181 results match your criteria: "and Toronto General Hospital[Affiliation]"

Article Synopsis
  • The 22q11.2 deletion syndrome is a genetic condition that's common and often linked to heart problems. Prenatal testing for this condition is becoming more common.
  • This study looked at how well babies do when they are diagnosed before they are born versus after they are born.
  • They found that, overall, the chance of dying in the first year didn't change much between those diagnosed early or late, but serious heart problems and when the baby was born affected the results.
View Article and Find Full Text PDF

Standardized Medical Terminology for Cardiac CT: What's in a Name?

Radiol Cardiothorac Imaging

August 2023

From the Department of Medical Imaging, Peter Munk Cardiac Center, Toronto General Hospital, University of Toronto, 585 University Ave, Toronto, ON, Canada M5G 2N2 (J.R., K.H.); Department of Medicine and Radiology, University of British Columbia, Vancouver, British Columbia, Canada (J.R.); and Toronto General Hospital Research Institute, Toronto, Ontario, Canada (K.H.).

View Article and Find Full Text PDF

The patient perspective on informed consent for anaesthesia when scheduled for cardiac surgery: An observational study.

Eur J Anaesthesiol

October 2023

From the Department of Anesthesiology and Intensive Care Medicine (MM, TGM, THK, WAvK), Department of Information Technology, University Medical Center Utrecht, Utrecht, The Netherlands (THK), Department of Anaesthesia and Pain Management, Toronto General Hospital, University Health Network (WavK), Department of Anesthesiology and Pain Medicine, Temerty Faculty of Medicine, University of Toronto (WavK) and Toronto General Hospital Research Institute, Toronto, ON, Canada (WavK).

View Article and Find Full Text PDF

Background: Preconditioning deceased organ donors with calcineurin inhibitors (CNIs) may reduce ischemia-reperfusion injury to improve transplant outcomes.

Methods: We searched MEDLINE, EMBASE, Cochrane Library, and conference proceedings for animal models of organ donation and transplantation, comparing donor treatment with CNIs with either placebo or no intervention, and evaluating outcomes for organ transplantation. Reviewers independently screened and selected studies, abstracted data, and assessed the risk of bias and clinical relevance of included studies.

View Article and Find Full Text PDF

Introduction: Foot ulcers are one of the most devastating complications of diabetes mellitus leading to leg amputations. In Canada, systematically marginalised and racialised populations are more prone to developing foot ulcers and at higher risk of limb amputations. Shortages of regulated healthcare have hindered efforts to provide foot care.

View Article and Find Full Text PDF

Congenital heart disease (CHD) affecting the conotruncal region of the heart, occurs in 40-50% of patients with 22q11.2 deletion syndrome (22q11.2DS).

View Article and Find Full Text PDF

Background: Most individuals with 22q11.2 deletion syndrome (22q11DS) have multi-system and lifelong needs requiring substantial support. Their primary caregivers are usually family members who dedicate lifelong time and effort to their role.

View Article and Find Full Text PDF

Cardiac surgery is associated with numerous peri- and post-operative haemostatic complications and blood transfusion requirements. Complex procedures such as redo-sternotomy heart transplantation or type A aortic dissection repairs are at high-risk for severe coagulopathy and significant transfusion requirements. However, current practice guidelines do not specifically address high-risk surgeries, resulting in variable practice.

View Article and Find Full Text PDF

Climate Change and Radiology: Impetus for Change and a Toolkit for Action.

Radiology

May 2023

From the Department of Radiology, University of British Columbia, Vancouver, BC, Canada (M.B.); Department of Radiology, Wake Forest University School of Medicine, Winston-Salem, NC (J.H.S.); Department of Radiology, Texas Children's Hospital/Baylor College of Medicine, Houston, Tex (J.G.); Department of Radiology and Radiological Sciences, Vanderbilt University Medical Center, Nashville, Tenn (R.A.O.); Department of Medical Imaging, University Medical Imaging Toronto, University of Toronto, Toronto, ON, Canada (K.H.); and Toronto General Hospital Research Institute, University Health Network (UHN), University of Toronto, 1 PMB-298, 585 University Ave, Toronto, ON, Canada M5G 2N2 (K.H.).

