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This form is used for the submission of influenza surveillance specimens and to record the associated patient and specimen details. It includes sections for patient information, facility information,
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How to fill out influenza surveillance specimen submission

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How to fill out Influenza Surveillance Specimen Submission & Results Form

01
Obtain the Influenza Surveillance Specimen Submission & Results Form from the designated health authority or online.
02
Fill in the 'Patient Information' section with the patient's name, age, gender, and other relevant details.
03
Provide the 'Specimen Information' by indicating the type of specimen collected (e.g., nasal swab, throat swab).
04
Specify the date of specimen collection and any relevant clinical information in the designated sections.
05
Include information about the healthcare provider submitting the form, including name, contact information, and facility details.
06
Ensure all mandatory fields are completed before submission.
07
Review the completed form for any errors or omissions.
08
Submit the form along with the specimen to the designated laboratory for testing.

Who needs Influenza Surveillance Specimen Submission & Results Form?

01
Healthcare providers who suspect influenza infection in patients.
02
Laboratories conducting influenza testing.
03
Public health officials monitoring influenza activity.
04
Research facilities studying influenza epidemiology.
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People Also Ask about

Influenza surveillance involves collection of both clinical and virological data. Clinical surveillance monitors the impact of the illness on the health service and the community, while virological surveillance confirms that influenza is circulating and also identifies the current strain.
Routine virologic surveillance allows situational awareness and novel influenza virus and antiviral resistance detection. It also provides specimens and viruses to CDC for annual vaccine virus selection.
Disease surveillance is an ongoing process that involves the systematic collection, analysis, interpretation, and dissemination of information regarding the occurrence of diseases in defined populations for public health action to reduce morbidity and mortality.
A nasopharyngeal (NP) swab is the optimal upper respiratory tract specimen collection method for influenza testing. However, such specimens cannot be collected from infants and many older patients may not allow an NP specimen to be collected.
Influenza surveillance is the collection, compilation and analysis of information on influenza activity in a defined population.
The CDC Laboratory Support for Influenza Surveillance (CLSIS) SharePoint Site is intended to facilitate technical support for domestic U.S. and international public health and research institutions performing influenza laboratory surveillance and/or research.
The California influenza surveillance system is a collaborative effort between CDPH and its many partners at local health departments, public health and clinical laboratories, vital statistics offices, healthcare providers, clinics, emergency departments, and the Centers for Disease Control and Prevention (CDC).
GISRS currently comprises institutions in 130 WHO Member States. FluNet is a global database of virologic surveillance for respiratory viruses conducted and reported through GISRS.

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The Influenza Surveillance Specimen Submission & Results Form is a standardized document used to collect and document information regarding samples submitted for influenza surveillance, monitoring, and research purposes.
Health care providers, laboratories, and institutions involved in collecting and submitting influenza specimens for surveillance purposes are required to file this form.
To fill out the form, follow the instructions provided, ensuring to accurately complete all required sections, including patient demographics, clinical information, specimen details, and submitter information.
The purpose of the form is to gather essential data on influenza cases and the virus's characteristics to aid in public health monitoring, research, and response strategies.
The form must report information such as patient demographics (age, sex), clinical symptoms, specimen type, collection date, geographical location, and any laboratory results associated with the submitted specimens.
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