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Morbidity and Mortality Weekly Report logoLink to Morbidity and Mortality Weekly Report
. 2022 Feb 18;71(7):264–270. doi: 10.15585/mmwr.mm7107e3

Effectiveness of Maternal Vaccination with mRNA COVID-19 Vaccine During Pregnancy Against COVID-19–Associated Hospitalization in Infants Aged <6 Months — 17 States, July 2021–January 2022

Natasha B Halasa 1, Samantha M Olson 2,, Mary A Staat 3, Margaret M Newhams 4, Ashley M Price 2, Julie A Boom 5, Leila C Sahni 5, Melissa A Cameron 6, Pia S Pannaraj 7, Katherine E Bline 8, Samina S Bhumbra 9, Tamara T Bradford 10, Kathleen Chiotos 11, Bria M Coates 12, Melissa L Cullimore 13, Natalie Z Cvijanovich 14, Heidi R Flori 15, Shira J Gertz 16, Sabrina M Heidemann 17, Charlotte V Hobbs 18, Janet R Hume 19, Katherine Irby 20, Satoshi Kamidani 21, Michele Kong 22, Emily R Levy 23, Elizabeth H Mack 24, Aline B Maddux 25, Kelly N Michelson 12, Ryan A Nofziger 26, Jennifer E Schuster 27, Stephanie P Schwartz 28, Laura Smallcomb 29, Keiko M Tarquinio 30, Tracie C Walker 28, Matt S Zinter 31, Suzanne M Gilboa 2, Kara N Polen 2, Angela P Campbell 2, Adrienne G Randolph 4,32, Manish M Patel 2; Overcoming COVID-19 Investigators1; Overcoming COVID-19 Network, Laura D Zambrano 2, Meghan Murdock 3, Mary Glas Gaspers 4, Connor P Kelley 5, Katri V Typpo 6, Peter M Mourani 7, Ronald C Sanders 8, Chelsea Smith 9, Masson Yates 10, Katheryn Crane 11, Geraldina Lionetti 12,13, Juliana Murcia-Montoya 14,15, Denise Villarreal-Chico 16, Daniel Hakimi 17, Adam L Skura 18, Imogene Carson 19, Justin M Lockwood 20, Emily Port 21, Brandon M Chatani 22, Nadine Baida 23, Laila Hussaini 24, Hassan A Khan 25, Simone T Rhodes 26, Courtney M Rowan 27, Mary Stumpf 28, Marla S Johnston 29, Laura Berbert 30, Benjamin J Boutselis 31, Sabrina R Chen 32, Jie He 33, Suden Kucukak 34, Timothy P McCadden 35, Amber O Orzel 36, Edie Weller 37, Patrick Moran 38, Ellen R Bruno 39, Lexie A Goertzen 40, Supriya Behl 41, Noelle M Drapeau 42, Lacy Malloch 43, Lora Martin 44, April Palmer 45, Roberto P Santos 46, Abigail Kietzman 47, Melissa Sullivan 48, Lauren A Hoody 49, Valerie H Rinehart 50, Paris C Bennett 51, Merry L Tomcany 52, Nicole A Twinem 53, Chelsea C Rohlfs 54, Amber Wolfe 55, Rebecca L Douglas 56, Kathlyn Phengchomphet 57, Megan M Bickford 58, Lauren E Wakefield 59, Meena Golchha 60, Laura S Stewart 61, Jennifer N Oates 62, Cindy Bowens 63, Mia Maamari 64
PMCID: PMC8853480  PMID: 35176002

COVID-19 vaccination is recommended for persons who are pregnant, breastfeeding, trying to get pregnant now, or who might become pregnant in the future, to protect them from COVID-19.§ Infants are at risk for life-threatening complications from COVID-19, including acute respiratory failure (1). Evidence from other vaccine-preventable diseases suggests that maternal immunization can provide protection to infants, especially during the high-risk first 6 months of life, through passive transplacental antibody transfer (2). Recent studies of COVID-19 vaccination during pregnancy suggest the possibility of transplacental transfer of SARS-CoV-2–specific antibodies that might provide protection to infants (35); however, no epidemiologic evidence currently exists for the protective benefits of maternal immunization during pregnancy against COVID-19 in infants. The Overcoming COVID-19 network conducted a test-negative, case-control study at 20 pediatric hospitals in 17 states during July 1, 2021–January 17, 2022, to assess effectiveness of maternal completion of a 2-dose primary mRNA COVID-19 vaccination series during pregnancy against COVID-19 hospitalization in infants. Among 379 hospitalized infants aged <6 months (176 with COVID-19 [case-infants] and 203 without COVID-19 [control-infants]), the median age was 2 months, 21% had at least one underlying medical condition, and 22% of case- and control-infants were born premature (<37 weeks gestation). Effectiveness of maternal vaccination during pregnancy against COVID-19 hospitalization in infants aged <6 months was 61% (95% CI = 31%–78%). Completion of a 2-dose mRNA COVID-19 vaccination series during pregnancy might help prevent COVID-19 hospitalization among infants aged <6 months.

