ada3 Flashcards

1
Q

Describe the characteristics of Metformin.

A

Metformin has high efficacy in lowering glucose levels, no cardiovascular effects, no renal effects, and a potential for weight loss. It is taken orally and has low cost. However, it is contraindicated in patients with an estimated glomerular filtration rate (eGFR) less than 30 mL/min.

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2
Q

What are the clinical considerations for Metformin?

A

When prescribing Metformin, clinicians should be aware of the potential for gastrointestinal side effects and consider slow dose titration, extended-release formulations, and administration with food to mitigate these effects. Regular monitoring for vitamin B12 deficiency is also recommended.

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3
Q

What are the characteristics of SGLT2 inhibitors?

A

SGLT2 inhibitors have intermediate efficacy in lowering glucose levels, no cardiovascular effects, no renal effects, and a potential for weight loss. They are taken orally and have high cost. However, they carry a risk of diabetic ketoacidosis (DKA) and genital mycotic infections. Renal dose considerations should be followed.

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4
Q

How do SGLT2 inhibitors affect glucose-lowering effect at lower eGFR?

A

The glucose-lowering effect of SGLT2 inhibitors is lower at lower eGFR. Therefore, caution should be exercised when using these medications in patients with reduced kidney function.

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5
Q

Describe the characteristics of GLP-1 RAs.

A

GLP-1 RAs have high to very high efficacy in lowering glucose levels, no cardiovascular effects, no renal effects, and a potential for weight loss. They can be administered subcutaneously or orally. However, there is a risk of thyroid C-cell tumors in rodents, and the human relevance is not determined. Renal dose considerations should be followed.

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6
Q

Describe the characteristics of GLP-1 RAs.

A

GLP-1 RAs have high to very high efficacy in lowering glucose levels, no cardiovascular effects, no renal effects, and a potential for weight loss. They can be administered subcutaneously or orally. However, there is a risk of thyroid C-cell tumors in rodents, and the human relevance is not determined. Renal dose considerations should be followed.

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7
Q

What are the clinical considerations for GLP-1 RAs?

A

When prescribing GLP-1 RAs, clinicians should monitor for thyroid C-cell tumors, counsel patients on potential gastrointestinal side effects, and provide guidance on dietary modifications to mitigate these effects. Renal function should be monitored when initiating or escalating doses in patients with renal impairment.

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8
Q

Describe the recommended glucose-lowering regimen for people with reduced estimated glomerular filtration rates (eGFR).

A

Table 10.3C and Section 10 recommend a glucose-lowering regimen independent of A1C, independent of metformin use, and considering person-specific factors.

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9
Q

What are the potential side effects associated with metformin use?

A

Metformin use is associated with vitamin B12 deficiency and worsening symptoms of neuropathy.

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10
Q

What are the potential side effects associated with metformin use?

A

Metformin use is associated with vitamin B12 deficiency and worsening symptoms of neuropathy.

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11
Q

What does the VERIFY trial suggest about initial combination therapy for type 2 diabetes?

A

The VERIFY trial suggests that initial combination therapy with metformin and the dipeptidyl peptidase 4 (DPP-4) inhibitor vildagliptin has a slower decline of glycemic control compared to metformin alone.

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12
Q

Define the term ‘glycemic targets’.

A

Glycemic targets refer to the desired levels of blood glucose control in individuals with diabetes.

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13
Q

How should medication choice be guided when selecting a glucose-lowering regimen?

A

Medication choice should be guided by efficacy in achieving individualized glycemic and weight management goals, avoidance of side effects, cost/access, and individual preferences.

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14
Q

How should medication choice be guided when selecting a glucose-lowering regimen?

A

Medication choice should be guided by efficacy in achieving individualized glycemic and weight management goals, avoidance of side effects, cost/access, and individual preferences.

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15
Q

Describe the principles in Figure 9.3 for pharmacologic approaches to glycemic treatment.

