Sterile Compounding of Hazardous Drugs...List of hazardous drugs and their risks Review of...
Transcript of Sterile Compounding of Hazardous Drugs...List of hazardous drugs and their risks Review of...
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Sterile Compounding of Hazardous Drugs
Session II
Pamella Ochoa, Pharm.D. Jose Vega, Pharm.D.
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Objectives � List requirements of secondary engineering controls for hazardous
compounding
� Explain requirements for environmental and personnel monitoring as it relates to hazardous drug handling and compounding
� Demonstrate use of a chemo spill kit
� State personnel qualifications and responsibilities for hazardous compounding
� Describe techniques and manipulations for hazardous compounding
� Summarize patient safety considerations for chemotherapy orders
� Explain the role and requirements of USP <800> for hazardous drug handling and compounding
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Interactive Activities
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INTEGRATED LEARNING
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Agenda � Part 2 (2 hour CE)
� Secondary Engineering Controls
� Handling Waste � Handling Chemo Spills
� Patient Safety Considerations � Documentation and Standard Operating Procedures � Personnel Training and Competency
� Aseptic Techniques and Manipulations
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Secondary Engineering Controls Design and Monitoring
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Buffer Room1
� ISO Class 7
� Negative pressure room � 0.01-0.03 inches of water column
� Minimum 30 air changes per hour (ACPH)
� If entry is through positive pressure buffer room not used for hazardous compounding, then: � Line of demarcation for garbing/degarbing within negative
pressure room � Method of transport in/out
� Pass-through � Sealed containers
� Must demonstrate effective containment
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1 USP <800> Hazardous Drugs—Handling in Healthcare Settings, PF 40(3) [May–Jun.2013].
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Ante-Area1 � Positive pressure
� 0.02 inches of water column relative to adjacent unclassified spaces
� ISO Class 7 or better
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1 USP <800> Hazardous Drugs—Handling in Healthcare Settings, PF 40(3) [May–Jun.2013].
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Unclassified Segregated Compounding Area
� May contain PEC
� Negative pressure � 0.01-0.03 inches of water column
� 12 ACPH of HEPA filtered air
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Compounding Areas -
Design1
� Areas where hazardous drugs are handled must: � Be restricted to authorized personnel
� Located away from break rooms/highly populated areas
� Have prominent sign outside of entrance designating hazard
� Dedicated area for unpacking � Negative pressure or neutral/normal
� NOT in sterile compounding areas � NOT in positive pressure areas
1 USP <800> Hazardous Drugs—Handling in Healthcare Settings, PF 40(3) [May–Jun.2013].
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Additional Design1
� Storage � Hazardous drugs for sterile compounding need to be
stored in negative pressure buffer room � At least 12 ACPH
� Dedicated refrigerator
� External ventilation through HEPA filtration
� Physical separation
� Sink must be available � At least one meter from entrance of buffer room
� Eye wash station
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1 USP <800> Hazardous Drugs—Handling in Healthcare Settings, PF 40(3) [May–Jun.2013].
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Cleaning � All chemotherapy vials must be decontaminated
with sodium hypochlorite wipes before shelving � Wear PPE when unpacking/decontaminating
� Wash hands after removal of PPE
� When decontaminating/cleaning/disinfecting, full PPE must be worn � Double chemotherapy gloves � Impermeable gown
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Quality Assurance � Environmental wipe sampling
� ChemoGLO™ � Quantify trace amounts of contaminants from the use of
7 antineoplastic agents � 6 wipes to test sites in compounding areas
� Testing areas should include:1
� Inside PEC and any equipment inside of it � Staging/work areas near PEC � Areas adjacent to PECs � Patient administration areas
� Initially (baseline) and at least every 6 months1
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1 USP <800> Hazardous Drugs—Handling in Healthcare Settings, PF 40(3) [May–Jun.2013].
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Handling Waste Proper Disposal and PPE
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Compounding Waste � Dispose waste inside PEC
� Hazardous waste bag
� Seal bag completely
� Dispose of bag in hazardous waste container
Images from: http://extww02a.cardinal.com/us/en/distributedproducts/ASP/8985-S.asp?cat=surgerycenter (sharps container) and http://medimart.com/product/chemotherapy-waste-handling-bag-yellow-12x15/ (waste bag)
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Disposal � Compliance
� Institutional policies and procedures
� State regulations
� Use licensed medical waste contractor
� Wear FULL PPE when handling waste
� Keep containers closed
Image from: http://img.ehowcdn.com/640/ehow/images/a05/7e/ug/medical-waste-disposed-of_-800x800.jpg
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PPE � All PPE used for compounding must be removed
and placed in an appropriate waste bin prior to exiting the buffer area
� PPE used for transport, administration, shelving, etc. must be disposed of in an appropriate waste bin
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Chemotherapy Spills Spill Kits and Handling Spills
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Have you ever cleaned up a chemotherapy spill using a spill kit? True: Yes False: No
PO
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Spill Kits � Used for containment and cleanup of spills involving
hazardous drugs � Supplies for absorption of up to 1000 mL
� Must be available in all areas in which hazardous drugs are: 1. Received1
2. Prepared 3. Transported 4. Administered
� Must be available to personnel involved in hazardous compounding
� Circumstances and management of spills must be documented
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1 USP <800> Hazardous Drugs—Handling in Healthcare Settings, PF 40(3) [May–Jun.2013].
