Instrumental variable (IV) methods were invented over 70 years ago but were used by epidemiologists only recently. Over the past decade or so, non-parametric versions of IV methods have appeared that connect IV methods to causal and measurement-error models important in epidemiological applications. An introduction to instrumental variables for epidemiologists (Int J Epidemiol 2000;29:722-9) presents those developments, illustrated by an application of IV methods to non-parametric adjustment for non-compliance in randomised trials. The author mentions a number of caveats but concludes that IV corrections can be valuable in many situations. Where IV assumptions are questionable, the corrections can still serve as part of the sensitivity analysis or external adjustment. Where the assumptions are more defensible, as in field trials and in studies that obtain validation or reliability data, IV methods can form an integral part of the analysis. A review of IV analysis for observational comparative effectiveness studies suggested that in the large majority of studies, in which IV analysis was applied, one of the assumption could be violated (Potential bias of instrumental variable analyses for observational comparative effectiveness research, Ann Intern Med. 2014;161(2):131-8).
A proposal for reporting instrumental variable analyses has been suggested in Commentary: how to report instrumental variable analyses (suggestions welcome) (Epidemiology. 2013;24(3):370-4). In particular the type of treatment effect (average treatment effect/homogeneity condition or local average treatment effect/monotonicity condition) and the testing of critical assumptions for valid IV analyses should be reported. In support of these guidelines, the standardized difference has been proposed to falsify the assumption that confounders are not related to the instrumental variable (Quantitative falsification of instrumental variables assumption using balance measures, Epidemiology. 2014;25(5):770-2).
The complexity of the issues associated with confounding by indication, channelling and selective prescribing is explored in Evaluating short-term drug effects using a physician-specific prescribing preference as an instrumental variable (Epidemiology 2006;17(3):268-75). A conventional, adjusted multivariable analysis, the author showed a higher risk of gastrointestinal toxicity for selective COX-2-inhibitors than for traditional NSAIDs, which is at odds with results from clinical trials.. However, a physician-level instrumental variable approach (a time-varying estimate of a physician’s relative preference for a given drug, where at least two therapeutic alternatives exist) yielded evidence of a protective effect due to COX-2 exposure, particularly for shorter term drug exposures. Despite the potential benefits of physician-level IVs their performance can vary across databases and strongly depends on the definition of IV used as discussed in Evaluating different physician's prescribing preference based instrumental variables in two primary care databases: a study of inhaled long-acting beta2-agonist use and the risk of myocardial infarction (Pharmacoepidemiol Drug Saf. 2016;25 Suppl 1:132-41).
Instrumental variable methods in comparative safety and effectiveness research (Pharmacoepidemiol Drug Saf 2010;19:537–54) is a practical guidance on IV analyses in pharmacoepidemiology. Instrumental variable methods for causal inference (Stat Med. 2014;33(13):2297-340) is a tutorial, including statistical code for performing IV analysis.
An important limitation of IV analysis is that weak instruments (small association between IV and exposure) lead to decreased statistical efficiency and biased IV estimates as detailed in Instrumental variables: application and limitations (Epidemiology 2006;17:260-7). For example, in the above mentioned study on non-selective NSAIDs and COX-2-inhibitors, the confidence intervals for IV estimates were in the order of five times wider than with conventional analysis. Performance of instrumental variable methods in cohort and nested case-control studies: a simulation study (Pharmacoepidemiol Drug Saf 2014; 2014;23(2):165-77) demonstrated that a stronger IV-exposure association is needed in nested case-control studies compared to cohort studies in order to achieve the same bias reduction. Increasing the number of controls reduces this bias from IV analysis with relatively weak instruments.
Selecting on treatment: a pervasive form of bias in instrumental variable analyses (Am J Epidemiol. 2015;181(3):191-7) warns against bias in IV analysis by including only a subset of possible treatment options.
|10. Specific topics|
|Annex 1.||Guidance on conducting systematic revies and meta-analyses of completed comparative pharmacoepidemiological studies of safety outcomes|