Reporting Serious Adverse Events

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    The author, Elisabeth Belmont, Esq., of MaineHealth,

    Portland, ME wishes to thank James W. Boswell, Esq., King

    and Spalding, LLP, Atlanta, GA; Jay A. Martus, Esq.,

    Sheridan Healthcare Inc., Sunrise, FL; and Sandra L.

    Parker, Esq., Maine Hospital Association, Augusta, ME for

    serving as peer reviewers for this publication.

    1 SeeC J., F F., S K., Cb M.J., Respectul Management o Serious Clinical Adverse Events

    (S E) (I H I), 14.

    2 U.S. Dept o Health & Human Servs., Oice o Inspector General, Adverse Events in Hospitals: Overview o

    Key Issues 16 (2008), available at://..///-06-07-00470. (OIG Adverse Events Overview

    Report). F -q (HAC), CMS b ://../HAqC/06_H-Aq_C.#TOP.

    3 S M D A 1990, Pb. L. N. 101-629, 104 S. 4511 (1990)( 21 U.S.C. 301 42 U.S.C.

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