Influenza: Seasonal Flu 2016-2017
Symptoms, Treatment, and Prevention
Online Continuing Education Course
Transmission, symptoms, diagnosis, and treatment of seasonal flu; 2016-2017 vaccines; preventing the spread of influenza viruses. Applicable for nursing, occupational and physical therapy, and EMS personnel.
Course Price: $18.00
Contact Hours: 2
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Influenza: Seasonal Flu 2016–2017
Symptoms, Treatment, and Prevention
Copyright © 2016 Wild Iris Medical Education, Inc. All Rights Reserved.
LEARNING OUTCOME AND OBJECTIVES: Upon completion of this course, you will be able to demonstrate an understanding of the symptoms, treatment, and prevention of seasonal influenza for 2016–17. Learning objectives for this course include:
- Discuss key concepts related to the transmission, symptoms, diagnosis, and treatment of influenza (flu).
- Explain the rationale for vaccination and other preventative measures against seasonal flu, based on the chain of infection.
TABLE OF CONTENTS
Influenza is a highly infectious viral illness. The disease has sickened and killed millions of people in local epidemics and global pandemics. The first documented pandemic that clearly fits the description of influenza was in 1580. The most lethal pandemic of record began in 1918, just after World War I, when an estimated 21 million people died from what was called the “Spanish” flu (CDC, 2015a).
Smith, Andrewes, and Laidlaw isolated influenza A virus in ferrets in 1933, and Francis isolated influenza B virus in 1936. In 1936, Burnet showed that the virus lost virulence when it was cultured in fertilized hens’ eggs. This led to the study of the characteristics of the virus and the development of inactivated vaccines. The protective efficacy of these inactivated vaccines was determined in the 1950s.
Since then, vaccination has limited the infection’s spread but has not prevented pandemics of the disease (CDC, 2015a). In 1957, the Asian flu swept around the world, killing 1 to 1.5 million people, and in 1968, a pandemic called Hong Kong flu killed nearly a million more (Kilbourne, 2006). Then, in 2009, a pandemic called swine flu, caused by a virus found in pigs, swept around the world (WHO, 2016a).
All influenza viruses belong to the Orthomyxoviridae family of RNA virus, including types A, B, C, Isa virus, thogotovirus, and others.
Type A viruses are the most virulent of influenza types, producing the most severe symptoms. Influenza A types contain two surface glycoprotein antigens, called subtypes hemagglutinin (H) and neuraminidase (N). The H antigen enables the virus to enter cells, while the N antigen facilitates cell-to-cell transmission. There are 18 different hemagglutinin subtypes and 11 different neuraminidase subtypes (H1 through H18 and N1 through N11, respectively).
Type A viruses can be further broken down into different strains that infect humans, other mammals, and birds and are the cause of all known pandemics, including:
- H1N1: Spanish flu of 1918 and swine flu of 2009
- H2N2: Asian flu of 1957
- H3N2: Hong Kong flu of 1968
- H5N1: Avian flu pandemic threat of 2008
Type B viruses infect humans and seals. They are not divided into subtypes but can be broken down into lineages and strains. Currently influenza B viruses belong to one of two lineages:
Type C viruses have one serotype, infect humans and pigs, and are relatively uncommon.
Isa virus infects fish and causes infectious anemia in salmon.
Thogotovirus is found in ticks, mosquitoes, and mammals; human epidemics from them are unknown.
Additional types of influenza viruses are being discovered, but to date, types A and B are known to pose the greatest threat to human health. The type A H1N1 virus that caused the 2009 swine flu pandemic is now a regular human flu virus and continues to circulate seasonally worldwide (CDC, 2014a).
When viruses laden with antigens infect a human or an animal, the body recognizes them as foreign substances and reacts in what is called an immune response. This response creates antibodies against the foreign substance. After recovery from the infection, the human or animal is usually immune to getting the same viral disease for years (perhaps a lifetime). Influenza vaccines help develop immunity by imitating an infection and causing the immune response that protects against the virus in the future (CDC, 2014b).
Antigen Drift and Shift
Influenza viruses change constantly. They do this in two ways: antigenic drift and antigenic shift.
Antigenic drift is caused by a slow accumulation of many small mutations that happen in both influenza A and B viruses. These mutations occur within both hemagglutinin (H) and neuraminidase (N) genes. When this happens, antibodies may only partially recognize the resultant viruses or may not recognize them at all. Thus, when an antigen drift occurs, the current vaccine may not provide protection against disease. This is the reason why influenza vaccines must be updated annually.
