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Aggressive Glucose Control for Acute Ischemic Stroke Patients by Insulin Infusion

BACKGROUND AND PURPOSE: Hyperglycemia after acute ischemic stroke (AIS) is associated with poor outcomes. However, there is no consensus as to the optimal method for glycemic control. We designed an insulin infusion protocol for aggressive glucose control and investigated its efficacy and safety. ME...

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Autores principales: Kim, Nayoung, Jhang, Yunsook, Park, Jong-Moo, Kim, Byung-Kun, Kwon, Ohyun, Lee, JungJu, Lee, Ji-Sung, Koo, Ja-Seong
Formato: Texto
Lenguaje:English
Publicado: Korean Neurological Association 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2806538/
https://www.ncbi.nlm.nih.gov/pubmed/20076797
http://dx.doi.org/10.3988/jcn.2009.5.4.167
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author Kim, Nayoung
Jhang, Yunsook
Park, Jong-Moo
Kim, Byung-Kun
Kwon, Ohyun
Lee, JungJu
Lee, Ji-Sung
Koo, Ja-Seong
author_facet Kim, Nayoung
Jhang, Yunsook
Park, Jong-Moo
Kim, Byung-Kun
Kwon, Ohyun
Lee, JungJu
Lee, Ji-Sung
Koo, Ja-Seong
author_sort Kim, Nayoung
collection PubMed
description BACKGROUND AND PURPOSE: Hyperglycemia after acute ischemic stroke (AIS) is associated with poor outcomes. However, there is no consensus as to the optimal method for glycemic control. We designed an insulin infusion protocol for aggressive glucose control and investigated its efficacy and safety. METHODS: We applied our protocol to patients within 48 hours after AIS or transient ischemic attack (TIA) with an initial capillary glucose level of between 100 and 399 mg/dL (5.6-22.2 mmol/L). An insulin solution comprising 40 or 50 U of human regular insulin in 500 mL of 5% dextrose was administered for 24 hours. Capillary glucose was measured every 2 hours and the infusion rate was adjusted according to a nomogram with a target range of 80-129 mg/dL (4.4-7.2 mmol/L). Changes in glucose and overall glucose levels during insulin infusion were analyzed according to the presence of diabetes or admission hyperglycemia (admission glucose >139 mg/dL or 7.7 mmol/L) by the generalized estimating equation method. RESULTS: The study cohort comprised 115 consecutive patients. Glucose was significantly lowered from 160±57 mg/dL (8.9±3.2 mmol/L) at admission to 93±28 mg/dL (5.2±1.6 mmol/L) during insulin infusion (p<0.05). Laboratory hypoglycemia (capillary glucose <80 mg/dL or 4.4 mmol/L) occurred in 91 (71%) patients, 11 (10%) of whom had symptomatic hypoglycemia. Although glucose levels were significantly lowered and maintained within the target range in all patients, overall glucose levels were significantly higher in patients with diabetes or hyperglycemia (p<0.05). CONCLUSIONS: Our insulin-infusion protocol was effective in glycemic control for patients with AIS or TIA. Further modification is needed to improve the efficacy and safety of this procedure, and tailored intervention should be considered according to glycemic status.
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spelling pubmed-28065382010-01-14 Aggressive Glucose Control for Acute Ischemic Stroke Patients by Insulin Infusion Kim, Nayoung Jhang, Yunsook Park, Jong-Moo Kim, Byung-Kun Kwon, Ohyun Lee, JungJu Lee, Ji-Sung Koo, Ja-Seong J Clin Neurol Original Article BACKGROUND AND PURPOSE: Hyperglycemia after acute ischemic stroke (AIS) is associated with poor outcomes. However, there is no consensus as to the optimal method for glycemic control. We designed an insulin infusion protocol for aggressive glucose control and investigated its efficacy and safety. METHODS: We applied our protocol to patients within 48 hours after AIS or transient ischemic attack (TIA) with an initial capillary glucose level of between 100 and 399 mg/dL (5.6-22.2 mmol/L). An insulin solution comprising 40 or 50 U of human regular insulin in 500 mL of 5% dextrose was administered for 24 hours. Capillary glucose was measured every 2 hours and the infusion rate was adjusted according to a nomogram with a target range of 80-129 mg/dL (4.4-7.2 mmol/L). Changes in glucose and overall glucose levels during insulin infusion were analyzed according to the presence of diabetes or admission hyperglycemia (admission glucose >139 mg/dL or 7.7 mmol/L) by the generalized estimating equation method. RESULTS: The study cohort comprised 115 consecutive patients. Glucose was significantly lowered from 160±57 mg/dL (8.9±3.2 mmol/L) at admission to 93±28 mg/dL (5.2±1.6 mmol/L) during insulin infusion (p<0.05). Laboratory hypoglycemia (capillary glucose <80 mg/dL or 4.4 mmol/L) occurred in 91 (71%) patients, 11 (10%) of whom had symptomatic hypoglycemia. Although glucose levels were significantly lowered and maintained within the target range in all patients, overall glucose levels were significantly higher in patients with diabetes or hyperglycemia (p<0.05). CONCLUSIONS: Our insulin-infusion protocol was effective in glycemic control for patients with AIS or TIA. Further modification is needed to improve the efficacy and safety of this procedure, and tailored intervention should be considered according to glycemic status. Korean Neurological Association 2009-12 2009-12-31 /pmc/articles/PMC2806538/ /pubmed/20076797 http://dx.doi.org/10.3988/jcn.2009.5.4.167 Text en Copyright © 2009 Korean Neurological Association
spellingShingle Original Article
Kim, Nayoung
Jhang, Yunsook
Park, Jong-Moo
Kim, Byung-Kun
Kwon, Ohyun
Lee, JungJu
Lee, Ji-Sung
Koo, Ja-Seong
Aggressive Glucose Control for Acute Ischemic Stroke Patients by Insulin Infusion
title Aggressive Glucose Control for Acute Ischemic Stroke Patients by Insulin Infusion
title_full Aggressive Glucose Control for Acute Ischemic Stroke Patients by Insulin Infusion
title_fullStr Aggressive Glucose Control for Acute Ischemic Stroke Patients by Insulin Infusion
title_full_unstemmed Aggressive Glucose Control for Acute Ischemic Stroke Patients by Insulin Infusion
title_short Aggressive Glucose Control for Acute Ischemic Stroke Patients by Insulin Infusion
title_sort aggressive glucose control for acute ischemic stroke patients by insulin infusion
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2806538/
https://www.ncbi.nlm.nih.gov/pubmed/20076797
http://dx.doi.org/10.3988/jcn.2009.5.4.167
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