TY - JOUR
T1 - Population Pharmacokinetics and Target Attainment of Allopurinol and Oxypurinol Before, During, and After Cardiac Surgery with Cardiopulmonary Bypass in Neonates with Critical Congenital Heart Disease
AU - the CRUCIAL trial consortium
AU - Chu, Wan Yu
AU - Nijman, Maaike
AU - Stegeman, Raymond
AU - Breur, Johannes M.P.J.
AU - Jansen, Nicolaas J.G.
AU - Nijman, Joppe
AU - van Loon, Kim
AU - Koomen, Erik
AU - Allegaert, Karel
AU - Benders, Manon J.N.L.
AU - Dorlo, Thomas P.C.
AU - Huitema, Alwin D.R.
AU - Beynum, Ingrid M.van
AU - ten Cate, Floris E.Udink
AU - Helbing, Willem A.
AU - Taverne, Yannick J.H.J.
AU - de Boode, Willem P.
AU - Bogers, Ad J.C.C.
AU - Joosten, Koen F.M.
AU - van de Woestijne, Pieter C.
AU - de Liefde, Inge I.
AU - van Dijk, Antony
AU - Meijer, Natasja I.F.
AU - Simons, Sinno H.P.H.P.
AU - van der Lee, Robin
AU - Cornette, Jérôme M.J.
AU - van Haren, Neeltje E.M.
AU - Bos, Arend F.
AU - Berger, Rolf M.F.
AU - Accord, Ryan E.
AU - Arrigoni, Sara C.
AU - Duin, Leonie K.
AU - Kneyber, Martin J.J.
AU - Kooi, Elisabeth M.W.
AU - van der Maaten, Joost M.A.A.
AU - Meiners, Linda C.
AU - Marchie, Gideon J.du Sarvaas
AU - Vanagt, Ward Y.
AU - Claessens, Nathalie H.P.
AU - van Wijk, Bram
AU - Talacua, Hanna
AU - Steenhuis, Trinette J.
AU - ter Heide, Henriette
AU - van Iperen, Gabrielle G.
AU - Bosch, Rian
AU - Groenendaal, Floris
AU - Derks, Jan B.
AU - de Heus, Roel
N1 - © 2024. The Author(s).
PY - 2024/8
Y1 - 2024/8
N2 - Background: The CRUCIAL trial (NCT04217421) is investigating the effect of postnatal and perioperative administration of allopurinol on postoperative brain injury in neonates with critical congenital heart disease (CCHD) undergoing cardiac surgery with cardiopulmonary bypass (CPB) shortly after birth.Objective: This study aimed to characterize the pharmacokinetics (PK) of allopurinol and oxypurinol during the preoperative, intraoperative, and postoperative phases in this population, and to evaluate target attainment of the current dosing strategy.Methods: Nonlinear mixed-effects modeling was used to develop population PK models in 14 neonates from the CRUCIAL trial who received up to five intravenous allopurinol administrations throughout the postnatal and perioperative periods. Target attainment was defined as achieving an allopurinol concentration >2 mg/L in at least two-thirds of the patients during the first 24 h after birth and between the start and 36 h after cardiac surgery with CPB.Results: A two-compartment model for allopurinol was connected to a one-compartment model for oxypurinol with an auto-inhibition effect on the conversion, which best described the PK. In a typical neonate weighing 3.5 kg who underwent cardiac surgery at a postnatal age (PNA) of 5.6 days, the clearance (CL) of allopurinol and oxypurinol at birth was 0.95 L/h (95% confidence interval 0.75–1.2) and 0.21 L/h (0.17–0.27), respectively, which subsequently increased with PNA to 2.97 L/h and 0.41 L/h, respectively, before CPB. During CPB, allopurinol and oxypurinol CL decreased to 1.38 L/h (0.9–1.87) and 0.12 L/h (0.05–0.22), respectively. Post-CPB, allopurinol CL increased to 2.21 L/h (1.74–2.83), while oxypurinol CL dropped to 0.05 L/h (0.01–0.1). Target attainment was 100%, 53.8%, and 100% at 24 h postnatally, 24 h after the start of CPB, and 36 h after the end of cardiac surgery, respectively. The combined concentrations of allopurinol and oxypurinol maintained ≥ 90% inhibition of xanthine oxidase (IC90XO) throughout the postnatal and perioperative period.Conclusions: The minimal target concentration of allopurinol was not achieved at every predefined time interval in the CRUCIAL trial; however, the dosing strategy used was deemed adequate, since it yielded concentrations well exceeding the IC90XO. The decreased CL of both compounds during CPB suggests influence of the hypothermia, hemofiltration, and the potential sequestration of allopurinol in the circuit. The reduced CL of oxypurinol after CPB is likely attributable to impaired kidney function.
AB - Background: The CRUCIAL trial (NCT04217421) is investigating the effect of postnatal and perioperative administration of allopurinol on postoperative brain injury in neonates with critical congenital heart disease (CCHD) undergoing cardiac surgery with cardiopulmonary bypass (CPB) shortly after birth.Objective: This study aimed to characterize the pharmacokinetics (PK) of allopurinol and oxypurinol during the preoperative, intraoperative, and postoperative phases in this population, and to evaluate target attainment of the current dosing strategy.Methods: Nonlinear mixed-effects modeling was used to develop population PK models in 14 neonates from the CRUCIAL trial who received up to five intravenous allopurinol administrations throughout the postnatal and perioperative periods. Target attainment was defined as achieving an allopurinol concentration >2 mg/L in at least two-thirds of the patients during the first 24 h after birth and between the start and 36 h after cardiac surgery with CPB.Results: A two-compartment model for allopurinol was connected to a one-compartment model for oxypurinol with an auto-inhibition effect on the conversion, which best described the PK. In a typical neonate weighing 3.5 kg who underwent cardiac surgery at a postnatal age (PNA) of 5.6 days, the clearance (CL) of allopurinol and oxypurinol at birth was 0.95 L/h (95% confidence interval 0.75–1.2) and 0.21 L/h (0.17–0.27), respectively, which subsequently increased with PNA to 2.97 L/h and 0.41 L/h, respectively, before CPB. During CPB, allopurinol and oxypurinol CL decreased to 1.38 L/h (0.9–1.87) and 0.12 L/h (0.05–0.22), respectively. Post-CPB, allopurinol CL increased to 2.21 L/h (1.74–2.83), while oxypurinol CL dropped to 0.05 L/h (0.01–0.1). Target attainment was 100%, 53.8%, and 100% at 24 h postnatally, 24 h after the start of CPB, and 36 h after the end of cardiac surgery, respectively. The combined concentrations of allopurinol and oxypurinol maintained ≥ 90% inhibition of xanthine oxidase (IC90XO) throughout the postnatal and perioperative period.Conclusions: The minimal target concentration of allopurinol was not achieved at every predefined time interval in the CRUCIAL trial; however, the dosing strategy used was deemed adequate, since it yielded concentrations well exceeding the IC90XO. The decreased CL of both compounds during CPB suggests influence of the hypothermia, hemofiltration, and the potential sequestration of allopurinol in the circuit. The reduced CL of oxypurinol after CPB is likely attributable to impaired kidney function.
UR - http://www.scopus.com/inward/record.url?scp=85201538343&partnerID=8YFLogxK
U2 - 10.1007/s40262-024-01401-3
DO - 10.1007/s40262-024-01401-3
M3 - Article
C2 - 39147988
SN - 0312-5963
VL - 63
SP - 1205
EP - 1220
JO - Clinical Pharmacokinetics
JF - Clinical Pharmacokinetics
IS - 8
ER -