Influenza: Difference between revisions
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'''Influenza''', commonly called “the ‘Flu”, is described as "an acute viral infection in humans involving the respiratory tract. It is marked by inflammation of the nasal mucosa; the pharynx; and conjunctiva, and by headache and severe, often generalized, myalgia".<ref name="pmid">{{cite journal |author=National Library of Medicine |title=Influenza |journal= |volume= |issue= |pages= |year= |pmid= |doi= |issn=}}</ref> It is contagious (easily passed from one person to another) and is caused by viruses of the [[Orthomyxoviridae]] family. | '''Influenza''', commonly called “the ‘Flu”, is described as "an acute viral infection in humans involving the respiratory tract. It is marked by inflammation of the nasal mucosa; the pharynx; and conjunctiva, and by headache and severe, often generalized, myalgia".<ref name="pmid">{{cite journal |author=National Library of Medicine |title=Influenza |journal= |volume= |issue= |pages= |year= |pmid= |doi= |issn=}}</ref> It is contagious (easily passed from one person to another) and is caused by viruses of the [[Orthomyxoviridae]] family. | ||
==Classification== | |||
There are three types of influenza viruses:<ref name="CDC-flu/avian/gen-info/flu-viruses.htm Influenza">Anonymous (2005)[http://www.cdc.gov/flu/avian/gen-info/flu-viruses.htm Influenza Viruses], [[Centers for Disease Control and Prevention]]</ref> | |||
* [[Influenza A virus]]. "Influenza A viruses are further classified by subtype on the basis of the two main surface glycoproteins hemagglutinin (HA) and neuraminidase (NA). Influenza A subtypes and B viruses are further classified by strains."<ref name="CDC-flu/avian/gen-info/flu-viruses.htm Influenza"/> | |||
** [[2009 H1N1 influenza virus]] | |||
* [[Influenza B virus]] | |||
* [[Influenza C virus]] | |||
==Hosts== | ==Hosts== | ||
===Influenza in humans=== | ===Influenza in humans=== | ||
In April, 2009, the [[2009 H1N1 influenza virus]] was first isolated and is a ''novel H1N1'' strain that was initially untypeable. The 2009 novel H1N1 influenza virus contains genes normally found in North American swine as well as two genes found in European and Asian swine and has been called a triple-reassortant of genes.<ref name="pmid19423869">{{cite journal| author=Novel Swine-Origin Influenza A (H1N1) Virus Investigation Team. Dawood FS, Jain S, Finelli L, Shaw MW, Lindstrom S et al.| title=Emergence of a novel swine-origin influenza A (H1N1) virus in humans. | journal=N Engl J Med | year= 2009 | volume= 360 | issue= 25 | pages= 2605-15 | pmid=19423869 | |||
| url=http://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&retmode=ref&cmd=prlinks&id=19423869 | doi=10.1056/NEJMoa0903810 }} <!--Formatted by http://sumsearch.uthscsa.edu/cite/--></ref><ref>[http://www.cdc.gov/h1n1flu/swineflu_you.htm Swine Flu & You]</ref> | |||
In the 2007-2008 season, the most common strains of influenza in the United States were:<ref>[http://www.cdc.gov/flu/weekly/weeklyarchives2007-2008/07-08summary.htm 2007-08 U.S. INFLUENZA SEASON SUMMARY], Centers for Disease Control and Prevention</ref> | |||
* [[influenza A virus]] (H1N1) 35% | |||
* [[influenza A virus]] (H3N2) 35% | |||
* [[influenza B virus]] 30% | |||
In the 1999-2000 season, the most common strains of influenza in the United States were:<ref>[http://www.cdc.gov/ncidod/diseases/flu/WeeklyArchives1999-2000/99-00summary2.htm 1999-2000 INFLUENZA SEASON SUMMARY], Centers for Disease Control and Prevention</ref> | |||
* [[influenza A virus]] (H1N1) 3% | |||
* [[influenza A virus]] (H3N2) 99% | |||
* [[influenza B virus]] 0.6% | |||
===Equine Influenza=== | ===Equine Influenza=== | ||
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==Epidemiology== | ==Epidemiology== | ||
[[Image:Labsummary06-07.GIF|right|thumb| | [[Image:Labsummary06-07.GIF|right|thumb|250px|{{#ifexist:Template:Labsummary06-07.GIF/credit|{{Labsummary06-07.GIF/credit}}<br/>|}}Seasonal influenza activity in the [[United States of America]] over four years. During the off season, the prevalence is < 2%. During the height of season, the prevalence may be 20-35%.<ref name="titleCDC - Influenza (Flu) | Flu Activity">{{cite web |url=http://www.cdc.gov/flu/weekly/fluactivity.htm |title=Flu Activity |accessdate=2007-11-29 |author=Centers for Disease Control and Prevention |authorlink= |coauthors= |date= |format= |work= |publisher= |pages= |language= |archiveurl= |archivedate= |quote=}}</ref>]] | ||
Current influenza activity can be monitored online: | |||
* In the [[United States of America]], the [[Centers for Disease Control and Prevention]] (CDC) maintains public statistics at http://www.cdc.gov/flu/weekly/fluactivitysurv.htm. | |||
* Google maintains statistics based on search terms (http://www.google.org/flutrends/).<ref name="urlGoogle Uses Web Searches to Track Flu’s Spread - NYTimes.com">{{cite web |url=http://www.nytimes.com/2008/11/12/technology/internet/12flu.html |title=Google Uses Web Searches to Track Flu’s Spread - NYTimes.com |author=Helft M |authorlink= |coauthors= |date=Nov 11, 2008 |format= |work= |publisher=New York Times Company |pages= |language= |archiveurl= |archivedate= |quote= |accessdate=2008-11-11}}</ref> | |||
* http://healthmap.org/ | |||
The prevalence of influenza among people who have an "influenza-like illness" varies strongly with the seasons of the year. In the [[United States]], the [[Centers for Disease Control and Prevention]] (CDC) maintains public statistics at http://www.cdc.gov/flu/weekly/fluactivity.htm. | The prevalence of influenza among people who have an "influenza-like illness" varies strongly with the seasons of the year. In the [[United States of America]], the [[Centers for Disease Control and Prevention]] (CDC) maintains public statistics at http://www.cdc.gov/flu/weekly/fluactivity.htm. | ||
* During the off season, | * During the off season, the prevalence is < 2%<ref name="titleCDC - Influenza (Flu) | Flu Activity"/> | ||
* During the height of season, the prevalence may be 20-35%.<ref name="titleCDC - Influenza (Flu) | Flu Activity"/> | * During the height of season, the prevalence may be 20-35%.<ref name="titleCDC - Influenza (Flu) | Flu Activity"/> | ||
