远端脑室腹腔分流导管移位至胃部,伴有或不伴有经口挤压:系统性文献综述和荟萃分析

R. Ghritlaharey
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The first case of migration of a VPS catheter into the stomach was reported in the year 1980, and the data were retrieved from 1980 to December 2022. Cases were categorized into two groups; Group A: Cases who had migration of the distal VPS catheter into the stomach and clinically presented with trans-oral extrusion of the same, and Group B: Cases who had migration of the distal VPS catheter into the stomach, but presented without trans-oral extrusion.\n RESULTS\n A total of n = 46 cases (n = 27; 58.69% male, and n = 19; 41.3% females) were recruited for the systematic review. Group A included n = 32, and Group B n = 14 cases. Congenital hydrocephalus was the indication for the primary VPS insertion for approximately half of the (n = 22) cases. Approximately sixty percent (n = 27) of them were children ≤ 5 years of age at the time of the diagnosis of the complication mentioned above. 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引用次数: 0

摘要

背景远端脑室腹腔分流(VPS)导管胃内移位,临床表现为或不伴有经口挤压,是VPS导管置入的罕见并发症之一。目的:探讨伴有或不伴有经口挤压的VPS远端导管胃内移位的患者的人口学特征、临床表现、临床表现和手术治疗结果。方法在线检索与上述VPS并发症相关的已发表/可获得的文献。论文从PubMed, PMC (PubMed Central), ResearchGate和Google Scholar数据库中检索,使用与VPS并发症相关的各种术语。第一例VPS导管移入胃的病例于1980年报道,数据检索时间为1980年至2022年12月。病例分为两组;A组:VPS远端导管移入胃,临床表现为经口挤压;B组:VPS远端导管移入胃,但未表现为经口挤压。结果共n = 46例(n = 27;男性58.69%,n = 19;(41.3%女性)纳入系统评价。A组32例,B组14例。先天性脑积水是约一半(n = 22)病例的原发性VPS插入指征。其中约60% (n = 27)为诊断上述并发症时≤5岁的儿童。在72% (n = 33)的病例中,该并发症在VPS插入/最后一次分流器翻修后24个月内被发现。A组全部病例临床诊断明显。采用多种诊断方法对B组病例进行诊断。两组共43例,采用多种手术方式处理并发症。在两例中,在尸检过程中检测到远端VPS导管的胃内移位。该审查记录了4例死亡。结论VPS导管腹膜端胃内移位是VPS导管植入术治疗脑积水的罕见并发症之一。虽然在成人和老年人中也有报道,但在儿童中更常见。对于一例临床表现为无经口挤压的远端VPS导管胃内移位病例的诊断,需要高度的临床怀疑。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Migration of the distal ventriculoperitoneal shunt catheter into the stomach with or without trans-oral extrusion: A systematic literature review and meta-analysis
BACKGROUND Intra-gastric migration of the distal ventriculoperitoneal shunt (VPS) catheter clinically presenting with or without trans-oral extrusion is one of the rare complications of VPS catheter insertion. AIM To identify the demographics, clinical presentation, clinical findings, and results of surgical therapy offered for the treatment of intra-gastric migration of the distal VPS catheter, clinically presented with or without trans-oral extrusion. METHODS An online search was performed for the extraction/retrieval of the published/ available literature pertaining to the above-mentioned VPS complication. Manuscripts were searched from PubMed, PMC (PubMed Central), ResearchGate, and Google Scholar databases using various terminology relating to the VPS complications. The first case of migration of a VPS catheter into the stomach was reported in the year 1980, and the data were retrieved from 1980 to December 2022. Cases were categorized into two groups; Group A: Cases who had migration of the distal VPS catheter into the stomach and clinically presented with trans-oral extrusion of the same, and Group B: Cases who had migration of the distal VPS catheter into the stomach, but presented without trans-oral extrusion. RESULTS A total of n = 46 cases (n = 27; 58.69% male, and n = 19; 41.3% females) were recruited for the systematic review. Group A included n = 32, and Group B n = 14 cases. Congenital hydrocephalus was the indication for the primary VPS insertion for approximately half of the (n = 22) cases. Approximately sixty percent (n = 27) of them were children ≤ 5 years of age at the time of the diagnosis of the complication mentioned above. In seventy-two percent (n = 33) cases, this complication was detected within 24 mo after the VPS insertion/last shunt revision. Clinical diagnosis was evident for the entire group A cases. Various diagnostic modalities were used to confirm the diagnosis for Group B cases. Various surgical procedures were offered for the management of the complication in n = 43 cases of both Groups. In two instances, intra-gastric migration of the distal VPS catheter was detected during the autopsy. This review documented four deaths. CONCLUSION Intra-gastric migration of the peritoneal end of a VPS catheter is one of the rare complications of VPS catheter implantation done for the treatment of hydrocephalus across all age groups. It was more frequently reported in children, although also reported in adults and older people. A very high degree of clinical suspicion is required for the diagnosis of a case of an intra-gastric migration of the distal VPS catheter clinically presenting without trans-oral extrusion.
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