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in patients whose therapy has changed
or who are not meeting glycemic targets
Microvascular complications
Macrovascular disease*
Preprandial capillary PG
Age/life expectancy
Comorbid conditions
Diabetes duration
Hypoglycemia status
Individual patient considerations
Known CVD/advanced microvascular complications
Any pharmacologic agents discussed are approved for use in the United States by the U.S. Food and Drug Administration (FDA)
unless otherwise noted. Consult individual prescribing information for approved uses outside of the United States.
January 2014
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Consider:
Efficacy
Cost
Potential side effects
Effects on weight
Comorbidities
Hypoglycemia risk
Patient preferences
Insulin eventually needed for many patients due to progressive nature of type 2 diabetes
GLP=glucagon-like peptide
Any pharmacologic agents discussed are approved for use in the United States by the U.S. Food and Drug Administration (FDA)
unless otherwise noted. Consult individual prescribing information for approved uses outside of the United States.
January 2014
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Results may be useful for guiding treatment and/or self-management for patients using less frequent
insulin injections or noninsulin therapies
Provide ongoing instruction and regular evaluation of SMBG technique and results and
patients ability to use data to adjust therapy
Any pharmacologic agents discussed are approved for use in the United States by the U.S. Food and Drug Administration (FDA)
unless otherwise noted. Consult individual prescribing information for approved uses outside of the United States.
January 2014
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promotional/commercial interest.
Treatment
Treatment targets
Treatment
*In certain individuals, if achieved without treatment burden ; If one class not tolerated, substitute other class
Any pharmacologic agents discussed are approved for use in the United States by the U.S. Food and Drug Administration (FDA)
unless otherwise noted. Consult individual prescribing information for approved uses outside of the United States.
January 2014
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Source:
Source:American
AmericanDiabetes
DiabetesAssociation.
Association.
Standards
Standardsofofmedical
medicalcare
careinindiabetes2014.
diabetes2014.Diabetes
DiabetesCare.
Care.2014;37(suppl
2014;37(suppl1):S14-S80.
1):S14-S80.
Refer
to
source
document
for
full
recommendations,
including
Targets
Lifestyle modification
Treatment
Overt CVD
No CVD, aged >40 yrs, 1 CVD risk factor
Consider statins in lower-risk patients (no overt CVD, aged <40 yrs)
if LDL-C >100 mg/dL or if multiple CVD risk factors
Any pharmacologic agents discussed are approved for use in the United States by the U.S. Food and Drug Administration (FDA)
unless otherwise noted. Consult individual prescribing information for approved uses outside of the United States.
January 2014
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promotional/commercial interest.
Aspirin: Secondary
prevention
Clopidogrel 75 mg/day
Men aged <50 yrs and women aged >60 yrs with no major additional CVD risk factors
ACEI=angiotensin-converting enzyme inhibitor; ACS=acute coronary syndrome; ARB=angiotensin receptor blocker; BP=blood pressure;
CAD=coronary artery disease; CVD=cardiovascular disease; DASH=Dietary Approaches to Stop Hypertension; DBP=diastolic blood pressure;
eGFR=estimated glomerular filtration rate; MI=myocardial infarction; SBP=systolic blood pressure; TZD=thiazolidinedione
Any pharmacologic agents discussed are approved for use in the United States by the U.S. Food and Drug Administration (FDA)
unless otherwise noted. Consult individual prescribing information for approved uses outside of the United States.
January 2014
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Annually measure urine albumin excretion in type 1 patients with 5-yr diabetes
duration, and all type 2 patients starting at diagnosis
Treatment
Nonpregnant with modest elevations Use ACEI or ARB (but not in combination)
(30-299 mg/24 h) or higher levels
(300 mg/24 h) of urinary albumin
excretion
Diabetic kidney disease
(albuminuria >30 mg/24 h)
Any pharmacologic agents discussed are approved for use in the United States by the U.S. Food and Drug Administration (FDA)
unless otherwise noted. Consult individual prescribing information for approved uses outside of the United States.
