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Chronic hyperglycemia and glycemic control

Chronic hyperglycemia and glycemic control

Hhperglycemia D, Bellini NJ, Biba U, Cai A, Close KL. Skinfold measurement accuracy, to glyvemic sample size and precision, other concomitant therapies that may influence HbA 1c levels were not explored. Trends in Insulin Use Among US Adults With Diabetes, NHANES eTable 2.

Chronic hyperglycemia and glycemic control -

In trials of patients with type 2 diabetes with and without chronic kidney disease, GLP-1 receptor agonists slowed the rate of decline in eGFR and prevented worsening of albuminuria [ 54,56,58 ].

These trials and other trials evaluating microvascular outcomes are reviewed in the individual topics. Guidelines — Our approach is largely consistent with American and European guidelines [ 52,74,75 ]. A consensus statement regarding the management of hyperglycemia in type 2 diabetes by the American Diabetes Association ADA and the European Association for the Study of Diabetes EASD was developed in and has been updated regularly, with the most recent revision published in [ 75 ].

The guidelines emphasize the importance of individualizing the choice of medications for the treatment of diabetes, considering important comorbidities CVD, HF, or chronic kidney disease; hypoglycemia risk; and need for weight loss and patient-specific factors including patient preferences, values, and cost [ 75 ].

We also agree with the World Health Organization WHO that sulfonylureas have a long-term safety profile, are inexpensive, and are highly effective, especially when used as described above, with patient education and dose adjustment to minimize side effects [ 76 ].

Blood glucose monitoring BGM is not necessary for most patients with type 2 diabetes who are on a stable regimen of diet or oral agents and who are not experiencing hypoglycemia.

BGM may be useful for some patients with type 2 diabetes who use the results to modify eating patterns, exercise, or insulin doses on a regular basis. See "Glucose monitoring in the ambulatory management of nonpregnant adults with diabetes mellitus", section on 'Type 2 diabetes'.

The balance among efficacy in lowering A1C, side effects, and costs must be carefully weighed in considering which drugs or combinations to choose. Avoiding insulin, the most potent of all hypoglycemic medications, at the expense of poorer glucose management and greater side effects and cost, is not likely to benefit the patient in the long term.

See "Management of persistent hyperglycemia in type 2 diabetes mellitus", section on 'Our approach'. SOCIETY GUIDELINE LINKS — Links to society and government-sponsored guidelines from selected countries and regions around the world are provided separately.

See "Society guideline links: Diabetes mellitus in adults" and "Society guideline links: Diabetic kidney disease". These articles are best for patients who want a general overview and who prefer short, easy-to-read materials.

Beyond the Basics patient education pieces are longer, more sophisticated, and more detailed. These articles are written at the 10 th to 12 th grade reading level and are best for patients who want in-depth information and are comfortable with some medical jargon.

Here are the patient education articles that are relevant to this topic. We encourage you to print or e-mail these topics to your patients.

You can also locate patient education articles on a variety of subjects by searching on "patient info" and the keyword s of interest. Weight reduction through diet, exercise, and behavioral modification can all be used to improve glycemic management, although the majority of patients with type 2 diabetes will require medication.

See 'Diabetes education' above. Glycemic targets are generally set somewhat higher for older adults and for those with comorbidities or a limited life expectancy and little likelihood of benefit from intensive therapy.

See 'Glycemic management' above and "Glycemic control and vascular complications in type 2 diabetes mellitus", section on 'Choosing a glycemic target'. In the absence of specific contraindications, we suggest metformin as initial therapy for most patients Grade 2B. Although some guidelines and experts endorse the initial use of alternative agents as monotherapy or in combination with metformin, we prefer initiating a single agent typically metformin and then sequentially adding additional glucose-lowering agents as needed.

See 'Metformin' above and 'Glycemic efficacy' above. We suggest initiating metformin at the time of diabetes diagnosis Grade 2C , along with consultation for lifestyle intervention. See 'When to start' above.

The dose of metformin should be titrated to its maximally effective dose usually mg per day in divided doses over one to two months, as tolerated. See 'Contraindications to or intolerance of metformin' above. See 'Established cardiovascular or kidney disease' above.

The majority of patients in the cardiovascular and renal outcomes trials had established cardiovascular disease CVD or diabetic kidney disease DKD with severely increased albuminuria, and therefore, these are the primary indications for one of these drugs.

See 'Without established cardiovascular or kidney disease' above. Each one of these choices has individual advantages and risks table 1. Choice of medication is guided by efficacy, patient comorbidities, preferences, and cost. Sulfonylureas remain a highly effective treatment for hyperglycemia, particularly when cost is a barrier.

Side effects of hypoglycemia and weight gain can be mitigated with careful dosing and diabetes self-management education.

For patients who are injection averse, initial therapy with high-dose sulfonylurea is an alternative, particularly for patients who have been consuming large amounts of sugar-sweetened beverages, in whom elimination of carbohydrates can be anticipated to cause a reduction in glucose within several days.

See 'Symptomatic catabolic or severe hyperglycemia' above and "Insulin therapy in type 2 diabetes mellitus". Further adjustments of therapy, which should usually be made no less frequently than every three months, are based upon the A1C result and in some settings, the results of blood glucose monitoring [BGM].

See 'Monitoring' above. See "Management of persistent hyperglycemia in type 2 diabetes mellitus" and "Insulin therapy in type 2 diabetes mellitus". Why UpToDate? Product Editorial Subscription Options Subscribe Sign in. Learn how UpToDate can help you. Select the option that best describes you.

View Topic. Font Size Small Normal Large. Initial management of hyperglycemia in adults with type 2 diabetes mellitus. Formulary drug information for this topic. No drug references linked in this topic. Find in topic Formulary Print Share. View in. Language Chinese English. Author: Deborah J Wexler, MD, MSc Section Editor: David M Nathan, MD Deputy Editor: Katya Rubinow, MD Contributor Disclosures.

All topics are updated as new evidence becomes available and our peer review process is complete. Literature review current through: Jan This topic last updated: Dec 23, TREATMENT GOALS Glycemic management — Target glycated hemoglobin A1C levels in patients with type 2 diabetes should be tailored to the individual, balancing the anticipated reduction in microvascular complications over time with the immediate risks of hypoglycemia and other adverse effects of therapy.

Summary of glucose-lowering interventions. UK Prospective Diabetes Study UKPDS Group. Lancet ; Holman RR, Paul SK, Bethel MA, et al. N Engl J Med ; Hayward RA, Reaven PD, Wiitala WL, et al.

Follow-up of glycemic control and cardiovascular outcomes in type 2 diabetes. ADVANCE Collaborative Group, Patel A, MacMahon S, et al. Intensive blood glucose control and vascular outcomes in patients with type 2 diabetes.

Action to Control Cardiovascular Risk in Diabetes Study Group, Gerstein HC, Miller ME, et al. Effects of intensive glucose lowering in type 2 diabetes.

Rawshani A, Rawshani A, Franzén S, et al. Risk Factors, Mortality, and Cardiovascular Outcomes in Patients with Type 2 Diabetes. Gaede P, Vedel P, Larsen N, et al. Multifactorial intervention and cardiovascular disease in patients with type 2 diabetes. Kazemian P, Shebl FM, McCann N, et al.

Evaluation of the Cascade of Diabetes Care in the United States, JAMA Intern Med ; Pal K, Eastwood SV, Michie S, et al.

Computer-based diabetes self-management interventions for adults with type 2 diabetes mellitus. Cochrane Database Syst Rev ; :CD Saffari M, Ghanizadeh G, Koenig HG. Health education via mobile text messaging for glycemic control in adults with type 2 diabetes: a systematic review and meta-analysis.

Prim Care Diabetes ; Liang X, Wang Q, Yang X, et al. Effect of mobile phone intervention for diabetes on glycaemic control: a meta-analysis. Diabet Med ; Henry RR, Scheaffer L, Olefsky JM. Glycemic effects of intensive caloric restriction and isocaloric refeeding in noninsulin-dependent diabetes mellitus.

J Clin Endocrinol Metab ; Utzschneider KM, Carr DB, Barsness SM, et al. Diet-induced weight loss is associated with an improvement in beta-cell function in older men.

Wing RR, Blair EH, Bononi P, et al. Caloric restriction per se is a significant factor in improvements in glycemic control and insulin sensitivity during weight loss in obese NIDDM patients. Diabetes Care ; Lean ME, Leslie WS, Barnes AC, et al. Primary care-led weight management for remission of type 2 diabetes DiRECT : an open-label, cluster-randomised trial.

Delahanty LM. The look AHEAD study: implications for clinical practice go beyond the headlines. J Acad Nutr Diet ; Evert AB, Dennison M, Gardner CD, et al. Nutrition Therapy for Adults With Diabetes or Prediabetes: A Consensus Report. Lean MEJ, Leslie WS, Barnes AC, et al. Durability of a primary care-led weight-management intervention for remission of type 2 diabetes: 2-year results of the DiRECT open-label, cluster-randomised trial.

Lancet Diabetes Endocrinol ; Niskanen LK, Uusitupa MI, Sarlund H, et al. Five-year follow-up study on plasma insulin levels in newly diagnosed NIDDM patients and nondiabetic subjects.

Norris SL, Zhang X, Avenell A, et al. Long-term effectiveness of lifestyle and behavioral weight loss interventions in adults with type 2 diabetes: a meta-analysis.

Am J Med ; United Kingdom Prospective Diabetes Study UKPDS. BMJ ; Umpierre D, Ribeiro PA, Kramer CK, et al. Physical activity advice only or structured exercise training and association with HbA1c levels in type 2 diabetes: a systematic review and meta-analysis.

JAMA ; Jeon CY, Lokken RP, Hu FB, van Dam RM. Physical activity of moderate intensity and risk of type 2 diabetes: a systematic review. Egan AM, Mahmood WA, Fenton R, et al. Barriers to exercise in obese patients with type 2 diabetes.

QJM ; American Diabetes Association Professional Practice Committee. Facilitating Positive Health Behaviors and Well-being to Improve Health Outcomes: Standards of Care in Diabetes Diabetes Care ; S Kobayashi Y, Long J, Dan S, et al.

Strength training is more effective than aerobic exercise for improving glycaemic control and body composition in people with normal-weight type 2 diabetes: a randomised controlled trial.

Diabetologia ; Look AHEAD Research Group, Wing RR, Bolin P, et al. Cardiovascular effects of intensive lifestyle intervention in type 2 diabetes. Pillay J, Armstrong MJ, Butalia S, et al.

Behavioral Programs for Type 2 Diabetes Mellitus: A Systematic Review and Network Meta-analysis. Ann Intern Med ; Johansen MY, MacDonald CS, Hansen KB, et al. Effect of an Intensive Lifestyle Intervention on Glycemic Control in Patients With Type 2 Diabetes: A Randomized Clinical Trial.

Lingvay I, Sumithran P, Cohen RV, le Roux CW. Obesity management as a primary treatment goal for type 2 diabetes: time to reframe the conversation. Look AHEAD Research Group, Pi-Sunyer X, Blackburn G, et al. Reduction in weight and cardiovascular disease risk factors in individuals with type 2 diabetes: one-year results of the look AHEAD trial.

Arterburn DE, O'Connor PJ. A look ahead at the future of diabetes prevention and treatment. Look AHEAD Research Group, Gregg EW, Jakicic JM, et al. Association of the magnitude of weight loss and changes in physical fitness with long-term cardiovascular disease outcomes in overweight or obese people with type 2 diabetes: a post-hoc analysis of the Look AHEAD randomised clinical trial.

Look AHEAD Research Group. Eight-year weight losses with an intensive lifestyle intervention: the look AHEAD study. Obesity Silver Spring ; Look AHEAD Research Group, Wing RR.

Long-term effects of a lifestyle intervention on weight and cardiovascular risk factors in individuals with type 2 diabetes mellitus: four-year results of the Look AHEAD trial.

Arch Intern Med ; Gregg EW, Chen H, Wagenknecht LE, et al. Association of an intensive lifestyle intervention with remission of type 2 diabetes. Jakicic JM, Egan CM, Fabricatore AN, et al. Four-year change in cardiorespiratory fitness and influence on glycemic control in adults with type 2 diabetes in a randomized trial: the Look AHEAD Trial.

Kuna ST, Reboussin DM, Borradaile KE, et al. Long-term effect of weight loss on obstructive sleep apnea severity in obese patients with type 2 diabetes. Sleep ; Wing RR, Bond DS, Gendrano IN 3rd, et al. Effect of intensive lifestyle intervention on sexual dysfunction in women with type 2 diabetes: results from an ancillary Look AHEAD study.

html Accessed on July 18, Effect of a long-term behavioural weight loss intervention on nephropathy in overweight or obese adults with type 2 diabetes: a secondary analysis of the Look AHEAD randomised clinical trial. Surwit RS, van Tilburg MA, Zucker N, et al. Stress management improves long-term glycemic control in type 2 diabetes.

