Skip to content

Diagnosis of Lymphohistiocytic Hemophagocytosis in Intensive Care

Diagnosis of Lymphohistiocytic Hemophagocytosis in Intensive Care: Relevance of the Hscore and Search for the Best Diagnostic Markers

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT07343037
Acronym
SAMICU
Enrollment
100
Registered
2026-01-15
Start date
2025-08-29
Completion date
2026-08-29
Last updated
2026-01-15

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Cirrhosis, Liver, Hepatic Insufficiency

Keywords

Hepatic Insufficiency, Cirrhosis, Liver, Lymphohistiocytic hemophagocytosis, Hepatocellular insufficiency, Invasive aspergillosis, Azole antifungals, Liver dysfunction.

Brief summary

Patients with hepatocellular insufficiency and/or cirrhosis are at risk of developing invasive fungal infections, particularly in critical care settings. In international recommendations, voriconazole is positioned as the first-line treatment for invasive aspergillosis. However, this molecule-and the azole class of antifungals-is associated with frequent hepatic toxicity. Available since 2018, isavuconazole appears to be better tolerated in patients without pre-existing liver dysfunction. The aim of this study is to retrospectively evaluate the validity of the hscore in intensive care and resuscitation patients.

Interventions

None listed

Sponsors

University Hospital, Strasbourg, France
Lead SponsorOTHER

Study design

Observational model
CASE_ONLY
Time perspective
RETROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Adult patient (≥18 years old) * Patient admitted to the intensive care unit at Hautepierre Hospital, Strasbourg University Hospital, between January 1, 2014, and December 31, 2024 * At least 3 biological signs of HLH: * ferritin \> 2000 ng/mL * triglycerides \> 1.5 g/L * at least one cytopenia (leukocytes ≤ 5000 G/L, platelets ≤ 110 G/L, hemoglobin ≤ 9.2 g/dL).

Exclusion criteria

Refusal to participate in the study

Design outcomes

Primary

MeasureTime frameDescription
hscoreUp to 12 monthsThe HScore adds up points assigned to 9 clinical, biological, and histological criteria: The higher the total score, the greater the likelihood of HLH: Possible total score: 0 to 337: HScore: Probability of HLH: \< 90 points → Very low * 130 points → ≈ 10-20% 168 points → high probability of HL

Countries

France

Contacts

Primary ContactAntonin HUGEROT, MD
antonin.hugerot@chru-strasbourg.fr33 3 88 12 79 24

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026