Tags

Type your tag names separated by a space and hit enter

Association of a Third Dose of BNT162b2 Vaccine With Incidence of SARS-CoV-2 Infection Among Health Care Workers in Israel.
JAMA. 2022 01 25; 327(4):341-349.JAMA

Abstract

Importance

Administration of a BNT162b2 booster dose (Pfizer-BioNTech) to fully vaccinated individuals aged 60 years and older was significantly associated with lower risk of SARS-CoV-2 infection and severe illness. Data are lacking on the effectiveness of booster doses for younger individuals and health care workers.

Objective

To estimate the association of a BNT162b2 booster dose with SARS-CoV-2 infections among health care workers who were previously vaccinated with a 2-dose series of BNT162b2.

Design, Setting, and Participants

This was a prospective cohort study conducted at a tertiary medical center in Tel Aviv, Israel. The study cohort included 1928 immunocompetent health care workers who were previously vaccinated with a 2-dose series of BNT162b2, and had enrolled between August 8 and 19, 2021, with final follow-up reported through September 20, 2021. Screening for SARS-CoV-2 infection was performed every 14 days. Anti-spike protein receptor binding domain IgG titers were determined at baseline and 1 month after enrollment. Cox regression with time-dependent analysis was used to estimate hazard ratios of SARS-CoV-2 infection between booster-immunized status and 2-dose vaccinated (booster-nonimmunized) status.

Exposures

Vaccination with a booster dose of BNT162b2 vaccine.

Main Outcomes and Measures

The primary outcome was SARS-CoV-2 infection, as confirmed by reverse transcriptase-polymerase chain reaction.

Results

Among 1928 participants, the median age was 44 years (IQR, 36-52 years) and 1381 were women (71.6%). Participants completed the 2-dose vaccination series a median of 210 days (IQR, 205-213 days) before study enrollment. A total of 1650 participants (85.6%) received the booster dose. During a median follow-up of 39 days (IQR, 35-41 days), SARS-CoV-2 infection occurred in 44 participants (incidence rate, 60.2 per 100 000 person-days); 31 (70.5%) were symptomatic. Five SARS-CoV-2 infections occurred in booster-immunized participants and 39 in booster-nonimmunized participants (incidence rate, 12.8 vs 116 per 100 000 person-days, respectively). In a time-dependent Cox regression analysis, the adjusted hazard ratio of SARS-CoV-2 infection for booster-immunized vs booster-nonimmunized participants was 0.07 (95% CI, 0.02-0.20).

Conclusions and Relevance

Among health care workers at a single center in Israel who were previously vaccinated with a 2-dose series of BNT162b2, administration of a booster dose compared with not receiving one was associated with a significantly lower rate of SARS-CoV-2 infection over a median of 39 days of follow-up. Ongoing surveillance is required to assess durability of the findings.

