pediatric population

儿科人群
  • 文章类型: Journal Article
    背景:Dupilumab可有效治疗特应性皮炎(AD);然而,它在阻止特应性游行中的作用仍然不确定。
    目的:研究dupilumab对小儿AD患者特应性行军的影响,与常规免疫调节剂相比。
    方法:这项回顾性队列研究利用了TriNetX美国合作网络(2011-2024)的数据。小儿AD患者(≤18岁)分为DUPI队列(新处方dupilumab)或CONV队列(处方常规免疫调节剂,不含dupilumab)。1:1倾向得分匹配后,我们分析了特应性行军进展,定义为哮喘或过敏性鼻炎(AR)。累积发病率用Kaplan-Meier作图,通过Cox回归进行风险评估。
    结果:该研究包括每个队列中的2192名患者。在DUPI队列中,特应性行军进展的3年累积发生率低于CONV队列(20.09%vs27.22%;P<.001)。DUPI队列显示特应性行军进展的风险显着降低(风险比[HR]0.68,95%CI0.55-0.83),个体哮喘(HR0.60,0.45-0.81),和个体AR(HR0.69,0.54-0.88)。使用dupilumab的年轻患者表现出更大的特应性进展和个体哮喘的风险降低,与个体AR的年龄相关模式相反。
    结论:观察性研究。
    结论:在小儿AD患者中,与常规治疗相比,dupilumab与特应性进展风险降低相关.
    BACKGROUND: Dupilumab effectively treats atopic dermatitis (AD); however, its role in halting the atopic march remains uncertain.
    OBJECTIVE: To investigate dupilumab\'s effect on atopic march in pediatric AD patients versus conventional immunomodulators.
    METHODS: This retrospective cohort study utilized data from the TriNetX US Collaborative Network (2011-2024). Pediatric AD patients (≤18 years) were categorized into DUPI-cohort (newly prescribed dupilumab) or CONV-cohort (prescribed conventional immunomodulators without dupilumab). After 1:1 propensity-score matching, we analyzed atopic march progression, defined by the incident asthma or allergic rhinitis (AR). Cumulative incidence was plotted using Kaplan-Meier, with risk assessment via Cox regression.
    RESULTS: The study included 2192 patients in each cohort. The 3-year cumulative incidence of atopic march progression was lower in the DUPI-cohort than the CONV-cohort (20.09% vs 27.22%; P < .001). The DUPI-cohort demonstrated significant risk reduction in atopic march progression (hazard ratio [HR] 0.68, 95% CI 0.55-0.83), individual asthma (HR 0.60, 0.45-0.81), and individual AR (HR 0.69, 0.54-0.88). Younger patients on dupilumab exhibited a greater risk reduction for atopic march progression and individual asthma, contrasting with the opposite age-related pattern for individual AR.
    CONCLUSIONS: Observational study.
    CONCLUSIONS: Among pediatric AD patients, dupilumab was associated with reduced risk of atopic march progression compared with conventional therapies.
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  • 文章类型: Journal Article
    Objective.通常推荐用于成人和儿童的药物包括质子泵抑制剂(PPI),被证明对治疗胃溃疡等消化性疾病有效,GERD,1岁以上儿童的幽门螺杆菌感染。然而,长期使用PPI会带来更高的不良反应风险,提示本研究的分析。方法。我们已经对30篇文章进行了系统的回顾,其中包括762505名儿科患者。结果。在6.98%的人口中遇到了不良反应。最常见的5种不良反应是呼吸道并发症,胃肠道并发症,尿路感染,哮喘,和耳鼻喉科感染。结论。因此,PPI应仅在必要时规定,和医生应该优先考虑患者的教育,当考虑他们的使用。
    Objective. Commonly recommended drugs for adults and children include proton pump inhibitors (PPIs), proven effective for treating peptic diseases like stomach ulcers, GERD, and Helicobacter pylori infections in children over 1-year-old. Yet, prolonged PPI use carries higher risks of adverse reactions, prompting this study\'s analysis. Methods. We have performed a systematic review of 30 articles, which include a total of 762 505 pediatric patients. Results. Adverse effects were encountered in 6.98% of the population. The 5 most common adverse effects were respiratory tract complications, gastrointestinal complications, urinary tract infections, asthma, and ENT infections. Conclusion. Hence, PPIs should be prescribed only when necessary, and physicians should prioritize patient education when considering their use.
