Pediatric

儿科
  • 文章类型: Journal Article
    目的:当腹膜腔不能作为远端分流终点时,非腹膜分流术,通常终止于心房或胸膜腔,使用。尚未评估这两种终点站选择的相对有效性。作者直接比较了儿科队列中心室房室(VA)和心室胸膜(VPl)分流的分流生存率和并发症发生率。
    方法:脑积水临床研究网络核心数据项目用于识别年龄≤18岁接受VA或VPl分流插入的儿童。主要结果是分流失败的时间。次要结果包括远端部位并发症和6、12和24个月时分流失败的频率。
    结果:搜索标准产生了来自14个中心的416名患有VA(n=318)或VPl(n=98)分流的儿童,包括从脑室腹膜分流术转换的那些。VA分流的儿童在插入时的中位年龄较低(6.1岁vs12.4岁,p<0.001)。在那些有VA分流的孩子中,与早产儿继发脑室出血(IVH)的病因相比,早产儿继发脑室出血(IVH)的比例更高(47.0%vs31.2%),而脊髓膜膨出的比例更低(17.8%vs27.3%)(p=0.024)。24个月时,VA分流的修订累积数量较高(48.6%对38.9%,p=0.038)。当在分流管插入时按患者年龄分层时,在小于6岁的儿童中,VA分流具有最低的分流存活率(p<0.001,对数秩检验)。在控制了年龄和病因后,多变量分析未发现分流类型(VAvsVPl)可预测分流失败的时间。并发症的累积频率没有差异(VA6.0%vsVPl9.2%,p=0.257),但VPl队列中气胸的发生率较高(3.1%vs0%,p=0.013)。
    结论:VA和VPl分流的分流生存相似,虽然VA分流器更常用,尤其是年轻患者。<6岁的VA分流儿童似乎有最短的分流生存期,这可能是VA组早产儿继发IVH病例较多的结果;然而,当年龄和病因被纳入多变量模型时,分流位置(心房与胸膜间隙)与至衰竭的时间无关。用VA与VPl分流治疗的儿童之间的基线差异可能解释了当前的实践模式。
    OBJECTIVE: When the peritoneal cavity cannot serve as the distal shunt terminus, nonperitoneal shunts, typically terminating in the atrium or pleural space, are used. The comparative effectiveness of these two terminus options has not been evaluated. The authors directly compared shunt survival and complication rates for ventriculoatrial (VA) and ventriculopleural (VPl) shunts in a pediatric cohort.
    METHODS: The Hydrocephalus Clinical Research Network Core Data Project was used to identify children ≤ 18 years of age who underwent either VA or VPl shunt insertion. The primary outcome was time to shunt failure. Secondary outcomes included distal site complications and frequency of shunt failure at 6, 12, and 24 months.
    RESULTS: The search criteria yielded 416 children from 14 centers with either a VA (n = 318) or VPl (n = 98) shunt, including those converted from ventriculoperitoneal shunts. Children with VA shunts had a lower median age at insertion (6.1 years vs 12.4 years, p < 0.001). Among those children with VA shunts, a hydrocephalus etiology of intraventricular hemorrhage (IVH) secondary to prematurity comprised a higher proportion (47.0% vs 31.2%) and myelomeningocele comprised a lower proportion (17.8% vs 27.3%) (p = 0.024) compared with those with VPl shunts. At 24 months, there was a higher cumulative number of revisions for VA shunts (48.6% vs 38.9%, p = 0.038). When stratified by patient age at shunt insertion, VA shunts in children < 6 years had the lowest shunt survival rate (p < 0.001, log-rank test). After controlling for age and etiology, multivariable analysis did not find that shunt type (VA vs VPl) was predictive of time to shunt failure. No differences were found in the cumulative frequency of complications (VA 6.0% vs VPl 9.2%, p = 0.257), but there was a higher rate of pneumothorax in the VPl cohort (3.1% vs 0%, p = 0.013).
    CONCLUSIONS: Shunt survival was similar between VA and VPl shunts, although VA shunts are used more often, particularly in younger patients. Children < 6 years with VA shunts appeared to have the shortest shunt survival, which may be a result of the VA group having more cases of IVH secondary to prematurity; however, when age and etiology were included in a multivariable model, shunt location (atrium vs pleural space) was not associated with time to failure. The baseline differences between children treated with a VA versus a VPl shunt likely explain current practice patterns.
