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      Incidence and Estimated Vaccine Effectiveness Against Hospitalizations for All-Cause Pneumonia Among Older US Adults Who Were Vaccinated and Not Vaccinated With 13-Valent Pneumococcal Conjugate Vaccine

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          Abstract

          This cohort study estimates the association between vaccination with 13-valent pneumococcal conjugate vaccine and hospitalizations for all-cause pneumonia and lower respiratory tract infection among older adults in a large health care system in California.

          Key Points

          Question

          What is the estimated vaccine effectiveness of 13-valent pneumococcal conjugate vaccine (PCV13) against hospitalized all-cause pneumonia and lower respiratory tract infections (LRTI) in US adults aged 65 years or older?

          Findings

          In this cohort study including 192 061 adults, PCV13 was associated with an adjusted vaccine effectiveness of 10.0% against hospitalized pneumonia and 9.4% against hospitalized LRTI, both of which were statistically significant.

          Meaning

          PCV13 vaccination in older adults may have broad public health benefit in preventing hospitalizations associated with all-cause pneumonia and LRTI.

          Abstract

          Importance

          Following routine use of 13-valent pneumococcal conjugate vaccine (PCV13) in children in 2010, invasive pneumococcal disease rates have decreased substantially in children and adults. In 2014, the Advisory Committee for Immunization Practices recommended routine use of PCV13 among adults aged 65 years or older; previously only 23-valent pneumococcal polysaccharide vaccine (PPV23) was recommended.

          Objective

          To estimate the association between the incidence of hospitalized all-cause pneumonia and lower respiratory tract infections (LRTI) and PCV13 vaccination among older adults at Kaiser Permanente Northern California (KPNC).

          Design, Setting, and Participants

          This retrospective cohort study included adults at KPNC aged 65 years or older between July 1, 2015, and June 30, 2018, born after 1936 with no known history of PPV23 or PCV13 receipt before age 65. The study took place at an integrated health care system with an annual membership more than 4 million individuals, approximately 15% of whom are 65 years or older and broadly representative of the region. Data analysis took place from July 2018 to December 2021, and data collection took place from November 2016 to June 2018.

          Exposures

          PCV13 vaccination status was ascertained from the electronic medical record (EMR). Individuals were considered vaccinated 14 days following immunization.

          Main Outcomes and Measures

          First hospitalized all-cause pneumonia was identified in the EMR using primary/secondary discharge diagnosis International Classification of Diseases, Ninth Revision and International Statistical Classification of Diseases and Related Health Problems, Tenth Revision codes. First hospitalized LRTI was identified using pneumonia codes and acute bronchitis codes. Relative risk (RR) of first pneumonia or LRTI hospitalization of individuals who were PCV13 vaccinated vs PCV13 unvaccinated was estimated using Poisson regressions adjusted for sex, race, ethnicity, age, influenza vaccine receipt, PPV23 receipt since age 65, pneumonia risk factors, health care use, and season. Vaccine effectiveness (VE) was estimated as (1–RR) × 100%.

          Results

          Of 192 061 adults, 107 957 (56%) were female and 139 024 (72%) were White individuals. PCV13 coverage increased from 0 in 2014 to 135 608 (76.9%) by 2018. There were 3488 individuals with 3766 pneumonia hospitalizations and 3846 individuals with 4173 LRTI hospitalizations. PCV13 was associated with an adjusted VE of 10.0% (95% CI, 2.4-17.0; P = .01) against hospitalized pneumonia and 9.4% (95% CI, 2.1-16.1; P = .01) against hospitalized LRTI.

          Conclusions and Relevance

          In the context of a robust pediatric PCV13 immunization program, PCV13 vaccination of adults aged 65 years or older was associated with significant reductions in hospitalizations for all-cause pneumonia and LRTI. Vaccinating older adults with PCVs may provide broader public health benefit against pneumonia hospitalizations.

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          Most cited references43

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          Adapting a clinical comorbidity index for use with ICD-9-CM administrative databases

          R Deyo (1992)
          Administrative databases are increasingly used for studying outcomes of medical care. Valid inferences from such data require the ability to account for disease severity and comorbid conditions. We adapted a clinical comorbidity index, designed for use with medical records, for research relying on International Classification of Diseases (ICD-9-CM) diagnosis and procedure codes. The association of this adapted index with health outcomes and resource use was then examined with a sample of Medicare beneficiaries who underwent lumbar spine surgery in 1985 (n = 27,111). The index was associated in the expected direction with postoperative complications, mortality, blood transfusion, discharge to nursing home, length of hospital stay, and hospital charges. These associations were observed whether the index incorporated data from multiple hospitalizations over a year's time, or just from the index surgical admission. They also persisted after controlling for patient age. We conclude that the adapted comorbidity index will be useful in studies of disease outcome and resource use employing administrative databases.
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            Polysaccharide conjugate vaccine against pneumococcal pneumonia in adults.

