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__NOTOC__
{{Pneumonia}}
{{Pneumonia}}
'''Editor(s)-in-Chief:''' [[C. Michael Gibson, M.S., M.D.]] [mailto:mgibson@perfuse.org] Phone:617-632-7753; Associate Editor(s)-In-Chief:''' [[Priyamvada Singh|Priyamvada Singh, M.D.]] [mailto:psingh@perfuse.org][[Philip Marcus, M.D., M.P.H.]][mailto:pmarcus192@aol.com]
{{CMG}}; {{AE}} {{HQ}}, [[Priyamvada Singh|Priyamvada Singh, M.D.]] [mailto:psingh13579@gmail.com][[Philip Marcus, M.D., M.P.H.]][mailto:pmarcus192@aol.com]
==Overview==
==Overview==
The risk factors for pneumonia includes: smoking, age, immuno-suppression, exposure to chemicals, underlying lung disease, and exposure to chemicals.
The risk factors for pneumonia include: smoking, age>65, immuno-suppression, exposure to chemicals, and underlying lung disease.
==Risk factors==
 
====Obstruction====
==Risk Factors==
* When part of the airway ([[bronchi]]) leading to the alveoli is obstructed, the lung is not able to clear fluid when it accumulates. This can lead to infection of the fluid resulting in CAP.
====Airway Obstruction====
* When part of the airway ([[bronchi]]) leading to the alveoli is obstructed, the lung is not able to clear fluid when it accumulates. This can lead to infection of the fluid resulting in community-acquired pneumonia (CAP).
* One cause of obstruction, especially in young children, is inhalation of a foreign object such as a marble or toy. The object is lodged in the small airways and pneumonia can form in the trapped areas of lung.
* One cause of obstruction, especially in young children, is inhalation of a foreign object such as a marble or toy. The object is lodged in the small airways and pneumonia can form in the trapped areas of lung.
* Another cause of obstruction is [[lung cancer]], which can grow into the airways block the flow of air.
* Another cause of obstruction is [[lung cancer]], which can grow into the airways blocking the flow of air.
====Lung disease====
 
* Diseases such as [[emphysema]], and [[Tobacco smoking|smoking]] results in more frequent and more severe bouts of CAP.
====Lung Disease====
* [[Tobacco smoking|Smoking]], and diseases such as [[emphysema]], result in more frequent and severe bouts of CAP.
* In children, recurrent episodes of CAP may be the first clue to diseases such as [[cystic fibrosis]] or [[pulmonary sequestration]].
* In children, recurrent episodes of CAP may be the first clue to diseases such as [[cystic fibrosis]] or [[pulmonary sequestration]].
====Immune problems====
 
====Immune Compromise====
* People who have [[Immunodeficiency|immune system problems]] are more likely to get CAP.
* People who have [[Immunodeficiency|immune system problems]] are more likely to get CAP.
* Risk factors for increased mortality from community acquired pneumonia are: active [[malignancy]], immuno-suppression, neurological disease, [[congestive heart failure]], [[coronary artery disease]], and [[diabetes mellitus]]
* Risk factors for increased mortality from community acquired pneumonia are: active [[malignancy]], immuno-suppression, neurological disease, [[congestive heart failure]], [[coronary artery disease]], and [[diabetes mellitus]]
* People who have [[AIDS]] are much more likely to develop CAP. Pneumonia could be the first manifestation of an underlying undiagnosed [[HIV]]. It is thus recommended by Centers for Disease Control (CDC) for HIV screening in all patients aged 13 to 64 in a medical setting regardless of known risk factors. The American College of Physicians and HIV Medicine Association recommends to broaden screening for HIV from age 13 to 75 <ref name="pmid19047021">{{cite journal |author= |title=Summaries for patients. Screening for HIV infection in health care settings: a guidance statement from the American College of Physicians and HIV Medicine Association |journal=[[Annals of Internal Medicine]] |volume=150 |issue=2 |pages=I–44 |year=2009 |month=January |pmid=19047021 |doi= |url=http://www.annals.org/article.aspx?volume=150&page=I |accessdate=2012-09-04}}</ref>, <ref name="pmid19047022">{{cite journal |author=Qaseem A, Snow V, Shekelle P, Hopkins R, Owens DK |title=Screening for HIV in health care settings: a guidance statement from the American College of Physicians and HIV Medicine Association |journal=[[Annals of Internal Medicine]] |volume=150 |issue=2 |pages=125–31 |year=2009 |month=January |pmid=19047022 |doi= |url=http://www.annals.org/article.aspx?volume=150&page=125 |accessdate=2012-09-04}}</ref>.
* People who have [[AIDS]] are much more likely to develop CAP. Pneumonia could be the first manifestation of an underlying undiagnosed [[HIV]]. It is thus recommended by the Center for Disease Control (CDC) that all patients aged 13 to 64 in a medical setting regardless of known risk factors be screened for HIV. The American College of Physicians and HIV Medicine Association recommends expanding screening for HIV from age 13 to 75 <ref name="pmid19047021">{{cite journal |author= |title=Summaries for patients. Screening for HIV infection in health care settings: a guidance statement from the American College of Physicians and HIV Medicine Association |journal=[[Annals of Internal Medicine]] |volume=150 |issue=2 |pages=I–44 |year=2009 |month=January |pmid=19047021 |doi= |url=http://www.annals.org/article.aspx?volume=150&page=I |accessdate=2012-09-04}}</ref>, <ref name="pmid19047022">{{cite journal |author=Qaseem A, Snow V, Shekelle P, Hopkins R, Owens DK |title=Screening for HIV in health care settings: a guidance statement from the American College of Physicians and HIV Medicine Association |journal=[[Annals of Internal Medicine]] |volume=150 |issue=2 |pages=125–31 |year=2009 |month=January |pmid=19047022 |doi= |url=http://www.annals.org/article.aspx?volume=150&page=125 |accessdate=2012-09-04}}</ref>.
* Other immune problems range from severe immune deficiencies of childhood such as [[Wiskott-Aldrich syndrome]] to less severe deficiencies such as [[common variable immunodeficiency]].{{ref|Mundy}}
* Other immune problems range from severe immune deficiencies of childhood such as [[Wiskott-Aldrich syndrome]] to less severe deficiencies such as [[common variable immunodeficiency]].{{ref|Mundy}}
* Elderly are affected with increased incidence and severity of community acquired pneumonia. It is the fifth commonest cause of death among individuals who are > 65 years of age, and fourth in individuals who are 85years and more. The clinical picture in elderly could be subtle and could present only as delirium without any fever, cough or sputum. Therefore, a high index of suspicion should be kept in these group of population.
* Elderly people are affected with increased incidence and severity of community acquired pneumonia. It is the fifth most common cause of death among individuals who are > 65 years of age, and fourth in individuals who are 85 years or older. The clinical picture in elderly could be subtle and could present only as delirium without any fever, cough or sputum. Therefore, a high index of suspicion should be kept in these groups of people.
 