* During local outbreaks, the prevalence may be 50-80% according to studies.<ref name=" | * During local outbreaks, the prevalence may be 50-80% according to studies.<ref name="pmid12361816">{{cite journal | author = Smith K, Roberts M | title = Cost-effectiveness of newer treatment strategies for influenza. | journal = Am J Med | volume = 113 | issue = 4 | pages = 300-7 | year = 2002 | doi = 10.1016/S0002-9343(02)01222-6 | id = PMID 12361816}}</ref><ref name="pimd12965940">{{cite journal | author = Rothberg M, Bellantonio S, Rose D | title = Management of influenza in adults older than 65 years of age: cost-effectiveness of rapid testing and antiviral therapy. | journal = Ann Intern Med | volume = 139 | issue = 5 Pt 1 | pages = 321-9 | year = 2003 | url = http://www.annals.org/cgi/content/abstract/139/5_Part_1/321 | id = PMID 12965940}}</ref> Unfortunately, the CDC does not report sufficient details to determine where local outbreaks are occurring. | ||
In addition to seasonal variations, there have been several worldwide influenza [[epidemic]]s, resulting in millions of deaths. | In addition to seasonal variations, there have been several worldwide influenza [[epidemic]]s, resulting in millions of deaths. | ||
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==Diagnosis== | ==Diagnosis== | ||
===History and physical examination=== | ===History and physical examination=== | ||
Since anti-viral drugs are effective in treating influenza if given early (see treatment section, below), it can be important to identify cases early. A [[systematic review]] by the [http:// | Since anti-viral drugs are effective in treating influenza if given early (see treatment section, below), it can be important to identify cases early. A [[systematic review]] by the [http://jama.ama-assn.org/cgi/collection/rational_clinical_exam Rational Clinical Examination] concluded that the best findings for excluding the diagnosis of influenza are:<ref name="pmid15728170">{{cite journal| author=Call SA, Vollenweider MA, Hornung CA, Simel DL, McKinney WP| title=Does this patient have influenza? | journal=JAMA | year= 2005 | volume= 293 | issue= 8 | pages= 987-97 | pmid=15728170 | ||
| url=http://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&retmode=ref&cmd=prlinks&id=15728170 | doi=10.1001/jama.293.8.987 }} [http://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&retmode=ref&cmd=prlinks&id=16247902 Review in: Evid Based Nurs. 2005 Oct;8(4):121]</ref> | |||
{| class="wikitable" | {| class="wikitable" | ||
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! style="text-align:center"|Finding: !! [[sensitivity (tests)|Sensitivity]] !! [[specificity (tests)|Specificity]] | ! style="text-align:center"|Finding: !! [[sensitivity (tests)|Sensitivity]] !! [[specificity (tests)|Specificity]] | ||
|- | |- | ||
! | ! Fever† | ||
| style="text-align:center"|86% ||style="text-align:center"| 25% | | style="text-align:center"|86%† ||style="text-align:center"| 25% | ||
|- | |||
! Cough† | |||
| style="text-align:center"|98%† ||style="text-align:center"| 23% | |||
|- | |||
! Sore throat | |||
| style="text-align:center"|~80%† ||style="text-align:center"| ~30% | |||
|- | |- | ||
! | ! Nasal congestion† | ||
| style="text-align:center"| | | style="text-align:center"|70–90%† || style="text-align:center"|20–40% | ||
|- | |- | ||
! | ! Absence of vaccination | ||
| style="text-align:center"| | | style="text-align:center"|83-97% || style="text-align:center"|14-19%<ref name="pmid11742606">{{cite journal |author=Hulson TD, Mold JW, Scheid D, ''et al'' |title=Diagnosing influenza: the value of clinical clues and laboratory tests |journal=J Fam Pract |volume=50 |issue=12 |pages=1051–6 |year=2001 |month=December |pmid=11742606 |doi= |url=http://www.jfponline.com/Pages.asp?AID=2406 |issn=}}</ref><ref name="pmid11510391">{{cite journal |author=van Elden LJ, van Essen GA, Boucher CA, ''et al'' |title=Clinical diagnosis of influenza virus infection: evaluation of diagnostic tools in general practice |journal=Br J Gen Pract |volume=51 |issue=469 |pages=630–4 |year=2001 |month=August |pmid=11510391 |pmc=1314072 |doi= |url=http://openurl.ingenta.com/content/nlm?genre=article&issn=0960-1643&volume=51&issue=469&spage=630&aulast=van |issn=}}</ref> | ||
|- | |- | ||
| colspan="3" | '''Note:'''<br> | | colspan="3" | '''Note:'''<br>† All three findings, especially fever, were less sensitive in patients over 60 years of age.<ref name="pmid15728170"/> | ||
|- | |- | ||
|} | |} | ||
Using the symptoms listed above, the ''combinations'' of findings below can improve diagnostic accuracy.<ref name="pmid11088084">{{cite journal | author = Monto A, Gravenstein S, Elliott M, Colopy M, Schweinle J | title = Clinical signs and symptoms predicting influenza infection. | journal = Arch Intern Med | volume = 160 | issue = 21 | pages = 3243–7 | year = 2000 | url http://archinte.ama-assn.org/cgi/content/abstract/160/21/3243 | id = PMID 11088084}}</ref> Unfortunately, even combinations of findings are imperfect. However, [[Bayes Theorem]] can combine pretest probability with clinical findings to adequately diagnose or exclude influenza in some patients. The pretest probability has a strong seasonal variation; the current prevalence of influenza among patients in the United States receiving sentinel testing is available at the [[Centers for Disease Control and Prevention|CDC]].<ref>Centers for Disease Control and Prevention. [http://www.cdc.gov/flu/weekly/ Weekly Report: Influenza Summary Update.] Accessed January 1, 2007.</ref> Using the CDC data, the following table shows how the likelihood of influenza varies with prevalence: | Using the symptoms listed above, the ''combinations'' of findings below can improve diagnostic accuracy.<ref name="pmid11088084">{{cite journal | author = Monto A, Gravenstein S, Elliott M, Colopy M, Schweinle J | title = Clinical signs and symptoms predicting influenza infection. | journal = Arch Intern Med | volume = 160 | issue = 21 | pages = 3243–7 | year = 2000 | url http://archinte.ama-assn.org/cgi/content/abstract/160/21/3243 | id = PMID 11088084}}</ref> Unfortunately, even combinations of findings are imperfect. Studies of combining symptoms have included use of recursive partitioning; however, this study combined two cohorts with different prevalences of influenza.<ref name="pmid22427440">{{cite journal| author=Afonso AM, Ebell MH, Gonzales R, Stein J, Genton B, Senn N| title=The use of classification and regression trees to predict the likelihood of seasonal influenza. | journal=Fam Pract | year= 2012 | volume= | issue= | pages= | pmid=22427440 | doi=10.1093/fampra/cms020 | pmc= | url=http://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=22427440 }} </ref> However, [[Bayes Theorem]] can combine pretest probability with clinical findings to adequately diagnose or exclude influenza in some patients. The pretest probability has a strong seasonal variation; the current prevalence of influenza among patients in the United States receiving sentinel testing is available at the [[Centers for Disease Control and Prevention|CDC]].<ref>Centers for Disease Control and Prevention. [http://www.cdc.gov/flu/weekly/ Weekly Report: Influenza Summary Update.] Accessed January 1, 2007.</ref> Using the CDC data, the following table shows how the likelihood of influenza varies with prevalence: | ||
