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Keywords Ventriculoperitoneal shunt in ...

Ventriculoperitoneal shunt in congenital hydrocephalus

https://read.qxmd.com/read/38604086/utility-of-intracranial-pressure-monitoring-as-a-diagnostic-tool-in-pediatric-ventriculomegaly
#1
JOURNAL ARTICLE
Mason M Richardson, Thomas Larrew, Steven Lin, Mohammed Alshareef, Joseph T Vasas, Libby Infinger, Ramin Eskandari
OBJECTIVE: Intracranial pressure (ICP) monitoring is commonly utilized for identifying pathologic ICP in cases of traumatic brain injury; however, its utility in hydrocephalic children has not been elucidated. Although patients with typical (pressure-active) hydrocephalus present with clear signs and/or symptoms and the need for cerebrospinal fluid (CSF) diversion is often clear, others may have arrested or pressure-compensated hydrocephalus with pathologic ICP elevation masked by ambiguous signs or are completely asymptomatic...
April 6, 2024: Clinical Neurology and Neurosurgery
https://read.qxmd.com/read/38558721/diagnostic-pitfalls-of-macrocephaly-and-intracranial-dural-arteriovenous-fistulas-connecting-the-dots-with-the-red-flags
#2
Alina Andrei, Thomas Saliba, Boris Lubicz, Christophe Fricx
Macrocephaly is defined as an abnormal increase in head circumference greater than two standard deviations above the mean for a given age and sex. We present the case of a 16-month-old boy with congenital progressive macrocephaly, who was referred to our hospital for a ventriculoperitoneal shunt placement for external hydrocephalus diagnosed at 13 months of age. The patient had a febrile seizure 12 hours after the shunt was placed and the emergency CT exam revealed collapsed ventricles and a right frontal subdural collection, suggestive of an over-drainage and intracranial hypotension...
February 2024: Curēus
https://read.qxmd.com/read/38449361/congenital-toxoplasmosis-and-long-term-outcomes
#3
JOURNAL ARTICLE
Ozlem Ozgur Gundeslioglu, Zeliha Haytoglu, Ebru Esen, Derya Alabaz, Ummuhan Cay, Ferda Ozlu, Filiz Kibar, Salih Cetiner
OBJECTIVE: Congenital toxoplasmosis (CT) can have severe early and late sequelae in children. In this study, we aimed to evaluate the demographic, clinical, treatment characteristics of patients diagnosed with congenital Toxoplasma infection and to highlight the long-term complications of the patients. METHODS: Patients with CT were included in this study who were followed between 2010 and 2022 in Cukurova University Medical Faculty Hospital. Demographic, clinical and treatment characteristics were searched retrospectively...
March 5, 2024: Türkiye Parazitolojii Dergisi
https://read.qxmd.com/read/38358179/anesthetic-management-in-a-huge-hydrocephalus
#4
Neha Kumari, Amritha Sai, Aditya Sharma, Archana Kachhap, Dipali Singh, Tushar Kumar
The pediatric age group with massive hydrocephalus posted for ventriculoperitoneal (VP) shunt presents a lot of confrontation to anesthesiologists due to macrocephalus and associated congenital anomalies. Here, we presented a case report with massive hydrocephalus with aqueduct stenosis, posted for VP shunt placement, and retained a difficult airway.
2024: Annals of African Medicine
https://read.qxmd.com/read/38357406/an-atypical-presentation-of-pancreatitis-secondary-to-a-ventriculoperitoneal-shunt
#5
Tasciana T Gordon, Katherine Goodall, Joanne Dale
Ventriculoperitoneal (VP) shunts are catheters inserted to drain excess cerebrospinal fluid (CSF) when there is an obstruction in the normal outflow or a decreased absorption of the fluid leading to hydrocephalus. Recognised complications of placement of the distal catheter are malposition, obstruction, pseudocysts and infection. Here, we present a case of a 23-year-old female with acute pancreatitis following the placement of a VP shunt in the lesser sac. The patient originally had a VP shunt placed in infancy for congenital hydrocephalus with one revision at four years old...
