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Protein Kinase N1 Level Predicts Acute Kidney Injury in Patients Undergoing Cardiac Surgery: A Prospective Cohort Study. 预测心脏手术患者急性肾损伤的蛋白激酶 N1 水平:一项前瞻性队列研究。
IF 3 3区 医学 Q1 Medicine Pub Date : 2024-01-01 Epub Date: 2024-01-16 DOI: 10.1159/000536225
Lianjiu Su, Fangfang Zhu, Jiahao Zhang, Edward Z Cao, Cheng Yang, Haibing Sun, Xiaofang Jiang, Xiaozhan Wang, Jing Wang, Zhiyong Peng

Introduction: The objective of this study was to examine the utility of protein kinase N1 (PKN1) as a biomarker of cardiac surgery-associated AKI (CSA-AKI).

Methods: A prospective cohort study of 110 adults undergoing on-pump cardiac surgery was conducted. The associations between post-operative PKN1 and CSA-AKI, AKI severity, need for renal replacement therapy (RRT), duration of AKI, length of ICU stay, and post-operative hospital stay were evaluated.

Results: Patients were categorized into three groups according to PKN1 tertiles. The incidence of CSA-AKI in the third tertile was 3.4-fold higher than that in the first. PKN1 was an independent risk factor for CSA-AKI. The discrimination of PKN1 to CSA-AKI assessed by ROC curve indicated that the AUC was 0.70, and the best cutoff was 5.025 ng/mL. This group (>5.025 ng/mL) was more likely to develop CSA-AKI (p < 0.001). The combined AUC of EuroSCORE, aortic cross-clamp time, and PKN1 was 0.82 (p < 0.001). A higher level of PKN1 was related to increased need for RRT, longer duration of AKI, and length of ICU and post-operative hospital stays.

Conclusions: PKN1 could be a potential biomarker for the prediction of CSA-AKI. The combination of PKN1, EuroSCORE, and aortic cross-clamp time was likely to predict the occurrence of CSA-AKI.

简介本研究旨在探讨蛋白激酶 N1(PKN1)作为心脏手术相关性 AKI(CSA-AKI)生物标志物的效用:方法:对110名接受泵上心脏手术的成人进行了前瞻性队列研究。研究评估了术后 PKN1 与 CSA-AKI、AKI 严重程度、肾脏替代治疗(RRT)需求、AKI 持续时间、重症监护室住院时间和术后住院时间之间的关系:结果:根据PKN1三元组将患者分为三组。第三梯队的 CSA-AKI 发生率是第一梯队的 3.4 倍。PKN1是CSA-AKI的独立危险因素。用ROC曲线评估PKN1对CSA-AKI的区分度,结果显示AUC为0.70,最佳临界值为5.025ng/mL。该组(>5.025ng/mL)更有可能发展为 CSA-AKI(结论:PKN1 可能是一种潜在的生物指标:PKN1可能是预测CSA-AKI的潜在生物标志物。PKN1、EuroSCORE和主动脉瓣关闭时间的组合有可能预测CSA-AKI的发生。
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引用次数: 0
Seraph 100 Microbind Affinity Blood Filter Does Not Clear Antibiotics: An Analysis of Antibiotic Concentration Data from PURIFY-OBS. Seraph 100 微粘附亲和血液过滤器无法清除抗生素:PURIFY-OBS 抗生素浓度数据分析。
IF 3 3区 医学 Q1 Medicine Pub Date : 2024-01-01 Epub Date: 2024-01-13 DOI: 10.1159/000531951
Jesse P DeLuca, Daniel J Selig, Pooja Vir, Chau V Vuong, Jeffrey Della-Volpe, Ian M Rivera, Caroline Park, Benjamin Levi, Kathleen P Pratt, Ian J Stewart

Introduction: Novel hemoperfusion systems are emerging for the treatment of sepsis. These devices can directly remove pathogens, pathogen-associated molecular patterns, cytokines, and other inflammatory markers from circulation. However, significant safety concerns such as potential antibiotic clearance need to be addressed prior to these devices being used in large clinical studies.

Methods: Prospective, observational study of 34 participants undergoing treatment with the Seraph 100® Microbind Affinity Blood Filter (Seraph 100) device at 6 participating sites in the USA. Patients were included for analysis if they had a record of receiving an antibiotic concurrent with Seraph 100 treatment. Patients were excluded if there was missing information for blood flow rate. Blood samples were drawn pre- and post-filter at 1 h and 4 h after treatment initiation. These average pre- and post-filter time-concentration observations were then used to estimate antibiotic clearance in L/h (CLSeraph) due to the Seraph 100 device.

Results: Of the 34 participants in the study, 17 met inclusion and exclusion criteria for the antibiotic analysis. Data were obtained for 7 antibiotics (azithromycin, cefazolin, cefepime, ceftriaxone, linezolid, piperacillin, and vancomycin) and one beta-lactamase inhibitor. Mean CLSeraph for the antibiotics investigated ranged from -0.57 to 0.47 L/h. No antibiotic had a CLSeraph statistically significant from 0.

Discussion/conclusion: The Seraph 100 did not significantly clear any measured antibiotic in clinical samples. These data give further evidence to suggest that these therapies may be safely administered to critically ill patients and will not impact concentrations of administered antibiotics.

