© American Diabetes Association ®, Inc., 2005 Hyperglycemia in the Hospital
In Brief This article reviews the use of subcutaneous insulin for hospitalized patients. Topics include the rationale for using insulin; scheduled insulin therapy to cover basal and nutritional needs; correction therapy; dose determination; establishment of timing of insulin action appropriate to the pattern of carbohydrate exposure; education of caregivers; and the design of hospital systems that will promote quality and help staff to manage complexity.
This review will focus on the rationale and methodology for management of hospital hyperglycemia under conditions that do not require intravenous insulin infusion. For many years, tradition held that hospitalization was not the time in the life of a patient with diabetes to focus on glycemic control. The complications of diabetes were divided into 1) acute metabolic emergencies requiring patient stabilization rather than perfection of glycemic control and 2) chronic tissue complications, which had required months or years to evolve. It was thought that safety considerations dictated the prudence of avoiding hospital hypoglycemia. Nevertheless, adverse hospital outcomes have been linked to hyperglycemia. These include nosocomial infection, sepsis, cardiac mortality after myocardial infarction or cardiac surgery, atrial fibrillation after cardiac surgery, increased infarct size after stroke, acute graft rejection after transplantation, "unit" neuropathy, transfusion requirement and acute renal failure in critical care unit patients, prolongation of stay, and increased cost.121 Some of these outcomes, being multifactorial in etiology and not readily classifiable as a manifestation of microvascular or macro-vascular disease, were not linked intuitively to specific diabetes treatment actions. In fact, it took randomized, controlled trials to establish the relationship. The revolution in present-day thinking about the importance of inpatient glycemic control has occurred because of the findings of a large and long-running cardiac surgery series3,5,14 and because of the convincing evidence of randomized, controlled trials demonstrating, first, the causal nature of the relationship between hyperglycemia and some of the outcomes listed above, and, second, the ability of intensive insulin management to reduce those adverse outcomes.2227 (Readers are referred to the article by Goldberg and Inzucchi in this issue of Diabetes Spectrum, p. 2833.) The strongest evidence for hospital outcomes advantages was obtained, without significant complications from hypoglycemia, during and after the use of intravenous insulin infusion under conditions of intensive monitoring. For general medical conditions treated in hospital wards other than intensive care units, similar outcomes data do not exist. It will be necessary to show, from randomized trials prospectively conducted outside of the intensive care unit setting, that specific benefits will result from intensive subcutaneous insulin management, without prohibitive risk from hypoglycemia. It is necessary to define blood glucose (BG) targets and to determine whether there is any glycemic threshold, other than the upper limit of normal, above which those benefits are jeopardized. Pending the results of such research, upper limits of glycemic targets intended to provide clinicians with guidelines for promoting improved outcomes have been recommended (Table 1).28, 29
Conditions of hospitalization, such as trauma, hemorrhage, burns, hypoxia, infections, sepsis, or shock, may induce both insulin resistance and relative insulin secretory defect. Both peripheral and hepatic sites of insulin resistance have been implicated. The consequences include increased muscle protein degradation, decreased peripheral glucose disposal, lipolysis resulting in increased circulating nonesterified fatty acids, hyperlactatemia, and increased hepatic glucose output. Mechanisms of the observed defects of insulin signaling and relative ß-cell suppression during acute illness are the subject of active research.30 The targets for protective action of insulin in the hospital setting prominently include the heart, the endothelium (vasodilatory action, protection against vessel wall inflammatory processes), the inflammatory pathway, the coagulation pathway, host defenses against infection, and the nutritional status of the patient.
Protection may be conferred in part by metabolic control (correction of
hyperglycemia, reduction of circulating nonesterified fatty acids, reduction
of lactate, reversal of proteolysis, and protection against the downstream
nonmetabolic consequences of these abnormalities). Protection also may be
conferred by other direct or indirect nonmetabolic effects of insulin itself
(nitric oxidemediated improvement of endothelial function; regulation
of nuclear factor-
One of the first challenges on admission is to recognize the presence of diabetes or risk for hospital hyperglycemia by patient history and examination and by measurements of BG and potentially hemoglobin A1c (A1C).34 Another challenge is the need for the admitting team to identify type 1 diabetes and record the classification.28 The timing of BG monitoring should be planned with consideration of the pattern of exposure to carbohydrate and antihyperglycemic treatment (Figure 1). The purpose of monitoring is to determine a pattern that might require initiation or revision of daily therapy with antihyperglycemic medication (for example, during pregnancy postprandial testing should be included), to detect hypoglycemia, and to provide BG measurements at the times of day when correction doses might best be used.
