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Percutaneous endoscopic gastrostomy in amyotrophic lateral sclerosis: outcomes of a dedicated anesthesia and surgery protocol

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Abstract

Background

Patients requiring percutaneous endoscopic gastrostomy (PEG) for amyotrophic lateral sclerosis (ALS) related dysphagia represent a clinical challenge. Diminished pulmonary function and aspiration risks can lead to anesthesia-related complications, and gastric displacement from hemidiaphragm elevation may preclude safe gastric access. This study reports the efficacy and outcomes of a dedicated anesthesia/surgery management protocol for ALS patients undergoing PEG.

Methods

In 2013, a PEG placement protocol for ALS patients was developed emphasizing efficient pre-operative evaluation, rapidly metabolized anesthetic agents, and minimization of opioid use. Outcomes were analyzed retrospectively. Preoperative weight loss, pulmonary function tests, total analgesia, procedural time, and 90-day morbidity and mortality were recorded.

Results

From 2013–2019, 67 ALS patients (mean age 65.3 years, 52.2% female) received a PEG under the protocol. Mean percentage weight loss 6 months before PEG was 9.3 ± 5.1% with 38.8% of patients meeting criteria for severe malnutrition. Mean anesthesia time (propofol induction to anesthesia emergence) was 34.5 ± 10.8 min and mean operative time (endoscope insertion to dressing placement) was 16.4 ± 8.2 min. Regional anesthesia with liposomal bupivacaine was performed in 76.1%. All attempts at PEG placement were successful. With a mean follow-up of 6.1 ± 6.8 months, all PEGs were functional and there were no surgical site complications. Thirty-day readmission rate was 7.0% and 90-day mortality was 22.4% (46.7% occurring within 30 days). Mean time from surgery to death was 8.8 ± 7.8 months.

Conclusions

Protocols for optimizing PEG may help overcome challenges present in the ALS patient population. Despite patient comorbidities, protocol implementation and dedicated team members resulted in a high procedural success rate and low complication rate. Further study is warranted to optimize the timing of PEG placement in relation to ALS disease progression and determine the utility of regional anesthesia during PEG placement.

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Correspondence to David J. Morrell.

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Disclosures

Eric Pauli reports speaking and teaching honoraria Beckton, Dickinson and Company (BD), Medtronic, PLC, Ovesco Endoscopy AG and Boston Scientific Corp.; consultant fees from Boston Scientific Corp., Actuated Medical, Inc., Baxter International, Inc., Wells Fargo & Company, Cook Biotech, Inc., CMR Surgical, Neptune Medical, Surgimatix, Inc., Boehringer Laboratories, Inc., Allergan, PLC and Noah Medical; royalties from Springer and UpToDate, Inc.; financial interests in International Hernia Collaboration, Inc., Contamination Source Identification and Cranial Devices, Inc. Joshua Winder receives consultant fees from Boston Scientific Corp unrelated to this report. Vamsi Alli receives research support from Actuated Medical unrelated to this report. David Morrell, Marvin Chau, Edward Stredny, Elizabeth Sinz, Sprague Hazard and Zachary Simmons have no conflicts of interest or financial ties to disclose.

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Morrell, D.J., Chau, M.H., Winder, J.S. et al. Percutaneous endoscopic gastrostomy in amyotrophic lateral sclerosis: outcomes of a dedicated anesthesia and surgery protocol. Surg Endosc 37, 4338–4344 (2023). https://doi.org/10.1007/s00464-023-09896-w

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