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Depurative capacity toward medium molecules of the dialyzer Toray NV-U® Hydrolink™: A new hydrophilic membrane to perform online hemodiafiltration. 透析器东丽 NV-U® Hydrolink™ 对介质分子的去污能力:用于进行在线血液渗滤的新型亲水膜。
IF 1.4 4区 医学 Q4 ENGINEERING, BIOMEDICAL Pub Date : 2024-09-21 DOI: 10.1177/03913988241274735
Maria Kislikova, Almudena Vega, Eduardo Verde, Soraya Abad, Marco Vaca, Adriana Acosta, Angela González, Arturo Bascuñana, Antonia Mijailova, Coraima Nava, Miguel Villa, Juan Carlos Ruiz, Marian Goicoechea

Introduction: New dialysis membranes with new properties are being developed to improve efficacy and tolerance. The hemocompatibility of a polymeric biomaterial is influenced by the layer of water at the blood membrane interface. The new dialyzer TORAY NV-U® has a membrane Hydrolink™, designed to suppress platelet adhesion and to improve the hemocompatibility. Until now, there is no experience in online hemodiafiltration (OL-HDF).The objective of the present study is to evaluate the efficacy of this new membrane in OL-HDF therapy compared to another membrane commonly used. Other objectives are to evaluate the inflammatory response, hemodynamic tolerance, and the anticoagulation regimes.

Methods: This is a prospective pilot study performed in five anuric patients receiving OL-HDF. For 1 month patients were kept with their usual dialyzer FX1000® (FMC). Subsequently, the dialyzer was changed to TORAY NV-U® (Hydrolink®) for 1 month. In the last dialysis session of each dialyzer, blood tests were performed to evaluate inflammation and depurative capacity.

Results: We did not find differences in medium size removal molecules and convective volume: FX1000®: 31 ± 9 l per session and Hydrolink™ 30 ± 8 l; p = 0.7); β2microglobulin reduction ratio (RR) FX1000® FMC 83 ± 3%; Hydrolink™ 79 ± 4; p = 0.14; Myoglobin RR FX1000® FMC 72 ± 7%; Hydrolink™ 76 ± 4; p = 0.28. We did not find differences in inflammation parameters: serum IL6 with FX1000® 6.0 ± 4.2 pg/mL; Hydrolink™ 7.6 ± 5.0 pg/mL; p = 0.3.During all sessions with the two dialyzers there was adequate plasmatic filling, reaching 85 % filling. All patients had "good" dialyzer status in all dialysis sessions with TORAY NV-U®, while the dialyzer status with FX1000® was "good" in 20% of the sessions, "medium" in 30%, and "dirty" in the remaining 50% dialysis sessions.

Conclusions: The new dialyzer Hydrolink™, TORAY NV-U® is not inferior to perform OL-HDF compared to dialyzers usually used for this therapy, and could allow decrease heparin doses. Further studies with a bigger sample size and longer follow-up will answer if Hydrolink improves inflammation and assess a better hemodynamic tolerance.

