needles

针头
  • 文章类型: Journal Article
    过度运动是椎间盘退变(IVDD)的病因。工程化的细胞外囊泡(EV)对于疾病修饰治疗表现出优异的治疗潜力。在这里,我们制造了一种运动自供电的摩擦电响应微针(MN)测定法,可持续释放光基因工程EV用于IVDD修复。机械上,运动促进衰老髓核(NP)细胞(IVD稳态维持的主细胞群)的胞浆DNA传感介导的炎症激活,加速IVDD。TREX1作为一种关键的核酸酶,TRAM1-TREX1复合物的拆解会破坏TREX1的亚细胞定位,从而在NP细胞衰老过程中触发TREX1依赖性基因组DNA损伤。光基因工程电动汽车将TRAM1蛋白递送到衰老的NP细胞中,它有效地重建了TREX1的消除功能。摩擦电纳米发电机(TENG)收集机械能并触发工程电动汽车的可控释放。值得注意的是,基于光基因工程的EV靶向治疗策略用于IVDD的治疗,显示出治疗变性相关疾病的有希望的临床潜力。
    Excessive exercise is an etiological factor of intervertebral disc degeneration (IVDD). Engineered extracellular vesicles (EVs) exhibit excellent therapeutic potential for disease-modifying treatments. Herein, we fabricate an exercise self-powered triboelectric-responsive microneedle (MN) assay with the sustainable release of optogenetically engineered EVs for IVDD repair. Mechanically, exercise promotes cytosolic DNA sensing-mediated inflammatory activation in senescent nucleus pulposus (NP) cells (the master cell population for IVD homeostasis maintenance), which accelerates IVDD. TREX1 serves as a crucial nuclease, and disassembly of TRAM1-TREX1 complex disrupts the subcellular localization of TREX1, triggering TREX1-dependent genomic DNA damage during NP cell senescence. Optogenetically engineered EVs deliver TRAM1 protein into senescent NP cells, which effectively reconstructs the elimination function of TREX1. Triboelectric nanogenerator (TENG) harvests mechanical energy and triggers the controllable release of engineered EVs. Notably, an optogenetically engineered EV-based targeting treatment strategy is used for the treatment of IVDD, showing promising clinical potential for the treatment of degeneration-associated disorders.
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  • 文章类型: Journal Article
    原发性腋窝多汗症是一种特发性疾病,由于过度不受控制的出汗而造成严重的心理社会负担。已经描述了各种治疗剂,但每个都有自己的局限性。最近出现了分数微针射频的使用,并取得了有希望的结果。这项研究旨在确定与A型肉毒杆菌毒素(BT-A)相比,局部微针射频在原发性腋窝多汗症患者中的疗效和安全性。在这项随机对照临床试验中,20名患者(40侧)被随机分为部分微针射频(间隔3周进行4次治疗)或BT-A(单次治疗),双方都接受了一种治疗方式。使用Minor's淀粉碘试验在3、6和12个月测量疗效,HDSS评分,Hqol问卷,患者满意度。分数微针射频,虽然显示中等疗效,12个月时纵向疗效不如BT-A,以及患者的满意度。两种治疗方式显示同样安全,但是分数微针射频手术更痛苦。总之,在原发性腋窝多汗症中,分数微针射频不能为BT-A提供更好的替代品。BT-A显示更高的疗效,不那么痛苦,更便宜,并且需要较少的会话。
    Primary axillary hyperhidrosis is an idiopathic disorder that creates severe psycho-social burden due to excessive uncontrolled sweating. Various therapeutic agents have been described, but each has its own limitations. The use of fractional microneedling radiofrequency has emerged lately with promising results. This study aimed to determine the efficacy and safety of fractional microneedle radiofrequency in comparison to Botulinum toxin-A (BT-A) in patients with primary axillary hyperhidrosis. In this randomized controlled clinical trial, 20 patients (40 sides) were randomized to either fractional microneedle radiofrequency (4 sessions at 3-week intervals) or BT-A (single session), where each side received one of the treatment modalities. Efficacy was measured at 3, 6 and 12 months using Minor\'s starch iodine test, HDSS score, Hqol questionnaire, and patient satisfaction. Fractional microneedle radiofrequency, although showed moderate efficacy, is inferior to BT-A regarding longitudinal efficacy at 12 months, as well as patients\' satisfaction. Both treatment modalities showed to be equally safe, but fractional microneedle radiofrequency procedure was substantially more painful. In conclusion, fractional microneedle radiofrequency does not offer a better substitute to BT-A in primary axillary hyperhidrosis. BT-A shows higher efficacy, is less painful, less expensive, and needs a smaller number of sessions.
