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

2005 PAS Annual Meeting
May 14 – 17
Washington, DC 
 

Pulmonology

Back to Track Index
Daily Expanded Schedule
Alliance Programs
 

  

Last updated February 10, 2005


Saturday, MAY 14

1:00pm–3:00pm
4652—Neonatal Infectious Disease and Inflammation
PAS Original Science Abstracts - Platform Session

1:00pm–3:00pm
4654—Pulmonary Vascular Biology
PAS Original Science Abstracts - Poster Symposium

3:15pm–5:15pm
4842—Fetal Origins of Adult Disease
PAS Original Science Abstracts - Poster Symposium

3:15pm–5:15pm
4851—Pathogenesis of Bronchopulmonary Dysplasia
PAS Original Science Abstracts - Platform Session

Sunday, MAY 15

7:00am–8:00am
5057—Pulmonology
Career Development in Pediatric Pulmonary Medicine
PAS Meet the Professor Breakfast

Steven H. Abman, University of Colorado School of Medicine, Denver, CO

This session will discuss issues in career development for trainees and junior faculty who are interested in pediatric pulmonary and critical care medicine. Discussion will focus on issues regarding training in clinical research, expanding laboratory research skills, meeting clinical and research committees, balancing career with life style, developing collaborations, mentorship and related questions.

Target Audience: Trainee, junior faculty.

8:00am–10:00am
5101—ARDS: New Pathways and Treatments
PAS Topic Symposium
Chairs: Steven H. Abman, University of Colorado School of Medicine, Denver, CO; and Alan Jobe, Cincinnati Children's Hospital Medical Center, Cincinnati, OH

Acute respiratory distress syndrome (ARDS) remains a leading cause of morbidity and death in critically ill neonates, infants and children. ARDS is associated with diverse clinical disorders, including sepsis, trauma, aspiration and infection and is characterized by lung inflammation, non-hydrostatic pulmonary edema and poor lung compliance. Recent advances in the basic pathobiology of lung injury have led to new insights into the etiology and potential therapeutic approaches toward ARDS. In addition, recent clinical studies have examined differences between adult and pediatric ARDS, genetic susceptibility factors that may increase the risk for ARDS, interactive cellular and physiologic mechanisms that cause progressive lung injury and the role of different strategies of mechanical ventilation that can adversely or favorably determine the clinical outcomes of patients with ARDS. This symposium includes leading experts in the field of lung biology and critical care who will present state of the art information on basic pathophysiologic mechanisms of ARDS and new therapeutic approaches. These integrated topics are of marked interest to intensivists, neonatologists, pulmonologists, infectious disease and basic scientists in the field of lung biology.

Target Audience: Scientists and clinicians interested in basic mechanisms underlying the pathophysiology of acute lung injury and clinical strategies in the management of acute hypoxemic respiratory failure in neonates, infants and children.

New Insights into ARDS
Michael Matthay, University of California San Francisco Medical School, San Francisco, CA

Mechanisms of Tissue Injury in Sepsis/ARDS
Hector R. Wong, Cincinnati Children's Hospital Medical Center, Cincinnati, OH

Role of Permissive Hypercapnea in Acute Lung Injury
Brian Kavanagh, Hospital for Sick Children, Toronto, ON, Canada

Novel Ventilator Strategies in ARDS
John H. Arnold, Children's Hospital, Boston, MA
 

8:00am–10:00am
5140—Childhood Asthma
PAS Original Science Abstracts - Platform Session

8:00am–10:00am
5150—Vascular Mediators in Persistent Pulmonary Hypertension
PAS Original Science Abstracts - Platform Session

8:00am–11:00am
5201—New Care Models for Inner-City Asthma: How Expanding the Primary Care Role of the Pediatric Emergency Department Can Improve Patient Outcomes
PAS Mini Course
Chairs: Ellen F. Crain, Albert Einstein College of Medicine and Jacobi Medical Center, Bronx, NY; and Sandra J. Cunningham, Albert Einstein College of Medicine and Jacobi Medical Center, Bronx, NY

The prevalence of and morbidity from asthma is especially high among inner-city children, and these children disproportionately use the emergency department (ED) for care. While EDs provide excellent acute care, they are not equipped to provide the preventive care that these children need. There is a debate in the pediatric ED community about how much primary care is appropriate for the ED to take on, but most efforts in primary care settings to reduce ED use by inner-city children with asthma have not worked. In this session, participants will learn about several successful pediatric ED interventions to reduce ED use by inner-city children, which have required the addition of relatively modest primary care activities. The interventions, as well as their human, financial and implementation costs, and likely success in other settings will be described.

