{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,10,8]],"date-time":"2026-10-08T16:44:26Z","timestamp":1791477866054,"version":"4.3.4"},"reference-count":53,"publisher":"Wiley","issue":"6","license":[{"start":{"date-parts":[[2021,6,3]],"date-time":"2021-06-03T00:00:00Z","timestamp":1622678400000},"content-version":"vor","delay-in-days":0,"URL":"http:\/\/creativecommons.org\/licenses\/by\/4.0\/"}],"content-domain":{"domain":["onlinelibrary.wiley.com"],"crossmark-restriction":true},"short-container-title":["Influenza Resp Viruses"],"published-print":{"date-parts":[[2021,11]]},"abstract":"<jats:title>Abstract<\/jats:title>\n                  <jats:sec>\n                    <jats:title>Background<\/jats:title>\n                    <jats:p>Standard\u2010dose seasonal influenza vaccines often produce modest immunogenic responses in adults \u226565\u00a0years old. MF59 is intended to elicit a greater magnitude and increased breadth of immune response.<\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Objective<\/jats:title>\n                    <jats:p>To determine the effectiveness of seasonal MF59\u2010adjuvanted trivalent\/quadrivalent influenza vaccine (aTIV\/aQIV) relative to no vaccination or vaccination with standard or high\u2010dose egg\u2010based influenza vaccines among people \u226565\u00a0years old.<\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Methods<\/jats:title>\n                    <jats:p>Cochrane methodological standards and PRISMA\u2010P guidelines were followed. Real\u2010world evidence from non\u2010interventional studies published in peer\u2010reviewed journals and gray literature from 1997 through to July 15, 2020, including cluster\u2010randomized trials, were eligible. Two reviewers independently extracted data; risk of bias was assessed using the ROBINS\u2010I tool.<\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Results<\/jats:title>\n                    <jats:p>\n                      Twenty\u2010one studies conducted during the 2006\/07\u20132019\/20 influenza seasons were included in the qualitative review; 16 in the meta\u2010analyses. Meta\u2010analysis of test\u2010negative studies found that aTIV reduced medical encounters due to lab\u2010confirmed influenza with pooled estimates of 40.7% (95% CI: 21.9, 54.9;\n                      <jats:italic>I<\/jats:italic>\n                      <jats:sup>2<\/jats:sup>\n                      \u00a0=\u00a00%) for non\u2010emergency outpatient visits and 58.5% (40.7, 70.9;\n                      <jats:italic>I<\/jats:italic>\n                      <jats:sup>2<\/jats:sup>\n                      \u00a0=\u00a052.9%) for hospitalized patients. The pooled estimate of VE from case\u2010control studies was 51.3% (39.1, 61.1;\n                      <jats:italic>I<\/jats:italic>\n                      <jats:sup>2<\/jats:sup>\n                      \u00a0=\u00a00%) against influenza\u2010 or pneumonia\u2010related hospitalization. The pooled estimates for the relative VE of aTIV for the prevention of influenza\u2010related medical encounters were 13.9% (4.2, 23.5;\n                      <jats:italic>I<\/jats:italic>\n                      <jats:sup>2<\/jats:sup>\n                      \u00a0=\u00a095.9%) compared with TIV, 13.7% (3.1, 24.2;\n                      <jats:italic>I<\/jats:italic>\n                      <jats:sup>2<\/jats:sup>\n                      \u00a0=\u00a098.8%) compared with QIV, and 2.8% (\u22122.9, 8.5;\n                      <jats:italic>I<\/jats:italic>\n                      <jats:sup>2<\/jats:sup>\n                      \u00a0=\u00a094.5%) compared with HD\u2010TIV.\n                    <\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Conclusions<\/jats:title>\n                    <jats:p>Among adults \u226565\u00a0years, aTIV demonstrated significant absolute VE, improved relative VE compared to non\u2010adjuvanted standard\u2010dose TIV\/QIV, and comparable relative VE to high\u2010dose TIV.<\/jats:p>\n                  <\/jats:sec>","DOI":"10.1111\/irv.12871","type":"journal-article","created":{"date-parts":[[2021,6,4]],"date-time":"2021-06-04T07:21:32Z","timestamp":1622791292000},"page":"813-823","update-policy":"https:\/\/doi.org\/10.1002\/crossmark_policy","source":"Crossref","is-referenced-by-count":109,"title":["Effectiveness of the MF59\u2010adjuvanted trivalent or quadrivalent seasonal influenza vaccine among adults 65 years of age or older, a systematic review and meta\u2010analysis"],"prefix":"10.1111","volume":"15","author":[{"ORCID":"https:\/\/orcid.org\/0000-0002-7144-4827","authenticated-orcid":false,"given":"Brenda L.","family":"Coleman","sequence":"first","affiliation":[{"name":"Sinai Health  Toronto ON Canada"},{"name":"Dalla Lana School of Public Health  Toronto ON Canada"},{"name":"Western University  London ON Canada"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Ruth","family":"Sanderson","sequence":"additional","affiliation":[{"name":"Sinai Health  Toronto ON Canada"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Mendel D. 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