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1.
Tijdschr Psychiatr ; 63(7): 557-564, 2021.
Artigo em Holandês | MEDLINE | ID: mdl-34523708

RESUMO

BACKGROUND: Lithium use during peripartum requires careful consideration due to a risk of teratogenic effects, adverse side effects and risk of neonatal complications. However, given the effectiveness of lithium, use during the peripartum period may be indicated. AIM: To provide an overview of the current evidence regarding the clinical use of lithium during peripartum, including risk of relapse in case of (dis)continuation and evolution of lithium levels. METHOD: A review was performed in the Medline and ScienceDirect database. RESULTS: Ten studies were included. Six studies concerned the risk of relapse in case of (dis)continuation of lithium during the peripartum. Four studies concerned the evolution of lithium levels throughout the peripartum. Lithium discontinuation during pregnancy leads to an increased risk of relapse during pregnancy and postpartum. At the same dose, lithium levels are lower than preconceptual in all trimesters. CONCLUSION: Risk and benefits of lithium use during the peripartum should be carefully considered, if possible prior to conception. Close monitoring of maternal lithium levels and renal function is necessary due to significant fluctuations during peripartum.


Assuntos
Transtorno Bipolar , Complicações na Gravidez , Transtorno Bipolar/tratamento farmacológico , Feminino , Humanos , Recém-Nascido , Lítio/uso terapêutico , Período Periparto , Período Pós-Parto , Gravidez , Complicações na Gravidez/tratamento farmacológico
2.
Front Pharmacol ; 15: 1403747, 2024.
Artigo em Inglês | MEDLINE | ID: mdl-39211781

RESUMO

Background: Physiological changes in pregnancy may affect drug safety and efficacy, sometimes requiring dose adjustments. Pregnancy-adjusted doses, however, are missing for most medications. Increasingly, pharmacokinetic models can be used for antenatal dose finding. Given the novelty of this technique and questions regarding dose credibility, the acceptability of model-informed antenatal doses should be explored. Objective: We aimed to assess the willingness-to-use and preferred features for model-informed antenatal doses among healthcare practitioners (HCPs) and pregnant women in European countries. Methods: A cross-sectional, web-based study drawing on two open surveys was performed between 8 September and 30 November 2022. Each survey comprised statements drawn from prior focus groups, associated with Likert-scales. Themes included respondents' information needs, search behaviours along with their willingness-to-use and preferred features for model-informed antenatal doses. The surveys were disseminated through professional societies, pregnancy websites and social media. A descriptive analysis was performed. Results: In total, 608 HCPs from different specialties and 794 pregnant women across 15 countries participated, with 81% of respondents across both groups in the Netherlands or Belgium. Among pregnant women, 31% were medical professionals and 85% used medication during pregnancy. Eighty-three percent of HCPs found current antenatal pharmacotherapy suboptimal and 97% believed that model-informed antenatal doses would enhance the quality of antenatal care. Most HCPs (93%) and pregnant women (75%) would be willing to follow model-informed antenatal doses. Most HCPs desired access to the evidence (88%), including from pharmacokinetic modelling (62%). Most pregnant women (96%) wanted to understand antenatal dosing rationales and to be involved in dosing decisions (97%). Conclusion: The willingness-to-use model-informed antenatal doses is high among HCPs and pregnant women provided that certain information needs are met.

4.
Talanta ; 46(3): 395-405, 1998 Jul.
Artigo em Inglês | MEDLINE | ID: mdl-18967161

RESUMO

An optimized sample preparation procedure for organotin speciation in sediment samples has been applied to the analysis of sediments collected in the environment. The method is based on tropolone complexation of the ionic organotins, followed by extraction into a hexane-ethylacetate mixture and derivatization by NaBEt(4). The method was applied to the determination of organotin in various harbour, shipyard and dry-dock sediments in Belgium. Butyltin compounds were detected in all samples analyzed, often at high mg kg(-1) levels. A limited number of samples showed the presence of phenyltin compounds. Further, the method was adapted to the analysis of river sediments sampled from the vicinity of shipyards. Butyltin concentrations were detected at the microg kg(-1) level in the majority of samples.

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