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Report on the work of the Chief Pediatric Surgeon of the Ministry of Health of the Russian Federation in 2022 关于俄罗斯联邦卫生部首席儿科外科医生2022年工作的报告
Pub Date : 2023-02-15 DOI: 10.17816/psaic1490
D. Morozov
The editorial presents a report on the work of the Chief Pediatric Surgeon of the Ministry of Health of Russia for 2022. From the very beginning of his activity, he established regular interaction with the chief supernumerary pediatric surgeons and executive and legislative authorities of the regions of the Russian Federation, both remotely and visiting surgical clinics in 15 cities. Much attention was paid to the improvement of pediatric surgical care in the Far East with repeated trips to this region to prepare a program for the creation of interregional centers for specialized surgical care in the most popular medical specialties. As a result of joint work with leading specialists of the Russian Association of Pediatric Surgeons and chief pediatric surgeons of the regions of the Russian Federation, the first Regulations on Interregional Centers for Neonatal Surgery was created. Chief Pediatric Surgeons organized surgical care for children in the special military operation zone and border regions with business trips to Taganrog, Rostov-on-Don and Lugansk. Throughout the year, is coordinated round-the-clock assistance to injured children, dozens of telemedicine consultations were held. As a result of a systematic survey of the chief supernumerary pediatric surgeons of the regions of the Russian Federation, a consolidated report on the activities of the pediatric surgical service of the Russian Federation for 2021 was formed, which was necessary to develop prospects for its further development. The work plans of the chief pediatric surgeon for 2023 include the completion of important documents for the specialty: the The procedure for providing surgical care to children and the Professional standard for a pediatric surgeon. There is also a task to implement the concept of interregional neonatal surgery centers in the Far Eastern Federal District, expert, educational work and audit of children's surgical clinics will be continued.
这篇社论介绍了俄罗斯卫生部首席儿科外科医生2022年的工作报告。从他的活动开始,他就与俄罗斯联邦各地区的首席临时儿科外科医生以及行政和立法当局建立了定期互动,包括远程和访问15个城市的外科诊所。对改善远东地区的儿科外科护理给予了很大的关注,并多次前往该地区,为在最受欢迎的医学专业建立区域间专门外科护理中心制定了一项计划。由于与俄罗斯儿科外科医生协会的主要专家和俄罗斯联邦各地区的首席儿科外科医生共同努力,制定了第一个《新生儿手术区域间中心条例》。首席儿科外科医生组织了特别军事行动区和边境地区儿童的手术护理,并出差到塔甘罗格、顿河畔罗斯托夫和卢甘斯克。全年,为受伤儿童提供协调的24小时援助,举行了数十次远程医疗会诊。在对俄罗斯联邦各地区的首席儿科外科医生进行系统调查后,形成了2021年俄罗斯联邦儿科外科服务活动的综合报告,这对于发展其进一步发展的前景是必要的。首席儿科外科医生2023年的工作计划包括完成本专业的重要文件:《为儿童提供外科护理的程序》和《儿科外科医生的专业标准》。还有一项任务是在远东联邦区实施跨区域新生儿外科中心的概念,专家、教育工作和对儿童外科诊所的审计将继续进行。
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引用次数: 0
The results of treatment of newborns with right-sided and left-sided intrathoracic localization of the liver with diaphragmatic hernia 新生儿右、左侧胸内定位肝膈疝的治疗效果
Pub Date : 2023-01-19 DOI: 10.17816/psaic1291
O. Mokrushina, A. Razumovskiy, E. V. Yudina, I. Afukov, V. Shumikhin, S. Smirnova, E. Zilbert, L. Petrova, N. Erokhina, R. V. Halafov, T.O. Svetlichnaya
BACKGROUND: The right-sided congenital diaphragmatic hernia is the rare pathology. Results of diagnostics, prognosis and treatment usally published as a collection of cases. AIM: Comparition of treatment results of congenital diaphragmatic hernia with the liver as its content in dependancy of the side. MATERIALS AND METHODS: We present a retrospective analysis of 50 newborn patients with congenital diaphragmatic hernia. Patiens were divided in two groups, first with right-sided (19 patients), and second with left-sided hernia (31 patients). Groups were compared by gender and weigth. Comparition criteria was the results of prenatal and postnatal diagnostics, intraoperative data, postoperative period, complications and outcomes. RESULTS: We found predominance of prenatal diagnosis in the second group (48% vs 84%, p = 0,001). The lung-to-head circumference ratio were the same in both groups (0,52 in first, 0,46 in second, p = 0,058). Chance to use thoracoscopic approach in the second group was higer in 5,7 times (48% vs 84%). Postoperative period was easier in the group of right-sided congenital diaphragmatic hernia: artificial ventilation lasted on average 8 days (min 3; max 28) versus 11 (min 4; max 50) days in the first group (p = 0,036). Hospital stay was significantly lower in the second group 18 days (min 12; max 28), versus 50 days in the first group (min 13; max 64), p = 0,011. Recovery chance in patients with right-sided hernia was higher (45% vs 79%, confidence interval 0,0590,814). CONCLUSIONS: Every type of diaphragmatic hernia, including right-sided location, need to be the subgect of research of high compitantive center. Prognostic criteria for right-sided congenital diaphragmatic hernia require furter advanced study, wich is possible only in case of concentration of patients in the same center.
