Prevention and Control of Laboratory-Acquired Infections


EPIDEMIOLOGY

The characterization of a person’s infection as laboratory acquired is usually retrospective

and is based on the assumption that the only likely exposure occurred while the person was

in a laboratory. A trivial laboratory event may be considered the possible exposure because

no other circumstance outside the laboratory could account for infection (40, 44).

It is important, however, to appreciate that the total laboratory testing cycle begins well

before the sample actually reaches the laboratory (the preanalytic phase of laboratory

testing) and that exposures during the collection and transport of the sample should also be

considered. In the past, infections acquired during the collection of some samples were

included if it could be ascertained that the collection was solely for the purpose of a

laboratory investigation. Infections experienced by phlebotomists as a result of needlestick

injuries are now routinely considered laboratory-acquired infections (27). In contrast,

phlebotomist infections (e.g., chicken pox) acquired while collecting samples in patient

rooms are not included (24).

Although difficult to date precisely, the first microbiology laboratories of Pasteur and Koch

were active by 1840 to 1860. The first report of a laboratory-acquired infection,

Mediterranean fever, was in 1899 (7).

Various compilations of laboratory-acquired infection have been published over the past 60

years (20, 32, 33,69, 73, 74). The first survey published, in 1953, was a survey of 5,000

American laboratories by Sulkin and Pike. They provided additional updates in 1961, 1965,

and 1976. They cited 3,921 laboratory infections dating between 1930 and 1974, with a

mortality of 4.1%. Of note, 2,307 (58.8%) of the infections were reported from research

facilities, 677 (17.3%) were from diagnostic facilities, 134 (3.4%) were from the generation

of biological products (industry), and 106 (2.7%) were from teaching facilities. The

remaining 697 (17.8%) infections had an unspecified source.

Four series performed in the United Kingdom between 1971 and 1991 revealed that within

clinical facilities, the majority of infections were reported from workers in the microbiology

laboratory, followed by the autopsy service. Over this 20-year period, the number of

infections reported dropped over 80%, from 104 to only 17. While it is tempting to conclude

that laboratories are becoming safer, there are no active monitoring programs in place to

capture the true number of accidents and infections.

Compiled information tends to be limited to events that are reported in the literature or in

specific databases. Thus, while uncommon community infections, such as those associated

with Brucella species (1, 36a, 49a, 50a,55a, 73a, 76a), are commonly reported as

laboratory-acquired infections, very common infections such asStaphylococcus

aureus (including methicillin-resistant S. aureus) infection are rarely identified (70) as being

acquired in the laboratory. It is assumed that even complete listings reflect an immeasurable

minority of infections that actually occur (69).

More recently, Internet-based discussion groups have worked to create informationgathering

approaches (5,68). While these newer surveys have challenges similar to those of

former retrospective compilations, they demonstrate the potential for gathering important

information on laboratory safety and infection.

Two hundred cases of laboratory-acquired infections with parasites resulting from laboratory

accidents, from 1929 through 1999, have been published (40, 41). While the distribution of

cases changed from decade to decade, the number of cases identified in each decade (19 to

28) remained relatively constant. Sharps-related injuries (e.g., needles and glass) were

common factors, often associated with manipulation of research animals and the production

of blood smears for malaria.

LABORATORY SAFETY AND PERSONAL ATTRIBUTES Back to

top

A matched case-control study of 33 laboratory workers who experienced a laboratoryassociated

injury over a 2-year period was previously described (57). No differences were

noted related to age, length of employment, years of formal education, wearing of glasses,

use of prescription medications, or off-the-job accidents or driving record. On the other

hand, the accident-involved persons were significantly more likely to have had a laboratory

accident or laboratory infection prior to the 2-year study period and were significantly more

likely to have a low opinion of laboratory safety programs. When the conditions surrounding

the accidents were examined, 36% occurred when the employee was working too quickly,

either just before lunch or at the end of the day. In 30% of accidents, the employee

acknowledged a breach in safety regulations. In summary, in this study, attitudes and work

habits were important contributing factors to laboratory accidents. While this study may

seem to be unduly dated, in today’s circumstances, with increasing numbers of samples and

increasing complexity of tests, along with an aging and shrinking workforce, rush, stress,

and awareness of risk continue to be relevant issues (1a, 47).

