FEES Procedure Preparation and Documentation
FEES Procedure Preparation and Documentation is a clinical checklist for preparing, performing, and recording a Flexible Endoscopic Evaluation of Swallowing. It helps you capture consent, readiness, trial consistencies, tolerance, and findings in one repeatable workflow.
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Overview
FEES Procedure Preparation and Documentation is a task template for recording a Flexible Endoscopic Evaluation of Swallowing from start to finish. It is built for the clinical workflow where preparation, patient readiness, the exam itself, and the final note all need to stay aligned in one place.
Use this template when you need a repeatable record of consent, pre-procedure vitals, scope readiness, trial consistencies, patient tolerance, and post-procedure findings. It is especially useful when multiple clinicians touch the same encounter or when you need a clean audit trail for chart review, quality checks, or handoff. The checklist format helps keep the work atomic: each item should be answerable yes, no, or N/A, with a clear verification step.
Do not use this template as a substitute for clinical judgment, local policy, or a broader dysphagia care plan. If your workflow does not include FEES, or if you only need a general swallowing-screen note, this template is too specific. It is also not the right fit for purely administrative scheduling tasks or for procedures where the exam details are captured in a separate device report. The value here is in documenting the actual FEES procedure in a way that reduces omissions and makes follow-up easier.
Standards & compliance context
- This template supports documentation practices commonly expected in clinical records by making consent, procedure details, and findings explicit.
- It should be aligned with your facility’s scope-of-practice rules, credentialing requirements, and local policies for FEES performance.
- If your organization has privacy, retention, or chart amendment rules, configure the template to match those requirements before rollout.
- Any regulatory or accreditation obligations should be validated against your own clinical governance process rather than assumed from the template alone.
General regulatory context for orientation only — verify current requirements with counsel or the relevant agency before relying on this template for compliance.
How to use this template
- 1. Set up the template with your site’s FEES-specific fields, including the consistencies you trial, the observation terms you use, and any required consent language.
- 2. Assign the DRI to the clinician responsible for the exam and leave support tasks unassigned until your team imports the template into the correct workflow.
- 3. Complete the pre-procedure checklist items before starting the exam, verifying readiness, vitals, and consent as blocking steps.
- 4. Document each trialed food or liquid consistency during the procedure, then record tolerance, key findings, and any immediate recommendations as separate checklist items.
- 5. Review the completed record for missing verification steps, correct any incomplete documentation, and file the note according to your charting process.
Best practices
- Keep consent and readiness as blocking checklist items so the procedure cannot be documented as complete before the patient is prepared.
- Record each food or liquid consistency as its own checklist item instead of combining all trials into one note line.
- Use exact, observable language for tolerance and findings, such as cough, throat clear, residue, or refusal, rather than vague summaries.
- Capture pre-procedure vitals before the exam begins if your protocol requires them, and mark any abnormal values for follow-up.
- Separate what was observed from what was recommended so the findings stay auditable and the plan stays easy to review.
- Add local protocol items for infection control, equipment readiness, or transport only if they are part of your actual FEES workflow.
- Avoid priority inflation by reserving critical only for steps that affect safety, consent, or compliance.
What this template typically catches
Issues teams running this template most often surface in practice:
Common use cases
Frequently asked questions
What does this FEES template cover?
This template covers the full FEES workflow from pre-procedure readiness through post-procedure documentation. It is designed to capture scope readiness, patient consent, pre-procedure vitals, the food and liquid consistencies trialed, patient tolerance, and the final findings. It works as a checklist so each step can be verified and documented in order.
Who should use this template?
It is intended for clinicians and support staff involved in swallowing evaluations, especially speech-language pathologists and other trained providers who perform or assist with FEES. The DRI should be the clinician responsible for the exam, while nursing or support staff can complete preparation items that are non-blocking. If your workflow separates setup from interpretation, this template can still be used as the shared record.
How often is this checklist used?
Use it every time a FEES procedure is performed. It is not a recurring administrative task; it is a per-patient, per-procedure checklist that should be completed once for each exam. If your site performs repeat FEES studies, clone the template for each encounter so the documentation stays tied to the specific visit.
Is this template appropriate for outpatient, inpatient, or bedside FEES?
Yes, it can be adapted for outpatient clinics, inpatient units, and bedside evaluations as long as the same core steps are relevant. The exact setup items may differ by location, but the checklist should still verify readiness, consent, vitals, trial consistencies, tolerance, and findings. If your setting has additional infection-control or transport steps, add them as local checklist items.
What are the most common mistakes this template helps prevent?
Common misses include documenting the exam without confirming consent, skipping pre-procedure vitals, failing to note which consistencies were trialed, and recording findings without a clear tolerance statement. Another frequent issue is using vague language like 'tolerated well' without specifying what was observed. This template pushes each item into an independently verifiable checklist item.
Does this template help with regulatory or charting requirements?
It supports documentation practices commonly expected in clinical records by making consent, patient status, procedure details, and findings explicit. It does not replace your facility policy, scope-of-practice rules, or local documentation standards. You should align the final checklist with your organization’s clinical governance, privacy, and retention requirements.
Can we customize the consistencies and findings fields?
Yes, and you should. FEES documentation often needs local terminology for food and liquid consistencies, airway observations, residue patterns, and recommendations. Customize the checklist items so they match your protocol, but keep each item atomic and verifiable rather than combining multiple observations into one line.
How does this compare with ad-hoc note taking?
Ad-hoc notes are easier to start but often miss critical steps or bury them in free text. A checklist format makes the exam easier to run consistently, easier to review, and easier to audit later. It also helps separate blocking steps, like consent and readiness, from non-blocking documentation details.
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