Literature DB >> 34673751

Effectiveness of Pfizer-BioNTech mRNA Vaccination Against COVID-19 Hospitalization Among Persons Aged 12-18 Years - United States, June-September 2021.

Samantha M Olson, Margaret M Newhams, Natasha B Halasa, Ashley M Price, Julie A Boom, Leila C Sahni, Katherine Irby, Tracie C Walker, Stephanie P Schwartz, Pia S Pannaraj, Aline B Maddux, Tamara T Bradford, Ryan A Nofziger, Benjamin J Boutselis, Melissa L Cullimore, Elizabeth H Mack, Jennifer E Schuster, Shira J Gertz, Natalie Z Cvijanovich, Michele Kong, Melissa A Cameron, Mary A Staat, Emily R Levy, Brandon M Chatani, Kathleen Chiotos, Laura D Zambrano, Angela P Campbell, Manish M Patel, Adrienne G Randolph.   

Abstract

Pfizer-BioNTech COVID-19 vaccine is authorized for use in children and adolescents aged 12-15 years and is licensed by the Food and Drug Administration (FDA) for persons aged ≥16 (1). A randomized placebo-controlled trial demonstrated an efficacy of 100% (95% confidence interval [CI] = 75.3%-100%) in preventing outpatient COVID-19 in persons aged 12-15 years (2); however, data among adolescents on vaccine effectiveness (VE) against COVID-19 in real-world settings are limited, especially among hospitalized patients. In early September 2021, U.S. pediatric COVID-19 hospitalizations reached the highest level during the pandemic (3,4). In a test-negative, case-control study at 19 pediatric hospitals in 16 states during June 1-September 30, 2021, the effectiveness of 2 doses of Pfizer-BioNTech vaccine against COVID-19 hospitalization was assessed among children and adolescents aged 12-18 years. Among 464 hospitalized persons aged 12-18 years (179 case-patients and 285 controls), the median age was 15 years, 72% had at least one underlying condition, including obesity, and 68% attended in-person school. Effectiveness of 2 doses of Pfizer-BioNTech vaccine against COVID-19 hospitalization was 93% (95% CI = 83%-97%), during the period when B.1.617.2 (Delta) was the predominant variant. This evaluation demonstrated that 2 doses of Pfizer-BioNTech vaccine are highly effective at preventing COVID-19 hospitalization among persons aged 12-18 years and reinforces the importance of vaccination to protect U.S. youths against severe COVID-19.

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Year:  2021        PMID: 34673751      PMCID: PMC9361838          DOI: 10.15585/mmwr.mm7042e1

Source DB:  PubMed          Journal:  MMWR Morb Mortal Wkly Rep        ISSN: 0149-2195            Impact factor:   35.301


