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Effect of Wrist Angulation on Radial Artery Sonoanatomy in a Pediatric Population: An Observational Pilot Study. 手腕角度对儿童桡动脉超声解剖的影响:一项观察性先导研究。
Q3 Medicine Pub Date : 2025-07-01 Epub Date: 2025-05-05 DOI: 10.4103/jiaps.jiaps_280_24
Akhil Kant Singh, Puneet Khanna, Souvik Maitra, Dalim Kumar Baidya, Anil Aggarwal, Neha Pangasa, Anirban Som, Mahesh Kumar Arora

Background: The radial artery is the most preferred site for arterial cannulation in pediatric patients. The optimal wrist position which provides the largest size of the radial artery in pediatric patients is unknown.

Aim: We aimed to compare the sonoanatomy of the radial artery in different wrist positions (0°, 15°, 30°, 45°, 60°, and 75° extension) in pediatric patients to identify the optimal position which offered the largest diameter of the radial artery.

Materials and methods: Ninety-six patients aged 1-12 years undergoing elective surgery were included. After induction of general anesthesia, an ultrasound examination of bilateral radial arteries was done. The wrist was placed in six different positions: 0°, 15°, 30°, 45°, 60°, and 75° extension, and radial artery anteroposterior diameter (APD), transverse diameter (TD), and depth from the skin (depth) were measured bilaterally using ultrasound.

Results: The mean (±standard deviation [SD]) APD in the neutral wrist position was 1.79 (±0.45) mm and 1.76 (±0.47) mm on the right and left side, respectively. The mean (±SD) TD in the neutral wrist position was 2.32 (±0.47) mm and 2.35 (±0.68) mm on the right and left side, respectively. The mean (±SD) depth of the radial artery in the neutral wrist position was 1.75 (±0.70) mm and 1.65 (±0.76) mm on the right and left side, respectively. With increasing wrist angulation, both APD and TD did not show any significant change; however, depth decreased with increasing angulation. All measurements were comparable bilaterally.

Conclusions: In 1-12-year-old children, increasing wrist angulation leads to decreasing depth of the artery; however, the anteroposterior and Transverse diameter show no significant change.

背景:桡动脉是儿科患者动脉插管的首选部位。在小儿患者中提供最大桡动脉的最佳手腕位置尚不清楚。目的:我们旨在比较儿科患者不同腕位(0°、15°、30°、45°、60°和75°伸展)桡动脉的超声解剖,以确定桡动脉直径最大的最佳位置。材料与方法:选取96例年龄1 ~ 12岁的择期手术患者。全麻诱导后,行双侧桡动脉超声检查。将腕关节置于0°、15°、30°、45°、60°和75°六个不同的位置,双侧超声测量桡动脉前后径(APD)、横径(TD)和距皮肤深度(depth)。结果:中位腕位左右侧APD均值(±标准差[SD])分别为1.79(±0.45)mm和1.76(±0.47)mm。中位腕位的平均(±SD) TD分别为右侧2.32(±0.47)mm和左侧2.35(±0.68)mm。腕中性位桡动脉平均深度(±SD)分别为1.75(±0.70)mm和1.65(±0.76)mm。随着腕部角度的增加,APD和TD均无明显变化;然而,深度随着成角的增加而下降。所有测量结果均具有双边可比性。结论:在1-12岁儿童中,手腕角度增加导致动脉深度减小;而前后径和横径无明显变化。
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引用次数: 0
Navigating Ergonomic Challenges in Pediatric Laparoscopy: Insights from Indian Surgeons. 导航儿科腹腔镜的人体工程学挑战:来自印度外科医生的见解。
Q3 Medicine Pub Date : 2025-07-01 Epub Date: 2025-05-21 DOI: 10.4103/jiaps.jiaps_307_24
Sugandh Chadha, Lakshmi Sundararajan

Aim: The aim of the study was to assess the awareness and identify the issues faced by pediatric surgeons in India concerning laparoscopic ergonomics.

Methods: An online survey was conducted by circulating a questionnaire consisting of 18 questions among pediatric surgical consultants and trainees in 2023. The questions were used to assess the musculoskeletal issues faced by the surgeons while operating and they included gender, height, experience, complexity of the procedure performed, position of the monitor, operating table height, length of instruments used, and health issues faced due to bad ergonomics.

Statistical analysis used: Chi-square test, Pearson's score for correlation, ANOVA.