Using a test-negative, case-control study design, vaccine performance was assessed by comparing the odds of having completed a 2-dose primary mRNA COVID-19 vaccination series during pregnancy among mothers of case-infants and control-infants (those with negative SARS-CoV-2 test results) (6). Participating infants were aged <6 months and admitted outside of their birth hospitalization to one of 20 pediatric hospitals during July 1, 2021–January 17, 2022. During this period, the SARS-CoV-2 Delta variant was the predominant variant in the United States through mid-December, after which Omicron became predominant. Case-infants were hospitalized with COVID-19 as the primary reason for admission or had clinical symptoms consistent with acute COVID-19,** and case-infants had a positive SARS-CoV-2 reverse transcription–polymerase chain reaction (RT-PCR) or antigen test result. No case-infant received a diagnosis of multisystem inflammatory syndrome. Control-infants were those hospitalized with or without COVID-19 symptoms and with negative SARS-CoV-2 RT-PCR or antigen test results. Enrolled control-infants were matched to case-infants by site and were hospitalized within 3–4 weeks of a case-infant’s admission date. Baseline demographic characteristics, clinical information, and SARS-CoV-2 testing history were obtained through parent or guardian interviews performed by trained study personnel during hospitalization or after discharge, and electronic medical record review of the infant’s record. Mothers were asked about their COVID-19 vaccination history, including number of doses and whether a dose had been received during pregnancy, location where vaccine was received, vaccine manufacturer, and availability of a COVID-19 vaccination card. Study personnel reviewed documented sources, including state vaccination registries, electronic medical records, or other sources (e.g., documentation from primary care providers) to verify vaccination status.

Mothers were considered vaccinated against COVID-19 if they completed a 2-dose series of either Pfizer-BioNTech or Moderna mRNA COVID-19 vaccine, based on source documentation or by plausible self-report (provision of vaccination dates and location). Maternal COVID-19 vaccination status was categorized as 1) unvaccinated (mothers who did not receive COVID-19 vaccine before their infants’ hospitalization) or 2) vaccinated†† (mothers who completed their 2-dose primary mRNA COVID-19 vaccine series during pregnancy ≥14 days before delivery). SARS-CoV-2 infection status of the mother during pregnancy or after delivery was not documented in this evaluation. Mothers were excluded if they were partially vaccinated during pregnancy (1 dose during pregnancy and none before pregnancy) or vaccinated after pregnancy (71), received Janssen (Johnson & Johnson) COVID-19 vaccine (four), received 2 doses of COVID-19 vaccination before pregnancy (seven), or received >2 doses of COVID-19 vaccine ≥14 days before delivery (10).

Descriptive statistics (Pearson chi-square tests and Fisher’s exact tests for categorical outcomes or Wilcoxon rank-sum tests for continuous outcomes) were used to compare characteristics of case- and control-infants; p-values <0.05 were considered statistically significant. Effectiveness of maternal vaccination (i.e., vaccine effectiveness [VE]) against infant COVID-19 hospitalization was calculated using the equation VE = 100% × (1 – adjusted odds ratio of completing 2-doses of COVID-19 mRNA vaccines during pregnancy among mothers of case-infants and control-infants), determined from logistic regression models. Models were adjusted for infant age and sex, U.S. Census region, calendar time of admission, and race/ethnicity (6). Other factors were assessed (e.g., infant’s underlying health conditions, Social Vulnerability Index, and behavioral factors) but were not included in the final model because they did not change the odds ratio of vaccination by >5% or because data on many infants were not available (e.g., breastfeeding history, prematurity, or child care attendance). In a secondary analysis, effectiveness of maternal receipt of the second dose of COVID-19 vaccination early in pregnancy (within the first 20 weeks) and late in pregnancy (21 weeks through 14 days before delivery) was assessed. Statistical analyses were conducted using SAS (version 9.4; SAS Institute). Procedures were approved as public health surveillance by each participating site and CDC and were conducted consistent with applicable federal law and CDC policy.§§