简介:目前正在开发具有新特性的新型透析膜,以提高疗效和耐受性。高分子生物材料的血液相容性受血膜界面水层的影响。新型透析器 TORAY NV-U® 的膜 Hydrolink™ 可抑制血小板粘附并改善血液相容性。到目前为止,还没有在线血液透析滤过(OL-HDF)方面的经验。本研究的目的是评估这种新型膜与另一种常用膜相比在 OL-HDF 治疗中的疗效。其他目的还包括评估炎症反应、血液动力学耐受性和抗凝方案:这是一项前瞻性试验研究,在五名接受 OL-HDF 治疗的无尿患者中进行。在一个月的时间里,患者一直使用他们常用的透析器 FX1000®(FMC)。随后,透析器改为 TORAY NV-U® (Hydrolink®),为期 1 个月。在每种透析器的最后一次透析过程中,都进行了血液检测,以评估炎症和去污能力:结果:我们没有发现中型清除分子和对流容量方面的差异:FX100031±9升/次和Hydrolink™ 30±8升/次;p = 0.7);β2微球蛋白还原率(RR)FX1000® FMC 83±3%;Hydrolink™ 79±4;p = 0.14;肌红蛋白还原率FX1000® FMC 72±7%;Hydrolink™ 76±4;p = 0.28。我们没有发现炎症参数的差异:血清 IL6 FX1000® 6.0 ± 4.2 pg/mL;Hydrolink™ 7.6 ± 5.0 pg/mL;p = 0.3。所有患者在使用 TORAY NV-U® 的所有透析过程中,透析器状态均为 "良好",而使用 FX1000® 的透析过程中,20% 的透析器状态为 "良好",30% 的透析器状态为 "中等",其余 50% 的透析器状态为 "不佳":结论:新型透析器Hydrolink™、TORAY NV-U®在进行OL-HDF透析时的效果并不比通常用于该疗法的透析器差,而且可以减少肝素剂量。样本量更大、随访时间更长的进一步研究将回答 Hydrolink 是否能改善炎症并评估更好的血液动力学耐受性。
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引用次数: 0
ECMO in severe hypoxemia post liver transplant for hepatopulmonary syndrome. 肝移植后严重低氧血症的肝肺综合征 ECMO。
IF 1.4 4区 医学 Q4 ENGINEERING, BIOMEDICAL Pub Date : 2024-09-02 DOI: 10.1177/03913988241274252
Jesús Emilio Barrueco-Francioni, María Carmen Martínez-González, Juan Francisco Martínez-Carmona, María Palma Benítez-Moreno, Cesar Aragón-González, Manuel Enrique Herrera-Gutiérrez

Hepatopulmonary syndrome (HPS) poses a significant challenge in liver transplant patients, affecting between 10% and 30% of candidates. Historically, HPS was considered a contraindication for liver transplantation due to its association with high mortality rates. However, recent studies have shown improvements in pulmonary function post-transplant, leading to the inclusion of these patients as candidates. Despite this progress, approximately one-fifth of liver transplant recipients develop severe postoperative hypoxia, further complicating their clinical course and contributing to increased mortality. The management of post-transplant HPS involves various strategies, including extracorporeal membrane oxygenation (ECMO), although its use remains infrequently reported. Theoretical models suggest that oxygenation typically improves within 10 days post-transplant, while resolution of HPS may take 6-12 months, making ECMO an attractive possibility as a bridge to recovery in this population. We present a case were ECMO was used in this context.

肝肺综合征(HPS)是肝移植患者面临的一项重大挑战,10% 到 30% 的候选者会受到影响。一直以来,由于 HPS 与高死亡率有关,因此被认为是肝移植的禁忌症。然而,最近的研究表明,移植后肺功能有所改善,因此这些患者也被列为候选者。尽管取得了这一进展,但仍有约五分之一的肝移植受者在术后出现严重缺氧,使其临床过程进一步复杂化,并导致死亡率上升。移植后 HPS 的治疗涉及多种策略,包括体外膜肺氧合(ECMO),但其使用情况仍鲜有报道。理论模型表明,血氧饱和度通常在移植后 10 天内得到改善,而 HPS 的缓解可能需要 6-12 个月的时间,因此 ECMO 作为这一人群康复的桥梁具有吸引力。我们介绍了一例在这种情况下使用 ECMO 的病例。
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引用次数: 0
An analytic method to investigate hemodynamics of the cardiovascular system: Biventricular system. 研究心血管系统血液动力学的分析方法:双心室系统
IF 1.4 4区 医学 Q4 ENGINEERING, BIOMEDICAL Pub Date : 2024-09-01 Epub Date: 2024-08-08 DOI: 10.1177/03913988241260943
Yuxin Zhu, Xu Mei, Wanning Ge, Tingting Wu, Liudi Zhang, Polin Hsu

