Final (new information) Flashcards

1
Q

What are the 4 criteria for diagnosing diabetes

A

1) A1C ≥ 6.5%
2) FPG ≥ 126mg/dL (7.0mmol/L)
3) 2-h plasma glucose ≥ 200mg/dL(11.1 mmol/L) after eating 75g of anhydrous glucose dissolved in water
4) Random plasma glucose level ≥200mg/dL (11.1mmol/L) PLUS symptoms of hyperglycemia or hyperglycemic crisis

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2
Q

What are some diseases of the exocrine pancreas that can lead to diabetes?

A

Pancreatitis
Cystic fibrosis
Hemochromatosis

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3
Q

What are some endocrinopathies that can lead to diabetes?

A

Acromegaly
Cushing’s syndrome
Pheochromocytoma
Hyperthyroidism

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4
Q

T/F Diabetes can have drug or chemical induced etiology.

A

True

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5
Q

What is the cause of type I diabetes

A

Loss of pancreatic beta cells

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6
Q

What are the classic symptoms of diabetes

A

Polyuria (Peeing a lot)
Polydipsia (Increased thirst)
Weight loss
Polyphagia (Increased hunger)

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7
Q

What is the cause of ketoacidosis in diabetics?

A

Grossly deficient insulin levels:

1) Lapse in insulin medication
2) Acute infection or trauma that causes a loss of insulin

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8
Q

What can be smelled on the breath of a patient with ketoacidosis?

A

Acetone

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9
Q

What is metabolic syndrome/insulin resistance syndrome?

A

It is the clustering of risk factors for type II DM and cardiovascular disease.

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10
Q

What are the risk factors for metabolic acidosis/Insulin resistance syndrome?

A

1) Excess abdominal fat: apple shaped (>40 inch waist for males, >30 inch waist for females)
2) Insulin resistance (>100 fasting glucose)
3) Elevated serum triglycerides (>150mg/dL)
4) Decreased HDL (

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11
Q

What is the condition that clusters the risk factors for Type II diabetes and cardiovascular disease also puts males at an increased prevalence of sleep apnea and low testosterone/erectile dysfunction?

A

Metabolic syndrome/insulin resistance syndrome

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12
Q

What condition is associated with hyper-­pigmented, velvety plaques located commonly axilla, groin, neck and is also associated with skin tags?

A

Acanthosis Nigricans

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13
Q

What are the types of Acanthosis Nigricans?

A

Benign Type : insulin resistance, obesity, predilection of type II diabetes, stimulated by insulin growth factor
Familial Type: Insulin resistance secondary to mutations in the insulin receptors
Malignant type: Associated with several aggressive cancers.

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14
Q

What is the causal mechanism for Type II DM?

A

Mechanism is unclear, but there is a strong genetic component and most patients are obese (insulin secretion is abnormal and there is insulin resistance at peripheral tissues)

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15
Q

What is the fasting plasma glucose level and random blood glucose level needed to diagnose type II diabetes?

A

FPG: 7mmol/L

Random PG: 11.1mmol/L

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16
Q

How does nephropathy occur in diabetics?

A

Glomerular capillaries are occluded by basement membrane-like material (leads to renal failure)

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17
Q

What are the 3 major effects of neuropathy?

A

1) Distal symmetrical polyneuropathy: impaired touch and pain sensation that starts in the lower extremities.
2) Autonomic neuropathy: Impotence, GI disturbances, neurogenic bladder, orthostatic hypotension.
3) Cranial nerve palsies: usually pupil sparing CNIII and CN VI. Due to vascular occlusions, not neuropathy.

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18
Q

What is the reason why amputations are so common in diabetics?

A

accelerated artherosclerosis leads to GANGRENE secondary to vascular occlusions of the smaller arteries in the lower extremities

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19
Q

What is the anti-hypertensive drug of choice that is nephroprotective?

A

ACE inhibitors (“-pril” endings)

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20
Q

By how much can you reduce the risk of diabetic retinopathy if you reduce HbA1C by 2%?

A

5X reduction in risk!

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21
Q

What is the typical HbA1C goal for diabetics?

A
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22
Q

If a patient has poor control of blood glucose and has severe NPDR or PDR, what do you have to be concerned about if they decide to strictly control their sugar abruptly?

A

Sight threatening progression of retinopathy!

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23
Q

Acute hyperglycemia can cause which 2 types of refractive shifts?

A

Hyperopic and myopic shifts

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24
Q

T/F: Along with Syphilis, DM can cause a Argyll-Robertson pupil

A

True

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25
Q

Other than NVI, what other iris findings can be found in patients with DM?

A

Iris atrophy that leads to loss of the iris colarette

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26
Q

What anterior segment finding in DM can lead to glaucoma?

