analyze_dff: Differential facet functioning analysis

In mfrmr: Estimation and Diagnostics for Many-Facet Measurement Models

Differential facet functioning analysis

Description

Tests whether the difficulty of facet levels differs across a grouping variable (e.g., whether rater severity differs for male vs. female examinees, or whether item difficulty differs across rater subgroups).

analyze_dif() is retained for compatibility with earlier package versions. In many-facet workflows, prefer analyze_dff() as the primary entry point.

Usage

analyze_dff(
  fit,
  diagnostics,
  facet,
  group,
  data = NULL,
  focal = NULL,
  method = c("residual", "refit"),
  min_obs = 10,
  p_adjust = "holm"
)

analyze_dif(...)

Arguments

fit	Output from fit_mfrm().
diagnostics	Output from diagnose_mfrm().
facet	Character scalar naming the facet whose elements are tested for differential functioning (for example, "Criterion" or "Rater").
group	Character scalar naming the column in the data that defines the grouping variable (e.g., "Gender", "Site").
data	Optional data frame containing at least the group column and the same person/facet/score columns used to fit the model. If NULL (default), mfrmr tries to recover the data from fit$prep$data. That slot only holds the columns that fit_mfrm() actually modelled; if the grouping column was not among them (common for DIF screening), pass the original data frame via ⁠data = <df>⁠ explicitly. The same applies when the fit object has been serialized without the prep slot.
focal	Optional character vector of group levels to treat as focal. If NULL (default), all pairwise group comparisons are performed.
method	Analysis method: "residual" (default) uses the fitted model's residuals without re-estimation; "refit" re-estimates the model within each group subset. The residual method is faster and avoids convergence issues with small subsets.
min_obs	Minimum number of observations per cell (facet-level x group). Cells below this threshold are flagged as sparse and their statistics set to NA. Default 10.
p_adjust	Method for multiple-comparison adjustment, passed to stats::p.adjust(). Default is "holm".
...	Passed directly to analyze_dff().

Details

Differential facet functioning (DFF) occurs when the difficulty or severity of a facet element differs across subgroups of the population, after controlling for overall ability. In an MFRM context this generalises classical DIF (which applies to items) to any facet: raters, criteria, tasks, etc.

Differential functioning is a threat to measurement fairness: if Criterion 1 is harder for Group A than Group B at the same ability level, the measurement scale is no longer group-invariant.

Two methods are available:

Residual method (method = "residual"): Uses the existing fitted model's observation-level residuals. For each facet-level \times group cell, the observed and expected score sums are aggregated and a standardized residual is computed as:

z = \frac{\sum (X_{obs} - E_{exp})}{\sqrt{\sum \mathrm{Var}}}

Pairwise contrasts between groups compare the mean observed-minus-expected difference for each facet level, with uncertainty summarized by a Welch/Satterthwaite approximation. This method is fast, stable with small subsets, and does not require re-estimation. Because the resulting contrast is not a logit-scale parameter difference, the residual method is treated as a screening procedure rather than an ETS-style classifier.

Refit method (method = "refit"): Subsets the data by group, refits the MFRM model within each subset, anchors all non-target facets back to the baseline calibration when possible, and compares the resulting facet-level estimates using a Welch t-statistic:

t = \frac{\hat{\delta}_1 - \hat{\delta}_2} {\sqrt{SE_1^2 + SE_2^2}}

This provides group-specific parameter estimates on a common scale when linking anchors are available, but is slower and may encounter convergence issues with small subsets. ETS categories are reported only for contrasts whose subgroup calibrations retained enough linking anchors to support a common-scale interpretation and whose subgroup precision remained on the package's model-based MML path.

When facet refers to an item-like facet (for example Criterion), this recovers the familiar DIF case. When facet refers to raters or prompts/tasks, the same machinery supports DRF/DPF-style analyses.

For the refit method only, effect size is classified following the ETS (Educational Testing Service) DIF guidelines when subgroup calibrations are both linked and eligible for model-based inference:

• A (Negligible): |\Delta| < 0.43 logits

• B (Moderate): 0.43 \le |\Delta| < 0.64 logits

• C (Large): |\Delta| \ge 0.64 logits

Multiple comparisons are adjusted using Holm's step-down procedure by default, which controls the family-wise error rate without assuming independence. Alternative methods (e.g., "BH" for false discovery rate) can be specified via p_adjust.

Value

An object of class mfrm_dff (with compatibility class mfrm_dif) with:

• dif_table: data.frame of differential-functioning contrasts.