Under conditions of hospitalization, metformin commonly is contraindicated. In general, oral agents do not provide the flexibility necessary to gain control rapidly. Sometimes oral agents are stopped on admission but are reintroduced as a patient approaches discharge. Patients previously taking insulin temporarily may have a new total daily dose (TDD) requirement. In contrast to the ambulatory pattern of insulin requirement consisting of a fairly continuous basal demand with discrete prandial elevations, the hospital pattern of insulin requirement may reflect continuous delivery or interruption of nutrition. The best course of action for demonstrable hyperglycemia usually is to plan a program of scheduled insulin appropriate to the specific conditions of hospitalization.28
Scheduled (programmed) insulin Specific insulin products are not uniquely identified as replacement for particular physiological insulin functions (basal or nutritional). However, for purposes of calculation of an initial TDD of insulin and establishment of a pattern of delivery, it is useful to think of therapy as having the following components: basal, nutritional, and correction-dose insulin. To match the anticipated and changing patterns of insulin requirement under conditions of hospitalization, providers have a palette of insulins and insulin analogs, each having a characteristic peak and duration of action when given subcutaneously, with which to "paint" the day (Figure 1). Rapid-acting analog therapy (lispro, aspart) is efficacious for coverage of prandial needs for patients eating discrete meals or for correction of hyperglycemia. For acute severe hyperglycemia, BG monitoring and subcutaneous injection of rapid-acting insulin analog can be ordered every 22.5 hours until BG correction occurs. Given every 12 hours, rapid-acting analog has been used in the treatment of ketoacidosis.35 If perfusion of subcutaneous sites is impaired, however, after repeated doses of subcutaneous insulin, there is a danger of delayed effect occurring beyond the expected time frame of action, with consequent late hypoglycemia. Rapid-acting analog therapy is not well suited for coverage of basal requirements or insulin requirements resulting from continuous delivery of nutritional support or intravenous dextrose. Long-acting peakless analog (glargine) administered once daily for patients having type 1 diabetes ensures against inadvertent omission of needed basal insulin coverage. A correctly established dose of glargine providing basal coverage may be safely administered in type 1 diabetes, despite NPO (nothing by mouth) status.36 With realization that requirements for exogenous insulin may have been inflated because of overnutrition and may vanish during prolonged NPO status, a safe minimum dose estimating true basal requirements still may be replaced as glargine insulin during NPO status in type 2 diabetes. Because nutrition or dextrose suddenly may be interrupted, as a safety precaution against hypoglycemia in unstable hospitalized patients, the doses of glargine generally should not be titrated to meet nutritional requirements, but rather, they should meet only the estimated basal insulin requirement. Glargine is not recommended during pregnancy. NPH and subcutaneous regular insulin are especially useful for patients whose carbohydrate exposure is not delivered as discrete meals. When insulin is required, a regimen of mixed NPH and regular insulin given every 68 hours provides excellent coverage for NPO status, intravenous dextrose, or continuous enteral feedings. NPH and subcutaneous regular insulin can supplement intravenous insulin coverage used as an additive with total parenteral nutrition. NPH and subcutaneous regular insulin are well suited to cover transitional meal plans and corticosteroid therapy. Intermediate-acting insulin and regular insulin or rapid-acting analog also can be used to cover normal diet with discrete meals. NPH insulin is preferred to glargine for basal coverage during use of multiple daily injection therapy in pregnancy.
Starting doses of insulin
In type 2 diabetes, the apparent requirement for exogenous basal insulin
may vanish during prolonged NPO status. However, a safe minimum starting point
(in the absence of renal failure), which would be tolerated as replacement for
endogenous basal insulin production even if the requirement should trend
downward, is
For patients who are eating normal meals, there is a nutritional insulin
requirement approximately equal to the basal requirement. For patients
receiving intravenous dextrose or nutritional support, the nutritional
requirement can be initially estimated at The starting TDD of insulin can be envisioned as the sum of the basal and nutritional requirements, calculated as discussed above.
