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2
 Published annually in Clinical Diabetes
 Contains evidence-based recommendations most pertinent to primary care
 Recommendations are substantively the same as in the complete Standards of Care
 Access:
 Abridged Standards of Care — diabetesjournals.org/clinical
 Complete Standards of Care and all supporting references — professional.diabetes.org/standards
Abridged for Primary Care Professionals
STANDARDS OF CARE IN DIABETES 2024
Section 1
Improving Care and
Promoting Health in Populations
4
A multifaceted approach encompassing patient-level, system-level, and policy-level interventions is crucial for enhancing population health
in the context of diabetes. This approach may include the following key elements.
Improving Care and Promoting Health in Populations
STANDARDS OF CARE: SECTION 1
Section 2
Diagnosis and Classification of Diabetes
6
Diagnostic Tests for Diabetes
STANDARDS OF CARE: SECTION 2
7
Classification
STANDARDS OF CARE: SECTION 2
Classification of diabetes type is not always straightforward at presentation, and misdiagnosis is common.
8
Screening Criteria for Prediabetes and Type 2
Diabetes
STANDARDS OF CARE: SECTION 2
Informal assessment of risk
factors
Validated risk calculator
9
STANDARDS OF CARE: SECTION 2
Informal Risk Factor Assessment for Prediabetes
and Type 2 Diabetes
10
Additional Screening Guidelines
STANDARDS OF CARE: SECTION 2
Section 3
Prevention or Delay of Diabetes and
Associated Comorbidities
12
Diet and Physical Activity Recommendations for
Adults at Risk for Type 2 Diabetes
STANDARDS OF CARE: SECTION 3
13
STANDARDS OF CARE: SECTION 3
Person-Centered Care Goals for
Individuals at Risk of Type 2 Diabetes
14
STANDARDS OF CARE: SECTION 3
15
STANDARDS OF CARE: SECTION 3
16
Staging of Type 1 Diabetes
STANDARDS OF CARE: SECTION 3
Section 4
Comprehensive Medical Evaluation
and Assessment of Comorbidities
18
STANDARDS OF CARE: SECTION 4
Assessment of Comorbidities
19
STANDARDS OF CARE: SECTION 4
20
STANDARDS OF CARE: SECTION 4
21
STANDARDS OF CARE: SECTION 4
22
STANDARDS OF CARE: SECTION 4
Proposed Algorithm for Risk Stratification in Individuals with NAFLD or NASH.
23
STANDARDS OF CARE: SECTION 4
24
STANDARDS OF CARE: SECTION 4
Components of the Comprehensive Diabetes Medical Evaluation at Initial, Follow-Up, and Annual Visits
25
STANDARDS OF CARE: SECTION 4
Components of the Comprehensive Diabetes Medical Evaluation at Initial, Follow-Up, and Annual Visits
26
STANDARDS OF CARE: SECTION 4
Components of the Comprehensive Diabetes Medical Evaluation at Initial, Follow-Up, and Annual Visits
27
STANDARDS OF CARE: SECTION 4
Components of the Comprehensive Diabetes Medical Evaluation at Initial, Follow-Up, and Annual Visits
Section 5
Facilitating Positive Health Behaviors and
Well-Being to Improve Health Outcomes
29
STANDARDS OF CARE: SECTION 5
Building positive health behaviors and maintaining psychological well-being are foundational for achieving diabetes
management goals and maximizing quality of life.
