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Published on: March 7, 2017
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Effect of Time Since Death on Multipathogen Molecular Test Results of Postmortem Specimens Collected Using Minimally
Jeanette Dawa1,2, Edwin Walong2, Clayton Onyango3
1Washington State University, Global Health Programs (Kenya Office), Nairobi, Kenya.
Summary
Minimally invasive tissue sampling (MITS) can detect pathogens in respiratory illness deaths up to 4 days postmortem. However, inconsistent pathogen detection requires careful interpretation for determining causes of death.
Area of Science:
- Forensic pathology
- Molecular diagnostics
- Pediatric infectious diseases
Background:
- Respiratory illness is a leading cause of death in young children.
- Accurate determination of the cause of death is crucial for public health surveillance.
- Postmortem diagnostics face challenges related to tissue degradation over time.
Purpose of the Study:
- To evaluate the impact of postmortem interval on molecular pathogen detection using MITS.
- To assess the feasibility of MITS for pathogen identification in pediatric respiratory deaths.
- To determine the optimal window for sample collection after death.
Main Methods:
- Minimally invasive tissue sampling (MITS) was performed on 20 children (1-59 months) who died from respiratory illness.
- Serial lung, liver, and blood samples were collected at intervals up to 72 hours postmortem.
- Multipathogen TaqMan® array cards (TACs) were used for molecular pathogen detection.
Main Results:
- A median of 3 pathogens were detected in lung tissue, 3 in liver, and 2 in blood.
- No significant association was found between postmortem interval and the number of pathogens detected.
- Specimen suitability for testing was maintained throughout the 72-hour collection period.
Conclusions:
- MITS allows for pathogen detection in lung, liver, and blood samples up to 4 days postmortem in refrigerated bodies.
- Inconsistent pathogen detection necessitates caution when attributing etiologic causes of death based solely on molecular findings.
- Further research is needed to optimize molecular diagnostic protocols for postmortem samples.