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  • 文章类型: Journal Article
    背景:儿童和青少年是急性病毒性肝炎(AVH)的高危人群,但是针对它们的流行病学研究已经被成人慢性B和C所掩盖。我们提供全球,区域,以及国家对1990年至2019年20岁以下人群的AVH负担及其趋势的估计。
    方法:使用来自全球疾病负担研究(GBD)2019的AVH数据。计算了发病率和残疾调整寿命年(DALYs),用估计的年度百分比变化(EAPC)和Joinpoint回归分析趋势。
    结果:2019年,全球儿童和青少年中报告了156.39(95%不确定区间145.20-167.16)百万新的AVH病例,产生1.98(1.50-2.55)百万DALYs。幼儿发病率(<5岁),年龄较大的儿童(5-9岁),青少年(10-19岁)为12,799(11,068-14,513),5,108(4829-5411),和3020(2724-3339)每100,000人口,分别。全球AVH发病率显示线性下降,EAPC为-0.66(-0.68至-0.65)。高发地区包括撒哈拉以南非洲,大洋洲,南亚,中亚,印度,巴基斯坦,尼日利亚面临最大的负担。主要原因是甲型肝炎,其次是戊型肝炎,B,所有类型的肝炎都呈下降趋势,尤其是乙型肝炎。此外,我们证实了AVH发病率和社会经济学之间的关联,疫苗,和晚期肝病。
    结论:有效的乙型和丙型肝炎疫苗和治疗提供了根除的机会。扩大诊断和治疗覆盖面对于解决为儿童和青少年提供服务的差距至关重要。
    BACKGROUND: Children and adolescents are at high risk for acute viral hepatitis (AVH), but epidemiological research focusing on them has been overshadowed by adult chronic B and C. We provide global, regional, and national estimates of the AVH burden and their trends on people under 20 years from 1990 to 2019.
    METHODS: AVH data from Global Burden of Disease Study (GBD) 2019 was used. Incidence and disability-adjusted life years (DALYs) were calculated, analyzing trends with estimated annual percentage change (EAPC) and Joinpoint regression.
    RESULTS: In 2019, 156.39 (95% uncertainty interval 145.20-167.16) million new cases of AVH were reported among children and adolescents globally, resulting in 1.98 (1.50-2.55) million DALYs. Incidence rates for young children (< 5 years), older children (5-9 years), and adolescents (10-19 years) were 12,799 (11,068-14,513), 5,108 (4829-5411), and 3020 (2724-3339) per 100,000 population, respectively. The global AVH incidence displayed a linear decline with an EAPC of - 0.66 (- 0.68 to - 0.65). High-incidence regions included sub-Saharan Africa, Oceania, South Asia, and Central Asia, with India, Pakistan, and Nigeria facing the greatest burden. Leading causes were hepatitis A, followed by hepatitis E, B, and C. All hepatitis types showed declining trends, especially hepatitis B. Furthermore, we confirmed the association between the AVH incidence and the socioeconomics, vaccine, and advanced liver diseases.
    CONCLUSIONS: Effective vaccines and treatments for hepatitis B and C offer eradication opportunities. Broadening diagnostic and therapeutic coverage is vital to address disparities in service provision for children and adolescents.
