Monovalent Rotavirus Vaccine Effectiveness and Long-term Impact Among Children <5 years Old in Antananarivo, Madagascar, 2010-2022.
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December 2024
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Available in CDC Stacks on February 27, 2025, 12:00 AM
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Alternative Title:Vaccine, 2024, v. 42, no. 26: Monovalent Rotavirus Vaccine Effectiveness and Long-term Impact Among Children <5 years Old in Antananarivo, Madagascar, 2010-2022.
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Journal Article:Vaccine
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Personal Author:Raboba, Julia Liliane ; Rahajamanana, Vonintsoa Lalaina ; Rakotojoelimaria, Haganiaina Elsa ; Vuo Masembe, Yolande ; Martin, Patricia Rasoamihanta ; Weldegebriel, Goitom G. ; Diallo, Alpha Oumar ; Burnett, Eleanor ; Tate, Jaqueline E. ; Parashar, Umesh D. ; Mwenda, Jason M. ; Seheri, Mapaseka ; Magagula, Nonkululeko ; Mphahlele, Jeffrey ; Robinson, Annick Lalaina
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Description: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).
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).
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, G3P8 (76 %) and G2P4 (12 %) were the dominant genotypes detected. Although genotypes varied by surveillance year, G1P8 and G2P4 represented >50 % of the genotypes detected post-introduction.
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. -
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Source:Vaccine, 2024, v. 42, no. 26
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DOI:
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ISSN:0264-410X ; 1873-2518
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Pubmed ID:39260057
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Pubmed Central ID:PMC11866102
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Pages in Document:126321 (19 pdf pages)
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Volume:42
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Issue:26
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Main Document Checksum:urn:sha-512:0add296d55528b762c76820ecff08911fea2db6c1ae57e815c4523b30c02a739efcb306f5328edac696214abeae03f55e3412819fa329da3ce797e87558cc805
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