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Research Article| Volume 23, ISSUE 1, P25-30, January 01, 1988

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Treatment of psychosis, intermittent hyponatremia, and polydipsia (PIP Syndrome) using lithium and phenytoin

  • W.V.R. Vieweg
    Correspondence
    Address reprint requests to Dr.W.V.R. Vieweg, Western State Hospital, Box 2500, Staunton, VA 24401.
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  • N.M. Weiss
    Affiliations
    Clinical Evaluation Service, Western State Hospital, Department of Mental Health and Mental Retardation, Commonwealth of Virginia, Charlottesville, VAUSA

    Department of Behavioral Medicine and Psychiatry and the Department of Internal Medicine, University of Virginia School of Medicine, Charlottesville, VAUSA

    Endocrinology Division, Department of Internal Medicine, University of Chicago, School of Medicine, Chicago, ILUSA
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  • J.J. David
    Affiliations
    Clinical Evaluation Service, Western State Hospital, Department of Mental Health and Mental Retardation, Commonwealth of Virginia, Charlottesville, VAUSA

    Department of Behavioral Medicine and Psychiatry and the Department of Internal Medicine, University of Virginia School of Medicine, Charlottesville, VAUSA

    Endocrinology Division, Department of Internal Medicine, University of Chicago, School of Medicine, Chicago, ILUSA
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  • W.T. Rowe
    Affiliations
    Clinical Evaluation Service, Western State Hospital, Department of Mental Health and Mental Retardation, Commonwealth of Virginia, Charlottesville, VAUSA

    Department of Behavioral Medicine and Psychiatry and the Department of Internal Medicine, University of Virginia School of Medicine, Charlottesville, VAUSA

    Endocrinology Division, Department of Internal Medicine, University of Chicago, School of Medicine, Chicago, ILUSA
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  • L.S. Godleski
    Affiliations
    Clinical Evaluation Service, Western State Hospital, Department of Mental Health and Mental Retardation, Commonwealth of Virginia, Charlottesville, VAUSA

    Department of Behavioral Medicine and Psychiatry and the Department of Internal Medicine, University of Virginia School of Medicine, Charlottesville, VAUSA

    Endocrinology Division, Department of Internal Medicine, University of Chicago, School of Medicine, Chicago, ILUSA
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  • W.W. Spradlin
    Affiliations
    Clinical Evaluation Service, Western State Hospital, Department of Mental Health and Mental Retardation, Commonwealth of Virginia, Charlottesville, VAUSA

    Department of Behavioral Medicine and Psychiatry and the Department of Internal Medicine, University of Virginia School of Medicine, Charlottesville, VAUSA

    Endocrinology Division, Department of Internal Medicine, University of Chicago, School of Medicine, Chicago, ILUSA
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      Abstract

      Six patients [5 men and I woman, mean age 37.3 ± 8.2 (SD) years] with psychosis, intermittent hyponatremia, and polydipsia (PIP syndrome) underwent a sequence of treatments in an effort to normalize basal serum sodium levels and thereby protect the patients against complications, including hyponatremic seizures and coma. The morning baseline group mean basal serum sodium value was 132.5 ± 3.8 meqlliter. Over a 20-monthperiod, the sequence of treatments was salt-added diet, lithium and phenytoin, and lithium alone. Each treatment program yielded morning group mean basal serum sodium determinations superior to baseline values, except for the program of lithium alone, which could not be tolerated. The combination of lithium and phenytoin provided a morning group mean basal serum sodium level of 140.6 ±3.2 meqlliter, which was superior (p < 0.01) to all other treatment modalities. Early morning hyposthenuria persisted throughout the 20-month period of observation.
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