Cost-effectiveness of prophylaxis against Pneumocystis carinii pneumonia in patients with Wegener's granulomatosis undergoing immunosuppressive therapy
Jb. Chung et al., Cost-effectiveness of prophylaxis against Pneumocystis carinii pneumonia in patients with Wegener's granulomatosis undergoing immunosuppressive therapy, ARTH RHEUM, 43(8), 2000, pp. 1841-1848
Objective. To assess the incremental cost-effectiveness of 3 Pneumocystis c
arinii pneumonia (PCP) prophylaxis strategies in patients with Wegener's gr
anulomatosis (WG) receiving immunosuppressive therapies: 1) no prophylaxis;
2) trimethoprim/sulfamethoxazole (TMP/SMX) 160 mg/800 mg 3 times a week, w
hich is discontinued if patients experience an adverse drug reaction (ADR);
and 3) TMP/SMX 160 mg/800 mg 3 times a week, which is replaced by monthly
aerosolized pentamidine (300 mg) if patients experience an ADR.
Methods. A Markov state-transition model was developed to follow a hypothet
ical cohort of WG patients over their lifetimes starting from the time of i
nitial exposure to the immunosuppressive therapy. The effect of PCP prophyl
axis on life expectancy, quality-adjusted life expectancy, average discount
ed lifetime cost (ADLC), and incremental cost-effectiveness was estimated b
ased on data obtained from a literature review. Direct medical costs were e
xamined from a societal perspective, and costs and benefits were discounted
at 3% annually.
Results. No prophylaxis resulted in a life expectancy of 13.36 quality-adju
sted life years (QALY) at an ADLC of $4,538. In comparison, prophylaxis wit
h TMP/ SMX alone increased the QALY to 13.54 and was cost saving, with an A
DLC of $3,303. The addition of pentamidine in patients who had an ADR to TM
P/SMX resulted in 13.61 QALY, with an ADLC of $7,428. Compared with TMP/SMX
alone, TMP/SMX followed by pentamidine increased the QALY by 0.07 at an in
cremental cost of $58,037 per QALY. Both TMP/SMX alone and TMP/SMX followed
by pentamidine prophylaxis strategies dominated the no prophylaxis strateg
y until the incidence of PCP fell below 0.2% and 2.25%, respectively. Insti
tution of pentamidine therapy for patients with a TMP/SMX ADR increased qua
lity-adjusted life expectancy compared with that with TMP/ SMX alone until
the incidence of PCP rose above 7.5%.
Conclusion. Prophylaxis using TMP/SMX alone increased life expectancy and r
educed cost for patients with WG receiving immunosuppressive therapy. Repla
cing TMP/SMX with monthly aerosolized pentamidine in cases of ADR further i
ncreased life expectancy, although at an increased cost.