30
STANDARDS OF CARE: SECTION 5
31
STANDARDS OF CARE: SECTION 5
Psychosocial Care for All People With Diabetes:
Considerations and Recommendations
32
STANDARDS OF CARE: SECTION 5
Psychosocial Care for All People With Diabetes:
Considerations and Recommendations
33
STANDARDS OF CARE: SECTION 5
34
STANDARDS OF CARE: SECTION 5
MNT
There is a no one-size-fits-all eating pattern. Successful MNT programs are:
35
STANDARDS OF CARE: SECTION 5
36
STANDARDS OF CARE: SECTION 5
37
STANDARDS OF CARE: SECTION 5
38
STANDARDS OF CARE: SECTION 5
Section 6
Glycemic Goals and Hypoglycemia
40
STANDARDS OF CARE: SECTION 6
41
STANDARDS OF CARE: SECTION 6
42
STANDARDS OF CARE: SECTION 6
Glucose Assessment via CGM:
The Ambulatory Glucose Profile (AGP) Report
43
STANDARDS OF CARE: SECTION 6
Glucose Assessment via CGM:
The Ambulatory Glucose Profile (AGP) Report
44
STANDARDS OF CARE: SECTION 6
45
STANDARDS OF CARE: SECTION 6
46
STANDARDS OF CARE: SECTION 6
47
STANDARDS OF CARE: SECTION 6
Hypoglycemia Assessment, Prevention, and Treatment
48
STANDARDS OF CARE: SECTION 6
Hypoglycemia Assessment, Prevention, and Treatment
Section 7
Diabetes Technology
50
STANDARDS OF CARE: SECTION 7
51
STANDARDS OF CARE: SECTION 7
52
STANDARDS OF CARE: SECTION 7
53
STANDARDS OF CARE: SECTION 7
54
STANDARDS OF CARE: SECTION 7
55
STANDARDS OF CARE: SECTION 7
Section 8
Obesity and Weight Management for the
Prevention and Treatment of Type 2 Diabetes
57
STANDARDS OF CARE: SECTION 8
58
STANDARDS OF CARE: SECTION 8
59
STANDARDS OF CARE: SECTION 8
60
STANDARDS OF CARE: SECTION 8
61
STANDARDS OF CARE: SECTION 8
62
STANDARDS OF CARE: SECTION 8
Section 9
Pharmacologic Approaches to
Glycemic Treatment
64
STANDARDS OF CARE: SECTION 9
65
STANDARDS OF CARE: SECTION 9
66
STANDARDS OF CARE: SECTION 9 Use of Glucose-Lowering Medications in the
Management of Type 2 Diabetes
67
STANDARDS OF CARE: SECTION 9
Section 10
Cardiovascular Disease and Risk Management
69
STANDARDS OF CARE: SECTION 10
70
STANDARDS OF CARE: SECTION 10
71
STANDARDS OF CARE: SECTION 10
72
STANDARDS OF CARE: SECTION 10
73
STANDARDS OF CARE: SECTION 10
74
STANDARDS OF CARE: SECTION 10
Section 11
Chronic Kidney Disease and Risk Management
76
STANDARDS OF CARE: SECTION 11
77
STANDARDS OF CARE: SECTION 11
78
STANDARDS OF CARE: SECTION 11
79
STANDARDS OF CARE: SECTION 11
80
STANDARDS OF CARE: SECTION 11
Section 12
Retinopathy, Neuropathy, and Foot Care
82
STANDARDS OF CARE: SECTION 12
83
STANDARDS OF CARE: SECTION 12
84
STANDARDS OF CARE: SECTION 12
85
STANDARDS OF CARE: SECTION 12
86
STANDARDS OF CARE: SECTION 12
Neuropathy
Treatment
 Various drugs may reduce pain from DPN, and both drug and non-drug strategies may
ease symptoms of DPN and autonomic neuropathy.
 The safest and most evidence-based pharmacologic options for DPN include
gabapentinoids, serotonin-norepinephrine reuptake inhibitors, tricyclic antidepressants,
and sodium channel blockers.
 Refer to a neurologist or pain specialist when pain control is not achieved within the
scope of practice of the treating clinician.