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Contents Appropriate PPE
Spill pads
Disposable towels
At least 2 hazardous waste bags
One disposable scoop
One puncture resistant container
Supplies for decontamination
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Handling Chemo Spills
< 5 mL • Responsible
personnel > 5 mL • Environmental
services
CONTAIN FIRST!
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Chemotherapy Spill Kit
INT
EG
RAT
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Patient Safety Considerations for Chemotherapy Orders
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Preventing Errors in Orders
Use pre-printed orders
Developed by key qualified personnel
Based on best practice & evidence-
based medicine
Familiarize new personnel
NO verbal or telephone orders
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Preventing Errors in Orders
Develop protocols
Use usual dosage
Developed by key qualified personnel
Familiarize new personnel
Familiarize current personnel
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Components of a Chemotherapy Order
Components of an Order 1. Patient name
2. Height
3. Weight
4. Diagnosis
5. Cycle number
6. Patient specific chemotherapy protocol
7. Drug amount in mg/m2
8. Total daily dose
9. Total number of days for dose to be administered
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Image from: http://www.rollingwavesoftware.com/StandardizedEntries.aspx
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Standardization � Use standardization for the following:
� Administration times
� Protocols
� Procedures
� Drug concentrations � Packaging
� Labeling
� Delivery times
� Verification
� Order entry data and process
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Double Check Method � Implement a �double check� method
� A person not involved in the process or preparation
� Verifies all aspects of order
� Must be documented in log
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Verify With Original Order Diagnosis/contraindications
Number of doses
Number of days
Number of cycles
Which cycle patient is currently receiving
Dose and volume of drug
Concentration and volume of final preparation
Expiration dates of components
Adjunctive therapies
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Which of the following labs should be checked prior to dispensing a chemotherapy order? A: Serum creatinine B: Liver function tests C: Complete blood count D: All of the above
AS
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NT
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Documentation and Standard Operating
Procedures Inclusions and Requirements
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DOCUMENTATION
Acquisition
Preparation
Dispensing
Personnel training
Maintenance of
equipment/supplies
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1 USP <800> Hazardous Drugs—Handling in Healthcare Settings, PF 40(3) [May–Jun.2013].
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Standard Operating Procedures (SOP)
� Must be maintained for safe handling of hazardous drugs for all situations for use throughout facility
� Reviewed at least annually � Document review � Revisions must be communicated to personnel
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SOP Inclusions1
Hazardous communication program
Occupational safety program
Labeling
Procurement
Use of PECs
Use of PPE based on activity and exposure risk
Decontamination/deactivation, cleaning, disinfection
Transport
Environmental monitoring
Spill control
Medical surveillance
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1 USP <800> Hazardous Drugs—Handling in Healthcare Settings, PF 40(3) [May–Jun.2013].
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Standard Operating Procedures1
� Must be developed for PPE based on: � Risk of exposure � Activities performed
� Must be developed for hazardous drug: � Receiving � Labeling � Handling � Packaging � Transport � Storage � Use of Safety Data Sheets (SDS) � Cleaning
� Must address: � Prevention of accidental exposures/spills � Personnel training on response to exposure � Use of a spill kit
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1 USP <800> Hazardous Drugs—Handling in Healthcare Settings, PF 40(3) [May–Jun.2013].
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Hazardous Communication Program1
� Elements must include: � Written plan for implementation of standard
� All containers of hazardous chemicals must be labeled, tagged, or marked with identity � Appropriate hazard warnings
� SDS for each hazardous chemical � SDS are readily accessible to personnel � Personnel who may be exposed to hazardous
chemicals must be provided information and training � Before initial assignment to work
� Whenever hazard changes
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1 USP <800> Hazardous Drugs—Handling in Healthcare Settings, PF 40(3) [May–Jun.2013].
Best Practice: Document that info and training
has been provided
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Medical Surveillance1
� Personnel involved in hazardous compounding as regular part of job
� Includes assessment and documentation of: � Symptom complaint � Physical findings
� Laboratory values (blood count)
� Follow-up plan should be completed for workers with potential toxicity/acute exposure
� Exit examination
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1 USP <800> Hazardous Drugs—Handling in Healthcare Settings, PF 40(3) [May–Jun.2013].
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Do you think medical surveillance is needed? True: False:
PO
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Personnel Qualifications, Training, and Monitoring
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General Requirements � Qualifications must be specified
� Ordering hazardous drugs
� Handling hazardous drugs
� Responsibilities include:1
� Understanding fundamental practices and precautions
� Continuous evaluation of procedures � Continuous evaluation of quality of final hazardous
drug preparations
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1 USP <800> Hazardous Drugs—Handling in Healthcare Settings, PF 40(3) [May–Jun.2013].