Antigenic shift is an abrupt, major change in the influenza viruses, resulting in new H and/or N proteins, usually only occurring in influenza A viruses. As a result, a new vaccine must be made to combat the altered virus. For this reason, people must be vaccinated anew to be protected from the altered virus of seasonal influenza (CDC, 2014c).
|ANTIGENIC DRIFT||ANTIGENIC SHIFT|
Examples of influenza viruses with pandemic potential include avian influenza A H5, A H7, and A H9. These are nonhuman viruses (i.e., they are novel among humans and circulate in birds in parts of the world), so there is little to no immunity against these viruses among people. Human infections with these viruses have occurred rarely, but if either of these viruses was to change in such a way that it was able to infect humans easily and spread easily from person to person, an influenza pandemic could result.
Although avian influenza A viruses usually do not infect humans, rare cases of human infection with these viruses have been reported. Most human infections with avian influenza A viruses have occurred following direct or close contact with infected poultry.
- Avian A H5 influenza viruses have occurred in 16 countries, with a 60% mortality worldwide due to severe pneumonia.
- Avian A H7 influenza high pathogenic subtypes viruses have caused mild to severe illness, but in 2013 a new subtype was reported in China causing severe respiratory illness and death.
- Avian A H9 influenza viruses cause sporadic infections resulting in mild upper respiratory illness.
The spread of avian influenza A viruses from one ill person to another has been reported very rarely. However, because of the possibility that avian influenza A viruses could change and gain the ability to spread easily between people, monitoring for human infection and person-to-person transmission is extremely important for public health.
Seasonal influenza vaccination will not prevent infection with avian influenza A viruses but can reduce the risk of infection with both human and avian influenza A viruses. It is also possible to make a vaccine that can protect people against avian influenza viruses. For example, the United States government maintains a stockpile of vaccine to protect against avian influenza A H5N1.
Source: CDC, 2015b.
Because viruses change constantly, the World Health Organization (WHO) monitors the changes globally each season. The data obtained is then used to predict the strain that will be most prevalent during the next flu season and to publish vaccine recommendations to prevent what is called seasonal influenza (WHO, 2016b).
In 2016 a new strategy was developed that can predict flu mutations before they occur in nature by simulating the changes in a laboratory. This new laboratory-based method of predicting how current viral strains of influenza will mutate can also be used to help select the strains to be included in the next seasonal flu vaccine (NIAID, 2016).
The most common way influenza viruses spread from person to person is by droplet infection. Infected people exhale, cough, or sneeze, and virus-containing droplets fly through the air into the nose and throat of others or onto some intermediate surface such as a doorknob. When other people touch a contaminated surface, viruses may stick to their fingers. When they touch the mucous membranes of their body, they inoculate themselves with the virus. Studies have shown that human influenza viruses generally can survive on surfaces for between 2 to 8 hours (CDC, 2016a).
According to the CDC, sick adults are able to infect others beginning 1 day before symptoms appear and up to 5 to 7 days after they become ill. Sick children may be able to infect others beginning 1 day before symptoms appear and for more than 7 days after they become ill.
Symptoms develop 1 to 4 days after the virus enters the body. That means people may be able to pass on the flu virus to others even before they know they are sick. Any individual who is infected with viruses can infect others whether they show symptoms or not (CDC, 2014d).
Anyone can be infected with the flu virus, but the disease is more severe and the consequences more critical for some people than others. The most vulnerable are:
- Children under 5 years of age, especially those younger than 2 years of age
- Adults 65 years of age and older
- Pregnant women and women up to two weeks postpartum
- Residents of nursing homes and other long-term care facilities
- American Indians and Alaskan Natives
American Indians and Alaska Natives are more likely to be hospitalized from the flu than the general U.S. population. Experts are not sure exactly why, but reasons that these populations are at high risk of flu complications could include social and economic factors that often result in reduced access to healthcare and crowded living conditions (CDC, 2015c).