In a study in which laboratory practices were observed directly and then related to

laboratory environmental contamination with hepatitis B virus (HBV), contamination was

strongly related to flawed technique and high workload. Unsafe work practices were also

related, but to a lesser degree (32).

Over time, laboratorians have learned that even conventionally accepted practices can result

in serious infection. Mouth pipetting, marking of blood spots, transport of samples to the

laboratory in corked or sheathed sharps, recapping of needles, eating, and smoking were all

practiced commonly at one time in properly run medical laboratories. All of these practices

are now appreciated as risky and are prohibited.

Injuries with sharp objects continue to be identified as an area of concern (20). Examination

of bacterial culture plates with an eyeglass or sniffing plates to help identify organisms is

now controversial (3). Laboratory safety requires diligent review and ongoing critique of

current conventional practice, as well as openness to change when new risks are identified.

RISK-BASED CLASSIFICATION OF MICROORGANISMS Back

to top

As a foundation for determining environmental requirements and best laboratory practices,

the international community has developed a common risk-based classification of

microorganisms. Group 1 biological agents are unlikely to cause human disease. Group 2

biological agents can cause human disease and might be a hazard to workers but are

unlikely to spread to the community, and there is usually effective prophylaxis or treatment

available. Group 3 biological agents cause severe human disease and present a serious

hazard to workers. They may present a risk of spreading to the community, but there is

usually effective prophylaxis or treatment available. Group 4 biological agents cause severe

human disease and are a serious hazard to workers. They may present a high risk of

spreading to the community, and there is usually no effective prophylaxis or treatment

available. A partial list of microorganisms by category is shown in Table 1.



SAFETY EQUIPMENT AND THE CLINICAL LABORATORY Back

to top

Splashguards

Splashguards made of clear glass or plastic represent the minimum level of equipment for

protecting workers. They are more likely to protect workers from gross splashes than from

aerosols. They can be an appropriate alternative to biosafety cabinets for opening vacuum

blood tubes. They should be of sufficient size and should be cleanable to remove the

occasional blood splatter. The effectiveness of splashguards depends on appropriate

placement with respect to both work flow and worker height. It is inappropriate to obscure

vision by using splashguards as a convenient location for taped memos and procedures.

Biosafety Cabinets

Biosafety cabinets can protect the laboratory worker and the laboratory environment from

splashes and aerosols and can also reduce the opportunities for sample contamination

(73, 75). Biosafety cabinets are enclosed units with various degrees of openness and access

and with control of exhausted air. Class 1 cabinets have an open front but work under

negative pressure, exhausting their air through a HEPA filter. Exhausted air usually is

returned to the work area. Class 2 cabinets increase the level of safety by including a HEPAfiltered

downward-flow air curtain designed to increase the degree of separation between

room air and interior cabinet air. Class 2 cabinets may exhaust back to room air (class 2A) or

through an exhaust system to outside the building environment (class 2B). Class 2B cabinets

can be subclassified further based on additional features. Class 3 cabinets are completely

enclosed, providing gas-tight containment. They are accessible only through front-end glove

ports. Class 3 cabinets provide the most suitable containment for working with exotic

pathogens. Because class 1 and class 2A units exhaust to the laboratory air, they are

unacceptable for use with volatile chemicals and reagents. Biological safety cabinets cannot

be used as alternatives to chemical fume hoods.

All safety cabinets must be tested and certified by a qualified person on a regular basis to

ensure that they maintain their required face velocity and negative pressure.

Even properly maintained and certified cabinets can be a hazard if equipment and materials

are placed improperly inside the cabinet. Overcrowding the cabinet or stacking of equipment

against either the front or back grill will disrupt the airflow, resulting in backwash out the

front of the unit (46). This can result in a compound hazard because biological safety

cabinets are detrimental to worker dexterity, making for a greater potential for accidents

(66).

