44
O.V.R. AND SENTINEL O.V.R. AND SENTINEL EVENT EVENT

Occurrence variance report

Embed Size (px)

Citation preview

Page 1: Occurrence variance report

O.V.R. AND SENTINEL O.V.R. AND SENTINEL EVENTEVENT

Page 2: Occurrence variance report

OBJECTIVESTo define ;OccurrenceO.V.R.Sentinel eventNear missMalpracticeAdverse eventVariation

Page 3: Occurrence variance report

How to report an O.V.R.Policy and procedures of occurrence

variance reporting system.

Page 4: Occurrence variance report

Definitions OCCURRENCEAn unusual event which adversely affects or threatens the health or life of patient , visitor, employee or student which involves loss or damage to personal or hospital property.An occurrence also includes any event that might otherwise result in any other adverse situation or a claim against the organization.

Page 5: Occurrence variance report

Occurrence variance report• It is an internal form which is issued to

document the details of the occurrence/event and the investigation of an occurrence and the corrective actions taken.

Page 6: Occurrence variance report

A “Sentinel Event” is an unexpected

occurrence involving death or serious physical or psychological injury, or the risk

thereof, not related to the natural course of a patient’s illness or underlying condition.

Such events called “sentinel” because they signal

the need for immediate investigation and response.

Sentinel Event

Page 7: Occurrence variance report

The following events are considered Sentinel

Events even if the outcome is not death or major permanent loss of function

• Suicide• Homicide • Surgery on the wrong patient or body part

Page 8: Occurrence variance report

• Impairment (major/permanent loss of bodily function

– i.e. serious physical or psychological injury or the risk thereof) that is not the result of the patient’s underlying medical condition.

• Any unexpected death that is not the result of the patient’s underlying medical condition

• Rape • Child Abduction or discharge to the wrong family • Hemolytic Blood Transfusion

Page 9: Occurrence variance report

Near miss• An event or situation that could have

resulted in adverse event but did not , either by chance or through timely intervention.

Page 10: Occurrence variance report

Why should report near miss?

They have the same

root causes as the

sentinel events, so

they should also be

reported.

Page 11: Occurrence variance report

Mal practice• It is an improper or unethical conduct by a

holder of professional and official position .• It is often applied to denote negligent or

unskillful performance of duties when professional kills are obligatory.

Page 12: Occurrence variance report

Adverse event• Are unexpected incidents, iatrogenic

injuries or other adverse occurrences directly associated with care or services provided.

Page 13: Occurrence variance report

VariationThe differences in result obtained in measuring the same event more than once.The sources of variationI.Common cause.II.Special cause.

Page 14: Occurrence variance report

PurposeTo act as a problem identification

mechanism - quality improvement toolTo define the responsibility and authorities

of all individuals involved in the occurrence reporting activity.

To implement corrective measures through root cause analysis.

Page 15: Occurrence variance report

policy• It is the responsibility of all staffs to

immediately report details any occurrence , which negatively impacts the care of a patient.

• The OVR will be initiated immediately following the occurrence

• Submit to the immediate supervisor/head of department within the current work shift.

Page 16: Occurrence variance report

•This report is to be used to identify the facts surrounding the occurrence.•This report will not be used to criticize or speculate on actions of the staff involved.•Corrective actions shall be taken and documented.

Page 17: Occurrence variance report

Confidentiality• The occurrence report form should not place

in medical record• The term “incident” or “error” shall not be used

while documenting the occurrence.• Confidentiality:• All OVR shall be handled and maintained in a

confidential manner• Occurrence variance report shall not be

duplicated.(except TQM)

Page 18: Occurrence variance report

Confidentiality..• The information contained in the OVR cannot

and shall not be used against any individual except in extreme situation. eg. patient harm

• Hospital staffs are not allowed to discuss the contents of an occurrence except proper authorities

• Discussion of general issues on OVR for educational or instructional purposes to improve patient care ,is however strongly encourage

• Names of concerned person should not be used ,instead use the ID number.

Page 19: Occurrence variance report

Roles &Responsibilities

1.Responsibilities of employee:• The employee who witness or discovers

an occurrence has the responsibility to notify immediately;

o the Physician-on-call if it involves patient /employee injury or harm.

