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| Dizajn studije događaja sa heterogenim efektom tretmana× | Panel studija slučaja× | |
|---|---|---|
| Oblast | Kauzalno zaključivanje | Kauzalno zaključivanje |
| Porodica | Regression model | Regression model |
| Godina nastanka≠ | 2021 | 1990s–2020s (modern panel formulation) |
| Tvorac≠ | Sun & Abraham (2021); Callaway & Sant'Anna (2021) | Formalized by Freyaldenhoven, Hansen, Perez-Orive & Shapiro (2021); widely applied in finance (Fama et al. 1969) and policy evaluation |
| Tip≠ | Quasi-experimental causal inference | Quasi-experimental / causal panel design |
| Temeljni izvor≠ | Sun, L., & Abraham, S. (2021). Estimating dynamic treatment effects in event studies with heterogeneous treatment effects. Journal of Econometrics, 225(2), 175-199. DOI ↗ | Freyaldenhoven, S., Hansen, C., Perez-Orive, J., & Shapiro, J. M. (2021). Visualization, Identification, and Estimation in the Linear Panel Event-Study Design. NBER Working Paper 29170. National Bureau of Economic Research. link ↗ |
| Drugi nazivi | HTE event study, heterogeneous effects event study, group-time ATT event study, dynamic HTE design | event-study regression, dynamic DiD, relative-time regression, distributed-lag panel model |
| Srodne≠ | 3 | 4 |
| Sažetak≠ | Heterogeneous Treatment Effect Event Study Design is a causal-inference framework that uses event study regression to estimate how treatment effects vary across groups, cohorts, or time relative to a treatment event. Unlike classical two-way fixed-effects event studies — which assume a homogeneous effect — this approach explicitly models and recovers group-time average treatment effects (ATTs), addressing the contamination bias that arises when effects differ across treated units. | A panel event study estimates the dynamic causal effect of a treatment or policy by regressing an outcome on a full set of relative-time indicators — one for each period before and after the event — while controlling for unit and time fixed effects. The resulting coefficient plot shows how the treated units diverged from untreated units at each point in calendar time relative to their treatment date, making both pre-treatment trend violations and post-treatment effect trajectories immediately visible. |
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