Distribution of 13-Valent pneumococcal conjugate vaccine serotype streptococcus pneumoniae in adults 50 Years and Older presenting with community-acquired pneumonia in Israel

Background: Community acquired pneumonia (CAP) is a major cause of morbidity and mortality worldwide, and is a leading cause of hospitalization in previously healthy individuals without predisposing risk factors or comorbidities. In this study we determined PCV13 serotype distribution in adults aged...

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Published inHuman vaccines & immunotherapeutics Vol. 14; no. 10; pp. 2527 - 2532
Main Authors Regev-Yochay, Gili, Chowers, Michal, Chazan, Bibiana, Gonzalez, Elisa, Gray, Sharon, Zhang, Zhou, Pride, Michael
Format Journal Article
LanguageEnglish
Published United States Taylor & Francis 03.10.2018
Taylor & Francis Group
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Online AccessGet full text
ISSN2164-5515
2164-554X
2164-554X
DOI10.1080/21645515.2018.1475811

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Abstract Background: Community acquired pneumonia (CAP) is a major cause of morbidity and mortality worldwide, and is a leading cause of hospitalization in previously healthy individuals without predisposing risk factors or comorbidities. In this study we determined PCV13 serotype distribution in adults aged ≥50 years with radiographically confirmed CAP in Israel. Methods: Subjects aged ≥50 years were enrolled from one of three hospitals (Emek Medical Center, Meir Medical Center and Sheba Medical Center) from March 2014 to July 2015. Information was collected on subject demographics, comorbidities, risk factors, and pneumococcal vaccine immunization status. Subjects presented with suspected CAP supported by radiographic evidence, and provided a urine sample and informed consent. Subjects without radiographic confirmation of CAP or who received PPSV23 within 30 days of study enrollment were excluded from the final analysis. Serotype distribution was performed using the urinary antigen detection (UAD) assay and/or microbiological culture. Results: Overall, 498 subjects with radiographically confirmed CAP were enrolled in the study. Eighty subjects (16.1%) were positive for any S. pneumoniae serotype by ≥1 assay, and 38 (7.6%) were positive for PCV13 serotypes via the UAD. The overall 30-day mortality rate was 1.2%, though S. pneumoniae was not isolated from any case leading to death. Conclusion: Despite six years of high pneumococcal immunization coverage in children in Israel, we have shown that 7.6% of CAP cases among adults in Israel remain related to PCV13 serotypes; and that the burden of PCV13 may be as high as 47% of observed pneumococcal CAP.
AbstractList Community acquired pneumonia (CAP) is a major cause of morbidity and mortality worldwide, and is a leading cause of hospitalization in previously healthy individuals without predisposing risk factors or comorbidities. In this study we determined PCV13 serotype distribution in adults aged ≥50 years with radiographically confirmed CAP in Israel.BACKGROUNDCommunity acquired pneumonia (CAP) is a major cause of morbidity and mortality worldwide, and is a leading cause of hospitalization in previously healthy individuals without predisposing risk factors or comorbidities. In this study we determined PCV13 serotype distribution in adults aged ≥50 years with radiographically confirmed CAP in Israel.Subjects aged ≥50 years were enrolled from one of three hospitals (Emek Medical Center, Meir Medical Center and Sheba Medical Center) from March 2014 to July 2015. Information was collected on subject demographics, comorbidities, risk factors, and pneumococcal vaccine immunization status. Subjects presented with suspected CAP supported by radiographic evidence, and provided a urine sample and informed consent. Subjects without radiographic confirmation of CAP or who received PPSV23 within 30 days of study enrollment were excluded from the final analysis. Serotype distribution was performed using the urinary antigen detection (UAD) assay and/or microbiological culture.METHODSSubjects aged ≥50 years were enrolled from one of three hospitals (Emek Medical Center, Meir Medical Center and Sheba Medical Center) from March 2014 to July 2015. Information was collected on subject demographics, comorbidities, risk factors, and pneumococcal vaccine immunization status. Subjects presented with suspected CAP supported by radiographic evidence, and provided a urine sample and informed consent. Subjects without radiographic confirmation of CAP or who received PPSV23 within 30 days of study enrollment were excluded from the final analysis. Serotype distribution was performed using the urinary antigen detection (UAD) assay and/or microbiological culture.Overall, 498 subjects with radiographically confirmed CAP were enrolled in the study. Eighty subjects (16.1%) were positive for any S. pneumoniae serotype by ≥1 assay, and 38 (7.6%) were positive for PCV13 serotypes via the UAD. The overall 30-day mortality rate was 1.2%, though S. pneumoniae was not isolated from any case leading to death.RESULTSOverall, 498 subjects with radiographically confirmed CAP were enrolled in the study. Eighty subjects (16.1%) were positive for any S. pneumoniae serotype by ≥1 assay, and 38 (7.6%) were positive for PCV13 serotypes via the UAD. The overall 30-day mortality rate was 1.2%, though S. pneumoniae was not isolated from any case leading to death.Despite six years of high pneumococcal immunization coverage in children in Israel, we have shown that 7.6% of CAP cases among adults in Israel remain related to PCV13 serotypes; and that the burden of PCV13 may be as high as 47% of observed pneumococcal CAP.CONCLUSIONDespite six years of high pneumococcal immunization coverage in children in Israel, we have shown that 7.6% of CAP cases among adults in Israel remain related to PCV13 serotypes; and that the burden of PCV13 may be as high as 47% of observed pneumococcal CAP.
