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Infection Control Chapter 10 Created by Jennifer Majeske, Mineral Area College
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Page 1: Chapter 10 Created by Jennifer Majeske, Mineral Area College.

Created by Jennifer Majeske, Mineral Area College

Infection Control

Chapter 10

Page 2: Chapter 10 Created by Jennifer Majeske, Mineral Area College.

Created by Jennifer Majeske, Mineral Area College

Explain the role of pathogenic organisms in causing

disease. Distinguish among bacteria, viruses, fungi, and

protozoa. Discuss the advantages and disadvantages of

various forms of sterilization. Identify common modes of contamination and

preventive measures that can be taken to reduce or eliminate these risks.

Discuss the guidelines set forth by the Centers for Disease Control and Prevention that address preventing the transmission of infectious agents in the hospital.

Learning Objectives

Page 3: Chapter 10 Created by Jennifer Majeske, Mineral Area College.

Created by Jennifer Majeske, Mineral Area College

Understand the distinction between hand-

washing and hand-hygiene practices and the importance of these practices in infection control.

Discuss the importance of vaccinations for healthcare workers.

Discuss the USP Chapter <797> guidelines for sterile compounding and aseptic technique.

Identify procedures to minimize airborne contamination during the compounding of sterile preparations.

Learning Objectives

Page 4: Chapter 10 Created by Jennifer Majeske, Mineral Area College.

Created by Jennifer Majeske, Mineral Area College

Contrast a manufactured sterile product with

expiration dating vs. a compounded sterile preparation with beyond-use dating according to USP Chapter <797> guidelines.

Apply contamination risk level designations and appropriate beyond-use dating for compounded sterile preparations.

Identify the role of the Infection Control Committee within a hospital.

List Universal Precautions that protect hospital employees.

Learning Objectives

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Created by Jennifer Majeske, Mineral Area College

Compounded sterile preparations (CSPs), or

medications that are created by mixing one or more sterile products using aseptic technique.

Microbiology – the study of microorganisms. General understanding of the germ theory of

disease; various sources of contamination; and the process of sterilization and aseptic technique, is important by pharmacy personnel.

Awareness of infection control procedures is critical during sterile compounding.

Introduction

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Created by Jennifer Majeske, Mineral Area College

The cause of illnesses – until most recently – were not

completely understood. What were diseases attributed to?

Seventeenth-Century Scientists: Anton van Leeuwenhoek made the first crude microscope; 1673, confirmed the existence of a microculture of organisms.

Microorganisms – “animalcules” (little animals). Robert Hooke, observed the walls of dead plant cells. Spontaneous generation – the belief that some

forms of life could arise spontaneously from matter. Francesco Redi, maggots could not spontaneously arise.

The Development of the Germ Theory of Disease

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Created by Jennifer Majeske, Mineral Area College

1798 Edward Jenner discovered the principle

of immunization against disease. Louis Pasteur was instrumental is proving the

connection between microorganisms and disease by demonstrating that the fermentation process is caused by the growth of microorganisms.

Pasteurization – a process to kill most bacteria and mold in milk.

Germ theory of disease – the idea that microorganisms cause diseases.

Important Discoveries of Jenner and Pasteur

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Created by Jennifer Majeske, Mineral Area College

Joseph Lister “Father of Modern Antisepsis”,

began soaking dressings in carbolic acid, to kill bacteria.

Lister later developed antiseptic methods in surgery, these are the basis of sterile technique; these techniques reduced postoperative infections and saved lives.

1876, German physician Robert Koch defined a series of steps known as Koch’s postulates.

These postulates could be used to prove that a certain disease was caused by a specific microorganism.

Medical Advances of Lister and Koch

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Created by Jennifer Majeske, Mineral Area College

Page 10: Chapter 10 Created by Jennifer Majeske, Mineral Area College.

