Safe Medical Devices for Children (2006)

Chapter: Appendix A Study Origins and Activities

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Suggested Citation: "Appendix A Study Origins and Activities." Institute of Medicine. 2006. Safe Medical Devices for Children. Washington, DC: The National Academies Press. doi: 10.17226/11313.

Appendixes

Suggested Citation: "Appendix A Study Origins and Activities." Institute of Medicine. 2006. Safe Medical Devices for Children. Washington, DC: The National Academies Press. doi: 10.17226/11313.

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Suggested Citation: "Appendix A Study Origins and Activities." Institute of Medicine. 2006. Safe Medical Devices for Children. Washington, DC: The National Academies Press. doi: 10.17226/11313.

A
Study Origins and Activities

The Medical Device User Fee and Modernization Act of 2002 (P.L. 107–250) called for the Institute of Medicine (IOM) to conduct a study of postmarket surveillance of pediatric medical devices. IOM appointed a committee of 13 experts to oversee the study. Its task was to develop a report that specifically examined the system under the Federal Food, Drug, and Cosmetic Act for postmarket surveillance of medical devices to assess whether the system as administered by the U.S. Food and Drug Administration provides adequate safeguards for the use of devices in children. As called for in the legislation, the study committee assessed

  • the U.S. Food and Drug Administration’s monitoring and use of adverse reaction reports, registries, clinical studies, and other postmarket surveillance activities to identify unsafe or ineffective products;

  • the adequacy of the agency’s monitoring of commitments for further clinical studies made by manufacturers at the time of approval of specific medical devices;

  • the adequacy of postmarket surveillance studies to evaluate how children’s active lifestyles may affect implant failure rates and longevity; and

  • the length of studies, including whether they continue long enough to evaluate the impact of children’s growth and development given the expected length of time that a child will have an implant.

The committee met five times between April 2004 and March 2005. It organized two advisory panels to provide additional technical guidance on clinical and technical issues. It commissioned two background papers. The

Suggested Citation: "Appendix A Study Origins and Activities." Institute of Medicine. 2006. Safe Medical Devices for Children. Washington, DC: The National Academies Press. doi: 10.17226/11313.

committee conducted three meetings with public sessions, including one to hear the views of family support and advocacy organizations and health care groups (with written statements invited from additional organizations). The committee also met with parents and young people who had personal experiences with implants or other complex medical devices. The agendas and participants for the public meetings are listed below.

INSTITUTE OF MEDICINE

Committee on Postmarket Surveillance of Pediatric Medical Devices

Room 204, The Keck Center, National Academy of Sciences

500 Fifth Street NW, Washington, DC

Public Session—April 15, 2004

1:00

Welcome and introductions

1:10

FDA Context and Perspectives

 

Donna-Bea Tillman, Ph.D.

Deputy Director, Office of Device Evaluation

Center for Devices and Radiological Health

U.S. Food and Drug Administration

Rockville, MD

 

Thomas Gross, M.D.

Director, Division of Postmarket Surveillance

Center for Devices and Radiological Health

U.S. Food and Drug Administration

Rockville, MD

2:40

Break

3:00

Research on Postmarket Surveillance: Experience of Duke Center for Education and Research on Therapeutics

 

Judith M. Kramer, M.D.

Principal Investigator, Duke Center for Education and

Research on Therapeutics

Duke University Medical Center

Durham, NC

4:00

Analysis of FDA Adverse Event Reports

 

Mark Bruley, B.Sc.

Vice President, ECRI

Plymouth Meeting, PA

5:15

Adjourn

* * *

Suggested Citation: "Appendix A Study Origins and Activities." Institute of Medicine. 2006. Safe Medical Devices for Children. Washington, DC: The National Academies Press. doi: 10.17226/11313.

INSTITUTE OF MEDICINE

Committee on Postmarket Surveillance of Pediatric Medical Devices

Room 100, The Keck Center, National Academy of Sciences

500 Fifth Street NW, Washington, DC

Public Session—June 24, 2004

1:00

Welcome and introductions

1:10

Update from CDRH/FDA: Thomas Gross, M.D.