In addition, influenza can make chronic health problems worse. For example, individuals with asthma may suffer asthma attacks, and people with chronic congestive heart failure may experience an accumulation of fluid in the lungs, abdominal organs, and peripheral tissue. Generally speaking, people with the following medical conditions are more vulnerable to serious influenza-related complications:
- Neurological and neurodevelopmental conditions, including disorders of the brain, spinal cord, peripheral nerve, and muscles
- Chronic lung diseases such as chronic obstructive pulmonary disease and cystic fibrosis
- Heart diseases such as congestive heart failure, congenital heart disease, and coronary artery disease
- Blood disorders such as sickle cell disease
- Endocrine disorders such as diabetes
- Metabolic disorders such as inherited metabolic and mitochondrial disorders
- Weakened immune system due to disease or medication (such as HIV/AIDS or those on chronic steroids)
- Kidney disorders
- Liver disorders
- Inherited metabolic disorders and mitochondrial disorders
- Weakened immune system due to disease or medication (HIV, AIDS, cancer, steroids)
- Morbid obesity (body mass index >40) (found to be a risk factor, independent from other chronic illnesses, resulting in greater hospitalization and death during the H1N1 pandemic)
- Any condition in children younger than 19 years of age that requires long-term aspirin therapy (related to Reye’s syndrome, see below)
Symptoms and Severity
Influenza is a highly contagious infection of the respiratory tract. The signs and symptoms of influenza can vary by age, immune status, and presence of underlying medical conditions. It should not be confused with a gastrointestinal illness sometimes referred to as the “stomach flu.” Uncomplicated influenza can cause mild to severe illness and may include any or all of these signs and symptoms:
- Fever (usually high, however, not everyone with the flu has a fever, especially elderly persons)
- Dry cough
- Sore throat
- Runny or stuffy nose
- Muscle or body aches
- Conjunctivitis, rhinitis, and gastrointestinal symptoms (more common in infants and young children than adults)
(CDC, 2016c; Brook, 2016)
The indicators of influenza are referred to as “flu-like symptoms.” In the early stages of an infection, it may be difficult to distinguish between a common cold and influenza. However, the symptoms of flu are more severe and last longer than the common cold. A comparison of the usual symptoms of influenza and the common cold are listed below.
|Source: WDHS, 2016.|
|Fever||Characteristic, high (100 °F–102 °F), lasts three to four days||Rare|
|Headache||Sudden onset, may be severe||Rare, usually mild|
|Muscle aches||Usual, often severe||Mild|
|Fatigue||Often extreme, may last 2 to 3 weeks||Quite mild|
|Chills||In about 50% of cases||Not common|
|Rhinitis and runny nose||Sometimes||Common|
|Sore throat||May occur||Common|
|Nausea, vomiting, diarrhea||Not usual; most often in children||Unusual|
|Cough||Dry cough (no phlegm) that may be severe; may last several weeks||Common, generally mild to moderate, usually produces phlegm|
The diagnosis of influenza is based on presenting symptoms and viral tests. However, most individuals with flu symptoms do not require special testing because test results usually do not change their treatment. The CDC offers a guide for practitioners in considering influenza virus diagnostic tests for individual patients when influenza viruses are circulating in the community.
GUIDE FOR CONSIDERING INFLUENZA VIRUS DIAGNOSTIC TESTING
Source: CDC, 2016d.
There are a number of different tests used in diagnosing influenza. All can be obtained from a mucus specimen collected from the back of the throat or nose by a healthcare provider (see “How to Obtain a Nasopharyngeal Specimen” below).
Rapid influenza diagnostic tests (RIDT) for antigen detection yield results in 15 minutes or less and display the results as “positive” or “negative.” However, these results are not foolproof and may give a false negative when the patient is actually infected or a false positive when the patient is not infected with influenza viruses. This test can help differentiate influenza from other viral and bacterial infections with similar symptoms. It is best used within 48 hours of symptom onset.
These tests are used to detect influenza virus as the cause of respiratory infections, and public health authorities should be notified promptly of any suspected outbreaks, especially in institutions such as nursing homes, hospitals, schools, etc. Respiratory specimens should then be collected for ill persons and sent to a public health laboratory for more accurate influenza testing.
Viral tissue cell culture of a mucus specimen is the “gold standard” for identifying which influenza viruses and which strains of virus are present. However, traditional viral cultures can take up to 10 days for results.
Rapid cell culture (shell vials, cell mixtures) yields live virus and takes 1 to 3 days.