==Community Acquired Pneumonia==
The following are risk factors related to specific causative pathogens in community-acquired pneumonia:
 
{| style="border: 0px; font-size: 85%; margin: 3px; width:500px;" align=center
|valign=top|
|+
! style="background: #4479BA; color:#FFF;  width: 150px;" | Condition
! style="background: #4479BA; color:#FFF;  width: 350px;" | Most Common Pathogens
|-
| style="padding: 5px 5px; background: #DCDCDC;font-weight: bold" |  Alcoholism
| style="padding: 5px 5px; background: #F5F5F5;" | [[Streptococcus pneumoniae]], oral [[anaerobes]], [[Klebsiella pneumoniae]], [[Acinetobacter spp]], [[Mycobacterium tuberculosis]]
|-
| style="padding: 5px 5px; background: #DCDCDC;font-weight: bold" | COPD
| style="padding: 5px 5px; background: #F5F5F5;" |[[Haemophilus influenzae]], [[Pseudomonas aeruginosa]], [[Legionella spp]], [[S. pneumoniae]], [[Moraxella catarrhalis]], [[Chlamydophila pneumoniae]]
|-
| style="padding: 5px 5px; background: #DCDCDC;font-weight: bold" | Smoking
| style="padding: 5px 5px; background: #F5F5F5;" |[[Haemophilus influenzae]], [[Pseudomonas aeruginosa]], [[Legionella spp]], [[S. pneumoniae]], [[Moraxella catarrhalis]], [[Chlamydophila pneumoniae]]
|-
| style="padding: 5px 5px; background: #DCDCDC;font-weight: bold" | Aspiration
| style="padding: 5px 5px; background: #F5F5F5;" | Oral [[anaerobes]], [[Gram-negative]] enteric bacteria
|-
| style="padding: 5px 5px; background: #DCDCDC;font-weight: bold" | Lung Abscess
| style="padding: 5px 5px; background: #F5F5F5;" | Community-acquired [[MRSA]], [[M. tuberculosis]], oral [[anaerobes]], [[atypical mycobacteria]], endemic fungal infection
|-
| style="padding: 5px 5px; background: #DCDCDC;font-weight: bold" | Early HIV infection
| style="padding: 5px 5px; background: #F5F5F5;" | [[S. pneumoniae]], [[H. influenzae]], [[M. tuberculosis]]
|-
| style="padding: 5px 5px; background: #DCDCDC;font-weight: bold" | Late HIV infection
| style="padding: 5px 5px; background: #F5F5F5;" | [[S. pneumoniae]], [[H. influenzae]], [[M. tuberculosis]], [[Pneumocystis jirovecii]], [[Cryptococcus]], [[Histoplasma]], [[Aspergillus]], [[atypical mycobacteria]] (especially [[Mycobacterium kansasii]]), [[P.aeruginosa]]
|-
| style="padding: 5px 5px; background: #DCDCDC;font-weight: bold" | > 2 weeks of cough with whoop or vomiting
| style="padding: 5px 5px; background: #F5F5F5;" | [[Bordetella pertussis]]
|-
| style="padding: 5px 5px; background: #DCDCDC;font-weight: bold" | Structural lung disease
| style="padding: 5px 5px; background: #F5F5F5;" | [[P. aeruginosa]], [[Burkholderia cepacia]], [[S. aureus]] 
|-
| style="padding: 5px 5px; background: #DCDCDC;font-weight: bold" | IV drug use
| style="padding: 5px 5px; background: #F5F5F5;" |  [[S. aureus]], [[anaerobes]], [[M. tuberculosis]], [[S. pneumoniae]]
|-
| style="padding: 5px 5px; background: #DCDCDC;font-weight: bold" | Bioterrorism
| style="padding: 5px 5px; background: #F5F5F5;" | [[Bacillus anthracis]] ([[anthrax]]), [[Yersinia pestis]] ([[plague]]), [[Francisella tularensis]] ([[tularemia]])
|-
| style="padding: 5px 5px; background: #DCDCDC;font-weight: bold" | Endobronchial obstruction
| style="padding: 5px 5px; background: #F5F5F5;" | [[S. pneumoniae]], [[anaerobes]], [[H influenzae]], [[S. aureus]]
|-
| style="padding: 0px 5px; background: #DCDCDC;" colspan= 2|<small>Table adapted from IDSA/ATS Guidelines for CAP in Adults <ref name="MandellWunderink2007">{{cite journal|last1=Mandell|first1=L. A.|last2=Wunderink|first2=R. G.|last3=Anzueto|first3=A.|last4=Bartlett|first4=J. G.|last5=Campbell|first5=G. D.|last6=Dean|first6=N. C.|last7=Dowell|first7=S. F.|last8=File|first8=T. M.|last9=Musher|first9=D. M.|last10=Niederman|first10=M. S.|last11=Torres|first11=A.|last12=Whitney|first12=C. G.|title=Infectious Diseases Society of America/American Thoracic Society Consensus Guidelines on the Management of Community-Acquired Pneumonia in Adults|journal=Clinical Infectious Diseases|volume=44|issue=Supplement 2|year=2007|pages=S27–S72|issn=1058-4838|doi=10.1086/511159}}</ref></small>
|}
 
