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Oral immunotherapy in children with allergic diseases: past, present and future. 儿童过敏性疾病的口服免疫治疗:过去、现在和未来。
IF 1 Q3 PEDIATRICS Pub Date : 2025-09-10 DOI: 10.23736/S2724-5276.25.07879-6
Giulia Pecora, Francesca Galletta, Giuseppe F Parisi, Maria Papale, Santiago Presti, Monica Tosto, Sara Manti, Salvatore Leonardi

Allergen immunotherapy (AIT) is the only treatment capable of modifying the natural history of allergic diseases by promoting immune tolerance. Initially developed for respiratory allergies, AIT has expanded to include food allergies, particularly through oral immunotherapy (OIT). This review explores the historical evolution, current applications, and future directions of AIT in pediatric patients. Subcutaneous and sublingual immunotherapy (SCIT and SLIT) remain well-established approaches for allergic rhinitis, asthma, and hymenoptera venom allergy, demonstrating long-term benefits. Additionally, OIT has gained attention for food allergies, aiming to increase the threshold for allergic reactions and reduce the risk of severe reactions upon accidental exposure. Despite promising results, challenges remain, including safety concerns, adherence, and the durability of induced tolerance. Research continues to refine treatment protocols, improve safety profiles, and identify biomarkers to predict patient response. Advancements in immunology and personalized medicine continue to influence the future of AIT, with novel administration routes, adjuvants, and biologic therapies being explored to enhance efficacy and reduce adverse effects. While AIT has transformed the management of allergic diseases, optimizing patient selection, standardizing protocols, and ensuring broader accessibility remain key priorities. A deeper understanding of immune mechanisms will further improve individualized treatment approaches, maximizing long-term benefits for pediatric patients.

过敏原免疫疗法(AIT)是唯一能够通过促进免疫耐受来改变过敏性疾病自然史的治疗方法。AIT最初发展用于呼吸道过敏,现已扩展到包括食物过敏,特别是通过口服免疫疗法(OIT)。本文就AIT在儿科患者中的历史演变、应用现状及未来发展方向进行综述。皮下和舌下免疫治疗(SCIT和SLIT)仍然是治疗过敏性鼻炎,哮喘和膜翅目毒液过敏的行之有效的方法,显示出长期的益处。此外,OIT在食物过敏方面也引起了人们的关注,旨在提高过敏反应的阈值,降低意外接触时发生严重反应的风险。尽管结果令人鼓舞,但挑战依然存在,包括安全性问题、依从性和诱导耐受性的持久性。研究继续完善治疗方案,提高安全性,并确定生物标志物来预测患者的反应。免疫学和个体化医学的进步将继续影响AIT的未来,新的给药途径、佐剂和生物疗法正在被探索,以提高疗效和减少不良反应。虽然AIT已经改变了过敏性疾病的管理,但优化患者选择、标准化方案和确保更广泛的可及性仍然是关键的优先事项。对免疫机制的深入了解将进一步改善个体化治疗方法,最大限度地提高儿科患者的长期效益。
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引用次数: 0
Associations between depressive symptoms with suicide behaviors and negative relationships with mother and father in early adolescents: a population-based study. 青少年早期抑郁症状与自杀行为及与父母的负面关系之间的关系:一项基于人群的研究。
IF 1 Q3 PEDIATRICS Pub Date : 2025-08-01 Epub Date: 2023-11-10 DOI: 10.23736/S2724-5276.23.07274-9
Kénora Chau, Honessa Gherdaoui, Bernard Kabuth, Jean-Marc Bovin, Damien Gonthier

Background: Adolescent-parent negative relationships may favour depressive symptoms only (DSonly) and more strongly those plus suicide ideation (DSSI) or attempt (DSSA) in early adolescents (10-16 years). We assessed their associations which remain poorly addressed.

Methods: This study included 1256 middle-school adolescents from north-eastern France (mean age 13.5±1.3). They completed a questionnaire gathering socioeconomic features, academic performance, substance (alcohol, tobacco, cannabis and other substances) use, relationships with father and mother, depressive symptoms, last-12-month suicide ideation, and lifetime suicide attempt. For depressive symptoms and suicide attempt, the time of the first occurrence during adolescent's life course was also gathered. Data were analyzed using multinomial logistic regression models and Kaplan-Meier survival estimates.

