ICD / Pacemaker Implantation
3324933206wRVU: 6.96 — Insertion of permanent pacemaker with transvenous electrode(s); atrial33270wRVU: 8.87 — Insertion/replacement of subcutaneous ICD (S-ICD) system33208wRVU: 8.31 — Insertion of permanent pacemaker with transvenous electrode(s); atrial and ventricular
[Ventricular tachycardia / ventricular fibrillation / reduced EF <35 % block complete heart ii-iii nyha sick sinus span syndrome]< with>, requiring [ICD / permanent pacemaker] implantation Same [Dual-chamber ICD / single-chamber ICD / dual-chamber permanent pacemaker / CRT-D / CRT-P] implantation, [de novo / upgrade / generator change] [Attending name], MD/DO [EP/Cardiac Surgery] [Nurse/tech name] Monitored anesthesia care [/ general] with local: [X] mL 1% lidocaine The patient is a [age]-year-old [male/female] with [LVEF X% / recurrent VT/VF / complete heart block / sinus node dysfunction], meeting criteria for [ICD / PPM] implantation per [AHA/ACC/HRS guidelines]. The risks, benefits, and alternatives were discussed and informed consent was obtained. Venous access was obtained via the [left / right] subclavian [/ axillary / cephalic] vein. Lead impedances, sensing, and pacing thresholds were acceptable. [ICD: defibrillation threshold was [<25 j]< span> confirmed. R-wave sensing was [X] mV.] Device position was confirmed by fluoroscopy. The patient was positioned supine on the fluoroscopy table. The [left / right] chest was prepped and draped. Local anesthesia was infiltrated subcutaneously and along the dissection plane. A [5]-cm incision was made [2 cm below the clavicle] over the pectoralis fascia. The subclavian [/ cephalic / axillary] vein was accessed with a [modified Seldinger technique / direct cutdown (cephalic vein)]. A [7 Fr / 9 Fr] peel-away introducer was placed. [For dual-chamber: a second venous puncture was made for the second lead.] [VENTRICULAR LEAD:] A [screw-in / passive-fixation] [RV apical / septal] lead was advanced under fluoroscopic guidance through the right atrium, across the tricuspid valve, to the [right ventricular apex / mid-septum]. The lead was secured. Pacing threshold: [X] V at [0.4 ms] pulse width. R-wave amplitude: [X] mV. Impedance: [X] ohms. [ATRIAL LEAD:] A [screw-in] right atrial appendage lead was positioned. P-wave sensing: [X] mV. Pacing threshold: [X] V. Impedance: [X] ohms. [CRT / LV LEAD: The CS was cannulated and a LV lead was advanced to the [lateral / posterolateral] CS branch. LV threshold: [X] V. Impedance: [X] ohms.] [ICD: DFT testing was [performed / deferred]. Induced VF terminated at [X] J.] The leads were anchored to the pectoralis fascia with [0-Silk] suture. A pocket was created for the generator. The [model/manufacturer] [ICD / pacemaker] generator was connected, and the pocket was closed in [2-3] layers. A sterile dressing was applied. Final fluoroscopic images confirmed lead positions. None None Minimal None The patient was monitored post-procedure. Chest X-ray confirmed [appropriate lead positions / no pneumothorax / no hemothorax]. The device was interrogated and programmed per EP protocol. [Activity restriction: no overhead use of the ipsilateral arm for [4–6 weeks].] Generator change was performed for battery depletion [elective replacement indicator (ERI) reached]. The existing pocket was opened. The generator was disconnected from the leads. Lead impedances and sensing/pacing thresholds were measured and documented before and after generator exchange. A new [model/manufacturer] generator was connected. The pocket was irrigated and closed in layers. Lead parameters at the new generator: [thresholds as documented above]. No lead revisions were required.Epic SmartPhrase Version
PREOPERATIVE DIAGNOSIS: ***, requiring *** implantation
POSTOPERATIVE DIAGNOSIS: Same
PROCEDURE PERFORMED: *** (ICD/PPM) implantation, ***
ATTENDING: ***, MD/DO
ASSISTANT: ***
ANESTHESIA: MAC + local
INDICATIONS: .PTAGE-year-old .PTSEX with ***. LVEF ***%. Meets criteria for ***. Consent obtained.
FINDINGS: *** venous access. Lead parameters: RV threshold *** V, R-wave *** mV, impedance *** ohms. RA threshold *** V, P-wave *** mV. [DFT: VF terminated at *** J.]
PROCEDURE:
Supine, fluoro table. *** chest prepped. Local anesthesia. *** cm incision below clavicle. *** venous access, peel-away introducer. [RV lead: *** fixation to *** position, fluoroscopy confirmed.] [RA lead: RAA, fluoroscopy confirmed.] [LV lead: CS cannulated, *** branch.] Leads anchored to fascia. Generator pocket created. *** generator connected. Closed *** layers. CXR: leads appropriate, no PTX.
EBL: Minimal
COMPLICATIONS: None
DISPOSITION: Monitored. Device programmed. Arm restriction × 4–6 weeks.
Signed: .ME, .MYDEGREE
.TODAYVariants
Generator Change (Battery Depletion)
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