Synonym/Acronym:
cholinesterase: CHS; Acetylcholinesterase: AcCHS, RBC cholinesterase, red blood cell cholinesterase, erythrocyte cholinesterase, true cholinesterase; Pseudocholinesterase: PCHE.
Rationale
To assess for acquired or inherited pseudocholinesterase deficiency.
Patient Preparation
There are no food, fluid, activity, or medication restrictions unless by medical direction.
Normal Findings
Method: Spectrophotometry, kinetic.
| Test | Conventional Units |
|---|---|
| Acetylcholinesterase (AcCHS)/ RBC cholinesterase | 25–50 U/g Hgb |
| Test | Conventional Units |
|---|---|
| Pseudocholinesterase (PCHE) | |
| Males | 3,334–7,031 units/L |
| Females | 2,504–6,297 units/L |
| Dibucaine Number | Fraction (%) of Activity Inhibited |
|---|---|
| Normal homozygote | 79%–84% |
| Heterozygote | 55%–70% |
| Abnormal homozygote | 16%–28% |
Critical Findings and Potential Interventions
Timely notification to the requesting health-care provider (HCP) of any critical findings and related symptoms is a role expectation of the professional nurse. A listing of these findings varies among facilities.
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