February 2024: Curēus
https://read.qxmd.com/read/38342093/double-myelomeningocele-repair-by-fetal-surgery-with-a-single-micro-hysterotomy
#6
Felipe Chavelas-Ochoa, Ma de la Luz Bermúdez-Rojas, Virginia Medina-Jiménez, Antonio Helue-Mena, Savino Gil-Pugliese, Ivan Gutiérrez-Gómez, Miguel Martínez-Rodríguez, Carmen Julia Gaona-Tapia, Rosa Villalobos-Gómez, Karla Aguilar-Vidales, Rogelio Cruz-Martínez
INTRODUCTION: Open spina bifida (OSB) is the most common congenital anomaly of the central nervous system. It is associated with severe neurodevelopmental delay, motor impairment, hydrocephalus, and bowel and bladder dysfunction. In selected cases, intrauterine spina bifida repair has been shown to improve neonatal outcomes. Rarely, the spine can have a double defect compromising two different segments and there is a lack of evidence on the feasibility and benefits of intrauterine repair in these cases...
February 9, 2024: Pediatric Neurosurgery
https://read.qxmd.com/read/38234714/bowel-perforation-and-anal-ventriculoperitoneal-shunt-migration-a-systematic-review
#7
REVIEW
Khelifa Adel, Aichaoui Fayçal, Bennafaa Toufik, Morsli Abdelhalim
BACKGROUND: One of the most feared complications of hydrocephalus is shunt migration. Although rare, bowel migration is the most commonly encountered type of migration. The relatively high frequency of this occurrence allowed us to gather a substantial number of reports for study. OBJECTIVES: The aim of this study was to better understand this complication and aid in decreasing its incidence. METHODS: The PubMed and Scopus databases were searched for cases of anal shunt migration...
April 2024: Journal of Taibah University Medical Sciences
https://read.qxmd.com/read/38217730/navigating-the-complexities-of-encephalocraniocutaneous-lipomatosis-a-case-series-and-review
#8
JOURNAL ARTICLE
Marco Pavanello, Liliana Piro, Arianna Roggero, Andrea Rossi, Matteo Cataldi, Gianluca Piatelli
INTRODUCTION: Encephalocraniocutaneous lipomatosis (ECCL) is a rare congenital syndrome with complex skin, eye, and central nervous system (CNS) symptoms. Diagnosis and treatment are challenging due to its rarity and diverse manifestations. It often involves issues like porencephalic cysts, cortical atrophy, and low-grade gliomas in the CNS, resulting in developmental delays. The spinal cord is frequently affected, leading to problems like medullary compression and radiculopathy, causing back pain and sensory/motor deficits...
January 13, 2024: Child's Nervous System: ChNS: Official Journal of the International Society for Pediatric Neurosurgery
https://read.qxmd.com/read/38178931/migration-of-the-distal-ventriculoperitoneal-shunt-catheter-into-the-stomach-with-or-without-trans-oral-extrusion-a-systematic-literature-review-and-meta-analysis
#9
JOURNAL ARTICLE
Rajendra Kumar Ghritlaharey
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...
December 9, 2023: World Journal of Clinical Pediatrics
https://read.qxmd.com/read/38116348/closed-loop-bowel-obstruction-induced-by-ventriculoperitoneal-shunt-catheter-coiling-at-the-sigmoid-colon-a-case-report
#10
Rinad M AlJoaid, Hawra H Alshakhori, Arwaa Haji, Dunya Alfaraj, Murad F Alabbad
Intestinal obstruction is a rarely encountered complication in patients with ventriculoperitoneal (VP) shunt. The most common causes of bowel obstruction in this subset of patients include volvulus, formation of a spontaneous knot, and adhesions. Herein, we report a 21-year-old bedridden male with a history of congenital hydrocephalus on VP shunt, spina bifida, neurogenic bladder, and paraplegia who presented with a seven-day history of abdominal discomfort, distention, constipation, vomiting, and intolerance to oral intake...
November 2023: Curēus
https://read.qxmd.com/read/38113564/dandy-walker-malformation-associated-with-subarachnoid-hemorrhage-a-case-report
#11
Razan S Samman, Mohamed K Gomaa, Bassem Y Sheikh
INTRODUCTION: Dandy-Walker malformation is a rare congenital brain defect characterized by vermian agenesia with cystic dilatation of the fourth ventricle, and posterior fossa enlargement. The etiology is still poorly understood but is presupposed to be multifactorial, infrequently caused by intracranial hemorrhage. We describe a case of male newborn known to have Dandy-Walker malformation associated with subarachnoid bleeding after the delivery, which is a quiet rare presentation only discussed in a few literatures before...
