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DOI 10.1016/s0009-9236(97)90069-2

Медицинская библиотека · Clinical pharmacology and therapeutics · 1997

Role of duration of diuretic effect in preventing sodium retention.

Ferguson J A, Sundblad K J, Becker P K, Gorski J C, Rudy D W, Brater D C

Клиническое исследованиеСтатьяРандомизированное исследованиеПоддержка службы здравоохранения СШАПеревод в очереди

Аннотация

OBJECTIVE

To determine whether the duration of diuretic effect at the active nephron site enhances ability to excrete an exogenous salt load.

METHODS

We conducted a study that involved eight patients with New York Heart Association class II to III congestive heart failure. In a randomized, crossover manner, each patient received 3.25 mg intravenous bumetanide at 0 hours and again at 6 hours or a loading dose of 0.5 mg bumetanide at 0 hours followed by a continuous infusion of 0.5 mg/hr for 6 hours. Response was followed for 12 hours; a total of 6.5 mg of bumetanide was administered in each arm of the study. Eight hours after dosing began, we administered approximately 80 mEq sodium intravenously and examined its excretion over 4 hours.

RESULTS

The percentage of the load excreted was 86% +/- 15% versus 29% +/- 30% for the infusion and bolus regimens, respectively (p = 0.0005). More bumetanide was excreted during the infusion (667 +/- 133 micrograms versus 240 +/- 121 micrograms; p = 0.0002). During the infusion, however, more sodium was excreted relative to amounts of bumetanide, indicating that the efficiency of response was greater during the infusion, 0.10 +/- 0.02 mEq sodium per microgram bumetanide versus 0.07 +/- 0.05 mEq for the bolus (p = 0.0145).

CONCLUSIONS

These data support the notions that a long-acting loop diuretic maintains its efficacy and that a longer duration of action facilitates excretion of a sodium load, such as that which might occur during dietary indiscretion.

Для цитирования: Ferguson J A, Sundblad K J, Becker P K, Gorski J C, Rudy D W, Brater D C. Role of duration of diuretic effect in preventing sodium retention.. Clinical pharmacology and therapeutics. 1997. DOI: 10.1016/s0009-9236(97)90069-2.

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