Background: Community acquired pneumonia (CAP) is a major cause of morbidity and mortality worldwide, and is a leading cause of hospitalization in previously healthy individuals without predisposing risk factors or comorbidities. In this study we determined PCV13 serotype distribution in adults aged ≥50 years with radiographically confirmed CAP in Israel. Methods: Subjects aged ≥50 years were enrolled from one of three hospitals (Emek Medical Center, Meir Medical Center and Sheba Medical Center) from March 2014 to July 2015. Information was collected on subject demographics, comorbidities, risk factors, and pneumococcal vaccine immunization status. Subjects presented with suspected CAP supported by radiographic evidence, and provided a urine sample and informed consent. Subjects without radiographic confirmation of CAP or who received PPSV23 within 30 days of study enrollment were excluded from the final analysis. Serotype distribution was performed using the urinary antigen detection (UAD) assay and/or microbiological culture. Results: Overall, 498 subjects with radiographically confirmed CAP were enrolled in the study. Eighty subjects (16.1%) were positive for any S. pneumoniae serotype by ≥1 assay, and 38 (7.6%) were positive for PCV13 serotypes via the UAD. The overall 30-day mortality rate was 1.2%, though S. pneumoniae was not isolated from any case leading to death. Conclusion: Despite six years of high pneumococcal immunization coverage in children in Israel, we have shown that 7.6% of CAP cases among adults in Israel remain related to PCV13 serotypes; and that the burden of PCV13 may be as high as 47% of observed pneumococcal CAP.
Community acquired pneumonia (CAP) is a major cause of morbidity and mortality worldwide, and is a leading cause of hospitalization in previously healthy individuals without predisposing risk factors or comorbidities. In this study we determined PCV13 serotype distribution in adults aged ≥50 years with radiographically confirmed CAP in Israel. Subjects aged ≥50 years were enrolled from one of three hospitals (Emek Medical Center, Meir Medical Center and Sheba Medical Center) from March 2014 to July 2015. Information was collected on subject demographics, comorbidities, risk factors, and pneumococcal vaccine immunization status. Subjects presented with suspected CAP supported by radiographic evidence, and provided a urine sample and informed consent. Subjects without radiographic confirmation of CAP or who received PPSV23 within 30 days of study enrollment were excluded from the final analysis. Serotype distribution was performed using the urinary antigen detection (UAD) assay and/or microbiological culture. Overall, 498 subjects with radiographically confirmed CAP were enrolled in the study. Eighty subjects (16.1%) were positive for any S. pneumoniae serotype by ≥1 assay, and 38 (7.6%) were positive for PCV13 serotypes via the UAD. The overall 30-day mortality rate was 1.2%, though S. pneumoniae was not isolated from any case leading to death. Despite six years of high pneumococcal immunization coverage in children in Israel, we have shown that 7.6% of CAP cases among adults in Israel remain related to PCV13 serotypes; and that the burden of PCV13 may be as high as 47% of observed pneumococcal CAP.
