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BNT162b2 vaccine breakthrough: clinical characteristics of 152 fully vaccinated hospitalized COVID-19 patients in Israel.
Brosh-Nissimov, Tal; Orenbuch-Harroch, Efrat; Chowers, Michal; Elbaz, Meital; Nesher, Lior; Stein, Michal; Maor, Yasmin; Cohen, Regev; Hussein, Khetam; Weinberger, Miriam; Zimhony, Oren; Chazan, Bibiana; Najjar, Ronza; Zayyad, Hiba; Rahav, Galia; Wiener-Well, Yonit.
  • Brosh-Nissimov T; Infectious Diseases Unit, Samson Assuta Ashdod University Hospital, Ashdod, Israel; Faculty of Health Sciences, Ben Gurion University of the Negev, Beer Sheba, Israel. Electronic address: tbrosh@gmail.com.
  • Orenbuch-Harroch E; Division of Microbiology and Infectious Diseases, Hadassah Hebrew University Medical Centre, Jerusalem, Israel; School of Medicine, Hebrew University of Jerusalem, Jerusalem, Israel.
  • Chowers M; Meir Medical Centre, Kfar Saba, Israel; Sackler Faculty of Medicine, Tel Aviv University, Tel Aviv, Israel.
  • Elbaz M; Sackler Faculty of Medicine, Tel Aviv University, Tel Aviv, Israel; Department of Infectious Diseases, Tel Aviv Sourasky Medical Centre, Tel Aviv, Israel.
  • Nesher L; Faculty of Health Sciences, Ben Gurion University of the Negev, Beer Sheba, Israel; Infectious Disease Institute, Soroka Medical Centre, Beer Sheba, Israel.
  • Stein M; Infectious Disease and Infection Control Unit, Hillel Yaffe Medical Centre, Hadera, Israel; Rappaport Faculty of Medicine, Technion-Israel Institute of Technology, Haifa, Israel.
  • Maor Y; Sackler Faculty of Medicine, Tel Aviv University, Tel Aviv, Israel; Infectious Disease Unit, Wolfson Medical Centre, Holon, Israel.
  • Cohen R; Rappaport Faculty of Medicine, Technion-Israel Institute of Technology, Haifa, Israel; Infectious Diseases Unit, Sanz Medical Centre, Laniado Hospital, Netanya, Israel.
  • Hussein K; Rappaport Faculty of Medicine, Technion-Israel Institute of Technology, Haifa, Israel; Rambam Health Care Campus, Haifa, Israel.
  • Weinberger M; Sackler Faculty of Medicine, Tel Aviv University, Tel Aviv, Israel; Shamir (Assaf Harofe) Medical Centre, Zerifin, Israel.
  • Zimhony O; School of Medicine, Hebrew University of Jerusalem, Jerusalem, Israel; Infectious Diseases Unit, Kaplan Medical Centre, Rhovot, Israel.
  • Chazan B; Rappaport Faculty of Medicine, Technion-Israel Institute of Technology, Haifa, Israel; Infectious Diseases Unit, Emek Medical Centre, Afula, Israel.
  • Najjar R; Rappaport Faculty of Medicine, Technion-Israel Institute of Technology, Haifa, Israel; Carmel Medical Centre, Haifa, Israel.
  • Zayyad H; Infectious Disease Unit, The Baruch Padeh Medical Centre, Tiberias, Israel; The Azrieli Faculty of Medicine in the Galilee, Bar Ilan University, Safed, Israel.
  • Rahav G; Sackler Faculty of Medicine, Tel Aviv University, Tel Aviv, Israel; Infectious Diseases Unit, Sheba Medical Centre, Tel Hashomer, Israel.
  • Wiener-Well Y; School of Medicine, Hebrew University of Jerusalem, Jerusalem, Israel; Shaare Zedek Medical Centre, Jerusalem, Israel.
Clin Microbiol Infect ; 27(11): 1652-1657, 2021 Nov.
Article in English | MEDLINE | ID: covidwho-1300724
ABSTRACT

OBJECTIVES:

The mRNA coronavirus disease 2019 (COVID-19) vaccines have shown high effectiveness in the prevention of symptomatic COVID-19, hospitalization, severe disease and death. Nevertheless, a minority of vaccinated individuals might become infected and experience significant morbidity. Characteristics of vaccine breakthrough infections have not been studied. We sought to portray the population of Israeli patients, who were hospitalized with COVID-19 despite full vaccination.

METHODS:

A retrospective multicentre cohort study of 17 hospitals included patients fully vaccinated with Pfizer/BioNTech's BNT162b2 vaccine who developed COVID-19 more than 7 days after the second vaccine dose and required hospitalization. The risk for poor outcome, defined as a composite of mechanical ventilation or death, was assessed.

RESULTS:

A total of 152 patients were included, accounting for half of hospitalized fully vaccinated patients in Israel. Poor outcome was noted in 38 patients and mortality rate reached 22% (34/152). Notably, the cohort was characterized by a high rate of co-morbidities predisposing to severe COVID-19, including hypertension (108; 71%), diabetes (73; 48%), congestive heart failure (41; 27%), chronic kidney and lung diseases (37; 24% each), dementia (29; 19%) and cancer (36; 24%), and only six (4%) had no co-morbidities. Sixty (40%) of the patients were immunocompromised. Higher viral load was associated with a significant risk for poor outcome. Risk also appeared higher in patients receiving anti-CD20 treatment and in patients with low titres of anti-Spike IgG, but these differences did not reach statistical significance.

CONCLUSIONS:

We found that severe COVID-19 infection, associated with a high mortality rate, might develop in a minority of fully vaccinated individuals with multiple co-morbidities. Our patients had a higher rate of co-morbidities and immunosuppression compared with previously reported non-vaccinated hospitalized individuals with COVID-19. Further characterization of this vulnerable population may help to develop guidance to augment their protection, either by continued social distancing, or by additional active or passive vaccinations.
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Full text: Available Collection: International databases Database: MEDLINE Main subject: COVID-19 / BNT162 Vaccine Type of study: Cohort study / Observational study / Prognostic study Topics: Vaccines Limits: Humans Country/Region as subject: Asia Language: English Journal: Clin Microbiol Infect Journal subject: Communicable Diseases / Microbiology Year: 2021 Document Type: Article

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Full text: Available Collection: International databases Database: MEDLINE Main subject: COVID-19 / BNT162 Vaccine Type of study: Cohort study / Observational study / Prognostic study Topics: Vaccines Limits: Humans Country/Region as subject: Asia Language: English Journal: Clin Microbiol Infect Journal subject: Communicable Diseases / Microbiology Year: 2021 Document Type: Article