Previously, we found analytic solutions for single ventricular system based on the lumped parameter model (LPM). In this study, we generalized the method to biventricular system and derived its analytic solutions. LPM is just a set of differential equations, but it is difficult to solve due to time-varying ventricular elastance and high order. Mathematically, there exist no elementary solutions for time-varying equations. It turns out that instead of differential equations, according to volume conservation, a set of algebraic equations can be carried out. The solutions of the set of equations are just physiological states at end of systolic and diastolic phases such as end systolic/diastolic pressure/volume of left ventricle. As a preliminary application, the method is utilized to deduce the hemodynamic effects of VA ECMO. Left ventricular (LV) distension, a serious complication of VA ECMO, is usually attributed to factors such as increased afterload, inadequate LV unloading, reduced myocardial contractility or aortic valve regurgitation (AR), bronchial and Thebesian return in the absence of aortic valve (AoV) opening. Among these, reduced contractility and AR are strongly associated with LV distension. However, in the absence of reduced contractility or AR, it is less clear whether increased afterload or inadequate LV unloading alone can cause LV distension. This leads to the critical question: under what conditions does LV distension occur in the absence of reduced contractility or AR? The analytic formulas derived in this study give conditions for LV distension. Furthermore, the results show that the analytic hemodynamics are coincident with simulated results.

在此之前,我们基于块参数模型(LPM)找到了单心室系统的解析解。在这项研究中,我们将该方法推广到了双心室系统,并得出了其解析解。LPM 只是一组微分方程,但由于心室弹性时变且阶数较高,因此很难求解。在数学上,不存在时变方程的基本解。原来,根据体积守恒,可以用一组代数方程来代替微分方程。方程组的解只是收缩期和舒张期结束时的生理状态,如收缩末期/舒张末期压力/左心室容积。作为初步应用,该方法用于推断 VA ECMO 的血液动力学效应。左心室(LV)胀大是 VA ECMO 的一种严重并发症,通常归因于后负荷增加、左心室卸载不足、心肌收缩力降低或主动脉瓣反流(AR)、主动脉瓣(AoV)未开放时支气管和忒拜斯回流等因素。其中,心肌收缩力减弱和主动脉瓣反流与左心室扩张密切相关。然而,在没有收缩力降低或 AR 的情况下,后负荷增加或 LV 负荷不足是否会单独导致 LV 舒张还不太清楚。这就引出了一个关键问题:在没有收缩力减弱或 AR 的情况下,左心室扩张会在什么条件下发生?本研究得出的分析公式给出了左心室扩张的条件。此外,结果表明分析血流动力学与模拟结果相吻合。
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引用次数: 0
Study on the recovery of bladder function in patients with cervical cancer after operation by portable ultrasound combined. 通过便携式超声波联合检查宫颈癌患者术后膀胱功能恢复情况的研究。
IF 1.4 4区 医学 Q4 ENGINEERING, BIOMEDICAL Pub Date : 2024-09-01 Epub Date: 2024-07-30 DOI: 10.1177/03913988241262593
Yu-Ting Zhao, Shuai Guo, Zai-Chun Shang, Hong-Yi Ding, Jian-Hua Jin, Kai-Yue Chu, Bin-Bin Ge, Peng-Qin Xu

Background: Postoperative urination dysfunction is a common complication after surgery in patients with cervical cancer. Portable bladder ultrasound are commonly utilized in clinical practice for measuring residual urine volume. This study aimed to the effect of bladder function training combined with portable ultrasound monitoring on bladder function recovery in patients with cervical cancer after training.

Methods: A total of 40 postoperative patients with cervical cancer were randomly divided into a control group (A) and an experimental group (B) of 20 cases each. Group A was given routine postoperative care, while group B was given bladder function training. Urgent urine bladder volume were taken twice daily after removal of the urinary catheter and monitored for five consecutive days. The difference of urgent urine bladder volume and bladder filling rate were compared by t-test and chi-square test respectively. The 36-item Short Form Health Survey (SF-36) was used to evaluate the quality of life of patients before and after intervention, and compared by Mann-Whitney U test.

Results: There was no significant difference in preoperative urgent urine volume between the two groups. After catheter removal, the bladder volume of patients in the B increased, while the bladder volume of patients in the A increased less and fluctuated greatly. The bladder filling rate in the A was significantly lower than that in the B (5/15 vs 17/18, p < 0.05). After intervention, the quality of life of the experimental group was better than that of the control group, including scores of general health, mental health, vitality, and physical role (p < 0.05).