Background : Community acquired pneumonia (CAP) is a major cause of morbidity and mortality worldwide, and is a leading cause of hospitalization in previously healthy individuals without predisposing risk factors or comorbidities. In this study we determined PCV13 serotype distribution in adults aged ≥50 years with radiographically confirmed CAP in Israel. Methods : Subjects aged ≥50 years were enrolled from one of three hospitals (Emek Medical Center, Meir Medical Center and Sheba Medical Center) from March 2014 to July 2015. Information was collected on subject demographics, comorbidities, risk factors, and pneumococcal vaccine immunization status. Subjects presented with suspected CAP supported by radiographic evidence, and provided a urine sample and informed consent. Subjects without radiographic confirmation of CAP or who received PPSV23 within 30 days of study enrollment were excluded from the final analysis. Serotype distribution was performed using the urinary antigen detection (UAD) assay and/or microbiological culture. Results : Overall, 498 subjects with radiographically confirmed CAP were enrolled in the study. Eighty subjects (16.1%) were positive for any S. pneumoniae serotype by ≥1 assay, and 38 (7.6%) were positive for PCV13 serotypes via the UAD. The overall 30-day mortality rate was 1.2%, though S. pneumoniae was not isolated from any case leading to death. Conclusion : Despite six years of high pneumococcal immunization coverage in children in Israel, we have shown that 7.6% of CAP cases among adults in Israel remain related to PCV13 serotypes; and that the burden of PCV13 may be as high as 47% of observed pneumococcal CAP.
Background: Community acquired pneumonia (CAP) is a major cause of morbidity and mortality worldwide, and is a leading cause of hospitalization in previously healthy individuals without predisposing risk factors or comorbidities. In this study we determined PCV13 serotype distribution in adults aged ≥50 years with radiographically confirmed CAP in Israel. Methods: Subjects aged ≥50 years were enrolled from one of three hospitals (Emek Medical Center, Meir Medical Center and Sheba Medical Center) from March 2014 to July 2015. Information was collected on subject demographics, comorbidities, risk factors, and pneumococcal vaccine immunization status. Subjects presented with suspected CAP supported by radiographic evidence, and provided a urine sample and informed consent. Subjects without radiographic confirmation of CAP or who received PPSV23 within 30 days of study enrollment were excluded from the final analysis. Serotype distribution was performed using the urinary antigen detection (UAD) assay and/or microbiological culture. Results: Overall, 498 subjects with radiographically confirmed CAP were enrolled in the study. Eighty subjects (16.1%) were positive for any S. pneumoniae serotype by ≥1 assay, and 38 (7.6%) were positive for PCV13 serotypes via the UAD. The overall 30-day mortality rate was 1.2%, though S. pneumoniae was not isolated from any case leading to death. Conclusion: Despite six years of high pneumococcal immunization coverage in children in Israel, we have shown that 7.6% of CAP cases among adults in Israel remain related to PCV13 serotypes; and that the burden of PCV13 may be as high as 47% of observed pneumococcal CAP.
Author Gonzalez, Elisa
Gray, Sharon
Chowers, Michal
Zhang, Zhou
Chazan, Bibiana
Pride, Michael
Regev-Yochay, Gili
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Cites_doi 10.1128/JCM.43.10.4972-4976.2005
10.3810/pgm.2010.03.2130
10.1016/j.vaccine.2017.05.049
10.1371/journal.pone.0060273
10.1016/j.vaccine.2015.06.062
10.1378/chest.101.2.442
10.1097/01.inf.0000049347.42983.77
10.1128/CVI.00064-12
10.1097/00005792-200007000-00002
10.1093/cid/ciu006
10.1016/j.vaccine.2017.03.031
10.1128/JCM.41.7.2810-2813.2003
