Malaria prevalence and performance of diagnostic tests among patients hospitalized with acute undifferentiated fever in Zanzibar.


Journal

Malaria journal
ISSN: 1475-2875
Titre abrégé: Malar J
Pays: England
ID NLM: 101139802

Informations de publication

Date de publication:
19 Feb 2022
Historique:
received: 26 04 2021
accepted: 31 01 2022
entrez: 20 2 2022
pubmed: 21 2 2022
medline: 23 2 2022
Statut: epublish

Résumé

Control efforts in Zanzibar reduced the burden of malaria substantially from 2000 to 2015, but re-emergence of falciparum malaria has been observed lately. This study evaluated the prevalence of malaria and performance of routine diagnostic tests among hospitalized fever patients in a 1.5 years period in 2015 and 2016. From March 2015 to October 2016, paediatric and adult patients hospitalized with acute undifferentiated fever at Mnazi Mmoja Hospital, Zanzibar were included. The malaria prevalence, and performance of rapid diagnostic test (RDT) and microscopy, were assessed using polymerase chain reaction (PCR) as gold standard. The malaria prevalence was 9% (63/731). Children under 5 years old had lower malaria prevalence (5%, 14/260) than older children (15%, 20/131, p = 0.001) and persons aged 16 to 30 years (13%, 15/119, p = 0.02), but not different from persons over 30 years old (6%, 14/217, p = 0.7). All cases had Plasmodium falciparum infection, except for one case of Plasmodium ovale. Ten malaria patients had no history of visiting mainland Tanzania. The RDT had a sensitivity of 64% (36/56) and a specificity of 98% (561/575), and microscopy had a sensitivity of 50% (18/36) and  a specificity of 99% (251/254), compared to PCR. The malaria parasitaemia was lower in patients with false negative results on RDT (median 7 × 10 The study emphasizes that malaria was a frequent cause of febrile illness in hospitalized patients in Zanzibar in the years 2015-2016, particularly among school age children and young adults. We found evidence of autochthonous malaria transmission in Zanzibar. Compared to PCR, both RDT and microscopy had low sensitivity, and false negative results were associated with low parasitaemia. While low parasitaemia identified only by PCR in a semi-immune individual could be coincidental and without clinical relevance, clinicians should be aware of the risk of false negative results on routine tests.

Sections du résumé

BACKGROUND BACKGROUND
Control efforts in Zanzibar reduced the burden of malaria substantially from 2000 to 2015, but re-emergence of falciparum malaria has been observed lately. This study evaluated the prevalence of malaria and performance of routine diagnostic tests among hospitalized fever patients in a 1.5 years period in 2015 and 2016.
METHODS METHODS
From March 2015 to October 2016, paediatric and adult patients hospitalized with acute undifferentiated fever at Mnazi Mmoja Hospital, Zanzibar were included. The malaria prevalence, and performance of rapid diagnostic test (RDT) and microscopy, were assessed using polymerase chain reaction (PCR) as gold standard.
RESULTS RESULTS
The malaria prevalence was 9% (63/731). Children under 5 years old had lower malaria prevalence (5%, 14/260) than older children (15%, 20/131, p = 0.001) and persons aged 16 to 30 years (13%, 15/119, p = 0.02), but not different from persons over 30 years old (6%, 14/217, p = 0.7). All cases had Plasmodium falciparum infection, except for one case of Plasmodium ovale. Ten malaria patients had no history of visiting mainland Tanzania. The RDT had a sensitivity of 64% (36/56) and a specificity of 98% (561/575), and microscopy had a sensitivity of 50% (18/36) and  a specificity of 99% (251/254), compared to PCR. The malaria parasitaemia was lower in patients with false negative results on RDT (median 7 × 10
CONCLUSIONS CONCLUSIONS
The study emphasizes that malaria was a frequent cause of febrile illness in hospitalized patients in Zanzibar in the years 2015-2016, particularly among school age children and young adults. We found evidence of autochthonous malaria transmission in Zanzibar. Compared to PCR, both RDT and microscopy had low sensitivity, and false negative results were associated with low parasitaemia. While low parasitaemia identified only by PCR in a semi-immune individual could be coincidental and without clinical relevance, clinicians should be aware of the risk of false negative results on routine tests.

Identifiants

pubmed: 35183188
doi: 10.1186/s12936-022-04067-z
pii: 10.1186/s12936-022-04067-z
pmc: PMC8858509
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

54

Subventions

Organisme : Helse Vest
ID : PhD scholarship Project Number 912277
Organisme : Vestre Viken Hospital Trust (NO)
ID : Vestre Viken Hospital Trust (NO)

Informations de copyright

© 2022. The Author(s).

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Auteurs

Annette Onken (A)

Department of Clinical Science, University of Bergen, Bergen, Norway. annetteonken@yahoo.com.
Norwegian National Advisory Unit on Tropical Infectious Diseases, Department of Medicine, Haukeland University Hospital, Bergen, Norway. annetteonken@yahoo.com.
Department of Microbiology, Vestre Viken Hospital Trust, Postbox 800, 3004, Drammen, Norway. annetteonken@yahoo.com.

Christel Gill Haanshuus (CG)

Norwegian National Advisory Unit on Tropical Infectious Diseases, Department of Medicine, Haukeland University Hospital, Bergen, Norway.

Mohammed Khamis Miraji (MK)

Department of Internal Medicine, Mnazi Mmoja Hospital, Zanzibar, Tanzania.

Msafiri Marijani (M)

Pathology Laboratory Department, Mnazi Mmoja Hospital, Zanzibar, Tanzania.

Kibwana Omar Kibwana (KO)

Pathology Laboratory Department, Mnazi Mmoja Hospital, Zanzibar, Tanzania.

Khamis Ali Abeid (KA)

Department of Paediatrics, Mnazi Mmoja Hospital, Zanzibar, Tanzania.

Kristine Mørch (K)

Department of Clinical Science, University of Bergen, Bergen, Norway.
Norwegian National Advisory Unit on Tropical Infectious Diseases, Department of Medicine, Haukeland University Hospital, Bergen, Norway.

Marianne Reimers (M)

Department of Medicine, Haukeland University Hospital, Bergen, Norway.
Department of International Collaboration, Haukeland University Hospital, Bergen, Norway.

Nina Langeland (N)

Department of Clinical Science, University of Bergen, Bergen, Norway.
Norwegian National Advisory Unit on Tropical Infectious Diseases, Department of Medicine, Haukeland University Hospital, Bergen, Norway.

Fredrik Müller (F)

Department of Microbiology, Oslo University Hospital, Oslo, Norway.
Institute of Clinical Medicine, University of Oslo, Oslo, Norway.

Pål A Jenum (PA)

Department of Microbiology, Vestre Viken Hospital Trust, Postbox 800, 3004, Drammen, Norway.
Institute of Clinical Medicine, University of Oslo, Oslo, Norway.

Bjørn Blomberg (B)

Department of Clinical Science, University of Bergen, Bergen, Norway.
Norwegian National Advisory Unit on Tropical Infectious Diseases, Department of Medicine, Haukeland University Hospital, Bergen, Norway.

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Classifications MeSH