ISSN 2979-8582 · Article No. 081
Funke Florence AKEREDOLU: Afe Babalola University, Ado-Ekiti, Department of Medical Laboratory Science, Faculty of Medicine and Health Sciences, Nigeria
Victor Olukayode EKUNDINA: Afe Babalola University, Ado-Ekiti, Department of Medical Laboratory Science, Faculty of Medicine and Health Sciences, Nigeria
Idowu Emmanuel AKEREDOLU: Federal University of Technology, Department of Physics, School of Physical Sciences, Akure, Ondo State, Nigeria
Oluwagbenga Tosin ALADE: Federal University of Technology, Department of Physics, School of Physical Sciences, Akure, Ondo State, Nigeria
Mary Olajumoke ADELODUN: Hospital Management Board, State Specialist Hospital, Ikere-Ekiti, Nigeria
Olubunmi Kikelomo OGUNDARE: Hospital Management Board, State Specialist Hospital, Ikere-Ekiti, Nigeria
ORCID
Funke Florence AKEREDOLU 0000-0001-7839-0676
Victor Olukayode EKUNDINA 0000-0001-5274-0949
Idowu Emmanuel AKEREDOLU 0009-0009-2633-714X
Oluwagbenga Tosin ALADE 0009-0008-7957-458X
Mary Olajumoke ADELODUN 0009-0005-5576-394X
Olubunmi Kikelomo OGUNDARE 0009-0008-8517-032X
Background: Septic shock is a time-critical medical emergency with mortality escalating exponentially for every hour targeted antimicrobial therapy is delayed. Microbiological diagnostic cultures represent the definitive standard for pathogen identification and targeted therapy. However, delayed processing, improper critical-value reporting, or missed diagnostic reports present serious medico-legal vulnerabilities. Methodology: A narrative search across Medline, Scopus, PubMed, and legal commentary databases synthesized clinical protocols, microbiology lab turnaround metrics, and malpractice litigation case law concerning diagnostic delays in sepsis. Results: Legal analysis demonstrates that while empirical antibiotic administration is the clinical baseline, failure to escalate, modify, or audit diagnostic cultures constitutes a breach of the standard of care. Institutional negligence frequently centers on communication breakdowns—specifically the failure of diagnostic laboratories to transmit urgent "critical values" (e.g., positive blood cultures) directly to ordering clinicians. Conclusion: Bridging the gap between microbiological laboratory timelines and clinical execution requires standardized critical-value reporting protocols, automated EHR alerting systems, and clear institutional legal frameworks governing shared diagnostic responsibility.
Keywords
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British Journal of Contemporary Research
Open Access · Peer Reviewed · Published by Bexford Publishing Ltd
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