Challenges in diagnosing scrub typhus among hospitalized patients with undifferentiated fever at a national tertiary hospital in northern Vietnam.


Journal

PLoS neglected tropical diseases
ISSN: 1935-2735
Titre abrégé: PLoS Negl Trop Dis
Pays: United States
ID NLM: 101291488

Informations de publication

Date de publication:
12 2019
Historique:
received: 15 03 2019
accepted: 14 11 2019
revised: 17 12 2019
pubmed: 6 12 2019
medline: 26 2 2020
entrez: 6 12 2019
Statut: epublish

Résumé

Scrub typhus (ST) is a leading cause of non-malarial febrile illness in Southeast Asia, but evidence of its true disease burden is limited because of difficulties of making the clinical diagnosis and lack of adequate diagnostic tests. To describe the epidemiology and clinical characteristics of ST, we conducted an observational study using multiple diagnostic assays at a national tertiary hospital in Hanoi, Vietnam. We enrolled 1,127 patients hospitalized with documented fever between June 2012 and May 2013. Overall, 33 (2.9%) patients were diagnosed with ST by PCR and/or screening of ELISA for immunoglobulin M (IgM) with confirmatory tests: 14 (42.4%) were confirmed by indirect immunoperoxidase assay (IIP), and 19 (57.6%) were by IIP and PCR. Living by farming, conjunctival injection, eschar, aspartate aminotransferase elevation, and alanine aminotransferase elevation were significantly associated with ST cases (adjusted odds ratios (aORs): 2.8, 3.07, 48.8, 3.51, and 4.13, respectively), and having a comorbidity and neutrophilia were significantly less common in ST cases (aORs: 0.29 and 0.27, respectively). The majority of the ST cases were not clinically diagnosed with rickettsiosis (72.7%). Dominant IIP reactions against a single antigen were identified in 15 ST cases, whereas indistinguishably high reactions against multiple antigens were seen in 11 ST cases. The most frequently observed dominant IIP reaction was against Karp antigen (eight cases) followed by Gilliam (four cases). The highest diagnostic accuracy of IgM ELISA in acute samples was 78%. In a phylogenetic analysis of the 56-kDa type-specific antigen gene, the majority (14 cases) were located in the Karp-related branch followed by the Gilliam-related (two cases), Kato-related (two cases), and TA763-related clades (one case). Both the clinical and laboratory diagnoses of ST remain challenging at a tertiary hospital. Implementation of both serological and nucleic acid amplification assays covering endemic O. tsutsugamushi strains is essential.

Sections du résumé

BACKGROUND
Scrub typhus (ST) is a leading cause of non-malarial febrile illness in Southeast Asia, but evidence of its true disease burden is limited because of difficulties of making the clinical diagnosis and lack of adequate diagnostic tests. To describe the epidemiology and clinical characteristics of ST, we conducted an observational study using multiple diagnostic assays at a national tertiary hospital in Hanoi, Vietnam.
METHODOLOGY/PRINCIPAL FINDINGS
We enrolled 1,127 patients hospitalized with documented fever between June 2012 and May 2013. Overall, 33 (2.9%) patients were diagnosed with ST by PCR and/or screening of ELISA for immunoglobulin M (IgM) with confirmatory tests: 14 (42.4%) were confirmed by indirect immunoperoxidase assay (IIP), and 19 (57.6%) were by IIP and PCR. Living by farming, conjunctival injection, eschar, aspartate aminotransferase elevation, and alanine aminotransferase elevation were significantly associated with ST cases (adjusted odds ratios (aORs): 2.8, 3.07, 48.8, 3.51, and 4.13, respectively), and having a comorbidity and neutrophilia were significantly less common in ST cases (aORs: 0.29 and 0.27, respectively). The majority of the ST cases were not clinically diagnosed with rickettsiosis (72.7%). Dominant IIP reactions against a single antigen were identified in 15 ST cases, whereas indistinguishably high reactions against multiple antigens were seen in 11 ST cases. The most frequently observed dominant IIP reaction was against Karp antigen (eight cases) followed by Gilliam (four cases). The highest diagnostic accuracy of IgM ELISA in acute samples was 78%. In a phylogenetic analysis of the 56-kDa type-specific antigen gene, the majority (14 cases) were located in the Karp-related branch followed by the Gilliam-related (two cases), Kato-related (two cases), and TA763-related clades (one case).
CONCLUSIONS/SIGNIFICANCE
Both the clinical and laboratory diagnoses of ST remain challenging at a tertiary hospital. Implementation of both serological and nucleic acid amplification assays covering endemic O. tsutsugamushi strains is essential.