A

The principles in Figure 9.3 include reinforcement of behavioral interventions such as weight management and physical activity, as well as provision of DSMES (Diabetes Self-Management Education and Support) to meet individualized treatment goals.

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16
Q

What are the recommended injectable therapies to reduce A1C in most individuals prior to insulin?

A

GLP-1 RA (Glucagon-Like Peptide-1 Receptor Agonist) or GIP/GLP-1 RA (Glucose-Dependent Insulinotropic Polypeptide/Glucagon-Like Peptide-1 Receptor Agonist) are recommended prior to insulin in most individuals.

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17
Q

How should the basal insulin dose be initiated and titrated?

A

The basal insulin dose should be initiated at an appropriate starting dose for the selected agent and titrated to a maintenance dose. The specific starting and titration doses vary within the class of basal insulin.

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18
Q

When should prandial insulin be considered and how should it be dosed?

A

Prandial insulin should be considered if A1C remains above target and the individual is not already on a GLP-1 RA or dual GIP and GLP-1 RA. It can be dosed individually or mixed with NPH as appropriate, usually with the largest meal or the meal with the greatest postprandial glucose excursion.

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19
Q

Describe the pharmacologic approaches to glycemic treatment.

A

Pharmacologic approaches to glycemic treatment involve the use of medications such as insulin therapy, GLP-1 receptor agonists, and SGLT2 inhibitors to manage blood sugar levels in individuals with diabetes.

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20
Q

What are the benefits associated with GLP-1 receptor agonists?

A

GLP-1 receptor agonists have been shown to have greater efficacy and durability of glycemic treatment compared to NPH insulin. They also reduce the risk of symptomatic and nocturnal hypoglycemia.

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21
Q

How do longer-acting basal insulin analogs differ from U-100 glargine or detemir?

A

Longer-acting basal insulin analogs, such as U-300 glargine or degludec, have a lower hypoglycemia risk when used in combination with oral agents compared to U-100 glargine.

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22
Q

Define overbasalization in insulin therapy.

A

Overbasalization in insulin therapy refers to the excessive use of basal insulin, which can lead to high bedtime-morning or postprandial glucose differentials, hypoglycemia, and high variability in blood sugar levels.

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23
Q

Describe the impact of chronic kidney disease (CKD) on treatment choices for diabetes.

A

Chronic kidney disease (CKD) can impact treatment choices for diabetes. Some medications, such as SGLT2 inhibitors, have been shown to have beneficial effects on indices of CKD. Clinicians should consider CKD when selecting treatment options.

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24
Q

What is the median AWP of metformin 850 mg (IR)?

A

$106 ($5, $189)

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25
Q

Describe the dosage strength of glimepiride.

A

4 mg

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26
Q

What is the maximum approved daily dose of glyburide?

A

5 mg

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27
Q

Define NADAC.

A

National Average Drug Acquisition Cost

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28
Q

How much does a 30-day supply of dulaglutide 4.5 mg mL pen cost according to NADAC?

A

$852

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29
Q

Do SGLT2 inhibitors lower blood glucose levels?

A

Yes

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30
Q

Describe the dosage strength of exenatide (extended release).

A

2 mg powder for suspension or pen

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31
Q

What is the median NADAC of miglitol 100 mg?

A

NA

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32
Q

How much does a 30-day supply of bromocriptine 0.8 mg cost according to AWP?

A

$1,118

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33
Q

Describe the median cost of Lispro follow-on product in U-100 vial calculated as AWP.

A

The median cost of Lispro follow-on product in U-100 vial calculated as AWP is $118.

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34
Q

What is the median cost of Glulisine in U-100 prefilled pen calculated as NADAC?

A

The median cost of Glulisine in U-100 prefilled pen calculated as NADAC is $351.

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35
Q

How much does the U-500 prefilled pen of concentrated human regular insulin cost?

A

The U-500 prefilled pen of concentrated human regular insulin costs $230.

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36
Q

Do the AWP and NADAC data presented include vials of regular human insulin and NPH available at Walmart?

