Michael W. Chu

Dr. Michael W. Chu


Research Focus & Metrics

Academic Career Length

26Years (2001-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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1 February 2010 in Anesthesia & Analgesia
Verified
Journal Article
Closed access
JMJohn M. Murkin
John M. Murkin
FFFlorian Falter
Florian Falter
JGJeff Granton
Jeff Granton
BYBryan Young
Bryan Young
CBChristiana Burt
Christiana Burt
MCMichael W. Chu
Michael W. Chu
In 2 separate centers, we observed a notable increase in the incidence of postoperative convulsive seizures from 1.3% to 3.8% in patients having undergone major cardiac surgical procedures. These events were temporally coincident with the initial use of high-dose tranexamic acid (TXA) therapy after withdrawal of aprotinin from general clinical usage. The purpose of this review was to perform a retrospective analysis to examine whether there was a relation between TXA usage and seizures after cardiac surgery. An in-depth chart review was undertaken in all 24 patients who developed perioperative seizures. Electroencephalographic activity was recorded in 11 of these patients, and all patients had a formal neurological evaluation and brain imaging studies. Twenty-one of the 24 patients did not have evidence of new cerebral ischemic injury, but seizures were likely due to ischemic brain injury in 3 patients. All patients with seizures did not have permanent neurological abnormalities. All 24 patients with seizures received high doses of TXA intraoperatively ranging from 61 to 259 mg/kg, had a mean age of 69.9 years, and 21 of 24 had undergone open chamber rather than coronary bypass procedures. All but one patient were managed using cardiopulmonary bypass. No evidence of brain ischemic, metabolic, or hyperthermia-induced causes for their seizures was apparent. Our results suggest that use of high-dose TXA in older patients in conjunction with cardiopulmonary bypass and open-chamber cardiac surgery is associated with clinical seizures in susceptible patients.

1 November 2004 in The Annals of Thoracic Surgery
Verified
Journal Article
Closed access
MCMichael W. Chu
Michael W. Chu
SWSteve R. Wilson
Steve R. Wilson
RNRichard J. Novick
Richard J. Novick
LSLarry W. Stitt
Larry W. Stitt
MQMacKenzie A. Quantz
MacKenzie A. Quantz

1 June 2008 in European Journal of Cardio-Thoracic Surgery
Verified
Journal Article
Closed access
TWThomas Walther
Thomas Walther
VFVolkmar Falk
Volkmar Falk
JKJörg Kempfert
Jörg Kempfert
MBMichael Borger
Michael Borger
JFJens Fassl
Jens Fassl
FMFriedrich W. Mohr
Friedrich W. Mohr
To evaluate the feasibility of minimally invasive transapical beating heart aortic valve implantation (TAP-AVI) for high-risk patients with aortic stenosis. TAP-AVI was performed via a small anterolateral minithoracotomy in 50 patients from February 2006 to March 2007. A balloon expandable transcatheter xenograft (Edwards SAPIEN THV, Edwards Lifesciences, Irvine, CA, USA) was used. Mean age was 82.4+/-5 years and 39 (78%) were female. Implantation was performed in a hybrid operative theatre using fluoroscopic and echocardiographic visualization. Average EuroSCORE predicted risk for mortality was 27.6+/-12%. Seven (14%) patients were re-operations with patent bypass grafts. TAP-AVI (13 patients 23 mm and 37 patients 26 mm) was successfully performed on the beating heart under temporary rapid ventricular pacing in 47 (94%) patients, and implantation was performed completely off-pump in 34 (68%) patients. Three patients required early conversion; two of them were successfully discharged. There was no prosthesis migration or embolization observed. Echocardiography revealed good hemodynamic function in all and minor incompetence in 23 patients, mostly paravalvular, without any signs of hemolysis. Mortality was due to the overall health condition and non-valve related in all patients. Actuarial survival at 1 month, 6 months and 1 year was 92+/-3.8%, 73.9+/-6.2% and 71.4+/-6.5%, respectively. Transapical minimally invasive aortic valve implantation is feasible using an off-pump technique. Good results have been achieved in the initial 50 patients, especially when considering the overall high-risk profile of these patients.

