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1.
J Diabetes Sci Technol ; 9(4): 739-50, 2015 Jul.
Artigo em Inglês | MEDLINE | ID: mdl-26033922

RESUMO

BACKGROUND: Current methods of blood glucose (BG) monitoring and insulin delivery are labor intensive and commonly fail to achieve the desired level of BG control. There is great clinical need in the hospital for a user-friendly bedside device that can automatically monitor the concentration of BG safely, accurately, frequently, and reliably. METHODS: A 100-patient observation study was conducted at 6 US hospitals to evaluate the first generation of the Intravenous Blood Glucose (IVBG) System (Edwards Lifesciences LLC & Dexcom Inc). Device safety, accuracy, and reliability were assessed. A research nurse sampled blood from a vascular catheter every 4 hours for ≤ 72 hours and BG concentration was measured using the YSI 2300 STAT Plus Analyzer (YSI Life Sciences). The IVBG measurements were compared to YSI measurements to calculate point accuracy. RESULTS: The IVBG systems logged more than 5500 hours of operation in 100 critical care patients without causing infection or inflammation of a vein. A total of 44135 IVBG measurements were performed in 100 patients with 30231 measurements from the subset of 75 patients used for accuracy analysis. In all, 996 IVBG measurements were time-matched with reference YSI measurements. These pairs had a mean absolute difference (MAD) of 11.61 mg/dl, a mean absolute relative difference (MARD) of 8.23%, 93% met 15/20% accuracy defined by International Organization for Standardization 15197:2003 standard, and 93.2% were in zone A of the Clarke error grid. The IVBG sensors were exposed to more than 200 different medications with no observable effect on accuracy. CONCLUSIONS: The IVBG system is an automated and user-friendly glucose monitoring system that provides accurate and frequent BG measurements with great potential to improve the safety and efficacy of insulin therapy and BG control in the hospital, potentially leading to improved clinical outcomes.


Assuntos
Glicemia/análise , Sistemas de Infusão de Insulina , Monitorização Fisiológica/instrumentação , Monitorização Fisiológica/métodos , Adulto , Idoso , Automação , Calibragem , Cateterismo , Desenho de Equipamento , Feminino , Hospitalização , Humanos , Bombas de Infusão Implantáveis , Infusões Intravenosas/instrumentação , Infusões Intravenosas/métodos , Masculino , Pessoa de Meia-Idade , Segurança do Paciente , Estudos Prospectivos , Reprodutibilidade dos Testes , Estados Unidos
2.
J Diabetes Sci Technol ; 7(6): 1484-91, 2013 Nov 01.
Artigo em Inglês | MEDLINE | ID: mdl-24351174

RESUMO

BACKGROUND: Hyperglycemia and hypoglycemia in hospitalized patients have been associated with increased morbidity and mortality. Improvements in glucose monitoring technology may be helpful in the clinical management of critically ill patients with abnormal glucose levels. A first-generation intravenous blood glucose monitoring (IVBG) system was developed to facilitate glycemic control therapy in hospitalized patients. A nonrandomized, single-arm, multicenter study was performed to evaluate the safety and accuracy of the IVBG system in insulin-treated subjects with diabetes mellitus. METHODS: The IVBG system is a bedside monitor that automatically measures venous blood glucose (BG) concentration. In this study, BG was measured every 7.5 min by the IVBG system. Reference samples [venous blood samples measured on the Yellow Springs Instruments (YSI) glucose analyzer] were drawn every 15 min during inpatient studies on days 1, 2, and 3. Fifty insulin-treated healthy volunteers with diabetes were studied, and a maximum of 72 reference samples were collected. Effectiveness was primarily evaluated by assessing the proportion of IVBG BG measurements within the 15 mg/dl or 20% criterion [15 mg/dl (for YSI <75 mg/dl) or 20% (for YSI ≥75 mg/dl)] compared with YSI. Adverse events and adverse device effects were evaluated. RESULTS: A total of 95% of all IVBG values were within the 15 mg/dl or 20% criterion. The IVBG system BG measurement showed significant linear relationship with the laboratory YSI standard. Catheter insertion site irritation was mild and infrequent. No serious adverse events were reported. A total of 33% of the sensors were replaced during the 3-day use due to problematic IV lines or sensor/system errors. CONCLUSIONS: This clinical performance evaluation demonstrates that the IVBG system provides accurate and safe continuous BG measurements in healthy insulin-treated patients with diabetes.


Assuntos
Automonitorização da Glicemia/instrumentação , Automonitorização da Glicemia/métodos , Glicemia/análise , Diabetes Mellitus Tipo 1/sangue , Dispositivos de Acesso Vascular , Adulto , Automonitorização da Glicemia/efeitos adversos , Diabetes Mellitus Tipo 1/tratamento farmacológico , Desenho de Equipamento , Feminino , Humanos , Insulina/administração & dosagem , Insulina/uso terapêutico , Masculino , Monitorização Fisiológica/efeitos adversos , Monitorização Fisiológica/instrumentação , Monitorização Fisiológica/métodos , Análise de Regressão , Reprodutibilidade dos Testes , Método Simples-Cego
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