简介:用于治疗败血症的新型血液灌流系统不断涌现。这些设备可直接清除血液循环中的病原体、病原体相关分子模式、细胞因子和其他炎症标志物。然而,在将这些设备用于大型临床研究之前,需要解决潜在的抗生素清除等重大安全问题:前瞻性观察研究:在美国 6 个参与研究的机构对 34 名接受 Seraph 100® Microbind Affinity 血液过滤器(Seraph 100)治疗的患者进行观察。如果患者在接受赛拉弗 100 治疗的同时有接受抗生素治疗的记录,则纳入分析范围。如果血流量信息缺失,则排除患者。在开始治疗后一小时和四小时分别抽取过滤前和过滤后的血液样本。然后,利用这些过滤器前后的平均时间浓度观测值来估算瑟拉弗 100 设备的抗生素清除率,单位为升/小时(CLSeraph):在 34 位参与研究的人员中,有 17 位符合抗生素分析的纳入和排除标准。获得了 7 种抗生素(阿奇霉素、头孢唑啉、头孢吡肟、头孢曲松、利奈唑胺、哌拉西林和万古霉素)和 1 种β-内酰胺酶抑制剂的数据。所研究抗生素的平均 CLSeraph 值介于 -0.57 至 0.47 升/小时之间。没有一种抗生素的 CLSeraph 在统计学上显著低于 0.0:Seraph 100 不能明显清除临床样本中的任何抗生素。这些数据进一步证明,危重病人可以安全地使用这些疗法,而且不会影响抗生素的浓度。
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引用次数: 0
Efficacy of Therapeutic Apheresis for Cryoglobulinemic Vasculitis Patients with Renal Involvement: A Systematic Review. 单采治疗肾受累的冷球蛋白血症血管炎患者的疗效:系统评价。
IF 3 3区 医学 Q1 Medicine Pub Date : 2024-01-01 Epub Date: 2023-10-18 DOI: 10.1159/000534102
Jing Miao, Pajaree Krisanapan, Supawit Tangpanithandee, Charat Thongprayoon, Wisit Cheungpasitporn

Introduction: Therapeutic apheresis (TA) is commonly used for cryoglobulinemic vasculitis (CV) patients, but its efficacy remains uncertain. This systematic review aimed to assess the efficacy of different TA modalities, such as plasma exchange (PE), plasmapheresis (PP), and cryofiltration (CF), in treating CV patients with renal involvement.

Methods: Literature search of MEDLINE, EMBASE, and Cochrane Databases was conducted up to December 2022. Studies that reported the outcomes of TA in adult CV patients with renal involvement were assessed. The protocol for this systematic review has been registered with PROSPERO (No. CRD42023417727). The quality of each study was evaluated by the investigators using the validated methodological index for non-randomized studies (minors) quality score.

Results: 154 patients who encountered 170 episodes of serious events necessitating TA were evaluated across 76 studies. Among them, 51% were males, with a mean age ranging from 49 to 58 years. The CV types included 15 type I, 97 type II, and 13 type III, while the remaining patients exhibited mixed (n = 17) or undetermined CV types (n = 12). Among the treatment modalities, PE, PP, and CF were performed in 85 (56%), 52 (34%), and 17 patients (11%), respectively, with no identical protocol for TA treatment. The overall response rate for TA was 78%, with response rates of 84%, 77%, and 75% observed in type I, II, and III patients respectively. Most patients received steroids, immunosuppressants, and treatment targeting the underlying causative disease. The overall long-term renal outcome rate was 77%, with type I, II, and III patients experiencing response rates of 89%, 76%, and 90%, respectively. The renal outcomes in patients receiving PE, PP, and CF were comparable, with rates of 78%, 76%, and 81%, respectively.

Conclusions: This study presents compelling evidence that combination of TA with other treatments, especially immunosuppressive therapy, is a successful strategy for effectively managing severe renal involvement in CV patients. Among the TA modalities studied, including PE, PP, and CF, all demonstrated efficacy, with PE being the most frequently employed approach.

引言:治疗性单采(TA)通常用于冷球蛋白血症血管炎(CV)患者,但其疗效尚不确定。这项系统综述旨在评估不同TA模式,如血浆置换(PE)、血浆置换(PP)和冷冻过滤(CF),在治疗肾脏受累的CV患者中的疗效。方法:截至2022年12月,对MEDLINE、EMBASE和Cochrane数据库进行文献检索。对报告肾功能损害的成年CV患者TA结果的研究进行了评估。该系统审查的方案已在PROSPERO注册(编号CRD42023417727)。每项研究的质量由研究人员使用非随机研究(未成年人)质量评分的验证方法指数进行评估。结果:在76项研究中对154名患者进行了评估,他们遇到了170次需要TA的严重事件。其中,51%为男性,平均年龄在49至58岁之间。CV类型包括15种I型、97种II型和13种III型,而其余患者表现出混合型(n=17)或未确定的CV类型(n=12)。在治疗方式中,PE、PP和CF分别在85名(56%)、52名(34%)和17名(11%)患者中进行,TA治疗方案不相同。TA的总有效率为78%,在I型、II型和III型患者中观察到的有效率分别为84%、77%和75%。大多数患者接受了类固醇、免疫抑制剂和针对潜在病因的治疗。总的长期肾脏转归率为77%,I型、II型和III型患者的有效率分别为89%、76%和90%。接受PE、PP和CF治疗的患者的肾脏结果具有可比性,其发生率分别为78%、76%和81%。结论:本研究提供了令人信服的证据,证明TA与其他治疗,特别是免疫抑制治疗相结合,是有效管理CV患者严重肾脏受累的成功策略。在所研究的TA模式中,包括PE、PP和CF,均显示出疗效,PE是最常用的方法。
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引用次数: 0
Effects of Blood Hemoadsorption Therapy with HA-380 in Total Arch Replacement for Acute Type A Aortic Dissection: A Retrospective Observational Study. HA-380血液吸附治疗急性A型主动脉夹层全足弓置换术的疗效:回顾性观察研究。
IF 3 3区 医学 Q1 Medicine Pub Date : 2024-01-01 Epub Date: 2023-10-30 DOI: 10.1159/000534852
Juxiang Wang, Bin Chen, Junhao Xie, Huilong Chen, Lihua Li, Weiqun Zhang, Lin Lu