Results: Many adolescents suffered from DSonly (8.0%), DSSI (2.5%) and DSSA (3.9%) and from negative relationships with father only (NRfather, 11.2%), mother only (NRmother, 6.1%), and both parents (NRboth parents, 10.9%). DSSA was more strongly associated (P<0.001) with NRmother (sex-age-adjusted odds ratio saOR=14.34) and NRboth parents (saOR=12.15) than NRfather (saOR=4.57). Similar results were found for DSSI (saOR 12.90, 12.23 and 2.16, respectively) and DSonly (saOR 4.18, 4.84 and 3.18, respectively). These results remained strong when controlling for socioeconomic features, academic performance and substance use (contribution reaching 62%). The risk early began and then steadily increased over time.

Conclusions: Adolescent-parent negative relationships favor DSonly and more strongly DSSI and DSSA. Mother had a much higher role than father. The role and support of both parents should be considered for prevention and care to reduce adolescents' mental health difficulties.

背景:在青少年早期(10-16岁),青少年父母负向关系可能只倾向于抑郁症状(DSonly),更倾向于那些加上自杀意念(DSSI)或企图(DSSA)的症状。我们评估了它们之间的关联,这些关联仍然没有得到很好的处理。方法:本研究纳入了来自法国东北部的1256名中学生(平均年龄13.5±1.3)。他们完成了一份问卷调查,收集了社会经济特征、学习成绩、物质(酒精、烟草、大麻和其他物质)使用、与父母的关系、抑郁症状、最后12个月的自杀意念和终身自杀企图。对于抑郁症状和自杀未遂,还收集了青少年生命过程中首次出现的时间。使用多项逻辑回归模型和Kaplan-Meier生存率估计对数据进行分析。结果:许多青少年患有单纯DS(8.0%)、DSSI(2.5%)和DSSA(3.9%),以及与父亲(NRfather,11.2%)、母亲(NRmother,6.1%)的负面关系,父母双方(NRboth parents,10.9%)。DSSA与NRfather(saOR=4.57)的相关性更强(Pmort(经性别年龄调整的比值比saOR=14.34)和NRboth父母(saOR=12.15)。DSSI(saOR12.90、12.23和2.16)和DSonly(saOR4.18、4.84和3.18)的结果相似。当控制社会经济特征、学习成绩和药物使用时,这些结果仍然很强(贡献率达到62%)。风险很早就开始了,然后随着时间的推移稳步增加。结论:青少年父母负向关系倾向于DSonly,更倾向于DSSI和DSSA。母亲的地位远高于父亲。应考虑父母双方在预防和护理方面的作用和支持,以减少青少年的心理健康困难。
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引用次数: 0
Point-of-care ultrasound recognition of massive thymic hyperplasia. 大量胸腺增生的即时超声识别。
IF 1 Q3 PEDIATRICS Pub Date : 2025-08-01 Epub Date: 2025-03-13 DOI: 10.23736/S2724-5276.25.07821-8
Marco Denina, Giulia Tosoni, Irene Raffaldi, Angelo G Delmonaco, Antonio Pizzol, Matilde Piglione, Claudia Bondone
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引用次数: 0
Concordance between admission and discharge diagnosis of a child and adolescent psychiatry inpatient unit. 某儿童青少年精神科住院单位入院与出院诊断的一致性分析。
IF 1 Q3 PEDIATRICS Pub Date : 2025-08-01 Epub Date: 2023-06-19 DOI: 10.23736/S2724-5276.23.07225-7
Mahmoud Bashtawi, Nasreen Roberts, Kevin Parker, Mazin Alqhazo

Background: Psychiatry is arguably the most medical practice that is affected by culture. The pediatric literature is sparse with respect to the differences between child psychiatric units in different cultures and different countries. In this study, we aim to investigate the discordance between admission diagnosis and discharge diagnosis for child psychiatric disorders.

Methods: A retrospective analysis was conducted on 206 patients admitted to a university hospital inpatient child and adolescent psychiatry unit in Ontario, Canada. The data extracted from electronic charts were age, gender, DSM-IV-based diagnosis at admission, living arrangement before admission, length of stay (minimum one day), post-discharge diagnosis, and post-discharge outcomes.

