Contamination Control in Hospital Dispensing · Cytotoxic drug contamination of vials and packaging...
Transcript of Contamination Control in Hospital Dispensing · Cytotoxic drug contamination of vials and packaging...
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Contamination Control in Hospital Aseptic Dispensing
mel davis & associatesknowledge and education for better healthcare
X CONTAMINATION
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What’s it about?
X-CONTAMINATION in the hospitalpharmacy
• An intriguing mystery to solve
• A scary tale has become more scary
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Aseptic Dispensing in hospitals
Manufacture of injectionsand infusions notcommercially available:• unstable in solution• dose/volume patient specific• components not heat stablein combination
• no parenteral form accessible
TERMINAL STERILISATIONNOT POSSIBLE
Laminar Air Flow Workstations
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Aseptic Dispensing
Meticulous ‘no-touch’ techniquemandatory
Cytotoxic Drug Safety Cabinet
Trained and validated operators
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Products dispensed
Mainly parenteral nutrition solutions forintravenous feeding patients with intestinal failure and low birth weight infants and
Cytotoxic (anti-cancer) drugs
some antibiotics, analgesics, etc.
Monoclonal Antibodies
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Parenteral Nutrition (PN) solutions
Amino acids, glucose, fat emulsion, multi-vitamins,trace elements ...
=
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Notable PN Aseptic Dispensing Disasters
All solutionswere prepared by pharmacists or
techniciansin laminar air flow workstations or
isolators
Enterobacter cloacae (mostly), Serratia and Klebsiella sps.the primary causative organisms in every case – allmembers of Tribe Klebsielleae
Tribe Klebsielleae organisms originate in the human GI tract
• no airborne organisms involved
Year City Solution Outcome
1989 Johannesburg PN 2 infants died
1993 Johannesburg PN 8 infants died
1994 Manchester PN 2 infants died
1998 Roraima, Brazil PN 20 infants died
2000 Campinas, Brazil PN 7 infants died
2005 Malaysia PN 7 infants died
2007 Groningen, Neth PN 3 infants died
2010 Mainz Univ, Ger PN 3 infants died
2011 Alabama, USA PN 9 adults died
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Many were prepared in cleanrooms
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Purpose of cleanrooms
Control airborne particulates with limits established by relevant Standards
maintain low pathogen environments in whichpools of pathogens are eliminated or heldwithin very low limits specified by Standards
So where do the contaminants come from?
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People constantly shed skin cell debris
Activity Particles per minute (> 0.3mµ)
Sitting or standing still 100,000
Simple arm movement 500,000
Average arm, body movement 1,000,000
Walking slowly 5,000,000
Walking average pace 7,500,000
Walking fast pace 10,000,000
Boisterous activity 15 M - 30 M
Based on work by Dr. Phillip Austin ('Austin's Contamination Index')
Operators wearing cleanroom garments:
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Origin of cleanroom contaminants?
Skin squames shed fromall body surfaces
GI tract cells rapidly turn overbecause of digestive processes ‘Perineal
fallout’ *
* Perineal fallout or shedding – OR Infection Control terminology
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The need for “Packaging people"
cleanroom garments well-designed
effective cuff closures at ankles
Reference: Australian Standard AS 2013.1 - 1989
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A Possible Cause
few if any operators in the hospitalpharmacy cleanrooms appear tohave been wearing particle trappinggarments
too heavy reliance on laminar flow cabinets for sterility?
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But why so predominantly Tribe Klebsielleae micro-organisms?
E cloacae infection is associated with the highest mortality rate of all Enterobacter infections
The Enterobacter species are ubiquitous.
MedScape Reference:Enterobacter InfectionsAuthor: Susan L Fraser, MD; Chief Editor: Burke A Cunha, MD
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But why so predominantly Tribe Klebsielleae micro-organisms?
Surveillance and Control of Pathogens of Epidemiological Importance [SCOPE] project, 24,179 nosocomial bloodstream infections from 1995-2002
Nosocomial infections surveyed 1995-2002:
Enterobacter species the second-most-common
gram-negative organism behind Pseudomonas
aeruginosa
both represented 4.7% of bloodstream infections
in ICU settings
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So where are the Pseudomonads, Coliforms, the Staphs, Candida etc.
?
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48241260
*No strains tested
** Mean normalized concentration of all strains in group
Hours incubation at 25°C
Enterobacter (31)*Klebsiella (10)Serratia (10)
Candida (5)
Staphylococcus (13)Proteus (12)E. coli (11)Pseudomonas (10)Herellea (3)
Log c ± SEM c
Log c
**
0
1
2
3
4
5
6
7
-1
Growth curves of 106 microbial strains in D5%W at 25°C - Maki and Martin (J Infect Dis 1975;131:267)
Redrawn from:
Growth characteristics of bacteria in 5% Glucose (Dextrose)
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Sad Facts
Tribe Klebsielleae organismsappear to proliferate morerapidly in parenteral solutionsthan other micro-organismsthat may be present and areoften implicated in death of compromised patients
Tribe Klebsielleae organisms are endotoxinproducers that may precipitate septic shock
antibiotics used to treat infection may accelerate release of endotoxin
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Sad Facts
Tribe Klebsielleae organismsare opportunistic – cause infections only in certain circumstances or in certain patients
e.g.