Authors+Show Affiliations

Department of Oncology, Tel Aviv Sourasky Medical Center, Tel Aviv, Israel. Sackler Faculty of Medicine, Tel Aviv University, Tel Aviv, Israel. Department of Molecular Cell Biology, Weizmann Institute of Science, Rehovot, Israel.Sackler Faculty of Medicine, Tel Aviv University, Tel Aviv, Israel. Department of Anesthesia, Pain Management and Intensive Care, Tel Aviv Sourasky Medical Center, Tel Aviv, Israel. Department of Physician Affairs, Tel Aviv Sourasky Medical Center, Tel Aviv, Israel.Sackler Faculty of Medicine, Tel Aviv University, Tel Aviv, Israel.Sackler Faculty of Medicine, Tel Aviv University, Tel Aviv, Israel. Department of Emergency Medicine, Tel Aviv Sourasky Medical Center, Tel Aviv, Israel.Sackler Faculty of Medicine, Tel Aviv University, Tel Aviv, Israel. Department of Information Systems and Operations, Tel Aviv Sourasky Medical Center, Tel Aviv, Israel.Sackler Faculty of Medicine, Tel Aviv University, Tel Aviv, Israel. Department of Clinical Laboratories, Tel Aviv Sourasky Medical Center, Tel Aviv, Israel.Sackler Faculty of Medicine, Tel Aviv University, Tel Aviv, Israel. Department of Clinical Laboratories, Tel Aviv Sourasky Medical Center, Tel Aviv, Israel.Sackler Faculty of Medicine, Tel Aviv University, Tel Aviv, Israel. Department of Clinical Laboratories, Tel Aviv Sourasky Medical Center, Tel Aviv, Israel.Sackler Faculty of Medicine, Tel Aviv University, Tel Aviv, Israel. Department of Clinical Laboratories, Tel Aviv Sourasky Medical Center, Tel Aviv, Israel.Sackler Faculty of Medicine, Tel Aviv University, Tel Aviv, Israel. Tel Aviv Sourasky Medical Center, Tel Aviv, Israel.Sackler Faculty of Medicine, Tel Aviv University, Tel Aviv, Israel. Department of Internal Medicine "D," Tel Aviv Sourasky Medical Center, Tel Aviv, Israel.Sackler Faculty of Medicine, Tel Aviv University, Tel Aviv, Israel. Department of Internal Medicine "D," Tel Aviv Sourasky Medical Center, Tel Aviv, Israel.Sackler Faculty of Medicine, Tel Aviv University, Tel Aviv, Israel. Department of Internal Medicine "D," Tel Aviv Sourasky Medical Center, Tel Aviv, Israel.Sackler Faculty of Medicine, Tel Aviv University, Tel Aviv, Israel. Department of Infectious Diseases and Infection Control, Tel Aviv Sourasky Medical Center, Tel Aviv, Israel.Sackler Faculty of Medicine, Tel Aviv University, Tel Aviv, Israel. Department of Dermatology, Tel Aviv Sourasky Medical Center, Tel Aviv, Israel.Sackler Faculty of Medicine, Tel Aviv University, Tel Aviv, Israel. Department of Internal Medicine "D," Tel Aviv Sourasky Medical Center, Tel Aviv, Israel.Sackler Faculty of Medicine, Tel Aviv University, Tel Aviv, Israel. Department of Infectious Diseases and Infection Control, Tel Aviv Sourasky Medical Center, Tel Aviv, Israel.Sackler Faculty of Medicine, Tel Aviv University, Tel Aviv, Israel. Department of Dermatology, Tel Aviv Sourasky Medical Center, Tel Aviv, Israel.Sackler Faculty of Medicine, Tel Aviv University, Tel Aviv, Israel. Department of Rheumatology, Tel