Pediatric Academic Societies'
Annual Meeting
>

       HOME                                                                                                                                      SITE MAP  

   
 

Sponsored by the:
 
 
American Pediatric Society
  
Society for Pediatric Research
  
Ambulatory Pediatric Association 

Alliance Organizations

Program Information

Program Committee & Contacts

Abstracts

Awards

Registration & Housing

Exhibits

Sponsorship/Support

Future Meetings

Past Meetings

Meeting Profiles

Pediatric Related Links

Contact Information
Mail Address:
Suite B-7
3400 Research Forest Drive
The Woodlands, TX  77381 USA
Telephone:  281-419-0052
Facsimile:  281-419-0082

 

Pediatric Infectious Diseases Society
May 3 – 6, 2003
Washington State Convention and Trade Center

 


Invitation

Join us in Seattle, where the Pediatric Infectious Diseases Society (PIDS) and the Pediatric Academic Societies (PAS) will host tightly aligned programs again this year.  PIDS symposia, joint symposia and original science will all be held at the Washington State Convention and Trade Center.  Contact Christy Taylor at the PIDS Office for information regarding the PIDS Dinner and Awards program on Monday evening, May 5th.

Registration Information

As in the past, there will be a single registration fee for the meeting set at the PAS registration fee schedule.  

Register by March 7th for substantial savings.  


Hotel 
Reservations

PIDS attendees may reserve accommodations at any of the PAS meeting hotels.

For PIDS  
Information

Contact for PIDS information:
Christy Taylor, PIDS Staff Manager
PIDS Headquarters
66 Canal Center Plaza, Suite 600
Alexandria, VA  22314
Phone: 703-299-6764
Fax: 703-299-0473
Email: ctaylor@idsociety.org
URL: www.pids.org

Contact for housing, registration and general information:
PAS Program Office
3400 Research Forest Dr., Ste. B-7 
The Woodlands, TX  77381
Phone:  281-419-0052     Fax:  281-419-0082
Email:  info@pas-meeting.org

URL:  www.pas-meeting.org

 


Conference 
Objectives


At the conclusion of this educational activity the participant should be better able to:

  • Comprehend new information and skills in various areas of basic and clinical pediatric research.

  • Apply knowledge gained in all areas of pediatric investigation and practice.

  • Understand new tools for teaching and practicing of medicine related to pediatrics.

Continuing 
Education


Continuing Education is through the PAS, as follows:

This activity has been planned and implemented in accordance with the Essential Areas and Policies of the Accreditation Council for Continuing Medical Education (ACCME) through the joint sponsorship of Tulane University Health Sciences Center and the Pediatric Academic Societies. Tulane University Health Sciences Center is accredited by the Accreditation Council for Continuing Medical Education to provide continuing medical education for physicians.

Tulane University Health Sciences Center designates this educational activity for a maximum of 36.50 hours in category 1 credit toward the AMA Physician’s Recognition Award. Each physician should claim only those hours of credit that he/she actually spent in the educational activity.

Tulane University Health Sciences Center presents this activity for educational purposes only. Participants are expected to utilize their own expertise and judgment while engaged in the practice of medicine. The content of the presentations is provided solely by presenters who have been selected because of their recognized expertise.
 

PIDS
Program Schedule 
(as of December 2002)

 

 

Saturday, May 3, 2003

9:30am – 11:30am
PAS Educational Workshops
See the PAS Daily Program

12:00pm – 3:00pm
Mini Courses & Educational Workshops
See the PAS Daily Program

3:15pm – 5:15pm
Infectious Diseases and/or Neonatal Infectious Diseases Platform Session
PAS/PIDS Original Science Abstracts

5:15pm – 7:15pm
Neonatal Infectious Diseases and/or Infectious Diseases Posters I
Poster Session I, PAS Opening Reception & Exhibits
PAS/PIDS Original Science Abstracts
 


Sunday, May 4, 2003

7:00am – 8:00am
Meet the Professor Breakfasts
   TICKETED EVENTS 
VENT

  • Advance Sign Up Required.

  • Attendance is limited to maintain the intimate interactive format and only 25 tickets will be assigned to each of these special sessions. These sessions will fill quickly.

  • To register, use the registration form on page 69

4052    Infectious Diseases
PAS Meet the Professor Breakfast

The Challenges of Clinical Research in Infectious Diseases; The Good, The Bad and the Ugly
Kathryn M. Edwards, Vanderbilt University School of Medicine, Nashville, TN

In this session the speaker will use a randomized placebo controlled vaccine efficacy trial to demonstrate the needed elements of a well conducted clinical trial. In addition to discussing the fundamental elements of a clinical trial, the speaker will also discuss the practical implications of clinical research in one’s career, how one integrates clinical studies into the broader context of academic life and how one prepares for such a career. Ample time for discussion will be available to the participants about all phases of the presentation.
 