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  • 文章类型: Journal Article
    背景:金氏三针(JTN)是中国缺血性中风的常用治疗方法。镜像疗法(MT)也逐渐从治疗肢体不适过渡到恢复受损肢体的运动功能。对两种治疗作用机制的研究仍在进行中。我们在这项研究中使用功能磁共振成像(fMRI)技术来检查JTN联合镜像疗法MT对缺血性中风上肢功能障碍患者脑功能的影响。以及潜在的中央机制。目的是提供坚实的循证医学基础,以支持JTN组合MT的持续使用。
    方法:这项研究将是单盲的,随机化,和受控实验。采用随机分组法,将符合研究资格要求的20例患者分为JTN+MT治疗组或JTN对照组。每次干预将持续4周,每周治疗6天。JTN穴位为伤肢对面的3个颞部穴位,受伤上肢3个手部穴位,3个肩部穴位,仁中和百汇,(JTN+MT)组同时进行30分钟的MT。使用BOLD和T1加权图像对治疗前后的大脑进行fMRI。分析了在治疗前后表现出区域均匀性变化的大脑区域。
    结果:疗程结束时,金三针治疗加MT比单纯金三针治疗激活更多相关脑功能区,增加脑血氧灌注(P<0.05)。
    结论:在缺血性卒中后出现上肢损伤的患者中,JTN与MT可以改善相关区域的脑功能重建。
    BACKGROUND: Jin\'s three needle (JTN) is a commonly utilized treatment for ischemic stroke in China. Mirror therapy (MT) is also gradually transitioning from treating limb discomfort to restoring motor function in the damaged limb. Investigations into the 2 treatments\' mechanisms of action are still ongoing. We used functional magnetic resonance imaging (fMRI) technique in this study to examine the effects of JTN combined with mirror therapy MT on brain function in patients with upper limb dysfunction in ischemic stroke, as well as potential central mechanisms. The goal was to provide a solid evidence-based medical basis to support the continued use of JTN combination MT.
    METHODS: This study will be a single-blind, randomized, and controlled experiment. Randomization was used to assign 20 patients who met the study\'s eligibility requirements to the JTN + MT treatment group or the JTN control group. Each intervention will last for 4 weeks, with 6 days of treatment per week. The JTN acupuncture points are 3 temporal acupuncture points on the opposite side of the wounded limb, 3 hand acupuncture points on the injured upper limb, 3 shoulder acupuncture points, Renzhong and Baihui, The (JTN + MT) group simultaneously takes MT for 30 minutes. fMRI of the brain using BOLD and T1-weighted images was done both before and after therapy. Brain areas exhibiting changes in regional homogeneity during the pre and posttreatment periods were analyzed.
    RESULTS: By the end of the treatment course, Jin three-needle therapy plus MT activated more relevant brain functional regions and increased cerebral blood oxygen perfusion than Jin three-needle therapy alone (P <.05).
    CONCLUSIONS: In patients with upper limb impairment following an ischemic stroke, JTN with MT may improve brain function reconstruction in the relevant areas.