: | : | ||
<table border="1" cellpadding="5" class="wikitable"> | <table border="1" cellpadding="5" class="wikitable"> | ||
<caption>Combinations of findings for diagnosing influenza<ref name="pmid15728170"/></caption> | <caption>Combinations of findings for diagnosing influenza<ref name="pmid22218625">{{cite journal| author=Ebell MH, Afonso AM, Gonzales R, Stein J, Genton B, Senn N| title=Development and validation of a clinical decision rule for the diagnosis of influenza. | journal=J Am Board Fam Med | year= 2012 | volume= 25 | issue= 1 | pages= 55-62 | pmid=22218625 | doi=10.3122/jabfm.2012.01.110161 | pmc= | url=http://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=22218625 }} </ref><ref name="pmid15728170"/></caption> | ||
<tr> | <tr> | ||
<th rowspan="2">Combinations of findings </th> | <th rowspan="2">Combinations of findings </th> | ||
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<tr> | <tr> | ||
<td>Fever and cough</td> | <td>Fever and cough</td> | ||
<td align="center">64%</td> | <td align="center">64%<br/>61%<ref name="pmid22218625"/></td> | ||
<td align="center">67%</td> | <td align="center">67%<br/>80%<ref name="pmid22218625"/></td> | ||
<td align="center">79%</td> | <td align="center">79%<br/>86%<ref name="pmid22218625"/></td> | ||
<td align="center">49%</td> | <td align="center">49%<br/>49%<ref name="pmid22218625"/></td> | ||
<td align="center">39%</td> | <td align="center">39%<br/>50%<ref name="pmid22218625"/></td> | ||
<td align="center">15%</td> | <td align="center">15%<br/>14%<ref name="pmid22218625"/></td> | ||
<td align="center">4%</td> | <td align="center">4%<br/>6%<ref name="pmid22218625"/></td> | ||
<td align="center">1%</td> | <td align="center">1%<br/>1%<ref name="pmid22218625"/></td> | ||
</tr> | </tr> | ||
<tr> | <tr> | ||
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<td align="center">16</td> | <td align="center">16</td> | ||
<td align="center">4</td> | <td align="center">4</td> | ||
<td align="center">1</td> | |||
</tr> | |||
<tr> | |||
<td>Fever and cough and acute onset<ref name="pmid22218625"/></td> | |||
<td align="center">41</td> | |||
<td align="center">93</td> | |||
<td align="center">92</td> | |||
<td align="center">55</td> | |||
<td align="center">66</td> | |||
<td align="center">18</td> | |||
<td align="center">11</td> | |||
<td align="center">1</td> | <td align="center">1</td> | ||
</tr> | </tr> | ||
</table> | </table> | ||
===Laboratory tests=== | |||
{{Image|Flu-virus2.jpg|right|350px|An electron tomography of the influenza virus.}} | |||
Available tests are [http://www.cdc.gov/flu/professionals/diagnosis/labprocedures.htm listed at the CDC website]. | |||
[[Clinical practice guideline]]s address diagnosis.<ref name="pmid19281331">{{cite journal| author=Harper SA, Bradley JS, Englund JA, File TM, Gravenstein S, Hayden FG et al.| title=Seasonal influenza in adults and children--diagnosis, treatment, chemoprophylaxis, and institutional outbreak management: clinical practice guidelines of the Infectious Diseases Society of America. | journal=Clin Infect Dis | year= 2009 | volume= 48 | issue= 8 | pages= 1003-32 | pmid=19281331 | |||
| url=http://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&retmode=ref&cmd=prlinks&id=19281331 | doi=10.1086/598513 }} <!--Formatted by http://sumsearch.uthscsa.edu/cite/--></ref> | |||
Rapid tests using for influenza antigens include [[immunofluorescence]] assays, [[immunoenzyme technique]], and [[polymerase chain reaction]] testing. The [[sensitivity and specificity|sensitivity]] of these tests range from 63% to 95%.<ref>Beyer WE. Heterogeneity of case definitions used in vaccine effectiveness studies--and its impact on meta-analysis. Vaccine. 2006 Nov 10;24(44-46):6602-4. Epub 2006 Jun 8. | |||
PMID 16797799</ref><ref>Rodriguez WJ, Schwartz RH, Thorne MM. Evaluation of diagnostic tests for influenza in a pediatric practice. Pediatr Infect Dis J. 2002 Mar;21(3):193-6. PMID 12005080</ref> | |||
Rapid influenza diagnostic tests (RIDT) using [[immunosorbent technique]] for influenza antigens have a sensitivity of about 50% and specificity of about 85%<ref name="pmid19779397">{{cite journal| author=Centers for Disease Control and Prevention (CDC)| title=Performance of rapid influenza diagnostic tests during two school outbreaks of 2009 pandemic influenza A (H1N1) virus infection - Connecticut, 2009. | journal=MMWR Morb Mortal Wkly Rep | year= 2009 | volume= 58 | issue= 37 | pages= 1029-32 | pmid=19779397 | |||
| url=http://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&retmode=ref&cmd=prlinks&id=19779397 }}</ref> | |||
The [[polymerase chain reaction]] is the most [[sensitivity and specificity|sensitive]] test and is as sensitive as viral culture.<ref name="pmid19281331" /> | |||
===Differential diagnosis=== | ===Differential diagnosis=== | ||
''Influenza-like illness'' is defined as "fever (temperature of 100°F [37.8°C] or greater) and | ''Influenza-like illness'' is defined as "fever (temperature of 100°F [37.8°C] or greater) and cough and/or sore throat"<ref name="titleCDC">{{cite web |url=http://www.cdc.gov/flu/weekly/index.htm |title=Seasonal Influenza (Flu) |author=Centers for Disease Control and Prevention |accessdate=2012-11-11 |format= |work=|year=2012}}</ref> A study from [[Australia]] found that possible causes for influenza-like illness include respiratory syncytial virus, rhinovirus, [[human adenovirus|adenovirus]], parainfluenza viruses, coronaviruses, and metapneumovirus.<ref name="pmid15227858">{{cite journal |author=Kelly H, Birch C |title=The causes and diagnosis of influenza-like illness |journal=Australian family physician |volume=33 |issue=5 |pages=305–9 |year=2004 |pmid=15227858 |doi=}}</ref> | ||
