Baseline characteristics |
|
|
|
|
|
Age structure of infected population presenting to care |
|
|
Badri[8], Dorrington[28], IDB[29] |
15-25 years old |
34% |
|
|
|
25-35 years old |
39% |
|
|
|
35-50 years old |
27% |
|
|
|
CD4 count at presentation, cells/μl (mean ± SD) |
144 ± 121 |
|
ART-LINC[9] |
Viral load at presentation, log copies/ml (mean ± SD) |
5.0 ± 0.8 |
|
Badri[6] |
Disease Progression Variables |
|
|
|
|
|
Decline in CD4 (cells/μl/mo), viral load 103-106
|
|
|
Holmes[21], Mellors[30], Rodriguez[31], PLATO[32] |
Baseline CD4 >500 cells/μl |
3.9-5.9 |
± 50% |
|
|
Baseline CD4 351-500 cells/μl |
2.6-3.8 |
± 50% |
|
|
Baseline CD4 201-350 cells/μl |
1.7-2.6 |
± 50% |
|
|
Baseline CD4 <200 cells/μl |
1.3-2.0 |
± 50% |
|
|
Monthly probability of developing severe opportunistic diseases (%), by CD4 |
<50 cells/μl
|
51-200 cells/μl
|
201-350 cells/μl
|
>350 cells/μl
|
Holmes[21] |
Oral candidiasis |
3.50% |
2.04% |
1.26% |
0.57% |
|
Chronic diarrhea |
2.00% |
0.49% |
0.18% |
0.00% |
|
Esophageal candidiasis |
1.46% |
0.34% |
0.09% |
0.06% |
|
Wasting syndrome |
1.29% |
0.23% |
0.02% |
0.00% |
|
Severe bacterial |
1.15% |
0.04% |
0.03% |
0.00% |
|
Pulmonary TB |
1.15% |
0.71% |
0.47% |
0.11% |
|
Extrapulmonary TB |
0.98% |
0.47% |
0.18% |
0.05% |
|
PCP |
0.67% |
0.05% |
0.02% |
0.00% |
|
CMV |
0.52% |
0.07% |
0.02% |
0.00% |
|
Cryptococcal meningitis |
0.52% |
0.05% |
0.00% |
0.00% |
|
Risk of HIV death by CD4 cell count |
|
|
|
Badri[7], ART-LINC[9] |
CD4 <50 cells/μl |
2.1%/mo |
|
± 10% |
|
|
CD4 51-200 cells/μl |
1.7%/mo |
|
± 10% |
|
|
CD4 201-350 cells/μl |
1.1%/mo |
|
± 10% |
|
|
CD4 >350 cells/μl |
0.8%/mo |
|
± 10% |
|
|
Cumulative risks of toxicity and failure |
Year 1 |
|
Year 3 |
Range |
Source |
tenofovir + lamivudine + efavirenz |
|
|
|
|
|
Virologic failure |
12% |
|
24% |
± 4% |
Gallant, Arribas[10, 33] |
Lipoatrophy |
6% |
|
17% |
± 3% |
Haubrich[11] |
Renal failure |
1% |
|
1% |
± 1% |
Gallant[11] |
Myocardial infarction |
0.1% |
|
0.1% |
± 0.1% |
Gallant[12, 33, 34] |
tenofovir + lamivudine + nevirapine |
Year 1 |
|
Year 3 |
Range |
Source |
Virologic failure |
18% |
|
31% |
± 6% |
Gallant, Nachega, Smith[15, 33, 35] |
Lipoatrophy |
6% |
|
17% |
± 3% |
Haubrich[11] |
Renal failure |
1% |
|
1% |
± 1% |
Gallant[11] |
Hepatotoxicity |
6.3% |
|
6.3% |
± 5% |
Amoroso[14] |
zidovudine + lamivudine + efavirenz |
Year 1 |
|
Year 3 |
Range |
Source |
Virologic failure |
17% |
|
31% |
± 7% |
Gallant[33], Arribas[10] |
Lipoatrophy |
23% |
|
54% |
± 15% |
Arribas, Haubrich[10, 11] |
Anemia |
6% |
|
6% |
± 3% |
Gallant[33] |
Myocardial infarction |
0.2% |
|
0.2% |
± 0.2% |
Gallant[12, 33, 34] |
zidovudine + lamivudine + nevirapine |
Year 1 |
|
Year 3 |
Range |
Source |
Virologic failure |
25% |
|
46% |
± 12% |
Gallant, Arriba, Nachega, Smith [10, 15, 33, 35] |
Lipoatrophy |
23% |
|
54% |
± 15% |
Arribas, Haubrich[10, 11] |
Anemia |
6% |
|
6% |