Results: A total of 152 pediatric surgeons participated, of which 119 were males and 32 were females, with 96 (62%) working at a teaching institution. 73 (48%) were senior consultants with >10 years of experience. 79 (52%) performed advanced laparoscopic procedures. Neonatal surgeries (71%) were the most challenging. Fifty-four (36%) surgeons faced musculoskeletal illnesses. This was more prevalent among senior grade consultants (58%), female surgeons (50%), surgeons with heights between 155 and 175 cm (81.2%), surgeons older than 60 years (58%), and those performing advanced procedures (75%). Most participants (98%) were keen on improving their laparoscopic ergonomics. 140 (93%) surgeons noted that laparoscopic ergonomics was overlooked at their hospitals and 84 (56%) lacked institutional support for acquiring the necessary infrastructure.

Conclusion: Thirty-six percent of surgeons experienced musculoskeletal disorders while performing advanced procedures (75%), and height, female gender, and complexity of procedures were noted to have a positive correlation with the injury.

目的:本研究的目的是评估印度儿科外科医生对腹腔镜人体工程学的认识,并确定其面临的问题。方法:对2023年儿科外科会诊医师和培训生进行在线问卷调查,问卷共18个问题。这些问题被用来评估外科医生在手术时面临的肌肉骨骼问题,包括性别、身高、经验、手术的复杂性、监视器的位置、手术台的高度、使用的器械的长度,以及由于不良的人体工程学而面临的健康问题。统计分析采用:卡方检验、Pearson评分相关性、方差分析。结果:共有152名儿科外科医生参与调查,其中男119名,女32名,其中96名(62%)在教学机构工作。73人(48%)为资深顾问,拥有10年以上经验。79例(52%)进行了高级腹腔镜手术。新生儿手术(71%)是最具挑战性的。54名(36%)外科医生面临肌肉骨骼疾病。这在高级顾问医生(58%)、女外科医生(50%)、身高在155至175厘米之间的外科医生(81.2%)、年龄超过60岁的外科医生(58%)和进行高级手术的外科医生(75%)中更为普遍。大多数参与者(98%)热衷于改善腹腔镜的人体工程学。140名(93%)外科医生指出腹腔镜人体工程学在他们的医院被忽视,84名(56%)缺乏获得必要基础设施的机构支持。结论:36%的外科医生在进行高级手术时出现肌肉骨骼疾病(75%),身高、女性性别和手术复杂性与损伤呈正相关。
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引用次数: 0
Surgical Outcomes of Laparoscopic versus Open Inguinal Hernia Repair in Children: A 10-year Single-surgeon Study. 儿童腹腔镜与开放式腹股沟疝修补术的手术效果:一项10年单外科医生研究。
Q3 Medicine Pub Date : 2025-05-01 Epub Date: 2025-04-10 DOI: 10.4103/jiaps.jiaps_272_24
Amar Shah, Ria Sharma, Anirudh Shah

Aims: The aims of this study were to compare surgical outcomes of conventional open inguinal hernia repair (OR) with laparoscopic repair of inguinal hernia (LR) repair in Indian children operated by a single surgeon.

Materials and methods: This is a retrospective (historical) nonrandomized cohort study of 1595 children with unilateral inguinal hernia for 10 years. All children who presented with unilateral inguinal hernia were included in this study. The study was divided into two phases of 5 years each, and patients were classified into Group 1 and Group 2. In the first 5 years (Group 1), all the children with unilateral inguinal hernia underwent conventional open repair. Over the next 5 years (Group 2), all the children with unilateral inguinal hernia underwent laparoscopic repair. All the operations were performed by the same surgeon who was well acquainted with laparoscopic surgery. Parameters studied included gender, side of the hernia, time of surgery, incidence of contralateral patent processus vaginalis (PPV), development of metachronous contralateral hernia, and complications.

Results: A total of 1595 children with unilateral inguinal hernia were studied. Nine hundred and forty-five patients underwent OR (Group 1), and 650 patients underwent LR (Group 2). The male-to-female ratio in Group 1 was 2.5:1, and in Group 2 was 2.4:1. Right inguinal hernia was present in 59%, whereas 41% had a left inguinal hernia. In Group 1, 8% of children developed metachronous contralateral hernias. In Group 2, the contralateral processus vaginalis was found to be patent in 260 children. However, only 10% (26) of these children developed metachronous contralateral hernia on follow-up. In the present study, a significantly higher recurrence rate (2.5%) was observed in the LR group as compared to the OR group (0.3%). The overall operative time was lesser in the OR group (15 ± 8.4 min) versus LR group (25 ± 10 min).

