African health sciences · 2023
The road to a polio-free Uganda; contribution of the Expanded Program on Immunization Laboratory (EPI-LAB) at Uganda Virus Research Institute.
СтатьяНазвание и аннотация: Перевод в очереди
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Nanteza Mary B, Tushabe Phionah, Bukenya Henry, Namuwulya Prossy, Kabaliisa Theopista, Birungi Molly, Tibanagwa Mayi, Ampeire Immaculate, Kakooza Proscovia, Katushabe Edson, Bwogi Josephine, Bakamutumaho Barnabas, Nanyunja Miriam, Byabamazima Charles R
Аннотация
BACKGROUND: The control of poliomyelitis in Uganda dates back as far as 1950 and acute flaccid paralysis (AFP) surveillance has since been used as a criterion for identifying wild polioviruses. Poliovirus isolation was initially pursued through collaborative research however, in 1993, the Expanded Program on Immunization Laboratory (EPI-LAB) was established as a member of the Global Poliovirus Laboratory Network (GPLN) and spearheaded this activity at Uganda Virus Research Institute.
OBJECTIVES: The aim of this report is to document the progress and impact of the EPI-LAB on poliovirus eradication in Uganda.
METHODS: Poliovirus detection and identification were achieved fundamentally through tissue culture and intra-typic differentiation of the poliovirus based on the real-time reverse transcriptase polymerase chain reaction (rRT PCR). The data obtained was entered into the national AFP database and analysed using EpiInfoTM statistical software.
RESULTS: Quantitative and qualitative detection of wild and Sabin polioviruses corresponded with the polio campaigns. The WHO target indicators for AFP surveillance were achieved essentially throughout the study period.
CONCLUSION: Virological tracking coupled with attaining standard AFP surveillance indicators has been pivotal in achieving and maintaining the national wild polio-free status. Laboratory surveillance remains key in informing the certification process of polio eradication.
OBJECTIVES: The aim of this report is to document the progress and impact of the EPI-LAB on poliovirus eradication in Uganda.
METHODS: Poliovirus detection and identification were achieved fundamentally through tissue culture and intra-typic differentiation of the poliovirus based on the real-time reverse transcriptase polymerase chain reaction (rRT PCR). The data obtained was entered into the national AFP database and analysed using EpiInfoTM statistical software.
RESULTS: Quantitative and qualitative detection of wild and Sabin polioviruses corresponded with the polio campaigns. The WHO target indicators for AFP surveillance were achieved essentially throughout the study period.
CONCLUSION: Virological tracking coupled with attaining standard AFP surveillance indicators has been pivotal in achieving and maintaining the national wild polio-free status. Laboratory surveillance remains key in informing the certification process of polio eradication.