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  • 文章类型: Journal Article
    目的:探讨单孔腹腔镜下行双改良疝穿刺针腹膜外闭合术(SLPEC组)和两孔腹腔镜下经皮腹膜外闭合术(TLPEC组)治疗小儿巨大腹股沟斜疝的疗效。我们对2019年1月至2021年12月在福建省儿童医院行腹腔镜疝囊高位结扎术的所有巨大腹股沟斜疝(内环口直径≥1.5cm)患儿进行了回顾性分析。我们从所有儿童的病历中收集数据,并分析了他们的临床特征以及与手术相关的和随访信息。总的来说,这项研究纳入了219例孤立性巨大腹股沟疝患者的队列,这些患者有完整的临床资料,并在我们中心接受了腹腔镜疝囊高位结扎术.在我们中心,对106例接受SLPEC的患者和113例接受TLPEC的患者成功进行了所有手术。患者年龄差异无统计学意义,性别,体重,SLPEC组与TLPEC组之间的随访时间或腹股沟疝侧(分别为P=0.123、0.613、0.121、0.076和0.081)。然而,出血量有显著差异,视觉模拟量表(VAS)评分,术后活动时间两组比较(P≤0.001)。TLPEC组手术时间明显长于SLPEC组(P=0.048),但两组间住院时间和住院费用无显著差异(P=0.244和0.073).SLPEC组2例,TLPEC组9例,切口瘢痕,两组间差异有统计学意义(P=0.04)。然而,同侧疝复发的发生率,手术部位感染,两组间缝合结反应和慢性腹股沟痛无显著差异(分别为P=0.332,0.301,0.332和0.599).SLPEC组仅有1名男童发生术后鞘膜积液,TLPEC组无男童发生术后鞘膜积液,两组间差异无统计学意义(P=0.310)。在这项研究中,没有睾丸萎缩或医源性睾丸上升的病例。与TLPEC组比拟,SLPEC组具有隐匿切口的优势,轻度疤痕,最小的侵入性,减少操作时间,出血最少,轻度疼痛和快速恢复。总之,SLPEC使用双改良疝针进行水切开和疝囊高位结扎术是一种安全的,有效和微创手术。美容效果令人印象深刻,后续成果很有希望。
    The objective was to explore the efficacy of single-port laparoscopic percutaneous extraperitoneal closure using double-modified hernia needles with hydrodissection (SLPEC group) and two-port laparoscopic percutaneous extraperitoneal closure (TLPEC group) for the treatment of giant indirect inguinal hernias in children. We performed a retrospective review of all children with giant indirect inguinal hernias (inner ring orifice diameter ≥ 1.5 cm) who underwent laparoscopic high ligation of the hernia sac at FuJian Children\'s Hospital from January 2019 to December 2021. We collected data from the medical records of all the children and analysed their clinical characteristics and operation-related and follow-up information. Overall, this study included a cohort of 219 patients with isolated giant inguinal hernias who had complete clinical data and who had undergone laparoscopic high ligation of the hernia sac at our centre. All procedures were successfully performed for the 106 patients who underwent SLPEC and for the 113 patients who underwent TLPEC at our centre. There were no statistically significant differences in patient age, sex, body weight, follow-up time or the side of inguinal hernia between the SLPEC group and the TLPEC group (P = 0.123, 0.613, 0.121, 0.076 and 0.081, respectively). However, there were significant differences in the bleeding volume, visual analogue scale (VAS) score, and postoperative activity time between the two groups (P ≤ 0.001). The operation times in the TLPEC group were significantly longer than those in the SLPEC group (P = 0.048), but there were no significant differences in hospital length of stay or hospitalization costs between the two groups (P = 0.244 and 0.073, respectively). Incision scars were found in 2 patients in the SLPEC group and 9 patients in the TLPEC group, and there was a significant difference between the two groups (P = 0.04). However, the incidence of ipsilateral hernia recurrence, surgical site infection, suture-knot reactions and chronic inguinodynia did not significantly differ between the two groups (P = 0.332, 0.301, 0.332 and 0.599, respectively). Postoperative hydrocele occurred in only 1 male child in the SLPEC group and in no male children in the TLPEC group, and there was no difference between the two groups (P = 0.310). In this study, there were no cases of testicular atrophy or iatrogenic ascent of the testis. Compared with the TLPEC group, the SLPEC group had the advantages of a concealed incision, light scarring, minimal invasiveness, a reduced operation time, minimal bleeding, mild pain and rapid recovery. In conclusion, SLPEC using double-modified hernia needles with hydrodissection and high ligation of the hernia sac is a safe, effective and minimally invasive surgery. The cosmetic results are impressive, and the follow-up results are promising.