Reverse transcription-polymerase chain reaction (RT-PCR) is a molecular assay that can identify the presence of influenza viral RNA or nucleic acid in respiratory secretions. It is used for hospitalized patients with suspected influenza and pneumonia if an upper respiratory tract specimen is negative and if positive testing would result in a change in clinical management. It is particularly useful in identifying influenza virus infection as a cause of respiratory outbreaks in institutions and in detecting novel influenza A strains. Results are generally available in 1 to 6 hours.
Immunofluorescence—direct (DFA) or indirect fluorescent-antibody (IFA) staining—is a type of antigen detection with results in 1 to 4 hours (AACC, 2016).
Rapid molecular assay is a new type of molecular influenza diagnostic test for upper respiratory tract specimens and takes approximately 20 minutes (CDC, 2016e; CDC, 2016f).
HOW TO OBTAIN A NASOPHARYNGEAL SPECIMEN
- Explain the procedure to the patient in order to obtain his or her cooperation.
- Ask the patient to blow his or her nose just prior to specimen collection. Provide tissues and a place to dispose of the contaminated tissues. Then, ask the patient to wash or sanitize his or her hands with alcohol wipes.
- Gather equipment: appropriate swab; transport media; and personal protective equipment (PPE), including gloves, gown, respiratory, and eye protection as prescribed by public health officials. Ideally, use a swab with a synthetic tip such as nylon. Specimen collection vials should contain 1 ml to 3 ml of viral transport medium containing protein stabilizer, antibiotics to discourage bacterial and fungal growth, and buffer solution.
- Wash or sanitize your hands and put on PPE.
- Tilt patient’s head back 70 degrees.
- Insert swab into nostril. (Swab should reach depth equal to the distance from nostrils to outer opening of the ear.) Leave swab in place for several seconds to absorb secretions.
- Slowly remove swab while rotating it. (Swab nostrils with same swab.)
- Place tip of swab into sterile viral transport media tube and snap/cut off the applicator stick.
Proper technique for obtaining a nasopharyngeal specimen. (Source: CDC, n.d.)
Comfort and Care
People young and old who are infected with the virulent viruses of influenza can be very ill. Such seriously ill people need rest, comfort, sleep, and extra fluids. They may benefit from analgesics and antipyretic medications such as ibuprofen (Advil) and acetaminophen (Tylenol). In spite of the misery for the first few days, most children and adults gradually recover in one to two weeks without complications or antiviral medications.
Children and adolescents under 18 years of age who are experiencing influenza symptoms should not be given any medication containing salicylates, such as acetylsalicylic acid (aspirin), because it has been linked with the risk of Reye’s syndrome, a rare, but potentially fatal disease (Mayo Clinic, 2015).
Antiviral medications can be used to treat or to prevent influenza. They can shorten the duration of fever and illness, reduce the risk of complications from influenza, and shorten the duration of hospitalization. Antiviral medications are approximately 70% to 90% effective in preventing influenza. The CDC does not recommend widespread or routine use of antiviral medications for chemoprophylaxis so as to limit the possibilities that antiviral-resistant viruses could emerge (2016g).
PERSONS RECOMMENDED FOR MEDICATION TREATMENT
The CDC (2016h) recommends these drugs be given as early as possible to any patient who has confirmed or suspected influenza and:
- Is hospitalized
- Has severe, complicated, or progressive illness
- Is at higher risk for influenza complications (as listed earlier in this course), including:
- Children younger than 2 years of age
- Adults 65 years and older
- Women who are pregnant or postpartum within 2 weeks of delivery
- Children and adolescents younger than 19 years who are receiving long-term aspirin therapy
- People with certain chronic medical conditions, including chronic pulmonary, cardiovascular, renal, hepatic, hematological, and metabolic disorders, or neurologic and neurodevelopment conditions
- People with immunosuppression, including those caused by medications or by HIV infection
- American Indians/Alaska Natives
- Persons who are morbidly obese (body mass index ≥40)
- Residents of nursing homes and other chronic care facilities
Although all children younger than 5 years are considered at higher risk for complications from influenza, the highest risk is for those younger than 2 years, with the highest hospitalization and death rates among infants younger than 6 months. Because many children with mild febrile respiratory illness might have other viral infections (e.g., respiratory syncytial virus), knowledge of other respiratory viruses as well as influenza virus strains circulating in the community is important for treatment decisions (CDC, 2016g).