January 2014
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promotional/commercial interest.
Treatment
ACEI=angiotensin-converting enzyme inhibitor; ARB=angiotensin receptor blocker; BP=blood pressure; CKD=chronic kidney disease;
eGFR=estimated glomerular filtration rate; NPDR=nonproliferative diabetic retinopathy; PDR=proliferative diabetic retinopathy; VEGF=vascular
endothelial growth factor
Any pharmacologic agents discussed are approved for use in the United States by the U.S. Food and Drug Administration (FDA)
unless otherwise noted. Consult individual prescribing information for approved uses outside of the United States.
January 2014
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promotional/commercial interest.
10
Retinopathy
Nephropathy
Neuropathy
CVD
Statins
ACEIs
ARBs
Most noninsulin therapies
Gestational Diabetes
Pregnant women with risk
factors
Glycemic targets
Any pharmacologic agents discussed are approved for use in the United States by the U.S. Food and Drug Administration (FDA)
unless otherwise noted. Consult individual prescribing information for approved uses outside of the United States.
January 2014
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promotional/commercial interest.
11
12
Two-Step (NIH)
*Threshold of 135 mg/dL in high-risk ethnic minorities with higher prevalence of GDM recommended by ACOG
ACEI=angiotensin-converting enzyme inhibitor; ACOG=American College of Obstetricians and Gynecologists; ARB=angiotensin receptor blocker;
CVD=cardiovascular disease; GDM=gestational diabetes mellitus; GLT=glucose load test; IADPSG=International Association of Diabetes and
Pregnancy Study Groups; NIH=National Institutes of Health; OGTT=oral glucose tolerance test; PG=plasma glucose
Any pharmacologic agents discussed are approved for use in the United States by the U.S. Food and Drug Administration (FDA)
unless otherwise noted. Consult individual prescribing information for approved uses outside of the United States.
January 2014
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promotional/commercial interest.
Prediabetes or diabetes
Achieve dietary fiber intake of 14 g/1,000 kcal and whole grains 50% of grain intake
Physical Activity
Adults with diabetes
Exercise programs should include
150 min/wk moderate-intensity aerobic activity (50%-70% max heart rate), spread over
3 days/wk with no more than 2 consecutive days without exercise
Resistance training 2 times/wk (in absence of contraindications)*
Evaluate patients for contraindications prohibiting certain types of exercise before recommending
exercise program
Consider age and previous level of physical activity
Children with diabetes, prediabetes
60 min physical activity/day
*Adults with type 2 diabetes
Eg, uncontrolled hypertension, severe autonomic or peripheral neuropathy, history of foot lesions,
unstable proliferative retinopathy
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13
Physical inactivity
First-degree relative with diabetes High-risk race/ethnicity
Women who delivered a baby >9 lb or were diagnosed with GDM
HDL-C <35 mg/dL TG >250 mg/dL
Hypertension (140/90 mm Hg or on therapy)
A1C 5.7%, IGT, or IFG on previous testing
Conditions associated with insulin resistance: severe obesity, acanthosis nigricans, PCOS
CVD history
Any pharmacologic agents discussed are approved for use in the United States by the U.S. Food and Drug Administration (FDA)
unless otherwise noted. Consult individual prescribing information for approved uses outside of the United States.
January 2014
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promotional/commercial interest.
14
January 2014
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promotional/commercial interest.
15
Any pharmacologic agents discussed are approved for use in the United States by the U.S. Food and Drug Administration (FDA)
unless otherwise noted. Consult individual prescribing information for approved uses outside of the United States.
January 2014
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promotional/commercial interest.
16
Most patients with type 1 diabetes: Consider screening for autoimmune diseases as appropriate
Screening
Inform individuals with type 1 diabetes of the opportunity to have relatives screened for risk of type 1
diabetes in the clinical research setting
Early diagnosis may limit complications, extend long-term endogenous insulin production
Any pharmacologic agents discussed are approved for use in the United States by the U.S. Food and Drug Administration (FDA)
unless otherwise noted. Consult individual prescribing information for approved uses outside of the United States.
