Vincent Chan
Current Organizations / Institutes
The organizations/institutes from the scholar's latest article
Previous Organizations / Institutes
The organizations / institutes from the scholar's other articles in the past ten years
Research Subjects
Vincent Chan has a total of 106 co-authors. Here are the top co-authors by number of shared publications:
- Anahi Perlas
Anesthesia and Pain Management, Toronto Western Hospital, Toronto, Ontario, Canada
3 shared publications - Adriana M. Mujal
Immunology Program, Memorial Sloan Kettering Cancer Center, New York, New York
2 shared publications - Alexandre Boissonnas
Inserm U1135, CNRS ERL 8255, Centre d'Immunologie et Des Maladies Infectieuses (CIMI‐Paris) Sorbonne Université Paris France
2 shared publications - Alexis J. Combes
Department of Pathology, University of California, San Francisco, USA
2 shared publications Anahi Perlas
Department of Anesthesia, Toronto Western Hospital, University Health Network, University of Toronto, Toronto, Ontario, Canada
2 shared publicationsAnne Agur
Division of Anatomy, Department of Surgery, University of Toronto, Toronto, Ontario, Canada
2 shared publications
Latest Publications
- 19 August 2026
- Published by Elsevier in British Journal of Anaesthesia
- Vol. 137 (4) , 968-971
Fascial plane blocks five years on: are we any closer to understanding them?
- 19 August 2026
- Published by Elsevier in British Journal of Anaesthesia
- Vol. 137 (4) , 968-971
Fascial plane blocks five years on: are we any closer to understanding them?
- Open Access
- 4 April 2023
- Published by American Association for Cancer Research (AACR)
Supplementary Table from Holistic Characterization of Tumor Monocyte-to-Macrophage Differentiation Integrates Distinct Immune Phenotypes in Kidney Cancer
Supplementary Table from Holistic Characterization of Tumor Monocyte-to-Macrophage Differentiation Integrates Distinct Immune Phenotypes in Kidney Cancer
- 4 April 2023
- Published by American Association for Cancer Research (AACR)
Open AccessSupplementary Table from Holistic Characterization of Tumor Monocyte-to-Macrophage Differentiation Integrates Distinct Immune Phenotypes in Kidney Cancer
Supplementary Table from Holistic Characterization of Tumor Monocyte-to-Macrophage Differentiation Integrates Distinct Immune Phenotypes in Kidney Cancer
- Open Access
- 4 April 2023
- Published by American Association for Cancer Research (AACR)
Supplementary Table from Holistic Characterization of Tumor Monocyte-to-Macrophage Differentiation Integrates Distinct Immune Phenotypes in Kidney Cancer
Supplementary Table from Holistic Characterization of Tumor Monocyte-to-Macrophage Differentiation Integrates Distinct Immune Phenotypes in Kidney Cancer
- 4 April 2023
- Published by American Association for Cancer Research (AACR)
Open AccessSupplementary Table from Holistic Characterization of Tumor Monocyte-to-Macrophage Differentiation Integrates Distinct Immune Phenotypes in Kidney Cancer
Supplementary Table from Holistic Characterization of Tumor Monocyte-to-Macrophage Differentiation Integrates Distinct Immune Phenotypes in Kidney Cancer
- 22 July 2022
- Published by Wolters Kluwer Health in Anesthesiology
- Vol. 137 (4) , 459-470
No Benefits of Adding Dexmedetomidine, Ketamine, Dexamethasone, and Nerve Blocks to an Established Multimodal Analgesic Regimen after Total Knee Arthroplasty
Background: An optimal opioid-sparing multimodal analgesic regimen to treat severe pain can enhance recovery after total knee arthroplasty. The hypothesis was that adding five recently described intravenous and regional interventions to multimodal analgesic regimen can further reduce opioid consumption. Methods: In a double-blinded fashion, 78 patients undergoing elective total knee arthroplasty were randomized to either (1) a control group (n = 39) that received spinal anesthesia with intrathecal morphine, periarticular local anesthesia infiltration, intravenous dexamethasone, and a single injection adductor canal block or (2) a study group (n = 39) that received the same set of analgesic treatments plus five additional interventions: local anesthetic infiltration between the popliteal artery and capsule of the posterior knee, intraoperative intravenous dexmedetomidine and ketamine, and postoperatively, one additional intravenous dexamethasone bolus and two additional adductor canal block injections. The primary outcome measure was 24-h cumulative opioid consumption after surgery and secondary outcomes were other analgesics, patient recovery, functional outcomes, and adverse events. Results: Opioid consumption was not different between groups at 24 h (oral morphine equivalents, mean ± SD; study: 