背景:右侧先天性膈疝是一种罕见的疾病。诊断、预后和治疗结果通常作为病例集发表。目的:比较以肝为内容的先天性膈疝侧边依赖性的治疗效果。材料与方法:我们对50例新生儿先天性膈疝患者进行回顾性分析。患者分为两组,一组为右侧疝(19例),二组为左侧疝(31例)。各组按性别和体重进行比较。比较标准为产前和产后诊断结果、术中资料、术后时间、并发症和结局。结果:我们发现产前诊断在第二组中占优势(48% vs 84%, p = 0.001)。两组肺头围比相同(第一组为0.52,第二组为0.46,p = 0.058)。第二组采用胸腔镜入路的几率为5,7次(48%对84%)。右侧先天性膈疝组术后时间较短,人工通气时间平均为8天(最短3天;最大28)vs 11(最小4;第一组最多50天(p = 0.036)。第二组患者住院时间明显缩短18天(最短12天;最长28天),而第一组为50天(最短13天;最大64),p = 0,011。右侧疝患者的康复率更高(45% vs 79%,可信区间0,0590,814)。结论:每一种类型的膈疝,包括右侧位置,都需要成为高竞争中心的研究对象。右侧先天性膈疝的预后标准需要进一步的深入研究,这只有在患者集中在同一中心的情况下才有可能。
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引用次数: 0
Fundamentals of photodynamic therapy, clinical practice and prospects for use in pediatric surgery. Review 光动力疗法的基本原理、临床实践及应用于儿科外科的前景。审查
Pub Date : 2023-01-19 DOI: 10.17816/psaic936
Saidkhasan M. Bataev, K. S. Tsilenko, A. Osipov, A. Reshetnikov, A. S. Bataev, S. P. Sosnova
The paper provides a review of domestic and foreign literature on photodynamic therapy, which is mainly used by oncologists in the treatment of adult patients and is little known to pediatric surgeons. The aim of this work is to describe the history of the formation, principles and mechanisms of photodynamic therapy, the main groups of photo sensitizers, areas of clinical application and prospects for wider use in pediatric surgery. Literature sources were searched in the databases in Russian eLibrary and English Medline and PubMed. The following keywords were specified for the search: photodynamic therapy, dysplasia, metaplasia, angiodysplasia, Barretts syndrome, children. 865 papers were found, of which 66 were fully consistent with the purpose of our study and were analyzed. The data presented in the review of the literature indicate the high efficiency of the method of photodynamic therapy in the treatment of a number of diseases, mostly in oncology. In addition, the work contains theoretical calculations and separate reports on the effectiveness of the method in the treatment of dysplasia of varying degrees in children. Taking into account the minimally invasiveness of the technique, the relative cheapness of photosensitizers and equipment for generating laser radiation, it is possible to create a basis for conducting research on the treatment of children with various dysplasias, epithelial metaplasia, and vascular malformations. Another promising direction is the development of technologies for the use of photodynamic methods for the treatment of severe forms of pyoinflammatory diseases in children. In childhood surgery, there are nosological forms of diseases where the method of photodynamic therapy has the prospect of effective use. Limitations on the scope of this article do not allow for a detailed analysis of the existing experience in the use of photodynamic therapy in children, which will need to be done in subsequent works.
