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Journal of Neonatal Surgery最新文献

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Triple atresia: Staged repair 三闭锁:分阶段修复
Journal of Neonatal Surgery Pub Date : 2023-01-03 DOI: 10.47338/jns.v12.1105
Meryem Unal, Muhammad Fadli Abdullah, Hazlina Mohd Khalid, Mughni Bahari
{"title":"Triple atresia: Staged repair","authors":"Meryem Unal, Muhammad Fadli Abdullah, Hazlina Mohd Khalid, Mughni Bahari","doi":"10.47338/jns.v12.1105","DOIUrl":"https://doi.org/10.47338/jns.v12.1105","url":null,"abstract":"","PeriodicalId":34201,"journal":{"name":"Journal of Neonatal Surgery","volume":" ","pages":""},"PeriodicalIF":0.0,"publicationDate":"2023-01-03","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"43249437","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
Constrained evidence-based practice 受限循证实践
Journal of Neonatal Surgery Pub Date : 2023-01-03 DOI: 10.47338/jns.v12.1174
Laraib Amjad Dudrah, Bilal Mirza
{"title":"Constrained evidence-based practice","authors":"Laraib Amjad Dudrah, Bilal Mirza","doi":"10.47338/jns.v12.1174","DOIUrl":"https://doi.org/10.47338/jns.v12.1174","url":null,"abstract":"","PeriodicalId":34201,"journal":{"name":"Journal of Neonatal Surgery","volume":" ","pages":""},"PeriodicalIF":0.0,"publicationDate":"2023-01-03","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"43474955","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
Fetal Lung Interstitial Tumor (FLIT): A case series 胎儿肺间质性肿瘤(FLIT):一个病例系列
Journal of Neonatal Surgery Pub Date : 2023-01-03 DOI: 10.47338/jns.v12.1141
Kah Ann Ho, N. Fuentes-Bolanos, A. Gifford, A. Jiwane, D. Wanaguru
{"title":"Fetal Lung Interstitial Tumor (FLIT): A case series","authors":"Kah Ann Ho, N. Fuentes-Bolanos, A. Gifford, A. Jiwane, D. Wanaguru","doi":"10.47338/jns.v12.1141","DOIUrl":"https://doi.org/10.47338/jns.v12.1141","url":null,"abstract":"Background: Fetal Lung Interstitial Tumor (FLIT) is a rare benign lung tumor. There have been 18 cases of FLIT described in the literature. FLIT is characterized by a region of arrested lung development and must be differentiated from other congenital lung lesions with poorer prognoses.\u0000Case Presentation: We report the first two known cases of FLIT in Australia and New Zealand. In both cases, the patients developed respiratory distress at birth requiring intubation. Imaging revealed solid lesions and echocardiography demonstrated pulmonary hypertension. The patients underwent surgical resection without any complications or recurrence.\u0000Conclusion: FLIT is a rare benign congenital lung tumor that can be adequately managed with surgical resection.","PeriodicalId":34201,"journal":{"name":"Journal of Neonatal Surgery","volume":" ","pages":""},"PeriodicalIF":0.0,"publicationDate":"2023-01-03","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"43707033","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: 2
Improvement of Broviac catheter-related outcomes after the implementation of a quality management system: A before-and-after prospective observational study 实施质量管理体系后布洛维亚克导管相关结果的改善:一项前后前瞻性观察研究
Journal of Neonatal Surgery Pub Date : 2023-01-03 DOI: 10.47338/jns.v12.1156
Manel Kammoun, A. Jarraya, S. Ammar, K. Kolsi
{"title":"Improvement of Broviac catheter-related outcomes after the implementation of a quality management system: A before-and-after prospective observational study","authors":"Manel Kammoun, A. Jarraya, S. Ammar, K. Kolsi","doi":"10.47338/jns.v12.1156","DOIUrl":"https://doi.org/10.47338/jns.v12.1156","url":null,"abstract":"Background: Because of the high rates of Broviac catheter complications, we started an urgent quality process to reduce this morbidity. The aim is to assess the efficiency of the main actions we have taken in enhancing our practice and improving Broviac outcomes.\u0000Methods: We included all neonates and young infants requiring surgical central venous access using a Broviac tunneled catheter. We compared the catheters’ outcomes before and after the implementation of a quality program based on a nurse teaching program, patient selection, and catheter management multidisciplinary protocol. The significance threshold was set at p<0.05.