RECOMMENDED ANTIVIRAL DRUGS
Antiviral drugs approved by the U. S. Food and Drug Administration (FDA) and recommended by the CDC for use during the 2016–17 influenza season are:
- Oral oseltamivir (Tamiflu): Oseltamivir is approved both to prevent flu (in people 3 months of age and older) and treat flu (in people of any age). The most common side effects are nausea and vomiting. The FDA requires that the package warn that people with the flu, especially children, may be at an increased risk of confusion and self-injury after taking the drug. Therefore, recipients should be monitored closely for signs of unusual behavior.
- Inhaled zanamivir (Relenza): Zanamivir is administered to the respiratory tract via an oral disk inhaler device. It is approved to treat flu in people 7 years of age and older and for prevention in people 5 years of age and older. Allergic reactions include oropharyngeal or facial edema. Common side effects are diarrhea, nausea, and sinusitis. It is contraindicated for those with underlying respiratory disease such as asthma or COPD.
- Intravenous peramivir (Rapivab): Peramivir may be used for treatment in people 18 years of age and older. It is not recommended for chemoprophylaxis. Side effects could include diarrhea and put patients at an increased risk for confusion and self-injury, as with oseltamivir.
Antiviral drugs work best when started within 48 hours of the onset of symptoms (without waiting for laboratory confirmation of the disease). Oseltamivir and zanamivir should be continued for at least 5 days. Recommendation for chemoprophylaxis is 7 days from last known exposure. Duration of treatment with intravenous peramivir is 1 day. Hospitalized patients may benefit from treatment even if the drug is started more than 48 hours after symptoms begin and treatment is continued for a minimum of five days (CDC, 2016g).
PREVENTION AND VACCINATION
The Chain of Infection
The process of transmission of an infectious agent such as the influenza virus can be best explained by the epidemiologic model called the chain of infection. An infectious disease results from specific interactions between the organism, host, and environment. Transmission occurs when the infectious organism leaves the reservoir or host through a portal of exit, travels by some mode of transmission, and enters through a portal of entry to infect another susceptible host (CDC, 2012).
Chain of infection. (Source: Wild Iris Medical Education.)
- A reservoir of an infectious agent is the habitat where the agent normally lives and grows. Reservoirs may be humans, animals, or the environment.
- The portal of exit is the path by which the infectious agent leaves its host (e.g., respiratory tract).
- Means of transmission is the mode in which the infectious agent is transmitted from its natural reservoir to a susceptible host (e.g., touching a doorknob that contains infectious particles or droplet spread). Transmission can occur in a mode that is direct or indirect.
- The portal of entry refers to the way in which the infectious agent enters the host (e.g., through one’s nose into the respiratory tract when breathing in airborne particles). The portal of entry must provide access to tissues in a way that allows the infectious agent to multiply and thrive.
- The final link is the vulnerable host. Susceptibility of a host depends on many factors, including immunity and the individual’s ability to resist infection (CDC, 2012).
By breaking any link of the chain of infection, healthcare professionals can prevent the occurrence of new infection. Infection prevention measures are designed to break the links and thereby prevent new infections. The chain of infection is the foundation of infection prevention.
|Link||Influenza Implications||Healthcare Provider Actions|
|Organism||Present in environment during flu season||Be aware of current strains and case reporting requirements|
|Reservoir||Potentially everyone, some higher risk||Promote vaccinations|
|Portal of Exit||Droplets||Teach/reinforce sneeze/cough etiquette and correct use/disposal of tissues|
|Transmission||Organism can remain active on environmental surfaces||Teach disinfection techniques|
|Portal of Entry||Nose/mouth||Teach/reinforce handwashing, not touching eyes/face, wearing masks|
|Vulnerable Hosts||Everyone; some people at greater risk||Promote vaccinations among high-risk groups|
Flu Prevention Measures
Because influenza produces such serious symptoms, the CDC issues prevention recommendations to the public:
- Take time to get flu vaccinations.
- Take everyday preventative actions:
- Try to avoid close contact with sick people.
- While sick with the flu, limit contact with others as much as possible to keep from infecting them.
- When sick with flu-like illness, stay home for at least 24 hours after your fever is gone except to get medical care or for other necessities. (Your fever should be gone for 24 hours without the use of a fever-reducing medicine.)
- Cover your nose and mouth with a tissue when you cough or sneeze. Throw the tissue in the trash after you use it.
- Wash your hands often with soap and water. If soap and water are not available, use an alcohol-based hand rub.
- Avoid touching your eyes, nose, and mouth. Germs spread this way.