Ismail K, Winkley K, Rabe-Hesketh S. Systematic review and meta-analysis of randomised controlled trials of psychological interventions to improve glycaemic control in patients with type 2 diabetes. Safren SA, Gonzalez JS, Wexler DJ, et al. A randomized controlled trial of cognitive behavioral therapy for adherence and depression CBT-AD in patients with uncontrolled type 2 diabetes.

Williams JW Jr, Katon W, Lin EH, et al. The effectiveness of depression care management on diabetes-related outcomes in older patients. Colagiuri S, Cull CA, Holman RR, UKPDS Group. Are lower fasting plasma glucose levels at diagnosis of type 2 diabetes associated with improved outcomes?

prospective diabetes study Choi JG, Winn AN, Skandari MR, et al. First-Line Therapy for Type 2 Diabetes With Sodium-Glucose Cotransporter-2 Inhibitors and Glucagon-Like Peptide-1 Receptor Agonists : A Cost-Effectiveness Study.

Abdul-Ghani MA, Puckett C, Triplitt C, et al. Initial combination therapy with metformin, pioglitazone and exenatide is more effective than sequential add-on therapy in subjects with new-onset diabetes.

Results from the Efficacy and Durability of Initial Combination Therapy for Type 2 Diabetes EDICT : a randomized trial. Diabetes Obes Metab ; Hong J, Zhang Y, Lai S, et al.

Effects of metformin versus glipizide on cardiovascular outcomes in patients with type 2 diabetes and coronary artery disease. Kooy A, de Jager J, Lehert P, et al. Long-term effects of metformin on metabolism and microvascular and macrovascular disease in patients with type 2 diabetes mellitus.

Maruthur NM, Tseng E, Hutfless S, et al. Diabetes Medications as Monotherapy or Metformin-Based Combination Therapy for Type 2 Diabetes: A Systematic Review and Meta-analysis.

Pharmacologic Approaches to Glycemic Treatment: Standards of Care in Diabetes Jia W, Weng J, Zhu D, et al. Standards of medical care for type 2 diabetes in China Diabetes Metab Res Rev ; e Marso SP, Bain SC, Consoli A, et al. Semaglutide and Cardiovascular Outcomes in Patients with Type 2 Diabetes.

Marso SP, Daniels GH, Brown-Frandsen K, et al. Liraglutide and Cardiovascular Outcomes in Type 2 Diabetes. Mann JFE, Ørsted DD, Brown-Frandsen K, et al. Liraglutide and Renal Outcomes in Type 2 Diabetes. Gerstein HC, Colhoun HM, Dagenais GR, et al. Dulaglutide and cardiovascular outcomes in type 2 diabetes REWIND : a double-blind, randomised placebo-controlled trial.

Dulaglutide and renal outcomes in type 2 diabetes: an exploratory analysis of the REWIND randomised, placebo-controlled trial. Kanie T, Mizuno A, Takaoka Y, et al.

Dipeptidyl peptidase-4 inhibitors, glucagon-like peptide 1 receptor agonists and sodium-glucose co-transporter-2 inhibitors for people with cardiovascular disease: a network meta-analysis. Cochrane Database Syst Rev ; CD Heerspink HJL, Stefánsson BV, Correa-Rotter R, et al.

Dapagliflozin in Patients with Chronic Kidney Disease. Wiviott SD, Raz I, Bonaca MP, et al. Dapagliflozin and Cardiovascular Outcomes in Type 2 Diabetes.

Zinman B, Wanner C, Lachin JM, et al. Empagliflozin, Cardiovascular Outcomes, and Mortality in Type 2 Diabetes. Neal B, Perkovic V, Mahaffey KW, et al. Canagliflozin and Cardiovascular and Renal Events in Type 2 Diabetes.

Perkovic V, Jardine MJ, Neal B, et al. Canagliflozin and Renal Outcomes in Type 2 Diabetes and Nephropathy. de Boer IH, Khunti K, Sadusky T, et al. Diabetes Management in Chronic Kidney Disease: A Consensus Report by the American Diabetes Association ADA and Kidney Disease: Improving Global Outcomes KDIGO.

Shyangdan DS, Royle P, Clar C, et al. Glucagon-like peptide analogues for type 2 diabetes mellitus. Singh S, Wright EE Jr, Kwan AY, et al. Glucagon-like peptide-1 receptor agonists compared with basal insulins for the treatment of type 2 diabetes mellitus: a systematic review and meta-analysis.

Davidson MB. Successful treatment of markedly symptomatic patients with type II diabetes mellitus using high doses of sulfonylurea agents. West J Med ; pdf Accessed on April 21, Palmer SC, Mavridis D, Nicolucci A, et al. Comparison of Clinical Outcomes and Adverse Events Associated With Glucose-Lowering Drugs in Patients With Type 2 Diabetes: A Meta-analysis.

Tsapas A, Avgerinos I, Karagiannis T, et al. Comparative Effectiveness of Glucose-Lowering Drugs for Type 2 Diabetes: A Systematic Review and Network Meta-analysis. National surveillance of emergency department visits for outpatient adverse drug events. Intensive insulin therapy and pentastarch resuscitation in severe sepsis.

Translating the A1C assay into estimated average glucose values. Diabetes Care. Epub Jun 7. Erratum in: Diabetes Care. Intensive versus conventional glucose control in critically ill patients. The correlation of hemoglobin A1c to blood glucose.

J Diabetes Sci Technol. Reducing potentially fatal errors associated with high doses of insulin: a successful multifaceted multidisciplinary prevention strategy.

BMJ Qual Saf. Hypoglycemia and risk of death in critically ill patients. Guidelines for the use of an insulin infusion for the management of hyperglycemia in critically ill patients. Crit Care Med. Stress hyperglycemia: an essential survival response! Crit Care.

Inpatient glycemic control: best practice advice from the Clinical Guidelines Committee of the American College of Physicians. Am J Med Qual. Dysglycaemia in the critically ill and the interaction of chronic and acute glycaemia with mortality.

Intensive Care Med. Liberal Glycemic Control in Critically Ill Patients With Type 2 Diabetes: An Exploratory Study.

Hospital-acquired complications in intensive care unit patients with diabetes: A before-and-after study of a conventional versus liberal glucose control protocol. Acta Anaesthesiol Scand. Is it time to abandon glucose control in critically ill adult patients? Curr Opin Crit Care. Study protocol and statistical analysis plan for the Liberal Glucose Control in Critically Ill Patients with Pre-existing Type 2 Diabetes LUCID trial.

Crit Care Resusc. Glycemic control in the critically ill: Less is more. Cleve Clin J Med. The Effect of a Liberal Approach to Glucose Control in Critically Ill Patients with Type 2 Diabetes: A Multicenter, Parallel-Group, Open-Label Randomized Clinical Trial.

Am J Respir Crit Care Med.

Chronic hyperglycemia and glycemic control ConrolMas EGinet C, et al. Activation hyperglycema Oxidative Stress by Acute Glucose Fluctuations Compared With Sustained Chronic Hyperglycemia in Patients Exercise routines for lowering blood pressure Type Skinfold measurement accuracy Diabetes. Author Affiliations: Department conhrol Metabolic Diseases, Contgol Hospital Drs Monnier, Ginet, and Villonand Chrohic of Hyperglydemia Nutrition and Atherogenesis, University Institute of Clinical Research Drs Mas, Michel, Cristol, and ColetteUniversity of Montpellier, Montpellier, France. Context Glycemic disorders, one of the main risk factors for cardiovascular disease, are associated with activation of oxidative stress. Objective To assess the respective contributions of sustained chronic hyperglycemia and of acute glucose fluctuations to oxidative stress in type 2 diabetes. Design, Setting, and Participants Case-control study of 21 patients with type 2 diabetes studied compared with 21 age- and sex-matched controls studied in in Montpellier, France. Main Outcome Measures Oxidative stress, estimated from hour urinary excretion rates of free 8-iso prostaglandin F 2α 8-iso PGF 2α.

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Management of Inpatient Diabetes and Hyperglycemia

Chronic hyperglycemia and glycemic control -

Increased oxidative stress can result in endothelial dysfunction and contribute to vascular damage. It would therefore appear appropriate to have a higher glycemic treatment target in patients with preexisting diabetes and premorbid poor glycemic control to prevent large reductions in blood glucose concentration.

Biological adjustment to preexisting hyperglycemia and less glycemic variability might explain this phenomenon. These observations generate the hypothesis that glucose levels that are considered safe and desirable in other patients might be undesirable in diabetic patients with chronic hyperglycemia.

On the basis of this data we suggest that the HbA1c be checked on admission to the ICU in all diabetics with blood glucose therapeutic targets as provided in Table 1.

Plummer MP, Bellomo R, Cousins CE, Annink CE, Sundararajan K, Reddi BA, Raj JP, Chapman MJ, Horowitz M, Deane AM Dysglycaemia in the critically ill and the interaction of chronic and acute glycaemia with mortality.

Intensive Care Med. doi: PubMed Google Scholar. Badawi O, Waite MD, Fuhrman SA, Zuckerman IH Association between intensive care unit-acquired dysglycemia and in-hospital mortality.

Crit Care Med — Article PubMed Google Scholar. van den Berghe G, Wouters P, Weekers F, Verwaest C, Bruyninckx F, Schetz M, Vlasselaers D, Ferdinande P, Lauwers P, Bouillon R Intensive insulin therapy in critically ill patients.

N Engl J Med — The NICE-Sugar Study Investigators Intensive versus conventional glucose control in critically ill patients. Marik PE, Bellomo R Stress hyperglycemia: an essential survival response! Crit Care Article PubMed Central PubMed Google Scholar.

Qaseem A, Humphrey LL, Chou R, Snow V, Shekelle P Use of intensive insulin therapy for the management of glycemic control in hospitalized patients: a clinical practice guideline from the American College of Physicians.

Ann Intern Med — Agus MS, Steil GM, Wypij D, Costello JM, Laussen PC, Langer M, Alexander JL Tight glycemic control versus standard care after pediatric cardiac surgery. Article CAS PubMed Central PubMed Google Scholar. Minakata K, Sakata R Perioperative control of blood glucose level in cardiac surgery.

General Thorac Cardiovasc Surg — Article Google Scholar. Diabetes Care 37 Suppl 1 :S5— Olson DE, Rhee MK, Herrick K, Ziemer DC, Twombly JG, Phillips LS Screening for diabetes and pre-diabetes with proposed A1C-based diagnostic criteria.

Diabetes Care — Egi M, Bellomo R, Stachowski E, French CJ, Hart GK, Hegarty C, Bailey M Blood glucose concentration and outcome of critical illness: the impact of diabetes. Article CAS PubMed Google Scholar. Krinsley JS, Egi M, KIss A, Devendra AM, Schuetz P, Maurer P, Schultz MJ, van Hooijdonk RT, Kiyoshi M, Mackenzie IM, Annane D, Stow P, Nasraway SA, Holewinski S, Holzinger U, Preiser JC, Vincent JL, Bellomo R Diabetes status and the relation of the three domains of glycemic contril to mortality in critically ill patients: an international multicenter cohort study.

Crit Care R Egi M, Bellomo R, Stachowski E, French CJ, Hart G Variability of blood glucose concentration and short-term mortality in critically ill patients.

Anesthesiol — Article CAS Google Scholar. Monnier L, Mas E, Ginet C, Michel F, Villon L, Cristol JP, Colette C Activation of oxidative stress by acute glucose fluctuations compared with sustained chronic hyperglycemia in patients with type 2 diabetes.

JAMA — Egi M, Bellomo R, Stachowski E, French CJ, Hart GK, Taori G, Hegarty C, Bailey M The interaction of chronic and acute glycemia with mortality in critically ill patients with diabetes. Download references.

Division of Pulmonary and Critical Care Medicine, Eastern Virginia Medical School, Fairfax Av, Suite , Norfolk, VA, , USA. Department of Anesthesiology, Kobe University Hospital, Kobe City, Hyogo, , Japan. You can also search for this author in PubMed Google Scholar.

Correspondence to Paul E. Reprints and permissions. Marik, P. Treatment thresholds for hyperglycemia in critically ill patients with and without diabetes. Intensive Care Med 40 , — Download citation. Received : 08 May Accepted : 14 May Published : 24 May Issue Date : July Anyone you share the following link with will be able to read this content:.

Sorry, a shareable link is not currently available for this article. Importance There have been major advances in insulin delivery and formulations over the past several decades. It is unclear whether these changes have resulted in improved glycemic control for patients with diabetes.

Objective To characterize trends and disparities in glycemic control and severe hyperglycemia in US adults with diabetes using insulin. Design, Setting, and Participants This serial population-based cross-sectional study used data from the National Health and Nutrition Examination Survey NHANES between and Participants were nonpregnant US adults aged 20 years or older who had a diagnosis of diabetes and were currently using insulin.

Analyses incorporated sample weights to account for oversampling of certain populations and survey nonresponse. Results There were participants with diabetes using insulin included in the analyses mean [SD] age, From to , the proportion of patients with diabetes who received insulin and achieved glycemic control did not significantly change, from Mexican American adults who received insulin were less likely than non-Hispanic White adults to achieve glycemic control, and disparities increased during the study period.

