long-term effect

长期效果
  • 文章类型: Journal Article
    已经记录了几种手术技术来接近和修复上半规管裂开综合征(SCDS)。这些技术包括跨中颅窝,乳突,内窥镜入路,和圆窗加固(RWR)。RWR需要放置有或没有软骨的结缔组织,并围绕圆窗小生境,限制圆窗的移动,以最小化第三窗口效应,并将骨迷宫恢复到更接近其正常状态。我们采用了多层RWR技术,2例患者术后明显改善,效果持续3.7年。这里,我们提出了临床发现,外科手术,和多层RWR的有效性。该技术由于其高效性,可以作为SCDS手术治疗的初始选择,更持久的效果,和最小的手术并发症的风险。
    Several surgical techniques have been documented for approaching and repairing superior semicircular canal dehiscence syndrome (SCDS). These techniques encompass the trans-middle cranial fossa, transmastoid, endoscopic approaches, and round window reinforcement (RWR). RWR entails the placement of connective tissue with or without cartilage and around the round window niche, restricting the round window\'s movement to minimize the 3rd window effect and restore the bony labyrinth closer to its normal state. We employed the multilayer RWR technique, resulting in significant postoperative improvement and long-lasting effects for 3.7 years in 2 cases. Here, we present the clinical findings, surgical procedures, and the effectiveness of multilayer RWR. This technique can be the initial choice for surgical treatments of SCDS due to its high effectiveness, longer-lasting effect, and minimal risk of surgical complications.
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  • 文章类型: Journal Article
    这个随机的,双盲,实验研究调查了每天锻炼前补充四周的效果(200毫克咖啡因,3.3g肌酸一水合物,3.2gβ-丙氨酸,6克瓜氨酸苹果酸,和5gBCAA)与安慰剂(等热量麦芽糊精)在厌氧(跳跃,冲刺,敏捷性,和基于运行的无氧冲刺测试:RAST)和有氧(Yo-Yo间歇恢复测试1级)性能,以及在赛季中训练有素的篮球运动员的身体成分和选择性肌肉损伤/与健康相关的血液标记。篮球运动员18名(年龄:24.4±6.3岁,身高:185.7±8.0厘米,重量:85.7±12.8kg,体脂:16.5±4.2%)被随机分为两组:锻炼前补充剂(PWS,n=10)或安慰剂(PL,n=8)。与PL相比,PWS消耗增加了有氧性能(PWS:8±6%;PL:-2±6%;p=0.004)。峰显著下降(F=7.0;p=0.017),平均值(F=10.7;p=0.005),和最小功率(F=5.1;p=0.039)补充4周后,两组。组间无其他显著变化(p>0.05)。总之,当前PWS在四个星期内的消耗似乎对赛季中训练有素的篮球运动员的有氧表现产生了积极影响。然而,它似乎并不能减轻观察到的无氧功率下降,也不影响跳跃的表现,冲刺,和敏捷性,或改变身体成分或选择性肌肉损伤/健康相关的血液标记。
    This randomized, double-blinded, experimental study investigated the effects of a four-week daily pre-workout supplementation (200 mg caffeine, 3.3 g creatine monohydrate, 3.2 g β-alanine, 6 g citrulline malate, and 5 g BCAA) vs. placebo (isocaloric maltodextrin) on anaerobic (jumping, sprinting, agility, and the running-based anaerobic sprint test: RAST) and aerobic (Yo-Yo intermittent recovery test level 1) performance, as well as on body composition and selective muscle damage/health-related blood markers in well-trained basketball players during the in-season period. Eighteen basketball players (age: 24.4 ± 6.3 years, height: 185.7 ± 8.0 cm, weight: 85.7 ± 12.8 kg, body fat: 16.5 ± 4.2%) were randomly assigned into two groups: pre-workout supplement (PWS, n = 10) or placebo (PL, n = 8). PWS consumption increased aerobic performance (PWS: 8 ± 6%; PL: -2 ± 6%; p = 0.004) compared to PL. A significant decrease was observed in peak (F = 7.0; p = 0.017), average (F = 10.7; p = 0.005), and minimum power (F = 5.1; p = 0.039) following 4 weeks of supplementation in both groups. No other significant changes were observed between groups (p > 0.05). In conclusion, the consumption of the current PWS over a four-week period appears to positively influence the aerobic performance of well-trained basketball players during the in-season period. However, it does not appear to mitigate the observed decline in anaerobic power, nor does it affect performance in jumping, sprinting, and agility, or alter body composition or selective muscle damage/health-related blood markers.
