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. 2013 Sep 2;5:437–445. doi: 10.2147/CEOR.S47486

Table 4.

Model costs by treatment, patient monitoring characteristic, and adverse event

Parameter Costa Distributionb Reference
Product acquisition costs
 First-line
  Atripla® 4,918 Gamma 1, 13
  Stribild™ 6,559
 Second-linec 6,977
 Third-lined 9,092
Patient monitoring costse
 No virologic failuref 914 Gamma 32
 Virologic failure
  CD4 ≥50 cells/mm3,g 1,561
  CD4 <50 cells/mm3,h 1,620
 Patient receiving new line of therapyi 113
Cost of treating adverse events
 Rash 226 Gamma 32
 Elevated lipids 186 13, 32
 CNS symptoms 226 32
 Renal abnormalities
 No acute kidney injury 914 32
  Acute kidney injury 33,594 14, 32
  Chronic kidney disease with dialysis 48,665 15
 Other adverse events causing discontinuation 226 32

Notes:

a

All costs are per 12-week cycle and are reported in 2012 US dollars;

b

distributions used in probabilistic sensitivity analysis;

c

second-line treatment defined as 50% receiving atazanavir with boosted ritonavir (atazanavir/r) and two NRTIs, 50% receiving darunavir with boosted ritonavir (darunavir/r) and two NRTIs;

d

third-line treatment defined as 50% receiving darunavir/r + etravirine, 50% receiving maraviroc + raltegravir + optimized background therapy;

e

all cost estimates were averages of high and low managed care rates;25

f

cost included baseline monitoring components, consisting of a 10-minute physician office visit, one blood draw, one chemistry panel, one complete blood count, one CD4 count, and one viral load assessment (ultrasensitive quantification);

g

cost included baseline patient monitoring plus a 15-minute physician office visit, one blood draw, and one viral load assessment;

h

cost included baseline patient monitoring plus a 25-minute physician office visit, one blood draw, and one viral load assessment;

i

cost included a 15-minute physician office visit.

Abbreviations: CNS, central nervous system; NRTIs, nucleoside reverse transcriptase inhibitors.