A

Neovascularization of the angle

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27
Q

What is a corneal complication that can be found in patients with DM?

A

Corneal epithelium has poor healing capabilities and the epithelium is more susceptible to damage.

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28
Q

Which anti-hypertensive medication can mask the symptoms of hyperglycemia?

A

Beta-blockers

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29
Q

What are the two cataracts associated with DM

A

PSC and snowflake cataract

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30
Q

What concerns should you have about doing cataract lens extraction with diabetic patients?

A

It can lead to progression in retinopathy and/or anterior segment neovascularization.

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31
Q

What happens to blood sugar when a diabetic undergoes any type of surgery?

A

The trauma and stress of the surgery can lead to an increase in blood sugar and the patients should be monitored carefully

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32
Q

What are the findings of asteroid hyalosis and what conditions is it associated with?

A

Unilateral finding of calcium soaps located in the vitreous in elderly patients. Associated with DM and gout.

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33
Q

What are the findings associated with synchysis scintillans?

A

Cholesterol crystals found bilaterally in the vitreous in younger patients after trauma. Vitreous is typically liquefied.

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34
Q

What is the mechanism behind cotton wool spot production?

A

CWS’s are the manifestations of capillary closure due to loss of Autoregulation of retinal vessels which is secondary to damage to Pericytes of the retinal capillaries.

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35
Q

What causes the formation of exudates and retinal edema in diabetic patients?

A

Microaneurysms and leaky capillaries.

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36
Q

What stage are blot hemes found in dm?

A

Advanced stages

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37
Q

What are some signs that are associated with proliferative diabetic retinopathy?

A

IRMA, venous beading, presence of new blood vessels, fibrous proliferation (scaffolding for the new blood vessels), and contraction of the vitreous and fibrous tissues (TRD)

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38
Q

In general, when is macular edema clinically significant in diabetic patients?

A

When the edema or hard exudates threaten the macula and treatment is necessary.

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39
Q

What is the criteria for treatment of CSME?

A

1) If edema is CLOSE to the retina (within 1/3DD of the macula)
2) If the edema is ASSOCIATED with the macula (hard exudates within 1/3DD of the macula with adjacent thickening.
3) If the edema is LARGE (if retinal thickening is greater than 1DD and within 1DD of the macula

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40
Q

Ketoacidosis puts diabetics at an increased risk for which life threatening fungal infection?

A

Mucormycosis

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41
Q

What is the treatment of Mucormycosis?

A

Amphotericin B

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42
Q

What are the signs of Mucormycosis?

A

Orbital cellulitis, eyelid edema, proptosis, external ophthalmoplegia, and fever
(not that important of a flashcard

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43
Q

What are the stages of diabetic retinopathy

A

Mild NPDR: Microaneurisms
Moderate NPDR: More than microaneurisms, but less than severe NPDR
Severe NPDR: 4-2-1 rule (4 quadrants of microaneurisms, 2 quadrants of venous beading, 1 quadrant of IRMA.)

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44
Q

What consists of the 4-2-1 rule?

A

At least 1 of the following:
4 quadrants of microaneurisms
2 quadrants of venous beading
1 quadrant of IRMA

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45
Q

What is the mechanism of action of Sulfonylureas (Diabetic medication)?

A

Stimulates insulin secretion and increases sensitivity to insulin.

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46
Q

What drug class is Meformin?

A

Biguanide

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47
Q

What is the MoA of Metformin?

A

Decreases hepatic glucose production

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48
Q

Braley’s sign is associated with thyroid orbitopathy. What is this sign?

A

Patients will have an increase in IOP on up gaze vs. primary gaze. (up to 8 mmHg)

49
Q

Restrictions of EOMs in 2 directions associated with thyroid eye disease puts the patient more at risk of what?

A

Optic nerve compression

50
Q

Patients with thyroid orbitopathy and complaints of diplopia and ptosis should have which tests ordered for them?

A

Tensilon or ice pack test (MG)

51
Q

What are some of the ocular signs of hyperthyroidism?

A

Dilated vessels over the horizontal rectus
Von Greafe sign: Delayed upper lid movement on down gaze
Dalrymple sign: Retraction of the upper eyelids in primary gaze
Choroidal folds can sometimes be present

52
Q

Restrictive myopathy can occur in patients with hyperthyroidism. List the muscles that are affected from most common to least common.

A

Inferior, medial, superior, lateral, obliques
(IM SLO)
notes: inferior is more common, but medial is going to be most bothersome because it mimics a CN VI palsy.

53
Q

What are the typical TSH, T3, T4 test results for some one with mild hypothyroidism?

A

TSH = High

T3, T4 = Normal

54
Q

What are the typical TSH, T3, T4 test results for some one with hypothyroidism?