During July 1, 2021–January 17, 2022, among 483 eligible infants in 20 pediatric hospitals in 17 states, 104 (22%) were excluded; 71 excluded infants were born to mothers partially vaccinated during pregnancy or vaccinated after delivery, 10 were born to mothers who received a third vaccine dose ≥14 days before delivery, and 23 were excluded for other reasons.¶¶ Among the remaining 379 hospitalized infants (176 case-infants and 203 control-infants), the median age was 2 months, 80 (21%) had at least one underlying medical condition, and 72 (22%) were born premature (Table 1). Among case-infants, 16% of mothers had received 2 COVID-19 vaccine doses during pregnancy, whereas 32% of control-infant mothers were vaccinated. Case- and control-infants had similar prevalences of underlying medical conditions (20% and 23%, respectively; p = 0.42) and prematurity (23% and 21%, respectively; p = 0.58). Case-infants were more commonly non-Hispanic Black (18%) and Hispanic (34%) than were control-infants (9% and 28%, respectively).

TABLE 1. Characteristics of infants aged <6 months hospitalized with COVID-19 (case-infants) and without COVID-19 (control-infants) — 20 pediatric hospitals, 17 states,* July 2021–January 2022.

Characteristic (no. missing) Case status, n/N (column %)
p-value§
Case-infants (N = 176) Control-infants (N = 203)
Median age, mos (IQR)
2 (1–3)
2 (1–3)
0.96
Age group, mos
0–2
129 (73.3)
153 (75.4)
0.64
3–5
47 (26.7)
50 (24.6)
Sex
Female
84 (47.7)
83 (40.9)
0.18
Race and ethnicity
Black, non-Hispanic
32 (18.2)
19 (9.4)
0.02
White, non-Hispanic
56 (31.8)
82 (40.4)
Other, non-Hispanic
10 (5.7)
21 (10.3)
Hispanic, any race
60 (34.1)
56 (27.6)
Unknown
18 (10.2)
25 (12.3)
Social Vulnerability Index, (IQR) (1)
0.71 (0.39–0.86)
0.61 (0.29–0.83)
0.06
U.S. Census region*
Northeast
30 (17.1)
29 (14.3)
0.08
Midwest
44 (25.0)
60 (29.6)
South
54 (30.7)
42 (20.7)
West
48 (27.3)
72 (35.5)
Month of admission
July
10 (5.7)
5 (2.5)
0.14
August
23 (13.1)
26 (12.8)
September
16 (9.1)
25 (12.3)
October
10 (5.7)
21 (10.3)
November
18 (10.2)
30 (14.8)
December
59 (33.5)
51 (25.1)
January**
40 (22.7)
45 (22.2)
Underlying health condition in infants
At least one underlying condition (5)
34/174 (19.5)
46/200 (23.0)
0.42
Respiratory disorder (6)
9/174 (5.2)
9/199 (4.5)
0.77
Cardiovascular system disorder (5)
15/174 (8.6)
19/200 (9.5)
0.77
Neurologic/Neuromuscular disorder (5)
4/174 (2.3)
7/200 (3.5)
0.49
Immunosuppression or autoimmune (5)
0/174 (—)
2/200 (1.0)
0.50
Other chronic conditions†† (6)
18/174 (10.3)
23/199 (11.6)
0.71
Preterm birth (born <37 weeks gestation) (50)
34/146 (23.3)
38/183 (20.8)
0.58
Maternal vaccination during pregnancy §§
28 (15.9)
65 (32.0)
<0.01
Timing of maternal vaccination¶¶ (3)

Early pregnancy (first 20 weeks)
17/165 (10.3)
26/164 (15.9)
0.14
Late pregnancy (21 weeks–14 days before delivery)
9/157 (5.7)
38/176 (21.6)
<0.01
Maternal vaccine type

Pfizer-BioNTech
20 (71.4)
35 (53.9)
0.11
Moderna
8 (28.6)
30 (46.2)
Behavioral factors***
Breastfeeding (103)
76/138 (55.1)
90/138 (65.2)
0.09
Child care (108) 6/135 (4.4) 9/136 (6.6) 0.43

Abbreviation: SVI = Social Vulnerability Index.

