David Turkel-Parrella
St. Michael's Hospital
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Featured researches published by David Turkel-Parrella.
Stroke | 2015
Airton Leonardo de Oliveira Manoel; Blessing N. R. Jaja; Menno R. Germans; Han Yan; Winnie Qian; Ekaterina Kouzmina; Tom R. Marotta; David Turkel-Parrella; Tom A. Schweizer; R. Loch Macdonald; Nima Etminan; Daniel Hänggi; David Hasan; S. Claiborne Johnston; Peter D. Le Roux; Stephan Mayer; Andrew Molyneux; Adam Noble; Audrey Quinn; Thomas Schenk; Julian Spears; Michael M. Todd; James C. Torner; Ming Tseng; William van den Bergh; Mervyn D.I. Vergouwen; George Kwok Chu Wong; Ming-Yuan Tseng
Background and Purpose— Patients are classically at risk of delayed cerebral ischemia (DCI) after aneurysmal subarachnoid hemorrhage. We validated a grading scale—the VASOGRADE—for prediction of DCI. Methods— We used data of 3 phase II randomized clinical trials and a single hospital series to assess the relationship between the VASOGRADE and DCI. The VASOGRADE derived from previously published risk charts and consists of 3 categories: VASOGRADE-Green (modified Fisher scale 1 or 2 and World Federation of Neurosurgical Societies scale [WFNS] 1 or 2); VASOGRADE-Yellow (modified Fisher 3 or 4 and WFNS 1–3); and VASOGRADE-Red (WFNS 4 or 5, irrespective of modified Fisher grade). The relation between the VASOGRADE and DCI was assessed by logistic regression models. The predictive accuracy of the VASOGRADE was assessed by receiver operating characteristics curve and calibration plots. Results— In a cohort of 746 patients, the VASOGRADE significantly predicted DCI (P<0.001). The VASOGRADE-Yellow had a tendency for increased risk for DCI (odds ratio [OR], 1.31; 95% CI, 0.77–2.23) when compared with VASOGRADE-Green; those with VASOGRADE-Red had a 3-fold higher risk of DCI (OR, 3.19; 95% CI, 2.07–4.50). Studies were not a significant confounding factor between the VASOGRADE and DCI. The VASOGRADE had an adequate discrimination for prediction of DCI (area under the receiver operating characteristics curve=0.63) and good calibration. Conclusions— The VASOGRADE results validated previously published risk charts in a large and diverse sample of subarachnoid hemorrhage patients, which allows DCI risk stratification on presentation after subarachnoid hemorrhage. It could help to select patients at high risk of DCI, as well as standardize treatment protocols and research studies.
Canadian Journal of Neurological Sciences | 2014
Airton Leonardo de Oliveira Manoel; David Turkel-Parrella; Menno Germans; Ekaterina Kouzmina; Priscila da Silva Almendra; Thomas R. Marotta; Julian Spears; Simon Abrahamson
OBJECTIVE The recent guidelines on management of aneurysmal subarachnoid hemorrhage (aSAH) advise pharmacological thromboprophylaxis (PTP) after aneurysm obliteration. However, no study has addressed the safety of PTP in the aSAH population. Therefore, the aim of this study was to assess the safety of early PTP after aSAH. METHODS Retrospective cohort of aSAH patients admitted between January 2012 and June 2013 in a single high-volume aSAH center. Traumatic SAH and perimesencephalic hemorrhage patients were excluded. Patients were grouped according to PTP timing: early PTP group (PTP within 24 hours of aneurysm treatment), and delayed PTP group (PTP started > 24 hours). RESULTS A total of 174 SAH patients (mean age 56.3±12.5 years) were admitted during the study period. Thirty-nine patients (22%) did not receive PTP, whereas 135 patients (78%) received PTP after aneurysm treatment or negative angiography. Among the patients who received PTP, 65 (48%) had an external ventricular drain. Twenty-eight patients (21%) received early PTP, and 107 (79%) received delayed PTP. No patient in the early treatment group and three patients in the delayed PTP group developed an intracerebral hemorrhagic complication. Two required neurosurgical intervention and one died. These three patients were on concomitant PTP and dual antiplatelet therapy. CONCLUSIONS The initiation of PTP within 24 hours may be safe after the treatment of a ruptured aneurysm or in angiogram-negative SAH patients with diffuse aneurysmal hemorrhage pattern. We suggest caution with concomitant use of PTP and dual antiplatelet agents, because it possibly increases the risk for intracerebral hemorrhage.
Critical Care | 2014
Airton Leonardo de Oliveira Manoel; Ann Mansur; Amanda Murphy; David Turkel-Parrella; Matt J. MacDonald; R. Loch Macdonald; Walter Montanera; Thomas R. Marotta; Aditya Bharatha; Khaled Effendi; Tom A. Schweizer
Neuroimaging is a key element in the management of patients suffering from subarachnoid haemorrhage (SAH). In this article, we review the current literature to provide a summary of the existing neuroimaging methods available in clinical practice. Noncontrast computed tomography is highly sensitive in detecting subarachnoid blood, especially within 6 hours of haemorrhage. However, lumbar puncture should follow a negative noncontrast computed tomography scan in patients with symptoms suspicious of SAH. Computed tomography angiography is slowly replacing digital subtraction angiography as the first-line technique for the diagnosis and treatment planning of cerebral aneurysms, but digital subtraction angiography is still required in patients with diffuse SAH and negative initial computed tomography angiography. Delayed cerebral ischaemia is a common and serious complication after SAH. The modern concept of delayed cerebral ischaemia monitoring is shifting from modalities that measure vessel diameter to techniques focusing on brain perfusion. Lastly, evolving modalities applied to assess cerebral physiological, functional and cognitive sequelae after SAH, such as functional magnetic resonance imaging or positron emission tomography, are discussed. These new techniques may have the advantage over structural modalities due to their ability to assess brain physiology and function in real time. However, their use remains mainly experimental and the literature supporting their practice is still scarce.
Critical Care | 2016
Airton Leonardo de Oliveira Manoel; Alberto Goffi; Fernando Godinho Zampieri; David Turkel-Parrella; Abhijit Duggal; Thomas R. Marotta; R. Loch Macdonald; Simon Abrahamson
Clinical and Investigative Medicine | 2016
Mohamad A. Hussain; Muhammad Mamdani; Gustavo Saposnik; Jack V. Tu; David Turkel-Parrella; Julian Spears; Mohammed Al-Omran
Neurology | 2018
Ashik Shrestha; Phillip Ye; Ting Zhou; Ambooj Tiwari; David Turkel-Parrella; Jeffrey Farkas; K Arcot; Danielle Crotty
Neurology | 2014
Airton Leonardo de Oliveira Manoel; David Turkel-Parrella; Alberto Goffi; Victoria A. McCredie; David Ben-Israel; Ekaterina Kouzmina; Julian Spears; Thomas R. Marotta; Simon Abrahamson
Neurology | 2014
David Ben-Israel; David Turkel-Parrella; Ekaterina Kouzmina; Thomas R. Marotta; Julian Spears; Airton Leonardo de Oliveira Manoel
Neurology | 2014
David Turkel-Parrella; Airton Leonardo de Oliveira Manoel; Thomas R. Marotta; Julian Spears
Neurology | 2014
Airton Leonardo de Oliveira Manoel; David Turkel-Parrella; Ekaterina Kouzmina; Simon Abrahamson; Thomas R. Marotta; Tom A. Schweizer; Julian Spears; Loch MacDonald