Clinical Pharmacokinetics: cram pack

Formula sheets, the key method steps for every topic and 8 practice problems, with full solutions at the back.

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1Formulas and methods

Clinical pharmacokinetics

Rate constant and half-life
k = ln 2/t½ = 0.693/t½
First-order decay
C = C₀·e−kt = C₀·(1/2)t/t½
Two levels
k = ln(C₁/C₂)/Δt
Volume and clearance
Vd = dose/C₀, CL = k·Vd
Loading dose
LD = Vd·C/(S·F)
Maintenance rate
R = CL·Css/(S·F)
Average steady state
Css,avg = S·F·D/(CL·τ)
Steady state
1 − (1/2)ⁿ after n half-lives; ≈ 97% after 5
Infusion
C = (R/CL)(1 − e−kt)
Interval and dose from peak and trough
τ = ln(Cpeak/Ctrough)/k, D = Vd·(Cpeak − Ctrough)
Cockcroft–Gault
CrCl = (140 − age) × kg/(72 × SCr mg/dL), × 0.85 for women
Renal adjustment
dose × CrCl/normal; Dettli Q = 1 − fe·(1 − CrCl/normal)

Method

  1. Convert the half-life to a rate constant: k = 0.693/t½.
  2. Turn per-kg values into totals: Vd (L) = L/kg × weight, CL (L/h) = L/kg/h × weight.
  3. Pick the relation: C = C₀·e−kt, LD = Vd·C/(S·F), maintenance rate = CL·Css/(S·F), τ = ln(Cpeak/Ctrough)/k.
  4. For kidney function, estimate CrCl with Cockcroft–Gault first, then scale the dose or the interval.
  5. Check the result: levels fall by half every half-life, and steady state takes about five half-lives.

Pharmacy calculations

Percentage strength
% w/v = g per 100 mL
Amount in a solution
g = % × mL / 100
Ratio strength
1:X = 1 g in X mL; % = 100 / X
Reconstitution
final volume = diluent + powder volume
Concentration
mg/mL = drug in vial / final volume
Alligation
parts of H = T − L, parts of L = H − T
Water or base
0%

Pediatric & critical-care dosing

Daily dose
mg/day = mg/kg/day × weight (kg)
Doses per day
number = 24 h / dosing interval (h)
Pounds to kilograms
kg = lb / 2.2
Infusion concentration
units/mL = units in bag / bag volume
Pump rate
mL/h = dose per hour / concentration
Titrated drip
mL/h = mcg/kg/min × kg × 60 / (mcg/mL)
Dose from pump rate
mcg/kg/min = mL/h × (mcg/mL) / (60 × kg)
Units
1 mg = 1000 mcg

2Practice problems

1.Clinical pharmacokineticsMedium
110100t (h)C (mg/L)1 h30 mg/L13 h9.1 mg/L

Practice exercise (made-up values, not clinical guidance). After an IV dose of vancomycin, the level is 30 mg/L at 1 h and 9.1 mg/L at 13 h. Assume first-order elimination. Find the elimination rate constant k.

C1 = 30 mg/L (1 h)C2 = 9.1 mg/L (13 h)
k = h⁻¹
2.Clinical pharmacokineticsHard
VCss,avg​ = ?450 mg · q8hCL = 0.03 L/kg/h84 kg · S = 0.8 · F = 1

Practice exercise (made-up values, not clinical guidance). An 84 kg patient takes oral aminophylline (S = 0.8, F = 1) every 8 h. The theophylline clearance is 0.03 L/kg/h. Each dose is 450 mg of aminophylline. Find the average steady-state level Css,avg.

CL = 0.03 L/kg/hτ = 8 hS = 0.8F = 184 kgD = 450 mg
Css,avg = mg/L
3.Pharmacy calculationsMedium
024681010 mL

A solution has a ratio strength of 1:10 000. You need 0.16 mg. Draw up the volume in the 10 mL syringe: what volume V is that?

1:10 0000.16 mg
V = mL
4.Pharmacy calculationsHard
5%30 g+1%coal tar? g2%coal tar

Practice exercise (made-up values, not clinical guidance). You have 30 g of 5% coal tar ointment. How many grams m of 1% coal tar ointment must you add to make a 2% ointment? Round to the nearest whole gram.

30 g · 5%1%2%
m = g
5.Pediatric & critical-care dosingMedium
heparin 5 000 units/mL60 units/kg · 64 kg → V = ? mL

Practice exercise (made-up values, not clinical guidance). A practice protocol calls for a heparin bolus of 60 units/kg for a patient who weighs 64 kg. The vial contains 5 000 units/mL. What volume V do you draw up? Round to two decimal places.

60 units/kg64 kg5 000 units/mL
V = mL
6.Pediatric & critical-care dosingHard
500 mg250 mLdobutamine26 mL/h59 kg? mcg/kg/min

Practice exercise (made-up values, not clinical guidance). A dobutamine infusion of 500 mg in 250 mL runs at 26 mL/h. The patient weighs 59 kg. What dose D in mcg/kg/min is the patient receiving? Round to one decimal place.

500 mg/250 mL26 mL/h59 kg
D = mcg/kg/min
7.PharmacologyMedium

Which group of effects would the nurse expect after a dose of an anticholinergic drug such as atropine?