23.7 ± 18.0 mg vs. control: 29.3 ± 18.7 mg; mean difference [95% CI], –5.6 mg [–2.7 to 13.9]; P = 0.189) and all other time points after surgery. There were no major differences in pain scores, quality of recovery, or time to reach rehabilitation milestones. Hypotensive episodes occurred more frequently in the study group (25 of 39 [64.1%] vs. 13 of 39 [33.3%]; P = 0.010). Conclusions: In the presence of periarticular local anesthesia infiltration, intrathecal morphine, single-shot adductor canal block and dexamethasone, the addition of five analgesic interventions—local anesthetic infiltration between the popliteal artery and capsule of the posterior knee, intravenous dexmedetomidine, intravenous ketamine, an additional intravenous dexamethasone dose, and repeated adductor canal block injections—failed to further reduce opioid consumption or pain scores or to improve functional outcomes after total knee arthroplasty. Editor’s Perspective: What We Already Know about This Topic: What This Article Tells Us That Is New:
- 22 July 2022
- Published by Wolters Kluwer Health in Anesthesiology
- Vol. 137 (4) , 459-470
No Benefits of Adding Dexmedetomidine, Ketamine, Dexamethasone, and Nerve Blocks to an Established Multimodal Analgesic Regimen after Total Knee Arthroplasty
Background: An optimal opioid-sparing multimodal analgesic regimen to treat severe pain can enhance recovery after total knee arthroplasty. The hypothesis was that adding five recently described intravenous and regional interventions to multimodal analgesic regimen can further reduce opioid consumption. Methods: In a double-blinded fashion, 78 patients undergoing elective total knee arthroplasty were randomized to either (1) a control group (n = 39) that received spinal anesthesia with intrathecal morphine, periarticular local anesthesia infiltration, intravenous dexamethasone, and a single injection adductor canal block or (2) a study group (n = 39) that received the same set of analgesic treatments plus five additional interventions: local anesthetic infiltration between the popliteal artery and capsule of the posterior knee, intraoperative intravenous dexmedetomidine and ketamine, and postoperatively, one additional intravenous dexamethasone bolus and two additional adductor canal block injections. The primary outcome measure was 24-h cumulative opioid consumption after surgery and secondary outcomes were other analgesics, patient recovery, functional outcomes, and adverse events. Results: Opioid consumption was not different between groups at 24 h (oral morphine equivalents, mean ± SD; study: 23.7 ± 18.0 mg vs. control: 29.3 ± 18.7 mg; mean difference [95% CI], –5.6 mg [–2.7 to 13.9]; P = 0.189) and all other time points after surgery. There were no major differences in pain scores, quality of recovery, or time to reach rehabilitation milestones. Hypotensive episodes occurred more frequently in the study group (25 of 39 [64.1%] vs. 13 of 39 [33.3%]; P = 0.010). Conclusions: In the presence of periarticular local anesthesia infiltration, intrathecal morphine, single-shot adductor canal block and dexamethasone, the addition of five analgesic interventions—local anesthetic infiltration between the popliteal artery and capsule of the posterior knee, intravenous dexmedetomidine, intravenous ketamine, an additional intravenous dexamethasone dose, and repeated adductor canal block injections—failed to further reduce opioid consumption or pain scores or to improve functional outcomes after total knee arthroplasty. Editor’s Perspective: What We Already Know about This Topic: What This Article Tells Us That Is New:
- 1 June 2022
- Published by Springer Nature
- p. 797-809
iPACK Block: Infiltration in the Interspace Between Popliteal Artery and Capsule of the Knee
- 1 June 2022
- Published by Springer Nature
- p. 797-809
iPACK Block: Infiltration in the Interspace Between Popliteal Artery and Capsule of the Knee
- 11 June 2021
- Published by Wolters Kluwer Health in Anesthesiology
- Vol. 135 (4) , 729-737
A Roadmap for Environmental Sustainability of Plastic Use in Anesthesia and the Perioperative Arena
- 11 June 2021
- Published by Wolters Kluwer Health in Anesthesiology
- Vol. 135 (4) , 729-737
A Roadmap for Environmental Sustainability of Plastic Use in Anesthesia and the Perioperative Arena
- Open Access
- 21 May 2021
- Published by Institute of Electrical and Electronics Engineers (IEEE) in IEEE Transactions on Green Communications and Networking
- Vol. 5 (2) , C3
IEEE Communications Society Information
Presents a listing of the editorial board, board of governors, current staff, committee members, and/or society editors for this issue of the publication.