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  • 文章类型: Journal Article
    背景:2013年ACC/AHA指南是脂质管理的范式转变,并确定了四个他汀类药物获益组。许多人研究了该指南的潜在影响,但很少有人调查它对MACE的潜在长期影响。此外,大多数研究也忽略了2011年12月阿托伐他汀较早释放的混杂效应.
    方法:为了评估2013年11月在美国发布的2013年ACC/AHA指南的潜在(长期)影响,我们调查了2013年ACC/AHA指南与5年MACE生存率和其他三个他汀类药物相关结局趋势变化的相关性(他汀类药物使用,最佳使用他汀类药物,和他汀类药物依从性),同时使用中断时间序列分析控制通用阿托伐他汀的可用性,称之为周氏测试。具体来说,我们进行了一项回顾性研究,使用美国全国范围内的去识别索赔和OptumLabs数据库仓库(OLDW)的电子健康记录,追踪2013年ACC/AHA指南中确定的4个他汀类药物获益组的5年MACE生存率和他汀类药物相关结局的趋势.然后,Chow检验用于辨别通用阿托伐他汀可用性和指南潜在影响之间的趋势变化。
    结果:纳入197,021例患者(ASCVD:19,060;高LDL:33,907;糖尿病:138,159;高ASCVD风险:5,895)。准则发布后,糖尿病组5年MACE生存率的长期趋势(斜率)显著改善(P=0.002).ASCVD组的最佳他汀类药物使用也显示出释放后的立即改善(截距)和长期积极变化(斜率)(P<0.001)。在所有他汀类药物获益组中,他汀类药物的使用没有显著的趋势变化,他汀类药物的依从性保持不变。尽管没有发现其他统计上显著的趋势变化,2013年ACC/AHA指南发布后,观察到总体正趋势变化或无变化.
    结论:2013年ACA/AHA指南的发布与糖尿病组的长期MACE生存率和ASCVD组的最佳他汀类药物使用的趋势改善有关。这些显著关联可能表明2013年ACA/AHA指南对一级预防组更好的健康结果具有潜在的积极长期影响,并对高风险组的他汀类药物处方行为具有直接的潜在影响。然而,需要进一步调查以确认2013年ACA/AHA指南的因果效应.
    BACKGROUND: The 2013 ACC/AHA Guideline was a paradigm shift in lipid management and identified the four statin-benefit groups. Many have studied the guideline\'s potential impact, but few have investigated its potential long-term impact on MACE. Furthermore, most studies also ignored the confounding effect from the earlier release of generic atorvastatin in Dec 2011.
    METHODS: To evaluate the potential (long-term) impact of the 2013 ACC/AHA Guideline release in Nov 2013 in the U.S., we investigated the association of the 2013 ACC/AHA Guideline with the trend changes in 5-Year MACE survival and three other statin-related outcomes (statin use, optimal statin use, and statin adherence) while controlling for generic atorvastatin availability using interrupted time series analysis, called the Chow\'s test. Specifically, we conducted a retrospective study using U.S. nationwide de-identified claims and electronic health records from Optum Labs Database Warehouse (OLDW) to follow the trends of 5-Year MACE survival and statin-related outcomes among four statin-benefit groups that were identified in the 2013 ACC/AHA Guideline. Then, Chow\'s test was used to discern trend changes between generic atorvastatin availability and guideline potential impact.
    RESULTS: 197,021 patients were included (ASCVD: 19,060; High-LDL: 33,907; Diabetes: 138,159; High-ASCVD-Risk: 5,895). After the guideline release, the long-term trend (slope) of 5-Year MACE Survival for the Diabetes group improved significantly (P = 0.002). Optimal statin use for the ASCVD group also showed immediate improvement (intercept) and long-term positive changes (slope) after the release (P < 0.001). Statin uses did not have significant trend changes and statin adherence remained unchanged in all statin-benefit groups. Although no other statistically significant trend changes were found, overall positive trend change or no changes were observed after the 2013 ACC/AHA Guideline release.
