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Characterising the Loss of Haemostasis in Haemorrhagic Fever With Renal Syndrome

L

Liverpool School of Tropical Medicine

Status

Not yet enrolling

Conditions

Haemorrhagic Fever With Renal Syndrome

Treatments

Other: Severity score calculation
Procedure: Blood draw for thromboelastography - admission
Procedure: Blood draw for transcriptomic analysis
Procedure: Blood draw for thromboelastography - follow-up
Other: Data collection - clinical/demographic/epidemiological data
Other: Data collection - routine laboratory parameters

Study type

Observational

Funder types

Other

Identifiers

Details and patient eligibility

About

Hantaviruses are globally distributed viruses that cause haemorrhagic fever with renal syndrome (HFRS) in Europe, a disease characterised by acute kidney failure and, in some cases, significant bleeding complications. The mechanisms underlying clotting abnormalities in HFRS remain poorly understood. This study aims to investigate the pathological mechanisms of clotting dysfunction in hospitalised HFRS patients, assess the impact of different hantavirus types on disease severity, and evaluate the accuracy of a severity scoring system developed in China for predicting mortality in European patients.

Hospitalised patients with laboratory-confirmed HFRS will be prospectively recruited from University Medical Centre Ljubljana, Slovenia. Blood samples will be analysed for routine laboratory markers, thromboelastography (TEG) will assess real-time clotting function, and transcriptomic analysis will identify hantavirus strains and gene expression patterns linked to disease severity. Patients will be stratified into haemorrhagic and non-haemorrhagic groups, with statistical analyses comparing clinical and laboratory parameters to identify predictors of bleeding risk. Findings from this study may contribute to improved risk stratification and potential therapeutic targets for HFRS.

Full description

Hantaviruses are globally distributed viruses that are transmitted to humans through the inhalation of viral particles found in the urine and faeces of infected rodents. In Europe, hantaviruses cause haemorrhagic fever with renal syndrome (HFRS), a disease characterised by acute kidney failure and, in some cases, significant bleeding complications. Despite advances in understanding HFRS, the mechanisms underlying these bleeding abnormalities remain poorly understood. Several hypotheses suggest that hantaviruses may interfere with the function of blood clotting factors, but definitive evidence is lacking.

Slovenia, a country in southern Europe, has one of the highest incidences of HFRS relative to its population, with recent years seeing large outbreaks. Discussions with leading hantavirus experts in Slovenia have highlighted the urgent need for further research, particularly to understand why some patients with HFRS develop severe bleeding complications. Currently, no licensed treatments exist for HFRS, raising concerns about future outbreaks, which are expected to become more frequent due to climate change. By investigating the mechanisms leading to clotting dysfunction, this study aims to identify potential targets for future therapeutic interventions.

This study will explore the pathological mechanisms driving clotting abnormalities and bleeding in hospitalised patients with HFRS. Additionally, it will assess whether different hantavirus types influence disease severity and haemorrhagic complications and evaluate the applicability of a severity scoring system-originally developed for HFRS cases in China-in predicting outcomes among Slovenian patients.

Patients with laboratory-confirmed HFRS will be prospectively recruited from University Medical Centre Ljubljana, Slovenia. Blood samples will be collected at multiple time points during their illness and tested for standard laboratory markers, including clotting factors, blood cell counts, kidney function, and liver function. Additionally, thromboelastography (TEG) will be performed to assess real-time clotting dynamics, providing a more detailed evaluation of clotting abnormalities.

An additional blood sample will undergo transcriptomic analysis using nanopore sequencing. This will identify the specific hantavirus strain in each patient and analyse gene expression patterns associated with disease severity and bleeding risk. Patients will also be assigned a severity score based on their clinical presentation, laboratory results, and symptoms, using a scoring system developed in China to predict HFRS-related mortality. This study will evaluate the reliability of this scoring system in a European cohort.

To better understand the factors contributing to bleeding in HFRS, patients will be categorised into two groups: those with haemorrhagic manifestations and those without. Statistical analyses will compare laboratory and clinical findings between these groups, aiming to identify key predictors of bleeding complications. The findings from this research may help inform future therapeutic strategies for HFRS.

Enrollment

62 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Patients aged 18 or older, including pregnant women
  • Laboratory-confirmed HFRS (serology and/or RT-PCR)
  • Willing and able to provide informed consent

Exclusion criteria

  • Patients under 18 years of age
  • Co-infections with other pathogens
  • Pre-existing coagulation disorders
  • Use of anticoagulant medication
  • Inability or refusal to provide consent

Trial design

62 participants in 2 patient groups

Non-haemorrhagic cases
Description:
This cohort will include laboratory confirmed cases of haemorrhagic fever with renal syndrome without any evidence of haemorrhagic manifestations.
Treatment:
Other: Data collection - routine laboratory parameters
Other: Data collection - clinical/demographic/epidemiological data
Procedure: Blood draw for thromboelastography - follow-up
Procedure: Blood draw for transcriptomic analysis
Other: Severity score calculation
Procedure: Blood draw for thromboelastography - admission
Haemorrhagic cases
Description:
This cohort will include laboratory confirmed cases of haemorrhagic fever with renal syndrome with evidence of haemorrhagic manifestations.
Treatment:
Other: Data collection - routine laboratory parameters
Other: Data collection - clinical/demographic/epidemiological data
Procedure: Blood draw for thromboelastography - follow-up
Procedure: Blood draw for transcriptomic analysis
Other: Severity score calculation
Procedure: Blood draw for thromboelastography - admission

Trial contacts and locations

0

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Central trial contact

Matthew J Riley, MBChB, MRes, DTMH, MRCP(UK)

Data sourced from clinicaltrials.gov

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