====Exposure to Animals====
{| style="border: 0px; font-size: 85%; margin: 3px; width:500px;" align=center
|valign=top|
|+
! style="background: #4479BA; color:#FFF;  width: 150px;" | Animals
! style="background: #4479BA; color:#FFF;  width: 350px;" | Most Common Pathogens
|-
| style="padding: 5px 5px; background: #DCDCDC;font-weight: bold" | Bat or bird droppings
| style="padding: 5px 5px; background: #F5F5F5;" | [[Histoplasma capsulatum]]
|-
| style="padding: 5px 5px; background: #DCDCDC;font-weight: bold" | Birds
| style="padding: 5px 5px; background: #F5F5F5;" | [[Chlamydophila psittaci]]
|-
| style="padding: 5px 5px; background: #DCDCDC;font-weight: bold" | Rabbits
| style="padding: 5px 5px; background: #F5F5F5;" | [[Francisella tularensis]]
|-
| style="padding: 5px 5px; background: #DCDCDC;font-weight: bold" | Farm animals or parturient cats
| style="padding: 5px 5px; background: #F5F5F5;" | [[Coxiella burnetti]] ([[Q fever]])
|-
| style="padding: 0px 5px; background: #DCDCDC;" colspan= 2|<small>Table adapted from IDSA/ATS Guidelines for CAP in Adults <ref name="MandellWunderink2007">{{cite journal|last1=Mandell|first1=L. A.|last2=Wunderink|first2=R. G.|last3=Anzueto|first3=A.|last4=Bartlett|first4=J. G.|last5=Campbell|first5=G. D.|last6=Dean|first6=N. C.|last7=Dowell|first7=S. F.|last8=File|first8=T. M.|last9=Musher|first9=D. M.|last10=Niederman|first10=M. S.|last11=Torres|first11=A.|last12=Whitney|first12=C. G.|title=Infectious Diseases Society of America/American Thoracic Society Consensus Guidelines on the Management of Community-Acquired Pneumonia in Adults|journal=Clinical Infectious Diseases|volume=44|issue=Supplement 2|year=2007|pages=S27–S72|issn=1058-4838|doi=10.1086/511159}}</ref></small>
|}
 
====Travel====
{| style="border: 0px; font-size: 85%; margin: 3px; width:500px;" align=center
|valign=top|
|+
! style="background: #4479BA; color:#FFF;  width: 150px;" | Condition
! style="background: #4479BA; color:#FFF;  width: 350px;" | Most Common Pathogens
|-
| style="padding: 5px 5px; background: #DCDCDC;font-weight: bold" | Hotel or cruise ship stay
| style="padding: 5px 5px; background: #F5F5F5;" | [[Legionella spp]]
|-
| style="padding: 5px 5px; background: #DCDCDC;font-weight: bold" | Travel to southwestern US
| style="padding: 5px 5px; background: #F5F5F5;" | [[Coccidioides spp]], [[Hantavirus]]
|-
| style="padding: 5px 5px; background: #DCDCDC;font-weight: bold" | Travel to southeast or east Asia
| style="padding: 5px 5px; background: #F5F5F5;" | [[Burkholderia pseudomallei]], [[avian influenza]], [[SARS]]
|-
| style="padding: 0px 5px; background: #DCDCDC;" colspan= 2|<small>Table adapted from IDSA/ATS Guidelines for CAP in Adults <ref name="MandellWunderink2007">{{cite journal|last1=Mandell|first1=L. A.|last2=Wunderink|first2=R. G.|last3=Anzueto|first3=A.|last4=Bartlett|first4=J. G.|last5=Campbell|first5=G. D.|last6=Dean|first6=N. C.|last7=Dowell|first7=S. F.|last8=File|first8=T. M.|last9=Musher|first9=D. M.|last10=Niederman|first10=M. S.|last11=Torres|first11=A.|last12=Whitney|first12=C. G.|title=Infectious Diseases Society of America/American Thoracic Society Consensus Guidelines on the Management of Community-Acquired Pneumonia in Adults|journal=Clinical Infectious Diseases|volume=44|issue=Supplement 2|year=2007|pages=S27–S72|issn=1058-4838|doi=10.1086/511159}}</ref></small>
|}
 
====Obstruction====
 
* Airway obstruction may cause fluid accumulation in the lungs and result in CAP if the fluids become infected.
 
* One cause of obstruction, especially in young children, is inhalation of a foreign object such as a marble or toy. The object is lodged in the small airways and [[pneumonia]] can form in the trapped areas of lung.
 
* Another cause of obstruction is [[lung cancer]], which can grow into the airways blocking the flow of air.
 
====Lung Disease====
 
* [[Tobacco smoking|Smoking]], and diseases such as [[emphysema]], result in more frequent and severe bouts of CAP.
 
* In children, recurrent episodes of CAP may be the first clue to diseases such as [[cystic fibrosis]] or [[pulmonary sequestration]].
 
* [[Hypoxemia]]
 
* [[Pulmonary edema]]
 
* [[Chronic obstructive pulmonary disease|Chronic obstructive pulmonary disease (COPD)]]
 
* Previous episode of [[pneumonia]] or [[chronic bronchitis]]
 
====Immune Problems====
 
* People who have [[Immunodeficiency|immune disorders]] are more likely to acquire CAP.
 
* Risk factors for increased mortality from community-acquired pneumonia are: active [[malignancy]], immunosuppression, neurological disease, [[congestive heart failure]], [[coronary artery disease]], and [[diabetes mellitus]].
 
* People who have [[AIDS]] are much more likely to develop CAP. Pneumonia could be the first manifestation of an underlying undiagnosed [[HIV]]. It is, thus, recommended by the Center for Disease Control (CDC) that all patients aged 13 to 64 in a medical setting, regardless of known risk factors, be screened for HIV. The American College of Physicians and HIV Medicine Association recommends expanding screening for [[HIV]] from age 13 to 75 <ref name="pmid19047021">{{cite journal |author= |title=Summaries for patients. Screening for HIV infection in health care settings: a guidance statement from the American College of Physicians and HIV Medicine Association |journal=[[Annals of Internal Medicine]] |volume=150 |issue=2 |pages=I–44 |year=2009 |month=January |pmid=19047021 |doi= |url=http://www.annals.org/article.aspx?volume=150&page=I |accessdate=2012-09-04}}</ref>, <ref name="pmid19047022">{{cite journal |author=Qaseem A, Snow V, Shekelle P, Hopkins R, Owens DK |title=Screening for HIV in health care settings: a guidance statement from the American College of Physicians and HIV Medicine Association |journal=[[Annals of Internal Medicine]] |volume=150 |issue=2 |pages=125–31 |year=2009 |month=January |pmid=19047022 |doi= |url=http://www.annals.org/article.aspx?volume=150&page=125 |accessdate=2012-09-04}}</ref>.
 