Conclusions: Only 10% of children with contralateral PPV in our study went on to develop a symptomatic hernia. Hence, we believe that upfront closure of the contralateral PPV with unilateral inguinal hernia may not be necessary. LR has a longer operating time and higher recurrence rates. The choice of technique depends on factors such as the availability of laparoscopic equipment and infrastructure, surgeon's preference, and expertise.

目的:本研究的目的是比较传统开放式腹股沟疝修补术(OR)与腹腔镜下腹股沟疝修补术(LR)在印度儿童中由单一外科医生操作的手术效果。材料和方法:这是一项回顾性(历史)非随机队列研究,1595名儿童单侧腹股沟疝10年。所有表现为单侧腹股沟疝的儿童都被纳入本研究。研究分为两期,每期5年,患者分为第1组和第2组。前5年(第一组),所有单侧腹股沟疝患儿均行常规开腹修补术。在接下来的5年中(第二组),所有单侧腹股沟疝患儿均行腹腔镜修补术。所有手术均由熟悉腹腔镜手术的同一位外科医生进行。研究参数包括性别、疝侧边、手术时间、对侧阴道突未闭发生率、异时性对侧疝发展及并发症。结果:对单侧腹股沟疝患儿1595例进行了研究。945例患者行OR(第一组),650例患者行LR(第二组)。组1男女比例为2.5:1,组2男女比例为2.4:1。右侧腹股沟疝占59%,左侧腹股沟疝占41%。在第1组中,8%的儿童发生异时性对侧疝。第二组260例患儿对侧阴道突未闭。然而,在随访中,这些儿童中只有10%(26)发生了异时性对侧疝。在本研究中,LR组的复发率(2.5%)明显高于OR组(0.3%)。OR组总手术时间(15±8.4 min)短于LR组(25±10 min)。结论:在我们的研究中,只有10%的对侧PPV患儿发展为有症状的疝气。因此,我们认为单侧腹股沟疝的对侧PPV可能没有必要预先关闭。LR手术时间长,复发率高。技术的选择取决于诸如腹腔镜设备和基础设施的可用性、外科医生的偏好和专业知识等因素。
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引用次数: 0
Urinary Bladder/ Posterior Urethra Morphology in Posterior Urethral Valves Outcome. 膀胱/后尿道形态与后尿道瓣膜预后的关系。
Q3 Medicine Pub Date : 2025-05-01 Epub Date: 2025-04-15 DOI: 10.4103/jiaps.jiaps_292_24
Ramesh Babu
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引用次数: 0
Evolution of Scientific Efforts to Define Cystometric Bladder Morphology in Neurogenic Bladder: A Narrated Review. 神经源性膀胱膀胱形态定义的科学进展:综述。
Q3 Medicine Pub Date : 2025-05-01 Epub Date: 2025-03-03 DOI: 10.4103/jiaps.jiaps_247_24
Arvind Sinha, Shrilakshmi Aithal

Children with high-pressure bladders are at an increased risk of upper tract deterioration, potentially leading to chronic renal failure if not adequately managed. Regular bladder pressure monitoring is essential, especially in patients with neurogenic bladders, often resulting from spinal dysraphism. Urodynamic studies (UDSs) are the gold standard for assessing bladder pressure but are invasive, resource-intensive, and uncomfortable for patients. Over the last many decades, there have been regular attempts to characterize the morphology of the neurogenic bladder, including the classical subjective appearance of the "Christmas Tree" bladder, to objectively define the shape of the bladder via the use of height-to-width ratio. The study explores the evolution of scientific efforts to define bladder morphology in neurogenic bladder and to describe the current state of evidence regarding the correlation of the shape of the bladder with the detrusor pressures and upper tract changes in children with neurogenic bladder.