Correction doses, "hold" orders, and daily revision of scheduled insulin Except for basal insulin in type 1 diabetes, orders might include a provision for nursing staff to withhold or reduce doses of scheduled insulin in the event of downward trending of BG or interruption of carbohydrate exposure. The dose of scheduled insulin should be recalculated daily based on BG response, the amount of insulin actually administered on the previous day, and the changing condition of the patient. Review of charted doses is necessary to discover withholding of ordered doses of scheduled insulin or use of correction doses. For both type 1 and type 2 diabetes, it is an important precaution to reduce the TDD of scheduled insulin in case of downward trending of BG or development of factors that might predispose to hypoglycemia, such as renal or hepatic failure or resolution of stress- or drug-related hyperglycemia.42
Consistent carbohydrate diets
Patient self-management of diabetes in the hospital
Hypoglycemia prevention
Discharge planning Hospitalization may provide an ideal opportunity to introduce patients with diabetes to strategies that might improve their preadmission control or reduce hypoglycemia, such as the addition of basal insulin to oral agents49,50 or intensification from use of regular and intermediate-acting insulin to multiple daily injections of insulin using a rapid-acting analog and basal insulin.5155 Outpatient follow-up over several visits with a diabetes educator and dietitian is necessary to establish the skill of matching prandial insulin to variable carbohydrate intake. This strategy (advanced carbohydrate counting), at least in type 1 diabetes, yields results superior to fixed-dose use of prandial insulin.56
Education of caregivers Baldwin et al.58 explored this issue further by designing a systematic approach to educate residents in inpatient insulin management. Residents were educated regarding management of hyperglycemia without using sliding scale insulin, which is ubiquitous in most inpatient settings and oftentimes is the sole means of blood glucose management. An endocrinologist supervised a basal-bolus regimen in all patients treated with insulin. A team consisting of two residents managed BG levels for all of the team's patients and rounded twice daily with the supervising endocrinologist. At the end of the rotation, all house officers felt confident in inpatient diabetes management without using a sliding scale. There was a significant decrease in the length of stay compared to a risk-matched control group, and the use of a sliding scale was effectively abolished in this particular training program. Interestingly, the use of a sliding scale on the surgical services not involved in this study also declined by 43%. This study exemplifies how intensive education, particularly for fellows, residents, and interns, can go a long way in improving glycemic control and achieving overall improved outcomes for diabetic patients. In the future, it would be helpful to have more data regarding the efficacy of different teaching models for education of house staff and other health care providers involved in diabetes management. Several methods of providing staff nurses with education about diabetes management have been reported in the literature. Adams and Cook59 compared the diabetes nursing care of two groups of home health agency nurses: those with a diabetes educator and those without. They found that although both groups scored similarly on a diabetes knowledge test, the nurses with the diabetes clinical nurse specialist scored higher in their care of diabetes patients on a nursing care intervention tool. The authors speculated that this resulted from the orientation modules, nursing care plans, and teaching tools provided to the staff nurses by the diabetes clinical nurse specialist. Self-directed learning about diabetes was the approach to educating staff nurses used by Dunning.60 The author developed a nursing care manual for the most frequent admission diagnoses for diabetes patients at a major teaching hospital. This manual was a unit resource for staff nurses. The manual was designed to improve the knowledge of nurses caring for diabetic patients and to be used as a springboard for developing nursing policies and standards for the nursing care of patients with diabetes. Parker et al.61 studied the impact of a diabetes education program on improving nurses' diabetes knowledge and changing nurse behavior in long-term care facilities. Nurses from two long-term care facilities participated in a multisession education program on diabetes treatment. Diabetes knowledge was assessed using both a pre- and postprogram test. Comparison was made with a control group of nurses from two other long-term care facilities who did not attend the education program. The nurses attending the education program had a significant increase in their postprogram knowledge score compared to those in the control group. However, a chart review revealed that there was no significant improvement postprogram in diabetes nursing care behaviors, such as giving insulin in the abdomen or giving carbohydrate after low blood glucose. The authors postulated that the lack of behavior change was because there was no opportunity for re-enforcement sessions and no contact with a diabetes nurse educator. The findings of Parker et al. were supported by the work of Asselin.62 She found that experienced hospital staff nurses primarily use new knowledge from unit-based resources to change their clinical practice. In only 1 of 29 examples given by these nurses was nursing practice changed by knowledge gained from attending a formal continuing education program. Asselin recommended that nursing staff development focus on unit-based resources and unit-based trainers. In addition, a network of multidisciplinary resource personnel and unit-based computer access to disease-specific knowledge bases would provide further information. A regular staff member from each unit thus might receive additional training and become a champion for diabetes to promulgate the spread of knowledge among his or her peers. A nursing clinical practice group can be defined as a group of nurses in the same nursing specialty at an institution who meet periodically to review their current nursing practice as it relates to standards of nursing care, institutional policies and procedures, and evidence-based practice. Clinical practice groups offer an avenue for communicating new ideas and new requirements and challenging the status quo. They allow for the use of critical thinking skills to evaluate current and future clinical practices and to discuss ways to improve nursing care for patients with specific diseases or conditions. This venue supports both novice and experienced nurses' perspectives on patient care. It enhances the likelihood that both the organization and its patients will benefit from performance improvement measures in order to provide the best diabetes care and education possible. Clinical practice groups are an excellent way to enhance clinical nursing practice.
