Endoscopic Sleeve Gastroplasty Procedure Note
Comprehensive procedure note template for Endoscopic Sleeve Gastroplasty (ESG) with integrated diagnostic EGD documentation. Includes ESG-specific technical parameters (suture pattern, count, anatomic extent), structured…
Document Type
clinical note / Procedure Note
Specialties
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Patient: [Patient name] DOB: [Date of birth] MRN: [Medical record number] Date of Service: [Date]
Start Time: [HH:MM] End Time: [HH:MM] Location: [Facility/Endoscopy suite] Setting: [inpatient / outpatient]
Primary Endoscopist: [Name, credentials] Assistant(s): [Name(s), credentials] Anesthesia Provider: [Name, credentials]
Procedures Performed
- [Diagnostic EGD / Upper GI endoscopy]
- [Endoscopic Sleeve Gastroplasty (ESG)]
- [Additional therapeutic maneuvers, e.g., hemostasis, clip placement, biopsy] (Only include if performed)
Diagnoses
Pre-procedure: [Primary indication(s) for ESG: obesity management with relevant metabolic comorbidities / bridge therapy / revision after weight regain]
Post-procedure: [ESG performed with technical outcome; key endoscopic findings, e.g., gastritis, hiatal hernia, erosions] (Do not infer findings not visualized.)
Indication and Clinical Context
[Brief statement of primary clinical reason for ESG, including baseline weight/BMI if available; relevant obesity-related comorbidities (e.g., T2DM, HTN, OSA, NAFLD); prior foregut or bariatric procedures impacting anatomy; presence/absence of contraindications evaluated (e.g., active gastric ulceration, large hiatal hernia)] (If specific data unavailable, enter "Not documented in record at time of note.")
Consent and Pre-procedure Verification
[Informed consent obtained prior to sedation, including discussion of risks (bleeding, perforation/leak, infection, aspiration, need for hospitalization or surgery, failure to achieve weight loss, need for repeat intervention) and alternatives.]
[Pre-procedure verification/time-out completed confirming correct patient, procedure, allergies, and anticoagulation status.] (Note anticoagulant/antiplatelet management if relevant.)
Prophylactic antibiotics: [Agent, dose, route, and timing relative to procedure start / Not administered]
Sedation/Anesthesia
Type: [moderate sedation / deep sedation / MAC / general anesthesia]
Administered by: [anesthesia service / endoscopy team]
[If endoscopist-directed sedation, list medications and doses; if anesthesia-managed, reference anesthesia record for details.] (Include notable sedation events only.)
Patient tolerance: [Tolerated well without events / Sedation-related event(s) and intervention(s) performed]
Equipment
- Gastroscope: [Manufacturer/model]
- Endoscopic suturing system: [Manufacturer/model]
- Accessories: [Tissue helix/retractor, overtube, distal cap, cinch/anchor device as applicable]
- Insufflation: [CO2 / room air]
- [Device lot/UDI identifiers] (Document here or per institutional policy.)
Pre-ESG Endoscopic Findings
[Extent and completeness of examination. If incomplete, state limitation and cause. Retroflexion and photo-documentation: performed / not performed with adequate / limited visualization.]
- Esophagus: [Mucosal appearance; presence/absence of esophagitis, varices, hiatal hernia]
- Stomach: [Fundus, body, antrum findings; presence/absence of ulcers, erosions, gastritis, polyps, retained contents] (Include pertinent negatives, e.g., "No gastric ulceration.")
- Duodenum: [Findings in bulb and second portion / Not examined with reason]
ESG Technique
[After diagnostic inspection confirmed no contraindications, ESG was performed transorally using the endoscopic suturing system to create full-thickness plications along the greater curvature, reducing gastric volume. Mucosal marking: performed / not performed.] (Provide concise narrative of plication sequence.)
- Suture pattern: [U / Z / triangular / site-specific] (Brief plain-language description.)
- Number of sutures/plications: [Total count]
- Start location: [e.g., distal body near incisura] End location: [e.g., proximal body; fundus spared / partially included]
- Additional technical details: [Bites per suture, anchor/cinch usage if tracked]
- Hemostasis: [Adequate throughout / Intervention performed with modality and site]
- Final assessment: [Sleeve configuration; luminal patency confirmed with ability to traverse to antrum/pylorus]
- Technical success: [complete / partial / aborted] (If partial or aborted, state reason.)
- Deviations/Challenges: [None / Description of mucosal tearing, device issue, bleeding requiring therapy, altered pattern with troubleshooting and outcome]
Specimens
Specimens: [None / List each with site, method, jar/label, and indication (e.g., Gastric antrum biopsy, Jar A, for H. pylori testing)] (If specimens obtained, note plan for pathology review and patient notification.)
Estimated Blood Loss and Complications
EBL: [mL value / minimal]
Immediate complications: [No immediate complications noted / Description with timing, severity, intervention performed, and outcome] (Relevant complications: bleeding requiring endoscopic therapy, suspected perforation/leak, pneumoperitoneum, aspiration, hemodynamic instability, unplanned admission.)
Impression
- [Key diagnostic findings from pre-ESG EGD with pertinent negatives]
- [ESG performed: suture pattern, total plications, technical outcome]
- [Additional intra-procedural therapies if any]
- [Overall tolerance and immediate post-procedure status]
Post-procedure Plan
- Recovery and disposition: [Recovery location; same-day discharge / observation / admission with reason; written instructions provided]
- Medications: [Acid suppression (agent/dose/duration); antiemetics; analgesia; antibiotics if prescribed; anticoagulation hold/resume plan]
- Diet: [Staged progression per ESG pathway: clear liquids → full liquids → soft/pureed → small solid portions with timeframes]
- Activity: [Return-to-work guidance; lifting restrictions; NSAID and tobacco avoidance per program]
- Follow-up: [Bariatric endoscopy follow-up timeframe; nutrition/dietitian appointment; behavioral/physical activity program]
- Return precautions: [Severe/worsening abdominal pain, fever, persistent vomiting, hematemesis/melena, chest pain/shortness of breath, inability to tolerate liquids] Contact: [Clinic number / After-hours number]
Communication
[Findings and plan reviewed with patient and/or family; questions addressed; report sent to referring provider] (Note interpreter use if applicable.)
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