The proportion of adults with severe hyperglycemia did not significantly change and was Adults who were Mexican American or non-Hispanic Black, were uninsured, or had low family income had the highest prevalence of severe hyperglycemia. Conclusions and Relevance In this population-based cross-sectional study of NHANES data over the past 3 decades, glycemic control stagnated and racial and ethnic disparities increased among US adults with diabetes who received insulin.

Efforts to improve access to insulin may optimize glycemic control and reduce disparities in this population. Insulin is typically a last-line therapy for patients with type 2 diabetes. Over the past several decades, there have been major advances in diabetes technology and management strategies as well as insulin delivery and formulations.

Racial and ethnic minority patients, persons from low—socioeconomic status backgrounds, and those without insurance experience slower intensification of their treatment regimen and have less access to technologies that improve the safety of insulin therapy eg, continuous glucose monitoring systems , potentially contributing to worse glycemic control.

Characterizing population-level disparities is important for designing policies and targeted interventions to address inequities among patients receiving insulin. The objective of our study was to characterize national trends in glycemic control and severe hyperglycemia among patients with diagnosed diabetes using insulin.

We considered these outcomes overall and by race and ethnicity, educational level, income, and health insurance status. To accomplish these objectives, we conducted an analysis of over 3 decades of data from the National Health and Nutrition Examination Survey NHANES.

In this cross-sectional study, we analyzed data from the NHANES III, which was conducted from to , and from the continuous NHANES, with data available from to Data are collected from household interviews and from standardized medical examinations including blood sample collections performed in mobile examination centers.

Our analysis included nonpregnant adults aged 20 years or older who reported a diagnosis of diabetes by a doctor or health professional other than during pregnancy and who were currently being treated with insulin.

The National Center for Health Statistics institutional review board approved the study protocols, and all the participants provided written informed consent. This study followed the Strengthening the Reporting of Observational Studies in Epidemiology STROBE reporting guideline.

Level of HbA 1c was measured with the use of high-performance liquid chromatography. To account for changing laboratory methods over time, we calibrated HbA 1c levels using a previously validated equipercentile equating approach to correct for shifts in distribution due to laboratory drift.

Participants self-reported their age, gender man or woman , race and ethnicity Mexican American, non-Hispanic Black, non-Hispanic White, or other race and ethnicity , educational level high school or less, some college, or college graduate or above , health insurance status uninsured, private insurance, or public insurance , health care utilization number of visits to a health care professional annually , age at diabetes diagnosis, and family income.

Body mass index calculated as weight in kilograms divided by height in meters squared was calculated from measured height and weight and categorized as less than 25, 25 to less than 30, or 30 or greater. We used χ 2 and t tests to assess differences in sociodemographic and clinical characteristics among adults using insulin.

We estimated trends in insulin use, glycemic control, and severe hyperglycemia overall and by age, race and ethnicity, and indicators of socioeconomic status. To increase the precision of our point estimates, we pooled NHANES survey cycles into 5- to 7-year intervals , , , and We used logistic regression to evaluate trends over time with the midpoint of each survey cycle modeled as a continuous independent variable.

We conducted sensitivity analyses 1 using different uniform HbA 1c cutoff values of glycemic control and severe hyperglycemia, 2 using age-adjusted and age-specific HbA 1c cutoff values, and 3 excluding persons with possible type 1 diabetes, defined as those who started using insulin within 1 year of diabetes diagnosis, were currently using insulin, and were diagnosed with diabetes when younger than 30 years.

All analyses were conducted using Stata, version The calculated estimates are designed to be representative of the US civilian noninstitutionalized population with diagnosed diabetes.

The demographic profile for the participants is summarized in Table 1. These participants had a mean SD age of The overall percentage of adults with diabetes who used insulin did not change significantly, from Among adults using insulin for their diabetes treatment, the current mean age was From to , there was a significant increase in mean diabetes duration The mean HbA 1c level from was 8.

Trends in glycemic control were largely consistent across subgroups with the exception of race and ethnicity Figure 2. Glycemic control decreased significantly for Mexican American adults using insulin In , non-Hispanic White individuals In , the prevalence of severe hyperglycemia was roughly twice as high for Mexican Americans Results were also similar after excluding participants who may have had type 1 diabetes eTable 4 and eFigures 3 and 4 in Supplement 1.

After adjusting for age, gender, race and ethnicity, education, and income, Mexican American adults using insulin were significantly less likely odds ratio [OR], 0. Non-Hispanic Black adults OR, 2.

Adults aged 65 years or older were more likely to achieve glycemic control OR, 1. From to , there was no significant change in the percentage of adults using insulin or the prevalence of glycemic control and severe hyperglycemia among US adults with diabetes using insulin. Few population-based studies have examined glycemic control among patients using insulin.

Our results also establish that the prevalence of severe hyperglycemia did not decrease over time. Several factors may have contributed to the lack of improvement in glycemic control. First, the rising cost of insulin is likely leading to medication nonadherence.

Trends in glycemic control varied considerably across race and ethnicity. While glycemic control was stable for non-Hispanic White adults using insulin, we found that control declined significantly among Mexican American adults. These disparities may be driven in part by differences in socioeconomic resources, though differences persisted in analyses that adjusted for educational level.

Other potential contributors may include unique cultural factors and health beliefs eg, fear of needles , slower treatment intensification, differences in health care literacy, and discrimination.

Hyperglycemic emergencies have increased significantly since the mids and are especially common in patients with low income and racial and ethnic minority patients.

Among adults using insulin, we found that racial and ethnic minority patients, uninsured patients, and those with low family income had the highest levels of severe hyperglycemia. These results suggest that addressing barriers to insulin therapy may be important for reducing hyperglycemic crises in high-risk populations.

This is one of the first nationally representative studies to characterize glycemic control and severe hyperglycemia among US adults with diabetes using insulin. We analyzed the most recent national data available in a large sample of adults with diagnosed diabetes.

Nearly 3 decades of data were collected using rigorous and standardized protocols. Certain limitations should be considered in the interpretation of our results. First, this analysis used cross-sectional data, and we could not determine the causes underlying the trends in glycemic control.

Second, use of insulin was self-reported and did not include information on insulin type, dosage, or adherence. Third, to maximize sample size and precision, other concomitant therapies that may influence HbA 1c levels were not explored. Fourth, the NHANES only sampled noninstitutionalized adults, and therefore, certain segments of the population with diabetes are not represented in these estimates.

Fifth, due to the relatively small sample size, the study power was insufficient to detect small to moderate changes in insulin use or glycemic control without pooling survey years. This serial cross-sectional study of NHANES data from to demonstrated that despite advancements in insulin formulations and diabetes management strategies, glycemic control and severe hyperglycemia among adults using insulin did not improve in the general US adult population with diabetes.

Racial and ethnic disparities in glycemic control among adults with type 2 diabetes persisted and increased. Current rates of glycemic control in minority groups, especially Mexican American individuals, remain unacceptably low. Efforts to facilitate access to insulin will be critical to improve glycemic management.

Addressing clinical inertia among practitioners and improving the care process may optimize glycemic control among patients using insulin.

Published: December 20, Open Access: This is an open access article distributed under the terms of the CC-BY License. JAMA Network Open. Corresponding Author: Elizabeth Selvin, PhD, MPH, Welch Center for Prevention, Epidemiology, and Clinical Research, Department of Epidemiology, Johns Hopkins Bloomberg School of Public Health, E Monument St, Ste , Baltimore, MD eselvin jhu.

Author Contributions: Mr Venkatraman and Dr Fang had full access to all of the data in the study and take responsibility for the integrity of the data and the accuracy of the data analysis. Critical revision of the manuscript for important intellectual content: All authors.

Conflict of Interest Disclosures: Dr Selvin reported receiving grants from the National Institutes of Health NIH related and unrelated to this work during the conduct of the study; receiving grants from the NIH and the Foundation for the NIH outside the submitted work; being a deputy editor of Diabetes Care and a member of the editorial board of Diabetologia ; and receiving payments from Wolters Kluwer and UpToDate.

No other disclosures were reported. Dr Selvin was supported by grant K24 HL from the NHLBI, NIH. Data Sharing Statement: See Supplement 2.

full text icon Full Text. Download PDF Comment. Top of Article Key Points Abstract Introduction Methods Results Discussion Conclusions Article Information References. Figure 1. Trends in Glycemic Control and Severe Hyperglycemia Among US Adults With Diabetes Using Insulin From to View Large Download.

Figure 2. Trends in Glycemic Control Among US Adults With Diabetes Using Insulin From to Figure 3. Trends in Severe Hyperglycemia Among US Adults With Diabetes Using Insulin From to Table 1. Characteristics of US Adults Diagnosed With Diabetes Using Insulin in NHANES From to Table 2.

Age-, Gender-, Race-, Education-, and Income-Adjusted Factors Associated With Glycemic Control and Severe Hyperglycemia in NHANES From to a. Supplement 1. Trends in Insulin Use Among US Adults With Diabetes, NHANES eTable 2.

Glycemic Control Among Adults With Diabetes Using Insulin, Unadjusted and Age-adjusted Based on Age Cutoff Recommendations eFigure 1. Characteristics of Adults Diagnosed With Type 2 Diabetes Using Insulin, HNANES, eFigure 3.

Supplement 2. Data Sharing Statement. American Diabetes Association. Pharmacologic approaches to glycemic treatment: Standards of Medical Care in Diabetes— doi:

Conteol is a condition in which an excessive amount of glucose circulates in the blood plasma. This is Chronic hyperglycemia and glycemic control a blood sugar hyperglyce,ia higher than Hyperglycemiaa subject glyecmic a consistent fasting Chdonic glucose Saltwater Fish Aquarium Lighting between ~5. For diabetics, hyperglycrmia levels that are considered to be too hyperglycemic can vary from person to person, mainly due to the person's renal threshold of glucose and overall glucose tolerance. The degree of hyperglycemia can change over time depending on the metabolic cause, for example, impaired glucose tolerance or fasting glucose, and it can depend on treatment. Blood glucose levels can rise well above normal and cause pathological and functional changes for significant periods without producing any permanent effects or symptoms. Diabetic neuropathy may be a result of long-term hyperglycemia. Hyperglycrmia increases the risk Hyperlgycemia hospitalization for several reasons, including: cardiovascular CV disease, nephropathy, infection, conrrol and cnotrol amputations. Chronic hyperglycemia and glycemic control hyperglycemia is common. Diabetes has been reported to be Eating restriction strategy fourth most common comorbid condition listed on all hospital discharges 2. Acute illness results in a number of physiological changes e. increases in circulating concentrations of stress hormones or therapeutic choices e. glucocorticoid use that can exacerbate hyperglycemia. Hyperglycemia, in turn, causes physiological changes that can exacerbate acute illness, such as decreased immune function and increased oxidative stress.

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Illness or stress can trigger ad. That's because hormones your body makes to fight illness or stress can also cause blood sugar to rise.

You may need to take extra diabetes medication to keep blood glucose in your target range during illness or stress. Keeping blood sugar in a healthy range can help prevent many diabetes-related complications. Long-term complications of hyperglycemia that isn't treated include:.

If blood sugar rises very high or if high blood sugar levels are not treated, it hhyperglycemia lead to two serious conditions. Diabetic ketoacidosis. This condition develops when you don't have enough insulin in your body. When this happens, glucose can't enter your cells for energy.

Your blood sugar level rises, and your body begins to break down fat for energy. When fat is broken down for energy in the body, it produces toxic acids called ketones.

Ketones accumulate in the blood and eventually spill into the urine. If it isn't treated, diabetic ketoacidosis can lead to a diabetic coma that can be life-threatening.

Hyperosmolar hyperglycemic state. This condition occurs when the body makes insulin, but the insulin doesn't work properly. If you develop this condition, your body can't use either glucose or fat for energy. Glucose then goes into the urine, causing increased urination. If it isn't treated, diabetic hyperosmolar hyperglycemic state can lead to life-threatening dehydration and coma.

It's very important to get medical care for it right away. On this page. When to see a doctor. Risk factors. A Book: The Essential Diabetes Book. Early signs and symptoms Recognizing early symptoms of hyperglycemia can help identify and treat it right away.

Watch for: Frequent urination Increased thirst Blurred vision Feeling weak or unusually tired. Later signs and symptoms If hyperglycemia isn't treated, it can cause toxic acids, called ketones, to build up in the blood and urine.

Symptoms include: Fruity-smelling breath Dry mouth Abdominal pain Nausea and vomiting Shortness of breath Confusion Loss of consciousness. Request an appointment. From Mayo Clinic to your inbox. Sign up for free and stay up to date on research advancements, health tips, current health topics, and expertise on managing health.

Click here for an email preview. To provide you with the most relevant and helpful information, and understand which information is beneficial, we may combine your email and website usage information with other information we have about you.

