Published online Sep 26, 2015. doi: 10.5662/wjm.v5.i3.122
Peer-review started: April 18, 2015
First decision: June 3, 2015
Revised: June 12, 2015
Accepted: August 13, 2015
Article in press: August 14, 2015
Published online: September 26, 2015
Processing time: 156 Days and 3.3 Hours
There are multiple biases in using observational studies to examine treatment effects such as those from prevalent drug users, immortal time and drug indications. We used renin angiotensin system (RAS) inhibitors and statins as reference drugs with proven efficacies in randomized clinical trials (RCTs) and examined their effectiveness in the prospective Hong Kong Diabetes Registry using adjustment methods proposed in the literature. Using time-dependent exposures to drug treatments yielded greatly inflated hazard ratios (HR) regarding the treatment effects of these drugs for cardiovascular disease (CVD) in type 2 diabetes. These errors were probably due to changing indications to use these drugs during follow up periods, especially at the time of drug commencement making time-dependent analysis extremely problematic. Using time-fixed analysis with exclusion of immortal time and adjustment for confounders at baseline and/or during follow-up periods, the HR of RAS inhibitors for CVD was comparable to that in RCT. The result supported the use of the Registry for performing pharmacoepidemiological analysis which revealed an attenuated low low-density lipoprotein cholesterol related cancer risk with RAS inhibitors. On the other hand, time-fixed analysis with including immortal time and adjustment for confounders at baseline and/or during follow-up periods, the HR of statins for CVD was similar to that in the RCT. Our results highlight the complexity and difficulty in removing these biases. We call for validations of the methods to cope with immortal time and drug use indications before applying them to particular research questions, so to avoid making erroneous conclusions.
Core tip: There are multiple biases in using observational studies to examine treatment effects. These biases include those due to prevalent drug users, immortal time and drug indications that must be taken into consideration. In this regard, we used drugs with proven effects in randomized controlled trials and applied those proposed methods by other groups to estimate their effects in a prospective cohort of patients with type 2 diabetes. Our results highlighted the importance of validating adjustment methods for immortal time and drug use indications before applying them to addressing research questions, so to avoid making erroneous conclusions.