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Dried blood spots and sparse sampling: a practical approach to estimating pharmacokinetic parameters of caffeine in preterm infants
Author(s) -
Patel Parul,
Mulla Hussain,
Kairamkonda Venkatesh,
Spooner Neil,
Gade Sonya,
Della Pasqua Oscar,
Field David J.,
Pandya Hitesh C.
Publication year - 2013
Publication title -
british journal of clinical pharmacology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.216
H-Index - 146
eISSN - 1365-2125
pISSN - 0306-5251
DOI - 10.1111/j.1365-2125.2012.04392.x
Subject(s) - caffeine , pharmacokinetics , dried blood , medicine , dried blood spot , blood sampling , population , anesthesia , chemistry , pharmacology , chromatography , environmental health
Aims Dried blood spots ( DBS ) alongside micro‐analytical techniques are a potential solution to the challenges of performing pharmacokinetic ( PK ) studies in children. However, DBS methods have received little formal evaluation in clinical settings relevant to children. The aim of the present study was to determine a PK model for caffeine using a ‘ DBS /microvolume platform’ in preterm infants. Methods DBS samples were collected prospectively from premature babies receiving caffeine for treatment of apnoea of prematurity. A non‐linear mixed effects approach was used to develop a population PK model from measured DBS caffeine concentrations. Caffeine PK parameter estimates based on DBS data were then compared with plasma estimates for agreement. Results Three hundred and thirty‐eight DBS cards for caffeine measurement were collected from 67 preterm infants (birth weight 0.6–2.11 kg). 88% of cards obtained were of acceptable quality and no child had more than 10 DBS samples or more than 0.5 ml of blood taken over the study period. There was good agreement between PK parameters estimated using caffeine concentrations from DBS samples ( CL = 7.3 ml h −1 kg −1 ; V = 593 ml kg −1 ; t 1/2 = 57 h) and historical caffeine PK parameter estimates based on plasma samples ( CL = 4.9–7.9 ml h −1 kg −1 ; V = 640–970 ml kg −1 ; t 1/2 = 101–144 h). We also found that changes in blood haematocrit may significantly confound estimates of caffeine PK parameters based on DBS data. Conclusions This study demonstrates that DBS methods can be applied to PK studies in a vulnerable population group and are a practical alternative to wet matrix sampling techniques.