87
STANDARDS OF CARE: SECTION 12
88
STANDARDS OF CARE: SECTION 12
Section 13
Older Adults
90
STANDARDS OF CARE: SECTION 13
91
STANDARDS OF CARE: SECTION 13
Simplification of Complex Insulin Therapy
Section 14
Children and Adolescents
93
STANDARDS OF CARE: SECTION 14
94
STANDARDS OF CARE: SECTION 14
95
STANDARDS OF CARE: SECTION 14
Addressing Probable New
Cases of Type 2 Diabetes in
Youth
Section 15
Management of Diabetes in Pregnancy
97
STANDARDS OF CARE: SECTION 15
98
STANDARDS OF CARE: SECTION 15
99
STANDARDS OF CARE: SECTION 15
100
STANDARDS OF CARE: SECTION 15
101
STANDARDS OF CARE: SECTION 15
Section 16
Diabetes Care in the Hospital
103
STANDARDS OF CARE: SECTION 16
104
STANDARDS OF CARE: SECTION 16
105
STANDARDS OF CARE: SECTION 16
106
STANDARDS OF CARE: SECTION 16
Summary of Revisions: Standards of Care in Diabetes—2024

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Summary of Revisions: Standards of Care in Diabetes—2024

Editor's Notes

  1. • There is insufficient evidence to support the use of continuous glucose monitoring for screening or diagnosing prediabetes or diabetes. • In the absence of unequivocal hyperglycemia (e.g., hyperglycemic crisis), diagnosis of type 2 diabetes requires confirmatory testing, which can be a different test on the same day or the same test on a different day. • Marked discordance between A1C and repeated blood glucose measurements should raise the possibility of a problem or interference with either test.
  2. Does statin therapy increase the risk of developing type 2 diabetes? • Statin therapy may slightly elevate type 2 diabetes risk in high-risk individuals. • In primary and secondary prevention of cardiovascular disease, statin benefits outweigh diabetes risk. • Discontinuing statins based on concerns about increased diabetes risk is not advised. Does pioglitazone have a role in secondary cardiovascular prevention in people at risk for type 2 diabetes? Pioglitazone could reduce stroke and myocardial infarction risks in people with a history of stroke and evidence of insulin resistance or prediabetes. However, the benefit must be weighed against potential weight gain, edema, and increased fracture risk. Lower doses may lessen these adverse effects.
  3. Diabetes treatment goals aim to prevent or delay complications and optimize quality of life. These goals should be developed collaboratively with people with diabetes to honor their preferences and values. Comprehensive diabetes care should be provided by an interprofessional team which may include but is not limited to diabetes care and education specialists, primary care and subspecialty clinicians, nurses, registered dietitian nutritionists, exercise specialists, pharmacists, dentists, podiatrists, behavioral health professionals, and community partners such as community health workers and community paramedics. Ongoing treatment necessitates regular follow-up and the active engagement of people with diabetes and their care partners. Comprehensive medical evaluations (described in the table below) and the provision of all recommended vaccinations (cdc.gov/vaccines) are essential components of ongoing diabetes care.
  4. ABI, ankle-brachial pressure index; ARBs, angiotensin receptor blockers; CGM, continuous glucose monitors; MDI, multiple daily injections; NAFLD, nonalcoholic fatty liver disease; OSA, obstructive sleep apnea; PAD, peripheral arterial disease. *At 65 years of age or older. +May be needed more frequently in people with diabetes with known chronic kidney disease or with changes in medications that affect kidney function and serum potassium #May also need to be checked after initiation or dose changes of medications that affect these laboratory values (i.e., diabetes medications, blood pressure medications, cholesterol medications, or thyroid medications). ^In people without dyslipidemia and not on cholesterol-lowering therapy, testing may be less frequent. **Should be performed at every visit in people with diabetes with sensory loss, previous foot ulcers, or amputations.
  5. ABI, ankle-brachial pressure index; ARBs, angiotensin receptor blockers; CGM, continuous glucose monitors; MDI, multiple daily injections; NAFLD, nonalcoholic fatty liver disease; OSA, obstructive sleep apnea; PAD, peripheral arterial disease. *At 65 years of age or older. +May be needed more frequently in people with diabetes with known chronic kidney disease or with changes in medications that affect kidney function and serum potassium #May also need to be checked after initiation or dose changes of medications that affect these laboratory values (i.e., diabetes medications, blood pressure medications, cholesterol medications, or thyroid medications). ^In people without dyslipidemia and not on cholesterol-lowering therapy, testing may be less frequent. **Should be performed at every visit in people with diabetes with sensory loss, previous foot ulcers, or amputations.
  6. ABI, ankle-brachial pressure index; ARBs, angiotensin receptor blockers; CGM, continuous glucose monitors; MDI, multiple daily injections; NAFLD, nonalcoholic fatty liver disease; OSA, obstructive sleep apnea; PAD, peripheral arterial disease. *At 65 years of age or older. +May be needed more frequently in people with diabetes with known chronic kidney disease or with changes in medications that affect kidney function and serum potassium #May also need to be checked after initiation or dose changes of medications that affect these laboratory values (i.e., diabetes medications, blood pressure medications, cholesterol medications, or thyroid medications). ^In people without dyslipidemia and not on cholesterol-lowering therapy, testing may be less frequent. **Should be performed at every visit in people with diabetes with sensory loss, previous foot ulcers, or amputations.