Centrifuges

Although the safety centrifuge was first described in 1975 (37), accidental contamination of

laboratory and personnel via centrifuges is regularly reported (18, 34). While other

equipment may result in greater aerosol dispersal, the frequency of use of centrifuges

increases their significance in accident risk assessment (6). Accidents occur because of a lack

of tight seals on containers and rotors. Centrifuges can be susceptible to contamination

because prolonged use without regular inspection can lead to worn O-ring container seals

(38). Plastic centrifuge tubes can crack or distort and result in increased risk (34). Accidents

can be avoided if centrifuges are used, cared for, and maintained in a safe manner. Lids

must be closed at all times during operation. The centrifuge should not be left until full

operating speed is attained and the machine is running safely without vibration. If vibration

does occur, the centrifuge should be stopped immediately and the load balances checked.

Swing-out buckets should be checked for clearance and support. Ideally, rotors and cups

should be cleaned and disinfected with noncorrosive cleaning solutions after each use. All

spills and breakage should be reported to the laboratory safety officer and should be cleaned

immediately, after giving time for aerosols to settle. In the context of quality control, a log

should be maintained and should include the rotor serial number, speed (revolutions per

minute), duration of spin, times of use, and operator’s name.

Chemical Fume Protection

A fume hood is a mechanically ventilated, partially enclosed workspace where harmful

volatile chemicals and reagents can be handled safely. The primary function of a fume hood

is to contain and remove gases and vapors.

Most fume hoods use ducts and a fan to ensure that heat and airborne contaminants are

captured, transported out of the work area, and eventually discharged into the atmosphere

outside the building. Chemical fume hoods differ from biosafety cabinets in that they are

usually ducted. They must be constructed of noncombustible materials, and they must also

be explosion proof.

Nonducted, or recirculating, fume hoods are of limited use in the laboratory and should not

be considered acceptable substitutes for ducted fume hoods for containment of volatile

chemicals (26).

Special fume hoods are designed to protect workers from specific highly corrosive reagents

or chemicals, such as perchloric acid or radioisotopes. Installation of fume hoods without

consideration of airflow and balance can result in increased risk due to backwash and room

contamination (26).

As with biological safety cabinets, chemical fume hoods require regular testing and

recertification. It is recommended that chemical fume hoods be tested for both face velocity

and containment by use of the ASHRAE 110 tracer gas test. Face velocity alone is not a valid

indication of containment (26).

Protection from Sharps

Scalpels, needles, broken glass, and other sharps are commonly associated with wound

injuries and laboratory-acquired infections (2). To the extent that it is possible, the use of

sharps should be eliminated or safety barriers should be implemented (29, 70). Sharps may

be contaminated with infectious or cytotoxic agents, or both. All sharps should be considered

potentially infectious and should be discarded in safety containers. Sharps containers

minimize injuries and transmission of potentially harmful agents, provided that they are

readily accessible and appropriately used.

Sharps containers used in medical laboratories should be designed specifically for the

containment and disposal of needles, syringes with needles, scalpel blades, clinical glass, and

other items capable of causing cuts or punctures (29, 71). If containers are not resistant to

penetration or compression, they pose a health risk to those involved in their handling and

disposal.

The characteristics of well-designed containers are that they are leakproof and puncture

resistant, do not degrade in autoclaves, either require no assembly or are easy to assemble,

are appropriately labeled, and come in a variety of sizes. Within this framework,

manufacturers can implement a variety of designs. Sharps containers should be stable

enough to resist toppling over and durable enough to withstand being dropped onto a hard

surface (13). Using locally available tin cans or other containers in lieu of designed

containers is inappropriate, as they do not address important aspects of containment.

Sharps containers must have a prominently displayed universal biohazard symbol. In

addition, sharps containers intended to contain sharps contaminated with cytotoxic

substances must display the cytotoxic hazard symbol. The international color code is yellow

for biohazardous medical sharps and red for cytotoxic medical sharps.

Containers should not be filled to more than three-quarters of their maximum capacity to

avoid accidents from overfilling, and sharps should never be forced into a container. Properly

designed containers have a designated fill line.

Most sharps containers are designed for a single use only. Once filled, they are securely and

irreversibly closed for containment. Following autoclave treatment, the containers should be

disposed of in accordance with local requirements. Containers with cytotoxic sharps or

probable prion proteins should not be autoclaved but rather require incineration.

To reduce the challenges associated with disposal of single-use containers, reuse container

services can provide collection and transport to an off-site location for safe, secure

reopening, emptying, and decontamination prior to redistribution for reuse.