    CONCLUSIONS: The 2013 ACA/AHA Guideline release is associated with trend improvements in the long-term MACE Survival for Diabetes group and optimal statin use for ASCVD group. These significant associations might indicate a potential positive long-term impact of the 2013 ACA/AHA Guideline on better health outcomes for primary prevention groups and an immediate potential impact on statin prescribing behaviors in higher-at-risk groups. However, further investigation is required to confirm the causal effect of the 2013 ACA/AHA Guideline.
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  • 文章类型: Journal Article
    背景:二十一世纪日益复杂的患者护理是由跨专业的医疗保健团队提供的。跨专业合作可以在跨专业教育中教授。然而,是否可以通过跨专业教育来实现合作能力的长期变化尚未得到充分研究。我们的研究问题是:跨专业教育干预后一年内,跨专业合作和跨专业合作技能的动机如何变化?它们如何相互关联?
    方法:在一年期间,本科医学和护理学生参加了四个跨专业(干预)或单专业(对照组)教育课程。以自决理论为理论框架。使用学业自我调节问卷计算跨专业合作的自主和受控动机分数,之前(T1),直接后(T2)和干预后一年(T3)。在T3,学生还填写了跨专业协作能力实现情况调查(ICCAS),通过回顾性测试前/测试后设计来衡量协作能力的感知成就。我们使用线性混合效应模型来分析动机得分,并对动机与能力之间的关系进行线性回归。
    结果:在跨专业组中,参与者的自主动机得分在T2明显较低。T1.控制动机得分在T3明显高于T1.在单职业组中,T2的受控动机得分显着高于跨职业组。感知能力与较高的自主动机得分有关。在T3,跨专业小组的学生之间的跨专业协作能力似乎有所增长。
    结论:在干预后,跨专业协作能力的增长至少持续了一年,并且可以通过ICCAS进行衡量。IPE学生的增长明显高于UPE学生。在跨专业合作的动机得分中发现的少数差异可能是由于不同时间点的护生与医学生的不平衡所致。这一发现表明,基于课堂的IPE可以在干预后至少长达一年的时间内促进护理和医学生的跨专业协作技能。
    BACKGROUND: The increasingly complex patient care in the twenty-first century is delivered by interprofessional health care teams. Interprofessional collaboration can be taught during interprofessional education. However, whether a long-term change in collaborative competencies can be achieved by interprofessional education has not been studied sufficiently. Our research questions were: How does motivation for interprofessional collaboration and interprofessional collaborative skills change up to one year after an interprofessional educational intervention? How are they related to each other?
    METHODS: During a one-year period, undergraduate medical and nursing students attended four interprofessional (intervention) or uniprofessional (control group) education sessions. Self-determination Theory was used as the theoretical framework. Autonomous and controlled motivation scores for interprofessional collaboration were calculated using the Academic Self-Regulation Questionnaire, before (T1), directly after (T2) and one year post-intervention (T3). At T3, the students also filled out the Interprofessional Collaborative Competencies Attainment Survey (ICCAS), which measured the perceived attainment of collaborative competencies by a retrospective pre-test/post-test design. We used linear mixed effects models to analyse the motivation scores and linear regression for the relation between motivation and competence.
    RESULTS: In the interprofessional group, autonomous motivation scores of the participants were significantly lower at T2 vs. T1. Controlled motivation scores were significantly higher at T3 vs. T1. Controlled motivation scores for T2 were significantly higher in the uniprofessional group than in the interprofessional group. Perceived competence was related to higher autonomous motivation scores. At T3 the interprofessional collaborative competencies seemed to have grown more among students in the interprofessional group.
    CONCLUSIONS: The perceived growth in interprofessional collaboration competence lasted at least up to one year after the intervention, and was measurable with the ICCAS. The growth was significantly more in the IPE students than in the UPE students. The few differences found in motivation scores for interprofessional collaboration were probably caused by an imbalance of nursing versus medical students over the different time points. This finding indicates that classroom based IPE can contribute to interprofessional collaboration skills of nursing and medical students at least up to one year after an intervention.