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  • 文章类型: Journal Article
    目的:这项关键研究旨在评估1型糖尿病(T1D)发病时儿童和青少年骨重建标志物的循环水平。此外,我们评估了它们与血糖控制的相关性,残余β细胞功能,以及演示的严重性。
    方法:在这项单中心横断面研究中,我们在三级糖尿病中心招募了新诊断为T1D的儿童和青少年.Anamnestic,人体测量学,临床,收集T1D诊断时的生化数据。评估了基础和刺激的C肽水平,以及以下骨重建生物标志物:骨钙蛋白(OC),碱性磷酸酶(ALP),甲状旁腺激素(PTH),25-OH维生素D(25OH-D),和1型胶原(CTX)的C端交联端肽。
    结果:我们招募了29名新诊断为T1D的患者,男性患病率较低(51.7%)。平均年龄为8.4±3.7岁。发现OC与刺激的C肽(R=0.538;p=0.026)之间以及PTH与血清HCO3-(R=0.544;p=0.025)之间呈正相关。未检测到骨重建生物标志物与临床变量之间的其他相关性。
    结论:我们的数据显示,儿童和青少年在T1D表现时,OC水平与残余β细胞功能之间呈正相关。需要进一步的纵向研究来评估患有T1D的儿科受试者的OC水平,以更好地了解骨骼和葡萄糖代谢之间的复杂相互作用。
    OBJECTIVE: This pivotal study aimed to evaluate circulating levels of bone remodeling markers in children and adolescents at the onset of type 1 diabetes (T1D). Additionally, we assessed their correlation with glucose control, residual β-cell function, and the severity of presentation.
    METHODS: In this single-center cross-sectional study, we recruited children and adolescents newly diagnosed with T1D at our tertiary-care Diabetes Centre. Anamnestic, anthropometric, clinical, and biochemical data at T1D diagnosis were collected. Basal and stimulated C-peptide levels were assessed, along with the following bone remodeling biomarkers: osteocalcin (OC), alkaline phosphatase (ALP), parathormone (PTH), 25-OH Vitamin D (25OH-D), and the C-terminal cross-linked telopeptide of type 1 collagen (CTX).
    RESULTS: We enrolled 29 individuals newly diagnosed with T1D, with a slight male prevalence (51.7%). The mean age was 8.4 ± 3.7 years. A positive correlation between OC and stimulated C-peptide (R = 0.538; p = 0.026) and between PTH and serum HCO3- (R = 0.544; p = 0.025) was found. No other correlations between bone remodeling biomarkers and clinical variables were detected.
    CONCLUSIONS: Our data showed a positive correlation between OC levels and residual β-cell function in children and adolescents at T1D presentation. Further longitudinal studies evaluating OC levels in pediatric subjects with T1D are needed to better understand the complex interaction between bone and glucose metabolisms.
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  • 文章类型: Journal Article
    目的:经脐腹腔镜辅助阑尾切除术(TULAA)是第一批由儿科医师进行的内镜手术之一。虽然手术时间通常比传统的腹腔镜阑尾切除术短,该手术的适应症尚不清楚,许多未知因素可以延长手术时间。我们进行了这项研究,以确定可能延长TULAA手术时间的因素。
    方法:本回顾性研究,单中心研究在2015年至2023年之间进行。我们通过分析受训者执行的TULAA程序,进行了多变量分析以确定与延长手术时间相关的因素。
    结果:该研究包括243名患者。中位手术时间为84分钟(四分位距,69-114分钟)。多变量分析表明,体重指数增加,C反应蛋白水平升高,急性阑尾炎保守治疗史,和阑尾穿孔,对于患者而言;手术外科医生毕业以来<6年的经验;以及缺乏日本儿科医师协会主管主治医师的董事会认证是延长手术时间的独立危险因素。
    结论:拥有一名主治医生,并获得日本儿科医生协会的主管委员会认证,有助于减少TULAA所需的手术时间。
    OBJECTIVE: Transumbilical laparoscopic-assisted appendectomy (TULAA) is one of the first endoscopic surgeries performed by trainee pediatric surgeons. While the operative time is generally shorter than for conventional laparoscopic appendectomy, the indications for this procedure are unclear and many unknown factors can prolong the operative time. We conducted this study to identify the factors that may prolong the operative time for TULAA.
