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Desflurane and remifentanil anesthesia in a child with citrin deficiency: A case report
1Department of Anesthesiology and Pain Medicine, Yeungnam University College of Medicine, Daegu, Republic of Korea.
Insights
General anesthesia using desflurane and remifentanil facilitates rapid emergence in citrin deficiency patients. Careful perioperative management, including medication and diet, is crucial to prevent hyperammonemia.
Area of Science:
- Anesthesiology
- Medical Genetics
- Metabolic Disorders
Background:
- Citrin deficiency (CD) poses risks for hyperammonemia and delayed emergence from general anesthesia, even in managed patients.
- Preoperative medication interruption can exacerbate hyperammonemia in CD patients.
- Genetic diagnosis of CD involves mutations in the SLC25A13 gene, identified via newborn screening.
Observation:
- A 5-year-old girl with CD experienced hyperammonemia after temporary medication cessation before blepharoplasty.
- Anesthesia was administered using desflurane and remifentanil, with careful monitoring of anesthetic depth.
- The patient regained consciousness promptly post-anesthesia with a minor ammonia level increase.
Findings:
- Short-duration general anesthesia with minimally metabolized agents like desflurane and remifentanil promotes rapid emergence in CD patients.
- Perioperative nitrogen scavenging medication and dietary management are vital for controlling ammonia levels.
- Serial ammonia monitoring is essential to prevent neurological complications.
Implications:
- Optimized anesthetic strategies can improve surgical outcomes for patients with metabolic disorders like CD.
- Continuous management of medication and diet is critical for preventing perioperative complications in CD.
- This case highlights the importance of tailored anesthetic and perioperative care for rare genetic metabolic diseases.
Rationale:
Hyperammonemia, metabolic derangement, and/or the prolonged effects of anesthetics may lead to delayed emergence from general anesthesia as well as the onset of type 2 citrullinemia, even in compensated patients with citrin deficiency.
Patient Concern:
A 5-year-old girl with citrin deficiency was scheduled for blepharoplasty under general anesthesia. She developed hyperammonemia with temporary interruption of medication for a few days before surgery.
Diagnosis:
The patient was genetically diagnosed as citrin deficiency with a mutation in the SLC25A13 gene via newborn screening for metabolic disorders. Her citrulline and ammonia levels were well-controlled with arginine medication and protein-rich diet. Her elevated ammonia level by temporary interruption of medication was corrected with resumption of arginine medication and protein-rich diet before surgery.
Interventions:
We used desflurane and remifentanil for general anesthesia to avoid hyperammonemia and delayed emergence. End-tidal desflurane concentration and anesthetic depth were carefully monitored to avoid excessive anesthesia.
Outcomes:
She recovered consciousness with slightly increased ammonia level immediately after anesthesia.
Lessions:
General anesthesia of the shortest duration with the least metabolized drugs using desflurane and remifentanil, would be beneficial for rapid emergence in surgical patients with citrin deficiency. Maintenance of nitrogen scavenging medication, a protein-rich diet, and serial measurement of ammonia levels in the perioperative period are also important for avoiding hyperammonemia-related neurological dysfunction.
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