* Infants were enrolled from 20 pediatric hospitals in 17 states. Northeast: Boston Children’s Hospital (Massachusetts), Cooperman Barnabas Medical Center (New Jersey), and Children’s Hospital of Philadelphia (Pennsylvania); Midwest: Akron Children’s Hospital (Ohio), Nationwide (Ohio), Children’s Mercy Kansas City (Missouri), Mayo Clinic (Minnesota), Riley Children’s (Indiana), Lurie Children’s Hospital (Illinois), Minnesota Masonic (Minnesota), and Children’s Hospital of Michigan (Michigan); South: Arkansas Children’s Hospital (Arkansas), University of North Carolina at Chapel Hill Children’s Hospital (North Carolina), Medical University of South Carolina Children’s Health (South Carolina), Texas Children’s Hospital (Texas), Children’s Hospital of New Orleans (Louisiana), and Children’s Healthcare of Atlanta, Emory (Georgia); West: Children’s Hospital Colorado (Colorado), Children’s Hospital Los Angeles (California), and University of California San Diego-Rady Children’s Hospital (California).

If N is less than total.

§ Testing for statistical significance was conducted using the Pearson chi-square test and Fisher’s exact test for comparisons with fewer than five observations. Wilcoxon rank-sum tests were used to compare continuous data.

CDC/Agency for Toxic Substances and Disease Registry SVI documentation is available at https://www.atsdr.cdc.gov/placeandhealth/svi/index.html. Median SVI for case-infants and control-infants are based on 2018 U.S. SVI data. The SVI ranges from 0 to 1.0, with higher scores indicating greater social vulnerability. One control-infant was missing an SVI score.

** January numbers do not reflect the entire month. Patients included were admitted through January 17, 2022.

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

§§ COVID-19 vaccination status included the following two categories: 1) unvaccinated (mothers who did not receive COVID-19 vaccine doses before their infant’s hospitalization) or 2) vaccinated (mothers who completed their 2-dose primary mRNA COVID-19 vaccination series during pregnancy and ≥14 days before delivery).

¶¶ Timing of vaccination is based on date of receipt of the second dose of a 2-dose primary mRNA COVID-19 vaccine series during pregnancy.

*** Behavioral factors are reported during interview with mother or proxy. Breastfeeding included any breastfeeding (either exclusive or partial).

Among case-infants, 43 (24%) were admitted to an intensive care unit (ICU) (Table 2). A total of 25 (15%) case-infants were critically ill and received life support during hospitalization, including mechanical ventilation, vasoactive infusions, or extracorporeal membrane oxygenation (ECMO); among these critically ill infants, one (0.4%) died. Of the 43 case-infants admitted to an ICU, 88% had mothers who were unvaccinated. The mothers of the one case-infant who required ECMO and one case-infant who died were both unvaccinated.

TABLE 2. Clinical outcomes and severity among case-infants aged <6 months hospitalized with COVID-19, by maternal vaccination status during pregnancy* — 20 pediatric hospitals, 17 states, July 2021–January 2022.

Characteristic (no. unknown) Maternal vaccination status during pregnancy, n/N (%)
Total 
(N = 176) Unvaccinated
(n = 148) Vaccinated (2-doses of mRNA COVID-19 vaccine) (n = 28)
Intensive care unit admission
43/176 (24.4)
38/148 (25.7)
5/28 (17.9)
Critically ill infants on life support (4)
25/172 (14.5)
21/144 (14.6)
4/28 (14.3)
Invasive mechanical ventilation (4)
11/172 (6.4)
10/144 (6.9)
1/28 (3.6)
Noninvasive mechanical ventilation (4)
18/172 (10.5)
15/144 (10.4)
3/28 (10.7)
Vasoactive infusions (4)
6/172 (3.5)
5/144 (3.5)
1/28 (3.6)
Extracorporeal membrane oxygenation (4)
1/172 (0.6)
1/144 (0.7)
0/28 (—)
Infants with discharge data, n/total N (%)
170/176 (96.6)
142/148 (96.0)
28/28 (100)
Hospital length of stay, median days§ (IQR) (8)
2 (1–3)
2 (1–3)
2 (1–5)
Died before discharge (6) 1/170 (0.6) 1/142 (0.7) 0/28 (—)

* COVID-19 vaccination status included the following two categories: 1) unvaccinated (mothers who did not receive COVID-19 vaccine doses before their infant’s hospitalization) or 2) vaccinated (mothers who completed their 2-dose primary mRNA COVID-19 vaccination series during pregnancy and ≥14 days before delivery).