8:00am – 10:00am
4102     Smallpox and Bioterrorism Preparedness Planning
PAS/PIDS Topic Symposium
Chair:  John F. Modlin, Children’s Hospital at Dartmouth/Dartmouth Medical School, Lebanon, NH

This program will give a “pediatric perspective” to smallpox bioterrorism preparedness planning efforts now under way within federal, state and local public health agencies. It will include a review of smallpox epidemiology, clinical disease, smallpox (vaccinia) vaccine and lessons learned from the WHO Smallpox Eradication Program. The nature of the current threat and responses to that threat will be discussed.

Smallpox Epidemiology and Clinical Disease
Walter A. Orenstein, National Immunization Program, Centers for Disease Control and Prevention, Atlanta, GA

Control and Eradication of Smallpox
J. Michael Lane, Emory University School of Medicine, Atlanta, GA

Smallpox (Vaccinia) Vaccine: Efficacy and Complications
John M. Neff, Children’s Hospital and Regional Medical Center, Seattle, WA

Smallpox Bioterrorism Preparedness Planning
John F. Modlin, Children’s Hospital at Dartmouth/Dartmouth Medical School, Lebanon, NH

Sponsored jointly with the Pediatric Infectious Diseases Society and the Pediatric Academic Societies
 

11:45am – 1:45pm
Neonatal Infectious Diseases and/or Infectious Diseases Posters II
PAS Poster Session II & Exhibits
PAS/PIDS Original Science Abstracts
 

2:30pm – 4:00pm
4731              Neonatal Herpes Simplex Virus (HSV) Infections: Current Controversies
PAS/PIDS State of the Art
Chair:  Richard J. Whitley, University of Alabama at Birmingham, Children’s Hospital, Birmingham, AL

This State of the Art Plenary will be of interest to practitioners, generalists, neonatologists and infectious diseases specialists and will explore current controversies in the diagnosis and management of neonatal HSV infection.  Speakers will present maternal factors that may allow interruption of maternal–fetal transmission of the virus, the latest strategies for diagnosis and treatment of newborns, and the potential prevention of neonatal HSV by use of pre-emptive antiviral therapy and vaccines.

Maternal–Fetal Transmission:  Risks and Opportunities
Ann M. Arvin, Stanford University School of Medicine, Stanford, CA

Diagnosis and Treatment of Neonatal HSV
Richard J. Whitley, University of Alabama at Birmingham, Children’s Hospital, Birmingham, AL

Prevention of Neonatal HSV Infection:  Are Vaccines the Answer?
Lawrence R. Stanberry, University of Texas Medical Branch, Galveston, TX

Discussion

Questions from the Audience and Answers from the Experts
Audience Moderators:  
Gail J. Demmler, Baylor College of Medicine, Houston, TX and Larry Givner, Wake Forest University, Winston-Salem, NC

Sponsored jointly with the Pediatric Infectious Diseases Society and the Pediatric Academic Societies
 

4:15pm – 6:15pm
4850     Current Research Issues in STDs and Adolescents: Chlamydia, Genital Herpes and Human Papillomavirus Infection
PAS/PIDS Topic Symposium
Chair:  Donald E. Greydanus, Michigan State University Kalamazoo Center for Medical Studies, Kalamazoo, MI

This session reviews current research principles in selected sexually transmitted diseases.  First, clinical epidemiology and prevention issues for Chlamydia trachomatis are considered, emphasizing rescreening (delayed retesting of infected persons), novel strategies for assuring partner treatment and the role of male screening in disease control.  Then, new directions in public health and prevention aspects of genital herpes are outlined.  An update of the HSV vaccine is presented.  Finally, human papillomavirus (HPV) is considered, including new recommendations in human papillomavirus testing, triage of abnormal Pap smears and the current status of HPV vaccines.  Questions are encouraged from the audience.

Chlamydia
H. Hunter Handsfield, University of Washington and Public Health - Seattle & King County, Seattle, WA

Genital Herpes
Anna Wald, University of Washington Virology Research Clinic, Seattle, WA

Human Papillomavirus Infection
Anna-Barbara Moscicki, Glaser Pediatric Research Network, University of California, San Francisco, CA

Epidemiology of STDs in Children and Adolescents: Perspectives from the World Health Organization
Nathalie Broutet, World Health Organization, Geneva, Switzerland

Sponsored jointly with the Pediatric Infectious Diseases Society and the Pediatric Academic Societies


Monday, May 5, 2003

8:00am – 10:00am
Neonatal Infectious Diseases and/or Infectious Diseases Abstract Session
PAS/PIDS Original Science Abstracts
 

1:00pm – 2:45pm
March of Dimes Prize in Developmental Biology Lectures
 

3:00pm – 5:00pm
5654               Vaccines—2003
PAS/PIDS Topic Symposium
Chair:  Stanley A. Plotkin, Aventis Pasteur and the University of Pennsylvania, Doylestown, PA

This symposium covers four issues in vaccination.  The American Academy of Pediatrics and CDC currently are moving toward a recommendation for universal annual vaccination of infants with killed or live influenza vaccine.  Why is this?  Now that Rotashield is off the market, a new rotavirus vaccine is needed and may be on the way.  Despite good protection of children by vaccination, pertussis infections are rising in adolescents and adults.  Can they be controlled?  Recent disruptions in vaccine supply have caused pediatricians significant problems.  What are the causes and solutions?