This special report discusses the importance of climate change for health care and radiology. The impact of climate change on human health and health equity, the contribution of health care and medical imaging to the climate crisis, and the impetus for change within radiology to create a more sustainable future are covered. The authors focus on actions and opportunities to address climate change in our role as radiologists.

View Article and Find Full Text PDF

Genetic Testing in Clinical Movement Disorders: A Case-Based Review.

Semin Neurol

February 2023

Division of Neurology, Department of Medicine, Ottawa Hospital Research Institute, University of Ottawa Brain and Mind Research Institute, The Ottawa Hospital, Ottawa, Ontario, Canada.

Article Synopsis
  • Understanding genetics is crucial for comprehending neurological diseases, especially movement disorders like Parkinson's and Huntington's disease.
  • Advancements in genetic testing have improved the chances of diagnosing these disorders, but clinicians still face challenges in selecting the right tests and interpreting results.
  • The review employs real case examples to explore key topics in genetic testing, including testing for Parkinson's disease, handling inconclusive results, and focusing on repeat expansion disorders like Huntington's.
View Article and Find Full Text PDF

Updated clinical practice recommendations for managing adults with 22q11.2 deletion syndrome.

Genet Med

March 2023

The Dalglish Family 22q Clinic, Toronto General Hospital, University Health Network, Toronto, Ontario, Canada; Department of Psychiatry, University of Toronto, Toronto, Ontario, Canada; Clinical Genetics Research Program and Campbell Family Mental Health Research Institute, Centre for Addiction and Mental Health, Toronto, Ontario, Canada; Department of Mental Health and Division of Cardiology, Department of Medicine, and Toronto General Hospital Research Institute, University Health Network, Toronto, Ontario, Canada. Electronic address:

This review aimed to update the clinical practice guidelines for managing adults with 22q11.2 deletion syndrome (22q11.2DS).

View Article and Find Full Text PDF

Background: Research participant feedback is rarely collected; therefore, investigators have limited understanding regarding stakeholders' (affected individuals/caregivers) motivation to participate. Members of the Genes to Mental Health Network (G2MH) surveyed stakeholders affected by copy number variants (CNVs) regarding perceived incentives for study participation, opinions concerning research priorities, and the necessity for future funding. Respondents were also asked about feelings of preparedness, research burden, and satisfaction with research study participation.

View Article and Find Full Text PDF

Prenatal Screening and Diagnostic Considerations for 22q11.2 Microdeletions.

Genes (Basel)

January 2023

Division of Human Genetics, The 22q and You Center, and Clinical Genetics Center, Children's Hospital of Philadelphia, Philadelphia, PA 19104, USA.

Diagnosis of a chromosome 22q11.2 microdeletion and its associated deletion syndrome (22q11.2DS) is optimally made early.

View Article and Find Full Text PDF

Clinical genetics of schizophrenia and related neuropsychiatric disorders.

Psychiatry Res

January 2023

Department of Psychiatry, University of Toronto, Toronto, Ontario, Canada; Clinical Genetics Research Program, and Campbell Family Mental Health Research Institute, Centre for Addiction and Mental Health, Toronto, Ontario, Canada; The Dalglish Family 22q Clinic, Department of Psychiatry and Division of Cardiology, Department of Medicine, and Toronto General Hospital Research Institute, University Health Network, Toronto, Ontario, Canada. Electronic address:

Rare structural variants have turned out to be the long sought for genetic variants of (relatively) high effect size for schizophrenia. Delineating the 22q11.2 microdeletion as the first molecular subtype of schizophrenia was a milestone in schizophrenia research, foreshadowing a more general role for rare copy number variation (CNV) in schizophrenia.

View Article and Find Full Text PDF

Tandem repeat expansions (TREs) are associated with over 60 monogenic disorders and have recently been implicated in complex disorders such as cancer and autism spectrum disorder. The role of TREs in schizophrenia is now emerging. In this study, we have performed a genome-wide investigation of TREs in schizophrenia.

View Article and Find Full Text PDF

Background: The indication for treatment of type 1 diabetes(T1D) with the sodium-glucose cotransporter 2 inhibitor (SGLT2i) dapagliflozin has been withdrawn in Europe likely because of concern for diabetic ketoacidosis (DKA). We calculated the incidence of DKA in people with T1D treated with SGLT2i in Denmark.