Introduction: This study aimed to evaluate whether the addition of a hemoadsorption (HA) cartridge, HA-380, in the cardiopulmonary bypass (CPB) circuit in acute type A aortic dissection (ATAAD) surgery reduced inflammatory cytokine levels and decreased postoperative complications.

Methods: A retrospective observational cohort study was conducted between March 1, 2021, and February 28, 2022. Patients with ATAAD undergoing emergent total arch replacement surgery were divided into the control (CON) and HA groups on the basis of the addition of the HA-380 cartridge in the CPB circuit.

Results: Overall, 121 patients met the eligibility criteria; 2 patients in each group who died within the first postoperative week were excluded. Further, 57 and 60 patients in the CON and HA groups, respectively, were included in the pooled analysis. The major perioperative data, baseline values of interleukin-6 (IL-6) and C-reactive protein, and therapeutic interventions were similar in the two groups (all, p > 0.05). The serum IL-6 levels increased more rapidly in the CON group than those in the HA group postoperatively (205.73 ± 174.72 vs. 146.13 ± 64.15 pg/mL, p = 0.020). The HA group had a lower incidence of postoperative acute kidney injury (AKI) and severe acute respiratory distress syndrome than the CON group (25.4 vs. 44.6%, p = 0.032 and 18.3 vs. 35.1%, p = 0.040, respectively). Logistic regression analyses showed that HA may be a protective factor against postoperative AKI. The incidence of bleeding, delirium, and stroke as well as the lengths of intensive care unit and hospital stay in both groups were similar (all, p > 0.05).

Conclusions: The use of HA-380 in the CPB circuit may attenuate inflammatory response and reduce major complications following ATAAD surgery. HA may be associated with lower rate of postoperative AKI.

引言:本研究旨在评估在急性a型主动脉夹层(ATAAD)手术的体外循环(CPB)回路中添加血液吸附(HA)墨盒HA-380是否降低了炎症细胞因子水平并减少了术后并发症。方法:在2021年3月1日至2022年2月28日期间进行了一项回顾性观察性队列研究。根据在体外循环回路中添加HA-380套筒,将接受紧急全足弓置换术的ATAAD患者分为对照组(CON)和HA组。结果:总体而言,121名患者符合资格标准;每组2名在术后第一周内死亡的患者被排除在外。此外,CON组和HA组分别有57名和60名患者被纳入合并分析。主要围手术期数据、白细胞介素-6(IL-6)和C反应蛋白的基线值,两组的治疗干预措施相似(均P>0.05)。CON组术后血清IL-6水平比HA组升高更快(205.73±174.72 vs.146.13±64.15 pg/mL,P=0.020)。HA组术后急性肾损伤(AKI)和严重急性呼吸窘迫综合征的发生率低于CON组(25.4%对44.6%,P=0.032;18.3%对35.1%,P=0.040)。Logistic回归分析表明HA可能是预防术后AKI的一个保护因素。两组出血、谵妄和中风的发生率以及重症监护室和住院时间相似(均P>0.05)。结论:在体外循环回路中使用HA-380可以减轻炎症反应,减少ATAAD手术后的主要并发症。HA可能与术后AKI发生率较低有关。
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引用次数: 0
Rapid and Effective Elimination of Myoglobin with CytoSorb® Hemoadsorber in Patients with Severe Rhabdomyolysis. CytoSorb®血液吸附器快速有效消除严重横纹肌溶解症患者的肌红蛋白。
IF 3 3区 医学 Q1 Medicine Pub Date : 2024-01-01 Epub Date: 2023-11-02 DOI: 10.1159/000534479
Frederic Albrecht, Stefan Schunk, Maren Fuchs, Thomas Volk, Juergen Geisel, Danilo Fliser, Andreas Meiser

Introduction: Rhabdomyolysis is characterized by destruction of muscle fibers by various causes and is diagnosed by increased creatine kinase concentrations in the blood. Myoglobin released into the blood may cause acute kidney injury. In this randomized controlled study, we hypothesized that myoglobin elimination would be faster when a hemoadsorber was added to a continuous veno-venous hemodialysis (CVVHD).