Other diagnoses to consider are: | Other diagnoses to consider are: | ||
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==Treatment== | ==Treatment== | ||
The two classes of | The two classes of [[antiviral agent]]s are neuraminidase inhibitors and M2 inhibitors ([[adamantane]] derivatives). Neuraminidase inhibitors are currently preferred for flu virus infections. | ||
Different strains of influenza virus have differing degrees of resistance against these antivirals and it is impossible to predict what degree of resistance a future pandemic strain might have.<ref> {{cite journal | last = Webster | first = Robert G. | title = H5N1 Influenza — Continuing Evolution and Spread | url=http://content.nejm.org/cgi/content/full/355/21/2174 | journal = N Engl J Med | volume = 355 | issue = 21 | pages = 2174–77 | year = 2006 | id = PMID 16192481}}</ref> | Different strains of influenza virus have differing degrees of resistance against these antivirals and it is impossible to predict what degree of resistance a future pandemic strain might have.<ref> {{cite journal | last = Webster | first = Robert G. | title = H5N1 Influenza — Continuing Evolution and Spread | url=http://content.nejm.org/cgi/content/full/355/21/2174 | journal = N Engl J Med | volume = 355 | issue = 21 | pages = 2174–77 | year = 2006 | id = PMID 16192481}}</ref> | ||
In the United States, the [[Centers for Disease Control and Prevention]] have issued recommendations for the use of [[antiviral agent]]s.<ref>Advisory Committee on Immunization Practices (2011) [http://www.cdc.gov/mmwr/preview/mmwrhtml/rr6001a1.htm Antiviral Agents for the Treatment and Chemoprophylaxis of Influenza]. Morbidity and Mortality Weekly Report</ref> The CDC recommends [[oseltamivir]] or [[zanamivir]]. | |||
===When to treat=== | ===When to treat=== | ||
According to two [[decision analysis]] studies of adults, treatment may be justified in the following settings: | According to two [[decision analysis]] studies of adults, treatment may be justified in the following settings: | ||
* Elderly patients if the probability of influenza is over | * Elderly patients if the probability of influenza is over 14%<ref name="pimd12965940"/> | ||
* Adults if the probability of influenza is over 30%<ref name=" | * Adults if the probability of influenza is over 30%<ref name="pmid12361816"/>. | ||
During ''local outbreaks'' of influenza, the prevalence will be over 50-80%<ref name="pmif12361816">{{cite journal | author = Smith K, Roberts M | title = Cost-effectiveness of newer treatment strategies for influenza. | journal = Am J Med | volume = 113 | issue = 4 | pages = 300-7 | year = 2002 | doi = 10.1016/S0002-9343(02)01222-6 | id = PMID 12361816}}</ref><ref name="pimd12965940">{{cite journal | author = Rothberg M, Bellantonio S, Rose D | title = Management of influenza in adults older than 65 years of age: cost-effectiveness of rapid testing and antiviral therapy. | journal = Ann Intern Med | volume = 139 | issue = 5 Pt 1 | pages = 321-9 | year = 2003 | url = http://www.annals.org/cgi/content/abstract/139/5_Part_1/321 | id = PMID 12965940}}</ref> and thus patients with any of the above combinations of symptoms may be treated with neuramidase inhibitors without testing. In the absence of a local outbreak, treatment may be justified in the elderly during the influenza season as long as the prevalence is over 15%.<ref name="pimd12965940"/> | During ''local outbreaks'' of influenza, the prevalence will be over 50-80%<ref name="pmif12361816">{{cite journal | author = Smith K, Roberts M | title = Cost-effectiveness of newer treatment strategies for influenza. | journal = Am J Med | volume = 113 | issue = 4 | pages = 300-7 | year = 2002 | doi = 10.1016/S0002-9343(02)01222-6 | id = PMID 12361816}}</ref><ref name="pimd12965940">{{cite journal | author = Rothberg M, Bellantonio S, Rose D | title = Management of influenza in adults older than 65 years of age: cost-effectiveness of rapid testing and antiviral therapy. | journal = Ann Intern Med | volume = 139 | issue = 5 Pt 1 | pages = 321-9 | year = 2003 | url = http://www.annals.org/cgi/content/abstract/139/5_Part_1/321 | id = PMID 12965940}}</ref> and thus patients with any of the above combinations of symptoms may be treated with neuramidase inhibitors without testing. In the absence of a local outbreak, treatment may be justified in the elderly during the influenza season as long as the prevalence is over 15%.<ref name="pimd12965940"/> | ||
===Neuraminidase inhibitors=== | ===Neuraminidase inhibitors=== | ||
These drugs are | These drugs are effective, but modestly so, against both influenza A and B.<ref name="pmid19995812">{{cite journal| author=Jefferson T, Jones M, Doshi P, Del Mar C| title=Neuraminidase inhibitors for preventing and treating influenza in healthy adults: systematic review and meta-analysis. | journal=BMJ | year= 2009 | volume= 339 | issue= | pages= b5106 | pmid=19995812 | ||
| url=http://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=clinical.uthscsa.edu/cite&email=badgett@uthscdsa.edu&retmode=ref&cmd=prlinks&id=19995812 | doi=10.1136/bmj.b5106 }}</ref><ref name="pmid20166059">{{cite journal| author=Jefferson T, Jones M, Doshi P, Del Mar C, Dooley L, Foxlee R| title=Neuraminidase inhibitors for preventing and treating influenza in healthy adults. | journal=Cochrane Database Syst Rev | year= 2010 | volume= 2 | issue= | pages= CD001265 | pmid=20166059 | |||
| url=http://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=clinical.uthscsa.edu/cite&retmode=ref&cmd=prlinks&id=20166059 | doi=10.1002/14651858.CD001265.pub3 }} </ref> Examples are [[oseltamivir]] (trade name Tamiflu) and [[zanamivir]] (trade name Relenza) are [[neuraminidase inhibitor]]s.<ref name= Neuraminidase_inhibitors>{{cite journal | last = Moscona | first = A | title = Neuraminidase inhibitors for influenza | url=http://content.nejm.org/cgi/content/full/353/13/1363 | journal = N Engl J Med | volume = 353 | issue = 13 | pages = 1363–73 | year = 2005 | id = PMID 16192481}}</ref> The [[Cochrane Collaboration]] concluded that these drugs reduce symptoms and complications.<ref name="pmid16855962">{{cite journal | last = Jefferson | first = T | coauthors = Demicheli V, Di Pietrantonj C, Jones M, Rivetti D | title = Neuraminidase inhibitors for preventing and treating influenza in healthy adults | journal = Cochrane Database Syst Rev | volume = 3 | issue = | pages = CD001265 | year = | doi = 10.1002/14651858.CD001265.pub2 | id = PMID 16855962}}</ref> Zanamivir, which must be delivered by inhalation, may cause bronchospasm in patients with asthma. | |||