A
TSH = High
T3 = Low or normal
T4 = Low
55
Q

What are the typical TSH, T3, T4 test results for some one with mild hyperthyroidism?

A

TSH = Low

T3, T4 = Normal

56
Q

What are the typical TSH, T3, T4 test results for some one with hyperthyroidism?

A

TSH = Low

T3, T4 = High or normal

57
Q

What are the typical TSH, T3, T4 test results for some one with nonthyroidal illness, or pituitary (secondary) hypothyroidism?

A

TSH = Low

T3, T4 = Low or normal

58
Q

What are the typical TSH, T3, T4 test results for some one with thyroid hormone resistance syndrome?

A

TSH = Normal

T3, T4 = High

59
Q

What is the disease process behind hypothyroidism?

A

Chronic autoimmune inflammation of the thyroid gland with lymphocytes.

60
Q

What is myxedema madness?

A

Depression, poor memory, hyper­-solmnescence and psychosis

61
Q

How do you interpret test results of low calcium levels and high levels of parathyroid hormone?

A

The parathyroid is acting normally. Additional testing should be done to see why the patient is hypocalcemic

62
Q

How do you interpret test results of low calcium levels and low or normal levels of parathyroid hormone?

A

Parathyroid is not working properly. Probably have hypoparathyroidism

63
Q

How do you interpret test results of high calcium levels and high levels of parathyroid hormone?

A

Parathyroid is producing too much parathyroid hormone. Do imaging for hyperparathyroidism

64
Q

How do you interpret test results of high calcium levels and low levels of parathyroid hormone?

A

Parathyroid is responding correctly. Do additional testing for hypercalcemia

65
Q

How do you interpret test results of normal calcium levels and high levels of parathyroid hormone?

A

Mild hyperparathyroidism

66
Q

What is the most common cause of hypercalcemia?

A

Excessive parathyroid hormone secretion

67
Q

What are some common causes of secondary hyperparathyroidism?

A

Renal failure
Osteogenesis imperfecta
Paget’s disease of the bone

68
Q

What are ocular signs of hyperparathyroidism?

A

Calcification of the conj and sclera.

Calcification of the cornea and band keratopathy.

69
Q

What is a common systemic cause of hyperparathyroidism that features extreme pain in the bladder and urethra?

A

Kidney stones

70
Q

What effects can occur in the CNS with hyperparathyroidsism?

A

Increased intracranial pressure

71
Q

What effects can occur in the mucocutaneous system with hyperparathyroidism?

A

Enamel hyperplasia
Coarse hair
Brittle nails

72
Q

What is a key ocular concern for patients with hypoparathyroidsm?

A

Papilledema

73
Q

What is multiple endocrine neoplasia syndrome (MENS)?

A

Syndrome characterized by tumors of the endocrine glands.

74
Q

Which type of multiple endocrine neoplasia syndrome (MENS) has specific ocular signs?

A

Type 2b

75
Q

What is multiple endocrine neoplasia syndrome (MENS) type 1 (Werner’s syndrome)?

A

Characterized by pituitary tumors, pancreatic islet cell tumor, and parathyroid hyperthyroidism

76
Q

what is multiple endocrine neoplasia syndrome (MENS) type 2 (Sipple’s syndrome)?

A

Characterized by medullary carcinoma, pheochromocytoma, and parathyroid hyperplasia.

77
Q

What is the ocular finding of multiple endocrine neoplasia syndrome (MENS) 2b?

A

Ganglioneuromas on the lids and conj. Bundles of enlarged corneal nerves.

78
Q

Pheochromocytoma is a tumor located where? What is a systemic concern with pheochromocytoma?

A

Tumor located in the adrenal medulla that secretes catecholamines. Pheochromocytoma causes HTN.

79
Q

What is the most common cause of symptoms in patients with pituitary adenomas?

A

Symptoms arise from the complications of have too much hormone secretions

80
Q

What type of symptoms occur in craniopharyngioma?

A

Symptoms of hypopituitarism

81
Q

What are the symptoms of excess luteinizing hormone and Follicle Stimulating Hormone?

A

Menstrual changes, low testosterone in males, and loss of libido

82
Q

What are the symptoms of reduced luteinizing hormone and Follicle Stimulating Hormone?

A

Amenorrhea, infertility, and decreased libido.

83
Q

What are the clinical manifestations of excess growth hormone?

A

acromegaly, gigantism, bony hypertrophy, sweating, HTN, and DM

84
Q

What are the clinical manifestations of decreased growth hormone?

A

Growth arrest and deficient lactation.

85
Q

What are the clinical manifestations of excess ACTH hormone?