* Other immune problems range from severe immune deficiencies from childhood, such as [[Wiskott-Aldrich syndrome]], to less severe deficiencies, such as [[common variable immunodeficiency]].{{ref|Mundy}}
 
* Elderly people are affected with increased incidence and severity of community-acquired pneumonia. It is the fifth most common cause of death amongst individuals who are greater than 65 years of age, and it is the fourth most common cause of death in individuals who are 85 years or older. The clinical picture in elderly could be subtle and it could be present only as [[delirium]] without any [[fever]], [[cough]] or [[sputum]]. Therefore, a high index of suspicion should be kept in these groups of people.
 
* [[Immotile cilia syndrome]]
* [[Kartagener's syndrome]] (ciliary dysfunction, [[situs inversus]], [[sinusitis]], [[bronchiectasis]])
* [[Young's syndrome]] ([[azoospermia]], [[sinusitis]], [[pneumonia]])
 
====Other Risk Factors====
 
A few other conditions may lead to [[pneumonia]] due to altered pulmonary defense mechanisms.<ref name="Almirall-1999">{{Cite journal  | last1 = Almirall | first1 = J. | last2 = Bolíbar | first2 = I. | last3 = Balanzó | first3 = X. | last4 = González | first4 = CA. | title = Risk factors for community-acquired pneumonia in adults: a population-based case-control study. | journal = Eur Respir J | volume = 13 | issue = 2 | pages = 349-55 | month = Feb | year = 1999 | doi =  | PMID = 10065680 }}</ref>
 
* [[Dysphagia]] due to esophageal lesions and motility problems
 
* [[HIV]] infection (especially for [[pneumococcal]] pneumonia)
 
====Drugs====
 
=====Acid-Suppressing Drugs=====
 
* Usage of [[H2 blocker]]s, [[proton pump inhibitor]]s, and [[antacid]]s may increase the pH and, as a result, may increase the risk of [[pneumonia]].<ref name="Laheij-2004">{{Cite journal  | last1 = Laheij | first1 = RJ. | last2 = Sturkenboom | first2 = MC. | last3 = Hassing | first3 = RJ. | last4 = Dieleman | first4 = J. | last5 = Stricker | first5 = BH. | last6 = Jansen | first6 = JB. | title = Risk of community-acquired pneumonia and use of gastric acid-suppressive drugs. | journal = JAMA | volume = 292 | issue = 16 | pages = 1955-60 | month = Oct | year = 2004 | doi = 10.1001/jama.292.16.1955 | PMID = 15507580 }}</ref><ref name="Gulmez-2007">{{Cite journal  | last1 = Gulmez | first1 = SE. | last2 = Holm | first2 = A. | last3 = Frederiksen | first3 = H. | last4 = Jensen | first4 = TG. | last5 = Pedersen | first5 = C. | last6 = Hallas | first6 = J. | title = Use of proton pump inhibitors and the risk of community-acquired pneumonia: a population-based case-control study. | journal = Arch Intern Med | volume = 167 | issue = 9 | pages = 950-5 | month = May | year = 2007 | doi = 10.1001/archinte.167.9.950 | PMID = 17502537 }}</ref><ref name="Hermos-2012">{{Cite journal  | last1 = Hermos | first1 = JA. | last2 = Young | first2 = MM. | last3 = Fonda | first3 = JR. | last4 = Gagnon | first4 = DR. | last5 = Fiore | first5 = LD. | last6 = Lawler | first6 = EV. | title = Risk of community-acquired pneumonia in veteran patients to whom proton pump inhibitors were dispensed. | journal = Clin Infect Dis | volume = 54 | issue = 1 | pages = 33-42 | month = Jan | year = 2012 | doi = 10.1093/cid/cir767 | PMID = 22100573 }}</ref>
 
* A similiar study showed increase risk of pneumonia after starting [[PPI]], especially within the first 48 hours.<ref name="Laheij-2004">{{Cite journal  | last1 = Laheij | first1 = RJ. | last2 = Sturkenboom | first2 = MC. | last3 = Hassing | first3 = RJ. | last4 = Dieleman | first4 = J. | last5 = Stricker | first5 = BH. | last6 = Jansen | first6 = JB. | title = Risk of community-acquired pneumonia and use of gastric acid-suppressive drugs. | journal = JAMA | volume = 292 | issue = 16 | pages = 1955-60 | month = Oct | year = 2004 | doi = 10.1001/jama.292.16.1955 | PMID = 15507580 }}</ref><ref name="Gulmez-2007">{{Cite journal  | last1 = Gulmez | first1 = SE. | last2 = Holm | first2 = A. | last3 = Frederiksen | first3 = H. | last4 = Jensen | first4 = TG. | last5 = Pedersen | first5 = C. | last6 = Hallas | first6 = J. | title = Use of proton pump inhibitors and the risk of community-acquired pneumonia: a population-based case-control study. | journal = Arch Intern Med | volume = 167 | issue = 9 | pages = 950-5 | month = May | year = 2007 | doi = 10.1001/archinte.167.9.950 | PMID = 17502537 }}</ref><ref name="Hermos-2012">{{Cite journal  | last1 = Hermos | first1 = JA. | last2 = Young | first2 = MM. | last3 = Fonda | first3 = JR. | last4 = Gagnon | first4 = DR. | last5 = Fiore | first5 = LD. | last6 = Lawler | first6 = EV. | title = Risk of community-acquired pneumonia in veteran patients to whom proton pump inhibitors were dispensed. | journal = Clin Infect Dis | volume = 54 | issue = 1 | pages = 33-42 | month = Jan | year = 2012 | doi = 10.1093/cid/cir767 | PMID = 22100573 }}</ref> However, the association between [[PPI]] and [[CAP]] may be cofounded.<ref name="Jena-2013">{{Cite journal  | last1 = Jena | first1 = AB. | last2 = Sun | first2 = E. | last3 = Goldman | first3 = DP. | title = Confounding in the association of proton pump inhibitor use with risk of community-acquired pneumonia. | journal = J Gen Intern Med | volume = 28 | issue = 2 | pages = 223-30 | month = Feb | year = 2013 | doi = 10.1007/s11606-012-2211-5 | PMID = 22956446 }}</ref>
 