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  • 文章类型: Journal Article
    目的:Lacosamide(LCM)是一种新一代抗癫痫药物,对局灶性癫痫发作有或没有继发泛化的患者均有效。直到现在,功效,安全,中国癫痫患者对LCM的耐受性仍然缺乏,特别是对于儿科人群和肾或肝损害患者。
    方法:本研究旨在建立基于生理学的药代动力学(PBPK)模型,以表征LCM在中国人群中的药代动力学,并预测LCM在中国儿科人群和肾或肝损害患者中的药代动力学。利用临床调查的数据,通过比较预测和观察到的血药浓度数据验证了开发的PBPK模型.
    结果:剂量应降至大约82%,75%,63%,和中国健康成人剂量的76%在轻度患者,中度,严重肾功能损害和终末期肾病;约89%,72%,ChildPugh-A患者的中国健康成人剂量为36%,B,和丙肝损害。对于儿科人群,新生儿的静脉注射剂量应调整为1.75mg/kg,幼儿2.5mg/kg,2.2mg/kgmg,适用于学龄前和学龄儿童,和2mg/kg的青少年,以达到2mg/kg的成人LCM的等效血浆暴露。幼儿的口服剂量应调整为20毫克,32毫克用于学龄前,45毫克的学龄儿童,和95mg的青少年达到大约相当于100mgLCM的成人血浆暴露。
    结论:LCM的PBPK模型可用于优化特殊人群的给药方案。
    Lacosamide (LCM) is a new-generation anti-seizure medication that is efficacious in patients with focal seizures with or without secondary generalization. Until now, the efficacy, safety, and tolerability of LCM are still lacking in Chinese epilepsy patients, particularly for pediatric populations and patients with renal or hepatic impairment.
    This study was conducted to develop a physiologically based pharmacokinetic (PBPK) model to characterize the pharmacokinetics of LCM in Chinese populations and predict the pharmacokinetics of LCM in Chinese pediatric populations and patients with renal or hepatic impairment. Using data from clinical investigations, the developed PBPK model was validated by comparing predicted and observed blood concentration data.
    Doses should be reduced to approximately 82%, 75%, 63%, and 76% of the Chinese healthy adult dose in patients with mild, moderate, and severe renal impairment and end-stage renal disease; and approximately 89%, 72%, and 36% of the Chinese healthy adult dose in patients with Child Pugh-A, B, and C hepatic impairment. For pediatric populations, intravenous doses should be adjusted to 1.75 mg/kg for newborns, 2.5 mg/kg for toddlers, 2.2 mg/kg mg for preschool and school age, and 2 mg/kg mg for adolescents to achieve an equivalent plasma exposure of 2 mg/kg LCM in adults. The oral doses should be adjusted to 20 mg for toddlers, 32 mg for preschool, 45 mg for school age, and 95 mg for adolescents to achieve an approximately equivalent plasma exposure of 100 mg LCM in adults.
    The PBPK model of LCM can be utilized to optimize dosage regimens for special populations.
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  • 文章类型: Journal Article
    背景:慢性乙型肝炎感染(CBI)对肝脏脂肪变性的影响,坏死性炎症,非酒精性脂肪性肝病(NAFLD)人群的纤维化尚不清楚。我们旨在研究CBI对肝脏脂肪变性的影响,并评估NAFLD儿科人群中同时存在的CBI和肝损伤之间的关联。
    方法:纳入经活检证实的NAFLD伴或不伴CBI的连续住院儿童。肝脏脂肪变性,通过NASHCRN系统和/或METAVIR评分系统评估坏死和纤维化,适当。使用多变量逻辑分析,我们确定了与肝脂肪变性和肝损伤相关的变量.
    结果:在223例经活检证实的NAFLD儿童中,161名没有CBI的NAFLD,62例NAFLD并存CBI。按轻度分组,中度和重度肝性脂肪变性,CBI与肝脏脂肪变性的严重程度呈负相关[奇数比(OR)0.037,95%置信区间(CI)0.014~0.098].此外,我们探讨了NAFLD儿童CBI与肝坏死性炎症和纤维化之间的关系.肝坏死性炎症和纤维化,分别,根据严重程度分为两组。CBI与肝坏死性炎症呈正相关(OR6.125,95CI1.958-19.158)。然而,CBI与显著肝纤维化之间无统计学独立关联.