Pfizer-BioNTech COVID-19 vaccine is authorized for use in children and adolescents aged 12–15 years and is licensed by the Food and Drug Administration (FDA) for persons aged ≥16 (). A randomized placebo-controlled trial demonstrated an efficacy of 100% (95% confidence interval [CI] = 75.3%–100%) in preventing outpatient COVID-19 in persons aged 12–15 years (); however, data among adolescents on vaccine effectiveness (VE) against COVID-19 in real-world settings are limited, especially among hospitalized patients. In early September 2021, U.S. pediatric COVID-19 hospitalizations reached the highest level during the pandemic (,). In a test-negative, case-control study at 19 pediatric hospitals in 16 states during June 1–September 30, 2021, the effectiveness of 2 doses of Pfizer-BioNTech vaccine against COVID-19 hospitalization was assessed among children and adolescents aged 12–18 years. Among 464 hospitalized persons aged 12–18 years (179 case-patients and 285 controls), the median age was 15 years, 72% had at least one underlying condition, including obesity, and 68% attended in-person school. Effectiveness of 2 doses of Pfizer-BioNTech vaccine against COVID-19 hospitalization was 93% (95% CI = 83%–97%), during the period when B.1.617.2 (Delta) was the predominant variant. This evaluation demonstrated that 2 doses of Pfizer-BioNTech vaccine are highly effective at preventing COVID-19 hospitalization among persons aged 12–18 years and reinforces the importance of vaccination to protect U.S. youths against severe COVID-19. This study used a test-negative design, similar to other postauthorization VE evaluations, in which vaccine performance is assessed by comparing the odds of antecedent vaccination among laboratory-confirmed case-patients hospitalized with COVID-19 and hospitalized controls without COVID-19 (). Participants were aged 12–18 years and were admitted to 19 pediatric hospitals in the CDC-funded Overcoming COVID-19 Network during June 1–September 30, 2021 (). Case-patients were hospitalized with symptomatic COVID-19–like illness and a positive SARS-CoV-2 reverse transcription–polymerase chain reaction (RT-PCR) or antigen test result; no case-patients received a diagnosis of multisystem inflammatory syndrome in children (MIS-C) during their enrolling hospitalization. Two hospitalized control groups were enrolled: 1) patients with symptoms compatible with COVID-19 with negative SARS-CoV-2 RT-PCR or antigen test results (test-negative) and 2) patients without COVID-19–associated symptoms who might or might not have received SARS-CoV-2 testing (syndrome-negative). Baseline demographic characteristics, clinical information about the current illness, and SARS-CoV-2 testing history were obtained through parent or guardian interviews performed by trained study personnel and review of electronic medical records. Parents or guardians were asked about COVID-19 vaccination history, including number of doses and whether the most recent dose occurred in the last 14 days, location where vaccination occurred, vaccine manufacturer, and availability of a COVID-19 vaccination card. Study personnel searched sources, including state vaccination registries, electronic medical records, or other sources (including documentation from pediatricians) to verify reported or unknown vaccination status. Patients were considered to have received COVID-19 vaccination based on source documentation or by plausible self-report (vaccination dates and location were provided). Because vaccination with Moderna or Janssen vaccine were not authorized for persons aged <18 years at the time of this evaluation, only receipt of Pfizer-BioNTech vaccine was assessed in this analysis. The study included fully vaccinated persons aged 12–18 years with COVID-19 vaccination status categorized as 1) unvaccinated (no receipt of any COVID-19 vaccine before illness onset) or 2) fully vaccinated (receipt of 2 doses of Pfizer-BioNTech vaccine, with the second dose administered ≥14 days before illness onset). Patients who were partially vaccinated (i.e., received only 1 dose or received a second dose <14 days before illness onset) were excluded from the analysis. Descriptive statistics were used to compare characteristics of case-patients and controls. Pearson chi-square tests (categorical outcomes) or Wilcoxon rank-sum test for medians (continuous outcomes) were used to make comparisons between groups; statistical significance was defined as p<0.05. VE against COVID-19 hospitalization was calculated by comparing the odds of full COVID-19 vaccination among case-patients and controls using the equation VE = 100 × (1 – adjusted odds ratio), determined from logistic regression models. Firth penalized regression was used for models with six or fewer vaccinated case-patients. Models were adjusted for U.S. Census region, calendar month of admission, age, sex, and race/ethnicity (). Other factors were assessed (underlying health conditions and social vulnerability index) but were not included in the final model because they did not change the odds ratio of vaccination by >5% (). Sensitivity analyses were performed to evaluate whether VE differed by control group. VE was also stratified by age groups (12–15 and 16–18 years). Statistical analyses were conducted using SAS (version 9.4; SAS Institute). This activity was reviewed by CDC and the other participating institutions and was conducted consistent with applicable federal law and CDC policy.** During June 1–September 30, 2021, among 572 eligible patients, 108 were excluded, including 56 who were partially vaccinated or who completed vaccination 0–13 days before illness onset, 20 who were hospitalized >14 days after illness onset, 14 case-patients who received a positive SARS-CoV-2 test result but were admitted for non–COVID-19 reasons, and 18 who were excluded for other reasons. The 464 patients in the final analysis comprised 179 case-patients and 285 controls (122 [43%] test-negative and 163 [57%] syndrome-negative). Among case-patients and all controls, the median age was 15 years, 72% had at least one underlying condition, including obesity, and 68% attended in-person school (Table 1). Vaccination coverage was 3% among case-patients and 33% among controls. Case-patients more frequently resided in areas with higher social vulnerability index scores (median = 0.67) than did controls (median = 0.58) (p = 0.02). The distribution of most underlying conditions was not significantly different between case-patients and controls; however, diabetes was more prevalent among case-patients (12%) than among controls (5%) (p = 0.01), and neurologic or neuromuscular disorders were more prevalent among controls (28%) than among case-patients (12%) (p<0.01).
TABLE 1

Characteristics of hospitalized COVID-19 case-patients and controls aged 12–18 years — 19 pediatric hospitals, 16 states,* June–September 2021

