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Pronunciation(noo moe KOK al pol i SAK a ride vak SEEN, pol i VAY lent)
U.S. Brand NamesPneumovax® 23
SynonymsPPV23; 23PS; 23-Valent Pneumococcal Polysaccharide Vaccine
Generic AvailableNo
Canadian Brand NamesPneumo 23™; Pneumovax® 23
UseChildren >2 years of age and adults who are at increased risk of pneumococcal disease and its complications because of underlying health conditions (including patients with cochlear implants); older adults, including all those 65 years of age Current Advisory Committee on Immunization Practices (ACIP) guidelines recommend pneumococcal 7-valent conjugate vaccine (PCV7) be used for children 2-23 months of age and, in certain situations, children up to 59 months of age
Pregnancy Risk FactorC
Pregnancy ImplicationsThe safety of vaccine in pregnant women has not been evaluated; it should not be given during pregnancy unless the risk of infection is high
ContraindicationsHypersensitivity to pneumococcal vaccine or any component of the formulation. Note: Epinephrine injection (1:1000) must be immediately available in the case of anaphylaxis.
Warnings/PrecautionsUse caution in patients with severe cardiovascular or pulmonary disease where a systemic reaction may pose a significant risk. Use caution and consider delay of vaccination in any active infection. Avoid use in pregnancy (unless potential benefit justifies possible risks). Use caution in individuals who have had episodes of pneumococcal infection within the preceding 3 years (pre-existing pneumococcal antibodies may result in increased reactions to vaccine); may cause relapse in patients with stable idiopathic thrombocytopenia purpura. Patients who will be receiving immunosuppressive therapy (including Hodgkin's disease, cancer chemotherapy, or transplantation) should be vaccinated at least 2 weeks prior to the initiation of therapy. Immune responses may be impaired for several months following intensive immunosuppressive therapy (up to 2 years in Hodgkin's disease patients). Patients who will undergo splenectomy should also be vaccinated 2 weeks prior to surgery, if possible. Patients with HIV should be vaccinated as soon as possible (following confirmation of the diagnosis). Not recommended in children 2 years of age.
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Adverse ReactionsAll serious adverse reactions must be reported to the U.S. Department of Health and Human Services (DHHS) Vaccine Adverse Event Reporting System (VAERS) 1-800-822-7967.>10%: Local: Induration and soreness at the injection site (~72%) (2-3 days)
<1%: Anaphylaxis, arthralgia, erythema, Guillain-Barré syndrome, low-grade fever, myalgia, paresthesia, rash
Drug InteractionsDecreased effect with immunosuppressive agents, immunoglobulin, other live vaccines within 1 month
StabilityRefrigerate
Mechanism of ActionAlthough there are more than 80 known pneumococcal capsular types, pneumococcal disease is mainly caused by only a few types of pneumococci. Pneumococcal vaccine contains capsular polysaccharides of 23 pneumococcal types which represent at least 98% of pneumococcal disease isolates in the United States and Europe. The pneumococcal vaccine with 23 pneumococcal capsular polysaccharide types became available in 1983. The 23 capsular pneumococcal vaccine contains purified capsular polysaccharides of pneumococcal types 1, 2, 3, 4, 5, 8, 9, 12, 14, 17, 19, 20, 22, 23, 26, 34, 43, 51, 56, 57, 67, 70 (American Classification). These are the main pneumococcal types associated with serious infections in the United States.
