Arbo-Score: A Rapid Score for Early Identification of Patients with Imported Arbovirosis Caused by Dengue, Chikungunya and Zika Virus.

Zika chikungunya dengue diagnosis imported score timing travelers

Journal

Microorganisms
ISSN: 2076-2607
Titre abrégé: Microorganisms
Pays: Switzerland
ID NLM: 101625893

Informations de publication

Date de publication:
04 Nov 2020
Historique:
received: 08 10 2020
revised: 31 10 2020
accepted: 02 11 2020
entrez: 7 11 2020
pubmed: 8 11 2020
medline: 8 11 2020
Statut: epublish

Résumé

Chikungunya (CHIKV), Dengue (DENV), and Zika (ZIKV) viruses present significant clinical and epidemiological overlap, making an accurate and rapid diagnosis challenging. Timely activation of preventive vector control measures is crucial to avoid outbreaks in non-endemic settings. Diagnosis is based on combination of serological and molecular assays which could be time consuming and sometimes disappointing. We report the results of a retrospective case-control study carried out at a tertiary teaching hospital in Italy, including all febrile subjects returning from tropical countries during the period 2014-2019. Controls were travelers with other febrile illnesses who tested negative in laboratory analysis for CHIKV, DENV, ZIKV arbovirosis. A score weighted on the regression coefficients for the independent predictors was generated. Ninety patients were identified: 34 cases (22 DENV, 4 CHIKV, and 8 ZIKV) and 56 controls. According to our results, myalgia, cutaneous rash, absence of respiratory symptoms, leukopenia, and hypertransaminasemia showed the strongest association with arbovirosis. Combining these variables, we generated a scoring model that showed an excellent performance (AUC 0.93). The best cut-off (>=2) presented a sensitivity of 82.35% and specificity of 96.43%. A handy and simple score, based on three clinical data (myalgia, cutaneous rash and absence of respiratory symptoms) and two laboratory results (leukopenia and hypertransaminasemia), provides a useful tool to help diagnose arboviral infections and appropriately activate vector control measures in order to avoid local transmission.

Sections du résumé

BACKGROUND BACKGROUND
Chikungunya (CHIKV), Dengue (DENV), and Zika (ZIKV) viruses present significant clinical and epidemiological overlap, making an accurate and rapid diagnosis challenging. Timely activation of preventive vector control measures is crucial to avoid outbreaks in non-endemic settings. Diagnosis is based on combination of serological and molecular assays which could be time consuming and sometimes disappointing.
METHODS METHODS
We report the results of a retrospective case-control study carried out at a tertiary teaching hospital in Italy, including all febrile subjects returning from tropical countries during the period 2014-2019. Controls were travelers with other febrile illnesses who tested negative in laboratory analysis for CHIKV, DENV, ZIKV arbovirosis. A score weighted on the regression coefficients for the independent predictors was generated.
RESULTS RESULTS
Ninety patients were identified: 34 cases (22 DENV, 4 CHIKV, and 8 ZIKV) and 56 controls. According to our results, myalgia, cutaneous rash, absence of respiratory symptoms, leukopenia, and hypertransaminasemia showed the strongest association with arbovirosis. Combining these variables, we generated a scoring model that showed an excellent performance (AUC 0.93). The best cut-off (>=2) presented a sensitivity of 82.35% and specificity of 96.43%.
CONCLUSION CONCLUSIONS
A handy and simple score, based on three clinical data (myalgia, cutaneous rash and absence of respiratory symptoms) and two laboratory results (leukopenia and hypertransaminasemia), provides a useful tool to help diagnose arboviral infections and appropriately activate vector control measures in order to avoid local transmission.

Identifiants

pubmed: 33158274
pii: microorganisms8111731
doi: 10.3390/microorganisms8111731
pmc: PMC7716211
pii:
doi:

Types de publication

Journal Article

Langues

eng

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Auteurs

Iacopo Vellere (I)

Department of Experimental and Clinical Medicine, University of Florence, 50134 Florence, Italy.

Filippo Lagi (F)

Department of Experimental and Clinical Medicine, University of Florence, 50134 Florence, Italy.
Infectious and Tropical Diseases Unit, Careggi University Hospital, 50134 Florence, Italy.

Michele Spinicci (M)

Department of Experimental and Clinical Medicine, University of Florence, 50134 Florence, Italy.
Referral Centre for Tropical Diseases of Tuscany, Infectious and Tropical Diseases Unit, Careggi University Hospital, 50134 Florence, Italy.

Antonia Mantella (A)

Department of Experimental and Clinical Medicine, University of Florence, 50134 Florence, Italy.

Elisabetta Mantengoli (E)

Infectious and Tropical Diseases Unit, Careggi University Hospital, 50134 Florence, Italy.

Giampaolo Corti (G)

Department of Experimental and Clinical Medicine, University of Florence, 50134 Florence, Italy.
Infectious and Tropical Diseases Unit, Careggi University Hospital, 50134 Florence, Italy.

Maria Grazia Colao (MG)

Clinical Microbiology and Virology Unit, Careggi University Hospital, 50134 Florence, Italy.

Federico Gobbi (F)

Department of Infectious/Tropical Diseases and Microbiology, IRCCS Sacro Cuore Don Calabria Hospital, 37024 Negrar, Verona, Italy.

Gian Maria Rossolini (GM)

Department of Experimental and Clinical Medicine, University of Florence, 50134 Florence, Italy.
Clinical Microbiology and Virology Unit, Careggi University Hospital, 50134 Florence, Italy.

Alessandro Bartoloni (A)

Department of Experimental and Clinical Medicine, University of Florence, 50134 Florence, Italy.
Referral Centre for Tropical Diseases of Tuscany, Infectious and Tropical Diseases Unit, Careggi University Hospital, 50134 Florence, Italy.

Lorenzo Zammarchi (L)

Department of Experimental and Clinical Medicine, University of Florence, 50134 Florence, Italy.
Referral Centre for Tropical Diseases of Tuscany, Infectious and Tropical Diseases Unit, Careggi University Hospital, 50134 Florence, Italy.

Classifications MeSH