Infants were enrolled from 20 pediatric hospitals in 17 states. Northeast: Boston Children’s Hospital (Massachusetts), Cooperman Barnabas Medical Center (New Jersey), and Children’s Hospital of Philadelphia (Pennsylvania); Midwest: Akron Children’s Hospital (Ohio), Nationwide (Ohio), Children’s Mercy Kansas City (Missouri), Mayo Clinic (Minnesota), Riley Children’s (Indiana), Lurie Children’s Hospital (Illinois), Minnesota Masonic (Minnesota), and Children’s Hospital of Michigan (Michigan); South: Arkansas Children’s Hospital (Arkansas), University of North Carolina at Chapel Hill Children’s Hospital (North Carolina), Medical University of South Carolina Children’s Health (South Carolina), Texas Children’s Hospital (Texas), Children’s Hospital of New Orleans (Louisiana), and Children’s Healthcare of Atlanta, Emory (Georgia); West: Children’s Hospital Colorado (Colorado), Children’s Hospital Los Angeles (California), and University of California San Diego-Rady Children’s Hospital (California).

§ Hospital length of stay was missing for eight case-infants born to unvaccinated mothers.

VE of a completed 2-dose maternal primary mRNA COVID-19 vaccination series during pregnancy against COVID-19–associated hospitalization in infants aged <6 months was 61% (95% CI = 31% to 78%) (Table 3). Among 93 mothers classified as vaccinated, 90 (97%) had documented dates of vaccination. Effectiveness of a completed 2-dose COVID-19 vaccination series early in pregnancy (first 20 weeks) was 32% (95% CI = –43% to 68%), although the confidence interval was wide and should be interpreted with caution, and later in pregnancy (21 weeks through 14 days before delivery) was 80% (95% CI = 55% to 91%).

TABLE 3. Effectiveness* of maternal 2-dose primary mRNA COVID-19 vaccination against COVID-19-associated hospitalization in infants aged <6 months, by timing of maternal vaccination during pregnancy — 20 pediatric hospitals, 17 states,§ July 2021–January 2022.

Timing of maternal vaccination during pregnancy No. vaccinated/Total (%)
Vaccine effectiveness,* % (95% CI)
Case-infants Control-infants
Any time
28/176 (15.9)
65/203 (32.0)
61 (31 to 78)
Early (first 20 weeks)
17/165 (10.3)
26/164 (15.9)
32 (–43 to 68)
Late (21 weeks’ gestation through 14 days before delivery) 9/157 (5.7) 38/176 (21.6) 80 (55 to 91)

* Vaccine effectiveness estimates were based on odds of antecedent maternal vaccination during pregnancy in case-infants versus control-infants, adjusted for U.S. Census region, admission date (biweekly intervals), continuous age, sex, and race/ethnicity (non-Hispanic White, non-Hispanic Black, non-Hispanic other, Hispanic of any race, or unknown).

Timing of vaccination is based on date of receipt of the second dose of a 2-dose primary mRNA COVID-19 vaccination series during pregnancy. Gestational age was missing for seven of 90 (7.8%) infants born to vaccinated mothers with known timing of the second dose, and for these infants classification of vaccination timing was based on gestational age of 40 weeks.

§ Infants were enrolled from 20 pediatric hospitals in 17 states. Northeast: Boston Children’s Hospital (Massachusetts), Cooperman Barnabas Medical Center (New Jersey), and Children’s Hospital of Philadelphia (Pennsylvania); Midwest: Akron Children’s Hospital (Ohio), Nationwide (Ohio), Children’s Mercy Kansas City (Missouri), Mayo Clinic (Minnesota), Riley Children’s (Indiana), Lurie Children’s Hospital (Illinois), Minnesota Masonic (Minnesota), and Children’s Hospital of Michigan (Michigan); South: Arkansas Children’s Hospital (Arkansas), University of North Carolina at Chapel Hill Children’s Hospital (North Carolina), Medical University of South Carolina Children’s Health (South Carolina), Texas Children’s Hospital (Texas), Children’s Hospital of New Orleans (Louisiana), and Children’s Healthcare of Atlanta, Emory (Georgia); West: Children’s Hospital Colorado (Colorado), Children’s Hospital Los Angeles (California), and University of California San Diego-Rady Children’s Hospital (California).

COVID-19 vaccination status included the following two categories: 1) unvaccinated (mothers who did not receive COVID-19 vaccine doses before their infant’s hospitalization) or 2) vaccinated (mothers who completed their 2-dose primary mRNA COVID-19 vaccination series during pregnancy and ≥14 days before delivery).

