Postoperative Hyponatremic Encephalopathy in Menstruant Women

Abstract

Objectives: To determine factors associated with the development of encephalopathy and with its clinical course in patients with postoperative hyponatremia.

Setting: Consultation and referral services of two university medical centers and community hospitals.

Design: Case-control study (risk factors for encephalopathy) and cohort study (clinical course among patients with encephalopathy).

Patients: Case patients included 65 adults with postoperative hyponatremic encephalopathy; controls included 674 adult patients who had postoperative hyponatremia without encephalopathy and who were selected from 76 678 consecutive adult surgical inpatients.

Measurements: Age, gender, menstrual status, neurologic symptoms, time to development and degree of hyponatremia, arterial blood gas determinations, serum chemistries, morbidity and mortality.

Results: Case patients included 40 women (62%) and 25 men (38%) (P > 0.05); controls included 367 women (54%) and 307 men (46%) (P > 0.1). Of the 34 case patients who developed permanent brain damage or died, 33 (97%) were women (P < 0.001). Among the women with brain damage, 25 (76%) were menstruant (P < 0.001). The relative risk for death or permanent brain damage from hyponatremic encephalopathy in women compared with men was 28 (95% Cl, 5 to 141) and in menstruant women compared with postmenopausal women, 26 (Cl, 11 to 62). Arterial PO2 at diagnosis was significantly lower in female than in male case patients (34 ± 5 compared with 91 ± 3 mm Hg; P < 0.001). Further, of the 38 case patients who had respiratory arrest before the diagnosis of hyponatremic encephalopathy, 36 (95%) were women. Extent of or time to development of hyponatremia did not correlate with subsequent brain damage (P > 0.1).

Conclusions: Women and men are equally likely to develop hyponatremia and hyponatremic encephalopathy after surgery. However, when hyponatremic encephalopathy develops, menstruant women are about 25 times more likely to die or have permanent brain damage compared with either men or postmenopausal women.

Article and Author Information

  • From Baylor College of Medicine, Houston, Texas; and University of California, San Francisco, School of Medicine; and Veterans Affairs Medical Center, San Francisco, California. For current author addresses, see end of text.

  • Grant Support: In part by grant RO1AG08575 from the National Institute on Aging, Department of Health and Human Services, Bethesda, Maryland, and by the Research Service of the Veterans Affairs Medical Center, San Francisco, California.

  • Requests for Reprints: J. Carlos Ayus, MD, 4 Brompton Court, Houston, Texas 77024.

  • Current Author Addresses: Dr. Ayus: 4 Brompton Court, Houston, Texas 77024.

    Dr. Wheeler: Department of Obstetrics and Gynecology, Baylor College of Medicine, 1 Baylor Plaza, Houston, Texas 77030.

    Dr. Arieff: Department of Medicine (111 G), Veterans Affairs Medical Center, 4150 Clement Street, San Francisco, CA 94121.

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