Management of High-Alert Medications – Hospital Pharmacy..

 


Standard Operating Procedure (SOP)
Management of High-Alert Medications – Hospital Pharmacy

 

1. Purpose

To minimize the risk of serious medication errors associated with high-alert medications by ensuring safe prescribing, storage, dispensing, administration, and monitoring within the hospital.

2. Scope

This SOP applies to all high-alert medications used in the hospital, including pharmacy, OPD, IPD, ICU, OT, Emergency, and wards.

3. Responsibility

  • Hospital Management: Support and enforcement of medication safety policies
  • Pharmacy Manager / Chief Pharmacist: Identification, implementation, and monitoring of high-alert medication practices
  • Pharmacists: Safe dispensing, labeling, and counseling
  • Medical Officers: Safe prescribing and review
  • Nursing Staff: Safe administration and monitoring
  • Quality / Patient Safety Team: Audit and incident review

4. Definitions

  • High-Alert Medications: Drugs that have a high risk of causing significant patient harm when used in error
  • Independent Double Check: Verification by two qualified healthcare professionals independently

5. Examples of High-Alert Medications

(Common examples; hospital-specific list should be maintained)

  • Insulin (all types)
  • Heparin and Low Molecular Weight Heparin
  • Potassium chloride (concentrated)
  • Magnesium sulfate
  • Chemotherapy agents
  • Narcotic analgesics (e.g., morphine, fentanyl)
  • Thrombolytics
  • Neuromuscular blocking agents

6. Procedure

6.1 Identification and Listing

  • A High-Alert Medication List shall be:
    • Prepared by the Pharmacy Department
    • Approved by the Drugs & Therapeutics Committee (DTC)
    • Reviewed annually or as required
  • High-alert medications shall be clearly identified with warning labels

6.2 Prescribing

  • Prescriptions for high-alert medications must be:
    • Clear and legible
    • Include patient weight (where applicable)
    • Specify dose, route, frequency, and duration
  • Verbal orders shall be discouraged and minimized
  • Dose calculations must be double-checked

6.3 Storage

  • High-alert medications shall be:
    • Stored separately from routine medications
    • Clearly labeled “HIGH-ALERT MEDICATION.”
  • Concentrated electrolytes shall:
    • Not be stored in patient care areas (where possible)
  • Access shall be restricted

6.4 Dispensing

  • Dispensing shall be done only by authorized pharmacists
  • An independent double check shall be performed before dispensing
  • Dispensed medications shall be:
    • Clearly labeled
    • Accompanied by special handling instructions
  • Look-Alike / Sound-Alike (LASA) precautions shall be followed

6.5 Administration

  • Nursing staff shall:
    • Verify patient identity using two identifiers
    • Perform an independent double check before administration
    • Follow the “Five Rights” of medication administration
  • Infusion pumps shall be used where required
  • Administration shall be documented immediately

6.6 Monitoring

  • Patients receiving high-alert medications shall be:
    • Closely monitored for adverse effects
    • Monitored as per clinical guidelines
  • Any abnormal findings shall be reported immediately

6.7 Error Reporting

  • Medication errors or near misses involving high-alert medications shall be:
    • Reported immediately
    • Documented in the medication error reporting system
  • Root cause analysis shall be conducted

6.8 Education and Training

  • All healthcare staff shall receive:
    • Initial training on high-alert medications
    • Periodic refresher training
  • Training records shall be maintained

7. Documentation

  • High-Alert Medication List
  • Prescriptions and medication charts
  • Dispensing and administration records
  • Double-check documentation
  • Medication error reports

8. Audit and Quality Improvement

  • Regular audits shall be conducted to ensure compliance
  • Audit findings shall be reviewed and corrective actions implemented

9. Review

This SOP shall be reviewed:

  • Annually, or
  • When new high-alert medications are introduced

10. References

  • NABH Patient Safety Standards
  • WHO Patient Safety Guidelines
  • Institute for Safe Medication Practices (ISMP)
  • Hospital Pharmacy Policy

11. Approval

  • Prepared by: __________________
  • Reviewed by: __________________
  • Approved by: __________________
  • Effective Date: ________________
  • Review Date: __________________

 

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