Oseltamivir may<ref name="pmid10697061">{{cite journal |author=Treanor JJ, Hayden FG, Vrooman PS, ''et al'' |title=Efficacy and safety of the oral neuraminidase inhibitor oseltamivir in treating acute influenza: a randomized controlled trial. US Oral Neuraminidase Study Group |journal=JAMA |volume=283 |issue=8 |pages=1016–24 |year=2000 |pmid=10697061 |doi=}}</ref> or may not<ref name="pmid19995812">{{cite journal| author=Jefferson T, Jones M, Doshi P, Del Mar C| title=Neuraminidase inhibitors for preventing and treating influenza in healthy adults: systematic review and meta-analysis. | journal=BMJ | year= 2009 | volume= 339 | issue= | pages= b5106 | pmid=19995812 | |||
| url=http://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=clinical.uthscsa.edu/cite&email=badgett@uthscdsa.edu&retmode=ref&cmd=prlinks&id=19995812 | doi=10.1136/bmj.b5106 }}</ref> reduce the incidence of respiratory complications on one of 13 patients who take it ([[number needed to treat]] = 13). This trial only included patients up to 65 years old. | |||
Neither of these drugs can be administered by injection. For the 2009 pandemic, the U.S. [[Food and Drug Administration]] issued an emergency authorization for the use of intravenous peramavir, which had been in [[New Drug Application|Phase III clinical trials]]. <ref name=FDA-EUA-par>{{citation | |||
| url = http://cdc.gov/h1n1flu/eua/peramivir.htm | |||
| title = Emergency Use Authorization of Peramivir IV | |||
| publisher = [[Centers for Disease Control]]}}</ref> | |||
===M2 inhibitors (adamantanes) === | ===M2 inhibitors (adamantanes) === | ||
These drugs are sometimes effective against influenza A if given early in the infection, but are always ineffective against influenza B. Examples include the [[antiviral drug]]s [[amantadine]] and [[rimantadine]] which block a viral ion channel and prevent the virus from infecting cells. <ref name="pmid10459804"/> | These drugs are sometimes effective against influenza A if given early in the infection, but are always ineffective against influenza B. Examples include the [[antiviral drug]]s [[amantadine]] and [[rimantadine]] which block a viral ion channel and prevent the virus from infecting cells.<ref name="pmid10459804">{{cite journal| author=Stephenson I, Nicholson KG| title=Chemotherapeutic control of influenza. | journal=J Antimicrob Chemother | year= 1999 | volume= 44 | issue= 1 | pages= 6-10 | pmid=10459804 | doi= | pmc= | url=http://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=10459804 }} </ref> | ||
==Prevention== | ==Prevention== | ||
===Barriers=== | |||
{{Image|N95.jpg|right|350px|N95 mask. This mask is '''''NOT''''' better than a regular surgical mask.}} | |||
A regular surgical mask is adequate.<ref>{{Cite journal | |||
| doi = 10.1001/jama.2009.1466 | |||
| pages = 2009.1466 | |||
| last = Loeb | |||
| first = Mark | |||
| coauthors = Nancy Dafoe, James Mahony, Michael John, Alicia Sarabia, Verne Glavin, Richard Webby, Marek Smieja, David J. D. Earn, Sylvia Chong, Ashley Webb, Stephen D. Walter | |||
| title = Surgical Mask vs N95 Respirator for Preventing Influenza Among Health Care Workers: A Randomized Trial | |||
| journal = JAMA | |||
| accessdate = 2009-10-02 | |||
| date = 2009-10-01 | |||
| url = http://jama.ama-assn.org/cgi/content/abstract/2009.1466v1 | |||
}}</ref> | |||
===Vaccination=== | ===Vaccination=== | ||
In the [[United States]], the [[Centers for Disease Control and Prevention]] has | In the [[United States of America]], the [[Centers for Disease Control and Prevention]] has maintains recommendations on who should get the influenza vaccination.<ref name="titleCDC - Influenza (Flu) | Vaccination">{{cite web |url=http://www.cdc.gov/flu/professionals/vaccination/ |title=Seasonal Influenza Vaccination Resources for Health Professionals|accessdate=2014-12-16 |author=Centers for Disease Control and Prevention |authorlink= |coauthors= |date=2014|format= |work= |publisher= |pages= |language= |archiveurl= |archivedate= |quote=}}</ref> Protection from infection occurs by two weeks after vaccination and lasts one year.<ref name="titleCDC - Influenza (Flu) | Vaccination"/> | ||
The quality of the research on vaccination my be reduced by [[conflict of interest]] according to the [[Cochrane Collaboration]].<ref name="pmid20614424">{{cite journal| author=Jefferson T, Di Pietrantonj C, Rivetti A, Bawazeer GA, Al-Ansary LA, Ferroni E| title=Vaccines for preventing influenza in healthy adults. | journal=Cochrane Database Syst Rev | year= 2010 | volume= 7 | issue= | pages= CD001269 | pmid=20614424 | url=http://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=20614424 | doi=10.1002/14651858.CD001269.pub4 }} </ref> | |||
=== | {| class="wikitable" | ||
The [[ | ! | ||
! colspan="4" style="text-align: center;" | Inactivated | |||
! style="text-align: center;" | Live attenuated | |||
(intranasal) | |||
|- | |||
! | |||
! style="text-align: center;" | Mammalian cells | |||
! style="text-align: center;" | Recombinant | |||
! colspan="2" style="text-align: center;" | Embryonated chicken eggs | |||
! style="text-align: center;" | Normal | |||
|- | |||
! | |||
! style="text-align: center;" | Trivalent | |||
! style="text-align: center;" | Trivalent | |||
! style="text-align: center;" | Trivalent | |||
! style="text-align: center;" | Quadrivalent | |||
! style="text-align: center;" | Quadrivalent | |||
|- | |||
| High dose | |||
| style="text-align: center;" | | |||
| style="text-align: center;" | | |||
| style="text-align: center;" | Fluzone high-dose. | |||
[[Centers for Disease Control|CDC]] lists as an option for age > 65 years old | |||
| style="text-align: center;" | | |||
| style="text-align: center;" | | |||
|- | |||
| Standard dose | |||
| style="text-align: center;" | Flucelvax† | |||
| style="text-align: center;" | FluBlok† | |||
| style="text-align: center;" | Needle-free jet‡ | |||
| style="text-align: center;" | [[Centers for Disease Control|CDC]] lists as an option for age < 65 years old | |||
| style="text-align: center;" | | |||
|- | |||
| Low dose | |||
| style="text-align: center;" | | |||
| style="text-align: center;" | | |||
| style="text-align: center;" | Fluzone intradermal‡ | |||
| style="text-align: center;" | | |||
| style="text-align: center;" | | |||
|- | |||