患有高压膀胱的儿童上尿路恶化的风险增加,如果处理不当,可能导致慢性肾功能衰竭。定期监测膀胱压力是必要的,特别是在神经源性膀胱患者,通常是由脊柱异常所致。尿动力学研究(UDSs)是评估膀胱压力的金标准,但它是侵入性的,资源密集的,并且对患者不舒服。在过去的几十年里,人们经常尝试描述神经源性膀胱的形态特征,包括“圣诞树”膀胱的经典主观外观,通过使用高宽比客观地定义膀胱的形状。本研究探讨了神经源性膀胱的膀胱形态定义的科学进展,并描述了神经源性膀胱儿童膀胱形状与逼尿肌压力和上尿路变化之间相关性的证据现状。
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引用次数: 0
Chromosomal Microarray Analysis in Spina Bifida: Genetic Heterogeneity and Its Clinical Implications. 脊柱裂的染色体微阵列分析:遗传异质性及其临床意义。
Q3 Medicine Pub Date : 2025-05-01 Epub Date: 2025-04-28 DOI: 10.4103/jiaps.jiaps_217_24
Himani Pandey, Jyoti Sharma, Sourabh Kumar, Nakul Mohan, Vishesh Jain, Anjan Kumar Dhua, Devendra Kumar Yadav, Ashish Kumar Dubey, Prativa Choudhury, Prabudh Goel

Background: The etiology of spina bifida is multifactorial; the phenotype is the end result of both genetic and environmental influences. While whole exome sequencing has identified several pathogenic variants in Indian cohorts, the role of chromosomal imbalances and long contiguous stretches of homozygosity (LCSHs) remains largely unexplored in this population. Chromosomal microarray analysis (CMA) is an important tool that provides insights into such genetic aberrations, making it significant for evaluating patients with spina bifida.

Objective: To identify LCSHs and chromosomal imbalances in three spina bifida patients through CMA analysis as a pilot investigation.

Materials and methods: Genomic DNA was isolated from three spina bifida patients (P1: 10-year-old female, P2: 1-year-old male, and P3: 2.8-year-old male) and subjected to CMA using the Affymetrix 750K high-density array platform. The submicroscopic chromosomal imbalances and LCSHs were cross-referenced with public databases (Database of Genomic Variants, ClinVar, and OMIM) to evaluate their clinical significance. Functional annotations of the affected genes were performed to understand their role in neural tube development.

Results: CMA revealed significant LCSH on chromosomes 2, 3, and 7 involving the genes SOX11, WNT7A, FZD9, SEMA3A, and VHL, all of which are involved in neural tube closure. Mosaic Klinefelter syndrome (25.9% mosaicism) was identified in the second patient while the third patient had a normal genetic profile. The detection of significant genetic variations in two of three cases underscores the potential utility of CMA in spina bifida patients.

Conclusions: This study has generated valuable insights into the complex genetic landscape underlying the multifactorial etiopathogenesis of spina bifida. The findings not only underscore the importance of an integrated approach but also support the cause of a platform for large-scale investigations in the Indian population.