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  • 文章类型: Journal Article
    背景:尽管有许多技术进步,由于频繁的定位错误,支气管镜周围肺结节分析的诊断率仍然有限.基于针的共聚焦激光显微内窥镜(nCLE)可实现对针定位的实时显微反馈,有可能改善采样位置和诊断产量。以前的研究已经定义并验证了恶性肿瘤的nCLE标准,气道和肺实质。缺乏更大规模的研究证明nCLE对诊断产量的影响。我们的目的是研究与不使用nCLE的常规支气管镜检查相比,与常规支气管镜检查结合的nCLE成像是否会导致更高的诊断率。
    方法:这是一项平行组随机对照试验。招募在六个不同欧洲国家的大学和综合医院的肺科门诊诊所以及美国的一家医院进行。连续筛查怀疑有诊断性支气管镜检查指征的恶性周围肺结节(10-30mm)患者,将包括208名患者。将在两个程序之间进行基于网络的随机化(1:1)。主要结果是诊断产量。次要结果包括恶性肿瘤的诊断敏感性,针头重新定位,手术和透视持续时间,和并发症。病理学家将不知道程序类型;患者和内窥镜医师不会。
    背景:阿姆斯特丹大学医学中心伦理委员会的初步批准。传播涉及在同行评审的期刊上发表。
    背景:MaunaKeaTechnologies的财务和物质支持。
    背景:NCT06079970。
    BACKGROUND: Despite many technological advances, the diagnostic yield of bronchoscopic peripheral lung nodule analysis remains limited due to frequent mispositioning. Needle-based confocal laser endomicroscopy (nCLE) enables real-time microscopic feedback on needle positioning, potentially improving the sampling location and diagnostic yield. Previous studies have defined and validated nCLE criteria for malignancy, airway and lung parenchyma. Larger studies demonstrating the effect of nCLE on diagnostic yield are lacking. We aim to investigate if nCLE-imaging integrated with conventional bronchoscopy results in a higher diagnostic yield compared with conventional bronchoscopy without nCLE.
    METHODS: This is a parallel-group randomised controlled trial. Recruitment is performed at pulmonology outpatient clinics in universities and general hospitals in six different European countries and one hospital in the USA. Consecutive patients with a for malignancy suspected peripheral lung nodule (10-30 mm) with an indication for diagnostic bronchoscopy will be screened, and 208 patients will be included. Web-based randomisation (1:1) between the two procedures will be performed. The primary outcome is diagnostic yield. Secondary outcomes include diagnostic sensitivity for malignancy, needle repositionings, procedure and fluoroscopy duration, and complications. Pathologists will be blinded to procedure type; patients and endoscopists will not.
    BACKGROUND: Primary approval by the Ethics Committee of the Amsterdam University Medical Center. Dissemination involves publication in a peer-reviewed journal.
    BACKGROUND: Financial and material support from Mauna Kea Technologies.
    BACKGROUND: NCT06079970.
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  • 文章类型: Journal Article
    腭注射被认为是最痛苦的牙科手术之一。因此,重要的是要找到替代这种痛苦的注射,以改善儿童的合作。牙科文献提到使用EMLA乳膏作为常规注射的可能替代品,但它的麻醉效果引起了争论。因此,研究微针贴片对增强这种乳膏功效的影响是有价值的。这项随机对照临床试验的目的是比较7-11岁儿童不同麻醉方法的有效性和疼痛程度。这项研究比较了EMLA霜的使用,EMLA用微针,和常规腭注射.将90名儿童随机分为三组:第1组接受常规腭部麻醉(对照组),第2组仅接受EMLA霜,第3组接受带微针的EMLA。在三个不同的时间点使用FLACC和Wong-Baker量表评估疼痛水平:T1(麻醉期间),T2(腭探查),和T3(在提取期间)。FLACC量表显示仅在T1时两组之间的疼痛差异显着(P值=0.000)。发现常规pal注射组的疼痛程度高于仅使用EMLA乳膏和使用带有EMLA乳膏的微针贴片组(P值=0.000)。然而,其他组麻醉期间疼痛水平无显著差异(P值=1.00).同样,Wong-Baker量表还显示仅在T1时两组之间的疼痛差异有统计学意义(P值=0.000).发现常规pal注射组的疼痛程度高于仅使用EMLA乳膏和使用带有EMLA乳膏的微针贴片组(P值=0.000)。然而,其他组麻醉期间的疼痛水平无显著差异(P值=0.091).该研究得出的结论是,单独的EMLA乳膏和带有微针的EMLA都可以用作儿童常规腭麻醉的替代品。
    Palatal injections are considered to be one of the most painful dental procedures. As a result, it was important to find alternatives to this painful injection to improve children\'s cooperation. The dental literature mentioned using EMLA cream as a possible alternative to conventional injections, but its anesthetic effect was debated. Therefore, it was valuable to research the impact of microneedle patches to enhance the effectiveness of this cream. The purpose of this randomized controlled clinical trial was to compare the effectiveness of different methods of anesthesia and pain levels in children aged 7-11 years. The study compared the use of EMLA cream, EMLA with microneedles, and conventional palatal