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Chronic Hypokalemia and Alkalosis: Approach to Diagnosis | JAMA Internal Medicine | ÌÇÐÄvlog

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°¿³¦³Ù´Ç²ú±ð°ùÌý1980

Chronic Hypokalemia and Alkalosis: Approach to Diagnosis

Author Affiliations

From the Department of Medicine, University of Miami School of Medicine, and the Medical and Research Services, Veterans Administration Medical Center, Miami.

Arch Intern Med. 1980;140(10):1336-1337. doi:10.1001/archinte.1980.00330210084028
Abstract

In general, the etiology of hypokalemic, hypochloremic, metabolic alkalosis is straightforward, since the most commonly occurring causes are easily recognized on clinical grounds. In some cases, such as the one described herein, however, the cause is not readily apparent, and a comprehensive systematic approach is recommended.

REPORT OF A CASEÌý A 35-year-old obese practical nurse was hospitalized because of unexplained hypokalemia persisting for several months, despite oral supplementation of as much as 120 mEq of potassium chloride elixir daily. She repeatedly denied vomiting, diarrhea, and diuretic or laxative use.Physical examination results were unremarkable except for slight proximal muscle weakness. Laboratory data included the following values: serum sodium, 140 mEq/L; potassium, 2.7 mEq/ L; chloride, 91 mEq/L; bicarbonate, 35 mEq/L; creatinine, 0.9 mg/dL; and calcium, 9.7 mg/dL. Arterial blood pH was 7.50, and Paco2 was 45 mm Hg. Urinary values for potassium ranged from 30 to 50 mEq/L and

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