Results: There was 75% agreement with the discharge diagnosis. We found strong negative and positive associations between conduct disorder at discharge and the prescription of antipsychotics (+), antidepressants (-), and stimulants (-), and there was a strong association between a conduct disorder (CD) diagnosis and medication-free status. The powerful effect size of stimulant medication was specific to the association between a primary diagnosis of ADHD (vs. not-ADHD) and stimulant medication (c2=127.5, df=1, phi=0.79, P<0.0001).

Conclusions: We have found a significant agreement between admission and discharge diagnosis. It is suggested that the inpatient stay helped to refine the formulation and to improve the child's well-being.

背景:精神病学可以说是最受文化影响的医学实践。关于不同文化和不同国家的儿童精神科之间的差异,儿科文献很少。本研究旨在探讨儿童精神障碍入院诊断与出院诊断的不一致性。方法:对加拿大安大略省某大学医院儿童和青少年精神科206例住院患者进行回顾性分析。从电子图表中提取的数据包括年龄、性别、入院时基于dsm - iv的诊断、入院前的生活安排、住院时间(至少1天)、出院后诊断和出院后结局。结果:出院诊断符合率75%。我们发现出院时品行障碍与抗精神病药(+)、抗抑郁药(-)和兴奋剂(-)处方之间存在强烈的负相关和正相关,品行障碍(CD)诊断与无药物状态之间存在强烈的关联。兴奋剂药物的强大效应量特异于ADHD(相对于非ADHD)和兴奋剂药物的初步诊断之间的关联(c2=127.5, df=1, phi=0.79, p)。结论:我们发现入院和出院诊断之间存在显著的一致性。建议住院有助于完善配方和改善儿童的福祉。
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引用次数: 0
Platelet parameters as biomarker for bronchopulmonary dysplasia in very low birth weight neonates in the first two weeks of life. 血小板参数作为生命前两周极低出生体重新生儿支气管肺发育不良的生物标志物
IF 1 Q3 PEDIATRICS Pub Date : 2025-08-01 Epub Date: 2023-05-08 DOI: 10.23736/S2724-5276.23.07213-0
Sunil K Sati, Carolyn Springer, Roger Kim, Kusum Viswanathan, Fernanda E Kupferman

Background: The pathogenesis of bronchopulmonary dysplasia (BPD) is attributed to the arrested lung development in premature infants. Studies showed the negative impact of inflammatory markers on the developing lung with higher levels of IL1, 6 and 8. Platelets contribute to the acute phase response of inflammation and are a direct source of IL-1β.

Methods: We conducted a retrospective data review of all preterm babies with gestational age (GA) <32 weeks admitted to NICU to assess the relationship between platelet parameters in the first 2 weeks of life with the incidence and severity of BPD in very low birth weight (VLBW) neonates.

Results: Of 114 screened newborns, 92 were included after exclusion criteria. Of these, 62 (67.3%) developed BPD. Mean platelet count (PC) (P=0.008) and mean platelet mass index (PMI) (P=0.027) were significantly lower and mean platelet volume (MPV) (P=0.016) was significantly higher in the BPD group. The highest difference between groups was observed at 2nd week of life for PC and PMI and at 1st week for MPV. Using multivariate logistic analysis, only PC (P=0.017) showed statistical significance. MPV and PMI showed a positive interaction but did not achieve significance (P=0.066 for both).

Conclusions: We concluded that platelet parameters in the first 2 weeks of life were associated with the incidence of BPD in VLBW neonates. PC may also predict the severity of BPD in these infants.

背景:支气管肺发育不良(BPD)的发病机制是由于早产儿肺发育受阻。研究表明,炎症标志物对IL1、6和8水平较高的肺发育有负面影响。血小板有助于炎症的急性期反应,是IL-1β的直接来源。方法:我们对所有胎龄早产儿(GA)进行回顾性资料回顾。结果:114例筛查新生儿中,92例符合排除标准。其中62例(67.3%)发展为BPD。BPD组平均血小板计数(PC) (P=0.008)、平均血小板质量指数(PMI) (P=0.027)显著降低,平均血小板体积(MPV) (P=0.016)显著升高。两组间最大的差异出现在生命第2周的PC和PMI以及第1周的MPV。多因素logistic分析显示,只有PC (P=0.017)有统计学意义。MPV与PMI呈正交互作用,但均无显著性(P=0.066)。结论:我们的结论是,出生后2周的血小板参数与VLBW新生儿BPD的发病率相关。PC也可以预测这些婴儿BPD的严重程度。
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引用次数: 0
Management of nocturnal enuresis in children. 儿童夜间遗尿的处理。
IF 1 Q3 PEDIATRICS Pub Date : 2025-08-01 Epub Date: 2025-02-18 DOI: 10.23736/S2724-5276.25.07812-7
Ignazio Cammisa, Margherita Zona, Pietro Ferrara