  1. ADry mouth, faster heart rate and dilated pupils
  2. BHeavy salivation, slow heart rate and small pupils
  3. CBronchial secretions, wheeze and tearing of the eyes
  4. DDiarrhoea, frequent urination and sweating
8.PharmacologyHard

Probenecid has been used to raise plasma penicillin levels. How does it do this?

  1. AIt inhibits the liver metabolism of penicillin
  2. BIt displaces penicillin from plasma proteins
  3. CIt increases the absorption of penicillin from the small intestine
  4. DIt blocks the tubular secretion of penicillin in the kidney

3Solutions

1.Clinical pharmacokinetics

Answer: k = 0.09941 h⁻¹

Clearance and volume: at steady state the dosing rate equals the elimination rate, so the maintenance rate = CL × Css. A loading dose is LD = Vd × C/(S × F), with S the salt factor (fraction of active drug in the salt) and F the bioavailability (1 for IV). From two levels, k = ln(C₁/C₂)/Δt; for an IV bolus Vd = dose/C₀ and CL = k × Vd. The numbers are for practice only; at the bedside always follow local protocols and have high-risk doses double-checked.

Elimination rate constant

k = ln(30/9.1)/12 = 1.193/12 = 0.09941 h⁻¹

Answer

k = 0.09941 h⁻¹
2.Clinical pharmacokinetics

Answer: Css,avg = 17.86 mg/L

Designing a regimen: with rapid IV doses the level falls from peak to trough during the interval, so τ = ln(Cpeak/Ctrough)/k and the dose that restores the peak is Vd × (Cpeak − Ctrough). The average steady-state level is Css,avg = S·F·dose/(CL·τ). An infusion rises as C = (R/CL)(1 − e−kt). For a drug cleared by the kidneys, the dose is scaled with the creatinine clearance. The numbers are for practice only; at the bedside always follow local protocols and have high-risk doses double-checked.

Clearance

CL = 0.03·84 = 2.52 L/h

Average steady-state level

Css,avg = S·F·D/(CL·τ) = 0.8·1·450/(2.52·8) = 17.86 mg/L

Answer

Css,avg = 17.86 mg/L
3.Pharmacy calculations

Answer: V = 1.6 mL

Strength to volume: turn the strength into mg per mL first. A w/v percentage is grams per 100 mL, so x% = 10x mg/mL. A ratio strength 1:n is 1 g in n mL. After reconstitution the concentration is the powder's dose over the final volume (diluent + powder volume). Then volume = dose/concentration.

Strength in mg/mL

1000 mg/10 000 mL = 0.1 mg/mL

Volume

V = 0.16/0.1 = 1.6 mL

Answer

V = 1.6 mL
4.Pharmacy calculations

Answer: m = 90 g

Alligation: to mix a higher strength H and a lower strength L into a target strength T, take (T − L) parts of H and (H − T) parts of L. The parts are crossed: each stock gets the distance from the target to the other stock. Water or a plain base counts as 0%. The numbers are for practice only; at the bedside always follow local protocols and have high-risk doses double-checked.

Alligation parts

5%: 2 − 1 = 1 parts
1%: 5 − 2 = 3 parts

Scale to the amount you have

m = 30·3/1 = 90 g

Answer

m = 90 g

Check: 30 g + 90 g = 120 g of 2% ointment.

5.Pediatric & critical-care dosing

Answer: V = 0.77 mL

Heparin and insulin infusions: concentration = units in the bag/bag volume (units/mL). Pump rate (mL/h) = units per hour/concentration, and units per hour = mL/h × concentration. For a weight-based order, units/h = units/kg/h × weight first. A bolus volume = units needed/vial strength. The numbers are for practice only; at the bedside always follow local protocols and have high-risk doses double-checked.

Units needed

60·64 = 3 840 units

Volume

V = 3840/5000 = 0.768 ≈ 0.77 mL

Answer

V = 0.77 mL
6.Pediatric & critical-care dosing

Answer: D = 14.7 mcg/kg/min

Titrated drips: first find the concentration in mcg/mL (mg × 1000/mL). For a weight-based order, mcg/min = mcg/kg/min × weight. Then mL/h = mcg/min × 60/concentration. Working backwards, mcg/kg/min = mL/h × concentration/(60 × weight). The numbers are for practice only; at the bedside always follow local protocols and have high-risk doses double-checked.

Concentration

500 000/250 = 2000 mcg/mL

Micrograms per minute

26·2000 = 52000 mcg/h
52000/60 = 866.7 mcg/min

Per kilogram

D = 866.7/59 = 14.69 ≈ 14.7 mcg/kg/min

Answer

D = 14.7 mcg/kg/min
7.Pharmacology

Answer: A · Dry mouth, faster heart rate and dilated pupils

Why this is the answer

Anticholinergic drugs block muscarinic receptors, so parasympathetic effects are reduced. This gives dry mouth, tachycardia, dilated pupils, constipation and urinary retention.

Answer

A · Dry mouth, faster heart rate and dilated pupils
8.Pharmacology

Answer: D · It blocks the tubular secretion of penicillin in the kidney

Why this is the answer

Penicillins are excreted largely by organic anion transporters in the proximal tubule. Probenecid competes for these transporters, so penicillin is excreted more slowly and its level stays higher.

Answer

D · It blocks the tubular secretion of penicillin in the kidney

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