A

No, the AWP and NADAC data presented do not include vials of regular human insulin and NPH available at Walmart.

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37
Q

What is the recommended spirometry testing for individuals who smoke or recently stopped smoking?

A

All individuals require spirometry (FEV1) testing to identify potential lung disease.

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38
Q

When initiating combination injectable therapy, what medication should be maintained?

A

When initiating combination injectable therapy, metformin therapy should be maintained.

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39
Q

What adjunctive medication may help improve control and reduce the amount of insulin needed in individuals with suboptimal blood glucose control?

A

In individuals with suboptimal blood glucose control, especially those requiring large insulin doses, adjunctive use of a thiazolidinedione or an SGLT2 inhibitor may help to improve control and reduce the amount of insulin needed.

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40
Q

Describe the importance of dose titration in a basal-bolus insulin regimen.

A

Once a basal-bolus insulin regimen is initiated, dose titration is important, with adjustments made in both mealtime and basal insulins based on the blood glucose levels and an understanding of the individual’s glycemic goals.

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41
Q

What is the purpose of advancing to combination injectable therapy?

A

If basal insulin has been titrated to an acceptable fasting blood glucose level and A1C remains above target, advancing to combination injectable therapy can help improve glycemic control.

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42
Q

Describe the importance of dose titration in a basal-bolus insulin regimen.

A

Once a basal-bolus insulin regimen is initiated, dose titration is important, with adjustments made in both mealtime and basal insulins based on the blood glucose levels and an understanding of the individual’s glycemic goals.

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43
Q

What is the purpose of advancing to combination injectable therapy?

A

If basal insulin has been titrated to an acceptable fasting blood glucose level and A1C remains above target, advancing to combination injectable therapy can help improve glycemic control.

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44
Q

Describe the importance of dose titration in a basal-bolus insulin regimen.

A

Once a basal-bolus insulin regimen is initiated, dose titration is important, with adjustments made in both mealtime and basal insulins based on the blood glucose levels and an understanding of the individual’s glycemic goals.

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45
Q

What is the purpose of advancing to combination injectable therapy?

A

If basal insulin has been titrated to an acceptable fasting blood glucose level and A1C remains above target, advancing to combination injectable therapy can help improve glycemic control.

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46
Q

Describe the purpose of the study published in the Lancet Diabetes Endocrinol in 2017.

A

To evaluate the efficacy and safety of liraglutide added to insulin treatment in type 1 diabetes.

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47
Q

What is the duration of the multicenter trial of closed-loop control in type 1 diabetes published in the New England Journal of Medicine in 2019?

A

12 weeks.

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48
Q

Define metformin.

A

A medication commonly used for the treatment of type 2 diabetes that helps control blood sugar levels.

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49
Q

How long was the trial in which the long-term treatment with metformin in type 2 diabetes and methylmalonic acid was analyzed?

A

4.3 years.

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50
Q

Describe the aim of the DEPICT-1 trial.

A

To assess the efficacy and safety of dapagliflozin in patients with inadequately controlled type 1 diabetes.

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51
Q

What organization published the American Diabetes Association/JDRF Type 1 Diabetes Sourcebook?

A

American Diabetes Association.

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52
Q

Do the FDA warnings regarding the use of diabetes medicine metformin apply to all patients?

A

No, the warnings are specific to certain patients.

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53
Q

Describe the findings of the randomized trial published in Diabetes Care in 2016 regarding the efficacy and safety of liraglutide added to capped insulin treatment in subjects with type 1 diabetes.

A

The trial found that liraglutide added to capped insulin treatment improved glycemic control and was well-tolerated.

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54
Q

Describe the TITRATE study.

A

The TITRATE study assessed the efficacy and safety of patient-directed titration for achieving glycemic goals using a once-daily basal insulin analogue.

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55
Q

What is the purpose of the PIONEER 4 study?

A

The PIONEER 4 study aimed to compare the efficacy and safety of oral semaglutide versus subcutaneous liraglutide and placebo in type 2 diabetes.