    METHODS: This retrospective, single-center study was conducted between 2015 and 2023. We performed multivariate analysis to identify the factors associated with prolonged operative time by analyzing TULAA procedures performed by trainees.
    RESULTS: The study included 243 patients. The median operative time was 84 min (interquartile range, 69-114 min). Multivariate analysis revealed that an increased body mass index, elevated C-reactive protein level, a history of conservative treatment for acute appendicitis, and appendix perforation, for the patient; < 6 years\' experience since graduation for the operating surgeon; and lack of board certification as a supervisor from the Japanese Society of Pediatric Surgeons for the attending surgeon were independent risk factors for prolonging the operative time.
    CONCLUSIONS: Having an attending surgeon with board certification as a supervisor by the Japanese Society of Pediatric Surgeons contributes to reducing the operative time required for TULAA.
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  • 文章类型: Journal Article
    目标:利那洛肽,鸟苷酸环化酶-C激动剂,最近在美国被批准用于治疗患有功能性便秘(FC)的6-17岁儿童。这项研究评估了剂量反应,安全,与安慰剂相比,利那洛肽在2-5岁FC儿童中的4周疗效。
    方法:在这个阶段2,随机,双盲,安慰剂对照,多剂量研究,35名FC儿童(基于罗马III标准)以3:1随机分配接受利那洛肽(18、36或72μg,对于第1、2和3组)和5:1分别接受利那洛肽9、18、36或72μg(第4组),或匹配的安慰剂。关键终点是总体自发排便(SBM)频率(SBM/周)相对于基线的变化,大便稠度,和紧张,以及研究干预期间大便失禁天数的比例。记录不良事件(AE)。
    结果:在随机分组的患者中,34(97.1%)完成了治疗期,33(94.3%)完成了治疗期。四个关键功效终点中的三个在治疗期间从基线的平均变化显示利那洛肽72μg组相对于安慰剂的更大改善。在接受利那洛肽的患者中,粪便稠度呈剂量反应趋势。四名随机接受利那洛肽治疗的患者经历了治疗引起的AE,其中之一是治疗相关的(轻度腹泻)。所有不良事件均为轻度或中度,无严重不良事件。
    结论:利那洛肽在该儿科人群中具有良好的耐受性,与安慰剂相比,利那洛肽72μg具有疗效趋势。
    OBJECTIVE: Linaclotide, a guanylate cyclase-C agonist, was recently approved in the United States for the treatment of children 6-17 years of age with functional constipation (FC). This study evaluated the dose-response, safety, and efficacy of 4 weeks of linaclotide compared with placebo in children 2-5 years of age with FC.
    METHODS: In this phase 2, randomized, double-blind, placebo-controlled, multidose study, 35 children with FC (based on Rome III criteria) were randomized 3:1 to receive linaclotide (18, 36, or 72 μg, for groups 1, 2, and 3, respectively) and 5:1 to receive linaclotide 9, 18, 36, or 72 μg (group 4), or matching placebo. Key endpoints were the changes from baseline in overall spontaneous bowel movement (SBM) frequency (SBMs/week), stool consistency, and straining, as well as the proportion of days with fecal incontinence during the study intervention period. Adverse events (AEs) were recorded.
    RESULTS: Of the randomized patients, 34 (97.1%) completed the treatment period and 33 (94.3%) completed the posttreatment period. Mean change from baseline over the treatment period for three of the four key efficacy endpoints showed greater improvement in the linaclotide 72 μg group versus placebo. A dose-response trend was seen for stool consistency in patients receiving linaclotide. Four patients randomized to linaclotide experienced treatment-emergent AEs, one of which was treatment-related (mild diarrhea). All AEs were mild or moderate and none were severe.
    CONCLUSIONS: Linaclotide was well tolerated in this pediatric population and an efficacy trend was seen with linaclotide 72 μg versus placebo.