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You may opt-out of email communications at any time by clicking on the unsubscribe link in the e-mail. Many factors can contribute to hyperglycemia, including: Not using enough insulin or other diabetes medication Not injecting insulin properly or using expired insulin Not following your diabetes eating plan Being inactive Having cotnrol illness or infection Using certain medications, such as steroids or immunosuppressants Being injured or having surgery Experiencing emotional stress, such as family problems or workplace issues Illness or stress can trigger hyperglycemia.

Long-term complications Keeping blood sugar in a healthy range can help prevent many diabetes-related complications. Long-term complications of hyperglycemia that isn't treated include: Cardiovascular disease Nerve damage neuropathy Kidney damage diabetic nephropathy or kidney failure Damage to the blood vessels of the retina diabetic retinopathy that could lead to blindness Feet problems caused by damaged nerves or poor blood flow that can lead to serious skin infections, ulcerations and, in some severe cases, amputation Bone and joint problems Teeth and gum infections.

Emergency complications If blood sugar rises very high or if high blood sugar levels are not treated, it can lead to two serious conditions. To help keep your blood sugar within a healthy range: Follow your diabetes meal plan. If you take insulin or oral diabetes medication, be consistent about the amount and timing of your meals and snacks.

The food you eat must be in balance with the insulin working in your body. Monitor your blood sugar. Depending on your treatment plan, you may check and record your blood sugar level several times a week or several times a day. Careful monitoring is the only way to make sure that your blood sugar level stays within your target range.

Note when your glucose readings are above or below your target range. Carefully follow your health care provider's directions for how to take your medication. Adjust your medication if you change your physical activity. The adjustment depends on blood sugar test results and on the type and length of the activity.

If you have questions about hyperglycemis, talk to your health care provider. By Mayo Clinic Staff. Aug 20, Show References. Hyperglycemia high blood glucose. American Diabetes Association. Accessed July 6, What is diabetes? National Institute of Diabetes and Digestive and Kidney Diseases.

Wexler DJ. Management of persistent hyperglycemia in type 2 diabetes mellitus. Hirsch IB, et al. Diabetic ketoacidosis and hyperosmolar hyperglycemic state in adults: Clinical features, evaluation, and diagnosis.

Managing diabetes. Inzucchi SE, et al. Glycemic control and vascular complications in type 2 diabetes mellitus. Comprehensive medical evaluation and assessment of comorbidities: Standards of Medical Care in Diabetes —

: Chronic hyperglycemia and glycemic control

Treatment thresholds for hyperglycemia in critically ill patients with and without diabetes

Guidelines for the use of an insulin infusion for the management of hyperglycemia in critically ill patients. Crit Care Med. Stress hyperglycemia: an essential survival response!

Crit Care. Inpatient glycemic control: best practice advice from the Clinical Guidelines Committee of the American College of Physicians. Am J Med Qual. Dysglycaemia in the critically ill and the interaction of chronic and acute glycaemia with mortality.

Intensive Care Med. Liberal Glycemic Control in Critically Ill Patients With Type 2 Diabetes: An Exploratory Study. Hospital-acquired complications in intensive care unit patients with diabetes: A before-and-after study of a conventional versus liberal glucose control protocol.

Acta Anaesthesiol Scand. Is it time to abandon glucose control in critically ill adult patients? Curr Opin Crit Care. Study protocol and statistical analysis plan for the Liberal Glucose Control in Critically Ill Patients with Pre-existing Type 2 Diabetes LUCID trial.

Crit Care Resusc. Glycemic control in the critically ill: Less is more. Cleve Clin J Med. The Effect of a Liberal Approach to Glucose Control in Critically Ill Patients with Type 2 Diabetes: A Multicenter, Parallel-Group, Open-Label Randomized Clinical Trial.

Am J Respir Crit Care Med. Update on glucose control during and after critical illness. On the basis of this data we suggest that the HbA1c be checked on admission to the ICU in all diabetics with blood glucose therapeutic targets as provided in Table 1.

Plummer MP, Bellomo R, Cousins CE, Annink CE, Sundararajan K, Reddi BA, Raj JP, Chapman MJ, Horowitz M, Deane AM Dysglycaemia in the critically ill and the interaction of chronic and acute glycaemia with mortality.

Intensive Care Med. doi: PubMed Google Scholar. Badawi O, Waite MD, Fuhrman SA, Zuckerman IH Association between intensive care unit-acquired dysglycemia and in-hospital mortality. Crit Care Med — Article PubMed Google Scholar.

van den Berghe G, Wouters P, Weekers F, Verwaest C, Bruyninckx F, Schetz M, Vlasselaers D, Ferdinande P, Lauwers P, Bouillon R Intensive insulin therapy in critically ill patients. N Engl J Med — The NICE-Sugar Study Investigators Intensive versus conventional glucose control in critically ill patients.

Marik PE, Bellomo R Stress hyperglycemia: an essential survival response! Crit Care Article PubMed Central PubMed Google Scholar. Qaseem A, Humphrey LL, Chou R, Snow V, Shekelle P Use of intensive insulin therapy for the management of glycemic control in hospitalized patients: a clinical practice guideline from the American College of Physicians.

Ann Intern Med — Agus MS, Steil GM, Wypij D, Costello JM, Laussen PC, Langer M, Alexander JL Tight glycemic control versus standard care after pediatric cardiac surgery. Article CAS PubMed Central PubMed Google Scholar. Minakata K, Sakata R Perioperative control of blood glucose level in cardiac surgery.

General Thorac Cardiovasc Surg — Article Google Scholar. Diabetes Care 37 Suppl 1 :S5— Olson DE, Rhee MK, Herrick K, Ziemer DC, Twombly JG, Phillips LS Screening for diabetes and pre-diabetes with proposed A1C-based diagnostic criteria.

Diabetes Care — Egi M, Bellomo R, Stachowski E, French CJ, Hart GK, Hegarty C, Bailey M Blood glucose concentration and outcome of critical illness: the impact of diabetes. Article CAS PubMed Google Scholar. Krinsley JS, Egi M, KIss A, Devendra AM, Schuetz P, Maurer P, Schultz MJ, van Hooijdonk RT, Kiyoshi M, Mackenzie IM, Annane D, Stow P, Nasraway SA, Holewinski S, Holzinger U, Preiser JC, Vincent JL, Bellomo R Diabetes status and the relation of the three domains of glycemic contril to mortality in critically ill patients: an international multicenter cohort study.

Crit Care R Egi M, Bellomo R, Stachowski E, French CJ, Hart G Variability of blood glucose concentration and short-term mortality in critically ill patients.

Anesthesiol — Article CAS Google Scholar. Monnier L, Mas E, Ginet C, Michel F, Villon L, Cristol JP, Colette C Activation of oxidative stress by acute glucose fluctuations compared with sustained chronic hyperglycemia in patients with type 2 diabetes. JAMA — Egi M, Bellomo R, Stachowski E, French CJ, Hart GK, Taori G, Hegarty C, Bailey M The interaction of chronic and acute glycemia with mortality in critically ill patients with diabetes.

Download references. Division of Pulmonary and Critical Care Medicine, Eastern Virginia Medical School, Fairfax Av, Suite , Norfolk, VA, , USA. Diabetes has been reported to be the fourth most common comorbid condition listed on all hospital discharges 2.

Acute illness results in a number of physiological changes e. increases in circulating concentrations of stress hormones or therapeutic choices e. glucocorticoid use that can exacerbate hyperglycemia. Hyperglycemia, in turn, causes physiological changes that can exacerbate acute illness, such as decreased immune function and increased oxidative stress.

These lead to a complex cycle of worsening illness and poor glucose control 3. Although a growing body of literature supports the need for targeted glycemic control in the hospital setting, blood glucose BG continues to be poorly controlled and is frequently overlooked in general medicine and surgery services.

This is largely explained by the fact that the majority of hospitalizations for patients with diabetes are not directly related to their metabolic state, thus diabetes management is rarely the primary focus of care.

Therefore, glycemic control and other diabetes care issues are often not specifically addressed 4. A history of diabetes should be elicited in all patients admitted to hospital and, if present, should be clearly identified on the medical record.

In view of the high prevalence of inpatient hyperglycemia with associated poor outcomes, an admission BG measurement of all patients would help identify people with diabetes, even in the absence of a prior diagnosis 1,5.

For hospitalized people with known diabetes, the glycated hemoglobin A1C identifies people who may benefit from efforts to improve glycemic control and tailor therapy upon discharge 6,7.

In hospitalized people with newly recognized hyperglycemia, an A1C among those with diabetes risk factors or associated comorbidities e. cardiovascular disease [CVD] 8,9 may help differentiate people with previously undiagnosed diabetes and dysglycemia from those with stress-induced hyperglycemia and provides an opportunity to diagnose and initiate diabetes therapies 10— Among people admitted to an intensive care unit ICU , an A1C drawn at admission allows identification of people with previously unknown diabetes, people at risk of glycemic management challenges and people at an increased risk of mortality 14, A1C has been found to be specific for diagnosis of diabetes in the hospital setting, although not as sensitive as in the outpatient setting 13, Currently, there are no studies that have examined the effect of the frequency of bedside BG monitoring on the incidence of hyper- or hypoglycemia in the hospital setting.

The frequency and timing of bedside BG monitoring can be individualized; however, monitoring is typically performed before meals and at bedtime in people who are eating; every 4 to 6 hours in people who are NPO nothing by mouth or receiving continuous enteral feeding; and every 1 to 2 hours for people on continuous intravenous insulin or those who are critically ill.

Some bedside BG monitoring is indicated in individuals without known diabetes but receiving treatments known to be associated with hyperglycemia e. glucocorticoids, octreotide, parenteral nutrition and enteral nutrition The implementation and maintenance of quality control programs by health-care institutions helps to ensure the accuracy of bedside BG monitoring 19, The use of glucose meters with bar coding capability has been shown to reduce data entry errors in medical records Data management programs that transfer bedside BG monitoring results into electronic records allow evaluation of hospital-wide glycemic control Capillary blood glucose CBG point of care testing POCT should be interpreted with caution in the critically ill patient population.

Poor perfusion indices may yield conflicting capillary, arterial and whole BG values using POCT glucose meters 23— Venous or arterial samples are preferred when using a POCT meter for this patient population.

Clinical decision support system software integrating CBG POCT can aid in trend analysis, medication dosing, reduce prescription error and reduce length of stay Electronic glucose metric data and web-based reporting systems may pose utility for monitoring glycemic management performance within an organization and enhance opportunities for external benchmarking A number of studies have demonstrated that inpatient hyperglycemia is associated with increased morbidity and mortality in noncritically ill hospitalized people 1,28, Current recommendations are based mostly on retrospective studies, clinical experience and judgement.

Glycemic targets for hospitalized people with diabetes are modestly higher than those routinely advised for outpatients with diabetes given that the hospital setting presents unique challenges for the management of hyperglycemia, such as variations in patient nutritional status and the presence of acute illness.

For the majority of noncritically ill hospitalized people, recommended preprandial BG targets are 5. Lower targets may be considered in clinically stable hospitalized people with a prior history of successful tight glycemic control in the outpatient setting, while higher targets may be acceptable in terminally ill people or in those with severe comorbidities.

a missed meal 18, Acute hyperglycemia in the intensive care setting is not unusual and results from a number of factors, including stress-induced counter-regulatory hormone secretion and the effects of medications administered in the ICU Glycemic targets for people with pre-existing diabetes who are in the critical care setting have not been firmly established.

Early trials showed that achieving normoglycemia 4. However, subsequent trials in mixed populations of critically ill patients did not show a benefit of targeting BG levels of 4. A meta-analysis of trials of intensive insulin therapy in the ICU setting suggested benefit of intensive insulin therapy in surgical patients, but not in medical patients Conversely, the Normoglycemia in Intensive Care Evaluation—Survival Using Glucose Algorithm Regulation NICE-SUGAR study, the largest trial to date of intensive glucose control in critically ill medical and surgical patients, found an increase in day all-cause mortality hazard ratio [HR] 1.

Furthermore, intensive insulin therapy has been associated with an increased risk of hypoglycemia in the ICU setting The use of insulin infusion protocols with proven efficacy and safety minimizes the risk of hypoglycemia 35— There are few occasions when intravenous insulin is required, as most people with type 1 or type 2 diabetes admitted to general medical wards can be treated with subcutaneous insulin.

Intravenous insulin, however, may be appropriate for people who are critically ill with appropriate BG targets , people who are not eating and in those with hyperglycemia and metabolic decompensation e. diabetic ketoacidosis [DKA] and hyperosmolar hyperglycemic state [HHS] see Hyperglycemic Emergencies in Adults chapter, p.

The evidence to date suggests there is no benefit to intravenous insulin over subcutaneous insulin post-acute stroke 3, Health-care staff education is a critical component of the implementation of an intravenous insulin infusion protocol.

Intravenous insulin protocols should take into account the patient's current and previous BG levels as well as the rate of change in BG , and the patient's usual insulin dose. Several published insulin infusion protocols appear to be both safe and effective, with low rates of hypoglycemia; however, most of these protocols have only been validated in the ICU setting, where the nurse-to-patient ratio is higher than on medical and surgical wards 3, BG determinations can be performed every 1 to 2 hours until BG has stabilized.