January 2024: International Journal of Surgery Case Reports
https://read.qxmd.com/read/38043518/persistent-hydrocephalus-shunt-and-subglottic-stenosis-in-a-newborn-with-plasminogen-deficiency-due-to-delayed-treatment-with-plasminogen-concentrates-a-case-report
#12
Benedikt Stephan Biesinger, Christoph Male, Veronika Kranebitter, Julia Binder, Martin B Niederle, Andrea Reinprecht, Christoph Binder
INTRODUCTION: Here we present the case of a newborn baby boy with severe plasminogen deficiency causing occlusive hydrocephalus and ligneous conjunctivitis. CASE PRESENTATION: Shortly after birth, the hydrocephalus was treated with a ventriculoperitoneal shunt implantation. However, the child had to be readmitted soon afterward because of shunt obstruction. Subglottic microtrauma caused by the necessary intubations then led to another life-threatening complication - subglottic stenosis with pseudomembrane formation...
December 1, 2023: Neonatology
https://read.qxmd.com/read/38024033/retrospective-examination-of-infants-with-congenital-neural-tube-defect
#13
JOURNAL ARTICLE
İsmail Hakki Özcan, Murat Yücel, Hasan Kahveci
INTRODUCTION: In the present study, neonates presenting with neural tube defects (NTDs) and undergoing observation within the confines of the neonatal intensive care unit (NICU) were subjected to a comprehensive assessment encompassing concurrent morbidities, clinical manifestations, laboratory parameters, and instituted interventions. MATERIALS AND METHODS: A retrospective examination was conducted on the medical records of 135 neonates diagnosed with congenital NTD within the temporal span from 2008 to 2018...
November 2023: Curēus
https://read.qxmd.com/read/37939879/profile-of-pediatric-neurosurgery-in-nigeria-from-1962-to-2021-a-systematic-review
#14
JOURNAL ARTICLE
Toyin A Oyemolade, Benjamin Mukumbya, Ehita N Oboh, Shiva A Nischal, Ifeanyichukwu Ozobu, Adhith Palla, Olaniyi D Ogundeji, Yesel Trillo-Ordonez, Evaristus E Nwaribe, Oluwakemi A Badejo, Oghenekevwe E Okere, Toluyemi A Malomo, Nancy Abu-Bonsrah, Oboh Ena, Andreas Seas, Megan E H Still, Isaac Asemota, Chiazam Ugorji, Padmavathi Reddy, Raphia Rahman, Romaric Waguia-Kouam, Di D Deng, Megan von Isenburg, Michael M Haglund, Anthony T Fuller, Amos O Adeleye, Alvan-Emeka K Ukachukwu
OBJECTIVE: This study aims to provide a comprehensive overview of pediatric neurosurgery in Nigeria, since 1962, by assessing epidemiological data, management strategies, and case outcomes. METHODS: A systematic bibliometric review of Nigerian neurosurgical literature was reported with the PRISMA guidelines. The Risk of Bias Assessment Tool was applied to all non-randomized studies, and a descriptive analysis was performed for all variables. RESULTS: We identified 12,295 pediatric patients from 196 published studies...
November 6, 2023: World Neurosurgery
https://read.qxmd.com/read/37933337/diagnosis-and-treatment-of-dandy-walker-syndrome-with-two-types-of-ventriculoperitoneal-vp-shunts-a-case-report
#15
Mohammed Khaleel I Kh Almadhoun, Abdallah Wasel Hattab, Nemer Nedal Alazzeh, Sufyan Taleb Aladwan, Osamah Ta'amneh
Dandy-Walker Syndrome (DWS) is a rare congenital neurological condition characterized by cerebellar and posterior fossa malformations, often presenting a variable clinical spectrum. Common complications include hydrocephalus, necessitating interventions like ventriculoperitoneal (VP) shunts, and endoscopic third ventriculostomy (ETV). We describe the case of a five-month-old infant conceived through in vitro fertilization (IVF), initially presenting with cold-like symptoms, later diagnosed with DWS. The patient underwent VP shunt placement for hydrocephalus management, with subsequent complications requiring shunt revisions and ETV...
