PMID- 38223849 OWN - NLM STAT- PubMed-not-MEDLINE LR - 20240116 IS - 2666-688X (Electronic) IS - 2666-688X (Linking) VI - 61 DP - 2024 TI - The Impact of Intra-Operative Heparin on Thromboembolism and Death in a Matched Cohort of Patients with a Ruptured Abdominal Aortic Aneurysm. PG - 20-26 LID - 10.1016/j.ejvsvf.2023.11.004 [doi] AB - OBJECTIVE: Portuguese nationwide estimates indicate that 20% of abdominal aortic aneurysms (AAAs) are treated when ruptured. In these cases, intra-operative unfractionated heparin (UFH) usage rates vary widely. Evidence on this topic is scarce and focused on patients treated by open repair (OSR). The aim was to determine the influence of UFH on peri-operative thromboembolic events (TEs) and death in a cohort of ruptured AAA (rAAA). METHODS: Retrospective, single-centre, comparative study. From 2011 to April 2023, all consecutive rAAAs (endovascular repair [EVAR] and OSR) were considered. Primary outcomes were 30-day TE free survival and TE rates. The secondary outcome was 30-day death. Safety endpoints were procedural blood loss, blood product requirements, and secondary interventions due to haemorrhage. Using propensity score matching (PSM) each UFH patient was matched with one no UFH patient in a 1:1 ratio. RESULTS: The study included 250 patients. After PSM, 190 patients were analysed (EVAR: 60.0% no-UFH vs. 64.4% UFH). TE free survival estimates favoured the UFH group (67.3% vs. 47.2%, p = .009; UFH adjusted odds ratio [aOR] 2.01, 95% confidence interval [CI] 1.04-4.17). TEs were more frequent in the no UFH group (20.0% vs. 44.2% patients, p < .001; UFH aOR 0.31, 95% CI 0.15-0.65 for any TE), driven by an increase in bowel ischaemia (17.9% no UFH vs. 3.2% UFH, p = .001). Most events occurred in the first 72 hours. EVAR was associated with reduced TE and improved TE free survival (aOR 0.20, 95% CI 0.09-0.45 and aOR 5.54, 95% CI 2.34-13.08, respectively). No significant differences in 30-day survival were noted (75% no-UFH vs. 83% UFH, p = .26; aOR 1.08, 95% CI 0.48-2.43) nor in blood loss, peri-operative red blood cell and fresh frozen plasma requirements, or secondary interventions due to haemorrhage (p = .10; p = .11; p = .13 and p = .18 respectively). CONCLUSION: In this cohort, intra-operative UFH was safe and associated with improved TE free survival, driven by a reduction in bowel ischaemia. Conversely, mortality remained unaffected. Randomised controlled trials are required to confirm these findings. CI - (c) 2023 The Author(s). FAU - Ribeiro, Tiago F AU - Ribeiro TF AD - Hospital de Santa Marta, Centro Hospitalar Universitario de Lisboa Central, Lisboa, Portugal. FAU - Correia, Ricardo AU - Correia R AD - Hospital de Santa Marta, Centro Hospitalar Universitario de Lisboa Central, Lisboa, Portugal. FAU - Soares Ferreira, Rita AU - Soares Ferreira R AD - Hospital de Santa Marta, Centro Hospitalar Universitario de Lisboa Central, Lisboa, Portugal. AD - NOVA Medical School|Faculdade de Ciencias Medicas, NMS|FCM, Universidade NOVA de Lisboa, Lisbon, Portugal. FAU - Bastos Goncalves, Frederico AU - Bastos Goncalves F AD - Hospital de Santa Marta, Centro Hospitalar Universitario de Lisboa Central, Lisboa, Portugal. AD - NOVA Medical School|Faculdade de Ciencias Medicas, NMS|FCM, Universidade NOVA de Lisboa, Lisbon, Portugal. AD - Hospital CUF Tejo, Lisbon, Portugal. FAU - Amaral, Carlos AU - Amaral C AD - Hospital de Santa Marta, Centro Hospitalar Universitario de Lisboa Central, Lisboa, Portugal. FAU - Ferreira, Maria Emilia AU - Ferreira ME AD - Hospital de Santa Marta, Centro Hospitalar Universitario de Lisboa Central, Lisboa, Portugal. LA - eng PT - Journal Article DEP - 20231124 PL - England TA - EJVES Vasc Forum JT - EJVES vascular forum JID - 101766732 PMC - PMC10784139 OTO - NOTNLM OT - Abdominal aortic aneurysm OT - Event free survival OT - Ruptured aortic aneurysms OT - Thromboembolism OT - Unfractionated heparin COIS- Frederico Bastos Goncalves has received speaker and proctoring fees from W.L. Gore, Medtronic, and Cook Medical. EDAT- 2024/01/15 06:42 MHDA- 2024/01/15 06:43 PMCR- 2023/11/24 CRDT- 2024/01/15 04:55 PHST- 2023/07/17 00:00 [received] PHST- 2023/10/17 00:00 [revised] PHST- 2023/11/19 00:00 [accepted] PHST- 2024/01/15 06:43 [medline] PHST- 2024/01/15 06:42 [pubmed] PHST- 2024/01/15 04:55 [entrez] PHST- 2023/11/24 00:00 [pmc-release] AID - S2666-688X(23)00091-6 [pii] AID - 10.1016/j.ejvsvf.2023.11.004 [doi] PST - epublish SO - EJVES Vasc Forum. 2023 Nov 24;61:20-26. doi: 10.1016/j.ejvsvf.2023.11.004. eCollection 2024.