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56
Q

Define network meta-analysis.

A

Network meta-analysis is a statistical technique that combines direct and indirect evidence from multiple studies to compare the effectiveness of different interventions.

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57
Q

How does insulin degludec compare to insulin glargine in the BEGIN Once Long trial?

A

The BEGIN Once Long trial found that insulin degludec was non-inferior to insulin glargine in terms of glycemic control in insulin-naive subjects with type 2 diabetes.

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58
Q

Describe the STAT study.

A

The STAT study investigated the efficacy of glucagon-like peptide-1 receptor agonist (GLP-1 RA) therapy in combination with titrated insulin glargine for glycemic control in patients with type 2 diabetes.

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59
Q

What is the purpose of the SURPASS-5 trial?

A

The SURPASS-5 trial aimed to compare the efficacy and safety of technosphere insulin versus insulin aspart in patients with type 2 diabetes over a 24-week period.

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60
Q

Define pharmacokinetics and pharmacodynamics.

A

Pharmacokinetics refers to the study of how a drug is absorbed, distributed, metabolized, and excreted by the body. Pharmacodynamics refers to the study of the drug’s effects on the body and the mechanisms of action.

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61
Q

How does LixiLan-L simplify insulin regimens?

A

LixiLan-L is a titratable fixed-ratio combination of insulin glargine and lixisenatide that simplifies insulin regimens by providing both basal and prandial insulin in a single injection.

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62
Q

What is the purpose of the American Diabetes Association (ADA) Standards of Care in Diabetes?

A

To provide clinical practice recommendations and tools for evaluating quality of care in diabetes.

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63
Q

What is the leading cause of morbidity and mortality for individuals with diabetes?

A

Atherosclerotic cardiovascular disease (ASCVD).

64
Q

What are the risk factors for ASCVD in individuals with diabetes?

A

Hypertension, dyslipidemia, and diabetes itself.

65
Q

Describe the relationship between controlling cardiovascular risk factors and ASCVD prevention in people with diabetes.

A

Controlling individual cardiovascular risk factors and addressing multiple risk factors simultaneously can prevent or slow the progression of ASCVD in people with diabetes.

66
Q

Where can readers comment on the ADA Standards of Care?

A

Readers can comment on the Standards of Care at professional.diabetes.org/SOC.

67
Q

Describe the relationship between controlling cardiovascular risk factors and ASCVD prevention in people with diabetes.

A

Controlling individual cardiovascular risk factors and addressing multiple risk factors simultaneously can prevent or slow the progression of ASCVD in people with diabetes.

68
Q

Where can readers comment on the ADA Standards of Care?

A

Readers can comment on the Standards of Care at professional.diabetes.org/SOC.

69
Q

What is the estimated annual cardiovascular-related spending associated with diabetes?

A

$37.3 billion.

70
Q

What is included in the ADA Standards of Care in Diabetes?

A

The ADA’s current clinical practice recommendations, components of diabetes care, general treatment goals and guidelines, and tools for evaluating quality of care.

71
Q

What is the role of the ADA Professional Practice Committee?

A

The committee is responsible for updating the Standards of Care annually or more frequently as warranted.

72
Q

What is the purpose of a risk calculator in cardiovascular disease management?

A

To assess the 10-year risk of a first ASCVD event and guide therapy.

73
Q

Describe the recommended approach to reducing the risk of diabetes-related complications.

A

A comprehensive approach that includes multiple evidence-based approaches to care.

74
Q

What are some modifiable risk factors for cardiovascular disease in people with diabetes?

A

Obesity/overweight, hypertension, dyslipidemia, smoking, and the presence of albuminuria.

75
Q

How does the overall risk prediction differ in people with and without diabetes?

A

The overall risk prediction does not differ, validating the use of risk calculators in people with diabetes.

76
Q

Define secondary prevention in the context of cardiovascular disease.

A

Secondary prevention refers to the management of individuals who are already at high risk for ASCVD.

77
Q

Describe the definition of hypertension.