Who should be the caregiver? The specialty training of caregivers may influence the hospital course for patients with diabetes. One study of diabetic ketoacidosis (DKA) by Levetan et al.63 compared outcomes in patients cared for by generalists to those cared for by endocrinologists. The endocrinologist-treated group had a significantly lower readmission rate for DKA as well as a significantly shorter length of stay. Endocrinologists treated patients more costeffectively than generalists, keeping their costs to almost half of their generalist counterparts. This savings resulted mainly from avoidance of unnecessary imaging and laboratory studies by those unfamiliar with DKA. In another study by Levetan et al.,64 the length of stay for patients with diabetes was shorter by 35% for those cared for by a diabetes consult team, which was a statistically significant difference. Koproski et al.65 randomly assigned 179 patients to either usual care or care by a diabetes team consisting of a nurse educator and an endocrinologist. The diabetes team intervention reduced the length of hospital stay, improved glycemic control, and reduced the rate of recurrent hospitalizations when compared to usual care. Clearly, the multidisciplinary diabetes care team approach is more effective than usual care, and there is some evidence that specialized nursing care contributes to the difference. Davies et al.66 showed that diabetic patients randomized to a diabetes specialist nursing service had shorter lengths of stay and lower costs of care. Patient satisfaction and knowledge of disease was superior in the intervention group.
Safety and quality
Managing complexity with a single signature: paper protocols and electronic health records Computerized provider order entry for diabetes is in its infancy. Nevertheless, computer prompting has been shown to reduce reliance on sliding scale monotherapy and increase the use of scheduled insulin.74 Computerized systems must make it convenient for users to select and implement the components of a comprehensive diabetes care plan under protocols or algorithms (Table 2). The design of any paper-based or computerized clinical order set based on accepted algorithms or protocols must: 1) query the electronic database or provider about weight, age, pregnancy, and risk for hypoglycemia; 2) encompass the desired input and output; 3) provide options for user override of defaults and for free text entries; 4) have flexibility to encompass future change; 5) accept input from diabetes experts and users and 6) ensure transparency of algorithms for review by the users.
Initiatives to intensify the treatment of hospital hyperglycemia result in improved patient outcomes and cost reductions. How can hospitals move in the direction of intensifying treatment? One part of the answer is the participation of diabetes experts and champions, not only in the direct care of patients, but also in the education of physicians, nursing staff, dietitians, pharmacists, and others. Another part of the solution, under enlightened hospital leadership, is the multidisciplinary design of systems that support improvements in hospital management of hyperglycemia. Such efforts potentially would affect screening for hyperglycemia; knowledge of appropriate glycemic targets; recognition of hyperglycemia as an indication for monitoring and treatment; spread of the use of intravenous insulin infusion; recognition and interception of unsafe situations leading potentially to hypoglycemia or ketosis; preservation of basal insulin regimens for type 1 diabetes; standardization of approaches to prevent hypoglycemia; facilitation of inpatient diabetes self-management for experienced and competent patients; elimination of sliding scale monotherapy; generation of effective orders for scheduled subcutaneous insulin therapy; creation of order sets and implementation of computerized clinical systems that facilitate regimen selection, intensification, and daily revision of insulin therapy; and appropriate patient education and discharge planning.
