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. 2022 Aug 6;19:38. doi: 10.1186/s12981-022-00457-0

Table 3.

Reasons for discontinuing RPV or EFV

RPV1 N (%) EFV2 N (%)
Median (IQR) duration of treatment at discontinuation (Months) 18.2 (6.7–34.2) 9.8 (3.4–23.1)
Treatment failure (virological, immunological, and/or clinical) 29 (5.8) 14 (9.5)
Toxicity 73 (14.7) 45 (30.4)
 Predominantly from central nervous system (CNS) 13 (2.6) 33 (22.3)
 Predominantly from kidneys 20 (4.0) 4 (2.7)
 Liver 6 (1.2) 3 (2.0)
 Hypersensitivity reaction (skin eruption etc.) 3 (0.6) 2 (1.4)
 Predominantly from abdomen/GI tract 13 (2.6) 1 (0.7)
 Abnormal fat redistribution 2 (0.4) 0 (0.0)
 Cardiovascular disease 2 (0.4) 0 (0.0)
 Dyslipidaemia 0 (0.0) 1 (0.7)
 Other side effects–not specified 14 (2.8) 1 (0.7)
Other
 Physician's decision, not specified 167 (33.5) 23 (15.5)
 Participant's wish/decision, not specified 38 (7.6) 18 (12.2)
 Availability of more effective treatment (not specifically failure or side effect related) 15 (3.0) 5 (3.4)
 Structured Treatment Interruption (STI) 3 (0.6) 0 (0.0)
 Enrolled in RCTs 2 (0.4) 0 (0.0)
 Other causes, not specified 91 (18.3) 23 (15.5)
 Unknown 80 (16.1) 20 (13.5)

Reasons listed are those for stopping either RPV or EFV

1Denominator is the number of participants who have discontinued RPV (n = 498)

2Denominator is the number of participants who have discontinued EFV (n = 148)

Reasons for discontinuation can be found at https://hicdep.org/Wiki/v/9/pt/4/Table/36/FieldID/439