Characteristic (no. unknown)Case status, no. (column %)
P-value
Total (N = 464)Case-patients (n = 179)Controls (n = 285)
Median age, yrs (IQR)
15 (14–17)
16 (14–17)
15 (14–17)
0.07
Age group, yrs
12–15
285 (61.4)
106 (59.2)
179 (62.8)
0.44
16–18
179 (38.6)
73 (40.8)
106 (37.2)
Sex
Female
210 (45.3)
90 (50.3)
120 (42.1)
0.09
Race/Ethnicity
White, non-Hispanic
193 (41.6)
68 (38.0)
125 (43.9)
0.27
Black, non-Hispanic
96 (20.7)
37 (20.7)
59 (20.7)
Hispanic, any race
125 (26.9)
57 (31.8)
68 (23.9)
Other, non-Hispanic
33 (7.1)
13 (7.3)
20 (7.0)
Unknown
17 (3.7)
4 (2.2)
13 (4.6)
Social vulnerability index,§ median (IQR) (1)
0.60 (0.34–0.82)
0.67 (0.37–0.85)
0.58 (0.32–0.80)
0.02
U.S. Census region*
Northeast
21 (4.5)
5 (2.8)
16 (5.6)
0.28
Midwest
60 (12.9)
28 (15.6)
32 (11.2)
South
283 (61.0)
106 (59.2)
177 (62.1)
West
100 (21.6)
40 (22.4)
60 (21.1)
Month of admission
June
21 (4.5)
7 (3.9)
14 (4.9)
0.03
July
50 (10.8)
29 (16.2)
21 (7.4)
August
159 (34.3)
58 (32.4)
101 (35.4)
September
234 (50.4)
85 (47.5)
149 (52.3)
Underlying health condition
At least one underlying condition (2)
333 (72.1)
131 (73.2)
202 (71.4)
0.67
Respiratory system disorder (4)
120 (26.1)
55 (30.9)
65 (23.1)
0.06
Asthma (6)
88 (19.2)
42 (23.7)
46 (16.4)
0.05
Cardiovascular system disorder (5)
29 (6.3)
7 (3.9)
22 (7.8)
0.09
Neurologic/Neuromuscular disorder (3)
100 (21.7)
21 (11.8)
79 (27.9)
<0.01
Active or prior oncologic disorder (3)
25 (5.4)
6 (3.4)
19 (6.7)
0.12
Nononcologic immunosuppressive disorder (5)
9 (2.0)
2 (1.1)
7 (2.5)
0.31
Endocrine disorder (3)
63 (13.7)
30 (16.8)
33 (11.7)
0.12
Diabetes (4)
35 (7.6)
21 (11.8)
14 (5.0)
0.01
Other chronic conditions (2)
226 (48.9)
100 (55.9)
126 (44.5)
0.02
Other characteristic
In-person school attendance (161)
205 (67.7)
80 (68.4)
125 (67.2)
0.83
Fully vaccinated**
99 (21.3)
6 (3.4)
93 (32.6)
<0.01
If fully vaccinated, median days from second vaccine to illness onset (IQR)††72 (45–97)55 (47–106)73 (43–97)0.68

Abbreviations: IQR = interquartile range; SVI = social vulnerability index.

* Patients were enrolled from 19 pediatric hospitals in 16 states. Northeast: Boston Children's Hospital (Massachusetts), Saint Barnabas Medical Center (New Jersey), Midwest: Akron Children’s Hospital (Ohio), Children’s Mercy Kansas City (Missouri), Children’s Hospital and Medical Center: Nebraska (Nebraska), Cincinnati Children’s Hospital Medical Center (Ohio), Mayo Clinic (Minnesota), South: Arkansas Children's Hospital (Arkansas), University of North Carolina at Chapel Hill Children’s Hospital (North Carolina), Children’s of Alabama (Alabama), Monroe Carell Jr. Children's Hospital at Vanderbilt (Tennessee), Medical University of South Carolina Children’s Health (South Carolina), Texas Children’s Hospital (Texas), Holtz Children’s Hospital (Florida), Children’s Hospital of New Orleans (Louisiana), West: University of California San Francisco Benioff Children’s Hospital Oakland (California), Children's Hospital Colorado (Colorado), Children’s Hospital Los Angeles (California), University of California San Diego-Rady Children’s Hospital (California).

† Testing for statistical significance was conducted using the Pearson chi-square test to compare categorical variables or Wilcoxon rank-sum test for medians to compare continuous data.

§ CDC/ATSDR SVI documentation is available at https://www.atsdr.cdc.gov/placeandhealth/svi/index.html. Median SVI for case-patients and controls are based on US 2018 SVI data.