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  • 文章类型: Journal Article
    这项研究是为了确定长期神经肌肉症状的患病率,包括疲劳,嗅觉缺失,头痛,肌痛,轻度住院的COVID-19幸存者的关节痛,中度,或全球严重感染。搜索一直进行到1月30日,2021年使用三个数据库(PubMed,Scopus,和WebofScience)以确定潜在的合格研究。有关研究特征的数据,后续特点,根据PRISMA指南收集住院期间COVID-19的严重程度。纽卡斯尔-渥太华量表用于评估相关文章的质量。在适当的情况下分析了特定延长神经肌肉症状的估计患病率以及COVID-19严重程度与延长神经肌肉症状发生之间的关系。数据库搜索产生4,050篇文章,其中22篇文章被纳入荟萃分析。在3,730名COVID-19幸存者中,估计的长期疲劳患病率为21.2%(95CI:11.9%-34.8%)。在2,600名COVID-19幸存者中,有239名记录到持续的失语症(9.7%,95CI:6.1%-15.2%)。在2,412名COVID-19幸存者中,有84人(8.9%,95CI:3.2%-22.6%),观察到长时间的头痛。在1,125例COVID-19患者中,共有53例(5.6%,95CI:2.1%-14.2%)即使在出院后仍抱怨持续性肌痛。长期关节痛的患病率为15.4%(95CI:8.2%-27.2%)。由于COVID-19严重程度和长期神经肌肉症状的数据匮乏,无法进行关联分析。在几项研究报告COVID-19幸存者出现长期症状后,人们普遍关注COVID-19的长期影响。已经提出了许多理论来解决这一问题;然而,由于对这种流行病的研究仍在进行中,还没有明确的解释。因此,有必要对COVID-19康复后的COVID-19幸存者进行随访研究,以确定长期症状的发病机制。PROSPERO注册:CRD42021242332。
    This study was conducted to determine the prevalence of prolonged neuromuscular symptoms, including fatigue, anosmia, headache, myalgia, and joint pain in COVID-19 survivors hospitalized with mild, moderate, or severe infections worldwide. The search was conducted up to January 30th, 2021 using three databases (PubMed, Scopus, and Web of Science) to identify potentially eligible studies. Data on study characteristics, follow-up characteristics, and severity of COVID-19 during hospitalization were collected in accordance with PRISMA guidelines. The Newcastle-Ottawa scale was used to assess the quality of relevant articles. The estimated prevalence of specific prolonged neuromuscular symptoms and the association between COVID-19 severity and occurrence of prolonged neuromuscular symptoms was analyzed wherever appropriate. Database search yielded 4,050 articles and 22 articles were included for meta-analysis. The estimated prevalence of prolonged fatigue was recorded in 21.2% (95%CI: 11.9%- 34.8%) of 3,730 COVID-19 survivors. Persistent anosmia was recorded in 239 of 2,600 COVID-19 survivors (9.7%, 95%CI: 6.1%-15.2%). In 84 out of 2,412 COVID-19 survivors (8.9%, 95%CI: 3.2%-22.6%), prolonged headache was observed. A total of 53 out of 1,125 COVID-19 patients (5.6%, 95%CI: 2.1%-14.2%) complained of persistent myalgia even after being discharged from the hospital. The prevalence of prolonged joint pain was in 15.4% (95%CI: 8.2%-27.2%) of subjects. Due to data scarcity on COVID-19 severity and prolonged neuromuscular symptoms, association analysis could not be conducted. Widespread concern regarding long-term impacts of COVID-19 was raised after several studies reported prolonged symptoms in COVID-19 survivors. Numerous theories have been proposed to address this concern; however, as the research on this pandemic is still ongoing, no explanation is definitive yet. Therefore, follow-up studies in COVID-19 survivors after recovery from COVID-19 are warranted to determine the pathogenesis of prolonged symptoms. PROSPERO registration: CRD42021242332.
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  • 文章类型: Journal Article
    目的:本临床研究的目的是评估结直肠癌(CRC)患者术中化疗(IOC)联合术中腹腔植入5-氟尿嘧啶(5-FU)的疗效和安全性。
    方法:在本研究中,选择165例接受结直肠根治术的患者,实验组中的111人接受了腹膜内5-氟尿嘧啶(5-FU)植入的手术治疗。对54例未进行5-FU腹膜内植入的患者进行匹配,以比较前者的无进展生存期(PFS)和总生存期(OS)。
    结果:我们还研究了两组手术前后不同生化指标变化的差异,白细胞有显著差异,中性粒细胞,前后淋巴细胞(P<0.05),而对于钠离子,钾离子,血小板,丙氨酸转氨酶,天冬氨酸转氨酶,肌酐,尿素,和白蛋白,没有显著差异。这可能与腹膜内化疗植入物进入血液循环有关。对于5年操作系统,5-FU组85/111(76.58%)(P=0.013),对照组35/54(64.81%);5年PFS,5-FU组84/111(75.68%),对照组29/54(53.70%)(P=0.02)。各实验组均优于对照组,实验结果差异有统计学意义。
    结论:对于CRC手术患者,腹腔植入缓释5-FU药物,这是一个安全而简单的程序,可以改善患者的预后。
    背景:本研究未进行临床试验。
    OBJECTIVE: The purpose of this clinical study was to evaluate the efficacy and safety of intraoperative chemotherapy (IOC) with intraoperative intraperitoneal implantation of 5-fluorouracil (5-FU) in colorectal cancer (CRC) patients.