本文对光动力疗法的国内外文献进行了综述。光动力疗法主要被肿瘤学家用于成人患者的治疗,而儿科外科医生对其知之甚少。本文旨在介绍光动力疗法的形成历史、原理和机制、光敏剂的主要种类、临床应用领域以及在儿科外科中广泛应用的前景。文献来源在俄语图书馆、英语Medline和PubMed数据库中检索。以下关键词被指定用于搜索:光动力治疗,发育不良,化生,血管发育不良,巴雷特综合征,儿童。共找到865篇论文,其中66篇完全符合我们的研究目的,并进行了分析。在文献综述中提出的数据表明,光动力治疗方法在治疗许多疾病,主要是肿瘤方面的高效率。此外,该工作还包含理论计算和关于该方法在治疗儿童不同程度发育不良方面的有效性的单独报告。考虑到该技术的微创性,光敏剂和产生激光辐射的设备的相对便宜,有可能为进行各种发育不良、上皮化和血管畸形儿童治疗的研究奠定基础。另一个有希望的方向是开发利用光动力学方法治疗儿童严重形式的热炎性疾病的技术。在儿童外科手术中,有病种形式的疾病,其中光动力治疗方法具有有效使用的前景。由于本文范围的限制,不允许对儿童使用光动力疗法的现有经验进行详细分析,这将需要在后续工作中进行。
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引用次数: 0
Pneumothorax in newborns with multisystem inflammatory syndrome associated with COVID-19: a case reports 与COVID-19相关的多系统炎症综合征新生儿气胸1例
Pub Date : 2023-01-19 DOI: 10.17816/psaic1303
R. K. Shangareeva, N. T. Absalyamova, Regina R. Fedorova, I. Tikhonova, Rano Kh. Mukhamedova, A. K. Alibaev, G. I. Minibaeva
Currently, there is more and more data on new manifestations of COVID-19, such as multisystem inflammatory syndrome in children, which occurs with severe complications, among which cases of pneumothorax have been recorded. The article presents the experience of treating 4 newborns with a new coronovirus infection who were admitted to the clinic during 2021. In all clinical cases, children were born to mothers with a burdened obstetric history. All children had a positive RNA polymerase chain reaction for SARS-CoV-2. Children were admitted with signs of respiratory, cerebral insufficiency, gastrointestinal syndrome and metabolic disorders. The clinical picture and laboratory data corresponded to the definition of a multisystem inflammatory syndrome and was characterized not only by lung damage, but also by changes in other organs. Pneumothorax was diagnosed on days 1521. In all children, a tension pneumothorax developed on the right, in the first two cases against the background of mechanical ventilation, in the remaining two with spontaneous breathing with additional oxygenation. In one case, the pneumothorax was bilateral. Drainage of the pleural cavity in three children was carried out according to Bulau and in one case with active aspiration. Pneumothorax resolved after 414 days. Computed tomography of the chest, performed during the period of rehabilitation treatment, shows pronounced sclerotic and bullous changes in the lung parenchyma. All patients were discharged from the hospital in a satisfactory condition. Since in all the above cases, pneumothorax occurred in newborns with a burdened obstetric history of mothers, it is difficult to differentiate the occurrence of pneumothorax associated with the underlying disease, the course of labor, complications of therapy, from the disease associated with COVID-19. Stronger evidence is needed from larger datasets and rigorous analysis.
