GESTATIONAL DIABETES MELLITUS Flashcards

(77 cards)

1
Q

– pregnancy-related hyoerglycemia

A

HUMAN PLACENTAL LACTOGEN

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2
Q

– similar to action of GH (inhibits insulin)

A

HUMAN CHORIONIC SOMAMOTROPIN

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3
Q

Glucose intolerance which develops in [?] of pregnancies

A

7%

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4
Q

Abnormal glucose concentration discovered for the 1st time during pregnancy

A

GESTATIONAL DIABETES MELLITUS

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5
Q

ONE-STEP STRATEGY

A

2011 Standards of Care – ADA

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6
Q

TWO-STEP STRATEGY

A

2013 – NIH

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7
Q

24 to 28 weeks of gestation

A

ONE-STEP STRATEGY
TWO-STEP STRATEGY

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8
Q

Step 1: Perform a 75-g OGTT (fasting, 1H, and 2H BGL)

A

ONE-STEP STRATEGY

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9
Q

Step 1: Perform a 50-g GLT (non-fasting)

A

TWO-STEP STRATEGY

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10
Q

1H PG measurements

A

TWO-STEP STRATEGY

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11
Q

If the 1H PG is [?], or [?], proceed to a [?]

A

> or = to 130 mg/dL
140 mg/dL
100-g OGTT

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12
Q

Step 2: The 100-g OGTT should be performed when the patient is fasting

A

TWO-STEP STRATEGY

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13
Q

ONE-STEP STRATEGY

Diagnosis of GDM is made when any or the PG values are = or > than any of the ff PG levels:

Fasting:

A

92 mg/dL (5.1 mmol/L)

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14
Q

ONE-STEP STRATEGY

Diagnosis of GDM is made when any or the PG values are = or > than any of the ff PG levels:

1 h:

A

180 mg/dL (10.0 mmol/L)

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15
Q

ONE-STEP STRATEGY

Diagnosis of GDM is made when any or the PG values are = or > than any of the ff PG levels:

2 h:

A

153 mg/dL (8.5 mmol/L)

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16
Q

TWO-STEP STRATEGY

Diagnosis of GDM is made if at least two values are = to or > than any of the ff PG levels:

Fasting:

A

105 mg/dL

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17
Q

TWO-STEP STRATEGY

Diagnosis of GDM is made if at least two values are = to or > than any of the ff PG levels:

1 h:

A

190 mg/dL

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18
Q

TWO-STEP STRATEGY

Diagnosis of GDM is made if at least two values are = to or > than any of the ff PG levels:

2 h:

A

165 mg/dL

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19
Q

TWO-STEP STRATEGY

Diagnosis of GDM is made if at least two values are = to or > than any of the ff PG levels:

3 h:

A

145 mg/dL

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20
Q

Results from an imbalance between glucose utilization and production

A

HYPOGLYCEMIA

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21
Q

Observable symptoms appear at about

A

50 to 55 mg/dL

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22
Q

ADRENALINE

A

EPINEPHRINE

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23
Q

 Triggered by the ANS

A

NEUROGENIC/ADRENERGIC

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24
Q

 Tremulousness, palpitations, anxiety

A

NEUROGENIC/ADRENERGIC

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25
 Diaphoresis (cold sweat)
NEUROGENIC/ADRENERGIC
26
 Hunger
NEUROGENIC/ADRENERGIC
27
 Paresthesias (numbness)
NEUROGENIC/ADRENERGIC
28
 CNS hypoglycemia
NEUROGLYCOPENIC
29
 Dizziness, tingling, difficulty in concentrating, blurred vision
NEUROGLYCOPENIC
30
 Confusion, behavioral changes, seizure, coma
NEUROGLYCOPENIC
31
aka fast Hgb, glycosylated Hgb
Glycohemoglobin
32
– major fraction; predominant form
HbA1c
33
Non-enzymatic condensation between glucose and the N-terminal valine of each B-chain
HbA1c
34
Occurs over the lifespan of the RBC (90 to 120 days)
HbA1c
35
[?] -------- [N-terminal of B]
Glucose + Valine
36
[?] (unstable aldimine) -------- [Amadori rearrangement]
SCHIFF BASE
37
(stable)
KETOAMINE
38
GHb testing provides an index of ave. BGL over the
past 2-4 months
39
Values for [?] have a high degree of correlation
total HbA1 & HbA1c
40
Labile fraction (Schiff base or pre-A1c): accounts for [?] of total HbA1
5 to 8%
41
GHb testing Advantages: 1. Provides objective means of 2. Additional confirmation of the
reflecting control of DM clinical impression of control
42
 Cation-exchange resin or carboxymethyl cellulose resin
ION-EXCHANGE CHROMATOGRAPHY
43
 HbA1 elutes from the column first
ION-EXCHANGE CHROMATOGRAPHY
44
 False elevation: labile fractions, HbF
ION-EXCHANGE CHROMATOGRAPHY
45
 Low values: Hb variants
ION-EXCHANGE CHROMATOGRAPHY
46
 Reference method
HPLC
47
 Separates and quantifies HbA1c and other haemoglobin types
HPLC
48
 Hb A1c --- acid --- 5-HMF
COLORIMETRY
49
 Specific for ketoaminelinked
COLORIMETRY
50
 Unaffected by HbF, Hb variants and labile intermediate
COLORIMETRY
51
 Routine
COLORIMETRY
52
 Antibodies against Hb A1c (sheep antiserum)
RADIOIMMUNOASSAY (RIA)
53
 Partial cross-reactivity w/ HbA1c
RADIOIMMUNOASSAY (RIA)
54
 Antiserum not commercially available
RADIOIMMUNOASSAY (RIA)
55
Citrate agar electrophoresis (pH 6.0-6.2) - Buffer:
Citrate agar buffer (acidic)
56
Citrate agar electrophoresis (pH 6.0-6.2) - Solid support:
agarose gel
57
HbF migrates to the same region as HbA1
Citrate agar electrophoresis
58
Cellulose acetate electrophoresis (pH 8.0) - Buffer:
Tris EDTA boric acid (alkaline)
59
Cellulose acetate electrophoresis (pH 8.0) - Solid support:
cellulose acetate
60
 Good resolution of Hb A & Hb A1
ELECTROPHORESIS
61
 No interference from Hb variants
ELECTROPHORESIS
62
 HbF migrates to the same region as HbA1
ELECTROPHORESIS
63
 Scanned on high-resolution microdensitometer
ISOELECTRIC FOCUSING
64
 Hb A1c is adequately resolved from HbA1a, A1b, S and F
ISOELECTRIC FOCUSING
65
ISOELECTRIC FOCUSING MEDIUM
Polyacrylamide gel
66
 Use of affinity gel columns
AFFINITY CHROMATOGRAPHY
67
AFFINITY CHROMATOGRAPHY ADVANTAGES:
o No interference from non-glycosylated Hb o Negligible interference from the labile intermediate o Minimal dependence on variations in ambient T
68
Total Hb A1 MEAN %
6.5
69
Total Hb A1 RANGE
5.0 – 8.0
70
Hb A1c only RANGE
3.0 – 6.0
71
Hb A1c only MEAN %
4.5
72
HbA1c (%) = Approximate Plasma Glucose mg/dL Mmol/L
73
For patients with inaccurate HbA1c assays (hemglobinopathies and hemolytic anemias)
o Affinity chromatography o Immunoassays
74
Turnover time of serum proteins: (primary albumin) 14 to 20 days
o Reflects glycemic control over narrower period of time
75
Most widely used to assess short-term (3 to 6 week) glycemic control
FRUCTOSAMINE ASSAYS
76
FRUCTOSAMINE ASSAYS ADVANTAGE:
Use of serum samples and automated equipment (simple to perform and low in cost)
77
More reliable than other glycosylated protein assays
FRUCTOSAMINE ASSAYS