    METHODS: In this study, 165 patients who underwent colorectal radical surgery were selected, of whom 111 in the experimental group received surgical treatment with an intraperitoneal 5-fluorouracil (5-FU) implantation. Fifty-four patients who did not undergo intraperitoneal implantation of 5-FU were matched to compare the progression-free survival (PFS) and overall survival (OS) with the former.
    RESULTS: We also studied the differences in the changes of different biochemical indicators between the two groups before and after surgery, and there were significant differences in leukocytes, neutrophils, and lymphocytes before and after (P < 0.05), while for sodium ions, potassium ions, platelets, alanine transaminase, aspartate transaminase, creatinine, urea, and albumin, there were no significant differences. This may be related to the intraperitoneal chemotherapy implant entering the blood circulation. For 5-year OS, there were 85/111 (76.58%) in the 5-FU group (P = 0.013) and 35/54 (64.81%) in the control group; for 5-year PFS, there were 84/111 (75.68%) in the 5-FU group and 29/54 (53.70%) in the control group (P = 0.02). All the experimental groups were better than the control group with a significant difference in the experimental results.
    CONCLUSIONS: For CRC surgery patients, intraperitoneal implantation of slow-release 5-FU drugs, which is a safe and simple procedure, can improve the prognosis of the patients.
    BACKGROUND: No clinical trials were performed in the study.
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  • 文章类型: Journal Article
    有效应对急性应激对促进心理健康和建立应激韧性具有重要意义。改善压力应对的干预措施通常需要长时间的培训。在这项研究中,我们提出了一种基于催眠的干预措施,在一次催眠治疗后产生长期效果.在那次会议上,我们建立了催眠后的安全建议,参与者可以通过提示激活,耶拿安全锚.在我们的研究中,我们测试了60名参与者,他们都接受了催眠会话和压力任务。安全小组在急性压力期间使用耶拿安全锚(特里尔社会压力测试,TSST)。对照组使用中性锚。我们通过自我报告测量主观应激反应,通过唾液和血液样本以及心率测量生理应激反应。一周后,所有参与者都填写了一项在线调查,以衡量催眠后安全建议的长期影响.我们发现,与对照组相比,在TSST期间使用耶拿安全锚的参与者报告的压力显着降低。在压力恢复阶段和1周后,安全性组报告的有关TSST表现的负面想法也明显少于对照组。所有参与者均表示,耶拿安全锚在成立后1周仍可工作。建议不影响耶拿安全锚的疗效。我们的研究结果表明,催眠后的安全建议可以改善压力,应对持久的影响,这使得它成为一个有希望的干预措施,以促进心理健康和建立在一个催眠会议的压力弹性。
    Effective coping with acute stress is important to promote mental health and to build stress resilience. Interventions improving stress coping usually require long training periods. In this study, we present a hypnosis-based intervention that produces long-term effects after a single hypnosis session. In that session, we established a post-hypnotic safety suggestion that participants can activate afterwards with a cue, the Jena Safety Anchor. We tested 60 participants in our study who all received the hypnosis session and a stress task. The safety group used the Jena Safety Anchor during acute stress (Trier Social Stress Test, TSST). The control group used a neutral anchor. We measured subjective stress responses via self-reports and physiological stress responses via saliva and blood samples as well as heart rate. One week later, all participants filled in an online survey to measure long-term effects of the post-hypnotic safety suggestion. We found that participants using the Jena Safety Anchor during the TSST reported significantly lower stress compared to the control group. The safety group also reported significantly fewer negative thoughts concerning their TSST performance than the control group during the stress recovery phase and 1 week later. All participants indicated that the Jena Safety Anchor still worked 1 week after its establishment. Suggestibility did not affect the efficacy of the Jena Safety Anchor. Our findings demonstrate that post-hypnotic safety suggestions improve stress coping with long-lasting effects, which makes it a promising intervention to promote mental health and establish stress resilience in just one hypnosis session.