aqueous solutions
blood
urinary tract
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Not only PN solutions contaminatedby Tribe Klebsielleae organisms
albumin fat emulsions cardioplegic (electrolyte) solutions sodium chloride 0.9% catheter flush solutions
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Year City Solution Outcome
1989 Johannesburg PN 2 infants died
1993 Johannesburg PN 8 infants died
1994 Manchester PN 2 infants died
1998 Roraima, Brazil PN 20 infants died
2000 Campinas, Brazil PN 7 infants died
2005 Malaysia PN 7 infants died
2007 Groningen, Neth PN 3 infants died
2010 Mainz Univ, Ger PN 3 infants died
2011 Alabama, USA PN 9 adults died
Analysis
In 3 cases, extrinsic contaminationoccurred because incoming solutions in vials or ampoules from external manufacturers were identified as the source
In 2 cases, bottles of amino acids or lipid emulsion become cracked during shipping and contaminated by Enterobacter cloacae prior to introduction into cleanrooms
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Question
Do mixed GI micro-organisms (including the Enterobacter species) colonising perineal skin squames circulate freely in uncontrolled environments?
And in at least some cleanroomenvironments?
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Question 2
Why don’t we detect Enterobacter et al. when performing routine airborne microbialmonitoring in cleanrooms and surrounding controlled environments?
swamped by normal airborne organisms? numbers below level of detection? requires fluid medium? any ideas?
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Go figure!
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Cytotoxic drugs dispensing
A scary tale has become more scary
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Cytotoxic drugs
Many supplied as lyophilised powders requiring reconstitution with saline or Water for Injections
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1/15,000th second
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Fluid Aerosols:
particle size distribution
No. ofParticles
micrometres0.01* 10 1,000mist spray
* not to scale From the Stanford Research Institute Chart
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Stoke's Law: Time taken for small spherical particles to fall in still air
Diameter of Particle(micrometres)
0.1
0.4
1.0
2.0
4.0
8.0
10.0
Calculated time to fall 1 metre
339 hrs
42 hrs
7.8 hrs
2.2 hrs
34 mins
8 mins
5.3 mins
Particle SG=1/Temperature=21 deg C USAF Technical Order 00-25-203
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Emerging consensus
certain cytotoxic drugs, particularly alkylatingagents, are carcinogenic in humans
many cytotoxic drugs are genotoxic, causingexcretion of mutagens
some cytotoxic drugs are teratogenic,capable of causing birth defects in offspringof exposed pregnant females
all cytotoxic drugs exhibit some, several,or all of these effects
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Leukemia risk following cancer chemotherapy,radiotherapy for Hodgkin’s Disease
0
1 2 3 4 5 6 7 8 9 100
Years after treatment
0.05
0.1
0.15
0.20
Blayney DW et al.
N Engl J Med 1987;316(12):710-4
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inhalation of CTX drug aerosols
absorption through the skin
mucosal absorption
needlestick injuries ?
inhalation of CTX drug vapour
Mechanisms of occupational exposure
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Engineering controls
Cytotoxic Drug Safety CabinetAS2567
Pharmaceutical Isolators
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Another source of contamination external to CDSCs and isolators
Cytotoxic drug contamination of vials and packaging
Hedmer M and others. Surface contamination of cyclophosphamide packaging and surface contamination with antineoplastic drugs in a hospital pharmacy in Sweden. Ann Occup Hyg 2005;49:629-637
Connor TH, Sessink PJM and others. Surface contamination of chemotherapy drugvials and evaluation of new vial-cleaning techniques: Results of three studies.Am J Health-Syst Pharm 2005;62:475-484
Connor, TH. External contamination of antineoplastic drug vials. Hosp Pharm Eur. 2005; Nov/Dec: 52-54.
Delporte JP, Chenoix P and Hubert P. Chemical contamination of the primary packaging of 5-fluorouracil RTU solutions commercially available on the Belgian market. Eur Hosp Pharm. 1999; 5:119-121.
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Several CTX drugs vapourise at 23 and 37°C
Drug 23°C Drug 37°C
Carmustine ++ Carmustine ++
Nitrogen mustard ++ Cyclophosphamide ++
Cyclophosphamide + Ifosphamide ++
Thiotepa ++
Nitrogen mustard ++
Fluorouracil ? Fluorouracil ?
Connor TH et al. Mutat Res Genet Toxicol Environ Mutagen 2000;470(1):85-92
Inhalation of Drug Vapour
BOLD – Class 1 human carcinogens
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Can settle on all surfaces within the area
Deposition of Vapourised Drug Residue
occupational exposure can occur inoperators not actively involved in asepticpreparation of drugs
chromosomal changes have been observed
Davis J, MacLauchlan R, Connor T. Exposure to hazardous drugs in Healthcare: An issue that will not go away. JOPP 2011;17(1):9-13
McDiarmid M and others. Chromosome 5 and 7 Abnormalities in Oncology Personnel Handling Anticancer Drugs. JOEM 2010;32(10):1028-43
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After 36 years …
No scientifically proven case of hospital pharmacy or medical stores staff suffering neoplastic disease from handling cytotoxic drugs
current safety practices are better thanat any time in the past
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X-Contamination in the hospital pharmacy
Two major areas of concern
Neither are addressed adequately by Code of Good Manufacturing Practice
Many practitioners inadequately informed
As a whole the profession is just waiting ...
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DISCUSSION