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Baclofen self-poisoning: Is renal replacement therapy efficient in patient with normal kidney function?
Brunet, Marion; Léger, Maxime; Billat, Pierre-André; Lelièvre, Bénédicte; Lerolle, Nicolas; Boels, David; Le Roux, Gaël.
Afiliação
  • Brunet M; Western Poison Control Center, University Hospital, 4 rue Larrey, 49100 Angers, France. Electronic address: marion.legeay@chu-angers.fr.
  • Léger M; Department of Medical Intensive Care and Hyperbaric Medicine, University Hospital, 4 rue Larrey, 49100 Angers, France.
  • Billat PA; MINT, UNIV Angers, INSERM 1066, CNRS 6021, Université Bretagne Loire, Angers, France.
  • Lelièvre B; Pharmacotoxicology Laboratory, University Hospital, Angers, France.
  • Lerolle N; Department of Medical Intensive Care and Hyperbaric Medicine, University Hospital, 4 rue Larrey, 49100 Angers, France.
  • Boels D; Western Poison Control Center, University Hospital, 4 rue Larrey, 49100 Angers, France.
  • Le Roux G; Western Poison Control Center, University Hospital, 4 rue Larrey, 49100 Angers, France.
Anaesth Crit Care Pain Med ; 39(6): 813-817, 2020 12.
Article em En | MEDLINE | ID: mdl-33068797
ABSTRACT

AIMS:

We aimed at assessing the effectiveness of renal replacement therapy in patients severely self-poisoned with baclofen and with normal kidney function.

METHODS:

A population pharmacokinetic model was built using analytical data extracted from 26 baclofen poisoning cases reported to a French Poison Centre 8 patients underwent renal replacement therapy (RRT), 18 did not. In the RRT group, 2 patients suffered from kidney failure. Mechanical ventilation was required for 20 patients with normal kidney function; 15 were not treated by RRT and 5 were. Pharmacokinetic profiles of baclofen were measured in 28 patients and further modelled by a non-parametric approach (PMetrics®). The total data set was divided into a building data set (26 patients, 57 observations) and a validation set (2 external patients, 6 observations). Then, the estimated elimination half-life of baclofen and the duration of intubation were compared in patients with or without RRT using Wilcoxon-Mann-Whitney test.

RESULTS:

A model using three parameters plus a lag time and bioavailability was necessary to determine the pharmacokinetics of baclofen. Estimated elimination half-life in the 'RRT' group and the 'no RRT' group were respectively 3.1 [2.2-4.8] h (n = 6 patients) and 3.4 [1.4-5.5] h (n = 19 patients, p = 0.53). The median duration of intubation was not significantly different between groups (72 [48-72] h and 72 [24-96] h, respectively; p = 0.38).

CONCLUSION:

Renal replacement therapy did not appear to significantly increase baclofen clearance in patients without kidney failure.
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Texto completo: 1 Bases de dados: MEDLINE Assunto principal: Baclofeno / Injúria Renal Aguda Tipo de estudo: Observational_studies Limite: Humans Idioma: En Revista: Anaesth Crit Care Pain Med Ano de publicação: 2020 Tipo de documento: Article

Texto completo: 1 Bases de dados: MEDLINE Assunto principal: Baclofeno / Injúria Renal Aguda Tipo de estudo: Observational_studies Limite: Humans Idioma: En Revista: Anaesth Crit Care Pain Med Ano de publicação: 2020 Tipo de documento: Article