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  • 文章类型: Journal Article
    背景:该研究旨在确定韩国国家戒烟服务(NSCS)使用者在12个月随访时与长期戒烟相关的预测因素。
    方法:为了衡量NSCS交付的长期效果,2018年在NSCS登记的5167名成年吸烟者的目标样本量为按比例随机抽样.多元逻辑回归分析(粗,进行调整)以确定最后一次NSCS登记后12个月随访时吸烟状况的变化以及与吸烟状况变化相关的潜在因素。
    结果:达到目标受试者数量的反应率为22.4%。41.2%的烟草使用者在基线时成功戒烟,以及12个月随访时戒烟的7天点患病率,通过电话调查,为34.4%。在12个月的随访中,与戒烟呈正相关的因素是戒烟经验更长,并且在有或没有NSCS注册的情况下尝试其他戒烟尝试,尽管每次使用NSCS的额外戒烟尝试都有更好的结果。此外,有一个成功的退出结果与NSCS使用在基线和有更满意的专业咨询或激励服务比其他由NSCS提供,在调整考虑的其他因素后,在随访时增加停止。
    结论:除了多次戒烟尝试外,更长的戒烟经验,以及在NSCS的额外注册,服务体验,以及对NSCS提供的内容的满意度,可能会提高禁欲的持久成功。这些结果可能被认为是为了改善NSCS的内容和协议,以获得更好的结果。
    BACKGROUND: The study aimed to identify predictors associated with long-term tobacco cessation at 12-month follow-up among users of the National Smoking Cessation Services (NSCS) in Korea.
    METHODS: To measure the long-term effect of NSCS delivery, the target sample size of 5167 adult smokers registered in the NSCS in 2018 was enrolled with proportional random sampling. A multiple logistic regression analysis (crude, adjusted) was performed to identify the changes in smoking status at the 12-month follow-up after the last NSCS enrollment and the potential factors associated with changes in smoking status.
    RESULTS: The response rate to reach the number of subjects targeted was 22.4%. A total of 41.2% of the tobacco users enrolled had successfully quit at baseline, and the 7-day point prevalence of tobacco cessation at the follow-up at 12 months, via a telephone survey, was 34.4%. Factors positively associated with cessation at the 12-month follow-up were longer experience with tobacco abstinence and additional quitting attempts with or without NSCS enrollment, although every additional quit attempt with NSCS use had a better outcome. In addition, having a successful quit outcome with NSCS use at the baseline and having more satisfaction with the service of professional counseling or incentives than others provided by NSCS, increased cessation at follow-up after adjustment of other factors considered.
    CONCLUSIONS: In addition to multiple quitting attempts, longer experience with tobacco abstinence, and additional enrollment in NSCS, the service experience, and satisfaction with the content that NSCS offered, might improve the lasting success of abstinence. These results might be considered to improve the contents and protocols of the NSCS for better outcomes.
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  • 文章类型: Journal Article
    Nusinersen是第一种被批准用于脊髓性肌萎缩症(SMA)治疗的药物。在这项研究中,我们的目的是评估nusinersen的长期安全性和有效性,根据治疗开始时机和基线运动功能评估治疗效果,并探索父母或患者对功能改善的看法,利用韩国3年全国随访数据。
    我们在国家健康保险范围内纳入了接受nusinersen治疗的SMA患者,提供完整的运动评分记录,最少治疗时间为6个月。评价患者的运动功能,Hammersmith婴儿神经学检查-2(HINE-2)用于1型患者,扩展Hammersmith功能运动量表(HFMSE)用于2型和3型患者。显著改善定义为1型患者的HINE-2评分增加≥5,2型和3型SMA患者的HFMSE评分≥3。评估治疗时机的影响。根据基线运动评分对2型患者进行进一步分类以进行结果分析。我们还分析了来自五家三级医院的第二个数据集,其中包含有关父母/患者报告的改善印象的信息。
    该研究包括137名患者,有21、103和13名患者代表1、2和3型SMA,分别。在3年的随访中,该分析包括7例1型患者,12例2型患者,无1例3型患者.几乎一半的SMA类型的所有登记患者(42.8、59.2和46.2%,分别)达到了2年的随访分析。1型SMA患者的运动功能逐渐改善超过1,2-,和3年随访(16、9和7例患者,分别)。2型SMA患者表现出超过1-的改善,2-,和3年随访(96、61和12例患者,分别)。对于1型和2型SMA患者,症状发作后的早期治疗可带来更好的预后。在第二个数据集中,108例患者中有90.7%在1年随访时报告主观改善。
    Nusinersen治疗1-3型SMA在长期随访中是安全有效的。早期开始治疗是影响长期运动结果的重要因素。
    UNASSIGNED: Nusinersen is the first drug approved for spinal muscular atrophy (SMA) treatment. In this study, we aimed to evaluate the long-term safety and efficacy of nusinersen, assess the therapeutic effects based on the treatment initiation timing and baseline motor function, and explore the perception of functional improvement from either parents or patients, utilizing 3-year nationwide follow-up data in South Korea.
