# Abdominal Compartment Syndrome Following Massive Transfusion in Upper Gastrointestinal Bleeding: A Case Report

**Authors:** Hudson Martins de Brito, Tiago de Almeida Macruz, Gisele J Wakim, Livia Dahmen Rodrigues, Arman Dagal

PMC · DOI: 10.7759/cureus.102969 · Cureus · 2026-02-04

## TL;DR

A patient with upper gastrointestinal bleeding developed severe abdominal compartment syndrome after massive transfusion, leading to multiple complications and highlighting the need for vigilance in such cases.

## Contribution

This case report highlights the rare but critical occurrence of abdominal compartment syndrome following massive transfusion in upper gastrointestinal bleeding.

## Key findings

- The patient developed intra-abdominal pressure of 85 mmHg, confirming severe abdominal compartment syndrome.
- Emergency decompressive laparotomy improved ventilatory parameters but the patient developed renal failure and ARDS.
- The case underscores the importance of clinical vigilance in patients undergoing massive transfusion.

## Abstract

Abdominal compartment syndrome (ACS) is defined as sustained intra-abdominal pressure (IAP) exceeding 20 mmHg, leading to organ hypoperfusion and dysfunction. Although most cases arise from intra-abdominal or retroperitoneal hemorrhage, ACS may also occur after massive transfusion due to capillary leak and fluid overload. We describe an 82-year-old man presenting with upper gastrointestinal bleeding from a duodenal ulcer who required massive transfusion. During resuscitation, he developed progressive ventilatory failure with rising airway pressures and refractory hypoxemia. Intra-vesical IAP measured 85 mmHg, confirming severe ACS. Emergency decompressive laparotomy evacuated over two liters of serous fluid and revealed a markedly distended bowel filled with intraluminal blood but no hemoperitoneum. Ventilatory parameters improved immediately after decompression. Despite timely surgical intervention and intensive supportive care, the patient developed renal failure, acute respiratory distress syndrome (ARDS), methicillin-resistant Staphylococcus aureus pneumonia, and progressive neurological decline, ultimately leading to transition to comfort measures. Although such presentations are uncommonly reported, this case highlighted the critical importance of maintaining high clinical vigilance in patients undergoing massive transfusion, particularly when acute respiratory deterioration occurs.

## Linked entities

- **Diseases:** renal failure (MONDO:0001106), acute respiratory distress syndrome (MONDO:0006502)

## Full-text entities

- **Genes:** ALB (albumin) [NCBI Gene 213] {aka FDAHT, HSA, PRO0883, PRO0903, PRO1341}, IAPP (islet amyloid polypeptide) [NCBI Gene 3375] {aka DAP, IAP}
- **Diseases:** impairment of the renal, gastrointestinal, cardiovascular, (MESH:D005767), effusions (MESH:D000080324), infection (MESH:D007239), cardiovascular or ventilatory deterioration (MESH:D002318), coagulopathy (MESH:D001778), acidosis (MESH:D000138), capillary leak (MESH:D019559), reperfusion injury (MESH:D015427), hypothermia (MESH:D007035), ascites (MESH:D001201), ruptured abdominal aortic aneurysm (MESH:D017544), anemia (MESH:D000740), melena (MESH:D008551), encephalopathy (MESH:D001927), fistula (MESH:D005402), sepsis (MESH:D018805), neuromuscular blockade (MESH:D020879), UGIB (MESH:D006471), Staphylococcus aureus (MESH:D013203), intra-abdominal bleeding (MESH:D000082122), abdominal distension (MESH:D000007), embolization (MESH:D004617), respiratory systems (MESH:D015619), dysfunction (MESH:D006331), renal failure (MESH:D051437), oliguria (MESH:D009846), edema (MESH:D004487), acute pancreatitis (MESH:D010195), blood loss (MESH:D016063), lung injury (MESH:D055370), pneumoperitoneum (MESH:D011027), ACS (MESH:D059325), abdominal pain (MESH:D015746), duodenal ulcer (MESH:D004381), hemoperitoneum (MESH:D006465), variceal bleeding (MESH:D014648), hematoma (MESH:D006406), critically ill (MESH:D016638), trauma (MESH:D014947), ARDS (MESH:D012128), duodenal diverticulum (MESH:D004382), hypotension (MESH:D007022), neurological decline (MESH:D009461), burn (MESH:D002056), esophagitis (MESH:D004941), hypoxemia (MESH:D000860), multi-organ dysfunction (MESH:D009102), Bleeding (MESH:D006470), artery extravasation (MESH:D005119), opacities (MESH:D003318), respiratory deterioration (MESH:D012131), hematemesis (MESH:D006396), pneumonia (MESH:D011014), ruptured aneurysm (MESH:D017542), hypercapnia (MESH:D006935)
- **Chemicals:** ceftriaxone (MESH:D002443), HCO3- (MESH:D001639), PRBC (-), pO2 (MESH:C093415), carbon dioxide (MESH:D002245), oxygen (MESH:D010100), octreotide (MESH:D015282), methicillin (MESH:D008712)
- **Species:** Staphylococcus aureus (species) [taxon 1280], Homo sapiens (human, species) [taxon 9606]

## Full text

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## References

19 references — full list in the complete paper: https://tomesphere.com/paper/PMC12966945/full.md

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Source: https://tomesphere.com/paper/PMC12966945