¶ Other chronic conditions included rheumatologic/autoimmune disorder, hematologic disorder, renal or urologic dysfunction, gastrointestinal/hepatic disorder, metabolic or confirmed or suspected genetic disorder (including obesity), or atopic or allergic condition.

** COVID-19 vaccination status included the following two categories: 1) unvaccinated, defined as no receipt of any SARS-CoV-2 vaccine before illness onset and 2) fully vaccinated, defined as receipt of both doses of a 2-dose Pfizer-BioNTech vaccination ≥14 days before illness onset.

†† Dates are based on those with documented vaccination, not plausible self-report. The date of illness onset was used for case-patients and controls with COVID-19–like illness with median value imputed if missing. For controls without COVID-19–like illness, the date of admission was used for a date of illness onset, also referred to as illness onset for this report.

Abbreviations: IQR = interquartile range; SVI = social vulnerability index. * Patients were enrolled from 19 pediatric hospitals in 16 states. Northeast: Boston Children's Hospital (Massachusetts), Saint Barnabas Medical Center (New Jersey), Midwest: Akron Children’s Hospital (Ohio), Children’s Mercy Kansas City (Missouri), Children’s Hospital and Medical Center: Nebraska (Nebraska), Cincinnati Children’s Hospital Medical Center (Ohio), Mayo Clinic (Minnesota), South: Arkansas Children's Hospital (Arkansas), University of North Carolina at Chapel Hill Children’s Hospital (North Carolina), Children’s of Alabama (Alabama), Monroe Carell Jr. Children's Hospital at Vanderbilt (Tennessee), Medical University of South Carolina Children’s Health (South Carolina), Texas Children’s Hospital (Texas), Holtz Children’s Hospital (Florida), Children’s Hospital of New Orleans (Louisiana), West: University of California San Francisco Benioff Children’s Hospital Oakland (California), Children's Hospital Colorado (Colorado), Children’s Hospital Los Angeles (California), University of California San Diego-Rady Children’s Hospital (California). † Testing for statistical significance was conducted using the Pearson chi-square test to compare categorical variables or Wilcoxon rank-sum test for medians to compare continuous data. § CDC/ATSDR SVI documentation is available at https://www.atsdr.cdc.gov/placeandhealth/svi/index.html. Median SVI for case-patients and controls are based on US 2018 SVI data. ¶ Other chronic conditions included rheumatologic/autoimmune disorder, hematologic disorder, renal or urologic dysfunction, gastrointestinal/hepatic disorder, metabolic or confirmed or suspected genetic disorder (including obesity), or atopic or allergic condition. ** COVID-19 vaccination status included the following two categories: 1) unvaccinated, defined as no receipt of any SARS-CoV-2 vaccine before illness onset and 2) fully vaccinated, defined as receipt of both doses of a 2-dose Pfizer-BioNTech vaccination ≥14 days before illness onset. †† Dates are based on those with documented vaccination, not plausible self-report. The date of illness onset was used for case-patients and controls with COVID-19–like illness with median value imputed if missing. For controls without COVID-19–like illness, the date of admission was used for a date of illness onset, also referred to as illness onset for this report. Among 179 COVID-19 case-patients, six (3%) were vaccinated and 173 (97%) were unvaccinated (Table 2). Overall, 77 (43%) case-patients were admitted to an intensive care unit, and 29 (16%) critically ill case-patients received life support during hospitalization, including invasive mechanical ventilation, vasoactive infusions, or extracorporeal membrane oxygenation; two of these 29 critically ill patients (7%) died. All 77 case-patients admitted to the intensive care unit, all 29 critically ill case-patients, and both deaths occurred among unvaccinated case-patients. Among 169 case-patients with available hospital discharge data, the median length of hospital stay was 5 days (interquartile range [IQR] = 2–9 days) for unvaccinated case-patients and 3 days (IQR = 2–4 days) for vaccinated case-patients.
TABLE 2

Clinical outcomes and severity among hospitalized COVID-19 case-patients aged 12–18 years, by vaccination status* — 19 pediatric hospitals, 16 states, June–September 2021

Characteristic (no. unknown)Case-patients hospitalized with COVID-19, no. (%)
Total (N = 179)Unvaccinated (n = 173)Fully vaccinated (n = 6)
ICU admission
77 (43.0)
77 (44.5)
0 (—)
Critically ill patients on life support
29 (16.2)
29 (16.8)
0 (—)
Invasive mechanical ventilation
21 (11.7)
21 (12.1)
0 (—)
Vasoactive infusions (1)
20 (11.2)
20 (11.6)
0 (—)
Extracorporeal membrane oxygenation (2)
7 (4.0)
7 (4.1)
0 (—)
Patients with discharge data, no./total no (%)
172/179 (96.1)
166/173 (96.0)
6/6 (100)
Hospital length of stay, median (IQR) (10)
5 (2–9)
5 (2–9)
3 (2–4)
Died before discharge (7)2 (1.2)2 (1.2)0 (—)

Abbreviations: ICU = intensive care unit; IQR = interquartile range.