10.1007/s10156-004-0351-1
10.1086/591405
10.1164/ajrccm.160.2.9808045
10.1128/JCM.42.8.3620-3625.2004
10.5603/PiAP.2016.0007
10.1111/j.1348-0421.2001.tb01284.x
10.1136/thoraxjnl-2015-207688
10.1016/j.vaccine.2012.08.012
10.1136/thx.51.2.179
10.1093/cid/cix1066
10.1093/tropej/fmq070
10.1086/528798
10.1136/thoraxjnl-2013-204282
10.1016/j.vaccine.2017.05.059
10.1093/clinids/14.4.801
10.1093/infdis/jit506
10.3109/00365548.2011.652162
10.1128/JCM.39.10.3495-3498.2001
10.1016/S0163-4453(94)90698-X
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Keywords pneumococcus
CAP
Israel
pneumonia
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References cit0011
cit0033
cit0012
cit0034
cit0010
cit0032
cit0030
Austrian R (cit0031) 1976; 43
cit0019
cit0017
cit0018
cit0015
cit0013
cit0035
cit0014
cit0022
Bandettini R (cit0028) 2012; 53
cit0001
cit0023
cit0020
File TM (cit0006) 2004; 117
cit0021
cit0008
cit0009
cit0007
cit0029
cit0004
cit0026
cit0005
cit0027
cit0002
cit0024
cit0003
cit0025
11574562 - J Clin Microbiol. 2001 Oct;39(10):3495-8
28554501 - Vaccine. 2017 Jun 22;35(29):3647-3654
28579230 - Vaccine. 2018 Aug 28;36(36):5477-5484
22263905 - Scand J Infect Dis. 2012 Jun;44(6):433-8
15297507 - J Clin Microbiol. 2004 Aug;42(8):3620-5
15614462 - J Infect Chemother. 2004 Dec;10(6):359-63
24532543 - Clin Infect Dis. 2014 Apr;58(7):918-24
18260752 - Clin Infect Dis. 2008 Mar 15;46(6):926-32
11293482 - Microbiol Immunol. 2001;45(2):159-62
18986290 - Clin Infect Dis. 2008 Dec 1;47 Suppl 3:S202-6
10430704 - Am J Respir Crit Care Med. 1999 Aug;160(2):397-405
1735270 - Chest. 1992 Feb;101(2):442-6
28342668 - Vaccine. 2017 Apr 25;35(18):2449-2456
29342250 - Clin Infect Dis. 2018 May 2;66(10):1504-1510
27238167 - Pneumonol Alergol Pol. 2016;84(2):95-103
23565216 - PLoS One. 2013;8(4):e60273
22939907 - Vaccine. 2012 Oct 12;30(46):6600-7
15360096 - Am J Med. 2004 Aug 2;117 Suppl 3A:39S-50S
26116251 - Vaccine. 2015 Aug 26;33(36):4623-9
7806880 - J Infect. 1994 Sep;29(2):171-82
12586987 - Pediatr Infect Dis J. 2003 Feb;22(2):e1-11
1576274 - Clin Infect Dis. 1992 Apr;14(4):801-7
20736384 - J Trop Pediatr. 2011 Jun;57(3):192-6
8711652 - Thorax. 1996 Feb;51(2):179-84
13297 - Mt Sinai J Med. 1976 Nov-Dec;43(6):699-709
22675155 - Clin Vaccine Immunol. 2012 Aug;19(8):1131-41
12843005 - J Clin Microbiol. 2003 Jul;41(7):2810-3
24130229 - Thorax. 2013 Nov;68(11):1057-65
16207950 - J Clin Microbiol. 2005 Oct;43(10):4972-6
24092845 - J Infect Dis. 2013 Dec 1;208(11):1813-20
10941350 - Medicine (Baltimore). 2000 Jul;79(4):210-21
20203464 - Postgrad Med. 2010 Mar;122(2):130-41
23240165 - J Prev Med Hyg. 2012 Jun;53(2):85-8
26888780 - Thorax. 2016 Jun;71(6):535-42
References_xml – ident: cit0035
  doi: 10.1128/JCM.43.10.4972-4976.2005
– ident: cit0003
  doi: 10.3810/pgm.2010.03.2130
– ident: cit0019
  doi: 10.1016/j.vaccine.2017.05.049
– ident: cit0018
  doi: 10.1371/journal.pone.0060273
– ident: cit0009
  doi: 10.1016/j.vaccine.2015.06.062
– ident: cit0002
  doi: 10.1378/chest.101.2.442
– ident: cit0030
  doi: 10.1097/01.inf.0000049347.42983.77
– ident: cit0017
  doi: 10.1128/CVI.00064-12
– ident: cit0025
  doi: 10.1097/00005792-200007000-00002
– volume: 117
  start-page: 39S
  issue: 3
  year: 2004
  ident: cit0006
  publication-title: Am J Med
– ident: cit0001
  doi: 10.1093/cid/ciu006
– ident: cit0010
  doi: 10.1016/j.vaccine.2017.03.031
– ident: cit0034
  doi: 10.1128/JCM.41.7.2810-2813.2003
– ident: cit0015
  doi: 10.1007/s10156-004-0351-1
– ident: cit0024
  doi: 10.1086/591405
– ident: cit0027
  doi: 10.1164/ajrccm.160.2.9808045
– ident: cit0013
  doi: 10.1128/JCM.42.8.3620-3625.2004
– ident: cit0020
  doi: 10.5603/PiAP.2016.0007
– ident: cit0033
  doi: 10.1111/j.1348-0421.2001.tb01284.x
– ident: cit0004
  doi: 10.1136/thoraxjnl-2015-207688
– ident: cit0008
  doi: 10.1016/j.vaccine.2012.08.012
– volume: 53