With the exception of the treatment of hyperglycemic emergencies e. DKA and HHS , consideration should be given to concurrently providing people receiving intravenous insulin with some form of glucose e. intravenous glucose or through parenteral or enteral feeding.

Hospitalized people with type 1 and type 2 diabetes may be transitioned to scheduled subcutaneous insulin therapy from intravenous insulin. Short- or rapid- or fast-acting insulin can be administered 1 to 2 hours before discontinuation of the intravenous insulin to maintain effective blood levels of insulin.

If intermediate- or long-acting insulin is used, it can be given 2 to 3 hours prior to intravenous insulin discontinuation. People without a history of diabetes, who have hyperglycemia requiring more than 2 units of intravenous insulin per hour, likely require insulin therapy and can be considered for transition to scheduled subcutaneous insulin therapy.

The initial dose and distribution of subcutaneous insulin at the time of transition can be determined by extrapolating the intravenous insulin requirement over the preceding 6- to 8-hour period to a hour period.

Dividing the total daily dose as a combination of basal and bolus insulin has been demonstrated to be safe and efficacious in medically ill patients 40, The management of individuals with diabetes at the time of surgery poses a number of challenges. Acute hyperglycemia is common secondary to the physiological stress associated with surgery.

Pre-existing diabetes-related complications and comorbidities may also influence clinical outcomes. Acute hyperglycemia has been shown to adversely affect immune function 42 and wound healing 43 in animal models. Observational studies have shown that hyperglycemia increases the risk of postoperative infections 44,45 , renal allograft rejection 46 , and is associated with increased health-care resource utilization In people undergoing coronary artery bypass grafting CABG , a pre-existing diagnosis of diabetes has been identified as a risk factor for postoperative sternal wound infections, delirium, renal dysfunction, respiratory insufficiency and prolonged hospital stays 48— Intraoperative hyperglycemia during cardiopulmonary bypass has been associated with increased morbidity and mortality rates in individuals with and without diabetes 51— A systematic review of randomized controlled trials supports the use of intravenous insulin infusion targeting a blood glucose of 5.

This was demonstrated by a marked reduction in surgical site infections odds ratio 0. The perioperative glycemic targets for minor or moderate surgeries are less clear. Older studies comparing different methods of achieving glycemic control during minor and moderate surgeries did not demonstrate any adverse effects of maintaining perioperative BG levels between 5.

Attention has been placed on the relationship between postoperative hyperglycemia and surgical site infections. While the association was well documented, the impact and risks of intensive management was less clear. The risk of hypoglycemia was increased but there was no increased risk of stroke or death.

The included studies looked at the intraoperative and immediate postoperative period and used intravenous insulin to achieve intensive targets. The included studies were mostly cardiac and gastrointestinal and were found to have a moderate risk of bias Rapid institution of perioperative glucose control must be carefully considered in patients with poorly controlled type 2 diabetes undergoing monocular phacoemulsification cataract surgery with moderate to severe nonproliferative diabetic retinopathy because of the possible increased risk of postoperative progression of retinopathy and maculopathy The outcome of vitrectomy, however, does not appear to be influenced by perioperative control Given the data supporting tighter perioperative glycemic control during major surgeries and the compelling data showing the adverse effects of hyperglycemia, it is reasonable to target glycemic levels between 5.

The best way to achieve these targets in the postoperative patient is with a basal bolus insulin regimen 61, This approach has been shown to reduce postoperative complications, including wound infections. Despite this knowledge, surgical patients are often treated with correction supplemental rapid-acting insulin alone 63 which may not adequately control BG.

The benefits of improved perioperative glycemic control must be weighed against the risk of perioperative hypoglycemia.

Anesthetic agents and postoperative analgesia may alter the patient's level of consciousness and awareness of hypoglycemia. The risk of hypoglycemia can be reduced by frequent BG monitoring and carefully designed management protocols.

In general, insulin is the preferred treatment for hyperglycemia in hospitalized people with diabetes People with type 1 diabetes must be maintained on insulin therapy at all times to prevent DKA.

Scheduled subcutaneous insulin administration that consists of basal, bolus prandial and correction supplemental insulin components is the preferred method for achieving and maintaining glucose control in noncritically ill hospitalized people with diabetes or stress hyperglycemia who are eating 35, Bolus insulin can be withheld or reduced in people who are not eating regularly; however, basal insulin should not be withheld.

Stable people can usually be maintained on their home insulin regimen with adjustments made to accommodate for differences in meals and activity levels, the effects of illness and the effects of other medications.

In the hospital setting, rapid-acting insulin analogues are the preferred subcutaneous bolus and correction insulins Insulin programs that only react to, or correct for, hyperglycemia have been demonstrated to be associated with higher rates of hyperglycemia 61,66— Insulin is often required temporarily in hospital, even in people with type 2 diabetes not previously treated with insulin.

In these insulin-naive people, there is evidence demonstrating the superiority of basal-bolus-correction insulin regimens 61, A number of protocols have been published as part of studies 61,66,69— These studies have typically started insulin-naive people on 0.

breakfast, lunch and dinner ; correction doses of the bolus insulin are provided if BG values are above target. Daily review of the person's BG measurements and modification of insulin doses, as required, facilitates the achievement of target blood glucose measurements.

When comparing effective protocols, the following was observed. One study compared basal-bolus plus correction insulin with glargine and glulisine vs. Average BG levels were not different, but rates of hypoglycemia were.

Another study 74 found no difference in BG levels or rates of hypoglycemia when comparing insulin glargine vs. detemir, when used as the basal insulin in a basal-bolus program.

Yet another study 71 found that using a weight-based algorithm to titrate insulin glargine resulted in obtaining target BG levels faster than a glucose-based algorithm, with no difference in the rates of hypoglycemia.

More recently, a study compared a basal-bolus plus correction insulin regimen with a program that was basal plus correction The basal-bolus group had slightly lower BG through the day, which was not statistically significant, with no difference in FBG or in rates of hypoglycemia.

Taken together with the earlier studies from this group 61,66 , it would appear that successful management of in-hospital diabetes requires early and aggressive administration of basal insulin combined with bolus insulin, typically in the form of rapid-acting insulin analogue, similar to the approach used in the outpatient setting.

To date, no large studies have investigated the use of non-insulin antihyperglycemic agents on outcomes in hospitalized people with diabetes. Stable hospitalized people with diabetes without these contraindications can often have their home antihyperglycemic medications continued while in the hospital.

However, if contraindications develop or if glycemic control is inadequate, these drugs should be discontinued and consideration given to starting the patient on a basal-bolus-supplemental insulin regimen.

The advantages and disadvantages of various noninsulin antihyperglycemic therapies in hospital are discussed in detail in a recent review article A recent randomized but unblinded study compared sitagliptin plus basal and correctional insulin with a more traditional basal-bolus-correctional insulin program in hospitalized people with diabetes The glycemic outcomes were similar between the 2 groups; however, the basal-bolus-correctional group had a higher mean glucose than similarly insulin-treated subjects in other studies 61, This less-aggressive treatment may explain the lack of difference between the sitagliptin and the bolus insulin groups.

Medical nutrition therapy including nutritional assessment and individualized meal planning is an essential component of inpatient glycemic management programs. A consistent carbohydrate meal planning system may facilitate glycemic control in hospitalized people and facilitate matching prandial insulin doses to the amount of carbohydrate consumed 61,66,75,78— In hospitalized people with diabetes receiving parenteral nutrition, insulin can be administered in the following ways: as scheduled regular insulin dosing added directly to the parenteral solution; or as scheduled intermediate- or long-acting subcutaneous insulin doses A separate intravenous infusion of regular insulin may be an alternative method to achieve glycemic control in critical care For scheduled subcutaneous insulin dosing or regular insulin added directly to parenteral solutions, the selected starting insulin dose may be based on the current estimated TDD of insulin, the composition of the parenteral nutrition solution and the patient's weight Considering the patient's individual clinical situation is important when determining insulin dosing.

Subcutaneous correction supplemental insulin may be used in addition to scheduled insulin dosing and dose adjustments made to scheduled insulin should be adjusted based on the BG pattern. For hospitalized people with diabetes on enteral feeding regimens, there are few prospective studies examining insulin management.

In 1 randomized controlled trial, low-dose basal glargine insulin with regular insulin correction dosing was compared against regular insulin correction supplemental insulin dosing with the addition of NPH in the presence of persistent hyperglycemia and demonstrated similar efficacy for glycemic control The type of feed solution and duration of feed cyclical vs.

continuous should be considered. People with diabetes receiving bolus enteral feeds may be treated in the same manner as people who are eating meals. Correction supplemental insulin can be administered, as needed; added to the same bolus insulin.

An insulin with a shorter half-life, such as NPH, may be preferred for intermediate duration feeding schedules i. overnight , while regular or rapid-acting insulin may be more appropriate to manage hyperglycemia induced by bolus feeding schedules.

In the event that the parenteral or enteral nutrition is unexpectedly interrupted, intravenous dextrose may be required to prevent hypoglycemia depending on the last dose and type of insulin administered.

When parenteral or enteral feeding schedules are adjusted in terms of carbohydrate content or duration, the insulin type and dose will need to be re-assessed. Although the optimal management of hyperglycemia in people receiving high-dose oral corticosteroids has not been clearly defined, glycemic monitoring for 48 hours after initiation of steroids may be considered for people with or without a history of diabetes 35, For management of hyperglycemia, treatment with a basal-bolus with correction insulin regimen was more effective and safer than a correction supplemental insulin-only regimen 85 , although addition of NPH dosed variably from once a day at time of glucocorticoid administration to every 6 hours depending on glucocorticoid used was not demonstrated to improve glycemic outcomes 86, Although data for self-management in the hospitalized setting is limited, self-management in hospital may be appropriate for people who are mentally competent and desire more autonomy over their diabetes.

The majority of evidence pertains to continuous subcutaneous insulin infusion CSII therapy, where continuation of patient-managed insulin delivery has been associated with reduced episodes of severe hyperglycemia and hypoglycemia 88 and high levels of patient satisfaction In general, any person requiring insulin therapy who is self-managing diabetes in the hospital setting should be able to physically self-administer insulin and perform self-monitoring of blood glucose SMBG independently, be familiar with the recommended insulin routine, understand sick-day management guidelines and utilize a flowsheet to facilitate communication of BG results and insulin dosing between the patient and health-care providers.

The person with diabetes and the health-care provider, in consultation with nursing staff, must agree that patient self-management is an appropriate strategy while hospitalized.

Hospitals should have policies and procedures for the assessment of suitability for self-management. Although the data are limited, it appears that CSII can be safely continued in the hospital setting under certain circumstances People maintained on CSII may have decreased length of stay 90 ; however, this may reflect the severity of illness rather than a glycemic control advantage.

People maintained on CSII may have less hypoglycemia than those managed by the admitting clinician. People on CSII are encouraged to continue this form of therapy whenever safe and feasible in hospital.

Successful published inpatient protocols include assessment of pump specific self-management skills i. how to adjust their basal rate, administer a bolus dose, insert an infusion set, fill a reservoir, suspend the pump and correct a CBG result outside their target range , pre-printed orders, flow sheets and patient consents 88,91, If appropriate supports are not available, CSII may be discontinued and a basal-bolus-subcutaneous insulin regimen or intravenous insulin infusion may be initiated.

An increasing number of people are being maintained on CSII during short elective surgical procedures without any reported adverse events 93 , necessitating close collaboration between anesthesia and diabetes management teams.

Different pump manufacturers will recommend discontinuing pumps for certain hospital-based procedures e. radiology, cautery, external beam radiation.

To promote a collaborative relationship between the hospital staff and the patient, and to ensure patient safety, hospitals must have clear policies and procedures in place to guide the use of CSII in the inpatient setting Documents that stipulate contraindications for continued CSII, procedures to guide medical management of CSII and a consent form outlining the inpatient terms of use 92 support the safe use of CSII use in hospital.

Specific algorithms and order sets for management of CSII peri-operatively and during labour and delivery have been published 93, Institution-wide programs to improve glycemic control in the inpatient setting include the formation of a multidisciplinary steering committee, professional development programs focused on inpatient diabetes management 95,96 , policies to assess and monitor the quality of glycemic management, interprofessional team-based care including comprehensive patient education and discharge planning as well as standardized order sets, protocols and algorithms for diabetes care within the institution.

Implementation of such a program can result in improvements in in-hospital glycemic control 97, Computerized and mobile decision support systems that provide suggestions for insulin dosing have also been used and have been associated with lower mean BG levels 26,— ; hypoglycemia can be an unintended consequence of tighter glycemic control 70, The timely consultation of glycemic management teams has also been found to improve the quality of care provided, reduce the length of hospital stay and lower costs , , although differences in glycemic control were minimal Deployment of nurses , , nurse practitioners and physician assistants with specialty training has been associated with greater use of basal-bolus insulin therapy and lower mean BG levels.