• cell_table: (residual method) per-cell detail table.

• summary: counts by screening or ETS classification.

• group_fits: (refit method) per-group facet estimates.

• gpcm_boundary: for bounded GPCM fits, a capability-boundary table.

• config: list with facet, group, method, min_obs, p_adjust settings.

Choosing a method

In most first-pass DFF screening, start with method = "residual". It is faster, reuses the fitted model, and is less fragile in smaller subsets. Use method = "refit" when you specifically want group-specific parameter estimates and can tolerate extra computation. Both methods should yield similar conclusions when sample sizes are adequate (N \ge 100 per group is a useful guideline for stable differential-functioning detection).

Interpreting output

• ⁠$dif_table⁠: one row per facet-level x group-pair with contrast, SE, t-statistic, p-value, adjusted p-value, effect metric, and method-appropriate classification. Includes Method, N_Group1, N_Group2, EffectMetric, ClassificationSystem, ContrastBasis, SEBasis, StatisticLabel, ProbabilityMetric, DFBasis, ReportingUse, PrimaryReportingEligible, and sparse columns.

• ⁠$cell_table⁠: (residual method only) per-cell detail with N, ObsScore, ExpScore, ObsExpAvg, StdResidual.

• ⁠$summary⁠: counts by screening result (method = "residual") or ETS category plus linked-screening and insufficient-linking rows (method = "refit").

• ⁠$group_fits⁠: (refit method only) list of per-group facet estimates and subgroup linking diagnostics.

• ⁠$gpcm_boundary⁠: for bounded GPCM fits, a capability-boundary table marking the DFF/DIF output as caveated screening evidence.

GPCM boundary

For bounded GPCM, DFF/DIF rows are available as slope-aware screening evidence over the fitted expected-score and residual scale. Keep residual-method contrasts and interaction cells in screening language. Refit contrasts require explicit subgroup linking and precision support before stronger subgroup-comparison language is used.

Typical workflow

1. Fit a model with fit_mfrm(). For RSM / PCM fairness review, prefer method = "MML".

2. Run diagnose_mfrm() and, for RSM / PCM, prefer diagnostic_mode = "both" so legacy and strict marginal screens remain visible together.

3. Run analyze_dff(fit, diagnostics, facet = "Criterion", group = "Gender", data = my_data).

4. Inspect ⁠$dif_table⁠ for flagged levels and ⁠$summary⁠ for counts.

5. Use dif_interaction_table() when you need cell-level diagnostics.

6. Use plot_dif_heatmap() or dif_report() for communication.

See Also

fit_mfrm(), estimate_bias(), compare_mfrm(), dif_interaction_table(), plot_dif_heatmap(), dif_report(), subset_connectivity_report(), mfrmr_linking_and_dff

Examples

toy <- load_mfrmr_data("example_bias")

fit <- fit_mfrm(toy, "Person", c("Rater", "Criterion"), "Score",
                 method = "MML", model = "RSM", quad_points = 7, maxit = 30)
diag <- diagnose_mfrm(fit, residual_pca = "none", diagnostic_mode = "both")
dff <- analyze_dff(fit, diag, facet = "Rater", group = "Group", data = toy)
dff$summary
# Look for: a small `FlaggedPairs` count relative to `Pairs`. Under
#   method = "residual", `ClassificationSystem` is "screening", not
#   ETS. "Screen positive" rows are prompts for substantive review.
head(dff$dif_table[, c("Level", "Group1", "Group2", "Contrast",
                       "Classification", "ClassificationSystem")])
# The residual contrast is an observed-minus-expected average contrast
# between groups. It is useful for screening, but it is not an ETS
# A/B/C logit-delta classification.
dff_refit <- analyze_dff(fit, diag, facet = "Rater", group = "Group",
                         data = toy, method = "refit")
unique(dff_refit$dif_table$ClassificationSystem)
# Look for: "ETS" only when subgroup calibration, linking, and precision
#   checks all support a common-scale model-based contrast.
sc <- subset_connectivity_report(fit, diagnostics = diag)
plot(sc, type = "design_matrix", draw = FALSE)
if ("ScaleLinkStatus" %in% names(dff_refit$dif_table)) {
  unique(dff_refit$dif_table$ScaleLinkStatus)
}
# Look for: "linked" in `ScaleLinkStatus` confirms the focal and
#   reference groups share enough common elements for a comparable
#   contrast; "demoted_*" rows lose linking under the refit branch
#   and should be read as exploratory.

mfrmr documentation built on June 13, 2026, 1:07 a.m.