| colspan="6" | † For egg allergy<br/>‡ For needle phobia | |||
|} | |||
====Adverse effects==== | |||
Several randomized placebo-controlled trials assess adverse effects<ref name="pmid7666874">{{cite journal| author=Nichol KL, Lind A, Margolis KL, Murdoch M, McFadden R, Hauge M et al.| title=The effectiveness of vaccination against influenza in healthy, working adults. | journal=N Engl J Med | year= 1995 | volume= 333 | issue= 14 | pages= 889-93 | pmid=7666874 | doi=10.1056/NEJM199510053331401 | pmc= | url=http://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=7666874 }} </ref> <ref name="pmid10411194">{{cite journal| author=Nichol KL, Mendelman PM, Mallon KP, Jackson LA, Gorse GJ, Belshe RB et al.| title=Effectiveness of live, attenuated intranasal influenza virus vaccine in healthy, working adults: a randomized controlled trial. | journal=JAMA | year= 1999 | volume= 282 | issue= 2 | pages= 137-44 | pmid=10411194 | doi= | pmc= | url=http://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=10411194 }} </ref>, including patients who have lung disease<ref name="pmid11794219">{{cite journal| author=| title=The safety of inactivated influenza vaccine in adults and children with asthma. | journal=N Engl J Med | year= 2001 | volume= 345 | issue= 21 | pages= 1529-36 | pmid=11794219 | doi=10.1056/NEJMoa011961 | pmc= | url=http://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=11794219 }} [http://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=12123261 Review in: Evid Based Nurs. 2002 Jul;5(3):77] [http://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=12093217 Review in: ACP J Club. 2002 Jul-Aug;137(1):18] </ref> or are elderly<ref name="pmid2200894">{{cite journal| author=Margolis KL, Nichol KL, Poland GA, Pluhar RE| title=Frequency of adverse reactions to influenza vaccine in the elderly. A randomized, placebo-controlled trial. | journal=JAMA | year= 1990 | volume= 264 | issue= 9 | pages= 1139-41 | pmid=2200894 | doi= | pmc= | url=http://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=2200894 }} </ref> <ref name="pmid8241913">{{cite journal| author=Govaert TM, Dinant GJ, Aretz K, Masurel N, Sprenger MJ, Knottnerus JA| title=Adverse reactions to influenza vaccine in elderly people: randomised double blind placebo controlled trial. | journal=BMJ | year= 1993 | volume= 307 | issue= 6910 | pages= 988-90 | pmid=8241913 | doi= | pmc=PMC1679213 | url=http://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=8241913 }} </ref>. | |||
Among health adults, vaccination may be associated with arm pain<ref name="pmid7666874">{{cite journal| author=Nichol KL, Lind A, Margolis KL, Murdoch M, McFadden R, Hauge M et al.| title=The effectiveness of vaccination against influenza in healthy, working adults. | journal=N Engl J Med | year= 1995 | volume= 333 | issue= 14 | pages= 889-93 | pmid=7666874 | doi=10.1056/NEJM199510053331401 | pmc= | url=http://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=7666874 }} </ref> and "runny nose or sore throat during the first 7 days after vaccination"<ref name="pmid10411194">{{cite journal| author=Nichol KL, Mendelman PM, Mallon KP, Jackson LA, Gorse GJ, Belshe RB et al.| title=Effectiveness of live, attenuated intranasal influenza virus vaccine in healthy, working adults: a randomized controlled trial. | journal=JAMA | year= 1999 | volume= 282 | issue= 2 | pages= 137-44 | pmid=10411194 | doi= | pmc= | url=http://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=10411194 }} </ref>. | |||
Among patients with asthma, vaccination was associated with body aches.<ref name="pmid11794219">{{cite journal| author=| title=The safety of inactivated influenza vaccine in adults and children with asthma. | journal=N Engl J Med | year= 2001 | volume= 345 | issue= 21 | pages= 1529-36 | pmid=11794219 | doi=10.1056/NEJMoa011961 | pmc= | url=http://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=11794219 }} [http://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=12123261 Review in: Evid Based Nurs. 2002 Jul;5(3):77] [http://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=12093217 Review in: ACP J Club. 2002 Jul-Aug;137(1):18] </ref> | |||
== | Among elderly patients, the influenza vaccine may increase arm pain.<ref name="pmid2200894">{{cite journal| author=Margolis KL, Nichol KL, Poland GA, Pluhar RE| title=Frequency of adverse reactions to influenza vaccine in the elderly. A randomized, placebo-controlled trial. | journal=JAMA | year= 1990 | volume= 264 | issue= 9 | pages= 1139-41 | pmid=2200894 | doi= | pmc= | url=http://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=2200894 }} </ref> <ref name="pmid8241913">{{cite journal| author=Govaert TM, Dinant GJ, Aretz K, Masurel N, Sprenger MJ, Knottnerus JA| title=Adverse reactions to influenza vaccine in elderly people: randomised double blind placebo controlled trial. | journal=BMJ | year= 1993 | volume= 307 | issue= 6910 | pages= 988-90 | pmid=8241913 | doi= | pmc=PMC1679213 | url=http://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=8241913 }} </ref> | ||
=== | |||
===Chemoprevention=== | |||
[[Chemoprevention]] (chemoprophylaxis) with neuraminidase inhibitors can prevent symptomatic influenza according to a [[meta-analysis]] by the [[Cochrane Collaboration]].<ref name="pmid16855962" />Zanamivir may cause bronchospasm in patients with asthma. Extended-duration (>4 weeks) chemoprevention may be effective as well.<ref name="pmid19652173">{{cite journal| author=Khazeni N, Bravata DM, Holty JE, Uyeki TM, Stave CD, Gould MK| title=Safety and Efficacy of Extended-Duration Antiviral Chemoprophylaxis Against Pandemic and Seasonal Influenza. | journal=Ann Intern Med | year= 2009 | volume= | issue= | pages= | pmid=19652173 | |||
| url=http://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&retmode=ref&cmd=prlinks&id=19652173 }}</ref> | |||
== | ==Pandemics and notable outbreaks== | ||
===Spanish influenza pandemic of 1918-1920=== | |||
A pandemic of Spanish Influenza, involving a highly pathogenic mutation of serotype H1N1, swept across the world in the wake of the Great War (1918-20). More people are believed to have died of the flu in the year after the war then in the Great War itself. Estimates vary but it is estimated that one third of the world's population were infected and up to 50 million people perished in this pandemic (it is possibly that fatalities world wide were as high as 100 million).<ref>http://www.cdc.gov/ncidod/EID/vol12no01/05-0979.htm</ref> Some comparisons are drawn between Spanish Flu and the Black Death (Bubonic Plague) of 1347 to 1351. Estimates are that the flu killed more people in one year than plague did in four. | |||