A

Hypertension is defined as a systolic blood pressure of 130 mmHg or higher, or a diastolic blood pressure of 80 mmHg or higher, based on an average of 2 measurements obtained on 2 occasions.

78
Q

What is the blood pressure target for individuals with hypertension and diabetes?

A

The blood pressure target for individuals with hypertension and diabetes is <130/80 mmHg, if it can be safely attained.

79
Q

Define the Systolic Blood Pressure Intervention Trial (SPRINT).

A

The Systolic Blood Pressure Intervention Trial (SPRINT) demonstrated that treatment to a target systolic blood pressure of <120 mmHg decreases cardiovascular event rates by 25% in high-risk patients.

80
Q

How should blood pressure be measured during routine clinical visits?

A

Blood pressure should be measured in the seated position, with feet on the floor and arm supported at heart level, after 5 minutes of rest.

81
Q

Describe the blood pressure threshold for diagnosing hypertension in pregnant individuals with diabetes and chronic hypertension.

A

In pregnant individuals with diabetes and chronic hypertension, a blood pressure threshold of 140/90 mmHg is used for initiation or titration of therapy.

82
Q

Describe the blood pressure target for intensive treatment in patients with cardiovascular disease and increased cardiovascular risk.

A

The blood pressure target for intensive treatment in these patients is a systolic blood pressure of 110 to <130 mmHg.

83
Q

What was the primary composite outcome in the trial comparing intensive blood pressure treatment to standard treatment?

A

The primary composite outcome was stroke, acute coronary syndrome, acute decompensated heart failure, coronary revascularization, atrial fibrillation, or death from cardiovascular causes.

84
Q

What was the risk reduction in major cardiovascular events associated with achieving a mean blood pressure of 133/76 mmHg compared to 140/81 mmHg?

A

There was a 14% risk reduction in major cardiovascular events.

85
Q

Define hypotension and its occurrence in the intensive treatment group.

A

Hypotension is low blood pressure. It occurred more frequently in the intensive treatment group, with a rate of 3.4%.

86
Q

How did more intensive blood pressure reduction to <130 mmHg affect the risk of stroke?

A

More intensive blood pressure reduction to <130 mmHg was associated with a further reduction in stroke risk.

87
Q

Describe the population of the ACCORD BP trial.

A

4,733 participants with type 2 diabetes aged 40-79 years with prior evidence of cardiovascular disease or multiple cardiovascular risk factors.

88
Q

What were the SBP targets for the intensive and standard treatment groups in the ACCORD BP trial?

A

Intensive: <120 mmHg, Standard: 130-140 mmHg.

89
Q

What was the primary composite end point in the ACCORD BP trial?

A

A composite of nonfatal myocardial infarction, nonfatal stroke, and cardiovascular death.

90
Q

Describe the outcomes of the ACCORD BP trial.

A

No benefit in the primary end point. Stroke risk reduced 41% with intensive control, but not sustained through follow-up beyond the period of active treatment. Adverse events more common in the intensive group.

91
Q

What were the SBP targets for the intensive and standard treatment groups in the ACCORD BP trial?

A

Intensive: <120 mmHg, Standard: 130-140 mmHg.

92
Q

What was the primary composite end point in the ACCORD BP trial?

A

A composite of nonfatal myocardial infarction, nonfatal stroke, and cardiovascular death.

93
Q

Describe the outcomes of the ACCORD BP trial.

A

No benefit in the primary end point. Stroke risk reduced 41% with intensive control, but not sustained through follow-up beyond the period of active treatment. Adverse events more common in the intensive group.

94
Q

What were the SBP targets for the intensive and standard treatment groups in the ACCORD BP trial?

A

Intensive: <120 mmHg, Standard: 130-140 mmHg.

95
Q

What was the primary composite end point in the ACCORD BP trial?

A

A composite of nonfatal myocardial infarction, nonfatal stroke, and cardiovascular death.

96
Q

Describe the outcomes of the ACCORD BP trial.