    UNASSIGNED: We enrolled patients with SMA who were treated with nusinersen under the National Health Insurance coverage, with complete motor score records available and a minimum treatment duration of 6 months. To evaluate the motor function of patients, the Hammersmith Infant Neurological Examination-2 (HINE-2) was used for type 1 and the Expanded Hammersmith Functional Motor Scale (HFMSE) was used for types 2 and 3 patients. A significant improvement was defined as a HINE-2 score gain ≥5 for patients with type 1 and an HFMSE score ≥ 3 for patients with types 2 and 3 SMA. Effects of treatment timing were assessed. Patients with type 2 were further categorized based on baseline motor scores for outcome analysis. We also analyzed a second dataset from five tertiary hospitals with the information on parents/patients-reported impressions of improvement.
    UNASSIGNED: The study comprised 137 patients, with 21, 103, and 13 patients representing type 1, 2, and 3 SMA, respectively. At the 3-year follow-up, the analysis encompassed 7 patients with type 1, 12 patients with type 2, and none with type 3. Nearly half of all enrolled patients across SMA types (42.8, 59.2 and 46.2%, respectively) reached the 2-year follow-up for analysis. Patients with type 1 SMA exhibited gradual motor function improvement over 1-, 2-, and 3-year follow-ups (16, 9, and 7 patients, respectively). Patients with type 2 SMA demonstrated improvement over 1-, 2-, and 3-year follow-ups (96, 61 and 12 patients, respectively). Early treatment from symptom onset resulted in better outcomes for patients with type 1 and 2 SMA. In the second dataset, 90.7% of 108 patients reported subjective improvement at the 1-year follow-up.
    UNASSIGNED: Nusinersen treatment for types 1-3 SMA is safe and effective in long-term follow-up. Early treatment initiation was a significant factor affecting long-term motor outcome.
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  • 文章类型: Journal Article
    UNASSIGNED: To determine the short-, mid-, and long-term complications after multisystem inflammatory syndrome in children (MIS-C) over a 24-month follow-up period in a hospital in Lima, Peru, 2020-2022, and to explore differences according to the immunomodulatory treatment received and type of SARS-CoV-2 virus circulating.
    UNASSIGNED: Ambispective 24-month follow-up study in children <14 years of age diagnosed with MIS-C at the Hospital Nacional Edgardo Rebagliati Martins (HNERM).
    UNASSIGNED: A total of 62 children were admitted with MIS-C. The most common short-term complications and serious events were intensive care unit (ICU) admission, invasive mechanical ventilation (IMV) due to respiratory failure, and shock; predominantly during the second pandemic wave (lambda predominance) and in children that received intravenous immunoglobulin (IVIG) plus a corticosteroid. Two patients died during the first wave due to MIS-C. During prospective follow-up (median of 24 months; IQR: 16.7-24), only 46.7% of patients were followed for >18-24 months. Of the total, seven (11.3%) patients were identified with some sequelae on discharge. Among the 43 remaining children, sequelae persisted in five (11.6%) cases (neurological, hematological, and skin problems). Six patients (13.9%) presented with new onset disease (hematologic, respiratory, neurological, and psychiatric disorders). One patient died due to acute leukemia during the follow-up period. None of them were admitted to the ICU or presented with MIS-C reactivation. Two patients presented persistence of coronary aneurysm until 8- and 24-month post-discharge.
    UNASSIGNED: In our hospital, children with MIS-C frequently developed short-term complications and serious events during the acute phase, with less frequent complications in the mid- and long-term. More studies are required to confirm these findings.
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