目前,关于COVID-19的新表现的资料越来越多,如儿童多系统炎症综合征,发生时伴有严重的并发症,其中有气胸的病例记录。本文介绍了2021年收治的4例新型冠状病毒感染新生儿的治疗经验。在所有临床病例中,儿童的母亲都有沉重的产科史。所有儿童的SARS-CoV-2 RNA聚合酶链反应均呈阳性。患儿入院时有呼吸、脑供血不足、胃肠综合征和代谢紊乱等症状。临床表现和实验室数据符合多系统炎症综合征的定义,不仅以肺损伤为特征,而且以其他器官的变化为特征。气胸是在1521天确诊的。所有患儿均出现右侧紧张性气胸,前两例为机械通气,其余两例为自发呼吸加氧。其中一例为双侧气胸。三名儿童胸膜腔引流是根据Bulau进行的,其中一例是主动抽吸。414天后气胸消退。在康复治疗期间进行的胸部计算机断层扫描显示肺实质明显硬化和大泡性改变。所有病人出院时情况都令人满意。由于在上述所有病例中,气胸发生在母亲有沉重产科史的新生儿中,因此很难区分与基础疾病、分娩过程、治疗并发症相关的气胸与与COVID-19相关的疾病的发生。需要从更大的数据集和严格的分析中获得更有力的证据。
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引用次数: 0
Respiratory parameters as a predictor of hospital outcomes in newborns requiring medical evacuation 呼吸参数作为需要医疗后送的新生儿医院结局的预测因子
Pub Date : 2023-01-19 DOI: 10.17816/psaic1292
R. Mukhametshin, O. Kovtun, N. S. Davydova
BACKGROUND: Assessment of the clinical condition, prediction of risks and possible outcomes during the transfer of newborns remains an important part of the work of transport teams. Respiratory disorders remain a significant indication for transfer to medical organizations of a higher level of care. AIM: To study the predictive value of the parameters of respiratory support in newborns requiring medical evacuation for the outcomes of treatment. MATERIALS AND METHODS: The observational, cohort, retrospective study included data from neonatal to patients on ventilators (286 newborns) in the period from August 1, 2017 to December 31, 2018. Anamnesis parameters, intensive care volume, respiratory support settings, and assessments on scales (KSHONN, NTISS, TRIPS) were evaluated. Analyzed: 24-hours mortality, 7 days mortality, hospital mortality, air leakage syndrome. The assessment and comparison of the predictive value of the parameters in relation to the hospital outcomes was performed. RESULTS: The AUC ROC of SpO2/FiO2 for predicting 24-hours mortality was 0.984 [0.9661.000], which is significantly higher than the ROC of the saturation oxygenation index (AUC 0.972 [0.9490.995], p = 0.004). The area under the ROC of the 24-hours mortality on the TRIPS scale does not significantly differ from the saturation index of oxygenation (AUC 0.972 [0.9490.995], p = 0.113) and the mean airway pressure (AUC 0.943 [0.8841.000], p = 0.107). When predicting 7-day mortality, the saturation oxygenation index has AUC ROC (0.702 [0.5490.854]) significantly lower than AUC ROC for SpO2/FiO2 (0.762 [0.6380.887], p = 0.001). SpO2/FiO2 predicts total mortality with AUC ROC (0.759 [0.6770.841]). CONCLUSIONS: The mean airway pressure, saturation oxygenation index and SpO2/FiO2 have a high (AUC 0,9) predictive value for 24-hours mortality, while only SpO2/FiO2 reliably predicts total mortality with AUC ROC 0,7.