背景:脊柱裂的病因是多因素的;表型是遗传和环境影响的最终结果。虽然全外显子组测序已经在印度人群中发现了几种致病变异,但染色体不平衡和长连续纯合延伸(LCSHs)的作用在该人群中仍未得到充分研究。染色体微阵列分析(CMA)是一种重要的工具,可以深入了解这种遗传畸变,使其对脊柱裂患者的评估具有重要意义。目的:通过CMA分析对3例脊柱裂患者LCSHs和染色体失衡进行初步研究。材料和方法:分离3例脊柱裂患者(P1: 10岁女性,P2: 1岁男性,P3: 2.8岁男性)的基因组DNA,使用Affymetrix 750K高密度阵列平台进行CMA检测。亚显微镜下的染色体不平衡和LCSHs与公共数据库(基因组变异数据库,ClinVar和OMIM)交叉参考,以评估其临床意义。对受影响的基因进行功能注释,以了解它们在神经管发育中的作用。结果:CMA显示,2、3、7号染色体上存在显著LCSH,涉及SOX11、WNT7A、FZD9、SEMA3A和VHL基因,这些基因都与神经管闭合有关。嵌合Klinefelter综合征(25.9%嵌合)在第二例患者中被确定,而第三例患者遗传谱正常。在三个病例中检测到两个显著的遗传变异,强调了CMA在脊柱裂患者中的潜在效用。结论:这项研究对脊柱裂多因素发病机制的复杂遗传格局产生了有价值的见解。研究结果不仅强调了综合方法的重要性,而且还支持在印度人口中建立大规模调查平台的事业。
{"title":"Chromosomal Microarray Analysis in Spina Bifida: Genetic Heterogeneity and Its Clinical Implications.","authors":"Himani Pandey, Jyoti Sharma, Sourabh Kumar, Nakul Mohan, Vishesh Jain, Anjan Kumar Dhua, Devendra Kumar Yadav, Ashish Kumar Dubey, Prativa Choudhury, Prabudh Goel","doi":"10.4103/jiaps.jiaps_217_24","DOIUrl":"10.4103/jiaps.jiaps_217_24","url":null,"abstract":"<p><strong>Background: </strong>The etiology of spina bifida is multifactorial; the phenotype is the end result of both genetic and environmental influences. While whole exome sequencing has identified several pathogenic variants in Indian cohorts, the role of chromosomal imbalances and long contiguous stretches of homozygosity (LCSHs) remains largely unexplored in this population. Chromosomal microarray analysis (CMA) is an important tool that provides insights into such genetic aberrations, making it significant for evaluating patients with spina bifida.</p><p><strong>Objective: </strong>To identify LCSHs and chromosomal imbalances in three spina bifida patients through CMA analysis as a pilot investigation.</p><p><strong>Materials and methods: </strong>Genomic DNA was isolated from three spina bifida patients (P1: 10-year-old female, P2: 1-year-old male, and P3: 2.8-year-old male) and subjected to CMA using the Affymetrix 750K high-density array platform. The submicroscopic chromosomal imbalances and LCSHs were cross-referenced with public databases (Database of Genomic Variants, ClinVar, and OMIM) to evaluate their clinical significance. Functional annotations of the affected genes were performed to understand their role in neural tube development.</p><p><strong>Results: </strong>CMA revealed significant LCSH on chromosomes 2, 3, and 7 involving the genes <i>SOX11</i>, <i>WNT7A</i>, <i>FZD9</i>, <i>SEMA3A</i>, and <i>VHL</i>, all of which are involved in neural tube closure. Mosaic Klinefelter syndrome (25.9% mosaicism) was identified in the second patient while the third patient had a normal genetic profile. The detection of significant genetic variations in two of three cases underscores the potential utility of CMA in spina bifida patients.</p><p><strong>Conclusions: </strong>This study has generated valuable insights into the complex genetic landscape underlying the multifactorial etiopathogenesis of spina bifida. The findings not only underscore the importance of an integrated approach but also support the cause of a platform for large-scale investigations in the Indian population.</p>","PeriodicalId":16069,"journal":{"name":"Journal of Indian Association of Pediatric Surgeons","volume":"30 3","pages":"290-295"},"PeriodicalIF":0.0,"publicationDate":"2025-05-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12094595/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144127590","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Transperitoneal Laparoscopic Adrenalectomy in Children - Initial Experience in an Emerging Tertiary Center in Eastern India. 儿童经腹膜腹腔镜肾上腺切除术-印度东部新兴三级中心的初步经验。
Q3 Medicine Pub Date : 2025-05-01 Epub Date: 2025-03-03 DOI: 10.4103/jiaps.jiaps_229_24
Avilash Sahu, Aditya Arvind Manekar, Subrat Kumar Sahoo, Bikasha Bihary Tripathy, Manoj Kumar Mohanty

Background: Adrenal tumors account for 0.2%-1% of all tumors in children. They can be benign or malignant, secretory or nonsecretory, and can arise either from the cortex or medulla. The common indication in children undergoing laparoscopic adrenalectomy (LA) is neuroblastic tumors (neuroblastoma, ganglioneuroma, and ganglioneuroblastoma).

Methodology: This is a retrospective observational study conducted from October 2021 to February 2024 (28 months) in the pediatric surgery unit at our institute. All children under 18 years of age referred to us for surgery of adrenal mass were included in this study. Any children with image-defined risk factors (IDRFs + ve) were excluded from the study. Children were worked up and managed according to the protocol of the Institute Pediatric Tumor Board. The laparoscopic transperitoneal approach was used for all. All adrenal lesions with IDRF +ve were excluded from the study and resected via open approaches.

Results: A total of six patients were included (three each in male and female groups). The mean age was 31 months (range 22 months-39 months). There were two cases of neuroblastoma, and one each of pheochromocytoma, adrenal adenoma, adrenocortical carcinoma, and paraganglioma. The median follow-up period was 24 months (range 7-32 months). On follow-up, there are no recurrences reported till date with zero mortality.