In the [[United States of America]], the epidemic led to closing of schools and banning of public meetings in order to successfully reduce mortality.<ref name="pmid17684187">{{cite journal |author=Markel H, Lipman HB, Navarro JA, ''et al'' |title=Nonpharmaceutical interventions implemented by US cities during the 1918-1919 influenza pandemic |journal=JAMA |volume=298 |issue=6 |pages=644–54 |year=2007 |pmid=17684187 |doi=10.1001/jama.298.6.644}}</ref> | |||
===Asian influenza pandemic of 1957 - 1963=== | |||
A/H2N2 virus was responsible for this outbreak | |||
===Hong Kong pandemic 1968-1970=== | |||
This was caused by serotype A/H3N2. | |||
==References== | ==References== | ||
{{reflist|2}}[[Category:Suggestion Bot Tag]] |
Latest revision as of 06:01, 1 September 2024
Influenza, commonly called “the ‘Flu”, is described as "an acute viral infection in humans involving the respiratory tract. It is marked by inflammation of the nasal mucosa; the pharynx; and conjunctiva, and by headache and severe, often generalized, myalgia".[1] It is contagious (easily passed from one person to another) and is caused by viruses of the Orthomyxoviridae family.
Classification
There are three types of influenza viruses:[2]
- Influenza A virus. "Influenza A viruses are further classified by subtype on the basis of the two main surface glycoproteins hemagglutinin (HA) and neuraminidase (NA). Influenza A subtypes and B viruses are further classified by strains."[2]
- Influenza B virus
- Influenza C virus
Hosts
Influenza in humans
In April, 2009, the 2009 H1N1 influenza virus was first isolated and is a novel H1N1 strain that was initially untypeable. The 2009 novel H1N1 influenza virus contains genes normally found in North American swine as well as two genes found in European and Asian swine and has been called a triple-reassortant of genes.[3][4]
In the 2007-2008 season, the most common strains of influenza in the United States were:[5]
- influenza A virus (H1N1) 35%
- influenza A virus (H3N2) 35%
- influenza B virus 30%
In the 1999-2000 season, the most common strains of influenza in the United States were:[6]
- influenza A virus (H1N1) 3%
- influenza A virus (H3N2) 99%
- influenza B virus 0.6%
Equine Influenza
This is a species-specific strain that infects horses, ponies, donkeys and mules. Humans do not catch this disease but are carriers of it. It is airborne and highly contagious. Equine influenza generally does not kill its victims, and affected horses display similar symptoms to those of humans.
In 2007, a horse flu epidemic began in New South Wales, Australia. The outbreak is believed to have begun as a result of infractions of proper quarantine procedure and is expected to cost millions of dollars in lost revenue. As of September, 2007, it had spread to the Victorian border, causing the cancellation of events at the Melbourne Show, and the possibility that the Spring Carnival, including the running of the Melbourne Cup horse race, would be canceled.
Avian flu
Avian flu, also known as Bird flu or H5N1, has led to recent outbreaks.[7][8]
Epidemiology
Current influenza activity can be monitored online:
- In the United States of America, the Centers for Disease Control and Prevention (CDC) maintains public statistics at http://www.cdc.gov/flu/weekly/fluactivitysurv.htm.
- Google maintains statistics based on search terms (http://www.google.org/flutrends/).[10]
- http://healthmap.org/
The prevalence of influenza among people who have an "influenza-like illness" varies strongly with the seasons of the year. In the United States of America, the Centers for Disease Control and Prevention (CDC) maintains public statistics at http://www.cdc.gov/flu/weekly/fluactivity.htm.
- During the off season, the prevalence is < 2%[9]
- During the height of season, the prevalence may be 20-35%.[9]
- During local outbreaks, the prevalence may be 50-80% according to studies.[11][12] Unfortunately, the CDC does not report sufficient details to determine where local outbreaks are occurring.
In addition to seasonal variations, there have been several worldwide influenza epidemics, resulting in millions of deaths.
Diagnosis
History and physical examination
Since anti-viral drugs are effective in treating influenza if given early (see treatment section, below), it can be important to identify cases early. A systematic review by the Rational Clinical Examination concluded that the best findings for excluding the diagnosis of influenza are:[13]
Finding: | Sensitivity | Specificity |
---|---|---|
Fever† | 86%† | 25% |
Cough† | 98%† | 23% |
Sore throat | ~80%† | ~30% |
Nasal congestion† | 70–90%† | 20–40% |
Absence of vaccination | 83-97% | 14-19%[14][15] |
Note: † All three findings, especially fever, were less sensitive in patients over 60 years of age.[13] |
Using the symptoms listed above, the combinations of findings below can improve diagnostic accuracy.[16] Unfortunately, even combinations of findings are imperfect. Studies of combining symptoms have included use of recursive partitioning; however, this study combined two cohorts with different prevalences of influenza.[17] However, Bayes Theorem can combine pretest probability with clinical findings to adequately diagnose or exclude influenza in some patients. The pretest probability has a strong seasonal variation; the current prevalence of influenza among patients in the United States receiving sentinel testing is available at the CDC.[18] Using the CDC data, the following table shows how the likelihood of influenza varies with prevalence:
Combinations of findings | Sensitivity | Specificity | Projected during local outbreaks (prevalence approx 66%[20][12]) |
Projected during influenza season (prevalence=25%) |
Projected in off-season (prevalence=2%) |
|||
---|---|---|---|---|---|---|---|---|
PPV | NPV | PPV | NPV | PPV | NPV | |||
Fever and cough | 64% 61%[19] |
67% 80%[19] |
79% 86%[19] |
49% 49%[19] |
39% 50%[19] |
15% 14%[19] |
4% 6%[19] |
1% 1%[19] |
Fever and cough and sore throat | 56 | 71 | 79 | 45 | 39 | 17 | 4 | 2 |
Fever and cough and nasal congestion | 59 | 74 | 81 | 48 | 43 | 16 | 4 | 1 |
Fever and cough and acute onset[19] | 41 | 93 | 92 | 55 | 66 | 18 | 11 | 1 |
Laboratory tests
Available tests are listed at the CDC website.