- Clean and disinfect surfaces and objects that may be contaminated with germs like the flu.
- Take flu antiviral drugs if recommended by a primary care provider.
- If an outbreak of flu occurs in your area, follow the advice given by public health officials. Such information may include how to increase distance between people and other measures.
FACEMASKS AND FLU PREVENTION
Although there is no proof that facemasks prevent transmission of the influenza virus, the CDC recommends the use of facemasks in the following situations:
- Healthcare personnel should don a facemask when entering the room of a patient with suspected or confirmed influenza.
- Patients with suspected influenza should be provided with a facemask when entering a healthcare facility.
- Patients with flu symptoms should be instructed to wear a facemask when leaving home.
- Patients under droplet precautions should wear a facemask when movement or transport outside of the room is necessary.
Source: CDC, 2016i.
Routine cleaning and disinfection strategies can also help prevent the spread of influenza. Management of laundry, utensils, and medical waste should be performed in accordance with established procedures.
John Smith, a 57-year-old man with a history of asthma, had been experiencing flu-like symptoms for three days. He was running a fever and, despite using his inhaler more frequently, found himself increasingly short of breath. At the urging of his wife, he went to the emergency department (ED) to be checked.
The ED intake staff noticed that Mr. Smith was frequently coughing, so they responded per facility policy by offering him a facemask to wear while he sat in the waiting room. As is consistent with their usual practice, the staff remembered to perform frequent hand hygiene. A few minutes later he was brought into triage, where the nurse confirmed that his symptoms were consistent with a contagious phase of influenza.
During triage, the nurse allowed Mr. Smith to remove his facemask for his comfort but donned a facemask herself to minimize the risk that she might become infected and transmit the virus to her family or other patients who had not yet been vaccinated. After sending the patient to the ED, the nurse remembered to clean all surfaces near the patient in the triage room, including the doorknobs, with an alcohol-based wipe prior to the next patient’s arrival.
During further diagnostic testing, the ED team continued the practice established by the triage nurse of wearing facemasks when they were within three feet of the patient while allowing him the comfort of not wearing a facemask.
Mr. Smith was admitted to the hospital with a diagnosis of left lower lobe pneumonia. On the advice of the infection prevention nurse, he was presumed to be infectious and was asked to wear a facemask when out of his room or being transported, while healthcare workers and visitors donned facemasks when they expected to come within three feet of him.
The infection prevention nurse explained to Mr. Smith and his family that, although there is no definitive evidence that facemasks decrease the spread of the influenza virus, it is still recommended to use facemasks as a prudent measure to decrease the spread of the virus.
Everyone 6 months of age and older should get vaccinated against the flu except for a few select individuals (see below). Vaccination is especially important for vulnerable individuals with chronic medical conditions, healthcare workers, and others who live with or care for high-risk people. Those who care for children younger than 6 months should be vaccinated (Grohskopf et al., 2016).
Due to their immature immune response systems, children 6 months to 8 years old who are receiving an influenza vaccine for the first time require an additional dose. An optimal immune response will be initiated by administering a second dose a minimum of four weeks after the first dose. For 2016–17, the Advisory Committee on Immunization Practice (ACIP) recommends that children aged 6 months through 8 years who have previously received ≥2 total doses of trivalent or quadrivalent influenza vaccine before July 1, 2016, require only 1 dose for 2016–17. The two previous doses need not have been given during the same season or consecutive seasons (Grohskopf et al, 2016).
Influenza vaccine dosing algorithm for children ages 6 months to 8 years. (Source: Grohskopf et al., 2016.)
Late in life, the immune system becomes less responsive. In answer to this, a high-dose trivalent influenza vaccine has been developed for those 65 years and over; it has been shown to induce significantly higher antibody responses and provide better protection against influenza illness. Progress is being made in the development of a high-dose vaccine for use in those under age 65 (CDC, 2016j).
POSSIBLE CONTRAINDICATIONS FOR VACCINATION
Those who should not be vaccinated before talking to their primary care provider include:
- Those who have had a severe allergic reaction to an influenza vaccination in the past (pain, swelling, and redness at the site of injection are not considered severe; any other symptoms should be reported to a physician prior to administration)
- Persons with moderate to severe acute illness with or without fever until symptoms are relieved
- Those who developed Guillain-Barré syndrome within six weeks of getting an influenza vaccine previously
VACCINATION AND EGG ALLERGY
The recommendations for people with egg allergies have been updated for this 2016–17 season.