背景:在新生儿转移过程中评估临床状况,预测风险和可能的结果仍然是转运团队工作的重要组成部分。呼吸系统疾病仍然是转移到更高护理水平的医疗机构的一个重要指标。目的:探讨需要医疗后送的新生儿呼吸支持参数对治疗结果的预测价值。材料与方法:该观察性、队列性、回顾性研究纳入了2017年8月1日至2018年12月31日期间新生儿至使用呼吸机患者(286名新生儿)的数据。评估了记忆参数、重症监护量、呼吸支持设置和量表评估(KSHONN、NTISS、TRIPS)。分析:24小时死亡率、7天死亡率、住院死亡率、漏气综合征。评估和比较与医院预后相关的参数的预测值。结果:SpO2/FiO2预测24小时死亡率的AUC ROC为0.984[0.9661.000],显著高于饱和氧合指数(AUC 0.972 [0.9490.995], p = 0.004)。24小时死亡率在TRIPS量表上的ROC下面积与氧合饱和度指数(AUC 0.972 [0.949 - 0.995], p = 0.113)和平均气道压力(AUC 0.943 [0.8841.000], p = 0.107)无显著差异。在预测7天死亡率时,饱和氧合指数AUC ROC(0.702[0.5490.854])显著低于SpO2/FiO2的AUC ROC (0.762 [0.63800.887], p = 0.001)。SpO2/FiO2预测总死亡率,AUC ROC(0.759[0.6770.841])。结论:平均气道压、饱和氧合指数和SpO2/FiO2对24小时死亡率具有较高的预测价值(AUC 0.9),而SpO2/FiO2仅可靠地预测总死亡率,AUC ROC为0.7。
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引用次数: 0
Chronic obstruction of the stomach as a result of congenital malformation in a child of 1 year 10 months. Case report 慢性胃阻塞作为先天性畸形的结果在1岁10个月的孩子。病例报告
Pub Date : 2023-01-19 DOI: 10.17816/psaic1283
Inna S. Schneider, N. Tsap, E. V. Gaydysheva, Maxim Yu. Timoshinov, Mikhail N. Ekimov, Snezhana E. Smirnova
Congenital malformation of the gastrointestinal tract in a rare case can cause partial obstruction and masquerade as functional disorders of the intestine for a long time. Atypical clinic of membranous gastric obstruction causes difficulties in diagnosis and determination of treatment tactics. The aim to determine and present to the surgical community the features of diagnosis, surgical treatment, possible complications of a rare malformation of the stomach in children in the form of a stomach membrane. The paper presents a clinical case of the stomach membrane in a child 1 year 10 months old with complaints of vomiting after each meal, bloating, lethargy for one month. The results of ultrasonography, X-ray examination with the passage of a contrast agent through the gastrointestinal tract, fibrogastroduodenoscopy established anatomical changes in the stomach in the form of pyloric stenosis up to 0.40.5 cm in diameter. Intraoperative revision of the stomach, supplemented by intraluminal endoscopic support, made it possible to reliably establish the presence of a perforated pyloric membrane. The membrane is radically cut along the entire circumference at the level of its base. The next postoperative period was uneventful. After 1.5 months, the child was again admitted to the pediatric surgical department on an emergency basis with a clinic of intestinal obstruction, including the childs anxiety, repeated vomiting, and bloating. X-ray and endoscopic picture corresponded to the diagnosis of cicatricial stenosis of the pyloric part of the stomach. Taking into account the presence of cicatricial deformity, due to the high risk of complications during resection of the stenotic part of the stomach and the imposition of gastroduodenoanastomosis, a bypass retrocolic gastrojejunoanastomosis with Brown fistula was formed. When examining a child of a child in the late postoperative period, no complications were identified. The presented clinical case confirms that congenital malformations of the gastrointestinal tract in the form of stenoses and membranes can have a long stage of compensation, their diagnosis is based on a comprehensive examination of the child using radiopaque and endoscopic studies.