Aviv Sourasky Medical Center, Tel Aviv, Israel.Sackler Faculty of Medicine, Tel Aviv University, Tel Aviv, Israel. Department of Dermatology, Tel Aviv Sourasky Medical Center, Tel Aviv, Israel.Sackler Faculty of Medicine, Tel Aviv University, Tel Aviv, Israel. Department of Infectious Diseases and Infection Control, Tel Aviv Sourasky Medical Center, Tel Aviv, Israel.Sackler Faculty of Medicine, Tel Aviv University, Tel Aviv, Israel. Department of Internal Medicine "D," Tel Aviv Sourasky Medical Center, Tel Aviv, Israel.Sackler Faculty of Medicine, Tel Aviv University, Tel Aviv, Israel. Department of Internal Medicine "D," Tel Aviv Sourasky Medical Center, Tel Aviv, Israel.Sackler Faculty of Medicine, Tel Aviv University, Tel Aviv, Israel. Department of Infectious Diseases and Infection Control, Tel Aviv Sourasky Medical Center, Tel Aviv, Israel.Sackler Faculty of Medicine, Tel Aviv University, Tel Aviv, Israel. Department of Rheumatology, Tel Aviv Sourasky Medical Center, Tel Aviv, Israel.Sackler Faculty of Medicine, Tel Aviv University, Tel Aviv, Israel. Department of Dermatology, Tel Aviv Sourasky Medical Center, Tel Aviv, Israel.Sackler Faculty of Medicine, Tel Aviv University, Tel Aviv, Israel. Department of Dermatology, Tel Aviv Sourasky Medical Center, Tel Aviv, Israel.Sackler Faculty of Medicine, Tel Aviv University, Tel Aviv, Israel. Department of Dermatology, Tel Aviv Sourasky Medical Center, Tel Aviv, Israel.Sackler Faculty of Medicine, Tel Aviv University, Tel Aviv, Israel. Department of Rheumatology, Tel Aviv Sourasky Medical Center, Tel Aviv, Israel.Sackler Faculty of Medicine, Tel Aviv University, Tel Aviv, Israel. Department of Rheumatology, Tel Aviv Sourasky Medical Center, Tel Aviv, Israel.Sackler Faculty of Medicine, Tel Aviv University, Tel Aviv, Israel. Department of Rheumatology, Tel Aviv Sourasky Medical Center, Tel Aviv, Israel.Sackler Faculty of Medicine, Tel Aviv University, Tel Aviv, Israel. Department of Rheumatology, Tel Aviv Sourasky Medical Center, Tel Aviv, Israel.Sackler Faculty of Medicine, Tel Aviv University, Tel Aviv, Israel. Department of Infectious Diseases and Infection Control, Tel Aviv Sourasky Medical Center, Tel Aviv, Israel.Department of Pathology, Tel Aviv Sourasky Medical Center, Tel Aviv, Israel.Sackler Faculty of Medicine, Tel Aviv University, Tel Aviv, Israel. Department of Pathology, Tel Aviv Sourasky Medical Center, Tel Aviv, Israel.Sackler Faculty of Medicine, Tel Aviv University, Tel Aviv, Israel. Department of Dermatology, Tel Aviv Sourasky Medical Center, Tel Aviv, Israel. Department of Research and Development, Tel Aviv Sourasky Medical Center, Tel Aviv, Israel.Sackler Faculty of Medicine, Tel Aviv University, Tel Aviv, Israel. Department of Infectious Diseases and Infection Control, Tel Aviv Sourasky Medical Center, Tel Aviv, Israel.Sackler Faculty of Medicine, Tel Aviv University, Tel Aviv, Israel. Department of Infectious Diseases and Infection Control, Tel Aviv Sourasky Medical Center, Tel Aviv, Israel.

