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The CPT® Code 90695 refers to the influenza virus vaccine specifically targeting the H5N8 strain, which is derived from cell cultures and is adjuvanted for intramuscular use. The H5N8 influenza virus is recognized as a virulent strain of the avian influenza, commonly known as bird flu, which can be transmitted from animals to humans, primarily through contact with infected poultry or environments contaminated by poultry. This vaccine is produced using mammalian cell cultures, a method that eliminates the need for egg-based production, thereby reducing the risk of allergic reactions associated with egg proteins. The inclusion of adjuvants, such as squalene, DL-α-tocopherol, and polysorbate 80, enhances the immune response, leading to a more robust defense against the virus. It is important to note that this code specifically pertains to the vaccine product itself, and the administration of the vaccine via intramuscular injection is reported separately under a different code.
© Copyright 2025 Coding Ahead. All rights reserved.
The H5N8 influenza virus vaccine is indicated for individuals who may be at risk of exposure to the H5N8 strain of the avian influenza virus. This includes, but is not limited to, individuals who work in environments with poultry or those who have close contact with birds. The vaccine is particularly important for healthcare professionals, poultry workers, and individuals living in areas where outbreaks of H5N8 have been reported.
The administration of the H5N8 influenza virus vaccine involves several key procedural steps to ensure proper delivery and effectiveness of the vaccine. First, the healthcare provider must verify the patient's eligibility for the vaccine, taking into account any contraindications or previous allergic reactions to vaccines. Next, the provider prepares the vaccine by ensuring it is at the appropriate temperature and inspecting the vial for any abnormalities. Following this, the provider selects an appropriate site for intramuscular injection, typically the deltoid muscle of the upper arm. The injection site is then cleaned with an antiseptic to minimize the risk of infection. The vaccine is administered using a sterile syringe and needle, ensuring that the injection is delivered deep into the muscle tissue. After the injection, the provider may apply a bandage to the site and monitor the patient for any immediate adverse reactions. Finally, proper documentation of the vaccine administration, including the date, lot number, and site of injection, is recorded in the patient's medical record.
After the administration of the H5N8 influenza virus vaccine, patients are typically monitored for a short period to observe for any immediate adverse reactions, such as allergic responses or injection site reactions. Common post-procedure care includes advising the patient to rest and hydrate adequately. Patients may experience mild side effects, such as soreness at the injection site, low-grade fever, or fatigue, which usually resolve within a few days. It is important for patients to be informed about these potential side effects and to seek medical attention if they experience severe or persistent symptoms. Additionally, patients should be advised to keep their vaccination records updated and to follow any recommended schedules for future vaccinations or boosters as indicated by public health guidelines.
Short Descr | H5N8 VACC DRV CLL CUL ADJ IM | Medium Descr | H5N8 VACCINE DRV CELL CUL ADJUVANTED FOR IM USE | Long Descr | Influenza virus vaccine, H5N8, derived from cell cultures, adjuvanted, for intramuscular use | APC Status Indicator | Non-Covered Service, not paid under OPPS | Type of Service (TOS) | 1 - Medical Care | Berenson-Eggers TOS (BETOS) | none | MUE | Not applicable/unspecified. |
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2025-01-01 | Added | First appearance in codebook |
2024-07-19 | Added | Code added. Effective upon receiving Emergency Use Authorization or approval from the Food and Drug Administration |
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