| Literature DB >> 21468244 |
Abstract
Type 2 diabetes is a major public health concern. Screening and early diagnosis followed by prompt and aggressive treatment interventions can help control progression of diabetes and its complications. Nurses are often the first healthcare team members to interact with patients and are being called on to apply their specialized knowledge, training, and skills to educate and motivate patients with diabetes about insulin use and practical ways to achieve treatment goals. Clinical nurse specialists possess specific training and skills to provide this level of care, while staff or office-based nurses may be trained by physicians to fulfill a task-specific role. This manuscript reviews the benefits of intensive glycemic control in type 2 diabetes, therapeutic goals and guidelines, advances in insulin therapy, and contribution of nurses in overcoming barriers to insulin initiation and related aspects of diabetes care. Nurses are particularly well positioned to fill the gap and improve efficiency in diabetes-related healthcare by assisting patients with insulin initiation and other aspects of glycemic self-management.Entities:
Keywords: diabetes; diabetes counseling; diabetes educator; hypoglycemia; insulin; insulin clinic; insulin pens
Year: 2011 PMID: 21468244 PMCID: PMC3065562 DOI: 10.2147/JMDH.S16451
Source DB: PubMed Journal: J Multidiscip Healthc ISSN: 1178-2390
Selected major evidence and rationale for intensive diabetes management
The UKPDS (United Kingdom Prospective Diabetes Study) found that poor glycemic control in patients with type 2 diabetes is associated with an increased risk of cardiovascular complications, including coronary heart disease, myocardial infarction, and peripheral vascular disease, as well as microvascular complications and death. The DCCT (Diabetes Control and Complications Trial) reported that maintaining fasting plasma glucose (FPG) between 70 and 120 mg/dL (3.89–6.67 mmol/L) and postprandial glucose (PPG) <180 mg/dL (10 mmol/L) helps sustain endogenous insulin secretion. The EDIC (Epidemiology of Diabetes Interventions and Complications) study found that early glycemic control reduces the risk of cardiovascular events. The ARIC (Atherosclerosis Risk in Communities) study reported that elevated HbA1C leads to atherosclerosis and cardiovascular disease. The Steno-2 study found that intensive, multifactorial intervention reduced diabetes-related mortality and cardiovascular events. The ADVANCE (Action in Diabetes and Vascular Disease) study found that intensive glucose control reduced major macrovascular and microvascular events, primarily due to a 21% reduction in nephropathy. Li et al Weng et al |
Figure 1Relationship of hemoglobin A1C (HbA1C) and incidence of diabetes complications.4 In the United Kingdom Prospective Diabetes Study (UKPDS), each percentage point reduction in HbA1C was linked with substantial risk reductions in diabetes-related morbidity and mortality.
Therapeutic goals for FPG, PPG, and HbA1C
| ADA | 90–130 mg/dL (5–7.22 mmol/L) | <180 mg/dL (10 mmol/L) | <7% |
| IDF | <110 mg/dL (6.11 mmol/L) | <145 mg/dL (8.06 mmol/) | <6.5% |
| ADA/EASD Consensus | 70–130 mg/dL (3.89–7.22 mmol/L) | <180 mg/dL (10 mmol/L) | <7% |
| AACE | <100 mg/dL (5.56 mmol/L) | <140 mg/dL (7.78 mmol/L) | ≤6.5% |
Abbreviations: FPG, fasting plasma glucose; PPG, postprandial glucose; HbA1C, hemoglobin A1C; ADA, American Diabetes Association; IDF, International Diabetes Federation, EASD, European Association for the Study of Diabetes; AACE, American Association of Clinical Endocrinologists.