- 21 May 2021
- Published by Institute of Electrical and Electronics Engineers (IEEE) in IEEE Transactions on Green Communications and Networking
- Vol. 5 (2) , C3
Open AccessIEEE Communications Society Information
Presents a listing of the editorial board, board of governors, current staff, committee members, and/or society editors for this issue of the publication.
- Open Access
- 1 October 2020
- Published by The Korean Society of Anesthesiologists in Korean Journal of Anesthesiology
- Vol. 73 (5) , 465-467
Impact of an ultrasound-guided regional anesthesia workshop on participants' confidence levels and clinical practice
- 1 October 2020
- Published by The Korean Society of Anesthesiologists in Korean Journal of Anesthesiology
- Vol. 73 (5) , 465-467
Open AccessImpact of an ultrasound-guided regional anesthesia workshop on participants' confidence levels and clinical practice
- 7 September 2020
- Published by BMJ in Regional Anesthesia & Pain Medicine
- Vol. 45 (12) , 1000-1005
Is the minimal clinically important difference (MCID) in acute pain a good measure of analgesic efficacy in regional anesthesia?
In the field of acute pain medicine research, we believe there is an unmet need to incorporate patient related outcome measures that move beyond reporting pain scores and opioid consumption. The term “minimal clinically important difference” (MCID) defines the clinical benefit of an intervention as perceived by the patient, as opposed to a mathematically determined statistically significant difference that may not necessarily be clinically significant. The present article reviews the concept of MCID in acute postoperative pain research, addresses potential pitfalls in MCID determination and questions the clinical validity of extrapolating MCID determined from chronic pain and non-surgical pain studies to the acute postoperative pain setting. We further suggest the concepts of minimal clinically important improvement, substantial clinical benefit and patient acceptable symptom state should also represent aspirational outcomes for future research in acute postoperative pain management.
- 7 September 2020
- Published by BMJ in Regional Anesthesia & Pain Medicine
- Vol. 45 (12) , 1000-1005
Is the minimal clinically important difference (MCID) in acute pain a good measure of analgesic efficacy in regional anesthesia?
In the field of acute pain medicine research, we believe there is an unmet need to incorporate patient related outcome measures that move beyond reporting pain scores and opioid consumption. The term “minimal clinically important difference” (MCID) defines the clinical benefit of an intervention as perceived by the patient, as opposed to a mathematically determined statistically significant difference that may not necessarily be clinically significant. The present article reviews the concept of MCID in acute postoperative pain research, addresses potential pitfalls in MCID determination and questions the clinical validity of extrapolating MCID determined from chronic pain and non-surgical pain studies to the acute postoperative pain setting. We further suggest the concepts of minimal clinically important improvement, substantial clinical benefit and patient acceptable symptom state should also represent aspirational outcomes for future research in acute postoperative pain management.