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1.
Br J Neurosurg ; 37(3): 476-479, 2023 Jun.
Artigo em Inglês | MEDLINE | ID: mdl-31852253

RESUMO

BACKGROUND: Syringomyelia is a rare disorder but its impact on patients' quality of life can be devastating. The exact pathophysiology remains unknown; the syrinx can either be idiopathic or associated with conditions such as Chiari malformation, scoliosis, malignancy, infection and trauma. Several techniques have been described to decompress syringomyelia with distal drainage to the subarachnoid space, pleura or peritoneum. METHOD: We present a modification of the syringosubarachnoid shunt insertion technique with minimal myelotomy and the use of a T shaped shunt which does not require suturing to the pia matter to prevent shunt migration. CONCLUSION: This technique for syringosubarachnoid shunt insertion is likely to prevent shunt migration and scarring whilst minimizing suturing and optimising syrinx decompression.


Assuntos
Malformação de Arnold-Chiari , Siringomielia , Humanos , Siringomielia/cirurgia , Siringomielia/complicações , Imageamento por Ressonância Magnética/métodos , Qualidade de Vida , Malformação de Arnold-Chiari/cirurgia , Descompressão Cirúrgica/métodos
2.
Acta Neurochir (Wien) ; 163(2): 317-329, 2021 02.
Artigo em Inglês | MEDLINE | ID: mdl-33222008

RESUMO

INTRODUCTION AND OBJECTIVES: The novel severe acute respiratory syndrome coronavirus 2 (COVID-19) pandemic has had drastic effects on global healthcare with the UK amongst the countries most severely impacted. The aim of this study was to examine how COVID-19 challenged the neurosurgical delivery of care in a busy tertiary unit serving a socio-economically diverse population. METHODS: A prospective single-centre cohort study including all patients referred to the acute neurosurgical service or the subspecialty multidisciplinary teams (MDT) as well as all emergency and elective admissions during COVID-19 (18th March 2020-15th May 2020) compared to pre-COVID-19 (18th of January 2020-17th March 2020). Data on demographics, diagnosis, operation, and treatment recommendation/outcome were collected and analysed. RESULTS: Overall, there was a reduction in neurosurgical emergency referrals by 33.6% and operations by 55.6% during the course of COVID-19. There was a significant increase in the proportion of emergency operations performed during COVID-19 (75.2% of total, n=155) when compared to pre-COVID-19 (n = 198, 43.7% of total, p < 0.00001). In contrast to other published series, the 30-day perioperative mortality remained low (2.0%) with the majority of post-operative COVID-19-infected patients (n = 13) having underlying medical co-morbidities and/or suffering from post-operative complications. CONCLUSION: The capacity to safely treat patients requiring urgent or emergency neurosurgical care was maintained at all times. Strategies adopted to enable this included proactively approaching the referrers to maintain lines of communications, incorporating modern technology to run clinics and MDTs, restructuring patient pathways/facilities, and initiating the delivery of NHS care within private sector hospitals. Through this multi-modal approach we were able to minimize service disruptions, the complications, and mortality.


Assuntos
COVID-19/complicações , Neurocirurgia , COVID-19/fisiopatologia , Estudos de Coortes , Comorbidade , Procedimentos Cirúrgicos Eletivos , Serviços Médicos de Emergência , Feminino , Saúde Global , Hospitalização , Humanos , Comunicação Interdisciplinar , Masculino , Procedimentos Neurocirúrgicos , Pandemias , Equipe de Assistência ao Paciente , Segurança do Paciente , Estudos Prospectivos , Encaminhamento e Consulta , SARS-CoV-2 , Medicina Estatal , Reino Unido
3.
Br J Neurosurg ; 26(6): 851-5, 2012 Dec.
Artigo em Inglês | MEDLINE | ID: mdl-22747194

RESUMO

Myelomeningocoele remains a significant neurosurgical challenge. We have carried out a retrospective study evaluating the practices of myelomeningocoele repair at our institute over the last 5 years. Additionally, for patients that have been followed up for at least 12 months, we have investigated parameters describing functional outcome up to this period. With the recent Management of Myelomeningocoele (MOMS) study re-igniting interest in the condition, we aim to provide contemporary practice and outcome data to add to the literature.


