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Association of Tdap vaccine guidelines with vaccine uptake during pregnancy
Julia D DiTosto1, Rebecca E Weiss2, Lynn M Yee1
1Division of Maternal-Fetal Medicine, Department of Obstetrics and Gynecology, Northwestern University Feinberg School of Medicine, Chicago, IL, United States of America.
Insights
Vaccine uptake for tetanus, diphtheria, and pertussis (Tdap) and influenza during pregnancy significantly increased after 2012 guidelines. However, racial disparities in vaccine access persist.
Area of Science:
- Obstetrics and Gynecology
- Immunology
- Public Health
Background:
- In 2012, universal recommendations for Tdap vaccination during pregnancy were issued.
- Maternal vaccination is crucial for protecting infants from preventable diseases.
Purpose of the Study:
- To evaluate changes in Tdap, influenza, and pneumococcal vaccine uptake during pregnancy after 2012.
- To identify factors associated with Tdap and influenza vaccine receipt post-2012.
Main Methods:
- Retrospective cohort study comparing pregnant individuals before (2011-2012) and after (2012-2015) Tdap guidelines.
- Analysis of vaccine uptake from medical records.
- Multivariable logistic regression to identify associated factors.
Main Results:
- Tdap uptake increased from 47.4% to 86.1% (p<0.001), with improved timing.
- Influenza vaccine uptake rose from 61.2% to 72.0% (p<0.001).
- Pneumococcal vaccine uptake remained low and unchanged; racial disparities were observed.
Conclusions:
- The 2012 guidelines successfully improved Tdap and influenza vaccine uptake during pregnancy.
- Significant racial disparities in vaccine receipt necessitate targeted interventions.
- Pneumococcal vaccine uptake remains a concern.
Objective:
In 2012, recommendations for universal tetanus toxoid, reduced diphtheria toxoid, and acellular pertussis (Tdap) vaccination during pregnancy were released. Our objective was to determine if Tdap, influenza, and pneumococcal vaccine uptake during pregnancy changed after the release of the guidelines, and identify factors associated with receiving the Tdap and influenza vaccine after 2012.
Methods:
We conducted a retrospective cohort study on pregnant individuals who initiated prenatal care before 20 weeks' gestation between 11/2011-11/2012 ("pre-guideline") and 12/2012-12/2015 ("post-guideline"). Vaccine uptake dates were abstracted from medical records. The pre and post-guideline cohorts were compared to determine if Tdap vaccine uptake and timing improved after the new Tdap guidelines. We additionally examined influenza and pneumococcal vaccine uptake before and after guidelines. Factors associated with receipt of the Tdap and influenza vaccine during pregnancy in the post-guideline cohort were evaluated using multivariable logistic regression models.
Results:
Of 2,294 eligible individuals, 1,610 (70.2%) received care in the post-guideline cohort. Among the pre-guideline cohort, 47.4% received Tdap, whereas Tdap uptake increased to 86.1% after the guidelines (p<0.001). Similarly, receiving the Tdap vaccine between the recommended time of 27-36 weeks gestational age improved from 52.5% to 91.8% after the guidelines (p<0.001). Vaccine frequency for influenza improved significantly from 61.2% to 72.0% (p<0.001), while frequency for pneumococcus were low and unchanged. An increased number of prenatal visits was associated with receiving the Tdap and influenza vaccines during pregnancy (respective, aOR 1.09 95% CI 1.05-1.13; aOR 1.50 95% CI 1.17-1.94). Non-Hispanic Black individuals were less likely to receive both the Tdap and influenza vaccines during pregnancy compared to non-Hispanic White individuals (respective, aOR 0.51 95% CI 0.33-0.80; aOR 0.68 95% CI 0.48-0.97).
Conclusions:
Receipt and timing of Tdap vaccine improved after implementation of the 2012 ACIP guidelines. Receipt of influenza vaccine uptake also improved during the study period, while uptake of the pneumococcal vaccine remained low. Significant racial disparities exist in receipt of Tdap and influenza vaccine during pregnancy.
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