Methods: Four patients in the control group received CVVHD with a high cut-off hemofilter using high blood and dialysate flows for 48 h. Four patients in the CytoSorb group received the same treatment, but in addition, the hemoadsorber CytoSorb® was inserted in front of the hemofilter and replaced once after 24 h. Blood samples were drawn simultaneously before (pre) and after (post) the hemofilter or else the hemoadsorber, after 5 and 30 min, as well as after 2, 4, 8, and 24 h. All measurements were repeated the next day after the hemoadsorber had been renewed in the CytoSorb group. Primary outcome was the area under the curve (AUC) of the relative myoglobin concentrations as percent of baseline. To evaluate the efficacy of myoglobin removal, relative reductions in myoglobin concentrations during one passage through each device at each time point were calculated.

Results: Patients in the CytoSorb group had a significantly lower AUC during the first 24 h (42 ± 10% vs. 63 ± 6%, p = 0.029) as well as during the observation period of 48 h (26 ± 7% vs. 51 ± 12%, p = 0.029). The relative reductions for myoglobin were considerably higher in the CytoSorb group compared to the control group during the first 8 h.

Conclusion: Myoglobin concentrations declined considerably faster when CytoSorb was added to a CVVHD. When compared to a high-cut-off hemofilter, efficacy of CytoSorb in myoglobin elimination was much better. Because of saturation after 8-12 h an exchange may be necessary.

简介:横纹肌溶解症的特点是由各种原因破坏肌肉纤维,并通过血液中肌酸激酶浓度升高来诊断。释放到血液中的肌红蛋白可能导致急性肾损伤。在这项随机对照研究中,我们假设在连续静脉-静脉血液透析(CVVHD)中加入血液吸附器会更快地消除肌红蛋白,将血液吸附器CytoSorb®插入血液过滤器前,并在24小时后更换一次。在血液过滤器或其他血液吸附剂之前(之前)和之后(之后),在5和30分钟后,以及在2、4、8和24小时后,同时抽取血液样本。在CytoSorb组更换血液吸附机后的第二天重复所有测量。主要结果是相对肌红蛋白浓度作为基线百分比的曲线下面积(AUC)。为了评估肌红蛋白去除的疗效,计算了在每个时间点通过每个装置的过程中肌红蛋白浓度的相对降低。结果:CytoSorb组患者在前24小时内AUC显著降低(42±10%vs.63±6%,p=0.029),在48小时观察期内AUC明显降低(26±7%vs.51±12%,p=0.029当CytoSorb被添加到CVVHD中时,速度要快得多。与高截止血液过滤器相比,CytoSorb在消除肌红蛋白方面的效果要好得多。由于8-12小时后饱和,可能需要进行交换。
{"title":"Rapid and Effective Elimination of Myoglobin with CytoSorb® Hemoadsorber in Patients with Severe Rhabdomyolysis.","authors":"Frederic Albrecht, Stefan Schunk, Maren Fuchs, Thomas Volk, Juergen Geisel, Danilo Fliser, Andreas Meiser","doi":"10.1159/000534479","DOIUrl":"10.1159/000534479","url":null,"abstract":"<p><strong>Introduction: </strong>Rhabdomyolysis is characterized by destruction of muscle fibers by various causes and is diagnosed by increased creatine kinase concentrations in the blood. Myoglobin released into the blood may cause acute kidney injury. In this randomized controlled study, we hypothesized that myoglobin elimination would be faster when a hemoadsorber was added to a continuous veno-venous hemodialysis (CVVHD).</p><p><strong>Methods: </strong>Four patients in the control group received CVVHD with a high cut-off hemofilter using high blood and dialysate flows for 48 h. Four patients in the CytoSorb group received the same treatment, but in addition, the hemoadsorber CytoSorb® was inserted in front of the hemofilter and replaced once after 24 h. Blood samples were drawn simultaneously before (pre) and after (post) the hemofilter or else the hemoadsorber, after 5 and 30 min, as well as after 2, 4, 8, and 24 h. All measurements were repeated the next day after the hemoadsorber had been renewed in the CytoSorb group. Primary outcome was the area under the curve (AUC) of the relative myoglobin concentrations as percent of baseline. To evaluate the efficacy of myoglobin removal, relative reductions in myoglobin concentrations during one passage through each device at each time point were calculated.</p><p><strong>Results: </strong>Patients in the CytoSorb group had a significantly lower AUC during the first 24 h (42 ± 10% vs. 63 ± 6%, p = 0.029) as well as during the observation period of 48 h (26 ± 7% vs. 51 ± 12%, p = 0.029). The relative reductions for myoglobin were considerably higher in the CytoSorb group compared to the control group during the first 8 h.</p><p><strong>Conclusion: </strong>Myoglobin concentrations declined considerably faster when CytoSorb was added to a CVVHD. When compared to a high-cut-off hemofilter, efficacy of CytoSorb in myoglobin elimination was much better. Because of saturation after 8-12 h an exchange may be necessary.</p>","PeriodicalId":8953,"journal":{"name":"Blood Purification","volume":null,"pages":null},"PeriodicalIF":3.0,"publicationDate":"2024-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"71420374","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"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
Low-Frequency/High-Frequency Ratio Is a Predictor of Death and Hospitalization in Patients on Maintenance Hemodialysis: A Prospective Study. 低频率/高频率比率是维持性血液透析患者住院和死亡的预测因素:一项前瞻性研究。
IF 2.2 3区 医学 Q3 HEMATOLOGY Pub Date : 2024-01-01 Epub Date: 2024-02-07 DOI: 10.1159/000536538
Yafei Chen, Xu Li, Li Zhu, Yan Wang, Liangying Gan, Li Zuo

Introduction: This study aimed to evaluate the predictive value of the low-frequency/high-frequency (LF/HF) ratio in all causes of death and hospitalizations in maintenance hemodialysis (MHD) patients.