Introduction: Nocturnal enuresis is defined as involuntary urination during sleep in children, particularly those aged 5 years or older. Treatment approaches include both pharmacological and non-pharmacological methods, with choices depending on the type and severity of nocturnal enuresis, as well as family dynamics. This review evaluates current knowledge on nocturnal enuresis treatment in children.

Evidence acquisition: A systematic review of studies published from 2000 to 2024 was conducted, assessing both pharmacological and non-pharmacological interventions.

Evidence synthesis: Nocturnal enuresis in children has been treated with various pharmacological and non-pharmacological interventions. Non-pharmacological therapies for nocturnal enuresis offer effective, low-risk options for managing this common pediatric condition, particularly when used in combination. Enuresis alarm therapy, considered the first-line treatment, has demonstrated success rates between 50% and 70%. On the other hand, bladder training, pelvic floor retraining and dietary modification play a supportive role in nocturnal enuresis management. Pharmacological interventions mainly include desmopressin and anticholinergics. Combination therapies, particularly desmopressin and anticholinergics, have demonstrated superior efficacy and faster results compared to monotherapy.

Conclusions: A variety of pharmacological and non-pharmacological treatments have been developed to manage nocturnal enuresis and improve the quality of life for affected children. The primary goal for healthcare providers is to tailor a treatment plan to each child, taking into consideration the individual needs of the child and their family.

导读:夜间遗尿症是指儿童,特别是5岁以上儿童在睡眠期间的不自主排尿。治疗方法包括药物和非药物方法,选择取决于夜间遗尿的类型和严重程度,以及家庭动态。这篇综述评价了目前关于儿童夜间遗尿治疗的知识。证据获取:对2000年至2024年发表的研究进行了系统回顾,评估了药物和非药物干预措施。证据综合:儿童夜间遗尿已被各种药物和非药物干预治疗。夜间遗尿的非药物治疗为管理这种常见的儿科疾病提供了有效、低风险的选择,特别是在联合使用时。遗尿报警疗法被认为是一线治疗方法,成功率在50%至70%之间。另一方面,膀胱训练、骨盆底再训练和饮食调整在夜间遗尿管理中起支持作用。药物干预主要包括去氨加压素和抗胆碱能药物。联合治疗,特别是去氨加压素和抗胆碱能药物,与单一治疗相比,已显示出更好的疗效和更快的结果。结论:已开发出多种药物和非药物治疗方法来管理夜间遗尿并改善患儿的生活质量。医疗保健提供者的主要目标是为每个儿童量身定制治疗计划,同时考虑到儿童及其家庭的个人需求。
{"title":"Management of nocturnal enuresis in children.","authors":"Ignazio Cammisa, Margherita Zona, Pietro Ferrara","doi":"10.23736/S2724-5276.25.07812-7","DOIUrl":"10.23736/S2724-5276.25.07812-7","url":null,"abstract":"<p><strong>Introduction: </strong>Nocturnal enuresis is defined as involuntary urination during sleep in children, particularly those aged 5 years or older. Treatment approaches include both pharmacological and non-pharmacological methods, with choices depending on the type and severity of nocturnal enuresis, as well as family dynamics. This review evaluates current knowledge on nocturnal enuresis treatment in children.</p><p><strong>Evidence acquisition: </strong>A systematic review of studies published from 2000 to 2024 was conducted, assessing both pharmacological and non-pharmacological interventions.</p><p><strong>Evidence synthesis: </strong>Nocturnal enuresis in children has been treated with various pharmacological and non-pharmacological interventions. Non-pharmacological therapies for nocturnal enuresis offer effective, low-risk options for managing this common pediatric condition, particularly when used in combination. Enuresis alarm therapy, considered the first-line treatment, has demonstrated success rates between 50% and 70%. On the other hand, bladder training, pelvic floor retraining and dietary modification play a supportive role in nocturnal enuresis management. Pharmacological interventions mainly include desmopressin and anticholinergics. Combination therapies, particularly desmopressin and anticholinergics, have demonstrated superior efficacy and faster results compared to monotherapy.</p><p><strong>Conclusions: </strong>A variety of pharmacological and non-pharmacological treatments have been developed to manage nocturnal enuresis and improve the quality of life for affected children. The primary goal for healthcare providers is to tailor a treatment plan to each child, taking into consideration the individual needs of the child and their family.</p>","PeriodicalId":56337,"journal":{"name":"Minerva Pediatrics","volume":" ","pages":"360-371"},"PeriodicalIF":1.0,"publicationDate":"2025-08-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143443001","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Thoracoscopic lobectomy for congenital pulmonary airway malformations before or after 5 months of age: evaluation of pulmonary function. 胸腔镜肺叶切除术治疗5月龄前后先天性肺气道畸形:肺功能评价。
IF 1 Q3 PEDIATRICS Pub Date : 2025-08-01 Epub Date: 2023-05-22 DOI: 10.23736/S2724-5276.23.07124-0
Luca Pio, Yaqoub Jafar, Lucas Carvalho, Liza Ali, Christrophe Delcaux, Florence Julien-Marsollier, Arnaud Bonnard

