42 The study population was selected from all women undergoing coronary arteriography at the Baptist Memorial Hospital, Memphis, Tennessee, between 1972 and 1989. Information on HRT use was obtained from the cardiac catheterization
reports and from annual follow-up questionnaires sent to the patients’ physician, while the outcome of death was established by reports from the physician or family until 1991. Subjects were defined as HRT users if treated with estrogens at the time of admission for angiography or if estrogen was listed as a current medication Inhibitors,research,lifescience,medical on any response to the follow-up questionnaire. As a result, 92 were noted to have received HRT, including 42 at the time of CABG and 50 any time Crizotinib ROS1 During follow-up. These were compared with 1,006 non-users who had not received HRT at baseline or any time during follow-up. Five- and ten-year survival was 98.8% and 81.4%, respectively, in the HRT users and 82.3% and 65.1% in the non-users. The Cox proportional hazards model resulted in a remarkable 62% reduction in mortality with HRT use (hazard ratio 0.38; P < 0.001). Inhibitors,research,lifescience,medical The authors concluded that HRT use after surgery significantly
improves the survival of postmenopausal women with coronary artery Inhibitors,research,lifescience,medical disease. Immortal time bias was introduced in this study classifying the 50 women who initiated HRT sometime during follow-up as exposed to HRT during the entire follow-up (Figure 3). Thus a woman who had her Inhibitors,research,lifescience,medical CABG in 1972 and only initiated HRT use in 1982 was called exposed to HRT when in fact she was not exposed between 1972 and 1982. The fact that she started in 1982 implies she was alive on that date, introducing a 10-year “immortal” period misclassified
as exposed to HRT instead of unexposed, which will necessarily generate immortal time bias in this study. Figure 3 Illustration of immortal time bias in the Sullivan et al. observational cohort study of HRT in patients undergoing CABG surgery.42 The second example is the Study of Osteoporotic Inhibitors,research,lifescience,medical Fractures, based on a prospective cohort identified from four US communities in this Oregon, Minnesota, Maryland, and Pennsylvania.43 The cohort included 9,704 women 65 years or older, Drug_discovery who were observed between 1986 and 1994. Of these, 14.1% reported use of HRT for at least 1 year. During an average follow-up of 6 years, 11.8% died, and after adjustment for confounders the all-cause mortality rate was 31% lower in users of HRT (RR 0.69; 95% CI 0.54–0.87). The RR was 0.95 (95% CI 0.68–1.32) among short-term users of HRT compared with 0.55 (95% CI 0.40–0.75) among long-term users. The authors concluded that HRT is associated with lower overall mortality rates. Immortal time bias was again introduced in this study by defining use of HRT, not exclusively at the baseline interview, but by updating this exposure information at the third clinical visit, i.e. 3.5 years after cohort entry. Here again, HRT exposure was misclassified as exposed during this 3.