  7. ABI, ankle-brachial pressure index; ARBs, angiotensin receptor blockers; CGM, continuous glucose monitors; MDI, multiple daily injections; NAFLD, nonalcoholic fatty liver disease; OSA, obstructive sleep apnea; PAD, peripheral arterial disease. *At 65 years of age or older. +May be needed more frequently in people with diabetes with known chronic kidney disease or with changes in medications that affect kidney function and serum potassium #May also need to be checked after initiation or dose changes of medications that affect these laboratory values (i.e., diabetes medications, blood pressure medications, cholesterol medications, or thyroid medications). ^In people without dyslipidemia and not on cholesterol-lowering therapy, testing may be less frequent. **Should be performed at every visit in people with diabetes with sensory loss, previous foot ulcers, or amputations.
  8. Hypoglycemia is categorized into three levels based on blood glucose concentrations and symptom severity. Level 1 is glucose <70 mg/dL (<3.9 mmol/L) but ≥54 mg/dL (≥3.0 mmol/L). Level 2 is glucose <54 mg/dL (<3.0 mmol/L). Level 3 is a severe event characterized by altered mental and/or physical status requiring assistance for treatment of hypoglycemia, irrespective of glucose level.
  9. Hypoglycemia is categorized into three levels based on blood glucose concentrations and symptom severity. Level 1 is glucose <70 mg/dL (<3.9 mmol/L) but ≥54 mg/dL (≥3.0 mmol/L). Level 2 is glucose <54 mg/dL (<3.0 mmol/L). Level 3 is a severe event characterized by altered mental and/or physical status requiring assistance for treatment of hypoglycemia, irrespective of glucose level.
  10. Learn More Section 7 of the complete ADA Standards of Care in Diabetes—2024 includes a wealth of additional information on blood glucose meters, evidence supporting the use of CGM, various insulin delivery systems, and digital health apps and online programs.
  11. * In people with HF, CKD, established CVD, or multiple risk factors for CVD, the decision to use a GLP-1 RA or SGLT2i with proven benefit should be independent of background use of metformin;† A strong recommendation is warranted for people with CVD and a weaker recommendation for those with indicators of high CV risk. Moreover, a higher absolute risk reduction and thus lower numbers needed to treat are seen at higher levels of baseline risk and should be factored into the shared decision-making process. See text for details; ^ Low-dose TZD may be better tolerated and similarly effective; § For SGLT2i, CV/renal outcomes trials demonstrate their efficacy in reducing the risk of composite MACE, CV death, all-cause mortality, MI, HHF, and renal outcomes in individuals with T2D with established/high risk of CVD; # For GLP-1 RA, CVOTs demonstrate their efficacy in reducing composite MACE, CV death, all-cause mortality, MI, stroke, and renal endpoints in individuals with T2D with established/high risk of CVD. ACEi, angiotensin-converting enzyme inhibitor; ACR, albumin-to-creatinine ratio; ARB, angiotensin receptor blocker; ASCVD, atherosclerotic cardiovascular disease; CGM, continuous glucose monitoring; CKD, chronic kidney disease; CV, cardiovascular; CVD, cardiovascular disease; CVOT, cardiovascular outcomes trial; DPP-4i, dipeptidyl peptidase 4 inhibitor; eGFR, estimated glomerular filtration rate; GLP-1 RA, glucagon-like peptide 1 receptor agonist; dual GIP/GLP-1 RA, dual glucose-dependent insulinotropic polypeptide and glucagon-like peptide 1 receptor agonist; HF, heart failure; HFpEF, heart failure with preserved ejection fraction; HFrEF, heart failure with reduced ejection fraction; HHF, hospitalization for heart failure; MACE, major adverse cardiovascular events; MI, myocardial infarction; SDOH, social determinants of health; SGLT2i, sodium-glucose cotransporter 2 inhibitor; T2D, type 2 diabetes; TZD, thiazolidinedione. Adapted from Davies MJ, D’Alessio DA, Fradkin J, et al. Management of hyperglycemia in type 2 diabetes, 2018: a consensus report by the American Diabetes Association (ADA) and the European Association for the Study of Diabetes (EASD). Diabetes Care 2018;41:2669–2701.
