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FIDDI — Family ICU Delirium Detection Instrument

2026

A five-item family-completed ICU questionnaire taking under five minutes. Initial work established feasibility, internal consistency and construct validity, but not diagnostic accuracy against an expert delirium reference standard.

Informant / caregiver-basedIntensive careScreening / case-findingNo eligible DTA study identifiedEmerging clinical record

Emerging clinical record

This record is at an emerging or derivation stage and is not counted as a mature independent family. This profile remains public for clinical and bibliographic context, but it does not add to the headline count of independent core families.

What this tool is and how to interpret its evidence

The Family ICU Delirium Detection Instrument, or FIDDI, is a five-item questionnaire designed for relatives who know the patient and may notice changes not apparent during a short professional encounter. It can be completed in under five minutes and was adapted from informant-focused delirium work for the adult intensive-care setting. Its intended role is to add family observation to routine clinical assessment, particularly when symptoms fluctuate.

The initial study involved 51 family members and examined usability, internal consistency and relationships with other measures. It did not test FIDDI against a blinded expert delirium diagnosis and therefore did not establish diagnostic sensitivity, specificity or a safe stand-alone threshold. Although the publication title uses the word validation, the evidence is best classified as instrument development with preliminary construct validation. The authors themselves called for clinical evaluation against an appropriate reference standard.

FIDDI merits an emerging-tool page because it is a named, purpose-built ICU instrument and family input is clinically valuable. The page must nevertheless state that it is a candidate adjunct, not a validated replacement for CAM-ICU, ICDSC or expert assessment. Five items, family completion and approximate timing can be described without reproducing the questions. No accuracy percentage should be inferred from internal consistency. Future independent studies should address feasibility across languages, family availability, pre-existing cognitive impairment and performance against contemporaneous specialist diagnosis.

Evidence and practical details

not established
Sensitivity*
not established
Specificity*
Full name
Family ICU Delirium Detection Instrument
Also known as
FIDDI
Catalogue class
Emerging clinical record
Record type
core-emerging
Family
fiddi-family
Purpose
Informant / caregiver-based, Intensive care, Screening / case-finding
Population
Adult
Setting
Intensive care
Items
5
Administration
<5 min
Evidence
No eligible DTA study identified
Evidence maturity
development-only
Evidence stage
emerging-development-or-derivation
DTA studies identified
0
Current audit status
canonical/source paper is not DTA; no eligible study yet identified
Reference type
Original/source paper; no eligible DTA study identified yet
Original/source citation
Krewulak KD, Arakawa NC, Deemer K, Jaworska N, Kissel KA, Longmore S, Maclean M, Mickelson P, Mok M, Oggy T, Poulin TG, Reyes J, Selig M, Sept B, Lee CH, Shulman RW, Stelfox HT, Fiest KM Development and Validation of the Family ICU Delirium Detection Instrument Critical care explorations. 2026;8(1):e1335. PMID 41481007

Format and clearly labelled links

FIDDI contains five family-observed indicators and is designed for completion in under five minutes. It should be used as an adjunct to clinical assessment, not as a validated replacement for bedside delirium examination.

Rights, version and permission record

Instrument access state
No verified public instrument form
Instrument host
No verified instrument host
Current instrument/version note
No version verified
Rights holder
Not yet verified
Licence / rights basis
No licence verified
Rights checked
2026-07-19
Rights-holder contact
Not yet verified

Permission scope recorded at the last check

  • Clinical use: Not verified; obtain the current authorised instrument and follow its terms.
  • Research use: Not verified; check with the developer or rights holder.
  • Web republication: Not verified; do not reproduce the form or item wording.
  • Translation/adaptation: Not verified; written permission may be required.
  • EHR/software integration: Not verified; check before implementation.
  • Commercial use: Not verified; check before use.

Site-text licence boundary: the CC BY 4.0 notice for original deliriumtools.com editorial text does not cover third-party instruments, item wording, forms, article text, logos, screenshots or linked material.

Page record and review status

Page version
3.1.0
Last factual/source check
2026-07-19
Last rights/link check
2026-07-19
Curator and responsible editor
Professor Alasdair M J MacLullich — Curator factual and source review complete (not an independent external reviewer)
Independent external clinical review
Not yet completed. No independent external reviewer, consortium endorsement or institutional endorsement is claimed.

Corrections and rights-holder notices can be submitted through the contribute and corrections page.

* Where shown, sensitivity/specificity are from the cited evaluation and are not pooled estimates. “DTA studies identified” describes the current audit, not a completed systematic-review count. Citation metadata checked against PubMed or a publisher record does not imply validation, study quality, endorsement or suitability for a setting. See Methodology.