MEDICAL WASTE AS AN INFECTION HAZARD Back to top

Medical facilities generate large volumes of waste that can be hazardous to workers and the

community (74). According to a recent survey, most university hospitals in the United States

continue to use autoclaves to sterilize medical waste, although many do not appear to

monitor autoclave effectiveness appropriately by use of biological indicators (50).

Contractual arrangements with biomedical waste management organizations may be an

economical or environmentally sound alternative. Alternatives such as microwave

inactivation can be considered, with recognition of the necessity of required rigorous

conditions (76). In some areas where economic or environmental issues are of extreme

concern, solar disinfection (21) of biomedical waste may be a viable consideration. In rare

circumstances in addressing zoonotic outbreaks, and more commonly in resource-limited

regions, incineration of medical waste continues to be performed, even though it has been

demonstrated to be harmful to health and the environment (31, 38, 50, 74a).

SAFETY AS A QUALITY MANAGEMENT INITIATIVE Back to top

There is an increasing interest in medical laboratory quality, safety, and risk, with a resulting

convergence of these issues (55). International Organization for Standardization Technical

Committee 212 has developed documents to improve the quality of medical laboratories,

including ISO 15189:2003 (Medical Laboratories—Particular Requirements for Quality and

Competence) and ISO 15190:2003 (Medical Laboratories—Requirements for

Safety) (41b, 41c). In those countries where laboratories are certified or accredited to the

requirements of the International Organization for Standardization, these documents are

considered essential standards.

With respect to safety, ISO 15190:2003 addresses management responsibility, safety

managers, safety manuals, safety programs, education, training, competence, and audit and

review. It states that laboratory management is respon sible for the safety of all employees

and visitors to the laboratory and that ultimate responsibility rests with the laboratory

director. The laboratory must identify an appropriately trained and experienced laboratory

safety officer to assist the laboratory director and managers with safety issues. The

laboratory safety officer must have the authority to stop activities that are deemed unsafe.

The laboratory safety officer is responsible for designing and maintaining the laboratory

safety program and is responsible for monitoring its effectiveness.

The elements of a laboratory safety program include development of the laboratory safety

manual, safety audits and inspections (see Table 4 for audits required by ISO 15190:2003),

risk assessments, and the maintenance of records. For further details, ISO 15190:2003 is

available through the International Organization for Standardization website (www.iso.org)

or the Clinical and Laboratory Standards Institute website (www.clsi.org).



HAND WASHING AND THE USE OF PERSONAL

PROTECTIVE EQUIPMENT Back to top

Hand Washing

Hand washing is the single most useful technique to stop the transmission of microorganisms

and acquisition of infection in medical laboratories (11). Hands can be contaminated during

sample collection, handling of sample containers, handling of contaminated equipment, and

touching of sample storage units.

While contamination can be reduced by the use of gloves, gloves alone are not completely

effective. Hand hygiene can be performed with running water and either plain or

antimicrobial soaps. Nonmedicated detergent-based soap products and water alone do not

disrupt the normal skin biota but can have some effect on reduction of the transient hand

biota, including both bacteria and viruses (11, 72). The efficacy is directly related to the

duration of hand washing. Plain soaps, similar to other products, can be associated with

detrimental effects, including skin drying and irritation.

It is less clear whether soaps containing antimicrobial products are essential for the vast

majority of hand-washing situations, even in the microbiology laboratory. For example, hand

washing with plain soap is as efficacious as that with antiseptic soap for

removing Clostridium difficile (36), nonenveloped viruses, andBacillus anthracis (79). For

short-term hand cleansing, the two product types are equally efficacious for the removal of

common bacterial pathogens (9, 72).

Most laboratories will continue to see value in regular use of antiseptic soaps. Selection of an

appropriate product for the laboratory depends upon both the types of organisms processed

by the laboratory and issues such as fragrance, consistency, and potential for irritation and

skin drying. Commonly used products contain chlorhexidine, iodophors, triclosan, or related

compounds. Other ingredients, such as those including tea tree oil, may be acceptable

alternatives (52).

