了 10 个重要的枢纽基因:TYROBP、PTPRC、整合素亚基 beta 2、ITGAM、PLEK、cathepsin S、淋巴细胞抗原 86、ITGAX、CCL4 和 FCER1G。研究结果发现了动脉粥样硬化和 AAA 之间的共同致病途径,其中整合素相关基因发挥了重要作用。发现的共同途径和枢纽基因为了解这两种疾病的共同机制提供了新的视角,有助于确定新的治疗靶点和预测生物制剂的治疗效果。
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引用次数: 0
The effects of rapid rehabilitation nursing on improving postoperative rehabilitation effect and life quality of early breast cancer patients. 快速康复护理对提高早期乳腺癌患者术后康复效果和生活质量的影响
IF 1.3 4区 医学 Q2 MEDICINE, GENERAL & INTERNAL Pub Date : 2024-11-15 DOI: 10.1097/MD.0000000000040533
Meng Wu, Lei Zhao, Meijie Chen, Shan Li, Yanyan Liao

This study was intended to determine whether rapid rehabilitation nursing can enhance postoperative rehabilitation and life quality for breast cancer (BC) patients. One hundred seventy-two patients with BC treated in our hospital from March 2020 to September 2022 were included in this retrospective study and divided into the observation group (n = 86) and control group (n = 86) based on the different nursing methods that they received. The control group accepted routine nursing care, and the observation group accepted rapid rehabilitation nursing intervention. The amount of intraoperative blood loss, anesthesia awake time, postoperative drainage tube removal time, postoperative time of getting out of bed, length of hospital stays, incidence of postoperative complications, and postoperative recovery rate of affected limb, Barthel index and quality of life instruments for cancer patients: breast cancer (QLICP-BR) of BC patients were analyzed. The amount of intraoperative bleeding in the observation group was less, and the difference was statistically significant (P < .05). The awake time of anesthesia, the time of pulling out the drainage tube after operation, the time of getting out of bed after operation and the time of hospitalization in the observation group were significant shorter (P < .05). The incidence of postoperative complications in the observation group was notably lower (P < .05). The excellent and good rate of postoperative rehabilitation of the affected limbs in the observation group was notably higher (P < .05). Before nursing, there exhibited no notable difference in the scores of Barthel index (P > .05). After 10 days of nursing, the score of Barthel index in the observation group was notably higher (P < .05). After 10 days of nursing, the QLICP-BR score of the observation group was significant higher (P < .05). Rapid rehabilitation nursing is beneficial to reduce the intraoperative blood loss of BC patients, shorten the recovery time of anesthesia, promote the excellent and good rate of rehabilitation of affected limbs, and improve the quality of life.

本研究旨在探讨快速康复护理能否提高乳腺癌(BC)患者的术后康复水平和生活质量。本次回顾性研究纳入了2020年3月至2022年9月在我院接受治疗的172例乳腺癌患者,根据患者接受的不同护理方法分为观察组(86例)和对照组(86例)。对照组接受常规护理,观察组接受快速康复护理干预。分析 BC 患者的术中失血量、麻醉清醒时间、术后拔除引流管时间、术后下床活动时间、住院时间、术后并发症发生率、术后患肢恢复率、Barthel 指数和癌症患者生活质量工具:乳腺癌(QLICP-BR)。观察组术中出血量较少,差异有统计学意义(P .05)。护理 10 天后,观察组的 Barthel 指数得分明显高于对照组(P.05)。
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