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1.
Int J Clin Pharm ; 43(1): 66-76, 2021 Feb.
Artigo em Inglês | MEDLINE | ID: mdl-32812096

RESUMO

Background Medication errors occur frequently in intensive care units (ICU). Voluntarily reported medication errors form an easily available source of information. Objective This study aimed to characterize prescribing, monitoring and medication transfer errors that were voluntarily reported in the ICU, in order to reveal medication safety issues. Setting This retrospective data analysis study included reports of medication errors from eleven Dutch ICU's from January 2016 to December 2017. Method We used data extractions from the incident reporting systems of the participating ICU's. The reports were transferred into one database and categorized into type of error, cause, medication (groups), and patient harm. Descriptive statistics were used to calculate the proportion of medication errors and the distribution of subcategories. Based on the analysis, ICU medication safety issues were revealed. Main outcome measure The main outcome measure was the proportion of prescribing, monitoring and medication transfer error reports. Results Prescribing errors were reported most frequently (n = 233, 33%), followed by medication transfer errors (n = 85, 12%) and monitoring errors (n = 27, 4%). Other findings were: medication transfer errors frequently caused serious harm, especially the omission of home medication involving the central nervous system and proton pump inhibitors; omissions and dosing errors occurred most frequently; protocol problems caused a quarter of the medication errors; and medications needing blood level monitoring (e.g. tacrolimus, vancomycin, heparin and insulin) were frequently involved. Conclusion This analysis of voluntarily reported prescribing, monitoring and medication transfer errors warrants several improvement measures in these processes, which may help to increase medication safety in the ICU.


Assuntos
Unidades de Terapia Intensiva , Erros de Medicação , Humanos , Erros de Medicação/prevenção & controle , Países Baixos/epidemiologia , Estudos Retrospectivos , Gestão de Riscos
2.
Neth J Med ; 76(3): 115-124, 2018 04.
Artigo em Inglês | MEDLINE | ID: mdl-29667584

RESUMO

INTRODUCTION: The risk of prescribing errors and related adverse drug events (ADE) on the intensive care unit (ICU) is high. Based on studies carried out in North America or the UK, a clinical pharmacy service can reduce ADEs and lower overall costs. This study looks into the clinical and financial impact of interventions made by pharmacists during patient rounds in two ICU settings in the Netherlands. MATERIALS AND METHODS: A quality improvement study was performed in a general teaching hospital (GTH) and a university hospital (UH) in the Netherlands. The improvement consisted of a review of medication orders and participation in patient rounds by an ICU-trained pharmacist. The main outcome measure was the proportion of accepted pharmacist interventions. Secondary outcome measures were the clinical relevance of the accepted interventions, the proportion of prevented potential ADEs (pADE) and a cost-benefit ratio. RESULTS: In the GTH 160 patients and in the UH 174 patients were included. A total of 332 and 280 interventions were analysed. Acceptance of the interventions was 67.3% in the GTH and 61.8% in the UH. The accepted interventions were mostly scored as clinically relevant, resulting in 0.16 and 0.11 prevented pADEs per patient. The cost benefit was €119 (GTH) and €136 (UH) per accepted intervention. CONCLUSION: This clinical pharmacy service in two ICUs resulted in high numbers of accepted and clinically relevant interventions. Our model appeared to be cost-effective in both ICU settings.


Assuntos
Efeitos Colaterais e Reações Adversas Relacionados a Medicamentos/prevenção & controle , Unidades de Terapia Intensiva/normas , Erros de Medicação/prevenção & controle , Farmacêuticos/normas , Serviço de Farmácia Hospitalar/normas , Visitas de Preceptoria/normas , Análise Custo-Benefício , Efeitos Colaterais e Reações Adversas Relacionados a Medicamentos/economia , Hospitais de Ensino/normas , Hospitais Universitários/normas , Humanos , Unidades de Terapia Intensiva/economia , Modelos Organizacionais , Países Baixos , Equipe de Assistência ao Paciente/normas , Serviço de Farmácia Hospitalar/economia , Papel Profissional , Melhoria de Qualidade , Visitas de Preceptoria/economia
3.
Ned Tijdschr Geneeskd ; 142(28): 1585-8, 1998 Jul 11.
Artigo em Holandês | MEDLINE | ID: mdl-9763837

RESUMO

Two patients, men aged 47 and 64 years, were found in a comatose condition in their homes, after a period of fatigue, polyuria and polydipsia. They had not been known to suffer from diabetes mellitus, but now displayed a hyperglycaemic hyperosmolar non-ketoacidotic disorder as the first manifestation of diabetes mellitus type 2. In that condition, just sufficient insulin is present to counteract ketone production, but not enough to prevent hyperglycaemia. Neurological and thromboembolic manifestations, possibly fatal, may result from severe dehydration brought about by a vicious circle in which osmotic diuresis reduces the effective circulating volume, causing renal function to decrease and hyperglycaemia to increase even more. Both patients recovered fully after adequate treatment with solutions of NaCl and glucose.


Assuntos
Diabetes Mellitus Tipo 2/complicações , Diabetes Mellitus Tipo 2/diagnóstico , Coma Hiperglicêmico Hiperosmolar não Cetótico/etiologia , Desidratação/etiologia , Hidratação , Humanos , Coma Hiperglicêmico Hiperosmolar não Cetótico/terapia , Masculino , Pessoa de Meia-Idade
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