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1.
J Med Biol Eng ; 35(1): 125-133, 2015.
Artigo em Inglês | MEDLINE | ID: mdl-25750607

RESUMO

Critically ill patients are occasionally associated with an abrupt decline in renal function secondary to their primary diagnosis. The effect and impact of haemodialysis (HD) on insulin kinetics and endogenous insulin secretion in critically ill patients remains unclear. This study investigates the insulin kinetics of patients with severe acute kidney injury (AKI) who required HD treatment and glycaemic control (GC). Evidence shows that tight GC benefits the onset and progression of renal involvement in precocious phases of diabetic nephropathy for type 2 diabetes. The main objective of GC is to reduce hyperglycaemia while determining insulin sensitivity. Insulin sensitivity (SI ) is defined as the body response to the effects of insulin by lowering blood glucose levels. Particularly, this study used SI to track changes in insulin levels during HD therapy. Model-based insulin sensitivity profiles were identified for 51 critically ill patients with severe AKI on specialized relative insulin nutrition titration GC during intervals on HD (OFF/ON) and after HD (ON/OFF). The metabolic effects of HD were observed through changes in SI over the ON/OFF and OFF/ON transitions. Changes in model-based SI at the OFF/ON and ON/OFF transitions indicate changes in endogenous insulin secretion and/or changes in effective insulin clearance. Patients exhibited a median reduction of -29 % (interquartile range (IQR): [-58, 6 %], p = 0.02) in measured SI after the OFF/ON dialysis transition, and a median increase of +9 % (IQR -15 to 28 %, p = 0.7) after the ON/OFF transition. Almost 90 % of patients exhibited decreased SI at the OFF/ON transition, and 55 % exhibited increased SI at the ON/OFF transition. Results indicate that HD commencement has a significant effect on insulin pharmacokinetics at a cohort and per-patient level. These changes in metabolic behaviour are most likely caused by changes in insulin clearance or/and endogenous insulin secretion.

2.
Comput Methods Programs Biomed ; 162: 149-155, 2018 Aug.
Artigo em Inglês | MEDLINE | ID: mdl-29903481

RESUMO

BACKGROUND AND OBJECTIVE: Blood glucose variability is common in healthcare and it is not related or influenced by diabetes mellitus. To minimise the risk of high blood glucose in critically ill patients, Stochastic Targeted Blood Glucose Control Protocol is used in intensive care unit at hospitals worldwide. Thus, this study focuses on the performance of stochastic modelling protocol in comparison to the current blood glucose management protocols in the Malaysian intensive care unit. Also, this study is to assess the effectiveness of Stochastic Targeted Blood Glucose Control Protocol when it is applied to a cohort of diabetic patients. METHODS: Retrospective data from 210 patients were obtained from a general hospital in Malaysia from May 2014 until June 2015, where 123 patients were having comorbid diabetes mellitus. The comparison of blood glucose control protocol performance between both protocol simulations was conducted through blood glucose fitted with physiological modelling on top of virtual trial simulations, mean calculation of simulation error and several graphical comparisons using stochastic modelling. RESULTS: Stochastic Targeted Blood Glucose Control Protocol reduces hyperglycaemia by 16% in diabetic and 9% in nondiabetic cohorts. The protocol helps to control blood glucose level in the targeted range of 4.0-10.0 mmol/L for 71.8% in diabetic and 82.7% in nondiabetic cohorts, besides minimising the treatment hour up to 71 h for 123 diabetic patients and 39 h for 87 nondiabetic patients. CONCLUSION: It is concluded that Stochastic Targeted Blood Glucose Control Protocol is good in reducing hyperglycaemia as compared to the current blood glucose management protocol in the Malaysian intensive care unit. Hence, the current Malaysian intensive care unit protocols need to be modified to enhance their performance, especially in the integration of insulin and nutrition intervention in decreasing the hyperglycaemia incidences. Improvement in Stochastic Targeted Blood Glucose Control Protocol in terms of uen model is also a must to adapt with the diabetic cohort.


Assuntos
Glicemia , Diabetes Mellitus/sangue , Unidades de Terapia Intensiva , Adulto , Idoso , Simulação por Computador , Cuidados Críticos , Estado Terminal , Complicações do Diabetes/sangue , Diabetes Mellitus Tipo 2/sangue , Feminino , Humanos , Hiperglicemia/tratamento farmacológico , Malásia , Masculino , Pessoa de Meia-Idade , Reprodutibilidade dos Testes , Estudos Retrospectivos , Processos Estocásticos
3.
Artigo em Inglês | MEDLINE | ID: mdl-24110484

RESUMO

Critically ill patients often develop renal failure in addition to their primary diagnosis. However, the effect and impact of haemodialysis (HD) on insulin sensitivity n critically ill patients remains unclear. Specifically, this study investigates insulin sensitivity of acute renal failure (ARF) patients with sepsis who underwent HD and glycaemic control. Model-based insulin sensitivity (SI) profiles were identified for 20 critically ill ARF patients on Specialized Relative Insulin Nutrition Titration (SPRINT) glycaemic control during intervals onto HD (OFF/ON), and after HD (ON/OFF). Patients exhibited a median -18% (IQR -36% to -5% p<0.05) reduction in measured SI after the OFF/ON dialysis transition, and a median 9% (IQR -5% to 37%, p<0.05) rise after the ON/OFF transition. Almost 80% of patients exhibited decreased SI at the OFF/ON interval, and 60% exhibited increased SI at the ON/OFF transition. Results indicate that HD commencement has significant effect on insulin pharmacokinetics at a cohort and per-patient level. These results provide the data to design conclusive studies of HD effects on SI, and to inform glycaemic control protocol development and implementation for this specific group of critically ill patients with ARF-sepsis.


Assuntos
Injúria Renal Aguda/fisiopatologia , Resistência à Insulina/fisiologia , Diálise Renal/efeitos adversos , Sepse/fisiopatologia , Idoso , Cuidados Críticos , Estado Terminal , Feminino , Humanos , Masculino , Pessoa de Meia-Idade , Modelos Biológicos
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