Assuntos
Meningomielocele/cirurgia , Derivação Ventriculoperitoneal/métodos , Criança , Pré-Escolar , Feminino , Seguimentos , Humanos , Lactente , Recém-Nascido , Masculino , Meningomielocele/patologia , Estudos Retrospectivos , Resultado do Tratamento , Derivação Ventriculoperitoneal/efeitos adversos
4.
Acta Neurochir (Wien) ; 152(7): 1175-9, 2010 Jul.
Artigo em Inglês | MEDLINE | ID: mdl-20349319

RESUMO

BACKGROUND: To enumerate possible intracranial vascular sequelae of sickle-cell disease, to identify risk factors and outline management strategies. METHOD: Retrospective review of a single unit experience managing vascular intracranial complications of sickle-cell disease from 1995 until 2005. Information such as homozygosity/heterozygosity, duration of disease, disease control as indicated by haematology follow-up, concurrent sickle-cell disease (SCD)-related health problems and neurosurgical management was recorded. The pattern of vascular disease was analysed to reveal possible contributory/risk factors towards development of vascular intracranial complications. SUBJECTS: All patients presenting with vascular intracranial complications of sickle-cell disease from 1995 to 2005 were evaluated. OUTCOME MEASURES: Classification of vascular intracranial complications into one or more of the following categories: aneurysmal subarachnoid haemorrhage, non-aneurysmal subarachnoid/intraventricular haemorrhage and vasculitis. FINDINGS: There were ten patients in the study. All symptomatic vascular intracranial complications of SCD requiring neurosurgical intervention were homozygous for SCD. Aneurysms were likely to be multiple. Ruptured aneursyms in SCD were small (average 4 mm). There was a propensity for aneurysms to occur in the posterior circulation, in particular the posterior cerebral artery was frequently involved. Patients with aneurysms and Moyamoya-type vasculitis were likely to have occlusive disease of the internal carotid arteries. CONCLUSIONS: The vascular intracranial complications of sickle-cell disease have an aggressive natural history. Tight control of SCD may reduce the possibility of complications. Complications that arise should be managed in the context of the disease entity rather than in isolation. Consideration should be given to bypass procedures, parent vessel ligations and revascularization techniques. Transcranial Doppler may be used to identify SCD patients with cerebrovascular occlusive disease, who may have increased risk of aneurysmal rupture.


Assuntos
Anemia Falciforme/complicações , Anemia Falciforme/epidemiologia , Transtornos Cerebrovasculares/classificação , Transtornos Cerebrovasculares/epidemiologia , Adolescente , Adulto , Transtornos Cerebrovasculares/fisiopatologia , Criança , Comorbidade , Feminino , Humanos , Masculino , Pessoa de Meia-Idade , Estudos Retrospectivos , Hemorragia Subaracnóidea/epidemiologia , Hemorragia Subaracnóidea/fisiopatologia , Adulto Jovem
5.
Surg Neurol Int ; 9: 119, 2018.
Artigo em Inglês | MEDLINE | ID: mdl-30009083

RESUMO

BACKGROUND: Intradural disc herniations (IDH) are rare, particularly in the cervical spine, where they account for less than 5% of all discs. Adhesions between the ossified/calcified posterior longitudinal ligament (OPLL), dura, and ossified/calcified disc herniations increase the complexity of resecting these cervical lesions. CASE DESCRIPTION: A 42-year-old male presented with a rapidly progressive cervical myelopathy over a 2-month period. This was attributed to an ossified/calcified intradural cervical disc herniation in conjunction with OPLL. The anterior cervical discectomy and fusion (ACDF) resulted in a dural defect but there was no cerebrospinal fluid (CSF) fistula as the arachnoid membrane remained intact. Had there been a CSF leak, it would have warranted both wound-peritoneal (WP) and lumbo-peritoneal shunts (LP). The surgeons should have anticipated that a CSF leak would likely occur prior to performing the ACDF, and should have prophylactically prepared and draped the abdomen for a potential WP, followed by a LP shunt. Three months postoperatively, the patient's proprioceptive deficit improved, and he almost completely recovered motor function. CONCLUSION: Performing an ACDF for resection of an intradural calcified/ossified disc with OPLL often results in both a dural defect and CSF fistula. As the arachnoid membrane rarely remains intact, the spine surgeon should be prepared to immediately perform both a WP shunt, and subsequently, an LP. In this case, following an ACDF, resection of an intradural ossified disc with OPLL resulted in an isolated dural defect without a CSF fistula and did not require no dural repair or shunting procedures.

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