Methods: This is a single-center prospective study with a 48-h electrocardiograph (ECG) recording. A total of 110 patients were enrolled in the study from October 1, 2021, to September 30, 2022. ECG recordings started before initiation of the hemodialysis (HD) session and lasted for 48 h, covering the intra- as well as inter-HD period. We divided our participants into two groups based on the median value of LF/HF, one of the frequency domain parameters of heart rate variability (HRV). Patients with LF/HF <1.33 were categorized as group A and those with LF/HF ≥1.33 were group B. The endpoint of the study was a composite event of death or hospitalization. We followed all patients until the composite endpoint or the end of the study on February 28, 2023. Multivariate Cox regression was used to assess the adjusted effect of LF/HF on the composite endpoint.

Results: Patients in group A were older and the number of patients with diabetes was more than that of group B. With regards to the laboratory data, group A had lower serum creatinine and uric acid and higher ferritin and NT-ProBNP. In the index HD session, systolic blood pressure was higher but diastolic blood pressure was significantly lower in group A. During the median follow-up period of 8.8 (7.6-9.8) months, 27 hospitalizations and 10 deaths were documented. Increased LF/HF ratio was an independent protective factor of composite endpoint events (HR = 0.357, 95% CI: 0.162-0.790, p = 0.011).

Conclusion: Risks of mortality and hospitalizations are higher among HD patients having decreased LF/HF ratios. LF/HF in the 48-h recording can be considered as a prognostic factor for risk stratification in HD patients.

导言本研究旨在评估低频/高频(LF/HF)比值对维持性血液透析(MHD)患者各种死亡原因和住院治疗的预测价值:这是一项单中心前瞻性研究,记录了 48 小时的心电图。从 2021 年 10 月 1 日至 2022 年 9 月 30 日,共有 110 名患者参与了这项研究。心电图记录从血液透析(HD)开始前开始,持续 48 小时,涵盖血液透析期间和透析间歇期。我们根据心率变异性(HRV)的频域参数之一 LF/HF 的中位值将参与者分为两组。LF/HF < 1.33 的患者为 A 组,LF/HF≥1.33 的患者为 B 组。我们对所有患者进行了随访,直至综合终点或研究于 2023 年 2 月 28 日结束。采用多变量 Cox 回归评估 LF/HF 对综合终点的调整效应:在实验室数据方面,A组患者的血清肌酐和尿酸较低,而铁蛋白和NT-ProBNP较高。在中位随访期 8.8(7.6-9.8)个月期间,记录到 27 例住院和 10 例死亡。LF/HF 比率的增加是综合终点事件的独立保护因素(HR = 0.357,95% CI 0.162-0.790,P = 0.011):结论:LF/HF比率降低的血液透析患者的死亡和住院风险更高。48小时记录中的LF/HF可作为对血液透析患者进行风险分层的预后因素。
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引用次数: 0
In vivo Assessment of a Manual Single Lumen Alternating Micro-Batch Hemodiafiltration System. 手动单腔交替微批次血液渗滤 (mSLAMB) 系统的体内评估。
IF 2.2 3区 医学 Q3 HEMATOLOGY Pub Date : 2024-01-01 Epub Date: 2024-03-27 DOI: 10.1159/000538358
Sabrina L Lanker, Christopher J Pino, H David Humes, Lakhmir Chawla, Kimberly A Johnston

Introduction: The manual single lumen alternating micro-batch hemodiafiltration (mSLAMB) system is a closed-loop dialysis system designed to provide kidney support in emergency situations (e.g., fluid overload, hyperkalemia, acidemia). If done repeatedly in small batches and at high flow rates, this system was found to achieve clearance levels comparable to traditional renal replacement therapy.

Methods: Using a porcine model, uremic toxins and exogenous fluorescent tracer concentrations were successfully lowered within just 1 h of treatment.

Results: With a maximal dialysate flow, mSLAMB can achieve decreases in serum potassium concentration of >0.5 mmol/L/h. With the mSLAMB hemodiafiltration system, micro-batch processing was also successful in removing up to 250 mL of ultrafiltrate in 8 cycles.

Conclusion: This process could create a better fluid balance allowing for administering therapeutic fluids such as sodium bicarbonate in the clinic. Electrolyte imbalance and volume overload remain severe life-threatening emergencies in low resource settings; therefore, mSLAMB should be explored further due to its modest vascular access requirements, low cost, and ability to be performed without electricity or batteries.

