{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,7,29]],"date-time":"2026-07-29T09:58:25Z","timestamp":1785319105003,"version":"3.55.0"},"reference-count":28,"publisher":"American Medical Association (AMA)","issue":"8","content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["JAMA Netw Open"],"abstract":"<jats:sec id=\"ab-zoi250704-4\"><jats:title>IMPORTANCE<\/jats:title><jats:p>Although the use of pneumococcal conjugate vaccines (PCV) has reduced the overall burden of pneumococcal disease, recent measurements of pneumococcal pneumonia incidence are lacking.<\/jats:p><\/jats:sec><jats:sec id=\"ab-zoi250704-5\"><jats:title>OBJECTIVE<\/jats:title><jats:p>To prospectively quantify the burden of pneumococcal pneumonia and to assess the potential impact of the recently approved adult-specific 21-valent pneumococcal conjugate vaccine (V116).<\/jats:p><\/jats:sec><jats:sec id=\"ab-zoi250704-6\"><jats:title>DESIGN, SETTINGS, AND PARTICIPANTS<\/jats:title><jats:p>This cross-sectional study for prospective active surveillance included adults residing in defined catchment areas in Tennessee and Georgia hospitalized with clinical and radiographical evidence of community-acquired pneumonia (CAP) at 3 hospitals between 2018 and 2022. Data were analyzed from July 2024 to January 2025.<\/jats:p><\/jats:sec><jats:sec id=\"ab-zoi250704-7\"><jats:title>MAIN OUTCOMES AND MEASURES<\/jats:title><jats:p>Pneumococcal etiology was determined using an on-market serotype-agnostic urinary antigen test, serotype-specific urinary antigen detection assays covering 30 serotypes, and routine clinical tests. Overall and age-stratified incidence rates for pneumonia hospitalizations were estimated accounting for the probability of enrollment and hospital market share of enrolling hospitals within the catchment area.<\/jats:p><\/jats:sec><jats:sec id=\"ab-zoi250704-8\"><jats:title>RESULTS<\/jats:title><jats:p>Among 2016 patients hospitalized for CAP, the median (IQR) age was 60.1 (47.0-70.2) years; 726 patients (36.0%) were Black, 81 (4.0%) were Hispanic, and 1209 (60.0%) were White; 1863 patients (92.4%) lived in a community dwelling. A total of 279 patients (13.8%) hospitalized for CAP had evidence of pneumococcal pneumonia, and 198 (9.8%) had detection of serotypes included in V116. The overall estimated annual incidence of hospitalizations for all-cause CAP was 340 per 100\u202f000 adults. The incidence of hospitalizations for pneumococcal CAP and pneumococcal CAP due to serotypes included in V116 was 43 and 30 per 100\u202f000 adults, respectively. The burden of all-cause and pneumococcal CAP was consistently highest among adults age 65 years or older.<\/jats:p><\/jats:sec><jats:sec id=\"ab-zoi250704-9\"><jats:title>CONCLUSIONS AND RELEVANCE<\/jats:title><jats:p>This prospective surveillance study demonstrated a large burden of hospitalizations for CAP among US adults, with the highest burden of disease among adults age 65 years or older. A sizable fraction of CAP was caused by <jats:italic>Streptococcus pneumoniae<\/jats:italic>, especially by serotypes included in V116.<\/jats:p><\/jats:sec>","DOI":"10.1001\/jamanetworkopen.2025.24783","type":"journal-article","created":{"date-parts":[[2025,8,6]],"date-time":"2025-08-06T15:00:27Z","timestamp":1754492427000},"page":"e2524783","source":"Crossref","is-referenced-by-count":4,"title":["All-Cause and Pneumococcal Community-Acquired Pneumonia Hospitalizations Among Adults in Tennessee and Georgia"],"prefix":"10.1001","volume":"8","author":[{"given":"Carlos G.","family":"Grijalva","sequence":"first","affiliation":[{"name":"Vanderbilt University Medical Center, Nashville, Tennessee"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Kelly D.","family":"Johnson","sequence":"additional","affiliation":[{"name":"Value & Implementation, Outcomes Research, Merck Sharp & Dohme LLC, a subsidiary of Merck & Co, Inc, Rahway, New Jersey"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"J. Jackson","family":"Resser","sequence":"additional","affiliation":[{"name":"Vanderbilt University Medical Center, Nashville, Tennessee"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Cynthia G.","family":"Whitney","sequence":"additional","affiliation":[{"name":"Emory University, Atlanta, Georgia"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Adrienne","family":"Baughman","sequence":"additional","affiliation":[{"name":"Vanderbilt University Medical Center, Nashville, Tennessee"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Mai","family":"Kio","sequence":"additional","affiliation":[{"name":"Emory University, Atlanta, Georgia"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Jessica","family":"Traenkner","sequence":"additional","affiliation":[{"name":"Emory University, Atlanta, 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Connecticut"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Thomas","family":"Weiss","sequence":"additional","affiliation":[{"name":"Value & Implementation, Outcomes Research, Merck Sharp & Dohme LLC, a subsidiary of Merck & Co, Inc, Rahway, New Jersey"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Craig S.","family":"Roberts","sequence":"additional","affiliation":[{"name":"Value & Implementation, Outcomes Research, Merck Sharp & Dohme LLC, a subsidiary of Merck & Co, Inc, Rahway, New Jersey"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Nadine","family":"Rouphael","sequence":"additional","affiliation":[{"name":"Emory University, Atlanta, Georgia"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Wesley H.","family":"Self","sequence":"additional","affiliation":[{"name":"Vanderbilt University Medical Center, Nashville, Tennessee"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"name":"PNEUMO 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