Cara L. Thompson MSN, APRN, BC-ADM, RD, LDN, CDE, is a diabetes clinical nurse education specialist in the Department of Nursing Practice Education and Research at the University of North Carolina Hospitals in Chapel Hill, N.C. Kelli C. Dunn, MD, and Meera C. Menon, MD, are second-year fellows in the Department of Endocrinology/Medicine at the same institution. Lauren E. Kearns, MSN, RN, BC, is a liver transplant coordinator at the same institution and is board certified in nursing informatics. Susan S. Braithwaite, MD, FACE, FACP, is a clinical professor of medicine at the University of North Carolina Diabetes Care Center in Durham, N.C. Note of disclosure: Dr. Braithwaite has received honoraria for speaking engagements from Aventis and research funding from Bristol-Myers Squibb. Both companies make insulin products for the treatment of hyperglycemia.
2 Pomposelli JJ, Baxter JK 3rd, Babineau TJ, Pomfret EA, Driscoll DF, Forse RA, Bistrian BR: Early postoperative glucose control predicts nosocomial infection rate in diabetic patients. JPEN J Parenter Enteral Nutr22 : 7781,1998[Abstract]
3 Furnary AP, Zerr
KJ, Grunkemeier GL, Starr A: Continuous intravenous insulin infusion reduces
the incidence of deep sternal wound infection in diabetic patients after
cardiac surgical procedures. Ann Thorac Surg67
: 352362,1999
4 Golden SH,
Peart-Vigilance C, Kao WHL, Brancati F: Perioperative glycemic control and the
risk of infectious complications in a cohort of adults with diabetes.
Diabetes Care 22:1408
1414, 1999 5 Furnary AP, Chaugle H, Zerr K, Grunkemeier G: Postoperative hyperglycemia prolongs length of stay in diabetic CABG patients (Abstract). Circulation 102 (II):556A , 2000 6 Thomas MC, Moran J, Mathew TH, Russ GR, Rao MM: Early peri-operative hyperglycaemia and renal allograft rejection in patients without diabetes. BMC Nephrol 1: 1,2000[Medline] 7 Thomas M, Mathew T, Russ G, Rao M, Moran J: Early peri-operative glycaemic control and allograft rejection in patients with diabetes mellitus: a pilot study. Transplantation 72:1321 1324, 2001[Medline] 8 Melin J, Hellberg L, Larsson E, Zezina L, Fellstrom B: Protective effect of insulin on ischemic renal injury in diabetes mellitus. Kidney Int61 : 13831392,2002[Medline]
9 Szabo Z, Hakanson
E, Svedjeholm R: Early postoperative outcome and medium-term survival in 540
diabetic and 2239 nondiabetic patients undergoing coronary artery bypass
grafting. Ann Thorac Surg 74:712
719, 2002
10 Umpierrez GE,
Isaacs SD, Bazargan N, You X, Thaler LM, Kitabchi AE: Hyperglycemia: an
independent marker of in-hospital mortality in patients with undiagnosed
diabetes. J Clin Endocrinol Metab87
: 978982,2002
11 Baird TA, Parsons
MW, Phanh T, Butcher KS, Desmond PM, Tress BM, Colman PG, Chambers BR, Davis
SM: Persistent poststroke hyperglycemia is independently associated with
infarct expansion and worse clinical outcome. Stroke34
: 22082214,2003
12 Finney SJ, Zekveld
C, Elia A, Evans TW: Glucose control and mortality in critically ill patients.
JAMA 290:2041
2047, 2003
13 Foo K, Cooper J,
Deaner A, Knight C, Suliman A, Ranjadayalan K, Timmis AD: A single serum
glucose measurement predicts adverse outcomes across the whole range of acute
coronary syndromes. Heart 89:512
516, 2003
14 Furnary AP, Gao G,
Grunkemeier GL, Wu Y, Zerr KJ, Bookin SO, Floten HS, Starr A: Continuous
insulin infusion reduces mortality in patients with diabetes undergoing
coronary artery bypass grafting. J Thorac Cardiovasc
Surg 125:1007
1021, 2003
15 McAlister FA, Man
J, Bistritz L, Amad H, Tandon P: Diabetes and coronary artery bypass surgery:
an examination of perioperative glycemic control and outcomes.