======Antipsychotic Drugs======
 
* A case control study has shown a significant correlation between the use of [[antipsychotic]] drugs and community-acquired pneumonia. A 60 percent increase in the rate of [[pneumonia]] can be seen in elderly patients who utilize antipsychotic medications.<ref name="Knol-2008">{{Cite journal  | last1 = Knol | first1 = W. | last2 = van Marum | first2 = RJ. | last3 = Jansen | first3 = PA. | last4 = Souverein | first4 = PC. | last5 = Schobben | first5 = AF. | last6 = Egberts | first6 = AC. | title = Antipsychotic drug use and risk of pneumonia in elderly people. | journal = J Am Geriatr Soc | volume = 56 | issue = 4 | pages = 661-6 | month = Apr | year = 2008 | doi = 10.1111/j.1532-5415.2007.01625.x | PMID = 18266664 }}</ref>
 
* The use of atypical antipsychotics was associated with an increases risk of community-acquired pneumonia.
 
======ACE Inhibitors======
 
* A randomized trial has shown that [[ACE inhibitor]]s reduce the risk of [[pneumonia]].<ref name="Caldeira-2012">{{Cite journal  | last1 = Caldeira | first1 = D. | last2 = Alarcão | first2 = J. | last3 = Vaz-Carneiro | first3 = A. | last4 = Costa | first4 = J. | title = Risk of pneumonia associated with use of angiotensin converting enzyme inhibitors and angiotensin receptor blockers: systematic review and meta-analysis. | journal = BMJ | volume = 345 | issue =  | pages = e4260 | month =  | year = 2012 | doi =  | PMID = 22786934 }}</ref>
 
==Hospital Acquired Pneumonia==
{| style="border: 0px; font-size: 85%; margin: 3px; width:400px;" align=center
|valign=top|
|+
! style="background: #4479BA; color:#FFF; " |  Major risk factors for hospital-acquired pneumonia
|-
| style="padding: 5px 5px; background: #DCDCDC;" |
*Primary admitting diagnosis of burns, trauma, or disease of the CNS
|-
| style="padding: 5px 5px; background: #F5F5F5;" |
*Thoraco-abdominal surgery
 
|-
| style="padding: 5px 5px; background: #DCDCDC;" |
*Depressed level of consciousness
 
|-
| style="padding: 5px 5px; background: #F5F5F5;" |
*Prior episode of a large-volume aspiration
 
|-
| style="padding: 5px 5px; background: #DCDCDC;" |
*Underlying chronic lung disease
|-
| style="padding: 5px 5px; background: #F5F5F5;" |
*>70 years of age
|-
| style="padding: 5px 5px; background: #DCDCDC;" |
*Fall-winter season
|-
| style="padding: 5px 5px; background: #F5F5F5;" |
*24-hour ventilator-circuit changes
 
|-
| style="padding: 5px 5px; background: #DCDCDC;" |
*Stress-bleeding prophylaxis with cimetidine with or without antacid
|-
| style="padding: 5px 5px; background: #F5F5F5;" |
*Administration of antimicrobial agents
|-
| style="padding: 5px 5px; background: #DCDCDC;" |
*Presence of a nasogastric tube
|-
| style="padding: 5px 5px; background: #F5F5F5;" |
*Severe trauma
 
|-
| style="padding: 5px 5px; background: #DCDCDC;" |
*Recent bronchoscopy
|-
| style="padding: 5px 5px; background: #F5F5F5;" |<Small>'''Table adapted from CDC<ref> {{cite web|url=http://www.cdc.gov/hicpac/pdf/guidelines/HApneu2003guidelines.pdf |title=CDC GUIDELINES FOR PREVENTING HEALTH-CARE-ASSOCIATED PNEUMONIA, 2003}}</ref></small>'''
|}
 
The following are major points for risk factors of adults with hospital-acquired, ventilator-associated, and healthcare-associated pneumonia:<ref name="pmid15699079">{{cite journal |author= |title=Guidelines for the management of adults with hospital-acquired, ventilator-associated, and healthcare-associated pneumonia |journal=[[American Journal of Respiratory and Critical Care Medicine]] |volume=171 |issue=4 |pages=388–416 |year=2005 |month=February |pmid=15699079 |doi=10.1164/rccm.200405-644ST |url=http://ajrccm.atsjournals.org/cgi/pmidlookup?view=long&pmid=15699079 |accessdate=2012-09-13}}</ref>
 
{{cquote|
===Major Points and Recommendations for Modifiable Risk Factors===                                         
====General Prophylaxis====
 
* Effective infection control measures: staff education, compliance with alcohol-based hand disinfection, and isolation to reduce        cross-infection with MDR pathogens should be used routinely (Level I).
 
* Surveillance of ICU infections, to identify and quantify endemic and new MDR pathogens, and preparation of timely data for            infection control and to guide appropriate, antimicrobial therapy in patients with suspected HAP or other nosocomial infections, are recommended (Level II).
===Intubation and Mechanical Ventilation===
* [[Intubation]] and reintubation should be avoided, if possible, as it increases the risk of VAP (Level I).
 
* Noninvasive ventilation should be used whenever possible in selected patients with respiratory failure (Level I).
 
* Orotracheal intubation and orogastric tubes are preferred over nasotracheal intubation and nasogastric tubes to prevent nosocomial    [[sinusitis]] and to reduce the risk of VAP, although direct causality has not been proved (Level II).
 
* Continuous aspiration of subglottic secretions can reduce the risk of early-onset VAP, and should be used, if available (Level I)
 
* The endotracheal tube cuff pressure should be maintained at greater than 20 cm H2O to prevent leakage of bacterial pathogens around the cuff into the lower respiratory tract.
 
* Contaminated condensate should be carefully emptied from ventilator circuits and condensate should be prevented from entering      either the [[endotracheal tube]] or in-line medication nebulizers (Level II).
 
* Passive humidifiers or heat–moisture exchangers decrease ventilator circuit colonization, but have not consistently reduced the incidence of VAP, and thus they cannot be regarded as a [[pneumonia]] prevention tool (Level I).
 
* Reduced duration of intubation and [[mechanical ventilation]] may prevent VAP and can be achieved by protocols to improve the use of sedation and to accelerate weaning (Level II).
 