Discussion

During July 2021–January 2022, maternal completion of a 2-dose primary mRNA COVID-19 vaccination series during pregnancy was associated with reduced risk for COVID-19 hospitalization among infants aged <6 months in a real-world evaluation at 20 U.S. pediatric hospitals during a period of Delta and Omicron variant circulation. Among 176 infants aged <6 months hospitalized with COVID-19, 148 (84%) were born to mothers who were not vaccinated during pregnancy. Although booster doses are recommended for pregnant women, VE of maternal booster doses received during pregnancy could not be assessed because of small sample size, which likely underestimated VE. Overall, these findings indicate that maternal vaccination during pregnancy might help protect against COVID-19 hospitalization among infants aged <6 months.

COVID-19 during pregnancy is associated with severe illness and death (7), and pregnant women with COVID-19 are more likely to experience preterm birth, stillbirth, and other pregnancy complications (8). Vaccination is recommended for pregnant women to prevent COVID-19, including severe illness and death. COVID-19 vaccination is safe and effective when administered during pregnancy (9,10). Receipt of COVID-19 vaccination during pregnancy is associated with detectable maternal antibodies in maternal sera at delivery, breast milk, and infant sera indicating transfer of maternal antibodies (35). The higher VE point estimates among infants born to women vaccinated later in pregnancy are consistent with the possibility of transplacental transfer of SARS-CoV-2–specific antibodies that might provide protection to infants. The optimal timing of maternal vaccination for the transfer of antibodies to protect the infant is currently uncertain, and the direct effect of maternal COVID-19 vaccination in preventing severe COVID-19 in infants has not previously been described. Further, with infants not currently age-eligible for vaccination and infant hospitalization rates remaining at the highest levels of the pandemic,*** this study suggests that maternal COVID-19 vaccination during pregnancy might protect infants aged <6 months from COVID-19–related hospitalization.

The findings in this report are subject to at least seven limitations. First, VE could not be assessed directly against specific variants. Second, the sample was too small to assess VE by pregnancy trimester of vaccination, and the small sample size resulted in wide confidence intervals for some estimates that should be interpreted with caution. Third, the analysis did not assess whether pregnant women were infected with SARS-CoV-2 before or during pregnancy, which might have provided maternal antibodies. Fourth, residual confounding such as additional differences in behaviors between vaccinated and unvaccinated mothers, including whether mothers had prenatal care, that might affect risk for infection cannot be excluded, and potential confounders (e.g., breastfeeding, child care attendance, and prematurity) could not be accounted for in the model because this information was not available for all infants. Fifth, because this analysis included self-reported data for a few participants, maternal vaccination status might be misclassified for a few infants, or there might be imperfect recollection of whether the mother completed COVID-19 vaccination during pregnancy. Sixth, immunocompromising maternal conditions were not collected to determine whether mothers needed an additional mRNA COVID-19 vaccine dose to complete their primary series. Finally, VE of maternal booster doses received during pregnancy could not be assessed because of small sample size.

Completion of a 2-dose primary mRNA COVID-19 vaccination series during pregnancy was associated with reduced risk for COVID-19–associated hospitalization among infants aged <6 months, and protection was higher among infants whose mothers were vaccinated later in pregnancy. Additional evaluation should examine timing of vaccination before pregnancy compared with during pregnancy. CDC recommends that women who are pregnant, are breastfeeding, are trying to get pregnant now, or might become pregnant in the future get vaccinated and stay up to date with COVID-19 vaccination.†††

Summary.

What is already known about this topic?

COVID-19 vaccination during pregnancy is recommended to prevent severe illness and death in pregnant women. Infants are at risk for COVID-19–associated complications, including respiratory failure and other life-threatening complications.

What is added by this report?

Effectiveness of maternal completion of a 2-dose primary mRNA COVID-19 vaccination series during pregnancy against COVID-19 hospitalization among infants aged <6 months was 61% (95% CI = 31% to 78%). Effectiveness of completion of the primary COVID-19 vaccine series early and later in pregnancy was 32% (95% CI = –43% to 68%) and 80% (95% CI = 55% to 91%), respectively.

What are the implications for public health practice?

Completion of a 2-dose mRNA COVID-19 vaccination series during pregnancy might help prevent COVID-19 hospitalization among infants aged <6 months.