简介:手动单腔交替微批次血液透析滤过(mSLAMB)系统是一种闭环透析系统,设计用于在紧急情况下(如液体超负荷、高钾血症、酸血症)提供肾脏支持。如果小批量、高流速地反复进行透析,该系统可达到与传统肾脏替代疗法(RRT)相当的清除水平:方法:使用猪模型,在治疗后 1 小时内成功降低了尿毒症毒素和外源性荧光示踪剂的浓度:结果:在最大透析流量下,mSLAMB 可使血清钾浓度下降 > 0.5 mmol/L/小时。使用 mSLAMB 血液透析过滤系统,微批处理也能在 8 个周期内成功去除多达 250 毫升的超滤液:结论:这一工艺可以改善体液平衡,从而在临床上使用治疗性液体,如碳酸氢钠。在资源匮乏的环境中,电解质失衡和容量超载仍然是严重威胁生命的紧急情况,因此,mSLAMB 因其对血管通路的要求不高、成本低廉以及无需电力或电池就能进行操作而值得进一步探索。
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引用次数: 0
Pediatric Emergent Peritoneal Dialysis in Intensive Care Units: Indications, Techniques, and Outcomes. 重症监护病房的儿科紧急腹膜透析:适应症、技术和结果。
IF 2.2 3区 医学 Q3 HEMATOLOGY Pub Date : 2024-01-01 Epub Date: 2024-05-26 DOI: 10.1159/000539512
Yi-Hsuan Huang, Chia-Man Chou, Sheng-Yang Huang, Hou-Chuan Chen

Introduction: This study aimed to identify risk factors affecting outcomes in pediatric patients requiring emergent peritoneal dialysis (PD) for all causes, focusing on survival rates, kidney function recovery, PD duration, complications, and quality of life.

Methods: A retrospective review was conducted on medical records of pediatric patients who received emergent bedside PD in the intensive care unit from January 2010 to February 2023. Thirty-four catheters were placed, with demographic, preoperative, and procedural data collected. MedCalc® Statistical Software was used for analysis with a significance level set at p < 0.05. Prophylactic antibiotics were administered prior to surgery, and catheters were placed using a consistent technique by a single team of pediatric surgeons.

Results: The median age at catheter placement was 39 days (range 2-2,286), and the median body weight was 3.53 kg (range 1.2-48.8). The majority were male (64.7%), with 17.6% preterm. The most common indication for PD was acute kidney injury (AKI) (88.2%), followed by hyperammonemia, metabolic acidosis, and abdominal compartment syndrome. The median waiting period for PD placement was 1 day, and the median duration of PD was 7 days. Complications included dialysate leakage (22.8%) and catheter obstruction leading to PD discontinuation (31.4%). The mortality rate was high at 71.4%.

Conclusion: It is advisable to advocate for the early initiation of PD in pediatric patients following cardiac surgery. AKI is a significant risk factor for mortality, while prematurity increases the risk of dialysate leakage. Omentectomy and the method of catheter exit did not significantly affect outcomes. The study's limitations highlight the need for larger prospective studies to better understand and improve emergent PD management in this vulnerable population.

导言:本研究旨在确定影响因各种原因需要紧急腹膜透析(PD)的儿科患者预后的风险因素,重点关注生存率、肾功能恢复、腹膜透析持续时间、并发症和生活质量:对2010年1月至2023年2月期间在重症监护室接受紧急床旁腹膜透析的儿科患者的病历进行了回顾性分析。共放置了 34 根导管,并收集了人口统计学、术前和手术数据。使用 MedCalc® 统计软件进行分析,显著性水平设定为 p <0.05。术前使用了预防性抗生素,导管由一个小儿外科医生团队以统一的技术置入:置入导管时的中位年龄为 39 天(范围 2-2286),中位体重为 3.53 千克(范围 1.2-48.8)。大多数为男性(64.7%),17.6%为早产儿。最常见的腹膜透析适应症是 AKI(88.2%),其次是高氨血症、代谢性酸中毒和腹腔隔室综合征。置入透析器的中位等待时间为一天,中位持续时间为七天。并发症包括透析液渗漏(22.8%)和导管阻塞导致腹膜透析中止(31.4%)。死亡率高达 71.4%:结论:对于心脏手术后的小儿患者,提倡尽早开始透析是明智的。AKI是导致死亡的重要风险因素,而早产则会增加透析液渗漏的风险。网膜切除术和导管出口方法对预后没有显著影响。这项研究的局限性突出表明,需要进行更大规模的前瞻性研究,以更好地了解和改善这一弱势群体的紧急透析管理。
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引用次数: 0
Japanese Study of the Effects of AMG (α1-Microglobulin) Reduction Rates on Survival (JAMREDS): A Protocol of a Multicenter Prospective Observational Cohort Study. 日本 AMG(α1-微球蛋白)降低率对生存的影响研究(JAMREDS):多中心前瞻性观察队列研究方案。
IF 3 3区 医学 Q1 Medicine Pub Date : 2024-01-01 Epub Date: 2024-02-04 DOI: 10.1159/000536537
Toshihide Naganuma, Yoshiaki Takemoto, Naohiro Kamada, Daijiro Kabata, Ayumi Shintani, Keiko Ota, Jun Minakuchi, Ken Tsuchiya, Hideki Kawanishi

Introduction: Recent advances in dialysis therapy have made it possible to remove middle molecules. Removal of small-middle molecules, such as β2-microglobulin, can now be achieved with conventional hemodialysis (HD), and removal of large-middle molecules has become a target, particularly for α1-microglobulin (AMG, 33 kD). The AMG reduction rate has emerged as a target for improvement of various clinical symptoms, but the effects on prognosis have yet to be determined. The "Japanese study of the effects of AMG (α1-microglobulin) reduction rates on survival" (JAMREDS) was started in April 2020, with the goal of determining if the AMG reduction rate associates with the risk of mortality and cardiovascular disease (CVD) events.