 

Briefing on Legislative Interest in Pediatric Medical Devices: Vipul Mankad, M.D. (Robert Wood Johnson Foundation fellow with Senate Health, Education, Labor and Pensions Committee)

1:30

Discussion with Clinical Advisory Panel

 

Jonathan Abramson, M.D.

Professor and Chair, Department of Pediatrics

Wake Forest University

Winston Salem, NC

 

Francis Sessions Cole, III, M.D.

Vice Chair and Park J. White Professor of Pediatrics

Washington University School of Medicine

Director, Division of Newborn Medicine

St. Louis Children’s Hospital

St. Louis, MO

 

Barbara Fivush, M.D.

Professor of Pediatrics

Johns Hopkins School of Medicine

Division Chief, Pediatric Nephrology

Johns Hopkins Hospital

Baltimore, MD

 

Susan T. Iannaccone, M.D., F.A.A.N.

Director, Neuromuscular Disease and Neurorehabilitation

Texas Scottish Rite Hospital for Children

Professor of Neurology

UT Southwestern Medical Center

Dallas, TX

 

John K. Niparko, M.D.

George T. Nager Professor

Director, Division of Otology, Neurotology & Skull Base Surgery

Johns Hopkins School of Medicine

Baltimore, MD

Suggested Citation: "Appendix A Study Origins and Activities." Institute of Medicine. 2006. Safe Medical Devices for Children. Washington, DC: The National Academies Press. doi: 10.17226/11313.

 

Ramon L. Ruiz, D.M.D., M.D.

Assistant Professor, Oral/Maxillofacial Surgery & Pediatrics

University of North Carolina at Chapel Hill

Director, Pediatric Oral/Maxillofacial Surgery

North Carolina Children’s Hospital

Chapel Hill, NC

 

Frederick J. Schoen, M.D., Ph.D.

Professor of Pathology and Health Sciences and Technology

Harvard Medical School

Executive Vice Chairman, Department of Pathology

Brigham and Women’s Hospital

Boston, MA

3:45

Break

4:00

Discussion with Methods Advisory Panel

 

Elizabeth B. Andrews, Ph.D., M.P.H.

Vice President

Pharmacoepidemiology and Risk Management

RTI Health Solutions

Research Triangle Park, NC

 

Roselie A. Bright, Sc.D.

Epidemiologist

Division of Postmarket Surveillance

Office of Surveillance and Biometrics

Center for Devices and Radiological Health

U.S. Food and Drug Administration

Rockville, MD

 

Robert T. Chen, M.D., M.A.

Chief, Immunization Safety Branch

National Immunization Program

Centers for Disease Control and Prevention

Atlanta, GA

 

Harry A. Guess, M.D., Ph.D.

Professor of Epidemiology

School of Public Health

University of North Carolina at Chapel Hill

Chapel Hill, NC

5:30

Adjourn

* * *

Suggested Citation: "Appendix A Study Origins and Activities." Institute of Medicine. 2006. Safe Medical Devices for Children. Washington, DC: The National Academies Press. doi: 10.17226/11313.

INSTITUTE OF MEDICINE

Committee on Postmarket Surveillance of Pediatric Medical Devices

Lecture Room, National Academy of Sciences

2101 Constitution Avenue, NW, Washington, DC

Public Session—August 31, 2004

8:20

Welcome

8:30

Advanced Medical Technology Association

 

Susan Alpert, M.D.

Vice President, Chief Quality and Regulatory Officer

Medtronic

Minneapolis, MN

9:00

American College of Cardiology, Congenital Heart Disease and Pediatric Cardiology Committee

 

Mark Boucek, M.D.

Director of Pediatric Heart Failure and Transplant Research Programs

The Children’s Hospital Denver

University of Colorado School of Medicine

Denver, CO

 

Pediatric Section, American Thoracic Society

 

Ann C. Halbower, M.D.

Assistant Professor of Pediatrics and Medical Director of Pediatric Sleep Disorders Program

Johns Hopkins University

Baltimore, MD

9:45

American Academy of Pediatrics

 

Jon Abramson, M.D.

Weston L. Kelsey Chair of Pediatrics

Wake Forest University Baptist Medical Center

Winston-Salem, NC

 

Pediatric Orthopedic Society of North America

Michael Vitale, M.D., M.P.H.