Created by Jennifer Majeske, Mineral Area College

Bacterium: a small, single-celled microorganism. Bacteria exist in three main forms:

Spherical (cocci) Rod shaped (bacilli) spirochettes

Gram positive (blue or purple) Gram negative (red) Bacteria cause a variety of illnesses:

Food poisoning, strep throat, ear infections, rheumatic fever, meningitis, pneumonia, tuberculosis, and conjunctivitis

Bacteria

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Created by Jennifer Majeske, Mineral Area College

Virus: a small microorganism that consists of

little more than a bit of genetic material enclosed by a casing of protein.

Viruses need a living host in order to reproduce.

Viruses cause a variety of diseases: Colds, mumps, measles, chickenpox, influenza, hepatitis, and HIV

Viruses

Page 12: Chapter 10 Created by Jennifer Majeske, Mineral Area College.

Created by Jennifer Majeske, Mineral Area College

Fungus: a parasite on living organisms (by feeding

on dead organic material) that reproduces by means of spores.

Spores and some fungi are microscopic plants that can occur as mold, mildew, or mushrooms; they can also travel through the air.

Penicillin is the result of a mold source. Fungal infections include:

Athlete’s foot, ringworm, vaginal yeast infections, and serious systemic fungal infections

Fungi

Cryptococcosis

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Created by Jennifer Majeske, Mineral Area College

Protozoan – a microscopic organism made up of a single

cell or a group of more or less identical cells. Protozoa live in water or as parasites inside other creatures. Examples of protozoa:

Paramecia Amoebas

Illnesses caused by protozoa: Amoebic dysentery Malaria Sleeping sickness: http://

www.nlm.nih.gov/medlineplus/ency/article/001362.htm

Protozoa

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Created by Jennifer Majeske, Mineral Area College

Microorganisms can be harmless or beneficial

(nonpathogenic) or harmful (pathogenic). Nonpathogenic Microorganisms: Some

microorganisms perform essential functions. Yogurt

Pathogenic Microorganisms: lead to widespread illness and disease.

Functions of Microorganisms

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Created by Jennifer Majeske, Mineral Area College

Epidemics and Pandemics:

Epidemic – increased incidence of a particular disease in a given area or among a certain group of people over a specific period.

Pandemic – affects a sizable population of several countries (epidemic of world-wide proportions). See pg. 404 for notable pandemics

Current Antimicrobial Medications: Antibiotics, antivirals, and antifungals Microorganisms can adapt and become resistant Resistance is caused by over prescribing or

incorrect administration.

Functions of Microorganisms

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Created by Jennifer Majeske, Mineral Area College

Transmission of microbes can occur by touch,

air, and water. Touch: the most common method of

contamination and the easiest to prevent. Air: microorganisms are found in the air, dust

particles and moisture droplets. Water: even tap water is not completely free

of microorganisms; moisture droplets after a sneeze or a cough often contain harmful microbes.

Sources of Contamination

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Created by Jennifer Majeske, Mineral Area College

Establishment of sterile practices in the 19th century. Asepsis – the absence of pathogenic microorganisms. Sterility – the absence of all microorganisms, brought

about by sterilization – a process that destroys the microorganisms.

Methods of Sterilization: Heat Dry heat Mechanical Gas Chemical

Asepsis and Sterility

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Created by Jennifer Majeske, Mineral Area College

Heat is available, effective, economical and easily

controlled. Boiling kills vegetative forms, viruses, and fungi in

about 10 minutes; more time is required to kill other organisms like, fungus spores and hepatitis virus.

Autoclave - a device that generates heat and pressure to sterilize.

Heat sterilization is being used less because of space requirements, equipment expense, and personnel training.

Heat Sterilization

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Created by Jennifer Majeske, Mineral Area College

Dry heat, like direct flaming, destroys all

microorganisms. It is used for the disposal of contaminated

objects, incineration. Proper sterilization using hot, dry air must be

at a temperature of 170°C and maintained for approximately 2 hours.

Why do you think a higher temperature is required for dry heat?

Dry Heat Sterilization

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Created by Jennifer Majeske, Mineral Area College

Filtration is the means by which mechanical

sterilization is achieved; the passage of a liquid or gas through a screen-like material with pores small enough to block microorganisms.

This is used for the sterilization of heat-sensitive materials like: culture media, enzymes, vaccines, and antibiotic solutions.