January 2014
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promotional/commercial interest.
17
Begin at admission
Clear diabetes management instructions
provided at discharge
Monitor glucose
Consider treating to same targets as patients
with known diabetes
Establish hypoglycemia management protocol and create a plan for each patient for treating and
preventing hypoglycemia
Any pharmacologic agents discussed are approved for use in the United States by the U.S. Food and Drug Administration (FDA)
unless otherwise noted. Consult individual prescribing information for approved uses outside of the United States.
January 2014
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promotional/commercial interest.
18
Persistent hyperglycemia:
Any pharmacologic agents discussed are approved for use in the United States by the U.S. Food and Drug Administration (FDA)
unless otherwise noted. Consult individual prescribing information for approved uses outside of the United States.
January 2014
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promotional/commercial interest.
19
20
Hepatitis B vaccine
Psychosocial Considerations
Reasonable to include psychological and social assessments of patient as part of
diabetes management
Psychosocial screening and follow-up may
include:
Screen on routine basis for depression and diabetes-related distress, anxiety, eating disorders, and
cognitive impairment
Any pharmacologic agents discussed are approved for use in the United States by the U.S. Food and Drug Administration (FDA)
unless otherwise noted. Consult individual prescribing information for approved uses outside of the United States.
January 2014
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promotional/commercial interest.
21
Functional
Cognitively intact
Expected to live long
enough to reap benefits
Glycemic targets: may be relaxed for some older adults based on individual criteria
Screening
Diagnosis
Treatment
Any pharmacologic agents discussed are approved for use in the United States by the U.S. Food and Drug Administration (FDA)
unless otherwise noted. Consult individual prescribing information for approved uses outside of the United States.
January 2014
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promotional/commercial interest.
22
After Diagnosis
Similar screening, treatment as for type 1 diabetes
for
Hypertension
Albumin excretion
Dyslipidemia
Retinopathy
January 2014
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promotional/commercial interest.
23
24
6-12 yrs
13-19 yrs
<8.5%
<8%
<7.5%
100-180 mg/dL
90-180 mg/dL
90-130 mg/dL
110-200 mg/dL
100-180 mg/dL
90-150 mg/dL
A1C
*If on basal-bolus: measure postprandial PG to monitor glycemic values and if discrepancy between
preprandial PG and A1C; modification of targets may be needed in children aged <7 yrs due to
hypoglycemic unawareness; Reasonable to consider lower target if achieved in absence of
excessive hypoglycemia
Microvascular Complications in Children & Adolescents With Type 1 Diabetes
Nephropathy
Screening
Aged 10 yrs or puberty onset (whichever occurs first) with 5-yr diabetes duration
Treatment
Retinopathy
Screening
Follow-up
Aged 10 yrs or puberty onset (whichever occurs first) with 3-5yr diabetes
duration
Yearly
Less frequently: per recommendation of eye care professional
ACEIs are not approved by the U.S. Food and Drug Administration (FDA) for treatment of
nephropathy. Not all ACEIs are indicated for use in children/adolescents by the FDA. Refer to full
prescribing information for indications and uses in pediatric populations.
Any pharmacologic agents discussed are approved for use in the United States by the U.S. Food and Drug Administration (FDA)
unless otherwise noted. Consult individual prescribing information for approved uses outside of the United States.
January 2014
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promotional/commercial interest.
Pharmacologic therapy
ACEI: initial treatment
*For age, sex, height; Provide counseling re: potential teratogenic effects.
Not all ACEIs are indicated for use in children/adolescents by the U.S. Food and Drug
Administration (FDA). Refer to full prescribing information for indications and uses in pediatric
populations.
