# Perioperative Management of a Patient With Very Long Chain Acyl-CoA Dehydrogenase Deficiency Undergoing Laparoscopic Sleeve Gastrectomy: First Report of Bariatric Surgery in VLCADD

**Authors:** Mirza Anwar Baig, Bennedict Williams

PMC · DOI: 10.1007/s11695-025-08347-w · 2025-12-05

## TL;DR

This paper reports the first bariatric surgery in a patient with VLCADD, a rare metabolic disorder, and discusses the challenges and outcomes of the procedure.

## Contribution

The first documented case of bariatric surgery in a patient with VLCADD, offering insights into perioperative management strategies.

## Key findings

- The patient developed postoperative rhabdomyolysis despite careful perioperative management.
- Long-term follow-up showed sustained weight loss and improved cardiometabolic profile.
- The case provides practical strategies for managing VLCADD patients during bariatric surgery.

## Abstract

Very Long Chain Acyl-CoA Dehydrogenase Deficiency (VLCADD) is a rare inherited disorder of mitochondrial fatty acid β-oxidation that predisposes patients to metabolic crises, rhabdomyolysis, and cardiomyopathy. Surgical stress, fasting, and anaesthesia may precipitate metabolic decompensation. We present the case of a 65-year-old female with late-onset VLCADD, multiple comorbidities, and chronic kidney disease (CKD) stage 3 who underwent laparoscopic sleeve gastrectomy. Despite perioperative glucose infusion, normothermia, and careful anaesthetic planning, she developed postoperative rhabdomyolysis. This case highlights perioperative challenges in VLCADD, provides practical strategies for anaesthetic and nutritional management, and, to our knowledge, represents the first report of bariatric surgery in a patient with VLCADD. Long-term follow-up demonstrated sustained weight loss, improved cardiometabolic profile, and stable muscle and renal function.

## Linked entities

- **Diseases:** Very Long Chain Acyl-CoA Dehydrogenase Deficiency (MONDO:0008723), rhabdomyolysis (MONDO:0005290), cardiomyopathy (MONDO:0004994), chronic kidney disease (MONDO:0005300)

## Full-text entities

- **Diseases:** inherited disorder (MESH:D030342), VLCADD (MESH:C536353), CKD (MESH:D051436), rhabdomyolysis (MESH:D012206), cardiomyopathy (MESH:D009202), weight loss (MESH:D015431)
- **Chemicals:** fatty acid (MESH:D005227), glucose (MESH:D005947)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Figures

1 figure with captions in the complete paper: https://tomesphere.com/paper/PMC12852248/full.md

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Source: https://tomesphere.com/paper/PMC12852248