- People who have experienced only hives after exposure to egg can get any licensed flu vaccine that is otherwise appropriate for their age and health.
- People who have symptoms other than hives after exposure to eggs (such as angioedema, respiratory distress, lightheadedness, or recurrent emesis) or who have needed epinephrine or any other emergency medical intervention also can get any licensed flu vaccine that is appropriate for their age and health, but the vaccine should be given in a medical setting and be supervised by a healthcare provider who is capable of recognizing and managing severe allergic conditions. Such settings include hospitals, clinics, health departments, and physician offices.
- People with egg allergies no longer have to wait 30 minutes after receiving their vaccine.
POSSIBLE SIDE EFFECTS FOLLOWING VACCINATION
Following vaccination, some individuals experience mild side effects. These may include:
- Soreness, redness, and swelling at the injection site
- Fainting, mainly in adolescents
- Low grade fever
Serious side effects include severe allergic reactions, usually beginning a few minutes to a few hours after receiving the flu shot, requiring immediate medical intervention. Their signs and symptoms include:
- Difficulty breathing
- Swelling around the eyes or lips
- Behavior changes
- High fever
TIMING OF VACCINATION
The optimal time period when vaccination should occur is before the onset of influenza activity in a community. Healthcare providers should begin offering vaccination by the end of October whenever possible. Children who require two doses should receive the first as soon as possible after the vaccine becomes available, and the second dose given at 4 weeks or later. Most adults will have a protective antibody response within 2 weeks following immunization. The vaccine should be offered continually as long as the influenza viruses are circulating and unexpired vaccine is available (Grohskopf et al, 2016).
VACCINATION FOR HEALTHCARE WORKERS
The CDC, the Advisory Committee on Immunization Practices, and the Healthcare Infection Control Practices Advisory Committee recommend that all U.S. healthcare workers get vaccinated annually against influenza. Healthcare workers include (but are not limited to):
- Nursing assistants
- Emergency medical service personnel
- Dental personnel
- Laboratory personnel
- Autopsy personnel
- Students and trainees
- Contractual staff not employed by the healthcare facility
- Persons not directly involved in patient care but potentially exposed to infectious agents:
VACCINES FOR THE 2016–17 FLU SEASON
Influenza vaccines are updated annually to provide a combination of the most likely flu strains to be in circulation. Traditional flu vaccines made to protect against three different flu viruses (trivalent) are available. Additionally, flu vaccines made to protect against four different flu viruses (quadrivalent) are available.
CDC recommends using injectable influenza vaccines only for the 2016–17 flu season. The nasal spray flu vaccine should not be used during 2016–17, as it has not demonstrated adequate effectiveness data. Options available this year include:
- Standard-dose trivalent shot manufactured using virus grown in eggs, given with a needle into the muscle of the arm. Different flu shots are approved for different age groups; one trivalent vaccine formulation can be given with a jet injector for persons aged 18 through 64.
- High-dose trivalent shot approved for people 65 and older
- Recombinant trivalent shot that is egg-free approved for people 18 years and older
- New trivalent shot made with adjuvant (an ingredient that helps create a stronger immune response) approved for people 65 years of age and older
- Quadrivalent shot approved for use in different age groups
- Intradermal quadrivalent shot injected into the skin and approved for people 18 through 64 years of age
- New quadrivalent shot containing virus grown in a cell culture and approved for persons 4 years of age and older
Trivalent vaccine protects against three different flu viruses: the two most common influenza A viruses (H1N1 and H3N2) and one influenza B virus, whichever is predicted to be circulating in a given year. The trivalent flu vaccine available for the 2016–17 flu season is made from the following viruses.
- A/California/7/2009 (H1N1)-like virus
- A/Hong Kong/4801/2014 (H3N2)-like virus
- B/Brisbane/60/2008-like virus (B/Victoria lineage)
This year’s quadrivalent vaccine contains the above three strains plus a B/Phuket/3073/2013-like virus (B/Yamagata lineage) (CDC, 2015k).
The increasing number of vaccination dosing and route options is leading to improved targeting and specificity in delivering influenza immunization while also allowing more people to be vaccinated than ever before. However, the variety of options is beyond what providers can commit to memory, particularly considering the frequency with which the options are updated.