A provincial survey of over 2, people with diabetes admitted to hospital found that people were more likely to be satisfied with their diabetes care in hospital if they had confidence that the team was knowledgeable about diabetes, presented a consistent message and acknowledged them in their diabetes care Programs that include self-management education, such as assessment of barriers and goal setting, have also been associated with improvements in glycemic control 97, Institutional implementation of hospital glycemic management programs require metrics to monitor progress, assess safety, length of stay and identify opportunities for improvement Implementation of inpatient hyperglycemia quality improvement programs evaluated with real-time metrics have been shown to improve glycemic control and safety of insulin ordering 97, To date, metrics for monitoring glycemic control programs in hospitals have not been established This lack of standardization limits the ability for benchmarking and comparison of different quality-improvement programs and protocols.

Further study into the development and implementation of appropriate standardized metrics for hospital glycemic management programs is warranted. Interventions that ensure continuity of care, such as arranging continuation of care after discharge 97 , telephone follow up and communication with primary providers at discharge , have been associated with a post-discharge reduction in A1C Providing people with diabetes and their family or caregivers with written and oral instructions regarding their diabetes management at the time of hospital discharge will facilitate transition to community care.

Comprehensive instructions may include recommendations for timing and frequency of home glucose monitoring; identification and management of hypoglycemia; a reconciled medication list, including insulin and other antihyperglycemic medications; and identification and contact information for health-care providers responsible for ongoing diabetes care and adjustment of glucose-lowering medications.

Communication of the need for potential adjustments in insulin therapy that may accompany adjustments of other medications prescribed at the time of discharge, such as corticosteroids or octreotide, to people with diabetes and their primary care providers is important.

Hypoglycemia remains a major barrier to achieving optimal glycemic control in hospitalized people with diabetes. Standardized treatment protocols that address mild, moderate and severe hypoglycemia may help mitigate this risk. Education of healthcare workers about factors that increase the risk of hypoglycemia, such as sudden reduction in oral intake, discontinuation of parenteral or enteral nutrition, unexpected transfer from the nursing unit after rapid-acting insulin administration or a reduction in corticosteroid dose 78 are important steps to reduce the risk of hypoglycemia.

Insulin is considered a high-alert medication and can be associated with risk of harm and severe adverse events. BG, blood glucose; CBG , capillary blood glucose; CABG , coronary artery bypass grafting; CSII , continuous subcutaneous insulin infusion; ICU , intensive care unit; NPH , neutral protamine Hagedorn; POC , point of care; TDD , total daily dose.

Chapter Glycemic Management in Adults With Type 1 Diabetes. Pharmacologic Glycemic Management of Type 2 Diabetes in Adults. Treatment of Diabetes in People With Heart Failure. Literature Review Flow Diagram for Chapter In-Hospital Management of Diabetes.

From: Moher D, Liberati A, Tetzlaff J, Altman DG, The PRISMA Group Preferred Reporting Items for Systematic Reviews and Meta-Analyses: The PRISMA Statement.

PLoS Med 6 6 : e pmed For more information, visit www. Halperin reports personal fees from Dexcom, Novo Nordisk, and QHR technologies, outside the submitted work.

Miller reports personal fees from Eli Lilly, Novo Nordisk, Sanofi, and AstraZeneca; and grants and personal fees from Boehringer Ingelheim, Janssen, Merck, outside the submitted work. Sarah Moore reports personal fees from Diabetes Care Alliance Boehringer Ingelheim Eli Lilly Alliance , and Merck Canada, outside the submitted work.

No other authors have anything to disclose. All content on guidelines. ca, CPG Apps and in our online store remains exactly the same. For questions, contact communications diabetes.

Stress Hyperglycemia in the ICU

Stress hyperglycemia is regarded as an evolutionary adaptive response which allows the host to survive during periods of severe stress [ 5 ]. The neuroendocrine response to stress is characterized by excessive gluconeogenesis, glycogenolysis, and insulin resistance, with increased hepatic output of glucose gluconeogenesis being the major cause of stress hyperglycemia.

Insects, worms, and all verterbrates including fish develop stress hyperglycemia when exposed to stress [ 5 ]. Stress hyperglycemia provides a source of fuel for the immune system and brain at a time of stress. While mild to moderate stress hyperglycemia is protective it is likely that severe stress hyperglycemia may be deleterious.

However, the blood glucose threshold above which stress hyperglycemia becomes harmful is unknown. Furthermore, we suggest that both the duration and the degree of hyperglycemia are important in determining whether hyperglycemia is protective or harmful [ 5 ]. It seems most unlikely that a few days of hyperglycemia would be harmful; indeed attempts at rapid correction of blood glucose in these patients may be harmful.

This recommendation is based largely on uncontrolled retrospective studies. Agus et al. In this study none of the outcome measures differed between groups. Current criteria used for the diagnosis of diabetes mellitus are i HbA1c level above 6.

Although diagnostic criteria based on HbA1c may be insensitive and not uniformly applicable to all patients [ 10 ], HbA1c level measured at admission to ICU is probably still the most useful test for undiagnosed diabetes, because glucose concentrations in critically ill patients increase even in the absence of diabetes.

International guidelines recommend the use of a protocolized approach to avoid acute hyperglycemia irrespective of the presence of diabetes mellitus [ 9 ]. Recent studies have shown that the relationship between hyperglycemia and outcomes is altered by the presence of diabetes mellitus [ 11 , 12 ].

Lowering the blood glucose levels in critically ill patients with chronic hyperglycemia will result in drastic and rapid changes of glucose concentrations. The degree of blood glucose change glycemic variability has been demonstrated to be an independent predictor of poor outcome in critically ill patients [ 13 ].

In patients with type II diabetes, glycemic variability has been demonstrated to increase oxidative stress [ 14 ]. Increased oxidative stress can result in endothelial dysfunction and contribute to vascular damage. It would therefore appear appropriate to have a higher glycemic treatment target in patients with preexisting diabetes and premorbid poor glycemic control to prevent large reductions in blood glucose concentration.

Biological adjustment to preexisting hyperglycemia and less glycemic variability might explain this phenomenon. These observations generate the hypothesis that glucose levels that are considered safe and desirable in other patients might be undesirable in diabetic patients with chronic hyperglycemia.

On the basis of this data we suggest that the HbA1c be checked on admission to the ICU in all diabetics with blood glucose therapeutic targets as provided in Table 1.

Plummer MP, Bellomo R, Cousins CE, Annink CE, Sundararajan K, Reddi BA, Raj JP, Chapman MJ, Horowitz M, Deane AM Dysglycaemia in the critically ill and the interaction of chronic and acute glycaemia with mortality.

Intensive Care Med. doi: PubMed Google Scholar. Badawi O, Waite MD, Fuhrman SA, Zuckerman IH Association between intensive care unit-acquired dysglycemia and in-hospital mortality. Crit Care Med — Article PubMed Google Scholar.

van den Berghe G, Wouters P, Weekers F, Verwaest C, Bruyninckx F, Schetz M, Vlasselaers D, Ferdinande P, Lauwers P, Bouillon R Intensive insulin therapy in critically ill patients. N Engl J Med — The NICE-Sugar Study Investigators Intensive versus conventional glucose control in critically ill patients.

Marik PE, Bellomo R Stress hyperglycemia: an essential survival response! Crit Care Article PubMed Central PubMed Google Scholar. Qaseem A, Humphrey LL, Chou R, Snow V, Shekelle P Use of intensive insulin therapy for the management of glycemic control in hospitalized patients: a clinical practice guideline from the American College of Physicians.

Ann Intern Med — Agus MS, Steil GM, Wypij D, Costello JM, Laussen PC, Langer M, Alexander JL Tight glycemic control versus standard care after pediatric cardiac surgery. Article CAS PubMed Central PubMed Google Scholar. Minakata K, Sakata R Perioperative control of blood glucose level in cardiac surgery.

General Thorac Cardiovasc Surg — Article Google Scholar. Diabetes Care 37 Suppl 1 :S5— Olson DE, Rhee MK, Herrick K, Ziemer DC, Twombly JG, Phillips LS Screening for diabetes and pre-diabetes with proposed A1C-based diagnostic criteria.

Diabetes Care — Egi M, Bellomo R, Stachowski E, French CJ, Hart GK, Hegarty C, Bailey M Blood glucose concentration and outcome of critical illness: the impact of diabetes. Article CAS PubMed Google Scholar. Krinsley JS, Egi M, KIss A, Devendra AM, Schuetz P, Maurer P, Schultz MJ, van Hooijdonk RT, Kiyoshi M, Mackenzie IM, Annane D, Stow P, Nasraway SA, Holewinski S, Holzinger U, Preiser JC, Vincent JL, Bellomo R Diabetes status and the relation of the three domains of glycemic contril to mortality in critically ill patients: an international multicenter cohort study.

Crit Care R Egi M, Bellomo R, Stachowski E, French CJ, Hart G Variability of blood glucose concentration and short-term mortality in critically ill patients.

Anesthesiol — Article CAS Google Scholar. Monnier L, Mas E, Ginet C, Michel F, Villon L, Cristol JP, Colette C Activation of oxidative stress by acute glucose fluctuations compared with sustained chronic hyperglycemia in patients with type 2 diabetes.

detemir, when used as the basal insulin in a basal-bolus program. Yet another study 71 found that using a weight-based algorithm to titrate insulin glargine resulted in obtaining target BG levels faster than a glucose-based algorithm, with no difference in the rates of hypoglycemia.

More recently, a study compared a basal-bolus plus correction insulin regimen with a program that was basal plus correction The basal-bolus group had slightly lower BG through the day, which was not statistically significant, with no difference in FBG or in rates of hypoglycemia.

Taken together with the earlier studies from this group 61,66 , it would appear that successful management of in-hospital diabetes requires early and aggressive administration of basal insulin combined with bolus insulin, typically in the form of rapid-acting insulin analogue, similar to the approach used in the outpatient setting.

To date, no large studies have investigated the use of non-insulin antihyperglycemic agents on outcomes in hospitalized people with diabetes. Stable hospitalized people with diabetes without these contraindications can often have their home antihyperglycemic medications continued while in the hospital.

However, if contraindications develop or if glycemic control is inadequate, these drugs should be discontinued and consideration given to starting the patient on a basal-bolus-supplemental insulin regimen.

The advantages and disadvantages of various noninsulin antihyperglycemic therapies in hospital are discussed in detail in a recent review article A recent randomized but unblinded study compared sitagliptin plus basal and correctional insulin with a more traditional basal-bolus-correctional insulin program in hospitalized people with diabetes The glycemic outcomes were similar between the 2 groups; however, the basal-bolus-correctional group had a higher mean glucose than similarly insulin-treated subjects in other studies 61, This less-aggressive treatment may explain the lack of difference between the sitagliptin and the bolus insulin groups.

Medical nutrition therapy including nutritional assessment and individualized meal planning is an essential component of inpatient glycemic management programs. A consistent carbohydrate meal planning system may facilitate glycemic control in hospitalized people and facilitate matching prandial insulin doses to the amount of carbohydrate consumed 61,66,75,78— In hospitalized people with diabetes receiving parenteral nutrition, insulin can be administered in the following ways: as scheduled regular insulin dosing added directly to the parenteral solution; or as scheduled intermediate- or long-acting subcutaneous insulin doses A separate intravenous infusion of regular insulin may be an alternative method to achieve glycemic control in critical care For scheduled subcutaneous insulin dosing or regular insulin added directly to parenteral solutions, the selected starting insulin dose may be based on the current estimated TDD of insulin, the composition of the parenteral nutrition solution and the patient's weight Considering the patient's individual clinical situation is important when determining insulin dosing.

Subcutaneous correction supplemental insulin may be used in addition to scheduled insulin dosing and dose adjustments made to scheduled insulin should be adjusted based on the BG pattern.

For hospitalized people with diabetes on enteral feeding regimens, there are few prospective studies examining insulin management. In 1 randomized controlled trial, low-dose basal glargine insulin with regular insulin correction dosing was compared against regular insulin correction supplemental insulin dosing with the addition of NPH in the presence of persistent hyperglycemia and demonstrated similar efficacy for glycemic control The type of feed solution and duration of feed cyclical vs.

continuous should be considered. People with diabetes receiving bolus enteral feeds may be treated in the same manner as people who are eating meals. Correction supplemental insulin can be administered, as needed; added to the same bolus insulin.

An insulin with a shorter half-life, such as NPH, may be preferred for intermediate duration feeding schedules i. overnight , while regular or rapid-acting insulin may be more appropriate to manage hyperglycemia induced by bolus feeding schedules. In the event that the parenteral or enteral nutrition is unexpectedly interrupted, intravenous dextrose may be required to prevent hypoglycemia depending on the last dose and type of insulin administered.

When parenteral or enteral feeding schedules are adjusted in terms of carbohydrate content or duration, the insulin type and dose will need to be re-assessed.

