Journal
CRITICAL CARE MEDICINE
Volume 30, Issue 2, Pages 343-348Publisher
LIPPINCOTT WILLIAMS & WILKINS
DOI: 10.1097/00003246-200202000-00013
Keywords
indomethacin; neonates; patent ductus arteriosus; pharmacodynamics; pharmacokinetics; critical concentration
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Objectives: To determine patent ductus arteriosus (PDA) closure rates, and indomethacin (INDO) toxicity rates in neonates dosed with INDO using an individualized pharmacokinetic/pharmacodynamic (PK/PD) dosing approach. In addition, develop PD curves evaluating dose-response and concentration-response relationships for closure and renal toxicity, especially in select subgroups historically known as poor responders (<1000 g and 10 days postnatal age). Design: Prospective, cohort study. Setting: Level III neonatal intensive care unit. Subjects: One hundred thirty-nine patients receiving 151 courses of INDO for PDA closure were evaluated. Interventions: Patients initially received 0.25 mg/kg of INDO, followed immediately by 1 mg/kg of furosemide. INDO concentrations were obtained 2 hrs and 8 hrs after the dose and were assayed using high-performance liquid chromatography. Individualized PK parameters were calculated with subsequent INDO dosing based on the individualized PK variables to increase trough serum concentrations by 0.3-0.5 mg/L. Measurements and Main Results: Ductal closure was successful in 127 patients (91%). Renal toxicity occurred in 21 (15%) patients and was temporary and reversible. No significant differences in response rates based on treatment weight or postnatal age were observed. PD curves were similar for neonates <1000 g vs. 1000 g. PD curves were also similar for neonates with postnatal age <10 days vs. greater than or equal to10 days. Statistically significant differences were noted between neonates categorized for postnatal age <10 days vs. greater than or equal to 10 days in total days of therapy (1.8 vs. 2.3 days), total number of doses required to close PDA (3.5 vs. 5.6 doses), critical INDO dose (0.9 vs. 1.4 mg/kg), critical INDO concentration (1.9 vs. 1.4 mg/L), and critical dose/critical concentration ratio (0.52 vs. 2.2). Conclusions. These findings support the hypothesis that the poor PDA closure rates with INDO for neonates >10 days postnatal age are the result of pharmacokinetic differences only and that weight does not impact response rates. Individualized pharmacokinetic/pharmacodynamic dosing of INDO continues to achieve higher closure rate than current dosing standards. Patients historically known as poor responders significantly benefit from this dosing approach.
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