Nurses who expect to be providing influenza vaccines should familiarize themselves with the CDC references and obtain copies of the most current vaccine dosing and administration tables so that, in consultation with medical providers, they are prepared to quickly ascertain the best vaccine options for their patients (see “Resources” at the end of this course).
TIPS FOR INTRAMUSCULAR VACCINE ADMINISTRATION
- Prepare vaccine out of line of sight of patient and/or parents (for children).
- Position patient so that the muscle is as relaxed as possible. If using the deltoid, allow the arm to swing freely and not rest on the patient’s lap, chair arm, or any other surface.
- Allow skin disinfectant to dry completely before injecting; this ensures adequate skin contact time and minimizes secondary pain from disinfectant.
- Select the appropriate skin manipulation (bunching, stretching flat) based on body habitus.
- Insert the needle fully into the muscle at a 90° angle and inject (do not attempt aspiration).
- Withdraw the needle and apply light pressure to the injection site for several seconds with a gauze pad.
Source: CDC, 2015d; VCH, 2013.
On a Friday afternoon in early September, Jeanine, a 55-year-old female patient, asked Maria Jones, RN, when she should receive her annual flu shot and if she could have the nasal spray so she didn’t need to have a shot. Maria told her she thought it was still a little early but did not yet have the information for the recommendations for this season. She reassured Jeanine that she would look into it and give her a call with further information.
Over the weekend, Maria went to the CDC website and read about the new recommendations for seasonal influenza vaccinations. She found a table that showed types of vaccines available, dosing, and route information. She also located information regarding when vaccinations should be provided. She printed the table and presented it to her nurse and physician coworkers when she came to work Monday morning. Together, they used the tables to determine the best option for a variety of their patients.
With a confirmation from the physician, Maria was then able to call her patient. She told Jeanine that the CDC recommends vaccines be given as soon as they are available and that the clinic expected to have their first doses available in early October. Maria informed her, however, that the new CDC recommendations did not include the use of nasal spray for this season, as it had not demonstrated adequate effectiveness.
PNEUMOCOCCAL VACCINE RECOMMENDATIONS FOR PERSONS AGE 65 AND OLDER
A serious complication of influenza is pneumococcal pneumonia caused by Streptococcus pneumonia. It is the leading cause of vaccine-preventable illness and death in the United States. Adults 65 years and older are at greater risk for contracting this disease. Also, because some strains of this bacterium have become resistant to drugs that were effective in the past, prevention through vaccination has become even more important.
The best prevention of pneumococcal pneumonia is by vaccination with both the influenza and pneumococcal vaccines. It is recommended that:
- Adults age 65 or older who have never received a pneumococcal vaccine or whose previous vaccination history is unknown should receive a dose of pneumococcal conjugate vaccine (PCV13) followed by a dose of PPSV23 at least 1 year later. PCV13 and PPSV23 should not be administered on the same day.
- Adults 65 years or older who received one or more doses of PPSV23 before age 65 years should receive one final dose of the vaccine at age 65 years or older if at least 5 years have elapsed since their previous PPSV23 dose.
- Adults age 65 or older who have not previously received one or more doses of PPSV23 and who have not previously received PCV13 should be given a dose of PVC13. This dose should be given at least 1 year after receipt of the most recent PPSV23 dose.
Source: CDC, 2015e.
Prevention of epidemics and pandemics depends on education of the public about the importance of vaccination and personal hygiene. The greater the number of vaccinated individuals, the fewer the cases of influenza. With increased prevention by individuals, such as covering a sneeze or cleansing the hands, the flu virus will be less likely to infect other people. For these reasons, healthcare providers have a special responsibility to encourage the general public to be vaccinated and to practice preventative measures.
Influenza continues to be a deadly disease, but due to the work of scientists and clinicians, people can be protected from infection by the ever-changing influenza viruses. With vaccination against the viruses and protective sanitary measures, infections can be reduced; and with antiviral medications, vulnerable individuals and those who are infected can be treated. Healthcare providers play an important role in delivering this message to those they serve.
Administering Vaccines: Dose, Route, Site, and Needle Size (Immunization Action Coalition)
Flu.gov (U.S. Department of Health and Human Services)
Influenza (National Institute of Allergy and Infectious Diseases)
Influenza vaccines—United States, 2016–17 influenza season (CDC)
Seasonal Influenza (Flu) (CDC)
NOTE: Complete URLs for references retrieved from online sources are provided in the PDF of this course (view/download PDF from the menu at the top of this page).
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