Universal Influenza Vaccination in Children
W. Paul Glezen, Baylor College of Medicine, Houston, TX

New Rotavirus Vaccines: After Rotashield
Paul A. Offit, Children’s Hospital of Philadelphia, Philadelphia, PA

Adolescent and Adult Pertussis Vaccination
Kathryn M. Edwards, Vanderbilt University School of Medicine, Nashville, TN

Vaccine Shortages: Causes and Effects
Walter A. Orenstein, National Immunization Program, Centers for Disease Control and Prevention, Atlanta, GA

Sponsored jointly with the Pediatric Infectious Diseases Society and the Pediatric Academic Societies
 

5:00pm – 6:00pm
PIDS Business Meeting
 

6:15pm
5955A  PIDS Annual Dinner & Awards Banquet
Grand Hyatt Seattle
 


Tuesday, May 6, 2003

8:00am – 10:00am
Related Infectious Diseases Abstract Session
PAS/PIDS Original Science Abstracts

10:15am – 11:45am
6302     New Directions in Newborn and Pediatric Sepsis and Multiple Organ Failure
PAS/PIDS State of the Art
Chair:  Joseph A. Carcillo, University of Pittsburgh School of Medicine, Pittsburgh, PA

Severe sepsis is an important and relatively neglected public health problem in the United States.  National estimates show that more children die with severe sepsis than die with cancer.   Despite improving national outcomes (10% mortality in 1995 and 9% mortality in 1999), the burden of severe sepsis continues to increase in the US with an estimated associated annual cost of 4 billion dollars. 

There is cause for continued optimism in the field.  In 1968, 96% of children with severe gram negative sepsis died.  Early recognition and aggressive fluid resuscitation has been credited with improved outcomes from septic shock (St. Mary’s Hospital reported a 5% mortality rate in meningococcal septic shock/purpura fulminans, and investigators in Vietnam reported a 0% mortality rate in Dengue shock in 2001).  Unlike adults, who die of vascular failure, newborns and children who die of fluid refractory septic shock do so from cardiac failure. The American College of Critical Care Medicine published age-specific evidence-based guidelines for management of newborn and pediatric shock in 2002. 

Understanding of the pathophysiology and potential treatment of sepsis-induced multiple organ failure is also rapidly advancing.  Thrombocytopenia associated multiple organ failure has been further characterized as a thrombotic microangiopathy.  Twenty percent of these patients have disseminated intravascular coagulation pathophysiology (unopposed tissue factor activity and consumptive coagulopathy), but 80% have thrombotic thrombocytopenic purpura pathophysiology (increased ultra large vWF multimers and decreased vWF cleaving protease activity).  This has great therapeutic implications because recombinant technology is rapidly producing human coagulation-related proteins (e.g., activated protein C, vWF cleaving protease, tissue plasminogen activator), and prolonged plasma exchange therapy is a proven therapy that reverses TTP pathophysiology.  Up to 80% of children who die with sepsis do so with multiple organ failure and uneradicated infection.  Primary and acquired immunodeficiency states contribute to most of these poor outcomes.  Prolonged neutropenia, lymphopenia, and hypogammaglobulinemia are readily measured in the clinical laboratory but research measurements (monocyte HLA-DR expression, and ex vivo whole blood TNF a response to LPS stimulation) are required to diagnose prolonged monocyte deactivation and immuneparalysis.  Diagnosis of these immunodeficiency syndromes can have great therapeutic implications as tapering of immune suppression and use of recombinant growth factors (e.g., G-CSF, GM-CSF, interferon) and prophylaxis strategies can improve outcome in these children.

Newborn and Pediatric Sepsis and Multiple Organ Failure
Joseph A. Carcillo, University of Pittsburgh School of Medicine, Pittsburgh, PA

Hypodynamic Septic Shock: The Heart as an Innate Immune Response Organ
Brett P. Giroir, University of Texas Southwestern Medical Center, Dallas, TX

Thrombocytopenia-Associated Multiple Organ Failure: The Role of ADAMTS13
Trung Nguyen, University of Pittsburgh School of Medicine, Pittsburgh, PA

Prolonged Monocyte Deactivation and Unresolving Multiple Organ Failure: A TH2-Like Paradigm
Mark Hall, Ohio State University School of Medicine, Columbus, OH

Sponsored jointly with the Pediatric Infectious Diseases Society and the Pediatric Academic Societies

Copyright:
All information contained in this Website is the property of the Pediatric Academic Societies unless otherwise noted.
Duplication of any information contained herein for reasons other than personal use requires the expressed written permission of PAS
.

For comments or concerns about the website, please contact webmaster@pas-meeting.org.

Last Updated: September 26, 2006