Breast Reconstruction Operative Note
Comprehensive operative note for breast reconstruction covering implant-based, autologous flap, and hybrid approaches. Includes FDA UDI-compliant device traceability, microsurgical documentation for free flaps, and ERAS-…
Document Type
clinical note / Operative Note
Specialties
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Date of Operation: [Date]
Facility/Location: [Facility and OR number]
Primary Surgeon: [Name, credentials]
Assistant(s): [Names and roles] (Omit if none.)
Anesthesia Type: [general / regional / MAC] (Include airway management and regional blocks if applicable.)
Preoperative Diagnosis: [Diagnosis with laterality]
Postoperative Diagnosis: [Diagnosis with laterality] (State "Same" if unchanged.)
Procedure(s) Performed: [Procedure title(s) with laterality and stage (e.g., Stage 1 / Stage 2 / Revision)]
Indication: [Brief statement of medical necessity for reconstruction] (1–2 sentences.)
Safety and Compliance
- Informed consent: [Verified with patient / surrogate]
- Operative site marking: [Marked / Not applicable]
- Time-out: [Completed confirming patient, procedure, laterality, and implants/materials]
- Antibiotic prophylaxis: [Agent, dose, timing / See anesthesia record]
- VTE prophylaxis: [Mechanical / Chemical / Both] [timing]
Intraoperative Summary
- Laterality: [Right / Left / Bilateral]
- Reconstruction Timing: [Immediate / Delayed / Delayed-immediate]
- Reconstructive Approach: [Implant-based / Autologous / Hybrid]
- Implant Plane/Pocket: [Prepectoral / Subpectoral / Dual-plane] (Include only if implant used.)
- Flap Type: [DIEP / MS-TRAM / SIEA / PAP / TUG / Latissimus pedicled / Other] (Include only if autologous.)
- Estimated Blood Loss: [mL]
- Drains Placed: [Number and locations]
- Specimens: [List / None]
- Complications: [None / List with brief management]
- Disposition: [Destination and condition]
Findings
(Document only clinically significant findings that influenced surgical decisions. Omit normal/expected findings.)
- [Mastectomy skin flap quality and perfusion]
- [Pocket or capsule condition]
- [Radiation changes or fibrosis]
- [Recipient vessel quality] (Autologous cases.)
- [Perfusion assessment results if performed]
- [Other findings that altered operative plan]
Counts and Hemostasis
[Sponge, needle, and instrument counts correct at case end. Hemostasis achieved.]
Wound Classification: [Class I / II / III / IV] (Include if required by facility.)
Specimens
(Omit this section entirely if no specimens were taken.)
- [Specimen name]: [Pathology / Research]; [Orientation/marking if applicable]
Implants, Devices, and Biologics
(Omit this section if no implants, expanders, ADM/mesh, or microvascular devices were used. Do not infer device identifiers—document from implant stickers or UDI scan. If unavailable, state "See implant log/UDI scan" or "Addendum pending.")
Right
-
Tissue Expander or Permanent Implant
- Device type: [Tissue expander / Permanent implant]
- Manufacturer and product: [Manufacturer, product line]
- Model/catalog number: [Number]
- Size and profile: [cc], [Profile]
- Serial/Lot/UDI: [Identifier(s) / See implant log / Addendum pending]
- Placement plane: [Prepectoral / Subpectoral / Dual-plane]
- Expander fill: Initial [cc]; End of case [cc] (Include only for expanders.)
-
ADM/Mesh/Biologic Scaffold
- Product and source: [Product name], [Human / Porcine / Bovine / Synthetic]
- Dimensions: [Size]
- Lot/tracking number: [Identifier / See implant log / Addendum pending]
- Configuration: [Sling / Wrap / Anterior coverage]
- Fixation: [Method and anchor points]
-
Microvascular Devices (Free flap cases only.)
- Venous coupler: [Brand], [Size mm]
- Implantable Doppler: [Device and location] (If placed.)
Left
-
Tissue Expander or Permanent Implant
- Device type: [Tissue expander / Permanent implant]
- Manufacturer and product: [Manufacturer, product line]
- Model/catalog number: [Number]
- Size and profile: [cc], [Profile]
- Serial/Lot/UDI: [Identifier(s) / See implant log / Addendum pending]
- Placement plane: [Prepectoral / Subpectoral / Dual-plane]
- Expander fill: Initial [cc]; End of case [cc] (Include only for expanders.)