injections. A total of 90 children were randomly assigned to three groups: Group 1 received conventional palatal anesthesia (control), Group 2 received EMLA cream only, and Group 3 received EMLA with microneedles. Pain levels were assessed using the FLACC and Wong-Baker scales at three different time points: T1(during anesthesia), T2(on palatal probing), and T3(during extraction). The FLACC scale revealed a significant difference in pain between groups only at T1 (P value = 0.000). It was found that the conventional palatal injection group had a higher pain level than the EMLA cream-only group and the group using microneedle patches with EMLA cream (P value = 0.000). However, the other groups did not show significant differences in pain levels during the anesthesia (P value  = 1.00). Similarly, the Wong-Baker scale also demonstrated a statistically significant difference in pain between groups only at T1 (P value  = 0.000). It was found that the conventional palatal injection group had a higher pain level than the EMLA cream-only group and the group using microneedle patches with EMLA cream (P value  = 0.000). However, the other groups did not show significant differences in pain levels during the anesthesia (P value  = 0.091). The study concludes that both EMLA cream alone and EMLA with microneedles can be used as an alternative to conventional palatal anesthesia for children.
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  • 文章类型: Journal Article
    经会阴激光消融是前列腺癌的微创热消融治疗,需要插入针以进行精确的光纤定位。针头插入软组织可能会导致组织运动和变形,导致组织损伤和针头定位错误。在这项研究中,我们提出了一种黄蜂启发的自推进针,它使用气动致动以零外部推力向前移动,从而避免大的组织运动和变形。针头由六个平行的0.25毫米直径的镍钛诺杆由气动致动系统驱动。气动致动系统由磁共振(MR)安全3D打印部件和现成的塑料螺钉组成。通过一个接一个地推进针段来实现自推进运动,然后同时收回它们。前进的针段必须克服切割力和摩擦力,而静止的针段在相反的方向上经受摩擦力。当五个静止的针段的摩擦力克服前进的针段的摩擦力和切割力的总和时,针自推进通过组织。我们根据针相对于体模或肝组织的滑移率,评估了原型在临床前磁共振成像(MRI)扫描仪内10重量%明胶体模和离体猪肝组织中的性能。我们的结果表明,针头能够自推进通过体模和肝组织,滑移率分别为0.912-0.955和0.88。该原型是朝着开发用于MRI引导的经会阴激光消融的自推进针作为治疗前列腺癌的方法迈出的有希望的一步。
    Transperineal laser ablation is a minimally invasive thermo-ablative treatment for prostate cancer that requires the insertion of a needle for accurate optical fiber positioning. Needle insertion in soft tissues may cause tissue motion and deformation, resulting in tissue damage and needle positioning errors. In this study, we present a wasp-inspired self-propelled needle that uses pneumatic actuation to move forward with zero external push force, thus avoiding large tissue motion and deformation. The needle consists of six parallel 0.25-mm diameter Nitinol rods driven by a pneumatic actuation system. The pneumatic actuation system consists of Magnetic Resonance (MR) safe 3D-printed parts and off-the-shelf plastic screws. A self-propelled motion is achieved by advancing the needle segments one by one, followed by retracting them simultaneously. The advancing needle segment has to overcome a cutting and friction force, while the stationary needle segments experience a friction force in the opposite direction. The needle self-propels through the tissue when the friction force of the five stationary needle segments overcomes the sum of the friction and cutting forces of the advancing needle segment. We evaluated the prototype\'s performance in 10-wt% gelatin phantoms and ex vivo porcine liver tissue inside a preclinical Magnetic Resonance Imaging (MRI) scanner in terms of the slip ratio of the needle with respect to the phantom or liver tissue. Our results demonstrated that the needle was able to self-propel through the phantom and liver tissue with slip ratios of 0.912-0.955 and 0.88, respectively. The prototype is a promising step toward the development of self-propelled needles for MRI-guided transperineal laser ablation as a method to treat prostate cancer.
