# The challenging diagnosis of ICU-related Mesenteric Ischaemia: a prospective, observational, multicentre cohort

**Authors:** Stefan Andrei, Jerome Allyn, Nicolas Allou, Sonia Yung, Gabriel Stefan, Peter Matthews, Mathieu Desmard, Laura Federici, Yves Castier, Lara Ribeiro Parenti, Philippe Montravers, Pascal Augustin

PMC · DOI: 10.1016/j.aicoj.2026.100028 · Annals of Intensive Care · 2026-01-21

## TL;DR

This study explores how to better predict necrotic bowel in ICU patients suspected of having acute mesenteric ischemia by combining clinical and biological factors.

## Contribution

The study is the first to propose a combined approach using multiple clinical and biological parameters to predict necrotic bowel in ICU patients with suspected AMI.

## Key findings

- Age, active fluid removal, gastrointestinal injury signs, and lactate dehydrogenase levels were independently associated with necrotic bowel.
- Lactate dehydrogenase showed the highest diagnostic accuracy among biomarkers.
- Surgical exploration is recommended for ICU patients with gastrointestinal injury signs and fluid removal or renal replacement therapy.

## Abstract

The diagnosis of acute mesenteric ischemia (AMI) is challenging, especially in the intensive care unit (ICU), where non-occlusive mesenteric ischemia (NOMI) predominates. In ICU patients, contrast-enhanced computed tomography (CT) provides limited diagnostic accuracy, and no single biomarker is sufficiently reliable. Transmural digestive necrosis, revealed as necrotic bowel (NB) during surgical exploration, is irreversible and requires bowel resection. We proposed an approach combining several clinical, biological, and therapeutic parameters to predict the presence of NB in ICU patients with high suspicion of AMI.

We conducted a prospective observational study in three ICUs. All consecutive patients with suspected AMI were enrolled. Patients with NB identified during surgical exploration were compared with those without NB. Patients who survived without undergoing surgery were considered not to have NB. Multivariable logistic regression analysis was used to identify parameters independently associated with NB.

A total of 202 patients were included. Among them, 74 (37%) had NB (including 70 with NOMI and 4 with occlusive AMI), while 128 (63%) did not. In the multivariable analysis, age (OR 1.068, 95% CI 1.027–1.111, p = 0.001), active fluid removal (OR 3.148 (1.19−8.33), p = 0.021), signs of gastrointestinal injury (3.432 (1.082−10.885), p = 0.036), need for renal replacement therapy (OR 3.834 (1.457−10.01), p = 0.006), and lactate dehydrogenase (log) at the time of AMI suspicion (OR 7.135 (2.1−24.235) p = 0.002) were independently associated with NB. Among biomarkers, lactate dehydrogenase, showed the highest area under the ROC curve.

This is the first study to propose a combined approach for predicting NB in ICU patients with suspected AMI. When AMI is highly suspected, surgical exploration should be considered in patients presenting with signs of gastrointestinal injury in a context of fluid removal or renal replacement therapy, as these findings are strongly suggestive of necrotic bowel.

## Full-text entities

- **Genes:** CMPK1 (cytidine/uridine monophosphate kinase 1) [NCBI Gene 51727] {aka CK, CMK, CMPK, UMK, UMP-CMPK, UMPK}, SLC17A5 (solute carrier family 17 member 5) [NCBI Gene 26503] {aka AST, ISSD, NSD, SD, SIALIN, SIASD}, FABP2 (fatty acid binding protein 2) [NCBI Gene 2169] {aka FABPI, I-FABP}, GPT (glutamic--pyruvic transaminase) [NCBI Gene 2875] {aka AAT1, ALT, ALT1, GPT1, SGPT}
- **Diseases:** colonic ischaemia (MESH:D003108), acute abdomen (MESH:D000006), necrosis (MESH:D009336), Coronary Artery Disease (MESH:D003324), abdominal conditions (MESH:D000007), acute organ dysfunctions (MESH:D019965), cardiovascular conditions (MESH:D002318), CKD (MESH:D012080), GI injury (MESH:D005767), Atrial Fibrillation (MESH:D001281), occlusive MI (MESH:D001157), death (MESH:D003643), melena (MESH:D008551), burns (MESH:D002056), non (MESH:C580335), paralytic ileus (MESH:D007418), ischaemia (MESH:D007511), diarrhea (MESH:D003967), Organ Failure (MESH:D009102), AMI (MESH:D065666), abdominal pain (MESH:D015746), Chronic Kidney Disease (MESH:D051436), acute pancreatitis (MESH:D010195), Failure (MESH:D051437), Non-occlusive mesenteric ischaemia (MESH:D008641), shock (MESH:D012769), NB (MESH:D012778)
- **Chemicals:** creatinine (MESH:D003404), catecholamines (MESH:D002395), D-lactate (-), citrulline (MESH:D002956), lactate (MESH:D019344), bilirubin (MESH:D001663)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## References

37 references — full list in the complete paper: https://tomesphere.com/paper/PMC12934417/full.md

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Source: https://tomesphere.com/paper/PMC12934417