AI Article Synopsis

  • Human monocytotropic ehrlichiosis (HME) is a tick-borne infection primarily caused by the bacteria Ehrlichia chaffeensis, with most data sourced from case studies rather than clinical trials.
  • HME is predominantly reported in North America, presenting as a fever and often accompanied by low platelet and white blood cell counts, along with abnormal liver tests; it significantly affects immunocompromised individuals.
  • Complications like acute respiratory distress syndrome and multi-organ failure are more common in immunocompromised patients, leading to a higher fatality rate of 16.3% compared to 9.9% in immunocompetent cases, although long-term effects are rare.

Article Abstract

Human monocytotropic ehrlichiosis (HME) is a tick-borne bacterial infection caused by Ehrlichia chaffeensis. Most available data come from case reports, case series and retrospective studies, while prospective studies and clinical trials are largely lacking. To obtain a clearer picture of the currently known epidemiologic distribution, clinical and paraclinical presentation, diagnostic aspects, complications, therapeutic aspects, and outcomes of HME, we systematically reviewed the literature and analyzed and summarized the data. Cases of HME are almost exclusively reported from North America. Human infections due to other (non-chaffeensis) Ehrlichia spp. are rare. HME primarily presents as an unspecific febrile illness (95% of the cases), often accompanied by thrombocytopenia (79.1% of the cases), leukopenia (57.8% of the cases), and abnormal liver function tests (68.1% of the cases). Immunocompromized patients are overrepresented among reviewed HME cases (26.7%), which indicates the role of HME as an opportunistic infection. The incidence of complications is higher in immunocompromized compared to immunocompetent cases, with ARDS (34% vs 19.8%), acute renal failure (34% vs 15.8%), multi organ failure (26% vs 14.9%), and secondary hemophagocytic lymphohistiocytosis (26% vs 14.9%) being the most frequent reported. The overall case fatality is 11.6%, with a significant difference between immunocompetent (9.9%) and immunocompromized (16.3%) cases, and sequelae are rare (4.2% in immunocompetent cases, 2.5% in immunocompromised cases).

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11324158PMC
http://dx.doi.org/10.1371/journal.pntd.0012377DOI Listing

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