Zobrazeno 1 - 10
of 22
pro vyhledávání: '"Aruna T. Nathan"'
Autor:
Aruna T. Nathan, Adam C. Adler
Publikováno v:
Anesthesiology clinics. 38(3)
Children and adults with congenital heart disease undergoing noncardiac surgery are at higher risk of perioperative adverse events. Patients have significant comorbidities and syndromic associations that increase perioperative risk further. The compl
Autor:
Yaniv Bar-Cohen, Naomi J. Kertesz, Macdonald Dick, Ronald J. Kanter, Joel A. Kirsh, Martin J. LaPage, John M. Clark, Christina Y. Miyake, Nicholas H. Von Bergen, Bryan C. Cannon, S Asirvatham, Francis X. McGowan, J. Philip Saul, Andreas Pflaumer, Frank Zimmerman, John D. Kugler, Andrew D. Blaufox, Anne Freter, William G. Stevenson, Allan C. Skanes, Aruna T. Nathan, Thomas Paul, John Papagiannis, Dominic Abrams
Publikováno v:
Heart Rhythm. 13:e251-e289
Dominic Abrams, MD, Sam Asirvatham, MD, Yaniv Bar-Cohen, MD, FAAP, FACC, FHRS, Andrew D. Blaufox, MD, FHRS, FACC, Bryan Cannon, MD, FHRS, John Clark, MD, Macdonald Dick, MD, FHRS, FACC, Anne Freter, MSN, FHRS, Naomi J. Kertesz, MD, FACC, FHRS, Joel A
Autor:
Aruna T. Nathan, Aditee P. Ambardekar, David L. Rodgers, Justin L. Lockman, Roberta Hales, Ellen S. Deutsch, Devika Singh, Harshad Gurnaney
Publikováno v:
Pediatric Anesthesia. 26:481-487
SummaryBackground Pediatric anesthesiologists must manage crises in neonates and children with timely responses and limited margin for error. Teaching the range of relevant skills during a 12-month fellowship is challenging. An experiential simulatio
Publikováno v:
Anesthesiology. 117:1117-1126
The long QT syndrome (LQTS) is characterized by prolonged ventricular repolarization, the electrocardiographic appearance of long QT intervals, an atypical polymorphic ventricular tachycardia known as torsades de pointes (TdP), and an increased risk
Autor:
Lisa M. Montenegro, Aruna T. Nathan, Susan C. Nicolson, David R. Jobes, Victoria L. Vetter, Darryl H. Berkowitz
Publikováno v:
Anesthesia & Analgesia. 112:1163-1168
Patients with congenital long QT syndrome (LQTS) are susceptible to an episodic malignant ventricular tachyarrhythmia known as torsade de pointes, which can result in a cardiac arrest and death. Patients can suffer severe cardiac events resulting in
Autor:
Susan C. Nicolson, K. Sarah Hoehn, Gil Wernovsky, Robert M. Nelson, Richard F. Ittenbach, J. William Gaynor, Aruna T. Nathan
Publikováno v:
Journal of Medical Ethics. 36:106-110
Objective To assess parental permission for a neonate9s research participation using the MacArthur competence assessment tool for clinical research (MacCAT-CR), specifically testing the components of understanding, appreciation, reasoning and choice.
Publikováno v:
Anesthesiology. 123(4)
Primary Erythromelalgia in a Child Responding to Intravenous Lidocaine and Oral Mexiletine Treatment
Publikováno v:
Pediatrics. 115:e504-e507
Erythromelalgia is a rare, chronic, debilitating condition characterized by redness, warmth, and severe burning pain of the distal extremities. The feet are more commonly affected than the hands. Pain is precipitated by increases in temperature and b
Publikováno v:
Anesthesia & Analgesia. 114:407-409
Long QT syndrome is characterized by electrocardiographic appearance of long QT intervals and propensity to polymorphic ventricular tachycardia. Aggressive anticipatory clinical management is required for a good outcome, especially in the symptomatic
Autor:
Jason G. Andrade, Susan P. Etheridge, Shubhayan Sanatani, Dorothy Myers, Ian H. Law, Prince J. Kannankeril, Aruna T. Nathan, Kathryn K. Collins, Jason Hayes, Scott C. Watkins, Simon D. Whyte
Publikováno v:
Anesthesia and analgesia. 119(4)
Patients with long QT syndrome (LQTS) may experience a clinical spectrum of symptoms, ranging from asymptomatic, through presyncope, syncope, and aborted cardiac arrest, to sudden cardiac death. Arrhythmias in LQTS are often precipitated by autonomic