Conclusion: Postoperative cervical cancer patients trained to hold urine by portable ultrasound monitoring are able to recover bladder function.

背景:术后排尿功能障碍是宫颈癌患者术后常见的并发症。临床上常用便携式膀胱超声测量残余尿量。本研究旨在探讨膀胱功能训练结合便携式超声监测对宫颈癌患者训练后膀胱功能恢复的影响:方法:将 40 例宫颈癌术后患者随机分为对照组(A 组)和实验组(B 组),每组 20 例。A 组给予常规术后护理,B 组给予膀胱功能训练。拔除导尿管后,每天两次测量膀胱急尿量,连续监测五天。分别用 t 检验和卡方检验比较急迫性膀胱尿量和膀胱充盈率的差异。采用 36 项简表健康调查(SF-36)评估干预前后患者的生活质量,并通过 Mann-Whitney U 检验进行比较:结果:两组患者术前急迫尿量无明显差异。拔除导尿管后,B 组患者的膀胱容量有所增加,而 A 组患者的膀胱容量增加较少且波动较大。A 组的膀胱充盈率明显低于 B 组(5/15 vs 17/18,p p 结论:通过便携式超声监测训练憋尿的宫颈癌术后患者能够恢复膀胱功能。
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引用次数: 0
Efficacy and safety of ertapenem dosing in patients with ESBL producing Enterobacterales infections utilizing renal replacement therapies. 使用肾脏替代疗法的 ESBL 产肠杆菌感染患者服用厄他培南的有效性和安全性。
IF 1.4 4区 医学 Q4 ENGINEERING, BIOMEDICAL Pub Date : 2024-09-01 Epub Date: 2024-07-30 DOI: 10.1177/03913988241264463
Wasim S El Nekidy, Iyad Ghazal, Emna Abidi, Diana Malaeb, Islam M Ghazi, Rania El Lababidi, Mohamad Mooty, Amir Malik, Muriel Ghosn, Jihad Mallat

Purpose: The clinical efficacy and safety of ertapenem use in patients undergoing renal replacement therapies (RRT) are not well-documented. Therefore, we aimed to investigate the safety and efficacy of ertapenem in patients with sepsis secondary to Enterobacterales who are undergoing RRT.

Methods: A retrospective cohort study was conducted on patients who met the inclusion criteria at our hospital between May 2015 and December 2021. The primary endpoint was 30-day mortality. Secondary endpoints included clinical cure, microbiologic cure, recurrence rate, and incidence of seizures.

Results: During the study period, 158 patients met the inclusion criteria. Of these, 86 were male (54.4%), the mean age was 66.4 ± 13.8 years, and the mean weight was 77 ± 22.4 kg. The most common diagnosis was bacteremia in 48 (30.4%) subjects, followed by urinary tract infection in 39 (24.7%) subjects, and pneumonia in 35 (22.2%) patients. The most isolated pathogens were Escherichia coli, followed by Klebsiella species. The median ertapenem dose was 0.5 g intravenously (IV) daily in those who received intermittent hemodialysis (IHD) and 1 g IV daily for those who received continuous veno-venous hemofiltration (CVVH). The 30-day mortality rate was 24%, the clinical cure rate was 89.2%, the microbiologic cure rate was 82%, the 30-day recurrence rate was 41.1%, and the incidence of seizures was 2.5%. Multivariate logistic regression analysis indicated that age (OR 1.04 [95% CI: 1.003-1.075]), being critically ill at therapy initiation (OR 2.9 [95% CI: 1.1-7.5]), and Enterobacterales other than Klebsiella species and Escherichia coli (OR 3.8 [95% CI: 1.1-12.5]) were significant independent risk factors associated with mortality in this population. Ertapenem dose was not associated with mortality.

Conclusion: Our findings suggest that the commonly used doses of ertapenem in patients undergoing IHD and CVVH are clinically effective but may pose a higher risk of seizures. A comprehensive pharmacokinetic study is needed to determine the most effective and safe dose for this population.