            Pneumococcal polysaccharide conjugate vaccines prevent pneumococcal disease in infants, but their efficacy against pneumococcal community-acquired pneumonia in adults 65 years of age or older is unknown.
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              A New Pneumococcal Capsule Type, 10D, is the 100th Serotype and Has a Large cps Fragment from an Oral Streptococcus

              The polysaccharide capsule is essential for the pathogenicity of pneumococcus, which is responsible for millions of deaths worldwide each year. Currently available pneumococcal vaccines are designed to elicit antibodies to the capsule polysaccharides of the pneumococcal isolates commonly causing diseases, and the antibodies provide protection only against the pneumococcus expressing the vaccine-targeted capsules. Since pneumococci can produce different capsule polysaccharides and therefore reduce vaccine effectiveness, it is important to track the appearance of novel pneumococcal capsule types and how these new capsules are created. Herein, we describe a new and the 100th pneumococcal capsule type with unique chemical and serological properties. The capsule type was named 10D for its serologic similarity to 10A. Genetic studies provide strong evidence that pneumococcus created 10D capsule polysaccharide by capturing a large genetic fragment from an oral streptococcus. Such interspecies genetic exchanges could greatly increase diversity of pneumococcal capsules and complicate serotype shifts.
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                Author and article information

                Journal
                JAMA Netw Open
                JAMA Netw Open
                JAMA Network Open
                American Medical Association
                2574-3805
                18 March 2022
                March 2022
                18 March 2022
                : 5
                : 3
                : e221111
                Affiliations
                [1 ]Kaiser Permanente Vaccine Study Center, Oakland, California
                [2 ]Pfizer Vaccine Medicines Development and Scientific Clinical Affairs, Collegeville, Pennsylvania
                Author notes
                Article Information
                Accepted for Publication: January 17, 2022.
                Published: March 18, 2022. doi:10.1001/jamanetworkopen.2022.1111
                Open Access: This is an open access article distributed under the terms of the CC-BY-NC-ND License. © 2022 Hsiao A et al. JAMA Network Open.
                Corresponding Author: Amber Hsiao, MPH, Senior Research Project Manager, Kaiser Permanente Vaccine Study Center, One Kaiser Plaza, 16th Flr, Oakland, CA 94612 ( Amber.Hyman@ 123456kp.org ).
                Author Contributions: Dr Klein and Ms Hsiao had full access to all of the data in the study and take responsibility for the integrity of the data and the accuracy of the data analysis.
                Concept and design: Lewis, Isturiz, McLaughlin, Gessner, Klein.
                Acquisition, analysis, or interpretation of data: Hsiao, Hansen, Timbol, Lewis, Isturiz, Alexander-Parrish, McLaughlin, Gessner.
                Drafting of the manuscript: Hsiao.
                Critical revision of the manuscript for important intellectual content: All authors.
                Statistical analysis: Hsiao, Hansen, Timbol, Lewis.
                Obtained funding: Gessner, Klein.
                Administrative, technical, or material support: Hsiao, Alexander-Parrish, Gessner.
                Supervision: Isturiz, Gessner, Klein.
                Conflict of Interest Disclosures : Dr Klein reported receiving grants from Sanofi Pasteur, GlaxoSmithKline, Merck, Pfizer, Protein Sciences (now Sanofi Pasteur), and the US Centers for Disease and Control outside of the submitted work. Ms Alexander-Parrish, Dr Gessner, Dr Isturiz, and Dr McLaughlin reported being employed by Pfizer and have ownership interests in Pfizer. No other conflicts were reported.
                Funding/Support: This work was funded by Pfizer, Inc.
                Role of the Funder/Sponsor: This study was conducted as a collaboration between Kaiser Permanente Northern California (KPNC) and Pfizer. KPNC is the study sponsor. KPNC and Pfizer coauthors were responsible for the design and conduct of the study; analysis and interpretation of the data; and preparation, review, and manuscript approval. The final decision to submit was made by the first and senior authors.
                Disclaimer: The findings and conclusions in this report are those of the authors and do not reflect the official positions of Kaiser Permanente Northern California and Pfizer.
                Article
                zoi220062
                10.1001/jamanetworkopen.2022.1111
                8933738
                35302634
                690ba0f4-08f1-4fb4-9fdf-ddb0cecb77d8
                Copyright 2022 Hsiao A et al. JAMA Network Open.

                This is an open access article distributed under the terms of the CC-BY-NC-ND License.

                History
                : 20 September 2021
                : 17 January 2022
                Categories
                Research
                Original Investigation
                Online Only
                Infectious Diseases

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