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  • 文章类型: Journal Article
    背景:疫苗接种是预防幼儿流感感染和并发症的主要方法。我们评估了单剂量MEDI3250(鼻内,四价,流感减毒活疫苗)在2016/17流感季节期间在健康的日本儿童中使用。
    方法:在这个多中心中,随机化,双盲,3期研究(jRCT2080223345),2-18岁的参与者接受MEDI3250或安慰剂(2:1),按年龄分层(2-6岁,7-18岁)。主要和次要终点是由流行的野生型毒株或疫苗匹配的毒株引起的确诊的流感症状发作的发生率。分别。安全性结果包括不良事件(AE)和疫苗相关AE的发生率。
    结果:总体而言,910名参与者接受MEDI3250(n=608)或安慰剂(n=302)。对于主要终点(无论流感亚型),流感发病的发生率为25.5%(MEDI3250)和35.9%(安慰剂);相对风险降低,28.8%(95%置信区间,12.5%至42.0%)。对于次要终点(疫苗匹配菌株),发病率为10.9%(MEDI3250)和17.2%(安慰剂);相对风险降低,36.6%(95%置信区间,6.5%至56.8%)。在67.6%(MEDI3250)和63.6%(安慰剂)中发生了诱发的AE。大多数事件为轻度;流鼻涕最常见(59.2%[MEDI3250]和52.6%[安慰剂])。36.0%(MEDI3250)和33.1%(安慰剂)发生非请求性不良事件。最常见的不请自来的疫苗相关不良事件是腹泻(2.3%,两组)。
    结论:与安慰剂相比,MEDI3250对日本儿童流感发作具有更大的预防作用;相对于MEDI3250的先前临床和上市后研究,未观察到新的安全性信号。
    BACKGROUND: Vaccination is the primary method of preventing influenza infection and complications in young children. We evaluated the efficacy and safety of a single dose of MEDI3250 (intranasal, quadrivalent, live attenuated influenza vaccine) in healthy Japanese children during the 2016/17 influenza season.
    METHODS: In this multicenter, randomized, double-blind, phase 3 study (jRCT2080223345), participants aged 2-18 years received MEDI3250 or placebo (2:1), stratified by age (2-6 years, 7-18 years). The primary and secondary endpoints were the incidence of confirmed symptomatic onset of influenza caused by a circulating wild-type strain or by a vaccine-matched strain, respectively. Safety outcomes included the incidence of adverse events (AEs) and vaccine-related AEs.
    RESULTS: Overall, 910 participants received MEDI3250 (n = 608) or placebo (n = 302). For the primary endpoint (regardless of the influenza subtype), the incidence of influenza onset was 25.5% (MEDI3250) and 35.9% (placebo); relative risk reduction, 28.8% (95% confidence interval, 12.5% to 42.0%). For the secondary endpoint (vaccine-matched strain), the incidence was 10.9% (MEDI3250) and 17.2% (placebo); relative risk reduction, 36.6% (95% confidence interval, 6.5% to 56.8%). Solicited AEs occurred in 67.6% (MEDI3250) and 63.6% (placebo). Most events were mild; nasal discharge was most common (59.2% [MEDI3250] and 52.6% [placebo]). Unsolicited AEs occurred in 36.0% (MEDI3250) and 33.1% (placebo). The most common unsolicited vaccine-related AE was diarrhea (2.3%, both groups).
    CONCLUSIONS: MEDI3250 had a greater preventive effect against influenza onset in Japanese children than placebo; no new safety signals were observed relative to previous clinical and post-marketing studies of MEDI3250.
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  • 文章类型: Journal Article
    暂无摘要。
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  • 文章类型: Journal Article
    这项研究的目的是探索影响儿童药物供应的因素,并建立机器学习模型,为后续相关政策的制定和完善提供实证依据。
    设计:横断面调查。设置:12个省,中国。来自25家公立医院的医生被招募。所有数据以7:3的比例随机分为训练集和验证集。三种预测模型,即随机森林(RF),逻辑回归(LR),和极端梯度提升(XGBoost),进行了开发和比较。使用受试者工作特征曲线(ROC)和相关曲线下面积(AUC)来评估三个模型。制定了药物可用性的列线图和临床影响曲线(CIC)。
    数据库中最有可能被选择的29个因素中的15个被考虑来建立预测模型。XGBoost模型(AUC=0.915)表现出比RF模型(AUC=0.902)和LR模型(AUC=0.890)更好的性能。根据Shapley加性解释值,在XGboost模型中,对儿童药物供应影响最大的五个因素是:儿童专用剂型数量相对较少;儿童无法负担的药物;关于儿童药物可及性和安全性的公共教育;医疗资源分配不均,导致儿童无法充分获得药物治疗;以及多年的医生服务。CIC用于评估因子预测列线图的实际适用性。
    XGBoost模型可用于建立预测模型,以筛选与儿童药物可用性相关的因素。模型的最重要的促成因素如下:儿童专用剂型相对较少;儿童无法负担的药物;关于儿童药物可及性和安全性的公共教育;医疗资源分配不均,导致儿童无法充分获得药物治疗;以及多年的医生服务。
    UNASSIGNED: The aim of the study was to explore the factors influencing the availability of medications for children, and establish a machine learning model to provide an empirical basis for the subsequent formulation and improvement of relevant policies.