目的:在接受肾脏替代疗法(RRT)的患者中使用厄他培南的临床疗效和安全性尚未得到充分证实。因此,我们旨在研究厄他培南在接受 RRT 的肠杆菌继发性败血症患者中的安全性和有效性:方法:我们对 2015 年 5 月至 2021 年 12 月期间本院符合纳入标准的患者进行了一项回顾性队列研究。主要终点是 30 天死亡率。次要终点包括临床治愈、微生物治愈、复发率和癫痫发作率:在研究期间,共有 158 名患者符合纳入标准。其中,86 名男性(54.4%),平均年龄(66.4±13.8)岁,平均体重(77±22.4)公斤。最常见的诊断是菌血症(48 人,占 30.4%),其次是尿路感染(39 人,占 24.7%)和肺炎(35 人,占 22.2%)。分离出的最多病原体是大肠埃希菌,其次是克雷伯氏菌。接受间歇性血液透析(IHD)的患者中位厄他培南剂量为每天静脉注射(IV)0.5 克,而接受持续静脉-静脉血液滤过(CVVH)的患者中位厄他培南剂量为每天静脉注射(IV)1 克。30天死亡率为24%,临床治愈率为89.2%,微生物治愈率为82%,30天复发率为41.1%,癫痫发作率为2.5%。多变量逻辑回归分析表明,年龄(OR 1.04 [95% CI:1.003-1.075])、开始治疗时病情危重(OR 2.9 [95% CI:1.1-7.5])以及除克雷伯菌属和大肠埃希菌以外的肠杆菌属(OR 3.8 [95% CI:1.1-12.5])是与该人群死亡率相关的重要独立风险因素。厄他培南的剂量与死亡率无关:我们的研究结果表明,IHD 和 CVVH 患者常用的厄他培南剂量在临床上是有效的,但可能会带来较高的癫痫发作风险。需要进行全面的药代动力学研究,以确定这一人群最有效、最安全的剂量。
{"title":"Efficacy and safety of ertapenem dosing in patients with ESBL producing <i>Enterobacterales</i> infections utilizing renal replacement therapies.","authors":"Wasim S El Nekidy, Iyad Ghazal, Emna Abidi, Diana Malaeb, Islam M Ghazi, Rania El Lababidi, Mohamad Mooty, Amir Malik, Muriel Ghosn, Jihad Mallat","doi":"10.1177/03913988241264463","DOIUrl":"10.1177/03913988241264463","url":null,"abstract":"<p><strong>Purpose: </strong>The clinical efficacy and safety of ertapenem use in patients undergoing renal replacement therapies (RRT) are not well-documented. Therefore, we aimed to investigate the safety and efficacy of ertapenem in patients with sepsis secondary to Enterobacterales who are undergoing RRT.</p><p><strong>Methods: </strong>A retrospective cohort study was conducted on patients who met the inclusion criteria at our hospital between May 2015 and December 2021. The primary endpoint was 30-day mortality. Secondary endpoints included clinical cure, microbiologic cure, recurrence rate, and incidence of seizures.</p><p><strong>Results: </strong>During the study period, 158 patients met the inclusion criteria. Of these, 86 were male (54.4%), the mean age was 66.4 ± 13.8 years, and the mean weight was 77 ± 22.4 kg. The most common diagnosis was bacteremia in 48 (30.4%) subjects, followed by urinary tract infection in 39 (24.7%) subjects, and pneumonia in 35 (22.2%) patients. The most isolated pathogens were <i>Escherichia coli</i>, followed by <i>Klebsiella</i> species. The median ertapenem dose was 0.5 g intravenously (IV) daily in those who received intermittent hemodialysis (IHD) and 1 g IV daily for those who received continuous veno-venous hemofiltration (CVVH). The 30-day mortality rate was 24%, the clinical cure rate was 89.2%, the microbiologic cure rate was 82%, the 30-day recurrence rate was 41.1%, and the incidence of seizures was 2.5%. Multivariate logistic regression analysis indicated that age (OR 1.04 [95% CI: 1.003-1.075]), being critically ill at therapy initiation (OR 2.9 [95% CI: 1.1-7.5]), and Enterobacterales other than <i>Klebsiella species</i> and <i>Escherichia coli</i> (OR 3.8 [95% CI: 1.1-12.5]) were significant independent risk factors associated with mortality in this population. Ertapenem dose was not associated with mortality.</p><p><strong>Conclusion: </strong>Our findings suggest that the commonly used doses of ertapenem in patients undergoing IHD and CVVH are clinically effective but may pose a higher risk of seizures. A comprehensive pharmacokinetic study is needed to determine the most effective and safe dose for this population.</p>","PeriodicalId":13932,"journal":{"name":"International Journal of Artificial Organs","volume":null,"pages":null},"PeriodicalIF":1.4,"publicationDate":"2024-09-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141792429","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Development of in situ forming autologous fibrin scaffold incorporating synthetic teriparatide peptide for bone tissue engineering. 为骨组织工程开发含有合成特立帕肽的原位成型自体纤维蛋白支架。
IF 1.4 4区 医学 Q4 ENGINEERING, BIOMEDICAL Pub Date : 2024-09-01 Epub Date: 2024-10-06 DOI: 10.1177/03913988241262907
Mohammad Reza Khalili, Azam Molafilabi, Sepideh Mousazadeh, Arezou Mehrabi, Jafar Kiani, Peiman Brouki Milan, Faezeh Ghasemi