A

No benefit in the primary end point. Stroke risk reduced 41% with intensive control, but not sustained through follow-up beyond the period of active treatment. Adverse events more common in the intensive group.

97
Q

What was the population of the ADVANCE trial?

A

11,140 participants with type 2 diabetes aged 55 years or older with prior evidence of cardiovascular disease or multiple cardiovascular risk factors.

98
Q

What was the intervention in the ADVANCE trial?

A

A single-pill, fixed-dose combination of perindopril and indapamide.

99
Q

What was the population of the ADVANCE trial?

A

11,140 participants with type 2 diabetes aged 55 years or older with prior evidence of cardiovascular disease or multiple cardiovascular risk factors.

100
Q

What was the intervention in the ADVANCE trial?

A

A single-pill, fixed-dose combination of perindopril and indapamide.

101
Q

What was the primary composite end point in the ADVANCE trial?

A

A composite of major macrovascular and microvascular events, death from any cause, and death from cardiovascular disease.

102
Q

Describe the outcomes of the ADVANCE trial.

A

Intervention reduced the risk of the primary composite end point by 9%. Reduction in risk of death in the intervention group attenuated but still significant during the 6-year observational follow-up.

103
Q

What was the primary composite end point in the ADVANCE trial?

A

A composite of major macrovascular and microvascular events, death from any cause, and death from cardiovascular disease.

104
Q

Describe the outcomes of the ADVANCE trial.

A

Intervention reduced the risk of the primary composite end point by 9%. Reduction in risk of death in the intervention group attenuated but still significant during the 6-year observational follow-up.

105
Q

What was the population of the HOT trial?

A

18,790 participants, including 1,501 with diabetes.

106
Q

What was the DBP target for the intensive and standard treatment groups in the HOT trial?

A

Intensive: <80 mmHg, Standard: <90 mmHg.

107
Q

What was the population of the HOT trial?

A

18,790 participants, including 1,501 with diabetes.

108
Q

What was the DBP target for the intensive and standard treatment groups in the HOT trial?

A

Intensive: <80 mmHg, Standard: <90 mmHg.

109
Q

What was the cardiovascular benefit observed in the HOT trial?

A

In the subpopulation with diabetes, an intensive DBP target was associated with a significantly reduced risk (51%) of cardiovascular disease events.

110
Q

What was the population of the SPRINT trial?

A

9,361 participants without diabetes.

111
Q

What was the cardiovascular benefit observed in the HOT trial?

A

In the subpopulation with diabetes, an intensive DBP target was associated with a significantly reduced risk (51%) of cardiovascular disease events.

112
Q

What was the population of the SPRINT trial?

A

9,361 participants without diabetes.

113
Q

What was the SBP target for the intensive and standard treatment groups in the SPRINT trial?

A

Intensive: <120 mmHg, Standard: <140 mmHg.

114
Q

What was the cardiovascular benefit observed in the HOT trial?

A

In the subpopulation with diabetes, an intensive DBP target was associated with a significantly reduced risk (51%) of cardiovascular disease events.

115
Q

What was the population of the SPRINT trial?

A

9,361 participants without diabetes.

116
Q

What was the SBP target for the intensive and standard treatment groups in the SPRINT trial?

A

Intensive: <120 mmHg, Standard: <140 mmHg.

117
Q

What was the primary composite outcome in the SPRINT trial?

A

A composite of myocardial infarction, acute coronary syndrome, stroke, heart failure, and death due to cardiovascular disease.

118
Q

What was the outcome of intensive therapy in the SPRINT trial?

A

Intensive therapy lowered the risk of the primary composite outcome by 25% and reduced the risk of death by 27%. However, it increased the risks of electrolyte abnormalities and acute kidney injury.

119
Q

What was the population of the STEP trial?

A

8,511 participants aged 60-80 years, including 1,627 with diabetes.

120
Q

What was the SBP target for the intensive and standard treatment groups in the STEP trial?

A

Intensive: <130 mmHg, Standard: <150 mmHg.

