儿童急性扁桃体炎治疗方案的优化

Q4 Medicine
O. Koloskova, A. Kosakovskyi, I. Horbatiuk, S. Tarnavska
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引用次数: 0

摘要

儿童急性扁桃体咽炎(Acute tonsillophyntis, ATP)是一个实际存在但尚未完全解决的问题,具有跨学科的重要性,需要优化诊断和治疗,以提高疾病的预后和儿童的生活质量。目的:通过结合抗炎和免疫调节药物的综合治疗,优化小儿ATP的治疗策略,并评价所提出的治疗方法的临床和免疫学指标的有效性。材料和方法。我们监测了51例临床诊断为ATP的住院儿童。所有患儿均接受复杂的临床及临床旁检查,入院时检测血清c反应蛋白(CRP),治疗第7天检测血清白细胞介素(IL) -4、-6、-8、肿瘤坏死因子α (TNFα)、干扰素-γ (γ-IFN)浓度作为治疗效果的标志。将患者随机分为2个临床组:1组28例患者(平均年龄- 8.0±0.9岁,男孩占53.5±6.1%)接受ATP治疗,根据说明书给予标准治疗和标准提取物培拉根EPs®7630 (Umckalor)及与年龄相关剂量的复方顺势疗法药物扁桃体曲仑。其余23例患儿作为临床第二组,平均年龄- 8.7±1.0岁(p>0.05),男孩占比- 56.5±8.3% (p>0.05),接受与ATP相同的标准治疗,作为对照组。各组的主要临床特征相匹配。结果。当Umckalor和Tonsilotren联合治疗时,我们获得了明显更好的治疗ATP儿童的结果,这是通过在治疗第3天(评估ATP - 10.0 mg/l, γ-IFN和IL-8>10.0 pg/ml)的临床病程较标准治疗有统计学可靠的机会来证明的。绝对风险降低20.8%,相对风险降低32.3%,最低需要治疗的患者数量为3.1。结论。在ATP患儿的综合治疗中,与相同的标准治疗相比,使用标准提取物Pelargonium sidoides EPs®7630 (Umckalor)和复方顺势疗法药物Tonsilotren的组合显示出更好的效果。这项研究是按照《赫尔辛基宣言》的原则进行的。研究方案经参与机构当地伦理委员会批准。获得患者的知情同意进行研究。作者未声明存在利益冲突。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Optimization of the treatment of acute tonsillopharyngitis in childhood
Acute tonsillopharyngitis (ATP) in children is an actual and not fully solved problem, which has interdisciplinary importance and requires optimization of diagnosis and treatment to improve the prognosis of the disease and the quality of life of children. Purpose - to optimize the tactics of treatment of children with ATP by supplementing the complex of therapy with drugs of anti-inflammatory and immunomodulatory action with the evaluation of clinical and immunological markers of the effectiveness of the proposed treatment. Materials and methods. We monitored 51 hospitalized children with a clinical diagnosis of ATP. All children underwent a complex clinical and paraclinical examination with the determination of C-reactive protein (CRP) in the blood serum upon admission to the hospital, and on the 7th day of treatment, the serum concentration of interleukin (IL) -4, -6, -8, tumor necrosis factor α (TNFα), and interferon-γ (γ-IFN) as markers of therapy effectiveness. The patients were randomly divided into 2 clinical groups: the Group 1 was formed by 28 patients (average age - 8.0±0.9 years, the share of boys - 53.5±6.1%) with ATP, who received standard treatment and standardized extract of Pelargonium sidoides EPs® 7630 (Umckalor) and the complex homeopathic drug Tonsilotren in age-related doses according to the instructions. The remaining 23 children formed the clinical Group 2 (average age - 8.7±1.0 years (p>0.05), the share of boys - 56.5±8.3% (p>0.05), and received the same standard treatment for ATP and served as a comparison group. The groups were matched for the main clinical characteristics. Results. We obtained significantly better results of treatment of children with ATP when using the combination of the drugs Umckalor and Tonsilotren in complex therapy, which are proven by the presence of statistically reliable chances of a milder clinical course of the disease on the 3rd day of treatment (assessment of the severity of ATP - <26 points): attribute risk - 59.8%, relative risk - 2.8 (95% CI: 1.1-7.2), odds ratio - 25.6 (9.0-72.6). The effectiveness of the proposed therapy was confirmed on the 7th day of treatment by the probably lower content of pro-inflammatory markers IL-8 (15.2±5.4 pg/ml vs 37.6±7.6 pg/ml) and γ-IFN (21.8±2.3 pg/ml vs. 30.0±1.2 pg/ml) compared to standard treatment, as well as twice lower TNF-α concentration (2.1±0.5 pg/ml vs. 4.5±2.5 pg/ml). The use of the combination of the drugs Umckalor and Tonsilotren was accompanied by a statistically significant reduction in the risk of maintaining a high serum concentration of pro-inflammatory cytokines (CRP - >10.0 mg/l, γ-IFN and IL-8>10.0 pg/ml) in relation to the standard treatment: absolute risk reduction - 20.8%, relative risk reduction - 32.3% with the minimum required number of patients to treat - 3.1. Conclusions. In the complex treatment of children with ATP, the use of a combination of the standardized extract of Pelargonium sidoides EPs® 7630 (Umckalor) and the complex homeopathic drug Tonsilotren demonstrated better effectiveness compared to the same standard treatment. The research was carried out in accordance with the principles of the Helsinki Declaration. The study protocol was approved by the Local Ethics Committee of the participating institution. The informed consent of the patient was obtained for conducting the studies. No conflict of interests was declared by the authors.
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来源期刊
Suchasna pediatriia Ukrayina
Suchasna pediatriia Ukrayina Medicine-Pediatrics, Perinatology and Child Health
CiteScore
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审稿时长
8 weeks
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