Assessment of the yellow fever outbreak in Angola from December 2015 through December 2016: A retrospective study

Author:

Manuel Eusebio12,Armando António2,Francisco Moisés3,Paixão Joana3,Aramburu Javier4,de Oliveira Miguel dos Santos2,Freitas Helga2,Pedro Alda Morais2,Jandondo Domingos3,Carderon Pablo Babrero5,Lamezon Sandra Lopez2,Fortes Filomeno6,Mariscal Jorge2,Cardoso Yolanda1,Moreira Rosa2,Morais Joana13,Francisco Ngiambudulu M.3ORCID

Affiliation:

1. Faculdade de Medicina Universidade Agostinho Neto Luanda Angola

2. Direcção Nacional de Saúde Pública Ministério da Saúde Luanda Angola

3. Grupo de Investigação Microbiana e Imunológica Instituto Nacional de Investigação em Saúde (National Institute for Health Research) Luanda Angola

4. World Health Organization (OMS, Angola) Luanda Angola

5. Clínica Girassol Luanda Angola

6. Instituto de Higiene e Medicina Tropical Universidade Nova de Lisboa Lisboa Portugal

Abstract

AbstractBackground and AimsThe acute tropical infectious disease known as yellow fever (YF) is caused by an arbovirus and is characterized by fever, jaundice, hemorrhage, headache, muscle pain, nausea, vomiting, and fatigue. Angola experienced a yellow fever virus (YFV) outbreak that was documented in December 2015. However, little is known about the outcome of this outbreak. We aimed to demonstrate epidemic features and lessons learned during the YF epidemic in Angola.MethodsA total of 4618 blood samples from suspected YF cases were sent to the Instituto Nacional de Investigação em Saúde (INIS), a national referral and public health laboratory, between December 5, 2015, and December 23, 2016. Sample analyses were conducted using enzyme‐linked immunosorbent assay (ELISA) and reverse transcription polymerase chain reaction (RT‐PCR) assays. Blood samples were sent from 16 out of the 18 provinces of Angola.ResultsWe detected 884 (19.1%) cases that were positive for ELISA, which were confirmed by RT‐PCR assay. Considering the positive cases, the incidence among male patients was around three times higher (n = 223; 10.9%) than in female patients (n = 59; 2.6%) in the 20–29 age group, followed by the age group 10–19 with n = 211 (6.8%) in males versus n = 108 (3.3%) in females; and the age group 30–39 had n = 68 (4.8%) in males versus n = 28 (1.8%) in females. The other groups had an incidence below 3.0%. The case fatality ratio for YF was in young adults in the age group 20–29 with n = 39 cases, followed by the age group 10–19 with n = 16 cases, and finally the age group 0–9 with n = 13 cases. The other age groups had several deaths by YF below 10 cases.ConclusionsThis study demonstrates features of the YF epidemic that occurred in Angola. Also, it demonstrates that YF causes deaths in young people but is preventable by high vaccine coverage. Thus, public health laboratory surveillance must be strengthened to reduce the possibility of emerging and re‐emerging human infections.

Publisher

Wiley

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