    结论:CBI与脂肪变性程度呈负相关,与严重肝坏死性炎症呈正相关,并且似乎不会影响小儿NAFLD儿童的显着肝纤维化。
    BACKGROUND: The influence of chronic hepatitis B infection (CBI) on hepatic steatosis, necroinflammation, and fibrosis in nonalcoholic fatty liver disease (NAFLD) population was unclear. We aimed to investigate the effect of CBI on hepatic steatosis and assess the association between NAFLD co-existed CBI and hepatic injury in NAFLD pediatric population.
    METHODS: Consecutive hospitalized children with biopsy-proven NAFLD with or without CBI were included. Hepatic steatosis, necroinflammation and fibrosis were evaluated by NASH CRN system and/or METAVIR scoring system, appropriately. Using multivariate logistic analysis, we identified variables associated with hepatic steatosis and liver injury.
    RESULTS: Of 223 biopsy-proven NAFLD children, 161 were NAFLD without CBI, and 62 were NAFLD co-existed CBI. Grouped by mild, moderate and severe hepatic steatosis, there was an inverse association between CBI and the severity of hepatic steatosis [odd ratio (OR) 0.037, 95% confidence interval (CI) 0.014-0.098]. In addition, we explored the relationship between CBI and hepatic necroinflammation and fibrosis in NAFLD children. Hepatic necroinflammation and fibrosis, respectively, were divided into two groups according to severity. And CBI was positively associated with hepatic necroinflammation (OR 6.125, 95%CI 1.958-19.158). However, there was no statistically independent association between CBI and significant hepatic fibrosis.
    CONCLUSIONS: CBI was inverse associated with the grade of steatosis and positively associated with severe hepatic necroinflammation, and does not appear to affect significant hepatic fibrosis in pediatric NAFLD children.
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  • 文章类型: Journal Article
    银屑病可影响所有年龄组的个体。虽然成人牛皮癣的流行病学已被广泛研究,专门调查儿科病例的研究有限。这项研究旨在调查台湾儿科患者中皮肤银屑病(PsO)和银屑病关节炎(PsA)的患病率和发病率。从国家健康保险研究数据库中纳入了2000-2013年期间的17535名18岁以下银屑病患者的全国队列,其中包括16129名PsO患者和2022名PsA患者。计算儿童PsO和PsA的年龄和性别标准化患病率和发病率。2007年一般人口按年龄和性别分列的年度报告被采纳为标准。结果显示,从2000年到2013年,儿童PsO的患病率从0.03%上升到0.07%,儿科PsA为0.003%至0.014%。在同一时期,小儿PsO的发病率略有下降,从19.81降至17.55/100000,但小儿PsA的发病率从1.02降至5.06/100000.青少年(12至<18岁)PsO和PsA的患病率和发病率高于儿童(≤12岁),在任何年龄组都没有观察到性别差异。PsO之前的PsA在儿童中比青少年更常见(27.07%vs.13.46%)。这项研究为儿童人群银屑病疾病的患病率和发病率提供了重要的见解。需要进一步的研究来确定小儿银屑病的危险因素并调查其长期健康结果。
    Psoriasis can affect individuals of all age groups. While the epidemiology of psoriasis in adults has been extensively studied, there is limited research specifically investigating pediatric cases. This study aimed to investigate the prevalence and incidence of skin psoriasis (PsO) and psoriatic arthritis (PsA) among pediatric patients in Taiwan. A nationwide cohort of 17 535 patients with psoriatic diseases under the age of 18 was enrolled from the National Health Insurance Research Database for the period 2000-2013, including 16 129 PsO patients and 2022 PsA patients. The age- and sex-standardized prevalence and incidence of pediatric PsO and PsA were calculated. The 2007 yearly reports of age- and sex-specific distribution of the general population was adopted as a standard. The results showed that between 2000 and 2013, the prevalence for pediatric PsO increased from 0.03% to 0.07%, and from 0.003% to 0.014% for pediatric PsA. During the same period, the incidence slightly decreased from 19.81 to 17.55 per 100 000 for pediatric PsO but increased from 1.02 to 5.06 per 100 000 for pediatric PsA. Adolescents (12 to <18 years) had higher prevalence and incidence rates of PsO and PsA than children (aged ≤ 12 years), with no sex difference observed in either age group. PsA preceding PsO was more common among children than adolescents (27.07% vs. 13.46%). This study provides important insights into the prevalence and incidence of psoriatic diseases in the pediatric population. Further research is needed to identify risk factors for pediatric psoriasis and to investigate its long-term health outcomes.