* Maintaining adequate staffing levels in the ICU can reduce length of stay, improve infection control practices, and reduce duration of mechanical ventilation (Level II).
====Aspiration, Body Position, and Enteral Feeding====
 
* Patients should be kept in the semirecumbent position (30–45°) rather than supine to prevent aspiration, especially when receiving    enteral feeding (Level I).
 
* Enteral nutrition is preferred over parenteral nutrition to reduce the risk of complications related to central intravenous catheters and to prevent reflux villous atrophy of the intestinal mucosa that may increase the risk of bacterial translocation (Level I).
===Modulation of Colonization: Oral Antiseptics and Antibiotics===
 
* Routine prophylaxis of HAP with oral antibiotics (selective decontamination of the digestive tract or SDD), with or without systemic antibiotics, reduces the incidence of ICU-acquired VAP, has helped contain outbreaks of MDR bacteria (Level I), but is not recommended for routine use, especially in patients who may be colonized with MDR pathogens (Level II).
 
* Prior administration of systemic antibiotics has reduced the risk of nosocomial pneumonia in some patient groups, but if a history of prior administration is present at the time of onset of infection, there should be increased suspicion of infection with MDR pathogens (Level II).
 
* Prophylactic administration of systemic antibiotics for 24 hours at the time of emergent intubation has been demonstrated to prevent ICU-acquired HAP in patients with closed head injury in one study, but its routine use is not recommended until more data become available (Level I).
 
* Modulation of oropharyngeal colonization by the use of oral [[chlorhexidine]] has prevented ICU-acquired HAP in selected patient populations such as those undergoing coronary bypass grafting, but its routine use is not recommended until more data become available (Level I).
 
* Use daily interruption or lightening of sedation to avoid constant heavy sedation and try to avoid paralytic agents, both of which can depress cough and thereby increase the risk of HAP (Level II).
 
* Stress bleeding prophylaxis, transfusion, and [[hyperglycemia]].
 
* Comparative data from randomized trials suggest a trend toward reduced VAP with [[sucralfate]], but there is a slightly higher rate of clinically significant gastric bleeding, compared with H2 antagonists. If needed, stress bleeding prophylaxis with either H2 antagonists or sucralfate is acceptable (Level I).
 
* Transfusion of red blood cell and other allogeneic blood products should follow a restricted transfusion trigger policy; leukocyte-depleted red blood cell transfusions can help to reduce HAP in selected patient populations (Level I).
 
* Intensive [[insulin]] therapy is recommended to maintain serum glucose levels between 80 and 110 mg/dl in ICU patients to reduce nosocomial blood stream infections, duration of mechanical ventilation, ICU stay, morbidity, and mortality (Level I).
}}
'''For Level of evidence and classes click [[ACC AHA Guidelines Classification Scheme|here]].'''


==References==
==References==
{{reflist|2}}
{{reflist|2}}
{{WH}}
{{WS}}


[[Category:Disease]]
[[Category:Pneumonia]]
[[Category:Pulmonology]]
[[Category:Pulmonology]]
[[Category:Infectious disease]]
[[Category:Pneumonia|Pneumonia]]
[[Category:Emergency medicine]]
[[Category:Emergency medicine]]
 
[[Category:Pediatrics]]
{{WH}}
[[Category:Disease]]
{{WS}}

Latest revision as of 23:45, 29 July 2020

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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief: Hamid Qazi, MD, BSc [2], Priyamvada Singh, M.D. [3]Philip Marcus, M.D., M.P.H.[4]

Overview

The risk factors for pneumonia include: smoking, age>65, immuno-suppression, exposure to chemicals, and underlying lung disease.

Risk Factors

Airway Obstruction

  • When part of the airway (bronchi) leading to the alveoli is obstructed, the lung is not able to clear fluid when it accumulates. This can lead to infection of the fluid resulting in community-acquired pneumonia (CAP).
  • One cause of obstruction, especially in young children, is inhalation of a foreign object such as a marble or toy. The object is lodged in the small airways and pneumonia can form in the trapped areas of lung.
  • Another cause of obstruction is lung cancer, which can grow into the airways blocking the flow of air.

Lung Disease

Immune Compromise

  • People who have immune system problems are more likely to get CAP.
  • Risk factors for increased mortality from community acquired pneumonia are: active malignancy, immuno-suppression, neurological disease, congestive heart failure, coronary artery disease, and diabetes mellitus
  • People who have AIDS are much more likely to develop CAP. Pneumonia could be the first manifestation of an underlying undiagnosed HIV. It is thus recommended by the Center for Disease Control (CDC) that all patients aged 13 to 64 in a medical setting regardless of known risk factors be screened for HIV. The American College of Physicians and HIV Medicine Association recommends expanding screening for HIV from age 13 to 75 [1], [2].
  • Other immune problems range from severe immune deficiencies of childhood such as Wiskott-Aldrich syndrome to less severe deficiencies such as common variable immunodeficiency.[5]
  • Elderly people are affected with increased incidence and severity of community acquired pneumonia. It is the fifth most common cause of death among individuals who are > 65 years of age, and fourth in individuals who are 85 years or older. The clinical picture in elderly could be subtle and could present only as delirium without any fever, cough or sputum. Therefore, a high index of suspicion should be kept in these groups of people.

Community Acquired Pneumonia

The following are risk factors related to specific causative pathogens in community-acquired pneumonia:

Condition Most Common Pathogens
Alcoholism Streptococcus pneumoniae, oral anaerobes, Klebsiella pneumoniae, Acinetobacter spp, Mycobacterium tuberculosis
COPD Haemophilus influenzae, Pseudomonas aeruginosa, Legionella spp, S. pneumoniae, Moraxella catarrhalis, Chlamydophila pneumoniae
Smoking Haemophilus influenzae, Pseudomonas aeruginosa, Legionella spp, S. pneumoniae, Moraxella catarrhalis, Chlamydophila pneumoniae
Aspiration Oral anaerobes, Gram-negative enteric bacteria
Lung Abscess Community-acquired MRSA, M. tuberculosis, oral anaerobes, atypical mycobacteria, endemic fungal infection
Early HIV infection S. pneumoniae, H. influenzae, M. tuberculosis
Late HIV infection S. pneumoniae, H. influenzae, M. tuberculosis, Pneumocystis jirovecii, Cryptococcus, Histoplasma, Aspergillus, atypical mycobacteria (especially Mycobacterium kansasii), P.aeruginosa
> 2 weeks of cough with whoop or vomiting Bordetella pertussis
Structural lung disease P. aeruginosa, Burkholderia cepacia, S. aureus
IV drug use S. aureus, anaerobes, M. tuberculosis, S. pneumoniae
Bioterrorism Bacillus anthracis (anthrax), Yersinia pestis (plague), Francisella tularensis (tularemia)
Endobronchial obstruction S. pneumoniae, anaerobes, H influenzae, S. aureus
Table adapted from IDSA/ATS Guidelines for CAP in Adults [3]