Chair, Evidence Analysis Work Group and Assistant Professor in the Division of Pediatric Orthopaedic Surgery Columbia University

New York, NY

10:30

Break

Suggested Citation: "Appendix A Study Origins and Activities." Institute of Medicine. 2006. Safe Medical Devices for Children. Washington, DC: The National Academies Press. doi: 10.17226/11313.

10:50

National Association of Children’s Hospitals and Related Institutions1

 

Joelle Mast, M.D., Ph.D.

Chief Medical Officer and Chief of Pediatrics

Blythedale Children’s Hospital

Valhalla, NY

 

Edwin Simpser, M.D.

Executive Vice President and Chief Medical Officer

St. Mary’s Hospital for Children

Assistant Professor of Clinical Pediatrics

New York University School of Medicine

New York, NY

11:30

National Consumers League

Alison Rein

Assistant Director, Food and Health Policy

Washington, DC

12:00

Adjourn

NOTE: The following organizations endorsed the statement of the American Academy of Pediatrics: Ambulatory Pediatric Association, American Pediatric Society, Association of Medical School Pediatric Department Chairs, Society for Pediatric Research. Additional written statements were provided by: Section on Neurological Surgery (of the American Academy of Pediatrics); Society for Pediatric Anesthesia; American Pediatric Surgical Association; and Anthony D. Slonim, M.D., M.P.H. (of Children’s National Medical Center, Washington, DC).

* * *

INSTITUTE OF MEDICINE

Committee on Postmarket Surveillance of Pediatric Medical Devices

Lecture Room, National Academy of Sciences

2101 Constitution Avenue, NW, Washington, DC

Public Session—August 31, 2004 (afternoon)

Meeting with Families

Wendy Baskins

Nancy Harder and Ben Harder

1  

Statements are those of guest speakers who represent member hospitals of NACHRI but who are not speaking for NACHRI.

Suggested Citation: "Appendix A Study Origins and Activities." Institute of Medicine. 2006. Safe Medical Devices for Children. Washington, DC: The National Academies Press. doi: 10.17226/11313.

Donya Hartley

Melisande Statz-Hill and Benjamin Hill

Penny Hill and Amanda Hill

Kim L. Katka

Karen Marston

Suggested Citation: "Appendix A Study Origins and Activities." Institute of Medicine. 2006. Safe Medical Devices for Children. Washington, DC: The National Academies Press. doi: 10.17226/11313.
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Suggested Citation: "Appendix A Study Origins and Activities." Institute of Medicine. 2006. Safe Medical Devices for Children. Washington, DC: The National Academies Press. doi: 10.17226/11313.
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Suggested Citation: "Appendix A Study Origins and Activities." Institute of Medicine. 2006. Safe Medical Devices for Children. Washington, DC: The National Academies Press. doi: 10.17226/11313.
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Suggested Citation: "Appendix A Study Origins and Activities." Institute of Medicine. 2006. Safe Medical Devices for Children. Washington, DC: The National Academies Press. doi: 10.17226/11313.
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Suggested Citation: "Appendix A Study Origins and Activities." Institute of Medicine. 2006. Safe Medical Devices for Children. Washington, DC: The National Academies Press. doi: 10.17226/11313.
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Suggested Citation: "Appendix A Study Origins and Activities." Institute of Medicine. 2006. Safe Medical Devices for Children. Washington, DC: The National Academies Press. doi: 10.17226/11313.
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Suggested Citation: "Appendix A Study Origins and Activities." Institute of Medicine. 2006. Safe Medical Devices for Children. Washington, DC: The National Academies Press. doi: 10.17226/11313.
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Suggested Citation: "Appendix A Study Origins and Activities." Institute of Medicine. 2006. Safe Medical Devices for Children. Washington, DC: The National Academies Press. doi: 10.17226/11313.
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Suggested Citation: "Appendix A Study Origins and Activities." Institute of Medicine. 2006. Safe Medical Devices for Children. Washington, DC: The National Academies Press. doi: 10.17226/11313.
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Next Chapter: Appendix B Medical Devices for Pediatric Care
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