Waterless alcohol-based products can be a rapid and convenient alternative to conventional

hand washing, especially when a sink with running water is not immediately accessible

(45, 72). When they are used correctly, alcohol-based hand gels are as active as traditional

70% alcohol for removing methicillin-resistant S. aureus, Serratia marcescens, and Candida

albicans from contaminated hands (81), but alcohol-based products may have reduced

efficacy if hands are contaminated with spore-forming organisms, including C. difficile and B.

anthracis (79), or with non enveloped viruses (72). Alcohol-based products should not be

relied upon when hands are visibly soiled, contaminated with proteinaceous materials, or

contaminated with materials that have a known high microbial load.

It is common in many laboratories to place alcohol- containing bottles by hand-washing

sinks. Others have noted that health care workers are more compliant with hand care when

agents are close to the site of contamination (25). Accordingly, laboratories might consider

having containers of alcohol-containing hand gel closer to workstations.

Gloves

Gloves can provide an important barrier within the laboratory, provided that they are used

appropriately. Clearly, gloves are essential to prevent damage when hands are exposed to

heat, cold, and toxic materials. Insulated gloves are essential for taking materials out of

−70°C freezers, exposure to liquid nitrogen, or removing materials from autoclaves.

General purpose utility gloves (“kitchen” or “rubber” gloves) provide ample protection for

cleaning biological spills, for general cleaning, and for decontamination. Utility gloves can be

cleaned and reused, although they should be examined regularly for cracks, tears, and

peeling. Damaged utility gloves should be discarded. Utility gloves may be inappropriate for

handling chemical solvents and should not be used. Chemical-resistant gloves should be

available in all laboratories that handle chemical solvents and other toxic chemicals and

dyes.

The degree of protection that gloves can provide depends upon many factors, including

composition, size, fit, grip, and thickness, all of which can affect user dexterity. Latexcontaining

gloves may provide superior fine finger dexterity, which could be associated with

fewer spills or accidents (65).

Disposable gloves of latex, vinyl, or nitrile can provide an effective barrier, especially for

handling blood, body fluids, and excrement. This is especially true because open abrasions

on hands can often go unnoticed (43). In specific settings, gloves of increased length, to

elbow or shoulder, may be appropriate. Gloves are easily torn. In-use durability studies

indicate that vinyl gloves may tear as often as 40% of the time, depending upon the

presence of powder and the length of the user’s fingernails (43). Latex gloves are more

durable but may be associated with atopic reactions.

It is critical for the user to remember that handling equipment and materials with

contaminated gloves can cause considerable environmental contamination. Gloves must be

removed either at the end of the task or when the task is interrupted.

Regardless of the type of gloves and their composition, it is essential that the user always

wash his or her hands as soon as gloves are removed, either with running water and soap or,

in many settings, with alcohol-containing hand hygiene products.

While it has become customary for phlebotomists to wear gloves during specimen collection,

this may not be essential if the risk of exposure to blood and body fluids is considered

sufficiently low and gloves of an appropriate size or material are not readily available.

Regardless of whether gloves are worn or not during the task of collection, hands should

always be cleansed immediately after the completion of the task. Contaminated gloves often

result in contamination of equipment (53) but can also contribute to transmission of serious

infection (59).

Disposable gloves do not provide significant protection against needlestick injury. If sharps

exposure and the risk of injury are possible, double gloving can provide some protection.

Cotton undergloves may provide more protection than a second vinyl or latex glove. In the

morgue, use of chain mail gloves may be appropriate.

Gloves provide an important protective barrier, but they may also be a source of harm. Use

of vinyl, latex, or cotton undergloves can reduce contact irritation noted with rubber gloves.

Excessive glove use can result in moisture damage to skin (12, 19, 61). Surveys of dentists

wearing gloves for 6 h daily indicated that many of them, especially young women with

preexisting eczema, suffered from glove intolerance (80).

IMMUNIZATION Back to top

Immunization provides protection against some laboratory-acquired infectious diseases but

should be considered secondary to mental alertness and good laboratory practices.

Immunization may not prevent infection but can protect against serious illness. All adults,

including pregnant women, should have a complete primary immunization with tetanus and

diphtheria toxoids and should receive a booster every 10 years (15).