0.22 micron filters are used for bacteria; 0.01 micron filters are used for viruses and some large proteins

Phlebitis – inflammation of the veins is reduced by the use of inline filters in IV administration sets.

Mechanical Sterilization

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Created by Jennifer Majeske, Mineral Area College

Gas sterilization, ethylene oxide, is used for objects

that are labile, or subject, to destruction by heat. Special equipment and aeration of materials is

required after application of the gas. The gas used is highly flammable and is used only

in large institutions. Some prepackaged IV fluids and bandages are

manufactured and sterilized in this manner. Ethylene oxide leaves only a slight, non-harmful

residue, which is detectable as an odor.

Gas Sterilization

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Created by Jennifer Majeske, Mineral Area College

Chemical sterilization involves the destruction

of microorganisms on inanimate objects by chemical means.

Chemicals rarely produce complete sterility, but can reduce microbial numbers to safe levels.

Disinfectant: a chemical applied to an object or topically to the body for sterilization purposes.

Topical disinfectants include: iodine, isopropyl alcohol (IPA) and bleach.

Chemical Sterilization

Page 23: Chapter 10 Created by Jennifer Majeske, Mineral Area College.

Created by Jennifer Majeske, Mineral Area College

Understanding disease transmission and

asepsis practices is necessary to infection control.

At the national level, the Centers for Disease Control and Prevention (CDC) and the United States Pharmacopeia (USP) set guidelines that must be followed by hospitals and healthcare workers.

At the local level, a hospital’s infection control committee develops hospital specific policies and procedures.

Organizations Overseeing Infection Control

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Created by Jennifer Majeske, Mineral Area College

Centers for Disease Control and Prevention

(CDC) - is a government agency the provides guidelines and recommendations on infection control.

The CDC publishes reports on the sensitivity and resistance of various bacteria, guidelines of drug choice, dosage, and duration of treatment for common infectious illnesses.

The CDC’s major focus is on the prevention of transmission of infectious agents in the hospital.

The CDC updates and publishes guidelines to protect the patient and the healthcare worker from infectious disease.

The Centers for Disease Control and Prevention

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Created by Jennifer Majeske, Mineral Area College

The guidelines are known as Universal Precautions. The CDC estimates that hospital patients acquire 1.7

million infectious disease during their hospital stays. Failure to train hospital employees or healthcare

personnel to follow proper infection control could produce a high incidence of HAIs (Healthcare-Associated Infections), or nosocomial infections.

Some of the infection control procedures outlined include: hand hygiene, protective clothing, and vaccinations of personnel.

The Centers for Disease Control and

Prevention

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Created by Jennifer Majeske, Mineral Area College

Simple hand washing and hand hygiene,

according to the CDC, are the single most important practices for minimizing touch contamination and reducing the transmission of infectious agents.

Hand washing – using plain or antiseptic soap and water.

Plain detergent soaps with minimal anti-microbial activity must be used for 20 to 30 seconds.

Adherence to proper hand-washing technique in the hospital remains less than 50%, according to the CDC.

Hand Washing

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Created by Jennifer Majeske, Mineral Area College

Hand hygiene - using special alcohol-based rinses, gels, or foams that do not require water.Alcohol based products are preferredbecause of their superior antimicrobial activity, shorter contact time, quick dryingeffect, minimal skin irritation, and convenience. Table 10.1 Hand Washing and Hand Hygiene Guidelineshttp://www.cdc.gov/cdctv/HandHygiene/

Hand Hygiene

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Created by Jennifer Majeske, Mineral Area College

PPE is critical to infection control in a facility,

protecting both healthcare workers and others from infectious diseases.

Gown or Apron: worn over the required uniform or scrubs with the opening in the back; ties should be secure.

Masks and Respirators: placed over the nose, mouth, and chin and secured to the back of the head using ties or elastic.

Goggles and Face Shields: positioned over the eyes or face and secured to the head with earpieces or elastic.

Personal Protective Equipment (PPE)

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Created by Jennifer Majeske, Mineral Area College

The CDC recommends that healthcare workers use

gloves, primarily to prevent the transmission of normal or pathogenic skin flora to patients.

