Foreign Body Removal Procedure Note (Ear/Nose)
Procedure note template for foreign body removal from the ear and/or nose. Includes site-conditional documentation for pre- and post-removal exams, high-risk object screening (button batteries, magnets), technique detail…
Document Type
clinical note / Procedure Note
Specialties
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Procedure Information
- Date/Time of Procedure: [Date and time]
- Location/Setting: [ED / urgent care / clinic / OR / other]
- Operator: [Name and credentials]
- Procedure Site(s): [right ear / left ear / both ears / right naris / left naris / both nares]
Indication and Clinical Context
[Brief narrative indication and context] (2–4 sentences summarizing indication for removal; time since insertion/incident if known; relevant symptoms such as pain, hearing change, discharge, bleeding, obstruction, rhinorrhea; and any prior removal attempts by caregivers or clinicians.)
- High-Risk Object Screening: [button battery: yes / no / suspected] · [magnet(s): yes / no / suspected] · [sharp object: yes / no / suspected] · [organic/vegetable matter: yes / no / suspected] · [live insect: yes / no / suspected] · [none identified] (If any high-risk object is present or suspected, document estimated dwell time and urgency considerations below.)
- If high-risk object present/suspected: [Estimated dwell time] · [Urgency considerations, tissue injury noted, escalations initiated] (Omit this line if no high-risk objects identified.)
Pre-Procedure Assessment
(Document each involved site separately. If any structure cannot be assessed, explicitly document the reason.)
Ear
(Include only if ear is involved.)
- Canal condition: [normal / edema / erythema / laceration / bleeding / discharge]
- Foreign body: [Visibility and depth; graspable edge: yes / no / unclear]
- Tympanic membrane: [intact / perforated / unable to assess: (reason)]
- Baseline hearing assessment: [Method and findings / unable to perform: (reason)]
Nose
(Include only if nose is involved.)
- Foreign body: [Visibility and location: anterior / posterior; relation to septum/turbinates]
- Mucosal condition: [normal / edema / erythema / ulceration / necrosis]
- Active bleeding: [none / minimal / moderate / severe]
- Aspiration concern: [yes / no] (If yes, state rationale.)
Consent
- Consent type: [verbal / written / both / emergency exception]
- Consent provided by: [patient / parent or guardian / other]
- [Risks, benefits, and alternatives discussed with opportunity for questions] (Risks include bleeding, pain, mucosal/canal laceration, infection, TM injury or hearing change for ear, posterior displacement or aspiration for nose, and potential need for sedation or ENT/OR removal.)
- (If consent not obtained due to emergency circumstances, document the clinical basis.)
Time-Out
- Time-out performed: [yes / no: (reason)]
- [Two patient identifiers confirmed]
- [Correct procedure confirmed]
- [Correct site and laterality confirmed]
- [Allergies reviewed]
- [Required equipment available]
Anesthesia and Analgesia
- Topical/local anesthesia: [none / agent, concentration, route, site]
- Nasal vasoconstrictor: [none / agent and concentration] (Include only for nasal procedures.)
- Analgesia: [none / medication, dose, route, time]
- Procedural sedation: [none / brief summary of medications with doses, routes, times; monitoring; adverse events] (Or reference separate sedation record by name/location.)
Procedure Details
[Narrative description of the procedure] (Describe patient positioning and immobilization if used; visualization tools such as otoscope, nasal speculum, headlamp, or endoscope; and stepwise technique. For live insects in the ear, document immobilization prior to extraction. For button batteries or magnets, emphasize urgency and document any visible tissue injury.)
- Techniques used: [irrigation / suction / forceps / hook / curette / loop / balloon catheter / positive-pressure / adhesive / magnet-assisted / other] (List in sequence of attempts.)
- Instruments: [Specific instruments utilized]
- Number of attempts: [Count]
- Bleeding during procedure: [none / minimal / moderate / severe] · [Hemostasis method if applicable]
Foreign Body Description
- Number removed: [Count]
- Material/type: [metal / plastic / organic / battery / magnet / insect / bead / other]
- Size and shape: [Approximate size; round and smooth / irregular / sharp edges]
- Integrity: [intact / fragmented / unknown until removal]
Removal Status
- Status: [complete / partial / unsuccessful / aborted]
- (If incomplete, unsuccessful, or aborted, document the reason and next steps including escalation plans such as ENT consult, imaging, sedation, or OR.)
Post-Removal Assessment
(Required even if findings are normal. If full exam not possible, document what was assessed and what could not be evaluated.)
Ear
(Include only if ear was involved.)
- Canal condition: [normal / abrasion / laceration / bleeding] (Describe extent and location if abnormal.)
- Tympanic membrane: [visualized and intact / suspected injury / unable to assess: (reason)]
- Post-procedure hearing: [Findings / unable to perform: (reason)] (Include only if baseline was assessed.)
Nose
(Include only if nose was involved.)
- Mucosal condition: [normal / abrasion / ulceration / necrosis / edema]
- Bleeding status: [none / controlled / persistent: (interventions)]
- Re-examination for additional foreign bodies: [yes / no] (Include contralateral naris; consider oral cavity and ear canals in young children or when multi-orifice insertion is suspected.)
Complications and Tolerance
- Patient tolerance: [well tolerated / poorly tolerated: (brief explanation)]
- Complications: [none / complication(s) with management provided] (Do not document "none" if complete post-procedure exam was not possible; instead state what is known and what could not be assessed.)
- Estimated blood loss: [none / minimal / quantified estimate]
Disposition and Follow-up
- Disposition: [discharge / observation / ENT consult / OR / transfer]
- Medications: [none / ear drops for canal trauma or otitis externa / nasal medications / analgesics] (Antibiotics are not routinely indicated after uncomplicated removal. List agent, dose, route, and duration when applicable.)
- Follow-up: [None indicated / ENT follow-up / Audiology follow-up / timeframe] (ENT follow-up indicated for button battery or magnet removal, significant mucosal/canal injury, suspected TM injury, retained fragments, or unsuccessful removal. Audiology if hearing loss or TM injury suspected.)
- Return precautions reviewed: [For ear: worsening pain, drainage, fever, hearing change, vertigo] · [For nose: recurrent or persistent bleeding, fever, worsening unilateral discharge or odor, increasing pain, breathing difficulty, concern for retained object]
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