* COVID-19 vaccination status included the following two categories: 1) unvaccinated, defined as no receipt of any SARS-CoV-2 vaccine before illness onset and 2) fully vaccinated, defined as receipt of both doses of a 2-dose Pfizer-BioNTech vaccination ≥14 days before illness onset.

† Patients were vaccinated and unvaccinated persons aged 12–18 years enrolled from 19 pediatric hospitals in 16 states. Northeast: Boston Children's Hospital (Massachusetts), Saint Barnabas Medical Center (New Jersey), Midwest: Akron Children’s Hospital (Ohio), Children’s Mercy Kansas City (Missouri), Children’s Hospital and Medical Center: Nebraska (Nebraska), Cincinnati Children’s Hospital Medical Center (Ohio), Mayo Clinic (Minnesota), South: Arkansas Children's Hospital (Arkansas), University of North Carolina at Chapel Hill Children’s Hospital (North Carolina), Children’s of Alabama (Alabama), Monroe Carell Jr. Children's Hospital at Vanderbilt (Tennessee), Medical University of South Carolina Children’s Health (South Carolina), Texas Children’s Hospital (Texas), Holtz Children’s Hospital (Florida), Children’s Hospital of New Orleans (Louisiana), West: University of California San Francisco Benioff Children’s Hospital Oakland (California), Children's Hospital Colorado (Colorado), Children’s Hospital Los Angeles (California), University of California San Diego-Rady Children’s Hospital (California).

Abbreviations: ICU = intensive care unit; IQR = interquartile range. * COVID-19 vaccination status included the following two categories: 1) unvaccinated, defined as no receipt of any SARS-CoV-2 vaccine before illness onset and 2) fully vaccinated, defined as receipt of both doses of a 2-dose Pfizer-BioNTech vaccination ≥14 days before illness onset. † Patients were vaccinated and unvaccinated persons aged 12–18 years enrolled from 19 pediatric hospitals in 16 states. Northeast: Boston Children's Hospital (Massachusetts), Saint Barnabas Medical Center (New Jersey), Midwest: Akron Children’s Hospital (Ohio), Children’s Mercy Kansas City (Missouri), Children’s Hospital and Medical Center: Nebraska (Nebraska), Cincinnati Children’s Hospital Medical Center (Ohio), Mayo Clinic (Minnesota), South: Arkansas Children's Hospital (Arkansas), University of North Carolina at Chapel Hill Children’s Hospital (North Carolina), Children’s of Alabama (Alabama), Monroe Carell Jr. Children's Hospital at Vanderbilt (Tennessee), Medical University of South Carolina Children’s Health (South Carolina), Texas Children’s Hospital (Texas), Holtz Children’s Hospital (Florida), Children’s Hospital of New Orleans (Louisiana), West: University of California San Francisco Benioff Children’s Hospital Oakland (California), Children's Hospital Colorado (Colorado), Children’s Hospital Los Angeles (California), University of California San Diego-Rady Children’s Hospital (California). VE against COVID-19 hospitalization was 93% (95% CI = 83%–97%) (Table 3), during the period when B.1.617.2 (Delta) was the predominant variant. Among all 99 patients classified as fully vaccinated, 96 (97%) had documentation of vaccination status. In a sensitivity analysis, VE was similar for each control group assessed independently (test-negative VE = 94%, 95% CI = 85%–98%; syndrome-negative VE = 92%, 95% CI = 80%–97%). In addition, VE was similar among 106 case-patients aged 12–15 years (VE = 91%) and 73 case-patients aged 16–18 years (VE = 94%).
TABLE 3

Vaccine effectiveness* against COVID-19 among hospitalized patients aged 12–18 years, by vaccination status — 19 pediatric hospitals, 16 states, July–September 2021

Age group, yrsNo. vaccinated/Total (%)
Vaccine effectiveness, % (95% CI)
Case-patientsControls
All
6/179 (3.4)
93/285 (32.6)
93 (83–97)
12–15
4/106 (3.8)
53/179 (29.6)
91 (74–97)
16–182/73 (2.7)40/106 (37.7)94 (78–99)

Abbreviation: CI = confidence interval.

