| Literature DB >> 31391841 |
Alba Maria Ropero Alvarez1, Barbara Jauregui1, Nathalie El Omeiri1.
Abstract
Maternal and neonatal immunization (MNI) is a core component of the new immunization model in the Americas, which transitioned from immunization of children to that of the entire family. Immunization during pregnancy protects the mother and the fetus by providing the neonate with maternal antibodies against disease. It has the potential to impact early childhood morbidity and mortality, and thus MNI has gained visibility and priority on the global health agenda. The Region of the Americas is a leader in MNI, as seen by its elimination of congenital rubella syndrome in 2015 and the progress made toward neonatal tetanus elimination. In the Americas, 31 countries currently target pregnant women for influenza vaccination; and 21 countries-over 90% of the Region's birth cohort-have nationwide newborn hepatitis B vaccination. This paper describes the status of MNI in the Americas and identifies gaps in the evidence, obstacles to optimal implementation, and opportunities for future improvements. Catalysts for MNI in the Region have been political commitment, endorsement by scientific societies, an established "culture of vaccination," widespread access to antenatal care, and context-specific communications; however, universal and equitable access for pregnant women and their newborns continues to be a formidable challenge, and additional vaccine safety and effectiveness evidence is needed. Continued efforts to integrate MNI with maternal and child health services will be critical to furthering the MNI platform as well.Entities:
Keywords: Americas; Immunity; immunization programs; maternally-acquired; prenatal care
Year: 2017 PMID: 31391841 PMCID: PMC6660888 DOI: 10.26633/RPSP.2017.159
Source DB: PubMed Journal: Rev Panam Salud Publica ISSN: 1020-4989
Figure 1.Upcoming vaccines in the development pipeline that are relevant to maternal and neonatal immunization, 2017
Vaccines and their recommended usage and timing in maternal and neonatal immunization programs, per recommendations of the Pan American Health Organization’s Technical Advisory Group (PAHO TAG), 2017
Timing and vaccine type | Pre-pregnancy | Pregnancy | Post-partum | Year of PAHO TAG recommendation |
|---|---|---|---|---|
Recommended during pregnancy |
|
|
|
|
Tetanus | Yes, ideal time. | Yes, two doses if not previously vaccinated. | Yes, to complete schedule. | 2017 |
Inactivated influenza |
| Yes, ideal time. | Yes, if not vaccinated during pregnancy, to protect tde newborn. | 2012 |
In special situations only |
|
|
|
|
Tetanus-diphtderia-pertussis |
| Yes, during outbreaks (ideally from 27 - 36 weeks of gestation). | Yes | 2014 |
Hepatitis B |
| Yes, IF incomplete schedule and IF under high-risk situation (e.g., more tdan one sexual partner during tde previous 6 montds, sexually transmitted disease, etc.) | Yes, to complete schedule (tdree doses). | NA |
Hepatitis A |
| Yes, during outbreaks. |
| 2013 |
Yellow fever | Yes, ideal moment (in endemic areas). | Yes, prior to travel to endemic areas under current outbreak, witd prior risk/benefit analysis. |
| 2013 |
Inactivated polio vaccine |
| Yes, prior to travel to endemic areas under current outbreak. |
| 2013 |
Oral polio vaccine |
| Yes, prior to travel to endemic areas under current outbreak. |
| 2015 |
Rabies |
| After high-risk exposure. |
| 2013 |
Meningococcus conjugate |
| Yes, during outbreaks |
| 2013 |
Meningococcus polysaccharide |
| Yes, during outbreaks |
| 2013 |
Contraindicated during pregnancy Rubella |
|
|
|
|
Rubella | Yes, ideal time, but avoid conception for 4 weeks. | No. | Yes, if not vaccinated during pre-pregnancy. | 2013 |
Measles |
|
|
| 2013 |
Mumps |
|
|
| 2013 |
Human papilloma virus | Yes, ideal time. | No. |
| 2013 |
Recommended for tde newborn |
|
|
|
|
Bacillus Calmette-Guérin vaccine |
|
| As soon as possible after birtd. | 2004 |
Hepatitis B vaccine |
|
| Before tde first 24 hours after birtd. | 2011 |
Prepared by the authors from the study data.