Diabetes Care 26:1518
1524, 2003 16 Ahmann A: Reduction of hospital costs and length of stay by good control of blood glucose levels. Endocr Pract 10 (Suppl. 2): 5356,2004 17 Chu VH, Cabell CH, Benjamin DK Jr, Kuniholm EF, Fowler VG Jr, Engemann J, Sexton DJ, Corey GR, Wang A: Early predictors of in-hospital death in infective endocarditis. Circulation 109:1745 1749, 2004[Medline]
18 Leigh R, Zaidat
OO, Suri MF, Lynch G, Sundararajan S, Sunshine JL, Tarr R, Selman W, Landis
DM, Suarez JI: Predictors of hyperacute clinical worsening in ischemic stroke
patients receiving thrombolytic therapy. Stroke35
: 19031907,2004
19 Lindsberg PJ,
Roine RO: Hyperglycemia in acute stroke. Stroke35
: 363364,2004
20 Schnell O, Schafer
O, Kleybrink S, Doering W, Standl E, Otter W: Intensification of therapeutic
approaches reduces mortality in diabetic patients with acute myocardial
infarction: the Munich registry. Diabetes Care27
: 455460,2004
21 Stranders I,
Diamant M, van Gelder RE, Spruijt HJ, Twisk JW, Heine RJ, Visser FC: Admission
blood glucose level as risk indicator of death after myocardial infarction in
patients with and without diabetes mellitus. Arch Intern
Med 164:982
988, 2004 22 Malmberg K, Ryden L, Efendic S, Herlitz J, Nicol P, Waldenstrom A, Wedel H, Welin L: Randomized trial of insulin-glucose infusion followed by subcutaneous insulin treatment in diabetic patients with acute myocardial infarction (DIGAMI study): effects on mortality at 1 year. J Am Coll Cardiol26 : 5765,1995[Abstract]
23 Malmberg K for the
DIGAMI Study Group: Prospective randomised study of intensive insulin
treatment on long term survival after acute myocardial infarction in patients
with diabetes mellitus. BMJ314
: 15121515,1997
24 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 345:1359
1367, 2001 25 Van den Berghe G, Wouters PJ, Bouillon R, Weekers F, Verwaest C, Schetz M, Vlasselaers D, Ferdinande P, Lauwers P: Outcome benefit of intensive insulin therapy in the critically ill: insulin dose versus glycemic control. Crit Care Med 31:359 366, 2003[Medline] 26 Lazar HL, Chipkin SR, Fitzgerald CA, Bao Y, Cabral H, Apstein CS: Tight glycemic control in diabetic coronary artery bypass graft patients improves perioperative outcomes and decreases recurrent ischemic events. Circulation109 : 14971502,2004[Medline] 27 Grey NJ, Perdrizet GA: Reduction of nosocomial infections in the surgical intensive-care unit by strict glycemic control. Endocr Pract10 (Suppl. 2): 4652,2004
28 Clement S,
Braithwaite SS, Magee MF, Ahmann A, Smith EP, Schafer RG, Hirsch IB, American
Diabetes Association Diabetes in Hospitals Writing Committee: Management of
diabetes and hyperglycemia in hospitals. Diabetes Care27
: 553591,2004 29 American College of Endocrinology: Position statement on inpatient diabetes and metabolic control. Endocr Pract 10:77 82, 2004[Medline] 30 Le Roith D: Molecular mechanisms by which metabolic control may improve outcomes. Endocr Pract 10 (Suppl. 2):57 62, 2004
31 Dandona P, Aljada
A, Mohanty P, Ghanim H, Hamouda W, Assian E, Ahmad S: Insulin inhibits
intranuclear nuclear factor kappaB and stimulates IkappaB in mononuclear cells
in obese subjects: evidence for an anti-inflammatory effect? J Clin
Endocrinol Metab 86:3257
3265, 2001 32 Chaudhuri A, Janicke D, Wilson MF, Tripathy D, Garg R, Bandyopadhyay A, Calieri J, Hoffmeyer D, Syed T, Ghanim H, Aljada A, Dandona P: Anti-inflammatory and profibrinolytic effect of insulin in acute ST-segment-elevation myocardial infarction. Circulation 109:849 854, 2004[Medline] 33 Hirsch IB: Effect of insulin therapy on nonglycemic variables during acute illness. Endocr Pract 10 (Suppl. 2):63 70, 2004
34 Greci LS, Kailasam
M, Malkani S, Katz DL, Hulinsky I, Ahmadi R, Nawaz H: Utility of HbA1c levels
for diabetes case finding in hospitalized patients with hyperglycemia.