Target Audience: Pediatric emergency medicine physicians, pulmonologists, epidemiologists, health service researchers.

Incorporating Primary Care into Emergency Department Treatment of Children with Asthma
Sandra J. Cunningham, Albert Einstein College of Medicine, Jacobi Medical Center, Bronx, NY

Successful Emergency Department Strategies To Improve Long-Term Care for Children with Asthma
Joseph J. Zorc, Children's Hospital of Philadelphia, Philadelphia, PA

The Asthma Coach Program
Sharon R. Smith, Connecticut Children's Medical Center, Hartford, CT

The Fast Track Clinic: An Emergency Department Intervention To Reduce Morbidity Among Children with Asthma
Stephen J. Teach, Children's National Medical Center, Washington, DC

Discussion
 

11:45am–1:45pm
Poster Session II
PAS Original Science Abstracts - Poster Session

Pulmonology:
5460—General

Neonatology:
5465—Apnea—Respiratory Control
5466—Control of Breathing
 

2:00pm–4:00pm
5521—Regulation of Alveolar Epithelial Repair—or, How Do We Put It All Back Together Again
PAS Topic Symposium
Chairs: Rita Ryan, State University of New York at Buffalo, Women and Children's Hospital of Buffalo, Buffalo, NY; and Heber Nielsen, Tufts University School of Medicine, Tufts-New England Medical Center, Boston, MA

Regulation of alveolar epithelial repair after many forms of lung injury remains incompletely understood. The type II cell is an important source of growth factors and there are autocrine and paracrine mediators that are altered during the repair process. Type I cells are the primary covering of the alveolar epithelium, and their restoration is critical to recapitulate normal repair. This symposium will focus on the fundamental mechanisms of epithelial repair after injury and examine connections with lung development. Finally, relevance to current clinical disease will be discussed.

Target Audience: Physician and basic scientists interested in how the alveolar epithelium repairs itself after injury and the relationship of lung repair with lung development.

Introduction
Rita M. Ryan, State University of New York at Buffalo, Women and Children's Hospital of Buffalo, Buffalo, NY
Heber C. Nielsen, Tufts New England Medical Center, Boston, MA

Type II Cell Mitogens
Timothy D. Le Cras, Cincinnati Children's Hospital Medical Center, Cincinnati, OH

Type II Cell Proliferation During Lung Injury and Repair
Michael A. O'Reilly, University of Rochester, Rochester, NY

Type I Cells in Alveolar Repair
Susan H. Guttentag, Children's Hospital of Philadelphia, Philadelphia, PA

Apoptosis in Alveolar Epithelial Repair
Lin L. Mantell, Institute for Medical Research at North Shore-Long Island Jewish, New York University School of Medicine, Manhasset, NY

Translating Alveolar Epithelial Repair Fundamentals to the Bedside
John S. Torday, Los Angeles Biomedical Research Institute at Harbor-UCLA Medical Center, Torrance, CA
 

2:00pm–4:00pm
5535—Neonatal Epidemiology and Follow-up
PAS Original Science Abstracts - Platform Session

4:15pm–5:45pm
5702—Identification of Asthma-Susceptibility Genes and Implications for New Pharmaceutical Development
PAS State of the Art Plenary
Chair: Clifford W. Bogue, Yale University School of Medicine, New Haven, CT

Asthma is rapidly emerging as a major public health disorder in childhood. Innovative strategies combining genetic mapping and gene expression profiling are providing the tools to identify genes that underpin asthma predisposition. This presentation not only has relevance for an important pediatric medical topic, but also establishes a paradigm that can be used for other complex genetic disorders that affect children.

