Ward based goal directed fluid therapy (GDFT) in acute pancreatitis (GAP) trial: A feasibility randomised controlled trial

医学 冲程容积 心输出量 随机对照试验 血流动力学 心率 麻醉 血压 急性胰腺炎 重症监护室 心脏病学 外科 内科学
作者
Farid Froghi,Fiammetta Soggiu,Federico Ricciardi,Cecilia Vindrola‐Padros,Lefteris Floros,Daniel Martín,Helder Filipe,M Varcada,Kurinchi Selvan Gurusamy,Satya Bhattacharya,Angela Fanshawe,Bogdan Delcea,Pawan Mathur,Brian R Davidson,Jonathan Costello,Dimitrios Tzelis,Christine Eastgate,Maria Jose Ciaponi,Margaret McNeil,Sara Mingo Garcia,Glykeria Pakou,Otto Schwalowsky-Monks,Gretchelle Asis,Atokoleka Osakanu,Rebekkah Troller,Nikolaos Dimitrokallis,Stephanos Pericleous,Amjad Khalil,Aliza Abeles,Charles W. Rees,Khalid Shakir Abdul-kareem,Mavroudis Voultsos
出处
期刊:International Journal of Surgery [Wolters Kluwer]
卷期号:104: 106737-106737 被引量:10
标识
DOI:10.1016/j.ijsu.2022.106737
摘要

Goal-directed fluid therapy (GDFT) reduces complications in patients undergoing major general surgery. There are no reports of cardiac output evaluation being used to optimise the fluid administration for patients with acute pancreatitis (AP) in a general surgery ward. 50 patients with AP were randomised to either ward-based GDFT (n = 25) with intravenous (IV) fluids administered based on stroke volume optimisation protocol or standard care (SC) (n = 25), but with blinded cardiac output evaluation, for 48-h following hospital admission. Primary outcome was feasibility. 50 of 116 eligible patients (43.1%) were recruited over 20 months demonstrating feasibility. 36 (72%) completed the 48-h of GDFT; 10 (20%) discharged within 48-h and 4 withdrawals (3 GDFT, 1 SC). Baseline characteristics were similar with only 3 participants having severe disease (6%, 1 GDFT, 2 SC). Similar volumes of IV fluids were administered in both groups (GDFT 5465 (1839) ml, SC 5211 (1745) ml). GDFT group had a lower heart rate, blood pressure and respiratory rate and improved oxygen saturations. GDFT was not associated with any harms. There was no evidence of difference in complications of AP (GDFT 24%, SC 32%) or in the duration of stay in intensive care (GDFT 0 (0), SC 0.7 (3) days). Length of hospital stay was 5 (2.9) days in GDFT and 6.3 (7.6) in SC groups. Ward-based GDFT is feasible and shows a signal of possible efficacy in AP in this early-stage study. A larger multi-site RCT is required to confirm clinical and cost effectiveness.
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