Chiraz Chaalala
Université de Montréal
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Featured researches published by Chiraz Chaalala.
Clinical Neurology and Neurosurgery | 2015
E. Magro; Jonathan Chainey; Chiraz Chaalala; Hosam Al Jehani; Jean-Yves Fournier; Michel W. Bojanowski
OBJECTIVE Posterior fossa arteriovenous malformations (pAVMs) are rare and because of their location at or close to vital structures, their treatment remains challenging despite overall improvements in the management of cerebrovascular lesions. We reviewed our recent series of ruptured pfAVMs in search of guiding principles in the management of these complex lesions. METHODS This is a retrospective series of consecutive patients admitted for a ruptured pfAVM from 2002 to 2013. We analyzed clinical and radiological data, as well as initial and definitive management. Outcome was assessed using the modified Rankin Scale (mRS) at 6 months. RESULTS The study included 34 patients (19 women and 15 men). Upon admission, 79% of patients presented with an intra-cerebellar hematoma, 42% of which required urgent drainage. Hydrocephaly was also present in 82% of patients, 56% of which required emergency ventriculostomy. There was an aneurysm associated with the AVM in 47% of cases. In 38% of the cases, the aneurysm was the source of the hemorrhage. Only 68% of patients were amenable to undergo treatment of the AVM: 24% exclusively by surgery, 9% by embolization, 3% by radiosurgery, and 32% using combined means. Five patients died within the first week: one as a direct result of the severity of the hemorrhage, and the other four due to re-bleeding before treatment. Outcome was favorable (mRS 0-2) in 71% of patients. CONCLUSION Patients with a ruptured pfAVM are often comatose upon admission, requiring emergency live-saving surgical treatment. An associated aneurysm is often the source of bleeding which if dealt with immediately, offers time to plan the most appropriate strategies to eliminate the AVM. Nevertheless, early re-bleeding is frequent, and a cause of concern as it often leads to death. Despite the gravity of the clinical condition upon admission, outcome is favorable for those amenable to treatment.
Journal of Neurology, Neurosurgery, and Psychiatry | 2017
Tim E. Darsaut; J. Max Findlay; Elsa Magro; Marc Kotowski; Daniel Roy; Alain Weill; Michel W. Bojanowski; Chiraz Chaalala; Daniela Iancu; Howard Lesiuk; John Sinclair; Félix Scholtes; Didier Martin; Michael M. Chow; C. O'Kelly; John H. Wong; Kenneth Butcher; Allan J. Fox; Adam Arthur; François Guilbert; Lu Tian; Miguel Chagnon; Suzanne Nolet; Guylaine Gevry; Jean Raymond
Background Unruptured intracranial aneurysms (UIAs) are increasingly diagnosed and are commonly treated using endovascular treatment or microsurgical clipping. The safety and efficacy of treatments have not been compared in a randomised trial. How to treat patients with UIAs suitable for both options remains unknown. Methods We randomly allocated clipping or coiling to patients with one or more 3–25 mm UIAs judged treatable both ways. The primary outcome was treatment failure, defined as: initial failure of aneurysm treatment, intracranial haemorrhage or residual aneurysm on 1-year imaging. Secondary outcomes included neurological deficits following treatment, hospitalisation >5 days, overall morbidity and mortality and angiographic results at 1 year. Results The trial was designed to include 260 patients. An analysis was performed for slow accrual: 136 patients were enrolled from 2010 through 2016 and 134 patients were treated. The 1-year primary outcome, available for 104 patients, was reached in 5/48 (10.4% (4.5%–22.2%)) patients allocated surgical clipping, and 10/56 (17.9% (10.0%–29.8%)) patients allocated endovascular coiling (OR: 0.54 (0.13–1.90), p=0.40). Morbidity and mortality (modified Rankin Scale>2) at 1 year occurred in 2/48 (4.2% (1.2%–14.0%)) and 2/56 (3.6% (1.0%–12.1%)) patients allocated clipping and coiling, respectively. New neurological deficits (15/65 vs 6/69; OR: 3.12 (1.05–10.57), p=0.031), and hospitalisations beyond 5 days (30/65 vs 6/69; OR: 8.85 (3.22–28.59), p=0.0001) were more frequent after clipping. Conclusion Surgical clipping or endovascular coiling of UIAs did not show differences in morbidity at 1 year. Trial continuation and additional randomised evidence will be necessary to establish the supposed superior efficacy of clipping.