Aseptic hand washing alone may not prevent the transmission of microorganisms if hands are heavily contaminated.

Gloves are made of latex or vinyl; both materials appear to offer comparable protection. Latex-free gloves should be available to those sensitive to latex.

Used gloves should be discarded in a designated area. Gloves should never be washed or reused.

Gloves

Page 30: Chapter 10 Created by Jennifer Majeske, Mineral Area College.

Created by Jennifer Majeske, Mineral Area College

More than 35,000 people die each year as a result of

flu complications; 200,000 are hospitalized. The CDC recommends if you are working in a

hospital setting that you receive an annual flu shot. Benefits of the Flu Vaccine: What are some of the

benefits associated with getting the flu vaccine? Administration of the Flu Vaccine: 63% of healthcare

workers get an annual flu shot; 60 to 70% effective. Administration of the Nasal Flu Vaccine: attenuated

virus – live, present in the nasal flu vaccine.

Vaccination

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Created by Jennifer Majeske, Mineral Area College

The United States Pharmacopeia (USP)

publishes guidelines on the preparation of sterile products with properly trained personnel and protective equipment.

2004, the USP developed the first official and enforceable requirements for sterile preparation compounding.

Guidelines were modified and updated in 2007 and approved in 2008.

USP Chapter <797> - focuses on sterility and stability of a compounded sterile preparation.

USP Chapter 797 Standards

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Created by Jennifer Majeske, Mineral Area College

Compounded sterile preparation (CSP) - a

sterile product that is prepared outside of the pharmaceutical manufacturer’s facility.

Sterility refers to the CSP being free of microorganisms.

Stability - refers to chemical and physical characteristics, such as pH, degradation, formation of precipitates, or unexpected color changes.

USP Chapter 797 Standards

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Created by Jennifer Majeske, Mineral Area College

Requirements for sterile compounds differ

from nonsterile compounds: Working in a defined clean-room environment Additional requirements for personnel garbing Personnel testing and training Environmental quality specifications Disinfection of gloves and surfaces

USP Chapter 797 Standards

Page 34: Chapter 10 Created by Jennifer Majeske, Mineral Area College.

Created by Jennifer Majeske, Mineral Area College

797 standards apply to all personnel involved in

the preparation, storage and transportation of CSP’s.

CSP’s include: drugs, biologicals, diagnostics, nutrients, and radioactive pharmaceuticals

797 standards also apply to all practice settings: Compounding Nuclear Home health Long-term healthcare pharmacy Clinics and physician’s offices

USP Chapter 797 Standards

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Created by Jennifer Majeske, Mineral Area College

Compounding facilities are designed to

minimize airborne contamination. High-efficiency particulate airflow (HEPA)

filter – minimizes airborne contamination. International Organization for

Standardization (ISO) - define the amount of particulate matter allowed in room air where CSPs are prepared.

The lower the ISO number, the less particulate matter is present in the air.

Sterile Compounding Facility

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Created by Jennifer Majeske, Mineral Area College

Figure 10.2 pg. 413 Sterile Compounding IV Room

Layout, is divided into two main areas: the anteroom and the clean room.

Personnel are responsible for maintaining the overall cleanliness of these areas.

Anteroom – where personnel perform aseptic hand washing and garbing procedures, gather supplies and check expiration dates, etc.; ISO Class 8.

Clean room – IV room or buffer area, the inner most room within the pharmacy; houses the laminar airflow hoods; ISO Class 7.

Sterile Compounding Areas

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Created by Jennifer Majeske, Mineral Area College

Only furniture, equipment and supplies

necessary for the preparation of CSPs should be allowed in defined compounding areas; long-term storage is not permitted.

Laminar Airflow Hoods: HEPA-filtered air to create an ISO Class 5 environment in the direct compounding area (DCA) of the hood. Horizontal LAFW (positive-pressure) Vertical LAFW (negative-pressure)

Compounding Equipment and Supplies

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Created by Jennifer Majeske, Mineral Area College

Air flows from the back of the hood, across the

work surface, and out into the room. As air passes through the hood it is prefiltered

by a high-efficiency particulate air (HEPA) filter.

