Volume 7, Number 5—October 2001
Synopsis
Cost-Effectiveness of a Potential Vaccine for Coccidioides immitis
Table A1
Input variable | Base-case estimate (range) | Quality of evidenceb | Source |
---|---|---|---|
Epidemiology (%) | |||
Vaccine effectiveness | 75 (20-90) | I | 77 |
Skin-test sensitivity | 70 (50-80) | II-2 | 78-80 |
Skin-test specificity | 90 (70-97) | II-2 | 79, 81, 82 |
Annual infection rate | 2 (0.25-3) | II-3 | 80, 83-91 |
Annual emigration among vaccinees out of highly endemic region | 0.5 (0-4.2) | II-2, III | c |
Symptomatic primary pulmonary disease after infection | 40 | II-2 | 93 |
Diagnosed symptomatic primary pulmonary disease | 10 (5-15) | III | d |
Death from primary pulmonary disease, given diagnosis | 0.5 (0-26) | II-2 | 94-101 |
Chronic pulmonary disease after diagnosed primary infection | 5 (1-10) | III | 99 |
Death from chronic pulmonary disease | 5 (0-20) | III | 99e |
Dissemination after infection | 0.38(0.25-0.55) | II-2 | 92 |
Meningitis, given dissemination | 33 (23-44) | II-2 | 96, 101 |
Death from meningeal dissemination | 7 (5-40) | II-2, III | 102d,e |
Moderate disability after meningeal dissemination | 50 (40-60) | III | 102d,e |
Severe disability after meningeal dissemination | 17 (10-30) | III | 102d,e |
Annual meningeal dissemination relapse rate, on treatment | 2 (0-5) | I, II-2 | 103-105 |
Death from nonmeningeal dissemination | 2 (0-10) | III | e |
Moderate disability after nonmeningeal dissemination | 33 (20-50) | III | d,e |
Annual nonmeningeal dissemination relapse rate, On treatment | 2 (0-5) | I, II-2, III | 79c |
Off treatment | 50 (35-65) | I, II-2, III | 106-109c |
Mild vaccine side effects | 25 (10-40) | II-2 | 110 |
Vaccine anaphylaxis, x 10-4 | 1.67 (0.1-10) | II-2 | 110 |
Direct medical costs ($) | |||
Three doses of vaccine | 180 (100-400) | III | 111,112 |
Skin test | 12 (9-15) | III | 113 |
Home care, per month | 2,450 (1,840-3,060) | II-2 | 114 |
Diagnosed pulmonary disease | 2,090 (1,570-2,610) | II-2, III | 115 |
Incident meningeal dissemination | 9,510 (7,130-11,890) | II-2 | 115 |
Medication and follow-up after Coccidioides immitis meningitis,f per month | 1,510 (1,130-1,890) | II-2 | 116e,g |
Incident nonmeningeal dissemination | 6,950 (5,210-8,690) | II-2 | 115 |
Medication and follow-up for chronic pulmonary infection and nonmeningeal dissemination,f per month | 530 (290-790) | II-2 | 116e,g |
Inpatient vaccine anaphylaxis treatment | 2,180 (1,640-2,730) | II-2 | 115 |
Time costsh | |||
Average wage ($ per hour) | 12 (9-15) | II-2 | d |
Average clinic visit (hours) | 1.25 (0.5-2) | III | Assumed |
Lost work due to undiagnosed primary pulmonary disease (days) | 5 (0-10) | III | Assumed |
For parents of sick children (days) | 3 (0-5) | III | Assumed |
Utilities | |||
Well | 0.94 to 0.70i | II-2 | 117 |
Diagnosed primary pulmonary infection | 0.90 (0.85-0.95) | III | d |
Chronic pulmonary infection (proxy, pulmonary tuberculosis) | 0.57 (0.29-0.84) | II-2, III | 117 |
Meningeal dissemination (proxy, paraplegia) | 0.40 (0.21-0.52) | II-2, III | 117 |
Nonmeningeal dissemination (proxy, orthopedic impairment) | 0.59 (0.34-0.84) | II-2, III | 117 |
Severe disability after meningitis (proxy, hemiplegia) | 0.27 (0.10-0.38) | II-2, III | 117 |
Moderate disability after meningitis (proxy, sciatica) | 0.72 (0.52-0.92) | II-2, III | 117 |
Moderate disability after nonmeningeal dissemination (proxy, arthritis) | 0.69 (0.51-0.92) | II-2, III | 117 |
Chronic azole treatment (proxy, warfarin treatment) | 0.98 (0.92-1.0) | II-2, III | 118 |
Dead | 0 | III | Assumed |
Vaccine side effect quality-of-life decrement (days) | 0.1 (0-0.2) | III | Assumed |
Other variables (%) | |||
Discount rate | 3 (0-5) | III | 119 |
aThe base-case estimate represents our best estimate for each value. All costs are in 2000 U.S. dollars.
bThe quality rating is derived from the U.S. Preventive Services Task Force Guide to Clinical Preventive Services (76). Source of evidence: I: at least one properly randomized controlled trial; II-1: well-designed controlled trial without randomization; II-2: well-designed cohort or case-control analytic studies; II-3: multiple time series with or without intervention; III: opinions of respected authorities; descriptive studies and case reports; or reports of expert committees (76).
cInternal Revenue Service, unpub. data.
dJohn Galgiani, pers. comm.
eHans Einstein, pers. comm.
fWe assumed that meningitis patients were treated with 800 mg of daily fluconazole, and chronic pulmonary and nonmeningeal dissemination patients with either 400 mg fluconazole or 400 mg ketoconazole daily (Royce Johnson, pers. comm., 1999). A 50:50 distribution of fluconazole and ketoconazole use represents our base case; the upper end of the range assumes all nonmeningeal dissemination patients receive fluconazole in follow-up, whereas the lower end assumes they receive the less expensive ketoconazole.
gRon Talbot, pers. comm.
hBased on a weighted adjusted gross income of $24,105 from taxpayers in the 10 highly endemic counties (Internal Revenue Service, unpub. data).
iMean HALex scores for healthy persons, by age group (when men and women had differing mean scores, we chose the higher of the two scores): <5=0.94; 5-17=0.93; 18-24= 0.92; 25-34=0.91; 35-44=0.90; 45-54=0.87; 55-64=0.81; 65-74=0.78; >75=0.70 (43).
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