Introduction: This study investigates the potential of an in-situ forming scaffold using a fibrin-based scaffold derived from autologous plasma combined with Synthetic Teriparatide (TP) for bone regeneration application. TP is known for its bone formation stimulation but has limited clinical use due to side effects. This autologous delivery system aims to provide precise, controlled, localized, and long-term release of TP for accelerating bone regeneration.

Methods: Fibrinogen from autologous plasma was extracted using ethanol, and thrombin was precipitated with ammonium sulfate to create the fibrin scaffold. Characterization of fibrinogen was done through FTIR, SDS-Page, porosity, SEM, degradation, and rheology tests. Viability was assessed by MTT in five groups with different concentrations of TP in fibrin scaffold (50, 100, and 150 µl/ml), fibrin alone, and a control group against HEK and Wharton's jelly cells. The release profile of different concentrations of TP in the fibrin scaffold was also examined.

Results: The formation time of the fibrin scaffold was 4 ± 0.2 s. The highest Infrared absorption for fibrinogen was confirmed. Rheology assessment revealed a higher elastic modulus than the viscous modulus. The created fibrin scaffold displayed a consistent three-dimensional microstructure with an interconnected porous network. Cytotoxicity assays demonstrated good biocompatibility and enhanced cell growth with different concentrations of TP in the fibrin scaffold. The TP release increased with higher concentrations, peaking at an average of 61% over 54 h.

Conclusion: Autologous plasma-derived fibrin scaffolds incorporating TP exhibit satisfactory release within the scaffold and hold promise as a versatile bone filler for clinical use, facilitating osteoregeneration.