Methods: JAMREDS is a prospective observational study in patients on HD to examine the effects of: (1) AMG reduction rate on survival outcome and CVD events; (2) dialysis treatment modalities (HD, intermittent infusion hemodiafiltration(iHDF), pre/post-dilution online HDF) on survival and CVD events (based on AMG reduction rates with treatment mode); and (3) AMG reduction rates on survival and CVD events in patients undergoing each therapy (iHDF, pre/post-dilution online HDF). The number of planned subjects was 4,000 in preplanning. Data are collected using RED-Cap, which is an EDC system. A total of 9,930 patients were enrolled at the beginning of the study at 59 registered facilities. The JAMREDS observation period will continue until the end of 2023, after which the data will be cleaned and confirmed before analysis.

Conclusion: This study may provide new evidence for the relationship between the amount of removed large-middle molecules (such as AMG) and the mortality and CVD risk. Comparisons with convection volumes will also be of interest.

导言:透析疗法的最新进展使清除中间分子成为可能。目前,传统血液透析可清除β2-微球蛋白(BMG)等中间小分子,而清除中间大分子已成为目标,尤其是1-微球蛋白(AMG,33 kD)。AMG减少率已成为改善各种临床症状的目标,但对预后的影响仍有待确定。日本 AMG(α1-微球蛋白)降低率对生存的影响研究"(JAMREDS)于 2020 年 4 月启动,旨在确定 AMG 降低率是否与死亡率和心血管疾病(CVD)事件风险相关:JAMREDS 是一项针对血液透析(HD)患者的前瞻性观察研究,旨在研究以下因素的影响:1)AMG 降低率对生存期的影响:1)AMG降低率对生存结果和心血管疾病事件的影响;2)透析治疗方式(HD、间歇输注血液透析(iHDF)、稀释前/后在线HDF)对生存结果和心血管疾病事件的影响(基于治疗方式的AMG降低率);3)AMG降低率对接受各种治疗(iHDF、稀释前/后在线HDF)的患者生存结果和心血管疾病事件的影响。在前期规划中,计划受试者人数为 4000 人。数据使用 EDC 系统 RED-Cap 收集。研究开始时,共有 9930 名患者在 59 家注册机构注册。JAMREDS 观察期将持续到 2023 年底,之后将对数据进行清理和确认,然后再进行分析:这项研究可能会为大中分子(如 AMG)的清除量与死亡率和心血管疾病风险之间的关系提供新的证据。与对流容量的比较也很有意义:UMIN000038457.2019年11月1日注册:https://center6.umin.ac.jp/cgi-open-bin/ctr/ctr_view.cgi?recptno=R000043823。
{"title":"Japanese Study of the Effects of AMG (α1-Microglobulin) Reduction Rates on Survival (JAMREDS): A Protocol of a Multicenter Prospective Observational Cohort Study.","authors":"Toshihide Naganuma, Yoshiaki Takemoto, Naohiro Kamada, Daijiro Kabata, Ayumi Shintani, Keiko Ota, Jun Minakuchi, Ken Tsuchiya, Hideki Kawanishi","doi":"10.1159/000536537","DOIUrl":"10.1159/000536537","url":null,"abstract":"<p><strong>Introduction: </strong>Recent advances in dialysis therapy have made it possible to remove middle molecules. Removal of small-middle molecules, such as β2-microglobulin, can now be achieved with conventional hemodialysis (HD), and removal of large-middle molecules has become a target, particularly for α1-microglobulin (AMG, 33 kD). The AMG reduction rate has emerged as a target for improvement of various clinical symptoms, but the effects on prognosis have yet to be determined. The \"Japanese study of the effects of AMG (α1-microglobulin) reduction rates on survival\" (JAMREDS) was started in April 2020, with the goal of determining if the AMG reduction rate associates with the risk of mortality and cardiovascular disease (CVD) events.</p><p><strong>Methods: </strong>JAMREDS is a prospective observational study in patients on HD to examine the effects of: (1) AMG reduction rate on survival outcome and CVD events; (2) dialysis treatment modalities (HD, intermittent infusion hemodiafiltration(iHDF), pre/post-dilution online HDF) on survival and CVD events (based on AMG reduction rates with treatment mode); and (3) AMG reduction rates on survival and CVD events in patients undergoing each therapy (iHDF, pre/post-dilution online HDF). The number of planned subjects was 4,000 in preplanning. Data are collected using RED-Cap, which is an EDC system. A total of 9,930 patients were enrolled at the beginning of the study at 59 registered facilities. The JAMREDS observation period will continue until the end of 2023, after which the data will be cleaned and confirmed before analysis.</p><p><strong>Conclusion: </strong>This study may provide new evidence for the relationship between the amount of removed large-middle molecules (such as AMG) and the mortality and CVD risk. Comparisons with convection volumes will also be of interest.</p>","PeriodicalId":8953,"journal":{"name":"Blood Purification","volume":null,"pages":null},"PeriodicalIF":3.0,"publicationDate":"2024-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"139680642","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"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
Sampling from Extracorporeal Circuit: A Step Forward for Dose Monitoring in Continuous Renal Replacement Therapy. 体外电路采样:CRRT中剂量监测的新进展。
IF 3 3区 医学 Q1 Medicine Pub Date : 2024-01-01 Epub Date: 2023-11-22 DOI: 10.1159/000535308
Maria Cristina Ruffa, Vittorio Bocciero, Sergio Fabbri, Francesca Nencini, Alessandra Fanelli, Stefano Romagnoli, Zaccaria Ricci, Valentina Cauda, Gianluca Villa