* Vaccine effectiveness estimates were based on odds of antecedent vaccination in case-patients vs controls adjusted for U.S. Census region, calendar month of admission, continuous age in years, sex, race/ethnicity (non-Hispanic White, non-Hispanic Black, non-Hispanic other, Hispanic of any race, or unknown). Firth penalized regression was used for models with six or fewer vaccinated cases.

† COVID-19 vaccination status included the following two categories: 1) unvaccinated, defined as no receipt of any SARS-CoV-2 vaccine before illness onset and 2) fully vaccinated, defined as receipt of both doses of a 2-dose Pfizer-BioNTech vaccination ≥14 days before illness onset.

§ Patients were enrolled from 19 pediatric hospitals in 16 states. Northeast: Boston Children's Hospital (Massachusetts), Saint Barnabas Medical Center (New Jersey), Midwest: Akron Children’s Hospital (Ohio), Children’s Mercy Kansas City (Missouri), Children’s Hospital and Medical Center: Nebraska (Nebraska), Cincinnati Children’s Hospital Medical Center (Ohio), Mayo Clinic (Minnesota), South: Arkansas Children's Hospital (Arkansas), University of North Carolina at Chapel Hill Children’s Hospital (North Carolina), Children’s of Alabama (Alabama), Monroe Carell Jr. Children's Hospital at Vanderbilt (Tennessee), Medical University of South Carolina Children’s Health (South Carolina), Texas Children’s Hospital (Texas), Holtz Children’s Hospital (Florida), Children’s Hospital of New Orleans (Louisiana), West: University of California San Francisco Benioff Children’s Hospital Oakland (California), Children's Hospital Colorado (Colorado), Children’s Hospital Los Angeles (California), University of California San Diego-Rady Children’s Hospital (California).

Abbreviation: CI = confidence interval. * Vaccine effectiveness estimates were based on odds of antecedent vaccination in case-patients vs controls adjusted for U.S. Census region, calendar month of admission, continuous age in years, sex, race/ethnicity (non-Hispanic White, non-Hispanic Black, non-Hispanic other, Hispanic of any race, or unknown). Firth penalized regression was used for models with six or fewer vaccinated cases. † COVID-19 vaccination status included the following two categories: 1) unvaccinated, defined as no receipt of any SARS-CoV-2 vaccine before illness onset and 2) fully vaccinated, defined as receipt of both doses of a 2-dose Pfizer-BioNTech vaccination ≥14 days before illness onset. § Patients were enrolled from 19 pediatric hospitals in 16 states. Northeast: Boston Children's Hospital (Massachusetts), Saint Barnabas Medical Center (New Jersey), Midwest: Akron Children’s Hospital (Ohio), Children’s Mercy Kansas City (Missouri), Children’s Hospital and Medical Center: Nebraska (Nebraska), Cincinnati Children’s Hospital Medical Center (Ohio), Mayo Clinic (Minnesota), South: Arkansas Children's Hospital (Arkansas), University of North Carolina at Chapel Hill Children’s Hospital (North Carolina), Children’s of Alabama (Alabama), Monroe Carell Jr. Children's Hospital at Vanderbilt (Tennessee), Medical University of South Carolina Children’s Health (South Carolina), Texas Children’s Hospital (Texas), Holtz Children’s Hospital (Florida), Children’s Hospital of New Orleans (Louisiana), West: University of California San Francisco Benioff Children’s Hospital Oakland (California), Children's Hospital Colorado (Colorado), Children’s Hospital Los Angeles (California), University of California San Diego-Rady Children’s Hospital (California).