Methods: Clinical data from adults with T1D in Denmark were collected from nine outpatient clinics.

View Article and Find Full Text PDF

Objectives: To compare the diagnostic performance of international hepatocellular carcinoma (HCC) guidelines with gadoxetic acid-enhanced MRI (EOB-MRI) and contrast-enhanced Computed tomography (CECT) and their impact on liver transplant (LT) allocation in cirrhotic patients with explant histopathology correlation.

Methods: In this prospective single-centre ethics-approved study, 101 cirrhotic patients were consecutively enrolled with informed consent from the pre-LT clinic. They underwent CECT and EOB-MRI alternately at three monthly intervals until LT or removal from LT list.

View Article and Find Full Text PDF

Decline in Ventilatory Ratio as a Predictor of Mortality in Adults With ARDS Receiving Prone Positioning.

Respir Care

August 2022

Interdepartmental Division of Critical Care Medicine, University of Toronto, Toronto, Ontario, Canada; Department of Medicine, Division of Respirology, Sinai Health System and University Health Network, Toronto, Ontario, Canada; and Toronto General Hospital Research Institute, Toronto, Ontario, Canada.

Background: Prone positioning reduces mortality in patients with moderate/severe ARDS. It remains unclear which physiological parameters could guide clinicians to assess which patients are likely to benefit from prone position. This study aimed to determine the association between relative changes in physiological parameters at 24 h of prone positioning and ICU mortality in adult subjects with ARDS.

View Article and Find Full Text PDF

Impact of cardiopulmonary bypass duration on efficacy of fibrinogen replacement with cryoprecipitate compared with fibrinogen concentrate: a post hoc analysis of the Fibrinogen Replenishment in Surgery (FIBRES) randomised controlled trial.

Br J Anaesth

September 2022

Department of Anesthesia and Pain Management, University Health Network, Sinai Health System, Women's College Hospital, University of Toronto, Toronto, ON, Canada; Peter Munk Cardiac Centre and Toronto General Hospital Research Institute, University Health Network, Toronto, ON, Canada; Institute of Health Policy Management and Evaluation, University of Toronto, Toronto, ON, Canada.

Background: Coagulopathy in cardiac surgery is frequently associated with acquired hypofibrinogenaemia, which can be treated with either purified fibrinogen concentrate (FC) or cryoprecipitate. Because the latter is not purified and therefore contains additional coagulation factors, it is thought to be more effective for treatment of coagulopathy that occurs after prolonged cardiopulmonary bypass (CPB). We examined the impact of CPB duration on the efficacy of the two therapies in cardiac surgery.

View Article and Find Full Text PDF

Objectives: Recurrent chromosome 22q11.2 deletions cause 22q11 deletion syndrome (22q11DS), a multisystem disorder associated with high rates of schizophrenia. Neuroanatomical changes on brain MRI have been reported in relation to 22q11DS.

View Article and Find Full Text PDF

Background: Hypofibrinogenaemia is associated with excessive bleeding after cardiac surgery. Our aim was to compare the efficacy and safety of weight-adjusted empiric dosing of fibrinogen replacement in cardiac surgery.

Methods: In the Fibrinogen Replenishment in Cardiac Surgery (FIBRES) RCT, patients (=735) received fibrinogen concentrate (4 g) or cryoprecipitate (10 units).

View Article and Find Full Text PDF

[Treatment-Emergent Central Sleep Apnea - Detection and Treatment].

Praxis (Bern 1994)

June 2022

Universitätsklinik für Pneumologie, Inselspital, Universitätsspital Bern, Universität Bern, Bern, Schweiz.

Treatment-Emergent Central Sleep Apnea - Detection and Treatment In treatment-emergent central sleep apnea (TECSA), affected patients with obstructive sleep apnea newly develop central sleep apnea (AHI central ≥5/h) under therapy with positive pressure ventilation which cannot be explained by other causes. The pathophysiology of TECSA is incompletely understood. PaCO2 and the associated apnea threshold seem to play a central role.

View Article and Find Full Text PDF