Introduction: Continuous renal replacement therapies (CRRTs) require constant monitoring and periodic treatment readjustments, being applied to highly complex patients, with rapidly changing clinical needs. To promote precision medicine in the field of renal replacement therapy and encourage dynamic prescription, the Acute Dialysis Quality Initiative (ADQI) recommends periodically measuring the solutes extracorporeal clearance with the aim of assessing the current treatment delivery and the gap from the therapeutic prescription (often intended as effluent dose). To perform this procedure, it is therefore necessary to obtain blood and effluent samples from the extracorporeal circuit to measure the concentrations of a target solute (usually represented by urea) in prefilter, postfilter, and effluent lines. However, samples must be collected simultaneously from the extracorporeal circuit ports, with the same suction flow at an unknown rate.

Methods: The proposed study takes the first step toward identifying the technical factors that should be considered in determining the optimal suction rate to collect samples from the extracorporeal circuit to measure the extracorporeal clearance for a specific solute.

Results: The results obtained identify the low suction rate (i.e., 1 mL/min) as an ideal parameter for an adequate sampling method. Low velocities do not perturb the external circulation system and ensure stability prevailing pressures in the circuit. Higher velocities can be performed only with blood flows above 120 mL/min preferably in conditions of appropriate filtration fraction.

Discussion/conclusions: The specific value of aspiration flow rate must be proportioned to the prescription of CRRT treatments set by the clinician.

简介:持续肾替代疗法(Continuous renal replacement therapy, CRRT)需要持续监测和定期调整治疗方案,应用于高度复杂的患者,临床需求变化迅速。为了促进肾脏替代治疗领域的精准医学并鼓励动态处方,急性透析质量倡议(ADQI)建议定期测量溶质体外清除率,目的是评估当前治疗交付和治疗处方(通常为流出剂量)的差距。因此,为了执行该程序,有必要从体外回路获取血液和流出液样本,以测量过滤前、过滤后和流出液中目标溶质(通常以尿素表示)的浓度。然而,样品必须同时从体外电路端口收集,以相同的吸流量,未知的速率。方法:本研究在确定体外循环采集样品的最佳吸力速率以测量特定溶质的体外清除时应考虑的技术因素方面迈出了第一步。结果:所获得的结果表明,低吸力(即1 ml/min)是适当取样方法的理想参数。低速不会扰乱外部循环系统,并确保回路中稳定的盛行压力。只有在血流量大于120ml /min的情况下才能允许更高的流速,最好在适当的过滤分数的条件下。讨论/结论:抽吸流量的具体数值必须与临床医生制定的CRRT治疗处方成比例。
{"title":"Sampling from Extracorporeal Circuit: A Step Forward for Dose Monitoring in Continuous Renal Replacement Therapy.","authors":"Maria Cristina Ruffa, Vittorio Bocciero, Sergio Fabbri, Francesca Nencini, Alessandra Fanelli, Stefano Romagnoli, Zaccaria Ricci, Valentina Cauda, Gianluca Villa","doi":"10.1159/000535308","DOIUrl":"10.1159/000535308","url":null,"abstract":"<p><strong>Introduction: </strong>Continuous renal replacement therapies (CRRTs) require constant monitoring and periodic treatment readjustments, being applied to highly complex patients, with rapidly changing clinical needs. To promote precision medicine in the field of renal replacement therapy and encourage dynamic prescription, the Acute Dialysis Quality Initiative (ADQI) recommends periodically measuring the solutes extracorporeal clearance with the aim of assessing the current treatment delivery and the gap from the therapeutic prescription (often intended as effluent dose). To perform this procedure, it is therefore necessary to obtain blood and effluent samples from the extracorporeal circuit to measure the concentrations of a target solute (usually represented by urea) in prefilter, postfilter, and effluent lines. However, samples must be collected simultaneously from the extracorporeal circuit ports, with the same suction flow at an unknown rate.</p><p><strong>Methods: </strong>The proposed study takes the first step toward identifying the technical factors that should be considered in determining the optimal suction rate to collect samples from the extracorporeal circuit to measure the extracorporeal clearance for a specific solute.</p><p><strong>Results: </strong>The results obtained identify the low suction rate (i.e., 1 mL/min) as an ideal parameter for an adequate sampling method. Low velocities do not perturb the external circulation system and ensure stability prevailing pressures in the circuit. Higher velocities can be performed only with blood flows above 120 mL/min preferably in conditions of appropriate filtration fraction.</p><p><strong>Discussion/conclusions: </strong>The specific value of aspiration flow rate must be proportioned to the prescription of CRRT treatments set by the clinician.</p>","PeriodicalId":8953,"journal":{"name":"Blood Purification","volume":null,"pages":null},"PeriodicalIF":3.0,"publicationDate":"2024-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"138294497","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"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
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Blood Purification
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