Discussion

During June–September 2021, receipt of 2 doses of Pfizer-BioNTech vaccine provided a high level of protection against COVID-19 hospitalization among children and adolescents aged 12–18 years in a real-world evaluation at 19 U.S. pediatric hospitals. This evaluation demonstrated that nearly all (97%) persons aged 12–18 years hospitalized with COVID-19 were unvaccinated (versus fully vaccinated) and reinforces the importance of vaccination to protect U.S. youths against severe COVID-19. These findings are consistent with efficacy data from the Pfizer-BioNTech clinical trial among persons aged 12–15 years, which found an observed vaccine efficacy of 100% (95% CI = 75.3%–100%) (). However, that trial was not powered to assess efficacy against hospitalized COVID-19. Another study reported VE against COVID-19 hospitalization of 81% for fully vaccinated patients aged 12–15 years; however, that study assessed only 45 cases and thus had wide CIs (–55% to 98%) (). One other evaluation from Israel evaluated Pfizer-BioNTech VE against SARS-CoV-2 infection in patients aged 12–15 years and found similarly high VE (91.5%; 95% CI = 88.2%–93.9%), but the study did not include enough cases to examine VE against hospitalized COVID-19 (). In this real-world analysis, in which all case-patients were hospitalized, vaccination reduced the risk for COVID-19 hospitalization in persons aged 12–18 years by 93%. Moreover, 16% of patients hospitalized with COVID-19 had critical illness requiring life support; all were unvaccinated. Taken together, these findings contribute to the growing knowledge regarding VE against pediatric COVID-19, as updated FDA Emergency Use Authorizations to expand COVID-19 vaccine eligibility to younger ages are considered. The findings in this report are subject to at least six limitations. First, VE could not be assessed directly against specific variants; the predominant variant during the evaluation period was B.1.617.2 (Delta) (). Second, the sample was too small to assess VE by underlying conditions or by other subgroups of interest, including against critical illness. Third, because this analysis included self-reported data from some participants, vaccination status might have been misclassified in a few case-patients or controls, or there might have been imperfect recollection of illness onset dates. Fourth, because of high levels of COVID-19 transmission in southern states during this period, the majority of patients in this analysis (61%) were from the South; this might limit the representativeness of the sample. Fifth, this report only assessed VE for the Pfizer-BioNTech vaccine. Finally, because vaccination of persons aged 12–15 years commenced only recently, evaluation of duration of protection was not possible. As of October 18, 2021, 46% of U.S. children and adolescents aged 12–15 years and 54% of those aged 16–17 years were fully vaccinated against COVID-19 (). In a multistate network of U.S. pediatric hospitals, this study found that receipt of 2 doses of Pfizer-BioNTech vaccine was highly effective in preventing COVID-19 hospitalization among persons aged 12–18 years. These data suggest that increasing vaccination coverage among this group could reduce the incidence of severe COVID-19 in the United States. Further, as in-person school attendance increases, multicomponent preventive measures to reduce the incidence of severe COVID-19 among adolescents, including vaccination, are imperative.

What is already known about this topic?

Persons aged 12–18 years are eligible to receive COVID-19 vaccine. Currently, data are lacking on real-world vaccine effectiveness against COVID-19 hospitalization in adolescents.

What is added by this report?

Among hospitalized U.S. patients aged 12–18 years, vaccine effectiveness of 2 doses of Pfizer-BioNTech vaccine against COVID-19 hospitalization during June–September 2021, was 93% (95% confidence interval = 83%–97%).

What are the implications for public health practice?

This evaluation demonstrated that 2 doses of Pfizer-BioNTech vaccine were highly effective in preventing COVID-19 hospitalization among persons aged 12–18 years. Findings reinforce the importance of vaccination to protect U.S. youths against severe COVID-19.
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Journal:  Bull Natl Res Cent       Date:  2022-09-16

2.  Post-vaccination infection rates and modification of COVID-19 symptoms in vaccinated UK school-aged children and adolescents: A prospective longitudinal cohort study.

Authors:  Erika Molteni; Liane S Canas; Kerstin Kläser; Jie Deng; Sunil S Bhopal; Robert C Hughes; Liyuan Chen; Benjamin Murray; Eric Kerfoot; Michela Antonelli; Carole H Sudre; Joan Capdevila Pujol; Lorenzo Polidori; Anna May; Prof Alexander Hammers; Jonathan Wolf; Prof Tim D Spector; Claire J Steves; Prof Sebastien Ourselin; Michael Absoud; Marc Modat; Prof Emma L Duncan
Journal:  Lancet Reg Health Eur       Date:  2022-07-08

3.  Association of Severe Acute Respiratory Syndrome Coronavirus 2 Vaccination or a Prior Positive Test Result in Adolescents during the Delta Variant Surge in Kentucky.

Authors:  Kevin B Spicer; Connor Glick; Alyson M Cavanaugh; Douglas Thoroughman
Journal:  J Pediatr       Date:  2022-05-27       Impact factor: 6.314

4.  Interim Estimate of Vaccine Effectiveness of BNT162b2 (Pfizer-BioNTech) Vaccine in Preventing SARS-CoV-2 Infection Among Adolescents Aged 12-17 Years - Arizona, July-December 2021.

