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. 2010 Mar;3(1):26–36. doi: 10.1111/j.1753-5174.2009.00028.x

Table 3.

Participants withdrawn prematurely from treatment, N (%)

All Participants Treatment- Naïve PI-Naïve but Treatment- Experienced Toxicity Switch from Other PI Regimen Toxicity Switch from Prior Non-PI Regimen HCV Coinfection Prior PI Prior Non-PI Regimen
Participants Initiating Study (N = 2122) (N = 413) (N = 265) (N = 161) (N = 201) (N = 287) (N = 1386) (N = 1640)
Reason for withdrawal
Adverse event 44 (2.1) 9 (2.2) 7 (2.6) 3 (1.9) 5 (2.5) 5 (1.7) 27 (1.9) 34 (2.1)
Lost to follow-up 42 (2.0) 17 (4.1) 1 (0.4) 2 (1.2) 1 (0.5) 12 (4.2) 23 (1.7) 23 (1.4)
Lack of adherence 26 (1.2) 5 (1.2) 4 (1.5) 1 (0.6) 4 (2.0) 7 (2.4) 17 (1.2) 20 (1.2)
Virologic failure 18 (0.8) 1 (0.2) 1 (0.6) 17 (1.2) 16 (1.0)
Intercurrent illness 11 (0.5) 4 (1.0) 2 (0.8) 2 (1.0) 5 (0.4) 7 (0.4)
Death 7 (0.3) 4 (1.0) 3 (1.0) 3 (0.2) 3 (0.2)
Other 43 (2.0) 9 (2.2) 5 (1.9) 1 (0.6) 6 (3.0) 3 (1.0) 28 (2.0) 33 (2.0)
None provided 23 (1.1) 4 (1.0) 5 (1.9) 2 (1.2) 3 (1.0) 14 (1.0) 19 (1.2)
All 214 (10.1) 53 (12.8) 24 (9.11) 10 (6.2) 18 (9.0) 33 (11.5) 134 (9.7) 155 (9.5)

HCV = hepatitis C virus; PI = protease inhibitor.