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  • 文章类型: Journal Article
    在中国,药物研发重点逐步从仿制药转向创新药。使用中国临床试验注册和信息透明平台,我们回顾性分析了过去10年在中国大陆进行的创新儿科药物的临床试验.这项工作的目的是更好地了解中国创新儿科药物研发(R&D)的特征和历史变化,并为政策制定者和其他利益相关者提供有效的数据支持。这项研究包括198个创新的儿科药物临床试验。数据显示,尽管中国在创新儿科药物的研发方面取得了一些进展,限制这一进步的许多因素仍然存在,如集中的研发领域,儿科参与者不足,和不平衡的来源分布。中国创新儿科药物研发水平目前落后于全球水平,还没有跟上中国抗肿瘤药物研发的步伐。为促进我国儿科药物的创新发展,中国政府必须制定研发监督框架,提高制药企业的动力和创新能力,并优化地区之间的源分布。
    In China, the focus of drug research and development has gradually shifted from generic to innovative drugs. Using the Chinese Clinical Trials Registry and Information Transparency Platform, we retrospectively analyzed clinical trials of innovative pediatric drugs conducted in mainland China over the last decade. The goal of this work was to better understand the characteristics of and historical changes in innovative pediatric drug research and development (R&D) in China and to provide effective data support for policy makers and other stakeholders. This study included 198 innovative pediatric drug clinical trials. The data showed that, although some progress has been made in the R&D of innovative pediatric drugs in China, many factors limiting this progress still exist, such as concentrated R&D areas, inadequate pediatric participants, and unbalanced source distributions. The level of innovative pediatric drug R&D in China currently lags behind the global level and has not kept pace with anti-neoplastic drug R&D in China. To promote the innovative development of pediatric drugs in China, the Chinese government must develop an R&D supervision framework, improve the motivation and innovation capabilities of pharmaceutical companies, and optimize the source distribution between regions.
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  • 文章类型: Case Reports
    背景:色素性视网膜炎是一组罕见的遗传性视网膜营养不良疾病,导致夜间视力困难,周边视野逐渐丧失(隧道视野),最终失去中心视力。然而,大约60%的病例无法确定遗传原因。
    方法:两个非近亲彝族家庭,有一个6.4岁男孩和一个0.5岁男孩,分别,被招募用于基因诊断。这里,我们使用全外显子组测序来检测色素性视网膜炎家族先证者基因的突变,和Sanger测序以确认通过全外显子组测序鉴定的因果突变。此外,我们报告了两例由RDH12(c.524C>T)和PRPF4(c.1273G>A)致病突变引起的色素性视网膜炎。
    结论:这些结果可能会扩展已知视网膜色素变性基因的突变谱,并为这两个云南彝族家庭提供更精确的遗传咨询和更具体的预后。
    BACKGROUND: Retinitis pigmentosa is a group of rare hereditary retinal dystrophy diseases that lead to difficulty seeing at night, progressive loss of peripheral field vision (tunnel vision), and eventual loss of central vision. However, a genetic cause cannot be determined in approximately 60% of cases.