Authors:  Karen Lutrick; Patrick Rivers; Young M Yoo; Lauren Grant; James Hollister; Krystal Jovel; Sana Khan; Ashley Lowe; Zoe Baccam; Hanna Hanson; Lauren E W Olsho; Ashley Fowlkes; Alberto J Caban-Martinez; Cynthia Porter; Sarang Yoon; Jennifer Meece; Manjusha Gaglani; Joy Burns; Julie Mayo Lamberte; Flavia Nakayima Miiro; Adam Bissonnette; Lindsay LeClair; Preeta K Kutty; James K Romine; Elisha Stefanski; Laura J Edwards; Katherine Ellingson; Joe K Gerald; Edward J Bedrick; Purnima Madhivanan; Karl Krupp; Lynn B Gerald; Mark Thompson; Jefferey L Burgess
Journal:  MMWR Morb Mortal Wkly Rep       Date:  2021-12-31       Impact factor: 17.586

5.  Safety and effectiveness of BNT162b2 mRNA Covid-19 vaccine in adolescents.

Authors:  Young June Choe; Seonju Yi; Insob Hwang; Jia Kim; Young-Joon Park; Eunhee Cho; Myoungyoun Jo; Hyunju Lee; Eun Hwa Choi
Journal:  Vaccine       Date:  2021-12-24       Impact factor: 3.641

6.  Effectiveness of BNT162b2 Vaccine against Critical Covid-19 in Adolescents.

Authors:  Samantha M Olson; Margaret M Newhams; Natasha B Halasa; Ashley M Price; Julie A Boom; Leila C Sahni; Pia S Pannaraj; Katherine Irby; Tracie C Walker; Stephanie P Schwartz; Aline B Maddux; Elizabeth H Mack; Tamara T Bradford; Jennifer E Schuster; Ryan A Nofziger; Melissa A Cameron; Kathleen Chiotos; Melissa L Cullimore; Shira J Gertz; Emily R Levy; Michele Kong; Natalie Z Cvijanovich; Mary A Staat; Satoshi Kamidani; Brandon M Chatani; Samina S Bhumbra; Katherine E Bline; Mary G Gaspers; Charlotte V Hobbs; Sabrina M Heidemann; Mia Maamari; Heidi R Flori; Janet R Hume; Matt S Zinter; Kelly N Michelson; Laura D Zambrano; Angela P Campbell; Manish M Patel; Adrienne G Randolph
Journal:  N Engl J Med       Date:  2022-01-12       Impact factor: 176.079

Review 7.  Considerations for the Safe Operation of Schools During the Coronavirus Pandemic.

Authors:  Ronan Lordan; Samantha Prior; Elizabeth Hennessy; Amruta Naik; Soumita Ghosh; Georgios K Paschos; Carsten Skarke; Kayla Barekat; Taylor Hollingsworth; Sydney Juska; Liudmila L Mazaleuskaya; Sarah Teegarden; Abigail L Glascock; Sean Anderson; Hu Meng; Soon-Yew Tang; Aalim Weljie; Lisa Bottalico; Emanuela Ricciotti; Perla Cherfane; Antonijo Mrcela; Gregory Grant; Kristen Poole; Natalie Mayer; Michael Waring; Laura Adang; Julie Becker; Susanne Fries; Garret A FitzGerald; Tilo Grosser
Journal:  Front Public Health       Date:  2021-12-16

Review 8.  Effectiveness of BNT162b2 and mRNA-1273 Vaccines against COVID-19 Infection: A Meta-Analysis of Test-Negative Design Studies.

Authors:  Shuailei Chang; Hongbo Liu; Jian Wu; Wenwei Xiao; Sijia Chen; Shaofu Qiu; Guangcai Duan; Hongbin Song; Rongguang Zhang
Journal:  Vaccines (Basel)       Date:  2022-03-18

9.  The COVID-19 pandemic in children and young people during 2020-2021: A complex discussion on vaccination.

Authors:  Igor Rudan; Davies Adeloye; Vittal Katikireddi; Josie Murray; Colin Simpson; Syed Ahmar Shah; Chris Robertson; Aziz Sheikh
Journal:  J Glob Health       Date:  2021-12-25       Impact factor: 7.664

Review 10.  Messenger ribonucleic acid vaccines for severe acute respiratory syndrome coronavirus-2 - a review.

Authors:  Christine M Akamine; Hana M El Sahly
Journal:  Transl Res       Date:  2021-12-23       Impact factor: 7.012

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