Laboratory workers should receive annual influenza immunizations. Similarly, all staff with

possible occupational exposure to human blood and body fluids should receive the hepatitis B

vaccine. The value of meningococcal immunization for laboratory workers has been discussed

previously (10, 14, 22). Cases of meningococcal illness possibly linked to laboratory

exposure have been published, and it has been recommended that microbiologists routinely

exposed to meningococci, especially aerosolized organisms, should consider meningococcal

immunization. Laboratorians working with specific pathogens and in specific situations should

consider additional immunizations, for example, human diploid cell rabies vaccine, typhoid

vaccine, and vaccinia vaccine (48, 51).

In the past, Mycobacterium bovis BCG vaccination has been considered valuable for health

care workers. However, it is no longer recommended as a primary tuberculosis control

strategy because the protective efficacy of the vaccine in health care workers is uncertain

and because immunization with BCG may cause difficulty in the interpretation of tuberculin

skin test responses caused by true infections with Mycobacterium tuberculosis. In laboratory

and other health care workers with positive tuberculin skin tests, the new gamma interferon

release assays can help to differentiate likely tuberculosis exposure (positive assay) from

BCG vaccination (negative assay).

LABORATORY-ACQUIRED HIV INFECTION, HEPATITIS B,

AND HEPATITIS C Back to top

Laboratory workers are at risk of blood-borne infections such as hepatitis C virus (HCV),

HBV, and human immunodeficiency virus (HIV) infections. However, the safeguards

introduced to medical laboratories have decreased the risk to workers. According to the

Division of Health Care Quality Promotion, Centers for Disease Control and Prevention

(http://www.cdc.gov/hai), between 1978 and December 2001, only 16 clinical laboratory

workers acquired HIV occupationally; 17 other persons may have been infected in the

laboratory. Following a deep-tissue exposure injury (e.g., needlestick), it is recommended

that workers consider postexposure prophylaxis (35), even though this prophylaxis does not

always prevent HIV infection following an exposure (31).

There is less information on the prevalence of hepatitis C in health care workers, although it

is estimated by the National Center for Infectious Diseases (28) that after needlestick or

sharps exposure to HCV-positive blood, about 2 (1.8%) health care workers of 100 will

become infected with HCV (range, 0% to 10%). Following the introduction of the hepatitis B

vaccine in 1982, the incidence of HBV infection was reduced by over 95% (70).

While blood-borne infection information may be thought to be well established, recent

knowledge surveys of health care workers have demonstrated that regular education

sessions to update existing staff and inform new staff are required (67).

LABORATORY-ACQUIRED INFECTIONS AND EXTERNAL

QUALITY ASSESSMENT Back to top

Infections acquired in the clinical laboratory are not always associated with clinical samples.

Documented clusters of bacterial infections have been associated with samples sent to

laboratories for proficiency testing (8). Contamination of other samples by quality control

organisms has also been documented (23), although no in-laboratory infections resulted.

Regardless of the source, all viable microorganisms processed in the clinical laboratory must

be handled with full awareness of appropriate biosafety practices.

PRIONS Back to top

Samples from patients with Creutzfeldt-Jakob disease (CJD) may be submitted to the

laboratory for investigation. To date, there are no known cases of laboratory-acquired CJD,

and there is no evidence that laboratorians are at increased risk of developing CJD. With that

being said, the progressive deteriorating nature of CJD raises concerns for those handling

samples from patients with CJD, especially for samples of neurological origin (64). This

represents a special problem in the medical laboratory because of the difficulty in

inactivating the underlying prions.

Current precautions while handling tissue samples require glove use. All tissue samples must

be discarded as medical waste. No special precautions are required for disposal of body

fluids.

Equipment that has been exposed to CJD tissues should either be discarded or, if tolerant to

heat, autoclaved at 134°C for 18 min (prevacuum sterilizer) or at 121 to 132°C for 1 h

(gravity displacement sterilizer). Autoclaving in water may be more effective than

autoclaving in its absence (33). Equipment may also be soaked in 1 N NaOH for 1 h (33, 42).

Work surfaces should be cleaned with a 1:10 dilution of sodium hypochlorite.

Milder chemical treatments based upon combinations of enzymes, including proteinase K and

pronase, in conjunction with detergents such as alkaline cleaners or sodium dodecyl sulfate,

have been shown to experimentally reduce PrPSc material to levels below detection and to

prevent infectivity. The advantages of these methods are that they are described as being

inexpensive, noncorrosive, and nonhazardous to staff (33, 42).