    METHODS: Two non-consanguineous Yi minority ethnic group families who have a 6.4-year-old boy and a 0.5-year-old boy, respectively, were recruited for genetic diagnosis. Here, we used whole-exome sequencing to detect mutations in the genes of the probands of the retinitis pigmentosa families, and Sanger sequencing to confirm the causal mutations identified by whole exome sequencing. In addition, we report two cases with retinitis pigmentosa caused by RDH12 (c.524C > T) and PRPF4 (c.1273G > A) pathogenic mutations.
    CONCLUSIONS: These results might extend the mutation spectrum of known retinitis pigmentosa genes and give these two Yi minority ethnic group families from Yunnan more precise genetic counseling and more specific prognoses.
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  • 文章类型: Clinical Trial
    背景:环境空气污染物可能对人体健康有害,特别是弱势儿童。尚未确定重症监护病房(ICU)之前和期间暴露于环境空气污染物对危重病患儿呼吸机相关性肺炎(VAP)发展的影响。我们旨在确定ICU中小儿心脏手术患者短期暴露于环境细颗粒物(PM2.5)与VAP之间的相关性。并探索延迟暴露的影响。
    方法:对2013年12月至2020年12月期间ICU需要人工通气的1755例儿童患者的病历进行分析。颗粒物的日平均浓度(PM2.5和PM10),二氧化硫(SO2),和臭氧(O3)是根据公开数据计算的。利用分布滞后非线性模型模拟了这些污染物与VAP之间的相互作用。
    结果:在这项研究中发现了348例(19.829%)的VAP,PM2.5、PM10、O3和SO2的平均浓度分别为58、118、98和26μg/m3。在VAP诊断前两天(滞后2天)暴露于PM2.5水平升高与VAP发展风险增加显着相关。即使PM2.5的10μg/m3略有增加,也可以转化为VAP发生率增加5.4%(95%CI:1.4%-9.5%),而VAP发生率增加至11.1%(95CI:4.5-19.5%)当PM2.5浓度远低于50μg/m3的国家环境空气质量标准(NAAQS)时。这种关联在3个月以下的人群中更为明显,体重指数低或患有肺动脉高压。
    结论:短期PM2.5暴露是儿科患者发生VAP的重要风险。即使PM2.5水平低于NAAQS,这种风险也存在。环境PM2.5可能是以前未被识别的肺炎危险因素,需要重新评估当前的环境污染标准以考虑易感人群。
    背景:该试验已在国家临床试验中心注册:环境空气污染与ICU并发症之间的相关性进行了心脏手术。
    背景:ChiCTR2000030507。注册日期:2020年3月5日。试验注册记录的URL:http://www。chictr.org.cn/index。aspx.
    Ambient air pollutants can be hazardous to human health, especially for vulnerable children. The impact of ambient air pollutant exposure before and during intensive care unit (ICU) stays on the development of ventilator-associated pneumonia (VAP) in critically ill children has not been established. We aimed to determine the correlations between short-term exposures to ambient fine particulate matter (PM2.5) and VAP in pediatric cardiac surgery patients in the ICU, and explore the effect of delayed exposure.
    The medical record of 1755 child patients requiring artificial ventilation in the ICU between December 2013 to December 2020, were analyzed. The daily average concentrations of particulate matters (PM2.5 and PM10), sulfur dioxide (SO2), and ozone (O3) were calculated from public data. Interactions between these pollutants and VAP were simulated with the distributed lag non-linear model.
