pre-IC11 Flashcards

1
Q

How many stages are there in T1DM? Which stage starts to become symptomatic?

A

3; Stage 3

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2
Q

Describe the pathophysiology of Type 1 DM

A

An absolute deficiency of pancreatic β-cell function

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3
Q

Describe the pathophysiology of Type 2 DM

A

Progressive loss of adequate β-cell insulin secretion on the background of insulin resistance

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4
Q

Signs and symptoms of hyperglycemia

A
  • extreme thirst (polydipsia)
  • hunger (polyphagia)
  • decreased healing
  • drowsiness
  • dry skin
  • frequent urination (polyuria)
  • blurred vision
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5
Q

Signs and symptoms of hypoglycemia

A
  • fast heartbeat
  • shaking
  • hunger
  • irritable
  • headache
  • dizziness
  • weakness fatigue
  • sweating
  • impaired vision
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6
Q

Diagnosis of DM

A

HbA1c 7% and above

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7
Q

Types of positive antibodies found in T1DM patients

A
  • islet cell autoantibodies and autoantibodies to GAD (GAD65)
  • insulin
  • tyrosine phosphatases IA-2 and IA-2b
  • zinc transporter 8 (ZnT8)
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8
Q

What substance is measured to prove absence of insulin in the body, and why is this measured instead of insulin?

A

C-peptide; insulin has a short half life

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9
Q

Explain insulin resistance

A

In the presence of insulin, glucose utilization is impaired and hepatic glucose output increased

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10
Q

Levels of glucose and insulin at an early stage of T2DM

A

Both elevated (hyperglycemia triggers insulin secretion)

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11
Q

Primary cause of Type 1 Vs Type 2 DM

A

T1: Autoimmune-mediated pancreatic beta-cell destruction; positive antibodies

T2: Insulin resistance, impaired insulin secretion, negative antibodies

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12
Q

Insulin production (C-peptide level) for Type 1 Vs Type 2 DM

A

T1: Absent
T2: Normal or abnormal

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13
Q

Age of onset for Type 1 Vs Type 2 DM

A

T1: Usually <30 years
T2: Often >40 years, although increasing prevalent in obese
children and younger adults

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14
Q

Onset of clinical presentation for Type 1 Vs Type 2 DM

A

T1: Abrupt
T2: Gradual

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15
Q

Physical appearance for Type 1 Vs Type 2 DM

A

T1: Often thin
T2: Often overweight

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16
Q

Proneness to ketosis for Type 1 Vs Type 2 DM

A

T1: Frequent
T2: Uncommon

17
Q

Onset and progress of hyperglycemia VS hypoglycemia

A

Hyper: gradual, may progress to diabetic coma
Hypo: sudden, may progress to insulin shock

18
Q

Measurement of fasting plasma glucose (FPG)

A

No calorie intake for ≥ 8hrs

19
Q

Measurement of Postprandial plasma glucose (PPG)

A

Glucose level measured after meal; usually after 2 hours

Can also be measured using a standardized 75-g oral glucose tolerance test (OGTT)

20
Q

Measurement of HbA1c

A

Measures the average amount of glucose in a person’s blood over the past 3 months.

HbA1c = Past 3 months Average of (FPG + PPG)

  • Glucose stays attached to hemoglobin for the lifespan of a red blood cell (~120 days)
21
Q

Contributor to high HbA1c

A

Greater extent contributed by fasting/ basal hyperglycemia

22
Q

Contributor to lower HbA1c

A

Greater extent contributed by postprandial hyperglycemia

23
Q

Frequency of glucometer use for T1DM, pregnant women, or insulin pump users

A
  • ≥ 4 times daily
  • Before meals/snacks, at bedtime, at 3 a.m.
24
Q

Frequency of glucometer use for T2DM

A
  • ≥ 3 times daily for patients on multiple injections of insulin
  • For patients using less frequent insulin injections, noninsulin therapies, or medical nutrition therapy alone, self monitoring of blood glucose (SMBG) may be useful as a guide to the success of therapy
25
Q

Frequency of glucometer use for practice setting

A

Patients are to check before breakfast (to see fasting glucose lvl) and 2hr after largest meal (2 times) (to see postprandial glucose)

26
Q

In the absence of diabetes risk factors, at what age should screening begin and how often should the screening be repeated?

A

40 y/o; every 3 years

27
Q

Significance of HbA1c of 6% and below

A

No diabetes

28
Q

Cutoff for 2h OGTT for diabetes

A

11.1 mmol/L and above

29
Q

Prevention of foot wound of diabetic patients

A

Maximizing Blood Glucose Control / Reduce risk factors
Self-Examination of the Foot
Foot Protection
Nail and Foot Care and Hygiene
Annual Foot Examination

30
Q

General DM medication adjustments during Ramadan

A

TDS to BD
* Reduce medications with high hypoglycemia potential
* Evening dose potency to be higher than morning

31
Q

Steps to Understanding patient views

A

Listen, Explain, Acknowledge, Recommend, Negotiate

32
Q

Most common causes of mild-to-moderate infections in diabetes

A

Gram positive cocci esp staphylococcus/ streptococcus

33
Q

Most common causes of chronic/severe infections

A

Mixed gram-positive cocci and gram-negative bacilli with or without anaerobic organisms

34
Q

TIME management for diabetic foot/ wound care

A
  • Tissue: Assessing for non-viable or necrotic tissue
  • Infection: Chronic wounds get “stuck” in inflammation due to bacteria
  • Moisture: Assessment and management of wound exudate
  • Edge of Wound: Assessment of non-advancing wound edges and condition of the periwound
35
Q

Risk factors for foot wounds in diabetes

A

Poor glycemic control
Peripheral artery disease
Peripheral neuropathy
Visual impairment
Smoking

35
Q

Risk factors for foot wounds in diabetes

A

Poor glycemic control
Peripheral artery disease
Peripheral neuropathy
Visual impairment
Smoking

36
Q

Can moisturiser be used btw toes?

A

No; may cause fungal infx

37
Q

Foot examination for PAD

A

Vascular assessment of pedal pulses

38
Q

Foot examination for peripheral neuropathy

A

Neurologic exam with monofilament