Journal of Neurosurgery | 2017
Elsa Magro; Jean-Christophe Gentric; André Lima Batista; Marc Kotowski; Chiraz Chaalala; David Roberge; Alain Weill; Christian Stapf; Daniel Roy; Michel W. Bojanowski; Tim E. Darsaut; Ruby Klink; Jean Raymond
OBJECTIVE The management of brain arteriovenous malformations (bAVMs) remains controversial. The Treatment of Brain AVMs Study (TOBAS) was designed to manage patients with bAVMs within a clinical research framework. The objective of this study was to study trial feasibility, recruitment rates, patient allocation to the various management groups, and compliance with treatment allocation. METHODS TOBAS combines two randomized care trials (RCTs) and a registry. Designed to be all-inclusive, the study offers randomized allocation of interventional versus conservative management to patients eligible for both options (first RCT), a second RCT testing the role of preembolization as an adjunct to surgery or radiotherapy, and a registry of patients managed using clinical judgment alone. The primary outcome of the first RCT is death from any cause or disabling stroke (modified Rankin Scale score > 2) at 10 years. A pilot phase was initiated at one center to test study feasibility, record the number and characteristics of patients enrolled in the RCTs, and estimate the frequency of crossovers. RESULTS All patients discussed at the multidisciplinary bAVM committee between June 2014 and June 2016 (n = 107) were recruited into the study; 46 in the randomized trials (23 in the first RCT with 21 unruptured bAVMs, 40 in the second RCT with 17 unruptured bAVMs, and 17 in both RCTs), and 61 patients in the registry. Three patients crossed over from surgery to observation (first RCT). CONCLUSIONS Clinical research was successfully integrated with normal practice using TOBAS. Recruitment rates in a single center are encouraging. Whether the trial will provide meaningful results depends on the recruitment of a sufficient number of participating centers. Clinical trial registration no.: NCT02098252 (clinicaltrials.gov).
Canadian Journal of Neurological Sciences | 2016
Charlotte Dandurand; Laurent Létourneau; Chiraz Chaalala; E. Magro; Michel W. Bojanowski
A 51-year-old male was brought to the emergency room with fever and depressed consciousness. The family reported a 3-day history of asthenia, myalgia, stiffness of the neck, chills, and confusion. His medical history was relevant for chronic alcohol abuse and gout. On physical examination, the patient was febrile (39.2°C), hypertensive, and tachypneic. He was unconscious with no focal neurological deficits. Urgent noncontrast computed tomography (CT) scan showed hydrocephalus with trans-ependymal edema with sparing of the fourth ventricle. The patient was intubated and an external ventricular drain was urgently inserted, which drained obviously purulent cerebrospinal fluid (CSF). The patient was started on a broad-spectrum antimicrobial therapy, which was later readjusted because CSF and blood cultures grew Streptococcus intermedius.The brain magnetic resonance imaging (Figure 1) scan revealed severe ventriculitis evidenced by intraventricular debris, intense enhancement of the ependymal lining of the ventricles associated with periventricular cerebritis, and multiple bilateral brain microabscesses. A chest and abdomen CT scan performed to search for a primary infection revealed a perforated diverticulitis complicated by multiple liver abscesses that were subsequently drained percutaneously. During hospitalization, the patient eventually developed multiloculated hydrocephalus that required multiple drains and finally a ventriculopleural shunt after endoscopic fenestration of the ventricular septations. The patient improved remarkably and was awaiting rehabilitation when he suddenly died of a respiratory complication.
Trials | 2015
Tim E. Darsaut; E. Magro; Jean-Christophe Gentric; André Lima Batista; Chiraz Chaalala; David Roberge; Michel W. Bojanowski; Alain Weill; Daniel Roy; Jean Raymond
Neurochirurgie | 2016
E. Magro; Jean-Christophe Gentric; Tim E. Darsaut; André Lima Batista; Chiraz Chaalala; David Roberge; Alain Weill; Daniel Roy; Michel W. Bojanowski; Jean Raymond
Journal of Neuroradiology | 2017
Robert Fahed; André Lima Batista; Tim E. Darsaut; Jean-Christophe Gentric; Célina Ducroux; Chiraz Chaalala; David Roberge; Michel W. Bojanowski; Alain Weill; Daniel Roy; Elsa Magro; Jean Raymond
Canadian Journal of Neurological Sciences | 2015
S Obaid; E. Magro; Chiraz Chaalala; C Jonathan; J Guimond; A Lesage; J Fournier; Michel W. Bojanowski
Neurochirurgie | 2013
E. Magro; Chiraz Chaalala; J. Chainey; H. Al-Jehani; J.-Y. Fournier; Michel W. Bojanowski
Neurochirurgie | 2013
E. Magro; Chiraz Chaalala; J. Chainey; J.-G. Guimond; A. Lesage; J.-Y. Fournier; Michel W. Bojanowski