A

Symptoms associated with Cushing syndrome (chronic elevated serum cortisol)

86
Q

What are the clinical manifestations of decreased adrenal function?

A

Symptoms associated with Addison’s disease (Low serum cortisol)

87
Q

What are the clinical manifestations of increased prolactin hormone?

A

Amenorrhea, decreased libido, infertility, galactorrhea, gynecomastia

88
Q

What are the clinical manifestations of decreased prolactin hormone?

A

Deficient lactation

89
Q

T/F: Vestibular, Auditory, and photoreceptors are derived from the same ciliated progenitors

A

True

90
Q

What is the inheritance of usher’s syndrome?

A

Autosomal recessive

91
Q

What is the triad of usher’s syndrome?

A

Hearing loss, RP, and metal disability

92
Q

Patients with usher’s syndrome will have reduced ERG or EOG?

A

ERG

93
Q

What is refsum’s disease?

A

Disease associated with hereditary retinal degeneration. Findings include autosomal recessive RP and increased serum phytanic acid.

94
Q

What systemic disease associated with hereditary retinal degeneration has symptoms of RP and fat intolerance?

A

Hereditary Abetaproteinemia

95
Q

What systemic disease associated with hereditary retinal degeneration has symptoms of RP before the age of 20 and cardiac conduction abnormality?

A

Kearn’s Sayre syndrome

96
Q

What disorder producing pseudo-retinitis pigmentosa is associated with hyper ornithemia and increased ornithine levels?

A

Gyrate atrophy

97
Q

What disorder producing pseudo-retinitis pigmentosa is associated with choroidal atrophy with macular sparing?

A

Choroidemia

98
Q

Which disease is associated with keratitis and hearing loss?

A

Cogan’s syndrome

99
Q

In Cogan’s syndrome, which becomes involved first, the cornea or the ear?

A

Either can become involved first.

100
Q

What is the treatment of Cogan’s?

A

Systemic steroids

101
Q

Which are the two most significant disorders that cause hearing loss/deafness

A

Usher’s syndrome and Cogan’s.

102
Q

What is barrett’s esophagitis?

A

Precancerous metaplasia of the stomach mucosa associated with GERD.

103
Q

What is the concern regarding anti-acids with GERD patients?

A

Anti-acids can cause a rebound acid reflux

104
Q

What is the gram negative organism that is present in the acidic conditions of the stomach that can contribute to symptoms of GERD?

A

Helicobacter Pylori

105
Q

What are the signs and symptoms of H. Pylori?

A

Dyspepsia (indigestion), Gastritis (inflammation of the gastric mucosa), Peptic ulcer disease (erosion of GI mucosa in the stomach)

106
Q

What are five causes of gastritis?

A

H. pylori, alcohol, stress, autoimmune, and NSAIDs

107
Q

What are the 3 tests based on endoscopic biopsy that are used to diagnose H. Pylori?

A

Biopsy urease test
Histology
Culture

108
Q

What are 3 non-invasive tests used to diagnose H. Pylori?

A

Serology, C urea breath test, stool antigen test.

109
Q

What is the algorithm for treating H. Pylori?

A

1) Test for pylori
2) If positive, treat with omeprazole, clarithromycin, and metronidazole (7-14 days).
3) If still positive, treat with omeprazole, clarithromycin, and amoxicillin (7-14 days).
4) If still positive, go to 3rd line of treatment (not important).
5) If still positive, refer to specialist.

110
Q

What is the cause of persistent pancreatitis?

A

Fibrosis and ductal strictures (narrowing). Typically caused by chronic alcoholism or can be idiopathic.

111
Q

What are the signs and symptoms of chronic pancreatitis?

A

recurrent attacks of pain

112
Q

What are some complications of chronic pancreatitis?

A

Mal-absorption and glucose intolerance (DM)

113
Q

What is the treatment of chronic pancreatitis?

A

Supportive, analgesics, diet modifications, and enzyme supplements.

114
Q

Ocular complications of pancreatitis include ischemic retinopathy that looks very similar to what retinal pathology?

A

Purtscher’s retinopathy (CWS, NFL hemorrhages, diffuse retinal edema, nonperfusion on FANG and ICG)

115
Q

T/F: ischemia can occur in pancreatitis?

A

true

116
Q

Which organs are involved in gastroenteritis?

A

Stomach and small intestine

117
Q

Gastroenteritis is typically caused by infection, but what infectious agent also ties gastroenteritis with reactive arthritis?

A

Bacteria! Specifically clostridium, salmonella, Shigella, Campylobacter, and E Coli

118
Q

Gardner syndrome is characterized by which findings?

A

Intestinal polyposis, Soft tissue tumors, benign osseous (bone) growths, RPE hypertrophy