121
Q

What was the primary composite outcome in the STEP trial?

A

A composite of stroke, acute coronary syndrome (acute myocardial infarction and hospitalization for unstable angina).

122
Q

What was the outcome of intensive therapy in the STEP trial?

A

Intensive therapy lowered the risk of the primary composite outcome by 26%.

123
Q

What is the recommended blood pressure range during pregnancy to reduce the risk of accelerated maternal hypertension?

A

110-135/85 mmHg

124
Q

What are the contraindicated medications for pregnant individuals with diabetes and hypertension?

A

ACE inhibitors, angiotensin receptor blockers (ARBs), and spironolactone

125
Q

Describe the lifestyle therapy for hypertension treatment.

A

It consists of reducing excess body weight through caloric restriction and engaging in at least 150 min of moderate-intensity aerobic activity per week.

126
Q

What is the purpose of controlling blood pressure in pregnant individuals with diabetes?

A

To reduce the risk of accelerated maternal hypertension and minimize impairment of fetal growth.

127
Q

How does lifestyle management contribute to hypertension treatment?

A

It lowers blood pressure, enhances the effectiveness of some antihypertensive medications, promotes metabolic and vascular health, and generally has few adverse effects.

128
Q

What are the potential adverse effects of using ACE inhibitors, ARBs, and spironolactone during pregnancy?

A

They may cause fetal damage.

129
Q

Describe the findings of a 2014 Cochrane systematic review on antihypertensive therapy in pregnant individuals with diabetes.

A

The review did not find any conclusive evidence for or against blood pressure treatment to reduce the risk of preeclampsia for the mother or effects on fetal growth.

130
Q

What is the recommended duration of moderate-intensity aerobic activity per week for hypertension treatment?

A

At least 150 minutes

131
Q

Describe the initial blood pressure threshold for starting treatment in people with confirmed hypertension and diabetes.

A

Initial BP 140/90 mmHg or Initial BP 160/100 mmHg.

132
Q

What are the two options for starting treatment if the blood pressure is below 160/100 mmHg in people with confirmed hypertension and diabetes?

A

Start one agent or Start two agents.

133
Q

When should an ACE inhibitor or angiotensin receptor blocker (ARB) be strongly recommended for treating hypertension in people with diabetes?

A

For individuals with urine albumin-to-creatinine ratio 300 mg/g creatinine.

134
Q

What is the preferred type of diuretic for reducing cardiovascular events in people with diabetes and hypertension?

A

Thiazide-like diuretic; long-acting agents such as chlorthalidone and indapamide.

135
Q

What is the recommended blood pressure goal for individuals with diabetes and hypertension?

A

<130/80 mmHg.

136
Q

What is the first-line therapy for hypertension in people with diabetes and coronary artery disease?

A

ACE inhibitors or angiotensin receptor blockers (ARBs).

137
Q

What is the recommended approach if blood pressure is not meeting the target or there are adverse effects on two agents in people with diabetes and hypertension?

A

Consider addition of a mineralocorticoid receptor antagonist or refer to a specialist with expertise in blood pressure management.

138
Q

How many drug classes are generally required to achieve blood pressure control in people with diabetes and hypertension?

A

Multiple-drug therapy is generally required.

139
Q

How many drug classes are generally required to achieve blood pressure control in people with diabetes and hypertension?

A

Multiple-drug therapy is generally required.

140
Q

What is the recommended first-line treatment for hypertension in people with diabetes and urinary albumin-to-creatinine ratio of 300 mg/g creatinine or 30-299 mg/g creatinine?

A

An ACE inhibitor or angiotensin receptor blocker, at the maximum tolerated dose, indicated for blood pressure treatment.

141
Q

Describe resistant hypertension.

A

Resistant hypertension is defined as blood pressure 140/90 mmHg despite a therapeutic strategy that includes appropriate lifestyle management plus a diuretic and two other antihypertensive drugs with complementary mechanisms of action at adequate doses.

