Category | Description | Level of Harm |
---|---|---|
A | An event that has the capacity to cause error. | No harm |
B | An event occurred, but did not reach the patient*. | No harm |
C | An event occurred that reached the patient, but did not cause harm. | No harm |
D | An event occurred that reached the patient and required monitoring to confirm that it resulted in no harm to the patient and/or required intervention to preclude harm. | No harm |
E | An event occurred that may have contributed to or resulted in temporary harm and required intervention. | Harm |
F | An event occurred that may have contributed to or resulted in temporary harm to the patient and required initial or prolonged hospitalization. | Harm |
G | An event occurred that may have contributed to or resulted in patient harm. | Harm |
H | An event occurred that required intervention necessary to sustain life. | Harm |
I | An event occurred that may have contributed to or resulted in the patient’s death. | Death |
Harm: Impairment of the physical, emotional, or psychological function or structure of the body and/or pain resulting therefrom. Monitoring: To observe or record relevant physiological or psychological signs. Intervention: May include change in therapy or active medical/surgical treatment. Intervention necessary to sustain life: Includes cardiovascular and respiratory support (e.g., CPR, defibrillation, intubation, etc.).
↵* Note: An error of omission reaches the patient. NCC MERP: National Coordinating Council for Medication Error Reporting and Prevention; M&MC: Morbidity and Mortality Conference. Adapted from McDonnell C, et al. Jt Comm J Qual Patient Saf 2010;36:117–25; with permission.