Exposure to Animals

Animals Most Common Pathogens
Bat or bird droppings Histoplasma capsulatum
Birds Chlamydophila psittaci
Rabbits Francisella tularensis
Farm animals or parturient cats Coxiella burnetti (Q fever)
Table adapted from IDSA/ATS Guidelines for CAP in Adults [3]

Travel

Condition Most Common Pathogens
Hotel or cruise ship stay Legionella spp
Travel to southwestern US Coccidioides spp, Hantavirus
Travel to southeast or east Asia Burkholderia pseudomallei, avian influenza, SARS
Table adapted from IDSA/ATS Guidelines for CAP in Adults [3]

Obstruction

  • Airway obstruction may cause fluid accumulation in the lungs and result in CAP if the fluids become infected.
  • One cause of obstruction, especially in young children, is inhalation of a foreign object such as a marble or toy. The object is lodged in the small airways and pneumonia can form in the trapped areas of lung.
  • Another cause of obstruction is lung cancer, which can grow into the airways blocking the flow of air.

Lung Disease

  • Smoking, and diseases such as emphysema, result in more frequent and severe bouts of CAP.

Immune Problems

  • People who have AIDS are much more likely to develop CAP. Pneumonia could be the first manifestation of an underlying undiagnosed HIV. It is, thus, recommended by the Center for Disease Control (CDC) that all patients aged 13 to 64 in a medical setting, regardless of known risk factors, be screened for HIV. The American College of Physicians and HIV Medicine Association recommends expanding screening for HIV from age 13 to 75 [1], [2].
  • Elderly people are affected with increased incidence and severity of community-acquired pneumonia. It is the fifth most common cause of death amongst individuals who are greater than 65 years of age, and it is the fourth most common cause of death in individuals who are 85 years or older. The clinical picture in elderly could be subtle and it could be present only as delirium without any fever, cough or sputum. Therefore, a high index of suspicion should be kept in these groups of people.

Other Risk Factors

A few other conditions may lead to pneumonia due to altered pulmonary defense mechanisms.[4]

  • Dysphagia due to esophageal lesions and motility problems

Drugs

Acid-Suppressing Drugs
  • A similiar study showed increase risk of pneumonia after starting PPI, especially within the first 48 hours.[5][6][7] However, the association between PPI and CAP may be cofounded.[8]
Antipsychotic Drugs
  • A case control study has shown a significant correlation between the use of antipsychotic drugs and community-acquired pneumonia. A 60 percent increase in the rate of pneumonia can be seen in elderly patients who utilize antipsychotic medications.[9]
  • The use of atypical antipsychotics was associated with an increases risk of community-acquired pneumonia.
ACE Inhibitors

Hospital Acquired Pneumonia

Major risk factors for hospital-acquired pneumonia
  • Primary admitting diagnosis of burns, trauma, or disease of the CNS
  • Thoraco-abdominal surgery
  • Depressed level of consciousness
  • Prior episode of a large-volume aspiration
  • Underlying chronic lung disease
  • >70 years of age
  • Fall-winter season
  • 24-hour ventilator-circuit changes
  • Stress-bleeding prophylaxis with cimetidine with or without antacid
  • Administration of antimicrobial agents
  • Presence of a nasogastric tube
  • Severe trauma
  • Recent bronchoscopy
Table adapted from CDC[11]

The following are major points for risk factors of adults with hospital-acquired, ventilator-associated, and healthcare-associated pneumonia:[12]

Major Points and Recommendations for Modifiable Risk Factors

General Prophylaxis

  • Effective infection control measures: staff education, compliance with alcohol-based hand disinfection, and isolation to reduce cross-infection with MDR pathogens should be used routinely (Level I).
  • Surveillance of ICU infections, to identify and quantify endemic and new MDR pathogens, and preparation of timely data for infection control and to guide appropriate, antimicrobial therapy in patients with suspected HAP or other nosocomial infections, are recommended (Level II).

Intubation and Mechanical Ventilation

  • Intubation and reintubation should be avoided, if possible, as it increases the risk of VAP (Level I).
  • Noninvasive ventilation should be used whenever possible in selected patients with respiratory failure (Level I).
  • Orotracheal intubation and orogastric tubes are preferred over nasotracheal intubation and nasogastric tubes to prevent nosocomial sinusitis and to reduce the risk of VAP, although direct causality has not been proved (Level II).
  • Continuous aspiration of subglottic secretions can reduce the risk of early-onset VAP, and should be used, if available (Level I)
  • The endotracheal tube cuff pressure should be maintained at greater than 20 cm H2O to prevent leakage of bacterial pathogens around the cuff into the lower respiratory tract.
  • Contaminated condensate should be carefully emptied from ventilator circuits and condensate should be prevented from entering either the endotracheal tube or in-line medication nebulizers (Level II).
  • Passive humidifiers or heat–moisture exchangers decrease ventilator circuit colonization, but have not consistently reduced the incidence of VAP, and thus they cannot be regarded as a pneumonia prevention tool (Level I).
  • Reduced duration of intubation and mechanical ventilation may prevent VAP and can be achieved by protocols to improve the use of sedation and to accelerate weaning (Level II).
  • Maintaining adequate staffing levels in the ICU can reduce length of stay, improve infection control practices, and reduce duration of mechanical ventilation (Level II).

Aspiration, Body Position, and Enteral Feeding

  • Patients should be kept in the semirecumbent position (30–45°) rather than supine to prevent aspiration, especially when receiving enteral feeding (Level I).
  • Enteral nutrition is preferred over parenteral nutrition to reduce the risk of complications related to central intravenous catheters and to prevent reflux villous atrophy of the intestinal mucosa that may increase the risk of bacterial translocation (Level I).