简介:本研究探讨了使用源自自体血浆的纤维蛋白基支架与合成特立帕肽(TP)相结合的原位成形支架在骨再生应用方面的潜力。合成特立帕肽(TP)以刺激骨形成而闻名,但由于其副作用,临床应用有限。这种自体给药系统旨在提供精确、可控、局部和长期的 TP 释放,以加速骨再生:方法:用乙醇提取自体血浆中的纤维蛋白原,并用硫酸铵沉淀凝血酶以形成纤维蛋白支架。通过傅立叶变换红外光谱、SDS-Page、孔隙率、扫描电镜、降解和流变测试对纤维蛋白原进行表征。用 MTT 评估了纤维蛋白支架中不同浓度 TP(50、100 和 150 µl/ml)的五组、单独纤维蛋白组以及 HEK 和沃顿果冻细胞对照组的活力。此外,还研究了纤维蛋白支架中不同浓度 TP 的释放情况:结果:纤维蛋白支架的形成时间为 4 ± 0.2 秒。纤维蛋白原的红外线吸收率最高。流变学评估显示弹性模量高于粘性模量。制成的纤维蛋白支架显示出一致的三维微观结构和相互连接的多孔网络。细胞毒性试验表明,纤维蛋白支架中不同浓度的 TP 具有良好的生物相容性,并能促进细胞生长。TP的释放量随着浓度的升高而增加,在54小时内达到峰值,平均释放量为61%:结论:含有 TP 的自体血浆衍生纤维蛋白支架在支架内的释放情况令人满意,有望作为一种多功能骨填充剂用于临床,促进骨再生。
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引用次数: 0
Performance study of dual heart assisted control system based on SL-SMC physiological combination controller. 基于 SL-SMC 生理组合控制器的双心脏辅助控制系统性能研究。
IF 1.4 4区 医学 Q4 ENGINEERING, BIOMEDICAL Pub Date : 2024-09-01 Epub Date: 2024-09-23 DOI: 10.1177/03913988241262911
Fangqun Wang, Fan Xu, Fenglian Zhu, Shaojun Wang, Chenyang He, Litao Ding, Mengping Li

The main challenges of Biventricular Assist Devices (BiVAD) as a treatment modality for patients with Bicardiac heart failure heart failure are the balance of systemic blood flow during changes in physiological activity and the prevention of ventricular suction. In this study, a model of the Biventricular Circulatory System (BCS) was constructed and a physiological combination controller based on Starling-Like controller and Sliding Mode Controller (SMC) was proposed. The effects of the physiological controller on the hemodynamics of the BCS were investigated by simulating two sets of physiological state change experiments: elevated pulmonary artery resistance and resting-exercise, with constant speed (CS) control and combined Starling-like and PI control (SL-PI) as controllers. Simulation and experimental results showed that the Starling-like and Sliding Mode Control (SL-SMC) physiological combination controller was effective in preventing the occurrence of ventricular suction, providing higher cardiac output, maintain balance of systemic blood flow, and have higher response speed and robustness in the face of physiological state changes.

双心室辅助装置(BiVAD)作为双心室心力衰竭患者的一种治疗方式,其主要挑战在于生理活动变化时全身血流的平衡和防止心室抽吸。本研究构建了双心室循环系统(BCS)模型,并提出了基于斯塔林样控制器和滑动模式控制器(SMC)的生理组合控制器。通过模拟肺动脉阻力升高和静息-运动两组生理状态变化实验,研究了生理控制器对 BCS 血液动力学的影响,控制器分别为恒速(CS)控制器和类 Starling 控制器与 PI 控制器组合(SL-PI)控制器。仿真和实验结果表明,类星凌和滑模控制(SL-SMC)生理组合控制器能有效防止心室抽吸的发生,提供更高的心输出量,维持全身血流平衡,并在生理状态变化时具有更高的响应速度和鲁棒性。
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引用次数: 0
Design and evaluation of mechanical strength of multi-material polymeric implants for mandibular reconstruction. 设计和评估用于下颌骨重建的多材料聚合物植入物的机械强度。
IF 1.4 4区 医学 Q4 ENGINEERING, BIOMEDICAL Pub Date : 2024-09-01 Epub Date: 2024-07-27 DOI: 10.1177/03913988241261817
Kalaithendral K, S Karuppudaiyan, Sandipan Roy

Reconstruction of mandible implants to address segmental abnormalities is still a challenging task, both in vitro and in vivo. The mechanical strength of the materials used is a critical factor that determines how well bone is regenerated. The reconstruction technique of mandibular abnormalities widely uses polymeric implants. It is critical to evaluate the mechanical resilience under different load cases, including axial, combined, and flexural loading conditions. This study developed implants for mandibular defects using a combination of four materials: polylactic acid (PLA), polyethylene terephthalate glycol (PETG), thermoplastic polyurethane (TPU), and polycaprolactone (PCL), with the aim of mimicking the inherent characteristics of cortical and cancellous bone structures and evaluating their mechanical properties to support bone Osseo integration. The eleven of these combinations of structures result below the micro strain threshold level of <3000 µε, and the five combinations of the structures result in micro strain above the threshold value. The intact bone study results show that the stress under axial, combined, and flexural loading conditions is 27.6, 38.9, and 64.9 MPa, respectively. This study's stress results are lower than those from the intact bone study. The study found that the combinations of PLA and TPU material were most preferred for the cortical and cancellous bone regions of polymeric implants. These materials are also compatible with 3D printing. The results of this study can be used to find multi-material combinations that are strong and flexible.