Diabetes Care 26:1064
1068, 2003
35 Umpierrez GE,
Cuervo R, Karabell A, Latif K, Freire AX, Kitabchi AE: Treatment of diabetic
ketoacidosis with subcutaneous insulin aspart. Diabetes
Care 27:1873
1878, 2004
36 Mucha GT, Merkel
S, Thomas W, Bantle JP: Fasting and insulin glargine in individuals with type
1 diabetes. Diabetes Care 27:1209
1210, 2004 37 Pitts DM, Kilo KA, Pontious SL: Nutritional support for the patient with diabetes. Crit Care Nurs Clin North Am 5:47 56, 1993[Medline] 38 Gearhart JG, Duncan JL, Replogle WH, Forbes RC, Walley EJ: Efficacy of sliding-scale insulin therapy: a comparison with prospective regimens. Fam Pract Res J 14:313 322, 1994[Medline] 39 Queale WS, Seidler AJ, Brancati FL: Glycemic control and sliding scale insulin use in medical inpatients with diabetes mellitus. Arch Intern Med157 : 545552,1997[Abstract]
40 Childs BP: Death
to the sliding scale! Diabetes Spectrum16
: 6869,2003
41 Trence DL, Kelly
JL, Hirsch IB: The rationale and management of hyperglycemia for inpatients
with cardiovascular disease: time for change. J Clin Endocrinol
Metab 88:2430
2437, 2003
42 Campbell KB,
Braithwaite SS: Hospital management of hyperglycemia. Clin
Diabetes 22:81
88, 2004 43 American Diabetes Association: Diabetes nutrition recommendations for health care institutions (Position Statement). Diabetes Care 27 (Suppl. 1):S55 S57, 2004
44 DeWitt DE, Hirsch
IB: Outpatient insulin therapy in type 1 and type 2 diabetes mellitus:
scientific review. JAMA 289:2254
2264, 2003 45 Lee SW, Im R, Magbual R: Current perspectives on the use of continuous subcutaneous insulin infusion in the acute care setting and overview of therapy. Crit Care Nurs 27:172 184, 2004 46 Fischer KF, Lees JA, Newman JH: Hypoglycemia in hospitalized patients. N Engl J Med 315:1245 1250, 1986[Abstract] 47 Braithwaite SS, Buie MM, Thompson CL, Baldwin DF, Oertel MD, Robertson BA, Mehrotra HP: Hospital hypoglycemia: not only treatment but also prevention. Endocr Pract 10 (Suppl. 2):71 -80, 2004 48 American Diabetes Association: Diagnosis and classification of diabetes mellitus (Position Statement). Diabetes Care 27 (Suppl. 1):S5 S10, 2004
49 Yki-JärvinenH, Bressler A, Ziemen M: Less nocturnal hypoglycemia
and better post-dinner glucose control with bedtime insulin glargine compared
with bedtime NPH insulin during insulin combination therapy in type 2
diabetes. Diabetes Care 23:1130
1136, 2000
50 Riddle MC,
Rosenstock J, Gerich J: The Treat-to-Target Trial: randomized addition of
glargine or human NPH insulin to oral therapy of type 2 diabetic patients.
Diabetes Care 26:3080
3086, 2003 51 Anderson JH Jr, Brunelle RL, Koivisto VA, Pfutzner A, Trautmann ME, Vignati L, DiMarchi R: Reduction of postprandial hyperglycemia and frequency of hypoglycemia in IDDM patients on insulin-analog treatment. Diabetes46 : 265270,1997[Abstract] 52 Anderson JH Jr, Brunelle RL, Keohane P, Koivisto VA, Trautmann ME, Vignati L, DiMarchi R: Mealtime treatment with insulin analog improves postprandial hyperglycemia and hypoglycemia in patients with non-insulin-dependent diabetes mellitus. Arch Intern Med 157:1249 1255, 1997[Abstract] 53 Lalli C, Ciofetta M, Del Sindaco P, Torlone E, Pampanelli S, Compagnucci P, Cartechini MG, Bartocci L, Brunetti P, Bolli GB: Long-term intensive treatment of type 1 diabetes with the short-acting insulin analog lispro in variable combination with NPH insulin at mealtime. Diabetes Care22 : 468477,1999[Abstract]
54 Lindholm A, McEwen
J, Riis AP: Improved postprandial glycemic control with insulin aspart.
