Ventricular Fibrillation, Automatic External Defibrillators, and the United States Food and Drug Administration: Confrontation Without Comprehension - 12/09/11
Doi : 10.1016/S0196-0644(95)70015-3
Abstract |
[Cummins RO, White RD, Pepe PE: Ventricular fibrillation, automatic external defibrillators, and the United States Food and Drug Administration: Confrontation without comprehension. Ann Emerg Med November 1995;26:621-631.]
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 | From the Department of Medicine, University of Washington, Seattle, Washington*; the Department of Anesthesiology, Mayo Clinic, Rochester, Minnesota‡; and the Departments of Medicine§, Surgery , and Pediatrics¶, Baylor College of Medicine, Houston, Texas. |
| Editor's note: Because of the critical nature of this article and because of the journals' policy to present balanced discussion of controversial topics, Annals invited a reply from the US Food and Drug Administration. That response follows this article. |
 | Full disclosure and conflict-of-interest information is provided at the end of the article. |
| Address for reprints: Richard O Cummins, MD, University of Washington Medical Center, Emergency Medicine Service BX356123, Seattle, Washington 98195-6123, 206-548-4228, Fax 206-325-9202 |
| ♢ | Reprint no. 47/1/64915 |
© 1995
Mosby, Inc. Tous droits réservés.
Vol 26 - N° 5
P. 621-631 - novembre 1995 Retour au numéro
Article précédent
- Need and Desire for Preventive Care Measures in Emergency Department Patients
- Robert M Rodriguez, William J Kreider, Larry J Baraff
- Automatic External Defibrillators and the United States Food and Drug Administration: An Invited Commentary
- D.Bruce Burlington
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