Saferating OceanView Demonstration Area
Hospital Incident Reporting Form
A sample hospital incident reporting form to replace a paper-based system.
NOTE: Fields marked with "
*
" are required.
THIS FORM IS NOT FOR MEDICATION OCCURRENCES
All major injuries or unanticipated death immediately contact administrative supervisor.
Patient Name of Visitors Identification:
OCCURRENCE REPORT
Confidential data, not to be disclosed, released, or copied. Not a part of patient medical record.
Date of Occurrence (mm/dd/yyyy):
Enter Time :
Enter Age in Years:
Location of Incident:
Select Location
Emergency
Outpatient
Inpatient
Visitor
On Campus
Choose Department Where Incident Occurred:
Select Department
NU100
NU200
NU3
SURGERY
ASU
ED
LAB
RADIOLOGY
PHYSICAL THERAPY
CARDIOLOGY
PHARMACY
CAMPUS
Location of Incident:
Select Location
Emergency
Outpatient
Inpatient
Visitor
On Campus
Falls Incident Information
Was Fall Witnessed?:
YES
NO
NA
Choose Most Appropriate
Fall Information:
Select Best Description
FOUND ON FLOOR
FALL FROM BED
FALL FROM CHAIR/COMMODE
FALL/ STANDING/WALKING
FALL/ MISCELLANEOUS
FALL/ ASSISTED TO FLOOR
Bed Rails:
Select Bedrail Position
UP
DOWN
BOTH
Ambulation Privileges:
Select Ambulation Status
UNLIMITED
LIMITED
WITH ASSISTANCE
RESTRAINED
NONE
Protective Device:
Select Precautions Ordered
ORDERED IN PLACE
ORDERED NOT IN PLACE
NOT ORDERED
BED ALARM ON
Balance:
Select Consition
DIZZY
FAINTED
TRIPPED
UNKNOWN
Surface Conditions:
Select Condition of Surface
DRY SMOOTH
UNEVEN
WET SLICK
SANDY
ICY
STICKY
Collision:
Select Best
OBJECT
PERSON
NONE
Medications Within Last 12 hrs:
YES
NO
NA
Lighting Conditions:
Select Lighting Conditions
BRIGHT
DIM
DARK
Treatment & Procedures
Incident:
Select Most Descriptive
CANCELED
NO CONSENT
INCOMPLETE CONSENT
UNPLANNED PROCEDURE
TECHNIQUE-PROCEDURE (Clinical)
TECHNIQUE-PERFORMANCE (Administrative)
IMPROPER IDENTIFICATION
READMISSION
RETURN FOR TREATMENT
Difference From Order:
Select Most Appropriate
PATIENT
OMITTED PROCEDURE
SITE
PROCEDURE
SEQUENCE
TIMELINESS
NOT APPLICABLE
Counts:
Select Most Descriptive
INITIAL COUNT NOT DONE
UNMATCHED INSTRUMENT COUNT
UNMATCHED NEEDLE COUNT
UNMATCHED SPONGE COUNT
ALL COUNTS UNMATCHED
NOT APPLICABLE
Specimen:
Select Specimen Category
UNLABELED
MISLABELED
MISSING
INCORRECT
NOT APPLICABLE
All other incident types
Other:
Patient condition prior to occurrence
Prior Condition:
Select Condition
AGITATED
ALERT
DEPRESSED
DISORIENTED
SEDATED
UNRESPONSIVE
UNABLE TO DETERMINE
Effects
Severity of Occurrence:
Select Severity
Patient not involved
No apparent harm or injury to patient
Minimal event no treatment required No change in vital signs
Minimal event treatment required need for increased patient monitoring
Moderate event physician intervention drug treatment required or LOS increased
Major event extended care required or suspected long term injury to patient
Pt death event may or may not have contributed
Effects (select most serious):
Select Most Appropriate
ABRASION BRUISE CONTUSION
AGGRAVATION OF PRE-EXISTING CONDITION
BLOOD LOSS
BURN
CIRCULATORY IMPAIRMENT
DAMAGED TISSUE SKIN
DECUBITUS ULCER
FOREIGN BODY
FRACTURE DISLOCATION
HEMORRHAGE WOUND DISRUPTION
INFECTION
LACERATION PERFORATION TEAR
MUSCULAR VASCULAR IMPAIRMENT
NEUROLOGICAL IMPAIRMENT
PAIN
RESPIRATORY DISTRESS
SPRAIN STRAIN
TOOTH TEETH INJURY
NONE NOT APPLICABLE NO APPARENT INJURY
UNABLE TO DETERMINE
Referred for Treatment:
YES
NO
NA
Physician:
Select Physician or Prescriber
James Smith MD
Jane Doe DO
Archie Wilson MD
Jonas Miller DO
Witness:
X Ray Ordered:
YES
NO
NA
Medical device failure form (safety index #808 812) completed:
YES
NO
NA
Evaluation (what was the occurrence):
Conclusions (why it happened):
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