先天性胃肠道畸形在一个罕见的情况下,可引起部分阻塞和伪装成肠道功能障碍很长一段时间。膜性胃梗阻临床不典型,给诊断和确定治疗策略带来困难。目的是确定和目前的外科社区的特点,诊断,手术治疗,可能的并发症的一种罕见的胃畸形的形式在儿童的胃膜。本文提出一个临床病例的胃膜在1岁10个月大的孩子抱怨呕吐后,每顿饭,腹胀,嗜睡一个月。超声检查、造影剂通过胃肠道的x线检查、纤维胃十二指肠镜检查的结果确定胃的解剖改变,其形式为幽门狭窄,直径达0.0.4 cm。术中胃翻修,辅以腔内内镜支持,可以可靠地确定幽门膜穿孔的存在。膜在其底部的水平沿整个圆周被彻底切割。下一个术后期平安无事。1.5个月后,患儿再次以肠梗阻门诊急诊入儿科外科,表现为患儿焦虑、反复呕吐、腹胀。x线及内窥镜影像符合胃幽门部瘢痕性狭窄的诊断。考虑到瘢痕畸形的存在,由于胃狭窄部分切除和胃十二指肠吻合术的并发症风险高,我们采用结肠后旁路胃空肠吻合布朗瘘。当在术后后期检查儿童的儿童时,未发现并发症。本临床病例证实,先天性胃肠道畸形以狭窄和膜的形式可以有一个长阶段的代偿,他们的诊断是基于对儿童的综合检查,使用不透射线和内窥镜研究。
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引用次数: 0
Commentary on the article "Chronic obstruction of the stomach as a result of congenital malformation in a child of 1.10 months. Case report" 《1例1.10个月儿先天畸形致慢性胃梗阻》一文评论。病例报告”
Pub Date : 2023-01-19 DOI: 10.17816/psaic1485
Y. Sokolov
Commentary on the article Schneider IS, Tsap NA, Gaydysheva EV, Timoshinov MYu, Ekimov MN, Smirnova SE. Chronic obstruction of the stomach as a result of congenital malformation in a child of 1.10 months. Case report published in the Russian Journal of Pediatric Surgery, Anesthesia and Intensive Care. 2022;12(4):513520. (In Russ.) DOI: https://doi.org/10.17816/psaic1283
文章评论Schneider IS, Tsap NA, Gaydysheva EV, Timoshinov MYu, Ekimov MN, Smirnova SE。一个1.10个月大的孩子,由于先天畸形导致慢性胃阻塞。病例报告发表在俄罗斯儿科外科、麻醉和重症监护杂志。2022;12(4):513520。(俄国人)。DOI: https://doi.org/10.17816/psaic1283
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引用次数: 0
Factors contributing to the late diagnosis of appendicitis in children: the results of a retrospective study 影响儿童阑尾炎晚期诊断的因素:一项回顾性研究的结果
Pub Date : 2023-01-19 DOI: 10.17816/psaic1260
Maria Yu. Yanitskaya, O. Kharkova, N. V. Markov, N. V. Zolotarev
BACKGROUND: The diagnosis of acute appendicitis in children is often established late, which leads to complications, lethal outcomes are recorded. AIM: To identify and analyze the factors contributing to the late diagnosis of acute appendicitis in children. MATERIALS AND METHODS: A retrospective analysis of 279 case histories of children was carried out. The duration of symptoms is divided into time 1 (before hospitalization) and time 2 (from hospitalization to surgery). Patients were divided into two groups: 1st with destructive uncomplicated appendicitis (phlegmonous, gangrenous), 2nd with complicated appendicitis (unrestricted peritonitis, infiltrate, abscess). The causes of late hospitalization, symptoms indicated in the case histories, examinations performed, postoperative complications were analyzed. The diagnosis was established on the basis of intraoperative data, histological examination. RESULTS: In the 1st group, time 1 and time 2 were significantly less than in the 2nd (p 0.001; 0.028). Late presentation (24 hours) in 21.9%, misdiagnosis in 12.2% of cases. In the hospital, the observation of the patient 12 hours in 21.1% of patients. The frequency of presence / absence of a description of clinical and laboratory signs of acute appendicitis is from 100 to 19.7%. The 2nd group was characterized by: duration of symptoms 24 hours, repeated vomiting (p 0.001), febrile condition (p 0.001), increase in neutrophils 90% (8792%). Ultrasound examination with evaluation of the appendix in 20.1% of cases with a diagnostic accuracy of 89.3%. Laparoscopic appendectomy in 53.2% Alvarado scores are significantly higher in 2nd group (810) than in 1st group (79, p 0.001). In 1st group, complications were significantly less than 3.4% than in 2nd group 22.7 % (p 0.001). CONCLUSIONS: Factors contributing to the late diagnosis of appendicitis in children are: late treatment, diagnostic errors at the prehospital stage, incomplete clinical examination and observation, insufficient use of laboratory and instrumental methods.