DosageI.M., SubQ: Children >2 years and Adults: 0.5 mL
Previously vaccinated with PCV7 vaccine: Children 2 years and Adults:
With sickle cell disease, asplenia, immunocompromised or HIV infection: 0.5 mL at 2 years of age and 2 months after last dose of PCV7; revaccination with PPV23 should be given 5 years for children >10 years of age and every 3-5 years for children 10 years of age; revaccination should not be administered <3 years after the previous PPV23 dose
With chronic illness: 0.5 mL at 2 years of age and 2 months after last dose of PCV7; revaccination with PPV23 is not recommended
Following bone marrow transplant (use of PCV7 under study): Administer one dose PPV23 at 12- and 24-months following BMT
Revaccination should be considered:
1. If 6 years since initial vaccination has elapsed, or
2. In patients who received 14-valent pneumococcal vaccine and are at highest risk (asplenic) for fatal infection or
3. At 6 years in patients with nephrotic syndrome, renal failure, or transplant recipients, or
4. 3-5 years in children with nephrotic syndrome, asplenia, or sickle cell disease
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AdministrationDo not inject I.V., avoid intradermal, administer SubQ or I.M. (deltoid muscle or lateral midthigh) For patients at risk of hemorrhage following intramuscular injection, the ACIP recommends "it should be administered intramuscularly if, in the opinion of the physician familiar with the patients bleeding risk, the vaccine can be administered with reasonable safety by this route. If the patient receives antihemophilia or other similar therapy, intramuscular vaccination can be scheduled shortly after such therapy is administered. A fine needle (23 gauge or smaller) can be used for the vaccination and firm pressure applied to the site (without rubbing) for at least 2 minutes. The patient should be instructed concerning the risk of hematoma from the injection."
Patient EducationThis vaccine is used to prevent pneumococcal disease which causes bacterial meningitis and pneumonia. It can be used in some children and in adults. Side effects from this vaccine include redness, tenderness, or swelling at the injection site and mild fever. Contact your prescriber immediately for high fever or signs of allergic reaction (respiratory difficulty, hoarseness or wheezing, hives, paleness, weakness, fast heartbeat, dizziness, swelling of the throat). Pregnancy/breast-feeding precautions: This vaccine is not usually given during pregnancy. Notify your prescriber if you are pregnant or breast-feeding.
Additional InformationInactivated bacteria vaccine. Federal law requires that the date of administration, the vaccine manufacturer, lot number of vaccine, and the administering person's name, title, and address be entered into the patient's permanent medical record.
Dental Health: Effects on Dental TreatmentNo significant effects or complications reported
Dental Health: Vasoconstrictor/Local Anesthetic PrecautionsNo information available to require special precautions
Mental Health: Effects on Mental StatusNone reported
Mental Health: Effects on Psychiatric TreatmentNone reported
Dosage FormsInjection, solution: 25 mcg each of 23 polysaccharide isolates/0.5 mL (0.5 mL, 2.5 mL)
ReferencesAdvisory Committee on Immunization Practices (ACIP), "Pneumococcal Vaccination for Cochlear Implant Recipients,"MMWR Morb Mortal Wkly Rep, 2002, 51(41):931.
Advisory Committee on Immunization Practices (ACIP), "Prevention of Pneumococcal Disease,"MMWR Recomm Rep, 1997, 46(RR-8):1-31.
Centers for Disease Control, "Recommendations of the Advisory Committee on Immunization Practices (ACIP): General Recommendations on Immunization,"MMWR Recomm Rep, 1994, 43(RR-1):23.
Davidson M, Bulkow LR, Grabman J, et al, "Immunogenicity of Pneumococcal Revaccination in Patients With Chronic Disease,"Arch Intern Med, 1994, 154(19):2209-14.
Gardner P and Schaffner W, "Immunization of Adults,"N Engl J Med, 1993, 328(17):1252-8.
"Preventing Pneumococcal Disease Among Infants and Young Children: Recommendations of the Advisory Committee on Immunization Practices (ACIP), Centers for Disease Control and Prevention,"MMWR Recomm Rep, 2000, 49(RR-9):1-35.
U.S. Department of Health and Human Services, "Prevention of Pneumococcal Disease. Recommendations of the Advisory Committee on Immunization Practices (ACIP),"MMWR Recomm Rep, 1997, 46(RR-8):1-24.
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International Brand NamesPneumo 23™ (CA); Pneumovax® 23 (CA)
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