\u0000Results: We included 94 patients: 51 in the protocol group and 43 in the control group. The complication rate was reduced from 60.3% to 25.5% with p=0.001. The lifetime of the catheter was improved from 11.3 ± 4.3 days to 19.1 ± 9 days with p=0.007. The catheter infection was reduced from 65.3% to 46.1% with p≤0.001.\u0000Conclusion: This quality improvement project shows the utility of a quality assurance program based on careful indications and patient selection, a nursing teaching program, and a multidisciplinary catheter management protocol, in reducing Broviac catheter-related morbidity.","PeriodicalId":34201,"journal":{"name":"Journal of Neonatal Surgery","volume":" ","pages":""},"PeriodicalIF":0.0,"publicationDate":"2023-01-03","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"44520945","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: 2
My journey with the Journal of Neonatal Surgery 我的新生儿外科杂志之旅
Journal of Neonatal Surgery Pub Date : 2022-12-27 DOI: 10.47338/jns.v11.1173
Parveen Kumar
{"title":"My journey with the Journal of Neonatal Surgery","authors":"Parveen Kumar","doi":"10.47338/jns.v11.1173","DOIUrl":"https://doi.org/10.47338/jns.v11.1173","url":null,"abstract":"","PeriodicalId":34201,"journal":{"name":"Journal of Neonatal Surgery","volume":" ","pages":""},"PeriodicalIF":0.0,"publicationDate":"2022-12-27","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"43550083","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
Hernia of umbilical cord containing gallbladder 含胆囊脐带疝
Journal of Neonatal Surgery Pub Date : 2022-12-12 DOI: 10.47338/jns.v11.1124
Krioudj Samia, Samari Bilel Zakaria, Zineddine Soualili
{"title":"Hernia of umbilical cord containing gallbladder","authors":"Krioudj Samia, Samari Bilel Zakaria, Zineddine Soualili","doi":"10.47338/jns.v11.1124","DOIUrl":"https://doi.org/10.47338/jns.v11.1124","url":null,"abstract":"An 11-day-old male neonate delivered by C-section presented to the emergency department with the misdiagnosis of umbilical hernia. The physical examination found a hernia of the umbilical cord with a defect of 3cm, and a small non-reducible umbilical mass covered with a thick and opaque membrane. The newborn has no other physical anomalies. Laboratory tests were also within normal ranges. The abdominal US was poorly contributive, and the radiologist concluded that there is an intraperitoneal structure within the sac without anomalies of the hepato-biliary and urinary tracts.","PeriodicalId":34201,"journal":{"name":"Journal of Neonatal Surgery","volume":" ","pages":""},"PeriodicalIF":0.0,"publicationDate":"2022-12-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"45658062","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: 1
Total colonic aganglionosis in a case of anorectal malformation: A case report 肛肠畸形致全结肠神经节病1例
Journal of Neonatal Surgery Pub Date : 2022-12-06 DOI: 10.47338/jns.v11.1100
D. K. Garnaik, Rajat Piplani, S. Tomar, P. Kothari
{"title":"Total colonic aganglionosis in a case of anorectal malformation: A case report","authors":"D. K. Garnaik, Rajat Piplani, S. Tomar, P. Kothari","doi":"10.47338/jns.v11.1100","DOIUrl":"https://doi.org/10.47338/jns.v11.1100","url":null,"abstract":"Background: Hirschsprung’s disease (HD) rarely co-occurs with anorectal malformation (ARM). If it occurs, the classical variety of HD is mostly associated. Total Colonic Aganglionosis (TCA) in a case with ARM is exceedingly rare.\u0000Case Presentation: A 3-day-old female neonate presented with neonatal intestinal obstruction. of such a rare association. Examination revealed a perineal fistula. A colostomy was formed for persistent abdominal distension, but it did not work properly. Re-exploration revealed TCA with a transition zone at the level of the terminal ileum.\u0000Conclusion: Though ARM is associated with several anomalies of various body systems, its association with TCA is exceedingly rare.","PeriodicalId":34201,"journal":{"name":"Journal of Neonatal Surgery","volume":" ","pages":""},"PeriodicalIF":0.0,"publicationDate":"2022-12-06","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"43106361","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