SARS CORONAVIRUS INFECTION AND OTHER SEVERE

VIRAL RESPIRATORY INFECTIONS Back to top

The 2002 outbreak of SARS associated with a coronavirus reinforced international health

concerns about the hazards of aerosol spread of communicable viruses. While laboratory

workers were at risk (56), containment was readily addressable (4), and laboratory workers

were among those with the lowest rates of illness or serological conversion (56). However,

microbiology and accessioning laboratory workers receiving respiratory samples, especially

via vacuum tube delivery systems, were deemed to be at increased risk. Since that time, the

concerns for similar events occurring with influenza viruses, including H2N2 (17), H5N1 (30),

H7N7 (43), and novel H1N1 (35) viruses, have pointed out the potential gaps in biosafety

protection for laboratory workers. Laboratories equipped and designed to biosafety level 2

should use practices more consistent with those for biosafety level 3, which require that all

samples be opened and handled only in a biosafety cabinet (4). In addition, centrifugation of

samples should be performed only by using sealed safety buckets that are opened within a

cabinet. Finally, personal protective equipment, including M95 respirators, should be

considered for additional protection. Frequent hand washing should be required (35), using

either soap and running water or alcohol-based hand gels. While caution and reasonable

practices have been demonstrated to contain outbreaks, effective influenza immunization is

most likely required in conjunction for optimal protection.

SAFETY AND POINT-OF-CARE TESTING Back to top

Medical laboratories are responsible for all aspects of laboratory testing throughout the total

testing cycle, even when the testing is performed outside the laboratory itself. Increasingly,

medical laboratories are responsible for point-of-care testing, such as blood glucose

monitoring, coagulation, and oxygenation. Despite improvements in equipment and hygiene

protocols, cases of hepatitis B and C continue to be associated with point-of-care devices.

Prevention of transmission requires strict adherence to infection control protocols for

equipment cleaning. The international standard ISO 22870:2006 [lsqb]Point-of-Care Testing

(POCT)—Requirements for Quality and Competence[rsqb] (41d) provides guidance on quality

management for point-of-care testing.

TRANSPORTATION OF SAMPLES Back to top

Laboratories have a responsibility to prevent exposure of individuals to infectious agents in

laboratory samples to the extent that is possible. This responsibility includes samples being

transported to and from the laboratory. For local transport within a clinic or hospital, the

laboratory should ensure that leakproof containers are available, are transported in secure

outer packaging such as a sealable plastic bag, and preferably are emblazoned with the

international biohazard label. For transport outside the facility, especially by road, rail, ship,

or air, local and federal regulations apply. Even for short distances, it is appropriate that

samples be transported in secure firm outer containers with sufficient absorbent materials

inside, in case of a spill. In most jurisdictions, transport of samples with infectious agents by

postal services is prohibited.

Air transport is under the authority of federal regulations directed by the requirements of the

International Civil Aviation Organization, as adopted by the International Air Transport

Association. The International Civil Aviation Organization specifies packaging and labeling

requirements, including proper shipping name, appropriate United Nations number (for

samples known to contain infectious agents based on the source of the sample), and the

likely pathogens contained. Every laboratory that transports samples is required to have at

least one person certified as knowledgeable with respect to packaging and transport

requirements, including the completion of shipping documents.

For additional information, direct reference can be made to the International Civil Aviation

Organization’sTechnical Instructions for the Safe Transport of Dangerous Goods by Air (41a)

or to federal requirements (58).

POSTEXPOSURE MANAGEMENT FOR ACCIDENTS

INVOLVING INFECTIOUS AGENTS Back to top

It is beyond the scope of this chapter to address the specifics of medical management

following accidents that involve infectious agents. However, it is important that the following

steps always be undertaken or considered. Every accident or injury, including those that are

seemingly trivial (40), should be reported to the appropriate safety officer or supervisor.

Scratches and puncture wounds should be cleaned immediately. For some injuries, especially

those involving blood exposures, time may be a critical factor (16). If it is deemed

appropriate to seek medical attention, it is important to identify that the accident was

laboratory acquired. If the likely or probable agent is known, bringing the microorganism

MSDS can be helpful and can save time. In research or animal facilities, preparation of

information sheets on specific organisms and availability of standardized investigation and

treatment protocols in the event of an accident can be invaluable.

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