Differentiating available diabetes therapies14,15,23–28
| Metformin | Weight neutral, inexpensive, oral | GI side effects, rare lactic acidosis |
| Thiazolidinediones | Improved lipid profile, oral | Fluid retention, weight gain, CHF, may not see reduction in glucose for several weeks, expensive, increased cardiovascular risk |
| Alpha-glucosidase inhibitors | Weight neutral, oral | Frequent GI side effects, 3 times/day dosing, expensive |
| Sulfonylureas | Inexpensive, oral | Weight gain, hypoglycemia |
| Glinides | Short duration | Hypoglycemia, 3 times/day dosing, expensive |
| DPP-4 inhibitors
Saxagliptin Sitagliptin | Weight neutral, less hypoglycemia, oral | Lack of long-term data regarding safety and efficacy |
| GLP-1 agonists
Exenatide Liraglutide | Less hypoglycemia, weight loss | Injections, lack of long-term data on safety and efficacy |
| Insulin | Inexpensive, no dose limit, improved lipid profile | Injections, monitoring, hypoglycemia, weight gain |
| Human insulin
Regular or short acting Intermediate acting (NPH) | Many physicians still most comfortable with standard insulin therapy | Limited pharmacokinetic/pharmacodynamic features, hypoglycemia, injections, monitoring, weight gain, variability in time-action profile |
| Insulin analogs
Rapid-acting analogs
○ Aspart ○ Lispro ○ Glulisine Long-acting basal analogs
○ Glargine ○ Detemir Premixed analogs
○ Biphasic insulin aspart 70/30 ○ Insulin lispro 75/25 ○ Insulin lispro 50/50 | Less hypoglycemia than human insulin, absorption more consistent, less weight gain; rapid- and long-acting formulations, predictable time–action profiles, simplified dosing with premixes | Injections, monitoring |
| Devices for insulin delivery | ||
| • Traditional vial and syringe | Some physicians most comfortable with standard vial and syringe insulin therapy | Can be complicated to administer, not discreet, time consuming, and potential for dosing errors; patients may have needle aversion |
| • Pen-injection devices | Convenient, discreet, simple, may improve confidence/adherence and reduce insulin-related adverse events, good for patients who have vision or dexterity problems, decreased dosing errors and more accurate dosing | Some patients are averse to injections in any form |
Abbreviations: GI, gastrointestinal; CHF, congestive heart failure; DPP-4, dipeptidyl peptidase-4; GLP-1, glucagon-like peptide 1; NPH, neutral protamine Hagedorn.
Insulin initiation strategies
| The AACE notes that insulin can be initiated by addition to any and all oral antidiabetic drug (OAD) therapies, as long as appropriate blood glucose monitoring is performed. Several different approaches are possible: 1) add a basal insulin, |
Basal initiation therapy aims to normalize fasting blood glucose and HbA1C Metformin is the preferred first-line OAD for patients with type 2 diabetes but can be expected to reduce HbA1C values by only ∼1.5%. To achieve target HbA1C goals, basal insulin is added to metformin, typically at a dose of 10 units/day. Adjustment of the daily dose will depend on the FPG and on the basal insulin selected. Two long-acting basal insulin analogs, insulin detemir and glargine, have pharmacodynamic profiles that provide up to 24-hour basal insulin levels, generally with a once-daily injection at bedtime. Because type 2 diabetes is a progressive disease, most patients will ultimately require the addition of rapid-acting bolus insulin injections at mealtimes to control postprandial glucose (PPG) (see below). A basal-bolus regimen is ideal for many patients, as it mimics the body’s constant release of insulin throughout the day and supplements the body’s need for insulin after a meal. |
Premixed insulins are formulated to combine both basal and rapid-acting components in 1 injection and thus provide a simple way to achieve near-normal insulin profiles at mealtime and between meals. Premixed insulins are easy to use, ensure that the correct amount of insulin is injected every time, and may improve adherence to therapy. They are especially helpful for patients who are older, averse to multiple injections, or prefer a simple insulin regimen. Premixed insulins are given in once-, twice-, or 3-times daily schedules, depending on the patient’s needs. When initiating a premixed insulin, metformin should be continued, but if the patient is currently taking a secretagogue, it should be discontinued. Individuals who eat regular meals on a schedule are ideally suited for premixed insulins; however, premixes are not a preferred option for patients with varied daily schedules or those who require flexibility around mealtimes. Specific dosing and titration information depend on the formulation chosen. |
