A 32-year-old primigravida at 38 weeks gestation is admitted to the labor and delivery unit for induction of labor due to preeclampsia with severe features. A continuous intravenous magnesium sulfate infusion is initiated for seizure prophylaxis. During the evening shift change, the departing nurse is urgently called to assist with a fetal deceleration in an adjacent room before completing a standardized bedside handoff. The incoming nurse assumes the patient's baseline deep tendon reflexes (DTRs) were recently checked and documented. Three hours later, the patient develops profound bradypnea and absent DTRs. Prompt administration of intravenous calcium gluconate reverses the patient's symptoms. A subsequent safety investigation reveals two key findings: the smart infusion pump library was inadvertently patched with a default loading dose rate instead of a maintenance rate, and the electronic health record (EHR) features a mandatory alert to check DTRs every 2 hours that only appears on the interface of the clinician who initially scanned the medication barcode.
Which of the following best classifies the EHR alert design flaw in this patient's care sequence?
- Latent errorCevap
- BActive error
- CSentinel event
- DNear miss
- EUnpreventable adverse event