All authors have completed and submitted the International Committee of Medical Journal Editors form for disclosure of potential conflicts of interest. Adrienne G. Randolph reports institutional support from the National Institute of Allergy and Infectious Diseases and National Institutes of Health (NIH) and being the UpToDate Pediatric Critical Care Section Editor. Matt S. Zinter reports institutional support from the National Heart, Lung, and Blood Institute (NHLBI), NIH and the American Thoracic Society. Laura Smallcomb reports support from the Medical University of South Carolina for conference attendance. Jennifer E. Schuster reports institutional support from Merck. Ryan A. Nofziger reports institutional support from NIH. Emily R. Levy reports institutional support from NIH. Michele Kong reports institutional support from NIH. Satoshi Kamidani reports institutional support from NIH and Pfizer. Janet R. Hume reports institutional support from the National Institute for Child Health and Development, NIH, and serving on a data safety monitoring board for an institutional study of magnesium for analgesia in complex medical patients. Charlotte V. Hobbs reports consultant fees from BioFire (bioMérieux). Natalie Z. Cvijanovich reports institutional support from NIH. Bria M. Coates reports institutional support from NHLBI, NIH, the American Lung Association, and the American Thoracic Society. Kathleen Chiotos reports institutional support from the Agency for Healthcare Research and Quality and serving as the Society for Healthcare Epidemiology of America Research Network Chair. Samina S. Bhumbra reports receipt of an NIH, National Institute for Allergy and Infectious Diseases training grant. Pia S. Pannaraj reports institutional support from AstraZeneca and Pfizer, consulting fees from Sanofi-Pasteur and Seqirus, payment from law firms for expert testimony, serving in the Division of Microbiology and Infectious Diseases, and unpaid service on the California Immunization Coalition. Mary A. Staat reports institutional support from NIH and receipt of lecture fees from the American Academy of Pediatrics for PREP ID Course. Natasha B. Halasa reports grant support from Sanofi and Quidel and honoraria from Genentech. No other potential conflicts of interest were disclosed.

Footnotes

*

These authors contributed equally to this report.

These senior authors contributed equally to this report.

**

Symptomatic COVID-19–like illness was defined as one or more of the following: fever, cough, shortness of breath, gastrointestinal symptoms (e.g., diarrhea, vomiting, or “stomachache”), use of respiratory support (high-flow oxygen by nasal cannula, new invasive or noninvasive ventilation) for the acute illness, or new pulmonary findings on chest imaging consistent with pneumonia. Four case-infants tested at an outside hospital or other facility had some missing data on positive test results and were not retested at the study hospital.

††

Mothers were defined as vaccinated after completing their 2-dose primary mRNA COVID-19 vaccine series during pregnancy, including both doses received during pregnancy or the first dose received before pregnancy and the second dose, completing their primary series, received during pregnancy. Data on maternal moderately or severely immunocompromising conditions were not recorded for mothers of enrolled infants to determine whether mothers needed an additional mRNA COVID-19 vaccine dose to complete their primary series.

§§

45 C.F.R. part 46.102(l)(2), 21 C.F.R. part 56; 42 U.S.C. Sect 241(d); 5 U.S.C. Sect 552a; 44 U.S.C. Sect 3501 et seq.

¶¶

Other reasons for excluding infants from the analysis included May or June hospital admission (two); birth to mothers who received Janssen (Johnson & Johnson) COVID-19 vaccine (four), who received their second dose of vaccine <14 days before delivery (three), who received a 2-dose primary mRNA COVID-19 vaccine before pregnancy (seven), or with unknown vaccination status (one); infants who received a positive SARS-CoV-2 test result but were admitted for non–COVID-19 reasons (four); and SARS-CoV-2 testing >10 days after illness onset or >3 days from hospitalization (two).

Contributor Information

Laura D. Zambrano, CDC

Meghan Murdock, Children’s of Alabama, Birmingham, Alabama.

Mary Glas Gaspers, University of Arizona, Tucson, Arizona.

Connor P. Kelley, University of Arizona, Tucson, Arizona

Katri V. Typpo, University of Arizona, Tucson, Arizona

Peter M. Mourani, Arkansas Children’s Hospital, Little Rock, Arkansas

Ronald C. Sanders, Arkansas Children’s Hospital, Little Rock, Arkansas

Chelsea Smith, Arkansas Children’s Hospital, Little Rock, Arkansas.

Masson Yates, Arkansas Children’s Hospital, Little Rock, Arkansas.

Katheryn Crane, Rady Children’s Hospital, San Diego, California.

Geraldina Lionetti, University of California; San Francisco Benioff Children’s Hospital Oakland, Oakland, California.

Juliana Murcia-Montoya, University of California; San Francisco Benioff Children’s Hospital Oakland, Oakland, California.

Denise Villarreal-Chico, University of California San Francisco Benioff Children’s Hospital, San Francisco, California.

Daniel Hakimi, Children’s Hospital Los Angeles, Los Angeles, California.

