TY - JOUR
T1 - Monovalent rotavirus vaccine effectiveness and long-term impact among children <5 years old in Antananarivo, Madagascar, 2010–2022
AU - Raboba, Julia Liliane
AU - Rahajamanana, Vonintsoa Lalaina
AU - Rakotojoelimaria, Haganiaina Elsa
AU - Masembe, Yolande Vuo
AU - Martin, Patricia Rasoamihanta
AU - Weldegebriel, Goitom G.
AU - Diallo, Alpha Oumar
AU - Burnett, Eleanor
AU - Tate, Jaqueline E.
AU - Parashar, Umesh D.
AU - Mwenda, Jason M.
AU - Seheri, Mapaseka
AU - Magagula, Nonkululeko
AU - Mphahlele, Jeffrey
AU - Robinson, Annick Lalaina
N1 - Publisher Copyright:
© 2024
PY - 2024/12/2
Y1 - 2024/12/2
N2 - Background: Monovalent rotavirus vaccine substantially reduced rotavirus disease burden after introduction (May 2014) in Madagascar. We examined the effectiveness and long-term impact on acute watery diarrhea and rotavirus-related hospitalizations among children <5 years old at two hospitals in Antananarivo, Madagascar (2010−2022). Methods: We used a test-negative case-control design to estimate monovalent rotavirus vaccine effectiveness (VE) against laboratory-confirmed rotavirus hospitalizations among children age 6–23 months with documented vaccination status adjusted for year of symptom onset, rotavirus season, age group, nutritional status, and clinical severity. To evaluate the impact, we expanded to children age 0–59 months with acute watery diarrhea. First, we used admission logbook data to compare the proportion of all hospitalizations attributed to diarrhea in the pre-vaccine (January 2010–December 2013), transition period (January 2014–December 2014), and post-vaccine (January 2015–December 2022) periods. Second, we used active surveillance data (June 2013–May 2022) to describe rotavirus positivity and detected genotypes by vaccine introduction period and surveillance year (1 June–31 May). Result: Adjusted VE of at least one dose against hospitalization due to rotavirus diarrhea among children age 6–23 months was 61 % (95 % CI: −39 %–89 %). The annual median proportion of hospitalizations attributed to diarrhea declined from 28 % in the pre-vaccine to 10 % in the post-vaccine period. Rotavirus positivity among hospitalized children age 0–59 months with acute watery diarrhea was substantially higher during the pre-vaccine (59 %) than the post-vaccine (23 %) period. In the pre-vaccine period, G3P[8] (76 %) and G2P[4] (12 %) were the dominant genotypes detected. Although genotypes varied by surveillance year, G1P[8] and G2P[4] represented >50 % of the genotypes detected post-introduction. Conclusions: Rotavirus vaccine has been successfully implemented in Madagascar's routine childhood immunization program and had a large impact on rotavirus disease burden, supporting continued use of rotavirus vaccines in Madagascar.
AB - Background: Monovalent rotavirus vaccine substantially reduced rotavirus disease burden after introduction (May 2014) in Madagascar. We examined the effectiveness and long-term impact on acute watery diarrhea and rotavirus-related hospitalizations among children <5 years old at two hospitals in Antananarivo, Madagascar (2010−2022). Methods: We used a test-negative case-control design to estimate monovalent rotavirus vaccine effectiveness (VE) against laboratory-confirmed rotavirus hospitalizations among children age 6–23 months with documented vaccination status adjusted for year of symptom onset, rotavirus season, age group, nutritional status, and clinical severity. To evaluate the impact, we expanded to children age 0–59 months with acute watery diarrhea. First, we used admission logbook data to compare the proportion of all hospitalizations attributed to diarrhea in the pre-vaccine (January 2010–December 2013), transition period (January 2014–December 2014), and post-vaccine (January 2015–December 2022) periods. Second, we used active surveillance data (June 2013–May 2022) to describe rotavirus positivity and detected genotypes by vaccine introduction period and surveillance year (1 June–31 May). Result: Adjusted VE of at least one dose against hospitalization due to rotavirus diarrhea among children age 6–23 months was 61 % (95 % CI: −39 %–89 %). The annual median proportion of hospitalizations attributed to diarrhea declined from 28 % in the pre-vaccine to 10 % in the post-vaccine period. Rotavirus positivity among hospitalized children age 0–59 months with acute watery diarrhea was substantially higher during the pre-vaccine (59 %) than the post-vaccine (23 %) period. In the pre-vaccine period, G3P[8] (76 %) and G2P[4] (12 %) were the dominant genotypes detected. Although genotypes varied by surveillance year, G1P[8] and G2P[4] represented >50 % of the genotypes detected post-introduction. Conclusions: Rotavirus vaccine has been successfully implemented in Madagascar's routine childhood immunization program and had a large impact on rotavirus disease burden, supporting continued use of rotavirus vaccines in Madagascar.
KW - Genotype
KW - Madagascar
KW - Rotavirus
KW - Rotavirus surveillance
KW - Rotavirus vaccine effectiveness
KW - Rotavirus vaccine impact
UR - http://www.scopus.com/inward/record.url?scp=85203408223&partnerID=8YFLogxK
U2 - 10.1016/j.vaccine.2024.126321
DO - 10.1016/j.vaccine.2024.126321
M3 - Article
C2 - 39260057
AN - SCOPUS:85203408223
SN - 0264-410X
VL - 42
JO - Vaccine
JF - Vaccine
IS - 26
M1 - 126321
ER -