Therapeutic drug monitoring of anti-epileptic drugs - a clinical verification of volumetric absorptive micro sampling.


Journal

Clinical chemistry and laboratory medicine
ISSN: 1437-4331
Titre abrégé: Clin Chem Lab Med
Pays: Germany
ID NLM: 9806306

Informations de publication

Date de publication:
28 04 2020
Historique:
received: 08 08 2019
accepted: 16 12 2019
pubmed: 12 2 2020
medline: 21 5 2021
entrez: 12 2 2020
Statut: ppublish

Résumé

Background Therapeutic drug monitoring (TDM) of antiepileptic drugs (AEDs) can serve as a valuable tool in optimising and individualising epilepsy treatment, especially in vulnerable groups such as pregnant women, the elderly and children. Unfortunately, TDM is often performed suboptimally due to limitations in blood collection. Therefore, we investigated volumetric absorptive micro sampling (VAMS) - a new home-sampling technique. We aimed to evaluate VAMS to determine and quantify the different AEDs and concentrations of 16 different AEDs in whole blood collected by VAMS. Methods Patient blood samples (n = 138) were collected via venepunctures at the Academic Centre for Epileptology Kempenhaeghe. AED concentrations were determined, and these concentrations were used to compare the VAMS method (whole blood) with the conventional method (serum). In addition, the recovery was examined as well as the impact of haematocrit. Finally, AED-spiked blood was used to test the stability of the AEDs inside the micro-sampler devices over a period of time and whether temperature had an effect on the stability. Results VAMS allows for an accurate detection of 16 different AEDs within 2 days after sampling. Deviation in recovery was less than 10% and high correlations were found between VAMS and conventional sampling. Moreover, haematocrit does not have an effect with values between 0.3 and 0.5 (L/L). Finally, although storage temperature of VAMS does affect some AEDs, most are unaffected. Conclusions VAMS enables an accurate detection of a wide variety of AEDs within 2 days after sampling.

Identifiants

pubmed: 32045349
doi: 10.1515/cclm-2019-0784
pii: /j/cclm.ahead-of-print/cclm-2019-0784/cclm-2019-0784.xml
doi:
pii:

Substances chimiques

Anticonvulsants 0
Primidone 13AFD7670Q
Carbamazepine 33CM23913M
Gabapentin 6CW7F3G59X

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

828-835

Auteurs

Thierry P I J M Canisius (TPIJM)

Laboratory Clinical Chemistry and Pharmacology, Academic Centre for Epileptology Kempenhaeghe Maastricht UMC+, VE Heeze, the Netherlands.

J W P Hans Soons (JWPH)

Laboratory Clinical Chemistry and Pharmacology, Academic Centre for Epileptology Kempenhaeghe Maastricht UMC+, VE Heeze, the Netherlands.

Pauline Verschuure (P)

Laboratory Clinical Chemistry and Pharmacology, Academic Centre for Epileptology Kempenhaeghe Maastricht UMC+, VE Heeze, the Netherlands.

Emmeke A Wammes-van der Heijden (EA)

Laboratory Clinical Chemistry and Pharmacology, Academic Centre for Epileptology Kempenhaeghe Maastricht UMC+, VE Heeze, the Netherlands.

Rob P W Rouhl (RPW)

Department of Neurology, Academic Centre for Epileptology Kempenhaeghe Maastricht UMC+, Heeze, the Netherlands.
School for Mental Health and Neuroscience, Maastricht University Medical Centre, Maastricht, the Netherlands.

H J Marian Majoie (HJM)

Department of Neurology, Academic Centre for Epileptology Kempenhaeghe Maastricht UMC+, Heeze, the Netherlands.
School for Mental Health and Neuroscience, Maastricht University Medical Centre, Maastricht, the Netherlands.
School of Health Professions Education, Faculty of Health, Medicine and Life Sciences, Maastricht University, Maastricht, the Netherlands.

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Classifications MeSH