Any pharmacologic agents discussed are approved for use in the United States by the U.S. Food and Drug Administration (FDA)
unless otherwise noted. Consult individual prescribing information for approved uses outside of the United States.
January 2014
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promotional/commercial interest.
25
Unknown
Unremarkable
Diabetes diagnosed prior to/post-puberty
Aged 10 yrs
Post-diagnosis*
Treatment
Initial
Control glucose
MNT: decrease saturated fat intake
Aged 10 yrs
Use American Heart Association Step 2 diet: saturated fat 7% of total calories; dietary cholesterol
200 mg/d
Statins are approved by the U.S. Food and Drug Administration for treatment of heterozygous
familial hypercholesterolemia in children and adolescents. Not all statins are FDA approved for use
under the age of 10 yrs; statins should generally not be used in children with type 1 diabetes before
age 10. Refer to full prescribing information for indications and uses in pediatric populations. For
postpubertal girls, pregnancy prevention is important as statins are contraindicated in pregnancy.
Any pharmacologic agents discussed are approved for use in the United States by the U.S. Food and Drug Administration (FDA)
unless otherwise noted. Consult individual prescribing information for approved uses outside of the United States.
January 2014
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promotional/commercial interest.
26
Screening for
Measuring TSH*
Celiac disease
Asymptomatic with
positive antibodies
If diagnosis confirmed
27
28
29
January 2014
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promotional/commercial interest.
30
January 2014
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promotional/commercial interest.
31
Any pharmacologic agents discussed are approved for use in the United States by the U.S. Food and Drug Administration (FDA)
unless otherwise noted. Consult individual prescribing information for approved uses outside of the United States.
January 2014
This content was created by KnowledgePoint360 Group, LLC, and was not associated with funding via an educational grant or a
promotional/commercial interest.
32
Any pharmacologic agents discussed are approved for use in the United States by the U.S. Food and Drug Administration (FDA)
unless otherwise noted. Consult individual prescribing information for approved uses outside of the United States.
January 2014
This content was created by KnowledgePoint360 Group, LLC, and was not associated with funding via an educational grant or a
promotional/commercial interest.
33
Refer to source document for full recommendations, including level of evidence rating.
Any pharmacologic agents discussed are approved for use in the United States by the U.S. Food and Drug Administration (FDA)
unless otherwise noted. Consult individual prescribing information for approved uses outside of the United States.
January 2014
This content was created by KnowledgePoint360 Group, LLC, and was not associated with funding via an educational grant or a
promotional/commercial interest.
34
Refer to source document for full recommendations, including level of evidence rating.
Any pharmacologic agents discussed are approved for use in the United States by the U.S. Food and Drug Administration (FDA)
unless otherwise noted. Consult individual prescribing information for approved uses outside of the United States.
January 2014
This content was created by KnowledgePoint360 Group, LLC, and was not associated with funding via an educational grant or a
promotional/commercial interest.
35
Refer to source document for full recommendations, including level of evidence rating.
Any pharmacologic agents discussed are approved for use in the United States by the U.S. Food and Drug Administration (FDA)
unless otherwise noted. Consult individual prescribing information for approved uses outside of the United States.
January 2014
This content was created by KnowledgePoint360 Group, LLC, and was not associated with funding via an educational grant or a
promotional/commercial interest.
36
Refer to source document for full recommendations, including level of evidence rating.
Any pharmacologic agents discussed are approved for use in the United States by the U.S. Food and Drug Administration (FDA)
unless otherwise noted. Consult individual prescribing information for approved uses outside of the United States.
January 2014
This content was created by KnowledgePoint360 Group, LLC, and was not associated with funding via an educational grant or a
promotional/commercial interest.
37
Any pharmacologic agents discussed are approved for use in the United States by the U.S. Food and Drug Administration (FDA)
unless otherwise noted. Consult individual prescribing information for approved uses outside of the United States.
January 2014
This content was created by KnowledgePoint360 Group, LLC, and was not associated with funding via an educational grant or a
promotional/commercial interest.