Tight control over PPG excursions can be exerted using mealtime bolus insulin injections. As beta-cell function declines with disease progression, prandial insulin injections will eventually be required by most patients with type 2 diabetes. Controlling PPG levels so they remain below 140 to 180 mg/dL (7.78–10 mmol/L) Adding a bolus injection of a rapid-acting mealtime insulin analog (lispro, aspart, or glulisine) is ideally suited for patients who require flexibility, since it may be given immediately before or even during a meal, ie, “inject and eat” rather than waiting 15 to 30 minutes with regular insulin. The dose can be varied based on the patient’s glucose levels or the size/type of meal. This approach is supported by AACE medical guidelines. |
Figure 2Approximate pharmacokinetic profiles of rapid- and long-acting insulin analogs as compared with an idealized profile of physiological insulin secretion.44
Copyright © 2007 [Lippincott, Williams & Wilkins] Reprinted with permission from Boyle PJ, Zrebiec J. Management of diabetes-related hypoglycemia. South Med J. 2007;100(2):183–194.44
Symptoms and management of hypoglycemia
| Hypoglycemia symptoms can vary considerably from patient to patient. |
Pallor Sweating Increased heart rate Feelings of shakiness Blurred vision Tingling sensation Difficulty concentrating Feeling weak Tiredness or clumsiness Feeling warm or cold Feeling hungry Changes in mood (manifesting as giddiness, anger or irritability, anxiety or frustration, or tearfulness) Seizures or loss of consciousness (if the hypoglycemia is very severe) |
Fast-acting carbohydrates (glucose tablets, fruit juices, drinks high in sugar content, or glucose gels). Five grams of carbohydrate raises plasma glucose by ∼15 mg/dL (0.83 mmol/L). A typical hypoglycemic episode is treated by ingesting 15 g of carbohydrate. If, after 15 minutes, plasma glucose remains <70 mg/dL (3.89 mmol/L), another carbohydrate-rich snack should be ingested (the 15/15 rule). Glucose gels are absorbed by the buccal mucosa and can be administered by an attendant in the event the patient is not alert. This may be followed by juice or food once the patient is more alert. Very severe hypoglycemia might require intravenous administration of glucose by trained medical personnel. In cases of severe or frequent hypoglycemia or hypoglycemic unawareness, it is prudent to instruct the patient and significant other(s) in the use of glucagon, an injectable treatment for hypoglycemia in the unconscious patient. |
Reasons for patient referral to insulin therapy evaluation clinics
Initiation of insulin for patients who are poorly controlled on OAD therapies Insulin dose adjustments for patients who are not achieving HbA1C goals with basal-bolus therapy Instruction on self-titration tools for basal insulin Instruction on carbohydrate counting and carbohydrate-to-insulin ratios Evaluation of patients’ ability to self inject (includes pen-vs-syringe demonstrations) General education about the role of insulin in diabetes management Instruction on the use of self-monitoring blood glucose monitors Hypoglycemia prevention and management |
Self-management and the chronic care model72
| Nearly half of all people with chronic illness have multiple conditions. Insurers have an interest in correcting specific issues in chronic disease management, including:
Practitioners who, because of high caseload, are too rushed to consult or follow established practice guidelines Lack of care coordination Lack of active follow-up to ensure the best outcomes Patients inadequately trained to manage their illnesses |
Notes: To overcome these issues, the Improving Chronic Illness Care organization created the Chronic Care Model, which summarizes basic elements for improving healthcare. The model draws on best practices and research findings and provides a foundation for collaborative programs, tools, and research aimed at improving care for the chronically ill (see http://www.improvingchroniccare.org for additional information and resources).72