Conclusion: LA is a safe and feasible operation in children without any IDRF. It should be preferred in children with small lesion with good plane between the tumor and normal tissues. For larger lesion and ACC, it should be used cautiously to prevent spillage. Thought difficult, laparoscopic resection is a safe approach for these adrenal tumors.

背景:肾上腺肿瘤占儿童所有肿瘤的0.2%-1%。它们可为良性或恶性,可为分泌性或非分泌性,可起源于皮层或髓质。儿童腹腔镜肾上腺切除术(LA)的常见适应症是神经母细胞瘤(神经母细胞瘤、神经节神经瘤和神经节神经母细胞瘤)。方法:这是一项回顾性观察性研究,于2021年10月至2024年2月(28个月)在我院儿科外科进行。所有到我们医院接受肾上腺肿块手术的18岁以下儿童都被纳入本研究。任何具有图像定义危险因素(IDRFs + 5)的儿童均被排除在研究之外。根据研究所儿童肿瘤委员会的协议对儿童进行治疗和管理。所有手术均采用腹腔镜经腹腔入路。所有伴有IDRF +ve的肾上腺病变均被排除在研究之外,并通过开放入路切除。结果:共纳入6例患者(男女组各3例)。平均年龄31个月(22 ~ 39个月)。神经母细胞瘤2例,嗜铬细胞瘤、肾上腺腺瘤、肾上腺皮质癌、副神经节瘤各1例。中位随访时间为24个月(范围7-32个月)。在随访中,到目前为止没有复发报告,死亡率为零。结论:对于无IDRF的患儿,LA手术是安全可行的。病灶小、肿瘤与正常组织间平面良好的患儿优先使用。对于较大的病变和ACC,应谨慎使用,防止外溢。虽然困难,但腹腔镜切除是治疗这些肾上腺肿瘤的安全方法。
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引用次数: 0
Redo Pull-through in Hirschsprungs Disease - A Meta-Analysis of Outcomes Based on type of Pull-through. hirschspsprung病的重新拔管-基于拔管类型结果的荟萃分析。
Q3 Medicine Pub Date : 2025-05-01 Epub Date: 2025-04-15 DOI: 10.4103/jiaps.jiaps_279_24
M Srinivasa Rao, D Kalyan Ravi Prasad, J Bhaskar Reddy

Purpose: The meta-analysis investigates the effects of redo pull-through (PT) surgeries on bowel function outcomes in patients with rectosigmoid and long-segment Hirschsprung's disease (HD) who have already undergone an initial PT. By comparing different redo PT techniques, this study explores whether specific approaches yield better postoperative bowel function.

Methodology: A literature search was conducted for articles on redo PT for HD; this included PubMed and ScienceDirect databases. The search terms or MeSH words "Hirschsprung disease" OR "congenital megacolon" AND "re-do pull through" OR "re-do" OR "reoperation," connected by two Boolean operators "OR" and "AND," were used to search the databases for relevant articles.

Results: Fifteen articles of interest comprising 374 patients receiving redo PT were selected for analysis. The results suggest that selecting a redo PT method tailored to the patient's unique anatomical and surgical history may substantially improve functional outcomes, highlighting the potential for individualized strategies to enhance recovery and long-term quality of life for those requiring reoperation.

Conclusion: The findings indicate that the Swenson redo PT approach yielded better bowel function outcomes compared to other techniques. While redo PT procedures were effective in reducing fecal incontinence, the incidence of enterocolitis remained consistent across the various approaches.

目的:本荟萃分析探讨了重拉通(PT)手术对已经接受过初始PT的直肠乙状结肠和长段巨结肠病(HD)患者肠功能结局的影响。通过比较不同的重拉通技术,本研究探讨了特定方法是否能产生更好的术后肠功能。方法:检索有关重做PT治疗HD的文章;这包括PubMed和ScienceDirect数据库。搜索词或MeSH词“巨结肠病”或“先天性巨冒号”和“重新拉过”或“重新做”或“再做”或“再操作”,由两个布尔运算符“或”和“与”连接,用于搜索数据库中的相关文章。结果:选取了15篇相关文章,包括374例接受重做PT的患者进行分析。结果表明,根据患者独特的解剖和手术史选择重做PT方法可能会大大改善功能结果,强调个性化策略的潜力,以提高需要再次手术的患者的恢复和长期生活质量。结论:研究结果表明,与其他技术相比,Swenson重做PT方法具有更好的肠功能预后。虽然重做PT手术在减少大便失禁方面是有效的,但小肠结肠炎的发生率在各种方法中保持一致。
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引用次数: 0
PostKasai Portoenterostomy Dissection of a Branch of the Right Hepatic Artery - A Rare Complication. 后开赛门肠造口术分离右肝动脉分支-一罕见并发症。
Q3 Medicine Pub Date : 2025-05-01 Epub Date: 2025-04-14 DOI: 10.4103/jiaps.jiaps_286_24
Charu Sharma, Nitinkumar Borkar, Revanth Kalla, C Ashwin, Nihar Kathrani