Background: Congenital pulmonary airway malformation (CPAM) is the most common pulmonary malformation. It can be managed via thoracoscopic lobectomy, which is safe and advantageous over thoracotomy. Some authors advocate the need for early resection to get an advantage over lung growth. Our study aimed to evaluate and compare the pulmonary function in patients who underwent thoracoscopic lobectomy for CPAM before and after 5 months of age.

Methods: This retrospective study was conducted between 2007 and 2014. Patients younger than 5 months were assigned to group 1 and those over 5 months of age were assigned to group 2. Pulmonary function tests (PFT) were requested for all the included patients. For patients who could not undergo full PFT, the function residual capacity (FRC) was evaluated by the helium dilution technique. The parameters evaluated in full PFT were forced expiratory volume in one second (FEV1), forced vital capacity (FVC), total lung capacity (TLC), and FEV1 to FVC ratio (FEV1/FVC). The Mann Whitney U test was used to compare both groups of patients.

Results: Seventy patients underwent thoracoscopic lobectomy during this period, 40 of which had CPAM. Twenty-seven patients tolerated and underwent PFT (group 1: 12 patients; group 2: 15 patients). Among them, 16 patients underwent full PFT and 11 patients had FRC measurement. FRC was similar in both groups (91% vs. 88.2%). FEV1 (83.9% vs. 86.4%), FVC (86.8% vs. 92.6%) and TLC (86.5% vs. 87.8%) were also similar between both groups. FEV1/FVC was slightly higher in group 1 (97.9% vs. 89.4%) but the difference was not statistically significant.

Conclusions: PFT for patients who underwent thoracoscopic lobectomy for CPAM before or after 5 months of age is normal and comparable between both groups. Surgical resection of CPAM can be performed safely early in life without any consequences for pulmonary function or more complications when older children undergo surgery.

背景:先天性肺气道畸形(Congenital pulmonary airway malformation, CPAM)是最常见的肺部畸形。胸腔镜下的肺叶切除术比开胸手术更安全、更有利。一些作者主张需要早期切除以获得优于肺生长的优势。我们的研究旨在评估和比较5月龄前后接受胸腔镜肺叶切除术的CPAM患者的肺功能。方法:回顾性研究时间为2007 - 2014年。小于5个月的患者被分配到1组,大于5个月的患者被分配到2组。所有患者均要求进行肺功能检查(PFT)。对于不能进行完全PFT的患者,采用氦稀释技术评估功能剩余容量(FRC)。全PFT时评估的参数为1秒用力呼气量(FEV1)、用力肺活量(FVC)、总肺活量(TLC)、FEV1/FVC比值(FEV1/FVC)。Mann Whitney U检验用于比较两组患者。结果:70例患者在此期间接受了胸腔镜肺叶切除术,其中40例有CPAM。27例患者耐受并接受了PFT治疗(第一组:12例;第二组:15例)。其中16例患者进行了完全PFT, 11例患者进行了FRC测量。两组FRC相似(91%对88.2%)。两组FEV1 (83.9% vs. 86.4%)、FVC (86.8% vs. 92.6%)、TLC (86.5% vs. 87.8%)相似。第一组FEV1/FVC略高(97.9%比89.4%),但差异无统计学意义。结论:在5个月前或5个月后接受胸腔镜肺叶切除术的CPAM患者的PFT正常,两组之间具有可比性。手术切除CPAM可以在生命早期安全地进行,不会对肺功能造成任何影响,当年龄较大的儿童接受手术时也不会出现更多并发症。
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引用次数: 0
Factors associated with the time to recover adequate nutrition in infants hospitalized for bronchiolitis, a French retrospective study. 与毛细支气管炎住院婴儿恢复充足营养时间相关的因素,一项法国回顾性研究。
IF 1 Q3 PEDIATRICS Pub Date : 2025-08-01 Epub Date: 2023-09-15 DOI: 10.23736/S2724-5276.23.07298-1
Arnaud Maugendre, Clément Medrinal, Tristan Bonnevie, Pascal LE Roux, Guillaume Prieur, Yann Combret

