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Commentary: Perioperative blood loss is a risk factor for postoperative delirium in geriatric hip fracture patients: a retrospective study

Abstract:
We commend Deng and colleagues for providing a timely and clinically relevant analysis of postoperative delirium (POD) in older adults undergoing hip fracture surgery (1). Prior work has long suggested an association between intraoperative physiological disturbance and delirium risk, but often lacked the granularity achieved here (2).The demonstration of a relationship between perioperative blood loss and POD risk is striking and warrants careful clinical interpretation. However, additional nuance is needed before blood loss can be viewed as an independent causal factor rather than a marker of underlying vulnerability. Patients who bleed more during hip fracture surgery are often those inherently more susceptible to delirium. In addition, several determinants of increased intraoperative bleeding are also well-established risk factors for delirium. (3) Pre-existing anticoagulation and antiplatelet therapy represent an important omission in this study. Many older adults with atrial fibrillation, coronary artery disease or peripheral vascular disease receive anticoagulation or antiplatelet therapy, all of which increase perioperative bleeding risk. These therapies also tend to cluster with conditions characterised by impaired cerebral autoregulation and vascular insufficiency, both contributors to delirium vulnerability (4). Without accounting for these medications, the association between blood loss and POD may instead reflect these underlying factors rather than blood loss itself. Frailty, sarcopenia, malnutrition and reduced physiological reserve also increase both bleeding tendency and delirium susceptibility. Frail individuals have reduced circulating volume, diminished haemostatic capacity and heightened inflammatory responses, all of which are strongly predictive of POD (3,5,6). However, no frailty index, cognitive baseline, functional status or nutritional marker was included. Similarly, the absence of fracture type or surgical approach introduces residual confounding, as unstable fractures are associated with greater blood loss and occur in individuals with her co-morbidity burden. Another important consideration is transfusion. The method used to calculate total blood loss incorporates transfused volume, yet transfusion was not analysed independently. Prior studies demonstrate that transfusion is itself associated with POD through inflammatory activation and endothelial dysfunction (3,8). Without separating the effects of anaemia, tissue hypoxia and transfusion-related mechanisms, it is difficult to determine the true mediator of delirium risk. Despite these limitations, Deng and colleagues are to be congratulated for highlighting a clinically important perioperative factor. Their work reinforces the close link between intraoperative physiology and postoperative cognitive outcomes and provides a useful foundation for future studies incorporating frailty, anticoagulation status, fracture complexity and transfusion dynamics.
Publication status:
Published
Peer review status:
Peer reviewed

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Publisher copy:
10.3389/fmed.2026.1753996

Authors

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Institution:
University of Oxford
Division:
MSD
Department:
Oncology
Sub department:
Oncology
Role:
Author


Publisher:
Frontiers Media
Journal:
Frontiers in Medicine More from this journal
Volume:
13
Article number:
1753996
Publication date:
2026-04-23
Acceptance date:
2026-04-06
DOI:
EISSN:
2296-858X
ISSN:
2296-858X


Language:
English
Keywords:
Subtype:
Comment
Source identifiers:
4021771
Deposit date:
2026-05-07
ARK identifier:
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