Diabetes Care 22:801
805, 1999
55 Raskin P, Guthrie
RA, Leiter L, Riis A, Jovanovic L: Use of insulin aspart, a fast-acting
insulin analog, as the mealtime insulin in the management of patients with
type 1 diabetes. Diabetes Care23
: 583588,2000
56 DAFNE Study Group: Training in flexible,
intensive insulin management to enable dietary freedom in people with type 1
diabetes: dose adjustment for normal eating (DAFNE) randomised controlled
trial. BMJ 325:746
752, 2002
57 Bernard A,
Anderson L, Cook C, Phillips L: What do internal medicine residents need to
enhance their diabetes care? Diabetes Care22
: 661666,1999 58 Baldwin D, Villanueva G, McNutt R: Eliminating the use of inpatient sliding scale (SS) insulin: a re-education project with medical housestaff (Abstract). Diabetes 53 (Suppl. 2):A118 , 2004 59 Adams CE, Cook DL: The impact of a diabetes nurse educator on nurses' knowledge of diabetes and nursing interventions in a home care setting. Diabetes Educ 20:49 53, 1994 60 Dunning T: Development of a nursing care manual to improve the knowledge of nurses caring for hospitalized patients with diabetes. J Contin Educ Nurs 26:261 266, 1995[Medline] 61 Parker MT, Leggett-Frazier N, Vincent PA, Swanson MS: The impact of an educational program on improving diabetes knowledge and changing behaviors of nurses in long-term care facilities. Diabetes Educ21 : 541545,1995 62 Asselin ME: Knowledge utilization among experienced staff nurses. J Nurses Staff Dev 17:115 122 [quiz 123124],2001[Medline]
63 Levetan CS,
Passaro MD, Jablonski KA, Ratner RE: Effect of physician specialty on outcomes
in diabetic ketoacidosis. Diabetes Care22
: 17901795,1999 64 Levetan CS, Salas JR, Wilets IF, Zumoff B: Impact of endocrine and diabetes team consultation on hospital length of stay for patients with diabetes. Am J Med 99:22 28, 1995[Medline] 65 Koproski J, Pretto Z, Poretsky L: Effects of an intervention by a diabetes team in hospitalized patients with diabetes. Diabetes Care290 : 15531555,1997 66 Davies M, Dixon S, Currie CJ, Davis RE, Peters JR: Evaluation of a hospital diabetes specialist nursing service: a randomized controlled trial. Diabet Med 18:301 307, 2001[Medline] 67 Roman SH, Linekin PL, Stagnaro-Green A: An inpatient diabetes QI program. Jt Comm J Qual Improv 21:693 699, 1995[Medline] 68 Gibney M, Cohen E, Roman SH: Inpatient diabetes care: strategies for disease management. Disease Man 2:13 23, 1999
69 Roman SH, Chassin
MR: Windows of opportunity to improve diabetes care when patients with
diabetes are hospitalized for other conditions. Diabetes
Care 24:1371
1376, 2001
70 Gilman JA: A
quality improvement project for better glycemic control in hospitalized
patients with diabetes. Diabetes Educ27
: 541546,2001 71 Hellman R: A systems approach to reducing errors in insulin therapy in the inpatient setting. Endocr Pract 10 (Suppl. 2): 8188,2004
72 Quevedo SF,
Sullivan E, Kington R, Rogers W: Improving diabetes care in the hospital using
guideline-directed orders. Diabetes Spectrum14
: 226233,2001
73 Bates DW, Ebell M,
Gotlieb E, Zapp J, Mullins HC: A proposal for electronic medical records in
U.S. primary care. J Am Med Inform Assoc10
: 110,2003 74 Achtmeyer CE, Payne TH, Anawalt BD: Computer order entry system decreased use of sliding scale insulin regimens. Meth Inf Med41 : 277281,2002[Medline] This article has been cited by other articles:
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