1. Hospital-onset adult invasive pneumococcal disease in Israel: Sicker patients, different pathogens
- Author
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Ariel Kenig, Gili Regev-Yochay, Shirley Khakshoor, Ronit Cohen-Poradosu, Jihad Bishara, Daniel Glikman, Mirit Hershman-Sarafov, Ron Dagan, Oren Zimhony, Marc Assous, Haim Ben-Zvi, Rita Bardenstein, Larissa Brik, Bibiana Chazan, Michal Chowers, Talia Finn, Alicia Embon, Sarit Freimann, Yuval Geffen, Danny Glikman, Mirit Hershman, Valery Istomin, Michal Katzir, Yoram Kennes, Camellia Khoury-Assi, Mandelbaum Sari, Yasmin Maor, Danny Miron, Ilana Oren, Yosi Paitan, Yael Paran, Nehama Peled, Avi Peretz, Nurit Porat, Israel Potasman, Galia Rahav, Hagai Rechnitzer, Klaris Reisenberg, Shifra Sela, David Schwartz, Orna Schwartz, Pninit Shaked-Mishan, Yehudit Sheindler, Gill Smollan, Itzhak Srugo, Michal Stein, Jacob Strahilevitz, Olga Sverdlob, Violetta Temper, Evgenia Tsyba, Yonit Wiener-Well, Gabriel Weber, and Miriam Weinberger
- Subjects
Infectious and parasitic diseases ,RC109-216 - Abstract
Objectives: Invasive pneumococcal disease (IPD) usually has its onset in the community (CO-IPD), but it can commence following hospitalization (HO-IPD). This study compared HO-IPD and CO-IPD cases during the implementation of the pneumococcal conjugate vaccine (PCV) program for children in Israel. Methods: This was a nationwide retrospective cohort study of adult (age >18 years) IPD patients covering the period from the implementation of the PCV7/13 program in 2009/2010 through 2015. HO-IPD and CO-IPD were defined as IPD with onset ≥4 and ≤2 days from admission, respectively. Patient characteristics, outcome measures, serotypes, and antimicrobial susceptibility were compared for the entire cohort, followed by a matched case–control analysis. Results: The study included 114 patients with HO-IPD and 2180 with CO-IPD. After matching HO-IPD to CO-IPD patients by age, sex, and comorbidities, the mortality rate and discharge to long-term care facility rate were significantly higher for HO-IPD patients than for CO-IPD patients (44.6% vs. 26.3% and 26.5% vs. 8.2%, respectively). HO-IPD isolates were less often covered by PCV13 (39.6% vs. 49.0%) and pneumococcal polysaccharide vaccine PPSV23 (56.6% vs. 71.3%) and more often resistant to penicillin (9.3% vs. 3.6%), ceftriaxone (3.8% vs. 0.75%), and levofloxacin (9.3% vs. 0.8%). Conclusions: HO-IPD was associated with higher morbidity and mortality than CO-IPD and was more often caused by non-vaccine serotypes (primarily non-PCV13 types) and antibiotic-resistant strains. Keywords: Streptococcus pneumoniae, Invasive pneumococcal disease, Pneumococcal conjugate vaccine, Hospital onset, Nosocomial infection
- Published
- 2019
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