无论是在体外还是在体内,重建下颌骨植入体以解决节段性畸形仍然是一项具有挑战性的任务。所用材料的机械强度是决定骨再生效果的关键因素。下颌骨畸形的重建技术广泛使用聚合物种植体。评估不同载荷情况下的机械弹性至关重要,包括轴向、联合和弯曲载荷条件。本研究使用聚乳酸(PLA)、聚对苯二甲酸乙二醇酯(PETG)、热塑性聚氨酯(TPU)和聚己内酯(PCL)四种材料的组合为下颌骨缺损开发了植入物,目的是模仿皮质骨和松质骨结构的固有特性,并评估其支持骨Osseo整合的机械性能。这些结构组合的十一种结果低于微应变阈值水平,即
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引用次数: 0
The effect of changes in intra-compartmental bioimpedance measurements with early intra-dialytic hypotension during haemodialysis. 在血液透析过程中,血液透析室内生物阻抗测量值的变化对早期透析室内低血压的影响。
IF 1.4 4区 医学 Q4 ENGINEERING, BIOMEDICAL Pub Date : 2024-08-21 DOI: 10.1177/03913988241269444
Sabrina Haroon, Andrew Davenport

Introduction: Intra-dialytic hypotension (IDH) remains the commonest problem associated with routine haemodialysis treatments. Fluid shifts from intracellular(ICW) and extracellular(ECW) compartments to refill plasma volume during haemodialysis with ultrafiltration.

Methods: We studied the effect of relative changes in ICW and ECW indifferent body segments using multifrequency segmental bioimpedance during haemodialysis and IDH episodes.

Results: Of 42 haemodialysis patients,16 patients (38.1%) developed IDH within the first hour of dialysis. Patients with and without early IDH were well-matched for demographics and starting bioimpedance measurements. However, after 60 min, the relative change in in ECW/ICW ratio between the non-fistula arm and leg was significantly different for the early IDH group median -1.07 (-3.33 to 0.8) versus 0.61 (-0.78 to 1.8), p < 0.05, whereas there no differences in ultrafiltration rate, relative blood volume monitoring or on-line clearance.

Conclusion: Monitoring serial changes in fluid status in different body compartments with bioimpedance may potentially prevent IDH in the future.

导言:透析内低血压(IDH)仍然是常规血液透析治疗中最常见的问题。在超滤血液透析过程中,液体会从细胞内(ICW)和细胞外(ECW)分区转移,以补充血浆容量:我们利用多频节段生物阻抗研究了血液透析和IDH治疗期间ICW和ECW相对变化对身体各节段的影响:在42名血液透析患者中,有16名患者(38.1%)在透析的第一个小时内出现了IDH。有早期 IDH 和没有早期 IDH 的患者在人口统计学和起始生物阻抗测量方面非常匹配。然而,60 分钟后,非瘘管手臂和腿部的 ECW/ICW 比率的相对变化在早期 IDH 组的中位数-1.07(-3.33 至 0.8)与 0.61(-0.78 至 1.8)之间存在显著差异,P 结论:利用生物阻抗监测身体各部分液体状态的连续变化有可能在未来预防 IDH。
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引用次数: 0
A special issue of our journal from the yESAO. yESAO 的特刊。
IF 1.4 4区 医学 Q4 ENGINEERING, BIOMEDICAL Pub Date : 2024-08-01 Epub Date: 2024-10-03 DOI: 10.1177/03913988241288365
Andrea Remuzzi
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引用次数: 0
期刊
International Journal of Artificial Organs
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