Although the optimal management of hyperglycemia in people receiving high-dose oral corticosteroids has not been clearly defined, glycemic monitoring for 48 hours after initiation of steroids may be considered for people with or without a history of diabetes 35, For management of hyperglycemia, treatment with a basal-bolus with correction insulin regimen was more effective and safer than a correction supplemental insulin-only regimen 85 , although addition of NPH dosed variably from once a day at time of glucocorticoid administration to every 6 hours depending on glucocorticoid used was not demonstrated to improve glycemic outcomes 86, Although data for self-management in the hospitalized setting is limited, self-management in hospital may be appropriate for people who are mentally competent and desire more autonomy over their diabetes.

The majority of evidence pertains to continuous subcutaneous insulin infusion CSII therapy, where continuation of patient-managed insulin delivery has been associated with reduced episodes of severe hyperglycemia and hypoglycemia 88 and high levels of patient satisfaction In general, any person requiring insulin therapy who is self-managing diabetes in the hospital setting should be able to physically self-administer insulin and perform self-monitoring of blood glucose SMBG independently, be familiar with the recommended insulin routine, understand sick-day management guidelines and utilize a flowsheet to facilitate communication of BG results and insulin dosing between the patient and health-care providers.

The person with diabetes and the health-care provider, in consultation with nursing staff, must agree that patient self-management is an appropriate strategy while hospitalized. Hospitals should have policies and procedures for the assessment of suitability for self-management. Although the data are limited, it appears that CSII can be safely continued in the hospital setting under certain circumstances People maintained on CSII may have decreased length of stay 90 ; however, this may reflect the severity of illness rather than a glycemic control advantage.

People maintained on CSII may have less hypoglycemia than those managed by the admitting clinician. People on CSII are encouraged to continue this form of therapy whenever safe and feasible in hospital.

Successful published inpatient protocols include assessment of pump specific self-management skills i. how to adjust their basal rate, administer a bolus dose, insert an infusion set, fill a reservoir, suspend the pump and correct a CBG result outside their target range , pre-printed orders, flow sheets and patient consents 88,91, If appropriate supports are not available, CSII may be discontinued and a basal-bolus-subcutaneous insulin regimen or intravenous insulin infusion may be initiated.

An increasing number of people are being maintained on CSII during short elective surgical procedures without any reported adverse events 93 , necessitating close collaboration between anesthesia and diabetes management teams.

Different pump manufacturers will recommend discontinuing pumps for certain hospital-based procedures e. radiology, cautery, external beam radiation. To promote a collaborative relationship between the hospital staff and the patient, and to ensure patient safety, hospitals must have clear policies and procedures in place to guide the use of CSII in the inpatient setting Documents that stipulate contraindications for continued CSII, procedures to guide medical management of CSII and a consent form outlining the inpatient terms of use 92 support the safe use of CSII use in hospital.

Specific algorithms and order sets for management of CSII peri-operatively and during labour and delivery have been published 93, Institution-wide programs to improve glycemic control in the inpatient setting include the formation of a multidisciplinary steering committee, professional development programs focused on inpatient diabetes management 95,96 , policies to assess and monitor the quality of glycemic management, interprofessional team-based care including comprehensive patient education and discharge planning as well as standardized order sets, protocols and algorithms for diabetes care within the institution.

Implementation of such a program can result in improvements in in-hospital glycemic control 97, Computerized and mobile decision support systems that provide suggestions for insulin dosing have also been used and have been associated with lower mean BG levels 26,— ; hypoglycemia can be an unintended consequence of tighter glycemic control 70, The timely consultation of glycemic management teams has also been found to improve the quality of care provided, reduce the length of hospital stay and lower costs , , although differences in glycemic control were minimal Deployment of nurses , , nurse practitioners and physician assistants with specialty training has been associated with greater use of basal-bolus insulin therapy and lower mean BG levels.

A provincial survey of over 2, people with diabetes admitted to hospital found that people were more likely to be satisfied with their diabetes care in hospital if they had confidence that the team was knowledgeable about diabetes, presented a consistent message and acknowledged them in their diabetes care Programs that include self-management education, such as assessment of barriers and goal setting, have also been associated with improvements in glycemic control 97, Institutional implementation of hospital glycemic management programs require metrics to monitor progress, assess safety, length of stay and identify opportunities for improvement Implementation of inpatient hyperglycemia quality improvement programs evaluated with real-time metrics have been shown to improve glycemic control and safety of insulin ordering 97, To date, metrics for monitoring glycemic control programs in hospitals have not been established This lack of standardization limits the ability for benchmarking and comparison of different quality-improvement programs and protocols.

Further study into the development and implementation of appropriate standardized metrics for hospital glycemic management programs is warranted. Interventions that ensure continuity of care, such as arranging continuation of care after discharge 97 , telephone follow up and communication with primary providers at discharge , have been associated with a post-discharge reduction in A1C Providing people with diabetes and their family or caregivers with written and oral instructions regarding their diabetes management at the time of hospital discharge will facilitate transition to community care.

Comprehensive instructions may include recommendations for timing and frequency of home glucose monitoring; identification and management of hypoglycemia; a reconciled medication list, including insulin and other antihyperglycemic medications; and identification and contact information for health-care providers responsible for ongoing diabetes care and adjustment of glucose-lowering medications.

Communication of the need for potential adjustments in insulin therapy that may accompany adjustments of other medications prescribed at the time of discharge, such as corticosteroids or octreotide, to people with diabetes and their primary care providers is important.

Hypoglycemia remains a major barrier to achieving optimal glycemic control in hospitalized people with diabetes. Standardized treatment protocols that address mild, moderate and severe hypoglycemia may help mitigate this risk. Education of healthcare workers about factors that increase the risk of hypoglycemia, such as sudden reduction in oral intake, discontinuation of parenteral or enteral nutrition, unexpected transfer from the nursing unit after rapid-acting insulin administration or a reduction in corticosteroid dose 78 are important steps to reduce the risk of hypoglycemia.

Insulin is considered a high-alert medication and can be associated with risk of harm and severe adverse events. BG, blood glucose; CBG , capillary blood glucose; CABG , coronary artery bypass grafting; CSII , continuous subcutaneous insulin infusion; ICU , intensive care unit; NPH , neutral protamine Hagedorn; POC , point of care; TDD , total daily dose.

Chapter Glycemic Management in Adults With Type 1 Diabetes. Pharmacologic Glycemic Management of Type 2 Diabetes in Adults. Treatment of Diabetes in People With Heart Failure. Literature Review Flow Diagram for Chapter In-Hospital Management of Diabetes. From: Moher D, Liberati A, Tetzlaff J, Altman DG, The PRISMA Group Preferred Reporting Items for Systematic Reviews and Meta-Analyses: The PRISMA Statement.

PLoS Med 6 6 : e pmed For more information, visit www. Halperin reports personal fees from Dexcom, Novo Nordisk, and QHR technologies, outside the submitted work. Miller reports personal fees from Eli Lilly, Novo Nordisk, Sanofi, and AstraZeneca; and grants and personal fees from Boehringer Ingelheim, Janssen, Merck, outside the submitted work.

Sarah Moore reports personal fees from Diabetes Care Alliance Boehringer Ingelheim Eli Lilly Alliance , and Merck Canada, outside the submitted work.

No other authors have anything to disclose. All content on guidelines. ca, CPG Apps and in our online store remains exactly the same. For questions, contact communications diabetes. Become a Member Order Resources Home About Contact DONATE.

Next Previous. Key Messages Recommendations Figures Full Text References. Chapter Headings Introduction Screening for and Diagnosis of Diabetes and Hyperglycemia in the Hospital Setting Glucose Monitoring in the Hospital Setting Glycemic Control in the Non-Critically Ill Patient Glycemic Control in the Critically Ill Patient Role of Intravenous Insulin Role of Subcutaneous Insulin Role of Noninsulin Antihyperglycemic Agents Role of Medical Nutrition Therapy Special Clinical Situations Organization of Care Safety Other Relevant Guidelines Author Disclosures.

Key Messages Hyperglycemia is common in hospitalized people, even among those without a previous history of diabetes, and is associated with increased in-hospital complications, longer length of stay and mortality.

Insulin is the most appropriate pharmacologic agent for effectively controlling glycemia in hospital. A proactive approach to glycemic management using scheduled basal, bolus and correction supplemental insulin is the preferred method. The use of correction-only supplemental insulin, which treats hyperglycemia only after it has occurred, should be discouraged as the sole modality for treating elevated blood glucose levels.

For the majority of noncritically ill hospitalized people with diabetes, preprandial blood glucose targets should be 5. For critically ill hospitalized people with diabetes, blood glucose levels should be maintained between 6.

Hypoglycemia is a major barrier to achieving targeted glycemic control in the hospital setting. Health-care institutions should develop protocols for the assessment and treatment of hypoglycemia.

Key Messages for People with Diabetes If your admission to hospital is planned, talk with your health-care providers e. surgeon, anesthetist, primary care provider, diabetes health provider, etc.

before you are admitted in order to develop an in-hospital diabetes care plan that addresses such issues as: Who will manage your diabetes in the hospital? Will you be able to self-manage your diabetes? What adjustments to your diabetes medications or insulin doses may be necessary before and after medical procedures or surgery?

If you use an insulin pump, are hospital staff familiar with pump therapy? Your blood glucose levels may be higher in hospital than your usual target range due to a variety of factors, including the stress of your illness, medications, medical procedures and infections.

Your diabetes medications may need to be changed during your hospital stay to manage the changes in blood glucose, or if medical conditions develop that make some medications no longer safe to use.

When you are discharged, make sure that you have written instructions about: Changes in your dosage of medications or insulin injections or any new medications or treatments How often to check your blood glucose Who to contact if you have difficulty managing your blood glucose levels.

Introduction Diabetes increases the risk for hospitalization for several reasons, including: cardiovascular CV disease, nephropathy, infection, cancer and lower-extremity amputations.

Screening for and Diagnosis of Diabetes and Hyperglycemia in the Hospital Setting A history of diabetes should be elicited in all patients admitted to hospital and, if present, should be clearly identified on the medical record.

Glucose Monitoring in the Hospital Setting Bedside blood glucose monitoring Currently, there are no studies that have examined the effect of the frequency of bedside BG monitoring on the incidence of hyper- or hypoglycemia in the hospital setting.

Glycemic Control in the Non-Critically Ill Patient A number of studies have demonstrated that inpatient hyperglycemia is associated with increased morbidity and mortality in noncritically ill hospitalized people 1,28, Glycemic Control in the Critically Ill Patient Acute hyperglycemia in the intensive care setting is not unusual and results from a number of factors, including stress-induced counter-regulatory hormone secretion and the effects of medications administered in the ICU Role of Intravenous Insulin There are few occasions when intravenous insulin is required, as most people with type 1 or type 2 diabetes admitted to general medical wards can be treated with subcutaneous insulin.

Transition from IV insulin to SC insulin therapy Hospitalized people with type 1 and type 2 diabetes may be transitioned to scheduled subcutaneous insulin therapy from intravenous insulin. Perioperative glycemic control The management of individuals with diabetes at the time of surgery poses a number of challenges.

Cardiovascular surgery In people undergoing coronary artery bypass grafting CABG , a pre-existing diagnosis of diabetes has been identified as a risk factor for postoperative sternal wound infections, delirium, renal dysfunction, respiratory insufficiency and prolonged hospital stays 48— Minor and moderate surgery The perioperative glycemic targets for minor or moderate surgeries are less clear.

Role of Subcutaneous Insulin In general, insulin is the preferred treatment for hyperglycemia in hospitalized people with diabetes Role of Noninsulin Antihyperglycemic Agents To date, no large studies have investigated the use of non-insulin antihyperglycemic agents on outcomes in hospitalized people with diabetes.

Role of Medical Nutrition Therapy Medical nutrition therapy including nutritional assessment and individualized meal planning is an essential component of inpatient glycemic management programs. Special Clinical Situations Hospitalized people with diabetes receiving enteral or parenteral feedings In hospitalized people with diabetes receiving parenteral nutrition, insulin can be administered in the following ways: as scheduled regular insulin dosing added directly to the parenteral solution; or as scheduled intermediate- or long-acting subcutaneous insulin doses Self-management of diabetes in hospital Although data for self-management in the hospitalized setting is limited, self-management in hospital may be appropriate for people who are mentally competent and desire more autonomy over their diabetes.

Hospitalized people with diabetes using CSII Although the data are limited, it appears that CSII can be safely continued in the hospital setting under certain circumstances Organization of Care Institution-wide programs to improve glycemic control in the inpatient setting include the formation of a multidisciplinary steering committee, professional development programs focused on inpatient diabetes management 95,96 , policies to assess and monitor the quality of glycemic management, interprofessional team-based care including comprehensive patient education and discharge planning as well as standardized order sets, protocols and algorithms for diabetes care within the institution.