-
ADM/Mesh/Biologic Scaffold
- Product and source: [Product name], [Human / Porcine / Bovine / Synthetic]
- Dimensions: [Size]
- Lot/tracking number: [Identifier / See implant log / Addendum pending]
- Configuration: [Sling / Wrap / Anterior coverage]
- Fixation: [Method and anchor points]
-
Microvascular Devices (Free flap cases only.)
- Venous coupler: [Brand], [Size mm]
- Implantable Doppler: [Device and location] (If placed.)
Drains
- Right breast: [Type (JP/Blake)], [Size], [Location], [Number]
- Left breast: [Type], [Size], [Location], [Number]
- Donor site: [Type], [Size], [Location], [Number] (Autologous cases only.)
Complications
[None] (Or list each complication with what occurred, immediate management, and outcome. For suspected events, document observations and actions without labeling as definitive complication.)
Procedure Description
(Narrate in chronological order. Use side-specific subheadings for bilateral cases.)
Positioning and Preparation
[Patient position]. [Areas prepped and draped in standard sterile fashion]. [Regional blocks if performed by surgeon: agent, concentration, volume].
Immediate Reconstruction Handoff
(Include only for immediate reconstruction.) [Handoff from ablative team including mastectomy pocket condition, hemostasis status, and skin viability assessment].
Implant-Based Reconstruction
(Include if implant-based or hybrid reconstruction.)
[Pocket assessment and preparation: plane selection, capsulotomy/capsulectomy/capsulorrhaphy as performed, hemostasis, irrigation].
[ADM/mesh placement: preparation, configuration, fixation technique] (If used.)
[Device placement: sizer use, expander or implant placement, fill volumes for expanders, port position confirmation, pocket closure technique].
[Drain placement, layered closure technique, skin closure method, dressings, support garment].
Autologous Reconstruction
(Include if autologous or hybrid reconstruction.)
Donor Site Harvest
[Flap design and type], [perforator selection], [pedicle dissection], [donor site closure including mesh with identifiers if used], [umbilical transposition for abdominal flaps], [donor site drains].
Recipient Site Preparation
[Vessel choice (internal mammary/thoracodorsal)], [exposure technique], [vessel quality assessment].
Microvascular Anastomosis
(Required for free flap cases.)
Ischemia time: [Start time] to [Reperfusion time]; Total: [minutes].
[Arterial anastomosis: hand-sewn or device-assisted, suture]. [Venous anastomosis: coupler size, number of anastomoses]. [Revisions if performed]. [Intraoperative anticoagulation if given].
Flap Inset and Shaping
[De-epithelialization], [skin paddle retention if applicable], [perfusion assessment result], [shaping technique], [breast pocket drains].
Adjunct Procedures
(Include relevant items as applicable.)
Latissimus dorsi flap: [Harvest details, tunneling/inset, donor drain, associated implant if used].
Fat grafting: [Harvest site], [processing], [volume injected per breast], [injection planes].
Contralateral symmetry procedure: [Mastopexy / Reduction / Augmentation], [technique], [specimens].
Nipple-areola reconstruction: [Technique].
Scar revision: [Location and technique].
Negative pressure incisional therapy: [Device and settings].
Postoperative Plan
- Disposition: [PACU to floor / PACU to ICU / Outpatient], [condition]
- Activity: [Mobilization plan], [arm restrictions if applicable]
- Diet: [Per ERAS pathway / Per anesthesia]
- Pain management: [Multimodal regimen per protocol]
- Antibiotics: [Regimen and duration]
- VTE prophylaxis: [Agent], [timing], [duration]
- Drain care: [Output recording], [removal criteria]
- Flap monitoring: [Frequency], [parameters (Doppler, color, capillary refill, temperature)], [escalation protocol] (Free flap cases only.)
- Wound surveillance: [Hematoma/seroma monitoring], [mastectomy skin assessment] (Implant-based cases.)
- Follow-up: [Timing], [triggers for earlier evaluation]
Signature
[Electronic signature, credentials]
[Date and time]
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