Background: Inadequate feeding is a frequent reason for hospital referring in infants with bronchiolitis and may leads to unnecessary prolonged hospitalization. Our objective was to identify the factors associated with the time to recover adequate feeding (TRAF) and the hospital length of stay (LOS) in infants hospitalized for bronchiolitis.

Methods: We conducted a single-center retrospective study including infants less than 12 months hospitalized for bronchiolitis at Le Havre Hospital (France) between September 2018 and February 2021. A multivariate logistic regression model was computed to investigate the factors associated with (1) TRAF, and (2) LOS.

Results: 268 infants were included to assess the TRAF and 478 infants to assess the LOS. The median age was 3.2 months (1.6-5.4) and the sex ratio M/F was 11/20. The use of accessory muscles, nutritional support, and RR ≥70/min or <30/min or apnea are associated (OR=1.5), from virtually no association (OR=1.0) to a significant positive association (OR=2.6) with the TRAF. Intense use of accessory muscles (OR=3.9; 95% CI 1.6-10.4) and "severe" clinical condition (OR=2.8; 95% CI 1.7-4.8) at admission, O2 supplementation (OR=2.0; 95% CI 1.3-3.1) were significantly related to prolonged LOS in the multivariate analysis.

Conclusions: The clinical severity on admission may be related to the TRAF, ranging from none to significant. Other known factors such as oxygen therapy and the new clinical severity scale proposed by the latest French guidelines appeared to be related to the LOS in this work. Further studies are needed to highlight these factors.

背景:喂养不足是毛细支气管炎婴儿转诊的常见原因,并可能导致不必要的延长住院时间。我们的目的是确定与毛细支气管炎住院婴儿恢复充足喂养时间(TRAF)和住院时间(LOS)相关的因素。方法:我们进行了一项单中心回顾性研究,包括2018年9月至2021年2月期间在法国勒阿弗尔医院因毛细支气管炎住院的12个月以下的婴儿。采用多元逻辑回归模型研究与(1)TRAF和(2)LOS相关的因素。结果:268名婴儿被纳入TRAF评估,478名婴儿被纳入LOS评估。中位年龄为3.2个月(1.6 ~ 5.4),性别比M/F为11/20。使用辅助肌肉,营养支持,RR≥70/min或2次补充(or =2.0;在多变量分析中,95% CI 1.3-3.1)与延长的LOS显著相关。结论:入院时的临床严重程度可能与TRAF有关,从无到显著。其他已知因素,如氧气治疗和最新法国指南提出的新的临床严重程度量表,似乎与本工作中的LOS有关。需要进一步的研究来突出这些因素。
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引用次数: 0
Management of children with acute post-viral cough: a primary care experience with levodropropizine. 病毒感染后急性咳嗽患儿的治疗:左旋多巴的基层医疗经验。
IF 1 Q3 PEDIATRICS Pub Date : 2025-08-01 Epub Date: 2024-10-31 DOI: 10.23736/S2724-5276.24.07691-2
Gian L Marseglia, Daniele Veraldi, Giorgio Ciprandi

Background: Acute post-viral cough (APVC) is a disturbing complaint that may also affect the quality of life. As a result, APVC requires an adequate managing with antitussive medications. In this regard, levodropropizine is an effective and safe peripheral antitussive drug.