    UNASSIGNED: Design: Cross-sectional survey. Setting: 12 provinces, China. Medical doctors from 25 public hospitals were enrolled. All data were randomly divided into a training set and a validation set at a ratio of 7:3. Three prediction models, namely random forest (RF), logistic regression (LR), and extreme gradient boosting (XGBoost), were developed and compared. The receiver operating characteristic curve (ROC) and the associated area under the curve (AUC) were used to evaluate the three models. A nomogram and clinical impact curve (CIC) for availability of medication were developed.
    UNASSIGNED: Fifteen of 29 factors in the database that were most likely to be selected were considered to establish the prediction model. The XGBoost model (AUC = 0.915) demonstrated better performance than the RF model (AUC = 0.902) and the LR model (AUC = 0.890). According to the Shapley additive explanation values, the five factors that most significantly affected the availability of medications for children in the XGboost model were as follows: the relatively small number of specialized dosage forms for children; unaffordable medications for children; public education on the accessibility and safety of medication for children; uneven distribution of medical resources, leading to insufficient access to medication for children; and years of service as a doctor. The CIC was used to assess the practical applicability of the factor prediction nomogram.
    UNASSIGNED: The XGBoost model can be used to establish a prediction model to screen the factors associated with the availability of medications for children. The most important contributing factors to the models were the following: the relatively small number of specialized dosage forms for children; unaffordable medications for children; public education on the accessibility and safety of medication for children; uneven distribution of medical resources, leading to insufficient access to medication for children; and years of service as a doctor.
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  • 文章类型: Journal Article
    目的:这项回顾性研究旨在评估小儿股骨颈骨折的手术效果并确定影响因素。
    方法:纳入23例接受股骨颈骨折手术治疗的儿科患者共25髋。包含患者人口统计信息的数据,骨折类型,外科技术,并发症,并对随访结果进行回顾性分析.骨折位移等因素,手术时机,固定方法,并对术后并发症进行复位质量评估。
    结果:从高处坠落占创伤机制的48%,血管坏死(AVN)是最常见的并发症(4髋)。虽然骨折位移,还原质量差,延迟手术在复杂病例中更为常见,没有达到统计学意义。该研究注意到缺血性坏死的存在与更差的临床结果之间的关联(rho:0.428,p:0.05,CI:95%)。
    结论:手术治疗取得了良好的临床效果;然而,由于研究的回顾性设计的局限性,样本量有限,单中心方法强调了更大的多中心研究的必要性。我们的研究结果强调需要进行全面的调查,以更好地了解和管理小儿股骨颈骨折,特别是关于影响AVN和长期结果的因素。
    OBJECTIVE: This retrospective study aimed to evaluate surgical outcomes and identify influential factors in pediatric femoral neck fractures.
    METHODS: A total of 25 hips from 23 pediatric patients who underwent surgical intervention for femoral neck fractures were included. Data encompassing patient demographics, fracture types, surgical techniques, complications, and follow-up outcomes were analyzed retrospectively. Factors such as fracture displacement, timing of surgery, fixation methods, and reduction quality were assessed concerning postoperative complications.
    RESULTS: Falling from a height accounted for 48% of the trauma mechanisms, and avascular necrosis (AVN) was the most prevalent complication (4 hips). Although fracture displacement, bad reduction quality, and delayed surgery were more common among complicated cases, statistical significance was not attained. The study noted an association between presence of avascular necrosis and worse clinical results(rho: 0.428, p: 0.05, CI: 95%).
    CONCLUSIONS: Surgical treatment yielded favorable clinical outcomes; however, limitations due to the study\'s retrospective design, limited sample size, and single-center approach underscore the necessity for larger multicenter studies. Our findings emphasize the need for comprehensive investigations to better understand and manage pediatric femoral neck fractures, especially regarding factors influencing AVN and long-term outcomes.