Clinical practice guidelines address diagnosis.[21]
Rapid tests using for influenza antigens include immunofluorescence assays, immunoenzyme technique, and polymerase chain reaction testing. The sensitivity of these tests range from 63% to 95%.[22][23]
Rapid influenza diagnostic tests (RIDT) using immunosorbent technique for influenza antigens have a sensitivity of about 50% and specificity of about 85%[24]
The polymerase chain reaction is the most sensitive test and is as sensitive as viral culture.[21]
Differential diagnosis
Influenza-like illness is defined as "fever (temperature of 100°F [37.8°C] or greater) and cough and/or sore throat"[25] A study from Australia found that possible causes for influenza-like illness include respiratory syncytial virus, rhinovirus, adenovirus, parainfluenza viruses, coronaviruses, and metapneumovirus.[26]
Other diagnoses to consider are:
- Parvovirus B19 - arthropathy is prominent
- Flaviviruses
- Dengue fever - bonebreak fever with retro-orbital pain
- West Nile virus - tremor is common
Treatment
The two classes of antiviral agents are neuraminidase inhibitors and M2 inhibitors (adamantane derivatives). Neuraminidase inhibitors are currently preferred for flu virus infections.
Different strains of influenza virus have differing degrees of resistance against these antivirals and it is impossible to predict what degree of resistance a future pandemic strain might have.[27]
In the United States, the Centers for Disease Control and Prevention have issued recommendations for the use of antiviral agents.[28] The CDC recommends oseltamivir or zanamivir.
When to treat
According to two decision analysis studies of adults, treatment may be justified in the following settings:
- Elderly patients if the probability of influenza is over 14%[12]
- Adults if the probability of influenza is over 30%[11].
During local outbreaks of influenza, the prevalence will be over 50-80%[20][12] and thus patients with any of the above combinations of symptoms may be treated with neuramidase inhibitors without testing. In the absence of a local outbreak, treatment may be justified in the elderly during the influenza season as long as the prevalence is over 15%.[12]
Neuraminidase inhibitors
These drugs are effective, but modestly so, against both influenza A and B.[29][30] Examples are oseltamivir (trade name Tamiflu) and zanamivir (trade name Relenza) are neuraminidase inhibitors.[31] The Cochrane Collaboration concluded that these drugs reduce symptoms and complications.[32] Zanamivir, which must be delivered by inhalation, may cause bronchospasm in patients with asthma.
Oseltamivir may[33] or may not[29] reduce the incidence of respiratory complications on one of 13 patients who take it (number needed to treat = 13). This trial only included patients up to 65 years old.
Neither of these drugs can be administered by injection. For the 2009 pandemic, the U.S. Food and Drug Administration issued an emergency authorization for the use of intravenous peramavir, which had been in Phase III clinical trials. [34]
M2 inhibitors (adamantanes)
These drugs are sometimes effective against influenza A if given early in the infection, but are always ineffective against influenza B. Examples include the antiviral drugs amantadine and rimantadine which block a viral ion channel and prevent the virus from infecting cells.[35]
Prevention
Barriers
A regular surgical mask is adequate.[36]
Vaccination
In the United States of America, the Centers for Disease Control and Prevention has maintains recommendations on who should get the influenza vaccination.[37] Protection from infection occurs by two weeks after vaccination and lasts one year.[37]
The quality of the research on vaccination my be reduced by conflict of interest according to the Cochrane Collaboration.[38]
Inactivated | Live attenuated
(intranasal) | ||||
---|---|---|---|---|---|
Mammalian cells | Recombinant | Embryonated chicken eggs | Normal | ||
Trivalent | Trivalent | Trivalent | Quadrivalent | Quadrivalent | |
High dose | Fluzone high-dose.
CDC lists as an option for age > 65 years old |
||||
Standard dose | Flucelvax† | FluBlok† | Needle-free jet‡ | CDC lists as an option for age < 65 years old | |
Low dose | Fluzone intradermal‡ | ||||
† For egg allergy ‡ For needle phobia |
Adverse effects
Several randomized placebo-controlled trials assess adverse effects[39] [40], including patients who have lung disease[41] or are elderly[42] [43].
Among health adults, vaccination may be associated with arm pain[39] and "runny nose or sore throat during the first 7 days after vaccination"[40].
Among patients with asthma, vaccination was associated with body aches.[41]
Among elderly patients, the influenza vaccine may increase arm pain.[42] [43]
Chemoprevention
Chemoprevention (chemoprophylaxis) with neuraminidase inhibitors can prevent symptomatic influenza according to a meta-analysis by the Cochrane Collaboration.[32]Zanamivir may cause bronchospasm in patients with asthma. Extended-duration (>4 weeks) chemoprevention may be effective as well.[44]
Pandemics and notable outbreaks
Spanish influenza pandemic of 1918-1920
A pandemic of Spanish Influenza, involving a highly pathogenic mutation of serotype H1N1, swept across the world in the wake of the Great War (1918-20). More people are believed to have died of the flu in the year after the war then in the Great War itself. Estimates vary but it is estimated that one third of the world's population were infected and up to 50 million people perished in this pandemic (it is possibly that fatalities world wide were as high as 100 million).[45] Some comparisons are drawn between Spanish Flu and the Black Death (Bubonic Plague) of 1347 to 1351. Estimates are that the flu killed more people in one year than plague did in four.
In the United States of America, the epidemic led to closing of schools and banning of public meetings in order to successfully reduce mortality.[46]
Asian influenza pandemic of 1957 - 1963
A/H2N2 virus was responsible for this outbreak
Hong Kong pandemic 1968-1970
This was caused by serotype A/H3N2.
References
- ↑ National Library of Medicine. "Influenza". [e]
- ↑ 2.0 2.1 Anonymous (2005)Influenza Viruses, Centers for Disease Control and Prevention
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