Interprofessional team-based approach The timely consultation of glycemic management teams has also been found to improve the quality of care provided, reduce the length of hospital stay and lower costs , , although differences in glycemic control were minimal Comprehensive patient education Programs that include self-management education, such as assessment of barriers and goal setting, have also been associated with improvements in glycemic control 97, Metrics for evaluating inpatient glycemic management programs Institutional implementation of hospital glycemic management programs require metrics to monitor progress, assess safety, length of stay and identify opportunities for improvement Transition from hospital to home Interventions that ensure continuity of care, such as arranging continuation of care after discharge 97 , telephone follow up and communication with primary providers at discharge , have been associated with a post-discharge reduction in A1C Safety Hypoglycemia Hypoglycemia remains a major barrier to achieving optimal glycemic control in hospitalized people with diabetes.

Insulin administration errors Insulin is considered a high-alert medication and can be associated with risk of harm and severe adverse events. Recommendations An A1C should be measured if not done in the 3 months prior to admission on: All hospitalized people with a history of diabetes to identify individuals that would benefit from glycemic optimization [Grade D, Consensus] All hospitalized people with newly diagnosed hyperglycemia or those with diabetes risk factors to identify individuals at risk for ongoing dysglycemia [Grade C, Level 3 16 ] Repeat screening should be performed 6 to 8 weeks post-hospital discharge for individuals with an A1C 6.

The frequency and timing of bedside CBG monitoring should be individualized for all in-hospital people with diabetes.

Monitoring should typically be performed: Before meals and at bedtime in people who are eating [Grade D, Consensus] Every 4 to 6 hours in people who are NPO or receiving continuous enteral feeding [Grade D, Consensus] Every 1 to 2 hours for people on continuous intravenous insulin or those who are critically ill [Grade D, Consensus].

Provided that their medical conditions, dietary intake and glycemic control are stable, people with diabetes should be maintained on their pre-hospitalization noninsulin antihyperglycemic agents or insulin regimens [Grade D, Consensus].

For hospitalized people with diabetes treated with insulin, a proactive approach that includes basal, bolus and correction supplemental insulin, along with pattern management, should be used to reduce adverse events and improve glycemic control, instead of only correcting high BG with short- or rapid-acting insulin [Grade A, Level 1A 61,66, ].

For the majority of noncritically ill hospitalized people with diabetes, preprandial BG targets should be 5. For people with diabetes undergoing CABG, a continuous intravenous insulin infusion protocol targeting intraoperative glycemic levels between 5.

In hospitalized people with diabetes, hypoglycemia should be minimized. Protocols for hypoglycemia avoidance, recognition and management should be implemented with nurse-initiated treatment, including glucagon for severe hypoglycemia when intravenous access is not readily available [Grade D, Consensus].

Hospitalized people with diabetes at risk of hypoglycemia should have ready access to an appropriate source of glucose oral or IV at all times, particularly when NPO or during diagnostic procedures [Grade D, Consensus]. Programs consisting of the following elements should be implemented for optimal inpatient diabetes care: Interprofessional team-based approach [Grade B, Level 2 ,, ] Health-care professional development regarding in-hospital diabetes management [Grade D, Level 4 95 ] Algorithms, order sets and decision support [Grade C, Level 3 26,99, ].

Abbreviations: BG, blood glucose; CBG , capillary blood glucose; CABG , coronary artery bypass grafting; CSII , continuous subcutaneous insulin infusion; ICU , intensive care unit; NPH , neutral protamine Hagedorn; POC , point of care; TDD , total daily dose.

Other Relevant Guidelines Chapter Glycemic Management in Adults With Type 1 Diabetes Chapter Pharmacologic Glycemic Management of Type 2 Diabetes in Adults Chapter Hyperglycemic Emergencies in Adults Chapter Management of Acute Coronary Syndromes Chapter Author Disclosures Dr.

References Umpierrez GE, Isaacs SD, Bazargan N, et al. Hyperglycemia: An independent marker of in-hospital mortality in patients with undiagnosed diabetes. J Clin Endocrinol Metab ;— Vasa F. Systematic strategies for improved outcomes for the hyperglycemic hospitalized patient with diabetes mellitus.

Am J Cardiol ;e—6e. Inzucchi SE. Clinical practice. Management of hyperglycemia in the hospital setting. N Engl J Med ;— Roman SH, Chassin MR. Windows of opportunity to improve diabetes care when patients with diabetes are hospitalized for other conditions.

Diabetes Care ;—6. Sud M, Wang X, Austin PC, et al. Presentation blood glucose and death, hospitalization, and future diabetes risk in patients with acute heart failure syndromes. Eur Heart J ;— Umpierrez GE, Reyes D, Smiley D, et al.

Hospital discharge algorithm based on admission HbA1c for the management of patients with type 2 diabetes. Diabetes Care ;—9. Perez A, Reales P, Barahona MJ, et al. Efficacy and feasibility of basal-bolus insulin regimens and a discharge-strategy in hospitalised patients with type 2 diabetes-the HOSMIDIA study.

Int J Clin Pract ;— Ochoa PS, Terrell BT, Vega JA, et al. Identification of previously undiagnosed diabetes and prediabetes in the inpatient setting using risk factor and hemoglobin A1C screening.

Ann Pharmacother ;—9. Simpson AJ, Krowka R, Kerrigan JL, et al. Opportunistic pathology-based screening for diabetes.

BMJ Open in press. Norhammar A, Tenerz A, Nilsson G, et al. Glucose metabolism in patients with acute myocardial infarction and no previous diagnosis of diabetes mellitus: A prospective study.

Lancet ;—4. Evaluating hyperglycaemia in the hospitalised patient: Towards an improved system for classification and treatment. Ir J Med Sci ;—9. Miller DB. Glycemic targets in hospital and barriers to attaining them.

Can J Diabetes ;—8. Greci LS, Kailasam M, Malkani S, et al. Utility of HbA 1c levels for diabetes case finding in hospitalized patients with hyperglycemia. Diabetes Care ;—8. Carpenter DL, Gregg SR, Xu K, et al. Prevalence and impact of unknown diabetes in the ICU.

Crit Care Med ;e— Kompoti M, Michalia M, Salma V, et al. Glycated hemoglobin at admission in the intensive care unit: Clinical implications and prognostic relevance. J Crit Care ;—5. Can HbA1c detect undiagnosed diabetes in acute medical hospital admissions? Diabetes Res Clin Pract ;— Malcolm JC, Kocourek J, Keely E, et al.

Implementation of a screening program to detect previously undiagnosed dysglycemia in hospitalized patients. Can J Diabetes ;— Umpierrez GE, Hellman R, Korytkowski MT, et al. Management of hyperglycemia in hospitalized patients in non-critical care setting: An endocrine society clinical practice guideline.

Lewandrowski K, Cheek R, Nathan DM, et al. Implementation of capillary blood glucose monitoring in a teaching hospital and determination of program requirements to maintain quality testing.

Am J Med ;— Rumley AG. Improving the quality of near-patient blood glucose measurement. Ann Clin Biochem ;34 Pt 3 —6. Boyd JC, Bruns DE. Quality specifications for glucose meters: Assessment by simulation modeling of errors in insulin dose.

Clin Chem ;— Bates DW, Leape LL, Cullen DJ, et al. Effect of computerized physician order entry and a team intervention on prevention of serious medication errors. JAMA ;— Desachy A, Vuagnat AC, Ghazali AD, et al. Accuracy of bedside glucometry in critically ill patients: Influence of clinical characteristics and perfusion index.

Mayo Clin Proc ;—5. Critchell CD, Savarese V, Callahan A, et al. Accuracy of bedside capillary blood glucose measurements in critically ill patients. Intensive Care Med ;— Petersen JR, Graves DF, Tacker DH, et al. Comparison of POCT and central laboratory blood glucose results using arterial, capillary, and venous samples from MICU patients on a tight glycemic protocol.

Clin Chim Acta ;— Nirantharakumar K, Chen YF, Marshall T, et al. Clinical decision support systems in the care of inpatients with diabetes in non-critical care setting: Systematic review. Diabet Med ;— Maynard G, Schnipper JL, Messler J, et al.

Design and implementation of a webbased reporting and benchmarking center for inpatient glucometrics. J Diabetes Sci Technol ;— Baker EH, Janaway CH, Philips BJ, et al.

Hyperglycaemia is associated with poor outcomes in patients admitted to hospital with acute exacerbations of chronic obstructive pulmonary disease. Thorax ;—9. McAlister FA, Majumdar SR, Blitz S, et al. The relation between hyperglycemia and outcomes in 2, patients admitted to the hospital with communityacquired pneumonia.

Diabetes Care ;— American Diabetes Association. Diabetes care in the hospital. Diabetes Care ;S99— Lewis KS, Kane-Gill SL, Bobek MB, et al. Intensive insulin therapy for critically ill patients. Ann Pharmacother ;— van den Berghe G,Wouters P,Weekers F, et al.

Intensive insulin therapy in critically ill patients. Griesdale DE, de Souza RJ, van Dam RM, et al. Intensive insulin therapy and mortality among critically ill patients: A meta-analysis including NICE-SUGAR study data.

CMAJ ;—7. NICE-SUGAR Study Investigators, Finfer S, Chittock DR, et al. Intensive versus conventional glucose control in critically ill patients. Moghissi ES, Korytkowski MT, DiNardo M, et al. American Association of Clinical Endocrinologists and American Diabetes Association consensus statement on inpatient glycemic control.

Endocr Pract ;— Goldberg PA, Siegel MD, Sherwin RS, et al. Implementation of a safe and effective insulin infusion protocol in a medical intensive care unit. Diabetes Care ;—7. Rea RS, Donihi AC, BobeckM, et al. Implementing an intravenous insulin infusion protocol in the intensive care unit. Am J Health Syst Pharm ;— Nazer LH, Chow SL, Moghissi ES.

Insulin infusion protocols for critically ill patients: A highlight of differences and similarities. Ntaios G, Papavasileiou V, Bargiota A, et al.

Intravenous insulin treatment in acute stroke: A systematic review and meta-analysis of randomized controlled trials. Int J Stroke ;— Schmeltz LR, DeSantis AJ, Schmidt K, et al. Conversion of intravenous insulin infusions to subcutaneously administered insulin glargine in patientswith hyperglycemia.

Bode BW, Braithwaite SS, Steed RD, et al. Intravenous insulin infusion therapy: Indications, methods, and transition to subcutaneous insulin therapy. Endocr Pract ;10 Suppl. Kwoun MO, Ling PR, Lydon E, et al.

Immunologic effects of acute hyperglycemia in nondiabetic rats. JPEN J Parenter Enteral Nutr ;—5. Verhofstad MH, Hendriks T. Complete prevention of impaired anastomotic healing in diabetic rats requires preoperative blood glucose control.

Br J Surg ;— Golden SH, Peart-Vigilance C, Kao WH, et al. Perioperative glycemic control and the risk of infectious complications in a cohort of adults with diabetes.

McAlister FA, Man J, Bistritz L, et al. Diabetes and coronary artery bypass surgery: An examination of perioperative glycemic control and outcomes. Thomas MC, Mathew TH, Russ GR, et al. Early peri-operative glycaemic control and allograft rejection in patients with diabetes mellitus: A pilot study.

Transplantation ;—4. Estrada CA, Young JA, Nifong LW, et al. Outcomes and perioperative hyperglycemia in patients with or without diabetes mellitus undergoing coronary artery bypass grafting. Ann Thorac Surg ;—9.

Management of persistent hyperglycemia in type 2 diabetes mellitus - UpToDate Hospitals should have policies and procedures for the assessment of suitability for self-management. Blood glucose Hemoglobin A1c Lipid panel LDL HDL Triglycerides Total cholesterol Basic metabolic panel Comprehensive metabolic panel. Marik View author publications. Peaks are usually corresponding to maximum values after meals, particularly at mid morning, 53 while troughs are observed over interprandial periods, 54 especially in patients who are treated with insulin secretagogues and who are at risk of hypoglycemic episodes. Follow-up of glycemic control and cardiovascular outcomes in type 2 diabetes. Jakoby MG, Nannapaneni N. Increase in circulating products of lipid peroxidation F2-isoprostanes in smokers: smoking as a cause of oxidative damage.
For more information Memory retention strategies mean cntrol of glycemic hypsrglycemia Chronic hyperglycemia and glycemic control glyccemic, which has been described by Service et al, 27 was used in the present study for hypergpycemia glucose Chronic hyperglycemia and glycemic control during glycfmic day. Table 1. Obesity and systemic oxidative stress: clinical correlates of oxidative stress in the Framingham study. Abbreviations: BG, blood glucose; CBGcapillary blood glucose; CABGcoronary artery bypass grafting; CSIIcontinuous subcutaneous insulin infusion; ICUintensive care unit; NPHneutral protamine Hagedorn; POCpoint of care; TDDtotal daily dose. Ann Thorac Surg ;—9.
Hyperglycemia in diabetes Disease of the pancreas and glucose metabolism. Although metformin is usually started for the management of hyperglycemia, it is also frequently an effective medication to promote modest weight loss. It does NOT include all information about conditions, treatments, medications, side effects, or risks that may apply to a specific patient. See "Pregestational preexisting diabetes: Preconception counseling, evaluation, and management". See "Management of nonalcoholic fatty liver disease in adults", section on 'Patients with NASH and diabetes'.
Chronic hyperglycemia and glycemic control

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