October 2023: Curēus
https://read.qxmd.com/read/37846534/surgery-of-cranial-deformity-following-ventricular-shunting-a-multicenter-study
#16
MULTICENTER STUDY
Burak Gezer, Mevlut Ozgur Taskapilioglu, Murat Zaimoglu, Tuba Morali Guler, Gokmen Kahilogullari, Hakan Karabagli
AIM: To review the cases of craniosynostosis secondary to ventricular shunting procedure. MATERIAL AND METHODS: We retrospectively evaluated the medical records of all pediatric patients with hydrocephalus who were treated with ventriculoperitoneal shunt procedure between the years 2017 and 2021 at the Selcuk University, Ankara University, and Bursa Uludag University. RESULTS: Twenty-one patients were included in the study. The median age at the time of insertion of ventriculoperitoneal shunt for hydrocephalus was 8...
2023: Turkish Neurosurgery
https://read.qxmd.com/read/37818495/recurrent-meningitis-and-its-rare-association-with-ligneous-conjunctivitis-and-congenital-plasminogen-deficiency
#17
Somayah A Alghubaishi, Muhammad Saeed, Fadi Abujamous, Hussam Osman, Badriah G Alasmari
This case report explores the rare association of recurrent meningitis, hydrocephalus, ligneous conjunctivitis, and congenital plasminogen deficiency in a term baby boy. Born at 39 weeks with a history of hydrocephalus, the neonate later developed ligneous conjunctivitis and a serious bout of meningitis. Genetic analyses confirmed a homozygous mutation in the PLG gene, indicative of congenital plasminogen deficiency. Despite intensive treatment, including a ventriculoperitoneal shunt for hydrocephalus and intravenous antibiotics for meningitis, the child succumbed to upper airway obstruction before reaching one year of age...
September 2023: Curēus
https://read.qxmd.com/read/37768257/cerebrospinal-fluid-as-vaginal-discharge-ventriculoperitoneal-shunt-migration-following-cesarean-section
#18
JOURNAL ARTICLE
Steffanie R Wright, Lauryn C Gabby, Brian T Nguyen
Congenital hydrocephalus was once a permanently disabling and even fatal disease. With the advent of ventriculoperitoneal shunts, affected women are now surviving to their reproductive years and beyond. Pregnancy outcomes in this population are generally positive. However due to possible shunt complications, including infection, migration, and organ perforation, perinatal care for pregnant individuals with a ventriculoperitoneal shunt is complex and requires input from both obstetric and neurosurgical providers...
October 2023: Minerva obstetrics and gynecology
https://read.qxmd.com/read/37715604/perinatal-presentation-of-a-congenital-intramedullary-capillary-hemangioma-in-a-neonate-born-with-hydrocephalus-and-paraplegia
#19
JOURNAL ARTICLE
Mohammad Ohadi, Seyed Farzad Maroufi, Keyvan Tayebi Meybodi, Moeinadin Safavi, Farideh Nejat, Zohreh Habibi
Spinal intramedullary capillary hemangioma is a rare condition. Although most spinal/spinal cord hemangiomas are inborn in origin, perinatal presentation is uncommon. We present a neonate with an intramedullary hemangioma, born with communicating hydrocephalus and complete paraplegia. Spinal imagining showed an intradural mass with hemorrhagic foci, a low-lying conus medullaris, and scalloping of dorsal elements. Ventriculoperitoneal shunting was performed in an emergent setting, with cerebrospinal fluid showing a brownish appearance with high viscosity which implied a possible old hemorrhage...
2023: Turkish Neurosurgery
https://read.qxmd.com/read/37700950/programmable-versus-differential-pressure-ventriculoperitoneal-shunts-for-pediatric-hydrocephalus-a-20-year-single-center-experience-from-saudi-arabia
#20
JOURNAL ARTICLE
Soha A Alomar, Rothina J Saiedi, Sultan M Albukhari, Majd M Ahmad, Ghaidaa Sindi, Mai Kadi, Saleh S Baeesa
Background Shunt malfunction is the most common complication after ventriculoperitoneal shunt (VPS) insertion for pediatric hydrocephalus. The incidence of shunt malfunction and the need for VPS revision may be related to the type of valve used in the shunt. Therefore, we aimed to compare the outcome of VPS in the pediatric age group stratified by differential pressure valves (DPV) and programmable shunt valves (PSV). Materials and methods This ethics-approved retrospective study was conducted at a tertiary care hospital in Saudi Arabia...
August 2023: Curēus
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