142
Q

Describe resistant hypertension.

A

Resistant hypertension is defined as blood pressure 140/90 mmHg despite a therapeutic strategy that includes appropriate lifestyle management plus a diuretic and two other antihypertensive drugs with complementary mechanisms of action at adequate doses.

143
Q

What is the risk of progressive kidney disease in patients with reduced glomerular filtration who are at increased risk of hyperkalemia and AKI?

A

The risk of progressive kidney disease is low in the absence of albuminuria, and ACE inhibitors and ARBs have not been found to afford superior cardioprotection.

144
Q

What is the risk of progressive kidney disease in patients with reduced glomerular filtration who are at increased risk of hyperkalemia and AKI?

A

The risk of progressive kidney disease is low in the absence of albuminuria, and ACE inhibitors and ARBs have not been found to afford superior cardioprotection.

145
Q

How can combinations of ACE inhibitors and angiotensin receptor blockers provide cardiovascular benefit without significantly increasing the risk of end-stage kidney disease?

A

Continuation of ACE inhibitor or ARB therapy as kidney function declines to estimated glomerular filtration rate (eGFR) <30 mL/min/1.73 may provide cardiovascular benefit without significantly increasing the risk of end-stage kidney disease.

146
Q

Define multiple-drug therapy in the context of hypertension treatment.

A

Multiple-drug therapy is often required to achieve blood pressure targets, particularly in the setting of diabetic kidney disease. It involves using a combination of antihypertensive drugs with complementary mechanisms of action at adequate doses.

147
Q

Describe the Mediterranean diet and its application in cardiovascular disease and risk management.

A

The Mediterranean diet is a dietary pattern that emphasizes the consumption of fruits, vegetables, whole grains, legumes, nuts, and olive oil. It also includes moderate intake of fish, poultry, and dairy products, while limiting red meat and processed foods. This diet has been shown to reduce the risk of cardiovascular disease in people with diabetes.

148
Q

What is the recommended frequency for obtaining a lipid profile in people with diabetes aged 40-75 at higher cardiovascular risk?

A

A lipid profile should be obtained at initiation of statins or other lipid-lowering therapy, 4-12 weeks after initiation or a change in therapy, and annually thereafter.

149
Q

Define high-intensity statin therapy and its role in reducing LDL cholesterol in people with diabetes.

A

High-intensity statin therapy refers to the use of statin medications at a higher dose to achieve a greater reduction in LDL cholesterol levels. It is recommended to reduce LDL cholesterol by > 50% of baseline and target an LDL cholesterol goal of <70 mg/dL in people with diabetes at higher cardiovascular risk.

150
Q

How can lifestyle therapy be intensified and glycemic control optimized for patients with elevated triglyceride levels in diabetes?

A

Lifestyle therapy can be intensified by promoting weight loss, increasing physical activity, and optimizing dietary choices. Additionally, glycemic control should be optimized through medication adjustments and adherence to prescribed treatment plans.

151
Q

Describe the recommended approach for lipid management in adults with diabetes aged >75 years already on statin therapy.

A

It is reasonable to continue statin treatment in adults with diabetes aged >75 years who are already on statin therapy. This approach helps to maintain lipid management and reduce the risk of cardiovascular disease.

152
Q

What is the recommended statin therapy for people with diabetes who are 75 years of age?

A

Moderate-intensity statin therapy

153
Q

Describe the evidence for the benefits of lipid-lowering therapy in older people with diabetes.

A

The relative benefit of lipid-lowering therapy has been uniform across most subgroups tested, including older age groups.

154
Q

What is the recommended statin therapy for people with diabetes who have known ASCVD and/or very high LDL cholesterol levels?

A

High-intensity statin therapy

155
Q

How should statin therapy be initiated in people with type 2 diabetes based on risk?

A

Statin therapy should be initiated based on risk, with downward titration of dose performed as needed.

156
Q

What is the recommended statin therapy for primary prevention in people without ASCVD?

A

Moderate-dose statin therapy