TABLE 4.
Research team’s Assessment of Likely Preventability of Errors Identified in Infusions That Were Not Given Via a Smart Infusion Device
| Observed Errors | Reported Errors | |
|---|---|---|
| Preventability Category* | No. errors | |
| Not preventable | 50 (32%) | 59 (51%) |
| Preventable with any pump | 21 (13%) | 9 (8%) |
| Possibly preventable with a standalone smart infusion device depending on limits set in drug library | 2 (1%) | 35 (30%) |
| Possibly preventable with a smart infusion device integrated with an electronic prescribing and barcode administration system | 80 (51%) | 9 (8%) |
| Unable to assess | — | 3 (3%) |
| Not applicable (blood products, or bolus) | 4 (3%) | — |
| Total | 157 (100%) | 115 (100%) |
*The categorization indicates the minimum level of functionality for preventability with a smart infusion device. For example, for errors classified as “preventable with any pump,” there would be no added value with the other technologies.