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  • 文章类型: Journal Article
    这项研究将空心微针阵列(HMNA)与新型水母形电化学传感器集成在一起,用于检测关键生物标志物,包括尿酸(UA),葡萄糖,pH值,在人工间质液中。水母形传感器通过差分脉冲伏安法(DPV)和计时电流法检测UA和葡萄糖时显示出线性响应,分别。值得注意的是,系统的开路电位(OCP)随pH变化呈线性变化,验证其pH传感能力。传感器系统在模拟表皮感测应用中在这些生物标志物的生理浓度范围内表现出优异的电化学响应性。UA的检测线性范围,葡萄糖,pH为0~0.8mM,0~7mM,分别为4.0~8.0。这些发现凸显了HMNA集成水母形传感器在现实世界表皮应用中的潜力,可用于全面的疾病诊断和健康监测。
    This study integrates hollow microneedle arrays (HMNA) with a novel jellyfish-shaped electrochemical sensor for the detection of key biomarkers, including uric acid (UA), glucose, and pH, in artificial interstitial fluid. The jellyfish-shaped sensor displayed linear responses in detecting UA and glucose via differential pulse voltammetry (DPV) and chronoamperometry, respectively. Notably, the open circuit potential (OCP) of the system showed a linear variation with pH changes, validating its pH-sensing capability. The sensor system demonstrates exceptional electrochemical responsiveness within the physiological concentration ranges of these biomarkers in simulated epidermis sensing applications. The detection linear ranges of UA, glucose, and pH were 0~0.8 mM, 0~7 mM, and 4.0~8.0, respectively. These findings highlight the potential of the HMNA-integrated jellyfish-shaped sensors in real-world epidermal applications for comprehensive disease diagnosis and health monitoring.
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  • 文章类型: Journal Article
    婴儿期血管瘤是婴儿期和儿童期最常见的血管瘤。尽管证明了普萘洛尔治疗的疗效,某些患者仍然遇到抵抗或面临复发。对频繁的日常用药的需要也对患者的依从性提出了挑战。博来霉素(BLM)已证明对血管异常有效,然而,它的使用受到剂量相关并发症的限制。解决这个问题,这项研究提出了一种使用BLM负载透明质酸(HA)的微针(MN)贴片治疗血管瘤的新方法。BLM在聚乳酸(PLA)微球(MPs)的合成过程中被包封。通过扫描电子显微镜(SEM)图像证实了PLAMPs和MN贴片的成功制备。HA微针在皮肤插入后迅速溶解,释放BLM@PLA议员。这些MP在28天内逐渐降解,提供BLM的持续释放。全面的安全评估,包括细胞活力,溶血率,和兔子的皮内反应,验证MN补丁的安全性。BLM@PLA-MN在鼠血管瘤模型中表现出对血管瘤形成的有效抑制效率。非常重要的是,RNA-seq分析显示BLM@PLA-MNs通过调节P53途径发挥对血管瘤的抑制作用。总之,BLM@PLA-MN成为有效治疗血管瘤的有希望的临床候选药物。
    Hemangioma of infancy is the most common vascular tumor during infancy and childhood. Despite the proven efficacy of propranolol treatment, certain patients still encounter resistance or face recurrence. The need for frequent daily medication also poses challenges to patient adherence. Bleomycin (BLM) has demonstrated effectiveness against vascular anomalies, yet its use is limited by dose-related complications. Addressing this, this study proposes a novel approach for treating hemangiomas using BLM-loaded hyaluronic acid (HA)-based microneedle (MN) patches. BLM is encapsulated during the synthesis of polylactic acid (PLA) microspheres (MPs). The successful preparation of PLA MPs and MN patches is confirmed through scanning electron microscopy (SEM) images. The HA microneedles dissolve rapidly upon skin insertion, releasing BLM@PLA MPs. These MPs gradually degrade within 28 days, providing a sustained release of BLM. Comprehensive safety assessments, including cell viability, hemolysis ratio, and intradermal reactions in rabbits, validate the safety of MN patches. The BLM@PLA-MNs exhibit an effective inhibitory efficiency against hemangioma formation in a murine hemangioma model. Of significant importance, RNA-seq analysis reveals that BLM@PLA-MNs exert their inhibitory effect on hemangiomas by regulating the P53 pathway. In summary, BLM@PLA-MNs emerge as a promising clinical candidate for the effective treatment of hemangiomas.