Hepatic artery branch dissection is a lesser-known complication after biliary atresia surgery. The presentation is massive upper gastrointestinal bleeding and rapid drop in hemoglobin levels. We present a 6-week-old infant with biliary atresia who had dissection of a branch of the right hepatic artery which was managed by angioembolization.

肝动脉分支剥离是胆道闭锁术后较不为人所知的并发症。表现为上消化道大量出血和血红蛋白水平迅速下降。我们提出了一个6周大的婴儿胆道闭锁谁有夹层的右肝动脉分支是由血管栓塞管理。
{"title":"PostKasai Portoenterostomy Dissection of a Branch of the Right Hepatic Artery - A Rare Complication.","authors":"Charu Sharma, Nitinkumar Borkar, Revanth Kalla, C Ashwin, Nihar Kathrani","doi":"10.4103/jiaps.jiaps_286_24","DOIUrl":"10.4103/jiaps.jiaps_286_24","url":null,"abstract":"<p><p>Hepatic artery branch dissection is a lesser-known complication after biliary atresia surgery. The presentation is massive upper gastrointestinal bleeding and rapid drop in hemoglobin levels. We present a 6-week-old infant with biliary atresia who had dissection of a branch of the right hepatic artery which was managed by angioembolization.</p>","PeriodicalId":16069,"journal":{"name":"Journal of Indian Association of Pediatric Surgeons","volume":"30 3","pages":"422-423"},"PeriodicalIF":0.0,"publicationDate":"2025-05-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12094607/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144127809","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Pediatric Lipoblastoma: A Case Report in a 2-year-old Girl. 小儿脂肪母细胞瘤:1例2岁女童。
Q3 Medicine Pub Date : 2025-05-01 Epub Date: 2025-02-20 DOI: 10.4103/jiaps.jiaps_239_24
Amar Shah, Ria Sharma, Anirudh Shah

Adipose tumors constitute only 6% of all soft-tissue neoplasms in the first two decades of life, with lipoblastomas accounting for one-third of these cases. Predominantly seen in children under 3 years old, preoperative diagnosis is challenging due to their heterogeneity and similarity to other lipomatous tumors. Surgical excision and histology remain essential for definitive diagnosis. We report the case of a 2-year-old girl with a right infraclavicular lipoblastoma.

在生命的前20年,脂肪肿瘤仅占所有软组织肿瘤的6%,而脂肪母细胞瘤占这些病例的三分之一。主要见于3岁以下儿童,由于其异质性和与其他脂肪瘤性肿瘤的相似性,术前诊断具有挑战性。手术切除和组织学检查仍然是明确诊断的必要条件。我们报告一例2岁女童右锁骨下脂肪母细胞瘤。
{"title":"Pediatric Lipoblastoma: A Case Report in a 2-year-old Girl.","authors":"Amar Shah, Ria Sharma, Anirudh Shah","doi":"10.4103/jiaps.jiaps_239_24","DOIUrl":"10.4103/jiaps.jiaps_239_24","url":null,"abstract":"<p><p>Adipose tumors constitute only 6% of all soft-tissue neoplasms in the first two decades of life, with lipoblastomas accounting for one-third of these cases. Predominantly seen in children under 3 years old, preoperative diagnosis is challenging due to their heterogeneity and similarity to other lipomatous tumors. Surgical excision and histology remain essential for definitive diagnosis. We report the case of a 2-year-old girl with a right infraclavicular lipoblastoma.</p>","PeriodicalId":16069,"journal":{"name":"Journal of Indian Association of Pediatric Surgeons","volume":"30 3","pages":"390-393"},"PeriodicalIF":0.0,"publicationDate":"2025-05-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12094579/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144127749","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
期刊
Journal of Indian Association of Pediatric Surgeons
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