    Three hundred forty-eight cases (19.829%) of VAP were identified in this study, while the average concentrations of PM2.5, PM10, O3 and SO2 were 58, 118, 98 and 26 μg/m3, respectively. Exposure to increased levels of PM2.5 two days prior (lag 2-day) to VAP diagnosis is significantly correlated with an enhanced risk for VAP development. Even a slight increase of 10 μg/m3 in PM2.5 can translate to a 5.4% increase in VAP incidence (95% CI: 1.4%-9.5%) while the VAP incidence increased to 11.1% (95%CI: 4.5-19.5%) when PM2.5 concentration is well below the National Ambient Air Quality standard (NAAQS) of 50 μg/m3. The association was more pronounced in those aged below 3-months, with low body mass index or suffered from pulmonary arterial hypertension.
    Short-term PM2.5 exposure is a significant risk for development of VAP in pediatric patients. This risk is present even with PM2.5 levels below the NAAQS. Ambient PM2.5 may represent a previously unrecognized risk factor for pneumonia and the current environmental pollution standards need to be reevaluated to consider susceptible populations.
    The trial was registered with the National Clinical Trial Center: The correlation between ambient air pollution and the complications in ICU underwent cardiac surgery.
    ChiCTR2000030507. Date of registration: March 5, 2020. URL of trial registry record: http://www.chictr.org.cn/index.aspx .
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  • 文章类型: Multicenter Study
    目的:比较儿童逆行肾内手术(RIRS)中使用低功率(高达30W)和高功率(高达120W)钬激光的结果,并分析激光技术和通路鞘的使用是否对结果有任何影响。
    方法:我们回顾性分析了2015年1月至2020年12月间接受钬激光治疗肾结石的9个儿童中心的数据。将患者分为两组:高功率和低功率钬激光。临床,分析围手术期变量和并发症。使用学生T检验对连续变量进行组间比较结果,分类变量的卡方检验和费舍尔精确检验。还进行了多变量逻辑回归分析模型。
    结果:包括314例患者。在97和217名患者中使用了高功率和低功率钬激光,分别。两组之间的临床和人口统计学变量具有可比性,除了小功率组治疗较大结石的结石大小(平均11.11mm对9.70mm;p0.018)。在高功率激光组中,发现手术时间缩短(平均64.29minvs75.27min;p<0.018),结石清除率(SFR)显著较高(平均81.4%vs59%;p<0.001).我们发现并发症发生率没有统计学差异。多因素logistic回归模型显示低功率钬组SFR较低,尤其是较大(p=0.011)和多个结石(p<0.001)。
    结论:我们的真实世界儿科多中心研究支持高功率钬激光,并确定其在儿童中的安全性和有效性。.
    Objectives: To compare the outcomes of using low-power (up to 30 W) vs high-power (up to 120 W) holmium lasers in retrograde intrarenal surgery (RIRS) in children and to analyze if lasering techniques and the use of access sheath have any influence on the outcomes. Methods: We retrospectively reviewed data from 9 centers of children who underwent RIRS with holmium laser for the treatment of kidney stones between January 2015 and December 2020. Patients were divided into two groups: high-power and low-power holmium laser. Clinical, perioperative variables and complications were analyzed. Outcomes were compared between groups using Student\'s t-test for continuous variables, and Chi-square and Fisher\'s exact test for categorical variables. A multivariable logistic regression analysis model was also performed. Results: A total of 314 patients were included. A high-power and low-power holmium laser was used in 97 and 217 patients, respectively. Clinical and demographic variables were comparable between both groups, except for stone size where the low-power group treated larger stones (mean 11.11 vs 9.70 mm, p = 0.018). In the high-power laser group, a reduction in surgical time was found (mean 64.29 vs 75.27 minutes, p = 0.018) with a significantly higher stone-free rate (SFR) (mean 81.4% vs 59%, p < 0.001). We found no statistical differences in complication rates. The multivariate logistic regression model showed lower SFR in the low-power holmium group, especially with larger (p = 0.011) and multiple stones (p < 0.001). Conclusion: Our real-world pediatric multicenter study favors high-power holmium laser and establishes its safety and efficacy in children.
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