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Designee � Designated person qualified and trained to:1
� Developing and implementing appropriate procedures
� Overseeing compliance � Ensuring environmental control
� Ensuring competency of personnel
� Designated person must conduct continuous monitoring of facility and maintaining reports of testing/sampling1
� Must contain cause of contamination if applicable
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1 USP <800> Hazardous Drugs—Handling in Healthcare Settings, PF 40(3) [May–Jun.2013].
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Competency � Specific for hazardous compounding
� Different competencies for pharmacists and pharmacy technicians
� Frequency: � All new personnel involved in hazardous compounding � At least annually for current personnel
� Components: � Written evaluation
� Including handling of hazardous drugs
� Media fill test � Observation of simulated chemotherapy preparation
� Using fluorescein dye
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Fluorescein Dye Surrogate
• Evaluates for contamination • Handling
• Compounding
• QI Medical • ChemoTest
http://www.qimedical.com/wp-content/uploads/2014/04/DFU022-D-8-10.pdf
• Covidien • ChemoPlus
http://products.covidien.com/pages.aspx?page=ProductDetail&id=147640&cat=Chemo&cat2=Default
Image accessed from: http://www.patientcare-edu.com/imageServer.aspx?contentID=28339&contenttype=application/pdf
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Personnel Training � Didactic training
� Skills training
Topics (minimum)1
List of hazardous drugs and their risks
Review of institution standard operating procedures related to handling of hazardous drugs
Proper use of PPE
Proper use of equipment and devices
Spill management
Response to known or suspected hazardous drug exposure
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1 USP <800> Hazardous Drugs—Handling in Healthcare Settings, PF 40(3) [May–Jun.2013].
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Fluorescein Dye for Personnel Monitoring IN
TE
GR
ATE
D
LEA
RN
ING
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Aseptic Technique and Manipulations
For Hazardous Compounding
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The manner in which a syringe is held when compounding in a BSC is the same for both hazardous and non-hazardous drugs? True or False
AS
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SS
ME
NT
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BSC Work Zone � Must adapt compounding techniques to account for
directional differences of first air
� Recommended area for compounding in BSC is: � Between front and rear air intake grilles � At least 4 inches from the front grille
� Six inches from each side of the BSC
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Work Zone
6 in
ches
Rear Intake Grille
6 inches
WORK ZONE
Front Intake Grille 4 inches
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Compounding Considerations
� �Three-fourths rule� � Syringe should be
large enough that it will never be more than ¾ full after prescribed volume is drawn up
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Compounding Considerations � Avoid positive pressure to prevent spraying or dripping
of drug
� Use negative pressure � Too much negative pressure can cause leakage from the
needle when withdrawing the needle from vial
� Use slight negative pressure to draw large volume of fluid
� Use closed system drug transfer device � Mechanically prevents escape of drug during transfer
� PhaSeal™ � OnGuard™ � LifeShield™ ChemoClave™
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Compounding Techniques & Manipulations
INT
EG
RAT
ED
LE
AR
NIN
G
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Updates in Sterile Compounding
Key Updates
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USP Chapter <800> April 29th:
Updated notice of intent to
revise (published as errata)
May 26th:
Errata published
June 1st:
USP Chapter <800> becomes
official
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USP Chapter <797>
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July 2010: Revision
process began
Nov/Dec 2015:
USP Chapter <797>
published for public
comment
January 2016:
Public commentary
due
May 2016: Public
comments under review
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TSBP � Met February 2016
� Discussion and passing of amendments to §291.133 � Update requirements for sterility testing
� Clarify requirements for temperature and humidity
� Clarify requirements for blood labeling procedures
� Compounding Stakeholders Meeting � March 1st
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Board of Pharmacy Specialties
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Additional Resources For Hazardous Drug Handling and Compounding
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Additional Resources � American Society of Hospital Pharmacists. ASHP guidelines on handling
hazardous drugs. Am J Health Sys Pharm. 2006; 63: 1172-93. http://www.ashp.org/s_ashp/docs/files/bp07/prep_gdl_hazdrugs.pdf.
� National Institute for Occupational Safety and Health (NIOSH) � NIOSH alert: preventing occupational exposure to anti-neoplastic and other
hazardous drugs in health care settings. http://www.cdc.gov/niosh/docs/2004-165/pdfs/2004-165.pdf
� List of Antineoplastic and Other Hazardous Drugs in Healthcare Settings, 2014http://www.cdc.gov/niosh/docs/2014-138/pdfs/2014-138.pdf.
� American Society of Clinical Oncology/Oncology Nursing Society. � Chemotherapy Administration Safety Standards, 2013.
https://www.ons.org/practice-resources/standards-reports/chemotherapy
� Eisenberg S. Safe handling and administration of antineoplastic chemotherapy. J Infus Nurs. 2009 Jan-Feb;32(1):23-32.
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THANK YOU! We enjoyed the opportunity.
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