Target Audience: This session will be of interest to a broad audience including practicing pediatricians, geneticists, pulmonologists, pharmacologists, critical care specialists and allergist/immunologists

Marsha Wills-Karp, Children's Hospital Medical Center, Cincinnati, OH
 

4:15pm–6:15pm
5743—Pediatric Nutrition and Metabolism
PAS Original Science Abstracts - Platform Session

Monday, MAY 16

8:00am–10:00am
6101—Understanding the New Pediatric Morbidities: Evidence from the Centers for Children’s Environmental Health and Disease Prevention Research
PAS Topic Symposium
Chair: Ruth A. Etzel, George Washington University School of Public Health and Human Services, Washington, DC

Learning disorders, ADHD, developmental delay, asthma and depression are among the chronic conditions referred to as the “new pediatric morbidities.” There is growing evidence that environmental disruption and chronic exposure to synthetic chemicals contribute to these new morbidities. The 12 Centers for Children’s Environmental Health and Disease Prevention Research funded by the National Institute of Environmental Health Sciences and the U.S. EPA are contributing to our understanding of the effects of environmental exposures on children’s health. Participants in this session will learn about findings related to asthma and neurobehavioral impairment and gain new understanding of conditions that affect growing numbers of U.S. children.

Target Audience: Pediatricians, academic generalists, health services researchers, environmental health scientists, developmental–behavioral pediatricians and pediatric pulmonologists.

Centers for Children's Environmental Health and Disease Prevention Research: Progress Since 1998
Ruth A. Etzel, George Washington University School of Public Health and Health Services, Washington, DC

Prenatal Exposure to Pesticides, Maternal Paraoxonase Levels and Small Heads at Birth: A Possible Gene–Environment Interaction
Trudy Berkowitz, Mount Sinai School of Medicine, New York, NY

PCBs, Mercury and Neurobehavioral Impairment
Susan Schantz, University of Illinois at Urbana-Champaign, Urbana, IL

Air Pollution, Smoking and Asthma in Southern California Children
Frank Gilliland, University of Southern California, Los Angeles, CA

Discussion
 

8:00am–10:00am
6132—Clinical Trials in Perinatal and Neonatal Medicine I
PAS Original Science Abstracts - Platform Session

8:00am–10:00am
6133—Development Biology
PAS Original Science Abstracts - Platform Session.

3:00pm–5:00pm
6730—Cardiac and Pulmonary Development
PAS Original Science Abstracts - Platform Session

3:00pm–5:00pm
6732—Neonatal Hyperoxia and the Lung
PAS Original Science Abstracts - Platform Session

5:15pm–6:45pm
Poster Session III
PAS Original Science Abstracts - Poster Session

Neonatal Pulmonology:
6840—Lung Injury

Developmental Biology:
6852—Lung

Neonatal Pulmonology:
6861—Neonatal Ventilating
6862—Bronchopulmonary Dysplasia

Neonatology:
6872—Steroids and Lung Development
 

6:45pm–8:00pm
6950A—Lung Club
 Club

Oxygen Therapy in the Newborn: Elixir of Life or Nectar of Death?
Ola Didrik Saugstad, Professor, Department of Pediatric Research, Rikshospitalet University Hospital, Oslo, Norway

Contact:
Roberta A. Ballard, M.D.
Children's Hospital of Philadelphia
Phone: 215-590-1653
Email: ballard@email.chop.edu

Sponsored by an educational grant from Ross Products Division, Abbott Laboratories
 

Tuesday, MAY 17

8:00am–10:00am
7101—Inner-City Asthma Intervention Program: Research to Practice
PAS Topic Symposium
Chair: Pamela R. Wood, University of Texas Health Sciences Center at San Antonio, San Antonio, TX

The National Cooperative Inner City Asthma Intervention (NCICAIS) is an asthma counselor (AC), social-worker-driven intervention for inner-city children with persistent asthma. Although the AC intervention was shown to decrease symptom days in a randomized, controlled trial, there were no data on implementation of this intervention outside the research setting. In 2001, the Centers for Disease Control and Prevention funded a 4-year program to implement the asthma counselor model in 22 sites. This “research to practice” session will explore lessons learned through the implementation process and the implications for researchers, clinicians and policy makers.

Target Audience: General pediatricians, pulmonologists, allergists and other health professionals who care for children with asthma; health services researchers; and program planners.