  12. Atherosclerotic cardiovascular disease (ASCVD), encompassing coronary heart disease, cerebrovascular disease, and peripheral artery disease (PAD) presumed to be of atherosclerotic origin, is the primary cause of morbidity and mortality in individuals with diabetes, leading to significant health care costs. Managing multiple risk factors simultaneously can prevent or slow the progression of ASCVD. Heart failure is another major cause of morbidity and mortality from cardiovascular disease. Legend: *An ACE inhibitor (ACEi) or angiotensin receptor blocker (ARB) is suggested to treat hypertension for people with coronary artery disease (CAD) or urine albumin-to-creatinine ratio (UACR) 30–299 mg/g creatinine and strongly recommended for individuals with UACR ≥300 mg/g creatinine. †Dihydropyridine calcium channel blocker (CCB). ‡Thiazide-like diuretic; long-acting agents shown to reduce cardiovascular events, such as chlorthalidone and indapamide, are preferred. BP, blood pressure. Adapted from de Boer IH, Bangalore S, Benetos A, et al. Diabetes and hypertension: a position statement by the American Diabetes Association. Diabetes Care 2017;40:1273–1284
  13. eGFR is presented in units of mL/min/1.73 m2. *ACEi or ARB (at maximal tolerated doses) should be first-line therapy for hypertension when albuminuria is present. Otherwise, dihydropyridine CCB or diuretic can also be considered; all three classes are often needed to attain BP targets. †Finerenone is currently the only nonsteroidal MRA with proven clinical kidney and cardiovascular benefits. ACEi, ACE inhibitor; ACR, albumin-to creatinine ratio; ARB, angiotensin receptor blocker; ASCVD, atherosclerotic cardiovascular disease; BP, blood pressure; CCB, calcium channel blocker; CVD, cardiovascular disease; GLP-1 RA, glucagon-like peptide 1 receptor agonist; HTN, hypertension; MRA, mineralocorticoid receptor antagonist; PCSK9i, proprotein convertase subtilisin/kexin type 9 inhibitor; RAS, renin- angiotensin system; SGLT2i, sodium–glucose cotransporter 2 inhibitor; T1D, type 1 diabetes; T2D, type 2 diabetes. Adapted from 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). Diabetes Care 2022;45:3075–3090.
  14. Algorithm to simplify insulin plans for older adults with type 2 diabetes. eGFR, estimated glomerular filtration rate. *Basal insulins: glargine U-100 and U-300, detemir, degludec, and human NPH. †Prandial insulins: short-acting (regular human insulin) or rapid-acting (lispro, aspart, and glulisine). ‡Premixed insulins: 70/30, 75/25, and 50/50 products. §Examples of noninsulin agents include metformin, sodium–glucose cotransporter 2 inhibitors, dipeptidyl peptidase 4 inhibitors, and glucagon-like peptide 1 receptor agonists. ||See previous page for more information. Adapted with permission from Munshi MN, Slyne C, Segal AR, Saul N, Lyons C, Weinger K. Simplification of insulin regimen in older adults and risk of hypoglycemia. JAMA Intern Med 2016;176:1023–1025.
  15. Management of new-onset diabetes in you with overweight or obesity with clinical suspicion of type 2 diabetes. A1C 8.5% = 69 mmol/mol. Adapted from Arslanian S, Bacha F, Grey M, Marcus MD, White NH, Zeitler P. Evaluation and management of youth-onset type 2 diabetes: a position statement by the American Diabetes Association. Diabetes Care 2018;41:2648–2668. BGM, blood glucose monitoring; DKA, diabetic ketoacidosis: HHNK, hyperosmolar hyperglycemic nonketotic syndrome; IV, intravenous; MDI, multiple daily injection.
  16. The preconception care of people with diabetes is detailed in Table 15.1 in the complete ADA Standards of Care in Diabetes—2024.