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1.
Neurochirurgie ; 69(5): 101464, 2023 Sep.
Article in English | MEDLINE | ID: mdl-37393989

ABSTRACT

PURPOSE: To assess the viability and effectiveness of mono-segmental percutaneous screw fixation in the treatment of unstable type B thoracolumbar fracture due to ankylosing spondylitis. METHODS: We report here all 40 patients treated by mono-segmental screw fixation in this indication, between January 2018 and January 2022, with follow-up at 3 and 9 months. Study variables comprised operating time, length of stay, fusion, stabilization quality, and peri-operative morbidity and mortality. RESULTS: One patient showed early displacement of rods caused by technical error. None of the others showed secondary displacement of rods or screws. Mean age was 73 years (range 18-93), mean hospital stay 4.8 days (range 2-15), mean operative time 52minutes (range 26-95minutes) and mean estimated blood loss 40ml. There were 2 deaths caused by intensive care unit complications. All patients except those in intensive care were verticalized within 24hours after surgery. Parker score was unchanged for each patient before and after surgery and during follow-up. CONCLUSION: Mono-segmental percutaneous screw fixation in the treatment of unstable type B thoracolumbar fracture due to ankylosing spondylitis was safe and effective. This study showed that this surgery reduced length of hospital stay, operative time, blood loss and complications compared to open or extended percutaneous surgery, and allowed fast rehabilitation in this vulnerable population.


Subject(s)
Pedicle Screws , Spinal Fractures , Spondylitis, Ankylosing , Humans , Adolescent , Young Adult , Adult , Middle Aged , Aged , Aged, 80 and over , Spinal Fractures/surgery , Spinal Fractures/etiology , Spondylitis, Ankylosing/complications , Spondylitis, Ankylosing/surgery , Fracture Fixation, Internal/adverse effects , Pedicle Screws/adverse effects , Lumbar Vertebrae/surgery , Thoracic Vertebrae/surgery , Treatment Outcome , Retrospective Studies
2.
Neurochirurgie ; 66(4): 195-202, 2020 Aug.
Article in English | MEDLINE | ID: mdl-32645393

ABSTRACT

INTRODUCTION: The management of antithrombotic therapy (AT) after surgery for chronic subdural hematoma (cSDH) requires taking account of the balance of risk between hemorrhage recurrence (HR) and the prophylactic thromboembolic effect (TE). The goal of the present study was to evaluate the prevalence of vascular events (VE: TE and/or HR) in the first 3 postoperative months after cSDH evacuation in patients previously treated by AT. The impact of AT resumption was also evaluated. PATIENTS AND METHODS: This observational prospective multicenter collaborative study (14 French neurosurgery centers) included patients with cSDH treated by AT and operated on between May 2017 and March 2018. Data collection used an e-CRF, and was principally based on an admission questionnaire and outcome/progression at 3 months. RESULTS: In this cohort of 211 patients, VE occurred in 58 patients (27.5%): HR in 47 (22.3%), TE in 17 (8%), with mixed event in 6 cases (2%). Median overall time to onset of complications 26 days±31.5, and specifically 43.5 days±29.25 for HR. Non-resumption of AT significantly increased the relative risk of VE [OR: 4.14; 95% CI: 2.08 - 8.56; P <0.001] and especially of TE [OR: 7.5; 95% CI: 1.2 - 42; P<0.001]. The relative risk of HR was significantly increased when AT was resumed at less than 30 days (P=0.015). CONCLUSION: The occurrence of VE in patients operated on for cSDH and previously treated by AT was statistically significant (27.5%). HR was the most common event (22.3%), whereas TE accounted for only the 8%, although with shorter time to onset. In order to prevent TE risk, AT should be restarted after 30 days, as HR risk is greatly decreased beyond this time.


Subject(s)
Fibrinolytic Agents/therapeutic use , Hematoma, Subdural, Chronic/surgery , Aged , Aged, 80 and over , Drainage , Female , France , Hematoma, Subdural, Chronic/prevention & control , Humans , Longitudinal Studies , Male , Neurosurgical Procedures , Postoperative Complications/epidemiology , Prevalence , Prospective Studies , Recurrence , Risk Factors , Surveys and Questionnaires , Treatment Outcome
3.
Neurochirurgie ; 62(1): 53-9, 2016 Feb.
Article in French | MEDLINE | ID: mdl-26657112

ABSTRACT

INTRODUCTION: Ventriculoperitoneal shunting (VPS) is a treatment of the hydrocephalus that may dysfunction. The clinical presentation of shunt dysfunction is variable. We therefore decided to focus on the clinical presentation of VPS malfunction in children, as this condition requires immediate emergency treatment and because of the sometimes confusing signs of intracranial hypertension in a shunted child. MATERIALS AND METHODS: We searched PubMed with the following groups of keywords: (dysfunction OR blockage) AND shunting AND hydrocephalus; shunt complications AND hydrocephalus; hydrocephalus AND shunt AND malfunction. Articles dealing with ventriculo-atrial shunt were excluded. A total of 79 articles were retained for analysis (English and French). Case reports were excluded. RESULTS: The clinical presentation varies by age: vomiting and alterated level of consciousness are the most frequent signs in older children, whereas infants present more often with raised intracranial pressure symptoms such as nausea, vomiting, irritability and bulging fontanel. Drowsiness is a good predictor of VPS dysfunction. An asymptomatic presentation is rare but possible. Abdominal presentation is also possible, ranging from abdominal discomfort to peritonitis. Fever, occurring a short time after the last intervention, and irritability are good predictors of shunt infection. Pumping the chamber of the VPS has a weak positive predictive value (12%). Shunt dysfunction can lead to death, with an estimated mortality rate at 1% per year during the first years. CONCLUSION: It is essential to be aware of the variability of the clinical presentation of VPS dysfunction, because of the potential severity of this condition. Also it is important to pay attention to the comments of the parents, especially if the child experienced a previous shunt malfunction.


Subject(s)
Equipment Failure , Hydrocephalus/surgery , Postoperative Complications/etiology , Postoperative Complications/therapy , Ventriculoperitoneal Shunt/adverse effects , Child , Fever/complications , Humans , Hydrocephalus/complications , Hydrocephalus/diagnosis , Postoperative Complications/diagnosis , Ventriculoperitoneal Shunt/methods , Vomiting/complications
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