  start-page: 85
  issue: 2
  year: 2012
  ident: cit0028
  publication-title: J Prev Med Hyg
– ident: cit0007
  doi: 10.1136/thx.51.2.179
– ident: cit0023
  doi: 10.1093/cid/cix1066
– ident: cit0012
  doi: 10.1093/tropej/fmq070
– ident: cit0026
  doi: 10.1086/528798
– ident: cit0005
  doi: 10.1136/thoraxjnl-2013-204282
– ident: cit0011
  doi: 10.1016/j.vaccine.2017.05.059
– ident: cit0032
  doi: 10.1093/clinids/14.4.801
– ident: cit0021
  doi: 10.1093/infdis/jit506
– volume: 43
  start-page: 699
  issue: 6
  year: 1976
  ident: cit0031
  publication-title: Mt Sinai J Med
– ident: cit0022
  doi: 10.3109/00365548.2011.652162
– ident: cit0014
  doi: 10.1128/JCM.39.10.3495-3498.2001
– ident: cit0029
  doi: 10.1016/S0163-4453(94)90698-X
– reference: 24532543 - Clin Infect Dis. 2014 Apr;58(7):918-24
– reference: 7806880 - J Infect. 1994 Sep;29(2):171-82
– reference: 15360096 - Am J Med. 2004 Aug 2;117 Suppl 3A:39S-50S
– reference: 22939907 - Vaccine. 2012 Oct 12;30(46):6600-7
– reference: 22675155 - Clin Vaccine Immunol. 2012 Aug;19(8):1131-41
– reference: 18986290 - Clin Infect Dis. 2008 Dec 1;47 Suppl 3:S202-6
– reference: 15614462 - J Infect Chemother. 2004 Dec;10(6):359-63
– reference: 11574562 - J Clin Microbiol. 2001 Oct;39(10):3495-8
– reference: 20203464 - Postgrad Med. 2010 Mar;122(2):130-41
– reference: 1576274 - Clin Infect Dis. 1992 Apr;14(4):801-7
– reference: 24092845 - J Infect Dis. 2013 Dec 1;208(11):1813-20
– reference: 13297 - Mt Sinai J Med. 1976 Nov-Dec;43(6):699-709
– reference: 12843005 - J Clin Microbiol. 2003 Jul;41(7):2810-3
– reference: 28579230 - Vaccine. 2018 Aug 28;36(36):5477-5484
– reference: 10430704 - Am J Respir Crit Care Med. 1999 Aug;160(2):397-405
– reference: 1735270 - Chest. 1992 Feb;101(2):442-6
– reference: 22263905 - Scand J Infect Dis. 2012 Jun;44(6):433-8
– reference: 10941350 - Medicine (Baltimore). 2000 Jul;79(4):210-21
– reference: 24130229 - Thorax. 2013 Nov;68(11):1057-65
– reference: 23240165 - J Prev Med Hyg. 2012 Jun;53(2):85-8
– reference: 26888780 - Thorax. 2016 Jun;71(6):535-42
– reference: 28342668 - Vaccine. 2017 Apr 25;35(18):2449-2456
– reference: 27238167 - Pneumonol Alergol Pol. 2016;84(2):95-103
– reference: 12586987 - Pediatr Infect Dis J. 2003 Feb;22(2):e1-11
– reference: 11293482 - Microbiol Immunol. 2001;45(2):159-62
– reference: 15297507 - J Clin Microbiol. 2004 Aug;42(8):3620-5
– reference: 28554501 - Vaccine. 2017 Jun 22;35(29):3647-3654
– reference: 26116251 - Vaccine. 2015 Aug 26;33(36):4623-9
– reference: 29342250 - Clin Infect Dis. 2018 May 2;66(10):1504-1510
– reference: 16207950 - J Clin Microbiol. 2005 Oct;43(10):4972-6
– reference: 23565216 - PLoS One. 2013;8(4):e60273
– reference: 18260752 - Clin Infect Dis. 2008 Mar 15;46(6):926-32
– reference: 20736384 - J Trop Pediatr. 2011 Jun;57(3):192-6
– reference: 8711652 - Thorax. 1996 Feb;51(2):179-84
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Snippet Background: Community acquired pneumonia (CAP) is a major cause of morbidity and mortality worldwide, and is a leading cause of hospitalization in previously...
Community acquired pneumonia (CAP) is a major cause of morbidity and mortality worldwide, and is a leading cause of hospitalization in previously healthy...
Background : Community acquired pneumonia (CAP) is a major cause of morbidity and mortality worldwide, and is a leading cause of hospitalization in previously...
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SubjectTerms CAP
Israel
pneumococcus
pneumonia
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Title Distribution of 13-Valent pneumococcal conjugate vaccine serotype streptococcus pneumoniae in adults 50 Years and Older presenting with community-acquired pneumonia in Israel
URI https://www.tandfonline.com/doi/abs/10.1080/21645515.2018.1475811
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