The HEPA filter removes 99.97% of all particles 0.5 micron or larger.

When working in the hood it is necessary to work at least 6 inches inside the hood.

Horizontal LAFW

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Created by Jennifer Majeske, Mineral Area College

Placement of supplies should not impede the

sterile airflow that moves across the work surface and around and over supplies.

Horizontal LAFW

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Created by Jennifer Majeske, Mineral Area College

Vertical laminar airflow workbench (LAFW) is

used for the preparation of hazardous CSPs. Air flows from the top of the hood down, through a

pre-filter and a HEPA filter onto the work area. The air is then recirculated through another HEPA

filter, and vented 100% to outside air minimize human exposure.

When working in and cleaning a vertical LAFW a technician should wear: Eye protection, a mask, and proper apparel – gown,

gloves, and hair covering

Vertical LAFW

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Created by Jennifer Majeske, Mineral Area College

Horizontal and vertical laminar airflow hoods are regularly

cleaned according to USP Chapter <797> guidelines. The hood must be cleaned at the beginning of each shift,

before each batch compounding session, and every 30 minutes during continuous sterile compounding.

The hood should run for at least 30 minutes after being turned off, before being used to prepare CSPs.

The entire LAFW should be cleaned first with sterile water and then with 70% isopropyl alcohol.

During cleaning the blower should remain on, and the technician should be in full protective garb.

Cleaning the Horizontal LAFW

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Created by Jennifer Majeske, Mineral Area College

Start with the hood’s hang bar and hooks;

hood’s ceiling – overlapping, side-to-side strokes; both sides of the hood – overlapping, down-and-up strokes, from the innermost part of the hood to the exterior ; and the work surface.

Page 43: Chapter 10 Created by Jennifer Majeske, Mineral Area College.

Created by Jennifer Majeske, Mineral Area College

Clean the entire hood with sterile water, then by 70%

isopropyl alcohol; the vertical hood must be allowed to run continuously during cleaning and decontamination.

Biological safety cabinet (BSC) is one of the most commonly used vertical hoods.

The HEPA-filter is located in the ceiling of the hood rather than the back, with the air flow downward toward the hood’s work surface, changing the cleaning order as well as direction of cleaning strokes.

Prefilter and HEPA Filter Maintenance: the prefilter must be replaced every 30 days; the HEPA filter must be recertified every 6 months.

Cleaning the Vertical LAFW

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Created by Jennifer Majeske, Mineral Area College

Clean room access is limited to those personnel

trained to prepare CSPs. No cosmetics, perfume, hair spray, artificial nails,

or nail polish can be worn while performing sterile compounding procedures.

Individuals with certain medical conditions (respiratory infections, weeping sores, rashes, and sunburn) are banned from the sterile compounding area.

No food or beverages in the anteroom or clean room; no horseplay and no gum.

Sterile Compounding Personnel

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Created by Jennifer Majeske, Mineral Area College

Strict sequence, moving from the most dirtiest

(shoe covers on shoes) to the cleanest item (donning sterile gloves).

Personnel must remove all outwear (coats, sweaters, hats, etc.), prior to entering the ante area.

Shoe Covers: placed over the technician’s closed-toed shoes to keep dirt and other substances from contaminating the floor of the clean room.

Garbing of Sterile Compounding Personnel

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Created by Jennifer Majeske, Mineral Area College

Hair Cover: secured to the head; avoids

contamination of the hood or CSP. Face Mask: covers nose and mouth during compounding; catches bacteria contained in the liquid droplets and aerosols that emanate from the nose and mouth.

Garbing of Sterile Compounding Personnel

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Created by Jennifer Majeske, Mineral Area College

Aseptic hand washing must be performed

using an acceptable cleansing agent such as chlorhexidine gluconate.

Aseptic hand washing procedures are rigorous and require personnel to follow a specific sequence; the sequence lasts 2-4 minutes.

Gowning and Gloving: last two procedures before beginning sterile compounding.

Gowning: sterile, disposable, nonshedding gown.

