The guidelines do not address sporadic infections with influenza C virus, and do not address sporadic human infections with novel influenza A viruses of animal origin. CDCHAN-00425. A pooled meta-analysis of observational studies with individual-level data from >29000 hospitalized patients (86% with laboratory-confirmed influenza, 14% clinically diagnosed with influenza) reported survival benefit of NAI treatment (primarily oseltamivir) in adults compared with no treatment, with significantly greater survival benefit with early (within 2 days of illness onset) compared with later initiation (>2 days after onset) of NAI treatment [16]. Clinicians should test respiratory specimens for influenza if influenza-associated neurologic complications are suspected. In the 2009/2010 pandemic, a new swine-origin influenza virus strain, a novel influenza A/H1N1 (variant) virus, has spread worldwide, causing more than . V. For patients who are recommended to receive antiviral treatment for suspected or confirmed influenza, which antiviral should be prescribed, at what dosing, and for what duration? Who should be considered for antiviral chemoprophylaxis to prevent influenza in the absence of exposure or an institutional outbreak (preexposure chemoprophylaxis)? Accessed Nov. 29, 2018. The pooled efficacy against laboratory-confirmed symptomatic influenza was 81% (95% CI, 55%92%) [398]. Oseltamivir (tablets or oral suspension formulation) may be administered to all pediatric age groups with influenza, including premature infants [216]. VIII. Mayo Clinic; 2020. The doctor may also offer symptomatic treatment for a fever, sore throat, runny nose and cough to alleviate your child's discomfort. "Mayo," "Mayo Clinic," "MayoClinic.org," "Mayo Clinic Healthy Living," and the triple-shield Mayo Clinic logo are trademarks of Mayo Foundation for Medical Education and Research. This is because aspirin has been linked to Reye's syndrome, a rare but potentially life-threatening condition, in such children. Signs and symptoms. Although no other factors have been demonstrated to be associated with the risk of outbreaks, biological plausibility and expert opinion suggest that volume and patterns of air flow, degree of crowding in rooms or public areas, the effectiveness of policies excluding ill visitors and ill staff, and the ability to reduce interresident and staff contact in response to a single identified influenza case may all influence whether introduction of a single case of influenza will result in an outbreak [430]. We also discuss some of the potential cons of antiviral . It represents a year-round disease burden. In contrast, NAI resistance has been reported among severely immunocompromised patients more frequently than immunocompetent patients during prolonged influenza viral replication and antiviral treatment, and after postexposure antiviral chemoprophylaxis [289, 335342]. Humans generally acquire the disease through direct contact with infected animals, by eating or drinking contaminated animal products or by inhaling airborne agents. There is no need to discontinue breastfeeding due to the use of oral oseltamivir. A large autopsy series of 100 fatal cases found no evidence of extrapulmonary influenza A(H1N1) pdm09 virus infection [167]. Consultation should be sought with an expert on management of patients with antiviral-resistant influenza virus infection. Therefore, facility medical directors should plan for prescribing antivirals (including renal dosing adjustments if needed) by facility physicians vs referral to external providers. Several respiratory syndromes can be associated with either bacterial or viral pathogen infections or coinfections, including community-acquired pneumonia, sinusitis, pharyngitis, and acute otitis media. Panel judgments were made throughout the guidelines based on consensus. Collection of upper respiratory tract specimens from immunocompetent outpatients with influenza >34 days after illness onset may yield negative results because of substantially decreased influenza viral shedding, especially in older children and adults. However, lack of clinical improvement while receiving adequate antiviral treatment can occur in severely ill patients with influenza. Seasonal influenza A or B virus infections can cause a wide range of manifestations, from asymptomatic infection, uncomplicated illness with or without fever (Table 2), to complications that may result in severe disease (Table 3). You should focus on relieving your symptoms and preventing the spread of the H1N1 to other people. Patients with significant hypoxemia who are not receiving mechanical ventilation may not be able to reliably use the disk inhaler device needed to effectively deliver inhaled zanamivir. AA. XVIII. The threshold for declaring an outbreak in hospital units with longer-stay patients should be the same as that in long-term care facilities for the elderly. During an influenza outbreak at a long-term care facility, should antiviral chemoprophylaxis be administered to residents only on affected units or to all residents in the facility? Most people recover from fever and other symptoms within a week . 