背景:儿童急性阑尾炎的诊断往往确立较晚,这导致并发症,致命的结果记录。目的:探讨影响儿童急性阑尾炎晚期诊断的因素。材料与方法:对279例儿童病例进行回顾性分析。症状持续时间分为时间1(住院前)和时间2(从住院到手术)。患者分为两组:一组为破坏性无并发症阑尾炎(痰性、坏疽性),二组为复杂性阑尾炎(无限制腹膜炎、浸润性、脓肿性)。分析延迟住院的原因、病史表现、检查情况及术后并发症。诊断依据术中资料及组织学检查。结果:第1组患者第1、2时间均显著少于第2组患者(p 0.001;0.028)。发病晚(24小时)占21.9%,误诊占12.2%。在医院,观察患者12小时的患者占21.1%。有/没有描述急性阑尾炎的临床和实验室体征的频率为100 - 19.7%。第二组患者症状持续24小时,反复呕吐(p 0.001),发热(p 0.001),中性粒细胞增加90%(8792%)。超声检查伴阑尾评估的病例占20.1%,诊断准确率为89.3%。第二组的Alvarado评分(810分)明显高于第一组(79分,p 0.001)。第1组并发症发生率低于第2组的22.7% (p < 0.001)。结论:导致儿童阑尾炎诊断晚的因素有:治疗晚、院前诊断错误、临床检查观察不全、实验室和仪器方法使用不充分。
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引用次数: 0
To the 75th Anniversary of Viktor V. Nesterov 为维克托·v·涅斯捷罗夫诞辰75周年干杯
Pub Date : 2023-01-19 DOI: 10.17816/psaic1309
Valery F. Blandinsky
The paper describes the professional activities and merits of the pediatric surgeon Viktor V. Nesterov in celebration of his anniversary.
本文描述的专业活动和功绩的儿科外科医生维克多·v·涅斯捷罗夫庆祝他的周年纪念日。
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引用次数: 0
Spontaneous biliary perforation in a child: case report and review 儿童自发性胆道穿孔1例报告及复习
Pub Date : 2023-01-19 DOI: 10.17816/psaic1285
P. Pavlushin, I. Porshennikov, Vladimir N. Pavlik, V. Tsyganok, A. Gramzin
Spontaneous perforation of the external biliary tract is an extremely rare pathology in childhood, presented in the literature by description of clinical cases. To date, a unified approach to the treatment of children with this pathology has not been developed. The paper presents a clinical case of spontaneous perforation of the anterior wall of the common hepatic duct in a child of seven months, with the development of bilioperitoneum against the background of obstruction of the common bile duct by bilirubin calculi. CASE REPORT. The disease began acutely with repeated vomiting, stool acholia, dark urine, and an increase in the size of the abdomen in a 7-month-old child. Examination in the hospital revealed ascites, cholecystitis and shadows of calculi in the projection of the hepatoduodenal ligament. According to the results of laparocentesis, bilioperitoneum was noted. The patient underwent laparotomy, 300 ml of serous-biliary effusion was removed from the abdominal cavity. On the anterior semicircle of the common hepatic duct there is a defect from which bile flows. Suturing of the perforation of the biliary tree, cholecystectomy and drainage of the external bile ducts through the stump of the cystic duct were performed. The cholangiostomy was removed after 1.5 months. Follow-up 1 year and 3 months, pathology is not determined during the examination. CONCLUSIONS. Sewing up the site of primary perforation with drainage of the external biliary tract can help accelerate the reparative process with a decrease in the risk of developing a biliary fistula. Performing primary reconstructive interventions on the abdominal cavity compromised by bilioperitoneum, in our opinion, is too risky.
自发性外胆道穿孔是一种极其罕见的儿童病理,在文献中通过临床病例的描述来呈现。到目前为止,还没有一个统一的方法来治疗患有这种病理的儿童。本文报告一例7个月大的儿童肝总管前壁自发穿孔,胆红素结石梗阻,并发胆道腹膜。病例报告。7个月大的婴儿发病时表现为反复呕吐、大便空泻、尿色深和腹部增大。医院检查发现腹水、胆囊炎及肝十二指肠韧带投影处结石影。根据腹腔镜检查结果,记录胆道腹膜。患者行开腹手术,从腹腔取出300 ml浆液性胆道积液。在肝总管前半圆处有一个缺损,胆汁由此流出。行胆道穿孔缝合、胆囊切除及外胆管残端引流术。1.5个月后切除胆管造口术。随访1年3个月,检查时未确定病理。结论。用外胆道引流缝合原发穿孔部位有助于加速修复过程,降低发生胆道瘘的风险。在我们看来,对胆腹受损的腹腔进行初级重建干预风险太大。
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Russian Journal of Pediatric Surgery, Anesthesia and Intensive Care
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