Methods: The present retrospective observational study collected data from children with APVC and treated with levodropropizine for up to seven days. Cough intensity and frequency, impact on children's and parents' sleep, school and games, treatment days, satisfaction, and adverse events were considered.

Results: Data from 92 children (mean age 5.5 years) were analyzed globally. Levodropropizine reduced cough intensity and frequency in most children and improved school and game activities and sleep quality in children and their parents. The treatment was safe. Most parents were highly satisfied with the results.

Conclusions: This experience showed that levodropropizine was an effective and safe remedy for children with acute post-viral cough.

背景:病毒感染后急性咳嗽(APVC)是一种令人不安的主诉,也可能影响生活质量。因此,急性病毒后咳嗽需要适当的止咳药物治疗。在这方面,左旋多巴是一种有效、安全的外周止咳药:本回顾性观察研究收集了患有 APVC 并接受左旋多巴治疗长达七天的儿童的数据。研究考虑了咳嗽强度和频率、对儿童和家长睡眠、学习和游戏的影响、治疗天数、满意度和不良反应等因素:对 92 名儿童(平均年龄 5.5 岁)的数据进行了全面分析。左旋多巴嗪降低了大多数儿童的咳嗽强度和频率,改善了儿童及其父母的学校和游戏活动以及睡眠质量。治疗是安全的。大多数家长对治疗效果非常满意:这一经验表明,左旋多巴嗪是治疗病毒感染后急性咳嗽患儿的一种有效而安全的药物。
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引用次数: 0
An Italian multidisciplinary Delphi Consensus on managing children and adolescents with acute fever using ketoprofen lysine salt. 意大利多学科德尔菲共识管理儿童和青少年急性发烧使用酮洛芬赖氨酸盐。
IF 1 Q3 PEDIATRICS Pub Date : 2025-07-17 DOI: 10.23736/S2724-5276.25.07830-9
Gianluigi Marseglia, Michele Miraglia Del Giudice, Francesco Scaglione, Amelia Licari, Giorgio Ciprandi

Fever is a common symptom and sign in children and adolescents. Italian pediatric guidelines recommend pharmacologically treating fever if discomfort is present. In addition, guidelines state that ibuprofen among NSAIDs and acetaminophen are the first-choice medications for relieving fever in children; however, among NSAIDs, also ketoprofen lysine salt (KLS) is indicated in young patients 6 years of age and older and proved to exert antipyretic effects. The present multidisciplinary Delphi Consensus, promoted by the Italian Society of Allergy and Clinical Immunology (SIAIP), aimed at proposing practical statements about fever management and the possible use of KLS to relieve acute pediatric fever. A multidisciplinary panel of 33 qualified experts discussed and anonymously voted on the statements drafted by a steering committee. The results confirmed a large agreement about the para-physiological role of fever and underlined the concept of not indiscriminately reducing fever. In addition, there was agreement that KLS displays efficacy and safety overlapping with ibuprofen and acetaminophen in modulating fever. Some discordances concerned the advantages of quickly relieving fever and the safety profile. Therefore, the steering committee hopes for new methodologically robust comparative trials. In conclusion. KLS could be considered a reasonable option for managing children and adolescents with fever. However, further studies are required to provide more robust evidence.

发烧是儿童和青少年的常见症状和体征。意大利儿科指南建议,如果出现不适,可以用药物治疗发烧。此外,指南指出,在非甾体抗炎药和对乙酰氨基酚中,布洛芬是儿童退烧的首选药物;然而,在非甾体抗炎药中,酮洛芬赖氨酸盐(KLS)也适用于6岁及以上的年轻患者,并被证明具有解热作用。目前,由意大利过敏和临床免疫学学会(SIAIP)推动的多学科德尔菲共识旨在提出有关发烧管理和可能使用KLS缓解急性儿科发烧的实用声明。一个由33名合格专家组成的多学科小组对指导委员会起草的声明进行了讨论和匿名投票。研究结果证实了发热的超生理作用在很大程度上是一致的,并强调了不能不加区分地退烧的概念。此外,KLS在调节发烧方面与布洛芬和对乙酰氨基酚具有重叠的有效性和安全性。一些不一致涉及到快速退烧的优点和安全性。因此,指导委员会希望有新的方法可靠的比较试验。在结论。KLS可以被认为是治疗发烧儿童和青少年的合理选择。然而,需要进一步的研究来提供更有力的证据。
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Minerva Pediatrics
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