FIDDI — Family ICU Delirium Detection Instrument
2026A 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.
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
- 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.