Aseptic Hand Washing

Page 48: Chapter 10 Created by Jennifer Majeske, Mineral Area College.

Created by Jennifer Majeske, Mineral Area College

Gowning and Gloving: last two procedures

before beginning sterile compounding. Gowning: sterile, disposable, nonshedding

gown. Gloving: sterile, powder-free gloves; disinfect the gloves with 70% isopropyl alcohol every time gloves touch a nonsterile surface.

Aseptic Hand Washing

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Created by Jennifer Majeske, Mineral Area College

Specific situations regarding garbing, address

by USP Chapter <797> guidelines. Repeating the entire garbing and hand-

washing process after leaving the clean room, but the same gown can be worn again upon return to the clean room.

Double gloving – wearing a second pair of gloves, is done when a technician is working with hazardous drugs.

Other Garbing Regulations

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Created by Jennifer Majeske, Mineral Area College

Risk levels are assigned based on the probability of

microbial, chemical, or physical contamination. Expiration date: shelf life. Beyond-use date is for a

compounded product. Low-risk CSPs: sterile products that have been manipulated

using aseptic technique for a single-volume transfer. Medium-risk CSPs: multiple sterile products combined

using automated devices. High-risk CSPs: products that have been compounded from

nonsterile ingredients and sterile products w/o preservatives.

Immediate-use CSPs: any CSPs made outside of a Class 5 ISO.

Contamination Risk Levels

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Created by Jennifer Majeske, Mineral Area College

Technicians working in the hospital pharmacy

IV are hold important and responsible position. Skills and experience are necessary to

practice in a clean-room environment. Written tests and skill assessments must be

passed to meet USP guidelines and Joint Commission accreditation standards.

Additional certifications and experience for technicians if often rewarded in salary.

Training Required to Work with CSPs

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Created by Jennifer Majeske, Mineral Area College

Infection control is the responsibility of all

healthcare workers. Infection Control Committee (ICC) – is

responsible for implementing CDC and USP guidelines and oversees training of all healthcare workers.

The ICC monitors the incidence of HAIs and the proper use of antibiotics within the hospital.

The ICC plays a major role in ensuring that the hospital is in compliance with the Joint Commission.

Generally made up of physicians, nursing staff, infection control practitioners, and many others.

Infection Control Committee

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Created by Jennifer Majeske, Mineral Area College

The primary role of the ICC is to prevent, identify,

and control healthcare associated infections (HAIs).

Nosocomial infection: healthcare-associated infection occurs when bacteria found in the hospital from any sources can cause a patient to develop an infectious disease.

2 million patients develop new infections in the hospital each year, according to the CDC.

HAIs result in additional costs from extended hospital stays to antibiotics.

Role and Responsibilities of the ICC

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Created by Jennifer Majeske, Mineral Area College

Infection control policy include:

Surveillance of nosocomial infections, antibiotic and other product evaluations, investigation of infection outbreaks and infection clusters, development of infection control procedures, patient education

The committee may evaluate which disinfectant should be used.

Educational programs are conducted for hospital employees including proper handling and disposal of medical waste, and discarding of sharps into a special container.

Roles and Responsibilities of the ICC

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Created by Jennifer Majeske, Mineral Area College

Due to exposure to blood and bodily fluids the

ICC oversees the implementation and training of personnel in universal precautions.

Universal precautions: procedures to prevent such infection as a result of exposure to blood or other bodily fluids.

Table 10.4 Universal Precautions Following procedures outlined in this chapter

protects personnel and patients from unnecessary risk of infection.

Implementation of Universal Precautions

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Created by Jennifer Majeske, Mineral Area College

This workforce solution was funded by a grant awarded by the U.S. Department of Labor’s Employment and Training Administration. The solution was created by the grantee and does not necessarily reflect the official position of the U.S. Department of Labor. The Department of Labor makes not guarantees, warranties, or assurances of any kind, express or implied, with respect to such information, including any information on linked sites and including, but not limited to, accuracy of the information or tis completeness, timeliness, usefulness, adequacy, continued availability, or ownership.

This work by Mineral Area College is licensed under the Creative Commons Attribution 4.0 International License.


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