± 3% |
Gallant[33] |
Myocardial infarction |
0.1% |
|
0.1% |
± 0.1% |
Gallant[12, 33, 34] |
Hepatotoxicity |
6.3% |
|
6.3% |
± 5% |
Amoroso[14] |
stavudine + lamivudine + nevirapine |
Year 1 |
|
Year 3 |
Range |
Source |
Virologic failure |
18% |
|
31% |
± 6% |
Gallant, Nachega, Smith[15, 33, 35] |
Lipoatrophy |
30% |
|
66% |
± 20% |
Haubrich[11] |
Neuropathy |
25% |
|
25% |
± 10% |
Gallant[11] |
Myocardial infarction |
0.3% |
|
0.3% |
± 0.3% |
Gallant[12, 33, 34] |
Hepatotoxicity |
6.3% |
|
6.3% |
± 5% |
Amoroso[14] |
Lactic acidosis |
0.5% |
|
0.5% |
± 0.2% |
John, Boubaker [36, 37] |
Quality of life weights and duration of toxicities |
|
|
|
|
|
HIV without HAART |
0.84 |
|
|
0.84-1 |
Cleary[38] |
HIV with HAART |
0.91 |
|
|
0.91-1 |
Cleary[38] |
Lipoatrophy |
0.87 |
Irreversible |
0.8-0.95 |
Rosen[23, 39] |
Anemia |
0.58 |
4 mo |
0.5-0.66 |
Kimel[40] |
Renal failure |
0.7 |
4 mo |
0.6-0.8 |
Rosen[23, 39] |
Neuropathy |
0.87 |
Irreversible after 1 year |
0.8-0.95 |
Gallant[12] |
Lactic acidosis |
0.5 |
3 mo |
0.4-0.6 |
Rosen[23, 39] |
MI |
0.6 |
2 mo |
0.4-0.8 |
Assumption |
Hepatotoxicity |
0.7 |
2 mo |
0.5-0.9 |
Assumption |
Utilization and cost variables |
|
|
|
|
|
Annual number of inpatient days without a severe opportunistic disease |
|
|
|
Badri et al[6, 41] |
|
CD4>350 (on/off HAART) |
0.14 / 1.9 |
|
± 50% |
|
|
CD4 201-350 (on/off HAART) |
0.39 / 3 |
|
± 50% |
|
|
CD4<=200 (on/off HAART) |
0.26 / 7.7 |
|
± 50% |
|
|
Annual number of inpatient days with a severe opportunistic disease |
|
|
|
Badri et al[6, 41] |
|
CD4>350 (on/off HAART) |
0.37 / 5.7 |
|
± 50% |
|
|
CD4 201-350 (on/off HAART) |
0.52 / 10.8 |
|
± 50% |
|
|
CD4<=200 (on/off HAART) |
1.8 / 17.7 |
|
± 50% |
|
|
Annual number of outpatient visits |
|
|
|
Badri et al[6, 41] |
|
CD4>350 (on/off HAART) |
4.3 / 4.1 |
|
± 50% |
|
|
CD4 201-350 (on/off HAART) |
3.9 / 5.0 |
|
± 50% |
|
|
CD4<=200 (on/off HAART) |
4.7 / 6.6 |
|
± 50% |
|
|
Monitoring Costs (2009 USD) |
|
|
|
|
|
Inpatient Day |
$182 |
|
± 50% |
Badri; Cleary[6, 38] |
|
Outpatient visit |
$26 |
|
± 50% |
Badri; Cleary[6, 38] |
|
Cost per CD4 test |
$15 |
|
± 50% |
Badri, Zijeneh[6, 42] |
|
HAART Costs (2009 USD) |
|
|
|
WHO[43] |
|
tenofovir + lamivudine + efavirenz |
$675 |
|
$100-675 |
|
|
tenofovir + lamivudine + nevirapine |
$538 |
|
$100-538 |
|
|
zidovudine + lamivudine + efavirenz |
$384 |
|
$100-384 |
|
|
zidovudine + lamivudine + nevirapine |
$247 |
|
$100-247 |
|
|
stavudine + lamivudine + nevirapine |
$121 |
|
$100-121 |
|
|
Second line HAART |
$769 |
|
$100-769 |
|
|
Toxicity costs |
|
|
|
|
|
Lipoatrophy |
$121 |
|
$60-242 |
Rosen[23] |
|
Anemia |
$136 |
|
$68-272 |
Cantor[44] |
|
Renal failure |
$213 |
|
$106-8,477 |
Rosen[23] |
|
Neuropathy |
$130 |
|
$65-260 |
Rosen[23] |
|
Lactic acidosis |
$192 |
|
$96-7,999 |
Rosen[23] |
|
MI |
$300 |
|
$150-600 |
Assumption |
|
Hepatotoxicity |
$300 |
|
$150-600 |
Assumption |
|