MLSCI 262 - Osmolality

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Last updated 12:36 AM on 10/18/26
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99 Terms

1
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What is the anion gap?

The difference between routinely measured cations and anions; estimates unmeasured anions.

2
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What is the formula for the anion gap?

AG = [Na+] - ([Cl-] + [HCO3-]).

3
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What is the lecture reference interval for the anion gap?

4–16 mmol/L.

4
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Why is K+ excluded from the standard anion gap formula?

Its extracellular concentration is relatively low.

5
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Which four electrolytes are routinely measured in the clinical lab?

Na+, K+, Cl-, and HCO3-.

6
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Why do measured plasma cations appear to exceed measured anions?

Not all ions are routinely measured; total positive and negative charges actually balance.

7
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What is the principle of electroneutrality?

Total positive charge equals total negative charge in a solution.

8
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Name unmeasured anions that contribute to the anion gap.

Albumin/proteins, phosphate, sulfate, organic acids such as lactate and ketoacids.

9
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Calculate AG: Na+ 140, Cl- 100, HCO3- 25 mmol/L.

140 - (100 + 25) = 15 mmol/L; within lecture reference interval.

10
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What is the most common general reason for an increased anion gap?

Increased unmeasured anions.

11
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Which organic acids may increase the anion gap?

Lactate, ketoacids (beta-hydroxybutyrate/acetoacetate), formate, oxalate, and salicylate.

12
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Why can renal failure increase the anion gap?

Failure to eliminate metabolic acids, including phosphate and sulfate species.

13
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How can alkalosis increase the anion gap?

Increases the net negative charge on proteins.

14
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How can low calcium or magnesium affect the anion gap?

Decreased unmeasured cations can increase the gap.

15
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Why is a decreased anion gap less common?

It is less likely than an increased gap, according to the lecture.

16
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What changes in unmeasured anions can decrease the anion gap?

Low albumin or low phosphate.

17
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What changes in unmeasured cations can decrease the anion gap?

High calcium or high magnesium.

18
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How can multiple myeloma decrease the anion gap?

Increased positively charged antibodies/proteins act as unmeasured cations.

19
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Calculate AG: Na+ 138, Cl- 105, HCO3- 24 mmol/L.

138 - (105 + 24) = 9 mmol/L; within lecture reference interval.

20
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Calculate AG: Na+ 142, Cl- 99, HCO3- 15 mmol/L.

142 - (99 + 15) = 28 mmol/L; increased.

21
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What collection issues should be avoided for electrolyte testing?

Hemolysis, delayed cell separation, exercise before collection, and fist pumping.

22
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Which anticoagulants may be in green-top tubes for electrolyte testing?

Lithium or ammonium heparin.

23
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Which listed tubes contain no anticoagulant?

Red tiger-striped serum separator, red-top, and gold-top tubes.

24
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Define a mole.

6.022 × 10^23 particles (Avogadro’s number).

25
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Define an osmole.

An amount producing 6.022 × 10^23 osmotically active particles in solution.

26
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How do moles and osmoles differ?

Moles count formula units/molecules; osmoles count dissolved osmotically active particles.

27
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How many osmoles are produced by 1 mol of glucose?

1 Osmol, because glucose does not dissociate.

28
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How many ideal osmoles are produced by 1 mol of NaCl?

2 Osmol: Na+ and Cl-.

29
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How many ideal osmoles are produced by 1 mol of CaCl2?

3 Osmol: one Ca2+ and two Cl-.

30
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What is n in the theoretical osmole calculation?

Number of dissolved particles/ions produced per formula unit.

31
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What is the theoretical formula for osmoles from a dissociating solute?

Osmoles = moles × n.

32
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Why may the theoretical number of ions overestimate osmoles in biological fluids?

Ions do not behave as fully independent particles; the lecture accounts for incomplete dissociation.

33
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What is the Van’t Hoff factor i in the lecture?

Effective particle factor: i = n × Φ, where Φ is the osmotic coefficient.

34
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Calculate ideal osmoles from 0.5 mol of NaCl.

0.5 × 2 = 1 Osmol.

35
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Calculate ideal osmoles from 0.2 mol of CaCl2.

0.2 × 3 = 0.6 Osmol.

36
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Define molarity and give its unit.

Amount of an individual solute per volume; mol/L.

37
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Define molality and give its unit.

Amount of an individual solute per mass of solvent; mol/kg.

38
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Define osmolarity and give its unit.

Total osmotically active particles per volume; Osmol/L.

39
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Define osmolality and give its unit.

Total osmotically active particles per mass of solvent; Osmol/kg.

40
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Which two concentration terms use volume as denominator?

Molarity and osmolarity.

41
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Which two concentration terms use mass as denominator?

Molality and osmolality.

42
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Which terms count individual solute amount rather than total osmotically active particles?

Molarity and molality.

43
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Why is osmolality preferred over osmolarity for consistent measurement?

Mass is unaffected by temperature/pressure, while volume can change.

44
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What is the mass of 1 L of water approximately?

1 kg.

45
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What is the lecture reference interval for serum osmolality?

280–300 mOsm/kg.

46
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What is a solute?

The substance being dissolved.

47
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What is a solvent?

The medium that dissolves a solute.

48
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Define osmosis.

Movement of solvent across a semipermeable membrane according to solute concentration.

49
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In which direction does solvent move during osmosis?

From higher solvent concentration (lower solute) to lower solvent concentration (higher solute).

50
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Define osmotic pressure.

Pressure needed to prevent solvent movement across a semipermeable membrane.

51
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What determines osmotic pressure?

