TABLE 3.
30+ day pharmacy |
60+ day pharmacy |
90-day visit |
180-day visit |
|||||
---|---|---|---|---|---|---|---|---|
Risk factor | HR | P value | HR | P value | HR | P value | HR | P value |
Site | ||||||||
Hôpital St. Michel in Jacmel vs. Hôpital St. Antoine in Jérémie |
0.58 | < 0.001 | 0.53 | < 0.001 | 0.46 | < 0.001 | 0.95 | 0.69 |
Post vs. pre-earthquake | 0.94 | 0.66 | 0.77 | 0.14 | 0.38 | < 0.001 | 0.51 | < 0.01 |
Gender (male=reference) | ||||||||
Female (not pregnant) | 0.99 | 0.92 | 1.07 | 0.67 | 1.08 | 0.40 | 1.02 | 0.90 |
Female (pregnant) | 1.08 | 0.71 | 1.20 | 0.54 | 1.16 | 0.42 | 1.44 | 0.22 |
Age (10 years or more) | 1.05 | 0.20 | 0.98 | 0.75 | 0.92 | 0.02 | 0.84 | < 0.01 |
Proximity (same commune=reference) | ||||||||
Adjacent commune | 1.69 | < 0.001 | 1.44 | 0.02 | 1.03 | 0.77 | 1.20 | 0.25 |
Non-adjacent commune | 1.89 | < 0.001 | 2.37 | < 0.001 | 1.65 | < 0.001 | 2.58 | < 0.001 |
Body mass index (< 18.5=reference) | ||||||||
>18.5 | 1.19 | 0.06 | 1.18 | 0.21 | 1.18 | 0.04 | 1.40 | 0.02 |
Year of ART start (2005-2006=reference) | ||||||||
2007–2008 | 0.66 | < 0.001 | 0.91 | 0.56 | 2.02 | < 0.001 | 1.14 | 0.36 |
2009–2010 | 0.60 | < 0.01 | 1.09 | 0.71 | 1.67 | < 0.001 | 0.81 | 0.41 |
2011 | 0.37 | < 0.001 | 0.54 | 0.13 | 2.20 | < 0.01 | 0.88 | 0.77 |
Baseline CD4 (< 100=reference) | ||||||||
100–249 | 1.06 | 0.58 | 1.01 | 0.97 | 1.06 | 0.54 | 0.75 | 0.05 |
≥ 250 | 1.15 | 0.33 | 0.98 | 0.92 | 1.04 | 0.74 | 0.78 | 0.18 |
ART regimenb (AZT-3TC-EFV=reference) | ||||||||
AZT-3TC-NVP | 1.14 | 0.23 | 0.94 | 0.70 | 0.87 | 0.16 | 0.79 | 0.15 |
d4T or TDF + 3TC-EFV | 0.67 | 0.10 | 0.47 | 0.07 | 1.01 | 0.97 | 1.08 | 0.81 |
d4T or TDF + 3TC-NVP | 0.86 | 0.51 | 0.78 | 0.45 | 0.73 | 0.09 | 0.66 | 0.21 |
non-standard regimens | 2.04 | 0.01 | 1.04 | 0.94 | 0.54 | 0.07 | 1.17 | 0.73 |
World Health Organization clinical stage (Stage I or II = reference) |
||||||||
Stage III or IV | 1.16 | 0.07 | 1.19 | 0.15 | 1.11 | 0.13 | 1.09 | 0.51 |
Tuberculosis status (No suspicion, prophylaxis or diagnosis = reference) |
||||||||
Yes | 0.91 | 0.32 | 0.95 | 0.75 | 0.94 | 0.48 | 1.03 | 0.81 |
Any Stage IV symptom (No=reference) | ||||||||
Yes | 0.84 | 0.22 | 0.77 | 0.21 | 0.94 | 0.64 | 1.16 | 0.47 |
Pre-ART duration (30 day increase) | 0.99 | 0.01 | 0.99 | 0.07 | 0.99 | < 0.01 | 0.98 | 0.01 |
Counseling sessions prior to ART start (None = reference) | ||||||||
1 | 0.84 | 0.07 | 0.92 | 0.52 | 1.11 | 0.22 | 1.05 | 0.73 |
≥ 2 | 0.74 | 0.06 | 0.83 | 0.42 | 0.99 | 0.93 | 0.92 | 0.75 |
Main effects model using alternative definitions for ART attrition; items in bold represent statistically significant hazard ratios.
ART regimen: AZT = zidovudine; 3TC =l amivudine; EFV = efavirenz; NVP = nevirapine; d4T = stavudine; TDF = tenofovir.