Identifiants

pubmed: 31805053
doi: 10.1371/journal.pntd.0007928
pii: PNTD-D-19-00394
pmc: PMC6917290
doi:

Types de publication

Journal Article Observational Study Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

e0007928

Déclaration de conflit d'intérêts

The authors have declared that no competing interests exist.

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Auteurs

Shungo Katoh (S)

Department of Clinical Medicine, Institute of Tropical Medicine (NEKKEN), Nagasaki University, Nagasaki, Japan.
Nagasaki University Graduate School of Biomedical Sciences, Nagasaki, Japan.
Department of General Internal Medicine, Nagasaki Rosai Hospital, Nagasaki, Japan.

Ngo Chi Cuong (NC)

Nagasaki University Graduate School of Biomedical Sciences, Nagasaki, Japan.
Department of Infectious Diseases, Bach Mai Hospital, Hanoi, Vietnam.

Sugihiro Hamaguchi (S)

Department of General Internal Medicine, Fukushima Medical University, Fukushima, Japan.

Pham Thanh Thuy (PT)

Department of Infectious Diseases, Bach Mai Hospital, Hanoi, Vietnam.
The Partnership for Health Advancement in Vietnam (HAIVN), Hanoi, Vietnam.

Do Duy Cuong (DD)

Department of Infectious Diseases, Bach Mai Hospital, Hanoi, Vietnam.

Le Kim Anh (LK)

Vietnam Research Station, Institute of Tropical Medicine (NEKKEN), Nagasaki University, Hanoi, Vietnam.

Nguyen Thi Hien Anh (NTH)

National Institute of Hygiene and Epidemiology, Hanoi, Vietnam.

Dang Duc Anh (DD)

National Institute of Hygiene and Epidemiology, Hanoi, Vietnam.

Eiichiro Sando (E)

Department of Clinical Medicine, Institute of Tropical Medicine (NEKKEN), Nagasaki University, Nagasaki, Japan.
Nagasaki University Graduate School of Biomedical Sciences, Nagasaki, Japan.
Department of General Internal Medicine, Kameda Medical Center, Chiba, Japan.

Motoi Suzuki (M)

Department of Clinical Medicine, Institute of Tropical Medicine (NEKKEN), Nagasaki University, Nagasaki, Japan.
School of Tropical Medicine and Global Health, Nagasaki University, Nagasaki, Japan.

Hiromi Fujita (H)

Mahara Institute of Medical Acarology, Tokushima, Japan.

Michio Yasunami (M)

Department of Clinical Medicine, Institute of Tropical Medicine (NEKKEN), Nagasaki University, Nagasaki, Japan.
Saga-Ken Medical Centre Koseikan, Saga, Japan.

Keisuke Yoshihara (K)

Department of Paediatric Infectious Diseases, Institute of Tropical Medicine (NEKKEN), Nagasaki University, Nagasaki, Japan.

Lay-Myint Yoshida (LM)

Nagasaki University Graduate School of Biomedical Sciences, Nagasaki, Japan.
Department of Paediatric Infectious Diseases, Institute of Tropical Medicine (NEKKEN), Nagasaki University, Nagasaki, Japan.

Daniel Henry Paris (DH)

Department of Medicine, Swiss Tropical and Public Health Institute, Basel, Switzerland.
Faculty of Medicine, University of Basel, Basel, Switzerland.

Koya Ariyoshi (K)

Department of Clinical Medicine, Institute of Tropical Medicine (NEKKEN), Nagasaki University, Nagasaki, Japan.
Nagasaki University Graduate School of Biomedical Sciences, Nagasaki, Japan.
School of Tropical Medicine and Global Health, Nagasaki University, Nagasaki, Japan.

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