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  • 文章类型: Journal Article
    背景:Dupuytren挛缩(DC)是手部皮肤下的纤维索,导致一个或多个手指逐渐且不可逆地向手掌卷曲。这些挛缩通常是无痛的,但可导致手功能丧失。Dupuytren挛缩的两种治疗方法在英国国家卫生服务(NHS)中被广泛使用:通过手术(有限的筋膜切除术)去除挛缩和通过插入皮肤的针来分裂挛缩(针筋膜切开术)。这项研究旨在建立临床和成本效益针筋膜切开术(NF)与有限筋膜切除术(LF)治疗DC在NHS,在患者报告的手功能和资源利用方面。
    方法:Hand-2是一个全国性的多中心,双臂,随机平行组,非自卑审判。如果患者年龄在18岁或以上,则有资格参加试验。至少有一个先前未治疗的手指,其清晰的Dupuytren挛缩为30°或更大,会导致功能问题,适用于LF或NF治疗。只有远端指间关节挛缩的患者不合格。符合条件的同意患者将以1:1的比例随机接受NF或LF,并在治疗后随访24个月。QuinteT招聘干预将用于优化招聘。主要结果指标是参与者报告的手功能评估,在治疗后12个月通过患者评估措施(PEM)问卷的手健康概况进行评估。次要结果包括其他患者报告的指标,失去手指的运动,和成本效益,报告在治疗后24个月。嵌入式定性研究将探索患者经验和手术后2年的可接受性。
    结论:本研究将确定在治疗后12个月患者报告的手功能方面,针状筋膜切开术治疗是否不低于有限筋膜切除术。
    背景:国际标准注册临床/社会sudyISRCTN12525655。于2020年9月18日注册。
    BACKGROUND: Dupuytren\'s contractures (DC) are fibrous cords under the skin of the hand that cause one or more fingers to curl gradually and irreversibly towards the palm. These contractures are usually painless but can cause a loss of hand function. Two treatments for Dupuytren\'s contractures are widely used within the National Health Service (NHS) in the UK: removal of the contractures via surgery (limited fasciectomy) and division of the contractures via a needle inserted through the skin (needle fasciotomy). This study aims to establish the clinical and cost-effectiveness of needle fasciotomy (NF) versus limited fasciectomy (LF) for the treatment of DC in the NHS, in terms of patient-reported hand function and resource utilisation.
    METHODS: Hand-2 is a national multi-centre, two-arm, parallel-group randomised, non-inferiority trial. Patients will be eligible to join the trial if they are aged 18 years or older, have at least one previously untreated finger with a well-defined Dupuytren\'s contracture of 30° or greater that causes functional problems and is suitable for treatment with either LF or NF. Patients with a contracture of the distal interphalangeal joint only are ineligible. Eligible consenting patients will be randomised 1:1 to receive either NF or LF and will be followed up for 24 months post-treatment. A QuinteT Recruitment Intervention will be used to optimise recruitment. The primary outcome measure is the participant-reported assessment of hand function, assessed by the Hand Health Profile of the Patient Evaluation Measure (PEM) questionnaire at 12 months post-treatment. Secondary outcomes include other patient-reported measures, loss of finger movement, and cost-effectiveness, reported over the 24-month post-treatment. Embedded qualitative research will explore patient experiences and acceptability of treatment at 2 years post-surgery.
    CONCLUSIONS: This study will determine whether treatment with needle fasciotomy is non-inferior to limited fasciectomy in terms of patient-reported hand function at 12 months post-treatment.
    BACKGROUND: International Standard Registered Clinical/soCial sTudy ISRCTN12525655. Registered on 18th September 2020.
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