Page 20: Occurrence variance report

o The immediate supervisor.• Initiating the OVR form before the end of

the current shift.• Submit OVR form to immediate superviosr

/head of department for completion.

Page 21: Occurrence variance report

2. The area supervisor/head of department•Ensure that all employees are aware of occurrence variance reporting system and how to report and process OVR form.•Conducting the immediate follow up of the occurrence by initiating and documenting on the OVR form the actions taken.•Indicate category and contributing factors of the occurrence.

Page 22: Occurrence variance report

• Complete the occurrence with their recommendation.

• Forward the completed original OVR form to TQM within 72 hours of the occurrence

• Conducting any further investigation and document findings of the occurrence upon request from the hospital administration or the safety committee.

Page 23: Occurrence variance report

3. Physician •Physician who attends the patient/employee involved in occurrence is responsible for examination and management of affected person.•Document a brief statement of his actions on the OVR form

Page 24: Occurrence variance report

4. Quality management department: is responsible for Monitoring all OVR for follow up with concerned

department Take steps to resolve the situation if necessary. Monthly summary and quarterly report. Maintaining file of all OVR forms for 3 years

Page 25: Occurrence variance report

5. Safety officer• Investigate all safety related occurrence

referred for investigation• Activate a review team of selected

committee members for investigation• Document the investigation result and

corrective actions taken on the OVR form.• Then return OVR form to QM office.

Page 26: Occurrence variance report

Procedure for OVR

• Write in clear legible handwriting ,can use blue or black ink avoid pencil.

• OVR consists of 5 sections• Part –A :Occurrence details• Filled by employee who witness or discover an

occurrence.Event detailsPerson’s affectedBrief description of occurrence.

Page 27: Occurrence variance report
Page 28: Occurrence variance report
Page 29: Occurrence variance report
Page 30: Occurrence variance report

Part-B :Immediate supervisor notification

• Immediate action taken• Evaluate the occurrence if it is sentinel or

not according to sentinel event criteria.• Document if the occurrence needs

physician evaluation.

Page 31: Occurrence variance report

Part- C: Physician follow up

• If a physician was notified and actually attended the patient ,the physician is responsible for recording a brief statement.

Page 32: Occurrence variance report

SEVERITY OF INJURY:

Severity of the incident is categorized in to “4”a.Slight /minor treatment: the incident resulted in abrasion , reddening of the skin or other minor damage to tissue.Treatment required – non-invasive treatment. ( e.g. Dressing , topical ointment etc.).

Page 33: Occurrence variance report

• b. Moderate injury: The incident resulted in hemorrhage , tissue

impairment and required clinical intervention.

e.g. suturing, first and second degree burns.Medication incidents with potential for

serious outcomes that require intervention and monitoring.

Page 34: Occurrence variance report

c. Serious injury:The incident resulted in fracture ,hemorrhage, aspiration third degree burns, serious drug reaction or the incident resulted in increase in length of stay(inpatient) or admission(out patient).d. Death.

Page 35: Occurrence variance report

Part-D: Action taken by

Involves corrective and recommendations to prevent recurrence of the incident.•To be filled by concerned /involved department.•QM will return back the OVR for if it is not completed.•The supervisor or head of department will verify and return the OVR form within the same day.

Page 36: Occurrence variance report

Part-E :TQM Comments

• To be filled by QM• Explain status of actions taken by

concerned department .• According to severity of the incident refer

to the safety officer for investigation.

Page 37: Occurrence variance report
Page 38: Occurrence variance report
Page 39: Occurrence variance report
Page 40: Occurrence variance report
Page 41: Occurrence variance report

• If occurrence happened after working hours:• Area supervisor should submit OVR form to

head of department next day.• Departmental OVR log sheet should be used

during transfer of the form.• The original copy of all monthly departmental

OVR log sheet should be kept in Quality department.

Page 42: Occurrence variance report

Remember…• OVR is a systematic standardized mechanism to

identify and develop preventive and improvement programs

• Shall be used as a system for monitoring ,quality improvement in a non-punitive manner.

• The information contained in the OVR form cannot and shall not be used against any individual as the sole basis for disciplinary action

Page 43: Occurrence variance report
Page 44: Occurrence variance report