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A Murine Model of Dengue Virus-induced Acute Viral Encephalitis-like Disease
Published on: April 28, 2019
Crimean-Congo hemorrhagic fever in a dengue-endemic region: lessons for the future
Farheen Ali1, Taimur Saleem, Umair Khalid
1Department of Medicine, Aga Khan University, Karachi, Pakistan. farheen.ali@aku.edu
Insights
Differentiating Crimean-Congo hemorrhagic fever and dengue hemorrhagic fever is challenging due to similar symptoms. Early diagnosis and increased surveillance are crucial for better patient outcomes and cost containment in Pakistan.
Area of Science:
- Epidemiology
- Infectious Diseases
- Public Health
Background:
- Crimean-Congo hemorrhagic fever (CCHF) and dengue hemorrhagic fever (DHF) are endemic in Pakistan.
- Overlapping geographic distribution and early clinical presentations complicate differential diagnosis.
- Accurate early diagnosis is critical for effective patient management and public health interventions.
Observation:
- A 16-year-old male presented with hematemesis and high-grade fever, initially suspected as DHF.
- Despite supportive care, the patient's condition deteriorated; Dengue IgM was negative.
- The patient expired; CCHF viral RNA PCR results confirmed CCHF post-mortem.
Findings:
- Delayed diagnosis of CCHF led to significant resource expenditure on contact tracing and ribavirin prophylaxis for healthcare workers.
- The case highlights the diagnostic challenges posed by co-endemic viral hemorrhagic fevers.
- Late confirmation of CCHF underscores the need for rapid diagnostic tools.
Implications:
- Early recognition and treatment of CCHF are vital to mitigate financial and health burdens on contacts, especially healthcare workers in developing countries.
- Enhanced surveillance for both CCHF and DHF is necessary to develop reliable, cost-effective diagnostic predictors.
- Improved diagnostic strategies can lead to better case management and cost containment in resource-limited settings.
Abstract:
Crimean-Congo hemorrhagic fever and dengue hemorrhagic fever are endemic in Pakistan. However, the overlap of geographic distribution and early clinical features between the two conditions make a reliable diagnosis difficult in the initial stage of illness. A 16-year-old boy presented with a history of hematemesis and high-grade fever. A preliminary diagnosis of dengue hemorrhagic fever was made and supportive treatment was instituted; however, the patient continued to deteriorate clinically. Dengue IgM antibody testing was negative on the third day of admission. Qualitative polymerase chain reaction test for Crimean-Congo hemorrhagic fever viral RNA was sent but the patient expired shortly after the results became available on the sixth day of admission. Considerable resources had to be expended on contact tracing and administration of ribavirin prophylaxis to all the health-care workers who had come in contact with the patient. It is crucial that Crimean-Congo hemorrhagic fever be recognized and treated at an early stage because of longer term financial and health implications for contacts such as health-care workers in the setting of a developing country. Increased surveillance of dengue and Crimean-Congo hemorrhagic fever cases is warranted for the derivation of reasonably reliable, cost-effective and prompt predictors of disease diagnosis. These predictors can help guide future decisions in the management of similar cases. Ultimately, such a strategy may translate into better cost containment in resource-poor settings. Institution of ribavirin prophylaxis in selected patients also merits consideration.
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