Introduction
Pamela R. Wood, University of Texas Health Sciences Center at San Antonio, San Antonio, TX

NCICAIS Intervention: Differences Between Research and Clinical Settings
Meyer Kattan, Mount Sinai School of Medicine, New York, NY

Asthma Risk Factor Assessment: What Are the Needs of Inner-City Families?
Karen Warman, Children's Hospital at Montefiore, Albert Einstein College of Medicine, Bronx, NY

The Asthma Counselor Speaks: Barriers and Successes
Laudy Rodriguez, Mount Sinai Medical Center, New York, NY

Aligning Incentives For Optimal Asthma Care
Cathy Carroll, Children's Mercy Hospitals and Clinics, Kansas City, MO

Discussion
 

8:00am–10:00am
7102—Transitioning Complex Pediatric Patients to Adult Care
PAS/ASPN/LWPES Hot Topic
Chair: Sandra L. Watkins, University of Washington, Seattle, WA

Transitions are a part of everyone's life experience. Most young people with special health care needs and disabilities (SHCN/D) become independent members of adult society, but some need deliberate guidance and support. With increasing success in reducing the mortality of once devastating pediatric diseases, the latter group is growing in number. A new consensus statement from the American Academy of Pediatrics and the U.S. Federal Government (Healthy People 2010) has focused attention on the need to assist young people with SHCN/D in attaining their potential in adulthood. This symposium will discuss the growing number of young people with SHCN/D and present approaches for effecting these transitions.  Specific disease-related examples will be used to highlight the issues, the barriers and the key elements of successful programs that transition patients from pediatric care to the adult system.

Target Audience:

All Grown Up and Wondering What To Do: Transitioning Complex Pediatric Patients to Adult Care
Patience H. White, George Washington University School of Medicine, Washington, DC

Transition Best Practices
Cecily L. Betz, University Center For Excellence in Development Disabilities, Children's Hospital Los Angeles, CA

Transition to Adult Care in the Nephrology Population–Renal Failure or Success
Maria Ferris, University of North Carolina-Chapel Hill, NC

Training and Workforce Issues for Successful Transition
Roberta G. Williams, University of Southern California, Los Angeles, CA

Discussion

Sponsored jointly by the American Society of Pediatric Nephrology, Lawson Wilkins Pediatric Endocrine Society and the Pediatric Academic Societies
 

8:00am–10:00am
7156—Genetic Basis of Cardiopulmonary Disease
PAS Original Science Abstracts - Platform Session

8:00am–10:00am
7157—Lung Maturation, Septation and Growth
PAS Original Science Abstracts - Platform Session

8:00am–10:00am
7158—Mechanisms of Childhood Lung Disease
PAS Original Science Abstracts - Platform Session

10:15am–11:45am
7301—Genetic Mechanisms of Respiratory Distress in the Newborn Infant
PAS State of the Art Plenary
Chair: F. Sessions Cole, Washington University School of Medicine, St. Louis Children's Hospital, St. Louis, MO

Improved survival of newborn infants with lung disease has unmasked distinct genetic mechanisms that contribute to acute, chronic and lethal pulmonary insufficiency. Mutations in the surfactant protein genes B and C and a lamellar body transporter gene (ATP-binding cassette transporter A3 or ABCA3) may disrupt pulmonary surfactant function and alveolar type 2 pneumocyte metabolism. After discussing the clinical aspects of the surfactant protein deficiencies, we will discuss how more common polymorphisms in the surfactant protein genes may be related to respiratory distress and our current understanding of the pathogenetic contribution of mutations in the ABCA3 gene to both acute neonatal and chronic interstitial lung disease in children.

Target Audience: Neonatologists, pulmonologists and geneticists.

Introduction
F. Sessions Cole, Washington University School of Medicine, St. Louis Children's Hospital, St. Louis, MO

Clinical Aspects of Surfactant Protein Deficiencies
Aaron Hamvas, Washington University School of Medicine, St. Louis Children's Hospital, St. Louis, MO

Polymorphisms in the Surfactant Protein Genes
Mikko Hallman, University of Oulu, Oulu, Finland

ABCA3 and the Genetic Basis of Interstitial Lung Disease
Lawrence M. Nogee, Johns Hopkins School of Medicine, Baltimore, MD

Summary
F. Sessions Cole, Washington University School of Medicine, St. Louis Children's Hospital, St. Louis, MO

Supported in part by an unrestricted educational grant from Dey, LP
 

12:00pm–1:30pm
Poster Session IV
PAS Original Science Abstracts - Poster Session

Neonatal Pulmonology:
7420—Surfactants
7421—Vascular Biology

Neonatology:
7430—Oxygen/Oxidative Stress
7432—Nitric Oxide
 

1:45pm–3:45pm
7601—New Therapeutic Strategies for Classical Pediatric Diseases
PAS Hot Topic
Chairs: David Cornfield, University of Minnesota School of Medicine, Minneapolis, MN; and Nina F. Schor, Children's Hospital of Pittsburgh, Pittsburgh, PA