Coexistence of ‘Friemann-Dahl sign’ and ‘Neuhauser’s sign’ in a newborn: A diagnostic dilemma 新生儿“Friemann-Dahl征”和“Neuhauser征”的共存：诊断困境
Journal of Neonatal Surgery Pub Date : 2022-12-05 DOI: 10.47338/jns.v11.1137
Venkatachalam Raveenthiran
{"title":"Coexistence of ‘Friemann-Dahl sign’ and ‘Neuhauser’s sign’ in a newborn: A diagnostic dilemma","authors":"Venkatachalam Raveenthiran","doi":"10.47338/jns.v11.1137","DOIUrl":"https://doi.org/10.47338/jns.v11.1137","url":null,"abstract":"Friemann-Dahl sign is the radiological appearance of three dense lines in the abdomen converging towards the left iliac fossa. It is caused by the apposing walls of the twisted sigmoid colon (sigmoid volvulus). [1] This appearance is also variously known as the ‘omega sign’, ‘bent inner-tube sign’, ‘horse-shoe sign’, ‘convergence sign’, or ‘coffee-bean sign’. Neuhauser’s sign is a soap-bubble like appearance in the right iliac fossa. It is caused by tiny air bubbles entrapped within the viscid meconium of cystic fibrosis. [2] Originally this sign was considered pathognomonic of meconium ileus; but subsequently, it was also reported in necrotizing enterocolitis, Hirschsprung disease, and anal stenosis. [3, 4] Concomitance of both the Friemann-Dahl’s sign and the Neuhauser’s sign in a neonate caused a diagnostic dilemma.","PeriodicalId":34201,"journal":{"name":"Journal of Neonatal Surgery","volume":" ","pages":""},"PeriodicalIF":0.0,"publicationDate":"2022-12-05","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"46283649","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
Double meningomyelocele - a rare variant of neural tube defect: A case series 双脊膜膨出-一种罕见的神经管缺损:一个病例系列
Journal of Neonatal Surgery Pub Date : 2022-11-29 DOI: 10.47338/jns.v11.1126
Md Mokarram Ali, Y. Kadian
{"title":"Double meningomyelocele - a rare variant of neural tube defect: A case series","authors":"Md Mokarram Ali, Y. Kadian","doi":"10.47338/jns.v11.1126","DOIUrl":"https://doi.org/10.47338/jns.v11.1126","url":null,"abstract":"Background: A neural tube defect is a common congenital malformation and it commonly presents as an isolated cystic swelling on the back, anywhere from occiput to sacrum. However, multiple neural tube defects are rare with less than 100 cases reported worldwide.\u0000Case Presentation: We are reporting two cases of multiple neural tube defects that presented in the newborn period with a history of concurrent swellings along the midline on the back. They were evaluated with ultrasonography and the diagnosis of double meningomyelocele was confirmed. Subsequently, they were operated on, both the lesions were excised, and the defects were repaired simultaneously.\u0000Conclusion: Double meningomyelocele is a rare form of neural tube defect. Due to its rarity, exact embryogenesis is not known and thus, there is a need for further study on its embryology.","PeriodicalId":34201,"journal":{"name":"Journal of Neonatal Surgery","volume":" ","pages":""},"PeriodicalIF":0.0,"publicationDate":"2022-11-29","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"42410852","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
Idiopathic congenital lymphedema in a neonate 新生儿特发性先天性淋巴水肿
Journal of Neonatal Surgery Pub Date : 2022-11-27 DOI: 10.47338/jns.v11.1140
Sengua Koipapi, D. Msuya, Joshua Tadayo, J. Lodhia
{"title":"Idiopathic congenital lymphedema in a neonate","authors":"Sengua Koipapi, D. Msuya, Joshua Tadayo, J. Lodhia","doi":"10.47338/jns.v11.1140","DOIUrl":"https://doi.org/10.47338/jns.v11.1140","url":null,"abstract":"A 16-day-old male neonate was referred with","PeriodicalId":34201,"journal":{"name":"Journal of Neonatal Surgery","volume":" ","pages":""},"PeriodicalIF":0.0,"publicationDate":"2022-11-27","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"47041325","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
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