5. While some studies have suggested that young children with uncomplicated influenza may also be at higher risk for the emergence of drug resistance during or after NAI use based on molecular detection methods, presumably due to longer viral shedding, no effect on illness resolution has been reported [246, 333, 334, 343]. They can reduce the severity of symptoms and possibly the risk of complications. Centers for Disease Control and Prevention. In a cluster randomized trial over 3 seasons in Australia comparing oseltamivir treatment of symptomatic persons and provision of oseltamivir chemoprophylaxis for elderly long-term care residents and staff, researchers found that chemoprophylaxis reduced the influenza attack rate among residents compared with treatment of symptomatic persons [407]. Performance of these assays depends heavily on laboratory expertise and the quality of the specimen collected (ie, specimens must include respiratory epithelium cells; requires a florescent microscope and an experienced laboratory technician). Based on pharmacokinetic modeling, a 30% dose increase of oseltamivir phosphate was estimated to be needed to attain comparable systemic exposure of oseltamivir carboxylate to nonpregnant women (105 mg once daily for prophylaxis and 105 mg twice daily for treatment) [270]. These are tiny droplets that are made when a person who has the virus. 2017; doi:10.1542/peds.2017-2550. During periods of low influenza activity: Clinicians should test for influenza on admission in all patients requiring hospitalization with acute respiratory illness, with or without fever, who have an epidemiological link to a person diagnosed with influenza, an influenza outbreak or outbreak of acute febrile respiratory illness of uncertain cause, or who recently traveled from an area with known influenza activity, Clinicians can consider testing for influenza in patients with acute, febrile respiratory tract illness, especially children and adults who are immunocompromised or at high risk of complications, or if the results might influence antiviral treatment or chemoprophylaxis decisions for high-risk household contacts (see recommendations 4143), Clinicians should collect upper respiratory tract specimens from outpatients for influenza testing as soon after illness onset as possible, preferably within 4 days of symptom onset, Nasopharyngeal specimens should be collected over other upper respiratory tract specimens to increase detection of influenza viruses, If nasopharyngeal specimens are not available, nasal and throat swab specimens should be collected and combined together for influenza testing over single specimens from either site (particularly over throat swabs) to increase detection of influenza viruses, Mid-turbinate nasal swab specimens should be collected over throat swab specimens to increase detection of influenza viruses, Flocked swab specimens should be collected over nonflocked swab specimens to improve detection of influenza viruses, Clinicians should collect nasopharyngeal (optimally, as for outpatients), mid-turbinate nasal, or combined nasalthroat specimens from hospitalized patients without severe lower respiratory tract disease for influenza testing as soon as possible, Clinicians should collect endotracheal aspirate or bronchoalveolar lavage fluid specimens from hospitalized patients with respiratory failure receiving mechanical ventilation, including patients with negative influenza testing results on upper respiratory tract specimens, for influenza testing as soon as possible, Clinicians should not collect or routinely test specimens for influenza from nonrespiratory sites such as blood, plasma, serum, cerebrospinal fluid, urine, and stool, Clinicians should not collect serum specimens, including single or paired sera, for serological diagnosis of seasonal influenza virus infection for clinical management purposes, Clinicians should use rapid molecular assays (ie, nucleic acid amplification tests) over rapid influenza diagnostic tests (RIDTs) in outpatients to improve detection of influenza virus infection, Clinicians should use reverse-transcription polymerase chain reaction (RT-PCR) or other molecular assays over other influenza tests in hospitalized patients to improve detection of influenza virus infection, Clinicians should use multiplex RT-PCR assays targeting a panel of respiratory pathogens, including influenza viruses, in hospitalized immunocompromised patients, Clinicians can consider using multiplex RT-PCR assays targeting a panel of respiratory pathogens, including influenza viruses, in hospitalized patients who are not immunocompromised if it might influence care (eg, aid in cohorting decisions, reduce testing, or decrease antibiotic use), Clinicians should not use immunofluorescence assays for influenza virus antigen detection in hospitalized patients except when more sensitive molecular assays are not available, Clinicians should not use RIDTs in hospitalized patients except when more sensitive molecular assays are not available, Clinicians should not use viral culture for initial or primary diagnosis of influenza because results will not be available in a timely manner to inform clinical management, Clinicians should not use serologic testing for diagnosis of influenza because results from a single serum specimen cannot be reliably interpreted, and collection of paired (acute/convalescent) sera 23 weeks apart are needed for serological testing. 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