Pub Type(s)

Journal Article
Research Support, Non-U.S. Gov't

Language

eng

PubMed ID

35006256

Citation

Spitzer, Avishay, et al. "Association of a Third Dose of BNT162b2 Vaccine With Incidence of SARS-CoV-2 Infection Among Health Care Workers in Israel." JAMA, vol. 327, no. 4, 2022, pp. 341-349.
Spitzer A, Angel Y, Marudi O, et al. Association of a Third Dose of BNT162b2 Vaccine With Incidence of SARS-CoV-2 Infection Among Health Care Workers in Israel. JAMA. 2022;327(4):341-349.
Spitzer, A., Angel, Y., Marudi, O., Zeltser, D., Saiag, E., Goldshmidt, H., Goldiner, I., Stark, M., Halutz, O., Gamzu, R., Slobodkin, M., Amrami, N., Feigin, E., Elbaz, M., Furman, M., Bronstein, Y., Chikly, A., Eshkol, A., Furer, V., ... Henig, O. (2022). Association of a Third Dose of BNT162b2 Vaccine With Incidence of SARS-CoV-2 Infection Among Health Care Workers in Israel. JAMA, 327(4), 341-349. https://doi.org/10.1001/jama.2021.23641
Spitzer A, et al. Association of a Third Dose of BNT162b2 Vaccine With Incidence of SARS-CoV-2 Infection Among Health Care Workers in Israel. JAMA. 2022 01 25;327(4):341-349. PubMed PMID: 35006256.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR T1 - Association of a Third Dose of BNT162b2 Vaccine With Incidence of SARS-CoV-2 Infection Among Health Care Workers in Israel. AU - Spitzer,Avishay, AU - Angel,Yoel, AU - Marudi,Or, AU - Zeltser,David, AU - Saiag,Esther, AU - Goldshmidt,Hanoch, AU - Goldiner,Ilana, AU - Stark,Moshe, AU - Halutz,Ora, AU - Gamzu,Ronni, AU - Slobodkin,Marina, AU - Amrami,Nadav, AU - Feigin,Eugene, AU - Elbaz,Meital, AU - Furman,Moran, AU - Bronstein,Yotam, AU - Chikly,Amanda, AU - Eshkol,Anna, AU - Furer,Victoria, AU - Mayer,Talia, AU - Meijer,Suzy, AU - Melloul,Ariel, AU - Mizrahi,Michal, AU - Yakubovsky,Michal, AU - Rosenberg,Dana, AU - Safir,Ari, AU - Spitzer,Liron, AU - Taleb,Eyal, AU - Elkayam,Ori, AU - Silberman,Adi, AU - Eviatar,Tali, AU - Elalouf,Ofir, AU - Levinson,Tal, AU - Pozyuchenko,Katia, AU - Itzhaki-Alfia,Ayelet, AU - Sprecher,Eli, AU - Ben-Ami,Ronen, AU - Henig,Oryan, PY - 2022/1/11/pubmed PY - 2022/2/2/medline PY - 2022/1/10/entrez SP - 341 EP - 349 JF - JAMA JO - JAMA VL - 327 IS - 4 N2 - Importance: Administration of a BNT162b2 booster dose (Pfizer-BioNTech) to fully vaccinated individuals aged 60 years and older was significantly associated with lower risk of SARS-CoV-2 infection and severe illness. Data are lacking on the effectiveness of booster doses for younger individuals and health care workers. Objective: To estimate the association of a BNT162b2 booster dose with SARS-CoV-2 infections among health care workers who were previously vaccinated with a 2-dose series of BNT162b2. Design, Setting, and Participants: This was a prospective cohort study conducted at a tertiary medical center in Tel Aviv, Israel. The study cohort included 1928 immunocompetent health care workers who were previously vaccinated with a 2-dose series of BNT162b2, and had enrolled between August 8 and 19, 2021, with final follow-up reported through September 20, 2021. Screening for SARS-CoV-2 infection was performed every 14 days. Anti-spike protein receptor binding domain IgG titers were determined at baseline and 1 month after enrollment. Cox regression with time-dependent analysis was used to estimate hazard ratios of SARS-CoV-2 infection between booster-immunized status and 2-dose vaccinated (booster-nonimmunized) status. Exposures: Vaccination with a booster dose of BNT162b2 vaccine. Main Outcomes and Measures: The primary outcome was SARS-CoV-2 infection, as confirmed by reverse transcriptase-polymerase chain reaction. Results: Among 1928 participants, the median age was 44 years (IQR, 36-52 years) and 1381 were women (71.6%). Participants completed the 2-dose vaccination series a median of 210 days (IQR, 205-213 days) before study enrollment. A total of 1650 participants (85.6%) received the booster dose. During a median follow-up of 39 days (IQR, 35-41 days), SARS-CoV-2 infection occurred in 44 participants (incidence rate, 60.2 per 100 000 person-days); 31 (70.5%) were symptomatic. Five SARS-CoV-2 infections occurred in booster-immunized participants and 39 in booster-nonimmunized participants (incidence rate, 12.8 vs 116 per 100 000 person-days, respectively). In a time-dependent Cox regression analysis, the adjusted hazard ratio of SARS-CoV-2 infection for booster-immunized vs booster-nonimmunized participants was 0.07 (95% CI, 0.02-0.20). Conclusions and Relevance: Among health care workers at a single center in Israel who were previously vaccinated with a 2-dose series of BNT162b2, administration of a booster dose compared with not receiving one was associated with a significantly lower rate of SARS-CoV-2 infection over a median of 39 days of follow-up. Ongoing surveillance is required to assess durability of the findings. SN - 1538-3598 UR - https://www.unboundmedicine.com/medline/citation/35006256/Association_of_a_Third_Dose_of_BNT162b2_Vaccine_With_Incidence_of_SARS_CoV_2_Infection_Among_Health_Care_Workers_in_Israel_ DB - PRIME DP - Unbound Medicine ER -