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  • 文章类型: Journal Article
    本研究旨在评估使用动画作为家庭授权计划的教育材料的有效性,以帮助其孩子接受神经外科手术的护理人员进行围手术期护理。
    总共204名护理人员被随机分配到面对面口腔护理教育组(口腔组)或动画辅助护理教育组(动画组)。护理教育主要侧重于指导护理人员手动振动方法。这项研究的主要结果是参与者的知识水平,由10项问卷收集。次要结果包括儿童患者的临床数据,包括住院天数,治疗,和肺炎的迹象。
    动画组的参与者在围手术期护理知识评估中表现出明显更高的准确性,与口服组相比,该组患者需要雾化治疗的机会较低。
    动画辅助护理教育计划有效地增强了儿科护理人员的知识,减少手术后的呼吸道并发症,并为将来使用此类程序指导护理人员的研究提供了有价值的见解。
    UNASSIGNED: This study aimed to evaluate the effectiveness of using animation as education material for family empowerment program on perioperative care for caregivers whose children were to undergo neurosurgery.
    UNASSIGNED: A total of 204 caregivers were randomly assigned to either the face-to-face oral nursing educated group (Oral Group) or the animation-assisted nursing educated group (Animated Group). The nursing education primarily focused on instructing caregivers about the manual vibration method. The primary outcome of interest in this study was participants\' knowledge level, collected by a 10-item questionnaire. Secondary outcomes included child patients\' clinical data, including hospitalization days, treatments, and signs of pneumonia.
    UNASSIGNED: Participants in the Animated Group exhibited significantly higher accuracy in perioperative care knowledge assessment, and patients in this group had a lower chance of requiring atomization therapy compared to the Oral Group.
    UNASSIGNED: The animation-assisted nursing education program effectively enhances pediatric caregivers\' knowledge, reduces respiratory complications after surgery, and offers valuable insights for future studies on the use of such programs to instruct caregivers.
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  • 文章类型: Journal Article
    目的:我们旨在探讨影响小儿体外心肺复苏(ECPR)预后的因素。
    方法:回顾性研究纳入了2007年7月至2022年12月期间住院和院外心脏骤停后接受ECPR的77例儿科病例(7例新生儿和70例儿童)。主要终点是并发症,次要终点包括全因住院死亡率.
    结果:在45例并发症中,4名新生儿和41名儿童同时出现多种并发症,25例主要是神经系统问题。此外,11例发生器官衰竭,在两个病例中存在免疫缺陷。此外,9例发生出血事件,13例显示血栓形成。有并发症的患者体重较低,更短的ECMO持续时间,和更长的CPR持续时间。非幸存者的CPR持续时间较长,ECMO持续时间较短,ICU停留,与幸存者相比,机械通气。并发症在非幸存者中更为普遍,尤其是器官衰竭和出血事件。
    结论:体重,CPR持续时间,ECMO持续时间与并发症相关,建议优化治疗区域。非幸存者并发症发生率较高,强调了早期发现和管理以提高生存率的重要性。我们的研究结果表明,临床医生在预后评估中考虑这些因素,以提高ECPR计划的有效性。
    OBJECTIVE: We aimed to investigate the prognostic factors of pediatric extracorporeal cardiopulmonary resuscitation (ECPR).
    METHODS: The retrospective study included a total of 77 pediatric cases (7 neonates and 70 children) who underwent ECPR after in-hospital and out-of-hospital cardiac arrest between July 2007 and December 2022. Primary endpoints were complications, while secondary endpoints included all-cause in-hospital mortality.
    RESULTS: Among the 45 cases experiencing complications, 4 neonates and 41 children had multiple simultaneous complications, primarily neurological issues in 25 cases. Additionally, organ failure occurred in 11 cases, and immunodeficiency was present in two cases. Furthermore, 9 cases experienced bleeding events, and 13 cases showed thrombosis. Patients with complications had lower weight, shorter ECMO durations, and longer CPR durations. Non-survivors had longer CPR durations and shorter durations of ECMO, ICU stay, and mechanical ventilation compared to survivors. Complications were more prevalent in non-survivors, particularly organ failure and bleeding events.
    CONCLUSIONS: Weight, CPR duration, and ECMO duration were associated with complications, suggesting areas for treatment optimization. The higher occurrence of complications in non-survivors underscores the importance of early detection and management to improve survival rates. Our findings suggest clinicians consider these factors in prognostic assessments to enhance the effectiveness of ECPR programs.
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