Modulation of Colonization: Oral Antiseptics and Antibiotics

  • Routine prophylaxis of HAP with oral antibiotics (selective decontamination of the digestive tract or SDD), with or without systemic antibiotics, reduces the incidence of ICU-acquired VAP, has helped contain outbreaks of MDR bacteria (Level I), but is not recommended for routine use, especially in patients who may be colonized with MDR pathogens (Level II).
  • Prior administration of systemic antibiotics has reduced the risk of nosocomial pneumonia in some patient groups, but if a history of prior administration is present at the time of onset of infection, there should be increased suspicion of infection with MDR pathogens (Level II).
  • Prophylactic administration of systemic antibiotics for 24 hours at the time of emergent intubation has been demonstrated to prevent ICU-acquired HAP in patients with closed head injury in one study, but its routine use is not recommended until more data become available (Level I).
  • Modulation of oropharyngeal colonization by the use of oral chlorhexidine has prevented ICU-acquired HAP in selected patient populations such as those undergoing coronary bypass grafting, but its routine use is not recommended until more data become available (Level I).
  • Use daily interruption or lightening of sedation to avoid constant heavy sedation and try to avoid paralytic agents, both of which can depress cough and thereby increase the risk of HAP (Level II).
  • Comparative data from randomized trials suggest a trend toward reduced VAP with sucralfate, but there is a slightly higher rate of clinically significant gastric bleeding, compared with H2 antagonists. If needed, stress bleeding prophylaxis with either H2 antagonists or sucralfate is acceptable (Level I).
  • Transfusion of red blood cell and other allogeneic blood products should follow a restricted transfusion trigger policy; leukocyte-depleted red blood cell transfusions can help to reduce HAP in selected patient populations (Level I).
  • Intensive insulin therapy is recommended to maintain serum glucose levels between 80 and 110 mg/dl in ICU patients to reduce nosocomial blood stream infections, duration of mechanical ventilation, ICU stay, morbidity, and mortality (Level I).

For Level of evidence and classes click here.

References

  1. 1.0 1.1 "Summaries for patients. Screening for HIV infection in health care settings: a guidance statement from the American College of Physicians and HIV Medicine Association". Annals of Internal Medicine. 150 (2): I–44. 2009. PMID 19047021. Retrieved 2012-09-04. Unknown parameter |month= ignored (help)
  2. 2.0 2.1 Qaseem A, Snow V, Shekelle P, Hopkins R, Owens DK (2009). "Screening for HIV in health care settings: a guidance statement from the American College of Physicians and HIV Medicine Association". Annals of Internal Medicine. 150 (2): 125–31. PMID 19047022. Retrieved 2012-09-04. Unknown parameter |month= ignored (help)
  3. 3.0 3.1 3.2 Mandell, L. A.; Wunderink, R. G.; Anzueto, A.; Bartlett, J. G.; Campbell, G. D.; Dean, N. C.; Dowell, S. F.; File, T. M.; Musher, D. M.; Niederman, M. S.; Torres, A.; Whitney, C. G. (2007). "Infectious Diseases Society of America/American Thoracic Society Consensus Guidelines on the Management of Community-Acquired Pneumonia in Adults". Clinical Infectious Diseases. 44 (Supplement 2): S27–S72. doi:10.1086/511159. ISSN 1058-4838.
  4. Almirall, J.; Bolíbar, I.; Balanzó, X.; González, CA. (1999). "Risk factors for community-acquired pneumonia in adults: a population-based case-control study". Eur Respir J. 13 (2): 349–55. PMID 10065680. Unknown parameter |month= ignored (help)
  5. 5.0 5.1 Laheij, RJ.; Sturkenboom, MC.; Hassing, RJ.; Dieleman, J.; Stricker, BH.; Jansen, JB. (2004). "Risk of community-acquired pneumonia and use of gastric acid-suppressive drugs". JAMA. 292 (16): 1955–60. doi:10.1001/jama.292.16.1955. PMID 15507580. Unknown parameter |month= ignored (help)
  6. 6.0 6.1 Gulmez, SE.; Holm, A.; Frederiksen, H.; Jensen, TG.; Pedersen, C.; Hallas, J. (2007). "Use of proton pump inhibitors and the risk of community-acquired pneumonia: a population-based case-control study". Arch Intern Med. 167 (9): 950–5. doi:10.1001/archinte.167.9.950. PMID 17502537. Unknown parameter |month= ignored (help)
  7. 7.0 7.1 Hermos, JA.; Young, MM.; Fonda, JR.; Gagnon, DR.; Fiore, LD.; Lawler, EV. (2012). "Risk of community-acquired pneumonia in veteran patients to whom proton pump inhibitors were dispensed". Clin Infect Dis. 54 (1): 33–42. doi:10.1093/cid/cir767. PMID 22100573. Unknown parameter |month= ignored (help)
  8. Jena, AB.; Sun, E.; Goldman, DP. (2013). "Confounding in the association of proton pump inhibitor use with risk of community-acquired pneumonia". J Gen Intern Med. 28 (2): 223–30. doi:10.1007/s11606-012-2211-5. PMID 22956446. Unknown parameter |month= ignored (help)
  9. Knol, W.; van Marum, RJ.; Jansen, PA.; Souverein, PC.; Schobben, AF.; Egberts, AC. (2008). "Antipsychotic drug use and risk of pneumonia in elderly people". J Am Geriatr Soc. 56 (4): 661–6. doi:10.1111/j.1532-5415.2007.01625.x. PMID 18266664. Unknown parameter |month= ignored (help)
  10. Caldeira, D.; Alarcão, J.; Vaz-Carneiro, A.; Costa, J. (2012). "Risk of pneumonia associated with use of angiotensin converting enzyme inhibitors and angiotensin receptor blockers: systematic review and meta-analysis". BMJ. 345: e4260. PMID 22786934.
  11. "CDC GUIDELINES FOR PREVENTING HEALTH-CARE-ASSOCIATED PNEUMONIA, 2003" (PDF).
  12. "Guidelines for the management of adults with hospital-acquired, ventilator-associated, and healthcare-associated pneumonia". American Journal of Respiratory and Critical Care Medicine. 171 (4): 388–416. 2005. doi:10.1164/rccm.200405-644ST. PMID 15699079. Retrieved 2012-09-13. Unknown parameter |month= ignored (help)

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