The pathogenesis of numerous single-gene disorders has been effectively delineated. However, the application of this knowledge to patient care has lagged far behind. This symposium will present recent progress made in the development of therapeutic strategies for four classical pediatric disorders. First, novel genetic therapies for hematologic diseases will be discussed. Second, interventions that reverse the key abnormalities in signal transduction underlying autosomal dominant polycystic kidney disease, a leading cause of end-stage renal disease, will be presented. Third, we will discuss a treatment strategy that normalizes the intracellular processing and function of the mutated cystic fibrosis transmembrane conductance regulator (CFTR), which underlies the majority of cases of CF. Fourth, pharmacologic strategies against muscular dystrophy will be presented. These four innovative approaches provide great hope for patients suffering from these disorders, and they serve as exciting examples of potential means to combat other devastating pediatric conditions.

Target Audience: Scientists and clinicians involved with the development of new therapeutic strategies for a variety of childhood disorders.

Embryonic Globins as Therapeutic Agents for Hemoglobinopathies and Thalassemias
J. Eric Russell, The Children's Hospital of Philadelphia, Philadelphia, PA

Novel Therapies for Renal Cystic Diseases
Vicente E. Torres, Mayo Clinic, Rochester, MN

Treatment of Cystic Fibrosis with Curcumin
Marie E. Egan, Yale University School of Medicine, New Haven, CT

Pharmacologic Strategies Against Muscular Dystrophy
Tejvir S. Khurana, University of Pennsylvania School of Medicine, Philadelphia, PA
 

1:45pm–3:45pm
7602—Pulmonary Hypertension: Mechanisms and Management
PAS Hot Topic
Chair: Steve H. Abman, University of Colorado School of Medicine, Denver, CO

Pulmonary hypertension contributes significantly to high morbidity and mortality in diverse clinical settings, including term or near-term newborns with hypoxemic respiratory failure, premature infants with RDS, congenital heart disease, idiopathic or primary pulmonary hypertension and other diseases. Recent advances in molecular biology, genetics and physiology have led to novel therapeutic strategies that are now available for the treatment of severe pulmonary hypertension. This symposium will present novel mechanisms in the pathogenesis of pulmonary hypertension, as well as critical appraisal of treatment options for neonates, infants and children with pulmonary hypertension. First, basic molecular and cellular mechanisms that underlie the development of pulmonary hypertension will be presented. This will be followed by a discussion of the physiologic basis for current therapeutic approaches to persistent pulmonary hypertension of the newborn and ongoing controversies in patient management. The next speaker will discuss the use of inhaled nitric oxide (iNO) in premature infants. Although approved for use in the term or near-term neonate with hypoxemic respiratory failure, the potential role for iNO in premature newborns for the treatment of acute lung disease or the prevention of bronchopulmonary dysplasia has been highly controversial. Finally, we will learn of novel treatment strategies for children with chronic pulmonary hypertension, including clinical approaches that utilize separate or combined therapies, such as prostacyclin analogues, endothelin receptor antagonists and PDE5 inhibitors.

Target Audience: Scientists and clinicians from diverse clinical backgrounds, including neonatology, cardiology, pulmonary medicine and critical care who are involved with newborns and children with acute and chronic pulmonary hypertension. This symposium will describe recent advances in the basic science and clinical management strategies of pulmonary hypertension.

Novel Mechanisms in the Pathogenesis of Pulmonary Hypertension
Marlene Rabinovitch, Stanford University School of Medicine, Stanford, CA

New Insights in the Pathophysiology and Treatment of PPHN
Robin H. Steinhorn, Northwestern University Medical School, Chicago, IL

Controversies in the Use of Inhaled NO in Premature Newborns
John P. Kinsella, University of Colorado School of Medicine, Children's Hospital, Denver, CO

Novel Therapeutic Strategies for the Treatment of Pulmonary Hypertension
Robyn J. Barst, Columbia University College of Physicians & Surgeons, New York, NY

Supported by an unrestricted educational grant from INO Therapeutics

 

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