Diferencia entre revisiones de «H1N1 (swine) flu»
(Created page with "CDC 2009 -March/April 2009, an outbreak of H1N1 influenza A virus infection was first detected in Mexico. -June 11, 2009, WHO raised its pandemic alert level to the highest lev...") |
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==High-risk groups== | |||
#Pregnant- incr rates of SAB, preterm labor | |||
#Chronic lung disease | |||
#Immunosuppressed | |||
#Cardiac | |||
#DM | |||
High-risk groups | |||
Pregnant- incr rates of SAB, preterm labor | |||
Chronic lung disease | |||
Immunosuppressed | |||
Cardiac | |||
DM | |||
==Screening== | |||
Individuals with an acute febrile respiratory illness (a measured temperature of 100ºF or higher and recent onset of at least one of the following: rhinorrhea, nasal congestion, sore throat, or cough) or sepsis-like syndrome- HIGH PRIORITY for hospitalized patients and those at high-risk for severe disease. | Individuals with an acute febrile respiratory illness (a measured temperature of 100ºF or higher and recent onset of at least one of the following: rhinorrhea, nasal congestion, sore throat, or cough) or sepsis-like syndrome- HIGH PRIORITY for hospitalized patients and those at high-risk for severe disease. | ||
==Diagnosis== | |||
#Rapid Flu nasal swab 60-80% sensitive in detecting influenza A | |||
#If patient is negative, severely ill and will be hospitalized, send viral culture | |||
#PCR is the recommended confirmatory test | |||
==Treatment== | |||
#All hospitalized patients with confirmed, probable or suspected novel influenza (H1N1) | |||
#Patients who are at higher risk for seasonal influenza complications | |||
Most effective when started within 48 hours of illness onset. | Most effective when started within 48 hours of illness onset. | ||
Adult: 75-mg capsule twice per day for 5 days | Adult: 75-mg capsule twice per day for 5 days | ||
===Post-exposure chemoprophylaxis=== | |||
#Tamiflu 75mg po daily x 10 days (10 days after the last known exposure to novel (H1N1) influenza.) | |||
Post-exposure | |||
Tamiflu 75mg po daily x 10 days (10 days after the last known exposure to novel (H1N1) influenza.) | |||
If the contact occurred with a patient after 7 days of symtpom onset, then chemoprophylaxis is not necessary. This is the presumed post-infectious period. | If the contact occurred with a patient after 7 days of symtpom onset, then chemoprophylaxis is not necessary. This is the presumed post-infectious period. | ||
[[Category:ID]] | [[Category:ID]] | ||
Revisión del 13:17 12 mar 2011
High-risk groups
- Pregnant- incr rates of SAB, preterm labor
- Chronic lung disease
- Immunosuppressed
- Cardiac
- DM
Screening
Individuals with an acute febrile respiratory illness (a measured temperature of 100ºF or higher and recent onset of at least one of the following: rhinorrhea, nasal congestion, sore throat, or cough) or sepsis-like syndrome- HIGH PRIORITY for hospitalized patients and those at high-risk for severe disease.
Diagnosis
- Rapid Flu nasal swab 60-80% sensitive in detecting influenza A
- If patient is negative, severely ill and will be hospitalized, send viral culture
- PCR is the recommended confirmatory test
Treatment
- All hospitalized patients with confirmed, probable or suspected novel influenza (H1N1)
- Patients who are at higher risk for seasonal influenza complications
Most effective when started within 48 hours of illness onset.
Adult: 75-mg capsule twice per day for 5 days
Post-exposure chemoprophylaxis
- Tamiflu 75mg po daily x 10 days (10 days after the last known exposure to novel (H1N1) influenza.)
If the contact occurred with a patient after 7 days of symtpom onset, then chemoprophylaxis is not necessary. This is the presumed post-infectious period.