20 July 2005 in JAMA
Verified
Journal Article
Closed access
PDF file
KBKaren E. A. Burns
Karen E. A. Burns
MCMichael W. Chu
Michael W. Chu
RNRichard J. Novick
Richard J. Novick
SFStephanie A. Fox
Stephanie A. Fox
KGKerri Gallo
Kerri Gallo
LMLouise Moist
Louise Moist
Research from JAMA — Perioperative N-acetylcysteine to Prevent Renal Dysfunction in High-Risk Patients Undergoing CABG Surgery — A Randomized Controlled Trial — ContextRenal dysfunction is a complication of coronary artery bypass graft (CABG) surgery performed with cardiopulmonary bypass (CPB) that is associated with increased morbidity and mortality. N-acetylcysteine, an antioxidant and vasodilator, counteracts renal ischemia and hypoxia.ObjectiveTo determine whether perioperative intravenous (IV) N-acetylcysteine preserves renal function in high-risk patients undergoing CABG surgery with CPB compared with placebo.Design, Setting, and PatientsRandomized, quadruple blind, placebo-controlled trial (October 2003-September 2004) in operating rooms and general intensive care units (ICUs) of 2 Ontario tertiary care centers. The 295 patients required elective or urgent CABG and had at least 1 of the following: preexisting renal dysfunction, at least 70 years old, diabetes mellitus, impaired left ventricular function, or undergoing concomitant valve or redo surgery.InterventionsPatients received 4 (2 intraoperative and 2 postoperative) doses of IV N-acetylcysteine (600 mg) (n = 148) or placebo (n = 147) over 24 hours.Main Outcome MeasuresThe primary outcome was the proportion of patients developing postoperative renal dysfunction, defined by an increase in serum creatinine level greater than 0.5 mg/dL (44 μmol/L) or a 25% increase from baseline within the first 5 postoperative days. Secondary outcomes included postoperative interventions and complications, the requirement for renal replacement therapy (RRT), adverse events, hospital mortality, and ICU and hospital length of stay.ResultsThere was no difference in the proportion of patients with postoperative renal dysfunction (29.7% vs 29.0%, P = .89; relative risk [RR], 1.03 [95% confidence interval {CI}, 0.72-1.46]) in the N-acetylcysteine and placebo groups, respectively. We noted nonsignificant differences in postoperative interventions and complications, the need for RRT (0.7% vs 2.1%; P = .37), total (6.1% vs 9.6%; P = .26) and serious adverse events, hospital mortality (3.4% vs 2.7%; P>.99), and ICU and hospital length of stay between the N-acetylcysteine and placebo groups. A post hoc subgroup analysis of patients (baseline creatinine level >1.4 mg/dL [120 μmol/L]) showed a nonsignificant trend toward fewer patients experiencing postoperative renal dysfunction in the N-acetylcysteine group compared with the placebo group (25.0% vs 37.1%; P = .29).ConclusionsN-acetylcysteine did not prevent postoperative renal dysfunction, interventions, complications, or mortality in high-risk patients undergoing CABG surgery with CPB. Further research is required to identify CABG patients at risk for postoperative renal events, valid markers of renal dysfunction, and to establish renal thresholds associated with important clinical outcomes.

1 August 2008 in The Journal of Thoracic and Cardiovascular Surgery
Verified
Journal Article
Closed access
WCW. Randolph Chitwood
W. Randolph Chitwood
EREvelio Rodriguez
Evelio Rodriguez
MCMichael W. Chu
Michael W. Chu
AHAnsar Hassan
Ansar Hassan
TFT. Bruce Ferguson
T. Bruce Ferguson
LNL. Wiley Nifong
L. Wiley Nifong

1 August 2017 in JACC
Verified
Journal Article
Closed access
EGEberhard Grube
Eberhard Grube
NMNicolas M. Van Mieghem
Nicolas M. Van Mieghem
SBSabine Bleiziffer
Sabine Bleiziffer
TMThomas Modine
Thomas Modine
JBJohan Bosmans
Johan Bosmans
DHDavid Hildick-Smith
David Hildick-Smith