Adam L. Skura, Children’s Hospital Los Angeles, Los Angeles, California

Imogene Carson, Children’s Hospital Colorado, Aurora, Colorado.

Justin M. Lockwood, Children’s Hospital Colorado, Aurora, Colorado

Emily Port, Children’s Hospital Colorado, Aurora, Colorado.

Brandon M. Chatani, Holtz Children’s Hospital, Miami, Florida

Nadine Baida, Emory University School of Medicine and Children’s Healthcare of Atlanta, Atlanta, Georgia.

Laila Hussaini, Emory University School of Medicine and Children’s Healthcare of Atlanta, Atlanta, Georgia.

Hassan A. Khan, Ann & Robert H. Lurie Children’s Hospital of Chicago, Chicago, Illinois

Simone T. Rhodes, Ann & Robert H. Lurie Children’s Hospital of Chicago, Chicago, Illinois

Courtney M. Rowan, Riley Hospital for Children, Indianapolis, Indiana

Mary Stumpf, Riley Hospital for Children, Indianapolis, Indiana.

Marla S. Johnston, Children’s Hospital of New Orleans, New Orleans, Louisiana

Laura Berbert, Boston Children’s Hospital, Boston, Massachusetts.

Benjamin J. Boutselis, Boston Children’s Hospital, Boston, Massachusetts

Sabrina R. Chen, Boston Children’s Hospital, Boston, Massachusetts

Jie He, Boston Children’s Hospital, Boston, Massachusetts.

Suden Kucukak, Boston Children’s Hospital, Boston, Massachusetts.

Timothy P. McCadden, Boston Children’s Hospital, Boston, Massachusetts

Amber O. Orzel, Boston Children’s Hospital, Boston, Massachusetts

Edie Weller, Boston Children’s Hospital, Boston, Massachusetts.

Patrick Moran, University of Michigan CS Mott Children’s Hospital, Ann Arbor, Michigan.

Ellen R. Bruno, University of Minnesota Masonic Children’s Hospital, Minneapolis, Minnesota

Lexie A. Goertzen, University of Minnesota Masonic Children’s Hospital, Minneapolis, Minnesota

Supriya Behl, Mayo Clinic, Rochester, Minnesota.

Noelle M. Drapeau, Mayo Clinic, Rochester, Minnesota

Lacy Malloch, Children’s Hospital of Mississippi, Jackson, Mississippi.

Lora Martin, Children’s Hospital of Mississippi, Jackson, Mississippi.

April Palmer, Children’s Hospital of Mississippi, Jackson, Mississippi.

Roberto P. Santos, Children’s Hospital of Mississippi, Jackson, Mississippi

Abigail Kietzman, Children’s Mercy Kansas City, Kansas City, Missouri.

Melissa Sullivan, Children’s Mercy Kansas City, Kansas City, Missouri.

Lauren A. Hoody, Children’s Hospital & Medical Center, Omaha, Nebraska

Valerie H. Rinehart, Children’s Hospital & Medical Center, Omaha, Nebraska

Paris C. Bennett, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina

Merry L. Tomcany, Akron Children’s Hospital, Akron, Ohio

Nicole A. Twinem, Akron Children’s Hospital, Akron, Ohio

Chelsea C. Rohlfs, Cincinnati Children’s Hospital, Cincinnati, Ohio

Amber Wolfe, Nationwide Children’s Hospital, Columbus, Ohio.

Rebecca L. Douglas, Children’s Hospital of Philadelphia, Philadelphia, Pennsylvania

Kathlyn Phengchomphet, Children’s Hospital of Philadelphia, Philadelphia, Pennsylvania.

Megan M. Bickford, Medical University of South Carolina Children’s Health, Charleston, South Carolina

Lauren E. Wakefield, Medical University of South Carolina Children’s Health, Charleston, South Carolina

Meena Golchha, Monroe Carell Jr. Children’s Hospital at Vanderbilt, Nashville, Tennessee.

Laura S. Stewart, Monroe Carell Jr. Children’s Hospital at Vanderbilt, Nashville, Tennessee

Jennifer N. Oates, Texas Children’s Hospital and Baylor College of Medicine, Houston, Texas

Cindy Bowens, University of Texas Southwestern, Children’s Medical Center Dallas, Dallas, Texas.

Mia Maamari, University of Texas Southwestern, Children’s Medical Center Dallas, Dallas, Texas.

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Articles from Morbidity and Mortality Weekly Report are provided here courtesy of Centers for Disease Control and Prevention

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