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Am J Perinatol ; 27(8): 655-62, 2010 Sep.
Article in English | MEDLINE | ID: mdl-20232280

ABSTRACT

We evaluated the efficacy, safety, and biological mechanisms of digoxin immune Fab (DIF) treatment of severe preeclampsia. Fifty-one severe preeclamptic patients were randomized in double-blind fashion to DIF ( N = 24) or placebo ( N = 27) for 48 hours. Primary outcomes were change in creatinine clearance (CrCl) at 24 to 48 hours and antihypertensive drug use. Serum sodium pump inhibition, a sequela of endogenous digitalis-like factors (EDLF), was also assessed. CrCl in DIF subjects was essentially unchanged from baseline versus a decrease with placebo (-3 +/- 10 and -34 +/- 10 mL/min, respectively, P = 0.02). Antihypertensive use was similar between treatments (46 and 52%, respectively, P = 0.7). Serum sodium pump inhibition was decreased with DIF compared with placebo at 24 hours after treatment initiation (least squares mean difference, 19 percentage points, P = 0.03). DIF appeared to be well tolerated. These results suggest DIF prevents a decline in renal function in severe preeclampsia by neutralizing EDLF. Sodium pump inhibition was significantly improved. Further research is warranted.


Subject(s)
Antihypertensive Agents/administration & dosage , Immunoglobulin Fab Fragments/administration & dosage , Pre-Eclampsia/drug therapy , Adult , Antihypertensive Agents/adverse effects , Cardenolides/blood , Digoxin/immunology , Double-Blind Method , Female , Humans , Immunoglobulin Fab Fragments/analysis , Kidney Function Tests , Pre-Eclampsia/blood , Pre-Eclampsia/diagnosis , Pre-Eclampsia/physiopathology , Pregnancy , Pregnancy Outcome , Saponins/blood , Sodium-Potassium-Exchanging ATPase/antagonists & inhibitors , Treatment Outcome , Young Adult
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