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. 2017 Sep 13;31(15):2095–2106. doi: 10.1097/QAD.0000000000001594

Table 2.

Observation (follow-up) time and time to event by outcomes of interest and treatment group.

Observation time (days) Time to event (days)
Outcome Exposure N Mean (SD) Median (Q1, Q3) n Mean (SD) Median (Q1, Q3)
MI All ARVs 9500 394 (626) 145 (59, 409) 80a 489 (622) 243 (67, 690)
ATV 1529 370 (598) 144 (61, 363) 8 363 (440) 180 (46, 637)
Non-ATV 7971 399 (631) 146 (59, 419) 72 503 (640) 250 (77, 690)
Other PIs 2053 279 (450) 116 (51, 282) 16 598 (821) 249 (128, 821)
NNRTI 5307 459 (704) 161 (61, 511) 50 502 (610) 256 (53, 701)
INSTI 611 276 (336) 145 (66, 361) 6 260 (223) 233 (98, 345)
Stroke All ARVs 9500 390 (622) 144 (59, 404) 170b 403 (593) 144 (28, 575)
ATV 1529 367 (601) 143 (60, 357) 16 163 (215) 72 (18, 280)
Non-ATV 7971 394 (626) 144 (58, 416) 154 428 (615) 151 (31, 691)
Other PIs 2053 277 (451) 113 (51, 281) 34 249 (323) 104 (31, 357)
NNRTI 5307 454 (698) 160 (60, 509) 105 521 (696) 175 (37, 799)
INSTI 611 271 (326) 144 (64, 360) 15 186 (284) 41 (8, 289)
All-cause mortality All ARVs 9500 397 (630) 147 (59, 413) 190c 501 (632) 204 (70, 698)
ATV 1529 373 (604) 144 (61, 364) 25 609 (864) 127 (63, 894)
Non-ATV 7971 402 (635) 147 (59, 428) 165 484 (591) 210 (71, 694)
Other PIs 2053 282 (455) 116 (51, 284) 37 410 (561) 119 (55, 515)
NNRTI 5307 463 (708) 164 (61, 516) 118 523 (616) 270 (88, 722)
INSTI 611 278 (339) 146 (66, 365) 10 302 (293) 165 (84, 453)

N = number of patients in each treatment group; n = number of events in each treatment group. ARV, antiretroviral; ATV, atazanavir; INSTI, integrase strand transfer inhibitor; MI, myocardial infarction; NNRTI, nonnucleoside reverse transcriptase inhibitor; PI, protease inhibitor; Q1, first quartile; Q3, third quartile.

aA total of 8692 patients were censored due to a 30-day gap in medication and 728 were administratively censored at the end of study period.

bA total of 8627 patients were censored due to a 30-day gap in medication and 703 were administratively censored at the end of study period.

cA total of 8575 patients were censored due to a 30-day gap in medication and 735 were administratively censored at the end of study period.