38
Any pharmacologic agents discussed are approved for use in the United States by the U.S. Food and Drug Administration (FDA)
unless otherwise noted. Consult individual prescribing information for approved uses outside of the United States.
January 2014
This content was created by KnowledgePoint360 Group, LLC, and was not associated with funding via an educational grant or a
promotional/commercial interest.
39
Refer to source document for full recommendations, including level of evidence rating.
January 2014
This content was created by KnowledgePoint360 Group, LLC, and was not associated with funding via an educational grant or a
promotional/commercial interest.
40
January 2014
This content was created by KnowledgePoint360 Group, LLC, and was not associated with funding via an educational grant or a
promotional/commercial interest.
41
January 2014
This content was created by KnowledgePoint360 Group, LLC, and was not associated with funding via an educational grant or a
promotional/commercial interest.
42
Any pharmacologic agents discussed are approved for use in the United States by the U.S. Food and Drug Administration (FDA)
unless otherwise noted. Consult individual prescribing information for approved uses outside of the United States.
January 2014
This content was created by KnowledgePoint360 Group, LLC, and was not associated with funding via an educational grant or a
promotional/commercial interest.
43
Refer to source document for full recommendations, including level of evidence rating.
Any pharmacologic agents discussed are approved for use in the United States by the U.S. Food and Drug Administration (FDA)
unless otherwise noted. Consult individual prescribing information for approved uses outside of the United States.
January 2014
This content was created by KnowledgePoint360 Group, LLC, and was not associated with funding via an educational grant or a
promotional/commercial interest.
44
January 2014
This content was created by KnowledgePoint360 Group, LLC, and was not associated with funding via an educational grant or a
promotional/commercial interest.
45
Any pharmacologic agents discussed are approved for use in the United States by the U.S. Food and Drug Administration (FDA)
unless otherwise noted. Consult individual prescribing information for approved uses outside of the United States.
January 2014
This content was created by KnowledgePoint360 Group, LLC, and was not associated with funding via an educational grant or a
promotional/commercial interest.
46
Any pharmacologic agents discussed are approved for use in the United States by the U.S. Food and Drug Administration (FDA)
unless otherwise noted. Consult individual prescribing information for approved uses outside of the United States.
January 2014
This content was created by KnowledgePoint360 Group, LLC, and was not associated with funding via an educational grant or a
promotional/commercial interest.
47
Any pharmacologic agents discussed are approved for use in the United States by the U.S. Food and Drug Administration (FDA)
unless otherwise noted. Consult individual prescribing information for approved uses outside of the United States.
January 2014
This content was created by KnowledgePoint360 Group, LLC, and was not associated with funding via an educational grant or a
promotional/commercial interest.
48
January 2014
This content was created by KnowledgePoint360 Group, LLC, and was not associated with funding via an educational grant or a
promotional/commercial interest.
49
Any pharmacologic agents discussed are approved for use in the United States by the U.S. Food and Drug Administration (FDA)
unless otherwise noted. Consult individual prescribing information for approved uses outside of the United States.
January 2014
This content was created by KnowledgePoint360 Group, LLC, and was not associated with funding via an educational grant or a
promotional/commercial interest.
50
Refer to source document for full recommendations, including level of evidence rating.
Any pharmacologic agents discussed are approved for use in the United States by the U.S. Food and Drug Administration (FDA)
unless otherwise noted. Consult individual prescribing information for approved uses outside of the United States.
January 2014
This content was created by KnowledgePoint360 Group, LLC, and was not associated with funding via an educational grant or a
promotional/commercial interest.
51
Source: American
Diabetes Association.
Standards of medical care in diabetes2014.
Diabetes Care. 2014;37(suppl 1):S14-S80.
Refer to source document for full recommendations, including level of evidence rating.
January 2014
This content was created by KnowledgePoint360 Group, LLC, and was not associated with funding via an educational grant or a
promotional/commercial interest.