Number/concentration of osmotically active solute particles.

52
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What osmotic pressure equation appears in the lecture?

π = iMRT (i: Van’t Hoff factor; M: molarity; R: gas constant; T: kelvin).

53
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Define osmometry.

Measurement of concentration of osmotically active solute particles.

54
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Which main plasma components appear in calculated osmolality?

Sodium-associated particles, glucose, and urea.

55
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What is the lecture’s calculated osmolality formula?

mOsm/kg = 1.86[Na+] + [glucose] + [urea] + 9 (inputs in mmol/L).

56
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What is the rough calculated osmolality formula?

mOsm/kg ≈ 2[Na+] + [glucose] + [urea] (inputs in mmol/L).

57
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Why is sodium approximately doubled in the rough osmolality formula?

Sodium is accompanied by counterions, which also contribute osmotic particles.

58
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Calculate rough osmolality: Na 140, glucose 5, urea 5 mmol/L.

2(140) + 5 + 5 = 290 mOsm/kg.

59
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Calculate osmolality with full formula: Na 140, glucose 5, urea 5.

1.86(140) + 5 + 5 + 9 = 279.4 mOsm/kg.

60
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What does a freezing-point osmometer measure directly?

Depression of the sample freezing point relative to pure water.

61
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Why does dissolved solute lower water’s freezing point?

Solute particles cause a colligative freezing-point depression; more particles cause a larger decrease.

62
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What is the freezing point of pure water?

0.00°C.

63
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What is the approximate freezing point of normal serum in the lecture?

−0.54°C.

64
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What is the molal freezing point depression constant of water?

1.86°C·kg/mol.

65
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What is Δ in freezing point depression calculations?

Freezing point of pure water minus freezing point of patient sample.

66
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What formula converts freezing point depression to osmolality?

Osmolality (mOsm/kg) = (Δ / 1.86) × 1000.

67
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Calculate osmolality if a sample freezes at −0.558°C.

(0.558 / 1.86) × 1000 = 300 mOsm/kg.

68
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Calculate osmolality if a sample freezes at −0.465°C.

(0.465 / 1.86) × 1000 = 250 mOsm/kg.

69
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How does greater solute particle concentration affect freezing point?

It causes a larger freezing point depression (more negative freezing temperature).

70
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What is a limitation of calculated osmolality?

It does not capture all unmeasured uncharged solutes.

71
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Define the osmolal gap.

Measured osmolality minus calculated osmolality.

72
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What is the lecture reference range for the osmolal gap?

≤10 mOsm/kg.

73
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What can an increased osmolal gap indicate?

Unmeasured osmotically active compounds, including alcohols, drugs, and metabolic by-products.

74
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Which alcohols are highlighted as possible osmolal gap contributors?

Ethanol, methanol, and ethylene glycol.

75
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What metabolic by-product is highlighted as contributing to the osmolal gap?

Acetone.

76
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Calculate osmolal gap: measured 320, calculated 290 mOsm/kg.

320 - 290 = 30 mOsm/kg; increased.

77
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Calculate osmolal gap: measured 295, calculated 289 mOsm/kg.

295 - 289 = 6 mOsm/kg; within lecture reference range.

78
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How do anion gap and osmolal gap differ?

Anion gap estimates unmeasured charged ions; osmolal gap detects additional osmotically active particles, often uncharged.

79
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What is specific gravity (SG)?

A measure of solute concentration based on density relative to water.

80
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What is density?

Mass per unit volume, e.g., g/mL.

81
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What is the specific gravity formula for urine?

SG = density of urine / density of an equal volume of water.

82
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What two solute properties influence specific gravity?

Number of solutes and their molecular weights.

83
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Does specific gravity have units?

No; it is a ratio of densities.

84
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What urine SG range is listed in the lecture?

1.002–1.040; average approximately 1.017 ± 0.007.

85
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What three methods are listed for urine SG testing?

Urinometer, specific gravity dipstick, and refractive index/refractometer.

86
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What does the urine SG dipstick primarily respond to?

Urine ionic concentration (ionic strength), via a polyelectrolyte reaction.

87
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What chemical principle underlies the urine SG dipstick?

Urine ions change dissociation/pKa behavior of pretreated polyelectrolytes in the pad.

88
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What happens to polyelectrolyte acid groups as urine ionic concentration increases?

More groups dissociate, releasing more H+.

89
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How does increased urine ionic concentration change the dipstick pad pH?

It makes the reagent pad more acidic.

90
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Which pH indicator is in the urine SG dipstick pad?

Bromothymol blue.

91
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How does the urine SG dipstick produce a readable result?

H+ released from polyelectrolytes changes pad pH; bromothymol blue changes color.

92
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What SG increments and range are listed for the dipstick?

Increments of 0.005, from 1.000 to 1.030.

93
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How does increasing urine SG affect the dipstick indicator color?

The slide chart shifts from blue/green at low SG toward yellow at high SG.

94
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What is the principle of refractometric SG measurement?

Solute-dependent bending of light (refractive index) provides an indirect SG estimate.

95
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What happens to refracted light at higher solute concentrations?

It bends more toward the normal.

96
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What is the “normal” in refraction diagrams?

An imaginary line perpendicular to the boundary between media.

97
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What law relates refractive indices and light angles?

Snell’s law: N1 sinθ1 = N2 sinθ2.

98
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How do dipstick and refractometer methods differ?

Dipstick responds mainly to ionic strength; refractometer responds to refractive index affected by solute concentration.

99
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Why can SG and osmolality respond differently to solute composition?

SG depends on density and molecular weight; osmolality depends on number of osmotically active particles.